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 *

244 related articles for article (PubMed ID: 11095060)

  • 21. 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]  

  • 22. A mutation within exon 14 of the TGFBI (BIGH3) gene on chromosome 5q31 causes an asymmetric, late-onset form of lattice corneal dystrophy.
    Stewart H; Black GC; Donnai D; Bonshek RE; McCarthy J; Morgan S; Dixon MJ; Ridgway AA
    Ophthalmology; 1999 May; 106(5):964-70. PubMed ID: 10328397
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Clinical outcome of eight BIGH3-linked corneal dystrophies.
    Ellies P; Renard G; Valleix S; Boelle PY; Dighiero P
    Ophthalmology; 2002 Apr; 109(4):793-7. PubMed ID: 11927442
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [Analysis of mutation of BIGH3 gene in Chinese patients with corneal dystrophies].
    Yu J; Zou LH; He JC; Liu NP; Zhang W; Lu L; Sun XG; Dong DS; Wu YY; Yin XT
    Zhonghua Yan Ke Za Zhi; 2003 Oct; 39(10):582-6. PubMed ID: 14766070
    [TBL] [Abstract][Full Text] [Related]  

  • 25. 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]  

  • 26. Kerato-epithelin mutations in four 5q31-linked corneal dystrophies.
    Munier FL; Korvatska E; Djemaï A; Le Paslier D; Zografos L; Pescia G; Schorderet DF
    Nat Genet; 1997 Mar; 15(3):247-51. PubMed ID: 9054935
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Survey of patients with granular, lattice, avellino, and Reis-Bücklers corneal dystrophies for mutations in the BIGH3 and gelsolin genes.
    Afshari NA; Mullally JE; Afshari MA; Steinert RF; Adamis AP; Azar DT; Talamo JH; Dohlman CH; Dryja TP
    Arch Ophthalmol; 2001 Jan; 119(1):16-22. PubMed ID: 11146721
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A novel mutation of the TGFBI gene found in a Vietnamese family with atypical granular corneal dystrophy.
    Ha NT; Cung le X; Chau HM; Thanh TK; Fujiki K; Murakami A; Kanai A
    Jpn J Ophthalmol; 2003; 47(3):246-8. PubMed ID: 12782158
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Double mutation (R124H, N544S) of TGFBI in two sisters with combined expression of Avellino and lattice corneal dystrophies.
    Yamada N; Kawamoto K; Morishige N; Chikama T; Nishida T; Nishioka M; Okayama N; Hinoda Y
    Mol Vis; 2009 May; 15():974-9. PubMed ID: 19461933
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Molecular genetic and histopathological examinations for genotype-phenotype analysis in patients with TGFBI-linked corneal dystrophy].
    Grünauer-Kloevekorn C; Braeutigam S; Weidle E; Wolter-Roessler M; Tost F; Auw-Haedrich C; Völcker HE; Heinritz W; Froster U; Duncker G
    Klin Monbl Augenheilkd; 2006 Oct; 223(10):829-36. PubMed ID: 17063427
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [Autosomal dominant inherited corneal dystrophies associated with TGFBI mutation].
    Mashima Y; Yamada M; Oguchi Y
    Nippon Ganka Gakkai Zasshi; 2001 Oct; 105(10):659-72. PubMed ID: 11692612
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. 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]  

  • 35. TGFBI gene mutation analysis in a Chinese pedigree of Reis-Bücklers corneal dystrophy.
    Ma K; Liu G; Yang Y; Yu M; Sui R; Yu W; Chen X; Deng Y; Yan N; Cao G; Liu X
    Mol Vis; 2010 Mar; 16():556-61. PubMed ID: 20360992
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Role of BIGH3 R124H mutation in the diagnosis of Avellino corneal dystrophy.
    Huerva V; Velasco A; Sanchez MC; Matias-Guiu X
    Eur J Ophthalmol; 2008; 18(3):345-50. PubMed ID: 18465714
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Pathogenic mutations of TGFBI and CHST6 genes in Chinese patients with Avellino, lattice, and macular corneal dystrophies.
    Huo YN; Yao YF; Yu P
    J Zhejiang Univ Sci B; 2011 Sep; 12(9):687-93. PubMed ID: 21887843
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. The classic form of granular corneal dystrophy associated with R555W mutation in the BIGH3 gene is rare in Japanese patients.
    Konishi M; Mashima Y; Yamada M; Kudoh J; Shimizu N
    Am J Ophthalmol; 1998 Sep; 126(3):450-2. PubMed ID: 9744382
    [TBL] [Abstract][Full Text] [Related]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 13.