Zobrazeno 1 - 10
of 61
pro vyhledávání: '"D J Bauer"'
Autor:
D. J. Bauer
Publikováno v:
Annals of the New York Academy of Sciences. 130:110-117
Autor:
D. J. Bauer
Publikováno v:
Archives of Dermatology. 129:855-858
Autor:
D. J. Bauer
Publikováno v:
Nature. 159(4039)
So far as is known, viruses appear to possess no enzyme activity ; the virus particles, in order to multiply, must presumably utilize the enzyme-substrate reactions of the host cells, or else have a selective affinity for the products of host metabol
Publikováno v:
Archives of dermatology. 130(7)
Publikováno v:
Archives of dermatology. 129(7)
The cutaneous eruptions due to allogeneic graft-vs-host disease, autologous graft-vs-host disease, and lymphocyte recovery occur in the setting of peripheral leukocyte reconstitution after marrow aplasia. Since the eruptions of lymphocyte recovery (E
Autor:
A Tomasz, Mirjana Nesin, S Projan, G. J. Noel, A M sa Figueiredo, Barry Kreiswirth, W Eisner, Paul J. Edelson, H. de Lencastre, D J Bauer
Publikováno v:
Scopus-Elsevier
Methicillin-resistant Staphylococcus aureus (MRSA) is an important cause of nosocomial infection. Outbreaks of infection caused by these pathogens are generally considered to be traceable to introduction of single strains into a hospital population.
Publikováno v:
Annals of the New York Academy of Sciences. 255:468-480
Autor:
Howard J. Schaeffer, Bart L. Dolmatch, Peter Collins, James A. Fyfe, Paul M. Keller, D. J. Bauer, Lilia M. Beauchamp
Publikováno v:
Journal of Medicinal Chemistry. 28:982-987
A group of compounds was prepared in which variations of the ring portion of the acyclovir (ACV) structure were made. These modifications included monocyclic (isocytosine, triazole, imidazole), bicyclic (8-azapurine, pyrrolo[2,3-d]pyrimidine, pyrazol
Publikováno v:
British Journal of Ophthalmology. 63:429-435
Acycloguanosine, a recently developed compound with high inhibitory activity against viruses belonging to the herpes group, has been evaluated in experimental herpes simplex keratitis in rabbits in comparison with trifluorothymidine and preparations