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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… 
National Institutes of Health

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12q12Homo sapiensLRRK2 geneLeucine-Rich Repeat Serine/Threonine-Protein Kinase 2

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Cognitive profile and 18F-fluorodeoxyglucose PET study in LRRK2-related Parkinson's disease.
2016
2016
Parkinson disease (PARK) genes are somatically mutated in cutaneous melanoma
Objective: To assess whether Parkinson disease (PD) genes are somatically mutated in cutaneous melanoma (CM) tissue, because CM… 
2015
2015
Status of the Parkinson’s disease gene family expression in non-small-cell lung cancer
BackgroundThe purpose of this study is to detect the Parkinson’s disease gene family mRNA relative expression in the non-small… 
Highly Cited
2009
Highly Cited
2009
Mutations in the LRRK2 Roc-COR tandem domain link Parkinson's disease to Wnt signalling pathways
Mutations in PARK8, encoding LRRK2, are the most common known cause of Parkinson's disease. The LRRK2 Roc-COR tandem domain… 
2009
2009
Novel GFAP Mutation in Patient with Adult-Onset Alexander Disease Presenting with Spastic Ataxia
Adult-onset Alexander disease is rare and clinically characterized by slowly progressive signs of brainstem and spinal cord… 
2008
2008
Genetic and environmental findings in early‐onset Parkinson's disease Brazilian patients
Parkinson's disease (PD) etiology has been attributed both to genetic and environmental factors. In this study, we investigated… 
2007
2007
Parkin polymorphisms and environmental exposure: decrease in age at onset of Parkinson's disease.
Highly Cited
2006
Highly Cited
2006
Isolation and expression profiling of genes upregulated in bone marrow-derived mononuclear cells of rheumatoid arthritis patients.
We have comprehensively identified the genes whose expressions are augmented in bone marrow-derived mononuclear cells (BMMC) from… 
Highly Cited
2005
Highly Cited
2005
An LRRK2 mutation as a cause for the parkinsonism in the original PARK8 family
We detected a missense mutation in the kinase domain of the LRRK2 gene in members with autosomal dominant Parkinson's disease of… 
Highly Cited
2005
Highly Cited
2005
Familial Parkinson's disease: Clinical and genetic analysis of four Basque families
During the last few years several loci have been linked to Mendelian forms of Parkinson's disease (PD). To date, 5 causative… 
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