118 related articles for article (PubMed ID: 15652848)
1. A novel missense mutation in a Japanese patient with gelatinous droplike corneal dystrophy.
Taniguchi Y; Tsujikawa M; Hibino S; Tsujikawa K; Tanaka T; Kiridoushi A; Tano Y
Am J Ophthalmol; 2005 Jan; 139(1):186-8. PubMed ID: 15652848
[TBL] [Abstract][Full Text] [Related]
2. Compound heterozygous mutations of M1S1 gene in gelatinous droplike corneal dystrophy.
Tian X; Fujiki K; Li Q; Murakami A; Xie P; Kanai A; Wang W; Liu Z
Am J Ophthalmol; 2004 Mar; 137(3):567-9. PubMed ID: 15013888
[TBL] [Abstract][Full Text] [Related]
3. A missense mutation in the M1S1 gene found in a turkish patient with gelatinous droplike corneal dystrophy.
Yildirim N; Muslumanoglu H; Isiksoy S; Sahin A; Baycu C; Artan S
Cornea; 2007 Sep; 26(8):1017-20. PubMed ID: 17721311
[TBL] [Abstract][Full Text] [Related]
4. Four mutations (three novel, one founder) in TACSTD2 among Iranian GDLD patients.
Alavi A; Elahi E; Tehrani MH; Amoli FA; Javadi MA; Rafati N; Chiani M; Banihosseini SS; Bayat B; Kalhor R; Amini SS
Invest Ophthalmol Vis Sci; 2007 Oct; 48(10):4490-7. PubMed ID: 17898270
[TBL] [Abstract][Full Text] [Related]
5. A novel mutation of M1S1 gene found in a Vietnamese patient with gelatinous droplike corneal dystrophy.
Ha NT; Chau HM; Cung le X; Thanh TK; Fujiki K; Murakami A; Kanai A
Am J Ophthalmol; 2003 Mar; 135(3):390-3. PubMed ID: 12614764
[TBL] [Abstract][Full Text] [Related]
6. A novel mutation in the M1S1 gene responsible for gelatinous droplike corneal dystrophy.
Tasa G; Kals J; Muru K; Juronen E; Piirsoo A; Veromann S; Jänes S; Mikelsaar AV; Lang A
Invest Ophthalmol Vis Sci; 2001 Nov; 42(12):2762-4. PubMed ID: 11687514
[TBL] [Abstract][Full Text] [Related]
7. Rapid detection of M1S1 mutations by the protein truncation test.
Tsujikawa M; Tsujikawa K; Maeda N; Watanabe H; Inoue Y; Mashima Y; Shimomura Y; Tano Y
Invest Ophthalmol Vis Sci; 2000 Aug; 41(9):2466-8. PubMed ID: 10937555
[TBL] [Abstract][Full Text] [Related]
8. Chromosomal sharing in atypical cases of gelatinous drop-like corneal dystrophy.
Tsujikawa M; Maeda N; Tsujikawa K; Hori Y; Inoue T; Nishida K
Jpn J Ophthalmol; 2010 Sep; 54(5):494-8. PubMed ID: 21052915
[TBL] [Abstract][Full Text] [Related]
9. Identification of the gene responsible for gelatinous drop-like corneal dystrophy.
Tsujikawa M; Kurahashi H; Tanaka T; Nishida K; Shimomura Y; Tano Y; Nakamura Y
Nat Genet; 1999 Apr; 21(4):420-3. PubMed ID: 10192395
[TBL] [Abstract][Full Text] [Related]
10. A spectrum of clinical manifestations of gelatinous drop-like corneal dystrophy in japan.
Ide T; Nishida K; Maeda N; Tsujikawa M; Yamamoto S; Watanabe H; Tano Y
Am J Ophthalmol; 2004 Jun; 137(6):1081-4. PubMed ID: 15183793
[TBL] [Abstract][Full Text] [Related]
11. Gelatinous drop-like corneal dystrophy.
Tsujikawa M
Cornea; 2012 Nov; 31 Suppl 1():S37-40. PubMed ID: 23038033
[TBL] [Abstract][Full Text] [Related]
12. Gelatinous drop-like corneal dystrophy with a novel mutation of TACSTD2 manifested in combination with spheroidal degeneration in a Chinese patient.
Zhang B; Yao YF
Mol Vis; 2010 Aug; 16():1570-5. PubMed ID: 20806038
[TBL] [Abstract][Full Text] [Related]
13. Spectrum of Clinical Signs and Genetic Characterization of Gelatinous Drop-Like Corneal Dystrophy in a Colombian Family.
Morantes S; Evans CJ; Valencia AV; Davidson AE; Hardcastle AJ; Ruiz Linares A; Tuft SJ; Cuevas M
Cornea; 2016 Aug; 35(8):1141-6. PubMed ID: 27227392
[TBL] [Abstract][Full Text] [Related]
14. Familial Gelatinous Drop-Like Corneal Dystrophy Caused by a Novel Nonsense TACSTD2 Mutation.
Cabral-Macias J; Zenteno JC; Ramirez-Miranda A; Navas A; Bermudez-Magner JA; Boullosa-Graña VM; Graue-Hernandez EO; Buentello-Volante B
Cornea; 2016 Jul; 35(7):987-90. PubMed ID: 27149532
[TBL] [Abstract][Full Text] [Related]
15. Establishment of a human corneal epithelial cell line lacking the functional TACSTD2 gene as an in vitro model for gelatinous drop-like dystrophy.
Kitazawa K; Kawasaki S; Shinomiya K; Aoi K; Matsuda A; Funaki T; Yamasaki K; Nakatsukasa M; Ebihara N; Murakami A; Hamuro J; Kinoshita S
Invest Ophthalmol Vis Sci; 2013 Aug; 54(8):5701-11. PubMed ID: 23868985
[TBL] [Abstract][Full Text] [Related]
16. A novel TACSTD2 mutation identified in two Chinese brothers with gelatinous drop-like corneal dystrophy.
Jing Y; Liu C; Wang L
Mol Vis; 2009 Aug; 15():1580-8. PubMed ID: 19693293
[TBL] [Abstract][Full Text] [Related]
17. [Gelatinous drop-like corneal dystrophy: mutation analysis of membrane component, chromosome 1, surface marker 1].
Yajima T; Fujiki K; Murakami A; Nakayasu K
Nippon Ganka Gakkai Zasshi; 2002 May; 106(5):265-72. PubMed ID: 12048921
[TBL] [Abstract][Full Text] [Related]
18. Two novel mutations of TACSTD2 found in three Japanese gelatinous drop-like corneal dystrophy families with their aberrant subcellular localization.
Nakatsukasa M; Kawasaki S; Yamasaki K; Fukuoka H; Matsuda A; Nishida K; Kinoshita S
Mol Vis; 2011 Apr; 17():965-70. PubMed ID: 21541270
[TBL] [Abstract][Full Text] [Related]
19. Exclusion of TACSTD2 in an Iranian GDLD pedigree.
Alavi A; Elahi E; Amoli FA; Tehrani MH
Mol Vis; 2007 Aug; 13():1441-5. PubMed ID: 17768381
[TBL] [Abstract][Full Text] [Related]
20. Q118X mutation of M1S1 gene caused gelatinous drop-like corneal dystrophy: the P501T of BIGH3 gene found in a family with gelatinous drop-like corneal dystrophy.
Ha NT; Fujiki K; Hotta Y; Nakayasu K; Kanai A
Am J Ophthalmol; 2000 Jul; 130(1):119-20. PubMed ID: 11004271
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]