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Wyszukujesz frazę ""Martinet, D."" wg kryterium: Autor


Tytuł :
Fast generation of high producer cho cell lines by an iterative transfection process
Autorzy :
Martinet D
Calabrese D
Grandjean M
Girod P-A
Beckmann J
Mermod N
Pokaż więcej
Temat :
Microbiology
QR1-502
Źródło :
Microbial Cell Factories, Vol 5, Iss Suppl 1, p S41 (2006)
Opis pliku :
electronic resource
Relacje :
https://doaj.org/toc/1475-2859
Dostęp URL :
https://doaj.org/article/6cb1794330e94aa9928e3eef05cbebd6
Czasopismo naukowe
Tytuł :
Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity.
Autorzy :
Walters, RG
Coin, LJM
Ruokonen, A
de Smith, AJ
Moustafa, JSE-S
Jacquemont, S
Elliott, P
Esko, T
Hartikainen, A-L
Laitinen, J
Maennik, K
Martinet, D
Meyre, D
Nauck, M
Schurmann, C
Sladek, R
Thorleifsson, G
Thorsteinsdottir, U
Valsesia, A
Waeber, G
Zufferey, F
Balkau, B
Pattou, F
Metspalu, A
Voelzke, H
Vollenweider, P
Stefansson, K
Jarvelin, M-R
Beckmann, JS
Froguel, P
Blakemore, AIF
Pokaż więcej
Temat :
Human Genetics
Kinesin
CIRCULAR BINARY SEGMENTATION
Genetic Loci
COPY NUMBER VARIATION
Forkhead Transcription Factors
Science & Technology - Other Topics
Female
Obesity
Case-Control Studies
MD Multidisciplinary
Biology
Genetics of Disease
Body Mass Index
Chromosomes, Human, Pair 16
WIDE ASSOCIATION
Heredity
SNP GENOTYPING DATA
Nutrition
HIDDEN-MARKOV MODEL
Science & Technology
Science
Cohort Studies
Adolescent
CHROMOSOME 16P11.2
Adult
Chromosome Deletion
Male
Child
Computational Biology
Research Article
COHORT
MULTIDISCIPLINARY SCIENCES
EARLY-ONSET
Genetics
Genomics
Child, Preschool
Structural Genomics
Clinical Research Design
Aged
Complex Traits
Medicine
Middle Aged
BODY-MASS INDEX
CHILDHOOD OBESITY
Genome-Wide Association Study
General Science & Technology
Genetic Association Studies
Adolescent Adult Aged Body Mass Index Child Child, Preschool *Chromosome Deletion Chromosomes, Human, Pair 16/*genetics Cohort Studies Female Forkhead Transcription Factors/genetics *Genetic Loci Genome-Wide Association Study Humans Kinesin/genetics Male Middle Aged Obesity/*genetics
Humans
Źródło :
PLoS ONE, Vol 8, Iss 3, p e58048 (2013)
Plos One, vol. 8, no. 3, pp. e58048
Opis pliku :
application/pdf
Tytuł :
A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.
Autorzy :
Zufferey, F
Sherr, E. H
Beckmann, N. D
Hanson, E
Maillard, A. M
Hippolyte, L
Macé, A
Ferrari, C
Kutalik, Z
Andrieux, J
Aylward, E
Barker, M
Bernier, R
Bouquillon, S
Conus, P
Delobel, B
Faucett, W. A
Goin-Kochel, R. P
Grant, E
Harewood, L
Hunter, J. V
Lebon, S
Ledbetter, D. H
Martin, C. L
Männik, K
Martinet, D
Mukherjee, P
Ramocki, M. B
Spence, S. J
Steinman, K. J
Tjernage, J
Spiro, J. E
Reymond, A
Beckmann, J. S
Chung, W. K
Jacquemont, S
Addor, M. C
Arveiler, B
Belfiore, M
Bena, F
Bernardini, L
Blanchet, P
Bonneau, D
Boute, O
Callier, P
Campion, D
Chiesa, J
Cordier, M. P
Cuisset, J. M
David, A
De Leeuw, N
De Vries, B
Didelot, G
Doco-Fenzy, M
Bedu, B. D
Dubourg, C
Dupuis-Girod, S
Fagerberg, C. R
Faivre, L
Fellmann, F
Fernandez, B. A
Fisher, R
Flori, E
Goldenberg, A
Heron, D
Holder, M
Hoyer, J
Isidor, B
Jaillard, S
Jonveaux, P
Joriot, S
Journel, H
Kooy, F
le Caignec, C
Leheup, B
Lemaitre, M. -P
Lewis, S
Malan, V
Mathieu-Dramard, M
Metspalu, A
Morice-Picard, F
Mucciolo, M
Oiglane-Shlik, E
Ounap, K
Pasquier, L
Petit, F
Philippe, A
Plessis, G
Prieur, F
Puechberty, J
Rajcan-Separovic, E
Rauch, A
Renieri, A
Rieubland, C
Rooryck, C
Rötzer, K. M
Ruiter, M
Sanlaville, D
Selmoni, S
Shen, Y
Siffredi, V
Thonney, J
Vallée, L
Van Binsbergen, E
Van der Aa, N
Van Haelst, M. M
Vigneron, J
Vincent-Delorme, C
Vittoria, D
Vulto-Van Silfhout, A. T
Witwicki, R. M
Zwolinski, S. A
Bowe, A
Beaudet, A. L
Brewton, C. M
Chu, Z
Dempsey, A. G
Evans, Y. L
Garza, S
Kanne, S. M
Laakman, A. L
Lasala, M. W
Llorens, A. V
Marzano, G
Moss, T. J
Nowell, K. P
Proud, M. B
Chen, Q
Vaughan, R
Berman, J
Blaskey, L
Hines, K
Kessler, S
Khan, S. Y
Qasmieh, S
Bibb, A. L
Paal, A. M
Page, P. Z
Smith-Packard, B
Buckner, R
Burko, J
Cavanagh, A. L
Cerban, B
Snow, A. V
Snyder, L. G
Keehn, R. M
Miller, D. T
Miller, F. K
Olson, J. E
Triantafallou, C
Visyak, N
Atwell, C
Benedetti, M
Fischbach, G. D
Greenup, M
Packer, A
Bukshpun, P
Cheong, M
Dale, C
Gobuty, S. E
Hinkley, L
Jeremy, R. J
Lee, H
Luks, T. L
Marco, E. J
Martin, A. J
Mcgovern, K. E
Nagarajan, S. S
Owen, J
Paul, B. M
Pojman, N. J
Sinha, T
Swarnakar, V
Wakahiro, M
Alupay, H
Aaronson, B
Ackerman, S
Ankenman, K
Elgin, J
Gerdts, J
Johnson, K
Reilly, B
Shaw, D
Stevens, A
Ward, T
Wenegrat, J
Roberts, T. P. L.
Pokaż więcej
Temat :
Adolescent
Adult
Body Mass Index
Child
Child Development Disorders, Pervasive/diagnosis
Child Development Disorders, Pervasive/genetics
Chromosome Deletion
Chromosomes, Human, Pair 16
Developmental Disabilities/diagnosis
Developmental Disabilities/genetics
Female
Gene Order
Heterozygote
Humans
Intelligence Tests
Male
Phenotype
Syndrome
Young Adult
Copy-Number Variation
Clinical genetics
Complex traits
[SDV]Life Sciences [q-bio]
Psychiatry
Obesity
Human medicine
Źródło :
Journal of Medical Genetics
Journal of medical genetics
Journal of Medical Genetics, BMJ Publishing Group, 2012, 49 (10), pp.660-8. ⟨10.1136/jmedgenet-2012-101203⟩
Journal of Medical Genetics, vol. 49, no. 10, pp. 660-668
Opis pliku :
application/pdf; pdf
Tytuł :
Presence of an oligodendroglioma-like component in newly diagnosed glioblastoma identifies a pathogenetically heterogeneous subgroup and lacks prognostic value: central pathology review of the EORTC_26981/NCIC_CE.3 trial
Autorzy :
Hegi, M.E.
Janzer, R.C.
Lambiv, W.L.
Gorlia, T
Kouwenhoven, M.C.
Hartmann, C.
von Deimling, A.
Martinet, D.
Besuchet Schmutz, N.
Diserens, A.C.
Hamou, M.F.
Bady, P.
Weller, M.
van den Bent, M.J.
Mason, W.P.
Mirimanoff, R.O.
Stupp, R.
Mokhtari, K.
Wesseling, P.
Pokaż więcej
Temat :
Clinic for Neurology
nervous system diseases
610 Medicine & health
Źródło :
Acta Neuropathologica, 123(6), 841 - 852. Springer Verlag
Acta Neuropathologica, 123, 841 - 852
Hegi, M E; Janzer, R C; Lambiv, W L; Gorlia, T; Kouwenhoven, M C M; Hartmann, C; von Deimling, A; Martinet, D; Besuchet Schmutz, N; Diserens, A C; Hamou, M F; Bady, P; Weller, M; van den Bent, M J; Mason, W P; Mirimanoff, R O; Stupp, R; Mokhtari, K; Wesseling, P (2012). Presence of an oligodendroglioma-like component in newly diagnosed glioblastoma identifies a pathogenetically heterogeneous subgroup and lacks prognostic value: central pathology review of the EORTC_26981/NCIC_CE.3 trial. Acta Neuropathologica, 123(6):841-852.
Opis pliku :
application/pdf
Tytuł :
A new highly penetrant form of obesity due to deletions on chromosome 16p11.2
Autorzy :
Walters, R. G.
Jacquemont, S.
Valsesia, A.
de Smith, A. J.
Martinet, D.
Andersson, J.
Falchi, M.
Chen, F.
Andrieux, J.
Lobbens, S.
Delobel, B.
Stutzmann, F.
Moustafa, J. S. El-Sayed
Chevre, J.-C.
Lecoeur, C.
Vatin, V.
Bouquillon, S.
Buxton, J. L.
Boute, O.
Holder-Espinasse, M.
Cuisset, J.-M.
Lemaitre, M.-P.
Ambresin, A.-E.
Brioschi, A.
Gaillard, M.
Giusti, V.
Fellmann, F.
Ferrarini, A.
Hadjikhani, N.
Campion, D.
Guilmatre, A.
Goldenberg, A.
Calmels, N.
Mandel, J.-L.
Le Caignec, C.
David, A.
Isidor, B.
Cordier, M.-P.
Dupuis-Girod, S.
Labalme, A.
Sanlaville, D.
Beri-Dexheimer, M.
Jonveaux, P.
Leheup, B.
Ounap, K.
Bochukova, E. G.
Henning, E.
Keogh, J.
Ellis, R. J.
MacDermot, K. D.
van Haelst, M. M.
Vincent-Delorme, C.
Plessis, G.
Touraine, R.
Philippe, A.
Malan, V.
Mathieu-Dramard, M.
Chiesa, J.
Blaumeiser, B.
Kooy, R. F.
Caiazzo, R.
Pigeyre, M.
Balkau, B.
Sladek, R.
Bergmann, S.
Mooser, V.
Waterworth, D.
Reymond, A.
Vollenweider, P.
Waeber, G.
Kurg, A.
Palta, P.
Esko, T.
Metspalu, A.
Nelis, M.
Elliott, P.
Hartikainen, A.-L.
McCarthy, M. I.
Peltonen, L.
Carlsson, L.
Jacobson, P.
Sjostrom, L.
Huang, N.
Hurles, M. E.
O'Rahilly, S.
Farooqi, I. S.
Maennik, K.
Jarvelin, M.-R.
Pattou, F.
Meyre, D.
Walley, A. J.
Coin, L. J. M.
Blakemore, A. I. F.
Froguel, P.
Beckmann, J. S.
Pokaż więcej
Temat :
MICRODELETION
CIRCULAR BINARY SEGMENTATION
MULTIDISCIPLINARY SCIENCES
INDIVIDUALS
AUTISM
Science & Technology
COPY NUMBER VARIATION
CHILDHOOD OBESITY
RISK LOCI
Science & Technology - Other Topics
GENOME-WIDE ASSOCIATION
MENTAL-RETARDATION
FRAMESHIFT MUTATION
Human medicine
Źródło :
463
Opis pliku :
pdf
Tytuł :
Recurrent Deletions and Reciprocal Duplications of 10q11.21q11.23 Including CHAT and SLC18A3 are Likely Mediated by Complex Low-Copy Repeats
Autorzy :
Stankiewicz, P.
Kulkarni, S.
Dharmadhikari, A.V.
Sampath, S.
Bhatt, S.S.
Shaikh, T.H.
Xia, Z.
Pursley, A.N.
Cooper, M.L.
Shinawi, M.
Paciorkowski, A.R.
Grange, D.K.
Noetzel, M.J.
Saunders, S.
Simons, P.
Summar, M.
Lee, B.
Scaglia, F.
Fellmann, F.
Martinet, D.
Beckmann, J.S.
Asamoah, A.
Platky, K.
Sparks, S.
Martin, A.S.
Madan-Khetarpal, S.
Hoover, J.
Medne, L.
Bonnemann, C.G.
Moeschler, J.B.
Vallee, S.E.
Parikh, S.
Irwin, P.
Dalzell, V.P.
Smith, W.E.
Banks, V.C.
Flannery, D.B.
Lovell, C.M.
Bellus, G.A.
Golden-Grant, K.
Gorski, J.L.
Kussmann, J.L.
McGregor, T.L.
Hamid, R.
Pfotenhauer, J.
Ballif, B.C.
Shaw, C.A.
Kang, S.H.
Bacino, C.A.
Patel, A.
Rosenfeld, J.A.
Cheung, S.W.
Shaffer, L.G.
Pokaż więcej
Temat :
Abnormalities, Multiple/genetics
Child
Child, Preschool
Chromosome Aberrations
Chromosome Mapping
Chromosomes, Human, Pair 10
DNA Copy Number Variations
Developmental Disabilities/complications
Developmental Disabilities/genetics
Female
Genetic Variation
Homologous Recombination
Humans
In Situ Hybridization, Fluorescence
Infant
Intellectual Disability/complications
Intellectual Disability/genetics
Male
Nerve Growth Factors/genetics
Oligonucleotide Array Sequence Analysis
Penetrance
Segmental Duplications, Genomic/genetics
Sequence Deletion
Vesicular Acetylcholine Transport Proteins/genetics
Article
Źródło :
Human Mutation, vol. 33, no. 1, pp. 165-179
Opis pliku :
application/pdf
Tytuł :
16q24.1 microdeletion in a premature newborn: Usefulness of array-based comparative genomic hybridization in persistent pulmonary hypertension of the newborn.
Autorzy :
Zufferey, F.
Martinet, D.
Osterheld, M.C.
Niel-Bütschi, F.
Giannoni, E.
Schmutz, N.B.
Xia, Z.
Beckmann, J.S.
Shaw-Smith, C.
Stankiewicz, P.
Langston, C.
Fellmann, F.
Pokaż więcej
Źródło :
Pediatric Critical Care Medicine, vol. 12, no. 6, pp. e427-e432
Opis pliku :
application/pdf
Tytuł :
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.
Autorzy :
Jacquemont, S.
Reymond, A.
Zufferey, F.
Harewood, L.
Walters, R.G.
Kutalik, Z.
Martinet, D.
Shen, Y.
Valsesia, A.
Beckmann, N.D.
Thorleifsson, G.
Belfiore, M.
Bouquillon, S.
Campion, D.
de Leeuw, N.
de Vries, B.B.
Esko, T.
Fernandez, B.A.
Fernández-Aranda, F.
Fernández-Real, J.M.
Gratacòs, M.
Guilmatre, A.
Hoyer, J.
Jarvelin, M.R.
Kooy, R.F.
Kurg, A.
Le Caignec, C.
Männik, K.
Platt, O.S.
Sanlaville, D.
Van Haelst, M.M.
Villatoro Gomez, S.
Walha, F.
Wu, B.L.
Yu, Y.
Aboura, A.
Addor, M.C.
Alembik, Y.
Antonarakis, S.E.
Arveiler, B.
Barth, M.
Bednarek, N.
Béna, F.
Bergmann, S.
Beri, M.
Bernardini, L.
Blaumeiser, B.
Bonneau, D.
Bottani, A.
Boute, O.
Brunner, H.G.
Cailley, D.
Callier, P.
Chiesa, J.
Chrast, J.
Coin, L.
Coutton, C.
Cuisset, J.M.
Cuvellier, J.C.
David, A.
de Freminville, B.
Delobel, B.
Delrue, M.A.
Demeer, B.
Descamps, D.
Didelot, G.
Dieterich, K.
Disciglio, V.
Doco-Fenzy, M.
Drunat, S.
Duban-Bedu, B.
Dubourg, C.
El-Sayed Moustafa, J.S.
Elliott, P.
Faas, B.H.
Faivre, L.
Faudet, A.
Fellmann, F.
Ferrarini, A.
Fisher, R.
Flori, E.
Forer, L.
Gaillard, D.
Gerard, M.
Gieger, C.
Gimelli, S.
Gimelli, G.
Grabe, H.J.
Guichet, A.
Guillin, O.
Hartikainen, A.L.
Heron, D.
Hippolyte, L.
Holder, M.
Homuth, G.
Isidor, B.
Jaillard, S.
Jaros, Z.
Jiménez-Murcia, S.
Helas, G.J.
Jonveaux, P.
Kaksonen, S.
Keren, B.
Kloss-Brandstätter, A.
Knoers, N.V.
Koolen, D.A.
Kroisel, P.M.
Kronenberg, F.
Labalme, A.
Landais, E.
Lapi, E.
Layet, V.
Legallic, S.
Leheup, B.
Leube, B.
Lewis, S.
Lucas, J.
MacDermot, K.D.
Magnusson, P.
Marshall, C.
Mathieu-Dramard, M.
McCarthy, M.I.
Meitinger, T.
Mencarelli, M.A.
Merla, G.
Moerman, A.
Mooser, V.
Morice-Picard, F.
Mucciolo, M.
Nauck, M.
Ndiaye, N.C.
Nordgren, A.
Pasquier, L.
Petit, F.
Pfundt, R.
Plessis, G.
Rajcan-Separovic, E.
Ramelli, G.P.
Rauch, A.
Ravazzolo, R.
Reis, A.
Renieri, A.
Richart, C.
Ried, J.S.
Rieubland, C.
Roberts, W.
Roetzer, K.M.
Rooryck, C.
Rossi, M.
Saemundsen, E.
Satre, V.
Schurmann, C.
Sigurdsson, E.
Stavropoulos, D.J.
Stefansson, H.
Tengström, C.
Thorsteinsdóttir, U.
Tinahones, F.J.
Touraine, R.
Vallée, L.
van Binsbergen, E.
Van der Aa, N.
Vincent-Delorme, C.
Visvikis-Siest, S.
Vollenweider, P.
Völzke, H.
Vulto-van Silfhout, A.T.
Waeber, G.
Wallgren-Pettersson, C.
Witwicki, R.M.
Zwolinksi, S.
Andrieux, J.
Estivill, X.
Gusella, J.F.
Gustafsson, O.
Metspalu, A.
Scherer, S.W.
Stefansson, K.
Blakemore, A.I.
Beckmann, J.S.
Froguel, P.
Pokaż więcej
Źródło :
Nature, vol. 478, no. 7367, pp. 97-102
Opis pliku :
application/pdf
Tytuł :
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus
Autorzy :
Jacquemont, S
Reymond, A
Zufferey, F
Harewood, L
Walters, R G
Kutalik, Z
Martinet, D
Shen, Y
Valsesia, A
Beckmann, N D
Thorleifsson, G
Belfiore, M
Bouquillon, S
Campion, D
De Leeuw, N
De Vries, B B A
Esko, T
Fernandez, B A
Fernández-Aranda, F
Fernández-Real, J M
Gratacòs, M
Guilmatre, A
Hoyer, J
Jarvelin, M R
Kooy, R F
Kurg, A
Le Caignec, C
Männik, K
Platt, O S
Sanlaville, D
Van Haelst, M M
Villatoro Gomez, S
Walha, F
Wu, B L
Yu, Y
Abourae, A
Addor, M C
Alembik, Y
Antonarakis, S E
Arveiler, B
Barth, M
Bednarek, N
Béna, F
Bergmann, S
Beri, M
Bernardini, L
Blaumeiser, B
Bonneau, D
Bottani, A
Boute, O
Brunner, H G
Cailley, D
Callier, P
Chiesa, J
Chrast, J
Coin, L
Coutton, C
Cuisset, J M
Cuvellier, J C
David, A
De Freminville, B
Delobel, B
Delrue, M A
Demeer, B
Descamps, D
Didelot, G
Dieterich, K
Disciglio, V
Doco-Fenzy, M
Drunat, S
Duban-Bedu, B
Dubourg, C
El-Sayed Moustafa, J S
Elliott, P
Faas, B H W
Faivre, L
Faudet, A
Fellmann, F
Ferrarini, A
Fisher, R
Flori, E
Forer, L
Gaillard, D
Gerard, M
Gieger, C
Gimelli, S
Gimelli, G
Grabe, H J
Guichet, A
Guillin, O
Hartikainen, A L
Heron, D
Hippolyte, L
Holder, M
Homuth, G
Isidor, B
Jaillard, S
Jaros, Z
Jiménez-Murcia, S
Helas, G J
Jonveaux, P
Kaksonen, S
Keren, B
Kloss-Brandstätter, A
Knoers, N V A M
Koolen, D A
Kroisel, P M
Kronenberg, F
Labalme, A
Landais, E
Lapi, E
Layet, V
Legallic, S
Leheup, B
Leube, B
Lewis, S
Lucas, J
MacDermot, K D
Magnusson, P
Marshall, C
Mathieu-Dramard, M
McCarthy, M I
Meitinger, T
Mencarelli, M A
Merla, G
Moerman, A
Mooser, V
Morice-Picard, F
Mucciolo, M
Nauck, M
Ndiaye, N C
Nordgren, A
Pasquier, L
Petit, F
Pfundt, R
Plessis, G
Rajcan-Separovic, E
Ramelli, G P
Rauch, A
Ravazzolo, R
Reis, A
Renieri, A
Richart, C
Ried, J S
Rieubland, C
Roberts, W
Roetzer, K M
Rooryck, C
Rossi, M
Saemundsen, E
Satre, V
Schurmann, C
Sigurdsson, E
Stavropoulos, D J
Stefansson, H
Tengström, C
Thorsteinsdóttir, U
Tinahones, F J
Touraine, R
Vallée, L
Van Binsbergen, E
Van Der Aa, N
Vincent-Delorme, C
Visvikis-Siest, S
Vollenweider, P
Völzke, H
Vulto-Van Silfhout, A T
Waeber, G
Wallgren-Pettersson, C
Witwicki, R M
Zwolinksi, S
Andrieux, J
Estivill, X
Gusella, J F
Gustafsson, O
Metspalu, A
Scherer, S W
Stefansson, K
Blakemore, A I F
Beckmann, J S
Froguel, P
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