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M Jarman

Showing results (131-140 of 189) with videos related to

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Bioorganic & Medicinal Chemistry Letters|March 31, 1999
Solid-phase synthesis of novel inhibitors of farnesyl transferaseA M Barber, I R Hardcastle, M G Rowlands, et al.
Journal of Medicinal Chemistry|October 13, 1995
Esters of 3-pyridylacetic acid that combine potent inhibition of 17 alpha-hydroxylase/C17,20-lyase (cytochrome P45017 alpha) with resistance to esterase hydrolysisM G Rowlands, S E Barrie, F Chan, et al.
British Journal of Cancer|January 1, 1997
The novel anti-oestrogen idoxifene inhibits the growth of human MCF-7 breast cancer xenografts and reduces the frequency of acquired anti-oestrogen resistanceS R Johnston, S Riddler, B P Haynes, et al.
Biochemical Pharmacology|August 15, 1973
Metabolism of aniline mustard (N,N-di-(2-chloroethyl)aniline)T A Connors, P B Farmer, A B Foster, et al.
Chemico-Biological Interactions|December 1, 1979
The metabolism of deuterated analogues of chlorambucil by the ratP B Farmer, A B Foster, M Jarman, et al.
Journal of Medicinal Chemistry|September 1, 1987
Analogues of 3-ethyl-3-(4-pyridyl)piperidine-2,6-dione as selective inhibitors of aromatase: derivatives with variable 1-alkyl and 3-alkyl substituentsC S Leung, M G Rowlands, M Jarman, et al.
Journal of Enzyme Inhibition|January 1, 1994
Evaluation of some 4-fluoro- and 4-cyano derivatives of delta 4,3-ketosteroids as inhibitors of testosterone 5 alpha-reductaseM Jarman, S E Barrie, J Houghton, et al.
Environmental Pollution (Barking, Essex : 1987)|January 1, 1993
Organochlorines, including chlordane compounds and their metabolites, in peregrine-falcon, prairie-falcon, and clapper-rail eggs from the USAW M Jarman, R J Norstrom, M Simon, et al.
Biomedical Mass Spectrometry|April 1, 1974
Observations on the mechanism of hydroxylation of cyclophosphamide by rat liver microsomes: the metabolism of cyclophosphamide-4-d2T A Connors, P J Cox, P B Farmer, et al.
Carcinogenesis|August 1, 1994
Reduced genotoxicity of [D5-ethyl]-tamoxifen implicates alpha-hydroxylation of the ethyl group as a major pathway of tamoxifen activation to a liver carcinogenD H Phillips, G A Potter, M N Horton, et al.
Pageof 19

Showing results (131-140 of 189) with videos related to

Sort By:
Pageof 19
Bioorganic & Medicinal Chemistry Letters|March 31, 1999
Solid-phase synthesis of novel inhibitors of farnesyl transferaseA M Barber, I R Hardcastle, M G Rowlands, et al.
Journal of Medicinal Chemistry|October 13, 1995
Esters of 3-pyridylacetic acid that combine potent inhibition of 17 alpha-hydroxylase/C17,20-lyase (cytochrome P45017 alpha) with resistance to esterase hydrolysisM G Rowlands, S E Barrie, F Chan, et al.
British Journal of Cancer|January 1, 1997
The novel anti-oestrogen idoxifene inhibits the growth of human MCF-7 breast cancer xenografts and reduces the frequency of acquired anti-oestrogen resistanceS R Johnston, S Riddler, B P Haynes, et al.
Biochemical Pharmacology|August 15, 1973
Metabolism of aniline mustard (N,N-di-(2-chloroethyl)aniline)T A Connors, P B Farmer, A B Foster, et al.
Chemico-Biological Interactions|December 1, 1979
The metabolism of deuterated analogues of chlorambucil by the ratP B Farmer, A B Foster, M Jarman, et al.
Journal of Medicinal Chemistry|September 1, 1987
Analogues of 3-ethyl-3-(4-pyridyl)piperidine-2,6-dione as selective inhibitors of aromatase: derivatives with variable 1-alkyl and 3-alkyl substituentsC S Leung, M G Rowlands, M Jarman, et al.
Journal of Enzyme Inhibition|January 1, 1994
Evaluation of some 4-fluoro- and 4-cyano derivatives of delta 4,3-ketosteroids as inhibitors of testosterone 5 alpha-reductaseM Jarman, S E Barrie, J Houghton, et al.
Environmental Pollution (Barking, Essex : 1987)|January 1, 1993
Organochlorines, including chlordane compounds and their metabolites, in peregrine-falcon, prairie-falcon, and clapper-rail eggs from the USAW M Jarman, R J Norstrom, M Simon, et al.
Biomedical Mass Spectrometry|April 1, 1974
Observations on the mechanism of hydroxylation of cyclophosphamide by rat liver microsomes: the metabolism of cyclophosphamide-4-d2T A Connors, P J Cox, P B Farmer, et al.
Carcinogenesis|August 1, 1994
Reduced genotoxicity of [D5-ethyl]-tamoxifen implicates alpha-hydroxylation of the ethyl group as a major pathway of tamoxifen activation to a liver carcinogenD H Phillips, G A Potter, M N Horton, et al.
Pageof 19