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16247488
Source:
http://linkedlifedata.com/resource/pubmed/id/16247488
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51
)
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0005586
,
umls-concept:C0006104
,
umls-concept:C0007407
,
umls-concept:C0017262
,
umls-concept:C0017431
,
umls-concept:C0036341
,
umls-concept:C0185117
,
umls-concept:C0205314
,
umls-concept:C0597298
,
umls-concept:C0679622
,
umls-concept:C0936012
,
umls-concept:C1280500
,
umls-concept:C2911684
pubmed:issue
2
pubmed:dateCreated
2006-1-26
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/9607835
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Catechol O-Methyltransferase
,
http://linkedlifedata.com/resource/pubmed/chemical/Methionine
,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Isoforms
,
http://linkedlifedata.com/resource/pubmed/chemical/Valine
pubmed:status
MEDLINE
pubmed:month
Feb
pubmed:issn
1359-4184
pubmed:author
pubmed-author:HarrisonP JPJ
,
pubmed-author:TunbridgeE MEM
,
pubmed-author:WeinbergerD RDR
pubmed:issnType
Print
pubmed:volume
11
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
116-7
pubmed:meshHeading
pubmed-meshheading:16247488-Amino Acid Substitution
,
pubmed-meshheading:16247488-Bipolar Disorder
,
pubmed-meshheading:16247488-Catechol O-Methyltransferase
,
pubmed-meshheading:16247488-Gene Expression
,
pubmed-meshheading:16247488-Gene Expression Regulation, Enzymologic
,
pubmed-meshheading:16247488-Genetic Predisposition to Disease
,
pubmed-meshheading:16247488-Humans
,
pubmed-meshheading:16247488-Methionine
,
pubmed-meshheading:16247488-Polymorphism, Genetic
,
pubmed-meshheading:16247488-Prefrontal Cortex
,
pubmed-meshheading:16247488-Protein Isoforms
,
pubmed-meshheading:16247488-Schizophrenia
,
pubmed-meshheading:16247488-Valine
pubmed:year
2006
pubmed:articleTitle
A novel protein isoform of catechol O-methyltransferase (COMT): brain expression analysis in schizophrenia and bipolar disorder and effect of Val158Met genotype.
pubmed:publicationType
Letter
,
Clinical Trial