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 *

232 related articles for article (PubMed ID: 21907015)

  • 21. Congenital megalocornea with zonular weakness and childhood lens-related secondary glaucoma - a distinct phenotype caused by recessive LTBP2 mutations.
    Khan AO; Aldahmesh MA; Alkuraya FS
    Mol Vis; 2011; 17():2570-9. PubMed ID: 22025892
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Abnormal eye development associated with Cat4a, a dominant mouse cataract mutation on chromosome 8.
    Grimes PA; Koeberlein B; Favor J; Neuhäuser-Klaus A; Stambolian D
    Invest Ophthalmol Vis Sci; 1998 Sep; 39(10):1863-9. PubMed ID: 9727409
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Clinical features and outcome of corneal opacity associated with congenital glaucoma.
    Kim YJ; Jeoung JW; Kim MK; Park KH; Yu YS; Oh JY
    BMC Ophthalmol; 2018 Aug; 18(1):190. PubMed ID: 30068309
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Proprotein Convertase Processing Enhances Peroxidasin Activity to Reinforce Collagen IV.
    Colon S; Bhave G
    J Biol Chem; 2016 Nov; 291(46):24009-24016. PubMed ID: 27697841
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Genetic heterogeneity in microcornea-cataract: five novel mutations in CRYAA, CRYGD, and GJA8.
    Hansen L; Yao W; Eiberg H; Kjaer KW; Baggesen K; Hejtmancik JF; Rosenberg T
    Invest Ophthalmol Vis Sci; 2007 Sep; 48(9):3937-44. PubMed ID: 17724170
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Anterior segment dysgenesis after overexpression of transforming growth factor-beta-induced gene, beta igh3, in the mouse eye.
    Kim JE; Han MS; Bae YC; Kim HK; Kim TI; Kim EK; Kim IS
    Mol Vis; 2007 Oct; 13():1942-52. PubMed ID: 17982418
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Reduced expression of Pax6 in lens and cornea of mutant mice leads to failure of chamber angle development and juvenile glaucoma.
    Kroeber M; Davis N; Holzmann S; Kritzenberger M; Shelah-Goraly M; Ofri R; Ashery-Padan R; Tamm ER
    Hum Mol Genet; 2010 Sep; 19(17):3332-42. PubMed ID: 20538882
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Novel
    Panagiotou ES; Fernandez-Fuentes N; Farraj LA; McKibbin M; Elçioglu NH; Jafri H; Cerman E; Parry DA; Logan CV; Johnson CA; Inglehearn CF; Toomes C; Ali M
    Mol Vis; 2022; 28():57-69. PubMed ID: 35693420
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Two Paired Box 6 mutations identified in Chinese patients with classic congenital aniridia and cataract.
    Lin Y; Gao H; Zhu Y; Chen C; Li T; Liu B; Lyu C; Huang Y; Li H; Wu Q; Jin C; Liang X; Huang X; Lu L
    Mol Med Rep; 2018 Nov; 18(5):4439-4445. PubMed ID: 30221735
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Variable expressivity of autosomal dominant microcornea with cataract.
    Salmon JF; Wallis CE; Murray AD
    Arch Ophthalmol; 1988 Apr; 106(4):505-10. PubMed ID: 3355418
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Mutations in the human forkhead transcription factor FOXE3 associated with anterior segment ocular dysgenesis and cataracts.
    Semina EV; Brownell I; Mintz-Hittner HA; Murray JC; Jamrich M
    Hum Mol Genet; 2001 Feb; 10(3):231-6. PubMed ID: 11159941
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Biallelic Deletion of
    Kim HK; Ham KA; Lee SW; Choi HS; Kim HS; Kim HK; Shin HS; Seo KY; Cho Y; Nam KT; Kim IB; Joe YA
    Int J Mol Sci; 2019 Dec; 20(24):. PubMed ID: 31817535
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Cataract formation in Peter's anomaly after trabeculotomy.
    Mullaney P; al-Awad A
    Ophthalmic Surg; 1995; 26(3):267-6. PubMed ID: 7651700
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Novel anterior segment phenotypes resulting from forkhead gene alterations: evidence for cross-species conservation of function.
    Lehmann OJ; Tuft S; Brice G; Smith R; Blixt A; Bell R; Johansson B; Jordan T; Hitchings RA; Khaw PT; John SW; Carlsson P; Bhattacharya SS
    Invest Ophthalmol Vis Sci; 2003 Jun; 44(6):2627-33. PubMed ID: 12766066
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Case of lattice corneal dystrophy due to L527R mutation in the TGFBI gene with asymmetric corneal opacity in eye laterality.
    Ohnishi T; Sakimoto T; Sawa M
    Jpn J Ophthalmol; 2010 Nov; 54(6):628-9. PubMed ID: 21191728
    [No Abstract]   [Full Text] [Related]  

  • 36. [Vitreoretinochoroidal heredo-dystrophy, microcornea, glaucoma and cataract].
    François P; Puech B; Hache JC; Laffineur Q
    J Fr Ophtalmol; 1993; 16(1):29-40. PubMed ID: 8482797
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma.
    Micheal S; Siddiqui SN; Zafar SN; Villanueva-Mendoza C; Cortés-González V; Khan MI; den Hollander AI
    PLoS One; 2016; 11(7):e0160016. PubMed ID: 27463523
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A novel mutation in GJA8 causing congenital cataract-microcornea syndrome in a Chinese pedigree.
    Hu S; Wang B; Zhou Z; Zhou G; Wang J; Ma X; Qi Y
    Mol Vis; 2010 Aug; 16():1585-92. PubMed ID: 20806042
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Unilateral Peters' anomaly complicated by a corneal tattoo.
    Pomella KM; Wagner H
    Optom Vis Sci; 1998 Sep; 75(9):635-9. PubMed ID: 9778695
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Two distinct kerato-epithelin mutations in Reis-Bücklers corneal dystrophy.
    Okada M; Yamamoto S; Tsujikawa M; Watanabe H; Inoue Y; Maeda N; Shimomura Y; Nishida K; Quantock AJ; Kinoshita S; Tano Y
    Am J Ophthalmol; 1998 Oct; 126(4):535-42. PubMed ID: 9780098
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.