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819 Possible Causes for Arabidopsis, Aldehyde, delta,, oxidase

Did you mean: Arabidopsis, Aldehyde, death, oxidase

  • Xanthinuria Type 2

    So I guess the main question is: What band size would you expect for catalyticly active xanthine oxidase, 150 kDa or 80 kDa?[abcam.com] Adenosylcobalamin Sythesis – Cbl A Defect in Adenosylcobalamin Sythesis – Cbl B Defect in Adenosylcobalamin Sythesis – Cbl C – HCU Defect in Adenosylcobalamin Sythesis – Cbl D -MMA Delta[climb.org.uk] Also Known As Xanthine dehydrogenase and xanthine aldehyde oxydase dual deficiency[codelay.com] In addition, XAN2 patients cannot metabolize allopurinol into oxypurinol due to dual deficiency of xanthine dehydrogenase and aldehyde oxidase.[malacards.org]

  • Molybdenum Cofactor Deficiency Complementation Group B

    Sulfite oxidase deficiency and molybdenum cofactor deficiency in the metabolism of sulfated amino acids. Pictured is an infant with sulfite oxidase deficiency.[emedicine.medscape.com] For the E. coli proteins MogA and MoeA and their putative homologs—cinnamon in Drososphila melanogaster ( 10 ) and Cnx1 in Arabidopsis thaliana ( 11 )—a function in the transfer[pnas.org] RAB3GAP1 2q21.3 Warburg micro syndrome 1 600118 RAB3GAP2 1q41 Martsolf syndrome 212720 Warburg micro syndrome 2 614225 RAG1 11p12 Alpha/beta T-cell lymphopenia with gamma/delta[institutobernabeu.com] […] catalysing diverse redox reactions, however, only four of them have been found in plants. (1) Nitrate reductase catalyses the key step in inorganic nitrogen assimilation, (2) aldehyde[paperity.org]

  • Xanthinuria

    The residual xanthine oxidase from the parents exhibited normal kinetics with respect to hypoxanthine.[ncbi.nlm.nih.gov] […] lack aldehyde oxidase activity.[emedicine.com] Creator: Ana Marcu Created On: September 10, 2018 at 15:49 Last Updated: September 10, 2018 at 15:49 PW012895 View Pathway metabolic Zeaxanthin Biosynthesis Arabidopsis thaliana[smpdb.ca] Mendel and Florian Bittner , Xanthine dehydrogenase AtXDH1 from Arabidopsis thaliana is a potent producer of superoxide anions via its NADH oxidase activity , Plant Molecular[doi.org]

    Missing: delta
  • Xanthinuria Type 1

    Allopurinol was metabolized to oxypurinol and pyrazinamide to 5-hydroxypyrazinamide in spite of no activity of xanthine oxidase, suggesting that aldehyde oxidase converted[ncbi.nlm.nih.gov] Adenosylcobalamin Sythesis – Cbl A Defect in Adenosylcobalamin Sythesis – Cbl B Defect in Adenosylcobalamin Sythesis – Cbl C – HCU Defect in Adenosylcobalamin Sythesis – Cbl D -MMA Delta[climb.org.uk] […] allopurinol to oxipurinol during an allopurinol loading test for determining the type of classical xanthinuria revealed that the patients had classical type 1 xanthinuria, because aldehyde[ncbi.nlm.nih.gov] In type II deficiency, mutations in the genes coding for both XOR and aldehyde oxidase are unlikely, because these genes are located far apart, albeit both on chromosome 2[jmg.bmj.com]

    Missing: Arabidopsis
  • 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] Intramolecular involvement of a gamma or delta hydroxyl group (as in examples #3 and 4) may occur, and is often more facile than the intermolecular reaction.[www2.chemistry.msu.edu] Some aldehydes are substrates for aldehyde dehydrogenase enzymes which metabolize aldehydes in the body.[en.wikipedia.org] KEYWORDS: aldehyde oxidase; animal models; in vitro–in vivo prediction; minipig[ncbi.nlm.nih.gov]

    Missing: Arabidopsis
  • Deficiency of Sulfite Oxidase

    Abstract Isolated sulfite oxidase (SO) deficiency is an autosomal recessively inherited inborn error of sulfur metabolism.[ncbi.nlm.nih.gov] Sulfite oxidase has homology in other species, including: Mouse, Rat, Arabidopsis, Zebrafish, Frog, Nematode, Chicken.[biocompare.com] The cofactor is essential for the function of the human enzymes sulfite oxidase, xanthine dehydrogenase, and aldehyde oxidase.[ommbid.mhmedical.com] Molybdenum cofactor is associated with the enzymes sulfite oxidase, xanthine dehydrogenase, and aldehyde oxidase (see the image below). [1] Molybdenum cofactor deficiency.[emedicine.medscape.com]

    Missing: delta
  • Pseudomonas Aeruginosa

    ANR may play an important role in preventing overexpression of the CIO in relation to other terminal oxidases.[doi.org] […] as well as on wild-type Arabidopsis plants primed with exogenous SA, a treatment known to enhance endogenous SA concentration.[ncbi.nlm.nih.gov] Moreover, using Delta exoU Delta exoY, Delta exoT Delta exoY, and Delta exoT Delta exoU double mutants, we determined that individual translocation of either ExoT or ExoU[ncbi.nlm.nih.gov] Ohta et al. ( 2005 ) discussed the expression of aldehyde dehydrogenase in Escherichia coli , and a cloned enzyme showed similarity to NAD (P)-dependent aldehyde dehydrogenase[doi.org]

  • Isolated Succinate-CoQ Reductase Deficiency

    […] peroxide. b) Oxidases catalyze reaction using oxygen as a hydrogen acceptor c) Oxidases catalyze reactions using Niacin as coenzyme d) Oxidases catalyze reactions of direct[namrata.co] delta aminolévulinique Ácido fenilpirúvico en orinaacide phénylpyruvique dans les urines ácido fenilpirúvico en sangreacide phénylpyruvique sanguin Ácido metilmalónicoacide[lexigene.com] Arabidopsis plants.[plantphysiol.org] […] amino-levulinic dehidrataza (ALAD)*10 Acid delta amino-levulinic in urina (ALAU)*10 Acid fenilglioxilic (PGLYU)*10 Acid fenilmercapturic in urina (PMER)*15 Acid glutamic[clinicamedicum.ro]

  • Variegate Porphyria

    Variegate porphyria is characterized by a partial reduction in the activity of protoporphyrinogen oxidase.[ncbi.nlm.nih.gov] Narita S, Tanaka R, Ito T, Okada K, Taketani S, Inokuchi H: Molecular cloning and characterization of a cDNA that encodes protoporphyrinogen oxidase of Arabidopsis thaliana[karger.com] […] neurological symptoms that included tremor, dysarthria, and loss of consciousness was diagnosed as having variegate porphyria, because of increased urinary excretion of delta-aminolevulinic[ncbi.nlm.nih.gov] […] aminoacid sequence alignment of eukaryotic PPOXs, revealed that mutations p.E34V and p.G332A affect residues that are conserved in mitochondrial PPOX2 from Nicotiana tabacum and Arabidopsis[biomedcentral.com]

    Missing: Aldehyde
  • Malignant Neoplasm

    Reduction of lysyl oxidase (LOX), a copper-dependent amine oxidase that catalyses the crosslinking of collagens, elastin, and fibrillin in the ECM [ 7 ] reduces matrix stiffening[doi.org] Antibodies to SIRT1 were also obtained from Delta Biolabs (DB083, Figure 3B & C ). Antibodies to EZH2 were from Cell Signaling Technologies (4905).[doi.org] Reznick and Dror Aizenbud , Oxidative damage in keratinocytes exposed to cigarette smoke and aldehydes , Toxicology in Vitro , 28 , 4 , (485) , (2014) .[doi.org] Weber , Deficient expression of aldehyde dehydrogenase 1A1 is consistent with increased sensitivity of Gorlin syndrome patients to radiation carcinogenesis , Molecular Carcinogenesis[dx.doi.org]

    Missing: Arabidopsis

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