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Journal Abstract Search

179 related items for PubMed ID: 15215498

  • 1. Loss of chondroitin 6-O-sulfotransferase-1 function results in severe human chondrodysplasia with progressive spinal involvement.
    Thiele H, Sakano M, Kitagawa H, Sugahara K, Rajab A, Höhne W, Ritter H, Leschik G, Nürnberg P, Mundlos S.
    Proc Natl Acad Sci U S A; 2004 Jul 06; 101(27):10155-60. PubMed ID: 15215498
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  • 2. Omani-type spondyloepiphyseal dysplasia with cardiac involvement caused by a missense mutation in CHST3.
    Tuysuz B, Mizumoto S, Sugahara K, Celebi A, Mundlos S, Turkmen S.
    Clin Genet; 2009 Apr 06; 75(4):375-83. PubMed ID: 19320654
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  • 3. Spondyloepiphyseal dysplasia, Omani type: further definition of the phenotype.
    van Roij MH, Mizumoto S, Yamada S, Morgan T, Tan-Sindhunata MB, Meijers-Heijboer H, Verbeke JI, Markie D, Sugahara K, Robertson SP.
    Am J Med Genet A; 2008 Sep 15; 146A(18):2376-84. PubMed ID: 18698629
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  • 4. Molecular cloning of squid N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase and synthesis of a unique chondroitin sulfate containing E-D hybrid tetrasaccharide structure by the recombinant enzyme.
    Yamaguchi T, Ohtake S, Kimata K, Habuchi O.
    Glycobiology; 2007 Dec 15; 17(12):1365-76. PubMed ID: 17893095
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  • 5. Chondroitin 4-O-sulfotransferase-2 regulates the number of chondroitin sulfate chains initiated by chondroitin N-acetylgalactosaminyltransferase-1.
    Izumikawa T, Koike T, Kitagawa H.
    Biochem J; 2012 Jan 15; 441(2):697-705. PubMed ID: 21942880
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  • 7. Synthesis of sulfated phenyl 2-acetamido-2-deoxy-D-galactopyranosides. 4-O-Sulfated phenyl 2-acetamido-2-deoxy-beta-D-galactopyranoside is a competitive acceptor that decreases sulfation of chondroitin sulfate by N-acetylgalactosamine 4-sulfate 6-O-sulfotransferase.
    Sawada T, Fujii S, Nakano H, Ohtake S, Kimata K, Habuchi O.
    Carbohydr Res; 2005 Sep 05; 340(12):1983-96. PubMed ID: 16024005
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  • 8. Spondyloepiphyseal dysplasia Omani type: CHST3 mutation spectrum and phenotypes in three Indian families.
    Srivastava P, Pandey H, Agarwal D, Mandal K, Phadke SR.
    Am J Med Genet A; 2017 Jan 05; 173(1):163-168. PubMed ID: 27753269
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  • 9. Chondroitin 4-O-sulfotransferase-1 is required for somitic muscle development and motor axon guidance in zebrafish.
    Mizumoto S, Mikami T, Yasunaga D, Kobayashi N, Yamauchi H, Miyake A, Itoh N, Kitagawa H, Sugahara K.
    Biochem J; 2009 Apr 15; 419(2):387-99. PubMed ID: 19125692
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  • 11. Regulation of the chondroitin/dermatan fine structure by transforming growth factor-beta1 through effects on polymer-modifying enzymes.
    Tiedemann K, Olander B, Eklund E, Todorova L, Bengtsson M, Maccarana M, Westergren-Thorsson G, Malmström A.
    Glycobiology; 2005 Dec 15; 15(12):1277-85. PubMed ID: 16118286
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  • 12. Molecular cloning and expression of a novel chondroitin 6-O-sulfotransferase.
    Kitagawa H, Fujita M, Ito N, Sugahara K.
    J Biol Chem; 2000 Jul 14; 275(28):21075-80. PubMed ID: 10781596
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  • 19. Congenital joint dislocations caused by carbohydrate sulfotransferase 3 deficiency in recessive Larsen syndrome and humero-spinal dysostosis.
    Hermanns P, Unger S, Rossi A, Perez-Aytes A, Cortina H, Bonafé L, Boccone L, Setzu V, Dutoit M, Sangiorgi L, Pecora F, Reicherter K, Nishimura G, Spranger J, Zabel B, Superti-Furga A.
    Am J Hum Genet; 2008 Jun 14; 82(6):1368-74. PubMed ID: 18513679
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  • 20. A novel CHST3 allele associated with spondyloepiphyseal dysplasia and hearing loss in Pakistani kindred.
    Waryah AM, Shahzad M, Shaikh H, Sheikh SA, Channa NA, Hufnagel RB, Makhdoom A, Riazuddin S, Ahmed ZM.
    Clin Genet; 2016 Jul 14; 90(1):90-5. PubMed ID: 26572954
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