(Phosphorylase, Glycogen, Muscle (PYGM))
Featured PYGM Categories
Recommended PYGM Antibodies
Recommended PYGM ELISA Kits
Recommended PYGM Proteins
Latest Publications for our PYGM products: "Combinatory high-resolution microdissection/ultra performance liquid chromatographic-mass spectrometry approach for small tissue volume analysis of rat brain glycogen." in: Journal of pharmaceutical and biomedical analysis, Vol. 178, pp. 112884, (2020) (PubMed).
: "Norepinephrine control of ventromedial hypothalamic nucleus glucoregulatory neurotransmitter expression in the female rat: Role of monocarboxylate transporter function." in: Molecular and cellular neurosciences, Vol. 95, pp. 51-58, (2019) (PubMed).
: "Hindbrain lactoprivic regulation of hypothalamic neuron transactivation and gluco-regulatory neurotransmitter expression: Impact of antecedent insulin-induced hypoglycemia." in: Neuropeptides, Vol. 77, pp. 101962, (2019) (PubMed).
: "Discovery of serum protein biomarkers in the mdx mouse model and cross-species comparison to Duchenne muscular dystrophy patients." in: Human molecular genetics, Vol. 23, Issue 24, pp. 6458-69, (2015) (PubMed).
: "PYGM expression analysis in white blood cells: A complementary tool for diagnosing McArdle disease?" in: Neuromuscular disorders : NMD, (2014) (PubMed).
: "AMP-activated protein kinase does not associate with glycogen alpha-particles from rat liver." in: Biochemical and biophysical research communications, Vol. 362, Issue 4, pp. 811-5, (2007) (PubMed).
: "cDNA microarray analysis of gene expression profiles in human placenta: up-regulation of the transcript encoding muscle subunit of glycogen phosphorylase in preeclampsia." in: Journal of the Society for Gynecologic Investigation, Vol. 10, Issue 8, pp. 496-502, (2003) (PubMed).
: "Loss of B cell identity correlates with loss of B cell-specific transcription factors in Hodgkin/Reed-Sternberg cells of classical Hodgkin lymphoma." in: Oncogene, Vol. 21, Issue 32, pp. 4908-20, (2002) (PubMed).
: "Molecular genetic study of myophosphorylase deficiency (McArdle's disease) in two Yemenite-Jewish families." in: Neuromuscular disorders : NMD, Vol. 12, Issue 9, pp. 824-7, (2002) (PubMed).
: "Two new mutations in the myophosphorylase gene in Italian patients with McArdle's disease." in: Neuromuscular disorders : NMD, Vol. 12, Issue 5, pp. 498-500, (2002) (PubMed).
Synonyms and alternative names related to PYGMglycogen phosphorylase, muscle associated (PYGM), glycogen phosphorylase, muscle form (THA_70), muscle glycogen phosphorylase (Pygm), phosphorylase, glycogen, muscle A (pygma), glycogen phosphorylase, muscle associated (Pygm), AI115133, im:7150327, Muscpho, PG, zgc:110706
Protein level used designations for PYGM
- glycogen phosphorylase
- glycogen phosphorylase, muscle form
- phosphorylase, glycogen; muscle (McArdle syndrome, glycogen storage disease type V)
- phosphorylase, glycogen. muscle
- Phosphorylase glycogen
- Phosphorylase, glycogen; muscle (McArdle syndrome)
- muscle (McArdle syndrome)
- muscle glycogen phosphorylase
- glycogen myophosphorylase
Did you look for something else?
- Pvt-Associated Transcript