Vinzenz Oji

Summary

Country: Germany

Publications

  1. ncbi Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Sorèze 2009
    Vinzenz Oji
    Department of Dermatology, University Hospital Munster, Munster, Germany
    J Am Acad Dermatol 63:607-41. 2010
  2. ncbi Ichthyosis vulgaris: novel FLG mutations in the German population and high presence of CD1a+ cells in the epidermis of the atopic subgroup
    V Oji
    Department of Dermatology, University of Munster, Von Esmarch Str 58, 48149 Munster, Germany
    Br J Dermatol 160:771-81. 2009
  3. ncbi Plasminogen activator inhibitor-2 is expressed in different types of congenital ichthyosis: in vivo evidence for its cross-linking into the cornified cell envelope by transglutaminase-1
    V Oji
    Department of Dermatology, University of Munster, Germany
    Br J Dermatol 154:860-7. 2006
  4. ncbi Ichthyoses: differential diagnosis and molecular genetics
    Vinzenz Oji
    Department of Dermatology, University Hospital, Von Esmarch Str 58, 48149 Munster, Germany
    Eur J Dermatol 16:349-59. 2006
  5. ncbi Ichthyosis: clinical manifestations and practical treatment options
    Vinzenz Oji
    Department of Dermatology, University of Munster, Munster, Germany
    Am J Clin Dermatol 10:351-64. 2009
  6. ncbi Loss of corneodesmosin leads to severe skin barrier defect, pruritus, and atopy: unraveling the peeling skin disease
    Vinzenz Oji
    Department of Dermatology, University Hospital Munster, 48149 Munster, Germany
    Am J Hum Genet 87:274-81. 2010
  7. ncbi Bathing suit ichthyosis is caused by transglutaminase-1 deficiency: evidence for a temperature-sensitive phenotype
    Vinzenz Oji
    Department of Dermatology, University of Muenster, Von Esmarch Str 58 D 48149, Munster, Germany
    Hum Mol Genet 15:3083-97. 2006
  8. ncbi Ichthyoses--Part 2: Congenital ichthyoses
    Markus Krug
    Department of Dermatology, University of Tubingen, Germany
    J Dtsch Dermatol Ges 7:577-88. 2009
  9. ncbi Ichthyoses - Part 1: Differential diagnosis of vulgar ichthyoses and therapeutic options
    Markus Krug
    Department of Dermatology, University of Tubingen, Germany
    J Dtsch Dermatol Ges 7:511-9. 2009
  10. ncbi The neuropeptide alpha-melanocyte-stimulating hormone is critically involved in the development of cytotoxic CD8+ T cells in mice and humans
    Karin Loser
    Department of Dermatology, University of Munster, Munster, Germany
    PLoS ONE 5:e8958. 2010

Collaborators

Detail Information

Publications15

  1. ncbi Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Sorèze 2009
    Vinzenz Oji
    Department of Dermatology, University Hospital Munster, Munster, Germany
    J Am Acad Dermatol 63:607-41. 2010
    ..Over the recent years, much progress has been made defining their molecular causes. However, there is no internationally accepted classification and terminology...
  2. ncbi Ichthyosis vulgaris: novel FLG mutations in the German population and high presence of CD1a+ cells in the epidermis of the atopic subgroup
    V Oji
    Department of Dermatology, University of Munster, Von Esmarch Str 58, 48149 Munster, Germany
    Br J Dermatol 160:771-81. 2009
    ..Ichthyosis vulgaris (IV) is a genetic disorder with a prevalence of 1:250-1000 caused by filaggrin (FLG) mutations, which also predispose to atopic diseases...
  3. ncbi Plasminogen activator inhibitor-2 is expressed in different types of congenital ichthyosis: in vivo evidence for its cross-linking into the cornified cell envelope by transglutaminase-1
    V Oji
    Department of Dermatology, University of Munster, Germany
    Br J Dermatol 154:860-7. 2006
    ..Protease inhibitors are essential for skin homeostasis and in particular for the regulation of the desquamation process. Therefore, an aberrant expression of PAI-2 could be involved in the pathogenesis of certain cornification disorders...
  4. ncbi Ichthyoses: differential diagnosis and molecular genetics
    Vinzenz Oji
    Department of Dermatology, University Hospital, Von Esmarch Str 58, 48149 Munster, Germany
    Eur J Dermatol 16:349-59. 2006
    ..The different pathomechanisms causing ichthyosis provide a fascinating insight into the role of various proteins, enzymes, lipids and metabolic pathways involved in terminal epidermal differentiation/keratinisation...
  5. ncbi Ichthyosis: clinical manifestations and practical treatment options
    Vinzenz Oji
    Department of Dermatology, University of Munster, Munster, Germany
    Am J Clin Dermatol 10:351-64. 2009
    ..Patients with lamellar ichthyosis or ichthyosiform erythroderma in particular profit from oral therapy with retinoids or retinoic acid metabolism-blocking agents...
  6. ncbi Loss of corneodesmosin leads to severe skin barrier defect, pruritus, and atopy: unraveling the peeling skin disease
    Vinzenz Oji
    Department of Dermatology, University Hospital Munster, 48149 Munster, Germany
    Am J Hum Genet 87:274-81. 2010
    ..Therefore, peeling skin disease will represent a new model disorder for atopic diseases, similarly to Netherton syndrome and ichthyosis vulgaris in the recent past...
  7. ncbi Bathing suit ichthyosis is caused by transglutaminase-1 deficiency: evidence for a temperature-sensitive phenotype
    Vinzenz Oji
    Department of Dermatology, University of Muenster, Von Esmarch Str 58 D 48149, Munster, Germany
    Hum Mol Genet 15:3083-97. 2006
    ..We conclude that BSI is caused by TGase-1 deficiency and suggest that it is a temperature-sensitive phenotype...
  8. ncbi Ichthyoses--Part 2: Congenital ichthyoses
    Markus Krug
    Department of Dermatology, University of Tubingen, Germany
    J Dtsch Dermatol Ges 7:577-88. 2009
    ..Patients with uncommon congenital ichthyoses often benefit from interdisciplinary management which involves specialized dermatological centers...
  9. ncbi Ichthyoses - Part 1: Differential diagnosis of vulgar ichthyoses and therapeutic options
    Markus Krug
    Department of Dermatology, University of Tubingen, Germany
    J Dtsch Dermatol Ges 7:511-9. 2009
    ..In this first part of the paper the vulgar ichthyoses as well as the diagnostic and therapeutic options are discussed. The second part focuses on the congenital ichthyoses and their differential diagnosis...
  10. ncbi The neuropeptide alpha-melanocyte-stimulating hormone is critically involved in the development of cytotoxic CD8+ T cells in mice and humans
    Karin Loser
    Department of Dermatology, University of Munster, Munster, Germany
    PLoS ONE 5:e8958. 2010
    ....
  11. ncbi Detection of functionally active melanocortin receptors and evidence for an immunoregulatory activity of alpha-melanocyte-stimulating hormone in human dermal papilla cells
    Markus Bohm
    Department of Dermatology, University of Munster, Von Esmarch Str 58, D 48149 Munster, Germany
    Endocrinology 146:4635-46. 2005
    ....
  12. ncbi SPINK5 and Netherton syndrome: novel mutations, demonstration of missing LEKTI, and differential expression of transglutaminases
    Michael Raghunath
    Department of Dermatology, University Hospital, University of Munster, Von Esmarch Strasse 58, D 48149 Munster, Germany
    J Invest Dermatol 123:474-83. 2004
    ....
  13. ncbi Loss-of-function variants of the filaggrin gene are not major susceptibility factors for psoriasis vulgaris or psoriatic arthritis in German patients
    Ulrike Huffmeier
    Institute of Human Genetics, University Erlangen Nuremberg, Erlangen, Germany
    J Invest Dermatol 127:1367-70. 2007
    ..The abnormal staining might reflect the altered epidermal differentiation. Our findings imply that the genetic background underlying the epidermal barrier defect in psoriasis is distinct from that found in atopic dermatitis...
  14. ncbi The alpha and beta subunits of the metalloprotease meprin are expressed in separate layers of human epidermis, revealing different functions in keratinocyte proliferation and differentiation
    Christoph Becker-Pauly
    Institute of Zoology, Johannes Gutenberg University, Johannes von Müller Weg 6, Mainz, Germany
    J Invest Dermatol 127:1115-25. 2007
    ....
  15. ncbi Deficiency of PORCN, a regulator of Wnt signaling, is associated with focal dermal hypoplasia
    Karl Heinz Grzeschik
    Department of Human Genetics, University of Marburg, Bahnhofstr 7, 35033 Marburg, Germany
    Nat Genet 39:833-5. 2007
    ..The findings implicate FDH as a developmental disorder caused by a deficiency in PORCN...