Linked Life Data

19387015

Source:http://linkedlifedata.com/resource/pubmed/id/19387015

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
17
pubmed:dateCreated
2009-4-23
pubmed:abstractText
The genetic cause of cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL), which is characterized by ischemic, nonhypertensive, cerebral small-vessel disease with associated alopecia and spondylosis, is unclear.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
1533-4406
pubmed:author
pubmed-author:ArimaKunimasaK, pubmed-author:ArisatoTakayoT, pubmed-author:FukutakeToshioT, pubmed-author:HaraKenjuK, pubmed-author:HirayamaMikioM, pubmed-author:IkedaMariM, pubmed-author:IkedaShu-ichiS, pubmed-author:IkeuchiTakeshiT, pubmed-author:KawataHirotoshiH, pubmed-author:KoyamaAkihideA, pubmed-author:KuwanoRyozoR, pubmed-author:MiyashitaAkinoriA, pubmed-author:NakanoImaharuI, pubmed-author:NishizawaMasatoyoM, pubmed-author:NozakiHiroakiH, pubmed-author:OnoderaOsamuO, pubmed-author:ShigaAtsushiA, pubmed-author:ShimoeYutakaY, pubmed-author:ShiotaHiroshiH, pubmed-author:TakahashiToshiakiT, pubmed-author:TamuraMasatoM, pubmed-author:TanakaAkiraA, pubmed-author:TsujiShojiS, pubmed-author:YamamotoTadashiT, pubmed-author:YanagawaSoheiS, pubmed-author:YokosekiAkioA, pubmed-author:YoshidaYutakaY
pubmed:copyrightInfo
2009 Massachusetts Medical Society
pubmed:issnType
Electronic
pubmed:day
23
pubmed:volume
360
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1729-39
pubmed:meshHeading
pubmed-meshheading:19387015-Adult, pubmed-meshheading:19387015-Aged, 80 and over, pubmed-meshheading:19387015-Alopecia, pubmed-meshheading:19387015-Cerebral Arterial Diseases, pubmed-meshheading:19387015-Cerebral Arteries, pubmed-meshheading:19387015-Cerebral Infarction, pubmed-meshheading:19387015-Female, pubmed-meshheading:19387015-Genes, Recessive, pubmed-meshheading:19387015-Humans, pubmed-meshheading:19387015-Male, pubmed-meshheading:19387015-Middle Aged, pubmed-meshheading:19387015-Mutation, pubmed-meshheading:19387015-Pedigree, pubmed-meshheading:19387015-Serine Endopeptidases, pubmed-meshheading:19387015-Signal Transduction, pubmed-meshheading:19387015-Spondylosis, pubmed-meshheading:19387015-Syndrome, pubmed-meshheading:19387015-Transcription, Genetic, pubmed-meshheading:19387015-Transforming Growth Factor beta, pubmed-meshheading:19387015-Tunica Intima
pubmed:year
2009
pubmed:articleTitle
Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease.
pubmed:affiliation
Niigata University, Niigata, Japan.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't