Clinical and Neuropathological Features Associated With Loss of RAB39B-Reference-Cited by-同舟云学术

Clinical and Neuropathological Features Associated With Loss of RAB39B

Published:2020-01-17 Issue:4 Volume:35 Page:687-693
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord

Author:

Gao Yujing¹²^ORCID,Martínez‐Cerdeño Verónica³⁴,Hogan Kirk J.⁵⁶,McLean Catriona A.⁷,Lockhart Paul J.¹²^ORCID

Affiliation:

1. Bruce Lefroy Centre for Genetic Health Research Murdoch Children's Research Institute Parkville Victoria Australia

2. Department of Pediatrics The University of Melbourne Melbourne Victoria Australia

3. Department of Pathology and Laboratory Medicine UC Davis School of Medicine; Institute for Pediatric Regenerative Medicine and Shriners Hospitals for Children of Northern California Davis, California USA

4. MIND Institute, UC Davis Medical Center Davis, California USA

5. Department of Anesthesiology University of Wisconsin School of Medicine and Public Health Madison Wisconsin USA

6. Wisconsin Alzheimer's Institute, University of Wisconsin School of Medicine and Public Health Madison Wisconsin USA

7. Anatomical Pathology Alfred Hospital Melbourne Victoria Australia

Funder

McCusker Alzheimer's Research Foundation

Michael J. Fox Foundation for Parkinson's Research

National Health and Medical Research Council

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mds.27951

Reference30 articles.

1. The clinical symptoms of Parkinson's disease

2. Parkinson disease

3. Genetics in Parkinson disease: Mendelian versus non-Mendelian inheritance

4. Mutations in RAB39B Cause X-Linked Intellectual Disability and Early-Onset Parkinson Disease with α-Synuclein Pathology

5. Loss-of-function mutations inRAB39Bare associated with typical early-onset Parkinson disease

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1. Peripheral cutaneous synucleinopathy characteristics in genetic Parkinson’s disease;Frontiers in Neurology;2024-05-01

2. Expression of human Ras-related protein Rab39B variant T168K in Caenorhabditis elegans leads to motor dysfunction and dopaminergic neuron degeneration;Heliyon;2024-03

3. Novel RAB39B variant associated intellectual disability and levodopa-responsive young-onset parkinsonism;Parkinsonism & Related Disorders;2023-11

4. Deficiency of RAB39B Activates ER Stress-Induced Pro-apoptotic Pathway and Causes Mitochondrial Dysfunction and Oxidative Stress in Dopaminergic Neurons by Impairing Autophagy and Upregulating α-Synuclein;Molecular Neurobiology;2023-01-30

5. Loss of RAB39B does not alter MPTP-induced Parkinson’s disease-like phenotypes in mice;Frontiers in Aging Neuroscience;2023-01-25