Effects of endurance training on skeletal muscle mitochondrial function in Huntington disease patients.

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Effects of endurance training on skeletal muscle mitochondrial function in Huntington disease patients.

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2017 nî lūn-bûn

@nan

2017年の論文

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2017年学术文章

@wuu

2017年学术文章

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2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

2017年學術文章

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name

Effects of endurance training ...... n Huntington disease patients.

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Effects of endurance training ...... n Huntington disease patients.

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type

Item

label

Effects of endurance training ...... n Huntington disease patients.

@en

Effects of endurance training ...... n Huntington disease patients.

@nl

prefLabel

Effects of endurance training ...... n Huntington disease patients.

@en

Effects of endurance training ...... n Huntington disease patients.

@nl

P1476

Effects of endurance training ...... n Huntington disease patients.

@en

P2093

Carsten Lundby

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Hans H Jung

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Jens A Petersen

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Marco Toigo

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Maria Ligon-Auer

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Natalia Khmara

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Sandro Manuel Mueller

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Saskia Maria Gehrig

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Sebastian Frese

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Violeta Mihaylova

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P2860

The kinetic properties of citrate synthase from rat liver mitochondria

Wheel running from a juvenile age delays onset of specific motor deficits but does not alter protein aggregate density in a mouse model of Huntington's disease.

Molecular and biochemical characterisation of a novel mutation in POLG associated with Alpers syndrome.

The relationship between skeletal muscle mitochondrial citrate synthase activity and whole body oxygen uptake adaptations in response to exercise training.

Combined effects of whole-body vibration, resistance exercise, and vascular occlusion on skeletal muscle and performance.

Aerobic high-intensity intervals improve VO2max more than moderate training.

Exercise attenuates neuropathology and has greater benefit on cognitive than motor deficits in the R6/1 Huntington's disease mouse model.

Pharmacologic activation of mitochondrial biogenesis exerts widespread beneficial effects in a transgenic mouse model of Huntington's disease

Enhanced mitochondrial biogenesis ameliorates disease phenotype in a full-length mouse model of Huntington's disease.

Mitochondria: isolation, structure and function.

P2888

s13023-017-0740-z

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184

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scholarly article

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10.1186/S13023-017-0740-Z

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P433

http://www.w3.org/2001/XMLSchema#string

P478

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P50

Jean-Marc Nuoffer

André Schaller

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2017-12-19T00:00:00Z

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P6179

1099721832

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P698

29258585

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P921

Huntington disease

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5735536

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