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1,462 Possible Causes for activity, glycine, reductase

  • Connective Tissue Disease

    […] intensity of the activity) by reducing the activity.[medicinenet.com] Treatment: Aggressive treatment of intercurrent illness, carnitine, Protein, lysine, and tryptophan restriction Saccharopinuria (268700) α -Aminoadipic semialdehyde-glutamate reductase[merck.com] Scleroderma – an activation of immune cells that produces scar tissue in the skin, internal organs, and small blood vessels.[en.wikipedia.org]

  • Influenza

    Seasonal influenza activity in the Southern Hemisphere was low overall, with influenza A(H1N1)pdm09 predominating in many regions.[ncbi.nlm.nih.gov] Immune-mediated necrotizing myopathy may be associated with myositis-specific autoantibodies including anti-single recognition particle and anti-3-hydroxy-3- methylglutaryl-coenzyme A reductase[ncbi.nlm.nih.gov] For example, the first row shows that the amino acid in position 5 of HA1 mutated from glycine (G, shown in light green) to valine (V, shown in burgundy) in November 1999,[dx.doi.org]

  • Chenodeoxycholic Acid

    Patient 2 received a combined treatment with LDL-apheresis, CDCA and HMG-CoA reductase inhibitor.[ncbi.nlm.nih.gov] The activation of ERK1/2 was responsible for the activating phosphorylation of C/EBPβ.[ncbi.nlm.nih.gov] […] spectrometric (LC-ESI-MS/MS) method for the quantification of chenodeoxycholic acid (CDCA) and glycochenodeoxycholic acid (GCDCA), representative primary non-amidated and glycine-conjugated[ncbi.nlm.nih.gov]

  • Tuberculosis

    A review of their phenotypes indicated that two of these strains were negative for nitrate reductase.[doi.org] However, the role of IGRAs for the diagnosis of active tuberculosis (TB) remains unclear.[ncbi.nlm.nih.gov] Ramakrishnan L, Federspiel NA, Falkow S (2000) Granuloma-specific expression of Mycobacterium virulence proteins from the glycine-rich PE-PGRS family.[springerlink.com]

  • Trimetrexate

    The most active quinazolines against both the P. carinii and the T. gondii enzyme were those with an ArCH2-NH or ArNHCH2 side chain.[ncbi.nlm.nih.gov] Abstract Drug Metabolism and Disposition November 1990, 18 (6) 980-986; Abstract The metabolic disposition of trimetrexate, a nonclassical inhibitor of dihydrofolate reductase[dmd.aspetjournals.org] Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA pre...[drugbank.ca]

  • Dihydrofolate Reductase Deficiency

    Activity of the liver-cell homogenate from the other patient, which was one quarter of the normal level, was restored to only half normal activity by high cation concentration[ncbi.nlm.nih.gov] […] metabolism Glycine encephalopathy, also known as Non-ketotic hyperglycinaemia GABA related disorders GABA-transaminase-deficiency Succinate-semialdehyde-dehydroxylase deficiency[intd-registry.org] Dihydrofolic acid reductase deficiency prevents the conversion of folic acid to tetrahydrofolic acid; the enzyme activity appears to differ in each patient.[nejm.org]

  • Nonketotic Hyperglycinemia

    The activity of the T-protein was normal.[ncbi.nlm.nih.gov] .- ) Marfan's syndrome ( Q87.4 ) 5-alpha-reductase deficiency ( E29.1 ) Metabolic disorders E72 ICD-10-CM Diagnosis Code E72 Other disorders of amino-acid metabolism 2016[icd10data.com] […] hyperglycinemia Non-ketotic hyperglycinemia (disorder) nonketotic hyperglycinemia Glycine synthase deficiency Hyperglycinemia, Transient Neonatal GLYCINE ENCEPHALOPATHY GLYCINE[wikidata.org]

  • Disorder of Sulfur-Bearing Amino Acid Metabolism

    […] annotations that may be applicable to E72.10 : E00-E89 2019 ICD-10-CM Range E00-E89 Endocrine, nutritional and metabolic diseases Note All neoplasms, whether functionally active[icd10data.com] Synonym initial insensitive preferred GB English Dihydrofolate reductase deficiency Synonym initial insensitive acceptable GB English Deficiency of dihydrofolate reductase[doctor.am] […] of glycine metabolism E72.8 Other specified disorders of amino-acid metabolism E72.81 Disorders of gamma aminobutyric acid metabolism E72.89 Other specified disorders of[healthprovidersdata.com]

  • Smith Lemli Opitz Syndrome

    Impaired DHCR7 function is associated with a spectrum of congenital malformations, intellectual impairment, epileptiform activity and autism spectrum disorder.[ncbi.nlm.nih.gov] Our data demonstrate that Smith-Lemli-Opitz syndrome is caused by mutations in the gene coding for 7-dehydrocholesterol reductase.[ncbi.nlm.nih.gov] The p.G366V is a novel mutation of the DHCR7 gene with guanine by thymine nucleotide exchange resulting in glycin by valin amino acid exchange in the dehydrocholesterol reductase[ncbi.nlm.nih.gov]

  • Fluvastatin

    Here, we explore whether this treatment could also increase telomerase activity.[ncbi.nlm.nih.gov] Product name Fluvastatin sodium salt, HMG-CoA reductase inhibitor Description Competitive HMG-CoA reductase inhibitor Biological description Competitive HMG-CoA reductase[abcam.com] Abstract In this paper, we have investigated the mechanism of phototoxicity of fluvastatin, an 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitor, in human keratinocytes[ncbi.nlm.nih.gov]