About: alpha-synuclein gene haplotypes are associated with Parkinson's disease

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rdf:type	Item
description	article (en) հոդված (hy) wetenschappelijk artikel (nl) наукова стаття, опублікована в серпні 2001 (uk) im August 2001 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q57905836-7C674828-9F84-46E1-A9FC-32AF7095CCC6
publication date	2001-08-01 00:00:00Z (xsd:dateTime)
author name string	wds:Q57905836-025BC587-26C6-4687-BB6B-CF503D74AF51 wds:Q57905836-41FEBE0B-EEF2-449B-BA58-584C54EA1F37 wds:Q57905836-4EF6F7BD-7BB8-49CC-B6A3-C57FC41156A8 wds:Q57905836-5FA49CF3-E408-4933-982F-9D634F289F48 wds:Q57905836-6DBA5340-B4F4-4CA2-8155-4955C656C8A5 wds:Q57905836-91B37EE8-92EE-46CA-A0EA-5DC28F81D635 wds:Q57905836-A2D71679-1E25-47DE-9F25-DB21297B3EFF wds:Q57905836-B68F3E0D-51E8-4420-9474-BEBE05F30851 wds:Q57905836-F14EC7D5-E314-4AB5-AC62-B3007422E0E0
author name string	J Hardy A West A Singleton M Farrer D Hernandez R de Silva D M Maraganore M de Andrade T G Lesnick
rdfs:label	alpha-synuclein gene haplotypes are associated with Parkinson's disease (en) alpha-synuclein gene haplotypes are associated with Parkinson's disease (nl)
skos:prefLabel	alpha-synuclein gene haplotypes are associated with Parkinson's disease (en) alpha-synuclein gene haplotypes are associated with Parkinson's disease (nl)
name	alpha-synuclein gene haplotypes are associated with Parkinson's disease (en) alpha-synuclein gene haplotypes are associated with Parkinson's disease (nl)
author	wds:Q57905836-F5735306-2264-4A6A-8875-1260C0A8575C
author	Paul J. Lockhart
title	wds:Q57905836-8FE2BBC9-35EC-4CA2-9701-3BACF2C1E6E5
title	alpha-Synuclein gene haplotypes are associated with Parkinson's disease (en)
page(s)	wds:Q57905836-4E204052-C5FF-4BA1-9A16-018015F1C22A
page(s)	1847-1851
instance of	wds:Q57905836-A46FF2E2-B2DE-4D41-905E-484AAC350D6D
instance of	scholarly article
main subject	wds:Q57905836-715819B6-123C-4376-90AF-EB6DD1C12E3A wds:Q57905836-785BBAC8-EC50-4EEE-B01F-DCD5272B3484
main subject	Parkinson's disease Synuclein
PubMed ID	wds:Q57905836-9F446BEB-03C4-4256-BFAB-65D29047A89F
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11532993
PubMed ID	11532993
published in	wds:Q57905836-DC537CEE-6E31-4BEC-94AE-D624D91D6766
published in	Human Molecular Genetics
issue	wds:Q57905836-873E42EE-6798-4871-B027-50CA426A0838
volume	wds:Q57905836-819B2742-11A5-4751-9BB2-EE10BE7548C1
issue	17
volume	10
DOI	wds:Q57905836-98FC81D4-D3D2-4B54-BDFE-91B7BA453E0A
DOI	http://dx.doi.org/10.1093/HMG/10.17.1847
DOI	10.1093/HMG/10.17.1847
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57905836
is cites work of	Functional dissection of the alpha-synuclein promoter: transcriptional regulation by ZSCAN21 and ZNF219 The alpha-synuclein gene in multiple system atrophy Advances in the genetics of Parkinson disease Genomewide association studies and human disease Genomic investigation of alpha-synuclein multiplication and parkinsonism Parkinson's disease: from monogenic forms to genetic susceptibility factors Neurodegenerative disorders: Parkinson's disease and Huntington's disease Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease Genome-wide association study confirms extant PD risk loci among the Dutch Parkinson's disease and dementia with Lewy bodies: a difference in dose? UCHL1 is a Parkinson's disease susceptibility gene. Head injury, α-synuclein Rep1, and Parkinson's disease Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations Genetics of Parkinson's disease and parkinsonism Pathways to Parkinsonism Stabilization of alpha-synuclein protein with aging and familial parkinson's disease-linked A53T mutation. Chasing genes in Alzheimer's and Parkinson's disease Parkinson's disease: mechanisms and models Alpha-synuclein locus duplication as a cause of familial Parkinson's disease Rare genetic mutations shed light on the pathogenesis of Parkinson disease The genetics of Parkinson's disease Parkinson's disease: one biochemical pathway to fit all genes? Traumatic brain injury in adult rats causes progressive nigrostriatal dopaminergic cell loss and enhanced vulnerability to the pesticide paraquat Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update Serine 129 phosphorylation reduces the ability of alpha-synuclein to regulate tyrosine hydroxylase and protein phosphatase 2A in vitro and in vivo. Expanding insights of mitochondrial dysfunction in Parkinson's disease. α-Synuclein genetic variants predict faster motor symptom progression in idiopathic Parkinson disease Environment, mitochondria, and Parkinson's disease Behavioral and histopathological consequences of paraquat intoxication in mice: effects of alpha-synuclein over-expression Genetic mouse models of parkinsonism: strengths and limitations The impact of genetic research on our understanding of Parkinson's disease Parkinson-associated risk variant in distal enhancer of α-synuclein modulates target gene expression Polymorphism in candidate genes: implications for the risk and treatment of idiopathic Parkinson's disease Genes and parkinsonism PINK, PANK, or PARK? A clinicians' guide to familial parkinsonism High-resolution whole-genome association study of Parkinson disease. The Tau Gene Haplotype H1 Confers a Susceptibility to Parkinson’s Disease Genetics of Parkinson's disease and biochemical studies of implicated gene products Elevated alpha-synuclein impairs innate immune cell function and provides a potential peripheral biomarker for Parkinson's disease The genetic epidemiology of neurodegenerative disease Molecular Pathways of Neurodegeneration in Parkinson's Disease The rotenone model of Parkinson's disease: genes, environment and mitochondria High LRRK2 levels fail to induce or exacerbate neuronal alpha-synucleinopathy in mouse brain

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