rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
11
|
pubmed:dateCreated |
2009-11-6
|
pubmed:abstractText |
We tested the hypothesis that genetic variation in vitamin D-dependent signaling is associated with congestive heart failure in human subjects with hypertension.
|
pubmed:grant |
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Nov
|
pubmed:issn |
1744-8042
|
pubmed:author |
|
pubmed:issnType |
Electronic
|
pubmed:volume |
10
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1789-97
|
pubmed:dateRevised |
2011-9-26
|
pubmed:meshHeading |
pubmed-meshheading:19891555-25-Hydroxyvitamin D3 1-alpha-Hydroxylase,
pubmed-meshheading:19891555-Adult,
pubmed-meshheading:19891555-Aged,
pubmed-meshheading:19891555-Female,
pubmed-meshheading:19891555-Genetic Variation,
pubmed-meshheading:19891555-Heart Failure,
pubmed-meshheading:19891555-Humans,
pubmed-meshheading:19891555-Hypertension,
pubmed-meshheading:19891555-Male,
pubmed-meshheading:19891555-Middle Aged,
pubmed-meshheading:19891555-Polymorphism, Single Nucleotide,
pubmed-meshheading:19891555-Vitamin D
|
pubmed:year |
2009
|
pubmed:articleTitle |
Genetic variation in CYP27B1 is associated with congestive heart failure in patients with hypertension.
|
pubmed:affiliation |
Medical College of Wisconsin, WI, USA.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|