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Wyszukujesz frazę ""Guanine Nucleotide Exchange Factors genetics"" wg kryterium: Temat


Tytuł :
IQSEC2-related encephalopathy in males and females: a comparative study including 37 novel patients
Autorzy :
Mignot, Cyril
McMahon, Aoife C.
Bar, Claire
Campeau, Philippe M.
Davidson, Claire
Buratti, Julien
Nava, Caroline
Jacquemont, Marie-Line
Tallot, Marilyn
Milh, Mathieu
Edery, Patrick
Marzin, Pauline
Barcia, Giulia
Barnerias, Christine
Besmond, Claude
Bienvenu, Thierry
Bruel, Ange-Line
Brunga, Ledia
Ceulemans, Berten
Coubes, Christine
Cristancho, Ana G.
Cunningham, Fiona
Dehouck, Marie-Bertille
Donner, Elizabeth J.
Duban-Bedu, Benedicte
Dubourg, Christele
Gardella, Elena
Gauthier, Julie
Genevieve, David
Gobin-Limballe, Stephanie
Goldberg, Ethan M.
Hagebeuk, Eveline
Hamdan, Fadi F.
Hancarova, Miroslava
Hubert, Laurence
Ioos, Christine
Ichikawa, Shoji
Janssens, Sandra
Journel, Hubert
Kaminska, Anna
Keren, Boris
Koopmans, Marije
Lacoste, Caroline
Lassuthova, Petra
Lederer, Damien
Lehalle, Daphne
Marjanovic, Dragan
Metreau, Julia
Michaud, Jacques L.
Miller, Kathryn
Minassian, Berge A.
Morales, Joannella
Moutard, Marie-Laure
Munnich, Arnold
Ortiz-Gonzalez, Xilma R.
Pinard, Jean-Marc
Prchalova, Darina
Putoux, Audrey
Quelin, Chloe
Rosen, Alyssa R.
Roume, Joelle
Rossignol, Elsa
Simon, Marleen E. H.
Smol, Thomas
Shur, Natasha
Shelihan, Ivan
Sterbova, Katalin
Vyhnalkova, Emilie
Vilain, Catheline
Soblet, Julie
Smits, Guillaume
Yang, Samuel P.
van der Smagt, Jasper J.
van Hasselt, Peter M.
van Kempen, Marjan
Weckhuysen, Sarah
Helbig, Ingo
Villard, Laurent
Heron, Delphine
Koeleman, Bobby
Moller, Rikke S.
Lesca, Gaetan
Helbig, Katherine L.
Nabbout, Rima
Verbeek, Nienke E.
Depienne, Christel
Pokaż więcej
Temat :
epilepsy
Seizures/epidemiology
isoforms
Infant, Newborn
Brain Diseases/epidemiology
Infant
Research Support, Non-U.S. Gov't
Intellectual Disability/epidemiology
Protein Isoforms/genetics
Female
Phenotype
Genetics(clinical)
X-linked inheritance
Guanine Nucleotide Exchange Factors/genetics
Article
Sex Characteristics
Pedigree
Mutation
IQSEC2
Brain/growth & development
[SDV]Life Sciences [q-bio]
Journal Article
[SDV.MHEP]Life Sciences [q-bio]/Human health and pathology
Humans
Human medicine
intellectual disability
Male
Źródło :
Genetics in Medicine, Nature Publishing Group, 2018, 21 (8), pp.1897-1898. ⟨10.1038/s41436-018⟩
Genetics in Medicine, 21(4), 837. Lippincott Williams and Wilkins
Mignot, C, McMahon, A C, Bar, C, Campeau, P M, Davidson, C, Buratti, J, Nava, C, Jacquemont, M-L, Tallot, M, Milh, M, Edery, P, Marzin, P, Barcia, G, Barnerias, C, Besmond, C, Bienvenu, T, Bruel, A-L, Brunga, L, Ceulemans, B, Coubes, C, Cristancho, A G, Cunningham, F, Dehouck, M-B, Donner, E J, Duban-Bedu, B, Dubourg, C, Gardella, E, Gauthier, J, Geneviève, D, Gobin-Limballe, S, Goldberg, E M, Hagebeuk, E, Hamdan, F F, Hančárová, M, Hubert, L, Ioos, C, Ichikawa, S, Janssens, S, Journel, H, Kaminska, A, Keren, B, Koopmans, M, Lacoste, C, Laššuthová, P, Lederer, D, Lehalle, D, Marjanovic, D, Métreau, J, Michaud, J L, Miller, K, Minassian, B A, Morales, J, Moutard, M-L, Munnich, A, Ortiz-Gonzalez, X R, Pinard, J-M, Prchalová, D, Putoux, A, Quelin, C, Rosen, A R, Roume, J, Rossignol, E, Simon, M E H, Smol, T, Shur, N, Shelihan, I, Štěrbová, K, Vyhnálková, E, Vilain, C, Soblet, J, Smits, G, Yang, S P, van der Smagt, J J, van Hasselt, P M, van Kempen, M, Weckhuysen, S, Helbig, I, Villard, L, Héron, D, Koeleman, B, Møller, R S, Lesca, G, Helbig, K L, Nabbout, R, Verbeek, N E & Depienne, C 2019, ' IQSEC2-related encephalopathy in males and females : a comparative study including 37 novel patients ', Genetics in Medicine, vol. 21, no. 4, pp. 837-849 . https://doi.org/10.1038/s41436-018-0268-1
Opis pliku :
pdf; image/pdf; application/pdf
Tytuł :
Variants in genes encoding small GTPases and association with epithelial ovarian cancer susceptibility.
Autorzy :
Dennis, Joe
Bruinsma, Fiona
Cunningham, Julie M.
Giles, Graham G.
Jakubowska, Anna
Li, Zheng
Sellers, Thomas A.
Pharoah, Paul D. P.
Goode, Ellen L.
Earp, Madalene
Tyrer, Jonathan P.
Winham, Stacey J.
Lin, Hui-Yi
Chornokur, Ganna
Aben, Katja K. H.
Anton‐Culver, Hoda
Antonenkova, Natalia
Bandera, Elisa V.
Bean, Yukie T.
Beckmann, Matthias W.
Bjorge, Line
Bogdanova, Natalia
Brinton, Louise A.
Brooks-Wilson, Angela
Bunker, Clareann H.
Butzow, Ralf
Campbell, Ian G.
Carty, Karen
Chang-Claude, Jenny
Cook, Linda S.
Cramer, Daniel W
Cybulski, Cezary
Dansonka-Mieszkowska, Agnieszka
Despierre, Evelyn
Doherty, Jennifer A.
Dörk, Thilo
du Bois, Andreas
Dürst, Matthias
Easton, Douglas F.
Eccles, Diana M.
Edwards, Robert P.
Ekici, Arif B.
Fasching, Peter A.
Fridley, Brooke L.
Gentry-Maharaj, Aleksandra
Glasspool, Rosalind
Goodman, Marc T.
Gronwald, Jacek
Harter, Philipp
Hein, Alexander
Heitz, Florian
Hildebrandt, Michelle A. T.
Hillemanns, Peter
Hogdall, Claus K.
Høgdall, Estrid
Hosono, Satoyo
Iversen, Edwin S.
Jensen, Allan
Ji, Bu-Tian
Jung, Audrey Y.
Karlan, Beth Y.
Kellar, Melissa
Kiemeney, Lambertus A.
Kiong Lim, Boon
Kjaer, Susanne K.
Krakstad, Camilla
Kupryjanczyk, Jolanta
Lambrechts, Diether
Lambrechts, Sandrina
Le, Nhu D.
Lele, Shashi
Lester, Jenny
Levine, Douglas A.
Liang, Dong
Lissowska, Jolanta
Lu, Karen
Lubinski, Jan
Lundvall, Lene
Massuger, Leon F. A. G.
Matsuo, Keitaro
McGuire, Valerie
McLaughlin, John R.
McNeish, Iain
Menon, Usha
Milne, Roger L.
Modugno, Francesmary
Moysich, Kirsten B.
Ness, Roberta B.
Nevanlinna, Heli
Odunsi, Kunle
Olson, Sara H.
Orlow, Irene
Orsulic, Sandra
Paul, James
Pejovic, Tanja
Pelttari, Liisa M.
Permuth, Jenny B.
Pike, Malcolm C.
Poole, Elizabeth M.
Rosen, Barry
Rossing, Mary Anne
Rothstein, Joseph H.
Runnebaum, Ingo B.
Rzepecka, Iwona K.
Schernhammer, Eva
Schwaab, Ira
Shu, Xiao-Ou
Shvetsov, Yurii B.
Siddiqui, Nadeem
Sieh, Weiva
Song, Honglin
Southey, Melissa C.
Spiewankiewicz, Beata
Sucheston-Campbell, Lara
Tangen, Ingvild L.
Teo, Soo-Hwang
Terry, Kathryn L.
Thompson, Pamela J.
Thomsen, Lotte
Tworoger, Shelley S.
van Altena, Anne M.
Vergote, Ignace
Vestrheim Thomsen, Liv Cecilie
Vierkant, Robert A.
Walsh, Christine S.
Wang-Gohrke, Shan
Wentzensen, Nicolas
Whittemore, Alice S.
Wicklund, Kristine G.
Wilkens, Lynne R.
Woo, Yin-Ling
Wu, Anna H.
Wu, Xifeng
Xiang, Yong-Bing
Yang, Hannah
Zheng, Wei
Ziogas, Argyrios
Lee, Alice W
Pearce, Celeste L.
Berchuck, Andrew
Schildkraut, Joellen M.
Ramus, Susan J.
Monteiro, Alvaro N. A.
Narod, Steven A.
Gayther, Simon A.
Kelemen, Linda E.
Chenevix-Trench, Georgia
Risch, Harvey A.
Phelan, Catherine M.
Pokaż więcej
Temat :
Cell Membranes
Human Genetics
Oncology
Research Support, Non-U.S. Gov't
endocrine system diseases
Signaling Molecules
Histology
Genome Analysis
Polymorphism, Single Nucleotide
Research Support, N.I.H., Intramural
Science & Technology - Other Topics
Female
Guanosine Triphosphatase
3122 Cancers
Risk Factors
MD Multidisciplinary
Biology and Life Sciences
Signal Transduction
Monomeric GTP-Binding Proteins/genetics
Guanine Nucleotide Exchange Factors
Enzymology
Genotype
Rho Guanine Nucleotide Exchange Factors
Ras Signaling
Science & Technology
Gene Regulation
Science
Research Support, U.S. Gov't, Non-P.H.S
Gene Expression
SUPER-ENHANCERS
Polymorphism, Single Nucleotide/genetics
Carcinoma, Ovarian Epithelial
Computational Biology
Research Article
TRAITS
3123 Gynaecology and paediatrics
Anatomy
Carcinoma, Ovarian Epithelial/genetics
Enzymes
Quantitative Trait Loci/genetics
Multidisciplinary Sciences
Quantitative Trait Loci
Research Support, U.S. Gov't, P.H.S
Membrane Proteins
Genetics
3111 Biomedicine
Invasive Tumors
Proteins
A Kinase Anchor Proteins/genetics
Genomics
Cancers and Neoplasms
Hydrolases
Medicine
Monomeric GTP-Binding Proteins
Cell Biology
Research Support, N.I.H., Extramural
Cellular Structures and Organelles
CARCINOMA
Biochemistry
Cell Signaling
General Science & Technology
Genetic Association Studies
Journal Article
Medicine and Health Sciences
Genetic Predisposition to Disease
GENOME-WIDE ASSOCIATION
A Kinase Anchor Proteins
Genome-Wide Association Studies
Humans
Rho Guanine Nucleotide Exchange Factors/genetics
Źródło :
Earp, M, Tyrer, J P, Winham, S J, Lin, H-Y, Chornokur, G, Dennis, J, Aben, K K H, Anton-Culver, H, Antonenkova, N, Bandera, E V, Bean, Y T, Beckmann, M W, Bjorge, L, Bogdanova, N, Brinton, L A, Brooks-Wilson, A, Bruinsma, F, Bunker, C H, Butzow, R, Campbell, I G, Carty, K, Chang-Claude, J, Cook, L S, Cramer, D W, Cunningham, J M, Cybulski, C, Dansonka-Mieszkowska, A, Despierre, E, Doherty, J A, Dörk, T, du Bois, A, Dürst, M, Easton, D F, Eccles, D M, Edwards, R P, Ekici, A B, Fasching, P A, Fridley, B L, Gentry-Maharaj, A, Giles, G G, Glasspool, R, Goodman, M T, Gronwald, J, Harter, P, Hein, A, Heitz, F, Hildebrandt, M A T, Hillemanns, P, Hogdall, C K, Høgdall, E, Hosono, S, Iversen, E S, Jakubowska, A, Jensen, A, Ji, B-T, Jung, A Y, Karlan, B Y, Kellar, M, Kiemeney, L A, Kiong Lim, B, Kjaer, S K, Krakstad, C, Kupryjanczyk, J, Lambrechts, D, Lambrechts, S, Le, N D, Lele, S, Lester, J, Levine, D A, Li, Z, Liang, D, Lissowska, J, Lu, K, Lubinski, J, Lundvall, L, Massuger, L F A G, Matsuo, K, McGuire, V, McLaughlin, J R, McNeish, I, Menon, U, Milne, R L, Modugno, F, Moysich, K B, Ness, R B, Nevanlinna, H, Odunsi, K, Olson, S H, Orlow, I, Orsulic, S, Paul, J, Pejovic, T, Pelttari, L M, Permuth, J B, Pike, M C, Poole, E M, Rosen, B, Rossing, M A, Rothstein, J H, Runnebaum, I B, Rzepecka, I K, Schernhammer, E, Schwaab, I, Shu, X-O, Shvetsov, Y B, Siddiqui, N, Sieh, W, Song, H, Southey, M C, Spiewankiewicz, B, Sucheston-Campbell, L, Tangen, I L, Teo, S-H, Terry, K L, Thompson, P J, Thomsen, L, Tworoger, S S, van Altena, A M, Vergote, I, Vestrheim Thomsen, L C, Vierkant, R A, Walsh, C S, Wang-Gohrke, S, Wentzensen, N, Whittemore, A S, Wicklund, K G, Wilkens, L R, Woo, Y-L, Wu, A H, Wu, X, Xiang, Y-B, Yang, H, Zheng, W, Ziogas, A, Lee, A W, Pearce, C L, Berchuck, A, Schildkraut, J M, Ramus, S J, Monteiro, A N A, Narod, S A, Sellers, T A, Gayther, S A, Kelemen, L E, Chenevix-Trench, G, Risch, H A, Pharoah, P D P, Goode, E L & Phelan, C M 2018, ' Variants in genes encoding small GTPases and association with epithelial ovarian cancer susceptibility ', PLoS ONE, vol. 13, no. 7, e0197561 . https://doi.org/10.1371/journal.pone.0197561
PLoS ONE, Vol 13, Iss 7, p e0197561 (2018)
Opis pliku :
application/pdf; Electronic-eCollection; text
Tytuł :
An interaction map of circulating metabolites, immune gene networks, and their genetic regulation
Autorzy :
Nath, Artika P.
Ritchie, Scott C.
Byars, Sean G.
Fearnley, Liam G.
Havulinna, Aki S.
Joensuu, Anni
Kangas, Antti J.
Soininen, Pasi
Wennerström, Annika
Milani, Lili
Metspalu, Andres
Männistö, Satu
Würtz, Peter
Kettunen, Johannes
Raitoharju, Emma
Kähönen, Mika
Juonala, Markus
Palotie, Aarno
Ala-Korpela, Mika
Ripatti, Samuli
Lehtimäki, Terho
Abraham, Gad
Raitakari, Olli
Salomaa, Veikko
Perola, Markus
Inouye, Michael
Pokaż więcej
Temat :
Cardiovascular Diseases/genetics
Gene Expression Regulation/immunology
NATURAL-KILLER-CELLS
Biolääketieteet - Biomedicine
YOUNG FINNS
ADIPOSE-TISSUE
Quantitative Trait Loci/immunology
Research
C-Reactive Protein/genetics
Research Support, Non-U.S. Gov't
318 Medical biotechnology
Gene Ontology
QH426-470
IDENTIFICATION
3111 Biomedicine
Genetics
1184 Genetics, developmental biology, physiology
Polymorphism, Single Nucleotide
B-Lymphocytes/immunology
CARDIOVASCULAR RISK
Basophils/immunology
Genome, Human
HOST-DEFENSE
Gene Regulatory Networks/immunology
B-CELLS
QH301-705.5
Amino Acids/immunology
Follow-Up Studies
INSULIN-RESISTANCE
RECEPTOR
Immunity, Innate
Metabolic Syndrome/genetics
Blood Platelets/immunology
Fatty Acids/immunology
Neutrophils/immunology
PLATELET
Lipoproteins/genetics
Journal Article
Humans
Metabolome/genetics
Biology (General)
Rho Guanine Nucleotide Exchange Factors/genetics
Źródło :
Genome Biology, Vol 18, Iss 1, Pp 1-15 (2017)
Nath, A P, Ritchie, S C, Byars, S G, Fearnley, L G, Havulinna, A S, Joensuu, A, Kangas, A J, Soininen, P, Wennerström, A, Milani, L, Metspalu, A, Männistö, S, Würtz, P, Kettunen, J, Raitoharju, E, Kähönen, M, Juonala, M, Palotie, A, Ala-Korpela, M, Ripatti, S, Lehtimäki, T, Abraham, G, Raitakari, O, Salomaa, V, Perola, M & Inouye, M 2017, ' An interaction map of circulating metabolites, immune gene networks, and their genetic regulation ', Genome Biology, vol. 18, 146 . https://doi.org/10.1186/s13059-017-1279-y
Opis pliku :
application/pdf; fulltext
Tytuł :
Brefeldin A-Inhibited Guanine Nucleotide-Exchange Factor 1 (BIG1) Governs the Recruitment of Tumor Necrosis Factor Receptor-Associated Factor 2 (TRAF2) to Tumor Necrosis Factor Receptor 1 (TNFR1) Signaling Complexes
Autorzy :
Noguchi, T.
Tsuchida, M.
Kogue, Y.
Spadini, C.
Hirata, Y.
Matsuzawa, A.
Pokaż więcej
Temat :
Chemistry
tumor necrosis factor-α (TNF-α)
JNK
QD1-999
Apoptosis/drug effects
Cell Line, Tumor
Gene Expression Regulation
Genes, Reporter
Guanine Nucleotide Exchange Factors/antagonists & inhibitors
Guanine Nucleotide Exchange Factors/genetics
Guanine Nucleotide Exchange Factors/metabolism
HeLa Cells
Humans
JNK Mitogen-Activated Protein Kinases/antagonists & inhibitors
JNK Mitogen-Activated Protein Kinases/genetics
JNK Mitogen-Activated Protein Kinases/metabolism
Luciferases/genetics
Luciferases/metabolism
NF-kappa B/antagonists & inhibitors
NF-kappa B/genetics
NF-kappa B/metabolism
Protein Binding
Protein Transport
Proteolysis/drug effects
RNA, Small Interfering/genetics
RNA, Small Interfering/metabolism
Receptors, Tumor Necrosis Factor, Type I/antagonists & inhibitors
Receptors, Tumor Necrosis Factor, Type I/genetics
Receptors, Tumor Necrosis Factor, Type I/metabolism
Signal Transduction/genetics
TNF Receptor-Associated Factor 2/antagonists & inhibitors
TNF Receptor-Associated Factor 2/genetics
TNF Receptor-Associated Factor 2/metabolism
Tumor Necrosis Factor-alpha/pharmacology
Ubiquitination/drug effects
TRAF2
apoptosis
Biology (General)
Article
BIG1
QH301-705.5
Źródło :
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 17, Iss 11, p 1869 (2016)
International journal of molecular sciences, vol. 17, no. 11, pp. 1869
Opis pliku :
application/pdf
Tytuł :
Isolated and Syndromic Retinal Dystrophy Caused by Biallelic Mutations in RCBTB1, a Gene Implicated in Ubiquitination
Autorzy :
Coppieters, Frauke
Ascari, Giulia
Dannhausen, Katharina
Nikopoulos, Konstantinos
Peelman, Frank
Karlstetter, Marcus
Xu, Mingchu
Brachet, Cécile
Meunier, Isabelle
Tsilimbaris, Miltiadis
Tsika, Chrysanthi
Blazaki, Styliani
Vergult, Sarah
Farinelli, Pietro
Van Laethem, Thalia
Bauwens, Miriam
De Bruyne, Marieke
Chen, Rui
Langmann, Thomas
Sui, Ruifang
Meire, Françoise
Rivolta, Carlo
Hamel, Christian
Leroy, Bart
De Baere, Elfride
Pokaż więcej
Temat :
CHRONIC LYMPHOCYTIC-LEUKEMIA
Genetics(clinical)
Biology and Life Sciences
TRANSCRIPTION FACTOR NRF2
PROTEASOME SYSTEM
EXPRESSION ANALYSIS
Biologie
DOMINANT RETINITIS-PIGMENTOSA
EPITHELIAL-CELLS
[SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics
CONJUGATING ENZYME
Génétique clinique
Genetics
RESPONSE ELEMENT
PROTEIN
CHROMOSOME 13Q14
Report
Medicine and Health Sciences
Adolescent
Adult
Age of Onset
Alleles
Child
Consanguinity
Cullin Proteins/metabolism
Exome/genetics
Female
Founder Effect
Genes, Recessive
Guanine Nucleotide Exchange Factors/genetics
Haplotypes/genetics
Homozygote
Humans
Lymphocytes/metabolism
Male
Mutation, Missense/genetics
NF-E2-Related Factor 2/metabolism
Pedigree
Phenotype
RNA, Messenger/genetics
Retina/metabolism
Retinal Dystrophies/genetics
Syndrome
Turkey
Ubiquitination/genetics
Źródło :
American journal of human genetics, vol. 99, no. 2, pp. 470-480
American Journal of Human Genetics
AMERICAN JOURNAL OF HUMAN GENETICS
American Journal of Human Genetics, Elsevier (Cell Press), 2016, 99 (2), pp.470 - 480. ⟨10.1016/j.ajhg.2016.06.017⟩
American journal of human genetics, 99 (2
Opis pliku :
application/pdf; 1 full-text file(s): application/pdf
Tytuł :
A local VE-cadherin and Trio-based signaling complex stabilizes endothelial junctions through Rac1
Autorzy :
Timmerman, I.
Heemskerk, N.
Kroon, J.
Schaefer, A.
van Rijssel, J.
Hoogenboezem, M.
van Unen, J.
Goedhart, J.
Gadella, T.W.J.
Yin, T.
Wu, Y.
Huveneers, S.
van Buul, J.D.
Pokaż więcej
Temat :
Antigens, CD/genetics
GTP Phosphohydrolases/metabolism
Intercellular Junctions/genetics
Signal Transduction/genetics
Capillary Permeability/genetics
Endothelial Cells/metabolism
Guanine Nucleotide Exchange Factors/genetics
Endothelium, Vascular/metabolism
Protein-Serine-Threonine Kinases/genetics
Actin Cytoskeleton/genetics
Human Umbilical Vein Endothelial Cells
rac1 GTP-Binding Protein/genetics
Correction
Cadherins/genetics
Humans
Źródło :
Journal of Cell Science, 128(16), 3041 - 54. Company of Biologists Ltd
Journal of Cell Science, 128(16), 3041 - 3054. Company of Biologists Ltd
Journal of cell science, 128(16), 3041 - 3054. Company of Biologists Ltd
Opis pliku :
application/pdf
Tytuł :
Human CalDAG-GEFI gene ( RASGRP2 ) mutation affects platelet function and causes severe bleeding
Autorzy :
Canault, Matthias
Ghalloussi, Dorsaf
Grosdidier, Charlotte
Guinier, Marie
Perret, Claire
Chelghoum, Nadjim
Germain, Marine
Raslova, Hana
Peiretti, Franck
Morange, Pierre E.
Saut, Noemie
Pillois, Xavier
Nurden, Alan T.
Cambien, François
Pierres, Anne
van den Berg, Timo K.
Kuijpers, Taco W.
Alessi, Marie-Christine
Tregouet, David-Alexandre
Pokaż więcej
Temat :
Hemorrhage/genetics
Protein Kinase C/genetics
Blood Coagulation Disorders, Inherited/genetics
[SDV.BC.BC]Life Sciences [q-bio]/Cellular Biology/Subcellular Processes [q-bio.SC]
Heterozygote
Guanine Nucleotide Exchange Factors/genetics
Article
Mutation
Platelet Glycoprotein GPIIb-IIIa Complex
[SDV.MHEP.HEM]Life Sciences [q-bio]/Human health and pathology/Hematology
Blood Platelets/metabolism
Guanosine Triphosphate/genetics
Platelet Aggregation/genetics
Adenosine Diphosphate/genetics
[SDV.BC.IC]Life Sciences [q-bio]/Cellular Biology/Cell Behavior [q-bio.CB]
Megakaryocytes/metabolism
Telomere-Binding Proteins/genetics
Female
Cell Line
Humans
Membrane Proteins/genetics
Neoplasm Proteins/genetics
Male
Homozygote
Źródło :
The Journal of Experimental Medicine
Journal of Experimental Medicine, Rockefeller University Press, 2014, 211 (7), pp.1349 - 1362. ⟨10.1084/jem.20130477⟩
Journal of Experimental Medicine 7 (211), 1346 - 1359. (2014)
Journal of Experimental Medicine
Journal of Experimental Medicine, 211(7), 1349 - 62. Rockefeller University Press
Journal of experimental medicine, 211(7), 1349 - 1362. Rockefeller University Press
Opis pliku :
application/pdf
Tytuł :
A genome-wide association study of anorexia nervosa.
Autorzy :
Boraska, Vesna
Franklin, Christopher S.
Floyd, James A. B.
Thornton, Laura M.
Huckins, Laura M.
Southam, Lorraine
Rayner, Nigel William
Tachmazidou, Ioanna
Klump, Kelly L.
Treasure, Janet
Lewis, Cathryn M.
Dedoussis, G.
Dikeos, D.
Gonidakis, F.
Tziouvas, K.
Tsitsika, A.
Papezova, H.
Slachtova, L.
Martaskova, D.
Kennedy, J. L.
Levitan, R. D.
Schmidt, U.
Yilmaz-Ergül, Zeynep
Huemer, J.
Koubek, D.
Merl, E.
Wagner, G.
Lichtenstein, P.
Breen, G.
Cohen-Woods, S.
Farmer, A.
McGuffin, P.
Tozzi, F.
Cichon, S.
Giegling, I.
Herms, S.
Rujescu, D.
Schreiber, S.
Wichmann, H.-E.
Dina, C.
Sladek, R.
Gambaro, G.
Soranzo, N.
Kiezebrink, K.
Julia, A.
Marsal, S.
Rabionet, R.
Gaborieau, V.
Dick, D. M.
Palotie, A.
Ripatti, S.
Widen, E.
Andreassen, O. A.
Espeseth, T.
Hebebrand, J.
Lundervold, A.
Reinvang, I.
Steen, V. M.
Le Hellard, S.
Mattingsdal, M.
Ntalla, I.
Bencko, V.
Foretova, L.
Janout, V.
Navratilova, M.
Gorwood, P.
Gallinger, S.
Pinto, D.
Scherer, S. W.
Aschauer, H.
Carlberg, L.
Schosser, A.
Alfredsson, L.
Ding, B.
Klareskog, L.
Padyukov, L.
Adan, R. A. H.
Courtet, P.
Guillaume, S.
Jaussent, I.
Finan, C.
Kalsi, G.
Roberts, M.
Logan, D. W.
Peltonen, L.
Ritchie, G. R. S.
Barrett, J. C.
Kas, M. J. H.
Estivill, X.
Hinney, A.
Sullivan, P. F.
Collier, D. A.
Zeggini, E.
Bulik, C. M.
Favaro, A.
Santonastaso, P.
Fernandez-Aranda, F.
Gratacos, M.
Rybakowski, F.
Dmitrzak-Weglarz, M.
Kaprio, J.
Keski-Rahkonen, A.
Raevuori, A.
Van Furth, E. F.
Slof-Op 't Landt, M. C. T.
Hudson, J. I.
Reichborn-Kjennerud, T.
Knudsen, G. P. S.
Monteleone, P.
Kaplan, A. S.
Karwautz, A.
Hakonarson, H.
Berrettini, W. H.
Guo, Y.
Li, D.
Schork, N. J.
Komaki, G.
Ando, T.
Inoko, H.
Esko, T.
Fischer, K.
Mannik, Katrin
Metspalu, A.
Baker, J. H.
Cone, R. D.
Dackor, J.
DeSocio, J. E.
Hilliard, C. E.
O'Toole, J. K.
Pantel, J.
Szatkiewicz, J. P.
Taico, C.
Zerwas, S.
Trace, S. E.
Davis, O. S. P.
Helder, S.
Buhren, K.
Burghardt, R.
de Zwaan, M.
Egberts, K.
Ehrlich, S.
Herpertz-Dahlmann, B.
Herzog, W.
Imgart, H.
Scherag, A.
Scherag, S.
Zipfel, S.
Boni, C.
Ramoz, N.
Versini, A.
Brandys, M. K.
Danner, U. N.
de Kovel, C.
Hendriks, J.
Koeleman, B. P. C.
Ophoff, R. A.
Strengman, E.
van Elburg, Anne-Marie A.
Bruson, Alice
Clementi, Maurizio
Degortes, Daniela
Forzan, Monica
Tenconi, Elodie
Docampo Martinez, Elisa
Escaramis, Geòrgia
Jimenez-Murcia, Susana
Lissowska, Jolanta
Rajewski, Andrzej
Szeszenia-Dabrowska, Neonila
Slopien, Agnieszka
Hauser, Joanna
Karhunen, Leila
Meulenbelt, Ingrid
Slagboom, P. E.
Tortorella, Alfonso
Maj, Mario
Pokaż więcej
Temat :
Anorexia Nervosa/genetics
Asian Continental Ancestry Group/genetics
Calcineurin/genetics
Carrier Proteins/genetics
Case-Control Studies
Cullin Proteins/genetics
European Continental Ancestry Group/genetics
Female
Genome-Wide Association Study
Guanine Nucleotide Exchange Factors/genetics
Humans
Japan
Male
Meta-Analysis as Topic
Nuclear Proteins/genetics
Polymorphism, Single Nucleotide
Genetics & genetic processes [Life sciences]
Génétique & processus génétiques [Sciences du vivant]
Źródło :
A genome-wide association study of anorexia nervosa. Molecular Psychiatry, 19(10), 1085-94., United Kingdom. (2014).

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