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Wyszukujesz frazę ""BRCA2 Protein genetics"" wg kryterium: Temat


Tytuł :
Tumour-infiltrating lymphocytes (TILs) and BRCA-like status in stage III breast cancer patients randomised to adjuvant intensified platinum-based chemotherapy versus conventional chemotherapy
Autorzy :
de Boo, Leonora
Pokaż więcej
Źródło :
In European Journal of Cancer March 2020 127:240-250
Czasopismo naukowe
Tytuł :
The predictive ability of the 313 variant–based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant
Autorzy :
Lakeman, Inge M. M.
Van Den Broek, Alexandra J.
Vos, Juliën A. M.
Barnes, Daniel R.
Adlard, Julian
Andrulis, Irene L.
Arason, Adalgeir
Arnold, Norbert
Arun, Banu K.
Balmaña, Judith
Barrowdale, Daniel
Giraud, Sophie
Golmard, Lisa
Hake, Christopher R.
Houdayer, Claude
Risch, Harvey A.
Lasset, Christine
Laurent, Maïté
Spurdle, Amanda B.
Hooning, Maartje J.
Hopper, John L.
Kets, Carolien M.
Leroux, Dominique
Longy, Michel
Mari, Véronique
Mazoyer, Sylvie
Mebirouk, Noura
Mortemousque, Isabelle
Blok, Marinus J.
Prieur, Fabienne
Hamann, Ute
Pujol, Pascal
Konstantopoulou, Irene
Heemskerk Gerritsen, Bernadette A. M.
Isaacs, Claudine
Saule, Claire
Piedmonte, Marion
Schuster, Helene
Sevenet, Nicolas
Sobol, Hagay
Sokolowska, Johanna
Gómez Garcia, Encarna B.
Venat Bouvet, Laurence
Claes, Kathleen B. M.
Ahmed, Munaza
Teixeira, Manuel R.
Barwell, Julian
Brady, Angela
Izatt, Louise
Hogervorst, Frans B. L.
Brennan, Paul
Harrington, Patricia A.
Henderson, Alex
Hodgson, Shirley
Kwong, Ava
Borg, Ake
Kennedy, M. John
Porteous, Mary E.
Rogers, Mark T.
Side, Lucy E.
Snape, Katie
Walker, Lisa
Collée, J. Margriet
Jakubowska, Anna
Couch, Fergus J.
Hahnen, Eric
Daly, Mary B.
Dennis, Joe
Teo, Soo Hwang
Jensen, Uffe Birk
Rantala, Johanna
Dhawan, Mallika
Benitez, Javier
Domchek, Susan M.
Eeles, Ros
Engel, Christoph
Legrand, Clémentine
Evans, D. Gareth
James, Paul A.
Feliubadaló i Elorza, Maria Lídia
Teulé-Vega, Àlex
Foretova, Lenka
Castera, Laurent
Friedman, Eitan
Frost, Debra
Rennert, Gad
Ganz, Patricia A.
Leslie, Goska
Garber, Judy
Hulick, Peter J.
Imyanitov, Evgeny N.
Glendon, Gord
Thomassen, Mads
Janavicius, Ramunas
Mulligan, Anna Marie
Hollestelle, Antoinette
Jager, Agnes
Koppert, Linetta B.
Cook, Jackie
Koudijs, Marco
Kriege, Mieke
Meijers Heijboer, Hanne E. J.
Schmutzler, Rita K.
Mensenkamp, Arjen R.
Dunning, Alison M.
Mooij, Thea M.
Oosterwijk, Jan C.
Caux Moncoutier, Virginie
Singer, Christian F.
Berthet, Pascaline
Caldés, Trinidad
Van den Ouweland, Ans M. W.
Van der Baan, Frederieke H.
Van der Hout, Annemieke H.
Van der Kolk, Lizet E.
Van der Luijt, Rob B.
Thull, Darcy L.
Van Deurzen, Carolien H. M.
Sharma, Priyanka
Van Doorn, Helena C.
Bignon, Yves Jean
Colas, Chrystelle
Van Engelen, Klaartje
Brewer, Carole
Van Hest, Liselotte P.
Van Os, Theo A. M.
Caligo, Maria A.
Verhoef, Senno
Tischkowitz, Marc
Vogel, Maartje J.
Wijnen, Juul T.
Lalloo, Fiona
Beesley, Jonathan
Fox, Stephen
Collonge Rame, Marie Agnès
Simard, Jacques
Holland, Helene
Jiao, Yue
John, Esther M.
Joseph, Vijai
Gerdes, Anne Marie
Karlan, Beth Y.
Lesueur, Fabienne
Loud, Jennifer T.
Lubiński, Jan
Manoukian, Siranoush
Mcguffog, Lesley
Miller, Austin
Coupier, Isabelle
Gomes, Denise Molina
Barouk Simonet, Emmanuelle
Montagna, Marco
Miller, Clare
Elan, Camille
Davidson, Rosemarie
Mouret Fourme, Emmanuelle
Gayther, Simon A.
Nathanson, Katherine L.
Neuhausen, Susan L.
Nevanlinna, Heli
Yie, Joanne Ngeow Yuen
Pauw, Antoine de
Olah, Edith
Morrison, Patrick J.
Olopade, Olufunmilayo I.
Van Asperen, Christi J.
Park, Sue K.
Parsons, Michael T.
Donaldson, Alan
Belotti, Muriel
Peterlongo, Paolo
Stadler, Zsofia
Stoppa Lyonnet, Dominique
Sutter, Christian
Ong, Kai Ren
Delnatte, Capucine
Tan, Yen Yen
Toland, Amanda E.
Tung, Nadine
Van Rensburg, Elizabeth J.
Vega, Ana
Wappenschmidt, Barbara
Devilee, Peter
Eason, Jacqueline
Chung, Wendy K.
Bernstein, Jonine L.
Offit, Kenneth
Aalfs, Cora M.
Hanson, Helen
Godwin, Andrew K.
Easton, Douglas F.
Bonadona, Valérie
Rookus, Matti A.
Chenevix-Trench, Georgia
Antoniou, Antonis C.
O’shaughnessy Kirwan, Aoife
Robson, Mark
Eccles, Diana M.
Schmidt, Marjanka K.
Adank, Muriel A.
Gemo Study Collaborators
Phillips, Kelly Anne
Embrace Collaborators
Ocgn Investigators
Goldgar, David E.
Hebon Investigators
Perkins, Jo
Kconfab Investigators
Bressac de Paillerets, Brigitte
Buecher, Bruno
Caputo, Sandrine
Ausems, Margreet G. E. M.
Gregory, Helen
Caron, Olivier
Faivre, Laurence
Fert Ferrer, Sandra
Gauthier Villars, Marion
Radice, Paolo
Gesta, Paul
Pokaż więcej
Temat :
Article
GEMO Study Collaborators
EMBRACE Collaborators
OCGN Investigators
HEBON Investigators
KconFab Investigators
Humans
Breast Neoplasms
Genetic Predisposition to Disease
BRCA1 Protein
BRCA2 Protein
Risk Factors
Retrospective Studies
Heterozygote
Mutation
Adult
Female
Genetics(clinical)
Prevention
Cancer
Aging
Breast Cancer
2.1 Biological and endogenous factors
Genetics & Heredity
Genetics
Clinical Sciences
BRCA1 Protein/genetics
BRCA2 Protein/genetics
Breast Neoplasms/diagnosis
MUTATION CARRIERS
SUSCEPTIBILITY ALLELES
CONSORTIUM
FAMILIES
OVARIAN
3111 Biomedicine
1184 Genetics, developmental biology, physiology
Medicine and Health Sciences
Càncer de mama
Factors de risc en les malalties
Risk factors in diseases
Źródło :
Genetics in medicine, 23(9), 1726-1737. Lippincott Williams and Wilkins
Lakeman, I M M, van den Broek, A J, Vos, J A M, Barnes, D R, Adlard, J, Andrulis, I L, Arason, A, Arnold, N, Arun, B K, Balmaña, J, Barrowdale, D, Benitez, J, Borg, A, Caldés, T, Caligo, M A, Chung, W K, Claes, K B M, Barouk-Simonet, E, Belotti, M, Berthet, P, Bignon, Y J, Bonadona, V, Bressac-de Paillerets, B, Buecher, B, Caputo, S, Caron, O, Castera, L, Caux-Moncoutier, V, Colas, C, Collonge-Rame, M A, Coupier, I, de Pauw, A, Delnatte, C, Elan, C, Faivre, L, Ferrer, S F, Gauthier-Villars, M, Gesta, P, Giraud, S, Golmard, L, Houdayer, C, Lasset, C, Laurent, M, Leroux, D, Longy, M, Mari, V, Mazoyer, S, Mebirouk, N, Mortemousque, I, Jensen, U B, GEMO Study Collaborators, EMBRACE Collaborators, OCGN Investigators, HEBON Investigators & KConFab Investigators 2021, ' The predictive ability of the 313 variant–based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant ', Genetics in Medicine, vol. 23, no. 9, pp. 1726-1737 . https://doi.org/10.1038/s41436-021-01198-7
Genetics in medicine : official journal of the American College of Medical Genetics, vol 23, iss 9
Lakeman, I M M, van den Broek, A J, Vos, J A M, Barnes, D R, Adlard, J, Andrulis, I L, Arason, A, Arnold, N, Arun, B K, Balmaña, J, Barrowdale, D, Benitez, J, Borg, A, Caldés, T, Caligo, M A, Chung, W K, Claes, K B M, Barouk-Simonet, E, Belotti, M, Berthet, P, Bignon, Y J, Bonadona, V, Bressac-de Paillerets, B, Buecher, B, Caputo, S, Caron, O, Castera, L, Caux-Moncoutier, V, Colas, C, Collonge-Rame, M A, Coupier, I, de Pauw, A, Delnatte, C, Elan, C, Faivre, L, Ferrer, S F, Gauthier-Villars, M, Gesta, P, Giraud, S, Golmard, L, Houdayer, C, Lasset, C, Laurent, M, Leroux, D, Longy, M, Mari, V, Mazoyer, S, Mebirouk, N, Gerdes, A M, Jensen, U B, Thomassen, M, GEMO Study Collaborators, EMBRACE Collaborators, OCGN Investigators, HEBON Investigators & kConFab Investigators 2021, ' The predictive ability of the 313 variant–based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant ', Genetics in Medicine, vol. 23, no. 9, pp. 1726-1737 . https://doi.org/10.1038/s41436-021-01198-7
GENETICS IN MEDICINE
Genetics in Medicine
Genetics in Medicine, 23(9), 1726-1737. Lippincott Williams and Wilkins
Genetics in Medicine. SPRINGERNATURE
Opis pliku :
Print-Electronic; application/pdf
Dostępność :
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fff307264df94c7ba3830c476324f06b
Tytuł :
Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk: an international prospective cohort of BRCA1 and BRCA2 mutation carriers
Autorzy :
Mavaddat, N.
Antoniou, A.C.
Mooij, T.M.
Hooning, M.J.
Heemskerk-Gerritsen, B.A.
Nogues, C.
Laborde, L.
Breysse, E.
Stoppa-Lyonnet, D.
Gauthier-Villars, M.
Buecher, B.
Caron, O.
Fourme-Mouret, E.
Fricker, J.P.
Lasset, C.
Bonadona, V.
Berthet, P.
Faivre, L.
Luporsi, E.
Mari, V.
Gladieff, L.
Gesta, P.
Sobol, H.
Eisinger, F.
Longy, M.
Dugast, C.
Colas, C.
Coupier, I.
Pujol, P.
Corsini, C.
Lortholary, A.
Vennin, P.
Adenis, C.
Nguyen, T.D.
Delnatte, C.
Tinat, J.
Tennevet, I.
Limacher, J.M.
Maugard, C.
Bignon, Y.J.
Demange, L.
Penet, C.
Dreyfus, H.
Cohen-Haguenauer, O.
Venat-Bouvet, L.
Leroux, D.
Zattara-Cannoni, H.
Fert-Ferrer, S.
Bera, O.
Ellis, S.
Barrowdale, D.
Frost, D.
Evans, D.G.
Izatt, L.
Adlard, J.
Eeles, R.
Brewer, C.
Tischkowitz, M.
Henderson, A.
Cook, J.
Eccles, D.
Hogervorst, F.B.L.
Collee, J.M.
Asperen, C.J. van
Mensenkamp, A.R.
Ausems, M.G.E.M.
Meijers-Heijboer, H.E.J.
Engelen, K. van
Blok, M.J.
Oosterwijk, J.C.
Verloop, J.
Broek, E. van den
Mourits, M.J.E.
Koppert, L.B.
Hopper, J.L.
John, E.M.
Chung, W.K.
Andrulis, I.L.
Daly, M.B.
Buys, S.S.
Benitez, J.
Caldes, T.
Jakubowska, A.
Simard, J.
Singer, C.F.
Tan, Y.
Olah, E.
Navratilova, M.
Foretova, L.
Gerdes, A.M.
Roos-Blom, M.J.
Leeuwen, F.E. van
Arver, B.
Olsson, H.
Schmutzler, R.K.
Engel, C.
Kast, K.
Phillips, K.A.
Terry, M.B.
Milne, R.L.
Goldgar, D.E.
Rookus, M.A.
Andrieu, N.
Easton, D.F.
GENEPSO
EMBRACE
HEBON
kConFab Investigators
IBCCS
kConFab
BCFR
Pokaż więcej
Temat :
Research Article
Breast cancer
BRCA1
BRCA2
Mutation
Risk-reducing salpingo-oophorectomy
association
consortium
kconfab
link
metaanalysis
ovarian
reduction
surgery
survival
women
[SDV]Life Sciences [q-bio]
[SDV.CAN]Life Sciences [q-bio]/Cancer
[SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie
[SDV.GEN]Life Sciences [q-bio]/Genetics
[SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics
Oncology
Cancer Research
Adult
BRCA1 Protein/genetics
BRCA2 Protein/genetics
Breast Neoplasms/epidemiology
Cohort Studies
Female
Humans
Incidence
International Agencies
Menopause
Middle Aged
Prospective Studies
Risk Reduction Behavior
Salpingo-oophorectomy/methods
Journal Article
Multicenter Study
Research Support, N.I.H., Intramural
Research Support, Non-U.S. Gov't
Obstetrics
medicine.medical_specialty
medicine
Surgical oncology
BRCA2 Mutation
medicine.disease
business.industry
business
Prospective cohort study
Brca1 protein
Natural menopause
Cohort study
lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens
lcsh:RC254-282
BRCA1 Protein
BRCA2 Protein
Breast Neoplasms
Salpingo-oophorectomy
skin and connective tissue diseases
endocrine system diseases
Źródło :
Breast Cancer Research, 22(1):8. BioMed Central Ltd
Breast Cancer Research, 22
Breast Cancer Research
Breast Cancer Research, BioMed Central, 2020, 22 (1), pp.8. ⟨10.1186/s13058-020-1247-4⟩
Breast cancer research, 22(1):8. BioMed Central Ltd.
Mavaddat, N, Antoniou, A C, Mooij, T M, Hooning, M J, Heemskerk-Gerritsen, B A, Noguès, C, Gauthier-Villars, M, Caron, O, Gesta, P, Pujol, P, Lortholary, A, Barrowdale, D, Frost, D, Evans, D G, Izatt, L, Adlard, J, Eeles, R, Brewer, C, Tischkowitz, M, Henderson, A, Cook, J, Eccles, D, van Engelen, K, Mourits, M J E, Ausems, M G E M, Koppert, L B, Hopper, J L, John, E M, Chung, W K, Andrulis, I L, Daly, M B, Buys, S S, Benitez, J, Caldes, T, Jakubowska, A, Simard, J, Singer, C F, Tan, Y, Olah, E, Navratilova, M, Foretova, L, Gerdes, A-M, Roos-Blom, M-J, Van Leeuwen, F E, Arver, B, Olsson, H, Schmutzler, R K, Engel, C, Kast, K, Phillips, K-A & GENEPSO 2020, ' Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk : an international prospective cohort of BRCA1 and BRCA2 mutation carriers ', Breast Cancer Research, vol. 22, no. 1, 8 . https://doi.org/10.1186/s13058-020-1247-4
Breast cancer research, 22(1):8. BioMed Central
Breast Cancer Research : BCR
Breast Cancer Research, Vol 22, Iss 1, Pp 1-11 (2020)
Breast Cancer Research, 22(1). BMC
essn: 1465-542X
nlmid: 100927353
Breast Cancer Research, 22(1):8. BioMed Central
Evans, D G & et al. 2020, ' Risk-reducing salpingo-oophorectomy, natural menopause and breast cancer risk : an international prospective cohort of BRCA1 and BRCA2 mutation carriers ', Breast Cancer Research . https://doi.org/10.1186/s13058-020-1247-4
Opis pliku :
application/pdf; text
Dostępność :
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::897204daf2b6489f47952598d573c042
Tytuł :
A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers
Autorzy :
Coignard, J. (Juliette)
Lush, M. (Michael)
Beesley, Jonathan
O’Mara, T.A. (Tracy A.)
Dennis, Joe
Tyrer, J.P. (Jonathan P.)
Barnes, Daniel
McGuffog, L. (Lesley)
Leslie, G. (Goska)
Bolla, M.K. (Manjeet K.)
Adank, Muriel
Agata, Simona
Ahearn, T. (Thomas)
Aittomäki, Kristiina
Andrulis, I.L. (Irene L.)
Anton-Culver, H. (Hoda)
Arndt, V. (Volker)
Arnold, N. (Norbert)
Aronson, K.J. (Kristan J.)
Arun, Banu
Augustinsson, A. (Annelie)
Azzollini, J.
Barrowdale, D. (Daniel)
Baynes, C. (Caroline)
Becher, H. (Heko)
Bermisheva, Marina
Bernstein, Leslie
Białkowska, K. (Katarzyna)
Blomqvist, Carl
Bojesen, Stig
Bonnani, Bernardo
Borg, Åke
Brauch, H. (Hiltrud)
Brenner, Hermann
Burwinkel, Barbara
Buys, S.S. (Saundra S.)
Caldes, Trinidad
Caligo, M.A. (Maria A.)
Campa, Daniele
Carter, B.D. (Brian D.)
Castelao, Jose
Chang-Claude, Jenny
Chanock, S.J. (Stephen J.)
Chung, W.K. (Wendy K.)
Claes, K.B.M. (Kathleen B. M.)
Clarke, C.L. (Christine L.)
Bertrand, O. (Ophélie)
Caputo, Sandrine
Dupré, A. (Anaïs)
Le Mentec, M. (Marine)
Belotti, Muriel
Birot, A.-M. (Anne-Marie)
Buecher, Bruno
Fourme, E. (Emmanuelle)
Gauthier-Villars, M. (Marion)
Golmard, Lisa
Houdayer, Claude
Moncoutier, Virginie
de Pauw, A. (Antoine)
Saule, C. (Claire)
Sinilnikova, O. (Olga)
Mazoyer, S. (Sylvie)
Damiola, F. (Francesca)
Barjhoux, L. (Laure)
Verny-Pierre, Carole
Léone, Mélanie
Boutry-Kryza, N.
Calender, Alain
Giraud, Sophie
Caron, Olivier
Guillaud-Bataille, Marine
Bressac-de Paillerets, Brigitte
Bignon, Yves-Jean
Uhrhammer, Nancy
Lasset, Christine
Bonadona, V. (Valérie)
Berthet, Pascaline
Vaur, Dominique
Castera, L. (Laurent)
Noguchi, T. (Tetsuro)
Popovici, C. (Cornel)
Sobol, Hagay
Bourdon, V. (Violaine)
Noguchi, Tetsuro
Remenieras, Audrey
Nogues, Catherine
Coupier, Isabelle
Pujol, P. (Pascal)
Dumont, A. (Aurélie)
Révillion, Françoise
Adenis, Claude
Muller, Danièle
Barouk-Simonet, Emmanuelle
Bonnet, Françoise
Bubien, Virginie
Sevenet, Nicolas
Longy, Michel
Toulas, Christine
Guimbaud, Rosine
Gladieff, L. (Laurence)
Feillel, Viviane
Leroux, Dominique
Dreyfus, Hélène
Rebischung, Christine
Peysselon, M. (Magalie)
Coron, Fanny
Faivre, Laurence
Baurand, A. (Amandine)
Jacquot, C. (Caroline)
Bertolone, G. (Geoffrey)
Lizard, S. (Sarab)
Prieur, Fabienne
Lebrun, Marine
Kientz, Caroline
Ferrer, S.F.
Mari, V. (Véronique)
Vénat-Bouvet, L. (Laurence)
Delnatte, C. (Capucine)
Bézieau, S. (Stéphane)
Mortemousque, I. (Isabelle)
Coulet, Florence
Colas, Chrystelle
Soubrier, Florent
Warcoin, M. (Mathilde)
Sokolowska, Johanna
Bronner, Myriam
Collonge-Rame, M.-A.
Damette, A. (Alexandre)
Gesta, P. (Paul)
Lallaoui, H. (Hakima)
Chiesa, J. (Jean)
Molina-Gomes, D. (Denise)
Ingster, O. (Olivier)
Gregory, Helen
Miedzybrodzka, Zosia
Morrison, P.J. (Patrick J.)
Ong, K.-R. (Kai-ren)
Donaldson, A. (Alan)
Rogers, Mark
Kennedy, M.J. (M. John)
Porteous, Mary
Brewer, C. (Carole)
Davidson, R. (Rosemarie)
Izatt, L. (Louise)
Brady, A.
Barwell, Julian
Adlard, Julian
Foo, Claire
Lalloo, Fiona
Side, L.E. (Lucy E.)
Eason, Jacqueline
Henderson, A. (Alex)
Walker, L. (Lisa)
Eeles, Rosalind
Cook, J. (Jackie)
Snape, K. (Katie)
Eccles, D. (Diana)
Murray, Alexandra
McCann, Emma
Collée, J.M. (J. Margriet)
Conroy, D.M. (Don M.)
Czene, Kamila
Daly, M.B. (Mary B.)
Devilee, Peter
Diez, O. (Orland)
Ding, Y.C. (Yuan Chun)
Domchek, Susan
Dörk, Thilo
Santos Silva, Isabel
Dunning, A.M. (Alison M.)
Dwek, M. (Miriam)
Eccles, D.M. (Diana M.)
Eliassen, A.H. (A. Heather)
Engel, C. (Christoph)
Eriksson, M. (Mikael)
Evans, D.G. (D. Gareth)
Fasching, Peter
Flyger, H. (Henrik)
Fostira, F. (Florentia)
Friedman, Eitan
Fritschi, L. (Lin)
Frost, D. (Debra)
Gago-Dominguez, Manuela
Gapstur, Susan M.
Garber, Judy
Garcia-Barberan, V. (Vanesa)
García-Closas, M. (Montserrat)
García-Sáenz, J.A. (José A.)
Gaudet, M.M. (Mia M.)
Gayther, Simon
Gehrig, A. (Andrea)
Georgoulias, V. (Vassilios)
Giles, G.G. (Graham G.)
Godwin, A.K. (Andrew K.)
Goldberg, Mark
Radice, Paolo
González-Neira, Anna
Greene, M.H. (Mark H.)
Guénel, Pascal
Haeberle, Lothar
Hahnen, E. (Eric)
Haiman, Christopher
Håkansson, N. (Niclas)
Hall, Per
Hamann, Ute
Harrington, P.A. (Patricia A.)
Hart, S.N. (Steven N.)
He, W. (Wei)
Hogervorst, F.B.L. (Frans B. L.)
Hollestelle, A. (Antoinette)
Hopper, John
Horcasitas, D.J. (Darling J.)
Hulick, P.J. (Peter J.)
Hunter, D.J. (David J.)
Imyanitov, Evgeny
Fox, Stephen
Campbell, Ian
Spurdle, A. (Amanda)
Webb, Penny
De Fazio, Anna
Tassell, M. (Margaret)
Kirk, J. (Judy)
Lindeman, Geoffrey
Price, Melanie
Southey, Melissa
Milne, Roger
Deb, S. (Sid)
Bowtell, David
Hout, Annemarie
Ouweland, Ans
Mensenkamp, A.R. (Arjen R.)
Deurzen, Carolien
Kets, Marleen
Seynaeve, Caroline
van Asperen, C.J. (Christi J.)
Aalfs, Cora
Gómez Garcia, E.B. (Encarna B.)
Leeuwen, Flora
Bock, Geertruida
Meijers-Heijboer, Hanne
Obdeijn, Inge-Marie
Gille, J.J.P. (J. J.P.)
Oosterwijk, Jan
Wijnen, Juul
Kolk, Lizet
Hooning, Maartje
Ausems, Margreet
Mourits, Marjan
Blok, M.J. (Marinus J.)
Rookus, Matti
van der Luijt, R.B. (Rob B.)
Cronenburg, T.C.T.E.F.
Pol, Carmen
Russell, Nicola
Siesling, Sabine
Overbeek, Lucy
Wijnands, R. (R.)
Lange, J.
Clarke, C. (Christine)
Graham, D. (Dinny)
Sachchithananthan, M. (Mythily)
Marsh, Deborah
Scott, Rodney
Baxter, R. (Robert)
Yip, Desmond
Carpenter, Adrian
Davis, A. (Alison)
Pathmanathan, N. (Nirmala)
Simpson, P. (Peter)
Jager, Agnes
Jakubowska, Anna
James, Margaret
Jensen, U.B. (Uffe Birk)
John, Esther
Jones, M.E. (Michael E.)
Kaaks, Rudolf
Kapoor, P.M. (Pooja Middha)
Karlan, Beth
Keeman, R. (Renske)
Khusnutdinova, Elza
Kiiski, J.I. (Johanna I.)
Ko, Y.-D. (Yon-Dschun)
Kosma, V.-M. (Veli-Matti)
Kraft, P. (Peter)
Kurian, A.W. (Allison W.)
Laitman, Y. (Yael)
Lambrechts, D. (Diether)
Le Marchand, Loic
Lester, J. (Jenny)
Lesueur, F. (Fabienne)
Lindstrom, T. (Tricia)
Lopez-Fernández, A. (Adria)
Loud, J.T. (Jennifer T.)
Luccarini, C. (Craig)
Mannermaa, Arto
Manoukian, Siranoush
Margolin, S. (Sara)
Martens, John
Mebirouk, Noura
Meindl, A. (Alfons)
Miller, A. (Austin)
Milne, R.L. (Roger L.)
Montagna, M. (Marco)
Nathanson, Katherine
Floris, O.A.M.
Nevanlinna, H. (Heli)
Nielsen, F.C. (Finn C.)
O’Brien, K.M. (Katie M.)
Olopade, Olofunmilayo
Olson, Janet
Olsson, H. (Håkan)
Osorio, Ana
Ottini, L. (Laura)
Park-Simon, T.-W. (Tjoung-Won)
Parsons, Marilyn
Pedersen, I.S. (Inge Sokilde)
Peshkin, B. (Beth)
Peterlongo, Paolo
Peto, Julian
Pharoah, Paul
Phillips, Kelly-Anne
Polley, E.C. (Eric C.)
Poppe, B. (Bruce)
Presneau, N. (Nadege)
Pujana, M.A. (Miquel Angel)
Punie, K. (Kevin)
Radice, P. (Paolo)
Rantala, J. (Johanna)
Rashid, Muhammad
Rennert, Gad
Rennert, H.S. (Hedy S.)
Robson, Mark
Romero, A. (Atocha)
Rossing, M. (Maria)
Saloustros, E. (Emmanouil)
Sandler, D.P. (Dale P.)
Santella, Regina
Scheuner, M.T. (Maren T.)
Schmidt, M.K. (Marjanka K.)
Schmidt, G. (Gunnar)
Scott, C. (Christopher)
Sharma, Priyanka
Soucy, P. (Penny)
Southey, M.C. (Melissa C.)
Spinelli, J.J. (John J.)
Steinsnyder, Z. (Zoe)
Stone, J. (Jennifer)
Stoppa-Lyonnet, Dominique
Swerdlow, Anthony
Tamimi, Rulla
Tapper, W.J. (William J.)
Taylor, J.A. (Jack A.)
Terry, Mary Beth
Teulé, A. (Alex)
Thull, D.L. (Darcy L.)
Tischkowitz, Marc
Toland, Amanda
Torres, Diana
Trainer, A.H. (Alison H.)
Truong, T. (Thérèse)
Tung, N. (Nadine)
Vachon, Celine
Vega, A. (Ana)
Joseph, Vijai
Wang, Q. (Qin)
Wappenschmidt, B. (Barbara)
Weinberg, C.R. (Clarice R.)
Weitzel, Jeffrey
Wendt, C. (Camilla)
Wolk, Kerstin
Yadav, S. (Siddhartha)
Yang, X.R. (Xiaohong R.)
Yannoukakos, D. (Drakoulis)
Zheng, Wei
Ziogas, Argyrios
Zorn, K.K. (Kristin K.)
Park, S.K. (Sue K.)
Thomassen, M. (Mads)
Offit, K. (Kenneth)
Schmutzler, Rita
Couch, Fergus
Simard, Jacques
Chenevix-Trench, Georgia
Adamo, Pio
Andrieu, Nadine
Antoniou, A.C. (Antonis C.)
Pokaż więcej
Temat :
Medical Genetics
Medicinsk genetik
Article
631/67/1347
631/67/2324
631/208/68
692/499
45/43
45/61
GEMO Study Collaborators
EMBRACE Collaborators
KConFab Investigators
HEBON Investigators
ABCTB Investigators
Humans
Breast Neoplasms
Genetic Predisposition to Disease
BRCA1 Protein
BRCA2 Protein
Risk Factors
Genotype
Linkage Disequilibrium
Mutation
Polymorphism, Single Nucleotide
Alleles
Quantitative Trait Loci
Adult
Middle Aged
Female
Genome-Wide Association Study
Breast cancer
Cancer epidemiology
Cancer genetics
Càncer de mama
Genètica
Genetics
BRCA1 Protein/genetics
BRCA2 Protein/genetics
Breast Neoplasms/genetics
Genetic Predisposition to Disease/genetics
Genome-Wide Association Study/methods
Quantitative Trait Loci/genetics
3111 Biomedicine
3122 Cancers
3123 Gynaecology and paediatrics
lcsh:Science
lcsh:Q
Chemistry(all)
Biochemistry, Genetics and Molecular Biology(all)
Physics and Astronomy(all)
General Physics and Astronomy
General Biochemistry, Genetics and Molecular Biology
General Chemistry
Polymorphism
Single Nucleotide
Prevention
Cancer
Genetic Testing
Human Genome
2.1 Biological and endogenous factors
Mama - Càncer - Aspectes genètics
Mama - Càncer - Factors de risc
Mutació (Biologia)
Neoplasms::Neoplasms by Site::Breast Neoplasms [DISEASES]
Other subheadings::Other subheadings::/genetics [Other subheadings]
Genetic Phenomena::Genetic Variation::Mutation [PHENOMENA AND PROCESSES]
neoplasias::neoplasias por localización::neoplasias de la mama [ENFERMEDADES]
Otros calificadores::Otros calificadores::/genética [Otros calificadores]
fenómenos genéticos::variación genética::mutación [FENÓMENOS Y PROCESOS]
Medicine and Health Sciences
skin and connective tissue diseases
endocrine system diseases
Źródło :
Nature Communications
Nature Communications, 12
Coignard, J, Lush, M, Beesley, J, O’Mara, T A, Dennis, J, Tyrer, J P, Barnes, D R, McGuffog, L, Leslie, G, Bolla, M K, Adank, M A, Agata, S, Ahearn, T, Aittomäki, K, Andrulis, I L, Anton-Culver, H, Arndt, V, Arnold, N, Aronson, K J, Arun, B K, Augustinsson, A, Azzollini, J, Barrowdale, D, Baynes, C, Becher, H, Bermisheva, M, Bernstein, L, Białkowska, K, Blomqvist, C, Bojesen, S E, Bonanni, B, Borg, A, Brauch, H, Brenner, H, Burwinkel, B, Buys, S S, Caldés, T, Caligo, M A, Campa, D, Carter, B D, Castelao, J E, Chang-Claude, J, Chanock, S J, Chung, W K, Claes, K B M, Clarke, C L, Bertrand, O, Caputo, S, Flyger, H, Jensen, U B, Nielsen, F C, Rossing, M, Pedersen, I S, Thomassen, M, GEMO Study Collaborators, EMBRACE Collaborators, kConFab Investigators, HEBON Investigators & ABCTB Investigators 2021, ' A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers ', Nature Communications, vol. 12, no. 1, 1078 . https://doi.org/10.1038/s41467-020-20496-3
Nature Communications, Vol 12, Iss 1, Pp 1-22 (2021)
Nature Communications, 12(1)
Nature Communications, 12(1):1078. Nature Publishing Group
Nature Communications, 12(1). NATURE RESEARCH
Coignard, J, Lush, M, Beesley, J, O’mara, T A, Dennis, J, Tyrer, J P, Barnes, D R, Mcguffog, L, Leslie, G, Bolla, M K, Adank, M A, Agata, S, Ahearn, T, Aittomäki, K, Andrulis, I L, Anton-culver, H, Arndt, V, Arnold, N, Aronson, K J, Arun, B K, Augustinsson, A, Azzollini, J, Barrowdale, D, Baynes, C, Becher, H, Bermisheva, M, Bernstein, L, Białkowska, K, Blomqvist, C, Bojesen, S E, Bonanni, B, Borg, A, Brauch, H, Brenner, H, Burwinkel, B, Buys, S S, Caldés, T, Caligo, M A, Campa, D, Carter, B D, Castelao, J E, Chang-claude, J, Chanock, S J, Chung, W K, Claes, K B M, Clarke, C L, Collée, J M, Conroy, D M, Czene, K, Daly, M B, Devilee, P, Diez, O, Ding, Y C, Domchek, S M, Dörk, T, Dos-santos-silva, I, Dunning, A M, Dwek, M, Eccles, D M, Eliassen, A H, Engel, C, Eriksson, M, Evans, D G, Fasching, P A, Flyger, H, Fostira, F, Friedman, E, Fritschi, L, Frost, D, Gago-dominguez, M, Gapstur, S M, Garber, J, Garcia-barberan, V, García-closas, M, García-sáenz, J A, Gaudet, M M, Gayther, S A, Gehrig, A, Georgoulias, V, Giles, G G, Godwin, A K, Goldberg, M S, Goldgar, D E, González-neira, A, Greene, M H, Guénel, P, Haeberle, L, Hahnen, E, Haiman, C A, Håkansson, N, Hall, P, Hamann, U, Harrington, P A, Hart, S N, He, W, Hogervorst, F B L, Hollestelle, A, Hopper, J L, Horcasitas, D J, Hulick, P J, Hunter, D J, Imyanitov, E N, Jager, A, Jakubowska, A, James, P A, Jensen, U B, John, E M, Jones, M E, Kaaks, R, Kapoor, P M, Karlan, B Y, Keeman, R, Khusnutdinova, E, Kiiski, J I, Ko, Y, Kosma, V, Kraft, P, Kurian, A W, Laitman, Y, Lambrechts, D, Le Marchand, L, Lester, J, Lesueur, F, Lindstrom, T, Lopez-fernández, A, Loud, J T, Luccarini, C, Mannermaa, A, Manoukian, S, Margolin, S, Martens, J W M, Mebirouk, N, Meindl, A, Miller, A, Milne, R L, Montagna, M, Nathanson, K L, Neuhausen, S L, Nevanlinna, H, Nielsen, F C, O’brien, K M, Olopade, O I, Olson, J E, Olsson, H, Osorio, A, Ottini, L, Park-simon, T, Parsons, M T, Pedersen, I S, Peshkin, B, Peterlongo, P, Peto, J, Pharoah, P D P, Phillips, K, Polley, E C, Poppe, B, Presneau, N, Pujana, M A, Punie, K, Radice, P, Rantala, J, Rashid, M U, Rennert, G, Rennert, H S, Robson, M, Romero, A, Rossing, M, Saloustros, E, Sandler, D P, Santella, R, Scheuner, M T, Schmidt, M K, Schmidt, G, Scott, C, Sharma, P, Soucy, P, Southey, M C, Spinelli, J J, Steinsnyder, Z, Stone, J, Stoppa-lyonnet, D, Swerdlow, A, Tamimi, R M, Tapper, W J, Taylor, J A, Terry, M B, Teulé, A, Thull, D L, Tischkowitz, M, Toland, A E, Torres, D, Trainer, A H, Truong, T, Tung, N, Vachon, C M, Vega, A, Vijai, J, Wang, Q, Wappenschmidt, B, Weinberg, C R, Weitzel, J N, Wendt, C, Wolk, A, Yadav, S, Yang, X R, Yannoukakos, D, Zheng, W, Ziogas, A, Zorn, K K, Park, S K, Thomassen, M, Offit, K, Schmutzler, R K, Couch, F J, Simard, J, Chenevix-trench, G, Easton, D F, Andrieu, N & Antoniou, A C 2021, ' A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers ', Nature Communications, vol. 12, no. 1 . https://doi.org/10.1038/s41467-020-20496-3
GEMO Study Collaborators, EMBRACE Collaborators, KConFab Investigators, HEBON Investigators & ABCTB Investigators 2021, ' A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers ', Nature Communications, vol. 12, no. 1, 1078 . https://doi.org/10.1038/s41467-020-20496-3
Nature communications, 12(1):1078. Nature Publishing Group
Nature communications, vol 12, iss 1
Scientia
NATURE COMMUNICATIONS
Opis pliku :
application/pdf; Electronic
Dostępność :
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19019e2b7195be3e05f9cb117543627e
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-440052
Tytuł :
Olaparib and durvalumab in patients with germline BRCA-mutated metastatic breast cancer (MEDIOLA):an open-label, multicentre, phase 1/2, basket study
Autorzy :
Saiama N. Waqar
Ding Wang
Haiyan Gao
Sakshi Gulati
Emma V. Jones
Iwanka Kozarewa
Matthew G Krebs
Helen K. Angell
Jean Pierre Delord
Sophie Postel-Vinay
Joon Rhee
Vidalba Rocher-Ros
Antoine Italiano
Susan M. Domchek
Zhongwu Lai
Benoit You
Anna M. L. Coenen-Stass
Sara Bastian
Bella Kaufman
P. Herbolsheimer
Jérôme Alexandre
Yeon Hee Park
Seock-Ah Im
L Opincar
M. Lanasa
Pokaż więcej
Temat :
Adolescent
Adult
Aged
Antibodies, Monoclonal/administration & dosage
B7-H1 Antigen/antagonists & inhibitors
BRCA1 Protein/genetics
BRCA2 Protein/genetics
Breast Neoplasms/drug therapy
Female
Germ-Line Mutation/genetics
Humans
Middle Aged
Neoplasm Metastasis
Neoplasm Recurrence, Local/drug therapy
Phthalazines/administration & dosage
Piperazines/administration & dosage
Young Adult
Oncology
Metastatic breast cancer
medicine.disease
medicine
Olaparib
chemistry.chemical_compound
chemistry
Lung cancer
Durvalumab
Breast cancer
Internal medicine
medicine.medical_specialty
Adverse effect
business.industry
business
Tolerability
Clinical trial
Źródło :
Domchek, S M, Postel-Vinay, S, Im, S-A, Park, Y H, Delord, J-P, Italiano, A, Alexandre, J, You, B, Bastian, S, Krebs, M G, Wang, D, Waqar, S N, Lanasa, M, Rhee, J, Gao, H, Rocher-Ros, V, Jones, E V, Gulati, S, Coenen-Stass, A, Kozarewa, I, Lai, Z, Angell, H K, Opincar, L, Herbolsheimer, P & Kaufman, B 2020, ' Olaparib and durvalumab in patients with germline BRCA-mutated metastatic breast cancer (MEDIOLA) : an open-label, multicentre, phase 1/2, basket study ', The Lancet. Oncology, vol. 21, no. 9, pp. 1155-1164 . https://doi.org/10.1016/S1470-2045(20)30324-7
Opis pliku :
application/vnd.openxmlformats-officedocument.wordprocessingml.document
Dostępność :
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c34416fb3adf2a299c05113cf960a2c
https://www.research.manchester.ac.uk/portal/en/publications/olaparib-and-durvalumab-in-patients-with-germline-brcamutated-metastatic-breast-cancer-mediola(5e0b81c7-c58f-4a44-98f4-47d6ec2731f4).html
Tytuł :
The genomic landscape of metastatic castration-resistant prostate cancers reveals multiple distinct genotypes with potential clinical impact
Autorzy :
van Dessel, Lisanne F.
van Riet, Job
Smits, Minke
Zhu, Yanyun
Hamberg, Paul
van der Heijden, Michiel S.
Bergman, Andries M.
van Oort, Inge M.
de Wit, Ronald
Voest, Emile E.
Steeghs, Neeltje
Yamaguchi, Takafumi N.
Livingstone, Julie
Boutros, Paul C.
Martens, John W. M.
Sleijfer, Stefan
Cuppen, Edwin
Zwart, Wilbert
van de Werken, Harmen J. G.
Mehra, Niven
Lolkema, Martijn P.
Pokaż więcej
Temat :
General Physics and Astronomy
General Biochemistry, Genetics and Molecular Biology
General Chemistry
Prostate
medicine.anatomical_structure
medicine
Tumor progression
Prostate cancer
medicine.disease
Genotype
Computational biology
Biology
Whole genome sequencing
Castration resistant
Tandem exon duplication
Microsatellite instability
BRCA2 Protein/genetics
Bone Neoplasms/genetics
Chromatin Immunoprecipitation Sequencing
Cyclin-Dependent Kinases/genetics
DNA Copy Number Variations
Enhancer Elements
Genetic/genetics
Humans
Liver Neoplasms/genetics
Lymph Nodes
Male
Microsatellite Instability
Neoplasm Metastasis
Oncogene Proteins
Fusion/genetics
Prostatic Neoplasms/genetics
Prostatic Neoplasms
Castration-Resistant/classification
Receptors
Androgen/genetics
Recombinational DNA Repair/genetics
Soft Tissue Neoplasms/genetics
Whole Genome Sequencing
SDG 3 - Good Health and Well-being
Science
Physics and Astronomy(all)
Chemistry(all)
Biochemistry
Genetics and Molecular Biology(all)
Journal Article
lcsh:Science
lcsh:Q
Article
Genetics research
Bone Neoplasms
Liver Neoplasms
Soft Tissue Neoplasms
Cyclin-Dependent Kinases
Fusion
BRCA2 Protein
Androgen
Genetic
Recombinational DNA Repair
Castration-Resistant
Biotechnology
Genetics
Cancer
Prostate Cancer
Urologic Diseases
Human Genome
Biochemistry, Genetics and Molecular Biology(all)
Enhancer Elements, Genetic/genetics
Oncogene Proteins, Fusion/genetics
Prostatic Neoplasms, Castration-Resistant/classification
Receptors, Androgen/genetics
Źródło :
Nature Communications, Vol 10, Iss 1, Pp 1-13 (2019)
Nature Communications, 10(1)
Nature Communications, 10
Nature Communications
Nature communications, vol 10, iss 1
Nature Communications, 10(1). Nature Publishing Group
Nature Communications, 10(1):5251. Nature Publishing Group
Nature communications, 10(1):5251. Nature Publishing Group
Opis pliku :
application/pdf; image/pdf
Dostępność :
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2882275e8ceb9ccb244ebae17d027bd1
Tytuł :
Clinical and molecular characterization of BRCA-associated breast cancer: results from the DBCG
Autorzy :
Anne-Marie Gerdes
Anne-Vibeke Laenkholm
Torben A Kruse
Martin Larsen
Inge Søkilde Pedersen
Torben Hansen
I M H Soenderstrup
Jens Ole Eriksen
M B Jensen
Bent Ejlertsen
Mads Thomassen
M Rossing
Pokaż więcej
Temat :
Radiology Nuclear Medicine and imaging
Oncology
Hematology
General Medicine
medicine.medical_specialty
medicine
Young adult
Risk assessment
Mastectomy
medicine.medical_treatment
Cancer
medicine.disease
Internal medicine
business.industry
business
Disease free survival
Breast cancer
Heterozygote advantage
Adolescent
Adult
Aged
BRCA1 Protein/genetics
BRCA2 Protein/genetics
Breast Neoplasms/genetics
Chemotherapy, Adjuvant
Denmark/epidemiology
Disease-Free Survival
Female
Genetic Predisposition to Disease
Heterozygote
Humans
Middle Aged
Mutation
Neoplasm Recurrence, Local/genetics
Registries
Young Adult
skin and connective tissue diseases
endocrine system diseases
Źródło :
Soenderstrup, I M H, Laenkholm, A V, Jensen, M B, Eriksen, J O, Gerdes, A M, Hansen, T V O, Kruse, T A, Larsen, M J, Pedersen, I S, Rossing, M, Thomassen, M & Ejlertsen, B 2018, ' Clinical and molecular characterization of BRCA-associated breast cancer : results from the DBCG ', Acta Oncologica, vol. 57, no. 1, pp. 95-101 . https://doi.org/10.1080/0284186X.2017.1398415
Dostępność :
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02537406100c692acaa8f486a2440693
https://www.tandfonline.com/doi/pdf/10.1080/0284186X.2017.1398415
Tytuł :
Subtypes in BRCA-mutated breast cancer
Autorzy :
Anne-Marie Gerdes
Maj-Britt Jensen
Martin Larsen
Bent Ejlertsen
Jens Ole Eriksen
Ida Marie Heeholm Sonderstrup
Mads Thomassen
Anne-Vibeke Lænkholm
Torben A Kruse
Pokaż więcej
Temat :
Adult
Aged
BRCA1 Protein/genetics
BRCA2 Protein/genetics
Breast Neoplasms/classification
Disease-Free Survival
Female
Germ-Line Mutation
Humans
Middle Aged
Young Adult
Journal Article
Research Support, Non-U.S. Gov't
Pathology and Forensic Medicine
Young adult
Proliferation index
Oncology
medicine.medical_specialty
medicine
Germline mutation
Cohort
Hormone receptor
Breast cancer
medicine.disease
Internal medicine
Confidence interval
business.industry
business
Immunohistochemistry
BRCA1
BRCA2
Intrinsic molecular subtypes
Survival
skin and connective tissue diseases
endocrine system diseases
Źródło :
Sønderstrup, I M H, Jensen, M-B R, Ejlertsen, B, Eriksen, J O, Gerdes, A-M, Kruse, T A, Larsen, M J, Thomassen, M & Lænkholm, A-V 2019, ' Subtypes in BRCA-mutated breast cancer ', Human Pathology, vol. 84, pp. 192-201 . https://doi.org/10.1016/j.humpath.2018.10.005
Sønderstrup, I, Jensen, M B, Ejlertsen, B, Eriksen, J O, Gerdes, A M, Kruse, T A, Larsen, M J, Thomassen, M & Lænkholm, A V 2019, ' Subtypes in BRCA-mutated breast cancer ', Human Pathology, vol. 84, pp. 192-201 . https://doi.org/10.1016/j.humpath.2018.10.005
Opis pliku :
application/pdf
Dostępność :
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff84836c194b97c102b30a50c7ce6b38
https://curis.ku.dk/portal/da/publications/subtypes-in-brcamutated-breast-cancer(1e028a04-c23a-4232-b6b4-e28aeb5ae098).html
Tytuł :
Genetic counselling and testing of susceptibility genes for therapeutic decision-making in breast cancer-an European consensus statement and expert recommendations
Autorzy :
Singer, Christian.F.
Balmaña Gelpí, Judith
Bürki, Nicole.
Delaloge, S.
Filieri, M.E.
Gerdes, A.M.
Grindedal, E.M.
Han, Suzette.
Johansson, Oskar.
Kaufman, Bella.
Krajc, Mateja.
Loman, Niklas.
Olah, Edith.
Paluch-Shimon, Shani.
Plavetic, Natalija Dedic
Pohlodek, Kamil.
Rhiem, Kerstin.
Teixeira, Manuel.
Evans, D.Gareth.
Universitat Autònoma de Barcelona
Pokaż więcej
Temat :
BRCA
BRCA1
BRCA2
Genetic counselling
Genetic testing
Hereditary breast cancer
Metastatic breast cancer
BRCA1 Protein/genetics
BRCA2 Protein/genetics
Biomarkers, Tumor/genetics
Breast Neoplasms/genetics
Consensus
Direct-To-Consumer Screening and Testing
Early Detection of Cancer
Female
Genetic Counseling
Genetic Predisposition to Disease
Heredity
Humans
Molecular Targeted Therapy
Mutation
Pedigree
Phenotype
Precision Medicine
Predictive Value of Tests
Reproducibility of Results
Risk Assessment
Risk Factors
Journal Article
Practice Guideline
Research Support, Non-U.S. Gov't
Cancer Research
Oncology
Susceptibility gene
Breast cancer
medicine.disease
medicine
medicine.diagnostic_test
Genetic predisposition
business.industry
business
Genetic counseling
Family medicine
medicine.medical_specialty
Family history
Therapeutic decision making
Metastatic breastcancer
Hereditary breastcancer
Źródło :
Singer, C F, Balmaña, J, Bürki, N, Delaloge, S, Filieri, M E, Gerdes, A-M, Grindedal, E M, Han, S, Johansson, O, Kaufman, B, Krajc, M, Loman, N, Olah, E, Paluch-Shimon, S, Plavetic, N D, Pohlodek, K, Rhiem, K, Teixeira, M & Evans, D G 2019, ' Genetic counselling and testing of susceptibility genes for therapeutic decision-making in breast cancer-an European consensus statement and expert recommendations ', European Journal of Cancer, vol. 106, pp. 54-60 . https://doi.org/10.1016/j.ejca.2018.10.007
Singer, C F, Balmaña, J, Bürki, N, Delaloge, S, Filieri, M E, Gerdes, A, Grindedal, E M, Han, S, Johansson, O, Kaufman, B, Krajc, M, Loman, N, Olah, E, Paluch-shimon, S, Plavetic, N D, Pohlodek, K, Rhiem, K, Teixeira, M & Evans, D G 2019, ' Genetic counselling and testing of susceptibility genes for therapeutic decision-making in breast cancer—an European consensus statement and expert recommendations ', European Journal of Cancer, vol. 106, pp. 54-60 . https://doi.org/10.1016/j.ejca.2018.10.007
Opis pliku :
Print-Electronic; application/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document
Dostępność :
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75253c7bf6f2079c7e463abd5dcf4bd7
https://lirias.kuleuven.be/handle/123456789/640223
Tytuł :
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification
Autorzy :
Parsons, Michael T.
Tudini, Emma
Li, Hongyan
Hahnen, Eric
Wappenschmidt, Barbara
Feliubadaló, Lidia
Aalfs, Cora M.
Agata, Simona
Aittomäki, Kristiina
Alducci, Elisa
Alonso‐Cerezo, María Concepción
Arnold, Norbert
Auber, Bernd
Austin, Rachel
Azzollini, Jacopo
Balmaña, Judith
Barbieri, Elena
Bartram, Claus R.
Blanco, Ana
Blümcke, Britta
Bonache, Sandra
Bonanni, Bernardo
Borg, Åke
Bortesi, Beatrice
Brunet, Joan
Bruzzone, Carla
Bucksch, Karolin
Cagnoli, Giulia
Caldés, Trinidad
Caliebe, Almuth
Caligo, Maria A.
Calvello, Mariarosaria
Capone, Gabriele L.
Caputo, Sandrine M.
Carnevali, Ileana
Carrasco, Estela
Caux‐Moncoutier, Virginie
Cavalli, Pietro
Cini, Giulia
Clarke, Edward M.
Concolino, Paola
Cops, Elisa J.
Cortesi, Laura
Couch, Fergus J.
Darder, Esther
Hoya, Miguel
Dean, Michael
Debatin, Irmgard
Del Valle, Jesús
Delnatte, Capucine
Derive, Nicolas
Diez, Orland
Ditsch, Nina
Domchek, Susan M.
Dutrannoy, Véronique
Eccles, Diana M.
Ehrencrona, Hans
Enders, Ute
Evans, D. Gareth
Farra, Chantal
Faust, Ulrike
Felbor, Ute
Feroce, Irene
Fine, Miriam
Foulkes, William D.
Galvao, Henrique C.R.
Gambino, Gaetana
Gehrig, Andrea
Gensini, Francesca
Gerdes, Anne‐Marie
Germani, Aldo
Giesecke, Jutta
Gismondi, Viviana
Gómez, Carolina
Garcia, Encarna B.
González, Sara
Grau, Elia
Grill, Sabine
Gross, Eva
Guerrieri‐Gonzaga, Aliana
Guillaud‐Bataille, Marine
Gutiérrez‐Enríquez, Sara
Haaf, Thomas
Hackmann, Karl
Hansen, Thomas V.O.
Harris, Marion
Hauke, Jan
Heinrich, Tilman
Hellebrand, Heide
Herold, Karen N.
Honisch, Ellen
Horvath, Judit
Houdayer, Claude
Hübbel, Verena
Iglesias, Silvia
Izquierdo, Angel
James, Paul A.
Janssen, Linda A.M.
Jeschke, Udo
Kaulfuß, Silke
Keupp, Katharina
Kiechle, Marion
Kölbl, Alexandra
Krieger, Sophie
Kruse, Torben A.
Kvist, Anders
Lalloo, Fiona
Larsen, Mirjam
Lattimore, Vanessa L.
Lautrup, Charlotte
Ledig, Susanne
Leinert, Elena
Lewis, Alexandra L.
Lim, Joanna
Loeffler, Markus
López‐Fernández, Adrià
Lucci‐Cordisco, Emanuela
Maass, Nicolai
Manoukian, Siranoush
Marabelli, Monica
Matricardi, Laura
Meindl, Alfons
Michelli, Rodrigo D.
Moghadasi, Setareh
Moles‐Fernández, Alejandro
Montagna, Marco
Montalban, Gemma
Monteiro, Alvaro N.
Montes, Eva
Mori, Luigi
Moserle, Lidia
Müller, Clemens R.
Mundhenke, Christoph
Naldi, Nadia
Nathanson, Katherine L.
Navarro, Matilde
Nevanlinna, Heli
Nichols, Cassandra B.
Niederacher, Dieter
Nielsen, Henriette R.
Ong, Kai‐ren
Pachter, Nicholas
Palmero, Edenir I.
Papi, Laura
Pedersen, Inge Sokilde
Peissel, Bernard
Perez‐Segura, Pedro
Pfeifer, Katharina
Pineda, Marta
Pohl‐Rescigno, Esther
Poplawski, Nicola K.
Porfirio, Berardino
Quante, Anne S.
Ramser, Juliane
Reis, Rui M.
Revillion, Françoise
Rhiem, Kerstin
Riboli, Barbara
Ritter, Julia
Rivera, Daniela
Rofes, Paula
Rump, Andreas
Salinas, Monica
Sánchez de Abajo, Ana María
Schmidt, Gunnar
Schoenwiese, Ulrike
Seggewiß, Jochen
Solanes, Ares
Steinemann, Doris
Stiller, Mathias
Stoppa‐Lyonnet, Dominique
Sullivan, Kelly J.
Susman, Rachel
Sutter, Christian
Tavtigian, Sean V.
Teo, Soo H.
Teulé, Alex
Thomassen, Mads
Tibiletti, Maria Grazia
Tischkowitz, Marc
Tognazzo, Silvia
Toland, Amanda E.
Tornero, Eva
Törngren, Therese
Torres‐Esquius, Sara
Toss, Angela
Trainer, Alison H.
Tucker, Katherine M.
Asperen, Christi J.
Mackelenbergh, Marion T.
Varesco, Liliana
Vargas‐Parra, Gardenia
Varon, Raymonda
Vega, Ana
Velasco, Ángela
Vesper, Anne‐Sophie
Viel, Alessandra
Vreeswijk, Maaike P. G.
Wagner, Sebastian A.
Waha, Anke
Walker, Logan C.
Walters, Rhiannon J.
Wang‐Gohrke, Shan
Weber, Bernhard H. F.
Weichert, Wilko
Wieland, Kerstin
Wiesmüller, Lisa
Witzel, Isabell
Wöckel, Achim
Woodward, Emma R.
Zachariae, Silke
Zampiga, Valentina
Zeder‐Göß, Christine
Investigators, KConFab
Lázaro, Conxi
Nicolo, Arcangela
Radice, Paolo
Engel, Christoph
Schmutzler, Rita K.
Goldgar, David E.
Spurdle, Amanda B.
Pokaż więcej
Temat :
BRCA1
BRCA2
quantitative
clinical
classification
multifactorial
variant
uncertain significance
Special Article
Special Articles
SEQUENCE VARIANTS
BREAST-CANCER
INTEGRATED EVALUATION
FUNCTIONAL ASSAYS
SPLICING ANALYSIS
GUIDELINES
CLINGEN
OVARIAN
RISKS
1184 Genetics, developmental biology, physiology
3111 Biomedicine
[SDV.MHEP]Life Sciences [q-bio]/Human health and pathology
Alternative Splicing
BRCA1 Protein/genetics
BRCA2 Protein/genetics
Computational Biology/methods
Early Detection of Cancer
Female
Genetic Predisposition to Disease
Humans
Likelihood Functions
Male
Multifactorial Inheritance
Mutation, Missense
Neoplasms/diagnosis
BRCA1 Protein
BRCA2 Protein
Computational Biology
Neoplasms
Settore MED/03 - GENETICA MEDICA
Genetics(clinical)
Genetics
Genetic analysis
Computational biology
Gene
Medical genetics
medicine.medical_specialty
medicine
Genetic variability
Population
education.field_of_study
education
Missense mutation
Biology
Posterior probability
ddc:610
Proteïnes
Genètica
Tumors
Proteins
BRCA1, BRCA2, quantitative, clinical, classification, multifactorial, variant, uncertain significance
Źródło :
Evans, D G, Lalloo, F, Woodward, E & et al. 2019, ' Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification ', Human Mutation . https://doi.org/10.1002/humu.23818
Human Mutation, 40(9), 1557-1578. WILEY
Human Mutation
Human Mutation, 40(9), 1557-1578. Wiley
Human Mutation, Wiley, 2019, 40 (9), pp.1557-1578. ⟨10.1002/humu.23818⟩
Parsons, M T, Tudini, E, Li, H, Hahnen, E, Wappenschmidt, B, Feliubadaló, L, Aalfs, C M, Agata, S, Aittomäki, K, Alducci, E, Alonso-Cerezo, M C, Arnold, N, Auber, B, Austin, R, Azzollini, J, Balmaña, J, Barbieri, E, Bartram, C R, Blanco, A, Blümcke, B, Bonache, S, Bonanni, B, Borg, Å, Bortesi, B, Brunet, J, Bruzzone, C, Bucksch, K, Cagnoli, G, Caldés, T, Caliebe, A, Caligo, M A, Calvello, M, Capone, G L, Caputo, S M, Carnevali, I, Carrasco, E, Caux-Moncoutier, V, Cavalli, P, Cini, G, Clarke, E M, Concolino, P, Cops, E J, Cortesi, L, Couch, F J, Darder, E, de la Hoya, M, Dean, M, Gerdes, A-M, Hansen, T V O, Wagner, S A & kConFab Investigators 2019, ' Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants : An ENIGMA resource to support clinical variant classification ', Human Mutation, vol. 40, no. 9, pp. 1557-1578 . https://doi.org/10.1002/humu.23818
Parsons, M T, Tudini, E, Li, H, Hahnen, E, Wappenschmidt, B, Feliubadaló, L, Aalfs, C M, Agata, S, Aittomäki, K, Alducci, E, Alonso-Cerezo, M C, Arnold, N, Auber, B, Austin, R, Azzollini, J, Balmaña, J, Barbieri, E, Bartram, C R, Blanco, A, Blümcke, B, Bonache, S, Bonanni, B, Borg, Å, Bortesi, B, Brunet, J, Bruzzone, C, Bucksch, K, Cagnoli, G, Caldés, T, Caliebe, A, Caligo, M A, Calvello, M, Capone, G L, Caputo, S M, Carnevali, I, Carrasco, E, Caux-Moncoutier, V, Cavalli, P, Cini, G, Clarke, E M, Concolino, P, Cops, E J, Cortesi, L, Couch, F J, Darder, E, de la Hoya, M, Dean, M, Debatin, I, del Valle, J, Delnatte, C, Derive, N, Diez, O, Ditsch, N, Domchek, S M, Dutrannoy, V, Eccles, D M, Ehrencrona, H, Enders, U, Evans, D G, Faust, U, Felbor, U, Feroce, I, Fine, M, Galvao, H C R, Gambino, G, Gehrig, A, Gensini, F, Gerdes, A-M, Germani, A, Giesecke, J, Gismondi, V, Gómez, C, Gómez Garcia, E B, González, S, Grau, E, Grill, S, Gross, E, Guerrieri-Gonzaga, A, Guillaud-Bataille, M, Gutiérrez-Enríquez, S, Haaf, T, Hackmann, K, Hansen, T V O, Harris, M, Hauke, J, Heinrich, T, Hellebrand, H, Herold, K N, Honisch, E, Horvath, J, Houdayer, C, Hübbel, V, Iglesias, S, Izquierdo, A, James, P A, Janssen, L A M, Jeschke, U, Kaulfuß, S, Keupp, K, Kiechle, M, Kölbl, A, Krieger, S, Kruse, T A, Kvist, A, Lalloo, F, Larsen, M, Lattimore, V L, Lautrup, C, Ledig, S, Leinert, E, Lewis, A L, Lim, J, Loeffler, M, López-Fernández, A, Lucci-Cordisco, E, Maass, N, Manoukian, S, Marabelli, M, Matricardi, L, Meindl, A, Michelli, R D, Moghadasi, S, Moles-Fernández, A, Montagna, M, Montalban, G, Monteiro, A N, Montes, E, Mori, L, Moserle, L, Müller, C R, Mundhenke, C, Naldi, N, Nathanson, K L, Navarro, M, Nevanlinna, H, Nichols, C B, Niederacher, D, Nielsen, H R, Ong, K, Pachter, N, Palmero, E I, Papi, L, Pedersen, I S, Peissel, B, Pérez-Segura, P, Pfeifer, K, Pineda, M, Pohl-Rescigno, E, Poplawski, N K, Porfirio, B, Quante, A S, Ramser, J, Rei, R M, Revillion, F, Rhiem, K, Riboli, B, Ritter, J, Rivera, D, Rofes, P, Rump, A, Salinas, M, Sánchez de Abajo, A M, Schmidt, G, Schoenwiese, U, Seggewiß, J, Solanes, A, Steinemann, D, Stiller, M, Stoppa-Lyonnet, D, Sullivan, K J, Susman, R, Sutter, C, Tavtigian, S V, Teo, S H, Teulé, A, Thomassen, M, Tibiletti, M G, Tognazzo, S, Toland, A E, Tornero, E, Törngren, T, Torres-Esquius, S, Toss, A, Trainer, A H, van Asperen, C J, van Mackelenbergh, M T, Varesco, L, Vargas-Parra, G, Varon, R, Vega, A, Velasco, Á, Vesper, A-S, Viel, A, Vreeswijk, M P G, Wagner, S A, Waha, A, Walker, L C, Walters, R J, Wang-Gohrke, S, Weber, B H F, Weichert, W, Wieland, K, Wiesmüller, L, Witzel, I, Wöckel, A, Woodward, E R, Zachariae, S, Zampiga, V, Zeder-Göß, C, KConFab Investigators, Lázaro, C, De Nicolo, A, Radice, P, Engel, C, Schmutzler, R K, Goldgar, D E & Spurdle, A B 2019, ' Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants : An ENIGMA resource to support clinical variant classification ', Human Mutation, vol. 40, no. 9, pp. 1557-1578 . https://doi.org/10.1002/humu.23818
Parsons, M T, Tudini, E, Li, H, Hahnen, E, Wappenschmidt, B, Feliubadaló, L, Aalfs, C M, Agata, S, Aittomäki, K, Alducci, E, Alonso-Cerezo, M C, Arnold, N, Auber, B, Austin, R, Azzollini, J, Balmaña, J, Barbieri, E, Bartram, C R, Blanco, A, Blümcke, B, Bonache, S, Bonanni, B, Borg, Å, Bortesi, B, Brunet, J, Bruzzone, C, Bucksch, K, Cagnoli, G, Caldés, T, Caliebe, A, Caligo, M A, Calvello, M, Capone, G L, Caputo, S M, Carnevali, I, Carrasco, E, Caux-Moncoutier, V, Cavalli, P, Cini, G, Clarke, E M, Concolino, P, Cops, E J, Cortesi, L, Couch, F J, Gerdes, A-M, Hansen, T V O, Kruse, T A, Nielsen, H R, Pedersen, I S, Lautrup, C K, Thomassen, M & kConFab Investigators 2019, ' Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants : An ENIGMA resource to support clinical variant classification ', Human Mutation, vol. 40, no. 9, pp. 1557-1578 . https://doi.org/10.1002/humu.23818
Opis pliku :
application/pdf
Dostępność :
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7e8c9e523f0496e5d186957a0c3bd3df
https://www.research.manchester.ac.uk/portal/en/publications/large-scale-multifactorial-likelihood-quantitative-analysis-of-brca1-and-brca2-variants-an-enigma-resource-to-support-clinical-variant-classification(754f8fe6-ac28-42ee-802a-e7b9ccff0fd3).html
Tytuł :
Enhanced response rate to pegylated liposomal doxorubicin in high grade serous ovarian carcinomas harbouring BRCA1 and BRCA2 aberrations
Autorzy :
Hollis, Robert L.
Meynert, Alison M.
Churchman, Michael
Rye, Tzyvia
Mackean, Melanie
Nussey, Fiona
Arends, Mark J.
Sims, Andrew H.
Semple, Colin A.
Herrington, C. Simon
Gourley, Charlie
Pokaż więcej
Temat :
Adult
Aged
Aged, 80 and over
Antibiotics, Antineoplastic/therapeutic use
BRCA1 Protein/genetics
BRCA2 Protein/genetics
Biomarkers, Tumor/genetics
Cystadenocarcinoma, Serous/drug therapy
Doxorubicin/analogs & derivatives
Female
Follow-Up Studies
Genetic Predisposition to Disease
Humans
Middle Aged
Mutation
Neoplasm Grading
Ovarian Neoplasms/drug therapy
Polyethylene Glycols/therapeutic use
Polymorphism, Single Nucleotide
Retrospective Studies
Survival Rate
Cancer Research
Genetics
Oncology
DNA repair
Internal medicine
medicine.medical_specialty
medicine
Surgical oncology
Survival rate
Population
education.field_of_study
education
Serous fluid
Ovarian carcinoma
business.industry
business
Chemotherapy
medicine.medical_treatment
Ovarian cancer
medicine.disease
Research Article
BRCA1
BRCA2
PLDH
lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens
lcsh:RC254-282
endocrine system diseases
skin and connective tissue diseases
Źródło :
Hollis, R L, Meynert, A M, Churchman, M, Rye, T, Mackean, M, Nussey, F, Arends, M J, Sims, A H, Semple, C A, Herrington, C S & Gourley, C 2018, ' Enhanced response rate to pegylated liposomal doxorubicin in high grade serous ovarian carcinomas harbouring BRCA1 and BRCA2 aberrations ', BMC Cancer, vol. 18, no. 1, pp. 16 . https://doi.org/10.1186/s12885-017-3981-2
BMC Cancer
BMC Cancer, Vol 18, Iss 1, Pp 1-8 (2018)
Opis pliku :
application/pdf
Dostępność :
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96400cfe4b9d479a18a0495e22787eaa
https://www.pure.ed.ac.uk/ws/files/50111950/RH_paper.pdf
Tytuł :
The BRCA2 c.68-7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicity
Autorzy :
Colombo, Mara
Lòpez-Perolio, Irene
Meeks, Huong D
Caleca, Laura
Parsons, Michael T
Li, Hongyan
De Vecchi, Giovanna
Tudini, Emma
Foglia, Claudia
Mondini, Patrizia
Manoukian, Siranoush
Behar, Raquel
Garcia, Encarna B Gómez
Meindl, Alfons
Montagna, Marco
Niederacher, Dieter
Schmidt, Ane Y
Varesco, Liliana
Wappenschmidt, Barbara
Bolla, Manjeet K
Dennis, Joe
Michailidou, Kyriaki
Wang, Jean
Aittomäki, Kristiina
Andrulis, Irene L
Anton-Culver, Hoda
Arndt, Volker
Beckmann, Matthias W
Beeghly-Fadel, Alicia
Benitez, Javier
Boeckx, Bram
Bogdanova, Natalia V
Bojesen, Stig E
Bonanni, Bernardo
Brauch, Hiltrud
Brenner, Hermann
Burwinkel, Barbara
Chang-Claude, Jenny
Conroy, Don M
Couch, Fergus J
Cox, Angela
Cross, Simon S
Czene, Kamila
Devilee, Peter
Dörk, Thilo
Eriksson, Mikael
Fasching, Peter A
Figueroa, Jonine
Fletcher, Olivia
Flyger, Henrik
Gabrielson, Marike
García-Closas, Montserrat
Giles, Graham G
González-Neira, Anna
Guénel, Pascal
Haiman, Christopher A
Hall, Per
Hamann, Ute
Hartman, Mikael
Hauke, Jan
Hollestelle, Antoinette
Hopper, John L
Jakubowska, Anna
Jung, Audrey
Kosma, Veli-Matti
Lambrechts, Diether
Le Marchand, Loid
Lindblom, Annika
Lubinski, Jan
Mannermaa, Arto
Margolin, Sara
Miao, Hui
Milne, Roger L
Neuhausen, Susan L
Nevanlinna, Heli
Olson, Janet E
Peterlongo, Paolo
Peto, Julian
Pylkäs, Katri
Sawyer, Elinor J
Schmidt, Marjanka K
Schmutzler, Rita K
Schneeweiss, Andreas
Schoemaker, Minouk J
See, Mee Hoong
Southey, Melissa C
Swerdlow, Anthony
Teo, Soo H
Toland, Amanda E
Tomlinson, Ian
Truong, Thérèse
Van Asperen, Christi J
Van Den Ouweland, Ans MW
Van Der Kolk, Lizet E
Winqvist, Robert
Yannoukakos, Drakoulis
Zheng, Wei
KConFab/AOCS Investigators
Dunning, Alison
Easton, Douglas
Henderson, Alex
Hogervorst, Frans BL
Izatt, Louise
Offitt, Kenneth
Side, Lucy E
Van Rensburg, Elizabeth J
Embrace, Study
Hebon, Study
McGuffog, Lesley
Antoniou, Antonis
Chenevix-Trench, Georgia
Spurdle, Amanda B
Goldgar, David E
Hoya, Miguel De La
Radice, Paolo
Pokaż więcej
Temat :
Genetics(clinical)
Genetics
Allele
Allele frequency
Gene mutation
Cancer
medicine.disease
medicine
Case-control study
Odds ratio
Digital polymerase chain reaction
Biology
Exon
kConFab/AOCS Investigators
Cell Line
Humans
Genetic Predisposition to Disease
Mitomycin
BRCA2 Protein
RNA, Messenger
Calibration
RNA Splicing
Base Sequence
Exons
Models, Genetic
Female
Genetic Variation
BRCA2
digital PCR
multifactorial likelihood analysis
quantitative real-time PCR
spliceogenic variants
Digital PCR
Multifactorial likelihood analysis
Quantitative real-time PCR
Spliceogenic variants
Journal Article
Research Article
Research Articles
quantitative real‐time PCR
BRCA2 Protein/genetics
Exons/genetics
Mitomycin/pharmacology
RNA Splicing/genetics
RNA, Messenger/genetics
Research Support, Non-U.S. Gov't
UNCLASSIFIED VARIANTS
FANCONI-ANEMIA
INTEGRATED EVALUATION
SEQUENCE VARIANTS
CANCER
GENES
MUTATIONS
BREAST
RISK
RNA
3111 Biomedicine
Źródło :
Human Mutation
Colombo, M, Lòpez-Perolio, I, Meeks, H D, Caleca, L, Parsons, M T, Li, H, De Vecchi, G, Tudini, E, Foglia, C, Mondini, P, Manoukian, S, Behar, R, Garcia, E B G, Meindl, A, Montagna, M, Niederacher, D, Schmidt, A Y, Varesco, L, Wappenschmidt, B, Bolla, M K, Dennis, J, Michailidou, K, Wang, Y-Q, Aittomäki, K, Andrulis, I L, Anton-Culver, H, Arndt, V, Beckmann, M W, Beeghly-Fadel, A, Benitez, J J, Boeckx, B, Bogdanova, N V, Bojesen, S E, Bonanni, B, Brauch, H, Brenner, H, Burwinkel, B, Chang-Claude, J, Conroy, D M, Couch, F J, Cox, A, Cross, S S, Czene, K, Devilee, P, Dörk, T, Eriksson, M, Fasching, P A, Figueroa, J, Fletcher, O, Flyger, H, Gabrielson, M, García-Closas, M, Giles, G G, González-Neira, A, Guénel, P, Haiman, C A, Hall, P, Hamann, U, Hartman, M, Hauke, J, Hollestelle, A, Hopper, J L, Jakubowska, A, Jung, A, Kosma, V-M, Lambrechts, D, Marchand, L L, Lindblom, A, Lubinski, J, Mannermaa, A, Margolin, S, Miao, H, Milne, R L, Neuhausen, S L, Nevanlinna, H, Olson, J E, Peterlongo, P, Peto, J, Pylkäs, K, Sawyer, E J, Schmidt, M K, Schmutzler, R K, Schneeweiss, A, Schoemaker, M J, See, M-H, Southey, M C, Swerdlow, A J, Teo, S-H, Toland, A E, Tomlinson, I, Truong, T, van Asperen, C J, van den Ouweland, A M W, van der Kolk, L, Winqvist, R, Yannoukakos, D, Zheng, W, Dunning, A M, Easton, D F, Henderson, R A, Hogervorst, F, Izatt, L, Offitt, K, Side, L E, van Rensburg, E J, Embrace, S, Hebon, S, McGuffog, L, Antoniou, A C, Chenevix-Trench, G, Spurdle, A B, Goldgar, D E, de la Hoya, M & Radice, P 2018, ' The BRCA2 c.68-7T > A variant is not pathogenic : A model for clinical calibration of spliceogenicity ', Human Mutation . https://doi.org/10.1002/humu.23411
Colombo, M; Lòpez-Perolio, I; Meeks, HD; Caleca, L; Parsons, MT; Li, H; et al.(2018). The BRCA2 c.68-7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicity.. Human mutation, 39(5), 729-741. doi: 10.1002/humu.23411. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/4zx2r18x
kConFab/AOCS Investigators 2018, ' The BRCA2 c.68-7T > A variant is not pathogenic : A model for clinical calibration of spliceogenicity ', Human Mutation, vol. 39, no. 5, pp. 729-741 . https://doi.org/10.1002/humu.23411
Human Mutation, 39(5), 729-741. Wiley
Human Mutation, 39(5), 729-741
Opis pliku :
Print-Electronic; application/pdf
Dostępność :
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::42ed0057e44305a3275d46682851b566
Tytuł :
Post-mortem testing; germline BRCA1/2 variant detection using archival FFPE non-tumor tissue. A new paradigm in genetic counseling
Autorzy :
Marianne Waldstrøm
Karina Dahl Steffensen
Henriette Roed Nielsen
Annabeth Høgh Petersen
Mads M. Aagaard
Anders Miki Bojesen
Pokaż więcej
Temat :
Article
Autopsy
BRCA1 Protein/genetics
BRCA2 Protein/genetics
Breast Neoplasms/diagnosis
False Positive Reactions
Female
Genetic Counseling/methods
Genetic Testing/methods
Germ-Line Mutation
Humans
Male
Pedigree
Sequence Analysis, DNA/methods
Tissue Fixation/methods
Genetics(clinical)
Genetics
Germline
Molecular genetics
medicine.medical_specialty
medicine
Germline mutation
Human genetics
Genetic linkage
Medical genetics
Genetic testing
medicine.diagnostic_test
Genetic counseling
Biology
Źródło :
European Journal of Human Genetics
Petersen, A H, Jørgensen, M M A, Nielsen, H R, Dahl Steffensen, K, Waldstrøm, M & Bojesen, A 2016, ' Post-mortem testing; germline BRCA1/2 variant detection using archival FFPE non-tumor tissue : A new paradigm in genetic counseling ', European Journal of Human Genetics, vol. 24, no. 8, pp. 1104-1111 . https://doi.org/10.1038/ejhg.2015.268
Dostępność :
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3f4764c76be36cea4ee58cb8b09f7ec
http://europepmc.org/articles/PMC4970683
Tytuł :
BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers
Autorzy :
Meeks, H.D.
Song, H.L.
Michailidou, K.
Bolla, M.K.
Dennis, J.
Wang, Q.
Barrowdale, D.
Frost, D.
McGuffog, L.
Ellis, S.
Feng, B.J.
Buys, S.S.
Hopper, J.L.
Southey, M.C.
Tesoriero, A.
James, P.A.
Bruinsma, F.
Campbell, I.G.
Broeks, A.
Schmidt, M.K.
Hogervorst, F.B.L.
Beckman, M.W.
Fasching, P.A.
Fletcher, O.
Johnson, N.
Sawyer, E.J.
Riboli, E.
Banerjee, S.
Menon, U.
Tomlinson, I.
Burwinkel, B.
Hamann, U.
Marme, F.
Rudolph, A.
Janavicius, R.
Tihomirova, L.
Tung, N.
Garber, J.
Cramer, D.
Terry, K.L.
Poole, E.M.
Tworoger, S.S.
Dorfling, C.M.
Rensburg, E.J. van
Godwin, A.K.
Guenel, P.
Truong, T.
Stoppa-Lyonnet, D.
Damiola, F.
Mazoyer, S.
Sinilnikova, O.M.
Isaacs, C.
Maugard, C.
Bojesen, S.E.
Flyger, H.
Gerdes, A.M.
Hansen, T.V.O.
Jensen, A.
Kjaer, S.K.
Hogdall, C.
Hogdall, E.
Pedersen, I.S.
Thomassen, M.
Benitez, J.
Gonzalez-Neira, A.
Osorio, A.
Hoya, M. de la
Segura, P.P.
Diez, O.
Lazaro, C.
Brunet, J.
Anton-Culver, H.
Eunjung, L.
John, E.M.
Neuhausen, S.L.
Ding, Y.C.
Castillo, D.
Weitzel, J.N.
Ganz, P.A.
Nussbaum, R.L.
Chan, S.B.
Karlan, B.Y.
Lester, J.
Wu, A.
Gayther, S.
Ramus, S.J.
Sieh, W.
Whittermore, A.S.
Monteiro, A.N.A.
Phelan, C.M.
Terry, M.B.
Piedmonte, M.
Offit, K.
Robson, M.
Levine, D.
Moysich, K.B.
Cannioto, R.
Olson, S.H.
Daly, M.B.
Nathanson, K.L.
Domchek, S.M.
Lu, K.H.
Liang, D.
Hildebrant, M.A.T.
Ness, R.
Modugno, F.
Pearce, L.
Goodman, M.T.
Thompson, P.J.
Brenner, H.
Butterbach, K.
Meindl, A.
Hahnen, E.
Wappenschmidt, B.
Brauch, H.
Bruning, T.
Blomqvist, C.
Khan, S.
Nevanlinna, H.
Pelttari, L.M.
Aittomaki, K.
Butzow, R.
Bogdanova, N.V.
Dork, T.
Lindblom, A.
Margolin, S.
Rantala, J.
Kosma, V.M.
Mannermaa, A.
Lambrechts, D.
Neven, P.
Claes, K.B.M.
Maerken, T. van
Chang-Claude, J.
Flesch-Janys, D.
Heitz, F.
Varon-Mateeva, R.
Peterlongo, P.
Radice, P.
Viel, A.
Barile, M.
Peissel, B.
Manoukian, S.
Montagna, M.
Oliani, C.
Peixoto, A.
Teixeira, M.R.
Collavoli, A.
Hallberg, E.
Olson, J.E.
Goode, E.L.
Hart, S.N.
Shimelis, H.
Cunningham, J.M.
Giles, G.G.
Milne, R.L.
Healey, S.
Tucker, K.
Haiman, C.A.
Henderson, B.E.
Goldberg, M.S.
Tischkowitz, M.
Simard, J.
Soucy, P.
Eccles, D.M.
Borresen-Dale, A.L.
Kristensen, V.
Salvesen, H.B.
Bjorge, L.
Bandera, E.V.
Risch, H.
Zheng, W.
Beeghly-Fadiel, A.
Cai, H.
Pylkas, K.
Tollenaar, R.A.E.M.
Ouweland, A.M.W. van der
Andrulis, I.L.
Knight, J.A.
Narod, S.
Devilee, P.
Winqvist, R.
Figueroa, J.
Greene, M.H.
Mai, P.L.
Loud, J.T.
Garcia-Closas, M.
Schoemaker, M.J.
Czene, K.
Darabi, H.
McNeish, I.
Siddiquil, N.
Glasspool, R.
Kwong, A.
Park, S.K.
Teo, S.H.
Yoon, S.Y.
Matsuo, K.
Hosono, S.
Woo, Y.L.
Gao, Y.T.
Foretova, L.
Singer, C.F.
Rappaport-Feurhauser, C.
Friedman, E.
Laitman, Y.
Rennert, G.
Imyanitov, E.N.
Hulick, P.J.
Olopade, O.I.
Senter, L.
Olah, E.
Doherty, J.A.
Schildkraut, J.
Koppert, L.B.
Kiemeney, L.A.
Massuger, L.F.A.G.
Cook, L.S.
Pejovic, T.
Li, J.M.
Borg, A.
Ofverholm, A.
Rossing, M.A.
Wentzensen, N.
Henriksson, K.
Cox, A.
Cross, S.S.
Pasini, B.J.
Shah, M.
Kabisch, M.
Torres, D.
Jakubowska, A.
Lubinski, J.
Gronwald, J.
Agnarsson, B.A.
Kupryjanczyk, J.
Moes-Sosnowska, J.
Fostira, F.
Konstantopoulou, I.
Slager, S.
Jones, M.
Antoniou, A.C.
Berchuck, A.
Swerdlow, A.
Chenevix-Trench, G.
Dunning, A.M.
Pharoah, P.D.P.
Hall, P.
Easton, D.F.
Couch, F.J.
Spurdle, A.B.
Goldgar, D.E.
EMBRACE
kConFab Investigators
Australia Ovarian Canc Study Grp
HEBON
GEMO Study Collaborators
OCGN
PRostate Canc Assoc Grp
Pokaż więcej
Temat :
Brjóstakrabbamein
Arfgengi
Eggjastokkar
Krabbamein
Krabbameinsrannsóknir
Blöðruhálskirtilskrabbamein
PTT12
Adult
Aged
BRCA2 Protein/genetics
Breast Neoplasms/genetics
Codon, Terminator
Female
Genetic Predisposition to Disease
Heterozygote
Humans
Logistic Models
Lysine/genetics
Male
Middle Aged
Neoplasm Invasiveness
Odds Ratio
Ovarian Neoplasms/genetics
Ovarian Neoplasms/pathology
Polymorphism, Single Nucleotide
Prostatic Neoplasms/genetics
Risk Assessment
Risk Factors Substances
Cancer Research
Oncology
medicine.medical_specialty
medicine
Prostate cancer
medicine.disease
Cancer
Estrogen receptor
Odds ratio
Breast cancer
Biology
Pancreatic cancer
Internal medicine
Ovarian cancer
Proportional hazards model
Gynecology
Article
SINGLE-NUCLEOTIDE POLYMORPHISMS
GERM-LINE MUTATION
PANCREATIC-CANCER
SUSCEPTIBILITY GENE
DNA RECOMBINATION
ESTROGEN-RECEPTOR
FAMILY-HISTORY
FANCONI-ANEMIA
LOCI
CONSORTIUM
BRCA2 Protein
Breast Neoplasms
Lysine
Ovarian Neoplasms
Prostatic Neoplasms
Risk Factors
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Źródło :
Journal of the National Cancer Institute, 108
Meeks, H D, Song, H, Michailidou, K, Bolla, M K, Dennis, J, Wang, Q, Barrowdale, D, Frost, D, McGuffog, L, Ellis, S, Feng, B, Buys, S S, Hopper, J L, Southey, M C, Tesoriero, A, James, P A, Bruinsma, F, Campbell, I G, Broeks, A, Schmidt, M K, Hogervorst, F B L, Beckman, M W, Fasching, P A, Fletcher, O, Johnson, N, Sawyer, E J, Riboli, E, Banerjee, S, Menon, U, Tomlinson, I, Burwinkel, B, Hamann, U, Marme, F, Rudolph, A, Janavicius, R, Tihomirova, L, Tung, N, Garber, J, Cramer, D, Terry, K L, Poole, E M, Tworoger, S S, Dorfling, C M, van Rensburg, E J, Godwin, A K, Guénel, P, Truong, T, Stoppa-Lyonnet, D, Gerdes, A-M, Thomassen, M & EMBRACE 2016, ' BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers ', Journal of the National Cancer Institute, vol. 108, no. 2, djv315 . https://doi.org/10.1093/jnci/djv315
JNCI: Journal of the National Cancer Institute, 108(2)
National Cancer Institute. Journal (Print), 108(2)
Jnci-Journal of the national cancer institute, 108(2):315. Oxford University Press
Meeks, H D, Song, H, Michailidou, K, Bolla, M K, Dennis, J, Wang, Q, Barrowdale, D, Frost, D, EMBRACE, McGuffog, L, Ellis, S, Feng, B, Buys, S S, Hopper, J L, Southey, M C, Tesoriero, A, kConFab Investigators, James, P A, Bruinsma, F, Campbell, I G, Broeks, A, Schmidt, M K, Hogervorst, F B L, HEBON, Beckman, M W, Fasching, P A, Fletcher, O, Johnson, N, Sawyer, E J, Riboli, E, Banerjee, S, Menon, U, Tomlinson, I, Burwinkel, B, Hamann, U, Marme, F, Rudolph, A, Janavicius, R, Tihomirova, L, Tung, N, Garber, J, Cramer, D, Terry, K L, Poole, E M, Tworoger, S S, Dorfling, C M, van Rensburg, E J, Godwin, A K, Guénel, P, Truong, T, GEMO Study Collaborators, Stoppa-Lyonnet, D, Damiola, F, Pedersen, I S, OCGN & PRostate cancer AssoCiation group To Investigate Cancer Associated aLterations in the genome 2016, ' BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers ', National Cancer Institute. Journal, vol. 108, no. 2, djv315 . https://doi.org/10.1093/jnci/djv315
Opis pliku :
application/pdf
Dostępność :
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb23f08642717d4e65f3010a25475b41
Tytuł :
A rare truncating BRCA2 variant and genetic susceptibility to upper aerodigestive tract cancer
Autorzy :
Vladimir Janout
Thangarajan Rajkumar
Paul Brennan
Marcin Lener
Sergio Koifman
Cristina Canova
Ewa Jaworowska
Maxime Vallée
Claire M. Healy
Jolanta Lissowska
W. Ahrens
Silvia Franceschi
José Eluf-Neto
Ana Paula de O. Menezes
Amélie Chabrier
Ioan Nicolae Mates
Paolo Boffetta
Ivana Holcatova
Eleonora Fabianova
Nalin S. Thakker
Luigi Barzan
David Zaridze
Stefania Boccia
Kristina Kjærheim
Tanuja A. Samant
Xavier Castellsagué
Ariana Znaor
Valerie Gaborieau
Leticia Fernández Garrote
V. Wünsch-Filho
Devasena Anantharaman
Keitaro Matsuo
Antonio Agudo
Jerry Polesel
Tatiana V. Macfarlane
Manon Delahaye-Sourdeix
Manoj B. Mahimkar
James McKay
Lorenzo Richiardi
Pagona Lagiou
Jan Lubinski
Maria Timofeeva
Graham Byrnes
Neonilia Szeszenia-Dabrowska
Maria Paula Curado
Lenka Foretová
David I. Conway
Vladimir Bencko
Pokaż więcej
Temat :
cancer
Japanese
breast cancer
neoplasms
genetics
smoking
BRAC2 gene
single nucleotide polymorphism
squamous cell carcinoma of lung
breast cancer risk
squamous cell carcinoma
upper aerodigestive tract
upper aerodigestive tract neoplasms
genetic predisposition to disease
BRCA2 protein
mutation
cancer risk
Adult Aged Alcohol Drinking/adverse effects/epidemiology BRCA2 Protein/*genetics Carcinoma
Squamous Cell/*genetics Case-Control Studies Female Genetic Predisposition to Disease Head and Neck Neoplasms/*genetics Humans Logistic Models Male Middle Aged Odds Ratio *Polymorphism
Single Nucleotide Risk Assessment Risk Factors Smoking/adverse effects/epidemiology
[SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie
Cancer Research
Oncology
Odds ratio
Internal medicine
medicine.medical_specialty
medicine
Case-control study
Carcinoma
medicine.disease
Breast cancer
Biology
Risk assessment
Genetic predisposition
Cancer
Single-nucleotide polymorphism
BRCA2 genetic variants - Breast cancer - Lung squamous cell carcinoma
Brief Communication
Adult
Aged
Alcohol Drinking
BRCA2 Protein
Carcinoma, Squamous Cell
Case-Control Studies
Female
Genetic Predisposition to Disease
Head and Neck Neoplasms
Humans
Logistic Models
Male
Middle Aged
Odds Ratio
Risk Assessment
Risk Factors
Smoking
Polymorphism, Single Nucleotide
Medicine (all)
Źródło :
Journal of the National Cancer Institute, 107(5):djv037
J Natl Cancer Inst
J Natl Cancer Inst, 2015, 107 (5), ⟨10.1093/jnci/djv037⟩
JNCI Journal of the National Cancer Institute
Opis pliku :
ELETTRONICO; application/pdf
Dostępność :
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31a466d710be0d4050ed73044d32b2f4
https://repository.publisso.de/resource/frl:6405165
Tytuł :
Common Variants at the 19p13.1 and ZNF365 Loci Are Associated with ER Subtypes of Breast Cancer and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers
Autorzy :
Couch, F.J.
Gaudet, M.M.
Antoniou, A.C.
Ramus, S.J.
Kuchenbaecker, K.B.
Soucy, P.
Beesley, J.
Chen, X.Q.
Wang, X.S.
Kirchhoff, T.
McGuffog, L.
Barrowdale, D.
Lee, A.
Healey, S.
Sinilnikova, O.M.
Andrulis, I.L.
Ozcelik, H.
Mulligan, A.M.
Thomassen, M.
Gerdes, A.M.
Jensen, U.B.
Skytte, A.B.
Kruse, T.A.
Caligo, M.A.
Wachenfeldt, A. von
Barbany-Bustinza, G.
Loman, N.
Soller, M.
Ehrencrona, H.
Karlsson, P.
Nathanson, K.L.
Rebbeck, T.R.
Domchek, S.M.
Jakubowska, A.
Lubinski, J.
Jaworska, K.
Durda, K.
Zlowocka, E.
Huzarski, T.
Byrski, T.
Gronwald, J.
Cybulski, C.
Gorski, B.
Osorio, A.
Duran, M.
Tejada, M.I.
Benitez, J.
Hamann, U.
Hogervorst, F.B.L.
Os, T.A. van
Leeuwen, F.E. van
Meijers-Heijboer, H.E.J.
Wijnen, J.
Blok, M.J.
Kets, M.
Hooning, M.J.
Oldenburg, R.A.
Ausems, M.G.E.M.
Peock, S.
Frost, D.
Ellis, S.D.
Platte, R.
Fineberg, E.
Evans, D.G.
Jacobs, C.
Eeles, R.A.
Adlard, J.
Davidson, R.
Eccles, D.M.
Cole, T.
Cook, J.
Paterson, J.
Brewer, C.
Douglas, F.
Hodgson, S.V.
Morrison, P.J.
Walker, L.
Porteous, M.E.
Kennedy, M.J.
Side, L.E.
Bove, B.
Godwin, A.K.
Stoppa-Lyonnet, D.
Fassy-Colcombet, M.
Castera, L.
Cornelis, F.
Mazoyer, S.
Leone, M.
Boutry-Kryza, N.
Bressac-de Paillerets, B.
Caron, O.
Pujol, P.
Coupier, I.
Delnatte, C.
Akloul, L.
Lynch, H.T.
Snyder, C.L.
Buys, S.S.
Daly, M.B.
Terry, M.
Chung, W.K.
John, E.M.
Miron, A.
Southey, M.C.
Hopper, J.L.
Goldgar, D.E.
Singer, C.F.
Rappaport, C.
Tea, M.K.M.
Fink-Retter, A.
Hansen, T.V.O.
Nielsen, F.C.
Arason, A.
Vijai, J.
Shah, S.
Sarrel, K.
Robson, M.E.
Piedmonte, M.
Phillips, K.
Basil, J.
Rubinstein, W.S.
Boggess, J.
Wakeley, K.
Ewart-Toland, A.
Montagna, M.
Agata, S.
Imyanitov, E.N.
Isaacs, C.
Janavicius, R.
Lazaro, C.
Blanco, I.
Feliubadalo, L.
Brunet, J.
Gayther, S.A.
Pharoah, P.P.D.
Odunsi, K.O.
Karlan, B.Y.
Walsh, C.S.
Olah, E.
Teo, S.H.
Ganz, P.A.
Beattie, M.S.
Rensburg, E.J. van
Dorfling, C.M.
Diez, O.
Kwong, A.
Schmutzler, R.K.
Wappenschmidt, B.
Engel, C.
Meindl, A.
Ditsch, N.
Arnold, N.
Heidemann, S.
Niederacher, D.
Preisler-Adams, S.
Gadzicki, D.
Varon-Mateeva, R.
Deissler, H.
Gehrig, A.
Sutter, C.
Kast, K.
Fiebig, B.
Heinritz, W.
Caldes, T.
Hoya, M. de la
Muranen, T.A.
Nevanlinna, H.
Tischkowitz, M.
Spurdle, A.B.
Neuhausen, S.L.
Ding, Y.C.
Lindor, N.M.
Fredericksen, Z.
Pankratz, V.S.
Peterlongo, P.
Manoukian, S.
Peissel, B.
Zaffaroni, D.
Barile, M.
Bernard, L.
Viel, A.
Giannini, G.
Varesco, L.
Radice, P.
Greene, M.H.
Mai, P.L.
Easton, D.F.
Chenevix-Trench, G.
Offit, K.
Simard, J.
OCGN
SWE-BRCA
HEBON
EMBRACE
GEMO Study Collaborators
kConFab Investigators
Consortium Investigators Modifiers
Pokaż więcej
Temat :
Adult
Aged
BRCA1 Protein
BRCA2 Protein
Breast Neoplasms
Chromosomes, Human, Pair 19
DNA-Binding Proteins
Female
Genetic Predisposition to Disease
Genome-Wide Association Study
Genotype
Humans
Immunoenzyme Techniques
Middle Aged
Mutation
Ovarian Neoplasms
Polymorphism, Single Nucleotide
Prognosis
Receptors, Estrogen
Risk Factors
Transcription Factors
United States
Oncology
Epidemiology
Cancer
medicine.disease
medicine
business.industry
business
Estrogen receptor
Breast cancer
Ovarian cancer
Genome-wide association study
Internal medicine
medicine.medical_specialty
Immunology
Risk factors for breast cancer
BRCA2 Protein - genetics
Chromosomes, Human, Pair 19 - genetics
Ovarian Neoplasms - epidemiology - genetics - metabolism
BRCA1 Protein - genetics
Breast Neoplasms - epidemiology - genetics - metabolism
Article
Źródło :
Cancer Epidemiology, Biomarkers & Prevention, 21, 645-657
Cancer Epidemiology, Biomarkers and Prevention, 21(4), 645-657
Cancer epidemiology, biomarkers & prevention, 21(4), 645-657. American Association for Cancer Research Inc.
Cancer Epidemiology, Biomarkers & Prevention, 21(4), 645-657
Couch, F J, Gaudet, M M, Antoniou, A C, Ramus, S J, Kuchenbaecker, K B, Soucy, P, Beesley, J, Chen, X, Wang, X, Kirchhoff, T, McGuffog, L, Barrowdale, D, Lee, A R, Healey, S, Sinilnikova, O M, Andrulis, I L, Ozcelik, H, Mulligan, A M, Thomassen, M, Gerdes, A-M A, Jensen, U B, Skytte, A-B S, Kruse, T A, Caligo, M A, von Wachenfeldt, A, Barbany-Bustinza, G, Loman, N, Soller, M, Ehrencrona, H, Karlsson, P W, Nathanson, K L, Rebbeck, T R, Domchek, S M, Jakubowska, A, Lubinski, J, Jaworska, K, Durda, K, Zlowocka, E, Huzarski, T, Byrski, T, Gronwald, J, Cybulski, C, Górski, B, Osorio, A, Durán, M, Tejada, M I, Benitez, J, Hamann, U, Hogervorst, F B L, van Os, T A & OCGN 2012, ' Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers ', Cancer Epidemiology, Biomarkers & Prevention, vol. 21, no. 4, pp. 645-57 . https://doi.org/10.1158/1055-9965.EPI-11-0888
Cancer Epidemiology Biomarkers and Prevention, 21(4), 645-657. American Association for Cancer Research Inc.
Couch, F J, Gaudet, M M, Antoniou, A C, Ramus, S J, Kuchenbaecker, K B, Soucy, P, Beesley, J, Chen, X, Wang, X, Kirchhoff, T, McGuffog, L, Barrowdale, D, Lee, A, Healey, S, Sinilnikova, O M, Andrulis, I L, Ozcelik, H, Mulligan, A M, Thomassen, M, Gerdes, A-M, Jensen, U B, Skytte, A-B, Kruse, T A, Caligo, M A, von Wachenfeldt, A, Barbany-Bustinza, G, Loman, N, Soller, M, Ehrencrona, H, Karlsson, P, Nathanson, K L, Rebbeck, T R, Domchek, S M, Jakubowska, A, Lubinski, J, Jaworska, K, Durda, K, Zlowocka, E, Huzarski, T, Byrski, T, Gronwald, J, Cybulski, C, Górski, B, Osorio, A, Durán, M, Tejada, M I, Benitez, J, Hamann, U, Hogervorst, F B L, van Os, T A & OCGN 2012, ' Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers ', Cancer Epidemiology, Biomarkers & Prevention, vol. 21, no. 4, pp. 645-57 . https://doi.org/10.1158/1055-9965.EPI-11-0888
Cancer Epidemiology Biomarkers & Prevention; Vol 21
Cancer Epidemiology Biomarkers & Prevention, 21(4), 645-657. American Association for Cancer Research Inc.
Dostępność :
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b949799806fed1689a9d24c254b3c62
Tytuł :
DNA Glycosylases Involved in Base Excision Repair May Be Associated with Cancer Risk in BRCA1 and BRCA2 Mutation Carriers
Autorzy :
Horwitz, Marshall S.
Osorio, Ana
Milne, Roger L.
Kuchenbaecker, Karoline
Vaclová, Tereza
Pita, Guillermo
Alonso, Rosario
Peterlongo, Paolo
Blanco, Ignacio
de la Hoya, Miguel
Duran, Mercedes
Díez, Orland
Ramón y Cajal, Teresa
Konstantopoulou, Irene
Martínez-Bouzas, Cristina
Andrés Conejero, Raquel
Soucy, Penny
McGuffog, Lesley
Barrowdale, Daniel
Lee, Andrew
SWE-BRCA, None
Arver, Brita
Rantala, Johanna
Loman, Niklas
Ehrencrona, Hans
Olopade, Olufunmilayo I.
Beattie, Mary S.
Domchek, Susan M.
Nathanson, Katherine
Rebbeck, Timothy R.
Arun, Banu K.
Karlan, Beth Y.
Walsh, Christine
Lester, Jenny
John, Esther M.
Whittemore, Alice S.
Daly, Mary B.
Southey, Melissa
Hopper, John
Terry, Mary B.
Buys, Saundra S.
Janavicius, Ramunas
Dorfling, Cecilia M.
van Rensburg, Elizabeth J.
Steele, Linda
Neuhausen, Susan L.
Ding, Yuan Chun
Hansen, Thomas v. O.
Jønson, Lars
Ejlertsen, Bent
Gerdes, Anne-Marie
Infante, Mar
Herráez, Belén
Moreno, Leticia Thais
Weitzel, Jeffrey N.
Herzog, Josef
Weeman, Kisa
Manoukian, Siranoush
Peissel, Bernard
Zaffaroni, Daniela
Scuvera, Giulietta
Bonanni, Bernardo
Mariette, Frederique
Volorio, Sara
Viel, Alessandra
Varesco, Liliana
Papi, Laura
Ottini, Laura
Tibiletti, Maria Grazia
Radice, Paolo
Yannoukakos, Drakoulis
Garber, Judy
Ellis, Steve
Frost, Debra
Platte, Radka
Fineberg, Elena
Evans, Gareth
Lalloo, Fiona
Izatt, Louise
Eeles, Ros
Adlard, Julian
Davidson, Rosemarie
Cole, Trevor
Eccles, Diana
Cook, Jackie
Hodgson, Shirley
Brewer, Carole
Tischkowitz, Marc
Douglas, Fiona
Porteous, Mary
Side, Lucy
Walker, Lisa
Morrison, Patrick
Donaldson, Alan
Kennedy, John
Foo, Claire
Godwin, Andrew K.
Schmutzler, Rita Katharina
Wappenschmidt, Barbara
Rhiem, Kerstin
Engel, Christoph
Meindl, Alfons
Ditsch, Nina
Arnold, Norbert
Plendl, Hans Jörg
Niederacher, Dieter
Sutter, Christian
Wang-Gohrke, Shan
Steinemann, Doris
Preisler-Adams, Sabine
Kast, Karin
Varon-Mateeva, Raymonda
Gehrig, Andrea
Stoppa-Lyonnet, Dominique
Sinilnikova, Olga M.
Mazoyer, Sylvie
Damiola, Francesca
Poppe, Bruce
Claes, Kathleen
Piedmonte, Marion
Tucker, Kathy
Backes, Floor
Rodríguez, Gustavo
Brewster, Wendy
Wakeley, Katie
Rutherford, Thomas
Caldés, Trinidad
Nevanlinna, Heli
Aittomäki, Kristiina
Rookus, Matti A.
van Os, Theo A. M.
van der Kolk, Lizet
de Lange, J. L.
Meijers-Heijboer, Hanne E. J.
van der Hout, A. H.
van Asperen, Christi J.
Gómez Garcia, Encarna B.
Hoogerbrugge, Nicoline
Collée, J. Margriet
van Deurzen, Carolien H. M.
van der Luijt, Rob B.
Devilee, Peter
HEBON, None
Olah, Edith
Lázaro, Conxi
Teulé, Alex
Menéndez, Mireia
Jakubowska, Anna
Cybulski, Cezary
Gronwald, Jacek
Lubinski, Jan
Durda, Katarzyna
Jaworska-Bieniek, Katarzyna
Johannsson, Oskar Th.
Maugard, Christine
Montagna, Marco
Tognazzo, Silvia
Teixeira, Manuel R.
Healey, Sue
Investigators, kConFab
Olswold, Curtis
Guidugli, Lucia
Lindor, Noralane
Slager, Susan
Szabo, Csilla I.
Vijai, Joseph
Robson, Mark
Kauff, Noah
Zhang, Liying
Rau-Murthy, Rohini
Fink-Retter, Anneliese
Singer, Christian F.
Rappaport, Christine
Geschwantler Kaulich, Daphne
Pfeiler, Georg
Tea, Muy-Kheng
Berger, Andreas
Phelan, Catherine M.
Greene, Mark H.
Mai, Phuong L.
Lejbkowicz, Flavio
Andrulis, Irene
Mulligan, Anna Marie
Glendon, Gord
Toland, Amanda Ewart
Bojesen, Anders
Pedersen, Inge Sokilde
Sunde, Lone
Thomassen, Mads
Kruse, Torben A.
Jensen, Uffe Birk
Friedman, Eitan
Laitman, Yael
Shimon, Shani Paluch
Simard, Jacques
Easton, Douglas F.
Offit, Kenneth
Couch, Fergus J.
Chenevix-Trench, Georgia
Antoniou, Antonis C.
Benitez, Javier
Pokaż więcej
Temat :
ddc:610
Càncer d'ovari
Genètica
Ovarian cancer
Genetics
Cancer--Risk factors
Cancer--Genetic aspects
FOS: Biological sciences
Single nucleotide polymorphisms
Biology
SINGLE-NUCLEOTIDE POLYMORPHISMS
BREAST-CANCER
OVARIAN-CANCER
GENETIC MODIFIERS
COMMON VARIANTS
NEIL2
OGG1
INVESTIGATORS
CONSORTIUM
DAMAGE
SWE-BRCA
HEBON
KConFab Investigators
Humans
Breast Neoplasms
Ovarian Neoplasms
Genetic Predisposition to Disease
DNA Glycosylases
BRCA1 Protein
BRCA2 Protein
Risk
DNA Repair
Genotype
Polymorphism, Single Nucleotide
Adolescent
Adult
Aged
Aged, 80 and over
Middle Aged
Female
Medical Genetics
BRCA1
BRCA2
Research Article
Biology and Life Sciences
Cancer Genetics
Cancer Research
Genetics(clinical)
Molecular Biology
Ecology, Evolution, Behavior and Systematics
Mutation
medicine.disease_cause
medicine
DNA repair
Cancer research
DNA glycosylase
Synthetic lethality
Base excision repair
Single-nucleotide polymorphism
lcsh:Genetics
lcsh:QH426-470
Brjóstakrabbamein
Arfgengi
Breast Neoplasms/genetics
DNA Glycosylases/genetics
DNA Repair/genetics
BRCA1 Protein/genetics
BRCA2 Protein/genetics
Ovarian Neoplasms/genetics
Polymorphism, Single Nucleotide/genetics
3111 Biomedicine
Glicosilasas
ADN
24 Ciencias de la Vida
Medicine and Health Sciences
Źródło :
Osorio, A, Milne, R L, Kuchenbaecker, K, Vaclová, T, Pita, G, Alonso, R, Peterlongo, P, Blanco, I, de la Hoya, M, Duran, M, Díez, O, Ramón Y Cajal, T, Konstantopoulou, I, Martínez-Bouzas, C, Andrés Conejero, R, Soucy, P, McGuffog, L, Barrowdale, D, Lee, A, Swe-Brca, Arver, B, Rantala, J, Loman, N, Ehrencrona, H, Olopade, O I, Beattie, M S, Domchek, S M, Nathanson, K, Rebbeck, T R, Arun, B K, Karlan, B Y, Walsh, C, Lester, J, John, E M, Whittemore, A S, Daly, M B, Southey, M, Hopper, J, Terry, M B, Buys, S S, Janavicius, R, Dorfling, C M, van Rensburg, E J, Steele, L, Neuhausen, S L, Ding, Y C, Hansen, T V O, Jønson, L, Ejlertsen, B, Gerdes, A-M, Infante, M, Herráez, B, Moreno, L T, Weitzel, J N, Herzog, J, Weeman, K, Manoukian, S, Peissel, B, Zaffaroni, D, Scuvera, G, Bonanni, B, Mariette, F, Volorio, S, Viel, A, Varesco, L, Papi, L, Ottini, L, Tibiletti, M G, Radice, P, Yannoukakos, D, Garber, J, Ellis, S, Frost, D, Platte, R, Fineberg, E, Evans, G, Lalloo, F, Izatt, L, Eeles, R, Adlard, J, Davidson, R, Cole, T, Eccles, D, Cook, J, Hodgson, S, Brewer, C, Tischkowitz, M, Douglas, F, Porteous, M, Side, L, Walker, L, Morrison, P, Donaldson, A, Kennedy, J, Foo, C, Godwin, A K, Schmutzler, R K, Wappenschmidt, B, Rhiem, K, Engel, C, Meindl, A, Ditsch, N, Arnold, N, Plendl, H J, Niederacher, D, Sutter, C, Wang-Gohrke, S, Steinemann, D, Preisler-Adams, S, Kast, K, Varon-Mateeva, R, Gehrig, A, Stoppa-Lyonnet, D, Sinilnikova, O M, Mazoyer, S, Damiola, F, Poppe, B, Claes, K, Piedmonte, M, Tucker, K, Backes, F, Rodríguez, G, Brewster, W, Wakeley, K, Rutherford, T, Caldés, T, Nevanlinna, H, Aittomäki, K, Rookus, M A, van Os, T A M, van der Kolk, L, de Lange, J L, Meijers-Heijboer, H E J, van der Hout, A H, van Asperen, C J, Gómez Garcia, E B, Hoogerbrugge, N, Collée, J M, van Deurzen, C H M, van der Luijt, R B, Devilee, P, Hebon, Olah, E, Lázaro, C, Teulé, A, Menéndez, M, Jakubowska, A, Cybulski, C, Gronwald, J, Lubinski, J, Durda, K, Jaworska-Bieniek, K, Johannsson, O T, Maugard, C, Montagna, M, Tognazzo, S, Teixeira, M R, Healey, S, Investigators, K, Olswold, C, Guidugli, L, Lindor, N, Slager, S, Szabo, C I, Vijai, J, Robson, M, Kauff, N, Zhang, L, Rau-Murthy, R, Fink-Retter, A, Singer, C F, Rappaport, C, Geschwantler Kaulich, D, Pfeiler, G, Tea, M-K, Berger, A, Phelan, C M, Greene, M H, Mai, P L, Lejbkowicz, F, Andrulis, I, Mulligan, A M, Glendon, G, Toland, A E, Bojesen, A, Pedersen, I S, Sunde, L, Thomassen, M, Kruse, T A, Jensen, U B, Friedman, E, Laitman, Y, Shimon, S P, Simard, J, Easton, D F, Offit, K, Couch, F J, Chenevix-Trench, G, Antoniou, A C & Benitez, J 2014, ' DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers ', P L o S Genetics, vol. 10, no. 4, pp. e1004256 . https://doi.org/10.1371/journal.pgen.1004256
PLoS genetics, 10(4):e1004256. PUBLIC LIBRARY SCIENCE
Osorio, A, Milne, R L, Kuchenbaecker, K, Vaclová, T, Pita, G, Alonso, R, Peterlongo, P, Blanco, I, de la Hoya, M, Duran, M, Díez, O, Ramón Y Cajal, T, Konstantopoulou, I, Martínez-Bouzas, C, Andrés Conejero, R, Soucy, P, McGuffog, L, Barrowdale, D, Lee, A, Swe-Brca, Arver, B, Rantala, J, Loman, N, Ehrencrona, H, Olopade, O I, Beattie, M S, Domchek, S M, Nathanson, K, Rebbeck, T R, Arun, B K, Karlan, B Y, Walsh, C, Lester, J, John, E M, Whittemore, A S, Daly, M B, Southey, M, Hopper, J, Terry, M B, Buys, S S, Janavicius, R, Dorfling, C M, van Rensburg, E J, Steele, L, Neuhausen, S L, Ding, Y C, Hansen, T V O, Jønson, L, Ejlertsen, B, Gerdes, A-M, Infante, M, Herráez, B, Moreno, L T, Weitzel, J N, Herzog, J, Weeman, K, Manoukian, S, Peissel, B, Zaffaroni, D, Scuvera, G, Bonanni, B, Mariette, F, Volorio, S, Viel, A, Varesco, L, Papi, L, Ottini, L, Tibiletti, M G, Radice, P, Yannoukakos, D, Garber, J, Ellis, S, Frost, D, Platte, R, Fineberg, E, Evans, G, Lalloo, F, Izatt, L, Eeles, R, Adlard, J, Davidson, R, Cole, T, Eccles, D, Cook, J, Hodgson, S, Brewer, C, Tischkowitz, M, Douglas, F, Porteous, M, Side, L, Walker, L, Morrison, P, Donaldson, A, Kennedy, J, Foo, C, Godwin, A K, Schmutzler, R K, Wappenschmidt, B, Rhiem, K, Engel, C, Meindl, A, Ditsch, N, Arnold, N, Plendl, H J, Niederacher, D, Sutter, C, Wang-Gohrke, S, Steinemann, D, Preisler-Adams, S, Kast, K, Varon-Mateeva, R, Gehrig, A, Stoppa-Lyonnet, D, Sinilnikova, O M, Mazoyer, S, Damiola, F, Poppe, B, Claes, K, Piedmonte, M, Tucker, K, Backes, F, Rodríguez, G, Brewster, W, Wakeley, K, Rutherford, T, Caldés, T, Nevanlinna, H, Aittomäki, K, Rookus, M A, van Os, T A M, van der Kolk, L, de Lange, J L, Meijers-Heijboer, H E J, van der Hout, A H, van Asperen, C J, Gómez Garcia, E B, Hoogerbrugge, N, Collée, J M, van Deurzen, C H M, van der Luijt, R B, Devilee, P, Hebon, Olah, E, Lázaro, C, Teulé, A, Menéndez, M, Jakubowska, A, Cybulski, C, Gronwald, J, Lubinski, J, Durda, K, Jaworska-Bieniek, K, Johannsson, O T, Maugard, C, Montagna, M, Tognazzo, S, Teixeira, M R, Healey, S, Investigators, K, Olswold, C, Guidugli, L, Lindor, N, Slager, S, Szabo, C I, Vijai, J, Robson, M, Kauff, N, Zhang, L, Rau-Murthy, R, Fink-Retter, A, Singer, C F, Rappaport, C, Geschwantler Kaulich, D, Pfeiler, G, Tea, M-K, Berger, A, Phelan, C M, Greene, M H, Mai, P L, Lejbkowicz, F, Andrulis, I, Mulligan, A M, Glendon, G, Toland, A E, Bojesen, A, Pedersen, I S, Sunde, L, Thomassen, M, Kruse, T A, Jensen, U B, Friedman, E, Laitman, Y, Shimon, S P, Simard, J, Easton, D F, Offit, K, Couch, F J, Chenevix-Trench, G, Antoniou, A C & Benitez, J 2014, ' DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers ', P L o S Genetics, vol. 10, no. 4, e1004256 . https://doi.org/10.1371/journal.pgen.1004256
Plos Genetics, 10, e1004256
Osorio, A, Milne, R L, Kuchenbaecker, K, Vaclová, T, Pita, G, Alonso, R, Peterlongo, P, Blanco, I, de la Hoya, M, Duran, M, Díez, O, Ramón Y Cajal, T, Konstantopoulou, I, Martínez-Bouzas, C, Andrés Conejero, R, Soucy, P, McGuffog, L, Barrowdale, D, Lee, A, Swe-Brca, Arver, B, Rantala, J, Loman, N, Ehrencrona, H, Olopade, O I, Beattie, M S, Domchek, S M, Nathanson, K, Rebbeck, T R, Arun, B K, Karlan, B Y, Walsh, C, Lester, J, John, E M, Whittemore, A S, Daly, M B, Southey, M, Hopper, J, Terry, M B, Buys, S S, Janavicius, R, Dorfling, C M, van Rensburg, E J, Steele, L, Neuhausen, S L, Ding, Y C, Hansen, T V O, Jønson, L, Ejlertsen, B, Gerdes, A-M, Infante, M, Herráez, B, Moreno, L T, Weitzel, J N, Herzog, J, Weeman, K, Manoukian, S, Peissel, B, Zaffaroni, D, Scuvera, G, Bonanni, B, Mariette, F, Volorio, S, Viel, A, Varesco, L, Papi, L, Ottini, L, Tibiletti, M G, Radice, P, Yannoukakos, D, Garber, J, Ellis, S, Frost, D, Platte, R, Fineberg, E, Evans, G, Lalloo, F, Izatt, L, Eeles, R, Adlard, J, Davidson, R, Cole, T, Eccles, D, Cook, J, Hodgson, S, Brewer, C, Tischkowitz, M, Douglas, F, Porteous, M, Side, L, Walker, L, Morrison, P, Donaldson, A, Kennedy, J, Foo, C, Godwin, A K, Schmutzler, R K, Wappenschmidt, B, Rhiem, K, Engel, C, Meindl, A, Ditsch, N, Arnold, N, Plendl, H J, Niederacher, D, Sutter, C, Wang-Gohrke, S, Steinemann, D, Preisler-Adams, S, Kast, K, Varon-Mateeva, R, Gehrig, A, Stoppa-Lyonnet, D, Sinilnikova, O M, Mazoyer, S, Damiola, F, Poppe, B, Claes, K, Piedmonte, M, Tucker, K, Backes, F, Rodríguez, G, Brewster, W, Wakeley, K, Rutherford, T, Caldés, T, Nevanlinna, H, Aittomäki, K, Rookus, M A, van Os, T A M, van der Kolk, L, de Lange, J L, Meijers-Heijboer, H E J, van der Hout, A H, van Asperen, C J, Gómez Garcia, E B, Hoogerbrugge, N, Collée, J M, van Deurzen, C H M, van der Luijt, R B, Devilee, P, Hebon, Olah, E, Lázaro, C, Teulé, A, Menéndez, M, Jakubowska, A, Cybulski, C, Gronwald, J, Lubinski, J, Durda, K, Jaworska-Bieniek, K, Johannsson, O T, Maugard, C, Montagna, M, Tognazzo, S, Teixeira, M R, Healey, S, Investigators, K, Olswold, C, Guidugli, L, Lindor, N, Slager, S, Szabo, C I, Vijai, J, Robson, M, Kauff, N, Zhang, L, Rau-Murthy, R, Fink-Retter, A, Singer, C F, Rappaport, C, Geschwantler Kaulich, D, Pfeiler, G, Tea, M-K, Berger, A, Phelan, C M, Greene, M H, Mai, P L, Lejbkowicz, F, Andrulis, I, Mulligan, A M, Glendon, G, Toland, A E, Bojesen, A, Pedersen, I S, Sunde, L, Thomassen, M, Kruse, T A, Jensen, U B, Friedman, E, Laitman, Y, Shimon, S P, Simard, J, Easton, D F, Offit, K, Couch, F J, Chenevix-Trench, G, Antoniou, A C & Benitez, J 2014, ' DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers ', PLoS genetics, vol. 10, no. 4, pp. e1004256 . https://doi.org/10.1371/journal.pgen.1004256
PLoS Genetics; 10(4), no e1004256 (2014)
PLoS Genetics, 10(4):e1004256. Public Library of Science
PLoS Genetics; Vol 10
PLoS Genetics, 10(4)
PLoS Genetics
PLoS Genetics, Vol 10, Iss 4, p e1004256 (2014)
PLoS genetics, 10(4). Public Library of Science
PL o S Genetics (Online), 10(4)
PLOS GENETICS
Opis pliku :
application/pdf; text; Electronic-eCollection
Dostępność :
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97eeeaf9408837a102bd70851ffb4cb2
https://opus.bibliothek.uni-wuerzburg.de/frontdoor/index/index/docId/11682
Tytuł :
Occupational Solvent Exposure, Genetic Variation of DNA Repair Genes, and Risk of Non-Hodgkin Lymphoma
Autorzy :
Brian P. Leaderer
Qian Deng
Qing Lan
Tongzhang Zheng
Jie Jiao
Zhao-lin Xia
Xiaofeng Bi
Theodore R. Holford
Peter Boyle
Yue Ba
Yingtai Chen
Yawei Zhang
Nathaniel Rothman
Christopher Kim
Stephen J. Chanock
Pokaż więcej
Temat :
Article
Adult Aged Aged
80 and over BRCA2 Protein/genetics Case-Control Studies Cell Cycle Proteins/genetics Connecticut/epidemiology DNA Modification Methylases/genetics DNA Repair/*genetics DNA Repair Enzymes/genetics Female Genetic Predisposition to Disease Humans Lymphoma
Follicular/epidemiology/*etiology Lymphoma
Large B-Cell
Diffuse/epidemiology/*etiology Middle Aged Nuclear Proteins/genetics Occupational Exposure/*adverse effects Polymorphism
Single Nucleotide/*genetics Prognosis Risk Factors Solvents/*adverse effects Tumor Markers
Biological/*genetics Tumor Suppressor Proteins/genetics Young Adult
[SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie
Cancer Research
Public Health, Environmental and Occupational Health
Oncology
Epidemiology
Internal medicine
medicine.medical_specialty
medicine
Case-control study
Solvent exposure
chemistry.chemical_compound
chemistry
Biology
Single-nucleotide polymorphism
Odds ratio
DNA repair
Non-Hodgkin's lymphoma
medicine.disease
Population
education.field_of_study
education
Follicular lymphoma
Immunology
Źródło :
Europe PubMed Central
European Journal of Cancer Prevention
European Journal of Cancer Prevention, Lippincott, Williams & Wilkins, 2012, 21 (6), pp.580-4. ⟨10.1097/CEJ.0b013e328351c762⟩
Dostępność :
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb40455fd9ffe1c1705a7e9640060f2c
https://europepmc.org/articles/PMC3397155/

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