EZ spheres: a stable and expandable culture system for the generation of pre-rosette multipotent stem cells from human ESCs and iPSCs.
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Self-Organizing 3D Human Neural Tissue Derived from Induced Pluripotent Stem Cells Recapitulate Alzheimer's Disease PhenotypesDerivation of myogenic progenitors directly from human pluripotent stem cells using a sphere-based culture.Human induced pluripotent stem cells are a novel source of neural progenitor cells (iNPCs) that migrate and integrate in the rodent spinal cord.Sensory neurons do not induce motor neuron loss in a human stem cell model of spinal muscular atrophyBack to the future: how human induced pluripotent stem cells will transform regenerative medicine.Genetic reprogramming of human amniotic cells with episomal vectors: neural rosettes as sentinels in candidate selection for validation assaysTargeting SR proteins improves SMN expression in spinal muscular atrophy cells.Stimulation of GABA-induced Ca2+ influx enhances maturation of human induced pluripotent stem cell-derived neuronsHD iPSC-derived neural progenitors accumulate in culture and are susceptible to BDNF withdrawal due to glutamate toxicity.The N-ethylmaleimide-sensitive factor and dysbindin interact to modulate synaptic plasticity.Bromodomain inhibitors regulate the C9ORF72 locus in ALSRapid and robust generation of long-term self-renewing human neural stem cells with the ability to generate mature astroglia.Neurite Aggregation and Calcium Dysfunction in iPSC-Derived Sensory Neurons with Parkinson's Disease-Related LRRK2 G2019S Mutation.Clinical Trials in a Dish: The Potential of Pluripotent Stem Cells to Develop Therapies for Neurodegenerative Diseases.Impact of a cytomegalovirus kinase inhibitor on infection and neuronal progenitor cell differentiationPhysiological normoxia and absence of EGF is required for the long-term propagation of anterior neural precursors from human pluripotent cells.Spinal muscular atrophy astrocytes exhibit abnormal calcium regulation and reduced growth factor productionIn vitro neurogenesis: development and functional implications of iPSC technology.Human-induced pluripotent stem cells: potential for neurodegenerative diseases.Proteome-wide analysis of neural stem cell differentiation to facilitate transition to cell replacement therapies.Developing therapies for spinal muscular atrophy.Astrocyte-produced miR-146a as a mediator of motor neuron loss in spinal muscular atrophy.Optimization of Morpholino Antisense Oligonucleotides Targeting the Intronic Repressor Element1 in Spinal Muscular Atrophy.Modeling simple repeat expansion diseases with iPSC technology.Developmental alterations in Huntington's disease neural cells and pharmacological rescue in cells and mice.Targeting ATM ameliorates mutant Huntingtin toxicity in cell and animal models of Huntington's disease.CD133-enriched Xeno-Free human embryonic-derived neural stem cells expand rapidly in culture and do not form teratomas in immunodeficient mice.Dormant cancer cells accumulate high protoporphyrin IX levels and are sensitive to 5-aminolevulinic acid-based photodynamic therapy.Huntington's Disease: Calcium Dyshomeostasis and Pathology ModelsSMN deficiency does not induce oxidative stress in SMA iPSC-derived astrocytes or motor neurons.Astrocytes influence the severity of spinal muscular atrophy.The Generation of Mouse and Human Huntington Disease iPS Cells Suitable for In vitro Studies on Huntingtin FunctionOptimization of trans-Splicing for Huntington's Disease RNA Therapy.An isogenic blood-brain barrier model comprising brain endothelial cells, astrocytes, and neurons derived from human induced pluripotent stem cells.A cGMP-applicable expansion method for aggregates of human neural stem and progenitor cells derived from pluripotent stem cells or fetal brain tissue.Huntington's Disease iPSC-Derived Brain Microvascular Endothelial Cells Reveal WNT-Mediated Angiogenic and Blood-Brain Barrier Deficits.Tetracycline-Inducible and Reversible Stable Gene Expression in Human iPSC-Derived Neural Progenitors and in the Postnatal Mouse Brain.Induction of early neural precursors and derivation of tripotent neural stem cells from human pluripotent stem cells under xeno-free conditions.Directed differentiation of human pluripotent stem cells to blood-brain barrier endothelial cells.Engineering the human blood-brain barrier in vitro.
P2860
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P2860
EZ spheres: a stable and expandable culture system for the generation of pre-rosette multipotent stem cells from human ESCs and iPSCs.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
2013年论文
@zh
2013年论文
@zh-cn
name
EZ spheres: a stable and expan ...... lls from human ESCs and iPSCs.
@en
EZ spheres: a stable and expan ...... lls from human ESCs and iPSCs.
@nl
type
label
EZ spheres: a stable and expan ...... lls from human ESCs and iPSCs.
@en
EZ spheres: a stable and expan ...... lls from human ESCs and iPSCs.
@nl
prefLabel
EZ spheres: a stable and expan ...... lls from human ESCs and iPSCs.
@en
EZ spheres: a stable and expan ...... lls from human ESCs and iPSCs.
@nl
P2093
P2860
P50
P1433
P1476
EZ spheres: a stable and expan ...... lls from human ESCs and iPSCs.
@en
P2093
Allison D Ebert
Amanda M Hurley
Brandon C Shelley
Clive N Svendsen
Dhruv Sareen
Ho Won Kim
Jered V McGivern
Soshana P Svendsen
Teresa N Patitucci
Valentina Castiglioni
P2860
P304
P356
10.1016/J.SCR.2013.01.009
P577
2013-02-04T00:00:00Z