132 related articles for article (PubMed ID: 11139648)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. Macular corneal dystrophy type I and type II are caused by distinct mutations in a new sulphotransferase gene.
Akama TO; Nishida K; Nakayama J; Watanabe H; Ozaki K; Nakamura T; Dota A; Kawasaki S; Inoue Y; Maeda N; Yamamoto S; Fujiwara T; Thonar EJ; Shimomura Y; Kinoshita S; Tanigami A; Fukuda MN
Nat Genet; 2000 Oct; 26(2):237-41. PubMed ID: 11017086
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. 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]
12. 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]
13. 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]
14. 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; 44(7):2949-53. PubMed ID: 12824236
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. 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]
19. BIGH3 exon 14 mutations lead to intermediate type I/IIIA of lattice corneal dystrophies.
Schmitt-Bernard CF; Guittard C; Arnaud B; Demaille J; Argiles A; Claustres M; Tuffery-Giraud S
Invest Ophthalmol Vis Sci; 2000 May; 41(6):1302-8. PubMed ID: 10798644
[TBL] [Abstract][Full Text] [Related]
20. Macular corneal dystrophy in a Chinese family related with novel mutations of CHST6.
Dang X; Zhu Q; Wang L; Su H; Lin H; Zhou N; Liang T; Wang Z; Huang S; Ren Q; Qi Y
Mol Vis; 2009; 15():700-5. PubMed ID: 19365571
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]