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Publications by Mei‑Ya Li

Mitochondrial tRNAAla 5601C>T Variant May Affect the Clinical Expression of the LHON‑related ND4 11778G>A Mutation in a Family

Molecular Medicine Reports

English

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The Mitochondrial tRNAAla T5655C Mutation May Modulate the Phenotypic Expression of tRNAMet and tRNAGln A4401G Mutation in a Han Chinese Family With Essential Hypertension

International Heart Journal

Medicine

Cardiovascular Medicine

Cardiology

2017

English

The ND4 G11696A Mutation May Influence the Phenotypic Manifestation of the Deafness-Associated 12S rRNA A1555G Mutation in a Four-Generation Chinese Family

Biochemical and Biophysical Research Communications

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The Mitochondrial Transfer RNAAsp A7551G Mutation May Contribute to the Clinical Expression of Deafness Associated With the A1555G Mutation in a Pedigree With Hearing Impairment

Molecular Medicine Reports

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Mitochondrial DNA Copy Number in Affected and Unaffected LHON Mutation Carriers

English

Mitochondrial tRNAIle A4317G Mutation May Be Associated With Hearing Impairment in a Han Chinese Family

Molecular Medicine Reports

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Heteroplasmy Rates of the M.14495A>G Variant in MT-ND6 May Not Predict the Phenotype of LHON

Translational Vision Science and Technology

Ophthalmology

Biomedical Engineering

2019

English

Mutation in the Novel Nuclear-Encoded Mitochondrial Protein CHCHD10 in a Family With Autosomal Dominant Mitochondrial Myopathy

Neurogenetics

Molecular Neuroscience

Genetics

Cellular

2014

English

Mitochondrial DNA Haplogroup Background Affects LHON, but Not Suspected LHON, in Chinese Patients

PLoS ONE

Multidisciplinary

2011

English

Hearing Loss Caused by a P2RX2 Mutation Identified in a MELAS Family With a Coexisting Mitochondrial 3243AG Mutation

Annals of Otology, Rhinology and Laryngology

Medicine

Otorhinolaryngology

2015

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Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Mei‑Ya Li

Mitochondrial tRNAAla 5601C>T Variant May Affect the Clinical Expression of the LHON‑related ND4 11778G>A Mutation in a Family

Related publications

The Mitochondrial tRNAAla T5655C Mutation May Modulate the Phenotypic Expression of tRNAMet and tRNAGln A4401G Mutation in a Han Chinese Family With Essential Hypertension

The ND4 G11696A Mutation May Influence the Phenotypic Manifestation of the Deafness-Associated 12S rRNA A1555G Mutation in a Four-Generation Chinese Family

The Mitochondrial Transfer RNAAsp A7551G Mutation May Contribute to the Clinical Expression of Deafness Associated With the A1555G Mutation in a Pedigree With Hearing Impairment

Mitochondrial DNA Copy Number in Affected and Unaffected LHON Mutation Carriers

Mitochondrial tRNAIle A4317G Mutation May Be Associated With Hearing Impairment in a Han Chinese Family

Heteroplasmy Rates of the M.14495A&gt;G Variant in MT-ND6 May Not Predict the Phenotype of LHON

Mutation in the Novel Nuclear-Encoded Mitochondrial Protein CHCHD10 in a Family With Autosomal Dominant Mitochondrial Myopathy

Mitochondrial DNA Haplogroup Background Affects LHON, but Not Suspected LHON, in Chinese Patients

Hearing Loss Caused by a P2RX2 Mutation Identified in a MELAS Family With a Coexisting Mitochondrial 3243AG Mutation

Heteroplasmy Rates of the M.14495A>G Variant in MT-ND6 May Not Predict the Phenotype of LHON