LRRK2 wt Allele

Known as: RIPK7, Leucine-Rich Repeat Kinase 2 wt Allele, DARDARIN 
Human LRRK2 wild-type allele is located in the vicinity of 12q12 and is approximately 144 kb in length. This allele, which encodes leucine-rich… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

2004-2018
02420042018

Papers overview

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2012
2012
Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene are the most common cause of autosomal-dominant familial Parkinson's… (More)
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2012
2012
Mutations in the LRRK2 (leucine-rich repeat kinase 2) gene have been identified in PARK8, a major form of autosomal-dominantly… (More)
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2009
2009
Mutations in PARK8, encoding LRRK2, are the most common known cause of Parkinson's disease. The LRRK2 Roc-COR tandem domain… (More)
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2009
2009
BACKGROUND Since the causative gene linked to PARK8 parkinsonism was identified as LRRK2, LRRK2 gene mutations have been found to… (More)
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Highly Cited
2007
Highly Cited
2007
Leucine-rich repeat kinase 2 (LRRK2), a product of a causative gene for the autosomal-dominant form of familial Parkinson's… (More)
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Highly Cited
2006
Highly Cited
2006
OBJECTIVE The PARK8 gene responsible for late-onset autosomal dominant Parkinson's disease encodes a large novel protein of… (More)
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2006
2006
We have comprehensively identified the genes whose expressions are augmented in bone marrow-derived mononuclear cells (BMMC) from… (More)
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Highly Cited
2005
Highly Cited
2005
Hertie Institute of Clinical Brain Research, Department of Medical Genetics and Department of Neuroradiology, University of T… (More)
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Highly Cited
2005
Highly Cited
2005
BACKGROUND Mutations in the gene Leucine-Rich Repeat Kinase 2 (LRRK2) were recently identified as the cause of PARK8 linked… (More)
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Highly Cited
2004
Highly Cited
2004
Recently, a new locus (PARK8) for autosomal dominant parkinsonism has been identified in one large Japanese family. Linkage has… (More)
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