Search Results - Eckl, Katja-Martina

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  1. 1

    Impaired epidermal ceramide synthesis causes autosomal recessive congenital ichthyosis and reveals the importance of ceramide acyl chain length by Eckl, Katja Martina (Author) , Tidhar, Rotem (Author) , Thiele, Holger (Author) , Oji, Vinzenz (Author) , Haußer-Siller, Ingrid (Author) , Brodesser, Susanne (Author) , Preil, Marie-Luise (Author) , Önal-Akan, Aysel (Author) , Stock, Friedrich (Author) , Müller, Dietmar (Author) , Becker, Kerstin (Author) , Casper, Ramona (Author) , Nürnberg, Gudrun (Author) , Altmüller, Janine (Author) , Nürnberg, Peter (Author) , Traupe, Heiko (Author) , Futerman, Anthony H. (Author) , Hennies, Hans C. (Author) ,


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  2. 2

    Mutations in CSTA, encoding cystatin A, underlie exfoliative ichthyosis and reveal a role for this protease inhibitor in cell-cell adhesion by Blaydon, Diana C. (Author) , Nitoiu, Daniela (Author) , Eckl, Katja-Martina (Author) , Cabral, Rita M. (Author) , Bland, Philip (Author) , Haußer-Siller, Ingrid (Author) , van Heel, David A. (Author) , Rajpopat, Shefali (Author) , Fischer, Judith (Author) , Oji, Vinzenz (Author) , Zvulunov, Alex (Author) , Traupe, Heiko (Author) , Hennies, Hans Christian (Author) , Kelsell, David P. (Author) ,


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  3. 3

    Loss of corneodesmosin leads to severe skin barrier defect, pruritus, and atopy: unraveling the peeling skin disease by Oji, Vinzenz (Author) , Eckl, Katja-Martina (Author) , Aufenvenne, Karin (Author) , Nätebus, Marc (Author) , Tarinski, Tatjana (Author) , Ackermann, Katharina (Author) , Seller, Natalia (Author) , Metze, Dieter (Author) , Nürnberg, Gudrun (Author) , Fölster-Holst, Regina (Author) , Schäfer-Korting, Monika (Author) , Haußer-Siller, Ingrid (Author) , Traupe, Heiko (Author) , Hennies, Hans Christian (Author) ,


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