Longitudinal expression of type I interferon responsive genes in systemic lupus erythematosus von Petri, M, Singh, S, Tesfasyone, H, Dedrick, R, Fry, K, Lal, PG, Williams, G, Bauer, JW, Gregersen, PK, Behrens, TW, Baechler, EC

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A common haplotype of interferon regulatory factor 5 ( IRF5 ) regulates splicing and expression and is associated with increased risk of systemic lupus erythematosus von Escribano, Ma Francisca González, Collaborative Groups, the Argentine and Spanish, Graham, Robert R, Baechler, Emily C, Reddy, M V Prasad Linga, Kozyrev, Sergey V, Bauer, Jason W, Martín, Javier, Gregersen, Peter K, Pons-Estel, Bernardo, Alarcón-Riquelme, Marta E, Behrens, Timothy W, Plenge, Robert M, Koeuth, Thearith, Daly, Mark, Altshuler, David, Ortmann, Ward A, Petri, Michelle

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Three functional variants of IFN regulatory factor 5 (IRF5) define risk and protective haplotypes for human lupus von Graham, Robert R, Kyogoku, Chieko, Sigurdsson, Snaevar, Vlasova, Irina A, Davies, Leela R.L, Baechler, Emily C, Plenge, Robert M, Koeuth, Thearith, Ortmann, Ward A, Hom, Geoffrey, Bauer, Jason W, Gillett, Clarence, Burtt, Noel, Cunninghame Graham, Deborah S, Onofrio, Robert, Petri, Michelle, Gunnarsson, Iva, Svenungsson, Elisabet, Rönnblom, Lars, Nordmark, Gunnel, Gregersen, Peter K, Moser, Kathy, Gaffney, Patrick M, Criswell, Lindsey A, Vyse, Timothy J, Syvänen, Ann-Christine, Bohjanen, Paul R, Daly, Mark J, Behrens, Timothy W, Altshuler, David

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Photodynamic therapy using topical methyl 5-aminolevulinate compared with cryotherapy for actinic keratosis: A prospective, randomized study von Szeimiesa, R.M., Karrera, S., Radakovic-Fijanb, S., Tanewb, A., Calzavara-Pintonc, P.G., Zanec, C., Sidoroffd, A., Hempele, M., Ulrichf, J., Proebstleg, T., Mefferth, H., Mulderi, M., Salomonj, D., Dittmark, H.C., Bauerl, J.W., Kernlandm, K., Braathenm, L.

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Type XVII collagen gene mutations in junctional epidermolysis bullosa and prospects for gene therapy von Bauer, J. W., Lanschuetzer, C.

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Expression of Neuropeptide Galanin and Galanin Receptors in Human Skin von Kofler, Barbara, Berger, Alexandra, Santic, Radmila, Moritz, Kerstin, Almer, Dietmar, Tuechler, Camilla, Lang, Roland, Emberger, Michael, Klausegger, Alfred, Sperl, Wolfgang, Bauer, Johann W.

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Safety and early efficacy outcomes for lentiviral fibroblast gene therapy in recessive dystrophic epidermolysis bullosa von Lwin, SM, Syed, F, Di, W-L, Kadiyirire, T, Liu, L, Guy, A, Petrova, A, Abdul-Wahab, A, Reid, F, Phillips, R, Elstad, M, Georgiadis, C, Aristodemou, S, Lovell, PA, McMillan, JR, Mee, J, Miskinyte, S, Titeux, M, Ozoemena, L, Pramanik, R, Serrano, S, Rowles, R, Maurin, C, Orrin, E, Martinez-Queipo, M, Rashidghamat, E, Tziotzios, C, Onoufriadis, A, Chen, M, Chan, L, Farzaneh, F, Del Rio, M, Tolar, J, Bauer, JW, Larcher, F, Antoniou, MN, Hovnanian, A, Thrasher, AJ, Mellerio, JE, Qasim, W, McGrath, JA

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Large melanocytic nevi in hereditary epidermolysis bullosa von Bauer, Johann W., Schaeppi, Herwig, Kaserer, Christine, Hantich, Birgit, Hintner, Helmut

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Epidermolysis bullosa naevi reveal a distinctive dermoscopic pattern von Lanschuetzer, C.M., Emberger, M., Laimer, M., Diem, A., Bauer, J.W., Soyer, H.P., Hintner, H.

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SCAVENGING BEHAVIOR IN PUMA von Bauer, Jim W, Logan, Kenneth A, Sweanor, Linda L, Boyce, Walter M

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Gene therapy of epidermolysis bullosa von Bauer, Johann W, Laimer, Martin

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Development of spliceosome-mediated RNA trans-splicing (SMaRT™) for the correction of inherited skin diseases von Dallinger, G., Puttaraju, M., Mitchell, L. G., Yancey, K. B., Yee, C., Klausegger, A., Hintner, H., Bauer, J. W.

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Private Safety Net: Childcare Resources from the Perspective of Rural Low-Income Families von Katras, Mary Jo, Zuiker, Virginia S., Bauer, Jean W.

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Revertant mosaicism: partial correction of a germ-line mutation in COL17A1 by a frame-restoring mutation von Darling, T N, Yee, C, Bauer, J W, Hintner, H, Yancey, K B

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Analysis of the LAMB3 gene in a junctional epidermolysis bullosa patient reveals exonic splicing and allele-specific nonsense-mediated mRNA decay von Buchroithner, Birgit, Klausegger, Alfred, Ebschner, Ulrike, Anton-Lamprecht, Ingrun, Pohla-Gubo, Gabriele, Lanschuetzer, Christoph M, Laimer, Martin, Hintner, Helmut, Bauer, Johann W

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A Compound Heterozygous One Amino-Acid Insertion/Nonsense Mutation in the Plectin Gene Causes Epidermolysis Bullosa Simplex with Plectin Deficiency von Bauer, Johann W., Rouan, Fatima, Kofler, Barbara, Rezniczek, Günther A., Kornacker, Iris, Muss, Wolfgang, Hametner, Rudolf, Klausegger, Alfred, Huber, Ariana, Pohla-Gubo, Gabriele, Wiche, Gerhard, Uitto, Jouni, Hintner, Helmut

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A localized variant of paraneoplastic pemphigus: acantholysis associated with malignant melanoma von Schaeppi, H., Bauer, J.W., Hametner, R., Metze, D., Ortiz‐Urda, S., Salmhofer, W., Rappersberger, K., Hintner, H.

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Introducing a fast and simple PCR-RFLP analysis for the detection of mutant thiopurine S-methyltransferase alleles TPMT3A and TPMT3C von Oender, K, Lanschuetzer, CM, Laimer, M, Klausegger, A, Paulweber, B, Kofler, B, Hintner, H, Bauer, JW

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Pathogenic mechanisms in epidermolysis bullosa naevi von LANSCHUETZER, Christoph M, EMBERGER, Michael, HAMETNER, Rudolf, KLAUSEGGER, Alfred, POHLA-GUBO, Gabriele, HINTNER, Helmut, BAUER, Johann W

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Skin grafting as a therapeutic approach in pretibially restricted junctional epidermolysis bullosa von Laimer, M., Bauer, J.W., Klausegger, A., Koller, J., Pohla-Gubo, G., Muss, W., Sadler, E., Emberger, M., Lanschuetzer, C.M., Hametner, R., Wally, V., Oender, K., Hintner, H.

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