Analysis of Mitochondrial Dysfunction by Microplate Reader in hiPSC-Derived Neuronal Cell Models of Neurodegenerative Disorders.- Generation and Hematopoietic Differentiation of Mesenchymal Stromal/Stem Cell-Derived Induced Pluripotent Stem Cell Lines for Disease Modeling of Hematopoietic and Immunological Diseases.- Establishment of Human Induced Pluripotent Stem Cells from Multiple Sclerosis Patients.- Monitoring Axonal Degeneration in Human Pluripotent Stem Cell Models of Hereditary Spastic Paraplegias.- Efficient Generation of Functional Hepatocytes from Human Induced Pluripotent Stem Cells for Disease Modeling and Disease Gene Discovery.- Autophagy Dysfunction as a Phenotypic Readout in hiPSC-Derived Neuronal Cell Models of Neurodegenerative Diseases.- Derivation of Induced Pluripotent Stem Cell (iPSC) Lines from Patient-Specific Peripheral Blood Mononuclear Cells (PBMC) Using Episomal Vectors.- Differentiating Induced Pluripotent Stem Cells toward Mesenchymal Stem/Stromal Cells.- A High-Efficiency Method for the Production of Endothelial Cells from Human Induced Pluripotent Stem Cells.- Image-Based Quantitation of Kainic Acid-Induced Excitotoxicity as a Model of Neurodegeneration in Human iPSC-Derived Neurons.- Amyloid β (Aβ) ELISA of Human iPSC-Derived Neuronal Cultures.- Creating Cell Model 2.0 for Pathogenic Mitochondrial DNA Mutation: iPSC Approach for LHON Mutation.- CRISPR Guide RNA Library Screens in Human Induced Pluripotent Stem Cells.- Generation and Encapsulation of Human iPSC-Derived Vascular Smooth Muscle Cells for Proangiogenic Therapy.- Methods to Induce Small-Scale Differentiation of iPS Cells into Dopaminergic Neurons and to Detect Disease Phenotypes.- Modeling Early Neural Crest Development via Induction from hiPSC-Derived Neural Plate Border-Like Cells.- Generation of Human Induced Pluripotent Stem Cells from Renal Epithelial Cells.- A Protocol for Stepwise Differentiation of Induced Pluripotent Stem Cells into Retinal Pigment Epithelium.- Genome Editing of Induced Pluripotent Stem Cells Using CRISPR/Cas9 Ribonucleoprotein Complexes to Model Genetic Ocular Diseases.- Generation of Cardiomyocytes and Endothelial Cells from Human iPSCs by Chemical Modulation of Wnt Signaling.- Immunoassay for Quantitative Detection of Antibody Transcytosis across the Blood-Brain Barrier In Vitro.- Generation of Cortical, Dopaminergic, Motor, and Sensory Neurons from Human Pluripotent Stem Cells.- CRISPR/Cas-Mediated Knock-In of Genetically Encoded Fluorescent Biosensors into the AAVS1 Locus of Human Induced Pluripotent Stem Cells.- Cancer Stem Cell Initiation by Tumor-Derived Extracellular Vesicles.- Genome Editing Using Cas9-gRNA Ribonucleoprotein in Human Pluripotent Stem Cells for Disease Modeling.

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