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Lewy bodies and parkinsonism in families with parkin mutations

Lewy bodies and parkinsonism in families with parkin mutations

http://www.wikidata.org/entity/Q28216308

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The prion hypothesis in Parkinson's disease: Braak to the future Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update Association between Parkinson's Disease and Cigarette Smoking, Rural Living, Well-Water Consumption, Farming and Pesticide Use: Systematic Review and Meta-Analysis Parkin-dependent degradation of the F-box protein Fbw7β promotes neuronal survival in response to oxidative stress by stabilizing Mcl-1 Dopamine covalently modifies and functionally inactivates parkin How does parkin ligate ubiquitin to Parkinson's disease?Neuregulin 1 transcripts are differentially expressed in schizophrenia and regulated by 5' SNPs associated with the disease Genetics of Parkinson disease Parkin mutation dosage and the phenomenon of anticipation: a molecular genetic study of familial parkinsonism Linking F-box protein 7 and parkin to neuronal degeneration in Parkinson's disease (PD)Analyzing the roles of multi-functional proteins in cells: The case of arrestins and GRKs The genetics and neuropathology of Parkinson's disease Pathologic and therapeutic implications for the cell biology of parkin Genetics of Parkinson's disease - a clinical perspective Genetics in Parkinson disease: Mendelian versus non-Mendelian inheritance Parkinson's Disease and Cognitive Impairment In Silico Analysis of SNPs in PARK2 and PINK1 Genes That Potentially Cause Autosomal Recessive Parkinson Disease.Copy number variation in familial Parkinson disease.Genetic mouse models of parkinsonism: strengths and limitations.Parkin disease: a clinicopathologic entity?Two large British kindreds with familial Parkinson's disease: a clinico-pathological and genetic study.Ubiquitin domain proteins in disease.Copy number variability in Parkinson's disease: assembling the puzzle through a systems biology approach Glycoproteomics in neurodegenerative diseases.Association study of neuregulin-1 gene polymorphisms in a North Indian schizophrenia sample.Olfaction in Parkin carriers in Chinese patients with Parkinson disease Mitochondrial dysfunction in the limelight of Parkinson's disease pathogenesis.The PARK8 locus in autosomal dominant parkinsonism: confirmation of linkage and further delineation of the disease-containing interval.Alternative splicing generates different parkin protein isoforms: evidences in human, rat, and mouse brain.Familial conformational diseases and dementias.How much phenotypic variation can be attributed to parkin genotype?HSPA1A-independent suppression of PARK2 C289G protein aggregation by human small heat shock proteins The genetic background of Parkinson's disease: current progress and future prospects.Biochemical analysis of Parkinson's disease-causing variants of Parkin, an E3 ubiquitin-protein ligase with monoubiquitylation capacity.Olfaction in Parkin heterozygotes and compound heterozygotes: the CORE-PD study.A meta-analysis of the relationship of the Parkin p.Val380Leu polymorphism to Parkinson's disease.The genetics of Parkinson disease.Diagnosis and treatment of Parkinson disease: molecules to medicine Genetics of parkinsonism.Genetic neuropathology of Parkinson's disease.

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P2860

Lewy bodies and parkinsonism in families with parkin mutations

http://www.wikidata.org/entity/Q28216308

description

2001 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2001 թվականի սեպտեմբերին հրատարակված գիտական հոդված

@hy

artículu científicu espublizáu en 2001

@ast

im September 2001 veröffentlichter wissenschaftlicher Artikel

@de

scientific article (publication date: September 2001)

@en

vedecký článok (publikovaný 2001-09)

@sk

vědecký článek publikovaný v roce 2001

@cs

wetenschappelijk artikel (gepubliceerd in 2001-09)

@nl

наукова стаття, опублікована у вересні 2001

@uk

مقالة علمية (نشرت في سبتمبر 2001)

@ar

name

Lewy bodies and parkinsonism in families with parkin mutations

@ast

Lewy bodies and parkinsonism in families with parkin mutations

@en

Lewy bodies and parkinsonism in families with parkin mutations

@nl

type

label

Lewy bodies and parkinsonism in families with parkin mutations

@ast

Lewy bodies and parkinsonism in families with parkin mutations

@en

Lewy bodies and parkinsonism in families with parkin mutations

@nl

prefLabel

Lewy bodies and parkinsonism in families with parkin mutations

@ast

Lewy bodies and parkinsonism in families with parkin mutations

@en

Lewy bodies and parkinsonism in families with parkin mutations

@nl

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P356

P1433

Annals of Neurology

P1476

Lewy bodies and parkinsonism in families with parkin mutations

@en

P2093

A Singleton

http://www.w3.org/2001/XMLSchema#string

C Tanner

http://www.w3.org/2001/XMLSchema#string

D Hernandez

http://www.w3.org/2001/XMLSchema#string

J Hussey

http://www.w3.org/2001/XMLSchema#string

J W Langston

http://www.w3.org/2001/XMLSchema#string

L Forno

http://www.w3.org/2001/XMLSchema#string

L Petrucelli

http://www.w3.org/2001/XMLSchema#string

L Tan

http://www.w3.org/2001/XMLSchema#string

M Farrer

http://www.w3.org/2001/XMLSchema#string

P Chan

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P2860

Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

RING for destruction?

Core assessment program for intracerebral transplantations (CAPIT)

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 Disease

Association between early-onset Parkinson's disease and mutations in the parkin gene

PolyPhred: automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencing

Widespread alterations of alpha-synuclein in multiple system atrophy

Differential expression of the parkin gene in the human brain and peripheral leukocytes.

Immunohistochemical and subcellular localization of Parkin protein: absence of protein in autosomal recessive juvenile parkinsonism patients.

P304

293-300

http://www.w3.org/2001/XMLSchema#string

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scholarly article

P3181

2252790

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P356

10.1002/ANA.1132

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P407

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3

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P478

50

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John Anthony Hardy

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2001-09-01T00:00:00Z

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11558785

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P921

Parkinson's disease