BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

134 related articles for article (PubMed ID: 14630904)

  • 1. Novel identification of a four-base-pair deletion mutation in PITX2 in a Rieger syndrome family.
    Wang Y; Zhao H; Zhang X; Feng H
    J Dent Res; 2003 Dec; 82(12):1008-12. PubMed ID: 14630904
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Morphology of the sella turcica in Axenfeld-Rieger syndrome with PITX2 mutation.
    Meyer-Marcotty P; Weisschuh N; Dressler P; Hartmann J; Stellzig-Eisenhauer A
    J Oral Pathol Med; 2008 Sep; 37(8):504-10. PubMed ID: 18331556
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Identification of the first intragenic deletion of the PITX2 gene causing an Axenfeld-Rieger Syndrome: case report.
    de la Houssaye G; Bieche I; Roche O; Vieira V; Laurendeau I; Arbogast L; Zeghidi H; Rapp P; Halimi P; Vidaud M; Dufier JL; Menasche M; Abitbol M
    BMC Med Genet; 2006 Nov; 7():82. PubMed ID: 17134502
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of a novel frameshift mutation in PITX2 gene in a Chinese family with Axenfeld-Rieger syndrome.
    Yin HF; Fang XY; Jin CF; Yin JF; Li JY; Zhao SJ; Miao Q; Song FW
    J Zhejiang Univ Sci B; 2014 Jan; 15(1):43-50. PubMed ID: 24390743
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A novel mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome.
    Brooks BP; Moroi SE; Downs CA; Wiltse S; Othman MI; Semina EV; Richards JE
    Ophthalmic Genet; 2004 Mar; 25(1):57-62. PubMed ID: 15255117
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.
    Seifi M; Footz T; Taylor SA; Elhady GM; Abdalla EM; Walter MA
    Acta Ophthalmol; 2016 Nov; 94(7):e571-e579. PubMed ID: 27009473
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A novel PITX2 mutation and a polymorphism in a 5-generation family with Axenfeld-Rieger anomaly and coexisting Fuchs' endothelial dystrophy.
    Kniestedt C; Taralczak M; Thiel MA; Stuermer J; Baumer A; Gloor BP
    Ophthalmology; 2006 Oct; 113(10):1791.e1-8. PubMed ID: 16876867
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel PITX2 mutation in non-syndromic orodental anomalies.
    Intarak N; Theerapanon T; Ittiwut C; Suphapeetiporn K; Porntaveetus T; Shotelersuk V
    Oral Dis; 2018 May; 24(4):611-618. PubMed ID: 29121437
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Novel mutations of FOXC1 and PITX2 in patients with Axenfeld-Rieger malformations.
    Weisschuh N; Dressler P; Schuettauf F; Wolf C; Wissinger B; Gramer E
    Invest Ophthalmol Vis Sci; 2006 Sep; 47(9):3846-52. PubMed ID: 16936096
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. A novel PITX2 mutation in a Chinese family with Axenfeld-Rieger syndrome.
    Li D; Zhu Q; Lin H; Zhou N; Qi Y
    Mol Vis; 2008; 14():2205-10. PubMed ID: 19052653
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Four novel mutations in the PITX2 gene in patients with Axenfeld-Rieger syndrome.
    Phillips JC
    Ophthalmic Res; 2002; 34(5):324-6. PubMed ID: 12381896
    [TBL] [Abstract][Full Text] [Related]  

  • 14. MSX1 gene is deleted in Wolf-Hirschhorn syndrome patients with oligodontia.
    Nieminen P; Kotilainen J; Aalto Y; Knuutila S; Pirinen S; Thesleff I
    J Dent Res; 2003 Dec; 82(12):1013-7. PubMed ID: 14630905
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A novel homeobox mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome associated with brain, ocular, and dental phenotypes.
    Idrees F; Bloch-Zupan A; Free SL; Vaideanu D; Thompson PJ; Ashley P; Brice G; Rutland P; Bitner-Glindzicz M; Khaw PT; Fraser S; Sisodiya SM; Sowden JC
    Am J Med Genet B Neuropsychiatr Genet; 2006 Mar; 141B(2):184-91. PubMed ID: 16389592
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 4q25 microdeletion encompassing PITX2: A patient presenting with tetralogy of Fallot and dental anomalies without ocular features.
    Vande Perre P; Zazo Seco C; Patat O; Bouneau L; Vigouroux A; Bourgeois D; El Hout S; Chassaing N; Calvas P
    Eur J Med Genet; 2018 Feb; 61(2):72-78. PubMed ID: 29100920
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Novel PITX2 mutations identified in Axenfeld-Rieger syndrome and the pattern of PITX2-related tooth agenesis.
    Fan Z; Sun S; Liu H; Yu M; Liu Z; Wong SW; Liu Y; Han D; Feng H
    Oral Dis; 2019 Nov; 25(8):2010-2019. PubMed ID: 31529555
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Novel c.300_301delinsT mutation in PITX2 in a Korean family with Axenfeld-Rieger syndrome.
    Yun JW; Cho HK; Oh SY; Ki CS; Kee C
    Ann Lab Med; 2013 Sep; 33(5):360-3. PubMed ID: 24003428
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Analysis of RNA splicing defects in PITX2 mutants supports a gene dosage model of Axenfeld-Rieger syndrome.
    Maciolek NL; Alward WL; Murray JC; Semina EV; McNally MT
    BMC Med Genet; 2006 Jul; 7():59. PubMed ID: 16834779
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.