LRRK2 pathobiology in Parkinson's disease-Reference-Cited by-同舟云学术

LRRK2 pathobiology in Parkinson's disease

Published:2014-10-10 Issue:5 Volume:131 Page:554-565
ISSN:0022-3042
Container-title:Journal of Neurochemistry
language:en
Short-container-title:J. Neurochem.

Author:

Martin Ian¹²,Kim Jungwoo Wren¹³,Dawson Valina L.¹²³⁴⁵,Dawson Ted M.¹²⁴⁵⁶

Affiliation:

1. Neuroregeneration and Stem Cell Programs; Institute for Cell Engineering; Johns Hopkins University School of Medicine; Baltimore Maryland USA

2. Department of Neurology; Johns Hopkins University School of Medicine; Baltimore Maryland USA

3. Department of Physiology; Johns Hopkins University School of Medicine; Baltimore Maryland USA

4. Solomon H. Snyder Department of Neuroscience; Johns Hopkins University School of Medicine; Baltimore Maryland USA

5. Adrienne Helis Malvin Medical Research Foundation; New Orleans Louisiana USA

6. Pharmacology and Molecular Sciences; Johns Hopkins University School of Medicine; Baltimore Maryland USA. Diana Helis Henry Medical Research Foundation; New Orleans Louisiana USA

Funder

NIH

NINDS

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/jnc.12949/fullpdf

Reference102 articles.

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3. Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease;Beilina;Proc. Natl Acad. Sci. USA,2014

4. Membrane localization of LRRK2 is associated with increased formation of the highly active LRRK2 dimer and changes in its phosphorylation;Berger;Biochemistry,2010

5. The pathophysiology of fragile X (and what it teaches us about synapses);Bhakar;Annu. Rev. Neurosci.,2012

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