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LRRK2-IN1

Known as: LRRK2-IN-1 
 
National Institutes of Health

Papers overview

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2019
2019
Mutations of LRRK2, encoding leucine-rich repeat kinase 2 (LRRK2), are the leading cause of autosomal dominant Parkinson's… Expand
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2015
2015
It has been uncertain whether specific disease-relevant biomarker phenotypes can be found using sporadic Parkinson’s disease (PD… Expand
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Highly Cited
2014
Highly Cited
2014
Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene have been associated with Parkinson’s disease, and its inhibition… Expand
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2014
2014
BackgroundDoublecortin-like kinase 1 (DCLK1) is emerging as a tumor specific stem cell marker in colorectal and pancreatic cancer… Expand
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2014
2014
Our understanding of Parkinson's disease (PD) has been revolutionized by the discovery of disease-causing genetic mutations. The… Expand
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Highly Cited
2013
Highly Cited
2013
A cluster of phosphorylation sites in LRRK2 (leucine-rich repeat kinase 2), including Ser910, Ser935, Ser955 and Ser973, is… Expand
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Highly Cited
2013
Highly Cited
2013
Mutations in leucine-rich repeat kinase 2 (LRRK2) are the most frequent known cause of late-onset Parkinson's disease (PD). To… Expand
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Highly Cited
2013
Highly Cited
2013
Recent studies indicate that the Parkinson's disease-linked leucine-rich repeat kinase 2 (LRRK2) modulates cytoskeletal functions… Expand
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Highly Cited
2012
Highly Cited
2012
Mutations in leucine-rich repeat kinase 2 (LRRK2) are the most common cause of familial Parkinson's disease. An amino terminal… Expand
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Highly Cited
2011
Highly Cited
2011
Mutations in leucine-rich repeat kinase 2 (LRRK2) are strongly associated with late-onset autosomal dominant Parkinson’s disease… Expand
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Is this relevant?