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Frontiers in Genetics|September 2, 2022
Case Report: Aarskog-scott syndrome caused by FGD1 gene variation: A family studyYijia Liang, Honglin Wu, Xiumei He, et al.
Frontiers in Molecular Neuroscience|September 26, 2022
Mitochondrial protein dysfunction in pathogenesis of neurological diseasesLiang Wang, Ziyun Yang, Xiumei He, et al.
Journal of Affective Disorders|July 28, 2022
Demographic characteristics, family environment and psychosocial factors affecting internet addiction in Chinese adolescentsWanling Zhang, Jianlin Pu, Ruini He, et al.
Journal of Cancer Research and Clinical Oncology|June 17, 2010
Evaluating mitochondrial DNA in patients with breast cancer and benign breast diseaseLijun Shen, Jia Wei, Tao Chen, et al.
Journal of Cell Science|April 8, 2024
GTPBP8 modulates mitochondrial fission through a Drp1-dependent processXiumei He, Liang Wang, Hoi Ying Tsang, et al.
Molecular Genetics and Metabolism|February 16, 2010
Maternally inherited hearing loss is associated with the novel mitochondrial tRNA Ser(UCN) 7505T>C mutation in a Han Chinese familyXiaowen Tang, Ronghua Li, Jing Zheng, et al.
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