Literature DB >> 6683244

Expression of the fragile site Xq27 in fibroblasts. I. Detection of fra(X)(q27) in fibroblast clones from males with X-linked mental retardation.

P Steinbach, G Barbi, S Baur, A Wiedenmann.   

Abstract

Twelve fibroblast clones from two males with X-linked mental retardation expressed the fragile site Xq27 in 3%-38% of metaphases analyzed. The number of in vitro doublings during the cloning procedure had no evident influence on the induction of fragile X expression. The variability of fragile X expression seems to depend on cell properties acquired during culture rather than on properties originally inherent in the cells.

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Year:  1983        PMID: 6683244     DOI: 10.1007/bf00274770

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


  8 in total

1.  Non-selective isolation, stability and longevity of hybrids between normal human somatic cells.

Authors:  H Hoehn; E M Bryant; P Johnston; T H Norwood; G M Martin
Journal:  Nature       Date:  1975-12-18       Impact factor: 49.962

2.  A marker X chromosome.

Authors:  H A Lubs
Journal:  Am J Hum Genet       Date:  1969-05       Impact factor: 11.025

3.  Increase in the incidence of the fragile site Xq27 in prometaphases.

Authors:  G Barbi; P Steinbach
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

4.  A simple method to demonstrate the fragile X chromosome in fibroblasts.

Authors:  C Fonatsch
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

5.  Expression in lymphocyte and fibroblast culture of the fragile X chromosome: a new technical approach.

Authors:  M G Mattei; J F Mattei; I Vidal; F Giraud
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

6.  X-linked mental retardation: a study of 7 families.

Authors:  P A Jacobs; T W Glover; M Mayer; P Fox; J W Gerrard; H G Dunn; D S Herbst
Journal:  Am J Med Genet       Date:  1980

7.  On the frequency of telomeric chromosomal changes induced by culture conditions suitable for fragile X expression.

Authors:  P Steinbach; G Barbi; T Böller
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

8.  X-linked mental retardation with the fragile X. A study of 15 families.

Authors:  J F Mattei; M G Mattei; C Aumeras; M Auger; F Giraud
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

  8 in total
  8 in total

1.  Intercellular NOR-Ag-variability in man. II. Search for determining factors, clonal analysis.

Authors:  O A Sozansky; A F Zakharov; S M Terekhov
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

2.  Fragile X syndrome: clinical, cytogenetic, biochemical and molecular features.

Authors:  J C Mixon; V G Dev
Journal:  Indian J Pediatr       Date:  1986 Jul-Aug       Impact factor: 1.967

3.  Manifestation of the fragile site Xq27 in fibroblasts. IV. Clones from a heterozygous female do not manifest this site homogeneously on either the early or late replicating X chromosome.

Authors:  G Barbi; P Steinbach; S Baur; W Vogel
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

4.  Fragile X expression and X inactivation. I. The expression of the fragile site at Xq27.3 is not suppressed on inactive X chromosomes separated from the active homologue.

Authors:  D Wöhrle; J P Fryns; P Steinbach
Journal:  Hum Genet       Date:  1990-10       Impact factor: 4.132

5.  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

6.  Rodent common fragile sites: are they conserved? Evidence from mouse and rat.

Authors:  F F Elder; T J Robinson
Journal:  Chromosoma       Date:  1989-05       Impact factor: 4.316

7.  Manifestation of the fragile site Xq27 in fibroblasts. III. A method to demonstrate R-type replication patterns and the fragile site.

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

8.  Mental impairment in Martin-Bell syndrome is probably determined by interaction of several genes: simple explanation of phenotypic differences between unaffected and affected males with the same X chromosome.

Authors:  P Steinbach
Journal:  Hum Genet       Date:  1986-03       Impact factor: 4.132

  8 in total

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