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  1. Increased PFKL and PFKM expression underlies increased glycolysis in pulmonary arterial...

  2. Mitochondrial and potassium channel dysfunction in pulmonary arterial hypertension

    Pulmonary arterial hypertension (PAH) is a rare, progressive and potentially fatal cardiopulmonary disorder, characterised by extensive remodelling and luminal narrowing of the small pulmonary arteries. Central to this remodelling is the

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