8 research outputs found

    Experimental signature of a topological quantum dot

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    9 pags., 6 figs., 2 tabs.M. S. would like to acknowledge the President’s PhD Scholarship programme at Imperial College London for financial support. C. M. would like to acknowledge the EPSRC award EP/M022250/1, and the award of a Royal Society University Research Fellowship by the UK Royal Society. M. S. R. is supported through a studentship in the Centre for Doctoral Training on Theory and Simulation of Materials at Imperial College London funded by EPSRC Grant No. EP/L015579/1. M. N.-C. acknowledges support from the University of Birmingham (Birmingham Fellowship) and the EPSRC (grant no. EP/S018395/1). V. G. acknowledges the Spanish Ministerio de Economia y Competitividad for financial support through the grant NANOTOPO (FIS2017-91413- EXP), and also the Ministerio de Ciencia, Innovación y Universidades through the grant MELODIA (PGC2018-095777- B-C21)

    Chromosome distribution studies in XXY karyotypes.

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    The method of 'generalised distances' was applied to characterise the relative position of the metaphase chromosomes in a population of XXY subjects (180 metaphases from 28 subjects). The most striking observation was that the presence of an extra gonosome coincided with a disturbance of the normally stable centromere-centre distribution pattern. The distribution analysis gave no clear cut evidence for the induction of gonosomal trisomy XXY by chromosome association. No significant association was observed between X and X or X and Y but there was a smaller distance between X and Y in XXY karyotypes than in XY karyotypes. As far as autosomes are concerned, the XXY karyotypes were characterised by a less central location of the acrocentrics without a clear decrease of association frequencies of these acrocentrics, and the C heterochromatin rich chromosomes were more often associated than in the XX and XY control populations. These data do not support the idea that gonosomal trisomies result from chromosome associations, but favour the hypothesis that spindle degeneration as a result of intrafollicular ageing of C heterochromatin polymorphism may be responsible for non-disjunctions
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