Zobrazeno 1 - 10
of 74
pro vyhledávání: '"G O Potts"'
Publikováno v:
Agents and Actions. 25:164-170
The purpose of the study was to determine if danazol was efficacious in the treatment of lupus MRL/MpJ (lpr) mice, as measured by longevity, proteinuria and serum amyloid protein (SAP) levels. Danazol, administered at an oral dose of 100 mg/kg, signi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41a9aad0a66e87f001cc5438db9c1996
https://doi.org/10.1007/bf01969108
https://doi.org/10.1007/bf01969108
Autor:
G. O. Potts, H.P. Schane
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 47:691-694
Spironolactone has progestational activity in the rabbit and rhesus monkey. It produced glandular development in the endometrium of the estrogen-primed immature female rabbit over the dosage range of 50 to 200 mg/kg and, at 400 mg/monkey, it delayed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d58359727d7dd267cebcbc5846106645
https://doi.org/10.1210/jcem-47-3-691
https://doi.org/10.1210/jcem-47-3-691
Autor:
G O, Potts
Publikováno v:
The Journal of international medical research. 5
We have established that danazol is an orally active pituitary gonadotrophin inhibitory agent devoid of oestrogenic and progestational activity. This steroid has weak, impeded androgenic activity. Danazol is unique in possessing such a profound separ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::84c82706e0d0583b945448467dc88ee3
https://pubmed.ncbi.nlm.nih.gov/410686
https://pubmed.ncbi.nlm.nih.gov/410686
Publikováno v:
Drugs. 19(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87b6921bfeecae029a9ff5a43ff466cd
https://pubmed.ncbi.nlm.nih.gov/6993179
https://pubmed.ncbi.nlm.nih.gov/6993179
Publikováno v:
Fertility and sterility. 30(1)
Azastene (4,4,17alpha-trimethylandrost-5-eno[2,3-d]isoxazol-17-ol), when given orally to rats at a dose of 12 mg/kg once on day 10 of pregnancy, induced resorption of all fetuses and a precipitous decline of circulating progesterone levels in all tes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0063126a0b18c39b70a75c8a610a5075
https://pubmed.ncbi.nlm.nih.gov/680188
https://pubmed.ncbi.nlm.nih.gov/680188
Publikováno v:
Biology of reproduction. 40(3)
The objective of these studies was to determine whether treatment of 10-day pregnant rats with a combination of epostane (a progesterone biosynthesis inhibitor) and either ZK 98299 or ZK 98734 (progesterone receptor antagonists) would result in addit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9cb56409634b96b97dc3ec53c007e50c
https://pubmed.ncbi.nlm.nih.gov/2758087
https://pubmed.ncbi.nlm.nih.gov/2758087
Publikováno v:
Fertility and sterility. 30(3)
Azastene is an orally effective "luteolytic" agent in rhesus monkeys. In nonpregnant monkeys it reverses the human chorionic gonadotropin-stimulated increase in progesterone production and delay in the onset of menstruation, and, in inseminated monke
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ffae87dc29a7037fa0bc5a2646b78f2f
https://pubmed.ncbi.nlm.nih.gov/101392
https://pubmed.ncbi.nlm.nih.gov/101392
Publikováno v:
Endocrinology. 67
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::9936521d2cc1f23ac468ecc9a6036997
https://pubmed.ncbi.nlm.nih.gov/13737525
https://pubmed.ncbi.nlm.nih.gov/13737525
Publikováno v:
Journal of medicinal chemistry. 7
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::52dc730f9ce9e1a68bd0b8de8cba7a0d
https://pubmed.ncbi.nlm.nih.gov/14221146
https://pubmed.ncbi.nlm.nih.gov/14221146
Publikováno v:
Experimental and molecular pathology. Supplement. 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::82ed440ac44cfe895adefaf4f483c039
https://pubmed.ncbi.nlm.nih.gov/14089659
https://pubmed.ncbi.nlm.nih.gov/14089659