What does acne genetics teach us about disease pathogenesis? von Common, J.E.A., Barker, J.N., Steensel, M.A.M.

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The Human Intermediate Filament Database: comprehensive information on a gene family involved in many human diseases von Szeverenyi, Ildiko, Cassidy, Andrew J., Chung, Cheuk Wang, Lee, Bernett T.K., Common, John E.A., Ogg, Stephen C., Chen, Huijia, Sim, Shu Yin, Goh, Walter L.P., Ng, Kee Woei, Simpson, John A., Chee, Li Lian, Eng, Goi Hui, Li, Bin, Lunny, Declan P., Chuon, Danny, Venkatesh, Aparna, Khoo, Kian Hoe, McLean, W.H. Irwin, Lim, Yun Ping, Lane, E. Birgitte

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A report and proposals for future activity from the inaugural Artificial Intelligence in Dermatology Symposium held at the International Societies for Investigative Dermatology 202... von Wongvibulsin, S, Sangers, T, Clibborn, C, Li, Y-CJ, Sharma, N, Common, JEA, Reynolds, NJ, Tanaka, RJ

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A functional SNP associated with atopic dermatitis controls cell type-specific methylation of the VSTM1 gene locus von Kumar, D, Puan, KJ, Andiappan, AK, Lee, B, Westerlaken, GHA, Haase, D, Melchiotti, R, Li, Z, Yusof, N, Lum, J, Koh, G, Foo, S, Yeong, J, Alves, AC, Pekkanen, J, Sun, LD, Irwanto, A, Fairfax, BP, Naranbhai, V, Common, JEA, Tang, M, Chuang, CK, Jarvelin, M-R, Knight, JC, Zhang, X, Chew, FT, Prabhakar, S, Liu, J, Wang, DY, Zolezzi, F, Poidinger, M, Lane, EB, Meyaard, L, Rotzschke, O

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Clinical and Genetic Heterogeneity of Erythrokeratoderma Variabilis von Common, John E.A., O'Toole, Edel A., Leigh, Irene M., Thomas, Anna, Griffiths, William A.D., Venning, Vanessa, Grabczynska, Sophie, Periš, Zdravko, Kansky, Aleksej, Kelsell, David P.

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Connexin interaction patterns in keratinocytes revealed morphologically and by FRET analysis von Di, Wei-Li, Gu, Yan, Common, John E. A, Aasen, Trond, O'Toole, Edel A, Kelsell, David P, Zicha, Daniel

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Further evidence for heterozygote advantage of GJB2 deafness mutations: a link with cell survival von Common, J E A, Di, W-L, Davies, D, Kelsell, D P

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Defective trafficking and cell death is characteristic of skin disease-associated connexin 31 mutations von Di, Wei-Li, Monypenny, James, Common, John E.A., Kennedy, Cameron T.C., Holland, Katalin A., Leigh, Irene M., Rugg, Elizabeth L., Zicha, Daniel, Kelsell, David P.

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A case of dermatopathia pigmentosa reticularis with wiry scalp hair and digital fibromatosis resulting from a recurrent KRT14 mutation von Goh, B. K., Common, J. E. A., Gan, W. H., Kumarasinghe, P.

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Functional studies of human skin disease- and deafness-associated connexin 30 mutations von Common, John E.A, Becker, David, Di, Wei-Li, Leigh, Irene M, O’Toole, Edel A, Kelsell, David P

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Specific loss of connexin 26 expression in ductal sweat gland epithelium associated with the deletion mutation del(GJB6-D13S1830) von Common, J. E. A., Bitner-Glindzicz, M., O'Toole, E. A., Barnes, M. R., Jenkins, L., Forge, A., Kelsell, D. P.

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Diagnosis and confirmation of epidermolytic palmoplantar keratoderma by the identification of mutations in keratin 9 using denaturing high-performance liquid chromatography von Rugg, E.L., Common, J.E.A., Wilgoss, A., Stevens, H.P., Buchan, J., Leigh, I.M., Kelsell, D.P.

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Connexin 26 Expression and Mutation Analysis in Epidermal Disease von Di, Wei-Li, Common, John E. A., Elsell, David P. K.

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