Literature DB >> 230280

In vivo and in vitro studies on the early embryonic lethal oligosyndactylism (Os) in the mouse.

H F Paterson.   

Abstract

The development of mouse embryos homozygous for oligosyndactylism (Os) is arrested during implantation. Histological investigations confirm a previous report that cells become blocked in mitosis, and air-dried spreads of the mutant embryos reveal that large numbers of cells accumulate in metaphase. Trophoblastic giant cells appear unaffected by the action of the mutant gene both in utero and during culture over the lethal phase. It is proposed that the form of endoreduplication undergone by giant cells renders them refractory to the metaphase block.

Entities:  

Mesh:

Year:  1979        PMID: 230280

Source DB:  PubMed          Journal:  J Embryol Exp Morphol        ISSN: 0022-0752


  4 in total

1.  Oligosyndactylism mice have an inversion of chromosome 8.

Authors:  Thomas L Wise; Dimitrina D Pravtcheva
Journal:  Genetics       Date:  2004-12       Impact factor: 4.562

Review 2.  Developmental genetics.

Authors:  C J Epstein
Journal:  Experientia       Date:  1986-10-15

3.  A transgene-induced mitotic arrest mutation in the mouse allelic with Oligosyndactylism.

Authors:  D D Pravtcheva; T L Wise
Journal:  Genetics       Date:  1996-12       Impact factor: 4.562

4.  Phenotyping by magnetic resonance imaging nondestructively measures glomerular number and volume distribution in mice with and without nephron reduction.

Authors:  Edwin J Baldelomar; Jennifer R Charlton; Scott C Beeman; Bradley D Hann; Luise Cullen-McEwen; Valeria M Pearl; John F Bertram; Teresa Wu; Min Zhang; Kevin M Bennett
Journal:  Kidney Int       Date:  2016-02       Impact factor: 10.612

  4 in total

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