Showing results (41-50 of 95) with videos related to
Sort By:
Pageof 10
Journal of Neurochemistry|January 7, 2012
Serine hydroxymethyltransferase 1 and 2: gene sequence variation and functional genomic characterizationScott J Hebbring, Yubo Chai, Yuan Ji, et al.Cancer Research|June 19, 2008
Glutathione s-transferase p1: gene sequence variation and functional genomic studiesAnn M Moyer, Oreste E Salavaggione, Tse-Yu Wu, et al.BMJ Open Ophthalmology|May 15, 2025
Associations between measures of oestrogen exposure and severity of Fuchs endothelial corneal dystrophyRedion B Petrela, Chandra Divyash Chhetri, Ahmad Najafi, et al.Molecular Genetics and Metabolism|May 7, 2008
Human betaine-homocysteine methyltransferase (BHMT) and BHMT2: common gene sequence variation and functional characterizationFang Li, Qiping Feng, Candace Lee, et al.Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|December 7, 2007
Glutathione S-transferase T1 and M1: gene sequence variation and functional genomicsAnn M Moyer, Oreste E Salavaggione, Scott J Hebbring, et al.Pharmacogenetics and Genomics|July 23, 2009
Cytosolic 5'-nucleotidase III (NT5C3): gene sequence variation and functional genomicsPinar Aksoy, Min Jia Zhu, Krishna R Kalari, et al.Cell & Bioscience|August 9, 2014
Clinical biomarkers of pulmonary carcinoid tumors in never smokers via profiling miRNA and target mRNABo Deng, Julian Molina, Marie C Aubry, et al.The Journal of Biological Chemistry|January 13, 2006
Human arsenic methyltransferase (AS3MT) pharmacogenetics: gene resequencing and functional genomics studiesThomas C Wood, Oreste E Salavagionne, Baidehi Mukherjee, et al.Circulation. Cardiovascular Genetics|March 16, 2013
Natriuretic peptide receptor-3 gene (NPR3): nonsynonymous polymorphism results in significant reduction in protein expression because of accelerated degradationNaveen L Pereira, Dong Lin, Linda Pelleymounter, et al.Investigative Ophthalmology & Visual Science|August 30, 2014
Comprehensive assessment of genetic variants within TCF4 in Fuchs' endothelial corneal dystrophyEric D Wieben, Ross A Aleff, Bruce W Eckloff, et al.Pageof 10