Dr Gillian Rice

Research Fellow

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Publications

  1. 1997
  2. Published

    The paraoxonase Gln-Arg 192 polymorphism in subjects with ischaemic heart disease.

    Rice, G. I., Ossei-Gerning, N., Stickland, M. H. & Grant, P. J., 3 Nov 1997, In : Coronary Artery Disease. 8, 11-12

    Research output: Contribution to journalArticle

  3. 1998
  4. Published

    FVIII coagulant activity and antigen in subjects with ischaemic heart disease.

    Rice, G. I. & Grant, P. J., Nov 1998, In : Thrombosis and Haemostasis. 80, 5

    Research output: Contribution to journalArticle

  5. 1999
  6. Published

    Angiotensin converting enzyme and angiotensin II type 1-receptor gene polymorphisms and risk of ischaemic heart disease.

    Rice, G. I., Foy, C. A. & Grant, P. J., Mar 1999, In : Cardiovascular research. 41, 3

    Research output: Contribution to journalArticle

  7. 2001
  8. Published

    Human endothelial cell-derived nuclear proteins that recognise polymorphic DNA elements in the von Willebrand factor gene promoter include YY1.

    Costa, M., Grant, P. J., Rice, G. I., Futers, T. S. & Medcalf, R. L., Aug 2001, In : Thrombosis and Haemostasis. 86, 2

    Research output: Contribution to journalArticle

  9. 2004
  10. Published

    Evaluation of angiotensin-converting enzyme (ACE), its homologue ACE2 and neprilysin in angiotensin peptide metabolism.

    Rice, G. I., Thomas, D. A., Grant, P. J., Turner, A. J. & Hooper, N. M., 1 Oct 2004, In : The Biochemical Journal. 383, Pt 1

    Research output: Contribution to journalArticle

  11. 2006
  12. Published

    Circulating activities of angiotensin-converting enzyme, its homolog, angiotensin-converting enzyme 2, and neprilysin in a family study

    Rice, G. I., Jones, A. L., Grant, P. J., Carter, A. M., Turner, A. J. & Hooper, N. M., Nov 2006, In : Hypertension. 48, 5, p. 914-920 6 p.

    Research output: Contribution to journalArticle

  13. 2007
  14. Published

    Heterozygous mutations in TREX1 cause familial chilblain lupus and dominant Aicardi-Goutières syndrome

    Rice, G., Newman, W. G., Dean, J., Patrick, T., Parmar, R., Flintoff, K., Robins, P., Harvey, S., Hollis, T., O'Hara, A., Herrick, A. L., Bowden, A. P., Perrino, F. W., Lindahl, T., Barnes, D. E. & Crow, Y. J., Apr 2007, In : American Journal of Human Genetics. 80, 4, p. 811-815 4 p.

    Research output: Contribution to journalArticle

  15. Published

    Clinical and molecular phenotype of Aicardi-Goutieres syndrome.

    Rice, G., Patrick, T., Parmar, R., Taylor, C. F., Aeby, A., Aicardi, J., Artuch, R., Montalto, S. A., Bacino, C. A., Barroso, B., Baxter, P., Benko, W. S., Bergmann, C., Bertini, E., Biancheri, R., Blair, E. M., Blau, N., Bonthron, D. T., Briggs, T., Brueton, L. A. & 100 othersBrunner, H. G., Burke, C. J., Carr, I. M., Carvalho, D. R., Chandler, K. E., Christen, H-J., Corry, P. C., Cowan, F. M., Cox, H., D'Arrigo, S., Dean, J., De Laet, C., De Praeter, C., Dery, C., Ferrie, C. D., Flintoff, K., Frints, S. G. M., Garcia-Cazorla, A., Gener, B., Goizet, C., Goutieres, F., Green, A. J., Guet, A., Hamel, B. C. J., Hayward, B. E., Heiberg, A., Hennekam, R. C., Husson, M., Jackson, A. P., Jayatunga, R., Jiang, Y-H., Kant, S. G., Kao, A., King, M. D., Kingston, H. M., Klepper, J., van der Knaap, M. S., Kornberg, A. J., Kotzot, D., Kratzer, W., Lacombe, D., Lagae, L., Landrieu, P. G., Lanzi, G., Leitch, A., Lim, M. J., Livingston, J. H., Lourenco, C. M., Lyall, E. G. H., Lynch, S. A., Lyons, M. J., Marom, D., McClure, J. P., McWilliam, R., Melancon, S. B., Mewasingh, L. D., Moutard, M-L., Nischal, K. K., Ostergaard, J. R., Prendiville, J., Rasmussen, M., Rogers, R. C., Roland, D., Rosser, E. M., Rostasy, K., Roubertie, A., Sanchis, A., Schiffmann, R., Scholl-Burgi, S., Seal, S., Shalev, S. A., Corcoles, C. S., Sinha, G. P., Soler, D., Spiegel, R., Stephenson, J. B. P., Tacke, U., Tan, T. Y., Till, M., Tolmie, J. L., Tomlin, P., Vagnarelli, F., Valente, E. M., Van Coster, R. N. A., Van der Aa, N., Vanderver, A., Vles, J. S. H., Voit, T., Wassmer, E., Weschke, B., Whiteford, M. L., Willemsen, M. A. A., Zankl, A., Zuberi, S. M., Orcesi, S., Fazzi, E., Lebon, P., Crow, Y. J., Østergaard, J. R. & Tiong, Y. T., Oct 2007, In : American Journal of Human Genetics. 81, 4, p. 713-725 12 p.

    Research output: Contribution to journalArticle

  16. 2008
  17. Published

    Aicardi-Goutières syndrome: Description of a late onset case

    D'arrigo, S., Riva, D., Bulgheroni, S., Chiapparini, L., Lebon, P., Rice, G., Crow, Y. J. & Pantaleoni, C., 2008, In : Developmental medicine and child neurology. 50, 8, p. 631-634 3 p.

    Research output: Contribution to journalArticle

  18. Published

    Cerebroretinal Microangiopathy with Calcifications and Cysts (CRMCC)

    Crow, Y., Briggs, T. A., Abdel-Salam, G. M. H., Balicki, M., Baxter, P., Bertini, E., Bishop, N., Browne, B. H., Chitayat, D., Chong, W. K., Eid, M. M., Halliday, W., Hughes, I., Klusmann-Koy, A., Kurian, M., Nischal, K. K., Rice, G. I., Stephenson, J. B. P., Surtees, R., Talbot, J. F. & 5 othersTehrani, N. N., Tolmie, J. L., Toomes, C., Van Der Knaap, M. S. & Crow, Y. J., 15 Jan 2008, In : American Journal of Medical Genetics, Part A. 146, 2, p. 182-190 8 p.

    Research output: Contribution to journalArticle

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