324 related articles for article (PubMed ID: 31286141)
1. HAND1 loss-of-function within the embryonic myocardium reveals survivable congenital cardiac defects and adult heart failure.
Firulli BA; George RM; Harkin J; Toolan KP; Gao H; Liu Y; Zhang W; Field LJ; Liu Y; Shou W; Payne RM; Rubart-von der Lohe M; Firulli AB
Cardiovasc Res; 2020 Mar; 116(3):605-618. PubMed ID: 31286141
[TBL] [Abstract][Full Text] [Related]
2. HAND transcription factors cooperatively specify the aorta and pulmonary trunk.
Vincentz JW; Firulli BA; Toolan KP; Osterwalder M; Pennacchio LA; Firulli AB
Dev Biol; 2021 Aug; 476():1-10. PubMed ID: 33757801
[TBL] [Abstract][Full Text] [Related]
3. Variation in a Left Ventricle-Specific Hand1 Enhancer Impairs GATA Transcription Factor Binding and Disrupts Conduction System Development and Function.
Vincentz JW; Firulli BA; Toolan KP; Arking DE; Sotoodehnia N; Wan J; Chen PS; de Gier-de Vries C; Christoffels VM; Rubart-von der Lohe M; Firulli AB
Circ Res; 2019 Aug; 125(6):575-589. PubMed ID: 31366290
[TBL] [Abstract][Full Text] [Related]
4. Gene replacement strategies to test the functional redundancy of basic helix-loop-helix transcription factor.
Firulli AB; Firulli BA; Wang J; Rogers RH; Conway SJ
Pediatr Cardiol; 2010 Apr; 31(3):438-48. PubMed ID: 20155416
[TBL] [Abstract][Full Text] [Related]
5. The HAND1 frameshift A126FS mutation does not cause hypoplastic left heart syndrome in mice.
Firulli BA; Toolan KP; Harkin J; Millar H; Pineda S; Firulli AB
Cardiovasc Res; 2017 Dec; 113(14):1732-1742. PubMed ID: 29016838
[TBL] [Abstract][Full Text] [Related]
6. Hand factor ablation causes defective left ventricular chamber development and compromised adult cardiac function.
Vincentz JW; Toolan KP; Zhang W; Firulli AB
PLoS Genet; 2017 Jul; 13(7):e1006922. PubMed ID: 28732025
[TBL] [Abstract][Full Text] [Related]
7. The Hand1 and Hand2 transcription factors regulate expansion of the embryonic cardiac ventricles in a gene dosage-dependent manner.
McFadden DG; Barbosa AC; Richardson JA; Schneider MD; Srivastava D; Olson EN
Development; 2005 Jan; 132(1):189-201. PubMed ID: 15576406
[TBL] [Abstract][Full Text] [Related]
8. The Hand1 bHLH transcription factor is essential for placentation and cardiac morphogenesis.
Riley P; Anson-Cartwright L; Cross JC
Nat Genet; 1998 Mar; 18(3):271-5. PubMed ID: 9500551
[TBL] [Abstract][Full Text] [Related]
9. Outflow tract cushions perform a critical valve-like function in the early embryonic heart requiring BMPRIA-mediated signaling in cardiac neural crest.
Nomura-Kitabayashi A; Phoon CK; Kishigami S; Rosenthal J; Yamauchi Y; Abe K; Yamamura K; Samtani R; Lo CW; Mishina Y
Am J Physiol Heart Circ Physiol; 2009 Nov; 297(5):H1617-28. PubMed ID: 19717734
[TBL] [Abstract][Full Text] [Related]
10. Ablation of Nkx2-5 at mid-embryonic stage results in premature lethality and cardiac malformation.
Terada R; Warren S; Lu JT; Chien KR; Wessels A; Kasahara H
Cardiovasc Res; 2011 Jul; 91(2):289-99. PubMed ID: 21285290
[TBL] [Abstract][Full Text] [Related]
11. Analysis of a Hand1 hypomorphic allele reveals a critical threshold for embryonic viability.
Firulli BA; McConville DP; Byers JS; Vincentz JW; Barnes RM; Firulli AB
Dev Dyn; 2010 Oct; 239(10):2748-60. PubMed ID: 20737509
[TBL] [Abstract][Full Text] [Related]
12. Cardiac-specific developmental and epigenetic functions of Jarid2 during embryonic development.
Cho E; Mysliwiec MR; Carlson CD; Ansari A; Schwartz RJ; Lee Y
J Biol Chem; 2018 Jul; 293(30):11659-11673. PubMed ID: 29891551
[TBL] [Abstract][Full Text] [Related]
13. Heart and extra-embryonic mesodermal defects in mouse embryos lacking the bHLH transcription factor Hand1.
Firulli AB; McFadden DG; Lin Q; Srivastava D; Olson EN
Nat Genet; 1998 Mar; 18(3):266-70. PubMed ID: 9500550
[TBL] [Abstract][Full Text] [Related]
14. Ablation of the CLP-1 gene leads to down-regulation of the HAND1 gene and abnormality of the left ventricle of the heart and fetal death.
Huang F; Wagner M; Siddiqui MA
Mech Dev; 2004 Jun; 121(6):559-72. PubMed ID: 15172687
[TBL] [Abstract][Full Text] [Related]
15. Epiblastic Cited2 deficiency results in cardiac phenotypic heterogeneity and provides a mechanism for haploinsufficiency.
MacDonald ST; Bamforth SD; Chen CM; Farthing CR; Franklyn A; Broadbent C; Schneider JE; Saga Y; Lewandoski M; Bhattacharya S
Cardiovasc Res; 2008 Aug; 79(3):448-57. PubMed ID: 18440989
[TBL] [Abstract][Full Text] [Related]
16. Hand factors as regulators of cardiac morphogenesis and implications for congenital heart defects.
Vincentz JW; Barnes RM; Firulli AB
Birth Defects Res A Clin Mol Teratol; 2011 Jun; 91(6):485-94. PubMed ID: 21462297
[TBL] [Abstract][Full Text] [Related]
17. Hypoxic regulation of hand1 controls the fetal-neonatal switch in cardiac metabolism.
Breckenridge RA; Piotrowska I; Ng KE; Ragan TJ; West JA; Kotecha S; Towers N; Bennett M; Kienesberger PC; Smolenski RT; Siddall HK; Offer JL; Mocanu MM; Yelon DM; Dyck JR; Griffin JL; Abramov AY; Gould AP; Mohun TJ
PLoS Biol; 2013 Sep; 11(9):e1001666. PubMed ID: 24086110
[TBL] [Abstract][Full Text] [Related]
18. A functional genetic study identifies HAND1 mutations in septation defects of the human heart.
Reamon-Buettner SM; Ciribilli Y; Traverso I; Kuhls B; Inga A; Borlak J
Hum Mol Genet; 2009 Oct; 18(19):3567-78. PubMed ID: 19586923
[TBL] [Abstract][Full Text] [Related]
19. Early exclusion of hand1-deficient cells from distinct regions of the left ventricular myocardium in chimeric mouse embryos.
Riley PR; Gertsenstein M; Dawson K; Cross JC
Dev Biol; 2000 Nov; 227(1):156-68. PubMed ID: 11076684
[TBL] [Abstract][Full Text] [Related]
20. Aryl Hydrocarbon Receptor Ablation in Cardiomyocytes Protects Male Mice From Heart Dysfunction Induced by NKX2.5 Haploinsufficiency.
Wang Q; Fan Y; Kurita H; Jiang M; Koch S; Rao MB; Rubinstein J; Puga A
Toxicol Sci; 2017 Nov; 160(1):74-82. PubMed ID: 28973413
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
