Keratins and skin disorders von Lane, EB, McLean, WHI

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Clinical and Pathological Features of Pachyonychia Congenita von Leachman, Sancy A., Kaspar, Roger L., Fleckman, Philip, Florell, Scott R., Smith, Frances J.D., McLean, W.H. Irwin, Lunny, Declan P., Milstone, Leonard M., van Steensel, Maurice A.M., Munro, Colin S., O'Toole, Edel A., Celebi, Julide T., Kansky, Aleksej, Lane, EBirgitte

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Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organization von McLean, W H, Pulkkinen, L, Smith, F J, Rugg, E L, Lane, E B, Bullrich, F, Burgeson, R E, Amano, S, Hudson, D L, Owaribe, K, McGrath, J A, McMillan, J R, Eady, R A, Leigh, I M, Christiano, A M, Uitto, J

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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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Phenotypes, genotypes and their contribution to understanding keratin function von Porter, Rebecca M., Birgitte Lane, E.

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Keratin 8/18 breakdown and reorganization during apoptosis von Schutte, Bert, Henfling, Mieke, Kölgen, Wendy, Bouman, Maartje, Meex, Stephan, Leers, Mathie P.G, Nap, Marius, Björklund, Viveka, Björklund, Peter, Björklund, Bertil, Lane, E.Birgitte, Omary, M.Bishr, Jörnvall, Hans, Ramaekers, Frans C.S

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The quest for the function of simple epithelial keratins von Owens, Dewi W., Lane, E. Birgitte

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Keratin mutations and intestinal pathology von Owens, DW, Lane, EB

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Keratin mutations of epidermolysis bullosa simplex alter the kinetics of stress response to osmotic shock von D'Alessandro, Mariella, Russell, David, Morley, Susan M, Davies, Anthony M, Lane, E Birgitte

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An Inhibitor of Nuclear Export Activates the p53 Response and Induces the Localization of HDM2 and p53 to U1A-Positive Nuclear Bodies Associated with the PODs von Laı́n, Sonia, Midgley, Carol, Sparks, Alison, Lane, E.Birgitte, Lane, David P.

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Human keratin 8 mutations that disturb filament assembly observed in inflammatory bowel disease patients von Owens, D W, Wilson, N J, Hill, A J M, Rugg, E L, Porter, R M, Hutcheson, A M, Quinlan, R A, van Heel, D, Parkes, M, Jewell, D P, Campbell, S S, Ghosh, S, Satsangi, J, Lane, E B

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Mutations in the plakophilin 1 gene result in ectodermal dysplasia/skin fragility syndrome von McGrath, John A, McMillan, James R, Shemanko, Carrie S, Runswick, Sarah K, Leigh, Irene M, Lane, E. Birgitte, Garrod, David R, Eady, Robin A.J

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Characterization of Early Assembly Intermediates of Recombinant Human Keratins von Herrmann, Harald, Wedig, Tatjana, Porter, Rebecca M., Lane, E.Birgitte, Aebi, Ueli

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An Unusual Ala12Thr Polymorphism in the 1A α-Helical Segment of the Companion Layer-Specific Keratin K6hf: Evidence for a Risk Factor in the Etiology of the Common Hair Disorder Ps... von Winter, Hermelita, Schissel, Daniel, Parry, David A.D., Smith, Thomasin A., Liovic, Mirjana, Birgitte Lane, E., Edler, Lutz, Langbein, Lutz, Jave-Suarez, Luis F., Rogers, Michael A., Wilde, Joseph, Peters, Gerald, Schweizer, Jürgen

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Binding of Integrin alpha 6 beta 4 to Plectin Prevents Plectin Association with F-Actin but Does Not Interfere with Intermediate Filament Binding von Geerts, D, Fontao, L, Nievers, M G, Schaapveld, QJ, Purkis, P E, Wheeler, G N, Lane, E B, Leigh, I M, Sonnenberg, A

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Modulation of Cell Proliferation by Cytokeratins K10 and K16 von Paramio, Jesús M., Casanova, M. Llanos, Segrelles, Carmen, Mittnacht, Sybille, Lane, E. Birgitte, Jorcano, José L.

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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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Plectin deficiency results in muscular dystrophy with epidermolysis bullosa von Leigh, I.M, Bryant, S.P, Milana, G, Kirtschig, G, Pulkkinen, L, Smith, F.J.D, McLean, W.H.I, Eady, R.A.J, Spurr, N.K, Owaribe, K, McMillan, J.R, Lane, E.B, Geddes, J.F, de Bono, A.G, Uitto, J, Wiche, G, Kelsell, D.P, Rugg, E.L

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Intermediate filaments in disease von Irwin McLean, W.H., Birgitte Lane, E.

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Generation and characterization of epidermolysis bullosa simplex cell lines: scratch assays show faster migration with disruptive keratin mutations von Morley, S.M., D'Alessandro, M., Sexton, C., Rugg, E.L., Navsaria, H., Shemanko, C.S., Huber, M., Hohl, D., Heagerty, A.I., Leigh, I.M., Lane, E.B.

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