B P Korge

Summary

Affiliation: University of Cologne
Country: Germany

Publications

  1. ncbi Identification of novel mutations in basic hair keratins hHb1 and hHb6 in monilethrix: implications for protein structure and clinical phenotype
    B P Korge
    Department of Dermatology and Venerology, University of Cologne, Germany
    J Invest Dermatol 113:607-12. 1999
  2. ncbi [Pityriasis rosea. Reactivation of human Herpesvirus 6 and 7 infection?]
    B Korge
    Klinik und Poliklinik fur Dermatologie und Venerologie, Cologne
    Hautarzt 54:78-9. 2003
  3. ncbi [Kaposi sarcoma-associated human herpesvirus 8 infection. With destabilization of cellular beta-catenin comes proliferation and tumor growth]
    B Korge
    Klinik und Polikinik für Dermatologie und Venerologie, Cologne
    Hautarzt 54:389-90. 2003
  4. ncbi A novel compound heterozygous mutation in Werner syndrome results in WRN transcript decay
    F B Muller
    Department of Dermatology, University of Cologne, Kerpener Str 62, 50937 Koln, Germany
    Br J Dermatol 152:1030-2. 2005
  5. ncbi Linkage of epidermolytic hyperkeratosis to the type II keratin gene cluster on chromosome 12q
    J G Compton
    Skin Biology Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, Maryland 20892
    Nat Genet 1:301-5. 1992

Collaborators

Detail Information

Publications5

  1. ncbi Identification of novel mutations in basic hair keratins hHb1 and hHb6 in monilethrix: implications for protein structure and clinical phenotype
    B P Korge
    Department of Dermatology and Venerology, University of Cologne, Germany
    J Invest Dermatol 113:607-12. 1999
    ..Other factors are required to explain the marked variation in clinical severity within and between cases...
  2. ncbi [Pityriasis rosea. Reactivation of human Herpesvirus 6 and 7 infection?]
    B Korge
    Klinik und Poliklinik fur Dermatologie und Venerologie, Cologne
    Hautarzt 54:78-9. 2003
  3. ncbi [Kaposi sarcoma-associated human herpesvirus 8 infection. With destabilization of cellular beta-catenin comes proliferation and tumor growth]
    B Korge
    Klinik und Polikinik für Dermatologie und Venerologie, Cologne
    Hautarzt 54:389-90. 2003
  4. ncbi A novel compound heterozygous mutation in Werner syndrome results in WRN transcript decay
    F B Muller
    Department of Dermatology, University of Cologne, Kerpener Str 62, 50937 Koln, Germany
    Br J Dermatol 152:1030-2. 2005
    ..Werner syndrome (WS) is a rare autosomal recessive progeroid disorder caused by mutations of the WRN gene encoding a protein of the RecQ-type family of DNA helicases...
  5. ncbi Linkage of epidermolytic hyperkeratosis to the type II keratin gene cluster on chromosome 12q
    J G Compton
    Skin Biology Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, Maryland 20892
    Nat Genet 1:301-5. 1992
    ..In the pedigree studied here, a type II keratin gene, very probably K1, is implicated as the site of the molecular defect causing EHK...