C P Maury

Summary

Affiliation: Helsinki University Central Hospital
Country: Finland

Publications

  1. pmc Danish type gelsolin related amyloidosis: 654G-T mutation is associated with a disease pathogenetically and clinically similar to that caused by the 654G-A mutation (familial amyloidosis of the Finnish type)
    C P Maury
    Department of Medicine, University of Helsinki, Finland
    J Clin Pathol 53:95-9. 2000
  2. ncbi request reprint Gelsolin-derived familial amyloidosis caused by asparagine or tyrosine substitution for aspartic acid at residue 187
    A de la Chapelle
    Department of Medical Genetics, University of Helsinki, Finland
    Nat Genet 2:157-60. 1992
  3. ncbi request reprint Finnish hereditary amyloidosis. Amino acid sequence homology between the amyloid fibril protein and human plasma gelsoline
    C P Maury
    Fourth Department of Medicine, University of Helsinki, Finland
    FEBS Lett 260:85-7. 1990
  4. ncbi request reprint Fibrillogenesis in gelsolin-related familial amyloidosis
    C P Maury
    Department of Medicine, University of Helsinki, Kasarmikatu 11 13, FIN 00130 Helsinki, Finland
    Amyloid 10:21-5. 2003
  5. ncbi request reprint Apolipoprotein E phenotypes in rheumatoid arthritis with or without amyloidosis
    C P Maury
    Department of Medicine, University of Helsinki, Finland
    Amyloid 8:270-3. 2001
  6. ncbi request reprint Familial amyloidosis, Finnish type: G654----a mutation of the gelsolin gene in Finnish families and an unrelated American family
    A de la Chapelle
    Department of Medical Genetics, University of Helsinki, Finland
    Genomics 13:898-901. 1992

Detail Information

Publications6

  1. pmc Danish type gelsolin related amyloidosis: 654G-T mutation is associated with a disease pathogenetically and clinically similar to that caused by the 654G-A mutation (familial amyloidosis of the Finnish type)
    C P Maury
    Department of Medicine, University of Helsinki, Finland
    J Clin Pathol 53:95-9. 2000
    ....
  2. ncbi request reprint Gelsolin-derived familial amyloidosis caused by asparagine or tyrosine substitution for aspartic acid at residue 187
    A de la Chapelle
    Department of Medical Genetics, University of Helsinki, Finland
    Nat Genet 2:157-60. 1992
    ..We conclude that substitution of the uncharged Asn or Tyr for the acidic Asp at residue 187 creates a conformation that may be preferentially amyloidogenic for GSN...
  3. ncbi request reprint Finnish hereditary amyloidosis. Amino acid sequence homology between the amyloid fibril protein and human plasma gelsoline
    C P Maury
    Fourth Department of Medicine, University of Helsinki, Finland
    FEBS Lett 260:85-7. 1990
    ..The results show that the amyloid fibril protein in Finnish hereditary amyloidosis represents a new type of amyloid protein that shows amino acid sequence homology with gelsoline, an actin-modulating protein...
  4. ncbi request reprint Fibrillogenesis in gelsolin-related familial amyloidosis
    C P Maury
    Department of Medicine, University of Helsinki, Kasarmikatu 11 13, FIN 00130 Helsinki, Finland
    Amyloid 10:21-5. 2003
    ....
  5. ncbi request reprint Apolipoprotein E phenotypes in rheumatoid arthritis with or without amyloidosis
    C P Maury
    Department of Medicine, University of Helsinki, Finland
    Amyloid 8:270-3. 2001
    ....
  6. ncbi request reprint Familial amyloidosis, Finnish type: G654----a mutation of the gelsolin gene in Finnish families and an unrelated American family
    A de la Chapelle
    Department of Medical Genetics, University of Helsinki, Finland
    Genomics 13:898-901. 1992
    ..We suggest two alternative explanations: (i) the mutation arose in a very early common ancestor or (ii) the Asn187 mutation is particularly, perhaps uniquely, amyloidogenic...