Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Bogdan Zabko-Potapovich"'
Autor:
Don E. Griswold, George Dytko, Brian Short, Jerry L. Adams, Bogdan Zabko-Potapovich, Bridget Brickson, Christine R. Albrightson
Publikováno v:
Kidney International. 45(5):1301-1310
Selective inhibition of 5-lipoxygenase attenuates glomerulonephritis in the rat. Three hours following injection of anti-GBM (glomerular basement membrane) antibody (10 mg/kg, i.v.) into rats, glomerular production of LTB4 was significantly increased
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0cb76cc6be99c088bf257a46c168a026
Autor:
Michael L. Moore, William M. Bryan, Christine R. Albrightson, George Dytko, Kieth Hoyle, Jeffrey M. Stadel, Bogdan Zabko-Potapovich
Publikováno v:
Cellular signalling. 6(7)
Thrombin stimulates cytosolic calcium mobilization and tritiated thymidine incorporation in rat glomerular mesangial cells. This effect may be mwediatyed by a a thrombin recepto similar to the receptor found in human platelets. In order to test this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f15de986a5ee586a337bc1f7eea9c9f3
https://pubmed.ncbi.nlm.nih.gov/7888301
https://pubmed.ncbi.nlm.nih.gov/7888301
Autor:
Barry M. Weichman, M A Wasserman, Barry A. Berkowitz, John G. Gleason, Bogdan Zabko-Potapovich, Thomas W. Ku, Mary E. McCarthy, Ruth R. Osborn, David A. Holden
Publikováno v:
Biochemical and Biophysical Research Communications. 117:732-739
A structural analog of LTD4, 4R-hydroxy-5S-cysteinylglycyl-6Z-nonadecenoic acid (4R, 5S, 6Z-2-nor-LTD1) has been synthesized and pharmacologically characterized. It significantly antagonized the contractile action of LTD4, LTC4 and LTE4 in guinea pig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::742f00b3bd33c278fb4b018bcbab1acf
https://doi.org/10.1016/0006-291x(83)91658-3
https://doi.org/10.1016/0006-291x(83)91658-3
Publikováno v:
European Journal of Pharmacology. 118:321-329
The alpha-adrenoceptor activity of fenoldopam was evaluated in three different in vitro tissue preparations. In rabbit isolated aortic rings fenoldopam displayed weak alpha 1-adrenoceptor antagonist activity (-log KB = 5.41) and displayed no alpha 1-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28d6c68d7b8e8c20eac484c6428ab6e4
https://doi.org/10.1016/0014-2999(85)90143-8
https://doi.org/10.1016/0014-2999(85)90143-8
Autor:
Charles B. Spainhour, Bogdan Zabko-Potapovich, David J. Newman, Edward G. Brann, Donald F. Colella, Joe R. Wardell
Publikováno v:
Biochemical pharmacology. 27(5)
A series of compounds drawn from a wide variety of chemical and pharmacologic classes were tested for their ability to act as inhibitors of a guinea pig tracheal cAMP-phosphodiesterase. Active compounds, defined as equal to or more potent than 1,3-di
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7f08b2e114232553b0fe42b45e18fca
https://pubmed.ncbi.nlm.nih.gov/207279
https://pubmed.ncbi.nlm.nih.gov/207279
Autor:
Cheng-Po Sung, Kazuhisa Shikano, Bogdan Zabko-Potapovich, Anthony J. Arleth, Barry A. Berkowitz
Publikováno v:
Biochemical pharmacology. 38(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bbce0450985f032e71300a8e7b199ac
https://pubmed.ncbi.nlm.nih.gov/2537087
https://pubmed.ncbi.nlm.nih.gov/2537087