University of Dundee

Molecular Medicine 2012

Brown, S. J., Kroboth, K., Sandilands, A., Campbell, L. E., Pohler, E., Kezic, S., Cordell, H. J., McLean, W. H. and Irvine, A. D. (2012) Intragenic copy number variation within filaggrin contributes to the risk of atopic dermatitis with a dose-dependent effect. J Invest Dermatol. 132, 98-104
doi. 10.1038/jid.2011.342
Pubmed. 22071473

Brown, S. J. and McLean, W. H. (2012) One remarkable molecule: filaggrin. J Invest Dermatol. 132, 751-762
doi. 10.1038/jid.2011.393
Pubmed. 22158554

Furusawa, Y., Fujiwara, Y., Campbell, P., Zhao, Q. L., Ogawa, R., Hassan, M. A., Tabuchi, Y., Takasaki, I., Takahashi, A. and Kondo, T. (2012) DNA double-strand breaks induced by cavitational mechanical effects of ultrasound in cancer cell lines. PLoS One. 7, e29012
doi. 10.1371/journal.pone.0029012
Pubmed. 22235259

Hassan, M. A., Ahmed, I. S., Campbell, P. and Kondo, T. (2012) Enhanced gene transfection using calcium phosphate co-precipitates and low-intensity pulsed ultrasound. Eur J Pharm Sci. 47, 768-773
doi. 10.1016/j.ejps.2012.08.007
Pubmed. 22921720

Kezic, S., O'Regan, G. M., Lutter, R., Jakasa, I., Koster, E. S., Saunders, S., Caspers, P., Kemperman, P. M., Puppels, G. J., Sandilands, A., Chen, H., Campbell, L. E., Kroboth, K., Watson, R., Fallon, P. G., McLean, W. H. and Irvine, A. D. (2012) Filaggrin loss-of-function mutations are associated with enhanced expression of IL-1 cytokines in the stratum corneum of patients with atopic dermatitis and in a murine model of filaggrin deficiency. J Allergy Clin Immunol. 129, 1031-1039 e1031
doi. 10.1016/j.jaci.2011.12.989
Pubmed. 22322004

Leslie Pedrioli, D. M., Fu, D. J., Gonzalez-Gonzalez, E., Contag, C. H., Kaspar, R. L., Smith, F. J. and McLean, W. H. (2012) Generic and personalized RNAi-based therapeutics for a dominant-negative epidermal fragility disorder. J Invest Dermatol. 132, 1627-1635
doi. 10.1038/jid.2012.28
Pubmed. 22402445

Sandilands, A., Brown, S. J., Goh, C. S., Pohler, E., Wilson, N. J., Campbell, L. E., Miyamoto, K., Kubo, A., Irvine, A. D., Thawer-Esmail, F., Munro, C. S., McLean, W. H., Kudoh, J., Amagai, M. and Matsui, T. (2012) Mutations in the SASPase gene (ASPRV1) are not associated with atopic eczema or clinically dry skin. J Invest Dermatol. 132, 1507-1510
doi. 10.1038/jid.2011.479
Pubmed. 22318384

Terrier, O., Marcel, V., Cartet, G., Lane, D. P., Lina, B., Rosa-Calatrava, M. and Bourdon, J. C. (2012) Influenza A viruses control expression of proviral human p53 isoforms p53beta and Delta133p53alpha. J Virol. 86, 8452-8460
doi. 10.1128/JVI.07143-11
Pubmed. 22647703

Uitto, J., Christiano, A. M., McLean, W. H. and McGrath, J. A. (2012) Novel molecular therapies for heritable skin disorders. J Invest Dermatol. 132, 820-828
doi. 10.1038/jid.2011.389
Pubmed. 22158553

Wilson, N. J., Perez, M. L., Vahlquist, A., Schwartz, M. E., Hansen, C. D., McLean, W. H. and Smith, F. J. (2012) Homozygous dominant missense mutation in keratin 17 leads to alopecia in addition to severe pachyonychia congenita. J Invest Dermatol. 132, 1921-1924
doi. 10.1038/jid.2011.484
Pubmed. 22336949