BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

117 related articles for article (PubMed ID: 25809640)

  • 21. Ocular developmental abnormalities and glaucoma associated with interstitial 6p25 duplications and deletions.
    Lehmann OJ; Ebenezer ND; Ekong R; Ocaka L; Mungall AJ; Fraser S; McGill JI; Hitchings RA; Khaw PT; Sowden JC; Povey S; Walter MA; Bhattacharya SS; Jordan T
    Invest Ophthalmol Vis Sci; 2002 Jun; 43(6):1843-9. PubMed ID: 12036988
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Human p32 is a novel FOXC1-interacting protein that regulates FOXC1 transcriptional activity in ocular cells.
    Huang L; Chi J; Berry FB; Footz TK; Sharp MW; Walter MA
    Invest Ophthalmol Vis Sci; 2008 Dec; 49(12):5243-9. PubMed ID: 18676636
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants.
    Souzeau E; Siggs OM; Zhou T; Galanopoulos A; Hodson T; Taranath D; Mills RA; Landers J; Pater J; Smith JE; Elder JE; Rait JL; Giles P; Phakey V; Staffieri SE; Kearns LS; Dubowsky A; Mackey DA; Hewitt AW; Ruddle JB; Burdon KP; Craig JE
    Eur J Hum Genet; 2017 Jun; 25(7):839-847. PubMed ID: 28513611
    [TBL] [Abstract][Full Text] [Related]  

  • 24. FOXC1 is required for cell viability and resistance to oxidative stress in the eye through the transcriptional regulation of FOXO1A.
    Berry FB; Skarie JM; Mirzayans F; Fortin Y; Hudson TJ; Raymond V; Link BA; Walter MA
    Hum Mol Genet; 2008 Feb; 17(4):490-505. PubMed ID: 17993506
    [TBL] [Abstract][Full Text] [Related]  

  • 25. FOXC1 variant in a family with anterior segment dysgenesis and normal-tension glaucoma.
    Or L; Barkana Y; Hecht I; Weiner C; Einan-Lifshitz A; Pras E
    Exp Eye Res; 2020 Nov; 200():108220. PubMed ID: 32905845
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. Axenfeld-Rieger anomaly: a novel mutation in the forkhead box C1 (FOXC1) gene in a 4-generation family.
    Mortemousque B; Amati-Bonneau P; Couture F; Graffan R; Dubois S; Colin J; Bonneau D; Morissette J; Lacombe D; Raymond V
    Arch Ophthalmol; 2004 Oct; 122(10):1527-33. PubMed ID: 15477465
    [TBL] [Abstract][Full Text] [Related]  

  • 28. The transcription factor gene FOXC1 exhibits a limited role in primary congenital glaucoma.
    Chakrabarti S; Kaur K; Rao KN; Mandal AK; Kaur I; Parikh RS; Thomas R
    Invest Ophthalmol Vis Sci; 2009 Jan; 50(1):75-83. PubMed ID: 18708620
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. Severe molecular defects of a novel FOXC1 W152G mutation result in aniridia.
    Ito YA; Footz TK; Berry FB; Mirzayans F; Yu M; Khan AO; Walter MA
    Invest Ophthalmol Vis Sci; 2009 Aug; 50(8):3573-9. PubMed ID: 19279310
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Haploinsufficiency of the transcription factors FOXC1 and FOXC2 results in aberrant ocular development.
    Smith RS; Zabaleta A; Kume T; Savinova OV; Kidson SH; Martin JE; Nishimura DY; Alward WL; Hogan BL; John SW
    Hum Mol Genet; 2000 Apr; 9(7):1021-32. PubMed ID: 10767326
    [TBL] [Abstract][Full Text] [Related]  

  • 32. FOXC1 modulates MYOC secretion through regulation of the exocytic proteins RAB3GAP1, RAB3GAP2 and SNAP25.
    Rasnitsyn A; Doucette L; Seifi M; Footz T; Raymond V; Walter MA
    PLoS One; 2017; 12(6):e0178518. PubMed ID: 28575017
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Structural and functional analyses of disease-causing missense mutations in the forkhead domain of FOXC1.
    Saleem RA; Banerjee-Basu S; Berry FB; Baxevanis AD; Walter MA
    Hum Mol Genet; 2003 Nov; 12(22):2993-3005. PubMed ID: 14506133
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Molecular analysis of FOXC1 in subjects presenting with severe developmental eye anomalies.
    Kaur K; Ragge NK; Ragoussis J
    Mol Vis; 2009 Jul; 15():1366-73. PubMed ID: 19626132
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A Novel Mutation of FOXC1 (R127L) in an Axenfeld-Rieger Syndrome Family with Glaucoma and Multiple Congenital Heart Diseases.
    Du RF; Huang H; Fan LL; Li XP; Xia K; Xiang R
    Ophthalmic Genet; 2016; 37(1):111-5. PubMed ID: 24914578
    [No Abstract]   [Full Text] [Related]  

  • 36. 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]  

  • 37. Childhood glaucoma genes and phenotypes: Focus on FOXC1 mutations causing anterior segment dysgenesis and hearing loss.
    Gauthier AC; Wiggs JL
    Exp Eye Res; 2020 Jan; 190():107893. PubMed ID: 31836490
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Axenfeld-Rieger syndrome-associated mutants of the transcription factor FOXC1 abnormally regulate
    Zhang Q; Liang D; Yue Y; He L; Li N; Jiang D; Hu P; Zhao Q
    J Biol Chem; 2020 Aug; 295(33):11902-11913. PubMed ID: 32631953
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. A novel variant in FOXC1 associated with atypical Axenfeld-Rieger syndrome.
    Wang R; Wang WQ; Li XQ; Zhao J; Yang K; Feng Y; Guo MM; Liu M; Liu X; Wang X; Yuan YY; Gao X; Xu JC
    BMC Med Genomics; 2021 Nov; 14(1):277. PubMed ID: 34809627
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.