Carole Todd
Laboratory Technician
Email: carole.todd@ncl.ac.uk Telephone: +44 (0) 191 222 7190 Address: Institute of Cellular Medicine Dermatological Sciences
2nd floor, W Leech Building
Medical School
University of Newcastle upon Tyne
NE2 4HH
Fearon P, Lonsdale-Eccles AA, Ross OK, Todd C, Sinha A, Allain F, Reynolds NJ. Keratinocyte secretion of cyclophilin B via the constitutive pathway is regulated through its cyclosporin binding site .
Journal of Investigative Dermatology 2011, 131 (5), 1085–1094.
Sinha A, Fearon P, Lonsdale-Eccles A, Forrester A, Todd C, Reynolds N. The cyclosporin A binding protein cyclophilin B is expressed in the granular layer of epidermis and regulates human keratinocyte growth and differentiation .
In: Journal of Investigative Dermatology: 41st Annual Meeting of the European Society for Dermatological Research . 2011, Barcelona, Spain: Nature Publishing Group.
Flanagan N, Ray AJ, Todd C, Birch-Machin MA, Rees JL. The relation between melanocortin 1 receptor genotype and experimentally assessed ultraviolet radiation sensitivity .
Journal of Investigative Dermatology 2001, 117 (5), 1314-1317.
Harding RM, Healy E, Ray AJ, Ellis NS, Flanagan N, Todd C, Dixon C, Sajantila A, Jackson IJ, Birch-Machin MA, Rees JL. Evidence for variable selective pressures at MC1R .
American Journal of Human Genetics 2000, 66 (4), 1351-1361.
Flanagan N, Healy E, Ray A, Philips S, Todd C, Jackson IJ, Birch-Machin MA, Rees JL. Pleiotropic effects of the melanocortin 1 receptor (MC1R) gene on human pigmentation .
Human Molecular Genetics 2000, 9 (17), 2531-2537.
Ruiz-Perez VL, Carter SA, Healy E, Todd C, Rees JL, Steijlen PM, Carmichael AJ, Lewis HM, Hohl D, Itin P, Vahlquist A, Gobello T, Mazzanti C, Reggazini R, Nagy G, Munro CS, Strachan T. ATP2A2 mutations in Darier's disease: Variant cutaneous phenotypes are associated with missense mutations, but neuropsychiatric features are independent of mutation class .
Human Molecular Genetics 1999, 8 (9), 1621-1630.