Literature DB >> 1924290

Physical map of human Xq27-qter: localizing the region of the fragile X mutation.

A Poustka1, A Dietrich, G Langenstein, D Toniolo, S T Warren, H Lehrach.   

Abstract

We describe a physical map of the end of the long arm of the human X chromosome encompassing the region from Xq27.2 to the q telomere, inclusive of the chromosomal band Xq28. This region is of particular interest, since it contains the highest density of genes associated with genetic diseases. The map covers a total of 12 megabases (Mb) of DNA and extends from the telomere to 3 Mb beyond the most likely position of the fragile X mutation, defined by a cluster of translocation breakpoints in somatic cell hybrids. The map determines order and position of loci throughout the Xq28 region and localizes cell line breakpoints marking the fragile X region to an interval of 300-700 kilobases between 8 and 8.7 Mb proximal of the Xq telomere.

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Year:  1991        PMID: 1924290      PMCID: PMC52496          DOI: 10.1073/pnas.88.19.8302

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  37 in total

1.  A marker X chromosome.

Authors:  H A Lubs
Journal:  Am J Hum Genet       Date:  1969-05       Impact factor: 11.025

2.  Characterization of the human factor VIII gene.

Authors:  J Gitschier; W I Wood; T M Goralka; K L Wion; E Y Chen; D H Eaton; G A Vehar; D J Capon; R M Lawn
Journal:  Nature       Date:  1984 Nov 22-28       Impact factor: 49.962

3.  Genetic mapping of the human X chromosome by using restriction fragment length polymorphisms.

Authors:  D Drayna; K Davies; D Hartley; J L Mandel; G Camerino; R Williamson; R White
Journal:  Proc Natl Acad Sci U S A       Date:  1984-05       Impact factor: 11.205

4.  Alu sequences transcription in X. laevis oocytes: nuclear-cytoplasmic partitioning and evidence for 3' end processing reactions.

Authors:  E Perlino; G Paonessa; G Ciliberto
Journal:  Nucleic Acids Res       Date:  1985-12-09       Impact factor: 16.971

5.  Expression of active human factor VIII from recombinant DNA clones.

Authors:  W I Wood; D J Capon; C C Simonsen; D L Eaton; J Gitschier; B Keyt; P H Seeburg; D H Smith; P Hollingshead; K L Wion; E Delwart; E G Tuddenham; G A Vehar; R M Lawn
Journal:  Nature       Date:  1984 Nov 22-28       Impact factor: 49.962

6.  Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids.

Authors:  P Wieacker; K E Davies; H J Cooke; P L Pearson; R Williamson; S Bhattacharya; J Zimmer; H H Ropers
Journal:  Am J Hum Genet       Date:  1984-03       Impact factor: 11.025

7.  Isolation of human glucose-6-phosphate dehydrogenase (G6PD) cDNA clones: primary structure of the protein and unusual 5' non-coding region.

Authors:  M G Persico; G Viglietto; G Martini; D Toniolo; G Paonessa; C Moscatelli; R Dono; T Vulliamy; L Luzzatto; M D'Urso
Journal:  Nucleic Acids Res       Date:  1986-03-25       Impact factor: 16.971

8.  Molecular genetics of human color vision: the genes encoding blue, green, and red pigments.

Authors:  J Nathans; D Thomas; D S Hogness
Journal:  Science       Date:  1986-04-11       Impact factor: 47.728

9.  Effects of nucleotides on expression of the folate sensitive fragile sites.

Authors:  G R Sutherland; E Baker
Journal:  Am J Med Genet       Date:  1986 Jan-Feb

10.  Defining the beginning and end of KpnI family segments.

Authors:  G Grimaldi; J Skowronski; M F Singer
Journal:  EMBO J       Date:  1984-08       Impact factor: 11.598

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  22 in total

1.  Molecular and genetic analysis of the Drosophila model of fragile X syndrome.

Authors:  Charles R Tessier; Kendal Broadie
Journal:  Results Probl Cell Differ       Date:  2012

2.  Further localization of X-linked hydrocephalus in the chromosomal region Xq28.

Authors:  P J Willems; L Vits; P Raeymaekers; J Beuten; P Coucke; J J Holden; C Van Broeckhoven; S T Warren; M Sagi; D Robinson
Journal:  Am J Hum Genet       Date:  1992-08       Impact factor: 11.025

3.  Characterization of a deletion at Xq27-q28 associated with unbalanced inactivation of the nonmutant X chromosome.

Authors:  J T Clarke; P J Wilson; C P Morris; J J Hopwood; R I Richards; G R Sutherland; P N Ray
Journal:  Am J Hum Genet       Date:  1992-08       Impact factor: 11.025

4.  Influence of single nucleotide polymorphisms in factor VIII and von Willebrand factor genes on plasma factor VIII activity: the ARIC Study.

Authors:  Marco Campos; Ashley Buchanan; Fuli Yu; Maja Barbalic; Yang Xiao; Lloyd E Chambless; Kenneth K Wu; Aaron R Folsom; Eric Boerwinkle; Jing-fei Dong
Journal:  Blood       Date:  2012-01-04       Impact factor: 22.113

5.  Evidence for the organization of chromatin in megabase pair-sized loops arranged along a random walk path in the human G0/G1 interphase nucleus.

Authors:  H Yokota; G van den Engh; J E Hearst; R K Sachs; B J Trask
Journal:  J Cell Biol       Date:  1995-09       Impact factor: 10.539

6.  Refining the genetic location of the gene for X linked hydrocephalus within Xq28.

Authors:  M Jouet; E Feldman; J Yates; D Donnai; J Paterson; D Siggers; S Kenwrick
Journal:  J Med Genet       Date:  1993-03       Impact factor: 6.318

7.  Genetic mapping of the X-linked dominant mutations striated (Str) and bare patches (Bpa) to a 600-kb region of the mouse X chromosome: implications for mapping human disorders in Xq28.

Authors:  T A Angel; C J Faust; J C Gonzales; S Kenwrick; R A Lewis; G E Herman
Journal:  Mamm Genome       Date:  1993       Impact factor: 2.957

8.  X-linked nephrogenic diabetes insipidus: from the ship Hopewell to RFLP studies.

Authors:  D G Bichet; G N Hendy; M Lonergan; M F Arthus; S Ligier; Z Pausova; R Kluge; H Zingg; P Saenger; E Oppenheimer
Journal:  Am J Hum Genet       Date:  1992-11       Impact factor: 11.025

9.  Emery-Dreifuss muscular dystrophy: linkage to markers in distal Xq28.

Authors:  J R Yates; J P Warner; J A Smith; F Deymeer; J P Azulay; I Hausmanowa-Petrusewicz; J Zaremba; J Borkowska; N A Affara; M A Ferguson-Smith
Journal:  J Med Genet       Date:  1993-02       Impact factor: 6.318

10.  X linked myotubular myopathy (MTM1) maps between DXS304 and DXS305, closely linked to the DXS455 VNTR and a new, highly informative microsatellite marker (DXS1684).

Authors:  N Dahl; F Samson; N S Thomas; L J Hu; W Gong; G Herman; J Laporte; P Kioschis; A Poustka; J L Mandel
Journal:  J Med Genet       Date:  1994-12       Impact factor: 6.318

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