Rokita SE - Search Results

1

Unraveling Reversible DNA Cross-Links with a Biological Machine.

Byrne SR, Rokita SE. Byrne SR, et al. Among authors: rokita se. Chem Res Toxicol. 2020 Nov 16;33(11):2903-2913. doi: 10.1021/acs.chemrestox.0c00413. Epub 2020 Nov 5. Chem Res Toxicol. 2020. PMID: 33147957 Free PMC article.

2

Nickel-dependent oxidative cross-linking of a protein.

Gill G, Richter-Rusli AA, Ghosh M, Burrows CJ, Rokita SE. Gill G, et al. Among authors: rokita se. Chem Res Toxicol. 1997 Mar;10(3):302-9. doi: 10.1021/tx960170i. Chem Res Toxicol. 1997. PMID: 9084910

3

Sequence-specific delivery of a quinone methide intermediate to the major groove of DNA.

Zhou Q, Pande P, Johnson AE, Rokita SE. Zhou Q, et al. Among authors: rokita se. Bioorg Med Chem. 2001 Sep;9(9):2347-54. doi: 10.1016/s0968-0896(01)00151-1. Bioorg Med Chem. 2001. PMID: 11553475

4

2'-Deoxyguanosine reacts with a model quinone methide at multiple sites.

Veldhuyzen WF, Lam YF, Rokita SE. Veldhuyzen WF, et al. Among authors: rokita se. Chem Res Toxicol. 2001 Sep;14(9):1345-51. doi: 10.1021/tx0101043. Chem Res Toxicol. 2001. PMID: 11559052

5

Thermodynamic versus kinetic products of DNA alkylation as modeled by reaction of deoxyadenosine.

Veldhuyzen WF, Shallop AJ, Jones RA, Rokita SE. Veldhuyzen WF, et al. Among authors: rokita se. J Am Chem Soc. 2001 Nov 14;123(45):11126-32. doi: 10.1021/ja011686d. J Am Chem Soc. 2001. PMID: 11697955

6

A transient product of DNA alkylation can be stabilized by binding localization.

Veldhuyzen WF, Pande P, Rokita SE. Veldhuyzen WF, et al. Among authors: rokita se. J Am Chem Soc. 2003 Nov 19;125(46):14005-13. doi: 10.1021/ja036943o. J Am Chem Soc. 2003. PMID: 14611237

7

Conjugation of a hairpin pyrrole-imidazole polyamide to a quinone methide for control of DNA cross-linking.

Kumar D, Veldhuyzen WF, Zhou Q, Rokita SE. Kumar D, et al. Among authors: rokita se. Bioconjug Chem. 2004 Jul-Aug;15(4):915-22. doi: 10.1021/bc049941h. Bioconjug Chem. 2004. PMID: 15264882

8

Time-dependent evolution of adducts formed between deoxynucleosides and a model quinone methide.

Weinert EE, Frankenfield KN, Rokita SE. Weinert EE, et al. Among authors: rokita se. Chem Res Toxicol. 2005 Sep;18(9):1364-70. doi: 10.1021/tx0501583. Chem Res Toxicol. 2005. PMID: 16167827

9

Substituents on quinone methides strongly modulate formation and stability of their nucleophilic adducts.

Weinert EE, Dondi R, Colloredo-Melz S, Frankenfield KN, Mitchell CH, Freccero M, Rokita SE. Weinert EE, et al. Among authors: rokita se. J Am Chem Soc. 2006 Sep 13;128(36):11940-7. doi: 10.1021/ja062948k. J Am Chem Soc. 2006. PMID: 16953635 Free PMC article.

10

Dynamic cross-linking is retained in duplex DNA after multiple exchange of strands.

Wang H, Rokita SE. Wang H, et al. Among authors: rokita se. Angew Chem Int Ed Engl. 2010 Aug 9;49(34):5957-60. doi: 10.1002/anie.201001597. Angew Chem Int Ed Engl. 2010. PMID: 20632342 No abstract available.

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