Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Susan E, Stred"'
Publikováno v:
AACE Clinical Case Reports, Vol 4, Iss 4, Pp e342-e345 (2018)
ABSTRACT: Objective: Hypothalamic obesity (HO) is an intractable form of obesity syndrome occurring in patients following hypothalamic insults. It is characterized by significant polyphagia, lack of satiety, and rapid weight gain not usually responsi
Externí odkaz:
https://doaj.org/article/70d3424d74df4c0c9974912e8835f678
Publikováno v:
AACE Clinical Case Reports, Vol 4, Iss 4, Pp e342-e345 (2018)
Objective: Hypothalamic obesity (HO) is an intractable form of obesity syndrome occurring in patients following hypothalamic insults. It is characterized by significant polyphagia, lack of satiety, and rapid weight gain not usually responsive to calo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14bea93acb6d92e198c68174f4aba976
https://doi.org/10.4158/accr-2018-0009
https://doi.org/10.4158/accr-2018-0009
Autor:
Susan E, Stred
Publikováno v:
Adolescent medicine: state of the art reviews. 26(2)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8ee7917fecd03321a04cb26b003ae4d0
https://pubmed.ncbi.nlm.nih.gov/26999882
https://pubmed.ncbi.nlm.nih.gov/26999882
Autor:
Susan E. Stred, Christin Carter-Su, J. R. Stubbart, F Talamantes, Lawrence S. Argetsinger, W C Smith, Jules A. Shafer
Publikováno v:
Endocrinology. 130:1626-1636
We have shown previously that GH receptors (GHRs) become phosphorylated on tyrosyl residues when GH-responsive cells are exposed to GH. In this work we investigate the molecular mechanism by which GH binding stimulates tyrosyl phosphorylation of GHR.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ad4b518f8c8deda136dc2c3cb46f224
https://doi.org/10.1210/endo.130.3.1537311
https://doi.org/10.1210/endo.130.3.1537311
Autor:
Ping Kaung K. Tai, Erela Gorin, Susan E. Stred, Christin Carter-Su, David F. Barton, J. Randall Stubbart, H. Maurice Goodman
Publikováno v:
Endocrinology. 129:1659-1670
GH stimulates tyrosyl phosphorylation of GH receptors in 3T3-F442A fibroblasts, and highly purified GH receptor preparations exhibit tyrosine kinase activity. Paradoxically, however, the GH receptor cloned from liver exhibits no sequence similarity t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc789ef45ffb62decd4b1294d76e9f96
https://doi.org/10.1210/endo-129-3-1659
https://doi.org/10.1210/endo-129-3-1659
Publikováno v:
Journal of athletic training. 42(3)
To describe the development of hypopituitarism in an adolescent athlete after multiple concussions and to raise awareness among sports medicine clinicians concerning the growing concern of hypopituitarism in concussion injury surveillance and managem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2bda1bd60357f107fa55cd926725253c
https://pubmed.ncbi.nlm.nih.gov/18060001
https://pubmed.ncbi.nlm.nih.gov/18060001
Publikováno v:
Molecular and cellular endocrinology. 204(1-2)
Hemopexin (Hx) is an acute-phase hepatic protein, whose transcription is upregulated by IL-6. The transcription rate of Hx was found to be increased 11-fold by the calcium ionophore A23187, 25-fold by the calcium ionophore ionomycin, and 4-5-fold by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1e4b09d6d1e28bdc63cbd70b2ccec28f
https://pubmed.ncbi.nlm.nih.gov/12850286
https://pubmed.ncbi.nlm.nih.gov/12850286
Autor:
Susan E. Stred, Joseph L. Messina
Publikováno v:
Molecular and cellular endocrinology. 204(1-2)
A cDNA library from the liver of a growth hormone (GH)-treated hypophysectomized rat was constructed and screened for GH-inducible genes (GIGs). Three cDNAs specific for putative GIG mRNAs (GIG-3, -7 and -12) were isolated and, when sequenced, were f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::351e0f65bf7b04bdfeb04c74b579464f
https://pubmed.ncbi.nlm.nih.gov/12850285
https://pubmed.ncbi.nlm.nih.gov/12850285
Publikováno v:
Clinical genetics. 49(6)
A third case of an interstitial deletion of the long arm of chromosome 6 with clinical features mimicking Prader-Willi syndrome (PWS) is presented. Although preliminary clinical evaluation in each case suggested PWS, further review revealed that the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34843a5d702b0403a58d2e169efddccf
https://pubmed.ncbi.nlm.nih.gov/8884080
https://pubmed.ncbi.nlm.nih.gov/8884080