Patient-Derived Stem Cell Models in HSP: Disease Modelling and Drug Discovery

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Patient-Derived Stem Cell Models in HSP: Disease Modelling and Drug Discovery

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wetenschappelijk artikel

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наукова стаття, опублікована в липні 2018

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Patient-Derived Stem Cell Models in HSP: Disease Modelling and Drug Discovery

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Patient-Derived Stem Cell Models in HSP: Disease Modelling and Drug Discovery

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Patient-Derived Stem Cell Models in HSP: Disease Modelling and Drug Discovery

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Patient-Derived Stem Cell Models in HSP: Disease Modelling and Drug Discovery

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Patient-Derived Stem Cell Models in HSP: Disease Modelling and Drug Discovery

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Patient-Derived Stem Cell Models in HSP: Disease Modelling and Drug Discovery

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P1476

Patient-Derived Stem Cell Models in HSP: Disease Modelling and Drug Discovery

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P2093

Carolyn M Sue

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Gautam Wali

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P2860

Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia

Hereditary spastic paraplegia proteins REEP1, spastin, and atlastin-1 coordinate microtubule interactions with the tubular ER network

Drosophila spastin regulates synaptic microtubule networks and is required for normal motor function

The axonal transport of mitochondria

HDAC6 regulates mitochondrial transport in hippocampal neurons

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

Delving into the complexity of hereditary spastic paraplegias: how unexpected phenotypes and inheritance modes are revolutionizing their nosology

Spastin, the protein mutated in autosomal dominant hereditary spastic paraplegia, is involved in microtubule dynamics

Multipotent stem cells from adult olfactory mucosa

Peroxisome biogenesis disorders

P304

142

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P31

scholarly article

P356

10.3390/BRAINSCI8080142

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P407

English

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P478

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P50

Alan Mackay-Sim

P577

2018-07-31T00:00:00Z

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30065201

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6120041

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