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European Journal of Human Genetics : EJHG|June 23, 2011
The tRNAMet 4435A>G mutation in the mitochondrial haplogroup G2a1 is responsible for maternally inherited hypertension in a Chinese pedigreeZhongqiu Lu, Hong Chen, Yanzi Meng, et al.
Human Molecular Genetics|June 6, 2013
Coronary heart disease is associated with a mutation in mitochondrial tRNAZidong Jia, Xinjian Wang, Yanwen Qin, et al.
Biochemical and Biophysical Research Communications|August 1, 2006
Extremely low penetrance of deafness associated with the mitochondrial 12S rRNA T1095C mutation in three Chinese familiesPu Dai, Yongyi Yuan, Deliang Huang, et al.
Investigative Ophthalmology & Visual Science|June 22, 2021
Leber's Hereditary Optic Neuropathy Arising From the Synergy Between ND1 3635G>A Mutation and Mitochondrial YARS2 MutationsXiaofen Jin, Juanjuan Zhang, Qiuzi Yi, et al.
Journal of Medicinal Food|July 25, 2009
The role of ribose on oxidative stress during hypoxic exercise: a pilot studyJohn G Seifert, Andrew W Subudhi, Min-Xin Fu, et al.
Journal of the American Heart Association|January 29, 2014
Mitochondrial tRNA variants in Chinese subjects with coronary heart diseaseYanwen Qin, Ling Xue, Pingping Jiang, et al.
Journal of Investigative Surgery : the Official Journal of the Academy of Surgical Research|July 22, 2024
Predicting the Risk of Postoperative Delirium in Elderly Patients Undergoing Hip Arthroplasty: Development and Assessment of a Novel NomogramYang Zhang, Li-Juan Xie, Ruo-Jie Wu, et al.
World Journal of Gastroenterology|December 20, 2011
CpG island methylator phenotype in plasma is associated with hepatocellular carcinoma prognosisJi-Bin Liu, Yi-Xin Zhang, Shu-Hui Zhou, et al.
World Journal of Gastroenterology|December 16, 2011
Plasma DNA methylation of Wnt antagonists predicts recurrence of esophageal squamous cell carcinomaJi-Bin Liu, Fu-Lin Qiang, Jing Dong, et al.
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