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 *

99 related articles for article (PubMed ID: 22261655)

  • 1. Molecular genetic analysis of macular corneal dystrophy patients from North India.
    Paliwal P; Sharma A; Tandon R; Sharma N; Titiyal JS; Sen S; Vajpayee RB
    Ophthalmic Res; 2012; 48(1):28-32. PubMed ID: 22261655
    [TBL] [Abstract][Full Text] [Related]  

  • 2. CHST6 mutations in North American subjects with macular corneal dystrophy: a comprehensive molecular genetic review.
    Klintworth GK; Smith CF; Bowling BL
    Mol Vis; 2006 Mar; 12():159-76. PubMed ID: 16568029
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Novel mutations of the carbohydrate sulfotransferase-6 (CHST6) gene causing macular corneal dystrophy in India.
    Sultana A; Sridhar MS; Jagannathan A; Balasubramanian D; Kannabiran C; Klintworth GK
    Mol Vis; 2003 Dec; 9():730-4. PubMed ID: 14735064
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of novel mutations in the carbohydrate sulfotransferase gene (CHST6) causing macular corneal dystrophy.
    El-Ashry MF; Abd El-Aziz MM; Wilkins S; Cheetham ME; Wilkie SE; Hardcastle AJ; Halford S; Bayoumi AY; Ficker LA; Tuft S; Bhattacharya SS; Ebenezer ND
    Invest Ophthalmol Vis Sci; 2002 Feb; 43(2):377-82. PubMed ID: 11818380
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Novel mutations in the carbohydrate sulfotransferase gene (CHST6) in American patients with macular corneal dystrophy.
    Aldave AJ; Yellore VS; Thonar EJ; Udar N; Warren JF; Yoon MK; Cohen EJ; Rapuano CJ; Laibson PR; Margolis TP; Small K
    Am J Ophthalmol; 2004 Mar; 137(3):465-73. PubMed ID: 15013869
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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]  

  • 9. Macular corneal dystrophy types I and II are caused by distinct mutations in the CHST6 gene in Iceland.
    Liu NP; Smith CF; Bowling BL; Jonasson F; Klintworth GK
    Mol Vis; 2006 Oct; 12():1148-52. PubMed ID: 17093400
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Allelic heterogeneity of the carbohydrate sulfotransferase-6 gene in patients with macular corneal dystrophy.
    Sultana A; Sridhar MS; Klintworth GK; Balasubramanian D; Kannabiran C
    Clin Genet; 2005 Nov; 68(5):454-60. PubMed ID: 16207214
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. Novel mutations of CHST6 in Iranian patients with macular corneal dystrophy.
    Birgani SA; Salehi Z; Houshmand M; Mohamadi MJ; Promehr LA; Mozafarzadeh Z
    Mol Vis; 2009; 15():373-7. PubMed ID: 19223992
    [TBL] [Abstract][Full Text] [Related]  

  • 17. An unusual presentation of macular corneal dystrophy associated with uniparental isodisomy and a novel Leu173Pro mutation.
    Yellore VS; Sonmez B; Chen MC; Rayner SA; Thonar EJ; Aldave AJ
    Ophthalmic Genet; 2007 Sep; 28(3):169-74. PubMed ID: 17896316
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Phenotype and genotype analysis in patients with macular corneal dystrophy.
    Nowinska AK; Wylegala E; Teper S; Wróblewska-Czajka E; Aragona P; Roszkowska AM; Micali A; Pisani A; Puzzolo D
    Br J Ophthalmol; 2014 Nov; 98(11):1514-21. PubMed ID: 24926691
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular analysis of the CHST6 gene in Korean patients with macular corneal dystrophy: Identification of three novel mutations.
    Park SH; Ahn YJ; Chae H; Kim Y; Kim MS; Kim M
    Mol Vis; 2015; 21():1201-9. PubMed ID: 26604660
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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; 44(8):3272-7. PubMed ID: 12882769
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.