Gamma-synucleinopathy: neurodegeneration associated with overexpression of the mouse protein

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Gamma-synucleinopathy: neurodegeneration associated with overexpression of the mouse protein is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1093/HMG/DDP090
P932PMC publication ID2671987
P698PubMed publication ID19246516
P5875ResearchGate publication ID24043769

P50authorVladimir BuchmanQ56441463
Steven J MillershipQ64495855
Owen M PetersQ42404100
P2093author name stringNatalia Ninkina
Herman van der Putten
Hatem Salem
P2860cites workEffects of Charcot-Marie-Tooth-linked mutations of the neurofilament light subunit on intermediate filament formationQ24318392
A new variant of Charcot-Marie-Tooth disease type 2 is probably the result of a mutation in the neurofilament-light geneQ24538715
Misfolded proteinase K-resistant hyperphosphorylated alpha-synuclein in aged transgenic mice with locomotor deterioration and in human alpha-synucleinopathiesQ24554351
alpha-Synuclein in filamentous inclusions of Lewy bodies from Parkinson's disease and dementia with lewy bodiesQ24653247
Residual structure, backbone dynamics, and interactions within the synuclein familyQ24671058
Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2−ΔΔCT MethodQ25938999
Persyn, a member of the synuclein family, influences neurofilament network integrityQ28512814
Synucleins in glaucoma: implication of gamma-synuclein in glaucomatous alterations in the optic nerveQ28580190
Distribution of α‐ and γ‐synucleins in the adult rat brain and their modification by high‐dose cocaine treatmentQ28581427
Formation of intermediate filament protein aggregates with disparate effects in two transgenic mouse models lacking the neurofilament light subunitQ28586151
Neurons Expressing the Highest Levels of γ-Synuclein Are Unaffected by Targeted Inactivation of the GeneQ28587583
???Q64770129
Discrete gene sets depend on POU domain transcription factor Brn3b/Brn-3.2/POU4f2 for their expression in the mouse embryonic retinaQ44770163
Decrease of Hsp25 protein expression precedes degeneration of motoneurons in ALS-SOD1 miceQ44971569
Early and progressive sensorimotor anomalies in mice overexpressing wild-type human alpha-synuclein.Q46441823
Progressive ganglion cell degeneration precedes neuronal loss in a mouse model of glaucomaQ46704887
Locomotor activity and evoked dopamine release are reduced in mice overexpressing A30P-mutated human alpha-synucleinQ46768370
Transgenic mice overexpressing tyrosine-to-cysteine mutant human alpha-synuclein: a progressive neurodegenerative model of diffuse Lewy body diseaseQ46780013
Retinal ganglion cells downregulate gene expression and lose their axons within the optic nerve head in a mouse glaucoma model.Q46815689
Sequence Determinants for Amyloid Fibrillogenesis of Human alpha-SynucleinQ46950603
Transgenic mice expressing mutant A53T human alpha-synuclein show neuronal dysfunction in the absence of aggregate formation.Q48165522
Pick's disease: alpha- and beta-synuclein-immunoreactive Pick bodies in the dentate gyrusQ48456409
Age-dependent cognitive decline and amygdala pathology in alpha-synuclein transgenic miceQ48461166
Neuronal alpha-synucleinopathy with severe movement disorder in mice expressing A53T human alpha-synucleinQ48581887
Alpha- and gamma-synuclein proteins are present in cerebrospinal fluid and are increased in aged subjects with neurodegenerative and vascular changes.Q49159052
CHIP overexpression reduces mutant androgen receptor protein and ameliorates phenotypes of the spinal and bulbar muscular atrophy transgenic mouse model.Q51580141
Protective effects of heat shock protein 27 in a model of ALS occur in the early stages of disease progression.Q51894120
A mutation in the small heat-shock protein HSPB1 leading to distal hereditary motor neuronopathy disrupts neurofilament assembly and the axonal transport of specific cellular cargoes.Q52567894
Disruption of neurofilament network with aggregation of light neurofilament protein: a common pathway leading to motor neuron degeneration due to Charcot-Marie-Tooth disease-linked mutations in NFL and HSPB1.Q52582284
Induction of neuronal death by α-synucleinQ58009056
Heat shock protein 70 chaperone overexpression ameliorates phenotypes of the spinal and bulbar muscular atrophy transgenic mouse model by reducing nuclear-localized mutant androgen receptor proteinQ73174347
Beta-synuclein inhibits formation of alpha-synuclein protofibrils: a possible therapeutic strategy against Parkinson's diseaseQ73196542
Neuropathology in mice expressing human alpha-synucleinQ74139704
Phenotypic analysis of neurofilament light gene mutations linked to Charcot-Marie-Tooth disease in cell culture modelsQ80391817
Accumulation of beta- and gamma-synucleins in the ubiquitin carboxyl-terminal hydrolase L1-deficient gad mouseQ80441003
Mouse model of multiple system atrophy alpha-synuclein expression in oligodendrocytes causes glial and neuronal degenerationQ81589639
Temporal profiles of neuronal degeneration, glial proliferation, and cell death in hNFL(+/+) and NFL(-/-) miceQ81791749
Alpha-synuclein cooperates with CSPalpha in preventing neurodegenerationQ28587785
Developmental loss and resistance to MPTP toxicity of dopaminergic neurones in substantia nigra pars compacta of gamma-synuclein, alpha-synuclein and double alpha/gamma-synuclein null mutant miceQ28594631
Persyn, a member of the synuclein family, has a distinct pattern of expression in the developing nervous systemQ28594866
Dopaminergic loss and inclusion body formation in alpha-synuclein mice: implications for neurodegenerative disordersQ29614754
Unraveling the mechanisms involved in motor neuron degeneration in ALSQ29619073
Human alpha-synuclein-harboring familial Parkinson's disease-linked Ala-53 --> Thr mutation causes neurodegenerative disease with alpha-synuclein aggregation in transgenic miceQ30476254
Development of a new treatment for Alzheimer's disease and Parkinson's disease using anti-aggregatory beta-synuclein-derived peptidesQ30845414
Modulation of alpha-synuclein expression in transgenic animals for modelling synucleinopathies--is the juice worth the squeeze?Q33392127
Characterization of progressive motor deficits in mice transgenic for the human Huntington's disease mutation.Q33857802
Further evidence that neurofilament light chain gene mutations can cause Charcot-Marie-Tooth disease type 2E.Q33935585
beta-amyloid peptides enhance alpha-synuclein accumulation and neuronal deficits in a transgenic mouse model linking Alzheimer's disease and Parkinson's diseaseQ33947152
Altered expression of the synuclein family mRNA in Lewy body and Alzheimer's diseaseQ34093055
beta-Synuclein inhibits alpha-synuclein aggregation: a possible role as an anti-parkinsonian factorQ34099593
Biophysical properties of the synucleins and their propensities to fibrillate: inhibition of alpha-synuclein assembly by beta- and gamma-synucleinsQ34111411
Beta-synuclein displays an antiapoptotic p53-dependent phenotype and protects neurons from 6-hydroxydopamine-induced caspase 3 activation: cross-talk with alpha-synuclein and implication for Parkinson's diseaseQ34214842
Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathyQ34318026
Beta-synuclein modulates alpha-synuclein neurotoxicity by reducing alpha-synuclein protein expressionQ34564479
Neuronal intermediate filaments and ALS: a new look at an old questionQ34574411
Part II: alpha-synuclein and its molecular pathophysiological role in neurodegenerative disease.Q35157623
Zeroing in on the pathogenic form of alpha-synuclein and its mechanism of neurotoxicity in Parkinson's diseaseQ35166364
Functions of intermediate filaments in neuronal development and diseaseQ35575907
Fiber diffraction of synthetic alpha-synuclein filaments shows amyloid-like cross-beta conformationQ35700288
Neurodegeneration with brain iron accumulation, type 1 is characterized by alpha-, beta-, and gamma-synuclein neuropathologyQ35745646
Selective insolubility of alpha-synuclein in human Lewy body diseases is recapitulated in a transgenic mouse modelQ35747138
Ubiquitination of alpha-synuclein is not required for formation of pathological inclusions in alpha-synucleinopathiesQ35791524
Cell systems and the toxic mechanism(s) of alpha-synucleinQ36440972
Transgenic mouse models of amyotrophic lateral sclerosisQ36468459
Mechanisms and models of alpha-synuclein-related neurodegeneration.Q36575028
Axon pathology in Parkinson's disease and Lewy body dementia hippocampus contains alpha-, beta-, and gamma-synucleinQ36677512
In vivo alpha-synuclein overexpression in rodents: a useful model of Parkinson's disease?Q36976137
Hsp70 Reduces alpha-Synuclein Aggregation and ToxicityQ40573441
Up-regulation of protein chaperones preserves viability of cells expressing toxic Cu/Zn-superoxide dismutase mutants associated with amyotrophic lateral sclerosisQ40975834
Parkinson's disease-associated alpha-synuclein is more fibrillogenic than beta- and gamma-synuclein and cannot cross-seed its homologsQ41755571
Differential neuropathological alterations in transgenic mice expressing alpha-synuclein from the platelet-derived growth factor and Thy-1 promotersQ42523541
An antiaggregation gene therapy strategy for Lewy body disease utilizing beta-synuclein lentivirus in a transgenic modelQ43865449
Motor dysfunction and gliosis with preserved dopaminergic markers in human alpha-synuclein A30P transgenic miceQ44260175
P433issue10
P921main subjectneurodegenerationQ1755122
overexpressionQ61643320
P304page(s)1779-1794
P577publication date2009-02-26
P1433published inHuman Molecular GeneticsQ2720965
P1476titleGamma-synucleinopathy: neurodegeneration associated with overexpression of the mouse protein
P478volume18

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