LRRK2 gene in Parkinson disease: Mutation analysis and case control association study-Reference-Cited by-同舟云学术

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LRRK2 gene in Parkinson disease: Mutation analysis and case control association study

Published:2005-06-15 Issue:5 Volume:65 Page:696-700
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Paisan-Ruiz C.,Lang A. E.,Kawarai T.,Sato C.,Salehi-Rad S.,Fisman G. K.,Al-Khairallah T.,St George-Hyslop P.,Singleton A.,Rogaeva E.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 158 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. How Parkinson’s Disease-Linked LRRK2 Mutations Affect Different CNS Cell Types;Journal of Parkinson's Disease;2024-06-15

2. Impaired Sonic Hedgehog Responsiveness of Induced Pluripotent Stem Cell-Derived Floor Plate Cells Carrying the LRRK2-I1371V Mutation Contributes to the Ontogenic Origin of Lower Dopaminergic Neuron Yield;Stem Cells and Development;2024-06-01

3. Parkinson's Disease Associated with G2019S LRRK2 Mutations without Lewy Body Pathology;Movement Disorders Clinical Practice;2024-05-16

4. Structural insights into the GTP-driven monomerization and activation of a bacterial LRRK2 homolog using allosteric nanobodies;eLife;2024-04-26

5. Structural insights into the GTP-driven monomerization and activation of a bacterial LRRK2 homolog using allosteric nanobodies;eLife;2024-04-26

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