Resultats de la cerca - Simon Collier

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  1. 1
    A de novo pathological point mutation at the 21–hydroxylase locus: implications for gene conversion in the human genome

    A de novo pathological point mutation at the 21–hydroxylase locus: implications for gene conversion in the human genome per Simon Collier, Mayada Tassabehji, Tom Strachan

    Publicat 1993
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  2. 2
    Genesis by meiotic unequal crossover of a de novo deletion that contributes to steroid 21-hydroxylase deficiency.

    Genesis by meiotic unequal crossover of a de novo deletion that contributes to steroid 21-hydroxylase deficiency. per P. J. Sinnott, Simon Collier, Colm Costigan, P. A. Dyer, R Harris, T Strachan

    Publicat 1990
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  3. 3
    Pulsed field gel electrophoresis identifies a high degree of variability in the number of tandem 21-hydroxylase and complement C4 gene repeats in 21-hydroxylase deficiency haplotypes.

    Pulsed field gel electrophoresis identifies a high degree of variability in the number of tandem 21-hydroxylase and complement C4 gene repeats in 21-hydroxylase deficiency haplotyp... per Simon Collier, P. J. Sinnott, P. A. Dyer, David A. Price, R Harris, T Strachan

    Publicat 1989
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  4. 4
    PCYT1A Regulates Phosphatidylcholine Homeostasis from the Inner Nuclear Membrane in Response to Membrane Stored Curvature Elastic Stress

    PCYT1A Regulates Phosphatidylcholine Homeostasis from the Inner Nuclear Membrane in Response to Membrane Stored Curvature Elastic Stress per Afreen Haider, Yu‐Chen Wei, Koini Lim, António Daniel Barbosa, Che Liu, Ursula Weber, Marek Mlodzik, Kadri Oras, Simon Collier, M. Mahmood Hussain, Dong Liang, Satish Patel, Anna Álvarez-Guaita, Vladimı́r Saudek, Benjamin Jenkins, Albert Koulman, Marcus K. Dymond, Roger Hardie, Symeon Siniossoglou, David B. Savage

    Publicat 2018
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