6.1-01 HLA typing in actinic prurigo; a new HLA association von Sheridan, D.P, Lane, P.R, Boychuk, C.L, Taylor, D.L, Irvine, J.D, Hogan, D.J

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Improvement to thin film CdTe solar cells with controlled back surface oxidation von Rugen-Hankey, S.L., Clayton, A.J., Barrioz, V., Kartopu, G., Irvine, S.J.C., McGettrick, J.D., Hammond, D.

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Study of thin film poly-crystalline CdTe solar cells presenting high acceptor concentrations achieved by in-situ arsenic doping von Kartopu, G., Oklobia, O., Turkay, D., Diercks, D.R., Gorman, B.P., Barrioz, V., Campbell, S., Major, J.D., Al Turkestani, M.K., Yerci, S., Barnes, T.M., Beattie, N.S., Zoppi, G., Jones, S., Irvine, S.J.C.

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Desmoglein 1 deficiency results in severe dermatitis, multiple allergies and metabolic wasting von Samuelov, Liat, Sarig, Ofer, Harmon, Robert M, Rapaport, Debora, Ishida-Yamamoto, Akemi, Isakov, Ofer, Koetsier, Jennifer L, Gat, Andrea, Goldberg, Ilan, Bergman, Reuven, Spiegel, Ronen, Eytan, Ori, Geller, Shamir, Peleg, Sarit, Shomron, Noam, Goh, Christabelle S M, Wilson, Neil J, Smith, Frances J D, Pohler, Elizabeth, Simpson, Michael A, McLean, W H Irwin, Irvine, Alan D, Horowitz, Mia, McGrath, John A, Green, Kathleen J, Sprecher, Eli

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Severe dermatitis, multiple allergies, and metabolic wasting syndrome caused by a novel mutation in the N-terminal plakin domain of desmoplakin von McAleer, Maeve A., MB, MRCP, Pohler, Elizabeth, PhD, Smith, Frances J.D., PhD, Wilson, Neil J., MSc, Cole, Christian, PhD, MacGowan, Stuart, PhD, Koetsier, Jennifer L., BS, Godsel, Lisa M., PhD, Harmon, Robert M., PhD, Gruber, Robert, MD, Crumrine, Debra, BS, Elias, Peter M., MD, McDermott, Michael, FRCPath, Butler, Karina, FRCPI, Broderick, Annemarie, MRCPI, Sarig, Ofer, PhD, Sprecher, Eli, MD, PhD, Green, Kathleen J., PhD, McLean, W.H. Irwin, PhD, DSc, FRS, FRSE, FMedSci, Irvine, Alan D., MD

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A comparative study of microstructural stability and sulphur diffusion in CdS/CdTe photovoltaic devices von Taylor, A.A., Major, J.D., Kartopu, G., Lamb, D., Duenow, J., Dhere, R.G., Maeder, X., Irvine, S.J.C., Durose, K., Mendis, B.G.

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Prevalent and Rare Mutations in the Gene Encoding Filaggrin Cause Ichthyosis Vulgaris and Predispose Individuals to Atopic Dermatitis von Sandilands, Aileen, O'Regan, Gráinne M., Liao, Haihui, Zhao, Yiwei, Terron-Kwiatkowski, Ana, Watson, Rosemarie M., Cassidy, Andrew J., Goudie, David R., Smith, Frances J.D., Irwin McLean, W.H., Irvine, Alan D.

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Loss-of-function mutations in the gene encoding filaggrin cause ichthyosis vulgaris von McLean, W H Irwin, Smith, Frances J D, Irvine, Alan D, Terron-Kwiatkowski, Ana, Sandilands, Aileen, Campbell, Linda E, Zhao, Yiwei, Liao, Haihui, Evans, Alan T, Goudie, David R, Lewis-Jones, Sue, Arseculeratne, Gehan, Munro, Colin S, Sergeant, Ann, O'Regan, Gráinne, Bale, Sherri J, Compton, John G, DiGiovanna, John J, Presland, Richard B, Fleckman, Philip

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Doping levels, trap density of states and the performance of co-doped CdTe(As,Cl) photovoltaic devices von Proskuryakov, Y.Y., Durose, K., Major, J.D., Al Turkestani, M.K., Barrioz, V., Irvine, S.J.C., Jones, E.W.

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Mutations in desmoglein 1 cause diverse inherited palmoplantar keratoderma phenotypes: implications for genetic screening von Lovgren, M.‐L., McAleer, M.A., Irvine, A.D., Wilson, N.J., Tavadia, S., Schwartz, M.E., Cole, C., Sandilands, A., Smith, F.J.D., Zamiri, M.

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Mitigating land degradation caused by wildfire: Application of the PESERA model to fire-affected sites in central Portugal von Esteves, T.C.J., Kirkby, M.J., Shakesby, R.A., Ferreira, A.J.D., Soares, J.A.A., Irvine, B.J., Ferreira, C.S.S., Coelho, C.O.A., Bento, C.P.M., Carreiras, M.A.

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A spectrum of mutations in keratins K6a, K16 and K17 causing pachyonychia congenita von Liao, Haihui, Sayers, Jane M, Wilson, Neil J, Irvine, Alan D, Mellerio, Jemima E, Baselga, Eulalia, Bayliss, Susan J, Uliana, Vera, Fimiani, Michele, Lane, E. Birgitte, McLean, W.H. Irwin, Leachman, Sancy A, Smith, Frances J.D

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Mutations in cornea-specific keratin K3 or K12 genes cause Meesmann's corneal dystrophy von Irvine, Alan D, Corden, Laura D, Swensson, Ole, Swensson, Beate, Moore, Jonathan E, Frazer, David G, Smith, Frances J.D, Knowlton, Robert G, Christophers, Enno, Rochels, Rainer, Uitto, Jouni, McLean, W.H. Irwin

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Development of allele-specific therapeutic siRNA in Meesmann epithelial corneal dystrophy von Liao, Haihui, Irvine, Alan D, Macewen, Caroline J, Weed, Kathryn H, Porter, Louise, Corden, Laura D, Gibson, A Bethany, Moore, Jonathan E, Smith, Frances J D, McLean, W H Irwin, Moore, C B Tara

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Haploinsufficiency for AAGAB causes clinically heterogeneous forms of punctate palmoplantar keratoderma von Pohler, Elizabeth, Mamai, Ons, Hirst, Jennifer, Zamiri, Mozheh, Horn, Helen, Nomura, Toshifumi, Irvine, Alan D, Moran, Benvon, Wilson, Neil J, Smith, Frances J D, Goh, Christabelle S M, Sandilands, Aileen, Cole, Christian, Barton, Geoffrey J, Evans, Alan T, Shimizu, Hiroshi, Akiyama, Masashi, Suehiro, Mitsuhiro, Konohana, Izumi, Shboul, Mohammad, Teissier, Sebastien, Boussofara, Lobna, Denguezli, Mohamed, Saad, Ali, Gribaa, Moez, Dopping-Hepenstal, Patricia J, McGrath, John A, Brown, Sara J, Goudie, David R, Reversade, Bruno, Munro, Colin S, McLean, W H Irwin

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Physics potential of a long-baseline neutrino oscillation experiment using a J-PARC neutrino beam and Hyper-Kamiokande von Anghel, I., Ariga, A., Ariga, T., Asfandiyarov, R., Back, J.J., Barker, G.J., Barr, G., Bay, F., Beltrame, P., Berardi, V., Bhadra, S., Boyd, S.B., Bravar, A., Cartwright, S.L., Catanesi, M.G., Cowan, G., Davies, G., Densham, C., Detwiler, J., Di Lodovico, F., Drapier, O., Finch, A., Fitton, M., Fujii, Y., Fukuda, Y., Fukuda, D., Ganezer, K., Gonin, M., Haesler, A., Haga, Y., Hartfiel, B., Hartz, M., Hayato, Y., Hierholzer, M., Huang, K., Ichikawa, A.K., Ikeda, M., Inoue, K., Ishitsuka, M., Itow, Y., Jang, H.I., Kajita, T., Kameda, J., Katori, T., Khabibullin, M., Khotjantsev, A., Konaka, A., Kutter, T., Kuze, M., Lagoda, J., Longhin, A., Ludovici, L., Ma, W., Mahn, K., Martin, J.F., Martins, P.P.J., McFarland, K.S., Miura, M., Monroe, J., Moriyama, S., Mueller, T., Muheim, F., Nakayama, S., Nirkko, M., Nishimura, Y., Nunokawa, H., Okumura, K., Oser, S.M., Owen, R.A., Oyama, Y., Pérez, J., Posiadala-Zezula, M., Poutissou, J.-M., Quinto, M., Radicioni, E., Rayner, M.A., Riccio, C., Rose, H.J., Ross-Lonergan, M., Rubbia, A., Sacco, R., Sakuda, M., Scantamburlo, E., Scott, M., Sekiya, H., Shaikhiev, A., Shimizu, I., Sinnis, G., Suda, Y., Suzuki, Y., Tanaka, H.K.M., Thompson, L.F., Tsukamoto, T., Vogelaar, R.B., Wascko, M.O., Wilking, M.J., Yamamoto, K., Yanagisawa, C., Yano, T., Yokoyama, M.

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Common loss-of-function variants of the epidermal barrier protein filaggrin are a major predisposing factor for atopic dermatitis von McLean, W H Irwin, Palmer, Colin N A, Irvine, Alan D, Terron-Kwiatkowski, Ana, Zhao, Yiwei, Liao, Haihui, Lee, Simon P, Goudie, David R, Sandilands, Aileen, Campbell, Linda E, Smith, Frances J D, O'Regan, Gráinne M, Watson, Rosemarie M, Cecil, Jo E, Bale, Sherri J, Compton, John G, DiGiovanna, John J, Fleckman, Philip, Lewis-Jones, Sue, Arseculeratne, Gehan, Sergeant, Ann, Munro, Colin S, El Houate, Brahim, McElreavey, Ken, Halkjaer, Liselotte B, Bisgaard, Hans, Mukhopadhyay, Somnath

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Filaggrin's Fuller Figure: A Glimpse into the Genetic Architecture of Atopic Dermatitis von Sandilands, Aileen, Smith, Frances J.D., Irvine, Alan D., Irwin McLean, W.H.

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Resolution of the plantar hyperkeratosis of pachyonychia congenita during chemotherapy for Ewing sarcoma von Higgins, E., Capra, M., Schwartz, M.E., Smith, F.J.D., McLean, W.H.I., Irvine, A.D.

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Study protocol for The GOAL Trial: comprehensive geriatric assessment for frail older people with chronic kidney disease to increase attainment of patient-identified goals-a cluste... von Logan, B, Viecelli, A K, Johnson, D W, Aquino, E M, Bailey, J, Comans, T A, Gray, L C, Hawley, C M, Hickey, L E, Janda, M, Jaure, A, Jose, M D, Kalaw, E, Kiriwandeniya, C, Matsuyama, M, Mihala, G, Nguyen, K H, Pascoe, E, Pole, J D, Polkinghorne, K R, Pond, D, Raj, R, Reidlinger, D M, Scholes-Robertson, N, Varghese, J, Wong, G, Hubbard, R E

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