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Integrative Analyses of Genes Associated With Right Ventricular Cardiomyopathy Induced by Tricuspid Regurgitation.
Tian C, Yang Y, Ke Y, Yang L, Zhong L, Wang Z, Huang H. Tian C, et al. Front Genet. 2021 Sep 17;12:708275. doi: 10.3389/fgene.2021.708275. eCollection 2021. Front Genet. 2021. PMID: 34603374 Free PMC article.
Tricuspid regurgitation (TR) induces right ventricular cardiomyopathy, a common heart disease, and eventually leads to severe heart failure and serious clinical complications. ...CTD-2314B22.3, hsa-miR-653-5p, and KIF17ceRNA; SRGAP3-AS2, hsa-miR-539-5p, and SHANK1; …
Tricuspid regurgitation (TR) induces right ventricular cardiomyopathy, a common heart disease, and eventually leads to severe hear …
Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot.
Page DJ, Miossec MJ, Williams SG, Monaghan RM, Fotiou E, Cordell HJ, Sutcliffe L, Topf A, Bourgey M, Bourque G, Eveleigh R, Dunwoodie SL, Winlaw DS, Bhattacharya S, Breckpot J, Devriendt K, Gewillig M, Brook JD, Setchfield KJ, Bu'Lock FA, O'Sullivan J, Stuart G, Bezzina CR, Mulder BJM, Postma AV, Bentham JR, Baron M, Bhaskar SS, Black GC, Newman WG, Hentges KE, Lathrop GM, Santibanez-Koref M, Keavney BD. Page DJ, et al. Circ Res. 2019 Feb 15;124(4):553-563. doi: 10.1161/CIRCRESAHA.118.313250. Circ Res. 2019. PMID: 30582441 Free PMC article.
RATIONALE: Familial recurrence studies provide strong evidence for a genetic component to the predisposition to sporadic, nonsyndromic Tetralogy of Fallot (TOF), the most common cyanotic congenital heart disease phenotype. Rare genetic variants have been identified as impo …
RATIONALE: Familial recurrence studies provide strong evidence for a genetic component to the predisposition to sporadic, nonsyndromic Tetra …
Conditional expression of Spry1 in neural crest causes craniofacial and cardiac defects.
Yang X, Kilgallen S, Andreeva V, Spicer DB, Pinz I, Friesel R. Yang X, et al. BMC Dev Biol. 2010 May 11;10:48. doi: 10.1186/1471-213X-10-48. BMC Dev Biol. 2010. PMID: 20459789 Free PMC article.
In addition, the domains of expression of several key transcription factors important to normal craniofacial and cardiac development including AP2, Msx2, Dlx5, and Dlx6 were reduced in Spry1;Wnt1-Cre transgenic embryos. CONCLUSION: Collectively, these data suggest that Spr …
In addition, the domains of expression of several key transcription factors important to normal craniofacial and cardiac development includi …
Mis-Expression of a Cranial Neural Crest Cell-Specific Gene Program in Cardiac Neural Crest Cells Modulates HAND Factor Expression, Causing Cardiac Outflow Tract Phenotypes.
Vincentz JW, Clouthier DE, Firulli AB. Vincentz JW, et al. J Cardiovasc Dev Dis. 2020 Apr 20;7(2):13. doi: 10.3390/jcdd7020013. J Cardiovasc Dev Dis. 2020. PMID: 32325975 Free PMC article.
Congenital heart defects (CHDs) occur with such a frequency that they constitute a significant cause of morbidity and mortality in both children and adults. ...The gene regulatory networks that identify cardiac NCCs as a distinct NCC population are not completely understoo …
Congenital heart defects (CHDs) occur with such a frequency that they constitute a significant cause of morbidity and mortality in bo …
Exclusion of Dlx5/6 expression from the distal-most mandibular arches enables BMP-mediated specification of the distal cap.
Vincentz JW, Casasnovas JJ, Barnes RM, Que J, Clouthier DE, Wang J, Firulli AB. Vincentz JW, et al. Proc Natl Acad Sci U S A. 2016 Jul 5;113(27):7563-8. doi: 10.1073/pnas.1603930113. Epub 2016 Jun 22. Proc Natl Acad Sci U S A. 2016. PMID: 27335460 Free PMC article.
Furthermore, the homeodomain proteins distal-less homeobox 5 (DLX5) and DLX6 reciprocally inhibit BMP/H2-mediated H1 enhancer regulation. ...
Furthermore, the homeodomain proteins distal-less homeobox 5 (DLX5) and DLX6 reciprocally inhibit BMP/H2-mediated H1 enhancer regulat …
Targeted deletion of a branchial arch-specific enhancer reveals a role of dHAND in craniofacial development.
Yanagisawa H, Clouthier DE, Richardson JA, Charité J, Olson EN. Yanagisawa H, et al. Development. 2003 Mar;130(6):1069-78. doi: 10.1242/dev.00337. Development. 2003. PMID: 12571099
The basic helix-loop-helix transcription factor dHAND is expressed in the mesenchyme of branchial arches and the developing heart. Mice homozygous for a dHAND (Hand2) null mutation die early in embryogenesis from cardiac abnormalities, precluding analysis of the potential …
The basic helix-loop-helix transcription factor dHAND is expressed in the mesenchyme of branchial arches and the developing heart. Mi …