Age at onset in two common neurodegenerative diseases is genetically controlled. - sprookjes - yvandenbroek - TriplyDB

Age at onset in two common neurodegenerative diseases is genetically controlled.

Age at onset in two common neurodegenerative diseases is genetically controlled.

http://www.wikidata.org/entity/Q37217180

about

Identification of risk and age-at-onset genes on chromosome 1p in Parkinson disease.High-resolution whole-genome association study of Parkinson disease.Genetics of Parkinson disease Association studies of 22 candidate SNPs with late-onset Alzheimer's disease The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson's disease in European populations Insulin-degrading enzyme regulates the levels of insulin, amyloid beta-protein, and the beta-amyloid precursor protein intracellular domain in vivo Genetic of Alzheimer's Disease: A Narrative Review Article PARK10 is a major locus for sporadic neuropathologically confirmed Parkinson disease Novel Folding and Stability Defects Cause a Deficiency of Human Glutathione Transferase Omega 1 Structural Insights into Omega-Class Glutathione Transferases: A Snapshot of Enzyme Reduction and Identification of a Non-Catalytic Ligandin Site Systems biology of neurodegenerative diseases Alzheimer's disease and environmental exposure to lead: the epidemiologic evidence and potential role of epigenetics Genome-wide scan linkage analysis for Parkinson's disease: the European genetic study of Parkinson's disease Parkinson disease loci in the mid-western Amish Expanded high-resolution genetic study of 109 Swedish families with Alzheimer's disease Genome-wide association analysis of age-at-onset in Alzheimer's disease Genomewide association study for onset age in Parkinson disease.Genomic variants, genes, and pathways of Alzheimer's disease: An overview.Replication study of genome-wide associated SNPs with late-onset Alzheimer's disease The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis study.Replication of association between ELAVL4 and Parkinson disease: the GenePD study.Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study Evidence for three loci modifying age-at-onset of Alzheimer's disease in early-onset PSEN2 families.Genome scan in familial late-onset Alzheimer's disease: a locus on chromosome 6 contributes to age-at-onset Association mapping of the PARK10 region for Parkinson's disease susceptibility genes Application of a rank-based genetic association test to age-at-onset data from the Collaborative Study on the Genetics of Alcoholism study.Alzheimer's disease risk genes and the age-at-onset phenotype.Genomic susceptibility Loci for brain atrophy, ventricular volume, and leukoaraiosis in hypertensive sibships Fine mapping of the alpha-T catenin gene to a quantitative trait locus on chromosome 10 in late-onset Alzheimer's disease pedigrees.Genome-wide scan for copy number variation association with age at onset of Alzheimer's disease.Ordered-subsets linkage analysis detects novel Alzheimer disease loci on chromosomes 2q34 and 15q22.Age-related macular degeneration--a genome scan in extended families.The PARK8 locus in autosomal dominant parkinsonism: confirmation of linkage and further delineation of the disease-containing interval.Disorder-specific effects of polymorphisms at opposing ends of the Insulin Degrading Enzyme gene.The genetic architecture of Alzheimer's disease: beyond APP, PSENs and APOE.The omega-class glutathione transferases: structure, function, and genetics.Modeling amyloid beta-peptide insertion into lipid bilayers Fine-mapping and candidate gene investigation within the PARK10 locus.A PIN1 polymorphism that prevents its suppression by AP4 associates with delayed onset of Alzheimer's disease.Exploratory data from complete genomes of familial alzheimer disease age-at-onset outliers.

P2860

Q24531223-C3D71965-328C-48B9-B2C1-0C1233348CCC Q24535861-104DB479-B11E-44AA-8B29-65D47685810F Q24558967-58D42DEA-8391-4A35-B180-CC1C8C7F5B4A Q24647572-D9154721-2960-4199-95B5-FF4A02343D61 Q24651395-78E807E8-1C73-48AD-A8F2-37D5E58DE270 Q24683214-6FDCBDD1-0428-4FA2-907A-CCA53C110068 Q27007467-35005796-C646-4890-9E41-1BF14415D485 Q27349225-07F3B974-E471-46D1-A03E-83C641680F2B Q27666060-F5527884-3377-4739-B02C-2A2033EAC204 Q27677424-50A7D1A7-E244-462F-8B9D-3AC3CA5539AE Q28080741-7F00ACE2-0AC1-44B9-BA0D-5F52843DE3FE Q28394199-8E85D5CD-BFD2-4A0F-9E43-2FC5719C477A Q28764371-4450663F-0CED-48E0-950A-CA69A56BB008 Q28943294-1E90B1A8-4856-4696-8BD1-BD2EE5322981 Q29301019-61020EB4-E74B-4DA2-9938-C254E72D997E Q29417033-9BDB94C6-96F7-4AEF-8DD6-B489D9ED7E8C Q29417034-E98D5F67-82C6-4190-B06A-BC7AF9FCE7CE Q30240093-AB31A90C-39BD-4937-BC40-13D8E41C47D5 Q30426556-DEC0DC8F-CB5E-4ADE-95A0-CEB88FF1DD4D Q30433658-B2096B27-89AE-4A3A-89CE-3F3D0F72EDF8 Q30439050-29125C28-1EA8-4627-8523-636F172F9CE9 Q30459046-9062E962-D9C1-4756-BCC1-184141F37044 Q30497920-E9E4F8CD-6839-4850-A386-6CD044538CB5 Q30539808-C5CA2285-F780-4796-BF9D-277F9FF8149F Q30573676-A2867378-AE36-4C25-AC0C-0558946BB918 Q31031554-AA3C25CC-0751-459C-9D81-3B22D09CADBB Q33685232-4BD093C6-C886-4D13-A828-2EDE0C08027E Q33689539-E0140C42-2022-4EE2-BE8A-A7B452335499 Q33719301-6697EBBA-2C60-42CB-A84F-3426E33F717E Q33790333-6E366B3E-F0A8-4C80-B5EE-35BC672746A5 Q33905584-08D6458A-3630-4467-AA2C-E211D282990D Q33906317-9EFB5A82-7AE2-4949-BAFD-A5B10E5E1AE7 Q33909482-BFB762C5-FCF8-41E4-A9F8-703B6665C163 Q34080209-BD1D9D3A-8150-4EF9-AF70-2D6503D09DC6 Q34123651-C810D7B8-95E9-4EBC-BF98-444A2FE893AE Q34178562-3D368274-BA97-4E73-9618-22D0977ABC56 Q34185973-A59E1783-A251-4897-BDE7-D15DA5D96BCB Q34325867-7DB21AA6-38FB-4629-8CCA-429B065FEFF4 Q34336304-161A5491-5778-4D02-A0EC-BAF491661DBA Q34350733-92F4207C-4D69-4A1A-8887-9AB909602F32

P2860

Age at onset in two common neurodegenerative diseases is genetically controlled.

http://www.wikidata.org/entity/Q37217180

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on March 2002

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Age at onset in two common neurodegenerative diseases is genetically controlled.

@en

Age at onset in two common neurodegenerative diseases is genetically controlled.

@nl

type

label

Age at onset in two common neurodegenerative diseases is genetically controlled.

@en

Age at onset in two common neurodegenerative diseases is genetically controlled.

@nl

prefLabel

Age at onset in two common neurodegenerative diseases is genetically controlled.

@en

Age at onset in two common neurodegenerative diseases is genetically controlled.

@nl

P1433

Q37217180-78955A97-706C-4490-BC71-C7872D13D9C7

P1476

Q37217180-8207FF06-27D4-41EB-9862-488B96FC2242

P2093

Q37217180-05317953-4DA4-49AD-BC6C-788D01DF6B6A

Q37217180-06C0D995-5002-4312-B34D-B78FFABF0ED5

Q37217180-0D78117A-A0EC-4BAF-B5FF-FCF46D672F10

Q37217180-1B616C67-E901-4A87-815B-883296EA81C7

Q37217180-25ADC9B7-3A63-4C12-A8EA-16B9A4055456

Q37217180-28BC0173-5C3D-48F1-BA11-BB6C19B7CE21

Q37217180-2FE3317A-F2EF-444D-A874-F5BCB3B231E7

Q37217180-35D7F6CC-BA75-4CD4-A244-EE6F7B5AA6A5

Q37217180-452D5C27-70A3-4431-B332-5F2CE58164DF

Q37217180-5289F1F2-554F-4A9E-AF42-BF1CAA9EDA99

P2860

Q37217180-08D1ED3B-1D57-4DE4-ADBD-DC3E1488696D

Q37217180-11087926-1AB9-4877-9180-6F1889D8AC9A

Q37217180-110A532E-C441-433D-B157-8936E578ED61

Q37217180-13ABAA00-8935-46A4-8352-023F65E488FF

Q37217180-1FDF4630-A979-4F5F-9D43-197A9DA42BC3

Q37217180-283DF7FD-899B-4DE1-84C9-AC529D052284

Q37217180-2A107922-DA39-423B-AE66-75C44839E52B

Q37217180-2A73B5F2-7ECA-4FA5-A9C6-DA7CA5F62D52

Q37217180-2A7B2514-6E4F-4E01-A224-7486621885BF

Q37217180-44CC3A31-B0E6-463F-B324-119A2C3F4931

P304

Q37217180-A173189C-EE6F-40AB-AD83-265F1403CD6C

P31

Q37217180-61D45B43-4894-434F-8643-49D259C9EFFE

P356

Q37217180-83A0D044-D624-4EBA-8D2A-0E0D6F7E7683

P407

Q37217180-4D1E22A0-E78D-4120-BFFF-CEF3AC932AF2

P433

Q37217180-3733DF58-C2DB-4883-A647-E313CA3BF004

P478

Q37217180-0802CFE0-F2CB-43F0-A133-9A990AE539B0

P50

Q37217180-2A4806E5-E422-4E11-927A-5AB987353AB6

Q37217180-764490EE-2903-4BB7-A4E8-59BFECAB1F1B

Q37217180-8670B9ED-1524-4ECD-B3B4-63D48A21E774

Q37217180-878F19F3-83DA-4E31-BAE7-86D975EF5BEA

Q37217180-879927AE-4F29-410C-9B45-D34E234F4F1A

Q37217180-8B704E45-F22C-49D6-9053-EFC2CA0153A6

Q37217180-B9E61E9E-DAF8-4A8F-A684-D597056FD4BC

Q37217180-C5CF2F49-2C62-478C-8068-D7FEDF6BB949

P577

Q37217180-C12A41AD-1ED5-41B0-8AB4-0087B2AE10D4

P5875

Q37217180-AC6A8669-18F6-47C6-81CD-2A37CA62B972

P698

Q37217180-9E80315B-313F-4BE6-A495-302A5DC1E92E

P921

Q37217180-F85D49B6-997A-4D9F-B05F-1676D356283F

P932

Q37217180-95155E18-457B-4AF3-8441-08CE8D4C96F3

P356

P1433

American Journal of Human Genetics

P1476

Age at onset in two common neurodegenerative diseases is genetically controlled.

@en

P2093

Allen D Roses

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

Allison D Reed

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

Ann M Saunders

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

Bradley C Hiner

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

Burton L Scott

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

Dale J Hedges

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

Donald E Schmechel

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

Fengyu Zhang

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

Frank Mastaglia

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

Fred A Allen

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

P2860

Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

Park7, a novel locus for autosomal recessive early-onset parkinsonism, on chromosome 1p36.

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

Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families

Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease

Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease

Mapping of a gene for Parkinson's disease to chromosome 4q21-q23

Candidate gene for the chromosome 1 familial Alzheimer's disease locus

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

Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases

P304

985-993

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

P31

scholarly article

P356

10.1086/339815

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

P407

P433

4

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

P478

70

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

P50

Margaret A. Pericak-Vance

Jeffery M. Vance

Rachel A Gibson

Joseph Jankovic

Christopher G. Goetz

Jonathan L Haines

P577

2002-03-01T00:00:00Z

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

P5875

11486456

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

P698

11875758

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

P921

neurodegeneration

P932

379130

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