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Publications by Caiming Chen

Molecular Characterization of a Pedigree Carrying the Hypertension‑associated Mitochondrial tRNAGln T4363C Mutation

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

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2017

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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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Novel Homozygous PANK2 Mutation Identified in a Consanguineous Chinese Pedigree With Pantothenate Kinase-Associated Neurodegeneration

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Sensorineural Hearing Loss Associated With Mitochondrial DNA Mutation

AUDIOLOGY JAPAN

2003

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Characterization of the Kyoto Circling (KCI) Rat Carrying a Spontaneous Nonsense Mutation in the Protocadherin 15 (Pcdh15) Gene

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A Novel GJB1 Mutation Associated With X‐linked Charcot–Marie–Tooth Disease in a Large Chinese Family Pedigree

Molecular genetics & genomic medicine

Genetics

Molecular Biology

2020

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A Novel Mutation (LEU396ARG) in OPA1 Is Associated With a Severe Phenotype in a Large Dominant Optic Atrophy Pedigree

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Characterization of a Tumor-Associated Activating Mutation of the P110β PI 3-Kinase

PLoS ONE

Multidisciplinary

2013

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A Novel BMPR2 Mutation Associated With Pulmonary Arterial Hypertension in an Octogenarian

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Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Caiming Chen

Molecular Characterization of a Pedigree Carrying the Hypertension‑associated Mitochondrial tRNAGln T4363C Mutation

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

Novel Homozygous PANK2 Mutation Identified in a Consanguineous Chinese Pedigree With Pantothenate Kinase-Associated Neurodegeneration

Sensorineural Hearing Loss Associated With Mitochondrial DNA Mutation

Characterization of the Kyoto Circling (KCI) Rat Carrying a Spontaneous Nonsense Mutation in the Protocadherin 15 (Pcdh15) Gene

A Novel GJB1 Mutation Associated With X‐linked Charcot–Marie–Tooth Disease in a Large Chinese Family Pedigree

A Novel Mutation (LEU396ARG) in OPA1 Is Associated With a Severe Phenotype in a Large Dominant Optic Atrophy Pedigree

Characterization of a Tumor-Associated Activating Mutation of the P110β PI 3-Kinase

A Novel BMPR2 Mutation Associated With Pulmonary Arterial Hypertension in an Octogenarian