Literature DB >> 1010312

Genetics of cortisone-induced cleft palate in the mouse-embryonic and maternal effects.

F G Biddle, F C Fraser.   

Abstract

Differences between mouse strains in frequency of embryonic, cortisone-induced cleft palate were examined. Probit analysis demonstrated a family of linear and parallel dose-response curves for different inbred and hybrid embryos. Since the differences between genotypes were not in the slopes of the response curves but rather in their location, it is proposed that the median effective dose (ED50) of cortisone required to induce cleft palate (or the tolerance) provides a more appropriate definition of the response trait and its difference that a frequency statement. The tolerance of C57BL/6J is dominant to that of A/J. A maternal effect of A/J relative to C57BL/6J dams caused a two-fold reduction in the embryonic tolerance of cortisone. Cortisone-induced cleft palate and mortality were separate response traits. In these and previous studies on cortisone- and other glucocorticoid-induced cleft palate in the mouse, the nature of the cleft-palate-response curve appeared to be the same for all glucocorticoids, and within-strain differences in tolerance could be used as measures of potency or bioassays for a particular effect of the glucocorticoids.

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Year:  1976        PMID: 1010312      PMCID: PMC1213605     

Source DB:  PubMed          Journal:  Genetics        ISSN: 0016-6731            Impact factor:   4.562


  5 in total

1.  Teratogenesis of acetazolamide in the CBA/J and SWV strains of mice. I. Teratology.

Authors:  F G Biddle
Journal:  Teratology       Date:  1975-02

2.  Sex of mouse (CDI) offspring not a factor in hydrocortisone induced cleft palate.

Authors:  H T Loevy; M A Wade
Journal:  Cleft Palate J       Date:  1972-07

3.  Annotation: the analysis of variance and the analysis of causes.

Authors:  R C Lewontin
Journal:  Am J Hum Genet       Date:  1974-05       Impact factor: 11.025

4.  Distribution and metabolism of triamcinolone acetonide in inbred mice with different cleft palate sensitivities.

Authors:  E F Zimmerman; D Bowen
Journal:  Teratology       Date:  1972-06

5.  Glucocorticoid induction of cleft palate in mice; no correlation with inhibition of mucopolysaccharide synthesis.

Authors:  F D Andrew; E F Zimmerman
Journal:  Teratology       Date:  1971-02
  5 in total
  7 in total

1.  Glucocorticoid-induced cleft palate genes in chromosome 17: genetic linkage and mapping analyses.

Authors:  J J Bonner; M L Tyan
Journal:  Immunogenetics       Date:  1984       Impact factor: 2.846

2.  The William Allan Memorial Award Address: evolution of a palatable multifactorial threshold model.

Authors:  F C Fraser
Journal:  Am J Hum Genet       Date:  1980-11       Impact factor: 11.025

Review 3.  Developmental genetics.

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

4.  Genetic differences among the A/J X C57BL/6J recombinant inbred mouse lines and their degree of association with glucocorticoid-induced cleft palate.

Authors:  S L Liu; R P Erickson
Journal:  Genetics       Date:  1986-07       Impact factor: 4.562

5.  Glucocorticoid-induced cleft palate in the mouse: two major histocompatibility complex, H-2, loci with different mechanisms.

Authors:  J J Bonner; M L Tyan
Journal:  Genetics       Date:  1983-02       Impact factor: 4.562

6.  Maternal exposure to life events during pregnancy and congenital heart disease in offspring: a case-control study in a Chinese population.

Authors:  Jing Li; Yujiao Du; Yini Liu; Jiaoyang Du; Ruo Zhang; Pengfei Qu; Hong Yan; Duolao Wang; Shaonong Dang
Journal:  BMC Pregnancy Childbirth       Date:  2021-10-06       Impact factor: 3.007

Review 7.  Receptor-dependent mechanisms of glucocorticoid and dioxin-induced cleft palate.

Authors:  R M Pratt
Journal:  Environ Health Perspect       Date:  1985-09       Impact factor: 9.031

  7 in total

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