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 *

199 related articles for article (PubMed ID: 19710953)

  • 21. Mutational spectrum of the ZEB1 gene in corneal dystrophies supports a genotype-phenotype correlation.
    Lechner J; Dash DP; Muszynska D; Hosseini M; Segev F; George S; Frazer DG; Moore JE; Kaye SB; Young T; Simpson DA; Churchill AJ; Héon E; Willoughby CE
    Invest Ophthalmol Vis Sci; 2013 May; 54(5):3215-23. PubMed ID: 23599324
    [TBL] [Abstract][Full Text] [Related]  

  • 22. In vivo laser confocal microscopy findings for Bowman's layer dystrophies (Thiel-Behnke and Reis-Bücklers corneal dystrophies).
    Kobayashi A; Sugiyama K
    Ophthalmology; 2007 Jan; 114(1):69-75. PubMed ID: 17198850
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Three autosomal dominant corneal dystrophies map to chromosome 5q.
    Stone EM; Mathers WD; Rosenwasser GO; Holland EJ; Folberg R; Krachmer JH; Nichols BE; Gorevic PD; Taylor CM; Streb LM
    Nat Genet; 1994 Jan; 6(1):47-51. PubMed ID: 8136834
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. Anticipation in familial lattice corneal dystrophy type I with R124C mutation in the TGFBI (BIGH3) gene.
    Romero P; Vogel M; Diaz JM; Romero MP; Herrera L
    Mol Vis; 2008 May; 14():829-35. PubMed ID: 18470323
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Genes in dizygote twins with Bowman layer corneal dystrophy.
    Hou YC; Hu FR; Wang IJ
    Optom Vis Sci; 2015 Apr; 92(4 Suppl 1):S20-4. PubMed ID: 25785536
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Two mutations in the TGFBI (BIGH3) gene associated with lattice corneal dystrophy in an extensively studied family.
    Klintworth GK; Bao W; Afshari NA
    Invest Ophthalmol Vis Sci; 2004 May; 45(5):1382-8. PubMed ID: 15111592
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A new, X-linked endothelial corneal dystrophy.
    Schmid E; Lisch W; Philipp W; Lechner S; Göttinger W; Schlötzer-Schrehardt U; Müller T; Utermann G; Janecke AR
    Am J Ophthalmol; 2006 Mar; 141(3):478-487. PubMed ID: 16490493
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Missense mutations in COL8A2, the gene encoding the alpha2 chain of type VIII collagen, cause two forms of corneal endothelial dystrophy.
    Biswas S; Munier FL; Yardley J; Hart-Holden N; Perveen R; Cousin P; Sutphin JE; Noble B; Batterbury M; Kielty C; Hackett A; Bonshek R; Ridgway A; McLeod D; Sheffield VC; Stone EM; Schorderet DF; Black GC
    Hum Mol Genet; 2001 Oct; 10(21):2415-23. PubMed ID: 11689488
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Heredity and in vivo confocal microscopy of punctiform and polychromatic pre-Descemet dystrophy.
    Henríquez-Recine MA; Marquina-Lima KS; Vallespín-García E; García-Miñaur S; Benitez Del Castillo JM; Boto de Los Bueis A
    Graefes Arch Clin Exp Ophthalmol; 2018 Sep; 256(9):1661-1667. PubMed ID: 29728753
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Corneal dystrophies.
    Klintworth GK
    Orphanet J Rare Dis; 2009 Feb; 4():7. PubMed ID: 19236704
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Mapping of Reis-Bücklers' corneal dystrophy to chromosome 5q.
    Small KW; Mullen L; Barletta J; Graham K; Glasgow B; Stern G; Yee R
    Am J Ophthalmol; 1996 Apr; 121(4):384-90. PubMed ID: 8604731
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A subset of patients with epithelial basement membrane corneal dystrophy have mutations in TGFBI/BIGH3.
    Boutboul S; Black GC; Moore JE; Sinton J; Menasche M; Munier FL; Laroche L; Abitbol M; Schorderet DF
    Hum Mutat; 2006 Jun; 27(6):553-7. PubMed ID: 16652336
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Variant lattice corneal dystrophy associated with compound heterozygous mutations in the
    Ann LB; Abbouda A; Frausto RF; Huseynli S; Gupta K; Alió JL; Aldave AJ
    Br J Ophthalmol; 2017 Apr; 101(4):509-513. PubMed ID: 27402970
    [TBL] [Abstract][Full Text] [Related]  

  • 36. 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]  

  • 37. Granular corneal dystrophy with homozygous mutations in the kerato-epithelin gene.
    Okada M; Yamamoto S; Watanabe H; Inoue Y; Tsujikawa M; Maeda N; Shimomura Y; Nishida K; Kinoshita S; Tano Y
    Am J Ophthalmol; 1998 Aug; 126(2):169-76. PubMed ID: 9727509
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Transforming growth factor beta-induced p.(L558P) variant is associated with autosomal dominant lattice corneal dystrophy type IV in a large cohort of Spanish patients.
    Campos-Mollo E; Varela-Conde Y; Arriola-Villalobos P; Cabrera-Beyrouti R; Benítez-Del-Castillo JM; Maldonado MJ; Escribano J
    Clin Exp Ophthalmol; 2019 Sep; 47(7):871-880. PubMed ID: 31056827
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Clinical and genetic profile of Avellino corneal dystrophy in 2 families from north India.
    Paliwal P; Gupta J; Tandon R; Sharma A; Vajpayee RB
    Arch Ophthalmol; 2009 Oct; 127(10):1373-6. PubMed ID: 19822856
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Coexistence of Meesmann Corneal Dystrophy and a Pseudo-Unilateral Lattice Corneal Dystrophy in a Patient With a Novel Pathogenic Variant in the Keratin K3 Gene: A Case Report.
    Abad-Morales V; Barbany M; Gris O; Güell JL; Pomares E
    Cornea; 2021 Mar; 40(3):370-372. PubMed ID: 33346999
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.