Source:http://linkedlifedata.com/resource/pubmed/id/10658742
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
2000-2-17
|
pubmed:abstractText |
OBJECTIVE: The aim of this study was to clarify the relationship between morphologic changes of the pituitary gland and the genotype of Prophet of Pit-1 (PROP1), a newly discovered gene responsible for congenital combined pituitary hormone deficiency, in a series of eight humans with this disorder. CONCLUSION: Congenital hypoplasia of the anterior pituitary gland is the most common MR imaging finding in patients with combined pituitary hormone deficiency. Our findings suggest a crucial role for PROP1 in pituitary organogenesis as well as anterior pituitary cell differentiation.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
AIM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Feb
|
pubmed:issn |
0361-803X
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
174
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
555-9
|
pubmed:dateRevised |
2008-2-15
|
pubmed:meshHeading |
pubmed-meshheading:10658742-Adolescent,
pubmed-meshheading:10658742-Adult,
pubmed-meshheading:10658742-Female,
pubmed-meshheading:10658742-Homeodomain Proteins,
pubmed-meshheading:10658742-Humans,
pubmed-meshheading:10658742-Magnetic Resonance Imaging,
pubmed-meshheading:10658742-Male,
pubmed-meshheading:10658742-Mutation,
pubmed-meshheading:10658742-Pituitary Gland,
pubmed-meshheading:10658742-Pituitary Hormones,
pubmed-meshheading:10658742-Transcription Factors
|
pubmed:year |
2000
|
pubmed:articleTitle |
MR imaging of the pituitary gland in children and young adults with congenital combined pituitary hormone deficiency associated with PROP1 mutations.
|
pubmed:affiliation |
Department of Pediatrics, Endocrinology Research Center, Moscow, Russia.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|