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  2. Glycogen phosphorylase - Wikipedia

    en.wikipedia.org/wiki/Glycogen_phosphorylase

    The glycogen phosphorylase monomer is a large protein, composed of 842 amino acids with a mass of 97.434 kDa in muscle cells. While the enzyme can exist as an inactive monomer or tetramer, it is biologically active as a dimer of two identical subunits.

  3. PYGL - Wikipedia

    en.wikipedia.org/wiki/PYGL

    Glycogen phosphorylase, liver form (PYGL), also known as human liver glycogen phosphorylase (HLGP), is an enzyme that in humans is encoded by the PYGL gene on chromosome 14. [1] [2] This gene encodes a homodimeric protein that catalyses the cleavage of alpha-1,4-glucosidic bonds to release glucose-1-phosphate from liver glycogen stores.

  4. Myophosphorylase - Wikipedia

    en.wikipedia.org/wiki/Myophosphorylase

    Myophosphorylase or glycogen phosphorylase, muscle associated (PYGM) is the muscle isoform of the enzyme glycogen phosphorylase and is encoded by the PYGM gene. This enzyme helps break down glycogen (a form of stored carbohydrate) into glucose-1-phosphate (not glucose), so it can be used within the muscle cell.

  5. PYGB - Wikipedia

    en.wikipedia.org/wiki/PYGB

    The PYGB gene encodes one of three major glycogen phosphorylase isoforms, which are distinguished by their different structures and subcellular localizations: brain (PYGB), muscle (PYGM), and liver . [2] [3] GPBB is the longest of the three isozymes, with a length of 862 residues, due to the extended 3'-UTR at the enzyme's C-terminal.

  6. Glycogen storage disease type V - Wikipedia

    en.wikipedia.org/wiki/Glycogen_storage_disease...

    In some cases, abnormal glycogen accumulation stained by periodic acid-Schiff can be seen with microscopy. [25] [9] Genetic sequencing of the PYGM gene (which codes for the muscle isoform of glycogen phosphorylase [49] [50]) may be done to determine the presence of gene mutations, determining if McArdle's is present. This type of testing is ...

  7. Glycogen storage disease type IX - Wikipedia

    en.wikipedia.org/wiki/Glycogen_storage_disease...

    Physical therapy, follow metabolic nutritionist [1] Glycogen storage disease type IX is a hereditary deficiency of glycogen phosphorylase kinase B that affects the liver and skeletal muscle tissue.

  8. Regenxbio's Gene Therapy Outlook Dims As Rival ... - AOL

    www.aol.com/regenxbios-gene-therapy-outlook-dims...

    Goldman Sachs downgraded Regenxbio Inc (NASDAQ:RGNX), citing gene therapy’s appeal for wet AMD and diabetic retinopathy is uncertain, as most patients are elderly and newer anti-VEGF treatments ...

  9. Glycogen synthase - Wikipedia

    en.wikipedia.org/wiki/Glycogen_synthase

    Glycogen synthase (UDP-glucose-glycogen glucosyltransferase) is a key enzyme in glycogenesis, the conversion of glucose into glycogen. It is a glycosyltransferase ( EC 2.4.1.11 ) that catalyses the reaction of UDP-glucose and (1,4- α - D -glucosyl) n to yield UDP and (1,4- α - D -glucosyl) n+1 .