Ye Chen

发表

Mitochondrial haplogroup B increases the risk for hearing loss among the Eastern Asian pedigrees carrying 12S rRNA 1555A>G mutation

M. Guan, Yi Zhu, Xiao-wen Tang, 2015, Protein & Cell.

Deletion of Mtu1 (Trmu) in zebrafish revealed the essential role of tRNA modification in mitochondrial biogenesis and hearing function

Xiao He, Qinghai Zhang, Danni Chen, 2018, Nucleic acids research.

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

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

Human blood-derived lymphoblastoid cybrids for assessment of mitochondrial tRNAs deficiency by MTO1 silence

Shixin Ye, Chao Chen, Ye Chen, 2021 .

Role of arsenic (+3 oxidation state) methyltransferase in arsenic mediated APL treatment: an in vitro investigation.

Khairul Islam, Chang Yang, Hua Naranmandura, 2018, Metallomics : integrated biometal science.

CXCR4-mediated signaling regulates autophagy and influences acute myeloid leukemia cell survival and drug resistance.

Yang Yang, M. Guan, S. Xue, 2018, Cancer letters.

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

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

Zebrafish as an emerging model to study gonad development

Mengling Ye, Ye Chen, 2020, Computational and structural biotechnology journal.

Mitochondrial DNA mutations associated with aminoglycoside induced ototoxicity

M. Guan, Ye Chen, Zewen Gao, 2017, Journal of otology.

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 mutation.

J. Qu, Xiaoling Liu, Taosheng Huang, 2016, Human molecular genetics.

A peep into mitochondrial disorder: multifaceted from mitochondrial DNA mutations to nuclear gene modulation

Chao Chen, M. Guan, Ye Chen, 2015, Protein & Cell.

Tissue-specific expression atlas of murine mitochondrial tRNAs

M. Guan, Yun Xiao, Ye Chen, 2021, The Journal of biological chemistry.

Contribution of a mitochondrial tyrosyl-tRNA synthetase mutation to the phenotypic expression of the deafness-associated tRNASer(UCN) 7511A>G mutation

N. Sondheimer, Wanzhong Ge, J. Mo, 2019, The Journal of Biological Chemistry.

The defective expression of gtpbp3 related to tRNA modification alters the mitochondrial function and development of zebrafish.

Miao Tian, Qinghai Zhang, Danni Chen, 2016, The international journal of biochemistry & cell biology.

Mutations of MAP1B encoding a microtubule-associated phosphoprotein cause sensorineural hearing loss

S. Yin, Chao Chen, M. Guan, 2020, JCI insight.

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

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

In vitro culture of mammalian inner ear hair cells

M. Guan, Xiaohui Cang, Lu-wen Zhang, 2018, Journal of Zhejiang University-SCIENCE B.

Novel mitochondrial gene variants in Northwestern Chinese probands with non-syndromic hearing loss by whole mitochondrial genome screening.

Jing Zheng, Xiao-wen Liu, Yufen Guo, 2018, Gene.

A Comprehensive Characterization of Mitochondrial Genome in Papillary Thyroid Cancer

T. Fahey, Hui-ling Wu, L. Teng, 2016, International journal of molecular sciences.

GJB2 Mutation Spectrum and Genotype-Phenotype Correlation in 1067 Han Chinese Subjects with Non-Syndromic Hearing Loss

Jing Zheng, Ye Chen, Min-Xin Guan, 2015, PloS one.

Mitochondrial tRNA(Ser(UCN)) variants in 2651 Han Chinese subjects with hearing loss.

M. Guan, Xiao-wen Tang, Jing Zheng, 2015, Mitochondrion.