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Temporal changes of Sall4 lineage contribution in developing embryos and the contribution of Sall4-lineages to postnatal germ cells in mice

Mutations in the SALL4 gene cause human syndromes with defects in multiple organs. Sall4 expression declines rapidly in post-gastrulation mouse embryos, and our understanding of the requirement of Sall4 in animal development is still limited. To assess the contributions of Sall4 expressing cells to...

詳細記述

保存先:
書誌詳細
出版年:Sci Rep
主要な著者: Tahara, Naoyuki, Kawakami, Hiroko, Zhang, Teng, Zarkower, David, Kawakami, Yasuhiko
フォーマット: Artigo
言語:Inglês
出版事項: Nature Publishing Group UK 2018
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC6219540/
https://ncbi.nlm.nih.gov/pubmed/30401915
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-018-34745-5
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