11370628

Source:http://linkedlifedata.com/resource/pubmed/id/11370628

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015127, umls-concept:C0020433, umls-concept:C0021289, umls-concept:C0022610, umls-concept:C0023175, umls-concept:C0026882, umls-concept:C0079941, umls-concept:C0086860, umls-concept:C0205081, umls-concept:C0522530, umls-concept:C0537026, umls-concept:C0542560, umls-concept:C1314792, umls-concept:C1704258, umls-concept:C1704675
pubmed:issue	4
pubmed:dateCreated	2001-5-22
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/1M01 RR12248-04, http://linkedlifedata.com/resource/pubmed/grant/DK 39137, http://linkedlifedata.com/resource/pubmed/grant/DK 46057, http://linkedlifedata.com/resource/pubmed/grant/P30-DK 41296
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985087R
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Codon, http://linkedlifedata.com/resource/pubmed/chemical/DNA, http://linkedlifedata.com/resource/pubmed/chemical/Glucuronosyltransferase, http://linkedlifedata.com/resource/pubmed/chemical/bilirubin...
pubmed:status	MEDLINE
pubmed:month	Apr
pubmed:issn	1468-6244
pubmed:author	pubmed-author:AriasI MIM, pubmed-author:ChowdhuryAA, pubmed-author:ChowdhuryJ RJR, pubmed-author:ChowdhuryN RNR, pubmed-author:ChowdhurySS, pubmed-author:GhoshS SSS, pubmed-author:KadakolAA, pubmed-author:LowenheimMM, pubmed-author:SantraAA, pubmed-author:SappalB SBS
pubmed:issnType	Electronic
pubmed:volume	38
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	244-9
pubmed:dateRevised	2008-11-21
pubmed:meshHeading	pubmed-meshheading:11370628-Adult, pubmed-meshheading:11370628-Animals, pubmed-meshheading:11370628-Base Sequence, pubmed-meshheading:11370628-Blotting, Western, pubmed-meshheading:11370628-COS Cells, pubmed-meshheading:11370628-Codon, pubmed-meshheading:11370628-Crigler-Najjar Syndrome, pubmed-meshheading:11370628-DNA, pubmed-meshheading:11370628-DNA Mutational Analysis, pubmed-meshheading:11370628-Female, pubmed-meshheading:11370628-Gilbert Disease, pubmed-meshheading:11370628-Glucuronosyltransferase, pubmed-meshheading:11370628-Humans, pubmed-meshheading:11370628-Infant, pubmed-meshheading:11370628-Infant, Newborn, pubmed-meshheading:11370628-Jaundice, Neonatal, pubmed-meshheading:11370628-Kernicterus, pubmed-meshheading:11370628-Male, pubmed-meshheading:11370628-Mutation, pubmed-meshheading:11370628-Mutation, Missense, pubmed-meshheading:11370628-Plasmids, pubmed-meshheading:11370628-Promoter Regions, Genetic
pubmed:year	2001
pubmed:articleTitle	Interaction of coding region mutations and the Gilbert-type promoter abnormality of the UGT1A1 gene causes moderate degrees of unconjugated hyperbilirubinaemia and may lead to neonatal kernicterus.
pubmed:publicationType	Letter, Research Support, U.S. Gov't, P.H.S.