Literature DB >> 1141013

Is the chromatid gap a folding defect due to protein change? Evidence from mercaptoethanol treatment of human lymphocyte chromosomes.

A Brogger.   

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Year:  1975        PMID： 1141013     DOI： 10.1111/j.1601-5223.1975.tb01507.x

Source DB:  PubMed          Journal:  Hereditas        ISSN： 0018-0661            Impact factor:   3.271


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  4 in total

1.  Psoralen/UVA treatment and chromosomes. I. Aberrations and sister chromatid exchange in human lymphocytes in vitro and synergism with caffeine.

Authors:  H Waksvik; A Brogger; J Stene
Journal:  Hum Genet       Date:  1977-09-22       Impact factor: 4.132

2.  The constitutional fragility of chromosome 12 in a case of 46,XX,var(12)(gh',RHG,CAG,CBG).

Authors:  E Donti; G Venti; V Bocchini; G Rosi; R Armellini; N Trabalza
Journal:  Hum Genet       Date:  1979-04-17       Impact factor: 4.132

3.  The effect of SH-SS transition in the structural organization of mitotic chromosomes.

Authors:  G Kosztolányi; E M Bühler
Journal:  Hum Genet       Date:  1978-05-16       Impact factor: 4.132

4.  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
  4 in total

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