Cotta-Ramusino

MI(25)113 M. Cotta Ramusino, M. Bartolomei, and L. Ruflni, J. Inclusion... 

Benigni, R., Andreoli, C., Conti, L., Tafani, P., Cotta-Ramusino, M., Carere, A., Crebelli, R. Quantitative structure-activity relationship models correctly predict the toxic and aneuploidizing properties of halogenated methanes in Aspergillus nidulans. Mutagenesis 1993, 8, 301-305. 

Benigni, R., Passerini, L., Gallo, G., Giorgi, F., and Cotta-Ramusino, M., QSAR models for discriminating between mutagenic and nonmutagenic aromatic and heteroaromatic amines, Environ. Mol. Mutagenesis, 32, 75-83, 1998. 

Benigni R, Cotta-Ramusino M, Gallo G, Giorgi F, Giuliani A, Vari MR. Deriving a quantitative chirality measure from molecular similarity indices. / Med Chem 2000 43 3699-703. 

Cotta Ramusino, M., Benigni, R., Passerini, L. and Giuliani, A. (2003) Looking for an unambiguous geometrical definition of organic series from 3-D molecular similarity indices./. Chem. Inf. Comput. Sci., 43, 248-254. 

Benigni R, Cotta-Ramusino M, Giorgi F, Gallo G. Molecular similarity matrixes and quantitative structure-activity relationships a case study with methodological implications. J Med Chem 1995 38 629-635. 

Benigni, R. Cotta-Ramusino, M. Andreoli, C. Giuliani, A. Electrophilicity as measured by K. molecular determinants, relationship with other physical-chemical and quantum mechanical parameters, and ability to predict rodent carcinogenicity. Carcinogenesis 1992,13, 547-553. 

Bartolomei M, Bertocchi P, Cotta Ramusino M, Santucci N, Valvo L. Physico-chemical characterisation of the modifications I and II of (R,S) propranolol hydrochloride solubihty and dissolution studies. 7 Pharm Biomed Ana/1999 21 (2) 299-309. 

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