Adenosine triphosphate-dependent copper transport in human liver.

No abstract is available for this paper.

• Publication year

  1996

• Venue

  Journal of Hepatology

• Publication date

  1996-07-01

• Fields of study

  Biology, Medicine, Chemistry

• Identifiers
  DOI 10.1016/S0168-8278(96)80325-4PMID 8836899
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• P-type ATPases of eukaryotes and bacteria: Sequence analyses and construction of phylogenetic trees

  2004cited by this paper
• Adenosine triphosphate-dependent copper transport in isolated rat liver plasma membranes.

  1995cited by this paper
• In vitro modeling of liver membrane copper transport.

  1995cited by this paper
• Identification of an ATP‐dependent copper transport system in endoplasmic reticulum vesicles isolated from rat liver.

  1995cited by this paper
• Regulation of biliary lipid secretion by mdr2 P-glycoprotein in the mouse.

  1995cited by this paper
• Copper pumping ATPases: Common concepts in bacteria and man

  1994cited by this paper
• Homozygous disruption of the murine mdr2 P-glycoprotein gene leads to a complete absence of phospholipid from bile and to liver disease.

  1993cited by this paper
• The Wilson disease gene is a putative copper transporting P–type ATPase similar to the Menkes gene

  1993cited by this paper
• Primary structure of two P-type ATPases involved in copper homeostasis in Enterococcus hirae.

  1993cited by this paper
• Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein

  1993cited by this paper
• Isolation of a partial candidate gene for Menkes disease by positional cloning

  1993cited by this paper
• ATP‐dependent transport systems for organic anions

  1993cited by this paper
• Mapping, cloning and genetic characterization of the region containing the Wilson disease gene

  1993cited by this paper
• Isolation and characterization of a human liver cDNA as a candidate gene for Wilson disease.

  1993cited by this paper
• Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper–transporting ATPase

  1993cited by this paper
• The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene

  1993cited by this paper
• The biology of the bile canaliculus, 1993

  1993cited by this paper
• Wilson Disease

  1992cited by this paper
• Adenosine triphosphate-dependent taurocholate transport in human liver plasma membranes.

  1992cited by this paper
• ATP-dependent bile-salt transport in canalicular rat liver plasma-membrane vesicles.

  1992cited by this paper
• Isolation and characterization of canalicular and basolateral plasma membrane fractions from human liver.

  1991cited by this paper
• ATP-dependent transport of taurocholate across the hepatocyte canalicular membrane mediated by a 110-kDa glycoprotein binding ATP and bile salt.

  1991cited by this paper
• Treatment of Wilson's disease with zinc. IX: Response of serum lipids.

  1991cited by this paper
• ATP-dependent S-(2,4-dinitrophenyl)glutathione transport in canalicular plasma membrane vesicles from rat liver.

  1991cited by this paper
• Wilson disease: clinical presentation, treatment, and survival.

  1991cited by this paper
• ATP-dependent primary active transport of cysteinyl leukotrienes across liver canalicular membrane. Role of the ATP-dependent transport system for glutathione S-conjugates.

  1990cited by this paper
• Two pathways for biliary copper excretion in the rat: The role of glutathione

  1990cited by this paper
• Perspectives on Wilson's disease

  1990cited by this paper
• Biliary copper excretion by hepatocyte lysosomes in the rat. Major excretory pathway in experimental copper overload.

  1989cited by this paper
• Two pathways for biliary copper excretion in the rat. The role of glutathione.

  1989cited by this paper
• The role of glutathione in copper metabolism and toxicity.

  1989cited by this paper
• The Metabolic basis of inherited disease

  1989cited by this paper
• Disorders of copper transport

  1989cited by this paper
• Extended preservation of the liver for clinical transplantation.

  1988cited by this paper
• In vitro interaction of organic copper (II) compounds with soluble glutathione S-transferases from rat liver.

  1986cited by this paper
• In vitro interaction of organic copper (II) compounds with soluble glutathione S-transferases from rat liver.

  1986cited by this paper
• A domain-specific marker for the hepatocyte plasma membrane. II. Ultrastructural localization of leucine aminopeptidase to the bile canalicular domain of isolated rat liver plasma membranes

  1984cited by this paper
• A domain-specific marker for the hepatocyte plasma membrane: localization of leucine aminopeptidase to the bile canalicular domain

  1983cited by this paper
• Copper and the liver.

  1980cited by this paper
• LYSOSOMAL PHYSIOLOGY IN TETRAHYMENA

  1973cited by this paper
• The colorimetric determination of leucine aminopeptidase in urine and serum of normal subjects and patients with cancer and other diseases

  1958cited by this paper
• Tissue fractionation studies. 6. Intracellular distribution patterns of enzymes in rat-liver tissue.

  1955cited by this paper

• Protective effect of curcumin against heavy metals-induced liver damage.

  2014cites this paper
• Metabolizm miedzi oraz charakterystyka dziedzicznych zespołów chorobowych, na tle niedoboru miedzi, spowodowanych zaburzeniami aktywności białka ATP7A

  2014cites this paper
• Structural and Functional Studies of ATP7B, the Copper(I)-transporting P-type ATPase Implicated in Wilson Disease

  2012cites this paper
• Liver Ischemia and Ischemia–Reperfusion Induces and Trafficks the Multi-specific Metal Transporter Atp7b to Bile Duct Canaliculi: Possible Preferential Transport of Iron into Bile

  2008cites this paper
• Copper in medicine: homeostasis, chelation therapy and antitumor drug design.

  2006cites this paper
• Is there a role for copper in neurodegenerative diseases?

  2005cites this paper
• Trace elements in human physiology and pathology. Copper.

  2003cites this paper
• Biological Effects of Chronic Copper Exposure

  2002cites this paper
• Copper Uptake in Eukaryotic Cells

  2002cites this paper
• Insights into the mechanism of copper transport by the Wilson and Menkes disease copper-transporting ATPases

  2002cites this paper
• Genetic Susceptibility to Heavy Metals in the Environment

  2002cites this paper
• Copper in disorders with neurological symptoms: Alzheimer's, Menkes, and Wilson diseases.

  2001cites this paper
• Mechanisms of cholestasis.

  2000cites this paper
• Copper-induced apical trafficking of ATP7B in polarized hepatoma cells provides a mechanism for biliary copper excretion.

  2000cites this paper
• Localization of the Wilson's disease protein in human liver.

  1999cites this paper
• Role of the Copper-binding Domain in the Copper Transport Function of ATP7B, the P-type ATPase Defective in Wilson Disease*

  1999cites this paper
• Molecular mechanisms of copper homeostasis.

  1999cites this paper
• ATP-dependent silver transport across the basolateral membrane of rainbow trout gills.

  1999cites this paper
• Differences in hepatic processing of dietary and intravenously administered copper in rats

  1997cites this paper
• Characterization of intracellular copper pools in rat hepatocytes using the chelator diamsar.

  1997cites this paper