| 1 |
33799212 | A novel PHKA1 mutation associating myopathy and cognitive impairment: Expanding the spectrum of phosphorylase kinase b (PhK) deficiency. | 2021 May 15 |
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| 2 |
34740118 | Generation of human induced pluripotent stem cell line, KRIBBi003-A, from urinary cells of a patient with glycogen storage disease type IXa. | 2021 Oct 22 |
4 |
| 3 |
32446205 | Glycogenolysis Is Crucial for Astrocytic Glycogen Accumulation and Brain Damage after Reperfusion in Ischemic Stroke. | 2020 May 6 |
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| 4 |
33014498 | Glycogen Storage Disease Type IX due to a Novel Mutation in PHKA2 Gene. | 2020 |
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| 5 |
31279057 | Kinetic regime of Ca2+ and Mg2+-induced aggregation of phosphorylase kinase at 40 °C. | 2019 Oct 1 |
1 |
| 6 |
29098736 | Structural characterization of the catalytic γ and regulatory β subunits of phosphorylase kinase in the context of the hexadecameric enzyme complex. | 2018 Feb |
2 |
| 7 |
27845042 | The regulatory α and β subunits of phosphorylase kinase directly interact with its substrate, glycogen phosphorylase. | 2017 Jan 8 |
2 |
| 8 |
26378249 | Sensitive, nonradioactive assay of phosphorylase kinase through measurement of enhanced phosphorylase activity towards fluorogenic dextrin. | 2016 Feb |
3 |
| 9 |
24389071 | Variability of disease spectrum in children with liver phosphorylase kinase deficiency caused by mutations in the PHKG2 gene. | 2014 Mar |
3 |
| 10 |
22899091 | Clinical application of massively parallel sequencing in the molecular diagnosis of glycogen storage diseases of genetically heterogeneous origin. | 2013 Feb |
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| 11 |
20604537 | The glucoamylase inhibitor acarbose is a direct activator of phosphorylase kinase. | 2010 Aug 10 |
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| 12 |
19141288 | The structure of phosphorylase kinase holoenzyme at 9.9 angstroms resolution and location of the catalytic subunit and the substrate glycogen phosphorylase. | 2009 Jan 14 |
2 |
| 13 |
18281058 | Structural evidence for co-evolution of the regulation of contraction and energy production in skeletal muscle. | 2008 Mar 28 |
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| 14 |
18950708 | 3D mapping of glycogenosis-causing mutations in the large regulatory alpha subunit of phosphorylase kinase. | 2008 Nov |
3 |
| 15 |
15362101 | Effect of molecular crowding on self-association of phosphorylase kinase and its interaction with phosphorylase b and glycogen. | 2004 Sep-Oct |
5 |
| 16 |
11796108 | Three-dimensional structure of phosphorylase kinase at 22 A resolution and its complex with glycogen phosphorylase b. | 2002 Jan |
2 |
| 17 |
10487978 | Phosphorylase kinase: the complexity of its regulation is reflected in the complexity of its structure. | 1999 Sep 15 |
2 |
| 18 |
10987651 | A mutation in GLUT2, not in phosphorylase kinase subunits, in hepato-renal glycogenosis with Fanconi syndrome and low phosphorylase kinase activity. | 1999 Sep |
1 |
| 19 |
9384616 | Liver glycogenosis due to phosphorylase kinase deficiency: PHKG2 gene structure and mutations associated with cirrhosis. | 1998 Jan |
3 |
| 20 |
9600238 | Variability of biochemical and clinical phenotype in X-linked liver glycogenosis with mutations in the phosphorylase kinase PHKA2 gene. | 1998 Apr |
2 |
| 21 |
9835437 | Clinical, biochemical and molecular findings in a patient with X-linked liver glycogenosis followed for 40 years. | 1998 Nov |
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| 22 |
8896567 | Mutations in the testis/liver isoform of the phosphorylase kinase gamma subunit (PHKG2) cause autosomal liver glycogenosis in the gsd rat and in humans. | 1996 Nov |
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| 23 |
7549948 | Isolation of cDNA encoding the human liver phosphorylase kinase alpha subunit (PHKA2) and identification of a missense mutation of the PHKA2 gene in a family with liver phosphorylase kinase deficiency. | 1995 Jul |
2 |
| 24 |
7711737 | Mutations in the phosphorylase kinase gene PHKA2 are responsible for X-linked liver glycogen storage disease. | 1995 Jan |
1 |
| 25 |
7511111 | Curcumin is a non-competitive and selective inhibitor of phosphorylase kinase. | 1994 Mar 14 |
1 |
| 26 |
21634085 | Phosphorylase Kinase Deficiency | 1993 |
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