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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Detalles Bibliográficos
Autores principales: Sah, Rajiv Kumar, Ma, Jun, Bah, Fatoumata Binta, Xing, Zhenkai, Adlat, Salah, Oo, Zin Ma, Wang, Yajun, Bahadar, Noor, Bohio, Ameer Ali, Nagi, Farooq Hayel, Feng, Xuechao, Zhang, Luqing, Zheng, Yaowu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7663123/
https://www.ncbi.nlm.nih.gov/pubmed/33153107
http://dx.doi.org/10.3390/ijms21218223

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