Phenotypes, genotypes and their contribution to understanding keratin function

This publication has 69 references indexed in Scilit:

• Type II Keratins Are Phosphorylated on a Unique Motif during Stress and Mitosis in Tissues and Cultured Cells
  Molecular Biology of the Cell, 2002
• Characterization of Early Assembly Intermediates of Recombinant Human Keratins
  Journal of Structural Biology, 2002
• Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
  Journal of Investigative Dermatology, 2001
• Focal Activation of a Mutant Allele Defines the Role of Stem Cells in Mosaic Skin Disorders
  The Journal of cell biology, 2001
• A keratin 14 ‘knockout’ mutation in recessive epidermolysis bullosa simplex resulting in less severe disease
  British Journal of Dermatology, 2000
• Epidermolysis bullosa simplex with mottled pigmentation: Clinical aspects and confirmation of the P24L mutation in theKRT5 gene in further patients
  American Journal of Medical Genetics, 1999
• Keratin 17 mutations cause either steatocystoma multiplex or pachyonychia congenita type 2
  British Journal of Dermatology, 1998
• Chronic hepatitis, hepatocyte fragility, and increased soluble phosphoglycokeratins in transgenic mice expressing a keratin 18 conserved arginine mutant.
  The Journal of cell biology, 1995
• Increased expression of keratin 16 causes anomalies in cytoarchitecture and keratinization in transgenic mouse skin.
  The Journal of cell biology, 1994
• Ectopic synthesis of epidermal cytokeratins in pancreatic islet cells of transgenic mice interferes with cytoskeletal order and insulin production.
  The Journal of cell biology, 1993