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21398422
Source:
http://linkedlifedata.com/resource/pubmed/id/21398422
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0015576
,
umls-concept:C0026882
,
umls-concept:C0205245
,
umls-concept:C0337810
,
umls-concept:C0683325
,
umls-concept:C0936012
,
umls-concept:C1412629
,
umls-concept:C1865322
pubmed:issue
7
pubmed:dateCreated
2011-5-23
pubmed:abstractText
To describe a new FHM kindred, and to analyse the functional consequences of the disease-associated ATP1A2 p.G301R mutation in human cellular models grown at 37°C.
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/8200710
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/ATP1A2 protein, human
,
http://linkedlifedata.com/resource/pubmed/chemical/Sodium-Potassium-Exchanging ATPase
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
1468-2982
pubmed:author
pubmed-author:AmbrosinoPaoloP
,
pubmed-author:FortunatoMaria RobertaMR
,
pubmed-author:IodiceRosaR
,
pubmed-author:ManganelliFioreF
,
pubmed-author:PisciottaChiaraC
,
pubmed-author:SantorelliFilippoF
,
pubmed-author:SantoroLucioL
,
pubmed-author:SoldovieriMaria VirginiaMV
,
pubmed-author:TaglialatelaMaurizioM
,
pubmed-author:TessaAlessandraA
pubmed:issnType
Electronic
pubmed:volume
31
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
808-19
pubmed:meshHeading
pubmed-meshheading:21398422-Adult
,
pubmed-meshheading:21398422-Aged
,
pubmed-meshheading:21398422-Blotting, Western
,
pubmed-meshheading:21398422-Cell Survival
,
pubmed-meshheading:21398422-Family
,
pubmed-meshheading:21398422-Female
,
pubmed-meshheading:21398422-Humans
,
pubmed-meshheading:21398422-Immunohistochemistry
,
pubmed-meshheading:21398422-Italy
,
pubmed-meshheading:21398422-Male
,
pubmed-meshheading:21398422-Microscopy, Confocal
,
pubmed-meshheading:21398422-Middle Aged
,
pubmed-meshheading:21398422-Migraine with Aura
,
pubmed-meshheading:21398422-Models, Molecular
,
pubmed-meshheading:21398422-Mutation, Missense
,
pubmed-meshheading:21398422-Pedigree
,
pubmed-meshheading:21398422-Protein Structure, Secondary
,
pubmed-meshheading:21398422-Reverse Transcriptase Polymerase Chain Reaction
,
pubmed-meshheading:21398422-Sodium-Potassium-Exchanging ATPase
,
pubmed-meshheading:21398422-Transfection
pubmed:year
2011
pubmed:articleTitle
A new Italian FHM2 family: clinical aspects and functional analysis of the disease-associated mutation.
pubmed:affiliation
Department of Neurological Sciences, University Federico II of Naples, Via Sergio Pansini 5, Naples, Italy. lusantor@unina.it
pubmed:publicationType
Journal Article