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Nature Genetics|July 1, 1994
Chromosome-specific microsatellite sets for fluorescence-based, semi-automated genome mappingP W Reed, J L Davies, J B Copeman, et al.Nature|September 8, 1994
A genome-wide search for human type 1 diabetes susceptibility genesJ L Davies, Y Kawaguchi, S T Bennett, et al.Plos One|March 12, 2015
First genome-wide association study in an Australian aboriginal population provides insights into genetic risk factors for body mass index and type 2 diabetesDenise Anderson, Heather J Cordell, Michaela Fakiola, et al.International Journal of Radiation Biology|September 3, 2010
The heritability of G2 chromosomal radiosensitivity and its association with cancer in Danish cancer survivors and their offspringGillian B Curwen, Kevin K Cadwell, Jeanette F Winther, et al.Aging|October 17, 2016
Transcriptional regulation of PNPLA3 and its impact on susceptibility to nonalcoholic fatty liver Disease (NAFLD) in humansWanqing Liu, Quentin M Anstee, Xiaoliang Wang, et al.Scientific Reports|July 21, 2018
Arylsulphatase A Pseudodeficiency (ARSA-PD), hypertension and chronic renal disease in Aboriginal AustraliansDave Tang, Michaela Fakiola, Genevieve Syn, et al.The Journal of Clinical Endocrinology and Metabolism|May 31, 2007
Genomic polymorphism at the interferon-induced helicase (IFIH1) locus contributes to Graves' disease susceptibilityAlison Sutherland, Jocelyn Davies, Catherine J Owen, et al.Blood|November 24, 1999
Lymphomas expressing ALK fusion protein(s) other than NPM-ALKB Falini, K Pulford, A Pucciarini, et al.Journal of Autoimmunity|December 5, 2021
rs9459874 and rs1012656 in CCR6/FGFR1OP confer susceptibility to primary biliary cholangitisYuki Hitomi, Yoshihiro Aiba, Kazuko Ueno, et al.Plos Genetics|December 4, 2018
Amino acid residues in five separate HLA genes can explain most of the known associations between the MHC and primary biliary cholangitisRebecca Darlay, Kristin L Ayers, George F Mells, et al.Pageof 27