Zobrazeno 1 - 5
of 5
pro vyhledávání: '"S H Kadwell"'
Autor:
G Chandra, J P Cogswell, L R Miller, M M Godlevski, S W Stinnett, S L Noel, S H Kadwell, T A Kost, J G Gray
Publikováno v:
The Journal of Immunology. 155:4535-4543
An intact cAMP response element (CRE) in the upstream regulatory sequence of IL-1 beta (-2755/-2762) has been shown to be essential for maintaining full IL-1 beta inducibility following treatment with LPS, PMA, or TNF-alpha. In the present study, usi
Autor:
J D, Stuart, F W, Lee, D, Simpson Noel, S H, Kadwell, L K, Overton, C R, Hoffman, T A, Kost, T K, Tippin, R L, Yeager, K W, Batchelor, H N, Bramson
Publikováno v:
Biochemical pharmacology. 62(7)
The interaction of baculovirus expressed rat steroid 5alpha-reductase types 1 and 2 (r5AR1 and r5AR2) with 17beta-N-(2,5-bis(trifluoromethyl)phenyl)carbamoyl-4-aza-5alpha-androst-1-en-3-one (GI198745) was investigated at pH 7 and 37 degrees. This 5al
Autor:
L M, Shewchuk, A M, Hassell, B, Ellis, W D, Holmes, R, Davis, E L, Horne, S H, Kadwell, D D, McKee, J T, Moore
Publikováno v:
Structure (London, England : 1993). 8(11)
Angiogenesis, the formation of new vessels from the existing vasculature, is a critical process during early development as well as in a number of disease processes. Tie2 (also known as Tek) is an endothelium-specific receptor tyrosine kinase involve
Autor:
M L, Moss, P, Kuzmic, J D, Stuart, G, Tian, A G, Peranteau, S V, Frye, S H, Kadwell, T A, Kost, L K, Overton, I R, Patel
Publikováno v:
Biochemistry. 35(11)
We have discovered that 17beta-[N,N-(diethyl)carbamoyl]-6-azaandrost-4-en-3-one is a time-dependent inhibitor of type II 5alpha-reductase, as is the drug finasteride. Unlike finasteride, the 6-aza-steroid is not a time-dependent inhibitor of type I 5
Autor:
G, Chandra, J P, Cogswell, L R, Miller, M M, Godlevski, S W, Stinnett, S L, Noel, S H, Kadwell, T A, Kost, J G, Gray
Publikováno v:
Journal of immunology (Baltimore, Md. : 1950). 155(10)
An intact cAMP response element (CRE) in the upstream regulatory sequence of IL-1 beta (-2755/-2762) has been shown to be essential for maintaining full IL-1 beta inducibility following treatment with LPS, PMA, or TNF-alpha. In the present study, usi