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Journal Abstract Search

242 related items for PubMed ID: 2010546

  • 1. Sialic acid storage diseases. A multiple lysosomal transport defect for acidic monosaccharides.
    Mancini GM, Beerens CE, Aula PP, Verheijen FW.
    J Clin Invest; 1991 Apr; 87(4):1329-35. PubMed ID: 2010546
    [Abstract] [Full Text] [Related]

  • 2. Characterization of a proton-driven carrier for sialic acid in the lysosomal membrane. Evidence for a group-specific transport system for acidic monosaccharides.
    Mancini GM, de Jonge HR, Galjaard H, Verheijen FW.
    J Biol Chem; 1989 Sep 15; 264(26):15247-54. PubMed ID: 2768261
    [Abstract] [Full Text] [Related]

  • 3. Functional reconstitution of the lysosomal sialic acid carrier into proteoliposomes.
    Mancini GM, Beerens CE, Galjaard H, Verheijen FW.
    Proc Natl Acad Sci U S A; 1992 Jul 15; 89(14):6609-13. PubMed ID: 1631163
    [Abstract] [Full Text] [Related]

  • 4. Defective glucuronic acid transport from lysosomes of infantile free sialic acid storage disease fibroblasts.
    Blom HJ, Andersson HC, Seppala R, Tietze F, Gahl WA.
    Biochem J; 1990 Jun 15; 268(3):621-5. PubMed ID: 2363700
    [Abstract] [Full Text] [Related]

  • 5. Infantile sialic acid storage disease: biochemical studies.
    Berra B, Gornati R, Rapelli S, Gatti R, Mancini GM, Ciana G, Bembi B.
    Am J Med Genet; 1995 Jul 31; 58(1):24-31. PubMed ID: 7573152
    [Abstract] [Full Text] [Related]

  • 6. Purification of the lysosomal sialic acid transporter. Functional characteristics of a monocarboxylate transporter.
    Havelaar AC, Mancini GM, Beerens CE, Souren RM, Verheijen FW.
    J Biol Chem; 1998 Dec 18; 273(51):34568-74. PubMed ID: 9852127
    [Abstract] [Full Text] [Related]

  • 7. Glucose transport in lysosomal membrane vesicles. Kinetic demonstration of a carrier for neutral hexoses.
    Mancini GM, Beerens CE, Verheijen FW.
    J Biol Chem; 1990 Jul 25; 265(21):12380-7. PubMed ID: 2373697
    [Abstract] [Full Text] [Related]

  • 8. Defective lysosomal egress of free sialic acid (N-acetylneuraminic acid) in fibroblasts of patients with infantile free sialic acid storage disease.
    Tietze F, Seppala R, Renlund M, Hopwood JJ, Harper GS, Thomas GH, Gahl WA.
    J Biol Chem; 1989 Sep 15; 264(26):15316-22. PubMed ID: 2768266
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  • 12. [Genetic disorders of N-acetylneuraminic acid metabolism: sialurias and sialidoses].
    Strecker G.
    C R Seances Soc Biol Fil; 1985 Sep 15; 179(5):567-76. PubMed ID: 2938684
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  • 13. Renal handling of free sialic acid in normal humans and patients with Salla disease or renal disease.
    Seppala R, Renlund M, Bernardini I, Tietze F, Gahl WA.
    Lab Invest; 1990 Aug 15; 63(2):197-203. PubMed ID: 2381164
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  • 14. Defective lysosomal release of glycoprotein-derived sialic acid in fibroblasts from patients with sialic acid storage disease.
    Mendla K, Baumkötter J, Rosenau C, Ulrich-Bott B, Cantz M.
    Biochem J; 1988 Feb 15; 250(1):261-7. PubMed ID: 2451509
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  • 15. Infantile sialic acid storage disease: the fate of biosynthetically labeled N-acetyl-(3H)-neuraminic acid in cultured human fibroblasts.
    Paschke E, Höfler G, Roscher A.
    Pediatr Res; 1986 Aug 15; 20(8):773-7. PubMed ID: 2942833
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  • 17. Biosynthesis of lysosomal proteinases in health and disease.
    Mach L.
    Biol Chem; 2002 May 15; 383(5):751-6. PubMed ID: 12108539
    [Abstract] [Full Text] [Related]

  • 18. A new gene, encoding an anion transporter, is mutated in sialic acid storage diseases.
    Verheijen FW, Verbeek E, Aula N, Beerens CE, Havelaar AC, Joosse M, Peltonen L, Aula P, Galjaard H, van der Spek PJ, Mancini GM.
    Nat Genet; 1999 Dec 15; 23(4):462-5. PubMed ID: 10581036
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  • 19. Genistein inhibits glucose and sulphate transport in isolated rat liver lysosomes.
    Chou HF, Chuang KH, Tsai YS, Chen YJ.
    Br J Nutr; 2010 Jan 15; 103(2):197-205. PubMed ID: 19747417
    [Abstract] [Full Text] [Related]

  • 20. A functional role for histidyl residues of the UDP-glucuronic acid carrier in rat liver endoplasmic reticulum membranes.
    Battaglia E, Radominska-Pandya A.
    Biochemistry; 1998 Jan 06; 37(1):258-63. PubMed ID: 9425046
    [Abstract] [Full Text] [Related]

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