BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

209 related articles for article (PubMed ID: 19509472)

  • 1. Heparan sulfate deficiency leads to Peters anomaly in mice by disturbing neural crest TGF-beta2 signaling.
    Iwao K; Inatani M; Matsumoto Y; Ogata-Iwao M; Takihara Y; Irie F; Yamaguchi Y; Okinami S; Tanihara H
    J Clin Invest; 2009 Jul; 119(7):1997-2008. PubMed ID: 19509472
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Exploration of the molecular mechanism of ocular development and the creation of animal models for ocular diseases].
    Inatani M
    Nippon Ganka Gakkai Zasshi; 2010 Mar; 114(3):280-96; discussion 297. PubMed ID: 20387539
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Conditional deletion of AP-2β in mouse cranial neural crest results in anterior segment dysgenesis and early-onset glaucoma.
    Martino VB; Sabljic T; Deschamps P; Green RM; Akula M; Peacock E; Ball A; Williams T; West-Mays JA
    Dis Model Mech; 2016 Aug; 9(8):849-61. PubMed ID: 27483349
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Compound developmental eye disorders following inactivation of TGFbeta signaling in neural-crest stem cells.
    Ittner LM; Wurdak H; Schwerdtfeger K; Kunz T; Ille F; Leveen P; Hjalt TA; Suter U; Karlsson S; Hafezi F; Born W; Sommer L
    J Biol; 2005; 4(3):11. PubMed ID: 16403239
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Targeted overexpression of TGF-α in the corneal epithelium of adult transgenic mice induces changes in anterior segment morphology and activates noncanonical Wnt signaling.
    Yuan Y; Yeh LK; Liu H; Yamanaka O; Hardie WD; Kao WW; Liu CY
    Invest Ophthalmol Vis Sci; 2013 Mar; 54(3):1829-37. PubMed ID: 23412089
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Primary cilia deficiency in neural crest cells models anterior segment dysgenesis in mouse.
    Portal C; Rompolas P; Lwigale P; Iomini C
    Elife; 2019 Dec; 8():. PubMed ID: 31845891
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Foxc1 and Foxc2 in the Neural Crest Are Required for Ocular Anterior Segment Development.
    Seo S; Chen L; Liu W; Zhao D; Schultz KM; Sasman A; Liu T; Zhang HF; Gage PJ; Kume T
    Invest Ophthalmol Vis Sci; 2017 Mar; 58(3):1368-1377. PubMed ID: 28253399
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Heparan sulfate deficiency in periocular mesenchyme causes microphthalmia and ciliary body dysgenesis.
    Iwao K; Inatani M; Ogata-Iwao M; Yamaguchi Y; Okinami S; Tanihara H
    Exp Eye Res; 2010 Jan; 90(1):81-8. PubMed ID: 19782070
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Development of the iridocorneal angle and congenital glaucoma].
    Tamm ER
    Ophthalmologe; 2011 Jul; 108(7):610-4, 616-7. PubMed ID: 21796509
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Anterior segment development relevant to glaucoma.
    Gould DB; Smith RS; John SW
    Int J Dev Biol; 2004; 48(8-9):1015-29. PubMed ID: 15558492
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Functional interactions between FOXC1 and PITX2 underlie the sensitivity to FOXC1 gene dose in Axenfeld-Rieger syndrome and anterior segment dysgenesis.
    Berry FB; Lines MA; Oas JM; Footz T; Underhill DA; Gage PJ; Walter MA
    Hum Mol Genet; 2006 Mar; 15(6):905-19. PubMed ID: 16449236
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Structural assessment of PITX2, FOXC1, CYP1B1, and GJA1 genes in patients with Axenfeld-Rieger syndrome with developmental glaucoma.
    Cella W; de Vasconcellos JP; de Melo MB; Kneipp B; Costa FF; Longui CA; Costa VP
    Invest Ophthalmol Vis Sci; 2006 May; 47(5):1803-9. PubMed ID: 16638984
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Axenfeld-Rieger syndrome. A spectrum of developmental disorders.
    Shields MB; Buckley E; Klintworth GK; Thresher R
    Surv Ophthalmol; 1985; 29(6):387-409. PubMed ID: 3892740
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Expression of the homeobox gene Pitx2 in neural crest is required for optic stalk and ocular anterior segment development.
    Evans AL; Gage PJ
    Hum Mol Genet; 2005 Nov; 14(22):3347-59. PubMed ID: 16203745
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.
    Vieira V; David G; Roche O; de la Houssaye G; Boutboul S; Arbogast L; Kobetz A; Orssaud C; Camand O; Schorderet DF; Munier F; Rossi A; Delezoide AL; Marsac C; Ricquier D; Dufier JL; Menasche M; Abitbol M
    Mol Vis; 2006 Dec; 12():1448-60. PubMed ID: 17167399
    [TBL] [Abstract][Full Text] [Related]  

  • 17. New hypothesis of developmental anomalies of the anterior chamber associated with glaucoma.
    Kupfer C; Kaiser-Kupfer MI
    Trans Ophthalmol Soc U K (1962); 1978; 98(2):213-5. PubMed ID: 286450
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Pax6 heterozygous eyes show defects in chamber angle differentiation that are associated with a wide spectrum of other anterior eye segment abnormalities.
    Baulmann DC; Ohlmann A; Flügel-Koch C; Goswami S; Cvekl A; Tamm ER
    Mech Dev; 2002 Oct; 118(1-2):3-17. PubMed ID: 12351165
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular and developmental mechanisms of anterior segment dysgenesis.
    Sowden JC
    Eye (Lond); 2007 Oct; 21(10):1310-8. PubMed ID: 17914434
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Potential role for Ext1-dependent heparan sulfate in regulating P311 gene expression in A549 carcinoma cells.
    Katta K; Sembajwe LF; Kusche-Gullberg M
    Biochim Biophys Acta Gen Subj; 2018 Jun; 1862(6):1472-1481. PubMed ID: 29580921
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.