Literature DB >> 2338491

The mouse mutation ulnaless on chromosome 2.

M T Davisson1, B M Cattanach.   

Abstract

The dominant skeletal mutation ulnaless (Ul) in the mouse causes extreme reduction of the radius and ulna and deformities of the tibia and fibula. Penetrance appears to be complete, but the homozygote is not known, as heterozygous males do not breed. We report the linkage of the Ul gene on Chromosome 2, 18 cM proximal to pallid (pa), and describe its phenotypic effects.

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Year:  1990        PMID： 2338491

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


  6 in total

Review 1.  Mouse chromosome 2.

Authors:  L D Siracusa; C M Abbott
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

Review 2.  Mouse chromosome 2.

Authors:  L D Siracusa; C M Abbott
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

3.  Genetic and physical mapping of the mouse Ulnaless locus.

Authors:  C L Peichel; C M Abbott; T F Vogt
Journal:  Genetics       Date:  1996-12       Impact factor: 4.562

4.  Monodactylous limbs and abnormal genitalia are associated with hemizygosity for the human 2q31 region that includes the HOXD cluster.

Authors:  M Del Campo; M C Jones; A N Veraksa; C J Curry; K L Jones; J T Mascarello; Z Ali-Kahn-Catts; T Drumheller; W McGinnis
Journal:  Am J Hum Genet       Date:  1999-07       Impact factor: 11.025

5.  Mapping the midkine family of developmentally regulated signaling molecules.

Authors:  C L Peichel; S W Scherer; L C Tsui; D R Beier; T F Vogt
Journal:  Mamm Genome       Date:  1993-11       Impact factor: 2.957

6.  Hoxa11 and Hoxd11 regulate chondrocyte differentiation upstream of Runx2 and Shox2 in mice.

Authors:  Stefanie Gross; Yvonne Krause; Manuela Wuelling; Andrea Vortkamp
Journal:  PLoS One       Date:  2012-08-20       Impact factor: 3.240
  6 in total

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