Jinhua Zheng

Zhengzhou 450003, PR China
Puerto Rico

Last Updated: 09/26/2026

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Found 12 publications

CXCR4 knockout induces neuropathological changes in the MPTP-lesioned model of Parkinson's disease.

CXCR4 knockout induces neuropathological changes in the MPTP-lesioned model of Parkinson's disease.

Journal: Biochimica et biophysica acta. Molecular basis of disease

Published: March 07, 2022

The long noncoding RNA GAS5 potentiates neuronal injury in Parkinson's disease by binding to microRNA-150 to regulate Fosl1 expression.

The long noncoding RNA GAS5 potentiates neuronal injury in Parkinson's disease by binding to microRNA-150 to regulate Fosl1 expression.

Journal: Experimental neurology

Published: July 07, 2021

Alpha-synuclein gene polymorphism affects risk of dementia in Han Chinese with Parkinson's disease.

Alpha-synuclein gene polymorphism affects risk of dementia in Han Chinese with Parkinson's disease.

Journal: Neuroscience letters

Published: March 28, 2018

Absence of association of the Ala58Val (rs17571) CTSD gene variant with Parkinson's disease or amyotrophic lateral sclerosis in a Han Chinese population.

Absence of association of the Ala58Val (rs17571) CTSD gene variant with Parkinson's disease or amyotrophic lateral sclerosis in a Han Chinese population.

Journal: Neuroscience letters

Published: May 27, 2017

No association of PARK10 polymorphism with Parkinson's disease in Han Chinese population.

No association of PARK10 polymorphism with Parkinson's disease in Han Chinese population.

Journal: Parkinsonism & related disorders

Published: April 27, 2017

HLA-DRA/HLA-DRB5 polymorphism affects risk of sporadic ALS and survival in a southwest Chinese cohort.

HLA-DRA/HLA-DRB5 polymorphism affects risk of sporadic ALS and survival in a southwest Chinese cohort.

Journal: Journal of the neurological sciences

Published: October 31, 2016

Association between gene polymorphism and depression in Parkinson's disease: A case-control study.

Association between gene polymorphism and depression in Parkinson's disease: A case-control study.

Journal: Journal of the neurological sciences

Published: October 24, 2016

Association between a heme oxygenase-2 genetic variant and risk of Parkinson's disease in Han Chinese.

Association between a heme oxygenase-2 genetic variant and risk of Parkinson's disease in Han Chinese.

Journal: Neuroscience letters

Published: August 09, 2016

Polymorphism in MIR4697 but not VPS13C, GCH1, or SIPA1L2 is associated with risk of Parkinson's disease in a Han Chinese population.

Polymorphism in MIR4697 but not VPS13C, GCH1, or SIPA1L2 is associated with risk of Parkinson's disease in a Han Chinese population.

Journal: Neuroscience letters

Published: June 06, 2016

Mutational analysis of CHCHD2 in Chinese patients with multiple system atrophy and amyotrophic lateral sclerosis.

Mutational analysis of CHCHD2 in Chinese patients with multiple system atrophy and amyotrophic lateral sclerosis.

Journal: Journal of the neurological sciences

Published: May 03, 2016

Mutational scanning of the CHCHD2 gene in Han Chinese patients with Parkinson's disease and meta-analysis of the literature.

Mutational scanning of the CHCHD2 gene in Han Chinese patients with Parkinson's disease and meta-analysis of the literature.

Journal: Parkinsonism & related disorders

Published: February 26, 2016

Association of the functional SNP rs2275294 in ZNF512B with risk of amyotrophic lateral sclerosis and Parkinson's disease in Han Chinese.

Association of the functional SNP rs2275294 in ZNF512B with risk of amyotrophic lateral sclerosis and Parkinson's disease in Han Chinese.

Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration

Published: August 28, 2015

Showing 1-12 of 12

Last Updated: 09/26/2026