R A Milsted|M Jarman - JoVE Visualize

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Anti-Cancer Drug Design|November 1, 1986

Analogues of tamoxifen: the role of the basic side-chain. Applications of a whole-cell oestrogen-receptor binding assay to N-oxides and quaternary saltsM Jarman, O T Leung, G Leclercq, et al.

Steroids|July 1, 1987

4-Hydroxyandrostenedione treatment for postmenopausal patients with advanced breast cancerR C Coombes, P E Goss, M Dowsett, et al.

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.

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.

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.

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Showing results (91-100 of 142) with videos related to

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Anti-Cancer Drug Design|November 1, 1986

Analogues of tamoxifen: the role of the basic side-chain. Applications of a whole-cell oestrogen-receptor binding assay to N-oxides and quaternary saltsM Jarman, O T Leung, G Leclercq, et al.

Steroids|July 1, 1987

4-Hydroxyandrostenedione treatment for postmenopausal patients with advanced breast cancerR C Coombes, P E Goss, M Dowsett, et al.

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.

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.

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.

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