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PUBMED FOR HANDHELDS

Journal Abstract Search


172 related items for PubMed ID: 9990120

  • 1. Measurement of activities of human serum sulfotransferases which transfer sulfate to the galactose residues of keratan sulfate and to the nonreducing end N-acetylglucosamine residues of N-acetyllactosamine trisaccharide: comparison between normal controls and patients with macular corneal dystrophy.
    Hasegawa N, Torii T, Nagaoka I, Nakayasu K, Miyajima H, Habuchi O.
    J Biochem; 1999 Feb; 125(2):245-52. PubMed ID: 9990120
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  • 2. Decreased GlcNAc 6-O-sulfotransferase activity in the cornea with macular corneal dystrophy.
    Hasegawa N, Torii T, Kato T, Miyajima H, Furuhata A, Nakayasu K, Kanai A, Habuchi O.
    Invest Ophthalmol Vis Sci; 2000 Nov; 41(12):3670-7. PubMed ID: 11053262
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  • 3. Human corneal GlcNac 6-O-sulfotransferase and mouse intestinal GlcNac 6-O-sulfotransferase both produce keratan sulfate.
    Akama TO, Nakayama J, Nishida K, Hiraoka N, Suzuki M, McAuliffe J, Hindsgaul O, Fukuda M, Fukuda MN.
    J Biol Chem; 2001 May 11; 276(19):16271-8. PubMed ID: 11278593
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  • 4. Serum sulfotransferase levels in patients with macular corneal dystrophy type I.
    Hassell JR, Klintworth GK.
    Arch Ophthalmol; 1997 Nov 11; 115(11):1419-21. PubMed ID: 9366673
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  • 5. Sulfation of sialyl N-acetyllactosamine oligosaccharides and fetuin oligosaccharides by keratan sulfate Gal-6-sulfotransferase.
    Torii T, Fukuta M, Habuchi O.
    Glycobiology; 2000 Feb 11; 10(2):203-11. PubMed ID: 10642612
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  • 6. Enzymatic sulfation of galactose residue of keratan sulfate by chondroitin 6-sulfotransferase.
    Habuchi O, Hirahara Y, Uchimura K, Fukuta M.
    Glycobiology; 1996 Jan 11; 6(1):51-7. PubMed ID: 8991509
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  • 10. Enzymes responsible for synthesis of corneal keratan sulfate glycosaminoglycans.
    Kitayama K, Hayashida Y, Nishida K, Akama TO.
    J Biol Chem; 2007 Oct 12; 282(41):30085-96. PubMed ID: 17690104
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  • 13. Altered fine structures of corneal and skeletal keratan sulfate and chondroitin/dermatan sulfate in macular corneal dystrophy.
    Plaas AH, West LA, Thonar EJ, Karcioglu ZA, Smith CJ, Klintworth GK, Hascall VC.
    J Biol Chem; 2001 Oct 26; 276(43):39788-96. PubMed ID: 11514545
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  • 15. Truncating mutations in the carbohydrate sulfotransferase 6 gene (CHST6) result in macular corneal dystrophy.
    Niel F, Ellies P, Dighiero P, Soria J, Sabbagh C, San C, Renard G, Delpech M, Valleix S.
    Invest Ophthalmol Vis Sci; 2003 Jul 26; 44(7):2949-53. PubMed ID: 12824236
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  • 16. Functional expression and genomic structure of human N-acetylglucosamine-6-O-sulfotransferase that transfers sulfate to beta-N-acetylglucosamine at the nonreducing end of an N-acetyllactosamine sequence.
    Sakaguchi H, Kitagawa H, Sugahara K.
    Biochim Biophys Acta; 2000 Oct 18; 1523(2-3):269-76. PubMed ID: 11042394
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  • 17. Mutations in the CHST6 gene in patients with macular corneal dystrophy: immunohistochemical evidence of heterogeneity.
    Iida-Hasegawa N, Furuhata A, Hayatsu H, Murakami A, Fujiki K, Nakayasu K, Kanai A.
    Invest Ophthalmol Vis Sci; 2003 Aug 18; 44(8):3272-7. PubMed ID: 12882769
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  • 18. Absence of normal keratan sulfate in the blood of patients with macular corneal dystrophy.
    Thonar EJ, Meyer RF, Dennis RF, Lenz ME, Maldonado B, Hassell JR, Hewitt AT, Stark WJ, Stock EL, Kuettner KE.
    Am J Ophthalmol; 1986 Nov 15; 102(5):561-9. PubMed ID: 2946233
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  • 19. The enzymatic sulfation of glycoprotein carbohydrate units: blood group T-hapten specific and two other distinct Gal:3-O-sulfotransferases as evident from specificities and kinetics and the influence of sulfate and fucose residues occurring in the carbohydrate chain on C-3 sulfation of terminal Gal.
    Chandrasekaran EV, Jain RK, Vig R, Matta KL.
    Glycobiology; 1997 Sep 15; 7(6):753-68. PubMed ID: 9376678
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  • 20. Macular dystrophy of the cornea. A systemic disorder of keratan sulfate metabolism.
    Edward DP, Thonar EJ, Srinivasan M, Yue BJ, Tso MO.
    Ophthalmology; 1990 Sep 15; 97(9):1194-200. PubMed ID: 2234853
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