Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
2007-9-28
pubmed:abstractText
Fibroblast growth factor (FGF) family signaling largely controls cellular homeostasis through short-range intercell paracrine communication. Recently FGF15/19, 21, and 23 have been implicated in endocrine control of metabolic homeostasis. The identity and location of the FGF receptor isotypes that mediate these effects are unclear. The objective was to determine the role of FGFR4, an isotype that has been proposed to mediate an ileal FGF15/19 to hepatocyte FGFR4 axis in cholesterol homeostasis, in metabolic homeostasis in vivo.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
1939-327X
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
56
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2501-10
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:17664243-Adipose Tissue, pubmed-meshheading:17664243-Animals, pubmed-meshheading:17664243-Blood Glucose, pubmed-meshheading:17664243-Body Weight, pubmed-meshheading:17664243-Dietary Fats, pubmed-meshheading:17664243-Fatty Liver, pubmed-meshheading:17664243-Gene Expression Regulation, pubmed-meshheading:17664243-Glucose, pubmed-meshheading:17664243-Homeostasis, pubmed-meshheading:17664243-Hyperlipidemias, pubmed-meshheading:17664243-Insulin, pubmed-meshheading:17664243-Insulin Resistance, pubmed-meshheading:17664243-Lipids, pubmed-meshheading:17664243-Liver, pubmed-meshheading:17664243-Mice, pubmed-meshheading:17664243-Mice, Knockout, pubmed-meshheading:17664243-Mice, Transgenic, pubmed-meshheading:17664243-Organ Size, pubmed-meshheading:17664243-RNA, Messenger, pubmed-meshheading:17664243-Receptor, Fibroblast Growth Factor, Type 4
pubmed:year
2007
pubmed:articleTitle
FGFR4 prevents hyperlipidemia and insulin resistance but underlies high-fat diet induced fatty liver.
pubmed:affiliation
Center for Cancer and Stem Cell Biology, Institute of Biosciences and Technology, Texas A&M Health Science Center, 2121 W. Holcombe Blvd., Houston, TX 77030, USA.
pubmed:publicationType
Journal Article, Research Support, N.I.H., Extramural