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    Article

    Are terminal chiasmata in male Schistocerca gregaria produced by telomere stickiness or by crossover processes?

    L. T. Douglas, D. F. Cupedo, R. M. Douglas in Genetica (1978)

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    Article

    Book reviews

    L. T. Douglas, R. Piechocki, E. Hofmann, K. Esser in Theoretical and Applied Genetics (1977)

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    Article

    Patterned disjunction in Drosophila melanogaster. I. Assortment of SPA pol /+ and X, Y in the stock N1

    N1 (= Nijmegen 1) ♂♂ D. melanogaster heterozygous for sparkling poliert (4) (= pol, here) were backcrossed as single pairs. When ♂♂ were not selected for departure from 1/1, pol/pol +, many exceptional ratios wer...

    L. T. Douglas, M. E. van Meekeren in Genetica (1972)

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    Article

    Meiosis VII: “Detorsive bending” as a basis for geometric shapes of late prophase bivalents

    A new model depending on mechanical properties of chromosomes is adduced as a basis for diplotene opening-out and for curvature occurring in grasshopper bivalents, during and subsequent to diplotene. Condition...

    L. T. Douglas in Genetica (1970)

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    Article

    Meiosis VI: A reinterpretation of tritium thymidine labelling of meiotic chromosomes, supporting the chiasmatype hypothesis

    Re-examination of data relating chiasmata per bivalent to tritium thymidine switch points per chromatid in male grasshoppers suggests that they are consistent with the chiasmatype hypothesis: that the number o...

    L. T. Douglas, H. W. Kroes in Genetica (1969)

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    Article

    A stock ofDrosophila melanogaster evidently showing drive and quasi-linkage in females

    Preliminary experiments on a laboratory stock ofDrosophila melanogaster are described, which lead to the conclusion that there is in this stock “meioti-drive” and quasi-linkage in females.

    L. T. Douglas, S. J. Geerts, Noordje Oomen in Genetica (1968)

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    Article

    Meiosis IV: Segregation from interchange multivalents as a Markov process

    A new model is adduced in explanation of known segregation ratios from quadrivalents and related multivalents. A Markov process consisting of the following three steps is proposed: (A) geometric ordering of ce...

    L. T. Douglas in Genetica (1968)

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    Article

    Meiosis III: The elastica, and markov proceses as models for non-random segregation from associated non-homologues inDrosophila

    Grell's (1964) “non-competitive” data describing segregation of markers on two non-homologous, non-crossover chromosomes inDrosophila melanogaster, called Dp and 4, are explained on the basis of the “elastica” b...

    L. T. Douglas in Genetica (1968)

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    Article

    Meiosis V: Matric and path coefficient solutions of tri- and quadrivalents

    Possible classes of spatial ordering between chromosomal components of multivalents and their motion with respect to each other are deduced on the basis of the propositions: (A) that the proximity of centromer...

    L. T. Douglas in Genetica (1968)

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    Article

    Meiosis, I: Association of non-homologous bivalents during spermatogenesis in white mice

    In Feulgen sqaushes from control and EDTA pretreated seminiferous tubules of white mice, association of non-homologous chromosomes has been observed in pachytene, diplotene and in secondary spermatocyte nuclei...

    L. T. Douglas in Genetica (1966)

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    Article

    Meiosis, II: A modified affinity model in mice

    In male mice, observations on MI clustering of nonhomologues in 4-armed tri-bivalent groups considered together with estimates of chiasma frequency in the same clusters, has suggested a modification of theWallce ...

    L. T. Douglas, S. J. Geerts in Genetica (1966)

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    Article

    Evidence for tandem arrangement of chromosomal elements in spermatid nuclei of the chinese hamster

    Incubation of living seminiferous tubules of the chinese hamster,Cricetulus barabensis, in EDTA-containing hypotonic salt solutions and subsequent Feulgen squashing gives preparations with tandemly-aligned chromo...

    L. T. Douglas in Genetica (1965)