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Peripheral immune cell traits and Parkinson's disease: A Mendelian randomization study

PloS one, 2024-03, Vol.19 (3), p.e0299026-e0299026

2024

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New Insights Into the Pathogenesis of Alzheimer's Disease

Frontiers in neurology, 2020-01, Vol.10, p.1312-1312

2020

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Supergene geochemistry of arsenic and activation mechanism of eucalyptus to arsenic source

Environmental geochemistry and health, 2022-11, Vol.44 (11), p.4017-4029

2022

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Peripheral immune markers and amyotrophic lateral sclerosis: a Mendelian randomization study

Frontiers in neuroscience, 2023-12, Vol.17, p.1269354-1269354

2023

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MicroRNA-381 reduces inflammation and infiltration of macrophages in polymyositis via downregulating HMGB1

International journal of oncology, 2018-09, Vol.53 (3), p.1332-1342

2018

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Microvascular and cellular dysfunctions in Alzheimer’s disease: an integrative analysis perspective

Scientific reports, 2024-09, Vol.14 (1), p.20944-15, Article 20944

2024

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Vitamin B supplementation, homocysteine levels, and the risk of cerebrovascular disease: a meta-analysis

Neurology, 2013-10, Vol.81 (15), p.1298-1307

2013

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AAV mediated carboxyl terminus of Hsp70 interacting protein overexpression mitigates the cognitive and pathological phenotypes of APP/PS1 mice

Neural regeneration research, 2025-01, Vol.20 (1), p.253-264

2025

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LRP10 Mutations May Correlate with Sporadic Parkinson’s Disease in China

Molecular neurobiology, 2021-03, Vol.58 (3), p.1212-1216

2021

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The Value of NOTCH2NLC Gene Detection and Skin Biopsy in the Diagnosis of Neuronal Intranuclear Inclusion Disease

Frontiers in neurology, 2021-05, Vol.12, p.624321-624321

2021

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Meningeal immunity and neurological diseases: new approaches, new insights

Journal of neuroinflammation, 2023-05, Vol.20 (1), p.125-125, Article 125

2023

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Early increased neutrophil-to-lymphocyte ratio is associated with poor 3-month outcomes in spontaneous intracerebral hemorrhage

PloS one, 2019-02, Vol.14 (2), p.e0211833-e0211833

2019

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Intelligence, education level, and risk of Parkinson's disease in European populations: A Mendelian randomization study

Frontiers in genetics, 2022-11, Vol.13, p.963163

2022

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Generation of an induced pluripotent stem cell line (ZZUi036-A) derived from skin fibroblasts of a Neuronal intranuclear inclusion disease patient with GGC repeat expansion in the NOTCH2NLC gene

Stem cell research, 2022-08, Vol.63, p.102844-102844, Article 102844

2022

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Increased PRR14 and VCAM-1 level in serum of patients with Parkinson's disease

Frontiers in neurology, 2022-09, Vol.13, p.993940-993940

2022

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Assessing the impact of novel risk loci on Alzheimer's and Parkinson's diseases in a Chinese Han cohort

Frontiers in neurology, 2024, Vol.15, p.1326692-1326692

2024

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CHCHD10 is involved in the development of Parkinson's disease caused by CHCHD2 loss-of-function mutation p.T61I

Neurobiology of aging, 2019-03, Vol.75, p.38-41

2019

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Manganese transporter Slc39a14 deficiency revealed its key role in maintaining manganese homeostasis in mice

Cell discovery, 2017-07, Vol.3 (1), p.17025-17025, Article 17025

2017

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Rare KCND3 Loss-of-Function Mutation Associated With the SCA19/22

Frontiers in molecular neuroscience, 2022-06, Vol.15, p.919199-919199

2022

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Corrigendum to “Generation of induced pluripotent stem cell line (ZZUi028-A) from a 52-year-old Chinese Han healthy female individual” [Stem Cell Res. 53 (2021) 102381]

Stem cell research, 2021-12, Vol.57, p.102603-102603, Article 102603

2021

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Generation of induced pluripotent stem cell line (ZZUi027-A) derived from skin fibroblasts from a Parkinson’s disease patient with RAB39B gene mutation

Stem cell research, 2021-08, Vol.55, p.102454-102454, Article 102454

2021

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Generation of induced pluripotent stem cell line (ZZUi028-A) from a 52-year-old Chinese Han healthy female individual

Stem cell research, 2021-05, Vol.53, p.102381-102381, Article 102381

2021

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Generation of induced pluripotent stem cell line (ZZUi019-A) derived from skin fibroblasts from a healthy volunteer

Stem cell research, 2021-05, Vol.53, p.102285-102285, Article 102285

2021

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Modeling Parkinson’s Disease Using Induced Pluripotent Stem Cells

Stem cells international, 2020, Vol.2020 (2020), p.1-15

2020

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A large pedigree study confirmed the CGG repeat expansion of RILPL1 Is associated with oculopharyngodistal myopathy

BMC medical genomics, 2023-10, Vol.16 (1), p.1-253, Article 253

2023

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Peripheral immune cell traits and Parkinson's disease: A Mendelian randomization study

New Insights Into the Pathogenesis of Alzheimer's Disease

Supergene geochemistry of arsenic and activation mechanism of eucalyptus to arsenic source

Peripheral immune markers and amyotrophic lateral sclerosis: a Mendelian randomization study

MicroRNA-381 reduces inflammation and infiltration of macrophages in polymyositis via downregulating HMGB1

Microvascular and cellular dysfunctions in Alzheimer’s disease: an integrative analysis perspective

Vitamin B supplementation, homocysteine levels, and the risk of cerebrovascular disease: a meta-analysis

AAV mediated carboxyl terminus of Hsp70 interacting protein overexpression mitigates the cognitive and pathological phenotypes of APP/PS1 mice

LRP10 Mutations May Correlate with Sporadic Parkinson’s Disease in China

The Value of NOTCH2NLC Gene Detection and Skin Biopsy in the Diagnosis of Neuronal Intranuclear Inclusion Disease

Meningeal immunity and neurological diseases: new approaches, new insights

Early increased neutrophil-to-lymphocyte ratio is associated with poor 3-month outcomes in spontaneous intracerebral hemorrhage

Intelligence, education level, and risk of Parkinson's disease in European populations: A Mendelian randomization study

Generation of an induced pluripotent stem cell line (ZZUi036-A) derived from skin fibroblasts of a Neuronal intranuclear inclusion disease patient with GGC repeat expansion in the NOTCH2NLC gene

Increased PRR14 and VCAM-1 level in serum of patients with Parkinson's disease

Assessing the impact of novel risk loci on Alzheimer's and Parkinson's diseases in a Chinese Han cohort

CHCHD10 is involved in the development of Parkinson's disease caused by CHCHD2 loss-of-function mutation p.T61I

Manganese transporter Slc39a14 deficiency revealed its key role in maintaining manganese homeostasis in mice

Rare KCND3 Loss-of-Function Mutation Associated With the SCA19/22

Corrigendum to “Generation of induced pluripotent stem cell line (ZZUi028-A) from a 52-year-old Chinese Han healthy female individual” [Stem Cell Res. 53 (2021) 102381]

Generation of induced pluripotent stem cell line (ZZUi027-A) derived from skin fibroblasts from a Parkinson’s disease patient with RAB39B gene mutation

Generation of induced pluripotent stem cell line (ZZUi028-A) from a 52-year-old Chinese Han healthy female individual

Generation of induced pluripotent stem cell line (ZZUi019-A) derived from skin fibroblasts from a healthy volunteer

Modeling Parkinson’s Disease Using Induced Pluripotent Stem Cells

A large pedigree study confirmed the CGG repeat expansion of RILPL1 Is associated with oculopharyngodistal myopathy

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