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July 1, 1976European Journal of BiochemistryOpen Access

The Molecular Basis of Skeletal Muscle Phosphorylase Kinase Deficiency

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Authors

PCPatricia T.W. CohenUniversidade do Estado do ParáABAni. BURCHELLUniversity of Dundee
Philip Cohen
Philip CohenMRC Protein Phosphorylation and Ubiquitylation Unit

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Implication

Mouse model links X-linked defect to phosphorylase kinase deficiency; leaves open human disease relevance.

Key Points

Key points are not available for this paper at this time.

Cite This Study

Cohen et al. (1976) studied this question.

synapsesocial.com/papers/6a845c01002ab1506fb2b043https://doi.org/10.1111/j.1432-1033.1976.tb10524.x
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Also Consider

Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENT1951 · 318,705 citations
  2. 2Characterization of the Phosphorylase b to a Converting Activity in Skeletal Muscle Extracts of Mice with the Phosphorylase b Kinase Deficiency Mutation1974 · 32 citations
  3. 3X‐Linked testicular feminization in the mouse as a non‐inducible regulatory mutation of the Jacob‐Monod type1970 · 103 citations
  4. 4The Subunit Structure of Rabbit‐Skeletal‐Muscle Phosphorylase Kinase, and the Molecular Basis of Its Activation Reactions1973 · 728 citations