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185 Possible Causes for catabolism, mannan

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  • Infectious Mononucleosis

    Imran Mahmud, Omar A Abdel-Mannan, Clare J Wotton and Michael J Goldacre , Maternal and perinatal factors associated with hospitalised infectious mononucleosis in children[dx.doi.org] Not only is IFN-γ itself elevated, but the catabolic product neopterin, which is produced by monocytes that are stimulated with IFN-γ, is also elevated (Table 3 ).[doi.org]

  • Glucomannan

    Because mannan catabolism results in the formation of Man-1-P (unpublished data), the requirement for a specific primer would prevent a futile cycle of mannan catabolism and[pnas.org] OBJECTIVE: To examine whether Konjac-mannan (KJM) fiber improves metabolic control as measured by glycemia, lipidemia, and blood pressure in high-risk type 2 diabetic patients[ncbi.nlm.nih.gov] Glucomannan Clinical Research Studies Clinical studies confirm that glucomannan in konjac mannan lowers cholesterol—both total cholesterol and low-density lipoprotein (LDL[cellhealthmakeover.com]

  • Mannose-Binding Lectin Deficiency

    MBL deficiency was defined using C4 deposition level 0.2 U/microl or mannan-binding level 0.5 microg/ml.[ncbi.nlm.nih.gov] Disease H00105 Mannose-binding lectin pathway component defects H00342 Tuberculosis Brite KEGG Orthology (KO) [BR: hsa00001 ] 09140 Cellular Processes 09141 Transport and catabolism[genome.jp] […] tested for serological evidence of H. pylori infection, and had their mannose-binding lectin status characterized by genotyping, and quantification of mannose-binding lectin mannan-binding[ncbi.nlm.nih.gov]

  • Immunodeficiency due to MASP-2 Deficiency

    Disease H00105 Mannose-binding lectin pathway component defects H00342 Tuberculosis Brite KEGG Orthology (KO) [BR: hsa00001 ] 09140 Cellular Processes 09141 Transport and catabolism[genome.jp] Accordingly, the addition of recombinant mannan-binding lectin to plasma from a subject with mannan-binding lectin deficiency restored the mannan-binding lectin pathway, whereas[nejm.org] The X-ray structure of human mannan-binding lectin-associated protein 19 (MAp19) and its interaction site with mannan-binding lectin and L -ficolin .[nature.com]

  • Pseudomonas

    The catabolic activity of the isolated strain differs from that of other PCP-degrading bacteria, which metabolize PCP through a chlorinated hydroquinone intermediate.[ncbi.nlm.nih.gov] Sharma, Aashu Kumar, Duraipandian Thavaselvam, Mannan Boopathi, Beer Singh and Yogesh K.[doi.org]

  • Invasive Candidiasis

    Abstract In studying the anti-mannan antibodies longitudinally in serial serum samples of three immunocompromised patients, it was observed that anti-mannan antibodies started[ncbi.nlm.nih.gov] Indoleamine 2,3-dioxygenase (IDO) catalyzes the first and limiting step in the kynurenine pathway of tryptophan catabolism.[asmscience.org] BACKGROUND: To assess the performance of Candida albicans germ tube antibody (CAGTA), (1 3)-ß-D-glucan (BDG), mannan antigen (mannan-Ag), anti-mannan antibodies (mannan-Ab[ncbi.nlm.nih.gov]

  • Organic Aciduria

    ( 29201734 ) Mosleh T....Mannan M.A. 2016 7 A Study on the Humoral and Complement Immune System of Patients with Organic Acidemia. ( 26725562 ) Alizadeh Najjarbashi F....Ghadimi[malacards.org] Branched chain organic acidurias are a group of disorders that result from an abnormality of specific enzymes involving the catabolism of branched chain amino acids (leucine[ncbi.nlm.nih.gov] Measures to prevent protein catabolism and intraoperative events that may precipitate metabolic acidosis, in addition to close monitoring of acid-base status during more extensive[ncbi.nlm.nih.gov]

  • Beta-Mannosidosis

    Chromosomal Location of Human Ortholog: 4q24 Cellular Component: intracellular membrane-bound organelle; lysosome Molecular Function: beta-mannosidase activity Biological Process: mannan[mybiosource.com] […] search lysosomal storage disease that has material basis in deficiency of the beta-A-manosidase enzyme resulting in the disruption of N-linked glycoprotein oligosaccharide catabolism[wikidata.org] Abstract Caprine beta-mannosidosis, an autosomal recessive disorder of glycoprotein catabolism, as yet undetected in man, was expressed in a 96/150 day gestation goat fetus[ncbi.nlm.nih.gov]

  • Alpha-Galactosidase

    BACKGROUND: Fabry disease is an X-linked genetic disorder involving sphingolipid catabolism, which is caused by lysosomal alpha-galactosidase A deficiency.[ncbi.nlm.nih.gov] Hydrolysis of legume seed D-galacto-D-mannans by α-D-galactosidases and β-D-mannanases. McCleary, B.[secure.megazyme.com] Abstract Fabry disease is an X-linked inborn error of sphingolipid catabolism resulting from deficient enzyme activity of alpha-galactosidase A.[ncbi.nlm.nih.gov]

  • Saccharomyces Cerevisiae

    Transgenic mice treated with mannan during allergen exposure had an equivalent response to non-mannan-treated allergic mice except for a prominent granulocytic influx into[ncbi.nlm.nih.gov] Also, metabolic engineering efforts to alter sucrose catabolism are presented in a chronological manner.[ncbi.nlm.nih.gov] The mean concentration of total nitrogen utilized during the catabolism of 1.11 M (200 g/L) glucose when all amino acids were in excess was 400 mg N/L with a range of 140[ajevonline.org]

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