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Targeted Disruption of Mouse Dip2B Leads to Abnormal Lung Development and Prenatal Lethality
Molecular and anatomical functions of mammalian Dip2 family members (Dip2A, Dip2B and Dip2C) during organogenesis are largely unknown. Here, we explored the indispensable role of Dip2B in mouse lung development. Using a LacZ reporter, we explored Dip2B expression during embryogenesis. This study sho...
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Main Authors: | , , , , , , , , , , , , |
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格式: | Artigo |
語言: | Inglês |
出版: |
MDPI AG
2020-11-01
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叢編: | International Journal of Molecular Sciences |
主題: | |
在線閱讀: | https://www.mdpi.com/1422-0067/21/21/8223 |
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