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Mutations in the gamma2 subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis.

Mutations in the gamma2 subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis.

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Bibliografiske detaljer
Main Authors: Blair, E, Redwood, C, Ashrafian, H, Oliveira, M, Broxholme, J, Kerr, B, Salmon, A, Ostman-Smith, I, Watkins, H
Format: Journal article
Udgivet: 2001
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  • Other Versions (1)
  • Lignende værker
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Beskrivelse
Summary:

Lignende værker

  • Mutations in the gamma(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis.
    af: Blair, E, et al.
    Udgivet: (2001)
  • Hypertrophic cardiomyopathy mutations in the gamma 2 subunit of AMP-activated kinase suggest a central role of energy compromise in disease pathogenesis
    af: Blair, E, et al.
    Udgivet: (2001)
  • Mutation analysis of AMP-activated protein kinase subunits in inherited cardiomyopathies: implications for kinase function and disease pathogenesis.
    af: Oliveira, S, et al.
    Udgivet: (2003)
  • Delineating the role of adenosine monophosphate (AMP)-activated protein kinase (AMP) gamma 2 subunit in hypertrophic cardiomyopathy (HCM)
    af: Grignani, R, et al.
    Udgivet: (2005)
  • Mutation analysis of genes encoding subunits of AMP-activated protein kinase (AMPK) in inherited cardiomyopathies
    af: Blair, E, et al.
    Udgivet: (2002)

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