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 *

120 related articles for article (PubMed ID: 33346999)

  • 61. Novel and known mutations of TGFBI, their genotype-phenotype correlation and structural modeling in 3 Chinese families with lattice corneal dystrophy.
    Zhong X; Chen S; Huang W; Yang J; Chen X; Zhou Y; Zhou Q; Wang Y
    Mol Vis; 2010 Feb; 16():224-30. PubMed ID: 20161820
    [TBL] [Abstract][Full Text] [Related]  

  • 62. Genotype-phenotype correlations in Chinese patients with TGFBI gene-linked corneal dystrophy.
    Long Y; Gu YS; Han W; Li XY; Yu P; Qi M
    J Zhejiang Univ Sci B; 2011 Apr; 12(4):287-92. PubMed ID: 21462384
    [TBL] [Abstract][Full Text] [Related]  

  • 63. Hereditary lattice corneal dystrophy is associated with corneal amyloid deposits enclosing C-terminal fragments of keratoepithelin.
    Stix B; Leber M; Bingemer P; Gross C; Rüschoff J; Fändrich M; Schorderet DF; Vorwerk CK; Zacharias M; Roessner A; Röcken C
    Invest Ophthalmol Vis Sci; 2005 Apr; 46(4):1133-9. PubMed ID: 15790870
    [TBL] [Abstract][Full Text] [Related]  

  • 64. [Type I lattice corneal dystrophy. Clinical and molecular genetic study of a large family].
    Meins M; Kohlhaas M; Richard G; Gal A
    Klin Monbl Augenheilkd; 1998 Mar; 212(3):154-8. PubMed ID: 9592740
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Isolation and chromosomal localization of a cornea-specific human keratin 12 gene and detection of four mutations in Meesmann corneal epithelial dystrophy.
    Nishida K; Honma Y; Dota A; Kawasaki S; Adachi W; Nakamura T; Quantock AJ; Hosotani H; Yamamoto S; Okada M; Shimomura Y; Kinoshita S
    Am J Hum Genet; 1997 Dec; 61(6):1268-75. PubMed ID: 9399908
    [TBL] [Abstract][Full Text] [Related]  

  • 66. Meesmann corneal dystrophy associated with epithelial basement membrane and posterior polymorphous corneal dystrophies.
    Cremona FA; Ghosheh FR; Laibson PR; Rapuano CJ; Cohen EJ
    Cornea; 2008 Apr; 27(3):374-7. PubMed ID: 18362674
    [TBL] [Abstract][Full Text] [Related]  

  • 67. H626R and R124C mutations of the TGFBI (BIGH3) gene caused lattice corneal dystrophy in Vietnamese people.
    Chau HM; Ha NT; Cung LX; Thanh TK; Fujiki K; Murakami A; Kanai A
    Br J Ophthalmol; 2003 Jun; 87(6):686-9. PubMed ID: 12770961
    [TBL] [Abstract][Full Text] [Related]  

  • 68. An R124C mutation in TGFBI caused lattice corneal dystrophy type I with a variable phenotype in three Chinese families.
    Liu Z; Wang YQ; Gong QH; Xie LX
    Mol Vis; 2008 Jun; 14():1234-9. PubMed ID: 18615206
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Lattice corneal dystrophy type II associated with familial amyloid polyneuropathy type IV.
    Akiya S; Nishio Y; Ibi K; Uozumi H; Takahashi H; Hamada T; Onishi A; Ishiguchi H; Hoshii Y; Nakazato M
    Ophthalmology; 1996 Jul; 103(7):1106-10. PubMed ID: 8684801
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Analysis of TGFBI gene mutations in Chinese patients with corneal dystrophies and review of the literature.
    Yang J; Han X; Huang D; Yu L; Zhu Y; Tong Y; Zhu B; Li C; Weng M; Ma X
    Mol Vis; 2010 Jun; 16():1186-93. PubMed ID: 20664689
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Arg124Cys mutation of the betaig-h3 bene in a Japanese family with lattice corneal dystrophy type I.
    Hotta Y; Fujiki K; Ono K; Fujimaki T; Nakayasu K; Yamaguchi T; Kanai A
    Jpn J Ophthalmol; 1998; 42(6):450-5. PubMed ID: 9886734
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Late-onset form of lattice corneal dystrophy caused by leu527Arg mutation of the TGFBI gene.
    Hirano K; Hotta Y; Nakamura M; Fujiki K; Kanai A; Yamamoto N
    Cornea; 2001 Jul; 20(5):525-9. PubMed ID: 11413411
    [TBL] [Abstract][Full Text] [Related]  

  • 73. The TGFBI A546D mutation causes an atypical type of lattice corneal dystrophy.
    Correa-Gomez V; Villalvazo-Cordero L; Zenteno JC
    Mol Vis; 2007 Sep; 13():1695-700. PubMed ID: 17893671
    [TBL] [Abstract][Full Text] [Related]  

  • 74. The molecular genetics of the corneal dystrophies--current status.
    Klintworth GK
    Front Biosci; 2003 May; 8():d687-713. PubMed ID: 12700042
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Spheroidal degeneration in H626R TGFBI variant lattice dystrophy: a multimodality analysis.
    Lai K; Reidy J; Bert B; Milman T
    Cornea; 2014 Jul; 33(7):726-32. PubMed ID: 24831201
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Genotype of lattice corneal dystrophy (R124C mutation in TGFBI) in a patient presenting with features of avellino corneal dystrophy.
    Edelstein SL; Huang AJ; Harocopos GJ; Waltman SR
    Cornea; 2010 Jun; 29(6):698-700. PubMed ID: 20458218
    [TBL] [Abstract][Full Text] [Related]  

  • 77. A novel variant of combined granular-lattice corneal dystrophy associated with the Met619Lys mutation in the TGFBI gene.
    Aldave AJ; Yellore VS; Sonmez B; Bourla N; Salem AK; Khan MA; Rayner SA; Glasgow BJ
    Arch Ophthalmol; 2008 Mar; 126(3):371-7. PubMed ID: 18332318
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Lattice corneal dystrophy type IIIA with hyaline component from a novel A620P mutation and distinct surgical treatments.
    Jung JW; Kim SA; Kang EM; Kim TI; Cho HS; Kim EK
    Cornea; 2014 Dec; 33(12):1324-31. PubMed ID: 25321938
    [TBL] [Abstract][Full Text] [Related]  

  • 79. A Novel Heterozygous TGFBI c.1613C>A Pathogenic Variant is Associated With Lattice Corneal Dystrophy in a Chinese Family.
    Fu M; Duan S; Zhang X; Wang J; Wang S; Chi ZL
    Am J Ophthalmol; 2023 Dec; 256():138-145. PubMed ID: 37567434
    [TBL] [Abstract][Full Text] [Related]  

  • 80.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.