Search Results - "GOLDMAN, A. S. H"
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Methyl methanesulfonate (MMS) produces heat-labile DNA damage but no detectable in vivo DNA double-strand breaks
Published in Nucleic acids research (01-07-2012)Get full text
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Evidence that MEK1 positively promotes interhomologue double-strand break repair
Published in Nucleic acids research (01-07-2010)“…During meiosis there is an imperative to create sufficient crossovers for homologue segregation. This can be achieved during repair of programmed DNA…”
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Meiotic Recombination Hotspots
Published in Annual review of genetics (01-01-1995)“…Meiotic recombination occurs more frequently in some regions of the eukaryotic genome than in others, with variations of several orders of magnitude observed…”
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Meiotic Studies of a Human Male Carrier of the Common Translocation, t(11;22), Suggests Postzygotic Selection rather than Preferential 3:1 MI Segregation as the Cause of Liveborn Offspring with an Unbalanced Translocation
Published in American journal of human genetics (01-09-2000)“…The t(11;22)(q23;q11) translocation is the only non-Robertsonian rearrangement for which there are a large number of unrelated families, apparently with the…”
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Meiotic analysis by FISH of a human male 46,XY,t(15;20)(q11.2;q11.2) translocation heterozygote : quadrivalent configuration, orientation and first meiotic segregation
Published in Chromosoma (1993)“…Understanding the segregational behaviour of reciprocal translocations in man is of both theoretical and clinical importance. Generally, information for…”
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Analysis of chiasma frequency and first meiotic segregation in a human male reciprocal translocation heterozygote, t(1;11)(p36.3;q13.1), using fluorescence in situ hybridisation
Published in Cytogenetics and cell genetics (1993)“…In this study we have used a testicular biopsy from a human male with a 46,XY,t(1;11)(p36.3;q13.1) karyotype. Fluorescence in situ hybridisation with whole…”
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Chromosome in situ suppression hybridisation in human male meiosis
Published in Journal of medical genetics (01-02-1992)“…Chromosome in situ suppression hybridisation with biotinylated whole chromosome libraries permits the unequivocable identification of specific human somatic…”
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Chromosome in situ suppression hybridisation in clinical cytogenetics
Published in Journal of medical genetics (01-09-1991)“…The use of chromosome in situ suppression hybridisation with whole chromosome libraries has previously been reported by various research laboratories to be an…”
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Meiotic and sperm chromosome analysis in a male carrier of an inverted insertion (3;10)(q13.2;p14p13)
Published in Journal of medical genetics (01-07-1992)“…A phenotypically normal male who fathered a son with the karyotype 46,XY,del(10)(p13) was found to be a balanced carrier of an inverted insertion (3;10)…”
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Subtelomeric breakage and chromosome exchange
Published in The Lancet (British edition) (16-12-1989)Get more information
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