UDP-N-acetylglucosamine-lysosomal-enzyme N-acetylglucosaminephosphotransferase — In enzymology, an UDP N acetylglucosamine lysosomal enzyme N acetylglucosaminephosphotransferase (EC number|2.7.8.17) is an enzyme that catalyzes the chemical reaction:UDP N acetyl D glucosamine + lysosomal enzyme D mannose ightleftharpoons UMP + … Wikipedia
UDP-N-acetylglucosamine–lysosomal-enzyme N-acetylglucosaminephosphotransferase — UDP N ac·e·tyl·glu·co·sa·mine–ly·so·so·mal en·zyme N ac·e·tyl·glu·co·sa·mine·phos·pho·trans·fer·ase (as″ə tēl″gloo kōsґə mēn li″so soґməl enґzīm as″ə tēl″gloo… … Medical dictionary
UDP-N-acetylglucosamine:lysosomal enzyme N-acetylglucosaminyl-1-phosphotransferase — An enzyme that participates in the posttranslational modification of a number of lysosomal proteins; a deficiency or defect in this enzyme results in two forms of mucolipidoses, I cell disease, and pseudo Hurler polydystrophy … Medical dictionary
Enzyme replacement therapy — Die Enzymersatztherapie (EET oder ERT von engl. Enzyme Replacement Therapy) ist ein therapeutisches Verfahren zur Behandlung von Enzymdefekten bei lysosomalen Speicherkrankheiten. Den Patienten werden dabei per Infusion oder Injektion… … Deutsch Wikipedia
lysosomal diseases — Diseases (also known as storage diseases) in which a deficiency of a particular lysosomal enzyme leads to accumulation of the undigested substrate for that enzyme within cells. Not immediately fatal, but within a few years lead to serious… … Dictionary of molecular biology
Enzyme replacement therapy — is a medical treatment replacing an enzyme in patients in whom that particular enzyme is deficient or absent. Usually this is done by giving the patient an intravenous (IV) infusion containing the enzyme. Enzyme replacement therapy is currently… … Wikipedia
Lysosomal storage disease — The lysosomal storage diseases are a group of over forty human genetic disorders that result from defects in lysosomal function. [cite journal |author=Winchester B, Vellodi A, Young E |title=The molecular basis of lysosomal storage diseases and… … Wikipedia
Enzyme, lysosomal — An enzyme in an organelle (a little organ) called the lysosome within the cell. Lysosomal enzymes degrade (break down) macromolecules (large molecules) and other materials (such as bacteria) that have been taken up by the cell during the process… … Medical dictionary
lysosomal — lyso|soma̱l: ein Lysosom betreffend, von ihm ausgehend (z. B. lysosomale Enzyme) … Das Wörterbuch medizinischer Fachausdrücke
Glycogen debranching enzyme — Amylo alpha 1, 6 glucosidase, 4 alpha glucanotransferase Identifiers Symbols AGL; GDE External IDs … Wikipedia