Ochronosis in a murine model of alkaptonuria is synonymous to that in the human condition

This publication has 23 references indexed in Scilit:

• Development of an in vitro model to investigate joint ochronosis in alkaptonuria
  Rheumatology, 2010
• Ultrastructural examination of tissue in a patient with alkaptonuric arthropathy reveals a distinct pattern of binding of ochronotic pigment
  Rheumatology, 2010
• Calculi and intracellular ochronosis in the submandibular tissues from a patient with alkaptonuria
  Journal of Clinical Pathology, 2010
• Alkaptonuria – a review of surgical and autopsy pathology
  Histopathology, 2008
• A novel therapeutic trial of homogentisic aciduria in a murine model of alkaptonuria
  Journal of Human Genetics, 1999
• Pharmacological correction of neonatal lethal hepatic dysfunction in a murine model of hereditary tyrosinaemia type I
  Nature Genetics, 1995
• The Human Gene for Alkaptonuria (AKU) Maps to Chromosome 3q
  Genomics, 1994
• Homozygosity mapping of the gene for alkaptonuria to chromosome 3q2
  Nature Genetics, 1993
• Ascorbic acid and alkaptonuria
  European Journal of Pediatrics, 1992
• Alkaptonuria in an orangutan (Pongo pygmaeus)
  American Journal of Physical Anthropology, 1973