451 related articles for article (PubMed ID: 11980846)
1. Foxe3 haploinsufficiency in mice: a model for Peters' anomaly.
Ormestad M; Blixt A; Churchill A; Martinsson T; Enerbäck S; Carlsson P
Invest Ophthalmol Vis Sci; 2002 May; 43(5):1350-7. PubMed ID: 11980846
[TBL] [Abstract][Full Text] [Related]
2. Abnormal eye development associated with Cat4a, a dominant mouse cataract mutation on chromosome 8.
Grimes PA; Koeberlein B; Favor J; Neuhäuser-Klaus A; Stambolian D
Invest Ophthalmol Vis Sci; 1998 Sep; 39(10):1863-9. PubMed ID: 9727409
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. A forkhead gene, FoxE3, is essential for lens epithelial proliferation and closure of the lens vesicle.
Blixt A; Mahlapuu M; Aitola M; Pelto-Huikko M; Enerbäck S; Carlsson P
Genes Dev; 2000 Jan; 14(2):245-54. PubMed ID: 10652278
[TBL] [Abstract][Full Text] [Related]
5. Loss of Msx2 function down-regulates the FoxE3 expression and results in anterior segment dysgenesis resembling Peters anomaly.
Zhao J; Kawai K; Wang H; Wu D; Wang M; Yue Z; Zhang J; Liu YH
Am J Pathol; 2012 Jun; 180(6):2230-9. PubMed ID: 22503753
[TBL] [Abstract][Full Text] [Related]
6. A novel, non-stop mutation in FOXE3 causes an autosomal dominant form of variable anterior segment dysgenesis including Peters anomaly.
Doucette L; Green J; Fernandez B; Johnson GJ; Parfrey P; Young TL
Eur J Hum Genet; 2011 Mar; 19(3):293-9. PubMed ID: 21150893
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Foxe3 is required for morphogenesis and differentiation of the anterior segment of the eye and is sensitive to Pax6 gene dosage.
Blixt A; Landgren H; Johansson BR; Carlsson P
Dev Biol; 2007 Feb; 302(1):218-29. PubMed ID: 17064680
[TBL] [Abstract][Full Text] [Related]
9. Mutations at the PAX6 locus are found in heterogeneous anterior segment malformations including Peters' anomaly.
Hanson IM; Fletcher JM; Jordan T; Brown A; Taylor D; Adams RJ; Punnett HH; van Heyningen V
Nat Genet; 1994 Feb; 6(2):168-73. PubMed ID: 8162071
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. PAX 6 is normal in most cases of Peters' anomaly.
Churchill AJ; Booth AP; Anwar R; Markham AF
Eye (Lond); 1998; 12 ( Pt 2)():299-303. PubMed ID: 9683959
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. A dominant mutation within the DNA-binding domain of the bZIP transcription factor Maf causes murine cataract and results in selective alteration in DNA binding.
Lyon MF; Jamieson RV; Perveen R; Glenister PH; Griffiths R; Boyd Y; Glimcher LH; Favor J; Munier FL; Black GC
Hum Mol Genet; 2003 Mar; 12(6):585-94. PubMed ID: 12620964
[TBL] [Abstract][Full Text] [Related]
14. First evidence of SOX2 mutations in Peters' anomaly: Lessons from molecular screening of 95 patients.
Chesneau B; Aubert-Mucca M; Fremont F; Pechmeja J; Soler V; Isidor B; Nizon M; Dollfus H; Kaplan J; Fares-Taie L; Rozet JM; Busa T; Lacombe D; Naudion S; Amiel J; Rio M; Attie-Bitach T; Lesage C; Thouvenin D; Odent S; Morel G; Vincent-Delorme C; Boute O; Vanlerberghe C; Dieux A; Boussion S; Faivre L; Pinson L; Laffargue F; Le Guyader G; Le Meur G; Prieur F; Lambert V; Laudier B; Cottereau E; Ayuso C; Corton-Pérez M; Bouneau L; Le Caignec C; Gaston V; Jeanton-Scaramouche C; Dupin-Deguine D; Calvas P; Chassaing N; Plaisancié J
Clin Genet; 2022 May; 101(5-6):494-506. PubMed ID: 35170016
[TBL] [Abstract][Full Text] [Related]
15. Whole exome sequence analysis of Peters anomaly.
Weh E; Reis LM; Happ HC; Levin AV; Wheeler PG; David KL; Carney E; Angle B; Hauser N; Semina EV
Hum Genet; 2014 Dec; 133(12):1497-511. PubMed ID: 25182519
[TBL] [Abstract][Full Text] [Related]
16. Characterization of a new, dominant V124E mutation in the mouse alphaA-crystallin-encoding gene.
Graw J; Löster J; Soewarto D; Fuchs H; Meyer B; Reis A; Wolf E; Balling R; Hrabé de Angelis M
Invest Ophthalmol Vis Sci; 2001 Nov; 42(12):2909-15. PubMed ID: 11687536
[TBL] [Abstract][Full Text] [Related]
17. Mutations in the human forkhead transcription factor FOXE3 associated with anterior segment ocular dysgenesis and cataracts.
Semina EV; Brownell I; Mintz-Hittner HA; Murray JC; Jamrich M
Hum Mol Genet; 2001 Feb; 10(3):231-6. PubMed ID: 11159941
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Bilateral anterior segment dysgenesis with the presumed Peters' anomaly in a cat.
Park S; Kim K; Kim Y; Seo K
J Vet Med Sci; 2018 Feb; 80(2):297-301. PubMed ID: 29249729
[TBL] [Abstract][Full Text] [Related]
20. Anterior segment dysgenesis (Peters' anomaly) in two snow leopard (Panthera uncia) cubs.
Hamoudi H; Rudnick JC; Prause JU; Tauscher K; Breithaupt A; Teifke JP; Heegaard S
Vet Ophthalmol; 2013 Jul; 16 Suppl 1():130-4. PubMed ID: 23217015
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
