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PUBMED FOR HANDHELDS

Journal Abstract Search


146 related items for PubMed ID: 6615884

  • 1. N-acetylneuraminic acid and sialoglycoconjugate metabolism in fibroblasts from a patient with generalized N-acetylneuraminic acid storage disease.
    Hancock LW, Horwitz AL, Dawson G.
    Biochim Biophys Acta; 1983 Oct 04; 760(1):42-52. PubMed ID: 6615884
    [Abstract] [Full Text] [Related]

  • 2. Impaired proteolytic processing of lysosomal N-acetyl-beta-hexosaminidase in cultured fibroblasts from patients with infantile generalized N-acetylneuraminic acid storage disease.
    Hancock LW, Ricketts JP, Hildreth J.
    Biochem Biophys Res Commun; 1988 Apr 15; 152(1):83-92. PubMed ID: 2965873
    [Abstract] [Full Text] [Related]

  • 3. Accumulation of [3H]sialyl-conjugates in sialidosis (sialidase-deficient) fibroblasts cultured in the presence of [3H]-N-acetylmannosamine.
    Scocca J, Thomas GH, Reynolds L, Miller CS.
    J Inherit Metab Dis; 1986 Apr 15; 9(1):79-88. PubMed ID: 3088328
    [Abstract] [Full Text] [Related]

  • 4. Studies on the defect underlying the lysosomal storage of sialic acid in Salla disease. Lysosomal accumulation of sialic acid formed from N-acetyl-mannosamine or derived from low density lipoprotein in cultured mutant fibroblasts.
    Renlund M, Kovanen PT, Raivio KO, Aula P, Gahmberg CG, Ehnholm C.
    J Clin Invest; 1986 Feb 15; 77(2):568-74. PubMed ID: 3944269
    [Abstract] [Full Text] [Related]

  • 5. Accumulation of N-acetylneuraminic acid (sialic acid) in human fibroblasts cultured in the presence of N-acetylmannosamine.
    Thomas GH, Scocca J, Miller CS, Reynolds LW.
    Biochim Biophys Acta; 1985 Jul 30; 846(1):37-43. PubMed ID: 4016156
    [Abstract] [Full Text] [Related]

  • 6. N-acetylneuraminic acid accumulation in a buoyant lysosomal fraction of cultured fibroblasts from patients with infantile generalized N-acetylneuraminic acid storage disease.
    Hildreth J, Sacks L, Hancock LW.
    Biochem Biophys Res Commun; 1986 Sep 14; 139(2):838-44. PubMed ID: 2945557
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. Free N-acetylneuraminic acid in tissues in Salla disease and the enzymes involved in its metabolism.
    Renlund M, Chester MA, Lundblad A, Parkkinen J, Krusius T.
    Eur J Biochem; 1983 Jan 17; 130(1):39-45. PubMed ID: 6297896
    [Abstract] [Full Text] [Related]

  • 9. Generalized N-acetylneuraminic acid storage disease: quantitation and identification of the monosaccharide accumulating in brain and other tissues.
    Hancock LW, Thaler MM, Horwitz AL, Dawson G.
    J Neurochem; 1982 Mar 17; 38(3):803-9. PubMed ID: 7057193
    [Abstract] [Full Text] [Related]

  • 10. Identification of the metabolic defect in sialuria.
    Weiss P, Tietze F, Gahl WA, Seppala R, Ashwell G.
    J Biol Chem; 1989 Oct 25; 264(30):17635-6. PubMed ID: 2808337
    [Abstract] [Full Text] [Related]

  • 11. Modification of sialic acid metabolism of murine erythroleukemia cells by analogs of N-acetylmannosamine.
    Schwartz EL, Hadfield AF, Brown AE, Sartorelli AC.
    Biochim Biophys Acta; 1983 Jul 14; 762(4):489-97. PubMed ID: 6871252
    [Abstract] [Full Text] [Related]

  • 12. Metabolic processing of gangliosides by normal and Salla human fibroblasts in culture. A study performed by administering radioactive GM3 ganglioside.
    Chigorno V, Tettamanti G, Sonnino S.
    J Biol Chem; 1996 Sep 06; 271(36):21738-44. PubMed ID: 8702969
    [Abstract] [Full Text] [Related]

  • 13. Identification of N-acetylhexosamines produced by enzymes of the N-acetylneuraminic acid metabolic pathway by borate complex anion-exchange chromatography of the corresponding N-acetylhexosaminitols.
    Scocca JR.
    Anal Biochem; 1986 Jul 06; 156(1):61-6. PubMed ID: 3740419
    [Abstract] [Full Text] [Related]

  • 14. The effect of D-(+)-glucosamine on levels of free N-acetylneuraminic acid and UDP-N-acetylhexosamines in infantile sialic acid storage disease (ISSD) fibroblasts.
    Paschke E, Höfler G, Roscher A.
    J Inherit Metab Dis; 1987 Jul 06; 10(1):48-51. PubMed ID: 3106716
    [Abstract] [Full Text] [Related]

  • 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 06; 20(8):773-7. PubMed ID: 2942833
    [Abstract] [Full Text] [Related]

  • 16. Free N-acetylneuraminic acid (NANA) storage disorders: evidence for defective NANA transport across the lysosomal membrane.
    Mancini GM, Verheijen FW, Galjaard H.
    Hum Genet; 1986 Jul 06; 73(3):214-7. PubMed ID: 3733077
    [Abstract] [Full Text] [Related]

  • 17. Synthesis of N-acetylneuraminic acid and of CMP-N-acetylneuraminic acid in the rat liver cell.
    Ferwerda W, Blok CM, Van Rinsum J.
    Biochem J; 1983 Oct 15; 216(1):87-92. PubMed ID: 6651781
    [Abstract] [Full Text] [Related]

  • 18. Studies on N-acetylneuraminic acid biosynthesis in chicken liver and hepatoma Mc-29 by using [14C]N-acetylmannosamine and [14C]glucosamine.
    Ivanov S, Gavazova E, Antonova M, Chelibonova-Lorer H.
    Int J Biochem; 1985 Oct 15; 17(10):1125-8. PubMed ID: 4065401
    [Abstract] [Full Text] [Related]

  • 19. 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
    [Abstract] [Full Text] [Related]

  • 20. Alterations in cultured fibroblasts of sibs with an infantile form of a free (unbound) sialic acid storage disorder.
    Thomas GH, Scocca J, Libert J, Vamos E, Miller CS, Reynolds LW.
    Pediatr Res; 1983 May 15; 17(5):307-12. PubMed ID: 6856393
    [Abstract] [Full Text] [Related]


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