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1,642 Possible Causes for activity, glycine, oxidase

  • Connective Tissue Disease

    Metabolism Disorders Disease (OMIM Number) Defective Proteins or Enzymes Defective Gene or Genes (Chromosomal Location) Comments Hyperprolinemia, type I (239500) Proline oxidase[merck.com] […] intensity of the activity) by reducing the activity.[medicinenet.com] Scleroderma – an activation of immune cells that produces scar tissue in the skin, internal organs, and small blood vessels.[en.wikipedia.org]

  • Infectious Mononucleosis

    […] subunit VIII, COX11; cytochrome c oxidase assembly protein, KCNA10; potassium voltage-gated channel, MGP; matrix Gla protein; ATP5L; ATP synthase).[dx.doi.org] The mitogen responses were decreased and natural killer (NK) cell activity was low.[dx.doi.org] […] antigen-1 through Epstein-Barr nuclear antigen-1's glycine/alanine repeat.[dx.doi.org]

  • Aldehyde

    An inhibition study suggested that monoamine oxidase-B (MAO-B) oxidizes KW-2449 to an iminium (intermediate) and aldehyde oxidase (AO) then metabolizes the intermediate to[ncbi.nlm.nih.gov] Maximum activation was observed at 1 μg/ml of cabbage extract with 2.6 fold increase in the activity.[ncbi.nlm.nih.gov] KEYWORDS: Betaine aldehyde dehydrogenase; Glycine betaine; Litopenaeus vannamei; Molecular characterization; Osmotic stress[ncbi.nlm.nih.gov]

  • Tuberculosis

    Maridonneau-Parini I (2000) Nonopsonic phagocytosis of zymosan and Mycobacterium kansasii by CR3 (CD11b/CD18) involves distinct molecular determinants and is or is not coupled with NADPH oxidase[springerlink.com] However, the role of IGRAs for the diagnosis of active tuberculosis (TB) remains unclear.[ncbi.nlm.nih.gov] In addition to INH activation, KatG also possesses peroxynitritase and NADH oxidase activities that are vital for bacterial defense against oxidative stress [108] – [109][ncbi.nlm.nih.gov]

  • Hereditary Coproporphyria

    This is the first mutation to be found at the coproporphyrinogen oxidase locus.[ncbi.nlm.nih.gov] […] clinical manifestation occur when the activity of uroporphyrinogen-I-synthase (E.C. 4.3.1.8) becomes rate-limiting for haem synthesis.[ncbi.nlm.nih.gov] This mutation results in a glycine to arginine substitution at amino acid 180.[ncbi.nlm.nih.gov]

  • Xanthinuria

    The residual xanthine oxidase from the parents exhibited normal kinetics with respect to hypoxanthine.[ncbi.nlm.nih.gov] Clinical Information An inborn error of metabolism resulting from a deficiency of hypoxanthine-guanine phosphoribosyltransferase (ec 2.4.2.8) with increased conversion of glycine[icd9data.com] […] mutation C2729T, while C3886T resulted in major residual activity of about 50% of the wild type.[ncbi.nlm.nih.gov]

  • Variegate Porphyria

    Variegate porphyria is characterized by a partial reduction in the activity of protoporphyrinogen oxidase.[ncbi.nlm.nih.gov] […] of clinical symptoms, excrete porphyrin metabolites in urine and stool similar to variegate porphyria, accompanied by a significant decrease of porphobilinogen deaminase activity[ncbi.nlm.nih.gov] In three other patients from two unrelated families we found a missense point mutation leading to glycine to arginine substitution (G232R) in exon 7.[ncbi.nlm.nih.gov]

  • Tranylcypromine

    Although monoamine oxidase (MAO) inhibitors, phytoestrogen and antioxidants used in chemotherapy have been systematically studied, their effects on cancer cell growth remain[ncbi.nlm.nih.gov] In particular, compound 19l had robust, selective LSD1 inhibitory activity, which was obviously higher than the inhibitory activity against homologues monoamine oxidase-A[ncbi.nlm.nih.gov] […] structure group: DG00949 Product (DG00949): D00826 US Efficacy Antidepressant, Monoamine oxidase (MAO) inhibitor Target MAO [HSA: 4128 4129 ] [KO: K00274 ] Pathway hsa00260 Glycine[kegg.jp]

  • Nonketotic Hyperglycinemia

    Polyglucosan Body Disease 147 Peroxisomes and Peroxisomal Disorders 151 Peroxisome Biogenesis Defects 154 Peroxisomal DBifunctional Protein Deficiency 167 Peroxisomal AcylCoA Oxidase[books.google.com] The activity of the T-protein was normal.[ncbi.nlm.nih.gov] The disease is caused by defects in the glycine cleavage system, an enzyme responsible for glycine catabolism.[en.wikipedia.org]

  • Deficiency of Sulfite Oxidase

    Abstract Isolated sulfite oxidase (SO) deficiency is an autosomal recessively inherited inborn error of sulfur metabolism.[ncbi.nlm.nih.gov] The deficiencies can be diagnosed prenatally by monitoring sulfite oxidase activity in chorionic villus sampling (CVS) tissue.[ncbi.nlm.nih.gov] […] dehydrogenase deficiency pathway GABA aminotransferase deficiency pathway glutaric aciduria type I pathway glutathione synthase deficiency pathway glutathionuria disease pathway glycine[rgd.mcw.edu]