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Frontiers in Bioscience (Landmark Edition)|May 30, 2026
Functional Heterogeneity of Hepatitis B Virus-Specific CD8+ T Cells Mediates the Clinical Outcomes of InfectionZhijun Shen, Xin Wang, Juan Zhao, et al.
Frontiers in Endocrinology|May 20, 2020
DUOX2 and DUOXA2 Variants Confer Susceptibility to Thyroid Dysgenesis and Gland-in-situ With Congenital HypothyroidismFengqi Wang, Yucui Zang, Miaomiao Li, et al.
International Journal of Clinical and Experimental Pathology|January 2, 2016
Association analysis between genetic variants in interleukin genes among different populations with hyperuricemia in Xinjiang Autonomous RegionBei Zhang, Yuping Sun, Yuanyuan Li, et al.
American Journal of Physiology. Endocrinology and Metabolism|February 4, 2010
Overexpression of nuclear receptor SHP in adipose tissues affects diet-induced obesity and adaptive thermogenesisImene Tabbi-Anneni, Robert Cooksey, Viswanath Gunda, et al.
The Journal of Gene Medicine|February 11, 2020
The role of SLITRK6 in the pathogenesis of Tourette syndrome: From the conclusion of a family-based study in the Chinese Han populationWenmiao Liu, Xuzhan Zhang, Ziwen Deng, et al.
The Journal of Gene Medicine|September 5, 2020
Compound heterozygous DYSF variants causing limb-girdle muscular dystrophy type 2B in a Chinese familyLiangshan Li, Zhongcui Jing, Lei Cheng, et al.
Molecular Vision|March 13, 2008
Mutation G61C in the CRYGD gene causing autosomal dominant congenital coralliform cataractsFeifeng Li, Shuzhen Wang, Chang Gao, et al.
Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology|November 9, 2016
Effects of GSTP1 and GPX1 Polymorphisms on the Risk of Preeclampsia in Chinese Han WomenHuijie Gao, Chao Liu, Ping Lin, et al.
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