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Analysis of aneuploidy in first-cleavage mouse embryos fertilized in vitro and in vivo.
First-cleavage mouse embryos, fertilized in vitro and in vivo, provide ideal material for chromosomal analysis. With the appropriate incubation in a mitotic inhibitor, syngamy is prevented and the sperm- and egg-derived chromosomes remain as separate clusters. Because the latter chromosomes undergo...
Autores principales: | , |
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Formato: | Texto |
Lenguaje: | English |
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1979
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1637642/ https://www.ncbi.nlm.nih.gov/pubmed/387395 |
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author | Fraser, L R Maudlin, I |
author_facet | Fraser, L R Maudlin, I |
author_sort | Fraser, L R |
collection | PubMed |
description | First-cleavage mouse embryos, fertilized in vitro and in vivo, provide ideal material for chromosomal analysis. With the appropriate incubation in a mitotic inhibitor, syngamy is prevented and the sperm- and egg-derived chromosomes remain as separate clusters. Because the latter chromosomes undergo condensation sooner than those from the spermatozoon, the parental source of chromosome sets can be identified even without a marker chromosome. Thus these embryos can be analyzed both for the primary incidence and the parental source of a number of chromosomal anomalies, including aneuploidy. By using fertilization in vitro to obtain the embryos, the synchrony of fertilization and nuclear development is such that 80% or more of the chromosomal preparations are suitable for analysis, compared with about 50% for embryos fertilized in vivo. |
format | Text |
id | pubmed-1637642 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1979 |
record_format | MEDLINE/PubMed |
spelling | pubmed-16376422006-11-17 Analysis of aneuploidy in first-cleavage mouse embryos fertilized in vitro and in vivo. Fraser, L R Maudlin, I Environ Health Perspect Research Article First-cleavage mouse embryos, fertilized in vitro and in vivo, provide ideal material for chromosomal analysis. With the appropriate incubation in a mitotic inhibitor, syngamy is prevented and the sperm- and egg-derived chromosomes remain as separate clusters. Because the latter chromosomes undergo condensation sooner than those from the spermatozoon, the parental source of chromosome sets can be identified even without a marker chromosome. Thus these embryos can be analyzed both for the primary incidence and the parental source of a number of chromosomal anomalies, including aneuploidy. By using fertilization in vitro to obtain the embryos, the synchrony of fertilization and nuclear development is such that 80% or more of the chromosomal preparations are suitable for analysis, compared with about 50% for embryos fertilized in vivo. 1979-08 /pmc/articles/PMC1637642/ /pubmed/387395 Text en |
spellingShingle | Research Article Fraser, L R Maudlin, I Analysis of aneuploidy in first-cleavage mouse embryos fertilized in vitro and in vivo. |
title | Analysis of aneuploidy in first-cleavage mouse embryos fertilized in vitro and in vivo. |
title_full | Analysis of aneuploidy in first-cleavage mouse embryos fertilized in vitro and in vivo. |
title_fullStr | Analysis of aneuploidy in first-cleavage mouse embryos fertilized in vitro and in vivo. |
title_full_unstemmed | Analysis of aneuploidy in first-cleavage mouse embryos fertilized in vitro and in vivo. |
title_short | Analysis of aneuploidy in first-cleavage mouse embryos fertilized in vitro and in vivo. |
title_sort | analysis of aneuploidy in first-cleavage mouse embryos fertilized in vitro and in vivo. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1637642/ https://www.ncbi.nlm.nih.gov/pubmed/387395 |
work_keys_str_mv | AT fraserlr analysisofaneuploidyinfirstcleavagemouseembryosfertilizedinvitroandinvivo AT maudlini analysisofaneuploidyinfirstcleavagemouseembryosfertilizedinvitroandinvivo |