Showing results (21-30 of 114) with videos related to
Sort By:
Pageof 12
Clinical Genetics|February 16, 2020
Functional analysis of SEMA3A variants identified in Chinese patients with isolated hypogonadotropic hypogonadismWenting Dai, Jia-Da Li, Yaguang Zhao, et al.Virchows Archiv : an International Journal of Pathology|January 26, 2026
CTNNB1 Mutational analysis enhances diagnostic precision in β-catenin-negative desmoid fibromatosis: a clinicopathological and molecular studyYang Wang, Ying Wang, Lin Sun, et al.Journal of Evidence-Based Medicine|June 10, 2024
Comparation of fixed-ratio (IDegLira and iGlarLixi) versus free combination of basal insulin and glucagon-like peptide-1 receptor agonist for uncontrolled type 2 diabetes: A systematic review and network meta-analysisJunling Weng, Ying Tao, Zian Xu, et al.Molecular Genetics & Genomic Medicine|October 12, 2021
Analysis of PLXNA1, NRP1, and NRP2 variants in a cohort of patients with isolated hypogonadotropic hypogonadismMeichao Men, Dan-Na Chen, Jia-Da Li, et al.Gene|March 28, 2019
Functional analysis of SOX10 mutations identified in Chinese patients with Kallmann syndromeWenting Dai, Jiayu Wu, Yaguang Zhao, et al.Eclinicalmedicine|September 25, 2024
Associations of socioeconomic status and healthy lifestyle with incident dementia and cognitive decline: two prospective cohort studiesKan Wang, Yuan Fang, Ruizhi Zheng, et al.FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|December 22, 2018
PROKR2 mutations in idiopathic hypogonadotropic hypogonadism: selective disruption of the binding to a Gα-protein leads to biased signalingYaguang Zhao, Jiayu Wu, Hong Jia, et al.European Journal of Endocrinology|June 11, 2020
Genotypic and phenotypic spectrum of CCDC141 variants in a Chinese cohort with congenital hypogonadotropic hypogonadismQiao Hou, Jiayu Wu, Yaguang Zhao, et al.Journal of Infection and Public Health|December 25, 2022
Comorbidities prolonged viral shedding of patients infected with SARS-CoV-2 omicron variant in Shanghai: A multi-center, retrospective, observational studyLei Pei, Ying Chen, Xiangtao Zheng, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 15, 2014
[Analysis of CYP21A2 gene mutations in two families with 21-hydroxylase deficiency]Ruizhi Zheng, Zhigang Zhao, Yanfang Wang, et al.Pageof 12