Age-related LRRK2 G2019S Mutation Impacts Microglial Dopaminergic Fiber Refinement and Synaptic Pruning Involved in Abnormal Behaviors

2021 ◽  
Author(s):  
Qiuyang Zhang ◽  
Xiaojuan Cheng ◽  
Wei Wu ◽  
Siyu Yang ◽  
Hanlin You ◽  
...  
Keyword(s):  
G2019s Mutation ◽  
Age Related ◽  
Lrrk2 G2019s ◽  
Abnormal Behaviors ◽  
Synaptic Pruning

Frequency and phenotypes of LRRK2 G2019S mutation in Italian patients with Parkinson's disease

2006 ◽  
Vol 21 (8) ◽  
pp. 1232-1235 ◽  
Author(s):  
Roberta Marongiu ◽  
Daniele Ghezzi ◽  
Tamara Ialongo ◽  
Francesco Soleti ◽  
Antonio Elia ◽  
...  
Keyword(s):  
Parkinson’S Disease ◽  
Parkinson's Disease ◽  
G2019s Mutation ◽  
Lrrk2 G2019s

Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease?

Neurology ◽  
2008 ◽  
Vol 71 (19) ◽  
pp. 1550-1552 ◽  
Author(s):  
S. Lesage ◽  
S. Belarbi ◽  
A. Troiano ◽  
C. Condroyer ◽  
N. Hecham ◽  
...  
Keyword(s):  
Parkinson Disease ◽  
North African ◽  
G2019s Mutation ◽  
Lrrk2 G2019s ◽  
The Common

scholarly journals LRRK2 G2019S mutation attenuates microglial motility by inhibiting focal adhesion kinase

2015 ◽  
Vol 6 (1) ◽  
Author(s):  
Insup Choi ◽  
Beomsue Kim ◽  
Ji-Won Byun ◽  
Sung Hoon Baik ◽  
Yun Hyun Huh ◽  
...  
Keyword(s):  
Focal Adhesion Kinase ◽  
Focal Adhesion ◽  
G2019s Mutation ◽  
Lrrk2 G2019s

Clinical and imaging markers in premotor LRRK2 G2019S mutation carriers

2015 ◽  
Vol 21 (10) ◽  
pp. 1170-1176 ◽  
Author(s):  
Dolores Vilas ◽  
Lourdes Ispierto ◽  
Ramiro Álvarez ◽  
Claustre Pont-Sunyer ◽  
María José Martí ◽  
...  
Keyword(s):  
G2019s Mutation ◽  
Mutation Carriers ◽  
Lrrk2 G2019s ◽  
Imaging Markers

scholarly journals Parkinson's disease-related LRRK2 G2019S mutation results from independent mutational events in humans

2010 ◽  
Vol 19 (10) ◽  
pp. 1998-2004 ◽  
Author(s):  
Suzanne Lesage ◽  
Etienne Patin ◽  
Christel Condroyer ◽  
Anne-Louise Leutenegger ◽  
Ebba Lohmann ◽  
...  
Keyword(s):  
Parkinson’S Disease ◽  
Parkinson's Disease ◽  
G2019s Mutation ◽  
Lrrk2 G2019s

Ashkenazi Parkinson’s disease patients with the LRRK2 G2019S mutation share a common founder dating from the second to fifth centuries

Neurogenetics ◽  
2009 ◽  
Vol 10 (4) ◽  
pp. 355-358 ◽  
Author(s):  
Anat Bar-Shira ◽  
Carolyn M. Hutter ◽  
Nir Giladi ◽  
Cyrus P. Zabetian ◽  
Avi Orr-Urtreger
Keyword(s):  
Parkinson’S Disease ◽  
Parkinson's Disease ◽  
G2019s Mutation ◽  
Lrrk2 G2019s ◽  
Common Founder

Fall risk and gait in Parkinson's disease: The role of the LRRK2 G2019S mutation

2013 ◽  
Vol 28 (12) ◽  
pp. 1683-1690 ◽  
Author(s):  
Anat Mirelman ◽  
Talia Heman ◽  
Kira Yasinovsky ◽  
Avner Thaler ◽  
Tanya Gurevich ◽  
...  
Keyword(s):  
Parkinson’S Disease ◽  
Parkinson's Disease ◽  
Fall Risk ◽  
G2019s Mutation ◽  
Lrrk2 G2019s

3.049 LEVODOPA-INDUCED DYSKINESIA IN PARKINSON'S DISEASE PATIENTS CARRYING THE LEUCINE-RICH REPEAT KINASE 2 (LRRK2) G2019S MUTATION

2012 ◽  
Vol 18 ◽  
pp. S181
Author(s):  
G. Yahalom ◽  
N. Kaplan ◽  
A. Vituri ◽  
O.S. Cohen ◽  
R. Inzelberg ◽  
...  
Keyword(s):  
Parkinson’S Disease ◽  
Parkinson's Disease ◽  
Leucine Rich Repeat ◽  
G2019s Mutation ◽  
Lrrk2 G2019s
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