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Huaxiao Yang

Researcher at University of North Texas

Publications -  42
Citations -  1024

Huaxiao Yang is an academic researcher from University of North Texas. The author has contributed to research in topics: Stem cell & Induced pluripotent stem cell. The author has an hindex of 17, co-authored 36 publications receiving 687 citations. Previous affiliations of Huaxiao Yang include Stanford University & Fudan University.

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Passive Stretch Induces Structural and Functional Maturation of Engineered Heart Muscle as Predicted by Computational Modeling.

TL;DR: The effects of varying passive stretch on engineered heart muscle (EHM) structural and functional maturation are tested and how to optimize cell alignment and calcium dynamics within EHMs is shown, which enables future scale‐up productions for clinical use in cardiovascular tissue engineering.
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An in Vivo miRNA Delivery System for Restoring Infarcted Myocardium

TL;DR: An in vivo delivery system using polymeric nanoparticles to carry miRNA (miNPs) for localized delivery within a shear-thinning injectable hydrogel to restore injured myocardium efficiently and safely is established.
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Modelling diastolic dysfunction in induced pluripotent stem cell-derived cardiomyocytes from hypertrophic cardiomyopathy patients

TL;DR: This study recapitulated DD in HCM at the single-cell level, and revealed novel cellular mechanisms and potential therapeutic targets of DD using patient-specific induced pluripotent stem cell-derived cardiomyocytes.
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A Premature Termination Codon Mutation in MYBPC3 Causes Hypertrophic Cardiomyopathy via Chronic Activation of Nonsense-Mediated Decay

TL;DR: iPSC-CMs carrying MYBPC3 PTC mutations displayed aberrant calcium signaling and molecular dysregulations in the absence of significant haploinsufficiency of MYB PC3 protein, providing the first evidence of the direct connection between the chronically activated nonsense-mediated decay pathway and HCM disease development.
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Molecular and functional resemblance of differentiated cells derived from isogenic human iPSCs and SCNT-derived ESCs

TL;DR: It is concluded that human iPSCs are capable of replacing SCNT for generating differentiated cells for drug testing and disease modeling and can replace nt-ESCs as alternatives for generating patient-specific differentiation cells for disease modeled and preclinical drug testing.