Zobrazeno 1 - 10
of 44
pro vyhledávání: '"R. Vesey"'
Autor:
A. Esaulov, A. L. Velikovich, V. Tangri, J. L. Giuliani, N. D. Ouart, A. Dasgupta, J. Schwarz, R. Vesey, D. J. Ampleford, M.-A. Schaeuble, B. M. Jones
Publikováno v:
2022 IEEE International Conference on Plasma Science (ICOPS).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a672fcb0208df3b91c0f4fc4e9f42219
https://doi.org/10.1109/icops45751.2022.9813108
https://doi.org/10.1109/icops45751.2022.9813108
Autor:
N. D. Ouart, A. Dasgupta, J. L. Giuliani, A. L. Velikovich, V. Tangri, M.-A. Schaeuble, J. Schwarz, D. J. Ampleford, R. Vesey, C. Jennings, B. M. Jones
Publikováno v:
2022 IEEE International Conference on Plasma Science (ICOPS).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6e6710c4cb0b490381d358a4021b9c4
https://doi.org/10.1109/icops45751.2022.9813276
https://doi.org/10.1109/icops45751.2022.9813276
Autor:
A. L. Velikovich, N. D. Ouart, A. Dasgupta, J. L. Giuliani, V. Tangri, A. J. Harvey-Thompson, M.-A. Schaeuble, J. Schwarz, C. Myers, D. J. Ampleford, R. Vesey, B. M. Jones, Y. Maron
Publikováno v:
2022 IEEE International Conference on Plasma Science (ICOPS).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44aea99d0e8980ca3f1377eec33d94fd
https://doi.org/10.1109/icops45751.2022.9813270
https://doi.org/10.1109/icops45751.2022.9813270
Autor:
Hooker, Joseph, Argyll, Duke of, Nares, George, Hamilton, R. Vesey, Wharton, Captain, Beresford, Charles, Turner, William, Flower, William H., Buchan, Alexander, Bruce, W. S.
Publikováno v:
The Geographical Journal, 1894 Jan 01. 3(1), 27-42.
Externí odkaz:
https://www.jstor.org/stable/1773600
Akademický článek
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Akademický článek
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K zobrazení výsledku je třeba se přihlásit.
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Autor:
Sandra E. Wilkinson, Janet L. Smith, Peter D. Davis, Harris William, David R. Vesey, John S. Nixon, Geoffrey Lawton, Christopher H. Hill, Trevor J. Hallam
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 4:1303-1308
A pharmacophore model for the localisation of the cationic binding site of bisindolylmaleimide PKC inhibitors is described. This model has been used to guide selection of further conformationally restricted tertiary amine analogues, culminating in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f5c019c3f6f3bbf635ab492fd02ea89b
https://doi.org/10.1016/s0960-894x(01)80349-8
https://doi.org/10.1016/s0960-894x(01)80349-8
Publikováno v:
Contributions to Plasma Physics. 34:175-179
The plasma transport, particle and energy fluxes, near the diverter plate with high recycling has been modeled by using an electron kinetic code (Fokker-Planck International) in conjunction with a two-fluid ambipolar code. We include the effects of i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4160efd139b68dd6197d0cd99b53e25
https://doi.org/10.1002/ctpp.2150340213
https://doi.org/10.1002/ctpp.2150340213
Publikováno v:
ChemInform. 22
A general Dieckmann/ring expansion approach to fused [1,2-a]indole systems is reported. This approach has allowed the synthesis of a large variety of substituted systems required for the preparation of a series of potent and selective inhibitors of P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2aecd85c651abb7f80e5e4b0be54c732
https://doi.org/10.1002/chin.199136180
https://doi.org/10.1002/chin.199136180
Autor:
I. Najera, Sophie Le Pogam, Graham Maile, Hobbs Christopher John, JH Merrett, Steven Swallow, Carl Laxton, Julie Hang, Rene Devos, Stewart J. Baker, Han Ma, Keshab Sarma, Julian Symons, Klaus Klumpp, David Bernard Smith, Vincent Leveque, David R. Vesey, Peter Blomgren, Mark D. Smith, Arkadius Pichota, Joseph Armstrong Martin, W.R. Jiang, Caroline Granycome, Nick Cammack
Publikováno v:
Bioorganicmedicinal chemistry letters. 17(9)
A series of 4'-substituted ribonucleoside derivatives has been prepared and evaluated for inhibition of hepatitis C virus (HCV) RNA replication in cell culture. The most potent and non-cytotoxic derivative was compound 28 (4'-azidocytidine, R1479) wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75a5e8af068b7cffce86f83a0bd1b0c8
https://pubmed.ncbi.nlm.nih.gov/17317178
https://pubmed.ncbi.nlm.nih.gov/17317178