Literature DB >> 949906

Further evidence of X-linkage of hypoxanthine phosphoribosyl-transferase in the mouse.

S Hashimi, O J Miller.   

Abstract

A variant of the HPRT-A9 mouse cell line was fused with wild type diploid mouse bone marrow cells to obtain an HPRT+ line. The unique chromosomal features of the A9 parent, including the presence of a t(X;3) translocation and the absence of normal chromosomes 15,16, 17, 18, and the X, have permitted use of this intraspecific hybrid for chromosome mapping. Back-selection of hybrid cells in 8-azaguanine for loss of HPRT resulted in the loss of the Xchromosome derived from the diploid parent, providing evidence of the X-linkage of the HPRT locus.

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Year:  1976        PMID: 949906     DOI: 10.1159/000130685

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN: 0301-0171


  4 in total

1.  Isoenzyme pattern of HPRT in murine erythrocytes: control by an autosomal locus.

Authors:  M N Nesbitt; B Bakay; M B Gardner; C Day
Journal:  Biochem Genet       Date:  1979-10       Impact factor: 1.890

2.  Electrophoretic variation for X chromosome-linked hypoxanthine phosphoribosyl transferase (HPRT) in wild-derived mice.

Authors:  V M Chapman; P G Kratzer; B A Quarantillo
Journal:  Genetics       Date:  1983-04       Impact factor: 4.562

3.  Comparative gene mapping: order of loci on the X chromosome is different in mice and humans.

Authors:  U Francke; R T Taggart
Journal:  Proc Natl Acad Sci U S A       Date:  1980-06       Impact factor: 11.205

4.  Phenotypic interaction studies of HPRT mutant and normal human fibroblasts.

Authors:  I Willers; S Singh; H W Goedde
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

  4 in total

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