BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

154 related articles for article (PubMed ID: 19693293)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. Identification and characterization of a novel TACSTD2 mutation in gelatinous drop-like corneal dystrophy.
    Paliwal P; Gupta J; Tandon R; Sharma N; Titiyal JS; Kashyap S; Sen S; Kaur P; Dube D; Sharma A; Vajpayee RB
    Mol Vis; 2010 Apr; 16():729-39. PubMed ID: 20454699
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Two novel mutations identified in two Chinese gelatinous drop-like corneal dystrophy families.
    Zhang B; Yao YF; Zhou P
    Mol Vis; 2007 Jun; 13():988-92. PubMed ID: 17653040
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel UBIAD1 mutation identified in a Chinese family with Schnyder crystalline corneal dystrophy.
    Jing Y; Liu C; Xu J; Wang L
    Mol Vis; 2009 Jul; 15():1463-9. PubMed ID: 19649163
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. 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-GraƱa VM; Graue-Hernandez EO; Buentello-Volante B
    Cornea; 2016 Jul; 35(7):987-90. PubMed ID: 27149532
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Gelatinous drop-like corneal dystrophy.
    Tsujikawa M
    Cornea; 2012 Nov; 31 Suppl 1():S37-40. PubMed ID: 23038033
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Road to a Genetic Model of Gelatinous Drop-Like Corneal Dystrophy.
    Tsujikawa M
    Cornea; 2018 Nov; 37 Suppl 1():S91-S93. PubMed ID: 30204612
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A novel TACSTD2 gene mutation in a Turkish family with a gelatinous drop-like corneal dystrophy.
    Markoff A; Bogdanova N; Uhlig CE; Groppe M; Horst J; Kennerknecht I
    Mol Vis; 2006 Dec; 12():1473-6. PubMed ID: 17167402
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. Corneal Opacity Induced by Light in a Mouse Model of Gelatinous Drop-Like Corneal Dystrophy.
    Nagahara Y; Tsujikawa M; Koto R; Uesugi K; Sato S; Kawasaki S; Maruyama K; Nishida K
    Am J Pathol; 2020 Dec; 190(12):2330-2342. PubMed ID: 33011110
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Tumor-associated calcium signal transducer 2 is required for the proper subcellular localization of claudin 1 and 7: implications in the pathogenesis of gelatinous drop-like corneal dystrophy.
    Nakatsukasa M; Kawasaki S; Yamasaki K; Fukuoka H; Matsuda A; Tsujikawa M; Tanioka H; Nagata-Takaoka M; Hamuro J; Kinoshita S
    Am J Pathol; 2010 Sep; 177(3):1344-55. PubMed ID: 20651236
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Two brothers with gelatinous drop-like dystrophy at different stages of the disease: role of mutational analysis.
    Yoshida S; Kumano Y; Yoshida A; Numa S; Yabe N; Hisatomi T; Nishida T; Ishibashi T; Matsui T
    Am J Ophthalmol; 2002 Jun; 133(6):830-2. PubMed ID: 12036680
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.