Diverse Regulation of Claudin-1 and Claudin-4 in Atopic Dermatitis von Gruber, Robert, Börnchen, Christian, Rose, Katharina, Daubmann, Anne, Volksdorf, Thomas, Wladykowski, Ewa, Vidal-y-Sy, Sabine, Peters, Eva M, Danso, Mogbekeloluwa, Bouwstra, Joke A, Hennies, Hans C, Moll, Ingrid, Schmuth, Matthias, Brandner, Johanna M

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Impaired Epidermal Ceramide Synthesis Causes Autosomal Recessive Congenital Ichthyosis and Reveals the Importance of Ceramide Acyl Chain Length von Eckl, Katja-Martina, Tidhar, Rotem, Thiele, Holger, Oji, Vinzenz, Hausser, Ingrid, Brodesser, Susanne, Preil, Marie-Luise, Önal-Akan, Aysel, Stock, Friedrich, Müller, Dietmar, Becker, Kerstin, Casper, Ramona, Nürnberg, Gudrun, Altmüller, Janine, Nürnberg, Peter, Traupe, Heiko, Futerman, Anthony H., Hennies, Hans C.

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Does the understanding of signalling pathways pave the way to therapies for keratinization disorders? von Hennies, Hans C

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hiPSC-Derived Epidermal Keratinocytes from Ichthyosis Patients Show Altered Expression of Cornification Markers von Lima Cunha, Dulce, Oram, Amanda, Gruber, Robert, Plank, Roswitha, Lingenhel, Arno, Gupta, Manoj K., Altmuller, Janine, Nurnberg, Peter, Schmuth, Matthias, Zschocke, Johannes, Saric, Tomo, Eckl, Katja M., Hennies, Hans C.

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A Gene Mutated in Nephronophthisis and Retinitis Pigmentosa Encodes a Novel Protein, Nephroretinin, Conserved in Evolution von Otto, Edgar, Hoefele, Julia, Ruf, Rainer, Mueller, Adelheid M., Hiller, Karl S., Wolf, Matthias T.F., Schuermann, Maria J., Becker, Achim, Birkenhäger, Ralf, Sudbrak, Ralf, Hennies, Hans C., Nürnberg, Peter, Hildebrandt, Friedhelm

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Wnt Signaling and Dupuytren's Disease von Dolmans, Guido H, Werker, Paul M, Hennies, Hans C, Furniss, Dominic, Festen, Eleonora A, Franke, Andre, Franke, Lude, Becker, Kerstin, van der Vlies, Pieter, Wolffenbuttel, Bruce H, Tinschert, Sigrid, Toliat, Mohammad R, Nothnagel, Michael, Klopp, Norman, Wichmann, H.-Erich, Nürnberg, Peter, Giele, Henk, Ophoff, Roel A, Wijmenga, Cisca

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Genome-Wide Association Scan of Dupuytren's Disease von Furniss, Dominic, DM, MA, Dolmans, Guido H.C.G., MD, Hennies, Hans C., PhD

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Induced Pluripotent Mesenchymal Stromal Cell Clones Retain Donor-derived Differences in DNA Methylation Profiles von Shao, Kaifeng, Koch, Carmen, Gupta, Manoj K, Lin, Qiong, Lenz, Michael, Laufs, Stephanie, Denecke, Bernd, Schmidt, Manfred, Linke, Matthias, Hennies, Hans C, Hescheler, Jürgen, Zenke, Martin, Zechner, Ulrich, Šarić, Tomo, Wagner, Wolfgang

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Effective Immunological Guidance of Genetic Analyses Including Exome Sequencing in Patients Evaluated for Hemophagocytic Lymphohistiocytosis von Ammann, Sandra, Lehmberg, Kai, zur Stadt, Udo, Klemann, Christian, Bode, Sebastian F. N., Speckmann, Carsten, Janka, Gritta, Wustrau, Katharina, Rakhmanov, Mirzokhid, Fuchs, Ilka, Hennies, Hans C., Ehl, Stephan

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Molecular Analysis of 250 Patients with Autosomal Recessive Congenital Ichthyosis: Evidence for Mutation Hotspots in ALOXE3 and Allelic Heterogeneity in ALOX12B von Eckl, Katja-Martina, de Juanes, Silvia, Kurtenbach, Janine, Nätebus, Marc, Lugassy, Jenny, Oji, Vinzenz, Traupe, Heiko, Preil, Marie-Luise, Martínez, Francisco, Smolle, Josef, Harel, Avikam, Krieg, Peter, Sprecher, Eli, Hennies, Hans C.

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MYO15A (DFNB3) mutations in Turkish hearing loss families and functional modeling of a novel motor domain mutation von Kalay, Ersan, Uzumcu, Abdullah, Krieger, Elmar, Çaylan, Refik, Uyguner, Oya, Ulubil-Emiroglu, Melike, Erdol, Hidayet, Kayserili, Hülya, Hafiz, Gunter, Başerer, Nermin, Heister, Angelien J.G.M., Hennies, Hans C., Nürnberg, Peter, Başaran, Seher, Brunner, Han G., Cremers, Cor W.R.J., Karaguzel, Ahmet, Wollnik, Bernd, Kremer, Hannie

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Medullary cystic kidney disease type 1: mutational analysis in 37 genes based on haplotype sharing von WOLF, Matthias T. F, MUCHA, Bettina E, HILDEBRANDT, Friedhelm, HENNIES, Hans C, ATTANASIO, Massimo, PANTHER, Franziska, ZALEWSKI, Isabella, KARLE, Stephanie M, OTTO, Edgar A, DELTAS, C. Constantinou, FUCHSHUBER, Arno

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Cystatin M/E knockdown by lentiviral delivery of shRNA impairs epidermal morphogenesis of human skin equivalents von Jansen, Patrick A. M., van den Bogaard, Ellen H., Kersten, Ferry F. J., Oostendorp, Corien, van Vlijmen-Willems, Ivonne M. J. J., Oji, Vinzenz, Traupe, Heiko, Hennies, Hans C., Schalkwijk, Joost, Zeeuwen, Patrick L. J. M.

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Mapping a new suggestive gene locus for autosomal dominant nephrolithiasis to chromosome 9q33.2–q34.2 by total genome search for linkage von Wolf, Matthias T. F., Zalewski, Isabella, Martin, Félix Claverie, Ruf, Rainer, Müller, Dominik, Hennies, Hans C., Schwarz, Stella, Panther, Franziska, Attanasio, Massimo, Acosta, Hilaria G., Imm, Anita, Lucke, Barbara, Utsch, Boris, Otto, Edgar, Nurnberg, Peter, Nieto, Victor Garcia, Hildebrandt, Friedhelm

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A gene locus for steroid-resistant nephrotic syndrome with deafness maps to chromosome 14q24.2 von RUF, Rainer G, WOLF, Matthias T. F, LENNERT, Thomas, FUCHSHUBER, Arno, NURNBERG, Peter, HILDEBRANDT, Friedhelm, HENNIES, Hans C, LUCKE, Barbara, ZINN, Christina, VARNHOLT, Verena, LICHTENBERGER, Anne, PASCH, Andreas, IMM, Anita, BRIESE, Sonia

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Telomeric refinement of the MCKD1 locuson chromosome 1q21 von Wolf, Matthias T.F., Van Vlem, Bruno, Hennies, Hans C., Zalewski, Isabella, Karle, Stephanie M., Puetz, Markus, Panther, Franziska, Otto, Edgar, Fuchshuber, Arno, Lameire, Norbert, Loeys, Bart, Hildebrandt, Friedhelm

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Dissecting the Development of Dupuytren Disease Through Human Genetics von Ng, Michael, Zeggini, Eleftheria, Hennies, Hans C., Werker, Paul M., Furniss, Dominic

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A Novel Homozygous Missense Mutation in SLURP1 Causing Mal de Meleda With an Atypical Phenotype von Gruber, Robert, Hennies, Hans C, Romani, Nikolaus, Schmuth, Matthias

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Cystatin M/E knockdown by lentiviral delivery of sh RNA impairs epidermal morphogenesis of human skin equivalents von Jansen, Patrick A. M., van den Bogaard, Ellen H., Kersten, Ferry F. J., Oostendorp, Corien, van Vlijmen‐Willems, Ivonne M. J. J., Oji, Vinzenz, Traupe, Heiko, Hennies, Hans C., Schalkwijk, Joost, Zeeuwen, Patrick L. J. M.

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Telomeric refinement of the MCKD1 locus on chromosome 1q21 von WOLF, Matthias T. F, VAN VLEM, Bruno, LOEYS, Bart, HILDEBRANDT, Friedhelm, HENNIES, Hans C, ZALEWSKI, Isabella, KARLE, Stephanie M, PUETZ, Markus, PANTHER, Franziska, OTTO, Edgar, FUCHSHUBER, Arno, LAMEIRE, Norbert

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