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  • About
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Viral-host interactions affecting neural differentiation of human progenitors

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  • Post published:May 9, 2025
  • Post category:

Human cytomegalovirus (HCMV) is the major cause of birth defects, almost all of which are neuronal in origin. Approximately 1% of newborns are infected, and of the 13% that are…

Continue ReadingViral-host interactions affecting neural differentiation of human progenitors

Correlated time-lapse imaging and single cell molecular analysis of human embryo development

  • Post author:
  • Post published:May 9, 2025
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We understand little about human development especially at the earliest stages. Yet human developmental biology is very important to stem cell biology and regenerative medicine for two reasons: 1) Understanding…

Continue ReadingCorrelated time-lapse imaging and single cell molecular analysis of human embryo development

Discovery of mechanisms that control epigenetic states in human reprogramming and pluripotent cells

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  • Post published:May 9, 2025
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The CIRM Basic Biology Award III was developed to support basic research that enables the realization of the full potential of human stem cells and reprogrammed cells for therapies and…

Continue ReadingDiscovery of mechanisms that control epigenetic states in human reprogramming and pluripotent cells

Molecular basis of human ES cell neurovascular differentiation and co-patterning

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  • Post published:May 9, 2025
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During human development, autonomic neurons align with and pattern alongside blood vessels. This patterning allows the autonomic nervous system to control the vascular function a phenomenon that is very useful…

Continue ReadingMolecular basis of human ES cell neurovascular differentiation and co-patterning

Investigation of synaptic defects in autism using patient-derived induced pluripotent stem cells

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  • Post published:May 9, 2025
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Autism spectrum disorders (ASD) are a group of neurodevelopmental diseases that occur in as many as 1 in 150 children in the United States. Three hallmarks of autism are dysfunctional…

Continue ReadingInvestigation of synaptic defects in autism using patient-derived induced pluripotent stem cells

Functional characterization of mutational load in nuclear reprogramming and differentiation

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  • Post published:May 9, 2025
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One of the most potentially powerful aspects of regenerative medicine is stem cell therapy. In this therapy, healthy tissues derived from stem cells will be implanted into patients with damaged…

Continue ReadingFunctional characterization of mutational load in nuclear reprogramming and differentiation

Phenotypic Analysis of Human ES Cell-Derived Muscle Stem Cells

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  • Post published:May 9, 2025
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We study human muscle development, and are actively investigating potential cell-based therapies for the treatment of degenerative muscle diseases, such as muscle dystrophy. This project will define the pathway that…

Continue ReadingPhenotypic Analysis of Human ES Cell-Derived Muscle Stem Cells

Triplet Repeat Instability in Human iPSCs

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  • Post published:May 9, 2025
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Over twenty human genetic diseases are caused by expansion of simple DNA sequences composed of repeats of three nucleotides (such as CAG, CTG, CGG and GAA) within essential genes. These…

Continue ReadingTriplet Repeat Instability in Human iPSCs

Neural and general splicing factors control self-renewal, neural survival and differentiation

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  • Post published:May 9, 2025
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Human embryonic and patient-specific induced pluripotent stem cells have the remarkable capacity to differentiate into many cell-types, including neurons, thus enabling the modeling of human neurological diseases in vitro, and…

Continue ReadingNeural and general splicing factors control self-renewal, neural survival and differentiation

Mechanisms of Direct Cardiac Reprogramming

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  • Post published:May 9, 2025
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Heart disease is a leading cause of adult and childhood mortality. The underlying pathology is typically loss of heart muscle cells that leads to heart failure, or improper development of…

Continue ReadingMechanisms of Direct Cardiac Reprogramming
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