Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36 - Test2 - elhamkhani - TriplyDB

Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36

Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36

http://www.wikidata.org/entity/Q24536382

about

Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update The genetic epidemiology of neurodegenerative disease.Biochemical aspects of the neuroprotective mechanism of PTEN-induced kinase-1 (PINK1)Pharmacological rescue of mitochondrial deficits in iPSC-derived neural cells from patients with familial Parkinson's disease.Park7, a novel locus for autosomal recessive early-onset parkinsonism, on chromosome 1p36.Genetics of Parkinson disease Mutations in the GIGYF2 (TNRC15) gene at the PARK11 locus in familial Parkinson disease A linkage study of candidate loci in familial Parkinson's Disease The Genetic Basis of Cognitive Impairment and Dementia in Parkinson's Disease Deconvoluting the complexity of autophagy and Parkinson's disease for potential therapeutic purpose Mouse models of Parkinson's disease associated with mitochondrial dysfunction Autophagy and neurodegeneration Miro, MCU, and calcium: bridging our understanding of mitochondrial movement in axons Genetics of Parkinson's disease - a clinical perspective Genetics in Parkinson disease: Mendelian versus non-Mendelian inheritance GDNF-Ret signaling in midbrain dopaminergic neurons and its implication for Parkinson disease Genomics and bioinformatics of Parkinson's disease Genome-wide scan linkage analysis for Parkinson's disease: the European genetic study of Parkinson's disease Genomewide association study for onset age in Parkinson disease.Huntington CAG repeat size does not modify onset age in familial Parkinson's disease: the GenePD study.PARK3 influences age at onset in Parkinson disease: a genome scan in the GenePD study.Effective quantitative real-time polymerase chain reaction analysis of the parkin gene (PARK2) exon 1-12 dosage.Significance of the parkin and PINK1 gene in Jordanian families with incidences of young-onset and juvenile parkinsonism T313M polymorphism of the PINK1 gene in Parkinson's disease A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2-q13.1.Parkinson's disease: Exit toxins, enter genetics Mutations in NR4A2 associated with familial Parkinson disease.How much phenotypic variation can be attributed to parkin genotype?Regulation of alpha-synuclein expression: implications for Parkinson's disease.Identification of the human ubiquitin specific protease 31 (USP31) gene: structure, sequence and expression analysis.G309D and W437OPA PINK1 mutations in Caucasian Parkinson's disease patients.Upregulation of human PINK1 gene expression by NFκB signalling The genetics of Parkinson disease.Genetics of population isolates.Genetics of parkinsonism.Programmed cell death and new discoveries in the genetics of parkinsonism.The genetic basis of Parkinson's disease Transgenic animal models of neurodegeneration based on human genetic studies.Familial Lewy body diseases.State of the art review: molecular diagnosis of inherited movement disorders. Movement Disorders Society task force on molecular diagnosis.

P2860

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P2860

Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36

http://www.wikidata.org/entity/Q24536382

description

2001 nî lūn-bûn

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2001 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2001 թվականի ապրիլին հրատարակված գիտական հոդված

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2001年の論文

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2001年論文

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2001年論文

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2001年論文

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2001年論文

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2001年論文

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2001年论文

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name

Localization of a novel locus ...... , on human chromosome 1p35-p36

@ast

Localization of a novel locus ...... , on human chromosome 1p35-p36

@en

Localization of a novel locus ...... , on human chromosome 1p35-p36

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type

label

Localization of a novel locus ...... , on human chromosome 1p35-p36

@ast

Localization of a novel locus ...... , on human chromosome 1p35-p36

@en

Localization of a novel locus ...... , on human chromosome 1p35-p36

@nl

prefLabel

Localization of a novel locus ...... , on human chromosome 1p35-p36

@ast

Localization of a novel locus ...... , on human chromosome 1p35-p36

@en

Localization of a novel locus ...... , on human chromosome 1p35-p36

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P1433

American Journal of Human Genetics

P1476

Localization of a novel locus ...... , on human chromosome 1p35-p36

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P2093

A Ferraris

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

A R Bentivoglio

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E M Valente

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M Frontali

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N W Wood

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P H Dixon

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T Ialongo

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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

Homozygosity and linkage-disequilibrium mapping of the urofacial (Ochoa) syndrome gene to a 1-cM interval on chromosome 10q23-q24

Localization of a gene for an autosomal recessive form of juvenile Parkinsonism to chromosome 6q25.2-27

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

Parkinsonism: onset, progression and mortality

Parkinson disease in twins: an etiologic study

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

Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children

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895-900

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1461426

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10.1086/319522

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P433

4

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68

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Alberto Albanese

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2001-04-01T00:00:00Z

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12078976

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11254447

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Parkinson's disease

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