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 *

131 related articles for article (PubMed ID: 26949635)

  • 1. Uncovering the profile of mutations of transforming growth factor beta-induced gene in Chinese corneal dystrophy patients.
    Hao XD; Zhang YY; Chen P; Li SX; Wang Y
    Int J Ophthalmol; 2016; 9(2):198-203. PubMed ID: 26949635
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Phenotype-genotype correlations in patients with TGFBI-linked corneal dystrophies in Taiwan.
    Hou YC; Wang IJ; Hsiao CH; Chen WL; Hu FR
    Mol Vis; 2012; 18():362-71. PubMed ID: 22355247
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Six different mutations of TGFBI (betaig-h3, keratoepithelin) gene found in Japanese corneal dystrophies.
    Fujiki K; Hotta Y; Nakayasu K; Yamaguchi T; Kato T; Uesugi Y; Ha NT; Endo S; Ishida N; Lu WN; Kanai A
    Cornea; 2000 Nov; 19(6):842-5. PubMed ID: 11095060
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genotypic Homogeneity in Distinctive Transforming Growth Factor-Beta Induced (TGFBI) Protein Phenotypes.
    Han SB; Anandalakshmi V; Wong CW; Ng SR; Mehta JS
    Int J Mol Sci; 2021 Jan; 22(3):. PubMed ID: 33513810
    [No Abstract]   [Full Text] [Related]  

  • 6. The spectrum of beta ig-h3 gene mutations in Japanese patients with corneal dystrophy.
    Yamamoto S; Okada M; Tsujikawa M; Morimura H; Maeda N; Watanabe H; Inoue Y; Shimomura Y; Kinoshita S; Tano Y
    Cornea; 2000 May; 19(3 Suppl):S21-3. PubMed ID: 10832717
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Investigation of TGFBI (transforming growth factor beta-induced) Gene Mutations in Families with Granular Corneal Dystrophy Type 1 in the Konya Region.
    Malkondu F; Arıkoğlu H; Erkoç Kaya D; Bozkurt B; Özkan F
    Turk J Ophthalmol; 2020 Apr; 50(2):64-70. PubMed ID: 32366062
    [TBL] [Abstract][Full Text] [Related]  

  • 8. TGFBI gene mutations causing lattice and granular corneal dystrophies in Indian patients.
    Chakravarthi SV; Kannabiran C; Sridhar MS; Vemuganti GK
    Invest Ophthalmol Vis Sci; 2005 Jan; 46(1):121-5. PubMed ID: 15623763
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutation analysis of the TGFBI gene in Vietnamese with granular and Avellino corneal dystrophy.
    Cung le X; Ha NT; Chau HM; Thanh TK; Fujiki K; Murakami A; Hiratsuka Y; Kanai A
    Jpn J Ophthalmol; 2004; 48(1):12-6. PubMed ID: 14767644
    [TBL] [Abstract][Full Text] [Related]  

  • 10. TGFBI and CHST6 gene analysis in Chinese stromal corneal dystrophies.
    Li Y; Li T; Song XS; Li JZ; Wu QS; Li HY
    Int J Ophthalmol; 2012; 5(3):301-6. PubMed ID: 22773977
    [TBL] [Abstract][Full Text] [Related]  

  • 11. TGFBI Gene Mutation Analysis of Clinically Diagnosed Granular Corneal Dystrophy Patients Prior to PTK: A Pilot Study from Eastern China.
    Zeng L; Zhao J; Chen Y; Zhao F; Li M; Chao-Shern C; Moore T; Marshall J; Zhou X
    Sci Rep; 2017 Apr; 7(1):596. PubMed ID: 28377594
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Analyses of TGFBI gene mutation spectrum in four Chinese families with corneal dystrophy].
    Zhang Y; Ying J; Zhou W; Zhu L; Cai J
    Zhonghua Yi Xue Za Zhi; 2015 Jan; 95(2):116-9. PubMed ID: 25876897
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. Genotype-phenotype correlation of TGFBI corneal dystrophies in Polish patients.
    Nowińska AK; Wylegala E; Janiszewska DA; Dobrowolski D; Aragona P; Roszkowska AM; Puzzolo D
    Mol Vis; 2011; 17():2333-42. PubMed ID: 21921985
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genotype-Phenotype Correlation for TGFBI Corneal Dystrophies Identifies p.(G623D) as a Novel Cause of Epithelial Basement Membrane Dystrophy.
    Evans CJ; Davidson AE; Carnt N; Rojas López KE; Veli N; Thaung CM; Tuft SJ; Hardcastle AJ
    Invest Ophthalmol Vis Sci; 2016 Oct; 57(13):5407-5414. PubMed ID: 27737463
    [TBL] [Abstract][Full Text] [Related]  

  • 17. TGFBI gene mutations analysis in Chinese families with corneal dystrophies.
    Wang X; Ying M; Fu C; Wang Y; Li N
    Mol Med Rep; 2017 May; 15(5):3198-3202. PubMed ID: 28358433
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular genetics of Chinese families with TGFBI corneal dystrophies.
    Zhang T; Yan N; Yu W; Liu Y; Liu G; Wu X; Lian J; Liu X
    Mol Vis; 2011 Feb; 17():380-7. PubMed ID: 21311742
    [TBL] [Abstract][Full Text] [Related]  

  • 19. TGFBI gene mutation analysis in families with hereditary corneal dystrophies from Ukraine.
    Pampukha VM; Drozhyna GI; Livshits LA
    Ophthalmologica; 2004; 218(6):411-4. PubMed ID: 15564760
    [TBL] [Abstract][Full Text] [Related]  

  • 20. R124C and R555W TGFBI mutations in Spanish families with autosomal-dominant corneal dystrophies.
    Blanco-Marchite C; Sánchez-Sánchez F; López-Sánchez E; Escribano J
    Mol Vis; 2007 Aug; 13():1390-6. PubMed ID: 17768377
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.