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NOTCH2NLC Intermediate‐Length Repeat Expansions Are Associated with Parkinson Disease

Annals of neurology, 2021-01, Vol.89 (1), p.182-187

2021

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Necroptosis in neurodegenerative diseases: a potential therapeutic target

Cell death & disease, 2017-06, Vol.8 (6), p.e2905-e2905

2017

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Reply to “NOTCH2NLC Intermediate‐Length Repeat Expansions Are Associated with Parkinson Disease”

Annals of neurology, 2021-03, Vol.89 (3), p.635-635

2021

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Molecular characteristics and stages of chronic hepatitis B virus infection

World journal of gastroenterology : WJG, 2009-07, Vol.15 (25), p.3099-3105

2009

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Shared Genetic Architecture between Parkinson's Disease and Brain Structural Phenotypes

Movement disorders, 2023-12, Vol.38 (12), p.2258-2268

2023

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CHIP as a therapeutic target for neurological diseases

Cell death & disease, 2020-09, Vol.11 (9), p.727-727, Article 727

2020

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Rab GTPases: The Key Players in the Molecular Pathway of Parkinson's Disease

Frontiers in cellular neuroscience, 2017-03, Vol.11, p.81-81

2017

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Genetic analysis of the ATP11B gene in Chinese Han population with cerebral small vessel disease

BMC genomics, 2022-12, Vol.23 (1), p.822-822

2022

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COVID-19-induced acute loss of consciousness in Marchiafava-Bignami disease: a case report

Journal of international medical research, 2024-04, Vol.52 (4), p.3000605241234555-3000605241234555

2024

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LRP10 in α-synucleinopathies

Lancet neurology, 2018-12, Vol.17 (12), p.1034-1035

2018

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A novel RAB39B gene mutation in X-linked juvenile parkinsonism with basal ganglia calcification

Movement disorders, 2016-12, Vol.31 (12), p.1905-1909

2016

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Association between inflammatory bowel disease and Parkinson's disease: a prospective cohort study of 468,556 UK biobank participants

Frontiers in aging neuroscience, 2024-01, Vol.15, p.1294879-1294879

2024

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CHCHD2 gene mutations in familial and sporadic Parkinson's disease

Neurobiology of aging, 2016-02, Vol.38, p.217.e9-217.e13

2016

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The Role of Pathogens and Anti-Infective Agents in Parkinson's Disease, from Etiology to Therapeutic Implications

Journal of Parkinson's disease, 2022-01, Vol.12 (1), p.27

2022

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Identifying causal genes for migraine by integrating the proteome and transcriptome

Journal of headache and pain, 2023-08, Vol.24 (1), p.111-111, Article 111

2023

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

Journal of neurology, 2019-07, Vol.266 (7), p.1796-1800

2019

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Genetic analysis of the TMEM230 gene in Chinese Han patients with Parkinson's disease

Scientific reports, 2017-04, Vol.7 (1), p.1190-3, Article 1190

2017

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Author Correction: Anisomycin prevents OGD-induced necroptosis by regulating the E3 ligase CHIP

Scientific reports, 2021-12, Vol.11 (1), p.24531-24531, Article 24531

2021

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Disrupted structure and aberrant function of CHIP mediates the loss of motor and cognitive function in preclinical models of SCAR16

PLoS genetics, 2018-09, Vol.14 (9), p.e1007664-e1007664

2018

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Bushen Jianpi Formula Combined with Entecavir for the Treatment of HBeAg-Negative Chronic Hepatitis B: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial

Evidence-based complementary and alternative medicine, 2022, Vol.2022, p.6097221-10

2022

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Anisomycin prevents OGD-induced necroptosis by regulating the E3 ligase CHIP

Scientific reports, 2018-04, Vol.8 (1), p.6379-12, Article 6379

2018

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NOTCH2NLC expanded GGC repeats in patients with cerebral small vessel disease

Stroke and vascular neurology, 2023-04, Vol.8 (2), p.161-168

2023

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

Frontiers in molecular neuroscience, 2019-06, Vol.12, p.159-159

2019

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Generation of an induced pluripotent stem cell line (ZZUi020-A) from a patient with Parkinson’s disease harboring the intermediate-length GGC repeat expansions in the NOTCH2NLC gene

Stem cell research, 2021-04, Vol.52, p.102257-102257, Article 102257

2021

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High promoter methylation levels of glutathione‐S‐transferase M3 predict poor prognosis of acute‐on‐chronic hepatitis B liver failure

Hepatology research, 2017-05, Vol.47 (6), p.566-573

2017

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NOTCH2NLC Intermediate‐Length Repeat Expansions Are Associated with Parkinson Disease

Necroptosis in neurodegenerative diseases: a potential therapeutic target

Reply to “NOTCH2NLC Intermediate‐Length Repeat Expansions Are Associated with Parkinson Disease”

Molecular characteristics and stages of chronic hepatitis B virus infection

Shared Genetic Architecture between Parkinson's Disease and Brain Structural Phenotypes

CHIP as a therapeutic target for neurological diseases

Rab GTPases: The Key Players in the Molecular Pathway of Parkinson's Disease

Genetic analysis of the ATP11B gene in Chinese Han population with cerebral small vessel disease

COVID-19-induced acute loss of consciousness in Marchiafava-Bignami disease: a case report

LRP10 in α-synucleinopathies

A novel RAB39B gene mutation in X-linked juvenile parkinsonism with basal ganglia calcification

Association between inflammatory bowel disease and Parkinson's disease: a prospective cohort study of 468,556 UK biobank participants

CHCHD2 gene mutations in familial and sporadic Parkinson's disease

The Role of Pathogens and Anti-Infective Agents in Parkinson's Disease, from Etiology to Therapeutic Implications

Identifying causal genes for migraine by integrating the proteome and transcriptome

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

Genetic analysis of the TMEM230 gene in Chinese Han patients with Parkinson's disease

Author Correction: Anisomycin prevents OGD-induced necroptosis by regulating the E3 ligase CHIP

Disrupted structure and aberrant function of CHIP mediates the loss of motor and cognitive function in preclinical models of SCAR16

Bushen Jianpi Formula Combined with Entecavir for the Treatment of HBeAg-Negative Chronic Hepatitis B: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial

Anisomycin prevents OGD-induced necroptosis by regulating the E3 ligase CHIP

NOTCH2NLC expanded GGC repeats in patients with cerebral small vessel disease

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

Generation of an induced pluripotent stem cell line (ZZUi020-A) from a patient with Parkinson’s disease harboring the intermediate-length GGC repeat expansions in the NOTCH2NLC gene

High promoter methylation levels of glutathione‐S‐transferase M3 predict poor prognosis of acute‐on‐chronic hepatitis B liver failure

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