BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

126 related articles for article (PubMed ID: 9366673)

  • 41. Immunohistochemical evidence of heterogeneity in macular corneal dystrophy.
    Yang CJ; SundarRaj N; Thonar EJ; Klintworth GK
    Am J Ophthalmol; 1988 Jul; 106(1):65-71. PubMed ID: 3293458
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Novel CHST6 nonsense and missense mutations responsible for macular corneal dystrophy.
    El-Ashry MF; Abd El-Aziz MM; Shalaby O; Wilkins S; Poopalasundaram S; Cheetham M; Tuft SJ; Hardcastle AJ; Bhattacharya SS; Ebenezer ND
    Am J Ophthalmol; 2005 Jan; 139(1):192-3. PubMed ID: 15652851
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Novel mutations in the CHST6 gene causing macular corneal dystrophy.
    Abbruzzese C; Kuhn U; Molina F; Rama P; De Luca M
    Clin Genet; 2004 Feb; 65(2):120-5. PubMed ID: 14984470
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Sulfation of endothelial mucin by corneal keratan N-acetylglucosamine 6-O-sulfotransferase (GST-4beta).
    Bartes A; Bhakta S; Hemmerich S
    Biochem Biophys Res Commun; 2001 Apr; 282(4):928-33. PubMed ID: 11352640
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Corneal alpha-galactosidase deficiency in macular corneal dystrophy.
    Bruner WE; Dejak TR; Grossniklaus HE; Stark WJ; Young E
    Ophthalmic Paediatr Genet; 1985 Apr; 5(3):179-83. PubMed ID: 2999674
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Mutations in corneal carbohydrate sulfotransferase 6 gene (CHST6) cause macular corneal dystrophy in Iceland.
    Liu NP; Dew-Knight S; Rayner M; Jonasson F; Akama TO; Fukuda MN; Bao W; Gilbert JR; Vance JM; Klintworth GK
    Mol Vis; 2000 Dec; 6():261-4. PubMed ID: 11139648
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Novel mutations in the CHST6 gene associated with macular corneal dystrophy in southern India.
    Warren JF; Aldave AJ; Srinivasan M; Thonar EJ; Kumar AB; Cevallos V; Whitcher JP; Margolis TP
    Arch Ophthalmol; 2003 Nov; 121(11):1608-12. PubMed ID: 14609920
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Purification of chondroitin 6-sulfotransferase secreted from cultured chick embryo chondrocytes.
    Habuchi O; Matsui Y; Kotoya Y; Aoyama Y; Yasuda Y; Noda M
    J Biol Chem; 1993 Oct; 268(29):21968-74. PubMed ID: 8408053
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Genetic analysis of
    Yaylacioglu Tuncay F; Kayman Kurekci G; Guntekin Ergun S; Pasaoglu OT; Akata RF; Dincer PR
    Mol Vis; 2016; 22():1267-1279. PubMed ID: 27829782
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Immunohistochemical classification of primary and recurrent macular corneal dystrophy in Germany: subclassification of immunophenotype I A using a novel keratan sulfate antibody.
    Cursiefen C; Hofmann-Rummelt C; Schlötzer-Schrehardt U; Fischer DC; Haubeck HD; Küchle M; Naumann GO
    Exp Eye Res; 2001 Nov; 73(5):593-600. PubMed ID: 11747360
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Research into the pathogenesis of macular corneal dystrophy.
    Klintworth GK
    Trans Ophthalmol Soc U K (1962); 1980 Apr; 100(Pt 1):186-94. PubMed ID: 6973846
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Molecular genetic study of Egyptian patients with macular corneal dystrophy.
    El-Ashry MF; Abd El-Aziz MM; Shalaby O; Bhattacharya SS
    Br J Ophthalmol; 2010 Feb; 94(2):250-5. PubMed ID: 19734134
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Macular corneal dystrophy type II: multiple studies on a cornea with low levels of sulphated keratan sulphate.
    Quantock AJ; Fullwood NJ; Thonar EJ; Waltman SR; Capel MS; Ito M; Verity SM; Schanzlin DJ
    Eye (Lond); 1997; 11 ( Pt 1)():57-67. PubMed ID: 9246278
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Sequencing of the CHST6 gene in Czech macular corneal dystrophy patients supports the evidence of a founder mutation.
    Liskova P; Veraitch B; Jirsova K; Filipec M; Neuwirth A; Ebenezer ND; Hysi PG; Hardcastle AJ; Tuft SJ; Bhattacharya SS
    Br J Ophthalmol; 2008 Feb; 92(2):265-7. PubMed ID: 17962390
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Mutation analysis of the carbohydrate sulfotransferase gene in Vietnamese with macular corneal dystrophy.
    Ha NT; Chau HM; Cung le X; Thanh TK; Fujiki K; Murakami A; Hiratsuka Y; Kanai A
    Invest Ophthalmol Vis Sci; 2003 Aug; 44(8):3310-6. PubMed ID: 12882775
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Protamine increases the affinity of 3'-phosphoadenosine 5'-phosphosulfate toward a sulfotransferase from chicken embryo epiphyseal cartilage.
    Salac ML; Santos JA; Mourão PA
    Biochim Biophys Acta; 1986 Oct; 883(3):605-9. PubMed ID: 3092873
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Macular corneal dystrophy in Iceland. A clinical, genealogic, and immunohistochemical study of 28 patients.
    Jonasson F; Oshima E; Thonar EJ; Smith CF; Johannsson JH; Klintworth GK
    Ophthalmology; 1996 Jul; 103(7):1111-7. PubMed ID: 8684802
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Different mutations in carbohydrate sulfotransferase 6 (CHST6) gene cause macular corneal dystrophy types I and II in a single sibship.
    Liu NP; Bao W; Smith CF; Vance JM; Klintworth GK
    Am J Ophthalmol; 2005 Jun; 139(6):1118-20. PubMed ID: 15953452
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Regulation of serum glycosaminoglycan sulfotransferase activities: inhibition by sulfated glycosaminoglycans and activation by polyamines and basic peptides including a polylysine-containing segment of the c-Ki-ras 2 protein.
    Sugahara K; Nakamura M; Nagisa J; Masuda M; Nunokawa Y; Fujii N; Yamashina I
    J Biochem; 1989 Nov; 106(5):910-9. PubMed ID: 2515192
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Elevated chondroitin 6-sulfotransferase activity in fetal bovine serum.
    Sugahara K; Shibamoto S; Yamashina I
    FEBS Lett; 1985 Apr; 183(1):43-6. PubMed ID: 3856526
    [TBL] [Abstract][Full Text] [Related]  

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