Literature DB >> 6863894

Four dominant autosomal mutations affecting skin and hair development in the mouse.

K F Stelzner.   

Abstract

Four new dominant autosomal mutations influencing the development of skin and hair in the mouse were tested for allelism with each other and with hairless, hr. Three of the mutations probably constitute an allelic series and have been given the symbols Frl1, Frlb, and Frlc. The Frl series shows no evidence of linkage with hr. The fourth mutation, Hrn, is a dominant and homozygous viable allele at the hr locus. With the possible exception or Frlb, all mutants were of spontaneous origin. Because of their unique characteristics, these new mutants are of potential value as mouse model systems in studies of skin carcinogenesis and related areas of research.

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Year:  1983        PMID: 6863894     DOI: 10.1093/oxfordjournals.jhered.a109761

Source DB:  PubMed          Journal:  J Hered        ISSN: 0022-1503            Impact factor:   2.645


  6 in total

1.  The gene for hypotrichosis of Marie Unna maps between D8S258 and D8S298: exclusion of the hr gene by cDNA and genomic sequencing.

Authors:  M van Steensel; F J Smith; P M Steijlen; I Kluijt; H P Stevens; A Messenger; H Kremer; M G Dunnill; C Kennedy; C S Munro; V R Doherty; J A McGrath; S P Covello; C M Coleman; J Uitto; W H McLean
Journal:  Am J Hum Genet       Date:  1999-08       Impact factor: 11.025

2.  Hair lost in translation.

Authors:  Lorin Weiner; Janice L Brissette
Journal:  Nat Genet       Date:  2009-02       Impact factor: 38.330

3.  Genomic organization and analysis of the hairless gene in four hypotrichotic rat strains.

Authors:  Hyunmi Kim; Andrey A Panteleyev; Colin A B Jahoda; Yoshiyaki Ishii; Angela M Christiano
Journal:  Mamm Genome       Date:  2004-12       Impact factor: 2.957

4.  Structure and expression of the hairless gene of mice.

Authors:  M B Cachon-Gonzalez; S Fenner; J M Coffin; C Moran; S Best; J P Stoye
Journal:  Proc Natl Acad Sci U S A       Date:  1994-08-02       Impact factor: 11.205

5.  A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis.

Authors:  In Cheol Baek; Jeong Ki Kim; Kyu-Hyuk Cho; Dal-Sun Cha; Jae-Woo Cho; Jong Keun Park; Chang-Woo Song; Sungjoo Kim Yoon
Journal:  Mamm Genome       Date:  2009-06-10       Impact factor: 2.957

6.  Insertional mutation of the hairless locus on mouse chromosome 14.

Authors:  J M Jones; J T Elder; K Simin; S A Keller; M H Meisler
Journal:  Mamm Genome       Date:  1993-11       Impact factor: 2.957

  6 in total

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