Zobrazeno 1 - 9
of 9
pro vyhledávání: '"D E, Magee"'
Publikováno v:
Endocrinology. 138:1794-1800
Estrogen inhibits postmenopausal bone loss and decreases fracture risk. Unfortunately, estrogen replacement therapy has many undesirable side effects, the majority of which are due to stimulation of reproductive tissues. Tissue specific estrogen agon
Publikováno v:
Endocrinology. 134:2283-2288
Tissue-specific estrogen agonists may be useful in protecting against osteoporosis and the increased risk of coronary heart disease in postmenopausal women with minimal undesired effects on reproductive tissues. The actions of the mixed estrogen agon
Autor:
N, Bowling, W E, Bloomquist, M L, Cohen, H U, Bryant, H W, Cole, D E, Magee, E R, Rowley, C J, Vlahos
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 281(1)
Ethinyl estradiol (EE2), administered orally to ovariectomized (ovex) rats, has been shown to prevent loss of bone mineral density and to decrease serum cholesterol levels. Radioligand binding studies with the dihydropyridine (DHP) [3H]PN200-110 were
Publikováno v:
Laboratory animal science. 47(1)
Publikováno v:
Endocrinology. 137(10)
Estrogen (E) treatment has proven to be effective in preventing bone loss after menopause with, however, some undesirable side effects. Many of these side effects are related to the hormone's actions on reproductive tissues. Raloxifene is an organ-se
Autor:
Raymond F. Kauffman, D C Williams, A Bekele, E R Rowley, W R Bensch, R Bendele, Larry John Black, D E Magee, Masahiko Sato, G J Cullinan
There is a medical need for an agent with the positive effects of estrogen on bone and the cardiovascular system, but without the negative effects on reproductive tissue. Raloxifene (LY139481 HCI) is a benzothiophene derivative that binds to the estr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb6238e4e6c949a9bb93215c390e1cf6
https://europepmc.org/articles/PMC293730/
https://europepmc.org/articles/PMC293730/
Publikováno v:
Advances in prostaglandin, thromboxane, and leukotriene research.
Publikováno v:
Molecular pharmacology. 39(1)
Thromboxane A2 (TXA2) and prostaglandin H2 (PGH2) are potent constrictors of airway smooth muscle and may mediate some of the pulmonary effects of leukotrienes. To date, the TXA2/PGH2 receptor in lung has not been well characterized. In this report,
Publikováno v:
Eicosanoids. 3(2)
A variety of lipoxygenase products such as 12- and 15-hydroxyeicosatetraenoic acid (12- and 15-HETE) inhibit thromboxane A2 (TXA2) mimetic induced human platelet aggregation in a stereoselective manner. The mechanism of this inhibition remains unclea