Literature DB >> 3198111

Population cytogenetics of folate-sensitive fragile sites. I. Common fragile sites.

M Kähkönen1.   

Abstract

The location and frequency of folate-sensitive common fragile sites (CFS) were studied in three populations: (1) 111 mentally retarded children of school age, (2) 240 mentally subnormal children attending special schools, and (3) 85 healthy children attending normal schools. Common fragile sites were found at 54 chromosomal bands including also the band Xq27, where gaps and breaks were detected in 4% of the children. The most frequent CFS were FRA3B (at 3p14.2), FRA6E (at 6q26), and FRA16D (at 16q23) seen in 73%, 65%, and 58% of the individuals totally studied. The frequencies of CFS-positive individuals did not differ among the populations. The variation found in the distribution of CFS among the populations was primarily assumed to be due to sampling differences and study method. The rate of expression of the most frequent CFS varied significantly among the individuals, seeming to suggest that polymorphism exists at those CFS.

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Year:  1988        PMID: 3198111     DOI: 10.1007/bf00273649

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


  22 in total

1.  Nonrandom distribution of chromosome breaks in cultured lymphocytes of normal subjects.

Authors:  S Aymé; J F Mattei; M G Mattei; Y Aurran; F Giraud
Journal:  Hum Genet       Date:  1976-02-29       Impact factor: 4.132

2.  Distribution of spontaneous chromosome breaks in human chromosomes.

Authors:  P Aula; H von Koskull
Journal:  Hum Genet       Date:  1976-05-19       Impact factor: 4.132

3.  Fragile sites update.

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

Review 4.  Chromosomal fragile sites and cancer-specific rearrangements.

Authors:  M M Le Beau
Journal:  Blood       Date:  1986-04       Impact factor: 22.113

5.  Fragile sites and chromosome breakpoints in constitutional rearrangements II. Spontaneous abortions, stillbirths and newborns.

Authors:  F Hecht; B K Hecht
Journal:  Clin Genet       Date:  1984-09       Impact factor: 4.438

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.  Frequency of rare fragile sites among mentally subnormal schoolchildren.

Authors:  M Kähkönen; J Leisti; C J Thoden; S Autio
Journal:  Clin Genet       Date:  1986-09       Impact factor: 4.438

8.  Induction of sister chromatid exchanges at common fragile sites.

Authors:  T W Glover; C K Stein
Journal:  Am J Hum Genet       Date:  1987-11       Impact factor: 11.025

9.  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

10.  Fragile sites, chromosome evolution, and human neoplasia.

Authors:  R Miró; I C Clemente; C Fuster; J Egozcue
Journal:  Hum Genet       Date:  1987-04       Impact factor: 4.132

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  8 in total

1.  Genetic determination of fragile-site expression.

Authors:  D Smeets; A Arets
Journal:  Am J Hum Genet       Date:  1990-08       Impact factor: 11.025

2.  Population cytogenetics of aphidicolin-induced fragile sites.

Authors:  B Tedeschi; P Vernole; M L Sanna; B Nicoletti
Journal:  Hum Genet       Date:  1992-07       Impact factor: 4.132

3.  Population cytogenetics of folate-sensitive fragile sites. II. Autosomal rare fragile sites.

Authors:  M Kähkönen; C Tengström; T Alitalo; R Matilainen; M Kaski; E Airaksinen
Journal:  Hum Genet       Date:  1989-04       Impact factor: 4.132

4.  Chromosome lesions which could be interpreted as "fragile sites" on the distal end of Xq.

Authors:  M G Butler; G A Allen; J L Haynes; S J Clark
Journal:  Am J Med Genet       Date:  1990-10

5.  12-year-old boy with a 4q35.2 microdeletion and involvement of MTNR1A, FAT1, and F11 genes.

Authors:  Erin L Youngs; Rebecca S Henkhaus; Jessica A Hellings; Merlin G Butler
Journal:  Clin Dysmorphol       Date:  2012-04       Impact factor: 0.816

6.  FREQUENCY AND DISTRIBUTION OF CHROMOSOME FRAGILE SITES OR LESIONS IN MALES WITH MENTAL RETARDATION: A DESCRIPTIVE STUDY.

Authors:  Merlin G Butler
Journal:  J Tenn Acad Sci       Date:  1998 Jul-Oct

7.  Discovery of structural alterations in solid tumor oligodendroglioma by single molecule analysis.

Authors:  Mohana Ray; Steve Goldstein; Shiguo Zhou; Konstantinos Potamousis; Deepayan Sarkar; Michael A Newton; Elizabeth Esterberg; Christina Kendziorski; Oliver Bogler; David C Schwartz
Journal:  BMC Genomics       Date:  2013-07-26       Impact factor: 3.969

Review 8.  Are common fragile sites merely structural domains or highly organized "functional" units susceptible to oncogenic stress?

Authors:  Alexandros G Georgakilas; Petros Tsantoulis; Athanassios Kotsinas; Ioannis Michalopoulos; Paul Townsend; Vassilis G Gorgoulis
Journal:  Cell Mol Life Sci       Date:  2014-09-20       Impact factor: 9.261

  8 in total

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