Search Results - (Author, Cooperation:G. Rodighiero)
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1M. J. Page ; M. Symeonidis ; J. D. Vieira ; B. Altieri ; A. Amblard ; V. Arumugam ; H. Aussel ; T. Babbedge ; A. Blain ; J. Bock ; A. Boselli ; V. Buat ; N. Castro-Rodriguez ; A. Cava ; P. Chanial ; D. L. Clements ; A. Conley ; L. Conversi ; A. Cooray ; C. D. Dowell ; E. N. Dubois ; J. S. Dunlop ; E. Dwek ; S. Dye ; S. Eales ; D. Elbaz ; D. Farrah ; M. Fox ; A. Franceschini ; W. Gear ; J. Glenn ; M. Griffin ; M. Halpern ; E. Hatziminaoglou ; E. Ibar ; K. Isaak ; R. J. Ivison ; G. Lagache ; L. Levenson ; N. Lu ; S. Madden ; B. Maffei ; G. Mainetti ; L. Marchetti ; H. T. Nguyen ; B. O'Halloran ; S. J. Oliver ; A. Omont ; P. Panuzzo ; A. Papageorgiou ; C. P. Pearson ; I. Perez-Fournon ; M. Pohlen ; J. I. Rawlings ; D. Rigopoulou ; L. Riguccini ; D. Rizzo ; G. Rodighiero ; I. G. Roseboom ; M. Rowan-Robinson ; M. Sanchez Portal ; B. Schulz ; D. Scott ; N. Seymour ; D. L. Shupe ; A. J. Smith ; J. A. Stevens ; M. Trichas ; K. E. Tugwell ; M. Vaccari ; I. Valtchanov ; M. Viero ; L. Vigroux ; L. Wang ; R. Ward ; G. Wright ; C. K. Xu ; M. Zemcov
Nature Publishing Group (NPG)
Published 2012Staff ViewPublication Date: 2012-05-12Publisher: Nature Publishing Group (NPG)Print ISSN: 0028-0836Electronic ISSN: 1476-4687Topics: BiologyChemistry and PharmacologyMedicineNatural Sciences in GeneralPhysicsPublished by: -
2Daddi, E. ; Renzini, A. ; Cassata, P. ; Vanzella, E. ; Pozzetti, L. ; Cristiani, S. ; Fontana, A. ; Rodighiero, G. ; Mignoli, M. ; Zamorani, G. ; Cimatti, A.
[s.l.] : Macmillian Magazines Ltd.
Published 2004Staff ViewISSN: 1476-4687Source: Nature Archives 1869 - 2009Topics: BiologyChemistry and PharmacologyMedicineNatural Sciences in GeneralPhysicsNotes: [Auszug] More than half of all stars in the local Universe are found in massive spheroidal galaxies, which are characterized by old stellar populations with little or no current star formation. In present models, such galaxies appear rather late in the history of the Universe as the culmination of a ...Type of Medium: Electronic ResourceURL: -
3Rodighiero, G. ; Musajo, L. ; Dall'acqua, F. ; Marciani, S. ; Caporale, G. ; Ciavatta, L.
Amsterdam : ElsevierStaff ViewISSN: 0005-2787Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002Topics: BiologyType of Medium: Electronic ResourceURL: -
4Staff View
ISSN: 0005-2787Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002Topics: BiologyType of Medium: Electronic ResourceURL: -
5Staff View
ISSN: 0014-5793Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002Topics: BiologyChemistry and PharmacologyPhysicsType of Medium: Electronic ResourceURL: -
6Staff View
ISSN: 0014-5793Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002Topics: BiologyChemistry and PharmacologyPhysicsType of Medium: Electronic ResourceURL: -
7Staff View
ISSN: 0040-4020Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002Topics: Chemistry and PharmacologyType of Medium: Electronic ResourceURL: -
8Staff View
ISSN: 0014-5793Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002Topics: BiologyChemistry and PharmacologyPhysicsType of Medium: Electronic ResourceURL: -
9Chandra, P. ; Marciani, S. ; Dall'Acqua, F. ; Vedaldi, D. ; Rodighiero, G. ; Biswa, R.K.
Amsterdam : ElsevierStaff ViewISSN: 0014-5793Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002Topics: BiologyChemistry and PharmacologyPhysicsType of Medium: Electronic ResourceURL: -
10Staff View
ISSN: 1420-9071Source: Springer Online Journal Archives 1860-2000Topics: BiologyMedicineNotes: Riassunto Le furocumarine possono legarsi in vitro al DNA ed, in misura molto minore, all'RNA. Per irradizione UV (3655 Å) in presenza di psoralene, tre virus a DNA sono stati inattivati, mentre nessun effetto è stato notato su altri tre virus ad RNA.Type of Medium: Electronic ResourceURL: -
11Staff View
ISSN: 1420-9071Source: Springer Online Journal Archives 1860-2000Topics: BiologyMedicineNotes: Riassunto Modificazioni negli spettri di fluorescenza si hanno irradiando (3655 Å) soluzioni di DNA o di nucleosidi e nucleotidi pirimidinici in presenza di furocumarine fotosensibilizzatrici. La formazione di nuovi composti nelle fotoreazioni tra psoralene e nucleosidi pirimidinici è stata confermata per cromatografia su carta.Type of Medium: Electronic ResourceURL: -
12Staff View
ISSN: 1420-9071Source: Springer Online Journal Archives 1860-2000Topics: BiologyMedicineType of Medium: Electronic ResourceURL: -
13Staff View
ISSN: 0040-4039Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002Topics: Chemistry and PharmacologyType of Medium: Electronic ResourceURL: -
14Staff View
ISSN: 1420-9071Source: Springer Online Journal Archives 1860-2000Topics: BiologyMedicineType of Medium: Electronic ResourceURL: -
15Staff View
ISSN: 1420-9071Source: Springer Online Journal Archives 1860-2000Topics: BiologyMedicineNotes: Riassunto Ricerche eseguite con bergaptene-O14CH3 confermano che tra questa sostanza ed il DNA avviene una fotoreazione in seguito ad irradiazione a 3655 å, che porta alla formazione di una stabile combinazione tra la furocumarina e lo stesso DNA.Type of Medium: Electronic ResourceURL: -
16Rodighiero, G. ; Musajo, L. ; Dall'Acqua, F. ; Marciani, S. ; Caporale, G. ; Ciavatta, M. L.
Springer
Published 1969Staff ViewISSN: 1420-9071Source: Springer Online Journal Archives 1860-2000Topics: BiologyMedicineNotes: Riassunto È stata determinata la fotoreattività con DNA nativo di un gruppo di furocumarine per irradiazione a 365 nm. I valori ottenuti sono risultati in accordo con quelli di attività fotosensibilizzatrice cutanea posseduti dalle stesse sostanze.Type of Medium: Electronic ResourceURL: -
17Staff View
ISSN: 1420-9071Source: Springer Online Journal Archives 1860-2000Topics: BiologyMedicineNotes: Riassunto Alcuni metil-derivati del psoralene hanno una attività fotosensibilizzatrice cutanea notevolmente più forte dello stesso psoralene, considerato finora la più attiva sostanza di questo gruppo. Il derivato, finora trovato con maggiore potere fotosensibilizzante è l'8-metilpsoralene.Type of Medium: Electronic ResourceURL: -
18Rodighiero, G. ; Dall'Acqua, F. ; Marciani, S. ; Chandra, P. ; Feller, H. ; Götz, A. ; Wacker, A.
Springer
Published 1971Staff ViewISSN: 1432-2099Source: Springer Online Journal Archives 1860-2000Topics: BiologyPhysicsNotes: Summary The angelicin-thymine photoadduct formed by irradiation (365 nm) of an aqueous solution of angelicin and tritiated thymine was isolated by preparative paper chromatography. Reirradiation of this photoadduct at wavelengths shorter than 334 nm splits the adduct, forming again the two parent compounds. A DNA-angelicin combination (8.30 μg angelicin per mg of DNA) was prepared by irradiating (365 nm) an aqueous solution of DNA with3H-angelicin. Reirradiation of this combination at wavelengths shorter than 312 nm releases3H-angelicin. The above mentioned conditions were employed to reactivate the photodamaged bacterial cells by angelicin. No reactivation was observed at shorter wavelengths; on the contrary, the lethality was higher after reirradiation. We conclude therefore, that the damage produced directly by the shorter wavelength radiations (formation of pyrimidine dimers) is greater than the small repair produced under our experimental conditions. Reirradiation of bacterial cells with visible light is a condition which activates the photoreactivating enzymes, which are able to provoke the cleavage of pyrimidine dimers. The inability to repair the photodamage caused by furocoumarins under these conditions suggests that this enzyme is highly specific for pyrimidine dimers. Though in both cases,i.e. pyrimidine-pyrimidine and pyrimidine-furocoumarine dimers a cyclo-butane ring is involved, the latter is not recognized by the photoreactivating enzyme.Type of Medium: Electronic ResourceURL: