Mitochondrial and metabolic-based protective strategies in Huntington's disease: the case of creatine and coenzyme Q. - Wikidata - wikimedia - TriplyDB

Mitochondrial and metabolic-based protective strategies in Huntington's disease: the case of creatine and coenzyme Q.

Mitochondrial and metabolic-based protective strategies in Huntington's disease: the case of creatine and coenzyme Q.

http://www.wikidata.org/entity/Q37965763

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Mechanisms of RNA-induced toxicity in CAG repeat disorders Coenzyme q10 therapy Downregulation of genes involved in metabolism and oxidative stress in the peripheral leukocytes of Huntington's disease patients.

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Mitochondrial and metabolic-based protective strategies in Huntington's disease: the case of creatine and coenzyme Q.

http://www.wikidata.org/entity/Q37965763

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article scientifique

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Mitochondrial and metabolic-ba ...... se of creatine and coenzyme Q.

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Mitochondrial and metabolic-ba ...... se of creatine and coenzyme Q.

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Mitochondrial and metabolic-ba ...... se of creatine and coenzyme Q.

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Mitochondrial and metabolic-ba ...... se of creatine and coenzyme Q.

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Reviews in the Neurosciences

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Mitochondrial and metabolic-ba ...... se of creatine and coenzyme Q.

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A Cristina Rego

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Luana Naia

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Maria João Ribeiro

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P2860

Huntingtin is a cytoplasmic protein associated with vesicles in human and rat brain neurons

AMP kinase is required for mitochondrial biogenesis in skeletal muscle in response to chronic energy deprivation.

Mitochondria, calcium and cell death: a deadly triad in neurodegeneration

PGC-1alpha deficiency causes multi-system energy metabolic derangements: muscle dysfunction, abnormal weight control and hepatic steatosis

The whole structure of the 13-subunit oxidized cytochrome c oxidase at 2.8 A

A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes.

Surfing the p53 network

Huntingtin aggregation and toxicity in Huntington's disease

Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation

The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease

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13-28

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scholarly article

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10.1515/RNS.2011.060

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1

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23

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2011-12-02T00:00:00Z

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51860436

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22150069

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P921

Huntington disease