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One or more keywords matched the following properties of Zhou, Bin
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overview The Zhou laboratory studies factors and mechanisms that control heart and coronary vessel development to understand the pathogenesis of congenital heart disease and to gain insights into potential repairing mechanisms to combat both congenital and acquired heart diseases. Our research uses mice, mouse and human stem cells as model systems. We apply an integrated approach of genetics, developmental, molecular and systems biology as well as advanced single cell technologies and CRISPR gene editing to address three major questions: (1) How individual cardiac cells and lineages are specified, maintained, or diversified during heart and coronary vessel development, disease, aging or regeneration (Wu et al. Circ Res 2011, Wu et al. Cell 2012, Lu et al. Nat Commun 2022, Lu et al. Dev Cell 2023)? (2) How cell-cell, or cell-environment communications are modulated to control cardiac functions under these conditions (Wang et al. Eur Heart J 2015, Wang et al. Nat Commun 2017, Lu et al. Nat Cell Biol 2021)? (3) How fetal cardiac gene program is controlled during development and reactivated in the diseased or failing heart (Wang et al. Cardiovasc Res 2017, Lu et al. Circ Res 2022)?
One or more keywords matched the following items that are connected to Zhou, Bin
Item TypeName
Concept Alleles
Concept Amino Acid Sequence
Concept Base Sequence
Concept Oncogenes
Concept Molecular Sequence Data
Concept Gene Library
Concept Cell Adhesion Molecules
Concept Genes, Tumor Suppressor
Concept Genes, Reporter
Concept Consensus Sequence
Concept Transgenes
Concept Single-Cell Analysis
Concept Platelet Endothelial Cell Adhesion Molecule-1
Concept Genes, Developmental
Concept Genome, Human
Concept Genes, erbB-2
Concept Transcriptome
Concept Nuclear Export Signals
Grant Molecular and Cellular Mechanisms in Coronary Artery Development and Anomalies
Grant Mouse Model of Human Calcific Aortic Valve Stenosis
Grant Mechanisms of Coronary Ostium Formation and Coronary Artery Patterning
Grant Molecular and Cellular Mechanisms of Calcific Aortic Stenosis
Grant TRANSCRIPTIONAL REGULATION OF ENDOCARDIAL DEVELOPMENT
Grant Molecular and cellular mechanisms in cardiac outflow tract formation and defects
Academic Article Robust integration of multiple single-cell RNA sequencing datasets using a single reference space.
Academic Article BMP2 expression in the endocardial lineage is required for AV endocardial cushion maturation and remodeling.
Academic Article Single-Cell Lineage Tracing Reveals that Oriented Cell Division Contributes to Trabecular Morphogenesis and Regional Specification.
Academic Article GATA4 regulates Fgf16 to promote heart repair after injury.
Academic Article Vertebrate Fidgetin Restrains Axonal Growth by Severing Labile Domains of Microtubules.
Academic Article Accelerated coronary angiogenesis by vegfr1-knockout endocardial cells.
Academic Article Regulation of the murine Nfatc1 gene by NFATc2.
Academic Article Inner cell mass-specific expression of a cell adhesion molecule (PECAM-1/CD31) in the mouse blastocyst.
Academic Article Microtubule-associated protein 1 light chain 3 is a fibronectin mRNA-binding protein linked to mRNA translation in lamb vascular smooth muscle cells.
Grant Molecular signaling in aortic valve development and congenital aortic valve defect
Grant Developmental mechanisms of human congenital heart disease
Grant Molecular aspects of CRKL in heart development and human disease
Grant Single Cell RNA-seq to Identify Endocardial Ontogenic Factors for the Heart
Academic Article EGFR phosphorylates and inhibits lung tumor suppressor GPRC5A in lung cancer.
Academic Article Akt-mediated phosphorylation of EZH2 suppresses methylation of lysine 27 in histone H3.
Academic Article The SNAG domain of Snail1 functions as a molecular hook for recruiting lysine-specific demethylase 1.
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