×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease.
15680456
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
Phosphorylation of amyloid precursor protein by mutant LRRK2 promotes AICD activity and neurotoxicity in Parkinson's disease.
28720718
2017
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
RAB7L1 interacts with LRRK2 to modify intraneuronal protein sorting and Parkinson's disease risk.
23395371
2013
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
Crystal structure of the WD40 domain dimer of LRRK2.
30635421
2019
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease*.
16251215
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
Mutations in LRRK2 increase phosphorylation of peroxiredoxin 3 exacerbating oxidative stress-induced neuronal death.
21850687
2011
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
LRRK2 R1441G in Spanish patients with Parkinson's disease.
15925109
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
An LRRK2 mutation as a cause for the parkinsonism in the original PARK8 family.
15880653
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease.
16333314
2006
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
A common LRRK2 mutation in idiopathic Parkinson's disease.
15680457
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
Rab29 activation of the Parkinson's disease-associated LRRK2 kinase.
29212815
2018
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease.
15680455
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
Clinical features of LRRK2-associated Parkinson's disease in central Norway.
15852371
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
G2019S LRRK2 mutation in French and North African families with Parkinson's disease.
16240353
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
Systematic review and UK-based study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset Parkinson's disease.
22956510
2012
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
Structural interface between LRRK2 and 14-3-3 protein.
28202711
2017
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
LRRK2 mutations in Parkinson disease.
16157908
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
Lrrk2 pathogenic substitutions in Parkinson's disease.
16172858
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
Parkinson's disease-associated mutations in leucine-rich repeat kinase 2 augment kinase activity.
16269541
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
Clinical and positron emission tomography of Parkinson's disease caused by LRRK2.
15732108
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology.
15541309
2004
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
LRRK2 mutations and Parkinsonism.
15811454
2005
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
Parkinson's disease and LRRK2: frequency of a common mutation in U.S. movement disorder clinics.
16250030
2006
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
The familial Parkinsonism gene LRRK2 regulates neurite process morphology.
17114044
2006
×
Entrez Id:
120892
Gene Symbol:
LRRK2
LRRK2
PARKINSON DISEASE 8 (disorder)
0.930
GeneticVariation
UNIPROT
Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data.
16272164
2005