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 *

130 related articles for article (PubMed ID: 9886734)

  • 41. 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]  

  • 42. Varied appearance of cornea of patients with corneal dystrophy associated with R124H mutation in the BIGH3 gene.
    Konishi M; Yamada M; Nakamura Y; Mashima Y
    Cornea; 1999 Jul; 18(4):424-9. PubMed ID: 10422854
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Q118X mutation of M1S1 gene caused gelatinous drop-like corneal dystrophy: the P501T of BIGH3 gene found in a family with gelatinous drop-like corneal dystrophy.
    Ha NT; Fujiki K; Hotta Y; Nakayasu K; Kanai A
    Am J Ophthalmol; 2000 Jul; 130(1):119-20. PubMed ID: 11004271
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Genotype-phenotype correlation in 2 Indian families with severe granular corneal dystrophy.
    Kannabiran C; Sridhar MS; Chakravarthi SK; Vemuganti GK; Lakshmipathi M
    Arch Ophthalmol; 2005 Aug; 123(8):1127-33. PubMed ID: 16087849
    [TBL] [Abstract][Full Text] [Related]  

  • 45. 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]  

  • 46. 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]  

  • 47. [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]  

  • 48. BIGH3 gene analysis in the differential diagnosis of corneal dystrophies.
    Kocak-Altintas AG; Kocak-Midillioglu I; Akarsu AN; Duman S
    Cornea; 2001 Jan; 20(1):64-8. PubMed ID: 11189007
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Triple anterior chamber after full-thickness lamellar keratoplasty for lattice corneal dystrophy.
    Hirano K; Kojima T; Nakamura M; Hotta Y
    Cornea; 2001 Jul; 20(5):530-3. PubMed ID: 11413412
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Lattice corneal dystrophy type 1: an epithelial or stromal entity?
    Lisch W; Seitz B
    Cornea; 2014 Oct; 33(10):1109-12. PubMed ID: 25055147
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Lattice corneal dystrophy type III in patients with a homozygous L527R mutation in the TGFBI gene.
    Funayama T; Mashima Y; Kawashima M; Yamada M
    Jpn J Ophthalmol; 2006; 50(1):62-4. PubMed ID: 16453189
    [No Abstract]   [Full Text] [Related]  

  • 52. Histologic phenotype-genotype correlation of corneal dystrophies associated with eight distinct mutations in the TGFBI gene.
    Dighiero P; Niel F; Ellies P; D'Hermies F; Savoldelli M; Renard G; Delpech M; Valleix S
    Ophthalmology; 2001 Apr; 108(4):818-23. PubMed ID: 11297504
    [TBL] [Abstract][Full Text] [Related]  

  • 53. A new L527R mutation of the betaIGH3 gene in patients with lattice corneal dystrophy with deep stromal opacities.
    Fujiki K; Hotta Y; Nakayasu K; Yokoyama T; Takano T; Yamaguchi T; Kanai A
    Hum Genet; 1998 Sep; 103(3):286-9. PubMed ID: 9799082
    [TBL] [Abstract][Full Text] [Related]  

  • 54. 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]  

  • 55. Amyloid and Pro501 Thr-mutated (beta)ig-h3 gene product colocalize in lattice corneal dystrophy type IIIA.
    Kawasaki S; Nishida K; Quantock AJ; Dota A; Bennett K; Kinoshita S
    Am J Ophthalmol; 1999 Apr; 127(4):456-8. PubMed ID: 10218700
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Clinical, histologic, and ultrastructural features of the corneal dystrophy caused by the R124L mutation of the BIGH3 gene.
    Dighiero P; Valleix S; D'Hermies F; Drunat S; Ellies P; Savoldelli M; Pouliquen Y; Delpech M; Legeais JM; Renard G
    Ophthalmology; 2000 Jul; 107(7):1353-7. PubMed ID: 10889112
    [TBL] [Abstract][Full Text] [Related]  

  • 57. 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]  

  • 58. Association of autosomal dominantly inherited corneal dystrophies with BIGH3 gene mutations in Japan.
    Mashima Y; Yamamoto S; Inoue Y; Yamada M; Konishi M; Watanabe H; Maeda N; Shimomura Y; Kinoshita S
    Am J Ophthalmol; 2000 Oct; 130(4):516-7. PubMed ID: 11024425
    [TBL] [Abstract][Full Text] [Related]  

  • 59. An analysis of BIGH3 mutations in patients with corneal dystrophies in the Kyushu district of Japan.
    Yoshida S; Kumano Y; Yoshida A; Hisatomi T; Matsui H; Nishida T; Ishibashi T; Matsui T
    Jpn J Ophthalmol; 2002; 46(4):469-71. PubMed ID: 12225829
    [TBL] [Abstract][Full Text] [Related]  

  • 60. A novel phenotype-genotype correlation with an Arg555Trp mutation of TGFBI gene in Thiel-Behnke corneal dystrophy in a Chinese pedigree.
    Yu Y; Qiu P; Zhu Y; Li J; Wu M; Zhang B; Yao K
    BMC Ophthalmol; 2015 Oct; 15():131. PubMed ID: 26464103
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.