Recessive Epidermolytic Hyperkeratosis Caused by a Previously Unreported Termination Codon Mutation in the Keratin 10 Gene von Terheyden, Patrick, Grimberg, Gundula, Hausser, Ingrid, Rose, Christian, Korge, Bernhard P., Krieg, Thomas, Arin, Meral J.

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A Missense Mutation in Connexin26, D66H, Causes Mutilating Keratoderma with Sensorineural Deafness (Vohwinkel's Syndrome) in Three Unrelated Families von Maestrini, Elena, Korge, Bernhard P., Ocaña-Sierra, Juan, Calzolari, Elisa, Cambiaghi, Stefano, Scudder, Pat M., Hovnanian, Alain, Monaco, Anthony P., Munro, Colin S.

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Genes Encoding Structural Proteins of Epidermal Cornification and S100 Calcium-Binding Proteins Form a Gene Complex (“Epidermal Differentiation Complex”) on Human Chromosome 1q21... von Mischke, Dietmar, Korge, Bernhard P., Marenholz, Ingo, Volz, Armin, Ziegler, Andreas

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A human keratin 10 knockout causes recessive epidermolytic hyperkeratosis von Müller, Felix B., Huber, Marcel, Kinaciyan, Tamar, Hausser, Ingrid, Schaffrath, Christina, Krieg, Thomas, Hohl, Daniel, Korge, Bernhard P., Arin, Meral J.

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Desmosome Assembly and Keratin Network Formation After Ca2+/Serum Induction and UVB Radiation in Hailey–Hailey Keratinocytes von Bernards, Markus, Korge, Bernhard P.

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Novel and recurrent mutations in keratin KRT5 and KRT14 genes in epidermolysis bullosa simplex: implications for disease phenotype and keratin filament assembly von Müller, Felix B., Küster, Wolfgang, Wodecki, Kerstin, Almeida Jr, Hiram, Bruckner-Tuderman, Leena, Krieg, Thomas, Korge, Bernhard P., Arin, Meral J.

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Linkage of epidermolytic hyperkeratosis to the type II keratin gene cluster on chromosome 12q von Compton, John G, DiGiovanna, John J, Santucci, Sandra K, Kearns, Kathleen S, Amos, Christopher I, Abangan, Donita L, Korge, Bernhard P, McBride, O. Wesley, Steinert, Peter M, Bale, Sherri J

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A leucine→proline mutation in the H1 subdomain of keratin 1 causes epidermolytic hyperkeratosis von Chipev, Constantin C., Korge, Bernhard P., Markova, Nedialka, Bale, Sherri J., DiGiovanna, John J., Compton, John G., Steinert, Peter M.

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Genetic Analysis of the Epidermal Differentiation Complex (EDC) on Human Chromosome 1q21: Chromosomal Orientation, New Markers, and a 6-Mb YAC Contig von Marenholz, Ingo, Volz, Armin, Ziegler, Andreas, Davies, Angela, Ragoussis, Ioannis, Korge, Bernhard P., Mischke, Dietmar

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Physical Mapping of a Functional Cluster of Epidermal Differentiation Genes on Chromosome 1q21 von Volz, Armin, Korge, Bernhard P., Compton, John G., Ziegler, Andreas, Steinert, Peter M., Mischke, Dietmar

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Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype von Korge, Bernhard P., Hamm, Henning, Jury, Catherine S., Traupe, Heiko, Irvine, Alan D., Healy, Eugene, Birch-Machin, Mark, Rees, Jonathan L., Messenger, Andrew G., Holmes, Susan C., Parry, David A.D., Munro, Colin S.

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Extensive Size Polymorphism of the Human Keratin 10 Chain Resides in the C-Terminal V2 Subdomain Due to Variable Numbers and Sizes of Glycine Loops von Korge, Bernhard P., Gan, Song-Qing, McBride, O. Wesley, Mischke, Dietmar, Steinert, Peter M.

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Altered Proliferation, Synthetic Activity, and Differentiation of Cultured Human sebocytes in the Absence of Vitamin A and Their Modulation by Synthetic Retinoids von Zouboulis, Christos C, Korge, Bernhard P, Mischke, Dietmar, Orfanos, Constantin E

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The Two Size Alleles of Human Keratin 1 Are Due to a Deletion in the Glycine-Rich Carboxyl-Terminal V2 Subdomain von Korge, Bernhard P, Compton, John G, Steinert, Peter M, Mischke, Dietmar

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Novel K5 and K14 Mutations in German Patients with the Weber–Cockayne Variant of Epidermolysis Bullosa Simplex von Müller, Felix B., Küster, Wolfgang, Bruckner-Tuderman, Leena, Korge, Bernhard P.

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Keratin and keratinization von Smack, David Phillips, Korge, Bernhard P., James, William D.

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Novel and recurrent mutations in keratin KRT5 and KRT14 genes in epidermolysis bullosa simplex: implications for disease phenotype and keratin filament assembly von Mueller, Felix B, Kuester, Wolfgang, Wodecki, Kerstin, Almeida Jr, Hiram, Bruckner-Tuderman, Leena, Krieg, Thomas, Korge, Bernhard P, Arin, Meral J

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A Premature Stop Codon Mutation in the 2B Helix Termination Peptide of Keratin 5 in a German Epidermolysis Bullosa Simplex Dowling–Meara Case von Müller, Felix B., Korge, Bernhard P., Anton-Lamprecht, Ingrun, Küster, Wolfgang

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A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients von Korge, Bernhard P., Healy, Eugene, Munro, Colin S., Birch-Machin, Mark, Holmes, Susan C., Darlington, Silke, Hamm, Henning, Messenger, Andrew G., Rees, Jonathan L., Traupe, Heiko, Pünter, Claudia

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Desmosome formation in cultured Hailey-Hailey keratinocytes cannot be impaired by UV-B radiation von Bernards, Markus, Korge, Bernhard P

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