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rdf:type |
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|
lifeskim:mentions |
|
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pubmed:issue |
4
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pubmed:dateCreated |
2008-3-14
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pubmed:abstractText |
The protein polymorphism of the GH receptor caused by genomic deletion of exon 3 (d3) has been linked to the magnitude of the first-year-growth response to GH in girls with Turner syndrome. Here, we studied the long-term effect of GH therapy in Turner syndrome in correlation to this polymorphism.
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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 |
|
|
pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
1365-2265
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pubmed:author |
|
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pubmed:issnType |
Electronic
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pubmed:volume |
68
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
567-72
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pubmed:meshHeading |
pubmed-meshheading:17973940-Body Mass Index,
pubmed-meshheading:17973940-Child,
pubmed-meshheading:17973940-Female,
pubmed-meshheading:17973940-Genotype,
pubmed-meshheading:17973940-Homozygote,
pubmed-meshheading:17973940-Hormone Replacement Therapy,
pubmed-meshheading:17973940-Human Growth Hormone,
pubmed-meshheading:17973940-Humans,
pubmed-meshheading:17973940-Polymorphism, Genetic,
pubmed-meshheading:17973940-Receptors, Somatotropin,
pubmed-meshheading:17973940-Recombinant Proteins,
pubmed-meshheading:17973940-Retrospective Studies,
pubmed-meshheading:17973940-Treatment Outcome,
pubmed-meshheading:17973940-Turner Syndrome
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pubmed:year |
2008
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|
pubmed:articleTitle |
Homozygosity of the d3-growth hormone receptor polymorphism is associated with a high total effect of GH on growth and a low BMI in girls with Turner syndrome.
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pubmed:affiliation |
University Children's Hospital Tuebingen, Pediatric Endocrinology Section, Tuebingen, Germany. gerhard.binder@med.uni-tuebingen.de
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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