Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
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1 |
Material Type: Artigo
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Functional Correction of Type VII Collagen Expression in Dystrophic Epidermolysis BullosaMurauer, Eva M. ; Gache, Yannick ; Gratz, Iris K. ; Klausegger, Alfred ; Muss, Wolfgang ; Gruber, Christina ; Meneguzzi, Guerrino ; Hintner, Helmut ; Bauer, Johann W.Journal of investigative dermatology, 2011-01, Vol.131 (1), p.74-83 [Periódico revisado por pares]New York, NY: Elsevier IncTexto completo disponível |
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2 |
Material Type: Artigo
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Correction of Dog Dystrophic Epidermolysis Bullosa by Transplantation of Genetically Modified Epidermal AutograftsGache, Yannick ; Pin, Didier ; Gagnoux-Palacios, Laurent ; Carozzo, Claude ; Meneguzzi, GuerrinoJournal of investigative dermatology, 2011-10, Vol.131 (10), p.2069-2078 [Periódico revisado por pares]New York, NY: Elsevier IncTexto completo disponível |
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3 |
Material Type: Artigo
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Two major 5′-untranslated regions for type XVII collagen mRNAvan Zalen, Sebastiaan ; Nijenhuis, Miranda ; Jonkman, Marcel F. ; Pas, Hendri H.Journal of dermatological science, 2006-07, Vol.43 (1), p.11-19 [Periódico revisado por pares]Netherlands: Elsevier Ireland LtdTexto completo disponível |
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4 |
Material Type: Artigo
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Epidermolysis Bullosa: Novel and De Novo Premature Termination Codon and Deletion Mutations in the Plectin Gene Predict Late-Onset Muscular DystrophyRouan, Fatima ; Pulkkinen, Leena ; LaForgia, Sal ; Hyde, Patrice ; Richard, Gabriele ; Uitto, Jouni ; Meneguzzi, Guerrino ; Kim, Dae UnJournal of investigative dermatology, 2000-02, Vol.114 (2), p.381-387 [Periódico revisado por pares]Danvers, MA: Elsevier IncTexto completo disponível |
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5 |
Material Type: Artigo
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A founder effect of c.1938delC in ITGB4 underlies junctional epidermolysis bullosa and its application for prenatal testingNatsuga, Ken ; Nishie, Wataru ; Shinkuma, Satoru ; Nakamura, Hideki ; Arita, Ken ; Yoneda, Kozo ; Kusaka, Takashi ; Yanagihara, Toshihiro ; Kosaki, Rika ; Sago, Haruhiko ; Akiyama, Masashi ; Shimizu, HiroshiExperimental dermatology, 2011-01, Vol.20 (1), p.74-76 [Periódico revisado por pares]Oxford, UK: Blackwell Publishing LtdTexto completo disponível |
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6 |
Material Type: Artigo
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Progress towards genetic and pharmacological therapies for keratin genodermatoses: current perspective and future promiseChamcheu, Jean Christopher ; Wood, Gary S. ; Siddiqui, Imtiaz A. ; Syed, Deeba N. ; Adhami, Vaqar M. ; Teng, Joyce M. ; Mukhtar, HasanExperimental dermatology, 2012-07, Vol.21 (7), p.481-489 [Periódico revisado por pares]Oxford: Blackwell Publishing LtdTexto completo disponível |
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7 |
Material Type: Artigo
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Fibroblasts Show More Potential as Target Cells than Keratinocytes in COL7A1 Gene Therapy of Dystrophic Epidermolysis BullosaGoto, Maki ; Sawamura, Daisuke ; Ito, Kei ; Abe, Masataka ; Nishie, Wataru ; Sakai, Kaori ; Shibaki, Akihiko ; Akiyama, Masashi ; Shimizu, HiroshiJournal of investigative dermatology, 2006-04, Vol.126 (4), p.766-772 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
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8 |
Material Type: Artigo
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Development and characterization of a canine skin equivalentSerra, Montserrat ; Brazís, Pilar ; Puigdemont, Anna ; Fondevila, Dolors ; Romano, Víctor ; Torre, Celina ; Ferrer, LluísExperimental dermatology, 2007-02, Vol.16 (2), p.135-142 [Periódico revisado por pares]Oxford, UK: Blackwell Publishing LtdTexto completo disponível |
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9 |
Material Type: Artigo
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Dynamic Characterization of the Molecular Events During In Vitro Epidermal Wound HealingRezzonico, Roger ; Yeow, Karen ; Loubat, Agnès ; Ferrua, Bernard ; Lenegrate, Gaëlle ; Turchi, Laurent ; Amandine Chassot, Anne ; Ortonne, Jean Paul ; Ponzio, GillesJournal of investigative dermatology, 2002-07, Vol.119 (1), p.56-63 [Periódico revisado por pares]Danvers, MA: Elsevier IncTexto completo disponível |
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10 |
Material Type: Artigo
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Hemidesmosomal variants of epidermolysis bullosaPulkkinen, L. ; Uitto, J.Experimental dermatology, 1998-06, Vol.7 (2-3), p.46-64 [Periódico revisado por pares]Oxford, UK: Blackwell Publishing LtdTexto completo disponível |