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A genetic disease in humans de...
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A genetic disease in humans demonstrates the importance of hypoxia-inducible factor in skeletal muscle metabolism
Manylion Llyfryddiaeth
Prif Awduron:
Formenti, F
,
Clarke, K
,
Dorrington, K
,
Edwards, L
,
Emmanuel, Y
,
Lappin, T
,
McMullin, M
,
McNamara, C
,
Mills, W
,
Murphy, J
,
O'Connor, D
,
Percy, M
,
Smith, T
,
Treacy, M
,
Robbins, P
Fformat:
Journal article
Cyhoeddwyd:
2009
Daliadau
Disgrifiad
Eitemau Tebyg
Dangos Staff
Eitemau Tebyg
Regulation of human metabolism by hypoxia-inducible factor.
gan: Formenti, F, et al.
Cyhoeddwyd: (2010)
A 'GAIN-OF-FUNCTION' MUTATION IN THE HYPOXIA-INDUCIBLE FACTOR 2 alpha GENE DOES NOT REDUCE EXERCISE CAPACITY IN HUMANS
gan: Formenti, F, et al.
Cyhoeddwyd: (2009)
Cardiopulmonary function in two human disorders of the hypoxia-inducible factor (HIF) pathway: von Hippel-Lindau disease and HIF-2α gain-of-function mutation.
gan: Formenti, F, et al.
Cyhoeddwyd: (2011)
Acclimatization of skeletal muscle mitochondria to high-altitude hypoxia during an ascent of Everest.
gan: Levett, D, et al.
Cyhoeddwyd: (2012)
Proteins modulation in human skeletal muscle in the early phase of adaptation to hypobaric hypoxia.
gan: Viganò, A, et al.
Cyhoeddwyd: (2008)