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21565790
Source:
http://linkedlifedata.com/resource/pubmed/id/21565790
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0008059
,
umls-concept:C0020676
,
umls-concept:C0020792
,
umls-concept:C0026882
,
umls-concept:C0205245
,
umls-concept:C0205314
,
umls-concept:C0679622
,
umls-concept:C0936012
,
umls-concept:C1421916
,
umls-concept:C1744681
pubmed:issue
8
pubmed:dateCreated
2011-8-5
pubmed:abstractText
Congenital hypothyroidism (CH) associated with goiter or a gland of normal size has been linked to dual oxidase 2 (DUOX2) mutations in the presence of iodide organification defect.
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/0375362
pubmed:citationSubset
AIM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/DUOX2 protein, human
,
http://linkedlifedata.com/resource/pubmed/chemical/NADPH Oxidase
pubmed:status
MEDLINE
pubmed:month
Aug
pubmed:issn
1945-7197
pubmed:author
pubmed-author:AgrettiPatriziaP
,
pubmed-author:BagattiniBrunellaB
,
pubmed-author:BrozziFedericaF
,
pubmed-author:CeccarelliClaudiaC
,
pubmed-author:De MarcoGiuseppinaG
,
pubmed-author:De ServiMelissaM
,
pubmed-author:Di CosmoCaterinaC
,
pubmed-author:DimidaAntonioA
,
pubmed-author:FerrariniEleonoraE
,
pubmed-author:Freitas FerreiraAndrea ClaudiaAC
,
pubmed-author:MolinaroAngeloA
,
pubmed-author:MontanelliLuciaL
,
pubmed-author:PincheraAldoA
,
pubmed-author:TonaccheraMassimoM
,
pubmed-author:VittiPaoloP
pubmed:issnType
Electronic
pubmed:volume
96
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
E1335-9
pubmed:meshHeading
pubmed-meshheading:21565790-Adult
,
pubmed-meshheading:21565790-Aged
,
pubmed-meshheading:21565790-Child
,
pubmed-meshheading:21565790-Child, Preschool
,
pubmed-meshheading:21565790-Congenital Hypothyroidism
,
pubmed-meshheading:21565790-Female
,
pubmed-meshheading:21565790-Gene Deletion
,
pubmed-meshheading:21565790-HeLa Cells
,
pubmed-meshheading:21565790-Humans
,
pubmed-meshheading:21565790-Male
,
pubmed-meshheading:21565790-Middle Aged
,
pubmed-meshheading:21565790-NADPH Oxidase
,
pubmed-meshheading:21565790-Oligonucleotide Array Sequence Analysis
,
pubmed-meshheading:21565790-Point Mutation
,
pubmed-meshheading:21565790-Severity of Illness Index
,
pubmed-meshheading:21565790-Thyroid Gland
pubmed:year
2011
pubmed:articleTitle
Identification and functional analysis of novel dual oxidase 2 (DUOX2) mutations in children with congenital or subclinical hypothyroidism.
pubmed:affiliation
Dipartimento di Endocrinologia, Università di Pisa, Via Paradisa 2, 56124, Cisanello, Pisa, Italy.
pubmed:publicationType
Journal Article
,
Research Support, Non-U.S. Gov't