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 *

318 related articles for article (PubMed ID: 21278591)

  • 1. Axenfeld-Rieger syndrome in monozygotic twins.
    Ma J; Zhong Y; Zhao C; Zhang X; Sui R; Chu P; Zhao J
    J Glaucoma; 2011 Dec; 20(9):584-6. PubMed ID: 21278591
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. A novel mutation in the FOXC1 gene in a family with Axenfeld-Rieger syndrome and Peters' anomaly.
    Weisschuh N; Wolf C; Wissinger B; Gramer E
    Clin Genet; 2008 Nov; 74(5):476-80. PubMed ID: 18498376
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Novel mutation in FOXC1 wing region causing Axenfeld-Rieger anomaly.
    Panicker SG; Sampath S; Mandal AK; Reddy AB; Ahmed N; Hasnain SE
    Invest Ophthalmol Vis Sci; 2002 Dec; 43(12):3613-6. PubMed ID: 12454026
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Axenfeld-Rieger syndrome: new perspectives.
    Chang TC; Summers CG; Schimmenti LA; Grajewski AL
    Br J Ophthalmol; 2012 Mar; 96(3):318-22. PubMed ID: 22199394
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Axenfeld-Rieger syndrome in the age of molecular genetics.
    Alward WL
    Am J Ophthalmol; 2000 Jul; 130(1):107-15. PubMed ID: 11004268
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Screening for mutations of Axenfeld-Rieger syndrome caused by FOXC1 gene in Japanese patients.
    Kawase C; Kawase K; Taniguchi T; Sugiyama K; Yamamoto T; Kitazawa Y; Alward WL; Stone EM; Nishimura DY; Sheffield VC
    J Glaucoma; 2001 Dec; 10(6):477-82. PubMed ID: 11740218
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Molecular characterization of Axenfeld-Rieger spectrum and other anterior segment dysgeneses in a sample of Mexican patients.
    Hernández-Martínez N; González-Del Angel A; Alcántara-Ortigoza MA; González-Huerta LM; Cuevas-Covarrubias SA; Villanueva-Mendoza C
    Ophthalmic Genet; 2018 Dec; 39(6):728-734. PubMed ID: 30457409
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A family with Axenfeld-Rieger syndrome and Peters Anomaly caused by a point mutation (Phe112Ser) in the FOXC1 gene.
    Honkanen RA; Nishimura DY; Swiderski RE; Bennett SR; Hong S; Kwon YH; Stone EM; Sheffield VC; Alward WL
    Am J Ophthalmol; 2003 Mar; 135(3):368-75. PubMed ID: 12614756
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Genetic analysis of PITX2 and FOXC1 in Rieger Syndrome patients from Brazil.
    Borges AS; Susanna R; Carani JC; Betinjane AJ; Alward WL; Stone EM; Sheffield VC; Nishimura DY
    J Glaucoma; 2002 Feb; 11(1):51-6. PubMed ID: 11821690
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25.
    Mirzayans F; Gould DB; Héon E; Billingsley GD; Cheung JC; Mears AJ; Walter MA
    Eur J Hum Genet; 2000 Jan; 8(1):71-4. PubMed ID: 10713890
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Cardiac anomalies in Axenfeld-Rieger syndrome due to a novel FOXC1 mutation.
    Gripp KW; Hopkins E; Jenny K; Thacker D; Salvin J
    Am J Med Genet A; 2013 Jan; 161A(1):114-9. PubMed ID: 23239455
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutation spectrum of FOXC1 and clinical genetic heterogeneity of Axenfeld-Rieger anomaly in India.
    Komatireddy S; Chakrabarti S; Mandal AK; Reddy AB; Sampath S; Panicker SG; Balasubramanian D
    Mol Vis; 2003 Feb; 9():43-8. PubMed ID: 12592227
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.