1963
DOI: 10.1016/0014-4827(63)90109-5
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Effets de la mitomycine sur l'incorporation de la thymidine tritiée dans les embryons d'amphibiens au stade morula

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Cited by 8 publications
(1 citation statement)
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“…The mitomycins also are instrumental in the stimulation of chromosomal exchanges and crossing-over (SHAW and CoHEN, 1965;SuzuKI, 1965) and for genetic recombination (lrJIMA and HAGAWARA, 1960;YuKI, 1962;HoLLIDAY, 1964), and in its inhibition . They cause fragmentation of chromosomes and other cell structures (BACH and MAGEE, 1962;BIELIAVSKY, 1963; CoHEN and SHAW, 1964;KERSTEN and THEMANN, 1962; 218 W. SzYBALSKI and V. N. lYER: KIMURA, 1963;KOSAKA, 1964;KURODA and FURUYAMA, 1963; LAPIS and BERN-HARD, 1965;MERZ, 1961; SHATKIN et al, 196Z; TRUHAUT and DEYSSON, 1960) resulting in inhibition of the development of pleurodele embryos blocked in the morula stage (BIELIAVSKY, 1963), giant cell formation (SHATKIN etal., 1962), and other abnormal growth as e.g., filament formation, an effect already mentioned.Mitomycin was also found to inhibit postirradiation repair of fragmented chromosomes (MATSUURA et al, 196Z, 1963;IWABUCHI et al, 1966).The mitomycins were found to influence the action of the polymerases, including stimulation of DNA polymerase activity in mammalian cells (BACH and MAGEE, 196Z; MAGEE and MILLER, 196Z) but not in bacteria (NAKATA et al, 196Z; SEKIGUCHI and TAKAGI, 1960a) and 60 to 75% impairment WEISS-BACH, 1964, 1965) or little impairment (TAKAGI, 1963;KONTANI, 1964) of the in vitro priming capacity of DNA for the DNA polymerase but not for the DNAdependent RNA polymerase. No changes in RNA base composition were detected in mitomycin-treated Ehrlich ascites cell (AKAMATSU et al, 1963).…”
mentioning
confidence: 99%
“…The mitomycins also are instrumental in the stimulation of chromosomal exchanges and crossing-over (SHAW and CoHEN, 1965;SuzuKI, 1965) and for genetic recombination (lrJIMA and HAGAWARA, 1960;YuKI, 1962;HoLLIDAY, 1964), and in its inhibition . They cause fragmentation of chromosomes and other cell structures (BACH and MAGEE, 1962;BIELIAVSKY, 1963; CoHEN and SHAW, 1964;KERSTEN and THEMANN, 1962; 218 W. SzYBALSKI and V. N. lYER: KIMURA, 1963;KOSAKA, 1964;KURODA and FURUYAMA, 1963; LAPIS and BERN-HARD, 1965;MERZ, 1961; SHATKIN et al, 196Z; TRUHAUT and DEYSSON, 1960) resulting in inhibition of the development of pleurodele embryos blocked in the morula stage (BIELIAVSKY, 1963), giant cell formation (SHATKIN etal., 1962), and other abnormal growth as e.g., filament formation, an effect already mentioned.Mitomycin was also found to inhibit postirradiation repair of fragmented chromosomes (MATSUURA et al, 196Z, 1963;IWABUCHI et al, 1966).The mitomycins were found to influence the action of the polymerases, including stimulation of DNA polymerase activity in mammalian cells (BACH and MAGEE, 196Z; MAGEE and MILLER, 196Z) but not in bacteria (NAKATA et al, 196Z; SEKIGUCHI and TAKAGI, 1960a) and 60 to 75% impairment WEISS-BACH, 1964, 1965) or little impairment (TAKAGI, 1963;KONTANI, 1964) of the in vitro priming capacity of DNA for the DNA polymerase but not for the DNAdependent RNA polymerase. No changes in RNA base composition were detected in mitomycin-treated Ehrlich ascites cell (AKAMATSU et al, 1963).…”
mentioning
confidence: 99%