Results 81 to 90 of about 19,899 (238)
Mutations in leucine-rich repeat kinase 2 (LRRK2) are strongly associated with late-onset autosomal dominant Parkinson's disease. LRRK2 is highly expressed in immune cells and recent work points towards a link between LRRK2 and innate immunity.
Nicolas Dzamko +12 more
doaj +1 more source
Macrophage‐derived S100 calcium‐binding protein A9 (S100A9) promotes the pathological progression of pulmonary arterial hypertension (PAH). S100A9 upregulates the interaction between signal‐transducing adaptor protein 2 and leucine‐rich repeat kinase 2, thereby regulating mitochondria–endoplasmic reticulum (ER) contact.
Chen Gong +15 more
wiley +1 more source
The general LRRK2 interactome.
A) Nodes (n = 407) represent LRRK2 interactors that were with FS > 2 and were reviewed by the UniprotKB. Node fill colour and node size are weighted on the final score (FS). Larger size and darker colour indicate higher FS.
Claudia Manzoni (204029) +6 more
core +1 more source
Clinical features and progression of Parkinson's disease with LRRK2 variants: A prospective study
Objective We established a prospective cohort study to investigate the differences in motor and non‐motor symptoms between idiopathic Parkinson's disease (IPD) and Parkinson's disease in carriers of leucine‐rich repeat kinase 2 (LRRK2) gene risk variants
Tingwei Song +9 more
doaj +1 more source
Socio‐Occupational Functioning after Subthalamic Deep Brain Stimulation in Parkinson's Disease
Abstract Background Socio‐occupational functioning in patients with Parkinson's disease (PD) treated with subthalamic nucleus deep brain stimulation (STN‐DBS) is not fully captured by standard motor and quality‐of‐life scales. Objectives To characterize patient‐reported socio‐occupational functioning after STN‐DBS and explore associated clinical and ...
Gabriele Imbalzano +7 more
wiley +1 more source
Impaired inflammatory responses in murine Lrrk2-knockdown brain microglia. [PDF]
LRRK2, a Parkinson's disease associated gene, is highly expressed in microglia in addition to neurons; however, its function in microglia has not been evaluated.
Beomsue Kim +9 more
doaj +1 more source
Caught in the act: LRRK2 in exosomes [PDF]
Abstract Mutations in the leucine-rich repeat kinase 2 (LRRK2) gene are a frequent genetic cause of late-onset Parkinson's disease (PD) and a target for therapeutic approaches. LRRK2 protein can influence vesicle trafficking events in the cytosol, with action both in endosomal and lysosomal pathways in different types of cells.
Shijie Wang, Andrew B. West
openaire +2 more sources
LRRK2 Kinase Activity Does Not Alter Cell-Autonomous Tau Pathology Development in Primary Neurons
Background: Mutations in leucine-rich repeat kinase 2 (LRRK2) are the most common cause of familial Parkinson’s disease (PD) and are also associated with genetic risk in idiopathic PD.
Michael X. Henderson +3 more
doaj +1 more source
Abstract Background Parkinson's disease (PD) is clinically heterogeneous, with variable progression rates that complicate clinical trial design. The data‐driven diffuse malignant (DM), intermediate (IM), and mild‐motor predominant (MMP) subtyping model has prognostic value but lacks disease duration–specific thresholds for prospective use in disease ...
Ahmed Negida +4 more
wiley +1 more source
LRRK2 phosphorylates ArfGAP1, and ArfGAP1 enhances LRRK2 kinase activity.
(A) In vitro kinase assay with [32P]-γ-ATP, recombinant WT, R1441C, G2019S or D1994A human LRRK2 (Δ970, residues 970–2527) and GST-tagged ArfGAP1.
Darren J. Moore (154952) +5 more
core +1 more source

