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17beta-hydroxysteroid dehydrogenase Type 1, and not Type 12, is a target for endocrine therapy of hormone-dependent breast cancer
17beta-hydroxysteroid dehydrogenase Type 1, and not Type 12, is a target for endocrine therapy of hormone-dependent breast cancer
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17beta-hydroxysteroid dehydrogenase Type 1, and not Type 12, is a target for endocrine therapy of hormone-dependent breast cancer

Day, Joanna M ; Foster, Paul A ; Tutill, Helena J ; Parsons, Michael F C ; Newman, Simon P ; Chander, Surinder K ; Allan, Gillian M ; Lawrence, Harshani R ; Vicker, Nigel ; Potter, Barry V L ; Reed, Michael J ; Purohit, Atul

International journal of cancer, 2008-05, Vol.122 (9), p.1931 [Periódico revisado por pares]

United States

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2
2-MeOE2bisMATE and 2-EtE2bisMATE induce cell cycle arrest and apoptosis in breast cancer xenografts as shown by a novel ex vivo technique
2-MeOE2bisMATE and 2-EtE2bisMATE induce cell cycle arrest and apoptosis in breast cancer xenografts as shown by a novel ex vivo technique
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2-MeOE2bisMATE and 2-EtE2bisMATE induce cell cycle arrest and apoptosis in breast cancer xenografts as shown by a novel ex vivo technique

Foster, Paul A. ; Ho, Yaik T. ; Newman, Simon P. ; Kasprzyk, Philip G. ; Leese, Mathew P. ; Potter, Barry V. L. ; Reed, Michael J. ; Purohit, Atul

Breast cancer research and treatment, 2008-09, Vol.111 (2), p.251-260 [Periódico revisado por pares]

Boston: Springer US

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3
2-Methoxyoestradiol-3,17-O,O-bis-sulphamate and 2-deoxy-D-glucose in combination: a potential treatment for breast and prostate cancer
2-Methoxyoestradiol-3,17-O,O-bis-sulphamate and 2-deoxy-D-glucose in combination: a potential treatment for breast and prostate cancer
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2-Methoxyoestradiol-3,17-O,O-bis-sulphamate and 2-deoxy-D-glucose in combination: a potential treatment for breast and prostate cancer

Tagg, S L C ; Foster, P A ; Leese, M P ; Potter, B V L ; Reed, M J ; Purohit, A ; Newman, S P

British journal of cancer, 2008-12, Vol.99 (11), p.1842-1848 [Periódico revisado por pares]

England: Nature Publishing Group

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4
2-Substituted Estradiol Bis-sulfamates, Multitargeted Antitumor Agents:  Synthesis, In Vitro SAR, Protein Crystallography, and In Vivo Activity
2-Substituted Estradiol Bis-sulfamates, Multitargeted Antitumor Agents:  Synthesis, In Vitro SAR, Protein Crystallography, and In Vivo Activity
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2-Substituted Estradiol Bis-sulfamates, Multitargeted Antitumor Agents:  Synthesis, In Vitro SAR, Protein Crystallography, and In Vivo Activity

Leese, Mathew P ; Leblond, Bertrand ; Smith, Andrew ; Newman, Simon P ; Di Fiore, Anna ; De Simone, Giuseppina ; Supuran, Claudiu T ; Purohit, Atul ; Reed, Michael J ; Potter, Barry V. L

Journal of medicinal chemistry, 2006-12, Vol.49 (26), p.7683-7696 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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5
26S proteasome inhibition induces apoptosis and limits growth of human pancreatic cancer
26S proteasome inhibition induces apoptosis and limits growth of human pancreatic cancer
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26S proteasome inhibition induces apoptosis and limits growth of human pancreatic cancer

Shah, Shimul A. ; Potter, Michael W. ; McDade, Theodore P. ; Ricciardi, Rocco ; Perugini, Richard A. ; Elliott, Peter J. ; Adams, Julian ; Callery, Mark P.

Journal of cellular biochemistry, 2001-07, Vol.82 (1), p.110-122 [Periódico revisado por pares]

New York: John Wiley & Sons, Inc

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6
3,17-Disubstituted 2-Alkylestra-1,3,5(10)-trien-3-ol Derivatives:  Synthesis, In Vitro and In Vivo Anticancer Activity
3,17-Disubstituted 2-Alkylestra-1,3,5(10)-trien-3-ol Derivatives:  Synthesis, In Vitro and In Vivo Anticancer Activity
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3,17-Disubstituted 2-Alkylestra-1,3,5(10)-trien-3-ol Derivatives:  Synthesis, In Vitro and In Vivo Anticancer Activity

Bubert, Christian ; Leese, Mathew P ; Mahon, Mary F ; Ferrandis, Eric ; Regis-Lydi, Sandra ; Kasprzyk, Philip G ; Newman, Simon P ; Ho, Yaik T ; Purohit, Atul ; Reed, Michael J ; Potter, Barry V. L

Journal of medicinal chemistry, 2007-09, Vol.50 (18), p.4431-4443 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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7
A-Ring-Substituted Estrogen-3-O-sulfamates:  Potent Multitargeted Anticancer Agents
A-Ring-Substituted Estrogen-3-O-sulfamates:  Potent Multitargeted Anticancer Agents
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A-Ring-Substituted Estrogen-3-O-sulfamates:  Potent Multitargeted Anticancer Agents

Leese, Mathew P ; Hejaz, Hatem A. M ; Mahon, Mary F ; Newman, Simon P ; Purohit, Atul ; Reed, Michael J ; Potter, Barry V. L

Journal of medicinal chemistry, 2005-08, Vol.48 (16), p.5243-5256 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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8
Abnormal Contractile Function in Transgenic Mice Expressing a Familial Hypertrophic Cardiomyopathy-linked Troponin T (I79N) Mutation
Abnormal Contractile Function in Transgenic Mice Expressing a Familial Hypertrophic Cardiomyopathy-linked Troponin T (I79N) Mutation
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Abnormal Contractile Function in Transgenic Mice Expressing a Familial Hypertrophic Cardiomyopathy-linked Troponin T (I79N) Mutation

Miller, Todd ; Szczesna, Danuta ; Housmans, Philippe R. ; Zhao, Jiaju ; de Freitas, Fatima ; Gomes, Aldrin V. ; Culbreath, Lieneke ; McCue, Jessica ; Wang, Yi ; Xu, Yuanyuan ; Kerrick, W. Glenn L. ; Potter, James D.

The Journal of biological chemistry, 2001-02, Vol.276 (6), p.3743-3755 [Periódico revisado por pares]

United States: Elsevier Inc

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9
Activation and antitumor activity of CPT-11 in plasma esterase-deficient mice
Activation and antitumor activity of CPT-11 in plasma esterase-deficient mice
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Activation and antitumor activity of CPT-11 in plasma esterase-deficient mice

MORTON, Christopher L ; IACONO, Lisa ; HYATT, Janice L ; TAYLOR, Kody R ; CHESHIRE, Pamela J ; HOUGHTON, Peter J ; DANKS, Mary K ; STEWART, Clinton F ; POTTER, Philip M

Cancer chemotherapy and pharmacology, 2005-12, Vol.56 (6), p.629-636 [Periódico revisado por pares]

Berlin: Springer

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10
Adamantyl Ethanone Pyridyl Derivatives: Potent and Selective Inhibitors of Human 11β-Hydroxysteroid Dehydrogenase Type 1
Adamantyl Ethanone Pyridyl Derivatives: Potent and Selective Inhibitors of Human 11β-Hydroxysteroid Dehydrogenase Type 1
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Adamantyl Ethanone Pyridyl Derivatives: Potent and Selective Inhibitors of Human 11β-Hydroxysteroid Dehydrogenase Type 1

Su, Xiangdong ; Pradaux-Caggiano, Fabienne ; Vicker, Nigel ; Thomas, Mark P. ; Halem, Heather ; Culler, Michael D. ; Potter, Barry V. L.

ChemMedChem, 2011-09, Vol.6 (9), p.1616-1629 [Periódico revisado por pares]

Weinheim: WILEY-VCH Verlag

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