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 *

205 related articles for article (PubMed ID: 19062536)

  • 1. [TGFBI gene mutations in the Ukrainian patients with inherited corneal stromal dystrophies].
    Pampukha VN; Kravchenko SA; Tereshchenko F; Drozhzhina GI; Livshits LA
    Genetika; 2008 Oct; 44(10):1392-6. PubMed ID: 19062536
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Novel L558P mutation of the TGFBI gene found in Ukrainian families with atypical corneal dystrophy.
    Pampukha VM; Kravchenko SA; Tereshchenko FA; Livshits LA; Drozhyna GI
    Ophthalmologica; 2009; 223(3):207-14. PubMed ID: 19221447
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Clinical and genetic features of TGFBI-linked corneal dystrophies in Mexican population: description of novel mutations and novel genotype-phenotype correlations.
    Zenteno JC; Correa-Gomez V; Santacruz-Valdez C; Suarez-Sanchez R; Villanueva-Mendoza C
    Exp Eye Res; 2009 Aug; 89(2):172-7. PubMed ID: 19303004
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A unique corneal dystrophy of Bowman's layer and stroma associated with the Gly623Asp mutation in the transforming growth factor beta-induced (TGFBI) gene.
    Aldave AJ; Rayner SA; King JA; Affeldt JA; Yellore VS
    Ophthalmology; 2005 Jun; 112(6):1017-22. PubMed ID: 15885785
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. TGFBI mutational analysis in a New Zealand population of inherited corneal dystrophy patients.
    Vincent AL; de Karolyi B; Patel DV; Wheeldon CE; McGhee CN
    Br J Ophthalmol; 2010 Jul; 94(7):836-42. PubMed ID: 19948560
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Gene symbol: TGFBI. Disease: Corneal dystrophy, lattice type.
    Livshits L; Pampukha VM; Tereshchenko FA; Drozhyna GI
    Hum Genet; 2008 Oct; 124(3):296-7. PubMed ID: 18846615
    [No Abstract]   [Full Text] [Related]  

  • 9. A corneal dystrophy associated with transforming growth factor beta-induced Gly623Asp mutation an amyloidogenic phenotype.
    Auw-Haedrich C; Agostini H; Clausen I; Reinhard T; Eberwein P; Schorderet DF; Gruenauer-Kloevekorn C
    Ophthalmology; 2009 Jan; 116(1):46-51. PubMed ID: 19019446
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Lattice corneal dystrophy associated with the Ala546Asp and Pro551Gln missense changes in the TGFBI gene.
    Aldave AJ; Gutmark JG; Yellore VS; Affeldt JA; Meallet MA; Udar N; Rao NA; Small KW; Klintworth GK
    Am J Ophthalmol; 2004 Nov; 138(5):772-81. PubMed ID: 15531312
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [A research on TGFBI gene mutations in Chinese families with corneal dystrophies].
    Qi YH; He HD; Li Y; Lin H; Gu JZ; Su H; Huang SZ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Jun; 23(3):310-2. PubMed ID: 16767671
    [TBL] [Abstract][Full Text] [Related]  

  • 12. TGFBI gene mutations in Brazilian patients with corneal dystrophy.
    Solari HP; Ventura MP; Perez AB; Sallum JM; Burnier MN; Belfort R
    Eye (Lond); 2007 May; 21(5):587-90. PubMed ID: 16440005
    [TBL] [Abstract][Full Text] [Related]  

  • 13. TGFBI (BIGH3) gene mutations in German families: two novel mutations associated with unique clinical and histopathological findings.
    Gruenauer-Kloevekorn C; Clausen I; Weidle E; Wolter-Roessler M; Tost F; Völcker HE; Schulze DP; Heinritz W; Reinhard T; Froster U; Duncker G; Schorderet D; Auw-Haedrich C
    Br J Ophthalmol; 2009 Jul; 93(7):932-7. PubMed ID: 19001012
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Corneal dystrophies in Japan.
    Fujiki K; Nakayasu K; Kanai A
    J Hum Genet; 2001; 46(8):431-5. PubMed ID: 11501939
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Spontaneous and inheritable R555Q mutation in the TGFBI/BIGH3 gene in two unrelated families exhibiting Bowman's layer corneal dystrophy.
    Zhao XC; Nakamura H; Subramanyam S; Stock LE; Gillette TE; Yoshikawa S; Ma X; Yee RW
    Ophthalmology; 2007 Nov; 114(11):e39-46. PubMed ID: 17980739
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. A novel variant lattice corneal dystrophy caused by association of mutation (V625D) in TGFBI gene.
    Tian X; Fujiki K; Zhang Y; Murakami A; Li Q; Kanai A; Wang W; Hao Y; Ma Z
    Am J Ophthalmol; 2007 Sep; 144(3):473-5. PubMed ID: 17765440
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Expanding the mutational spectrum in TGFBI-linked corneal dystrophies: Identification of a novel and unusual mutation (Val113Ile) in a family with granular dystrophy.
    Zenteno JC; Ramirez-Miranda A; Santacruz-Valdes C; Suarez-Sanchez R
    Mol Vis; 2006 Apr; 12():331-5. PubMed ID: 16636649
    [TBL] [Abstract][Full Text] [Related]  

  • 19. TGFBI (BIGH3) gene mutations in Hungary--report of the novel F547S mutation associated with polymorphic corneal amyloidosis.
    Takács L; Losonczy G; Matesz K; Balogh I; Sohajda Z; Tóth K; Fazakas F; Vereb G; Berta A
    Mol Vis; 2007 Oct; 13():1976-83. PubMed ID: 17982422
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 11.