Search Results - (Author, Cooperation:F. Berardinelli)
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1L. Senovilla ; I. Vitale ; I. Martins ; M. Tailler ; C. Pailleret ; M. Michaud ; L. Galluzzi ; S. Adjemian ; O. Kepp ; M. Niso-Santano ; S. Shen ; G. Marino ; A. Criollo ; A. Boileve ; B. Job ; S. Ladoire ; F. Ghiringhelli ; A. Sistigu ; T. Yamazaki ; S. Rello-Varona ; C. Locher ; V. Poirier-Colame ; M. Talbot ; A. Valent ; F. Berardinelli ; A. Antoccia ; F. Ciccosanti ; G. M. Fimia ; M. Piacentini ; A. Fueyo ; N. L. Messina ; M. Li ; C. J. Chan ; V. Sigl ; G. Pourcher ; C. Ruckenstuhl ; D. Carmona-Gutierrez ; V. Lazar ; J. M. Penninger ; F. Madeo ; C. Lopez-Otin ; M. J. Smyth ; L. Zitvogel ; M. Castedo ; G. Kroemer
American Association for the Advancement of Science (AAAS)
Published 2012Staff ViewPublication Date: 2012-09-29Publisher: American Association for the Advancement of Science (AAAS)Print ISSN: 0036-8075Electronic ISSN: 1095-9203Topics: BiologyChemistry and PharmacologyComputer ScienceMedicineNatural Sciences in GeneralPhysicsKeywords: Animals ; Calreticulin/immunology ; Cell Line, Tumor ; Common Variable Immunodeficiency/genetics ; DNA, Neoplasm/analysis/genetics ; Endoplasmic Reticulum Stress/*immunology ; Eukaryotic Initiation Factor-2/metabolism ; Humans ; Immunocompetence ; *Immunologic Surveillance ; Mice ; Mice, Inbred BALB C ; Neoplasms/chemically induced/*genetics/*immunology ; Phosphorylation ; *PloidiesPublished by: -
2Berardinelli, F. M. ; Dolce, T. J. ; Walling, Cheves
New York, NY [u.a.] : Wiley-Blackwell
Published 1965Staff ViewISSN: 0021-8995Keywords: Chemistry ; Polymer and Materials ScienceSource: Wiley InterScience Backfile Collection 1832-2000Topics: Chemistry and PharmacologyMechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision MechanicsPhysicsNotes: Acetal copolymers prepared from trioxane and ethylene oxide consist of polyoxymethylene segments with oxyethylene units distributed in the chain. These oxyethylene units profoundly affect the thermal and chemical behavior of the polymer. The presence of the oxyethylene units renders the copolymer amenable to thermal or base hydrolytic treatment which results in a final product with stable endgroups. The copolymers so obtained are significantly more stable, thermally and chemically, than acetylated polyoxymethylene homopolymer.Additional Material: 3 Ill.Type of Medium: Electronic ResourceURL: -
3Collins, G. L. ; Greene, R. K. ; Berardinelli, F. M. ; Ray, W. H.
New York : Wiley-Blackwell
Published 1981Staff ViewISSN: 0360-6376Keywords: Physics ; Polymer and Materials ScienceSource: Wiley InterScience Backfile Collection 1832-2000Topics: Chemistry and PharmacologyNotes: A comprehensive mechanistic scheme that accounts for the unique experimental features of the copolymerization of bulk trioxane (TOX) with 2% (wt/wt) ethylene oxide (EO) was developed. The formation of the primary initiating species is shown as the diffusion-limited reaction of trace water with boron triflouride dibutyletherate [BF3O(Bu)2] to form a Bronsted acid. This acid complexes principally with the more basic EO and partly with the less basic TOX. The acid-complexed TOX depolymerizes to formaldehyde which can react with acid-complexed EO in an insertion reaction to form an acid-complexed dioxolane. Further insertion of formaldehyde yields an acid-complexed trioxepane. This sequence is generalized into a propagation scheme that involves propagation by expansion and ring opening. Displacement of complexed dioxolane and trioxepane can occur in the event that the more basic EO attacks the oxonium-active site at the reactive position outside the oxonium ring. These displacement reactions account for the observation of formation of dioxolane and trioxepane. The polymerization of formaldehyde is not considered significant until all EO has been consumed. During the latter stages of polymerization, cyclic oxonium-active sites are transformed into oxocarbenium sites that are stabilized by complexation with the polymer chain. This complexation is the origin of the phenomena of transacetalization and hydride transfer.Additional Material: 3 Ill.Type of Medium: Electronic ResourceURL: