Pages that link to "Q24313555"
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The following pages link to Characterization of TBX20 in human hearts and its regulation by TFAP2 (Q24313555):
Displaying 34 items.
- T-box transcription factor 20 (Q21127368) (← links)
- A gain-of-function TBX20 mutation causes congenital atrial septal defects, patent foramen ovale and cardiac valve defects (Q24317048) (← links)
- T-box transcription factor TBX20 mutations in Chinese patients with congenital heart disease (Q24318968) (← links)
- Tbx20 regulates a genetic program essential to adult mouse cardiomyocyte function (Q24634382) (← links)
- Of mice and men: molecular genetics of congenital heart disease (Q26995476) (← links)
- Lack of genetic interaction between Tbx20 and Tbx3 in early mouse heart development (Q28534871) (← links)
- Characterization of the novel interaction between muskelin and TBX20, a critical cardiogenic transcription factor (Q28587409) (← links)
- Prediction of cardiac transcription networks based on molecular data and complex clinical phenotypes (Q31156132) (← links)
- Molecular genetics of congenital atrial septal defects (Q33696535) (← links)
- A Gro/TLE-NuRD corepressor complex facilitates Tbx20-dependent transcriptional repression (Q33702644) (← links)
- The BMP pathway acts to directly regulate Tbx20 in the developing heart. (Q33840093) (← links)
- Xenopus: An emerging model for studying congenital heart disease (Q35075360) (← links)
- Mutations of TFAP2B in congenital heart disease patients in Mysore, South India (Q35646873) (← links)
- Cellular Mechanisms of Drosophila Heart Morphogenesis. (Q35904328) (← links)
- Cooperative and antagonistic roles for Irx3 and Irx5 in cardiac morphogenesis and postnatal physiology (Q36321332) (← links)
- Transcriptional Regulation of Heart Development in Zebrafish (Q36855391) (← links)
- Silencing of TBX20 gene expression in rat myocardial and human embryonic kidney cells leads to cell cycle arrest in G2 phase (Q37297481) (← links)
- iPSC-derived cardiomyocytes reveal abnormal TGF-β signalling in left ventricular non-compaction cardiomyopathy. (Q37297762) (← links)
- Mechanisms of T-box gene function in the developing heart (Q37865969) (← links)
- Alternative splicing of T-box transcription factor genes. (Q37920357) (← links)
- Transcription factor pathways and congenital heart disease. (Q37997218) (← links)
- A molecular and genetic outline of cardiac morphogenesis. (Q38072446) (← links)
- Perturbations of heart development and function in cardiomyocytes from human embryonic stem cells with trisomy 21. (Q38913781) (← links)
- A Functional Variant Associated with Atrial Fibrillation Regulates PITX2c Expression through TFAP2a (Q41974431) (← links)
- Formation of a TBX20-CASZ1 protein complex is protective against dilated cardiomyopathy and critical for cardiac homeostasis (Q42370926) (← links)
- Tbx20 drives cardiac progenitor formation and cardiomyocyte proliferation in zebrafish (Q46447680) (← links)
- A Matter of the Heart: The African Clawed Frog Xenopus as a Model for Studying Vertebrate Cardiogenesis and Congenital Heart Defects (Q49328900) (← links)
- Understanding Tissue-Specific Gene Regulation (Q50082931) (← links)
- Association of TBX20 gene polymorphism with congenital heart disease in Han Chinese neonates. (Q54181235) (← links)
- [Detection of promoter and 3' UTR mutation in A20 gene of a case with T cell lymphoma cell leukemia] (Q58122384) (← links)
- Role of cardiac TBX20 in dilated cardiomyopathy (Q63440914) (← links)
- DNA methylation status of TBX20 in patients with tetralogy of Fallot. (Q64949321) (← links)
- Tbx20 Is Required in Mid-Gestation Cardiomyocytes and Plays a Central Role in Atrial Development (Q89107305) (← links)
- A Chromosomal Inversion of 46XX, inv (6) (p21.3p23) Connects to Congenital Heart Defects (Q98771887) (← links)