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The Journal of Investigative Dermatology|December 2, 2006
Follow-up analysis of PSORS9 in 151 Chinese families confirmed the linkage to 4q31-32 and refined the evidence to the families of early-onset psoriasisKai-Lin Yan, Wei Huang, Xue-Jun Zhang, et al.Medrxiv : the Preprint Server for Health Sciences|September 4, 2024
Endogenous adenine is a potential driver of the cardiovascular-kidney-metabolic syndromeIan Tamayo, Hak Joo Lee, M Imran Aslam, et al.Environmental Science and Pollution Research International|September 3, 2022
Effect modification by aging on the associations of nicotine exposure with cognitive impairment among Chinese elderlyJian Hou, Chao Huang, Bo Zhu, et al.Journal of Medical Genetics|September 28, 2013
Association analyses identifying two common susceptibility loci shared by psoriasis and systemic lupus erythematosus in the Chinese Han populationYang Li, Hui Cheng, Xian-bo Zuo, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|July 25, 2016
Genetic variants in the receptor for advanced glycation end products (RAGE) gene were associated with circulating soluble RAGE level but not with renal function among Asians with type 2 diabetes: a genome-wide association studySu Chi Lim, Rajkumar Dorajoo, Xiao Zhang, et al.Nature Genetics|December 27, 2011
A genome-wide association study in Han Chinese identifies multiple susceptibility loci for IgA nephropathyXue-Qing Yu, Ming Li, Hong Zhang, et al.Journal of the American Society of Nephrology : JASN|September 11, 2020
Genome-Wide Meta-Analysis Identifies Three Novel Susceptibility Loci and Reveals Ethnic Heterogeneity of Genetic Susceptibility for IgA NephropathyMing Li, Ling Wang, Dian-Chun Shi, et al.Diabetologia|December 2, 2024
Metabolomics profiling in multi-ancestral individuals with type 2 diabetes in Singapore identified metabolites associated with renal function declineYuqing Chen, Federico Torta, Hiromi W L Koh, et al.Journal of Medical Genetics|September 14, 2012
Exome sequencing identifies a COL14A1 mutation in a large Chinese pedigree with punctate palmoplantar keratodermaBi-Rong Guo, Xin Zhang, Gang Chen, et al.Journal of Medical Genetics|October 27, 2012
Exome sequencing identified a missense mutation of EPS8L3 in Marie Unna hereditary hypotrichosisXin Zhang, Bi-Rong Guo, Li-Qiong Cai, et al.Pageof 34