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Biochemical and Biophysical Research Communications|December 29, 2005
Clinical and molecular analysis of a four-generation Chinese family with aminoglycoside-induced and nonsyndromic hearing loss associated with the mitochondrial 12S rRNA C1494T mutationQiuju Wang, Qing-Zhong Li, Dongyi Han, et al.
Blood|February 17, 2022
Inhibition of LDHA to induce eEF2 release enhances thrombocytopoiesisQidi Chen, Min Xin, Lingjun Wang, et al.
Cell|February 21, 2012
Mitochondrial stress engages E2F1 apoptotic signaling to cause deafnessNuno Raimundo, Lei Song, Timothy E Shutt, et al.
Ophthalmology|January 27, 2009
Extremely low penetrance of Leber's hereditary optic neuropathy in 8 Han Chinese families carrying the ND4 G11778A mutationJia Qu, Xiangtian Zhou, Juanjuan Zhang, et al.
Yi Chuan = Hereditas|February 24, 2010
[Leber's hereditary optic neuropathy and limbs abnormity claudication may be associated with the mitochondrial ND1 T3866C mutation]Yan Liu, Shu-Liu Zhuang, Yi Tong, et al.
Yi Chuan = Hereditas|October 14, 2016
Cellular models for mitochondrial DNA-based diseases: lymphoblastoid cell lines and transmitochondrial cybridsJi-ji Sun, Xiao-xu Zhao, Li-hua Qiao, et al.
Mitochondrial DNA. Part A, DNA Mapping, Sequencing, and Analysis|May 10, 2016
Mitochondrial haplogroup D4j specific variant m.11696G > a(MT-ND4) may increase the penetrance and expressivity of the LHON-associated m.11778G > a mutation in Chinese pedigreesShipeng Xie, Juanjuan Zhang, Jiji Sun, et al.
Molecular and Cellular Biology|May 11, 2016
A Hypertension-Associated tRNAAla Mutation Alters tRNA Metabolism and Mitochondrial FunctionPingping Jiang, Meng Wang, Ling Xue, et al.
Disease Models & Mechanisms|June 3, 2015
Phenotypic and functional characterization of Bst+/- mouse retinaHamidreza Riazifar, Guoli Sun, Xinjian Wang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 10, 2012
[Characterization of two Chinese families with aminoglycoside-induced and nonsyndromic hearing loss both carrying a mitochondrial 12S rRNA 1494C>T mutation]Sha-sha Gong, Bo-bei Chen, Guang-hua Peng, et al.
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