about
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Telomere shortening and loss of self-renewal in dyskeratosis congenita induced pluripotent stem cellsGenome-scale DNA methylation maps of pluripotent and differentiated cellsGenome-wide maps of chromatin state in pluripotent and lineage-committed cellsDirect conversion of fibroblasts to functional neurons by defined factorsAutism-associated SHANK3 haploinsufficiency causes Ih channelopathy in human neuronsAnalysis of conditional heterozygous STXBP1 mutations in human neuronsInduced neuronal cells: how to make and define a neuronComprehensive qPCR profiling of gene expression in single neuronal cellsNeurons generated by direct conversion of fibroblasts reproduce synaptic phenotype caused by autism-associated neuroligin-3 mutationAcute reduction in oxygen tension enhances the induction of neurons from human fibroblastsRapid single-step induction of functional neurons from human pluripotent stem cellsDirect lineage conversion of terminally differentiated hepatocytes to functional neuronsDirect conversion of mouse fibroblasts to self-renewing, tripotent neural precursor cellsInduction of human neuronal cells by defined transcription factorsGeneration of induced neuronal cells by the single reprogramming factor ASCL1In Vivo Reprogramming for Brain and Spinal Cord RepairMolecular roadblocks for cellular reprogrammingThe many roads to Rome: induction of neural precursor cells from fibroblastsm(6)A RNA modification controls cell fate transition in mammalian embryonic stem cells.A bivalent chromatin structure marks key developmental genes in embryonic stem cellsPolycomb complexes repress developmental regulators in murine embryonic stem cellsConnecting microRNA genes to the core transcriptional regulatory circuitry of embryonic stem cellsHierarchical mechanisms for direct reprogramming of fibroblasts to neuronsMyt1l safeguards neuronal identity by actively repressing many non-neuronal fates.Partial Reprogramming of Pluripotent Stem Cell-Derived Cardiomyocytes into Neurons.The novel tool of cell reprogramming for applications in molecular medicine.Generation of iPSCs from cultured human malignant cells.Induced neuronal reprogramming.The vast majority of bone-marrow-derived cells integrated into mdx muscle fibers are silent despite long-term engraftmentThe histone chaperone CAF-1 safeguards somatic cell identity.Direct lineage conversions: unnatural but useful?Generation of oligodendroglial cells by direct lineage conversion.Fifty ways to make a neuron: shifts in stem cell hierarchy and their implications for neuropathology and CNS repair.Direct reprogramming of terminally differentiated mature B lymphocytes to pluripotency.A continuous molecular roadmap to iPSC reprogramming through progression analysis of single-cell mass cytometryHuman COL7A1-corrected induced pluripotent stem cells for the treatment of recessive dystrophic epidermolysis bullosaEarly reprogramming regulators identified by prospective isolation and mass cytometry.In situ genetic correction of the sickle cell anemia mutation in human induced pluripotent stem cells using engineered zinc finger nucleases.Conditional deletion of L1CAM in human neurons impairs both axonal and dendritic arborization and action potential generation.Dissecting direct reprogramming from fibroblast to neuron using single-cell RNA-seq
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P50
description
professor of pathology
@en
name
Marius Wernig
@en
Marius Wernig
@nl
type
label
Marius Wernig
@en
Marius Wernig
@nl
altLabel
M Wernig
@en
M. Wernig
@en
Wernig M
@en
Wernig M.
@en
Wernig
@en
prefLabel
Marius Wernig
@en
Marius Wernig
@nl
P214
P244
P214
P244
no2012062285
P31
P496
0000-0002-5309-515X