Literature DB >> 1290160

Neural tube defects without neural crest defects in splotch mice.

T Franz1.   

Abstract

Homozygous Splotch mutant mice (Sp/Sp) die on day 14 of gestation with neural tube defects, curly tail, and malformations of neural crest derivatives. Sp1H mice, which have a radiation-induced allele of Splotch with a similar phenotype, were used for this study. The neural tube defects are always located in the lumbosacral region and in 50% of the cases also in the region of the hindbrain. In this report, rare cases of neural tube defects and tail defects among the offspring of crosses between Splotch (Sp1H) heterozygotes are presented, which are not associated with a neural crest defect. This suggests that the development of the neural tube and neural crest defects in this mutant is caused by independent mechanisms or is dependent on the dosage of the mutant gene, with different thresholds being pathogenetic in the neural tube and neural crest, respectively.

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Year:  1992        PMID: 1290160     DOI: 10.1002/tera.1420460609

Source DB:  PubMed          Journal:  Teratology        ISSN: 0040-3709


  4 in total

1.  Pax3 is essential for normal cardiac neural crest morphogenesis but is not required during migration nor outflow tract septation.

Authors:  Michael Olaopa; Hong-ming Zhou; Paige Snider; Jian Wang; Robert J Schwartz; Anne M Moon; Simon J Conway
Journal:  Dev Biol       Date:  2011-05-12       Impact factor: 3.582

2.  The Splotch (Sp1H) and Splotch-delayed (Spd) alleles: differential phenotypic effects on neural crest and limb musculature.

Authors:  T Franz
Journal:  Anat Embryol (Berl)       Date:  1993-04

3.  Tyrosine phosphatase MEG2 modulates murine development and platelet and lymphocyte activation through secretory vesicle function.

Authors:  Yingchun Wang; Eric Vachon; Jinyi Zhang; Vera Cherepanov; Joshua Kruger; Jun Li; Kan Saito; Patrick Shannon; Nunzio Bottini; Huong Huynh; Heyu Ni; Hong Yang; Colin McKerlie; Sue Quaggin; Zhizhuang Joe Zhao; Philip A Marsden; Tomas Mustelin; Katherine A Siminovitch; Gregory P Downey
Journal:  J Exp Med       Date:  2005-12-05       Impact factor: 14.307

4.  A new missense mutation in the paired domain of the mouse Pax3 gene.

Authors:  Tamio Ohno; Tomoki Maegawa; Hiroto Katoh; Yuki Miyasaka; Miyako Suzuki; Misato Kobayashi; Fumihiko Horio
Journal:  Exp Anim       Date:  2017-04-06
  4 in total

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