Zobrazeno 1 - 10
of 28
pro vyhledávání: '"Weldon B Jolley"'
Autor:
Donald F Smee, Howard B Cottam, Brahma S Sharma, Ganesh D Kini, Ganapathi R Revankar, Emmanuel A Ojo-Amaize, Robert W Sidwell, Weldon B Jolley, Roland K Robins
Publikováno v:
Canadian Journal of Infectious Diseases, Vol 3, Iss Suppl B, Pp 41-48 (1992)
7-thia-8-oxoguanosine (TOGuo) is the first reported structure of a family of modified guanosine analogues exhibiting antiviral activity in rodent models. Its spectrum of action includes interferon-sensitive viruses such as alphaviruses, bunyaviruses,
Externí odkaz:
https://doaj.org/article/c4c9e5228dba4f8a9eceddc11c64aceb
Autor:
Arend Mulder, Weldon B. Jolley, Johan W. Bruning, Cornelis J. M. Melief, Joke Blom, M.J. Kardol
Publikováno v:
Human Immunology. 36:186-192
We have developed an in vitro immunization system for the production of B-cell lines that secrete HLA-specific human mAbs. For this purpose, peripheral blood lymphocytes of parous women were stimulated with pools of allogeneic lymphocytes. Preferenti
Autor:
Roland K. Robins, Brahma S. Sharma, Howard B. Cottam, Ganesh D. Kini, Weldon B. Jolley, Donald F. Smee, Ganapathi R. Revankar, Robert W. Sidwell, Emmanuel A. Ojo-Amaize
Publikováno v:
Canadian Journal of Infectious Diseases, Vol 3, Iss Suppl B, Pp 41-48 (1992)
7-thia-8-oxoguanosine (TOGuo) is the first reported structure of a family of modified guanosine analogues exhibiting antiviral activity in rodent models. Its spectrum of action includes interferon-sensitive viruses such as alphaviruses, bunyaviruses,
Publikováno v:
Cellular Immunology. 126:414-419
Intraperitoneal treatment of mice with a novel guanosine analog, 7-thia-8-oxoguanosine (7-thia-8-oxoGuo), gives rise to activated splenic lymphocytes and peritoneal macrophages with enhanced capacity to mediate antibody-dependent cellular cytotoxicit
Autor:
Steven B. Larson, Ganesh D. Kini, Roland K. Robins, Birendra K. Bhattacharya, Steven S. Matsumoto, Yogesh S. Sanghvi, Ganapathi R. Revankar, Weldon B. Jolley
Publikováno v:
Journal of Medicinal Chemistry. 33:336-344
A series of 1,2,3-triazole (2), pyrazole (3 and 5), and pyrrole (4) ribonucleosides with two adjacent carbamoyl groups have been synthesized and evaluated for cell growth inhibition and induction of cellular differentiation of HL-60 cells in culture.
Autor:
Thomas L. Avery, Boanerges Rubalcava, Roland K. Robins, Steven S. Matsumoto, Howard B. Cottam, Weldon B. Jolley, Emmanuel A. Ojo-Amaize
Publikováno v:
Immunology Letters. 23:173-178
The capacity of certain guanine ribonucleosides (modified at the 7 and/or 8 positions) to enhance the respiratory burst of murine peritoneal phagocytes was evaluated. The results show that 8-mercaptoguanosine, 8-bromoguanosine, 7-methyl-8-oxoguanosin
Publikováno v:
Tissue antigens. 42(1)
In vitro immunization and subsequent immortalization of peripheral blood cells of a multiparous woman has resulted in the production of a stable human mouse heterohybridoma, 5C2A2, secreting an HLA-A2/A28-specific human monoclonal antibody. Although
Publikováno v:
Clinicalexperimental metastasis. 9(5)
We have recently reported that a synthetic nucleoside, 7-thia-8-oxoguanosine (7T8OG) is a potent activator of a number of effectors which are involved in anti-tumor immune responses. 7T8OG was found to induce interferon (IFN) production, to activate
Autor:
K Nagahara, Ganesh D. Kini, Brahma S. Sharma, Roland K. Robins, Jack D. Anderson, Steven B. Larson, N. K. Dalley, Donald F. Smee, Weldon B. Jolley, Ai Jin
Publikováno v:
Journal of medicinal chemistry. 33(1)
Novel analogues of the naturally occurring purine nucleosides were synthesized in the thiazolo[4,5-d]pyrimidine ring system to determine the immunomodulatory effects of insertion of a sulfur atom in place of nitrogen at position 7 of the purine ring.
Autor:
Yogeshi S. Sanghvi, Brahma S. Sharma, Roland K. Robins, Ganapathi R. Revankar, Weldon B. Jolley
Publikováno v:
International journal of immunopharmacology. 12(6)
We have examined the immunological activity of a unique α-nucleoside analog of 2′-deoxyguanosine in which the pyrimidine ring nitrogen in the 3 positionis replaced by CH [6-amino-1, 5- dihydro -1-(2- deoxy -α- D -erythro- pentofuranosy ) imidazo