149 related articles for article (PubMed ID: 21242781)
1. Novel CHST6 gene mutations in 2 unrelated cases of macular corneal dystrophy.
Patel DA; Harocopos GJ; Chang SH; Vora SC; Lubniewski AJ; Huang AJ
Cornea; 2011 Jun; 30(6):664-9. PubMed ID: 21242781
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. 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]
6. New histopathologic and ultrastructural findings in Reis-Bücklers corneal dystrophy caused by the Arg124Leu mutation of TGFBI gene.
Qiu WY; Zheng LB; Pan F; Wang BB; Yao YF
BMC Ophthalmol; 2016 Sep; 16(1):158. PubMed ID: 27590038
[TBL] [Abstract][Full Text] [Related]
7. Granular and lattice deposits in corneal dystrophy caused by R124C mutation of TGFBIp.
Patel DA; Chang SH; Harocopos GJ; Vora SC; Thang DH; Huang AJ
Cornea; 2010 Nov; 29(11):1215-22. PubMed ID: 20697279
[TBL] [Abstract][Full Text] [Related]
8. Immunophenotypes of macular corneal dystrophy in India and correlation with mutations in CHST6.
Sultana A; Klintworth GK; Thonar EJ; Vemuganti GK; Kannabiran C
Mol Vis; 2009; 15():319-25. PubMed ID: 19204788
[TBL] [Abstract][Full Text] [Related]
9. TGFBI, CHST6, and GSN gene analysis in Mexican patients with stromal corneal dystrophies.
Gonzalez-Rodriguez J; Ramirez-Miranda A; Hernandez-Da Mota SE; Zenteno JC
Graefes Arch Clin Exp Ophthalmol; 2014 Aug; 252(8):1267-72. PubMed ID: 24801599
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. 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]
13. 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]
14. A case of Korean patient with macular corneal dystrophy associated with novel mutation in the CHST6 gene.
Lee YK; Chang DJ; Chung SK
Korean J Ophthalmol; 2013 Dec; 27(6):454-8. PubMed ID: 24311932
[TBL] [Abstract][Full Text] [Related]
15. Macular corneal dystrophy related to novel mutations of CHST6 in a Chinese family and clinical observation after penetrating keratoplasty.
Li D; Tian L; Wang X; Chen M
BMC Med Genomics; 2021 Oct; 14(1):247. PubMed ID: 34645431
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. Association of macular corneal dystrophy with excessive cell senescence and apoptosis induced by the novel mutant CHST6.
Hao XD; Liu YN; Hu SH; Pan XJ; Chen P
Exp Eye Res; 2022 Jan; 214():108862. PubMed ID: 34826417
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]
