Zobrazeno 1 - 10
of 212
pro vyhledávání: '"L L, BENNETT"'
Autor:
L. L. Bennett, M. J. Williams, W. E. Kunkle, A. C. Hammond, M. F. Miller, D. D. Johnson, R L Preston
Publikováno v:
Journal of Animal Science. 73:1881-1887
Steers (n = 156) finished on rhizoma peanut (Arachis glabrata Benth.)-tropical grass pasture in Florida and slaughtered at Central Packing, Center Hill were compared with steers (n = 152) finished on a concentrate diet in Texas and slaughtered at Exc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9507d4bb54a112438f697eb04a30368
https://doi.org/10.2527/1995.7371881x
https://doi.org/10.2527/1995.7371881x
Publikováno v:
Endocrinology. 38
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1c560bdc31e85c93e11d4b56174cd3b3
https://pubmed.ncbi.nlm.nih.gov/21017050
https://pubmed.ncbi.nlm.nih.gov/21017050
Publikováno v:
2007 Conference on Lasers and Electro-Optics (CLEO).
We describe the operation of a compact CW liquid nitrogen cooled Yb:YAG laser with near diffraction-limited output > 200 W and slope efficiency > 63%.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::14b3bd6bb74618c36bf35928580a4619
https://doi.org/10.1109/cleo.2007.4453001
https://doi.org/10.1109/cleo.2007.4453001
Publikováno v:
SPIE Proceedings.
In this paper we discuss a CW Yb:YAG cryogenic laser program that has resulted in the design and demonstration of a novel high power laser. Cryogenically-cooled crystalline solid-state lasers, and Yb:YAG lasers in particular, are attractive sources o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f98da7e53db3044e0796131ae19d00f8
https://doi.org/10.1117/12.718312
https://doi.org/10.1117/12.718312
Autor:
W B, Parker, S C, Shaddix, L M, Rose, D S, Shewach, L W, Hertel, J A, Secrist, J A, Montgomery, L L, Bennett
Publikováno v:
Molecular pharmacology. 55(3)
In an effort to understand biochemical features that are important to the selective antitumor activity of 2-chloro-9-(2-deoxy-2-fluoro-beta-D-arabinofuranosyl)adenine [Cl-F( upward arrow)-dAdo], we evaluated the biochemical pharmacology of three stru
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6b4d7445517df705c9b947bfadebfc66
https://pubmed.ncbi.nlm.nih.gov/10051535
https://pubmed.ncbi.nlm.nih.gov/10051535
Autor:
L L, Bennett, P W, Allan, G, Arnett, Y F, Shealy, D S, Shewach, W S, Mason, I, Fourel, W B, Parker
Publikováno v:
Antimicrobial agents and chemotherapy. 42(5)
The carbocyclic analog of 2′-deoxyguanosine (CdG) has broad-spectrum antiviral activity. Because of recent observations with other nucleoside analogs that biological activity may be associated the l enantiomer rather than, as expected, with the d e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2c1d460c90ec98ab1dc74582ac64f241
https://pubmed.ncbi.nlm.nih.gov/9593124
https://pubmed.ncbi.nlm.nih.gov/9593124
Publikováno v:
Gene therapy. 1(4)
Inefficiency of gene delivery, together with inadequate bystander killing, represent two major hurdles in the development of a toxin-mediated gene therapy for human malignancy. The product of the Escherischia coli DeoD gene (purine nucleoside phospho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::93f80b1d2219e4915bdc74f9346f6623
https://pubmed.ncbi.nlm.nih.gov/7584086
https://pubmed.ncbi.nlm.nih.gov/7584086
Autor:
L L, Bennett, W B, Parker, P W, Allan, L M, Rose, Y F, Shealy, J A, Secrist, J A, Montgomery, G, Arnett, R L, Kirkman, W M, Shannon
Publikováno v:
Molecular pharmacology. 44(6)
CdG, the carbocyclic analog of 2'-deoxyguanosine, is active against herpes, hepatitis B, and human cytomegaloviruses. We have studied the interaction of the tritiated enantiomers of CdG with the herpes simplex virus type 1-specific thymidine kinase (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1b42ecce0509fc371e75732c37714bb8
https://pubmed.ncbi.nlm.nih.gov/8264563
https://pubmed.ncbi.nlm.nih.gov/8264563
Publikováno v:
The Journal of pharmacology and experimental therapeutics. 266(2)
Certain derivatives of 9-deazaguanine that contain arylmethyl, heteroarylmethyl or cycloalkylmethyl groups at the 9-position are potent inhibitors of purine nucleoside phosphorylase (PNP, E.C. 2.4.2.1). To determine whether these agents can produce m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::adfa2d0ba5e539c546165e2d4ad60138
https://pubmed.ncbi.nlm.nih.gov/8355201
https://pubmed.ncbi.nlm.nih.gov/8355201
Autor:
W B, Parker, S C, Shaddix, P W, Allan, G, Arnett, L M, Rose, W M, Shannon, Y F, Shealy, J A, Montgomery, J A, Secrist, L L, Bennett
Publikováno v:
Molecular pharmacology. 41(2)
The carbocyclic analog of 2'-deoxyguanosine (CdG) is active against herpes simplex virus (HSV), human cytomegalovirus, and human hepatitis-B virus. In order to understand the mechanism of action of this compound against HSV, we have evaluated (a) the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3a802a400d5467e8274a208ce9d8afad
https://pubmed.ncbi.nlm.nih.gov/1311407
https://pubmed.ncbi.nlm.nih.gov/1311407