Mutations in LRRK2 are the most common genetic cause of Parkinson's disease. Despite substantial research efforts, the physiological and pathological role of this multidomain protein remains poorly defined. In this study, we used a systematic approach to construct the general protein-protein interactome around LRRK2, which was then evaluated taking into consideration the differential expression patterns and the co-expression behaviours of the LRRK2 interactors in 15 different healthy tissue types. The LRRK2 interactors exhibited distinct expression features in the brain as compared to the peripheral tissues analysed. Moreover, a high degree of similarity was found for the LRRK2 interactors in putamen, caudate and nucleus accumbens, thus def...
Human LRRK2 (Leucine-Rich Repeat Kinase 2) has been associated with both familial and idiopathic Par...
Leucine-rich repeat kinase 2 (LRRK2) encodes a large and complex protein which is widely expressed i...
The leucine-rich repeat kinase 2 (LRRK2) gene was found to play a role in the pathogenesis of both f...
Mutations in LRRK2 are the most common genetic cause of Parkinson's disease. Despite substantial res...
A wide variety of different functions and an impressive array of interactors have been associated wi...
Mutations in LRRK2 are the most frequent cause of familial Parkinson’s disease (PD), with common LRR...
Mutations in leucine-rich repeat kinase 2 (LRRK2) cause Parkinson’s disease with a similar clinical ...
Since the discovery of leucine-rich repeat kinase 2 (LRRK2) as a protein that is likely central to t...
Parkinson disease (PD) is the most common movement disorder and the second most common age-related p...
Genetic studies show that LRRK2, and not its closest paralogue LRRK1, is linked to Parkinson's disea...
Mutations in LRRK2 are one of the primary genetic causes of Parkinson's disease (PD). LRRK2 contains...
Mutations in the leucine-rich repeat kinase 2 (LRRK2) encoding gene are the most common cause of mon...
Mutations in Park8, encoding for the multidomain Leucine-rich repeat kinase 2 (LRRK2) protein, compr...
Leucine-rich repeat kinase 2 (LRRK2) is a large, multidomain protein containing two catalytic domain...
Mutations in LRRK2 cause autosomal dominant Parkinsons disease (PD). LRRK2 encodes a multi-domain pr...
Human LRRK2 (Leucine-Rich Repeat Kinase 2) has been associated with both familial and idiopathic Par...
Leucine-rich repeat kinase 2 (LRRK2) encodes a large and complex protein which is widely expressed i...
The leucine-rich repeat kinase 2 (LRRK2) gene was found to play a role in the pathogenesis of both f...
Mutations in LRRK2 are the most common genetic cause of Parkinson's disease. Despite substantial res...
A wide variety of different functions and an impressive array of interactors have been associated wi...
Mutations in LRRK2 are the most frequent cause of familial Parkinson’s disease (PD), with common LRR...
Mutations in leucine-rich repeat kinase 2 (LRRK2) cause Parkinson’s disease with a similar clinical ...
Since the discovery of leucine-rich repeat kinase 2 (LRRK2) as a protein that is likely central to t...
Parkinson disease (PD) is the most common movement disorder and the second most common age-related p...
Genetic studies show that LRRK2, and not its closest paralogue LRRK1, is linked to Parkinson's disea...
Mutations in LRRK2 are one of the primary genetic causes of Parkinson's disease (PD). LRRK2 contains...
Mutations in the leucine-rich repeat kinase 2 (LRRK2) encoding gene are the most common cause of mon...
Mutations in Park8, encoding for the multidomain Leucine-rich repeat kinase 2 (LRRK2) protein, compr...
Leucine-rich repeat kinase 2 (LRRK2) is a large, multidomain protein containing two catalytic domain...
Mutations in LRRK2 cause autosomal dominant Parkinsons disease (PD). LRRK2 encodes a multi-domain pr...
Human LRRK2 (Leucine-Rich Repeat Kinase 2) has been associated with both familial and idiopathic Par...
Leucine-rich repeat kinase 2 (LRRK2) encodes a large and complex protein which is widely expressed i...
The leucine-rich repeat kinase 2 (LRRK2) gene was found to play a role in the pathogenesis of both f...