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Isomer-specific activity of dichlorodyphenyltrichloroethane with estrogen receptor in adult and suckling estrogen reporter mice.
Di Lorenzo D, Villa R, Biasiotto G, Belloli S, Ruggeri G, Albertini A, Apostoli P, Raviscioni M, Ciana P, Maggi A. Di Lorenzo D, et al. Endocrinology. 2002 Dec;143(12):4544-51. doi: 10.1210/en.2002-220448. Endocrinology. 2002. PMID: 12446581
The DDT isomers p,p'-DDT [1,1,1-trichloro2,2-bis(p-chlorophenyl) ethane] and o,p'-DDT [1,1,1-trichloro-2(p-chlorophenyl)-2-(o-chlorophenyl) ethane] were specifically selected as a weak and a strong estrogen, respectively. ...In all the organs an …
The DDT isomers p,p'-DDT [1,1,1-trichloro2,2-bis(p-chlorophenyl) ethane] and o,p'-DDT [1,1,1-trichloro-2(p
The environmental chemical tributyltin chloride (TBT) shows both estrogenic and adipogenic activities in mice which might depend on the exposure dose.
Penza M, Jeremic M, Marrazzo E, Maggi A, Ciana P, Rando G, Grigolato PG, Di Lorenzo D. Penza M, et al. Toxicol Appl Pharmacol. 2011 Aug 15;255(1):65-75. doi: 10.1016/j.taap.2011.05.017. Epub 2011 Jun 12. Toxicol Appl Pharmacol. 2011. PMID: 21683088
Estrogen receptor-mediated transcriptional activity of genistein in the mouse testis.
Montani C, Penza M, Jeremic M, Rando G, Ciana P, Maggi A, La Sala G, De Felici M, Di Lorenzo D. Montani C, et al. Ann N Y Acad Sci. 2009 Apr;1163:475-7. doi: 10.1111/j.1749-6632.2008.03657.x. Ann N Y Acad Sci. 2009. PMID: 19456391
Whole body action of xenoestrogens with different chemical structures in estrogen reporter male mice.
Penza M, Bonetti E, Villa R, Ganzerla S, Bergonzi R, Biasiotto G, Caimi L, Apostoli P, Ciana P, Maggi A, Di Lorenzo D. Penza M, et al. Toxicology. 2004 Dec 1;205(1-2):65-73. doi: 10.1016/j.tox.2004.06.038. Toxicology. 2004. PMID: 15458791
The present work tested the estrogenic activity of three weak environmental estrogens p,p'DDT [1,1,1-trichloro-2,2-bis(p-chlorophenyl) ethane], p,p'DDE [1,1-dichloro-2,2-bis(p-chlorophenyl)ethylene] and betaBHC [beta-benzene-hexachloride] …
The present work tested the estrogenic activity of three weak environmental estrogens p,p'DDT [1,1,1-trichloro-2,2-bis(p
Target-specific action of organochlorine compounds in reproductive and nonreproductive tissues of estrogen-reporter male mice.
Villa R, Bonetti E, Penza ML, Iacobello C, Bugari G, Bailo M, Parolini O, Apostoli P, Caimi L, Ciana P, Maggi A, Di Lorenzo D. Villa R, et al. Toxicol Appl Pharmacol. 2004 Dec 1;201(2):137-48. doi: 10.1016/j.taap.2004.05.007. Toxicol Appl Pharmacol. 2004. PMID: 15541753
Three weak estrogens were studied: p,p'DDT [1,1,1-trichloro2,2-bis(p-chlorophenyl) ethane], p,p'DDE [1,1-dichloro-2,2-bis(p-chlorophenyl)ethylene], and betaBHC [beta-benzene-hexachloride]. ...During fasting, betaBHC, p,p'DDT …
Three weak estrogens were studied: p,p'DDT [1,1,1-trichloro2,2-bis(p-chlorophenyl) ethane], p,p'DDE [1,1- …
The dynamics of estrogen receptor activity.
Ciana P, Scarlatti F, Biserni A, Ottobrini L, Brena A, Lana A, Zagari F, Lucignani G, Maggi A. Ciana P, et al. Maturitas. 2006 Jul 20;54(4):315-20. doi: 10.1016/j.maturitas.2006.04.016. Epub 2006 Jun 5. Maturitas. 2006. PMID: 16753274 Review.
Multimodality imaging: novel pharmacological applications of reporter systems.
Stell A, Belcredito S, Ramachandran B, Biserni A, Rando G, Ciana P, Maggi A. Stell A, et al. Q J Nucl Med Mol Imaging. 2007 Jun;51(2):127-38. Q J Nucl Med Mol Imaging. 2007. PMID: 17420714 Review.
Molecular imaging: a new way to study molecular processes in vivo.
Ottobrini L, Ciana P, Biserni A, Lucignani G, Maggi A. Ottobrini L, et al. Mol Cell Endocrinol. 2006 Feb 26;246(1-2):69-75. doi: 10.1016/j.mce.2005.11.013. Epub 2006 Jan 4. Mol Cell Endocrinol. 2006. PMID: 16388894 Review.
Reporter mice for the study of long-term effects of drugs and toxic compounds.
Rizzi N, Ramachandran B, Vantaggiato C, Ciana P, Maggi A. Rizzi N, et al. Methods Mol Biol. 2014;1204:45-58. doi: 10.1007/978-1-4939-1346-6_5. Methods Mol Biol. 2014. PMID: 25182760
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