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Verification of an iPSC line (LZUi002-A) from a patient with a novel mutation in the TBL1X gene

Stem cell research, 2022-05, Vol.61, p.102761-102761, Article 102761

2022

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Barhl 1 is required for the differentiation of inner ear hair cell-like cells from mouse embryonic stem cells

The international journal of biochemistry & cell biology, 2018-03, Vol.96, p.79-89

2018

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Mitochondrial biogenesis dysfunction and metabolic dysfunction from a novel mitochondrial tRNAMet 4467 C>A mutation in a Han Chinese family with maternally inherited hypertension

Scientific reports, 2017-06, Vol.7 (1), p.1-11, Article 3034

2017

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A Critical E-box in Barhl1 3' Enhancer Is Essential for Auditory Hair Cell Differentiation

Cells (Basel, Switzerland), 2019-05, Vol.8 (5), p.458

2019

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A homozygous mutation of TWNK identified in premature ovarian insufficiency warns of late-onset perrault syndrome

European journal of obstetrics & gynecology and reproductive biology, 2024-08, Vol.299, p.118-123

2024

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Voltage-dependent anion channel (VDAC) is involved in apoptosis of cell lines carrying the mitochondrial DNA mutation

BMC medical genetics, 2009-11, Vol.10 (1), p.114-114, Article 114

2009

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ATAD3B is a mitophagy receptor mediating clearance of oxidative stress‐induced damaged mitochondrial DNA

The EMBO journal, 2021-04, Vol.40 (8), p.e106283-n/a

2021

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A six-generation Chinese family in haplogroup B4C1C exhibits high penetrance of 1555A > G-induced hearing Loss

BMC medical genetics, 2010-09, Vol.11 (1), p.129-129, Article 129

2010

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5-hydroxymethylcytosine-mediated DNA demethylation in stem cells and development

Stem cells and development, 2014-05, Vol.23 (9), p.923

2014

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Barhl1 is required for the differentiation of inner ear hair cell-like cells from mouse embryonic stem cells

The international journal of biochemistry & cell biology, 2018-03, Vol.96, p.79-89

2018

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Clinical and genetic analysis of essential hypertension with mitochondrial tRNA Met 4435A>G and YARS2 mutation

Zhejiang da xue xue bao. Journal of Zhejiang University. Medical sciences. Yi xue ban, 2024-04, Vol.53 (2), p.184

2024

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A non-invasive method for detecting mitochondrial tRNA Thr 15927G>A mutation

Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2021-01, Vol.41 (1), p.151

2021

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携带CYB m.15024G>A突变的原发性高血压家系遗传学分析

浙江大学学报（医学版）, 2023-08, Vol.52 (4), p.510-517

2023

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Processing and properties of a low-fire, high-k dielectric in H 2 /N 2

Ceramics international, 2017-08, Vol.43, p.S270-S273

2017

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Corrigendum to “Barhl1 is required for the differentiation of inner ear hair cell-like cells from mouse embryonic stem cells” [Int. J. Biochem. Cell Biol. 96 (2018) 79–89]

The international journal of biochemistry & cell biology, 2018-04, Vol.97, p.128-129

2018

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Nucleotide modification of mitochondrial tRNA and mitochondrial diseases

Zhonghua yi xue yi chuan xue za zhi, 2017-04, Vol.34 (2), p.275

2017

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Mitochondrial tRNA mutations in Chinese hypertensive individuals

Mitochondrion, 2016-05, Vol.28, p.1-7

2016

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Processing and properties of a low-fire, high-k dielectric in H2/N2

Ceramics international, 2017-08, Vol.43, p.S270-S273

2017

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Effect of mitochondrial tRNA(Lys) mutation on the clinical and biochemical characteristics of Chinese essential hypertensive subjects

Biochemical and biophysical research communications, 2014-11, Vol.454 (4), p.500-504

2014

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Mutations of mitochondrial tRNA Ser(UCN) and their connection with hearing loss

Zhonghua yi xue yi chuan xue za zhi, 2017-02, Vol.34 (1), p.128

2017

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Effect of mitochondrial tRNALys mutation on the clinical and biochemical characteristics of Chinese essential hypertensive subjects

Biochemical and biophysical research communications, 2014-11, Vol.454 (4), p.500-504

2014

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Clinical practice guidelines for Leber's hereditary optic neuropathy

Zhonghua yi xue yi chuan xue za zhi, 2020-03, Vol.37 (3), p.284

2020

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Identification of mitochondrial DNA ND1 T3866C mutation in three ethnic Han Chinese families affected with Leber's hereditary optic neuropathy

Zhonghua yi xue yi chuan xue za zhi, 2015-04, Vol.32 (2), p.198

2015

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GW25-e4292 Systematic analysis of the clinical and biochemical characteristics of maternally inherited hypertension in Chinese Han families associated with mitochondrial genome mutations

Journal of the American College of Cardiology, 2014-10, Vol.64 (16), p.C55-C55

2014

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Mitochondrial tRNAHis 12201T>C mutation influence the deafness by altering the mitochondrial function

Mitochondrion, 2015-09, Vol.24, p.S29-S30

2015

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Verification of an iPSC line (LZUi002-A) from a patient with a novel mutation in the TBL1X gene

Barhl 1 is required for the differentiation of inner ear hair cell-like cells from mouse embryonic stem cells

Mitochondrial biogenesis dysfunction and metabolic dysfunction from a novel mitochondrial tRNAMet 4467 C>A mutation in a Han Chinese family with maternally inherited hypertension

A Critical E-box in Barhl1 3' Enhancer Is Essential for Auditory Hair Cell Differentiation

A homozygous mutation of TWNK identified in premature ovarian insufficiency warns of late-onset perrault syndrome

Voltage-dependent anion channel (VDAC) is involved in apoptosis of cell lines carrying the mitochondrial DNA mutation

ATAD3B is a mitophagy receptor mediating clearance of oxidative stress‐induced damaged mitochondrial DNA

A six-generation Chinese family in haplogroup B4C1C exhibits high penetrance of 1555A > G-induced hearing Loss

5-hydroxymethylcytosine-mediated DNA demethylation in stem cells and development

Barhl1 is required for the differentiation of inner ear hair cell-like cells from mouse embryonic stem cells

Clinical and genetic analysis of essential hypertension with mitochondrial tRNA Met 4435A>G and YARS2 mutation

A non-invasive method for detecting mitochondrial tRNA Thr 15927G>A mutation

携带CYB m.15024G>A突变的原发性高血压家系遗传学分析

Processing and properties of a low-fire, high-k dielectric in H 2 /N 2

Corrigendum to “Barhl1 is required for the differentiation of inner ear hair cell-like cells from mouse embryonic stem cells” [Int. J. Biochem. Cell Biol. 96 (2018) 79–89]

Nucleotide modification of mitochondrial tRNA and mitochondrial diseases

Mitochondrial tRNA mutations in Chinese hypertensive individuals

Processing and properties of a low-fire, high-k dielectric in H2/N2

Effect of mitochondrial tRNA(Lys) mutation on the clinical and biochemical characteristics of Chinese essential hypertensive subjects

Mutations of mitochondrial tRNA Ser(UCN) and their connection with hearing loss

Effect of mitochondrial tRNALys mutation on the clinical and biochemical characteristics of Chinese essential hypertensive subjects

Clinical practice guidelines for Leber's hereditary optic neuropathy

Identification of mitochondrial DNA ND1 T3866C mutation in three ethnic Han Chinese families affected with Leber's hereditary optic neuropathy

GW25-e4292 Systematic analysis of the clinical and biochemical characteristics of maternally inherited hypertension in Chinese Han families associated with mitochondrial genome mutations

Mitochondrial tRNAHis 12201T>C mutation influence the deafness by altering the mitochondrial function

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