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Personalized Medicine|May 23, 2015
The road from next-generation sequencing to personalized medicineManuel L Gonzalez-GarayJournal of Cell Science|August 3, 2002
Paclitaxel-dependent mutants have severely reduced microtubule assembly and reduced tubulin synthesisSteven B Barlow, Manuel L Gonzalez-Garay, Fernando CabralProceedings of the National Academy of Sciences of the United States of America|October 2, 2013
Personalized genomic disease risk of volunteersManuel L Gonzalez-Garay, Amy L McGuire, Stacey Pereira, et al.Annual Review of Medicine|November 6, 2013
Adult genetic risk screeningC Thomas Caskey, Manuel L Gonzalez-Garay, Stacey Pereira, et al.Molecular Syndromology|July 8, 2016
Whole Exome Sequencing Reveals a Mutation in CRYBB2 in a Large Mexican Family with Autosomal Dominant Pulverulent CataractOlga Messina-Baas, Manuel L Gonzalez-Garay, Luz M González-Huerta, et al.European Journal of Human Genetics : EJHG|November 17, 2022
Genome-wide association study of a lipedema phenotype among women in the UK Biobank identifies multiple genetic risk factorsYann C Klimentidis, Zhao Chen, Manuel L Gonzalez-Garay, et al.Journal of the American Society of Nephrology : JASN|November 18, 2015
Defective Store-Operated Calcium Entry Causes Partial Nephrogenic Diabetes InsipidusMykola Mamenko, Isha Dhande, Viktor Tomilin, et al.Circulation. Cardiovascular Genetics|November 5, 2014
Hypertensive renal injury is associated with gene variation affecting immune signalingMichael C Braun, Stacy M Herring, Nisha Gokul, et al.Translational Research : the Journal of Laboratory and Clinical Medicine|July 26, 2020
MicroRNA and protein-coding gene expression analysis in idiopathic pulmonary fibrosis yields novel biomarker signatures associated to survivalNancy G Casanova, Tong Zhou, Manuel L Gonzalez-Garay, et al.Nature Genetics|October 1, 2013
Truncating mutations of MAGEL2 cause Prader-Willi phenotypes and autismChristian P Schaaf, Manuel L Gonzalez-Garay, Fan Xia, et al.Pageof 3