Literature DB >> 2688541

Chromosome maps of man and mouse. IV.

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

Abstract

Current knowledge of man-mouse genetic homology is presented in the form of chromosomal displays, tables and a grid, which show locations of the 322 loci now assigned to chromosomes in both species, as well as 12 DNA segments not yet associated with gene loci. At least 50 conserved autosomal segments with two or more loci have been identified, twelve of which are over 20 cM long in the mouse, as well as five conserved segments on the X chromosome. All human and mouse chromosomes now have conserved regions; human 17 still shows the least evidence of rearrangement, with a single long conserved segment which apparently spans the centromere. The loci include 102 which are known to be associated with human hereditary disease; these are listed separately. Human parental effects which may well be the result of genomic imprinting are reviewed and the location of the factors concerned displayed in relation to mouse chromosomal regions which have been implicated in imprinting phenomena.

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Year:  1989        PMID: 2688541     DOI: 10.1111/j.1469-1809.1989.tb01777.x

Source DB:  PubMed          Journal:  Ann Hum Genet        ISSN: 0003-4800            Impact factor:   1.670


  52 in total

1.  Evidence for a prostate cancer-susceptibility locus on chromosome 20.

Authors:  R Berry; J J Schroeder; A J French; S K McDonnell; B J Peterson; J M Cunningham; S N Thibodeau; D J Schaid
Journal:  Am J Hum Genet       Date:  2000-05-16       Impact factor: 11.025

2.  Close linkage of retinoic acid receptor genes with homeobox- and keratin-encoding genes on paralogous segments of mouse chromosomes 11 and 15.

Authors:  J H Nadeau; J G Compton; V Giguère; J Rossant; S Varmuza
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

3.  Chromosomal mapping of the high affinity Fc gamma receptor gene.

Authors:  R J Oakey; T A Howard; P M Hogarth; K Tani; M F Seldin
Journal:  Immunogenetics       Date:  1992       Impact factor: 2.846

4.  The tyrosinase-positive oculocutaneous albinism locus maps to chromosome 15q11.2-q12.

Authors:  M Ramsay; M A Colman; G Stevens; E Zwane; J Kromberg; M Farrall; T Jenkins
Journal:  Am J Hum Genet       Date:  1992-10       Impact factor: 11.025

Review 5.  Genomic imprinting.

Authors:  J G Hall
Journal:  Arch Dis Child       Date:  1990-10       Impact factor: 3.791

Review 6.  Chromosome imbalance, normal phenotype, and imprinting.

Authors:  L Bortotto; E Piovan; R Furlan; H Rivera; O Zuffardi
Journal:  J Med Genet       Date:  1990-09       Impact factor: 6.318

Review 7.  Twinning and mitotic crossing-over: some possibilities and their implications.

Authors:  G B Côté; J Gyftodimou
Journal:  Am J Hum Genet       Date:  1991-07       Impact factor: 11.025

8.  A polymorphism in the human UGRP1 gene promoter that regulates transcription is associated with an increased risk of asthma.

Authors:  Tomoaki Niimi; Mitsuru Munakata; Catherine L Keck-Waggoner; Nicholas C Popescu; Roy C Levitt; Michie Hisada; Shioko Kimura
Journal:  Am J Hum Genet       Date:  2002-01-25       Impact factor: 11.025

9.  Induction of uteroglobin-related protein 2 (Ugrp2) expression by EGF and TGFalpha.

Authors:  Atsushi Yamada; Shioko Kimura
Journal:  FEBS Lett       Date:  2005-04-11       Impact factor: 4.124

10.  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

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