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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
6
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pubmed:dateCreated |
2004-9-23
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pubmed:abstractText |
Chronic allograft dysfunction (CAD) is a complex phenomenon caused by underlying kidney disease and superimposed environmental and genetic factors. We investigated the association of polymorphisms in the genes for angiotensin-converting enzyme (ACE), angiotensinogen (AGT), angiotensin II receptor type 1 (ATR1) and type 2 (ATR2), and endothelial nitric oxide synthase (ENOS) with the initiation of CAD.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Angiotensinogen,
http://linkedlifedata.com/resource/pubmed/chemical/DNA Primers,
http://linkedlifedata.com/resource/pubmed/chemical/NOS3 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide Synthase,
http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide Synthase Type III,
http://linkedlifedata.com/resource/pubmed/chemical/Peptidyl-Dipeptidase A,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Angiotensin, Type 1,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Angiotensin, Type 2
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
0041-1337
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:day |
27
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pubmed:volume |
78
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
892-8
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15385810-Adult,
pubmed-meshheading:15385810-Angiotensinogen,
pubmed-meshheading:15385810-Base Sequence,
pubmed-meshheading:15385810-DNA Primers,
pubmed-meshheading:15385810-Female,
pubmed-meshheading:15385810-Genotype,
pubmed-meshheading:15385810-Humans,
pubmed-meshheading:15385810-Introns,
pubmed-meshheading:15385810-Kidney Transplantation,
pubmed-meshheading:15385810-Male,
pubmed-meshheading:15385810-Nitric Oxide Synthase,
pubmed-meshheading:15385810-Nitric Oxide Synthase Type III,
pubmed-meshheading:15385810-Peptidyl-Dipeptidase A,
pubmed-meshheading:15385810-Polymorphism, Genetic,
pubmed-meshheading:15385810-Receptor, Angiotensin, Type 1,
pubmed-meshheading:15385810-Receptor, Angiotensin, Type 2,
pubmed-meshheading:15385810-Renin-Angiotensin System,
pubmed-meshheading:15385810-Retrospective Studies,
pubmed-meshheading:15385810-Treatment Failure
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pubmed:year |
2004
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pubmed:articleTitle |
Association of the genetic polymorphisms of the renin-angiotensin system and endothelial nitric oxide synthase with chronic renal transplant dysfunction.
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pubmed:affiliation |
Department of Nephrology, Baskent University Faculty of Medicine, Ankara, Turkey. akcayali@hotmail.com
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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