131,228 research outputs found
Aspetti della terapia nel Corpus Hippocraticum
No full textAtti del «IX Colloque International Hippocratique» (Pisa 25-29 settembre 1996), a cura di I. Garofalo, A. L., D. Manetti, A. Roselli, Accademia toscana di Scienze e Lettere «La Colombaria», vol. 183, Leo S. Olschki, Firenz
On the adjoint map of homotopy abelian Dg-lie algebras
No full textWe prove that a differential graded Lie algebra is homotopy abelian if its adjoint map into its cochain complex of derivations is trivial in cohomology. The converse is true for cofibrant algebras and false in general
R&D and innovative health technologies: towards the definition of a methodology for an Early Assessment
No full textSome structures for neural based A/D conversion
No full textSome structures for neural based A/D conversion are presented. Experimental results on the proposed topologies are reported. The structures described are particularly suitable for the realisation of a low-cost, easily expandable voltmeter for consumer application
Homotopy abelianity of the DG-Lie algebra controlling deformations of pairs (variety with trivial canonical bundle, line bundle)
No full textWe investigate the deformations of pairs (X,L), where L is a line bundle on a smooth projective variety X, defined over an algebraically closed field of characteristic 0. In particular, we prove that the DG-Lie algebra controlling the deformations of the pair (X,L) is homotopy abelian whenever X has trivial canonical bundle, and so these deformations are unobstructed
W. Cavini, M. C. Donnini Macciò, M. S. Funghi, D. Manetti, Studi su papiri greci di logica e medicína (Firenze : Olschki, 1985)
No full textW. Cavini, M. C. Donnini Macciò, M. S. Funghi, D. Manetti, Studi su papiri greci di logica e medicína (Firenze : Olschki, 1985). In: Revue d'histoire des sciences, tome 41, n°2, 1988. pp. 216-217
Synthesis, biological evaluation, and SAR study of novel pyrazole analogues as inhibitors of Mycobacterium tuberculosis: Part 2. Synthesis of rigid pyrazolones
No full textTwo series of novel rigid pyrazolone derivatives were synthesized and evaluated as inhibitors of Mycobacterium tuberculosis (MTB), the causative agent of tuberculosis. Two of these compounds showed a high activity against MTB (MIC = 4 μg/mL). The newly synthesized pyrazolones were also computationally investigated to analyze if their properties fit the pharmacophoric model for antitubercular compounds previously built by us. The results are in agreement with those reported by us previously for a class of pyrazole analogues and confirm the fundamental role of the p-chlorophenyl moiety at C4 in the antimycobacterial activity
- …
