Zobrazeno 1 - 10
of 39
pro vyhledávání: '"G W Carter"'
Autor:
G. W. Carter
Publikováno v:
Physical Review D. 67
We compute the axial vector current, form factor, and coupling for quarks in the instanton liquid model with two light flavors. Non-local current corrections are derived, as required by the effective 't Hooft interaction. We obtain a pion-mediated ax
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0efc4662f830c582a5fdc019b990fc28
https://doi.org/10.1103/physrevd.67.014008
https://doi.org/10.1103/physrevd.67.014008
We phenomenologically study whether partonic collisions responsible for the growth of hadron-hadron cross sections at high energy can be ascribed to instanton-induced processes. Although non-perturbative in nature, these interactions occur at the sem
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2ae8dfefb99c7ba0f6fca9172afe67d
http://arxiv.org/abs/hep-ph/0112036
http://arxiv.org/abs/hep-ph/0112036
Autor:
K W, Mollison, T A, Fey, D M, Gauvin, R M, Kolano, M P, Sheets, M L, Smith, M, Pong, N M, Nikolaidis, B C, Lane, J M, Trevillyan, J, Cannon, K, Marsh, G W, Carter, Y S, Or, Y W, Chen, G C, Hsieh, J R, Luly
Publikováno v:
The Journal of investigative dermatology. 112(5)
T lymphocytes play a critical part in inflammatory skin diseases but are targeted by available therapies that have only partial efficacy, significant side-effects, or both. Because psoriasis, atopic dermatitis, and allergic contact hypersensitivity a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7525d02e6e2fc0d77782e46551af1c83
https://pubmed.ncbi.nlm.nih.gov/10233764
https://pubmed.ncbi.nlm.nih.gov/10233764
Publikováno v:
Drug metabolism and disposition: the biological fate of chemicals. 25(9)
An in vitro glucuronidation assay was used to optimize a series of N-hydroxyurea-containing 5-lipoxygenase inhibitors for metabolic stability. The glucuronidation of these compounds in cynomolgus monkey microsomes followed Michaelis-Menten kinetics a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::74f7cee16f45f1f2886dee2af6ba98d1
https://pubmed.ncbi.nlm.nih.gov/9311617
https://pubmed.ncbi.nlm.nih.gov/9311617
Autor:
R L, Bell, R R, Harris, P E, Malo, J B, Bouska, T K, Shaughnessy, K I, Hulkower, C D, Brooks, G W, Carter
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 280(3)
Our primary goal has been to discover leukotriene biosynthesis inhibitors with characteristics that are appropriate for use as clinical agents. The success of the use of zileuton in the treatment of asthma led us to explore further the use of the N-h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bf17b1bbb45d6ada3145e144dfcdfc60
https://pubmed.ncbi.nlm.nih.gov/9067325
https://pubmed.ncbi.nlm.nih.gov/9067325
Autor:
K I, Hulkower, E R, Otis, J, Li, B W, Ennis, D J, Cugier, R L, Bell, G W, Carter, K B, Glaser
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 280(2)
These studies examined the signal transduction mechanisms by which prostaglandin (PG) E2 production can occur in human amnionic WISH cells in response to the stimuli okadaic acid, interleukin (IL)-1beta, tumor necrosis factor (TNF)-alpha, phorbol-12-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::906f7ee8c7ab6f9d7a53824408b9ae4f
https://pubmed.ncbi.nlm.nih.gov/9023325
https://pubmed.ncbi.nlm.nih.gov/9023325
Autor:
R L, Bell, R R, Harris, J B, Bouska, K I, Hulkower, J, Moore, P, Bhatia, P E, Malo, T, Kalosa, C D, Brooks, G W, Carter
Publikováno v:
Advances in experimental medicine and biology. 433
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::09dc86765f52a93da9387819fc3c6e73
https://pubmed.ncbi.nlm.nih.gov/9561111
https://pubmed.ncbi.nlm.nih.gov/9561111
Autor:
D H, Albert, R G, Conway, T J, Magoc, P, Tapang, D A, Rhein, G, Luo, J H, Holms, S K, Davidsen, J B, Summers, G W, Carter
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 277(3)
ABT-299 is an aqueous soluble prodrug that is converted rapidly in vivo to A-85783, a novel, highly potent, specific platelet activating factor (PAF) antagonist. The K, for inhibiting PAF binding to rabbit platelet membranes is 3.9 and 0.3 nM for hum
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::4fca4b574a066c2950a9819ae31000eb
https://pubmed.ncbi.nlm.nih.gov/8667228
https://pubmed.ncbi.nlm.nih.gov/8667228
Publikováno v:
Advances in experimental medicine and biology. 416
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ceb77946a8ecfa1645faf8b0306ee266
https://pubmed.ncbi.nlm.nih.gov/9131177
https://pubmed.ncbi.nlm.nih.gov/9131177
In vivo pharmacological evaluation of two novel type II (inducible) nitric oxide synthase inhibitors
Publikováno v:
Canadian journal of physiology and pharmacology. 73(5)
Les inhibiteurs selectifs de l'oxyde nitrique synthase (NOS) de type II ont plusieurs applications therapeutiques possibles, incluant le traitement de la septicemie, du diabete et des maladies autoimmunes. On a examine la capacite de deux nouveaux in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea78be9c0e8e7f7b9fdd1c36f374c9ee
https://pubmed.ncbi.nlm.nih.gov/7585335
https://pubmed.ncbi.nlm.nih.gov/7585335