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18 Possible Causes for II(Glc), enzyme

  • Imiglucerase

    […] groups of 122 patients each (enzyme therapy in Groups A, B, and C).[] […] of clinical and biological parameters; this corresponds to patients with hematological phenotype only (Figure S1 A). ii) Other patients showed variability of Glc uptake ([] Abstract The treatment of type 1 Gaucher disease has dramatically improved with the development of enzyme replacement therapy (ERT).[]

  • Polycystic Liver Disease

    Prothrombin time, albumin, and liver enzyme values were normal except for a mildly elevated gamma-glutamyl transpeptidase.[] PRKCSH codes for the beta-subunit of glucosidase II (hepatocystin), which cleaves two glucose residues of Glc(3)Man(9)GlcNAc(2) N-glycans on proteins.[] Laboratory data, including routine blood tests and liver enzymes, were collected before and 1, 3, 7, and 14 days, 1, 3, 6, and 12 months after TAE.[]

  • Hexokinase Deficiency

    The former enzyme was not detectable in the erythrocytes of the patient, whereas the presence of the latter enzyme could be demonstrated.[] Acts as a glucose sensor by trapping glucose inside the cell by catalyzing its phosphorylation to produce Glc-6-P.[] […] disorders 2016 2017 2018 2019 Non-Billable/Non-Specific Code Type 1 Excludes drug-induced enzyme deficiency anemia ( D59.2 ) Anemia due to enzyme disorders ICD-10-CM D55.2[]

  • Shigella Flexneri

    Non-functional activity of the apyrase enzyme in the constructed strain by colorimetric test indicated the successful mutation of the apyrase enzyme.[] )-α- l -Rha p III -(1 2)-α- l -Rha p II -(1 3)-α- l -Rha p I -(1 3)-β- d -Glc p NAc-(1 [5] .[] Mixed acid fermentation enzymes were highly expressed intracellularly, while tricarboxylic acid (TCA) cycle oxidoreductive enzymes and most electron transport chain proteins[]

  • Mycobacterium Leprae

    In silico analyses showed that oxidation of cholesterol to cholest-4-en-3-one (cholestenone), the first step of cholesterol degradation catalyzed by the enzyme 3β-hydroxysteroid[] This material proved to be made up of the M. leprae -specific phenolic glycolipids (PGL-I, PGL-II and PGL-III) and the related phthiocerol dimycocerosate (PDIM) [ 19 ].[] The expression levels of LDL receptors (LDL-R, CD36, SRA-1, SR-B1, and LRP-1) and enzymes involved in Cho biosynthesis were investigated by qRT-PCR and/or Western blot and[]

  • Dextroamphetamine

    Prior to randomization, 94nbsp;of patients to induce CYP450 enzymes is, .[] Karrer and Ehrhardt 15 originally prepared V from D-phenylalanine via the N,O-di-p-toluenesulfonate derivative of II .[] ., various synaptic proteins, synthetic enzymes, etc.).[]

  • Congenital Disorder of Glycosylation Type 1o

    The RFT1 homolog (human homolog of the yeast Rft1 enzyme) is a flippase enzyme that is responsible for the translocation of the Man 5 -GlcNAc 2 -P-P-Dol intermediate from[] Congenital disorders of glycosylation (CDGs) are very rare genetic disorders that lack enzymes needed for glycosylation.[] CDG is caused by a genetically inherited change or malfunction of one of these enzymes.[]

  • Isoniazid

    The mutant enzyme showed 86.5% of catalase and 45% of peroxidase activities in comparison to the wild type.[] ./25 mbar: 1.17 g (85%) biege crystals (GLC 98 area %, as trimethylsilylester). 1 H-NMR: (400 MHz, D 6 DMSO): δ 2.54 (s, 3H), 7.59 (dd, 1H), 7.70 (s, 1H), 8.60 (dd, 1H) ii[] BACKGROUND: Interactions between transcriptional inducers of cytochrome P450 (CYP450) enzymes and therapeutic drugs may be prevented by antagonizing the activation of a nuclear[]

  • Neisseria Meningitidis

    […] propose that studies of the relationship between bacterial virulence and gene expression should consider whether genetic variation could affect properties of biosynthetic enzymes[] The results of gas-liquid chromatography (GLC)-MS analysis of partially methylated/ethylated alditol acetates (PMAAs) is shown in Table II .[] This bacteria has also been found to be oxidase positive which means it contains the enzyme cytochrome c oxidase and is capable of using oxygen for energy via an electron[]

  • Congenital Disorder of Glycosylation Type 2

    Diagnosis can be made through blood work that allows enzyme function to be analyzed. Brain scans are normal in CDG type 2A.[] Type I) or genes that process the protein-bound N-glycans (Type II).[] A profoundly deficient activity of the Golgi enzyme N-acetylglucosaminyltransferase II (EC was demonstrated in fibroblasts.[]

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