BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

208 related articles for article (PubMed ID: 29660784)

  • 21. Zebrafish anterior segment mesenchyme progenitors are defined by function of tfap2a but not sox10.
    Vöcking O; Van Der Meulen K; Patel MK; Famulski JK
    Differentiation; 2023; 130():32-42. PubMed ID: 36563566
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Novel CYP1B1 and known PAX6 mutations in anterior segment dysgenesis (ASD).
    Chavarria-Soley G; Michels-Rautenstrauss K; Caliebe A; Kautza M; Mardin C; Rautenstrauss B
    J Glaucoma; 2006 Dec; 15(6):499-504. PubMed ID: 17106362
    [TBL] [Abstract][Full Text] [Related]  

  • 23. 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]  

  • 24. 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]  

  • 25. Generation and validation of a PITX2-EGFP reporter line of human induced pluripotent stem cells enables isolation of periocular mesenchymal cells.
    Okubo T; Hayashi R; Shibata S; Kudo Y; Ishikawa Y; Inoue S; Kobayashi Y; Honda A; Honma Y; Kawasaki S; Nishida K
    J Biol Chem; 2020 Mar; 295(11):3456-3465. PubMed ID: 32034090
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The Ocular Neural Crest: Specification, Migration, and Then What?
    Williams AL; Bohnsack BL
    Front Cell Dev Biol; 2020; 8():595896. PubMed ID: 33425902
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The homeobox gene Six3 is a potential regulator of anterior segment formation in the chick eye.
    Hsieh YW; Zhang XM; Lin E; Oliver G; Yang XJ
    Dev Biol; 2002 Aug; 248(2):265-80. PubMed ID: 12167403
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Genomics and anterior segment dysgenesis: a review.
    Ito YA; Walter MA
    Clin Exp Ophthalmol; 2014; 42(1):13-24. PubMed ID: 24433355
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Genotype-phenotype correlations in Axenfeld-Rieger malformation and glaucoma patients with FOXC1 and PITX2 mutations.
    Strungaru MH; Dinu I; Walter MA
    Invest Ophthalmol Vis Sci; 2007 Jan; 48(1):228-37. PubMed ID: 17197537
    [TBL] [Abstract][Full Text] [Related]  

  • 30. A new autosomal dominant Peters' anomaly phenotype expanding the anterior segment dysgenesis spectrum.
    Berker N; Alanay Y; Elgin U; Volkan-Salanci B; Simsek T; Akarsu N; Alikasifoglu M
    Acta Ophthalmol; 2009 Feb; 87(1):52-7. PubMed ID: 18616618
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A novel mouse model of anterior segment dysgenesis (ASD): conditional deletion of
    Hägglund AC; Jones I; Carlsson L
    Dis Model Mech; 2017 Mar; 10(3):245-257. PubMed ID: 28250050
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Role of the neural crest in anterior segment development and disease.
    Beauchamp GR; Knepper PA
    J Pediatr Ophthalmol Strabismus; 1984; 21(6):209-14. PubMed ID: 6502411
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Evaluating neural crest cell migration in a Col4a1 mutant mouse model of ocular anterior segment dysgenesis.
    Cozzitorto C; Peltz Z; Flores LM; Della Santina L; Mao M; Gould DB
    Cells Dev; 2024 May; ():203926. PubMed ID: 38729574
    [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. Anterior eye development and ocular mesenchyme: new insights from mouse models and human diseases.
    Cvekl A; Tamm ER
    Bioessays; 2004 Apr; 26(4):374-86. PubMed ID: 15057935
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Impairing retinoic acid signalling in the neural crest cells is sufficient to alter entire eye morphogenesis.
    Matt N; Ghyselinck NB; Pellerin I; Dupé V
    Dev Biol; 2008 Aug; 320(1):140-8. PubMed ID: 18539269
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Mutation Survey of Candidate Genes and Genotype-Phenotype Analysis in 20 Southeastern Chinese Patients with Axenfeld-Rieger Syndrome.
    Wang X; Liu X; Huang L; Fang S; Jia X; Xiao X; Li S; Guo X
    Curr Eye Res; 2018 Nov; 43(11):1334-1341. PubMed ID: 29939776
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Forkhead box transcription factor FoxC1 preserves corneal transparency by regulating vascular growth.
    Seo S; Singh HP; Lacal PM; Sasman A; Fatima A; Liu T; Schultz KM; Losordo DW; Lehmann OJ; Kume T
    Proc Natl Acad Sci U S A; 2012 Feb; 109(6):2015-20. PubMed ID: 22171010
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Identification of the IRXB gene cluster as candidate genes in severe dysgenesis of the ocular anterior segment.
    Chaabouni M; Etchevers H; De Blois MC; Calvas P; Waill-Perrier MC; Vekemans M; Romana SP
    Invest Ophthalmol Vis Sci; 2010 Sep; 51(9):4380-6. PubMed ID: 20164457
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Molecular genetics of Axenfeld-Rieger malformations.
    Lines MA; Kozlowski K; Walter MA
    Hum Mol Genet; 2002 May; 11(10):1177-84. PubMed ID: 12015277
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.