These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

135 related articles for article (PubMed ID: 3209585)

  • 21. Targeting of phosphomannosyl-deficient arylsulfatase A to lysosomes of I-cell fibroblasts.
    Waheed A; Van Etten RL; Koob R; Drenckhahn D
    Eur J Cell Biol; 1988 Feb; 45(2):262-7. PubMed ID: 2896590
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Correction of sphingomyelinase deficiency in Niemann-Pick type C fibroblasts by removal of lipoprotein fraction from culture media.
    Thomas GH; Tuck-Muller CM; Miller CS; Reynolds LW
    J Inherit Metab Dis; 1989; 12(2):139-51. PubMed ID: 2547109
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Presence of a lysosomal enzyme, arylsulfatase-A, in the prelysosome-endosome compartments of human cultured fibroblasts.
    Kelly BM; Yu CZ; Chang PL
    Eur J Cell Biol; 1989 Feb; 48(1):71-8. PubMed ID: 2568259
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The biochemical diagnosis of lysosomal storage diseases--a review of five years experience.
    Wallace IJ; McCusker CA; McCormick D
    Ir J Med Sci; 1990 Jul; 159(7):203-9. PubMed ID: 2283277
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Effects of dimethylsulfoxide on sphingomyelinase activities in normal and Niemann-Pick type A, B and C fibroblasts.
    Sato M; Yoshida Y; Sakuragawa N; Arima M
    Biochim Biophys Acta; 1988 Sep; 962(1):59-65. PubMed ID: 2843241
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Lysosomal enzyme variations in cultured normal skin fibroblasts.
    Milunsky A; Spielvogel C; Kanfer JN
    Life Sci II; 1972 Nov; 11(22):1101-7. PubMed ID: 4663811
    [No Abstract]   [Full Text] [Related]  

  • 27. Lysosomal acid hydrolases in lymphocytes of I-cell disease.
    Kato E; Yokoi T; Taniguchi N
    Clin Chim Acta; 1979 Jul; 95(2):285-90. PubMed ID: 43204
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Ultrastructural studies of the skin and cultured fibroblasts in I-cell disease.
    Endo H; Miyazaki T; Asano S; Sagami S
    J Cutan Pathol; 1987 Oct; 14(5):309-17. PubMed ID: 3316329
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Lysosomal biogenesis in lysosomal storage disorders.
    Karageorgos LE; Isaac EL; Brooks DA; Ravenscroft EM; Davey R; Hopwood JJ; Meikle PJ
    Exp Cell Res; 1997 Jul; 234(1):85-97. PubMed ID: 9223373
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Mucolipidosis II with unusual biochemical parameters].
    Morava E; Eduard P; Tóth G; Dobos M; Melegh B; Kosztolányi G
    Orv Hetil; 2002 Jan; 143(3):135-7. PubMed ID: 11883111
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Biochemical characteristics of a Korean patient with mucolipidosis III (pseudo-Hurler polydystrophy).
    Song J; Lee DS; Cho HI; Kim JQ; Cho TJ
    J Korean Med Sci; 2003 Oct; 18(5):722-6. PubMed ID: 14555827
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The subcellular localization of soluble and membrane-bound lysosomal enzymes in I-cell fibroblasts: a comparative immunocytochemical study.
    van Dongen JM; Willemsen R; Ginns EI; Sips HJ; Tager JM; Barranger JA; Reuser AJ
    Eur J Cell Biol; 1985 Nov; 39(1):179-89. PubMed ID: 2935398
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Effects of dimethylsulfoxide on sphingomyelinase in cultured human fibroblasts and correction of sphingomyelinase deficiency in fibroblasts from Niemann-Pick patients.
    Sakuragawa N; Sato M; Yoshida Y; Kamo I; Arima M; Satoyoshi E
    Biochem Biophys Res Commun; 1985 Jan; 126(2):756-62. PubMed ID: 2983689
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Lysosomal storage disorders. Diagnosis by ultrastructural examination of skin biopsy specimens.
    O'Brien JS; Bernett J; Veath ML; Paa D
    Arch Neurol; 1975 Sep; 32(9):592-9. PubMed ID: 809024
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Lysosomal integral membrane glycoproteins are expressed at high levels in the inclusion bodies of I-cell disease fibroblasts.
    Sandoval IV; Chen JW; Yuan L; August JT
    Arch Biochem Biophys; 1989 May; 271(1):157-67. PubMed ID: 2540710
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Methylamine accumulation in cultured cells as a measure of the aqueous storage compartment in the laboratory diagnosis of genetic lysosomal diseases.
    Kopitz J; Harzer K; Kohlschütter A; Zöller B; Blenck N; Cantz M
    Am J Med Genet; 1996 May; 63(1):198-202. PubMed ID: 8723110
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Brain lysosomal hydrolases in neuronal ceroid-lipofuscinoses.
    Prasad VV; Pullarkat RK
    Mol Chem Neuropathol; 1996; 29(2-3):169-79. PubMed ID: 8971694
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Comparison of the measurement of lysosomal hydrolase activity in mycoplasma-contaminated and non-contaminated human fibroblast cultures treated with mycoplasma removal agent.
    Souza FT; Souza Sostruznik L; Casagrande Scolari R; Maciel de Castro KJ; Giugliani R; Coelho JC
    Clin Biochem; 2007 May; 40(8):521-5. PubMed ID: 17367773
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Biochemical mechanisms of aminoglycoside cell toxicity. I. The uptake of gentamicin by cultured skin fibroblasts and the alteration of lysosomal enzyme activities.
    Oshima M; Hashiguchi M; Shindo N; Shibata S
    J Biochem; 1986 Dec; 100(6):1575-82. PubMed ID: 3571189
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Enzymological diagnosis of a group of lysosomal storage diseases. Review of 5-year experience of 1600 patient-sample referrals.
    Pollard AC; Carey WF; Nelson PV; Poulos A; Hill GN
    Med J Aust; 1980 Nov; 2(10):549-53. PubMed ID: 6780772
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.