Literature DB >> 2305264

Mini-mouse: disruption of the pygmy locus in a transgenic insertional mutant.

X Xiang1, K F Benson, K Chada.   

Abstract

A founder transgenic mouse harbored two different integration patterns of a transgene at the same locus, each of which gave rise to a similar autosomal recessive mutation. Mice of the mutant phenotype were of small stature but had normal levels of growth hormone. The disrupted locus was cloned, and a genetic and molecular analysis showed that the insertional mutants were allelic to a spontaneous mutant, pygmy. The mice should be a useful model for the growth hormone-resistant human dwarf syndromes and could lead to a greater understanding of the pathways involved in growth and development.

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Year:  1990        PMID: 2305264     DOI: 10.1126/science.2305264

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  34 in total

1.  Inherited haemolytic anaemia created by insertional inactivation of the alpha-spectrin gene.

Authors:  G Grimber; C Galand; M Garbarz; M G Mattei; C Cavard; A Zider; P Blanchet; P Boivin; P Briand; D Dhermy
Journal:  Transgenic Res       Date:  1992-11       Impact factor: 2.788

Review 2.  Mouse chromosome 10.

Authors:  B A Taylor; W N Frankel; R H Reeves
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

3.  The same genomic region is disrupted in two transgene-induced limb deformity alleles.

Authors:  T F Vogt; L Jackson-Grusby; A J Wynshaw-Boris; D C Chan; P Leder
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

Review 4.  Mouse chromosome 10.

Authors:  B A Taylor; M J Justice; R Reeves
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

Review 5.  Transgenic regulation in laboratory animals.

Authors:  S Rusconi
Journal:  Experientia       Date:  1991-09-15

6.  Molecular characterization of the mouse In(10)17Rk inversion and identification of a novel muscle-specific gene at the proximal breakpoint.

Authors:  Kathleen F Benson; Kiran Chada
Journal:  Genetics       Date:  2002-01       Impact factor: 4.562

7.  A genetic linkage map of mouse chromosome 10: localization of eighteen molecular markers using a single interspecific backcross.

Authors:  M J Justice; L D Siracusa; D J Gilbert; N Heisterkamp; J Groffen; K Chada; C M Silan; N G Copeland; N A Jenkins
Journal:  Genetics       Date:  1990-08       Impact factor: 4.562

8.  The gene for the human architectural transcription factor HMGI-C consists of five exons each coding for a distinct functional element.

Authors:  K Y Chau; U A Patel; K L Lee; H Y Lam; C Crane-Robinson
Journal:  Nucleic Acids Res       Date:  1995-11-11       Impact factor: 16.971

9.  Phenotypic characterization of the Komeda miniature rat Ishikawa, an animal model of dwarfism caused by a mutation in Prkg2.

Authors:  Atsuko Tsuchida; Norihide Yokoi; Misako Namae; Masanori Fuse; Taku Masuyama; Masashi Sasaki; Shoji Kawazu; Kajuro Komeda
Journal:  Comp Med       Date:  2008-12       Impact factor: 0.982

10.  A conditional system to specifically link disruption of protein-coding function with reporter expression in mice.

Authors:  Shin-Heng Chiou; Caroline Kim-Kiselak; Viviana I Risca; Megan K Heimann; Chen-Hua Chuang; Aurora A Burds; William J Greenleaf; Tyler E Jacks; David M Feldser; Monte M Winslow
Journal:  Cell Rep       Date:  2014-06-12       Impact factor: 9.423

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