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Elucidating Molecular Basis of Hypertrophic Cardiomyopathy with Human Induced Pluripotent Stem Cells

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  • Post published:February 17, 2026
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Familial hypertrophic cardiomyopathy (HCM) is the leading cause of sudden cardiac death in young people, including trained athletes, and is the most common inherited heart defect. Until now, studies in…

Continue ReadingElucidating Molecular Basis of Hypertrophic Cardiomyopathy with Human Induced Pluripotent Stem Cells

Characterization and Engineering of the Cardiac Stem Cell Niche

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  • Post published:February 17, 2026
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Despite therapeutic advances, cardiovascular disease remains a leading cause of mortality and morbidity in both California and Europe. New insights into disease pathology, models to expedite in vitro testing and…

Continue ReadingCharacterization and Engineering of the Cardiac Stem Cell Niche

Molecular Mechanisms Underlying Human Cardiac Cell Junction Maturation and Disease Using Human iPSC

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  • Post published:February 17, 2026
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Heart disease is the number one cause of death and disability in California and in the United States. Especially devastating is Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC), an inherited form of…

Continue ReadingMolecular Mechanisms Underlying Human Cardiac Cell Junction Maturation and Disease Using Human iPSC

Molecular determinants of accurate differentiation from human pluripotent stem cells

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  • Post published:February 17, 2026
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The use of human pluripotent stem cells for cell-based therapeutics is predicated on the ability to convert these cells into functional equivalents of those lost in disease or injury. However,…

Continue ReadingMolecular determinants of accurate differentiation from human pluripotent stem cells

Understanding the role of LRRK2 in iPSC cell models of Parkinson’s Disease

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  • Post published:February 17, 2026
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The goal of this research is to utilize novel research tools to investigate the molecular mechanisms that cause Parkinson’s disease (PD). The proposed work builds on previous funding from CIRM…

Continue ReadingUnderstanding the role of LRRK2 in iPSC cell models of Parkinson’s Disease

Identifying sources of mutation in human induced pluripotent stem cells by whole genome sequencing

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  • Post published:February 17, 2026
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Stem cell research offers new tools to help treat and cure diseases that affect diverse cells types in the body such as neurological diseases, heart disease and diabetes by producing…

Continue ReadingIdentifying sources of mutation in human induced pluripotent stem cells by whole genome sequencing

Induced Pluripotent Stem Cells for Tissue Regeneration

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  • Post published:February 17, 2026
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Induced pluripotent stem cells (iPSCs) have tremendous potential for patient-specific cell therapies, which bypasses immune rejection issues and ethical concerns for embryonic stem cells (ESCs). However, to fully harness the…

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Cellular tools to study brain diseases affecting synaptic transmission

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  • Post published:February 17, 2026
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There is a group of brain diseases that are caused by functional abnormalities. The brains of patients afflicted with these diseases which include autism spectrum disorders, schizophrenia, depression, and mania…

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Antibody tools to deplete or isolate teratogenic, cardiac, and blood stem cells from hESCs

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  • Post published:February 17, 2026
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Purity is as important for cell-based therapies as it is for treatments based on small-molecule drugs or biologics. Pluripotent stem cells possess two properties: they are capable of self regeneration…

Continue ReadingAntibody tools to deplete or isolate teratogenic, cardiac, and blood stem cells from hESCs

Use of iPS cells (iPSCs) to develop novels tools for the treatment of spinal muscular atrophy.

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  • Post published:February 17, 2026
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Spinal Muscular Atrophy (SMA) is one of the most common lethal genetic diseases in children. One in thirty five people carry a mutation in a gene called survival of motor…

Continue ReadingUse of iPS cells (iPSCs) to develop novels tools for the treatment of spinal muscular atrophy.
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