Zobrazeno 1 - 3
of 3
pro vyhledávání: '"John P. Galgani"'
Autor:
Mary Catherine Jensen, Bakula Trivedi, William H. Daughaday, Dennis M. Bier, Peter Rotwein, David P. Dempsher, Ellen Heath-Monnig, John P. Galgani, Sherida E. Tollefsen
Publikováno v:
Pediatric Research. 28:394-400
We studied the effects of growth hormone on retention of 15N-labeled amino acids in 34 short, prepubertal, growth hormone-sufficient children and three growth hormone-deficient subjects. All 34 non-growth hormone-deficient children had apparently nor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe76dd95a9f5550a3dd148319c6976eb
https://doi.org/10.1203/00006450-199010000-00018
https://doi.org/10.1203/00006450-199010000-00018
Publikováno v:
The Journal of clinical endocrinology and metabolism. 70(3)
In an attempt to identify genetic lesions contributing to human growth disorders, we evaluated a prospectively recruited group of children with growth failure for mutations in the insulin-like growth factor-I (IGF-I) gene. Two complementary approache
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f9e05eee897626ccbcf891d3b50eb44e
https://pubmed.ncbi.nlm.nih.gov/2155253
https://pubmed.ncbi.nlm.nih.gov/2155253
Autor:
Zvi Laron, Lillian R. Meacham, Peter Rotwein, Ruth Keret, William I. Wood, Paul J. Godowski, John S. Parks, John P. Galgani, Renate Hellmiss, David W. Leung
Publikováno v:
Proceedings of the National Academy of Sciences. 86:8083-8087
Laron-type dwarfism is an autosomal recessive genetic disorder that is characterized by high levels of growth hormone and low levels of insulin-like growth factor I in the circulation. Several lines of evidence suggest that this disease is caused by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::087fb9436180e8581ef0f1ede5915cd1
https://doi.org/10.1073/pnas.86.20.8083
https://doi.org/10.1073/pnas.86.20.8083