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Publication : ARNT-deficient mice and placental differentiation.

First Author  Kozak KR Year  1997
Journal  Dev Biol Volume  191
Issue  2 Pages  297-305
PubMed ID  9398442 Mgi Jnum  J:44365
Mgi Id  MGI:1099946 Doi  10.1006/dbio.1997.8758
Citation  Kozak KR, et al. (1997) ARNT-deficient mice and placental differentiation. Dev Biol 191(2):297-305
abstractText  We used homologous recombination in embryonic stem cells to generate mice heterozygous for an aryl hydrocarbon nuclear translocator (ARNT) null mutation. These mice were intercrossed, but no live homozygous Arnt-/- knockout mice were produced among 64 newborns. Homozygotes die in utero between 9.5 and 10.5 days of gestation. Abnormalities included neural tube closure defects, forebrain hypoplasia, delayed rotation of the embryo, placental hemorrhaging, and visceral arch abnormalities. However, the primary cause of lethality appears to be failure of the embryonic component of the placenta to vascularize and form the labyrinthine spongiotrophoblast. This may be related to ARNT's known role in hypoxic induction of angiogenesis. We found no defects in yolk sac circulation.
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