Showing results (341-350 of 362) with videos related to
Sort By:
Pageof 37
Gene|March 8, 2007
Very low penetrance of hearing loss in seven Han Chinese pedigrees carrying the deafness-associated 12S rRNA A1555G mutationXiaowen Tang, Li Yang, Yi Zhu, et al.Human Molecular Genetics|December 10, 2015
The exome sequencing identified the mutation in YARS2 encoding the mitochondrial tyrosyl-tRNA synthetase as a nuclear modifier for the phenotypic manifestation of Leber's hereditary optic neuropathy-associated mitochondrial DNA mutationPingping Jiang, Xiaofen Jin, Yanyan Peng, et al.Mitochondrion|July 22, 2008
Mutations at position 7445 in the precursor of mitochondrial tRNA(Ser(UCN)) gene in three maternal Chinese pedigrees with sensorineural hearing lossJing Chen, Huijun Yuan, Jianxin Lu, et al.Frontiers in Psychiatry|July 19, 2018
Risk Factors for Recent Suicide Attempts in Major Depressive Disorder Patients in China: Results From a National StudyLi-Min Xin, Lin Chen, Yun-Ai Su, et al.Biochemical and Biophysical Research Communications|December 27, 2005
Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA mutation in 16 Chinese families: implication for early detection and prevention of deafnessPu Dai, Xin Liu, Dongyi Han, et al.Stem Cells Translational Medicine|March 26, 2016
Genetic Correction of Induced Pluripotent Stem Cells From a Deaf Patient With MYO7A Mutation Results in Morphologic and Functional Recovery of the Derived Hair Cell-Like CellsZi-Hua Tang, Jia-Rong Chen, Jing Zheng, et al.Journal of Affective Disorders|December 30, 2018
Prevalence and clinical features of atypical depression among patients with major depressive disorder in ChinaLi-Min Xin, Lin Chen, Yun-Ai Su, et al.Human Molecular Genetics|January 1, 2019
Contribution of mitochondrial ND1 3394T>C mutation to the phenotypic manifestation of Leber's hereditary optic neuropathyYanchun Ji, Juanjuan Zhang, Jialing Yu, et al.Journal of Affective Disorders|January 17, 2022
Prevalence, clinical features and prescription patterns of psychotropic medications for patients with psychotic depression in ChinaLi-Min Xin, Yun-Ai Su, Feng Yan, et al.Biochemical and Biophysical Research Communications|July 31, 2007
Mitochondrial tRNASer(UCN) gene is the hot spot for mutations associated with aminoglycoside-induced and non-syndromic hearing lossLongjin Jin, Aifen Yang, Yi Zhu, et al.Pageof 37