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40 Possible Causes for activity, decarboxylase, orotidylic

  • Hereditary Orotic Aciduria

    In the cancer cells, the OPRT activity is paralleled with the UPRT activity.[ncbi.nlm.nih.gov] orotidylic pyrophosphorylase and orotidylic decarboxylase or a lack of orotidylic decarboxylase only) impairs the body's ability to break down orotic acid, leading to excessive[checkorphan.org] Orotate phosphoribosyltransferase: orotidylate decarboxylase (Ehrlich ascites cell).[ncbi.nlm.nih.gov]

  • Disorder of Pyrimidine Metabolism

    In the most common of the hyperuricemic metabolic disorders, deficiency of hypoxanthine phosphoribosyl transferase, the fundamental deficiency in the activity of an enzyme[ncbi.nlm.nih.gov] UMP Orotate phosphoribosyle Orotidylate deoxylase transpherase 34 Part II- Nucleotides degradation 35 Purine nucleotides (AMP and GMP) are degraded by a pathway in which[slideplayer.com] Uridine monophosphate is the enzyme that catalyzes orotate phosphoribosyltransferase and orotidine-5 ′ -monophosphate decarboxylase reactions.[merckmanuals.com]

  • Antimetabolite

    In this review, the recent literature describing investigations of the structural and thermodynamic basis for the anticancer activity of three antipyrimidines [1-beta-D-arabinofuranosyl[ncbi.nlm.nih.gov] […] myelogenous leukemia Adverse Effects: N ausea A lopecia S tomatitis S evere myelosuppression Azacitidine (IV administration): Mechanism of Action: active derivatives inhibit orotidylate[pharmacology2000.com] Abstract 2-Chlorodeoxyadenosine (2-CdA) is unique compared with traditional antimetabolites in that it is equally active against dividing and resting lymphocytes, which may[ncbi.nlm.nih.gov]

  • Disorder of Purine Metabolism

    In comparison with the activity in the brain and liver of an infant of 2 years, the activity of the organs of a fetus of 8 months as well as of an adult tended to be lower[jstage.jst.go.jp] Carbamoyl-aspartate Aspartate Aspartate transcarbamoylase Carbamoyl phosphate - Orotate PRPP OMP Orotate phosphoribosyl transferase UDP UTP 2 ATP UTP 2 ADP Gln ATP CTP Glu Pi ADP UMP Orotidylic[slideplayer.com] […] synthesis, UMP synthetase deficiency, in which a single gene mutation can cause deficiency of two enzyme activities, orotic phosphoribosyltransferase and orotidine monophosphate decarboxylase[ncbi.nlm.nih.gov]

  • Cross Syndrome

    Activating the Glutes through Exercise To preface: there are many ways that you can safely activate your gluteals.[askthetrainer.com] […] type Orofaciodigital syndrome Thurston type Orofaciodigital syndrome type 2 Orofaciodigital syndrome type1 Orotic aciduria hereditary Orotic aciduria purines-pyrimidines Orotidylic[wikidoc.org] […] syndrome 6 Orofaciodigital syndrome 8 Orofaciodigital syndrome 9 Orofaciodigital syndromes Oropharyngeal cancer adult Oropharyngeal cancer childhood Orotic aciduria type 1 Orotidylic[personalizedcause.com]

  • Hypoxanthine Guanine Phosphoribosyltransferase Partial Deficiency

    In this subject, hepatic xanthine oxidase activity showed a twelve-fold increase.[ncbi.nlm.nih.gov] Deficiency of this enzyme lead to subtypes orotate phosphoribosyltransferase deficiency and orotidylic acid decarboxylase deficiency.[clinicaladvisor.com] Increased erythrocyte concentration of NAD and rate of synthesis by intact erythrocytes were found in the patient; increased activities of nicotinic acid phosphoribosyltransferase[ncbi.nlm.nih.gov]

  • 6-Pyruvoyl-Tetrahydropterin Synthase Deficiency

    SCREENING OF 6-PYRUVOYL-TETRAHYDROPTERIN SYNTHASE ACTIVITY DEFICIENCY AMONG HYPERP HENYLALANINEMIC PATIENTS Abstract A deficiency of the phenylalanine hydroxylase activity[daru.tums.ac.ir] […] defective T & B cell function  Pyrimidine metabolism:- Hydroxy butyric aciduria- dihydropyrimidine dehydrogenase Orotic aciduria – Orotate phosphorybosyl transferase & orotidyl[de.slideshare.net] Aromatic L-amino acid decarboxylase deficiency: clinical features, treatment and prognosis . Neurology. 2004 ;62: 1058 - 1065 .[doi.org]

  • Oculo-Cerebral Hypopigmentation Syndrome Type Preus

    .), and/or a delay in the acquisition of skills requiring the coordination of muscular and mental activity (psychomotor retardation).[rarediseases.org] […] type Orofaciodigital syndrome Thurston type Orofaciodigital syndrome type 2 Orofaciodigital syndrome type1 Orotic aciduria hereditary Orotic aciduria purines-pyrimidines Orotidylic[wikidoc.org] Altered DNA ligase I activity in Bloom‘s syndrome cells. Nature 1987; 325: 357-9. Gretzula JC, Oscar Hevia BS, Weber PJ. Bloom‘s syndrome.[drmhijazy.com]

  • Cytosolic Acetoacetyl-CoA Thiolase Deficiency

    This study examined the activity of enzymes involved in butyrate oxidation in ulcerative colitis.[gut.bmj.com] Dihydrofolic acid Dihydrothymine Dihydrouracil dTDP dUDP dUMP FAD Fe2 Flavin Mononucleotide Hydrogen carbonate L-Dihydroorotic acid L-Glutamine Magnesium NADP NADPH Orotic acid Orotidylic[smpdb.ca] […] of oxygenase Deficiency of pancreatic elastase Deficiency of pantetheine kinase Deficiency of pantetheine-phosphate adenylyltransferase Deficiency of pantothenoylcysteine decarboxylase[icdlist.com]

  • Onycho-Tricho-Dysplasia-Neutropenia Syndrome

    Patients MEDcraze makes it possible for you to take charge of your diagnosis and become an active participant and informed patient on your healthcare journey.[medcraze.com] […] type Orofaciodigital syndrome Thurston type Orofaciodigital syndrome type 2 Orofaciodigital syndrome type1 Orotic aciduria hereditary Orotic aciduria purines-pyrimidines Orotidylic[starrepublic.org] “Trichodysplasia spinulosa is characterized by active polyomavirus infection”. Journal of Clinical Virology . 53 (3): 225–230. doi : 10.1016/j.jcv.2011.11.007 .[checkrare.com]