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  1. 0 資料タイプ別
  2. 01 学術雑誌論文
  1. 070 農学部
  2. 10 学術雑誌論文
  3. 10 査読済論文

Time-Lapse Videomicrographic Observations of Parthenogenetic Mouse Embryos during Early Development

http://hdl.handle.net/10191/7771
http://hdl.handle.net/10191/7771
1ce6aa14-e3d9-48f6-9af3-7267d45f3b37
名前 / ファイル ライセンス アクション
2009030023.pdf 2009030023.pdf (1.1 MB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2009-04-09
タイトル
タイトル Time-Lapse Videomicrographic Observations of Parthenogenetic Mouse Embryos during Early Development
言語 en
言語
言語 eng
キーワード
主題Scheme Other
主題 Parthenogenetic mouse embryo
キーワード
主題Scheme Other
主題 Early development
キーワード
主題Scheme Other
主題 Time-lapse videomicrography
資源タイプ
資源 http://purl.org/coar/resource_type/c_6501
タイプ journal article
著者 Niimura, Sueo

× Niimura, Sueo

WEKO 6732

en Niimura, Sueo

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Futatsumata, Nana

× Futatsumata, Nana

WEKO 6733

en Futatsumata, Nana

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著者別名
識別子Scheme WEKO
識別子 6734
姓名 新村, 末雄
言語 ja
著者別名
識別子Scheme WEKO
識別子 6735
姓名 二俣, ナナ
言語 ja
抄録
内容記述タイプ Abstract
内容記述 The process of early development in diploid parthenogenetic mouse embryos from the 2-cell to the blastocyst stages was observed by time-lapse videomicrography, and was compared with that in fertilized embryos. Parthenogenetic 2-cell embryos cleaved and developed to 8-cell embryos after 23.0 hrs of culture. Transformation of blastomeres occurred at the 8-cell stage: namely, outer blastomeres were flattened. The embryos compacted at the morula stage, and then developed to blastocysts after 54.0 hrs of culture. A slit in the zona pellucida was formed 42.7 hrs after blastocyst formation, and trophectoderm cells protruded out of the zona pellucida through the slit. Protrusion of trophectoderm cells from the zona pellucida could arise from either side, polar trophectoderm or mural trophectoderm. After 7.0 hrs, the blastocysts completely escaped from the zona pellucida in either state, expansion or contraction. Fertilized 2-cell embryos showed morphological changes similar to those of parthenogenetic embryos and developed to blastocysts after 51.9 hrs of culture. Fertilized blastocysts took a significantly shorter time, 31.1 hrs, to start hatching, but required a significantly longer time, 23.8 hrs, to complete hatching, compared with parthenogenetic blastocysts. Hatching patterns of fertilized blastocysts were consistent with those of parthenogenetic blastocysts, except that hatching began with protrusion of trophectoderm cells from small holes in zonae pellucidae of fertilized blastocysts. From these results, it was confirmed that the developmental ability of early diploid parthenogenetic embryos prepared by the treatment with ethanol and cytochalasin B is comparable to that in fertilized embryos.
言語 en
書誌情報 en : Journal of mammalian ova research

巻 16, 号 3, p. 124-129, 発行日 1999
出版者
出版者 Japanese Society of Mammalian Ova Research
言語 en
ISSN
収録物識別子タイプ ISSN
収録物識別子 1341-7738
書誌レコードID
収録物識別子タイプ NCID
収録物識別子 AA12018687
DOI
識別子タイプ DOI
関連識別子 http://doi.org/10.1274/jmor.16.124
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
著者版フラグ
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Niimura, Sueo, Futatsumata, Nana, 1999, Time-Lapse Videomicrographic Observations of Parthenogenetic Mouse Embryos during Early Development: Japanese Society of Mammalian Ova Research, 124–129 p.

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