348 related articles for article (PubMed ID: 10767326)
1. 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]
2. 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]
3. Haploinsufficient Bmp4 ocular phenotypes include anterior segment dysgenesis with elevated intraocular pressure.
Chang B; Smith RS; Peters M; Savinova OV; Hawes NL; Zabaleta A; Nusinowitz S; Martin JE; Davisson ML; Cepko CL; Hogan BL; John SW
BMC Genet; 2001; 2():18. PubMed ID: 11722794
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. 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]
7. 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]
8. Murine forkhead/winged helix genes Foxc1 (Mf1) and Foxc2 (Mfh1) are required for the early organogenesis of the kidney and urinary tract.
Kume T; Deng K; Hogan BL
Development; 2000 Apr; 127(7):1387-95. PubMed ID: 10704385
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. 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]
12. 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]
13. 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]
14. Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly.
Mears AJ; Jordan T; Mirzayans F; Dubois S; Kume T; Parlee M; Ritch R; Koop B; Kuo WL; Collins C; Marshall J; Gould DB; Pearce W; Carlsson P; Enerbäck S; Morissette J; Bhattacharya S; Hogan B; Raymond V; Walter MA
Am J Hum Genet; 1998 Nov; 63(5):1316-28. PubMed ID: 9792859
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. Expression of the Mf1 gene in developing mouse hearts: implication in the development of human congenital heart defects.
Swiderski RE; Reiter RS; Nishimura DY; Alward WL; Kalenak JW; Searby CS; Stone EM; Sheffield VC; Lin JJ
Dev Dyn; 1999 Sep; 216(1):16-27. PubMed ID: 10474162
[TBL] [Abstract][Full Text] [Related]
18. The wing 2 region of the FOXC1 forkhead domain is necessary for normal DNA-binding and transactivation functions.
Murphy TC; Saleem RA; Footz T; Ritch R; McGillivray B; Walter MA
Invest Ophthalmol Vis Sci; 2004 Aug; 45(8):2531-8. PubMed ID: 15277473
[TBL] [Abstract][Full Text] [Related]
19. Foxc1 and Foxc2 in the Neural Crest Are Required for Ocular Anterior Segment Development.
Seo S; Chen L; Liu W; Zhao D; Schultz KM; Sasman A; Liu T; Zhang HF; Gage PJ; Kume T
Invest Ophthalmol Vis Sci; 2017 Mar; 58(3):1368-1377. PubMed ID: 28253399
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
