Zhi-hua Yang

1 Jian She East Road
Zhengzhou, 450000, China

Last Updated: 09/26/2026

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Found 18 publications

Single-Cell RNA Sequencing Reveals Impaired CHIP-Mediated Heat Stress Response in SCA3 Pathogenesis.

Single-Cell RNA Sequencing Reveals Impaired CHIP-Mediated Heat Stress Response in SCA3 Pathogenesis.

Journal: Molecular neurobiology

Published: November 16, 2025

GGC repeat expansion in NOTCH2NLC induces dysfunction in ribosome biogenesis and translation.

GGC repeat expansion in NOTCH2NLC induces dysfunction in ribosome biogenesis and translation.

Journal: Brain : a journal of neurology

Published: July 29, 2022

No biallelic intronic AAGGG repeat expansion in RFC1 was found in patients with late-onset ataxia and MSA.

No biallelic intronic AAGGG repeat expansion in RFC1 was found in patients with late-onset ataxia and MSA.

Journal: Parkinsonism & related disorders

Published: October 14, 2019

Metabolic Profiling Reveals Biochemical Pathways and Potential Biomarkers of Spinocerebellar Ataxia 3.

Metabolic Profiling Reveals Biochemical Pathways and Potential Biomarkers of Spinocerebellar Ataxia 3.

Journal: Frontiers in molecular neuroscience

Published: March 26, 2019

SNCA but not DNM3 and GAK modifies age at onset of LRRK2-related Parkinson's disease in Chinese population.

SNCA but not DNM3 and GAK modifies age at onset of LRRK2-related Parkinson's disease in Chinese population.

Journal: Journal of neurology

Published: March 22, 2019

Carboxyl Terminus of Hsp70-Interacting Protein Is Increased in Serum and Cerebrospinal Fluid of Patients With Spinocerebellar Ataxia Type 3.

Carboxyl Terminus of Hsp70-Interacting Protein Is Increased in Serum and Cerebrospinal Fluid of Patients With Spinocerebellar Ataxia Type 3.

Journal: Frontiers in neurology

Published: March 17, 2019

Novel compound heterozygous GFPT1 mutations in a family with limb-girdle myasthenia with tubular aggregates.

Novel compound heterozygous GFPT1 mutations in a family with limb-girdle myasthenia with tubular aggregates.

Journal: Neuromuscular disorders : NMD

Published: February 07, 2019

Two Novel Mutations and a de novo Mutation in PSEN1 in Early-onset Alzheimer's Disease.

Two Novel Mutations and a de novo Mutation in PSEN1 in Early-onset Alzheimer's Disease.

Journal: Aging and disease

Published: October 02, 2018

Identification of a novel PAFAH1B1 missense mutation as a cause of mild lissencephaly with basal ganglia calcification.

Identification of a novel PAFAH1B1 missense mutation as a cause of mild lissencephaly with basal ganglia calcification.

Journal: Brain & development

Published: April 14, 2018

DNAJC12 mutation is rare in Chinese Han population with Parkinson's disease.

DNAJC12 mutation is rare in Chinese Han population with Parkinson's disease.

Journal: Neurobiology of aging

Published: April 02, 2018

Analysis of Single Nucleotide Polymorphisms of STK32B, PPARGC1A and CTNNA3 Gene With Sporadic Parkinson's Disease Susceptibility in Chinese Han Population.

Analysis of Single Nucleotide Polymorphisms of STK32B, PPARGC1A and CTNNA3 Gene With Sporadic Parkinson's Disease Susceptibility in Chinese Han Population.

Journal: Frontiers in neurology

Published: January 14, 2018

TGM6 gene mutations in undiagnosed cerebellar ataxia patients.

TGM6 gene mutations in undiagnosed cerebellar ataxia patients.

Journal: Parkinsonism & related disorders

Published: March 01, 2017

Showing 1-12 of 18

Last Updated: 09/26/2026