Literature DB >> 6859039

Heritable fragile sites on human chromosomes. X. New folate-sensitive fragile sites: 6p23, 9p21, 9q32, and 11q23.

G R Sutherland, P B Jacky, E Baker, A Manuel.   

Abstract

Four new folate-sensitive fragile sites are documented at 6p23, 9p21, 9q32, and 11q23. These have all been shown to be heritable except for the one at 9p21, which has been seen only in a single individual. As with the other autosomal fragile sites, these appear to be innocuous in heterozygotes.

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Year:  1983        PMID： 6859039      PMCID： PMC1685660     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


  9 in total

1.  Heritable fragile sites on human chromosomes I. Factors affecting expression in lymphocyte culture.

Authors:  G R Sutherland
Journal:  Am J Hum Genet       Date:  1979-03       Impact factor: 11.025

2.  Heritable fragile sites on human chromosomes II. Distribution, phenotypic effects, and cytogenetics.

Authors:  G R Sutherland
Journal:  Am J Hum Genet       Date:  1979-03       Impact factor: 11.025

3.  Heritable fragile sites on human chromosomes. VI. Characterization of the fragile site at 12q13.

Authors:  G R Sutherland; L Hinton
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

Review 4.  The fragile X chromosome.

Authors:  G R Sutherland
Journal:  Int Rev Cytol       Date:  1983

5.  [Genetic aspects of autosomal fragile sites. Apropos of 40 Cases].

Authors:  M Guichaoua; M G Matteï; J F Matteï; F Giraud
Journal:  J Genet Hum       Date:  1982-10

6.  5-Fluoro-2'-deoxyuridine induction of the fragile site on Xq28 associated with X linked mental retardation.

Authors:  N Tommerup; H Poulsen; K Brøndum-Nielsen
Journal:  J Med Genet       Date:  1981-10       Impact factor: 6.318

7.  Heritable fragile sites on human chromosomes. VIII. Preliminary population cytogenetic data on the folic-acid-sensitive fragile sites.

Authors:  G R Sutherland
Journal:  Am J Hum Genet       Date:  1982-05       Impact factor: 11.025

8.  Heritable fragile sites on human chromosomes. VII. Children homozygous for the BrdU-requiring fra(10)(q25) are phenotypically normal.

Authors:  G R Sutherland
Journal:  Am J Hum Genet       Date:  1981-11       Impact factor: 11.025

9.  FUdR induction of the X chromosome fragile site: evidence for the mechanism of folic acid and thymidine inhibition.

Authors:  T W Glover
Journal:  Am J Hum Genet       Date:  1981-03       Impact factor: 11.025
  9 in total
  12 in total

1.  Inhibition of condensation in human chromosomes induced by the thymidine analogue 5-iododeoxyuridine.

Authors:  G Ott; T Haaf; M Schmid
Journal:  Chromosome Res       Date:  1998-09       Impact factor: 5.239

2.  Rare, polymorphic, and common fragile sites: a classification.

Authors:  F Hecht
Journal:  Hum Genet       Date:  1986-10       Impact factor: 4.132

Review 3.  Jacobsen syndrome: report of a patient with severe eye anomalies, growth hormone deficiency, and hypothyroidism associated with deletion 11 (q23q25) and review of 52 cases.

Authors:  E K Pivnick; G V Velagaleti; R S Wilroy; M E Smith; S R Rose; R E Tipton; A T Tharapel
Journal:  J Med Genet       Date:  1996-09       Impact factor: 6.318

4.  Regional localization for HLA by recombination with a fragile site at 6p23.

Authors:  J C Mulley; J Hay; L J Sheffield; G R Sutherland
Journal:  Am J Hum Genet       Date:  1983-11       Impact factor: 11.025

5.  Nonrandom distribution of methotrexate-induced aberrations on human chromosomes. Detection of further folic acid sensitive fragile sites.

Authors:  G Barbi; P Steinbach; W Vogel
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

6.  Autosomal fragile sites and cancer.

Authors:  F Hecht; B K Hecht
Journal:  Am J Hum Genet       Date:  1984-05       Impact factor: 11.025

7.  Fragile sites and structural rearrangements in cancer.

Authors:  M De Braekeleer; B Smith; C C Lin
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

8.  Red blood cell folate is associated with the development of dysplasia and cancer in ulcerative colitis.

Authors:  B A Lashner
Journal:  J Cancer Res Clin Oncol       Date:  1993       Impact factor: 4.553

9.  Excess of mental retardation and/or congenital malformation in reciprocal translocations in man.

Authors:  J P Fryns; A Kleczkowska; E Kubień; H Van den Berghe
Journal:  Hum Genet       Date:  1986-01       Impact factor: 4.132

10.  Further localization of ETS1 indicates that the chromosomal rearrangement in Ewing sarcoma does not occur at fra(11)(q23).

Authors:  R N Simmers; G R Sutherland
Journal:  Hum Genet       Date:  1988-02       Impact factor: 4.132
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