These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
295 related articles for article (PubMed ID: 12223419)
1. The heartstrings mutation in zebrafish causes heart/fin Tbx5 deficiency syndrome. Garrity DM; Childs S; Fishman MC Development; 2002 Oct; 129(19):4635-45. PubMed ID: 12223419 [TBL] [Abstract][Full Text] [Related]
2. Tbx5-mediated expression of Ca(2+)/calmodulin-dependent protein kinase II is necessary for zebrafish cardiac and pectoral fin morphogenesis. Rothschild SC; Easley CA; Francescatto L; Lister JA; Garrity DM; Tombes RM Dev Biol; 2009 Jun; 330(1):175-84. PubMed ID: 19345202 [TBL] [Abstract][Full Text] [Related]
3. Zebrafish tbx5 paralogs demonstrate independent essential requirements in cardiac and pectoral fin development. Parrie LE; Renfrew EM; Wal AV; Mueller RL; Garrity DM Dev Dyn; 2013 May; 242(5):485-502. PubMed ID: 23441045 [TBL] [Abstract][Full Text] [Related]
4. Pdlim7 is required for maintenance of the mesenchymal/epidermal Fgf signaling feedback loop during zebrafish pectoral fin development. Camarata T; Snyder D; Schwend T; Klosowiak J; Holtrup B; Simon HG BMC Dev Biol; 2010 Oct; 10():104. PubMed ID: 20950450 [TBL] [Abstract][Full Text] [Related]
5. Distinct tissue-specific requirements for the zebrafish tbx5 genes during heart, retina and pectoral fin development. Pi-Roig A; Martin-Blanco E; Minguillon C Open Biol; 2014 Apr; 4(4):140014. PubMed ID: 24759614 [TBL] [Abstract][Full Text] [Related]
6. MicroRNA 19a replacement partially rescues fin and cardiac defects in zebrafish model of Holt Oram syndrome. Chiavacci E; D'Aurizio R; Guzzolino E; Russo F; Baumgart M; Groth M; Mariani L; D'Onofrio M; Arisi I; Pellegrini M; Cellerino A; Cremisi F; Pitto L Sci Rep; 2015 Dec; 5():18240. PubMed ID: 26657204 [TBL] [Abstract][Full Text] [Related]
7. sall4 acts downstream of tbx5 and is required for pectoral fin outgrowth. Harvey SA; Logan MP Development; 2006 Mar; 133(6):1165-73. PubMed ID: 16501170 [TBL] [Abstract][Full Text] [Related]
8. Fibin, a novel secreted lateral plate mesoderm signal, is essential for pectoral fin bud initiation in zebrafish. Wakahara T; Kusu N; Yamauchi H; Kimura I; Konishi M; Miyake A; Itoh N Dev Biol; 2007 Mar; 303(2):527-35. PubMed ID: 17196583 [TBL] [Abstract][Full Text] [Related]
9. Induction of apoptosis and inhibition of cell growth by tbx5 knockdown contribute to dysmorphogenesis in Zebrafish embryos. Lu J; Tsai T; Choo S; Yeh S; Tang R; Yang A; Lee H; Lu J J Biomed Sci; 2011 Oct; 18(1):73. PubMed ID: 21982178 [TBL] [Abstract][Full Text] [Related]
10. The paracrine effect of exogenous growth hormone alleviates dysmorphogenesis caused by tbx5 deficiency in zebrafish (Danio rerio) embryos. Tsai TC; Lu JK; Choo SL; Yeh SY; Tang RB; Lee HY; Lu JH J Biomed Sci; 2012 Jul; 19(1):63. PubMed ID: 22776023 [TBL] [Abstract][Full Text] [Related]
11. The bHLH transcription factor hand2 plays parallel roles in zebrafish heart and pectoral fin development. Yelon D; Ticho B; Halpern ME; Ruvinsky I; Ho RK; Silver LM; Stainier DY Development; 2000 Jun; 127(12):2573-82. PubMed ID: 10821756 [TBL] [Abstract][Full Text] [Related]
12. Identification and characterisation of the developmental expression pattern of tbx5b, a novel tbx5 gene in zebrafish. Albalat R; Baquero M; Minguillón C Gene Expr Patterns; 2010 Jan; 10(1):24-30. PubMed ID: 19925885 [TBL] [Abstract][Full Text] [Related]
13. Regulatory variation in a TBX5 enhancer leads to isolated congenital heart disease. Smemo S; Campos LC; Moskowitz IP; Krieger JE; Pereira AC; Nobrega MA Hum Mol Genet; 2012 Jul; 21(14):3255-63. PubMed ID: 22543974 [TBL] [Abstract][Full Text] [Related]
14. Tbx5a and Tbx5b paralogues act in combination to control separate vectors of migration in the fin field of zebrafish. Boyle-Anderson EAT; Mao Q; Ho RK Dev Biol; 2022 Jan; 481():201-214. PubMed ID: 34756968 [TBL] [Abstract][Full Text] [Related]
15. Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome. Basson CT; Bachinsky DR; Lin RC; Levi T; Elkins JA; Soults J; Grayzel D; Kroumpouzou E; Traill TA; Leblanc-Straceski J; Renault B; Kucherlapati R; Seidman JG; Seidman CE Nat Genet; 1997 Jan; 15(1):30-5. PubMed ID: 8988165 [TBL] [Abstract][Full Text] [Related]
16. Cascade effect of cardiac myogenesis gene expression during cardiac looping in tbx5 knockdown zebrafish embryos. Lu JH; Lu JK; Choo SL; Li YC; Yeh HW; Shiue JF; Yeh VC J Biomed Sci; 2008 Nov; 15(6):779-87. PubMed ID: 18661250 [TBL] [Abstract][Full Text] [Related]
17. Clinical and molecular characterisation of Holt-Oram syndrome focusing on cardiac manifestations. Jhang WK; Lee BH; Kim GH; Lee JO; Yoo HW Cardiol Young; 2015 Aug; 25(6):1093-8. PubMed ID: 25216260 [TBL] [Abstract][Full Text] [Related]
18. T-box gene tbx5 is essential for formation of the pectoral limb bud. Ahn DG; Kourakis MJ; Rohde LA; Silver LM; Ho RK Nature; 2002 Jun; 417(6890):754-8. PubMed ID: 12066188 [TBL] [Abstract][Full Text] [Related]
19. KLF13 is a genetic modifier of the Holt-Oram syndrome gene TBX5. Darwich R; Li W; Yamak A; Komati H; Andelfinger G; Sun K; Nemer M Hum Mol Genet; 2017 Mar; 26(5):942-954. PubMed ID: 28164238 [TBL] [Abstract][Full Text] [Related]