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Pingping Jiang

Showing results (221-230 of 228) with videos related to

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Investigative Ophthalmology & Visual Science|January 9, 2014
Frequency and spectrum of mitochondrial ND6 mutations in 1218 Han Chinese subjects with Leber's hereditary optic neuropathyMin Liang, Pingping Jiang, Feng Li, et al.
Mitochondrion|May 14, 2013
Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated m.14484T>C (MT-ND6) mutation in Chinese familiesJuanjuan Zhang, Fuxin Zhao, Qun Fu, et al.
Journal of Pediatric Gastroenterology and Nutrition|June 7, 2019
Correlates of Gut Function in Children Hospitalized for Severe Acute Malnutrition, a Cross-sectional Study in UgandaBetty Lanyero, Benedikte Grenov, Nicolette N Barungi, et al.
The Journal of Clinical Investigation|June 10, 2020
PRICKLE3 linked to ATPase biogenesis manifested Leber's hereditary optic neuropathyJialing Yu, Xiaoyang Liang, Yanchun Ji, et al.
Journal of Medical Genetics|September 21, 2011
Maternally transmitted late-onset non-syndromic deafness is associated with the novel heteroplasmic T12201C mutation in the mitochondrial tRNAHis geneXukun Yan, Xinjian Wang, Zhengmin Wang, et al.
JCI Insight|April 26, 2022
Heteroplasmic and homoplasmic m.616T>C in mitochondria tRNAPhe promote isolated chronic kidney disease and hyperuricemiaChengxian Xu, Lingxiao Tong, Jia Rao, 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.
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.
Pageof 23

Showing results (221-230 of 228) with videos related to

Sort By:
Pageof 23
You have reached the last page of results.This site can display upto 228 results.
Investigative Ophthalmology & Visual Science|January 9, 2014
Frequency and spectrum of mitochondrial ND6 mutations in 1218 Han Chinese subjects with Leber's hereditary optic neuropathyMin Liang, Pingping Jiang, Feng Li, et al.
Mitochondrion|May 14, 2013
Mitochondrial haplotypes may modulate the phenotypic manifestation of the LHON-associated m.14484T>C (MT-ND6) mutation in Chinese familiesJuanjuan Zhang, Fuxin Zhao, Qun Fu, et al.
Journal of Pediatric Gastroenterology and Nutrition|June 7, 2019
Correlates of Gut Function in Children Hospitalized for Severe Acute Malnutrition, a Cross-sectional Study in UgandaBetty Lanyero, Benedikte Grenov, Nicolette N Barungi, et al.
The Journal of Clinical Investigation|June 10, 2020
PRICKLE3 linked to ATPase biogenesis manifested Leber's hereditary optic neuropathyJialing Yu, Xiaoyang Liang, Yanchun Ji, et al.
Journal of Medical Genetics|September 21, 2011
Maternally transmitted late-onset non-syndromic deafness is associated with the novel heteroplasmic T12201C mutation in the mitochondrial tRNAHis geneXukun Yan, Xinjian Wang, Zhengmin Wang, et al.
JCI Insight|April 26, 2022
Heteroplasmic and homoplasmic m.616T>C in mitochondria tRNAPhe promote isolated chronic kidney disease and hyperuricemiaChengxian Xu, Lingxiao Tong, Jia Rao, 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.
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.
Pageof 23