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Biochimica Et Biophysica Acta. Molecular Basis of Disease|November 23, 2018
Mutations in glucokinase and other genes detected in neonatal and type 1B diabetes patient using whole exome sequencing may lead to disease-causing changes in protein activityDao-Chen Lin, Chi-Yu Huang, Wei-Hsin Ting, et al.
European Journal of Endocrinology|February 2, 2011
A unique exonic splicing mutation in the CYP17A1 gene as the cause for steroid 17{alpha}-hydroxylase deficiencyJie Qiao, Bing Han, Bing-Li Liu, et al.
Acta Pharmacologica Sinica|June 11, 2025
YOD1 mediates isoproterenol-induced cardiac remodeling by deubiquitinating PKM2 and reducing PKM2 tetramerization in cardiomyocytesQing-Song Zheng, Yong-Qiang Xiong, Jia-Chen Xu, et al.
Zhonghua Wai Ke Za Zhi [Chinese Journal of Surgery]|January 7, 2005
[The contrast study between single and double balloon bilateral dilatation of kyphoplasty]Hui-lin Yang, Guo-qi Niu, Dao-chen Liang, et al.
Diagnostics (Basel, Switzerland)|July 2, 2021
Thoracic Aortic Calcification and Pre-Clinical Hypertension by New 2017 ACC/AHA Hypertension GuidelinesYa-Ting Jan, Pei-Shan Tsai, Chris T Longenecker, et al.
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