Leucine-rich repeat kinase 2 (LRRK2), a complex kinase/GTPase mutated in Parkinson's disease, has been shown to physically and functionally interact with cytoskeletal-related components in different brain cells. Neurons greatly rely on a functional cytoskeleton for many homeostatic processes such as local and long-distance vesicle transport, synaptic plasticity, and dendrites/axons growth and remodeling. Here, we will review the available data linking LRRK2 and the cytoskeleton, and discuss how this may be functionally relevant for the well-established roles of LRRK2 in intracellular trafficking pathways and outgrowth of neuronal processes in health and disease conditions
: Leucine-rich repeat kinase 2 (LRRK2) is a complex GTPase/kinase orchestrating cytoskeletal dynamic...
Mutations in leucine-rich repeat kinase 2 (LRRK2) are the single most common cause of inherited Park...
Leucine-rich repeat kinase 2 (LRRK2) is a key player in the pathogenesis of Parkinson's disease. Mut...
Mutations in human leucine-rich repeat kinase 2 (Lrrk2), a protein of yet unknown function, are link...
Mutations in human leucine-rich repeat kinase 2 (Lrrk2), a protein of yet unknown function, are link...
Mutations in PARK8, encoding leucine-rich repeat kinase 2 (LRRK2), are a major cause of Parkinson's ...
LRRK2 is a protein that interacts with a plethora of signaling molecules, but the complexity of LRRK...
AbstractMutations in the leucine-rich repeat kinase 2 (LRRK2) gene represent the most common genetic...
It is now well established that chronic inflammation is a prominent feature of several neurodegenera...
The leucine-rich repeat kinase 2 (LRRK2) gene was found to play a role in the pathogenesis of both f...
<div><p>The leucine-rich repeat kinase 2 (<i>LRRK2</i>) gene was found to play a role in the pathoge...
The leucine-rich repeat kinase 2 (LRRK2) gene was found to play a role in the pathogenesis of both f...
Mutations in Leucine-rich repeat kinase 2 gene (LRRK2) are associated with familial and sporadic Par...
AbstractThe leucine rich repeat kinase 2 (LRRK2/dardarin) is implicated in autosomal dominant famili...
Leucine-rich repeat kinase 2 (LRRK2) encodes a large and complex protein which is widely expressed i...
: Leucine-rich repeat kinase 2 (LRRK2) is a complex GTPase/kinase orchestrating cytoskeletal dynamic...
Mutations in leucine-rich repeat kinase 2 (LRRK2) are the single most common cause of inherited Park...
Leucine-rich repeat kinase 2 (LRRK2) is a key player in the pathogenesis of Parkinson's disease. Mut...
Mutations in human leucine-rich repeat kinase 2 (Lrrk2), a protein of yet unknown function, are link...
Mutations in human leucine-rich repeat kinase 2 (Lrrk2), a protein of yet unknown function, are link...
Mutations in PARK8, encoding leucine-rich repeat kinase 2 (LRRK2), are a major cause of Parkinson's ...
LRRK2 is a protein that interacts with a plethora of signaling molecules, but the complexity of LRRK...
AbstractMutations in the leucine-rich repeat kinase 2 (LRRK2) gene represent the most common genetic...
It is now well established that chronic inflammation is a prominent feature of several neurodegenera...
The leucine-rich repeat kinase 2 (LRRK2) gene was found to play a role in the pathogenesis of both f...
<div><p>The leucine-rich repeat kinase 2 (<i>LRRK2</i>) gene was found to play a role in the pathoge...
The leucine-rich repeat kinase 2 (LRRK2) gene was found to play a role in the pathogenesis of both f...
Mutations in Leucine-rich repeat kinase 2 gene (LRRK2) are associated with familial and sporadic Par...
AbstractThe leucine rich repeat kinase 2 (LRRK2/dardarin) is implicated in autosomal dominant famili...
Leucine-rich repeat kinase 2 (LRRK2) encodes a large and complex protein which is widely expressed i...
: Leucine-rich repeat kinase 2 (LRRK2) is a complex GTPase/kinase orchestrating cytoskeletal dynamic...
Mutations in leucine-rich repeat kinase 2 (LRRK2) are the single most common cause of inherited Park...
Leucine-rich repeat kinase 2 (LRRK2) is a key player in the pathogenesis of Parkinson's disease. Mut...