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induced pluripotent stem cells

The Potential of Pancreatic Organoids for Diabetes Research and Therapy

[Islets] Scientists review the attempts over the past decade, to utilize the organoid cell culture principles in order to identify, expand, and differentiate the adult pancreatic stem cells from different compartments of mouse and human pancreata.

Human Microglia States Are Conserved across Experimental Models and Regulate Neural Stem Cell Responses in Chimeric Organoids

[Cell Stem Cell] Xenotransplantation of human microglia into cerebral organoids allowed us to characterize key transcriptional programs of developing microglia in vitro and revealed that microglia induced transcriptional changes in neural stem cells and decrease interferon signaling response genes.

Restoration of the Defect in Radial Glial Fiber Cell Migration and Cortical Plate Organization in Brain Organoid Model of Fukuyama Muscular Dystrophy

[iScience] Brain organoids successfully mimicked patient phenotypes not reliably reproduced by existing models, including decreased alpha dystroglycan glycosylation and abnormal radial glial cell fiber migration.

Kruppel-Like Factor 15 Induces the Development of Mature Hepatocyte-Like Cells from Hepatoblasts

[Scientific Reports] Kruppel-like factor 15 (KLF15) was identified as a new regulator of hepatic maturation through a comprehensive analysis of the expression of transcriptional regulators in mouse fetal and adult hepatocytes. KLF15 induced the overexpression of liver function genes in mouse embryonic hepatocytes.

CRISPR/Cas9 Mediated Gene Correction Ameliorates Abnormal Phenotypes in Spinocerebellar Ataxia Type 3 Patient-Derived Induced Pluripotent Stem Cells

[Translational Psychiatry] Spinocerebellar ataxia type 3 (SCA3)-iPSCs could be corrected by the replacement of the abnormal CAG expansions with normal repeats using CRISPR/Cas9-mediated homologous recombination strategy. Corrected SCA3-iPSCs retained pluripotent and normal karyotype, which could be differentiated into a neural stem cell and neuronal cells.

IQSEC2 Mutation Associated with Epilepsy, Intellectual Disability, and Autism Results in Hyperexcitability of Patient-Derived Neurons and Deficient Synaptic Transmission

[Molecular Psychiatry] Investigators used iPSC technology to obtain hippocampal neurons to investigate the neuropathology of IQSEC2-mediated disease. The neurons were characterized at three-time points during differentiation to assess developmental progression.

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