About: Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22

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About: Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22 Goto Sponge Distinct Permalink

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scientific article published on 01 October 2000

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в жовтні 2000 (uk) article scientifique publié en 2000 (fr) im Oktober 2000 veröffentlichter wissenschaftlicher Artikel (de) artículu científicu espublizáu n'ochobre de 2000 (ast) scientific article published on 01 October 2000 (en)
publication date	wds:Q73031723-11508B30-671A-4E61-87EB-E7F496E20F3B
publication date	2000-10-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q73031723-5469853E-7FEC-45CF-A332-7133B109CFDF
language of work or name	English
author name string	wds:Q73031723-0318B1D1-E1D9-4DC9-AB4C-210AC70567B8 wds:Q73031723-1D470C47-6A7F-4366-AD31-773215FE874B wds:Q73031723-47E57DC9-085F-4818-9ED8-35EA5C4022FF wds:Q73031723-63219DB2-67EB-4E35-A1C4-5A48AE7A111D wds:Q73031723-7437C9BB-C5B0-4F16-88B6-E5AAF7973AF2 wds:Q73031723-79A3DC18-85B7-4763-86B0-E4A5B040162B wds:Q73031723-7FD7B5E7-E224-4E66-AB9D-51B664233C72 wds:Q73031723-BD7D5493-8043-49AF-A6F9-66D2DC549F5B wds:Q73031723-C0B7BC56-087D-4D78-927E-FD71A9E892AB wds:Q73031723-CC91A936-5B87-444E-BB2D-3FF10FE6D5E3 wds:Q73031723-D0E35AAB-D5A0-44DA-BC5D-AA2ED2A71802 wds:Q73031723-D877CA1B-ABB6-4904-BA6D-5F8A763C0882 wds:Q73031723-EA2E7F4B-3EAF-4CB1-A9E5-9F32A73AD645 wds:Q73031723-EF5CC94A-8F29-4A3B-9051-CF4B36F42CEC
author name string	J L Haines M A Pericak-Vance J Kaplan W Y Hung R H Brown B A Hosler D McKenna-Yasek P C Sapp C Fan A Hossain M C Huang M Nance J R Daube W Sailor
rdfs:label	Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22 (en) Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22 (nl)
skos:prefLabel	Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22 (en) Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22 (nl)
name	Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22 (en) Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22 (nl)
author	wds:Q73031723-609734C4-D80B-4B83-9A96-B4E6B843764E wds:Q73031723-E33F6C1F-90AF-45D5-98C6-C7502974B951
author	H. Robert Horvitz Teepu Siddique
title	wds:Q73031723-521A1D88-1ACF-4518-AB4C-C5AA17BC00A3
title	Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22 (en)
page(s)	wds:Q73031723-5631FC52-4873-4CE0-B120-0FCBBA0D8A3C
page(s)	1664-1669
instance of	wds:Q73031723-03F59FC2-A2EA-482C-ADCD-990ACD6D704A
instance of	scholarly article
main subject	wds:Q73031723-2D52D181-D779-4D28-9C6C-CDEC58C51A6F wds:Q73031723-5BD786F3-322E-4DE4-8434-DE3B1FCB672F
main subject	amyotrophic lateral sclerosis frontotemporal dementia
PubMed ID	wds:Q73031723-F2B4E497-FA8A-4250-A31E-C1473577E193
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/11015796
PubMed ID	11015796
published in	wds:Q73031723-96716E7B-C169-4A03-886F-C0326060F961
published in	The Journal of the American Medical Association
issue	wds:Q73031723-EB6BCDAB-2E24-4894-8C0E-21FDB3059999
volume	wds:Q73031723-65A74AE4-C6E3-4880-BB4C-99E467096400
issue	13
volume	284
DOI	wds:Q73031723-9EA40ACF-801B-49BE-AF3B-88E563CE283E
DOI	http://dx.doi.org/10.1001/JAMA.284.13.1664
DOI	10.1001/JAMA.284.13.1664
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q73031723
is cites work of	A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2 Amyotrophic lateral sclerosis. unfolding the toxicity of the misfolded Granulin mutations associated with frontotemporal lobar degeneration and related disorders: an update Clinical delineation and localization to chromosome 9p13.3-p12 of a unique dominant disorder in four families: hereditary inclusion body myopathy, Paget disease of bone, and frontotemporal dementia Genetics of motor neuron disorders: new insights into pathogenic mechanisms TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis Complex genetics of amyotrophic lateral sclerosis Broad clinical phenotypes associated with TAR-DNA binding protein (TARDBP) mutations in amyotrophic lateral sclerosis ALS with variable phenotypes in a six-generation family caused by leu144phe mutation in the SOD1 gene A mutation in sigma-1 receptor causes juvenile amyotrophic lateral sclerosis A human phenome-interactome network of protein complexes implicated in genetic disorders Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6 Innate immune activation in neurodegenerative disease Molecular biology of amyotrophic lateral sclerosis: insights from genetics Frontotemporal dementia Presenile dementia syndromes: an update on taxonomy and diagnosis Recent advances in amyotrophic lateral sclerosis research From Charcot to Lou Gehrig: deciphering selective motor neuron death in ALS Recent advances in the genetics of amyotrophic lateral sclerosis The early neuropsychological and behavioral characteristics of frontotemporal dementia The genetic epidemiology of neurodegenerative disease Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia Update on recent molecular and genetic advances in frontotemporal lobar degeneration Amyotrophic lateral sclerosis: an emerging era of collaborative gene discovery Molecular and cellular pathways of neurodegeneration in motor neurone disease Frontotemporal and motor neurone degeneration with neurofilament inclusion bodies: additional evidence for overlap between FTD and ALS. Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval. A new familial amyotrophic lateral sclerosis locus on chromosome 16q12.1-16q12.2.

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