BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

347 related articles for article (PubMed ID: 25967385)

  • 21. Analyses of a novel L130F missense mutation in FOXC1.
    Ito YA; Footz TK; Murphy TC; Courtens W; Walter MA
    Arch Ophthalmol; 2007 Jan; 125(1):128-35. PubMed ID: 17210863
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Dysfunction of the stress-responsive FOXC1 transcription factor contributes to the earlier-onset glaucoma observed in Axenfeld-Rieger syndrome patients.
    Ito YA; Goping IS; Berry F; Walter MA
    Cell Death Dis; 2014 Feb; 5(2):e1069. PubMed ID: 24556684
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Novel mutations in the FOXC1 gene in Japanese patients with Axenfeld-Rieger syndrome.
    Fuse N; Takahashi K; Yokokura S; Nishida K
    Mol Vis; 2007 Jun; 13():1005-9. PubMed ID: 17653043
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. A Family with Axenfeld-Rieger Syndrome: Report of the Clinical and Genetic Findings.
    Yang HJ; Lee YK; Joo CK; Moon JI; Mok JW; Park MH
    Korean J Ophthalmol; 2015 Aug; 29(4):249-55. PubMed ID: 26240509
    [TBL] [Abstract][Full Text] [Related]  

  • 26. 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]  

  • 27. 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]  

  • 28. 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]  

  • 29. A novel forkhead box C1 gene mutation in a Korean family with Axenfeld-Rieger syndrome.
    Kim GN; Ki CS; Seo SW; Yoo JM; Han YS; Chung IY; Park JM; Kim SJ
    Mol Vis; 2013; 19():935-43. PubMed ID: 23687430
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The 6p25 deletion syndrome: An update on a rare neurocristopathy.
    de Vos IJ; Stegmann AP; Webers CA; Stumpel CT
    Ophthalmic Genet; 2017; 38(2):101-107. PubMed ID: 27070436
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Exome Sequencing in a Swiss Childhood Glaucoma Cohort Reveals
    Lang E; Koller S; Bähr L; Töteberg-Harms M; Atac D; Roulez F; Bahr A; Steindl K; Feil S; Berger W; Gerth-Kahlert C
    Transl Vis Sci Technol; 2020 Jun; 9(7):47. PubMed ID: 32832252
    [TBL] [Abstract][Full Text] [Related]  

  • 32. 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]  

  • 33. Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma.
    Siggs OM; Souzeau E; Pasutto F; Dubowsky A; Smith JEH; Taranath D; Pater J; Rait JL; Narita A; Mauri L; Del Longo A; Reis A; Chappell A; Kearns LS; Staffieri SE; Elder JE; Ruddle JB; Hewitt AW; Burdon KP; Mackey DA; Craig JE
    JAMA Ophthalmol; 2019 Apr; 137(4):348-355. PubMed ID: 30653210
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Identification and functional study of FOXC1 variants in Chinese families with glaucoma.
    Wang X; Liu X; Li Y; Yang B; Sun X; Yang P; Zhong Z; Chen J
    Am J Med Genet A; 2022 Feb; 188(2):540-547. PubMed ID: 34741396
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. 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]  

  • 37. Genotype-phenotype association of PITX2 and FOXC1 in Axenfeld-Rieger syndrome.
    Zhou L; Wang X; An J; Zhang Y; He M; Tang L
    Exp Eye Res; 2023 Jan; 226():109307. PubMed ID: 36442680
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. 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]  

  • 40. PITX2 and FOXC1 spectrum of mutations in ocular syndromes.
    Reis LM; Tyler RC; Volkmann Kloss BA; Schilter KF; Levin AV; Lowry RB; Zwijnenburg PJ; Stroh E; Broeckel U; Murray JC; Semina EV
    Eur J Hum Genet; 2012 Dec; 20(12):1224-33. PubMed ID: 22569110
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 18.