LRRK2 in Parkinson's disease: upstream regulation and therapeutic targeting-Reference-Cited by-同舟云学术

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LRRK2 in Parkinson's disease: upstream regulation and therapeutic targeting

Published:2024-08 Issue: Volume: Page:
ISSN:1471-4914
Container-title:Trends in Molecular Medicine
language:en
Short-container-title:Trends in Molecular Medicine

Author:

Xiong Yulan^ORCID,Yu Jianzhong

Funder

National Science Foundation Office of Diversity and Inclusion

National Institute of General Medical Sciences

National Science Foundation

National Institutes of Health

National Institute of Neurological Disorders and Stroke

Parkinson's Foundation Inc

Publisher

Elsevier BV

Reference145 articles.

1. Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology;Zimprich;Neuron,2004

2. Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease;Paisan-Ruiz;Neuron,2004

3. Parkinson's disease;Lees;Lancet,2009

4. LRRK2 in Parkinson's disease: protein domains and functional insights;Mata;Trends Neurosci.,2006

5. Leucine-rich repeat kinases;Alessi;Annu. Rev. Biochem.,2024

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