Literature DB >> 1675191

High-density molecular map of the central span of the mouse X chromosome.

N Brockdorff1, G Kay, S Smith, J T Keer, R M Hamvas, S D Brown, S Rastan.   

Abstract

A total of 17 linking clones previously sublocalized to the central span of the mouse X chromosome have been ordered by detailed analysis through interspecific Mus spretus/Mus musculus domesticus backcross progeny. These probes have been positioned with respect to existing DNA markers utilizing a new interspecific backcross segregating for the Tabby (Ta) locus. The density of clones within this 11.5-cM interval is now, on average, one clone every 1000 kb. This high-density map provides probes in the vicinity of a number of important genetic loci in this region which include the X-inactivation center, the Ta locus, and the mottled (Mo) locus, and therefore provides a molecular framework for identification of the genes encoded at these loci.

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Year:  1991        PMID: 1675191     DOI: 10.1016/0888-7543(91)90478-w

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


  13 in total

Review 1.  Mouse X chromosome.

Authors:  S D Brown; P Avner; G E Herman
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

Review 2.  X-chromosome inactivation and escape.

Authors:  Christine M Disteche; Joel B Berletch
Journal:  J Genet       Date:  2015-12       Impact factor: 1.166

Review 3.  Mouse X chromosome.

Authors:  S D Brown; P Avner; V M Chapman; R M Hamvas; G E Herman
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

Review 4.  Menkes disease: recent advances and new aspects.

Authors:  Z Tümer; N Horn
Journal:  J Med Genet       Date:  1997-04       Impact factor: 6.318

5.  The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains.

Authors:  A K Srivastava; J Pispa; A J Hartung; Y Du; S Ezer; T Jenks; T Shimada; M Pekkanen; M L Mikkola; M S Ko; I Thesleff; J Kere; D Schlessinger
Journal:  Proc Natl Acad Sci U S A       Date:  1997-11-25       Impact factor: 11.205

6.  Mapping of loci and translocation breakpoints in Xq13: isolation of a conserved locus that maps close to CCG1 in human and mouse.

Authors:  V Reed; S H Laval; V McCabe; H F Willard; Y Boyd
Journal:  Mamm Genome       Date:  1994-04       Impact factor: 2.957

7.  Mapping of a mouse homolog of a heterochromatin protein gene the X chromosome.

Authors:  R M Hamvas; W Reik; S J Gaunt; S D Brown; P B Singh
Journal:  Mamm Genome       Date:  1992       Impact factor: 2.957

8.  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

9.  Molecular genetic analysis of the Ta25H deletion: evidence for additional deleted loci.

Authors:  N Brockdorff; G Kay; B M Cattanach; S Rastan
Journal:  Mamm Genome       Date:  1991       Impact factor: 2.957

10.  Detection of a molecular deletion at the DXS732 locus in a patient with X-linked hypohidrotic ectodermal dysplasia (EDA), with the identification of a unique junctional fragment.

Authors:  J Zonana; J Gault; K J Davies; M Jones; D Browne; M Litt; N Brockdorff; S Rastan; A Clarke; N S Thomas
Journal:  Am J Hum Genet       Date:  1993-01       Impact factor: 11.025

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