282 related articles for article (PubMed ID: 11740218)
1. 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]
2. 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]
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. 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]
5. 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]
6. 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]
7. 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]
8. 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]
9. 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]
10. 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]
11. A novel (Pro79Thr) mutation in the FKHL7 gene in a Japanese family with Axenfeld-Rieger syndrome.
Suzuki T; Takahashi K; Kuwahara S; Wada Y; Abe T; Tamai M
Am J Ophthalmol; 2001 Oct; 132(4):572-5. PubMed ID: 11589884
[TBL] [Abstract][Full Text] [Related]
12. 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]
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. Whole exome sequencing reveals a novel de novo FOXC1 mutation in a patient with unrecognized Axenfeld-Rieger syndrome and glaucoma.
Pasutto F; Mauri L; Popp B; Sticht H; Ekici A; Piozzi E; Bonfante A; Penco S; Schlötzer-Schrehardt U; Reis A
Gene; 2015 Aug; 568(1):76-80. PubMed ID: 25967385
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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]
17. 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]
18. 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]
19. 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]
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]