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Neurobiology of Disease, ISSN 0969-9961, 2014, Volume 71, pp. 62 - 73
Journal Article
Expert Opinion on Therapeutic Targets, ISSN 1472-8222, 06/2017, Volume 21, Issue 6, pp. 601 - 610
Journal Article
JOURNAL OF PROTEOME RESEARCH, ISSN 1535-3893, 04/2010, Volume 9, Issue 4, pp. 1738 - 1745
Mutations in leucine-rich repeat kinase 2 (LRRK2) that increase its kinase activity associate with familial forms of Parkinson disease (PD). As phosphorylation... 
LRRK2 autophosphorylation | TANDEM | LEUCINE-RICH-REPEAT-KINASE-2 LRRK2 | LRRK2 | PHOSPHATASE | BIOCHEMICAL RESEARCH METHODS | Parkinson disease | IDENTIFICATION | GTP-BINDING | MASS-SPECTROMETRY | GENE | ENRICHMENT | MUTATIONS | AUTOPHOSPHORYLATION | Phosphopeptide enrichment
Journal Article
Neurobiology of Disease, ISSN 0969-9961, 2015, Volume 78, pp. 172 - 195
Journal Article
Movement Disorders, ISSN 0885-3185, 05/2017, Volume 32, Issue 5, pp. 726 - 738
Background: Asymptomatic, nonmanifesting carriers of leucine‐rich repeat kinase 2 mutations are at increased risk of developing PD. Clinical and neuroimaging... 
Parkinson's disease | mutations | nonmotor symptoms | prodromal phase | LRRK2 | LRRK2 mutations | LRRK2 G2019S MUTATION | R1441G MUTATION | IDENTIFICATION | CARRIERS | CLINICAL NEUROLOGY | SLEEP BEHAVIOR DISORDER | FEATURES | PENETRANCE | DYSFUNCTION | QUESTIONNAIRE | PREMOTOR PHASE | Dopamine Plasma Membrane Transport Proteins - metabolism | Brain - diagnostic imaging | Depression - physiopathology | REM Sleep Behavior Disorder - etiology | Humans | Middle Aged | Tomography, Emission-Computed, Single-Photon | Male | Cognition | Prodromal Symptoms | Primary Dysautonomias - physiopathology | Case-Control Studies | Brain - metabolism | Depression - etiology | Young Adult | Aged, 80 and over | Adult | Female | Surveys and Questionnaires | Parkinson Disease - complications | Parkinson Disease - diagnostic imaging | Primary Dysautonomias - etiology | Parkinson Disease - genetics | Parkinson Disease - physiopathology | REM Sleep Behavior Disorder - physiopathology | Adolescent | Aged | Mutation | Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 - genetics | Medicine, Experimental | Medical research | Amino acids | SPECT imaging | Neuroimaging | Medical imaging | Neurodegenerative diseases | Sleep (REM) | Leucine | Dysautonomia | Mental depression | Motor task performance | Sleep | Computed tomography | Olfaction | Dopamine transporter | LRRK2 protein | Movement disorders | Index Medicus
Journal Article
12/2011
Background : The frequency of leucine-rich repeat kinase 2 (LRRK2) G2019S mutation, the most common genetic cause of Parkinson′s disease (PD), shows... 
Parkinson′s disease | LRRK2 | G2019S mutation | India
Web Resource
Journal Article
Journal Article
The Journal of Physiology, ISSN 0022-3751, 07/2019, Volume 597, Issue 14, pp. 3511 - 3521
Journal Article