Search results

• Finished

  Validation of the C20orf54 gene associated with Brown-Vialetto-Van Laere syndrome as diagnostic marker for Amyotrophic lateral sclerosis and related disorders by means of clinical and molecular studies

  Green, P., Roberts, R. & Josifova, D.

  1/01/2011 → 31/12/2012

  Project: Research

• Whole gene sequencing in familial Crohn's Disease

  Mathew, C., Prescott, N., Green, P. & Sanderson, J.

  Crohn's and Colitis UK

  1/04/2010 → 1/03/2012

  Project: Research

• Genome-wide autozygosity mapping in a consanguineous family with a novel myotonic disorder.

  Green, P., Roberts, R., Gill, H. & Longman, D.

  Newlife Foundation

  1/09/2007 → 30/11/2009

  Project: Research

• NIHR Biomedical Research Centre

  Afzali, B., Antoniou, M., Barker, J., Barratt, B., Beighton, D., Bevan, S., Blower, P., Burchell, J., Cason, J., Chappell, L., Cope, A., Corrigan, C., Cunninghame Graham, D., Dontu, G., Edgeworth, J., Farzaneh, F., Gee, T., Gould, H., Green, P., Greenough, A., Grigoriadis, A., Hayday, A., Higginson, I., Kalra, L., Karagiannis, S., Kelly, F., Kemper, C., Lau-Walker, M., Lavender, P., Lee, T., Lempp, H., Lewis, C., Lombardi, G., Lord, G., Marber, M., Mason, J., Mathew, C., McGrath, J., Metcalfe, A., Molokhia, M., Mullen, G., Nagel, E., Neil, S., Nestle, F., Oakey, R., Parker, P., Peakman, M., Perera, D., Purushotham, A., Rasekh Ahmadi, K., Rashid, T., Razavi, R., Ridley, A., Robson, M., Sacks, S., Sanchez Fueyo, A., Santis, G., Sanz Moreno, V., Sawyer, E., Schaeffter, T., Shah, A., Sharpe, P., Simpson, M., Smith, R., Sorinola, I., Spector, T., Spicer, J., Taams, L., Tavassoli, M., Taylor, D., Tree, T., Trembath, R., Tribe, R., Tutt, A., Waltham, M., Watt, F., Webb, A., Wells, C., Whelan, K., Whitaker, J., Whittlesea, C., Williamson, C., Wolfe, C., Yu, V., academic, A., Hughes, S., Montana, G., Rhode, K., Schnabel, J. & Tziotzios, C.

  NIHR National Institute For Health & Care Research, DHSC Department of Health and Social Care

  1/04/2007 → 31/03/2017

  Project: Research

  • T-Helper Cell 100%
  • Inflammatory Arthritis 66%
  • Monocyte 36%
  • Tumor Necrosis Factor 36%
  • Cytotoxic T-Cell 33%

• Gene duplication and mutation detection in Haemophilia A.

  Green, P.

  Friends of Guy's & St.Thomas' Hospital

  1/12/2005 → 30/11/2006

  Project: Research

• The application of the MWG-Biotech Robot to the automation of Mutation Detection

  Green, P.

  MRC Medical Research Council

  1/01/2001 → 31/12/2001

  Project: Research

• A national database of haemophilia and pedigrees to optimise genetic service and promote national integration of laboratory activities related to genetic counselling in monogenic disorders

  Green, P.

  Guy's & St Thomas' Charity

  1/09/2000 → 31/08/2002

  Project: Research

• A fast and efficient mutation detection procedure for the molecular diagnosis of Alport Syndrome.

  Green, P.

  NKRF National Kidney Research Fund

  1/10/1999 → 30/09/2000

  Project: Research

• The use of Denaturing High-Performance Liquid Chromatography as a fast and accurate means of mutation detection in genetic disorders

  Green, P., Lanchbury, J. & academic, A.

  Special Trustees of Guys & St Thomas' Hospital

  20/07/1999 → 19/07/2002

  Project: Research

• A novel approach to the analysis of human genome variations investigating heterogeneity of both mutation and recombination

  Green, P. & Giannelli, F.

  BBSRC Biotechnology and Biological Sciences Research Council

  1/10/1998 → 1/10/2001

  Project: Research