Jialing Yu

发表

Generation of the human induced pluripotent stem cell line (ZJUi005-A) from a patient with Pelizaeus-Merzbacher disease (PMD) carrying a novel hemizygous mutation in PLP1 gene.

Jin Zhang, K. Yan, Yeqing Qian, 2020, Stem cell research.

A Hypertension-Associated tRNA Ala Mutation Alters tRNA Metabolism and Mitochondrial Function

H. Liu, Meng Wang, M. Guan, 2016 .

Aminoglycoside Stress Together with the 12S rRNA 1494C>T Mutation Leads to Mitophagy

Danni Chen, Chao Chen, M. Guan, 2014, PloS one.

[Application of single nucleotide polymorphism microarray in clinical diagnosis of intellectual disability or retardation].

Yeqing Qian, Minyue Dong, Yi-xi Sun, 2019, Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences.

[Single nucleotide polymorphism microarray in prenatal diagnosis of fetuses with absent nasal bone].

Yeqing Qian, Minyue Dong, Yi-xi Sun, 2019, Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences.

A Hypertension-Associated tRNAAla Mutation Alters tRNA Metabolism and Mitochondrial Function

H. Liu, Meng Wang, M. Guan, 2016, Molecular and Cellular Biology.

Case Report: Prenatal diagnosis of fetal tetrasomy 9p initially identified by non-invasive prenatal testing

Yeqing Qian, Min Chen, Minyue Dong, 2022, Frontiers in Genetics.

Mitochondrial DNA depletion, mitochondrial mutations and high TFAM expression in hepatocellular carcinoma

Pingping Jiang, G. Ru, Jialing Yu, 2017, Oncotarget.

Leber's Hereditary Optic Neuropathy Arising From the Synergy Between ND1 3635G>A Mutation and Mitochondrial YARS2 Mutations

J. Mo, M. Guan, Y. Tong, 2021, Investigative ophthalmology & visual science.

PRICKLE3 linked to ATPase biogenesis manifested Leber's hereditary optic neuropathy.

Taosheng Huang, Xiangtian Zhou, Cheng Ai, 2020, The Journal of clinical investigation.

Loss of MED1 triggers mitochondrial biogenesis in C2C12 cells.

M. Guan, Yanchun Ji, Pingping Jiang, 2014, Mitochondrion.

Contribution of mitochondrial ND1 3394T>C mutation to the phenotypic manifestation of Leber’s hereditary optic neuropathy

T. Zhu, Xiaoling Liu, Taosheng Huang, 2018, Human molecular genetics.

A Hypertension-Associated tRNAAla Mutation Alters tRNA Metabolism and Mitochondrial Function

H. Liu, Meng Wang, M. Guan, 2016, Molecular and Cellular Biology.