310 related articles for article (PubMed ID: 33607112)
1. Retinoic acid signaling restricts the size of the first heart field within the anterior lateral plate mesoderm.
Duong TB; Holowiecki A; Waxman JS
Dev Biol; 2021 May; 473():119-129. PubMed ID: 33607112
[TBL] [Abstract][Full Text] [Related]
2. Zebrafish second heart field development relies on progenitor specification in anterior lateral plate mesoderm and nkx2.5 function.
Guner-Ataman B; Paffett-Lugassy N; Adams MS; Nevis KR; Jahangiri L; Obregon P; Kikuchi K; Poss KD; Burns CE; Burns CG
Development; 2013 Mar; 140(6):1353-63. PubMed ID: 23444361
[TBL] [Abstract][Full Text] [Related]
3. HDAC1-mediated repression of the retinoic acid-responsive gene ripply3 promotes second heart field development.
Song YC; Dohn TE; Rydeen AB; Nechiporuk AV; Waxman JS
PLoS Genet; 2019 May; 15(5):e1008165. PubMed ID: 31091225
[TBL] [Abstract][Full Text] [Related]
4. Unique developmental trajectories and genetic regulation of ventricular and outflow tract progenitors in the zebrafish second heart field.
Paffett-Lugassy N; Novikov N; Jeffrey S; Abrial M; Guner-Ataman B; Sakthivel S; Burns CE; Burns CG
Development; 2017 Dec; 144(24):4616-4624. PubMed ID: 29061637
[TBL] [Abstract][Full Text] [Related]
5. Latent TGF-β binding protein 3 identifies a second heart field in zebrafish.
Zhou Y; Cashman TJ; Nevis KR; Obregon P; Carney SA; Liu Y; Gu A; Mosimann C; Sondalle S; Peterson RE; Heideman W; Burns CE; Burns CG
Nature; 2011 May; 474(7353):645-8. PubMed ID: 21623370
[TBL] [Abstract][Full Text] [Related]
6. Wnt signaling balances specification of the cardiac and pharyngeal muscle fields.
Mandal A; Holowiecki A; Song YC; Waxman JS
Mech Dev; 2017 Feb; 143():32-41. PubMed ID: 28087459
[TBL] [Abstract][Full Text] [Related]
7. Nr2f-dependent allocation of ventricular cardiomyocyte and pharyngeal muscle progenitors.
Dohn TE; Ravisankar P; Tirera FT; Martin KE; Gafranek JT; Duong TB; VanDyke TL; Touvron M; Barske LA; Crump JG; Waxman JS
PLoS Genet; 2019 Feb; 15(2):e1007962. PubMed ID: 30721228
[TBL] [Abstract][Full Text] [Related]
8. Hippo signaling determines the number of venous pole cells that originate from the anterior lateral plate mesoderm in zebrafish.
Fukui H; Miyazaki T; Chow RW; Ishikawa H; Nakajima H; Vermot J; Mochizuki N
Elife; 2018 May; 7():. PubMed ID: 29809141
[TBL] [Abstract][Full Text] [Related]
9. Chamber identity programs drive early functional partitioning of the heart.
Mosimann C; Panáková D; Werdich AA; Musso G; Burger A; Lawson KL; Carr LA; Nevis KR; Sabeh MK; Zhou Y; Davidson AJ; DiBiase A; Burns CE; Burns CG; MacRae CA; Zon LI
Nat Commun; 2015 Aug; 6():8146. PubMed ID: 26306682
[TBL] [Abstract][Full Text] [Related]
10. Continuous addition of progenitors forms the cardiac ventricle in zebrafish.
Felker A; Prummel KD; Merks AM; Mickoleit M; Brombacher EC; Huisken J; Panáková D; Mosimann C
Nat Commun; 2018 May; 9(1):2001. PubMed ID: 29784942
[TBL] [Abstract][Full Text] [Related]
11. Cyp26 enzymes are required to balance the cardiac and vascular lineages within the anterior lateral plate mesoderm.
Rydeen AB; Waxman JS
Development; 2014 Apr; 141(8):1638-48. PubMed ID: 24667328
[TBL] [Abstract][Full Text] [Related]
12. Retinoic acid deficiency alters second heart field formation.
Ryckebusch L; Wang Z; Bertrand N; Lin SC; Chi X; Schwartz R; Zaffran S; Niederreither K
Proc Natl Acad Sci U S A; 2008 Feb; 105(8):2913-8. PubMed ID: 18287057
[TBL] [Abstract][Full Text] [Related]
13. Tbx5a lineage tracing shows cardiomyocyte plasticity during zebrafish heart regeneration.
Sánchez-Iranzo H; Galardi-Castilla M; Minguillón C; Sanz-Morejón A; González-Rosa JM; Felker A; Ernst A; Guzmán-Martínez G; Mosimann C; Mercader N
Nat Commun; 2018 Jan; 9(1):428. PubMed ID: 29382818
[TBL] [Abstract][Full Text] [Related]
14. The LIM protein Ajuba restricts the second heart field progenitor pool by regulating Isl1 activity.
Witzel HR; Jungblut B; Choe CP; Crump JG; Braun T; Dobreva G
Dev Cell; 2012 Jul; 23(1):58-70. PubMed ID: 22771034
[TBL] [Abstract][Full Text] [Related]
15. Pbx4 limits heart size and fosters arch artery formation by partitioning second heart field progenitors and restricting proliferation.
Holowiecki A; Linstrum K; Ravisankar P; Chetal K; Salomonis N; Waxman JS
Development; 2020 Mar; 147(5):. PubMed ID: 32094112
[TBL] [Abstract][Full Text] [Related]
16. Patterning of vertebrate cardiac progenitor fields by retinoic acid signaling.
Duong TB; Waxman JS
Genesis; 2021 Nov; 59(11):e23458. PubMed ID: 34665508
[TBL] [Abstract][Full Text] [Related]
17. Tbx1 is required for second heart field proliferation in zebrafish.
Nevis K; Obregon P; Walsh C; Guner-Ataman B; Burns CG; Burns CE
Dev Dyn; 2013 May; 242(5):550-9. PubMed ID: 23335360
[TBL] [Abstract][Full Text] [Related]
18. Interactions between Cdx genes and retinoic acid modulate early cardiogenesis.
Lengerke C; Wingert R; Beeretz M; Grauer M; Schmidt AG; Konantz M; Daley GQ; Davidson AJ
Dev Biol; 2011 Jun; 354(1):134-42. PubMed ID: 21466798
[TBL] [Abstract][Full Text] [Related]
19. The AP-1 transcription factor component Fosl2 potentiates the rate of myocardial differentiation from the zebrafish second heart field.
Jahangiri L; Sharpe M; Novikov N; González-Rosa JM; Borikova A; Nevis K; Paffett-Lugassy N; Zhao L; Adams M; Guner-Ataman B; Burns CE; Burns CG
Development; 2016 Jan; 143(1):113-22. PubMed ID: 26732840
[TBL] [Abstract][Full Text] [Related]
20. A HCN4+ cardiomyogenic progenitor derived from the first heart field and human pluripotent stem cells.
Später D; Abramczuk MK; Buac K; Zangi L; Stachel MW; Clarke J; Sahara M; Ludwig A; Chien KR
Nat Cell Biol; 2013 Sep; 15(9):1098-106. PubMed ID: 23974038
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
