Connexin31-Deficiency in Mice Causes Transient Placental Dysmorphogenesis but Does Not Impair Hearing and Skin Differentiation

Author:

Plum Achim,Winterhager Elke,Pesch Joerg,Lautermann Juergen,Hallas Gaby,Rosentreter Boris,Traub Otto,Herberhold Claus,Willecke Klaus

Publisher

Elsevier BV

Subject

Cell Biology,Developmental Biology,Molecular Biology

Reference38 articles.

1. Current Protocols in Molecular Biology;Ausubel,1989

2. Differential expression of the gap junction proteins connexin45, -43, -40, -31, and -26 in mouse skin;Butterweck;Eur. J. Cell Biol.,1994

3. Segment-specific expression of a gap junction gene, connexin31, during hindbrain development;Dahl;Dev. Genes Evol.,1997

4. Expression of the gap junction proteins connexin31 and connexin43 correlates with communication compartments in extraembryonic tissues and in the gastrulating mouse embryo, respectively;Dahl;J. Cell Sci.,1996

5. Multiple members of the connexin gene family participate in preimplantation development of the mouse;Davies;Dev. Genet.,1996

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