Reprogramming Huntington monkey skin cells into pluripotent stem cells
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Pluripotent stem cells models for Huntington's disease: prospects and challengesModeling Huntington's disease with induced pluripotent stem cellsMonomeric, oligomeric and polymeric proteins in huntington disease and other diseases of polyglutamine expansionmRNA-Seq and microRNA-Seq whole-transcriptome analyses of rhesus monkey embryonic stem cell neural differentiation revealed the potential regulators of rosette neural stem cells.Reversal of cellular phenotypes in neural cells derived from Huntington's disease monkey-induced pluripotent stem cellsInduction of pluripotent stem cells from a cynomolgus monkey using a polycistronic simian immunodeficiency virus-based vector, differentiation toward functional cardiomyocytes, and generation of stably expressing reporter lines.Induced pluripotent stem cells: a new tool to confront the challenge of neuropsychiatric disordersDirect reprogramming of Huntington's disease patient fibroblasts into neuron-like cells leads to abnormal neurite outgrowth, increased cell death, and aggregate formationA panel of induced pluripotent stem cells from chimpanzees: a resource for comparative functional genomics.Nonhuman primate induced pluripotent stem cells in regenerative medicine.The Path to microRNA Therapeutics in Psychiatric and Neurodegenerative DisordersHuntington disease iPSCs show early molecular changes in intracellular signaling, the expression of oxidative stress proteins and the p53 pathwayInduced pluripotent stem cells to model and treat neurogenetic disordersmiR-196a Ameliorates Cytotoxicity and Cellular Phenotype in Transgenic Huntington's Disease Monkey Neural CellsGermline transmission in transgenic Huntington's disease monkeysPolyglutamine (polyQ) disorders: the chromatin connection.Pathogenic cellular phenotypes are germline transmissible in a transgenic primate model of Huntington's disease.Progress and prospects for genetic modification of nonhuman primate models in biomedical research.Derivation of induced pluripotent stem cells from the baboon: a nonhuman primate model for preclinical testing of stem cell therapies.Systematic review of induced pluripotent stem cell technology as a potential clinical therapy for spinal cord injury.Polyglutamine Aggregation in Huntington Disease: Does Structure Determine Toxicity?iPSC-based drug screening for Huntington's disease.Huntington Disease as a Neurodevelopmental Disorder and Early Signs of the Disease in Stem Cells.Clinical potential of human-induced pluripotent stem cells : Perspectives of induced pluripotent stem cells.Patient-specific pluripotent stem cells in neurological diseases.FOXOs modulate proteasome activity in human-induced pluripotent stem cells of Huntington's disease and their derived neural cells.
P2860
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P2860
Reprogramming Huntington monkey skin cells into pluripotent stem cells
description
2010 nî lūn-bûn
@nan
2010 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Reprogramming Huntington monkey skin cells into pluripotent stem cells
@ast
Reprogramming Huntington monkey skin cells into pluripotent stem cells
@en
Reprogramming Huntington monkey skin cells into pluripotent stem cells
@nl
type
label
Reprogramming Huntington monkey skin cells into pluripotent stem cells
@ast
Reprogramming Huntington monkey skin cells into pluripotent stem cells
@en
Reprogramming Huntington monkey skin cells into pluripotent stem cells
@nl
prefLabel
Reprogramming Huntington monkey skin cells into pluripotent stem cells
@ast
Reprogramming Huntington monkey skin cells into pluripotent stem cells
@en
Reprogramming Huntington monkey skin cells into pluripotent stem cells
@nl
P2093
P2860
P356
P1476
Reprogramming Huntington monkey skin cells into pluripotent stem cells
@en
P2093
Adam Neumann
Anthony W S Chan
Jin-Jing Yang
Pei-Hsun Cheng
P2860
P304
P356
10.1089/CELL.2010.0019
P577
2010-10-01T00:00:00Z