BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

293 related articles for article (PubMed ID: 820626)

  • 1. The mucopolysaccharidoses: inborn errors of glycosaminoglycan catabolism.
    Cantz M; Gehler J
    Hum Genet; 1976 Jun; 32(3):233-55. PubMed ID: 820626
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The Enzymatic Degradation of Heparan Sulfate.
    Griffin LS; Gloster TM
    Protein Pept Lett; 2017; 24(8):710-722. PubMed ID: 28741461
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mucopolysaccharide storage diseases and lysosomal hydrolases in cultured fibroblasts.
    den Tandt WR; Schaberg A
    Pathol Eur; 1973; 8(1):3-11. PubMed ID: 4269628
    [No Abstract]   [Full Text] [Related]  

  • 4. The mucopolysaccharidoses (a review).
    Dorfman A; Matalon R
    Proc Natl Acad Sci U S A; 1976 Feb; 73(2):630-7. PubMed ID: 813230
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The mucopolysaccharidoses: a synergism between clinical and basic investigation.
    Fluharty AL
    J Invest Dermatol; 1982 Jul; 79 Suppl 1():38s-44s. PubMed ID: 6806398
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Sanfilippo disease type D: deficiency of N-acetylglucosamine-6-sulfate sulfatase required for heparan sulfate degradation.
    Kresse H; Paschke E; von Figura K; Gilberg W; Fuchs W
    Proc Natl Acad Sci U S A; 1980 Nov; 77(11):6822-6. PubMed ID: 6450420
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Enzyme defects of glycosaminoglycan degradation in the mucopolysaccharidoses.
    Benson PF
    Dev Med Child Neurol; 1974 Aug; 16(4):534-9. PubMed ID: 4277471
    [No Abstract]   [Full Text] [Related]  

  • 8. Deficiencies of glucosamine-6-sulfate or galactosamine-6-sulfate sulfatases are responsible for different mucopolysaccharidoses.
    Di Ferrante N; Ginsberg LC; Donnelly PV; Di Ferrante DT; Caskey CT
    Science; 1978 Jan; 199(4324):79-81. PubMed ID: 17569489
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Lysosomal enzymes in cultured cells from mucopolysaccharidoses.
    Keyser AJ; Priest RE; Priest JH
    Lab Invest; 1972 Dec; 27(6):600-5. PubMed ID: 4264608
    [No Abstract]   [Full Text] [Related]  

  • 10. Macular corneal dystrophy. Studies of sulfated glycosaminoglycans in corneal explant and confluent stromal cell cultures.
    Klintworth GK; Smith CF
    Am J Pathol; 1977 Oct; 89(1):167-82. PubMed ID: 143892
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Defective heparan sulfate metabolism in the Sanfilippo syndrome and assay of this defect in the assessment of the mucopolysaccharidoses patient.
    Gordon BA; Feleki V; Budreau CH; Tyler L
    Clin Biochem; 1975 Jun; 8(3):184-93. PubMed ID: 238759
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Chemical definition of the mucopolysaccharidoses.
    Constantopoulos G; Dekaban AS
    Clin Chim Acta; 1975 Mar; 59(3):321-36. PubMed ID: 123832
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Characterization of glycosaminoglycans stored in mucopolysaccharidosis III A: evidence for a generally occuring degradation of heparan sulfate by endoglycosidases.
    Kindler A; Klein U; von Figura K
    Hoppe Seylers Z Physiol Chem; 1977 Nov; 358(11):1431-8. PubMed ID: 411726
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mucopolysaccharidosis in a cat with arylsulfatase B deficiency: a model of Maroteaux-Lamy syndrome.
    Jezyk PF; Haskins ME; Patterson DF; Mellman WJ; Greenstein M
    Science; 1977 Nov; 198(4319):834-6. PubMed ID: 144321
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A new biochemical subtype of the Sanfilippo syndrome: characterization of the storage material in cultured fibroblasts of Sanfilippo C patients.
    Kresse H; Von Figura K; Klein U
    Eur J Biochem; 1978 Dec; 92(2):333-9. PubMed ID: 153835
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Glycosaminoglycan accumulation and excretion in the mucopolysaccharidoses: characterization and basis of a diagnostic test for MPS.
    Byers S; Rozaklis T; Brumfield LK; Ranieri E; Hopwood JJ
    Mol Genet Metab; 1998 Dec; 65(4):282-90. PubMed ID: 9889015
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The mucopolysaccaridoses: clinical and biochemical correlations.
    Horwitz AL
    Am J Ment Defic; 1979 Sep; 84(2):113-23. PubMed ID: 115315
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Glycosaminoglycan levels in dried blood spots of patients with mucopolysaccharidoses and mucolipidoses.
    Kubaski F; Suzuki Y; Orii K; Giugliani R; Church HJ; Mason RW; Dũng VC; Ngoc CT; Yamaguchi S; Kobayashi H; Girisha KM; Fukao T; Orii T; Tomatsu S
    Mol Genet Metab; 2017 Mar; 120(3):247-254. PubMed ID: 28065440
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical and biochemical expression of a unique mucopolysaccharidosis.
    O'Brien JS; Nyhan WL; Sjear C; Schmidt L; Veath ML
    Clin Genet; 1976 Apr; 9(4):399-411. PubMed ID: 131013
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Storage correction in cells of patients suffering from mucopolysaccharidoses types IIIA and VII after treatment with genistein and other isoflavones.
    Arfi A; Richard M; Gandolphe C; Scherman D
    J Inherit Metab Dis; 2010 Feb; 33(1):61-7. PubMed ID: 20084460
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.