author_facet Ritter, E. J.
Scott, W. J.
Wilson, J. G.
Ritter, E. J.
Scott, W. J.
Wilson, J. G.
author Ritter, E. J.
Scott, W. J.
Wilson, J. G.
spellingShingle Ritter, E. J.
Scott, W. J.
Wilson, J. G.
Teratology
Relationship of temporal patterns of cell death and development to malformations in the rat limb. Possible mechanisms of teratogenesis with inhibitors of DNA synthesis
Health, Toxicology and Mutagenesis
Developmental Biology
Toxicology
Embryology
author_sort ritter, e. j.
spelling Ritter, E. J. Scott, W. J. Wilson, J. G. 0040-3709 1096-9926 Wiley Health, Toxicology and Mutagenesis Developmental Biology Toxicology Embryology http://dx.doi.org/10.1002/tera.1420070302 <jats:title>Abstract</jats:title><jats:p>Cytosine arabinoside palmitate (ara‐CP) is a sustained‐action form of the DNA‐synthesis‐inhibitor cytosine arabinoside (ara‐C). When given at day 12 of rat gestation ara‐CP caused moderate but prolonged depression of DNA synthesis, killed embryonic cells after 2–3 days, and led to severe limb and other defects and extreme growth retardation. The results were compared with those obtained in earlier studies with hydroxyurea and with ara‐C, both of which also caused depression of DNA synthesis, cell death, and limb defects, but at different times in relation to treatment. There was a relation between the time of maximal cell death in the limbs after treatment and the specific limb malformations seen at day 20. The relation of cell death to teratogenesis seen with these chemical agents is similar to that previously reported for X irradiation.</jats:p> Relationship of temporal patterns of cell death and development to malformations in the rat limb. Possible mechanisms of teratogenesis with inhibitors of DNA synthesis Teratology
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title Relationship of temporal patterns of cell death and development to malformations in the rat limb. Possible mechanisms of teratogenesis with inhibitors of DNA synthesis
title_unstemmed Relationship of temporal patterns of cell death and development to malformations in the rat limb. Possible mechanisms of teratogenesis with inhibitors of DNA synthesis
title_full Relationship of temporal patterns of cell death and development to malformations in the rat limb. Possible mechanisms of teratogenesis with inhibitors of DNA synthesis
title_fullStr Relationship of temporal patterns of cell death and development to malformations in the rat limb. Possible mechanisms of teratogenesis with inhibitors of DNA synthesis
title_full_unstemmed Relationship of temporal patterns of cell death and development to malformations in the rat limb. Possible mechanisms of teratogenesis with inhibitors of DNA synthesis
title_short Relationship of temporal patterns of cell death and development to malformations in the rat limb. Possible mechanisms of teratogenesis with inhibitors of DNA synthesis
title_sort relationship of temporal patterns of cell death and development to malformations in the rat limb. possible mechanisms of teratogenesis with inhibitors of dna synthesis
topic Health, Toxicology and Mutagenesis
Developmental Biology
Toxicology
Embryology
url http://dx.doi.org/10.1002/tera.1420070302
publishDate 1973
physical 219-225
description <jats:title>Abstract</jats:title><jats:p>Cytosine arabinoside palmitate (ara‐CP) is a sustained‐action form of the DNA‐synthesis‐inhibitor cytosine arabinoside (ara‐C). When given at day 12 of rat gestation ara‐CP caused moderate but prolonged depression of DNA synthesis, killed embryonic cells after 2–3 days, and led to severe limb and other defects and extreme growth retardation. The results were compared with those obtained in earlier studies with hydroxyurea and with ara‐C, both of which also caused depression of DNA synthesis, cell death, and limb defects, but at different times in relation to treatment. There was a relation between the time of maximal cell death in the limbs after treatment and the specific limb malformations seen at day 20. The relation of cell death to teratogenesis seen with these chemical agents is similar to that previously reported for X irradiation.</jats:p>
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author Ritter, E. J., Scott, W. J., Wilson, J. G.
author_facet Ritter, E. J., Scott, W. J., Wilson, J. G., Ritter, E. J., Scott, W. J., Wilson, J. G.
author_sort ritter, e. j.
container_issue 3
container_start_page 219
container_title Teratology
container_volume 7
description <jats:title>Abstract</jats:title><jats:p>Cytosine arabinoside palmitate (ara‐CP) is a sustained‐action form of the DNA‐synthesis‐inhibitor cytosine arabinoside (ara‐C). When given at day 12 of rat gestation ara‐CP caused moderate but prolonged depression of DNA synthesis, killed embryonic cells after 2–3 days, and led to severe limb and other defects and extreme growth retardation. The results were compared with those obtained in earlier studies with hydroxyurea and with ara‐C, both of which also caused depression of DNA synthesis, cell death, and limb defects, but at different times in relation to treatment. There was a relation between the time of maximal cell death in the limbs after treatment and the specific limb malformations seen at day 20. The relation of cell death to teratogenesis seen with these chemical agents is similar to that previously reported for X irradiation.</jats:p>
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imprint Wiley, 1973
imprint_str_mv Wiley, 1973
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spelling Ritter, E. J. Scott, W. J. Wilson, J. G. 0040-3709 1096-9926 Wiley Health, Toxicology and Mutagenesis Developmental Biology Toxicology Embryology http://dx.doi.org/10.1002/tera.1420070302 <jats:title>Abstract</jats:title><jats:p>Cytosine arabinoside palmitate (ara‐CP) is a sustained‐action form of the DNA‐synthesis‐inhibitor cytosine arabinoside (ara‐C). When given at day 12 of rat gestation ara‐CP caused moderate but prolonged depression of DNA synthesis, killed embryonic cells after 2–3 days, and led to severe limb and other defects and extreme growth retardation. The results were compared with those obtained in earlier studies with hydroxyurea and with ara‐C, both of which also caused depression of DNA synthesis, cell death, and limb defects, but at different times in relation to treatment. There was a relation between the time of maximal cell death in the limbs after treatment and the specific limb malformations seen at day 20. The relation of cell death to teratogenesis seen with these chemical agents is similar to that previously reported for X irradiation.</jats:p> Relationship of temporal patterns of cell death and development to malformations in the rat limb. Possible mechanisms of teratogenesis with inhibitors of DNA synthesis Teratology
spellingShingle Ritter, E. J., Scott, W. J., Wilson, J. G., Teratology, Relationship of temporal patterns of cell death and development to malformations in the rat limb. Possible mechanisms of teratogenesis with inhibitors of DNA synthesis, Health, Toxicology and Mutagenesis, Developmental Biology, Toxicology, Embryology
title Relationship of temporal patterns of cell death and development to malformations in the rat limb. Possible mechanisms of teratogenesis with inhibitors of DNA synthesis
title_full Relationship of temporal patterns of cell death and development to malformations in the rat limb. Possible mechanisms of teratogenesis with inhibitors of DNA synthesis
title_fullStr Relationship of temporal patterns of cell death and development to malformations in the rat limb. Possible mechanisms of teratogenesis with inhibitors of DNA synthesis
title_full_unstemmed Relationship of temporal patterns of cell death and development to malformations in the rat limb. Possible mechanisms of teratogenesis with inhibitors of DNA synthesis
title_short Relationship of temporal patterns of cell death and development to malformations in the rat limb. Possible mechanisms of teratogenesis with inhibitors of DNA synthesis
title_sort relationship of temporal patterns of cell death and development to malformations in the rat limb. possible mechanisms of teratogenesis with inhibitors of dna synthesis
title_unstemmed Relationship of temporal patterns of cell death and development to malformations in the rat limb. Possible mechanisms of teratogenesis with inhibitors of DNA synthesis
topic Health, Toxicology and Mutagenesis, Developmental Biology, Toxicology, Embryology
url http://dx.doi.org/10.1002/tera.1420070302