Spinal Muscular Atrophy Patient iPSC-Derived Motor Neurons Display Altered Proteomes at Early Stages of Differentiation | ACS Omega
A Skeletal Muscle Model of Infantile-onset Pompe Disease with Patient-specific iPS Cells | Scientific Reports
PAS-based quality scores for 12 iPSC lines. Shown for each iPSC line is... | Download Scientific Diagram
Mitochondrial deficits in human iPSC-derived neurons from patients with 22q11.2 deletion syndrome and schizophrenia | Translational Psychiatry
Frontiers | Human Induced Pluripotent Stem Cell-Derived TDP-43 Mutant Neurons Exhibit Consistent Functional Phenotypes Across Multiple Gene Edited Lines Despite Transcriptomic and Splicing Discrepancies
Pass LabsINT-25 - Pass Labs
Distribution of statistically significant PAS in ESC and iPSC lines.... | Download Scientific Diagram
A risk-based approach for cell line development, manufacturing and characterization of genetically engineered, induced pluripotent stem cell–derived allogeneic cell therapies - Cytotherapy
Pass LabsINT-25 - Pass Labs
Pass LabsINT-25 - Pass Labs
Nonviral Cell Labeling and Differentiation Agent for Induced Pluripotent Stem Cells Based on Mesoporous Silica Nanoparticles | ACS Nano
A Carbon-Based Biosensing Platform for Simultaneously Measuring the Contraction and Electrophysiology of iPSC-Cardiomyocyte Monolayers | ACS Nano
Human iPSC-derived motoneurons harbouring TARDBP or C9ORF72 ALS mutations are dysfunctional despite maintaining viability | Nature Communications
Integrity of Induced Pluripotent Stem Cell (iPSC) Derived Megakaryocytes as Assessed by Genetic and Transcriptomic Analysis | PLOS ONE
Functional characterization of iPSC-derived arterial- and venous-like endothelial cells | Scientific Reports
Frontiers | Electrophysiological Properties of Induced Pluripotent Stem Cell-Derived Midbrain Dopaminergic Neurons Correlate With Expression of Tyrosine Hydroxylase
A CDX2-GFP iPSC reporter line for intestinal differentiation a Detailed... | Download Scientific Diagram
Frontiers | iPSC-Derived Hepatocytes as a Platform for Disease Modeling and Drug Discovery
iPSC-Derived Intestinal Organoids from Cystic Fibrosis Patients Acquire CFTR Activity upon TALEN-Mediated Repair of the p.F508del Mutation: Molecular Therapy - Methods & Clinical Development
