Zobrazeno 1 - 6
of 6
pro vyhledávání: '"William C. Curtiss"'
Autor:
Gunther Stahl, Phillip Cruz, Richard D. Cramer, Farhad Soltanshahi, Brian Campbell, William C. Curtiss, Brian B. Masek
Publikováno v:
ChemInform. 40
Multiple R-groups (monovalent fragments) are implicitly accessible within most of the molecular structures that populate large structural databases. R-group searching would desirably consider pIC50 contribution forecasts as well as ligand similaritie
Autor:
William C. Curtiss, Richard D. Cramer, Brian B. Masek, Gunther Stahl, Phillip Cruz, Brian Campbell, Farhad Soltanshahi
Publikováno v:
Journal of chemical information and modeling. 48(11)
Multiple R-groups (monovalent fragments) are implicitly accessible within most of the molecular structures that populate large structural databases. R-group searching would desirably consider pIC50 contribution forecasts as well as ligand similaritie
Autor:
William C. Curtiss, Jeffrey A. Kramer, Kyle L. Kolaja, Carmen J. Jackson, Sandra W. Curtiss, Eric A. G. Blomme, Carl L. Alden, Roderick T. Bunch, Julio C. Davila
Publikováno v:
Chemical research in toxicology. 17(4)
Currently, the only way to identify nongenotoxic hepatocarcinogens is through long-term repeat dose studies such as the 2 year rodent carcinogenicity assay. Such assays are both time consuming and expensive and require large amounts of active pharmac
Autor:
Richard D. Cramer, Phillip Cruz, Gunther Stahl, William C. Curtiss, Brian Campbell, Brian B. Masek, Farhad Soltanshahi
Publikováno v:
Journal of Chemical Information & Modeling; Nov2008, Vol. 48 Issue 11, p2180-2195, 16p
Autor:
William C. Curtiss, John N. Vournakis
Publikováno v:
Journal of Molecular Evolution. 20:351-361
Eukaryotic 5S rRNA sequences from 34 diverse species were compared by the following method: (1) The sequences were aligned; (2) the positions of substitutions were located by comparison of all possible pairs of sequences; (3) the substitution sites w
The 5S rRNAs from Bombyx mori and Dictyostelium discoideum were end-labeled with [32-P] at either the 5' or 3' end and sequenced using enzymatic digestion. The secondary structure of these molecules was studied using the single-strand specific S1 nuc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::94b016eca644fc080c0977c693435a24
https://europepmc.org/articles/PMC326164/
https://europepmc.org/articles/PMC326164/