G2019S LRRK2 enhances the neuronal transmission of tau in the mouse brain.

scientific article published on 27 October 2017

G2019S LRRK2 enhances the neuronal transmission of tau in the mouse brain. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1093/HMG/DDX389
P698PubMed publication ID29088368

P50authorDarren J MooreQ87693446
P2093author name stringBernard L Schneider
Guillaume Daniel
Pamela Valdés
Md Shariful Islam
An Phu Tran Nguyen
P2860cites workDopaminergic neuronal loss, reduced neurite complexity and autophagic abnormalities in transgenic mice expressing G2019S mutant LRRK2.Q21135493
GTPase activity and neuronal toxicity of Parkinson's disease-associated LRRK2 is regulated by ArfGAP1Q21144926
Parkinson's disease-associated mutations in leucine-rich repeat kinase 2 augment kinase activityQ22254785
Impaired dopaminergic neurotransmission and microtubule-associated protein tau alterations in human LRRK2 transgenic miceQ24293070
Leucine-rich repeat kinase 2 (LRRK2) interacts with parkin, and mutant LRRK2 induces neuronal degenerationQ24298689
LRRK2 phosphorylates tubulin-associated tau but not the free molecule: LRRK2-mediated regulation of the tau-tubulin association and neurite outgrowthQ24304347
A direct interaction between leucine-rich repeat kinase 2 and specific β-tubulin isoforms regulates tubulin acetylationQ24310126
Functional interaction of Parkinson's disease-associated LRRK2 with members of the dynamin GTPase superfamilyQ24310218
Localization of LRRK2 to membranous and vesicular structures in mammalian brainQ24318643
LRRK2 phosphorylates novel tau epitopes and promotes tauopathyQ24338188
Genome-wide association study reveals genetic risk underlying Parkinson's diseaseQ24646654
Transmission and spreading of tauopathy in transgenic mouse brainQ24651334
Synapse loss and microglial activation precede tangles in a P301S tauopathy mouse modelQ28115206
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathologyQ28131833
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's diseaseQ28244731
CHIP and Hsp70 regulate tau ubiquitination, degradation and aggregationQ28245143
Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17Q28274687
Cloning of the gene containing mutations that cause PARK8-linked Parkinson's diseaseQ28292932
Enhanced striatal dopamine transmission and motor performance with LRRK2 overexpression in mice is eliminated by familial Parkinson's disease mutation G2019SQ28589899
Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's diseaseQ29614900
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control studyQ29614953
Tau-mediated neurodegeneration in Alzheimer's disease and related disordersQ29618148
Neurodegenerative tauopathiesQ29619895
An LRRK2 mutation as a cause for the parkinsonism in the original PARK8 family.Q30350674
Neurodegenerative phenotypes in an A53T α-synuclein transgenic mouse model are independent of LRRK2.Q30454029
Increasing microtubule acetylation rescues axonal transport and locomotor deficits caused by LRRK2 Roc-COR domain mutationsQ30596172
Tau deposition drives neuropathological, inflammatory and behavioral abnormalities independently of neuronal loss in a novel mouse modelQ30667424
Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic dataQ33226682
A preparation of Alzheimer paired helical filaments that displays distinct tau proteins by polyacrylamide gel electrophoresisQ33720044
Mutant LRRK2(R1441G) BAC transgenic mice recapitulate cardinal features of Parkinson's diseaseQ33754793
Leucine-rich repeat kinase 2 gene-associated disease: redefining genotype-phenotype correlationQ33808789
Differential LRRK2 expression in the cortex, striatum, and substantia nigra in transgenic and nontransgenic rodentsQ33825413
LRRK2 protein levels are determined by kinase function and are crucial for kidney and lung homeostasis in miceQ35288337
Zeroing in on LRRK2-linked pathogenic mechanisms in Parkinson's disease.Q37313530
Mechanisms of LRRK2-Mediated NeurodegenerationQ37996364
LRRK2 Facilitates tau Phosphorylation through Strong Interaction with tau and cdk5.Q38844125
Mechanisms of LRRK2-dependent neurodegeneration: role of enzymatic activity and protein aggregation.Q39137358
Propagation of Tau aggregatesQ39338832
Leucine-rich repeat kinase 2 phosphorylates brain tubulin-beta isoforms and modulates microtubule stability--a point of convergence in parkinsonian neurodegeneration?Q39834913
Parkinsonism, Lrrk2 G2019S, and tau neuropathologyQ40216459
Biochemical and pathological characterization of Lrrk2.Q40324969
Coordinate dual-gene transgenesis by lentiviral vectors carrying synthetic bidirectional promoters.Q40477022
LRRK2 Promotes Tau Accumulation, Aggregation and Release.Q40899192
Neuron-to-neuron wild-type Tau protein transfer through a trans-synaptic mechanism: relevance to sporadic tauopathiesQ41760966
Distinct tau prion strains propagate in cells and mice and define different tauopathiesQ41904960
Leucine-rich repeat kinase 2 functionally interacts with microtubules and kinase-dependently modulates cell migrationQ42826736
LRRK2 G2019S mutation induces dendrite degeneration through mislocalization and phosphorylation of tau by recruiting autoactivated GSK3ß.Q42873469
A rat model of progressive nigral neurodegeneration induced by the Parkinson's disease-associated G2019S mutation in LRRK2.Q43501182
Targeted overexpression of the parkin substrate Pael-R in the nigrostriatal system of adult rats to model Parkinson's diseaseQ43735682
Lrrk2 and Lewy body diseaseQ46912096
Study of LRRK2 variation in tauopathy: Progressive supranuclear palsy and corticobasal degenerationQ47161677
Nigrostriatal overabundance of α-synuclein leads to decreased vesicle density and deficits in dopamine release that correlate with reduced motor activity.Q48006941
Lack of exacerbation of neurodegeneration in a double transgenic mouse model of mutant LRRK2 and tau.Q48264748
Expression and localization of Parkinson's disease-associated leucine-rich repeat kinase 2 in the mouse brainQ48372083
P433issue1
P304page(s)120-134
P577publication date2018-01-01
P1433published inHuman Molecular GeneticsQ2720965
P1476titleG2019S LRRK2 enhances the neuronal transmission of tau in the mouse brain
P478volume27

Reverse relations

cites work (P2860)
Q55048859Cellular and Molecular Basis of Neurodegeneration in Parkinson Disease.
Q104504605Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study
Q98177378LRRK2 and Protein Aggregation in Parkinson's Disease: Insights From Animal Models
Q97066874LRRK2 and α-Synuclein: Distinct or Synergistic Players in Parkinson's Disease?
Q55122127Mutations in LRRK2 amplify cell-to-cell protein aggregate propagation: a hypothesis.
Q64059038Parkinson's disease-linked knockin mice manifest tau neuropathology and dopaminergic neurodegeneration
Q64265990Rab GTPases as Physiological Substrates of LRRK2 Kinase
Q92017939What Have We Learned from Cerebrospinal Fluid Studies about Biomarkers for Detecting LRRK2 Parkinson's Disease Patients and Healthy Subjects with Parkinson's-Associated LRRK2 Mutations?

Search more.