Glycogen Storage Disorder Type IXb: Exploring Clinical Patterns and Genetic Insights Into a Rare Phosphorylase Kinase B (PHKB)-Associated Case. [PDF]
Venkata Renuka I+4 more
europepmc +1 more source
Mass Spectrometric Analysis of Surface-Exposed Regions in the Hexadecameric Phosphorylase Kinase Complex. [PDF]
Rimmer MA+5 more
europepmc +1 more source
The Structure Of Phosphorylase Kinase Holoenzyme At Subnanometer Resolution, Location Of The Catalytic Subunit And The Substrate Glycogen Phosphorylase [PDF]
Slavica Jonić+7 more
openalex +1 more source
A rare co-occurrence of phosphorylase kinase deficiency (GSD type IXd) and alpha-glycosidase deficiency (GSD Type II) in a 53-year-old man presenting with an atypical glycogen storage disease phenotype. [PDF]
Picillo E+4 more
europepmc +1 more source
Molecular basis for the hormonal regulation of the tyrosine aminotransferase and tryptophane oxygenase genes [PDF]
Baxter J. D.+19 more
core +1 more source
The interaction of calmodulin with regulatory peptides of phosphorylase kinase.
Darmawi Juminaga+2 more
openalex +1 more source
Electrostatic changes in phosphorylase kinase induced by its obligatory allosteric activator Ca2+
Timothy S Priddy+2 more
semanticscholar +1 more source