Literature DB >> 3311967

Chromosome maps of man and mouse, III.

A G Searle1, J Peters, M F Lyon, E P Evans, J H Edwards, V J Buckle.   

Abstract

Data on loci whose positions are known in both man and mouse are presented in the form of chromosomal displays, a table, and autosomal and X-chromosomal grids. At least 40 conserved autosomal segments with two or more loci, as well as 17 homologous X-linked loci, are now known in the two species, in which mitochondrial DNA is also highly conserved. Apart from the Y, the only chromosome now lacking a conserved group is human 13. Human 17 has a single conserved group which includes both short and long arms, and so may have remained largely intact in mammalian evolution. Human and mouse chromosomal maps show the approximate locations of homologous genes while the mouse map also shows the positions of translocations used in gene location.

Entities:  

Mesh:

Year:  1987        PMID: 3311967     DOI: 10.1016/0888-7543(87)90099-1

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  27 in total

1.  Male-enhanced antigen gene is phylogenetically conserved and expressed at late stages of spermatogenesis.

Authors:  Y F Lau; K M Chan; R Sparkes
Journal:  Proc Natl Acad Sci U S A       Date:  1989-11       Impact factor: 11.205

2.  A genetic study of Hirschsprung disease.

Authors:  J A Badner; W K Sieber; K L Garver; A Chakravarti
Journal:  Am J Hum Genet       Date:  1990-03       Impact factor: 11.025

3.  Linkage disequilibrium and CF allele segregation analysis in cystic fibrosis families in Northern Ireland.

Authors:  A J Hill; C A Graham; E D Kelly; P J Morrison; N C Nevin
Journal:  Hum Genet       Date:  1989-11       Impact factor: 4.132

Review 4.  The 6's and 17's of developmental mutants near the major histocompatibility complex: the mouse t-complex does not have a human equivalent.

Authors:  R P Erickson
Journal:  Am J Hum Genet       Date:  1988-08       Impact factor: 11.025

Review 5.  Creating animal models of genetic disease.

Authors:  R P Erickson
Journal:  Am J Hum Genet       Date:  1988-11       Impact factor: 11.025

6.  X-linked hypohidrotic ectodermal dysplasia: localization within the region Xq11-21.1 by linkage analysis and implications for carrier detection and prenatal diagnosis.

Authors:  J Zonana; A Clarke; M Sarfarazi; N S Thomas; K Roberts; K Marymee; P S Harper
Journal:  Am J Hum Genet       Date:  1988-07       Impact factor: 11.025

Review 7.  Genetic markers on chromosome 7.

Authors:  L C Tsui
Journal:  J Med Genet       Date:  1988-05       Impact factor: 6.318

8.  Major effects on teratogen-induced facial clefting in mice determined by a single genetic region.

Authors:  J Karolyi; R P Erickson; S Liu; L Killewald
Journal:  Genetics       Date:  1990-09       Impact factor: 4.562

9.  High-resolution mapping of the X-linked hypohidrotic ectodermal dysplasia (EDA) locus.

Authors:  J Zonana; M Jones; D Browne; M Litt; P Kramer; H W Becker; N Brockdorff; S Rastan; K P Davies; A Clarke
Journal:  Am J Hum Genet       Date:  1992-11       Impact factor: 11.025

10.  Chromosomal location of three spectrin genes: relationship to the inherited hemolytic anemias of mouse and man.

Authors:  C S Birkenmeier; E C McFarland-Starr; J E Barker
Journal:  Proc Natl Acad Sci U S A       Date:  1988-11       Impact factor: 11.205

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.