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 TitleAuthors / EditorsDate
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αIIbβ3 variants defined by next-generation sequencing: predicting variants likely to cause Glanzmann thrombasthenia Buitrago, Lorena; Rendon, Augusto; Liang, Yupu 2015
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Y-chromosome specific YCAII, DYS19 and YAP polymorphisms in human populations: a comparative study Quintana-Murci, L.; Semino, O.; Poloni, Estella S.; Liu, A.; ... Santachiara-Benerecetti, A S. 1999
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Whole exome sequencing of a dominant retinitis pigmentosa family identifies a novel deletion in PRPF31 Villanueva, Adda; Willer, Jason R; Bryois, Julien; Dermitzakis, Emmanouil; ... Davis, Erica E 2014
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War exposure, 5-HTTLPR genotype and lifetime risk of depression Artero, Sylvaine; Touchon, Jacques; Dupuy, Anne-Marie; Malafosse, Alain; Ritchie, Karen 2011
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Type I and type II psoriasis show a similar usage of T-cell receptor variable regions Schmitt-Egenolf, M.; Boehncke, Wolf-Henning; Christophers, Enno; Stander, M.; Sterry, Wolfram 1991
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TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum Kern, Ilse 2011
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Transcriptome and genome sequencing uncovers functional variation in humans Lappalainen, Tuuli Emilia; Giger, Thomas; Padioleau, Ismael; Ongen, Halit; ... Dermitzakis, Emmanouil 2013
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TORC1 organized in inhibited domains (TOROIDs) regulate TORC1 activity Prouteau, Manoel; Desfosses, Ambroise; Sieben, Christian; Bourgoint, Clelia; ... Loewith, Robbie Joséph 2017
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TNFA -308G>A in two international population-based cohorts and risk of asthma Castro-Giner, F.; Kogevinas, M.; Mächler, M.; de Cid, R.; ... Probst-Hensch, Nicole M. 2008
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Tissue-specific effects of genetic and epigenetic variation on gene regulation and splicing Gutierrez Arcelus, Maria; Ongen, Halit; Lappalainen, Tuuli Emilia; Montgomery, Stephen; ... Dermitzakis, Emmanouil 2015
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The tetranucleotide repeat polymorphism D21S1245 demonstrates hypermutability in germline and somatic cells Talbot, C. C.; Avramopoulos, D.; Gerken, S.; Chakravarti, A.; ... Antonarakis, Stylianos 1995
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The TATA-binding protein-associated factor yTafII19p functionally interacts with components of the global transcriptional regulator Ccr4-Not complex and physically interacts with the Not5 subunit Lemaire, Marc; Collart, Martine 2000
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The probability of identifying a 10/10 HLA allele-matched unrelated donor is highly predictable Tiercy, Jean-Marie; Nicoloso, G; Passweg, Jakob; Schanz, U; ... Gratwohl, Alois 2007
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The mouse Hoxd13spdh mutation, a polyalanine expansion similar to human type II synpolydactyly (SPD), disrupts the function but not the expression of other Hoxd genes Bruneau, Sylvia; Johnson, Kenneth R.; Yamamoto, Masakazu; Kuroiwa, Atsushi; Duboule, Denis 2001
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The molecular determination of HLA-Cw alleles in the Mandenka (West Africa) reveals a close genetic relationship between Africans and Europeans Sanchez-Mazas, Alicia; Steiner, Q G.; Grundschober, C.; Tiercy, Jean-Marie 2000
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The molecular chaperone Cdc37 is required for Ste11 function and pheromone-induced cell cycle arrest Abbas-Terki, Toufik; Donze, Olivier; Picard, Didier 2000
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The HLA-B landscape of Africa: Signatures of pathogen-driven selection and molecular identification of candidate alleles to malaria protection Sanchez-Mazas, Alicia; Černý, Viktor; Di, Da; Buhler, Stéphane; ... Nunes, Jose Manuel 2017
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The genomic silencing of position-effect variegation in Drosophila melanogaster: interaction between the heterochromatin-associated proteins Su(var)3-7 and HP1 Delattre, Marion; Spierer-Royer, Anne; Tonka, Chia-Hwa; Spierer, Pierre 2000
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The forensic use of behavioral genetics in criminal proceedings: Case of the MAOA-L genotype McSwiggan, Sally; Elger, Bernice Simone; Appelbaum, Paul S 2017
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The essential function of Not1 lies within the Ccr4-Not complex Maillet, Laurent Jean Marie; Tu, Chi; Hong, Y K; Shuster, E O; Collart, Martine 2000
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