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T H Koch

Showing results (1-10 of 38) with videos related to

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Chemical Research in Toxicology|January 1, 1991
Redox chemistry of anthracycline antitumor drugs and use of captodative radicals as tools for its elucidation and controlG Gaudiano, T H Koch
Critical Reviews in Biochemistry and Molecular Biology|January 1, 1997
Photocross-linking of nucleic acids to associated proteinsK M Meisenheimer, T H Koch
Current Medicinal Chemistry|February 15, 2001
Nuclear targeting and retention of anthracycline antitumor drugs in sensitive and resistant tumor cellsD J Taatjes, T H Koch
Anticancer Research|June 16, 1999
Growth inhibition, nuclear uptake, and retention of anthracycline-formaldehyde conjugates in prostate cancer cells relative to clinical anthracyclinesD J Taatjes, T H Koch
Anticancer Research|November 29, 2001
Doxorubicin-formaldehyde conjugate, doxoform: induction of apoptosis relative to doxorubicinP J Burke, T H Koch
Photochemistry and Photobiology|December 1, 1987
Photochemical coupling of 5-bromouracil to tryptophan, tyrosine and histidine, peptide-like derivatives in aqueous fluid solutionT M Dietz, T H Koch
Photochemistry and Photobiology|February 1, 1989
Photochemical reduction of 5-bromouracil by cysteine derivatives and coupling of 5-bromouracil to cystine derivativesT M Dietz, T H Koch
Chemical Research in Toxicology|September 26, 1997
Production of formaldehyde and DNA-adriamycin or DNA-daunomycin adducts, initiated through redox chemistry of dithiothreitol/iron, xanthine oxidase/NADH/iron, or glutathione/ironD J Taatjes, G Gaudiano, T H Koch
Journal of Medicinal Chemistry|August 1, 1997
Doxoform and Daunoform: anthracycline-formaldehyde conjugates toxic to resistant tumor cellsD J Fenick, D J Taatjes, T H Koch
Journal of Medicinal Chemistry|May 9, 1998
Epidoxoform: a hydrolytically more stable anthracycline-formaldehyde conjugate toxic to resistant tumor cellsD J Taatjes, D J Fenick, T H Koch
Pageof 4

Showing results (1-10 of 38) with videos related to

Sort By:
Pageof 4
Chemical Research in Toxicology|January 1, 1991
Redox chemistry of anthracycline antitumor drugs and use of captodative radicals as tools for its elucidation and controlG Gaudiano, T H Koch
Critical Reviews in Biochemistry and Molecular Biology|January 1, 1997
Photocross-linking of nucleic acids to associated proteinsK M Meisenheimer, T H Koch
Current Medicinal Chemistry|February 15, 2001
Nuclear targeting and retention of anthracycline antitumor drugs in sensitive and resistant tumor cellsD J Taatjes, T H Koch
Anticancer Research|June 16, 1999
Growth inhibition, nuclear uptake, and retention of anthracycline-formaldehyde conjugates in prostate cancer cells relative to clinical anthracyclinesD J Taatjes, T H Koch
Anticancer Research|November 29, 2001
Doxorubicin-formaldehyde conjugate, doxoform: induction of apoptosis relative to doxorubicinP J Burke, T H Koch
Photochemistry and Photobiology|December 1, 1987
Photochemical coupling of 5-bromouracil to tryptophan, tyrosine and histidine, peptide-like derivatives in aqueous fluid solutionT M Dietz, T H Koch
Photochemistry and Photobiology|February 1, 1989
Photochemical reduction of 5-bromouracil by cysteine derivatives and coupling of 5-bromouracil to cystine derivativesT M Dietz, T H Koch
Chemical Research in Toxicology|September 26, 1997
Production of formaldehyde and DNA-adriamycin or DNA-daunomycin adducts, initiated through redox chemistry of dithiothreitol/iron, xanthine oxidase/NADH/iron, or glutathione/ironD J Taatjes, G Gaudiano, T H Koch
Journal of Medicinal Chemistry|August 1, 1997
Doxoform and Daunoform: anthracycline-formaldehyde conjugates toxic to resistant tumor cellsD J Fenick, D J Taatjes, T H Koch
Journal of Medicinal Chemistry|May 9, 1998
Epidoxoform: a hydrolytically more stable anthracycline-formaldehyde conjugate toxic to resistant tumor cellsD J Taatjes, D J Fenick, T H Koch
Pageof 4