Long-term faithful recapitulation of transglutaminase 1-deficient lamellar ichthyosis in a skin-humanized mouse model and insights from proteomic studies

Podobne zapisy

• Topical Enzyme-Replacement Therapy Restores Transglutaminase 1 Activity and Corrects Architecture of Transglutaminase-1-Deficient Skin Grafts
  od: Aufenvenne, Karin, i wsp.
  Wydane: (2013)
• Transglutaminase-1 Mutations in Omani Families with Lamellar Ichthyosis
  od: Al-Naamani, Aisha, i wsp.
  Wydane: (2013)
• Novel transglutaminase 1 mutations in patients affected by lamellar ichthyosis
  od: Terrinoni, A, i wsp.
  Wydane: (2012)
• Loss of Corneodesmosin Leads to Severe Skin Barrier Defect, Pruritus, and Atopy: Unraveling the Peeling Skin Disease
  od: Oji, Vinzenz, i wsp.
  Wydane: (2010)
• Genotype/phenotype correlation in autosomal recessive lamellar ichthyosis.
  od: Hennies, H C, i wsp.
  Wydane: (1998)