Pathogenesis of adult-onset type II citrullinemia caused by deficiency of citrin, a mitochondrial solute carrier protein: tissue and subcellular localization of citrin

Adv Enzyme Regul. 2001:41:325-42. doi: 10.1016/s0065-2571(00)00022-4.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Age Factors
  • Age of Onset
  • Aged
  • Aged, 80 and over
  • Animals
  • Blotting, Northern
  • Calcium-Binding Proteins / biosynthesis*
  • Calcium-Binding Proteins / chemistry
  • Calcium-Binding Proteins / deficiency*
  • Cell Line
  • Child
  • Citrullinemia / diagnosis*
  • Citrullinemia / pathology*
  • DNA Mutational Analysis
  • Endothelium / metabolism
  • Humans
  • Intestine, Small / metabolism
  • Kidney / metabolism
  • Kupffer Cells / metabolism
  • Liver / metabolism
  • Male
  • Mice
  • Mice, Inbred C3H
  • Microscopy, Fluorescence
  • Middle Aged
  • Mutation
  • Octoxynol / pharmacology
  • Organic Anion Transporters*
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Wistar
  • Reverse Transcriptase Polymerase Chain Reaction
  • Temperature
  • Time Factors
  • Tissue Distribution

Substances

  • Calcium-Binding Proteins
  • Organic Anion Transporters
  • RNA, Messenger
  • citrin
  • Octoxynol