Keratin diseases

This publication has 38 references indexed in Scilit:

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• Allelic Variations of Human Keratins K4 and K5 Provide Polymorphic Markers Within the Type II Keratin Gene Cluster on Chromosome 12
  Journal of Investigative Dermatology, 1993
• Peptides from the Conserved Ends of the Rod Domain of Desmin Disassemble Intermediate Filaments and Reveal Unexpected Structural Features: A Circular Dichroism, Fourier Transform Infrared, and Electron Microscopic Study
  Journal of Structural Biology, 1993
• Keratin Intermediate Filament Structure: Crosslinking Studies Yield Quantitative Information on Molecular Dimensions and Mechanism of Assembly
  Journal of Molecular Biology, 1993
• The Two Size Alleles of Human Keratin 1 Are Due to a Deletion in the Glycine-Rich Carboxyl-Terminal V2 Subdomain
  Journal of Investigative Dermatology, 1992
• Chemical cross‐linking indicates a staggered and antiparallel protofilament of desmin intermediate filaments and characterizes one higher‐level complex between protofilaments
  European Journal of Biochemistry, 1992
• Molecular interactions in paracrystals of a fragment corresponding to the alpha-helical coiled-coil rod portion of glial fibrillary acidic protein: evidence for an antiparallel packing of molecules and polymorphism related to intermediate filament structure.
  The Journal of cell biology, 1989
• Concerted gene duplications in the two keratin gene families
  Journal of Molecular Evolution, 1988
• Intermediate filament forming ability of desmin derivatives lacking either the amino-terminal 67 or the carboxy-terminal 27 residues
  Journal of Molecular Biology, 1985