Literature DB >> 2921033

Expression of folate-sensitive fragile sites in lymphocyte chromosomes.

C Fuster1, R Miró, C Templado, L Barrios, J Egozcue.   

Abstract

The expression of folate-sensitive fragile sites (FS) was analyzed using MTX as a fragility inducer in seven normal subjects [four unrelated persons and three members of one family (father, mother, and son)]; a woman heterozygous for fra Xq27.3 with a 47,XXX karyotype; and her son, affected by the fra-X syndrome. The mean expression of chromosome lesions (CL) other than Xq27.3 was 70.1% (686CL in 978 metaphases), and the coincidence between CL and FS was 68.9%. We propose six new c-fra sites: bands 4q33 and 11q22 because they were found in two members of the same family; band 13q32 because it had a frequency of expression of 3% of metaphases; and bands 3p13, 8q21, and Xq21 because they were observed in four of the nine individuals studied.

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Year:  1989        PMID: 2921033     DOI: 10.1007/BF00278997

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


  20 in total

1.  Different inducibility and possible significance of several concomitant "fragile sites" in two brothers.

Authors:  F Shabtai; J Orlin; J Hart; I Halbrecht; D Klar; J Friedman
Journal:  Hum Genet       Date:  1986-09       Impact factor: 4.132

2.  Fragile sites update.

Authors:  F Hecht
Journal:  Cancer Genet Cytogenet       Date:  1988-03

3.  Report of the committee on cytogenetic markers.

Authors:  G R Sutherland; J F Mattei
Journal:  Cytogenet Cell Genet       Date:  1987

4.  Clinical implications and classification of the constitutive fragile sites.

Authors:  A Daniel
Journal:  Am J Med Genet       Date:  1986 Jan-Feb

5.  Excess thymidine induces folate sensitive fragile sites.

Authors:  G R Sutherland; E Baker; A Fratini
Journal:  Am J Med Genet       Date:  1985-10

6.  DNA polymerase alpha inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes.

Authors:  T W Glover; C Berger; J Coyle; B Echo
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

7.  Constitutive fragile sites and cancer.

Authors:  J J Yunis; A L Soreng
Journal:  Science       Date:  1984-12-07       Impact factor: 47.728

8.  Carrier detection and X-inactivation studies in the fragile X syndrome. Cytogenetic studies in 63 obligate and potential carriers of the fragile X.

Authors:  K B Nielsen; N Tommerup; H Poulsen; P Jacobsen; B Beck; M Mikkelsen
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

9.  Familial fragile site found at the cancer breakpoint (1)(q32). Inducibility by distamycin A, concomitance with fragile (16)(q22).

Authors:  F Shabtai; J Hart; D Klar; I Halbrecht
Journal:  Hum Genet       Date:  1986-07       Impact factor: 4.132

10.  The most common fragile site in man is 3p14.

Authors:  D F Smeets; J M Scheres; T W Hustinx
Journal:  Hum Genet       Date:  1986-03       Impact factor: 4.132

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  3 in total

1.  Increased expression of 5q31 fragile site in a Bloom syndrome family.

Authors:  A F Fundia; N B Gorla; M M Bonduel; O Azpilicueta; H Lejarraga; F S Muriel; I B Larripa
Journal:  Hum Genet       Date:  1992-07       Impact factor: 4.132

2.  Telomere association of chromosomes induced by aphidicolin in a normal individual.

Authors:  C Fuster; R Miró; L Barrios; J Egozcue
Journal:  Hum Genet       Date:  1990-04       Impact factor: 4.132

3.  Cytogenetic studies in motile sperm from normal men.

Authors:  J Benet; A Genescà; J Navarro; J Egozcue; C Templado
Journal:  Hum Genet       Date:  1992-05       Impact factor: 4.132

  3 in total

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