Transport of organic anions by the lysosomal sialic acid transporter: a functional approach towards the gene for sialic acid storage disease

No abstract is available for this paper.

• Publication year

  1999

• Venue

  FEBS Letters

• Publication date

  1999-03-05

• Fields of study

  Biology, Medicine, Chemistry

• Identifiers
  DOI 10.1016/S0014-5793(99)00187-8PMID 10100616
• 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.

• Identification of multispecific organic anion transporter 2 expressed predominantly in the liver

  1998cited by this paper
• Major Facilitator Superfamily

  1998cited by this paper
• Purification of the Lysosomal Sialic Acid Transporter

  1998cited by this paper
• Functional characterization of the rat multispecific organic anion transporter OAT1 mediating basolateral uptake of anionic drugs in the kidney

  1998cited by this paper
• Unified inventory of established and putative transporters encoded within the complete genome of Saccharomyces cerevisiae

  1998cited by this paper
• Microbial genome analyses: global comparisons of transport capabilities based on phylogenies, bioenergetics and substrate specificities.

  1998cited by this paper
• Expression Cloning and Characterization of a Novel Multispecific Organic Anion Transporter*

  1997cited by this paper
• Characterization of a novel transporter family that includes multiple Escherichia coli gluconate transporters and their homologues.

  1997cited by this paper
• Cloning and Characterization of a Novel Multispecific Organic Anion Transporter *

  1997cited by this paper
• Isolation of a multispecific organic anion and cardiac glycoside transporter from rat brain.

  1997cited by this paper
• Expression Cloning and Characterization of ROAT1

  1997cited by this paper
• Derived structure of the putative sialic acid transporter from Escherichia coli predicts a novel sugar permease domain

  1995cited by this paper
• Lysosomal free sialic acid storage disorders with different phenotypic presentations--infantile-form sialic acid storage disease and Salla disease--represent allelic disorders on 6q14-15.

  1995cited by this paper
• Molecular cloning and characterization of a novel liver-specific transport protein.

  1994cited by this paper
• Functional expression cloning of the canalicular sulfate transport system of rat hepatocytes.

  1994cited by this paper
• Expression cloning of a rat liver Na(+)-independent organic anion transporter.

  1994cited by this paper
• Mechanisms mediating renal secretion of organic anions and cations.

  1993cited by this paper
• Functional reconstitution of the lysosomal sialic acid carrier into proteoliposomes.

  1992cited by this paper
• The transport systems of mammalian lysosomes.

  1991cited by this paper
• The PHO84 gene of Saccharomyces cerevisiae encodes an inorganic phosphate transporter

  1991cited by this paper
• Sialic acid storage diseases. A multiple lysosomal transport defect for acidic monosaccharides.

  1991cited by this paper
• Glucose transport in lysosomal membrane vesicles. Kinetic demonstration of a carrier for neutral hexoses.

  1990cited by this paper
• Characterization of a proton-driven carrier for sialic acid in the lysosomal membrane. Evidence for a group-specific transport system for acidic monosaccharides.

  1989cited by this paper
• Characterization of phosphate:hexose 6-phosphate antiport in membrane vesicles of Streptococcus lactis.

  1984cited by this paper

• Development and application of analytical tools to study the origin, fate and impact of the oncometabolite 2-hydroxyglutarate and its lactone

  2020cites this paper
• Membrane transporters and the diseases corresponding to functional defects

  2013cites this paper
• Molecular physiology and pathophysiology of lysosomal membrane transporters

  2008cites this paper
• Lysosomal Transporters and Associated Diseases

  2005cites this paper
• Varied Mechanisms Underlie the Free Sialic Acid Storage Disorders*♦

  2005cites this paper
• Functional characterization of wild‐type and mutant human sialin

  2004cites this paper
• Sialin expression in the CNS implicates extralysosomal function in neurons.

  2004cites this paper
• Budowa i funkcje bialek blony lizosomalnej

  2003cites this paper
• Nutritive metal uptake in teleost fish

  2003cites this paper
• Molecular pathogenesis of Salla disease

  2003cites this paper
• The Finnish disease heritage III: the individual diseases

  2003cites this paper
• Recommended Reading Materials

  2003cites this paper
• Sialic Acid Storage Disease and Related Disorders

  2003cites this paper
• Membrane Transporter Diseases

  2003cites this paper
• Lysosomal sialic acid transporter sialin (SLC17A5): sialic acid storage disease (SASD)

  2003cites this paper
• Review Nutritive metal uptake in teleost fish

  2003cites this paper
• Unraveling the molecular pathogenesis of free sialic acid storage disorders: altered targeting of mutant sialin.

  2002cites this paper
• An Italian severe Salla disease variant associated with a SLC17A5 mutation earlier described in infantile sialic acid storage disease

  2002cites this paper
• Multiple Neuroendocrine Disorder in Salla Disease

  2001cites this paper
• Lysosomal transport disorders

  2000cites this paper
• The proton-linked monocarboxylate transporter (MCT) family: structure, function and regulation.

  1999cites this paper
• A new gene, encoding an anion transporter, is mutated in sialic acid storage diseases

  1999cites this paper