Molecular Basis of the Accumulation of Abnormal Proteins in Progeria and Aging Fibroblasts



  • Rare Diseases, Aging, Adolescent, Adult, Aged, Aging, Amino Acid Sequence, Cells, Cultured, Culture Media, Fibroblasts, Glucosephosphate Dehydrogenase, Humans, Hypoxanthine Phosphoribosyltransferase, Middle Aged, Models, Molecular, Phosphogluconate Dehydrogenase, Progeria, Protein Conformation, Proteins, Triose-Phosphate Isomerase, Werner Syndrome
  • Digital Object Identifier (doi)

    Pubmed Id

  • 19581465
  • Start Page

  • 427
  • End Page

  • 442
  • Volume

  • 35