Parkinson disease: etiology, pathogenesis and future of gene therapy

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Parkinson disease: etiology, pathogenesis and future of gene therapy is …
instance of (P31):
scholarly articleQ13442814
review articleQ7318358

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P356DOI10.1016/S0168-0102(01)00254-1
P698PubMed publication ID11535288

P2093author name stringShastry BS
P2860cites workRING fingers mediate ubiquitin-conjugating enzyme (E2)-dependent ubiquitinationQ22010577
Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligaseQ22254584
Parkin functions as an E2-dependent ubiquitin- protein ligase and promotes the degradation of the synaptic vesicle-associated protein, CDCrel-1Q24290518
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonismQ24309753
Functional recovery in parkinsonian monkeys treated with GDNFQ24312738
Mutation in the alpha-synuclein gene identified in families with Parkinson's diseaseQ27860459
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A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's DiseaseQ28371129
Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's diseaseQ29547175
Chronic systemic pesticide exposure reproduces features of Parkinson's diseaseQ29614763
Aggresomes, inclusion bodies and protein aggregationQ29615253
Association between early-onset Parkinson's disease and mutations in the parkin geneQ29615733
A Drosophila model of Parkinson's diseaseQ29617052
Matrilineal inheritance of complex I dysfunction in a multigenerational Parkinson's disease familyQ30472923
A novel Cys212Tyr founder mutation in parkin and allelic heterogeneity of juvenile Parkinsonism in a population from North West Colombia.Q31859176
Aggregates in neurodegenerative disease: crowds and power?Q33633045
Membrane association and protein conformation of alpha-synuclein in intact neurons. Effect of Parkinson's disease-linked mutationsQ33893738
Progress in the clinical and molecular genetics of familial parkinsonismQ34030090
Association of coffee and caffeine intake with the risk of Parkinson diseaseQ34508881
Role of neuronal nitric oxide in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-induced dopaminergic neurotoxicityQ37597604
Origin of the mutations in the parkin gene in Europe: exon rearrangements are independent recurrent events, whereas point mutations may result from Founder effectsQ39412774
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Bilateral caudate and putamen grafts of embryonic mesencephalic tissue treated with lazaroids in Parkinson's diseaseQ39429074
Progression of parkinsonism and loss of cognitive function in Alzheimer diseaseQ39540404
Evidence for mitochondrial dysfunction in Parkinson's disease--a critical appraisalQ40758643
Biomedicine. Combating Parkinson's disease--step threeQ40826182
Epidemiology versus genetics in Parkinson's disease: progress in resolving an age-old debateQ40842073
Neurodegeneration prevented by lentiviral vector delivery of GDNF in primate models of Parkinson's diseaseQ40846012
Complete and long-term rescue of lesioned adult motoneurons by lentiviral-mediated expression of glial cell line-derived neurotrophic factor in the facial nucleus.Q40866683
Mesencephalic dopaminergic neurons protected by GDNF from axotomy-induced degeneration in the adult brainQ41379201
Long-term gene expression and phenotypic correction using adeno-associated virus vectors in the mammalian brainQ42280576
Tau is a candidate gene for chromosome 17 frontotemporal dementiaQ42456776
Molecular cloning, gene expression, and identification of a splicing variant of the mouse parkin geneQ42626667
Long-term behavioral recovery in parkinsonian rats by an HSV vector expressing tyrosine hydroxylaseQ43185222
Genetic analysis of families with Parkinson disease that carry the Ala53Thr mutation in the gene encoding alpha-synucleinQ43218554
The cellular chamber of doom.Q43513552
A five-year study of the incidence of dyskinesia in patients with early Parkinson's disease who were treated with ropinirole or levodopaQ45087241
A one-hit model of cell death in inherited neuronal degenerationsQ45300872
Transgenic mice with increased Cu/Zn-superoxide dismutase activity are resistant to N-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced neurotoxicityQ46070812
The ubiquitin pathway in Parkinson's diseaseQ48015939
Point mutations of mitochondrial genome in Parkinson's diseaseQ48075275
Point mutations (Thr240Arg and Gln311Stop) [correction of Thr240Arg and Ala311Stop] in the Parkin geneQ48398668
Dopaminergic neurons intrinsic to the primate striatum.Q48633399
Mitochondrial DNA polymorphism in substantia nigraQ48844431
Inhibition of neuronal nitric oxide synthase prevents MPTP-induced parkinsonism in baboonsQ48937244
Two novel point mutations of mitochondrial tRNA genes in histologically confirmed Parkinson diseaseQ49085090
Opportunism knocks?Q59079003
Molecular genetic analysis of a novelParkin gene in Japanese families with autosomal recessive juvenile parkinsonism: Evidence for variable homozygous deletions in theParkin gene in affected individualsQ60684231
Dopamine agonists in early therapy for Parkinson disease: promise and problemsQ64767712
Mutation analysis and association studies of the UCHL1 gene in German Parkinson's disease patientsQ64778242
Treatment of early Parkinson's diseaseQ64779682
GSTM1 and mEPHX polymorphisms in Parkinson's disease and age of onsetQ64787846
Deletions in the Parkin gene and genetic heterogeneity in a Greek family with early onset Parkinson's diseaseQ64866906
Mitochondrial oxidative phosphorylation defects in Parkinson's diseaseQ68060626
Deficiencies in complex I subunits of the respiratory chain in Parkinson's diseaseQ69356679
Immunocytochemical characterization of catecholaminergic neurons in the rat striatum following dopamine-depleting lesionsQ73189206
Prevalence of homozygous deletions of the parkin gene in a cohort of patients with sporadic and familial Parkinson's diseaseQ73532938
Exonic deletion mutations of the Parkin gene among sporadic patients with Parkinson's diseaseQ73807460
P433issue1
P921main subjectParkinson's diseaseQ11085
gene therapyQ213901
P304page(s)5-12
P577publication date2001-09-01
P1433published inNeuroscience ResearchQ15764280
P1476titleParkinson disease: etiology, pathogenesis and future of gene therapy
P478volume41

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cites work (P2860)
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