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pro vyhledávání: '"J. M. DENIS"'
Autor:
J M Denis, V Ganansia-Leymarie, Pierre Bischoff, Barbara Fischer, J. P. Bergerat, John Gueulette, S Benzina, Philippe Dufour
Publikováno v:
Canadian Journal of Physiology and Pharmacology. 82:140-145
L'utilisation de rayonnements a transfert lineique d'energie (TLE) eleve, tels que les neutrons rapides et les ions carbone (hadrontherapie) offre de prometteuses perspectives en radiotherapie. Bien qu'en combinant la radiotherapie et la chimiotherap
Akademický článek
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Autor:
Philippe Dufour, Pierre Bischoff, David Coelho, Holl, J M Denis, John Gueulette, J. P. Bergerat, Barbara Fischer
Publikováno v:
Canadian Journal of Physiology and Pharmacology. 80:644-649
The involvement of the tumor suppressor p53 gene in the sensitivity of many cell types towards low linear energy transfer (LET) radiation is now well established. However, little information is available on the relationship between p53 status of tumo
Autor:
J Mathieu, J M Denis, John Gueulette, David Coelho, I Florentin, Philippe Dufour, D. Weltin, Pierre Bischoff, V. Holl
Publikováno v:
Canadian Journal of Physiology and Pharmacology. 79:109-113
To assess the capacity of heavy ions to induce apoptosis in lymphocytes, mice have been irradiated with accelerated carbon ions (95 MeV/nucleon) at doses ranging from 0.1 to 4 Gy. Their spleens were removed 24 h later and gently dissociated to prepar
Autor:
Maciej Budzanowski, Stefaan Vynckier, Paweł Bilski, Michael P. R. Waligórski, J M Denis, T. Loncol, Pierre Scalliet, Pawel Olko
Publikováno v:
Radiation Protection Dosimetry. 84:179-184
Variation of Ti and Mg concentration is known to modify substantially the dosimetric characteristics of the standard LiF:Mg,Ti detector commonly used in radiotherapy. Preliminary studies conducted by the Institute of Nuclear Physics at Krakow suggest
Autor:
J. M. Denis, A. C. Gaumont
Publikováno v:
Chemical Reviews. 94:1413-1439
Publikováno v:
Synthesis. 1972:549-551
Publikováno v:
ChemInform. 42
Asymmetric formal [2 + 2] cycloaddition of N-sulfonylimines (I) and (IV) with allenoates (II) is efficiently catalyzed by a bifunctional glycinamide-containing quinidine organocatalyst to give azetidines (III) and (V), resp., in high enantioselectivi
Publikováno v:
Angewandte Chemie International Edition
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2011, 50 (23), pp.5356-5360. ⟨10.1002/anie.201100706⟩
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2011, 50 (23), pp.5356-5360. ⟨10.1002/anie.201100706⟩
Mix and go. The quinidine-amide (1)-catalyzed [2+2] cycloaddition between N-sulfonylimines (2) and alkyl 2,3-butadienoate (3) afforded the (R)-azetidines 4 in excellent yields and enantioselectivities. The (S)-enantiomer was obtained when a quinine-a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1370ac4f9518f7dab1cfcabb968b6379
https://hal.archives-ouvertes.fr/hal-00606163
https://hal.archives-ouvertes.fr/hal-00606163
Autor:
Raphael Olszewski, Hervé Reychler, Stefaan Vynckier, Francis Zech, L Frison, J M Denis, Guy Cosnard, Marcin Wisniewski
Publikováno v:
Clinical oral investigations. 17(1)
The purpose of this study is to compare the reproducibility of three-dimensional cephalometric landmarks on three-dimensional computed tomography (3D-CT) surface rendering using clinical protocols based on low-dose (35-mAs) spiral CT and cone-beam CT