Generation of induced pluripotent stem cell lines from Friedreich ataxia patients. - Wikidata - wikimedia - TriplyDB

Generation of induced pluripotent stem cell lines from Friedreich ataxia patients.

Generation of induced pluripotent stem cell lines from Friedreich ataxia patients.

http://www.wikidata.org/entity/Q39616684

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An Overview of Direct Somatic Reprogramming: The Ins and Outs of iPSCs Cardiovascular Disease Modeling Using Patient-Specific Induced Pluripotent Stem Cells Understanding the genetic and molecular pathogenesis of Friedreich's ataxia through animal and cellular models Utility of Induced Pluripotent Stem Cells for the Study and Treatment of Genetic Diseases: Focus on Childhood Neurological Disorders Induced pluripotent stem cell potential in medicine, specifically focused on reproductive medicine Modelling sarcomeric cardiomyopathies in the dish: from human heart samples to iPSC cardiomyocytes Generation and characterisation of Friedreich ataxia YG8R mouse fibroblast and neural stem cell models Rho/ROCK pathway is essential to the expansion, differentiation, and morphological rearrangements of human neural stem/progenitor cells induced by lysophosphatidic acid Neurons and cardiomyocytes derived from induced pluripotent stem cells as a model for mitochondrial defects in Friedreich's ataxia.Trichostatin A enhances differentiation of human induced pluripotent stem cells to cardiogenic cells for cardiac tissue engineering Friedreich's ataxia induced pluripotent stem cell-derived cardiomyocytes display electrophysiological abnormalities and calcium handling deficiency.Functional characterization of Friedreich ataxia iPS-derived neuronal progenitors and their integration in the adult brain.Genetic variations creating microRNA target sites in the FXN 3'-UTR affect frataxin expression in Friedreich ataxia.Stem cells on the brain: modeling neurodevelopmental and neurodegenerative diseases using human induced pluripotent stem cells.Probing disorders of the nervous system using reprogramming approaches.The current status of iPS cells in cardiac research and their potential for tissue engineering and regenerative medicine.Generation of disease-specific induced pluripotent stem cells from patients with different karyotypes of Down syndrome.Induced pluripotent stem cells to model and treat neurogenetic disorders Human pluripotent stem cells: applications and challenges in neurological diseases.Role of mismatch repair enzymes in GAA·TTC triplet-repeat expansion in Friedreich ataxia induced pluripotent stem cells.New lessons learned from disease modeling with induced pluripotent stem cells.Generation of human-induced pluripotent stem cells to model spinocerebellar ataxia type 2 in vitro.Neurodegeneration in Friedreich's ataxia: from defective frataxin to oxidative stress Stem cell technology for the study and treatment of motor neuron diseases.Human pluripotent stem cells for disease modelling and drug screening.Current status of drug screening and disease modelling in human pluripotent stem cells.Expanded complexity of unstable repeat diseases.Animal and cellular models of Friedreich ataxia.Diabetes in Friedreich ataxia.Human stem cell models of neurodegeneration: a novel approach to study mechanisms of disease development.Induced pluripotent stem cells for modeling of pediatric neurological disorders.Induced pluripotent stem cells for regenerative medicine Neural crest cells: from developmental biology to clinical interventions.Stem cell reprogramming: basic implications and future perspective for movement disorders.NEW DIRECTIONS IN BASIC RESEARCH IN HYPERTROPHY AND HEART FAILURE: RELEVANCE FOR PEDIATRIC CARDIOLOGY.Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes as a Model for Heart Development and Congenital Heart Disease.Induced pluripotent stem cell technology for modelling and therapy of cerebellar ataxia.Revisiting Mitochondrial Function and Metabolism in Pluripotent Stem Cells: Where Do We Stand in Neurological Diseases?Modeling simple repeat expansion diseases with iPSC technology.Unveiling a common mechanism of apoptosis in β-cells and neurons in Friedreich's ataxia.

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Generation of induced pluripotent stem cell lines from Friedreich ataxia patients.

http://www.wikidata.org/entity/Q39616684

description

2011 nî lūn-bûn

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2011年の論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年論文

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2011年论文

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2011年论文

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2011年论文

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name

Generation of induced pluripotent stem cell lines from Friedreich ataxia patients.

@en

Generation of induced pluripotent stem cell lines from Friedreich ataxia patients.

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type

label

Generation of induced pluripotent stem cell lines from Friedreich ataxia patients.

@en

Generation of induced pluripotent stem cell lines from Friedreich ataxia patients.

@nl

prefLabel

Generation of induced pluripotent stem cell lines from Friedreich ataxia patients.

@en

Generation of induced pluripotent stem cell lines from Friedreich ataxia patients.

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Stem Cell Reviews and Reports

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Generation of induced pluripotent stem cell lines from Friedreich ataxia patients

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Anna Michalska

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Jessie Leung

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Joseph P Sarsero

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Marguerite V Evans-Galea

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Martin B Delatycki

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Paul J Verma

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Robert Williamson

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P2860

Disease-specific induced pluripotent stem cells

Induced pluripotent stem cell lines derived from human somatic cells

Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors

Induction of pluripotent stem cells from adult human fibroblasts by defined factors

Embryonic stem cell lines derived from human blastocysts

Generation of germline-competent induced pluripotent stem cells

Reprogramming of human somatic cells to pluripotency with defined factors

Mouse models for Friedreich ataxia exhibit cardiomyopathy, sensory nerve defect and Fe-S enzyme deficiency followed by intramitochondrial iron deposits

Efficient and rapid generation of induced pluripotent stem cells from human keratinocytes

Generation of induced pluripotent stem cells without Myc from mouse and human fibroblasts

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