Search Results - "GOLDMAN, A. S. H"

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    Evidence that MEK1 positively promotes interhomologue double-strand break repair by Terentyev, Yaroslav, Johnson, Rebecca, Neale, Matthew J, Khisroon, Muhammad, Bishop-Bailey, Anna, Goldman, Alastair S.H

    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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    Journal Article
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    Meiotic Recombination Hotspots by Lichten, M, Goldman, A S H

    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 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 by GOLDMAN, A. S. H, HULTEN, M. A

    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 by Goldman, A S, Hultén, M A

    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 by Goldman, A S, Hultén, M A

    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 by Hulten, M A, Gould, C P, Goldman, A S, Waters, J J

    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) by GOLDMAN, A. S. H, MARTIN, R. H, JOHANNISSON, R, GOULD, C. P, DAVISON, E. V, EMSLIE, J. E, BURN, J, HULTEN, M. A

    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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