280 related articles for article (PubMed ID: 22303467)
1. pitx2 Deficiency results in abnormal ocular and craniofacial development in zebrafish.
Liu Y; Semina EV
PLoS One; 2012; 7(1):e30896. PubMed ID: 22303467
[TBL] [Abstract][Full Text] [Related]
2. A zebrafish model of axenfeld-rieger syndrome reveals that pitx2 regulation by retinoic acid is essential for ocular and craniofacial development.
Bohnsack BL; Kasprick DS; Kish PE; Goldman D; Kahana A
Invest Ophthalmol Vis Sci; 2012 Jan; 53(1):7-22. PubMed ID: 22125274
[TBL] [Abstract][Full Text] [Related]
3. PITX2 deficiency and associated human disease: insights from the zebrafish model.
Hendee KE; Sorokina EA; Muheisen SS; Reis LM; Tyler RC; Markovic V; Cuturilo G; Link BA; Semina EV
Hum Mol Genet; 2018 May; 27(10):1675-1695. PubMed ID: 29506241
[TBL] [Abstract][Full Text] [Related]
4. Knockdown of fbxl10/kdm2bb rescues chd7 morphant phenotype in a zebrafish model of CHARGE syndrome.
Balow SA; Pierce LX; Zentner GE; Conrad PA; Davis S; Sabaawy HE; McDermott BM; Scacheri PC
Dev Biol; 2013 Oct; 382(1):57-69. PubMed ID: 23920116
[TBL] [Abstract][Full Text] [Related]
5. Pegasus, the 'atypical' Ikaros family member, influences left-right asymmetry and regulates pitx2 expression.
John LB; Trengove MC; Fraser FW; Yoong SH; Ward AC
Dev Biol; 2013 May; 377(1):46-54. PubMed ID: 23499657
[TBL] [Abstract][Full Text] [Related]
6. Ambra1 knockdown in zebrafish leads to incomplete development due to severe defects in organogenesis.
Benato F; Skobo T; Gioacchini G; Moro I; Ciccosanti F; Piacentini M; Fimia GM; Carnevali O; Dalla Valle L
Autophagy; 2013 Apr; 9(4):476-95. PubMed ID: 23348054
[TBL] [Abstract][Full Text] [Related]
7. Potential novel mechanism for Axenfeld-Rieger syndrome: deletion of a distant region containing regulatory elements of PITX2.
Volkmann BA; Zinkevich NS; Mustonen A; Schilter KF; Bosenko DV; Reis LM; Broeckel U; Link BA; Semina EV
Invest Ophthalmol Vis Sci; 2011 Mar; 52(3):1450-9. PubMed ID: 20881290
[TBL] [Abstract][Full Text] [Related]
8. Mutations in zebrafish pitx2 model congenital malformations in Axenfeld-Rieger syndrome but do not disrupt left-right placement of visceral organs.
Ji Y; Buel SM; Amack JD
Dev Biol; 2016 Aug; 416(1):69-81. PubMed ID: 27297886
[TBL] [Abstract][Full Text] [Related]
9. A zebrafish model of PMM2-CDG reveals altered neurogenesis and a substrate-accumulation mechanism for N-linked glycosylation deficiency.
Cline A; Gao N; Flanagan-Steet H; Sharma V; Rosa S; Sonon R; Azadi P; Sadler KC; Freeze HH; Lehrman MA; Steet R
Mol Biol Cell; 2012 Nov; 23(21):4175-87. PubMed ID: 22956764
[TBL] [Abstract][Full Text] [Related]
10. Differences in neural crest sensitivity to ethanol account for the infrequency of anterior segment defects in the eye compared with craniofacial anomalies in a zebrafish model of fetal alcohol syndrome.
Eason J; Williams AL; Chawla B; Apsey C; Bohnsack BL
Birth Defects Res; 2017 Sep; 109(15):1212-1227. PubMed ID: 28681995
[TBL] [Abstract][Full Text] [Related]
11. Mechanistic Insights into Axenfeld-Rieger Syndrome from Zebrafish
French CR
Int J Mol Sci; 2021 Sep; 22(18):. PubMed ID: 34576164
[TBL] [Abstract][Full Text] [Related]
12. Investigation of Islet2a function in zebrafish embryos: Mutants and morphants differ in morphologic phenotypes and gene expression.
Moreno RL; Williams K; Jones KL; Ribera AB
PLoS One; 2018; 13(6):e0199233. PubMed ID: 29927984
[TBL] [Abstract][Full Text] [Related]
13. Disruption of foxc1 genes in zebrafish results in dosage-dependent phenotypes overlapping Axenfeld-Rieger syndrome.
Ferre-Fernández JJ; Sorokina EA; Thompson S; Collery RF; Nordquist E; Lincoln J; Semina EV
Hum Mol Genet; 2020 Sep; 29(16):2723-2735. PubMed ID: 32720677
[TBL] [Abstract][Full Text] [Related]
14. Requirement for Pdx1 in specification of latent endocrine progenitors in zebrafish.
Kimmel RA; Onder L; Wilfinger A; Ellertsdottir E; Meyer D
BMC Biol; 2011 Oct; 9():75. PubMed ID: 22034951
[TBL] [Abstract][Full Text] [Related]
15. Zebrafish pitx3 is necessary for normal lens and retinal development.
Shi X; Bosenko DV; Zinkevich NS; Foley S; Hyde DR; Semina EV; Vihtelic TS
Mech Dev; 2005 Apr; 122(4):513-27. PubMed ID: 15804565
[TBL] [Abstract][Full Text] [Related]
16. Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.
Vieira V; David G; Roche O; de la Houssaye G; Boutboul S; Arbogast L; Kobetz A; Orssaud C; Camand O; Schorderet DF; Munier F; Rossi A; Delezoide AL; Marsac C; Ricquier D; Dufier JL; Menasche M; Abitbol M
Mol Vis; 2006 Dec; 12():1448-60. PubMed ID: 17167399
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Rbfox-regulated alternative splicing is critical for zebrafish cardiac and skeletal muscle functions.
Gallagher TL; Arribere JA; Geurts PA; Exner CR; McDonald KL; Dill KK; Marr HL; Adkar SS; Garnett AT; Amacher SL; Conboy JG
Dev Biol; 2011 Nov; 359(2):251-61. PubMed ID: 21925157
[TBL] [Abstract][Full Text] [Related]
19. Craniofacial cartilage morphogenesis requires zebrafish col11a1 activity.
Baas D; Malbouyres M; Haftek-Terreau Z; Le Guellec D; Ruggiero F
Matrix Biol; 2009 Oct; 28(8):490-502. PubMed ID: 19638309
[TBL] [Abstract][Full Text] [Related]
20. Egr1 gene knockdown affects embryonic ocular development in zebrafish.
Hu CY; Yang CH; Chen WY; Huang CJ; Huang HY; Chen MS; Tsai HJ
Mol Vis; 2006 Oct; 12():1250-8. PubMed ID: 17110908
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
