Literature DB >> 7129443

Cocultivation studies with cells of patients bearing fragile X chromosomes.

G Eberle, H Zankl, M Zankl.   

Abstract

Fourteen cocultivation studies were carried out with cells of our patients with fragile X, one obligate and two possible female heterozygotes, two female controls, and a rabbit. In all cocultivations the number of fragile X chromosomes was sharply reduced in the patient cells. The strongest effect was causes by the animal cells. A distinct difference between the two controls in the reducing ability was observed. No such difference was found between the obligate and possible heterozygotes on the one hand and the controls on the other. To test the influence of the residual serum in the mixed blood cultures, the serum of a patient's blood sample was replaced by the serum of a control. The frequency of fragile X chromosomes was not decreased by this procedure. Therefore a soluble factor is supposed to exist which is produced by normal or heterozygote cells in culture and which reduces the expression of fragile sites in patient cells.

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Year:  1982        PMID: 7129443     DOI: 10.1007/bf00274210

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


  6 in total

1.  Methods of increasing the visibility of fragile X chromosomes.

Authors:  H Zankl; G Eberle
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

2.  Fragile sites in chromosomes.

Authors:  D Soudek; T McGregor
Journal:  Can Med Assoc J       Date:  1981-01-15       Impact factor: 8.262

3.  Rate of sister chromatid exchanges in Bloom syndrome fibroblasts reduced by co-cultivation with normal fibroblasts.

Authors:  H W Rüdiger; C R Bartram; W Harder; E Passarge
Journal:  Am J Hum Genet       Date:  1980-03       Impact factor: 11.025

4.  Prevention of chromosomal breakage in Fanconi's anemia by cocultivation with normal cells.

Authors:  I Nordenson; B Björksten; B Lundh
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

5.  High rate of sister chromatid exchanges of Bloom's syndrome chromosomes is corrected in rodent human somatic cell hybrids.

Authors:  B Alhadeff; M Velivasakis; I Pagan-Charry; W C Wright; M Siniscalco
Journal:  Cytogenet Cell Genet       Date:  1980

6.  Normalization by cell fusion of sister chromatid exchange in Bloom syndrome lymphocytes.

Authors:  Y Shiraishi; S Matsui; A A Sandberg
Journal:  Science       Date:  1981-05-15       Impact factor: 47.728

  6 in total
  5 in total

1.  Expression of the fragile site Xq27 in fibroblasts. II. Evidence for negative and positive clones from heterozygous females and possible relationship between frequency and phenotype.

Authors:  P Steinbach; G Barbi; S Baur; W Vogel
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

2.  Expression of fra(X)(q28) is suppressed in man-mouse hybrid cells.

Authors:  R D Wegner; B Geiseler; K Sperling
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

3.  A fragile X suppressor in the normal human blood?

Authors:  D Soudek; M Emanuel
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

4.  Mean corpuscular hemoglobin is increased in Martin-Bell syndrome.

Authors:  U Langenbeck; J Schmidtke; I Bartels; I Hansmann; H Knüppel
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

5.  Expression of the fragile (X) chromosome in an interspecific somatic cell hybrid.

Authors:  R L Nussbaum; S D Airhart; D H Ledbetter
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

  5 in total

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