Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Eric J. Schurter"'
Publikováno v:
Journal of Chemical Education. 97:4097-4102
In the first-year general chemistry laboratory course, instrumental data collection involving sample quantification has often been limited to absorption spectroscopy due to the inaccessibility of e...
Publikováno v:
Journal of Chemical Education. 88:1419-1421
This multi-technique experiment with a forensic theme was developed for a nonscience-major chemistry course. The students are provided with solid samples and informed that the samples are either co...
Autor:
Claudia Kent, Patricia Gee, Subramaniam Sanker, Eric J. Schurter, Erik R. P. Zuiderweg, Young-Seo Park
Publikováno v:
Journal of Biological Chemistry. 272:15161-15166
The CTP:glycerol-3-phosphate cytidylyltransferase (GCT) of Bacillus subtilis has been shown to be similar in primary structure to the CTP:phosphocholine cytidylyltransferases of several organisms. To identify the residues of this cytidylyltransferase
Autor:
Herman J. C. Yeh, Donald M. Jerina, David G. Gorenstein, Haruhiko Yagi, Xiaohong Liu, Eric J. Schurter, Jane M. Sayer
Publikováno v:
Polycyclic Aromatic Compounds. 10:145-152
The principal adducts formed between DNA and polycyclic aromatic hydrocarbon diol epoxides result from N-alkylation of the exocyclic amino groups of the purine bases by the benzylic carbon atom of the epoxide. To date, the solution conformations of m
Autor:
David G. Gorenstein, Mahesh K. Lakshman, Eric J. Schurter, A. S. Altieri, Haruhiko Yagi, R. A. Byrd, H. J. C. Yeh, Jane M. Sayer, Xiaohong Liu, Donald M. Jerina
Publikováno v:
Biochemistry. 34:13570-13581
A nonanucleotide, d(G1G2T3C4[BaP]A5C6G7A8G9), in which (+)-(7R,8S,9S,10R)-7,8-dihydroxy-9,10-epoxy-7,8,9,10- tetrahydrobenzo[a]pyrene (7-hydroxyl group and epoxide oxygen are trans) is covalently bonded to the exocyclic N6-amino group of deoxyadenosi
Autor:
Toshinari Oh-hara, Eric J. Schurter, David G. Gorenstein, Jane M. Sayer, Donald M. Jerina, Bruce A. Luxon, Herman J. E. Yeh, Haruhiko Yagi
Publikováno v:
Biochemistry. 34:9009-9020
The solution structure of a modified undecamer duplex containing (-)-(7R,8S,9R,10S)-7,8-dihydroxy-9,10-epoxy-7,8,9,10-tetrahydrobenzo[a] pyrene covalently bonded through trans ring opening at C10 of the epoxide by the N6-amino group of deoxyadenosine
Autor:
Mahesh K. Lakshman, Donald M. Jerina, Jane M. Sayer, David G. Gorenstein, Eric J. Schurter, Herman J. C. Yeh, Haruhiko Yagi
Publikováno v:
Biochemistry. 34:1364-1375
A nonanucleotide in which (-)-(7S,8R,9R,10S)-7,8-dihydroxy-9,10-epoxy- 7,8,9,10-tetrahydrobenzo[a]pyrene (7-hydroxy group and epoxide oxygen are trans) is covalently bonded to the exocyclic N6-amino group of deoxyadenosine through trans addition at C