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Publications by Yunhong Xu

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

Related publications

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

Molecular Medicine Reports

English

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

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

Molecular Medicine Reports

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

English

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

English

Obesity Associated With a Novel Mitochondrial tRNACys 5802A>G Mutation in a Chinese Family

English

Marked Intrafamilial Phenotypic Variation in a Family With SOD1 C111Y Mutation

Amyotrophic Lateral Sclerosis

2012

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

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

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Yunhong Xu

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

Related publications

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

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

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

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

Obesity Associated With a Novel Mitochondrial tRNACys 5802A&gt;G Mutation in a Chinese Family

Marked Intrafamilial Phenotypic Variation in a Family With SOD1 C111Y Mutation

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

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

Obesity Associated With a Novel Mitochondrial tRNACys 5802A>G Mutation in a Chinese Family