Literature DB >> 6686210

Regional localization of the human factor IX gene by molecular hybridization.

P F Chance, K A Dyer, K Kurachi, S Yoshitake, H H Ropers, P Wieacker, S M Gartler.   

Abstract

A cloned cDNA probe encoding human factor IX was used for detecting homologous sequences in rodent human X chromosome hybrids and in human metaphase chromosome preparations. The results of these studies indicate that human factor IX is localized to the Xq27 leads to Xqter region.

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Year:  1983        PMID： 6686210     DOI： 10.1007/bf00286666

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


  10 in total

1.  COMBINED HEMOPHILIA AND CHRISTMAS DISEASE.

Authors:  J H ROBERTSON; R G TRUEMAN
Journal:  Blood       Date:  1964-09       Impact factor: 22.113

2.  HAEMOPHILIA, CHRISTMAS DISEASE AND THE XG BLOOD GROUPS. OBSERVATIONS BASED ON THE HAEMOPHILIACS OF BIRMINGHAM.

Authors:  J F HARRISON
Journal:  Br J Haematol       Date:  1964-01       Impact factor: 6.998

3.  Linkage of color blindness to hemophilias A and B.

Authors:  D L WHITTAKER; D L COPELAND; J B GRAHAM
Journal:  Am J Hum Genet       Date:  1962-06       Impact factor: 11.025

4.  Detection of specific sequences among DNA fragments separated by gel electrophoresis.

Authors:  E M Southern
Journal:  J Mol Biol       Date:  1975-11-05       Impact factor: 5.469

5.  Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I.

Authors:  P W Rigby; M Dieckmann; C Rhodes; P Berg
Journal:  J Mol Biol       Date:  1977-06-15       Impact factor: 5.469

6.  Linkage relationships of X-linked enzymes glucose-6-phosphate dehydrogenase and hypoxanthine guanine phosphoribosyltransferase: recombination in female offspring of compound heterozygotes.

Authors:  U Francke; B Bakay; J D Connor; J G Coldwell; W L Nyhan
Journal:  Am J Hum Genet       Date:  1974-07       Impact factor: 11.025

7.  Christmas disease, color-blindness and blood group Xga.

Authors:  R L Wall; J McConnell; D Moore; C R Macpherson; A Marson
Journal:  Am J Med       Date:  1967-08       Impact factor: 4.965

8.  4th International Workshop on Human Gene Mapping. Report of the committee on the genetic constitution of the X and Y chromosomes.

Authors: 
Journal:  Cytogenet Cell Genet       Date:  1978

9.  Localization of the human insulin gene to the distal end of the short arm of chromosome 11.

Authors:  M E Harper; A Ullrich; G F Saunders
Journal:  Proc Natl Acad Sci U S A       Date:  1981-07       Impact factor: 11.205

10.  Isolation and characterization of a cDNA coding for human factor IX.

Authors:  K Kurachi; E W Davie
Journal:  Proc Natl Acad Sci U S A       Date:  1982-11       Impact factor: 11.205
  10 in total
  16 in total

1.  A new MspI restriction fragment length polymorphism in the hemophilia B locus.

Authors:  G Camerino; I Oberlé; D Drayna; J L Mandel
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

2.  The telomeric region of the human X chromosome long arm: presence of a highly polymorphic DNA marker and analysis of recombination frequency.

Authors:  I Oberlé; D Drayna; G Camerino; R White; J L Mandel
Journal:  Proc Natl Acad Sci U S A       Date:  1985-05       Impact factor: 11.205

3.  Linkage studies of X-linked mental retardation: high frequency of recombination in the telomeric region of the human X chromosome (fragile site/linkage/recombination/X chromosome).

Authors:  K E Davies; M G Mattei; J F Mattei; H Veenema; S McGlade; K Harper; N Tommerup; K B Nielsen; M Mikkelsen; P Beighton
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

4.  Characterization of a set of X-linked sequences and of a panel of somatic cell hybrids useful for the regional mapping of the human X chromosome.

Authors:  I Oberlé; G Camerino; C Kloepfer; J P Moisan; K H Grzeschik; B Hellkuhl; M C Hors-Cayla; N Van Cong; D Weil; J L Mandel
Journal:  Hum Genet       Date:  1986-01       Impact factor: 4.132

5.  An intragenic deletion of the factor IX gene in a family with hemophilia B.

Authors:  S H Chen; S Yoshitake; P F Chance; G L Bray; A R Thompson; C R Scott; K Kurachi
Journal:  J Clin Invest       Date:  1985-12       Impact factor: 14.808

6.  Heterogeneity of the factor IX locus in nine hemophilia B inhibitor patients.

Authors:  R J Matthews; D S Anson; I R Peake; A L Bloom
Journal:  J Clin Invest       Date:  1987-03       Impact factor: 14.808

7.  Two sisters with a distal deletion at the Xq26/Xq27 interface: DNA studies indicate that the gene locus for factor IX is present.

Authors:  C Schwartz; N Fitch; M C Phelan; C L Richer; R Stevenson
Journal:  Hum Genet       Date:  1987-05       Impact factor: 4.132

8.  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

9.  Localization by in situ hybridization of the coagulation factor IX gene and of two polymorphic DNA probes with respect to the fragile X site.

Authors:  M G Mattei; M A Baeteman; R Heilig; I Oberlé; K Davies; J L Mandel; J F Mattei
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

Review 10.  The contribution of DNA analysis to carrier detection and prenatal diagnosis of hemophilia A and B.

Authors:  A H Bröcker-Vriends; E Bakker; H H Kanhai; G J van Ommen; P H Reitsma; J J van de Kamp; E Briët
Journal:  Ann Hematol       Date:  1992-01       Impact factor: 3.673
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