Stelzner K F
J Hered. 1983 May-Jun;74(3):193-6. doi: 10.1093/oxfordjournals.jhered.a109761.
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.
对影响小鼠皮肤和毛发发育的四个新的显性常染色体突变进行了相互之间以及与无毛基因(hr)的等位性测试。其中三个突变可能构成一个等位基因系列,并已被赋予符号Frl1、Frl b和Frl c。Frl系列没有显示出与hr基因连锁的证据。第四个突变Hrn是hr基因座上的一个显性且纯合可存活等位基因。除了可能的Frl b之外,所有突变体均为自发产生。由于其独特的特性,这些新的突变体作为小鼠模型系统在皮肤癌发生及相关研究领域具有潜在价值。