Zobrazeno 1 - 10
of 149
pro vyhledávání: '"D Papadopoulo"'
Autor:
Nicholas J. Finnie, J.P. de Villartay, Marina Cavazzana-Calvo, N Nicolas, Alain Fischer, F Le Deist, D Papadopoulo, Stephen P. Jackson
Publikováno v:
European Journal of Immunology. 26:1118-1122
The initial step of the V(D)J recombination occurs through the generation of a DNA double-strand break (dsb). Defects in the DNA-dependent protein kinase complex (DNA-PK) result in an inability to perform either V(D)J recombination or any dsb repair
Autor:
Marina Cavazzana-Calvo, G de Saint Basile, J P de Villartay, Alain Fischer, D Papadopoulo, F Le Deist
Publikováno v:
Journal of Clinical Investigation. 91:1214-1218
We studied the radiosensitivity of granulocyte macrophage colony-forming units (GM-CFU) in patients with a severe combined immunodeficiency (SCID). Three patients lacking both mature T and B cells showed a twofold higher GM-CFU radiosensitivity calcu
Publikováno v:
Journal of molecular biology. 281(5)
The hallmark of Fanconi anemia (FA), a rare inherited cancer prone disorder, is a high level of chromosome breakage, spontaneous and induced by cross-linking agents. The increased genomic instability of FA is reflected at the gene level by an overpro
Publikováno v:
Radiation research. 133(1)
Survival and HPRT- mutant frequency were measured in human lymphoblastoid cells preexposed or not to a low dose of 0.02 Gy gamma rays and then treated with a high dose of 4.0 Gy. When compared to the high dose alone, the low-dose preexposure induced
Autor:
Ethel Moustacchi, D. Papadopoulo
Publikováno v:
Mutation research. 245(4)
The photobiological effects induced by the monofuctional 7-methylpyrido[3,4- c ]psoralen (MePyPs) in comparison to the bifunctional furocoumarin 8-methoxypsoralen (8-MOP) have been studied in a human lymphoblast cell line TK6. We report that, in huma
Fanconi anemia (FA) is an inherited human disorder associated with a predisposition to cancer and characterized by anomalies in the processing of DNA cross-links and certain monoadducts. We reported previously that the frequency of psoralen-photoindu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da94f6bc17c6b0573a8bf04c48f2cccb
https://europepmc.org/articles/PMC54960/
https://europepmc.org/articles/PMC54960/
Publikováno v:
Cancer research. 50(11)
The induction of mutants at the hypoxanthine-guanine phosphoribosyltransferase and Na+/K+ ATPase loci by photoaddition of two bifunctional psoralens was compared in normal and in Fanconi's anemia lymphoblasts from the genetic complementation group A.
Publikováno v:
Nouvelle revue francaise d'hematologie. 32(6)
Several features of Fanconi's anemia (FA) are reported: relative inefficiency in the processing of DNA cross-links and monoadducts, hypomutability at the two loci analysed, complementation of the cytogenetic defect by cocultivation with mouse cells a
Publikováno v:
Radiation Research. 133:94
Survival and $HPRT^{-}$ mutant frequency were measured in human lymphoblastoid cells preexposed or not to a low dose of 0.02 Gy γ rays and then treated with a high dose of 4.0 Gy. When compared to the high dose alone, the low-dose preexposure induce
Publikováno v:
British Journal of Cancer. 36:65-71
We have maintained in culture, for a prolonged period, untreated hamster cells from whole embryo, foetal brain and lung from newborn animals. Among the 7 lines studied we observed only one spontaneous transformation during the first year of culture.