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Journal of Human Genetics|December 14, 2018
Exome sequencing identifies a novel nonsense mutation of Ring Finger Protein 207 in a Chinese family with Long QT syndrome and syncopeLiang-Liang Fan, Ya-Qin Chen, Hao Huang, et al.
Frontiers in Human Neuroscience|April 18, 2025
Association of deep tiny flow voids with prognosis of acute middle cerebral artery atherosclerotic occlusionMan-Qiu Ding, Wei-Zhuang Yuan, Zi-Jue Wang, et al.
Frontiers in Cardiovascular Medicine|September 6, 2021
Case Report: BAF-Opathies/SSRIDDs Due to a de novo ACTL6A Variant, Previously Considered to Be Heart-Hand SyndromeZhuang-Zhuang Yuan, Xiao-Hui Xie, Heng Gu, et al.
Materials (Basel, Switzerland)|May 25, 2024
The Microstructure and Mechanical Properties of Si3N4f/BN/SiBCN Microcomposites Fabricated by the PIP ProcessZhiyou Gong, Zhongkai Xu, Jian Zhang, et al.
Clinical Genetics|August 23, 2021
A novel POF1B variant in a Chinese patient is associated with premature ovarian failureZhuang-Zhuang Yuan, Chen-Yu Wang, Jie-Yuan Jin, et al.
International Journal of Geriatric Psychiatry|May 18, 2010
Depression and hypertension among Chinese nonagenarians and centenariansZhao Wen, Dong Bi-Rong, Huang Chang-Quan, et al.
Frontiers in Neuroscience|August 2, 2021
Case Report: Mutant SCN9A Susceptible to Charcot Neuroarthropathy in a Patient With Congenital Insensitivity to PainXiao-Hui Xie, Jian-Guang Tang, Zhong-Hua Liu, et al.
World Journal of Gastroenterology|October 5, 2017
Dihydromyricetin-mediated inhibition of the Notch1 pathway induces apoptosis in QGY7701 and HepG2 hepatoma cellsCai-Jie Lu, Yi-Feng He, Wei-Zhuang Yuan, et al.
Molecular Medicine (Cambridge, Mass.)|February 19, 2025
RTN3 regulates collagen biosynthesis and profibrotic macrophage differentiation to promote pulmonary fibrosis via interacting with CRTH2Chen-Yu Wang, Ya-Qin Chen, Hao Huang, et al.
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