Literature DB >> 2989089

Construction of a human X-chromosome-enriched phage library which facilitates analysis of specific loci.

L M Kunkel, M Lalande, A P Monaco, A Flint, W Middlesworth, S A Latt.   

Abstract

A human X-chromosome-enriched MboI-partial-digest recombinant library in phage lambda Charon30 has been constructed. Twelve out of the thirteen X-chromosome DNA sequences that were tested were present in the library. Most regions were covered in overlapping phage inserts; mean insert size was 13.7 kb. One phage from the library allowed detection of a 225-bp insertion of DNA into a region near the Duchenne muscular dystrophy (DMD) locus. Another recombinant phage represents an expansion of a region which exhibits extensive and varying homology with other human chromosomes, including the Y, as well as with rodent DNA. The present library should have widespread use for examining DNA sequences on the human X chromosome.

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Year:  1985        PMID: 2989089     DOI: 10.1016/0378-1119(85)90232-x

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  13 in total

1.  Linkage relationship between retinoschisis and four marker loci.

Authors:  G Gellert; J Peterson; M Krawczak; B Zoll
Journal:  Hum Genet       Date:  1988-08       Impact factor: 4.132

2.  Repeated DNA sequences in the distal long arm of the human X chromosome.

Authors:  U Müller; U Tantravahi; A Monaco; H Stroh; L M Kunkel; S A Latt
Journal:  Hum Genet       Date:  1986-09       Impact factor: 4.132

3.  Anonymous DNA probes to human chromosome 16 derived from a flow-purified library.

Authors:  V J Hyland; S Grist; D F Callen; G R Sutherland
Journal:  Am J Hum Genet       Date:  1988-02       Impact factor: 11.025

4.  An extremely polymorphic locus on the short arm of the human X chromosome with homology to the long arm of the Y chromosome.

Authors:  R G Knowlton; C A Nelson; V A Brown; D C Page; H Donis-Keller
Journal:  Nucleic Acids Res       Date:  1989-01-11       Impact factor: 16.971

5.  Analysis of a terminal Xp22.3 deletion in a patient with six monogenic disorders: implications for the mapping of X linked ocular albinism.

Authors:  A Meindl; D Hosenfeld; W Brückl; S Schuffenhauer; J Jenderny; A Bacskulin; H C Oppermann; O Swensson; P Bouloux; T Meitinger
Journal:  J Med Genet       Date:  1993-10       Impact factor: 6.318

6.  Genetic linkage study between the loci for Duchenne and Becker muscular dystrophy and nine X-chromosomal DNA markers.

Authors:  E Wilichowski; M Krawczak; E Seemanova; F Hanefeld; J Schmidtke
Journal:  Hum Genet       Date:  1987-01       Impact factor: 4.132

7.  A long range restriction map of the distal human X chromosome short arm around the steroid sulfatase locus.

Authors:  X M Li; P Yen; T Mohandas; L J Shapiro
Journal:  Nucleic Acids Res       Date:  1990-05-11       Impact factor: 16.971

Review 8.  Advanced molecular cytogenetics in human and mouse.

Authors:  Kathleen Dorritie; Cristina Montagna; Michael J Difilippantonio; Thomas Ried
Journal:  Expert Rev Mol Diagn       Date:  2004-09       Impact factor: 5.225

9.  Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: molecular genetic evidence for deletions.

Authors:  U Francke; J F Harper; B T Darras; J M Cowan; E R McCabe; A Kohlschütter; W K Seltzer; F Saito; J Goto; J P Harpey
Journal:  Am J Hum Genet       Date:  1987-03       Impact factor: 11.025

10.  X linked lymphoproliferative disease in a United Kingdom family.

Authors:  P D Arkwright; G Makin; A M Will; M Ayres; D A Gokhale; W D Fergusson; G M Taylor
Journal:  Arch Dis Child       Date:  1998-07       Impact factor: 3.791

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