Missense mutations in leucine-rich repeat kinase 2 (LRRK2) contribute significantly to autosomal dominant Parkinsons disease (PD). Genome-wide association studies have further suggested that mutations in LRRK2 comprise a risk factor for sporadic PD. How LRRK2 contributes to PD however, is largely unknown. Recent work has shown that LRRK2 is highly expressed in tissue and circulating immune cells and is suggestive of a potential role for LRRK2 in innate immunity. These studies and theirpotential implications for PD will be discussed
It is now well established that chronic inflammation is a prominent feature of several neurodegenera...
Abstract Leucine-rich repeat kinase 2 (LRRK2) is a large multidomain kinase/GTPase that has been rec...
Sequence variants at or near the leucine-rich repeat kinase 2 (LRRK2) locus have been associated wit...
Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene are found in familial and idiopathic case...
The multiple hit hypothesis for Parkinson's disease (PD) suggests that an interaction between multip...
Mutations in the Leucine-Rich Repeat Kinase 2 (LRRK2) gene are associated with familial and sporadic...
Mutations in the leucine‐rich repeat kinase 2 (LRRK2, OMIM 609007) gene were first associated with a...
Interest in studying the biology of LRRK2 (leucine-rich repeat kinase 2) started in 2004 when missen...
A growing unmet need for better treatments of neurode-generative disorders, including Parkinson’s di...
The pathogenetic mechanisms leading to typical Parkinson's Disease (PD), the second most common huma...
Parkinson's disease (PD) is the most common neurodegenerative movement disorder. Although PD has lon...
Importance: Pathogenic variants in LRRK2 are a relatively common genetic cause of Parkinson disease ...
Leucine-rich repeat kinase 2 (LRRK2) is a large multidomain kinase/GTPase that has been recently lin...
IMPORTANCE Pathogenic variants in LRRK2 are a relatively common genetic cause of Parkinson disease (...
Mutations in Leucine-rich repeat kinase 2 (LRRK2) gene are the most common cause of sporadic and fam...
It is now well established that chronic inflammation is a prominent feature of several neurodegenera...
Abstract Leucine-rich repeat kinase 2 (LRRK2) is a large multidomain kinase/GTPase that has been rec...
Sequence variants at or near the leucine-rich repeat kinase 2 (LRRK2) locus have been associated wit...
Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene are found in familial and idiopathic case...
The multiple hit hypothesis for Parkinson's disease (PD) suggests that an interaction between multip...
Mutations in the Leucine-Rich Repeat Kinase 2 (LRRK2) gene are associated with familial and sporadic...
Mutations in the leucine‐rich repeat kinase 2 (LRRK2, OMIM 609007) gene were first associated with a...
Interest in studying the biology of LRRK2 (leucine-rich repeat kinase 2) started in 2004 when missen...
A growing unmet need for better treatments of neurode-generative disorders, including Parkinson’s di...
The pathogenetic mechanisms leading to typical Parkinson's Disease (PD), the second most common huma...
Parkinson's disease (PD) is the most common neurodegenerative movement disorder. Although PD has lon...
Importance: Pathogenic variants in LRRK2 are a relatively common genetic cause of Parkinson disease ...
Leucine-rich repeat kinase 2 (LRRK2) is a large multidomain kinase/GTPase that has been recently lin...
IMPORTANCE Pathogenic variants in LRRK2 are a relatively common genetic cause of Parkinson disease (...
Mutations in Leucine-rich repeat kinase 2 (LRRK2) gene are the most common cause of sporadic and fam...
It is now well established that chronic inflammation is a prominent feature of several neurodegenera...
Abstract Leucine-rich repeat kinase 2 (LRRK2) is a large multidomain kinase/GTPase that has been rec...
Sequence variants at or near the leucine-rich repeat kinase 2 (LRRK2) locus have been associated wit...