Ion transport and cystogenesis: the paradigm of autosomal dominant polycystic kidney disease

Adv Nephrol Necker Hosp. 1998:28:439-78.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Aquaporin 1
  • Aquaporin 2
  • Aquaporin 6
  • Aquaporins / physiology
  • Blood Group Antigens
  • Chlorides / metabolism
  • Cystic Fibrosis Transmembrane Conductance Regulator / physiology
  • Humans
  • Ion Transport*
  • Membrane Proteins / genetics
  • Polycystic Kidney, Autosomal Dominant / etiology
  • Polycystic Kidney, Autosomal Dominant / metabolism*
  • Proteins / genetics
  • Sodium-Potassium-Exchanging ATPase / physiology
  • TRPP Cation Channels

Substances

  • AQP1 protein, human
  • AQP2 protein, human
  • Aquaporin 2
  • Aquaporin 6
  • Aquaporins
  • Blood Group Antigens
  • CFTR protein, human
  • Chlorides
  • Membrane Proteins
  • Proteins
  • TRPP Cation Channels
  • polycystic kidney disease 1 protein
  • polycystic kidney disease 2 protein
  • Cystic Fibrosis Transmembrane Conductance Regulator
  • Aquaporin 1
  • Sodium-Potassium-Exchanging ATPase