Items where Author is "Scott, H. S."

2008

Ferguson, B. J. and Alexander, C. and Rossi, S. W. and Liiv, I. and Rebane, A. and Worth, C. L. and Wong, J. and Laan, M. and Peterson, P. and Jenkinson, E. J. and Anderson, G. and Scott, H. S. and Cooke, A. and Rich, T.. (2008) AIRE's CARD revealed, a new structure for central tolerance provokes transcriptional plasticity. Journal of biological chemistry, Vol. 283. pp. 1723-1731.

Irla, M. and Hugues, S. and Gill, J. and Nitta, T. and Hikosaka, Y. and Williams, I. R. and Hubert, F. X. and Scott, H. S. and Takahama, Y. and Holländer, G. A. and Reith, W.. (2008) Autoantigen-specific interactions with CD4+ thymocytes control mature medullary thymic epithelial cell cellularity. Immunity, Vol. 29, H. 3. pp. 451-463.

Alimohammadi, M. and Björklund, P. and Hallgren, A. and Pöntynen, N. and Szinnai, G. and Shikama, N. and Keller, M. P. and Ekwall, O. and Kinkel, S. A. and Husebye, E. S. and Gustafsson, J. and Rorsman, F. and Peltonen, L. and Betterle, C. and Perheentupa, J. and Akerström, G. and Westin, G. and Scott, H. S. and Holländer, G. A. and Kämpe, O.. (2008) Autoimmune polyendocrine syndrome type 1 and NALP5, a parathyroid autoantigen. The New England journal of medicine, Vol. 358, H. 10. pp. 1018-1028.

White, A. J. and Withers, D. R. and Parnell, S. M. and Scott, H. S. and Finke, D. and Lane, P. J. and Jenkinson, E. J. and Anderson, G.. (2008) Sequential phases in the development of Aire-expressing medullary thymic epithelial cells involve distinct cellular input. European Journal of Immunology, Vol. 38, H. 4. pp. 942-947.

2002

Wattenhofer, M. and Di Iorio, M. V. and Rabionet, R. and Dougherty, L. and Pampanos, A. and Schwede, T. and Montserrat-Sentis, B. and Arbones, M. L. and Iliades, T. and Pasquadibisceglie, A. and D'Amelio, M. and Alwan, S. and Rossier, C. and Dahl, H. H. M. and Petersen, M. B. and Estivill, X. and Gasparini, P. and Scott, H. S. and Antonarakis, S. E.. (2002) Mutations in the TMPRSS3 gene are a rare cause of childhood non-syndromic deafness in Caucasian patients. Journal of molecular medicine, Vol. 80. pp. 124-131.

2001

Masmoudi, S. and Antonarakis, S. E. and Schwede, T. and Ghorbel, A. M. and Gratri, M. and Pappasavas, M. P. and Drira, M. and Elgaied Boulila, A. and Wattenhofer, M. and Rossier, C. and Scott, H. S. and Ayadi, H. and Guipponi, M.. (2001) Novel missense mutations of TMPRSS3 in two consanguineous Tunisian families with non-syndromic autosomal recessive deafness. Human mutation, Vol. 18, no. 2. pp. 101-108.