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1,050 Possible Causes for 05, DECARBOXYLASE, OROTIDINE, PHOSPHATE

Did you mean: 05, DECARBOXYLASE, OROTIDINE, phosphene

  • Hereditary Orotic Aciduria

    […] decarboxylase (EC 4.1.1.23; orotidine-5′-phosphate carboxy-lyase).[pnas.org] Orotate phosphoribosyltransferase: orotidylate decarboxylase (Ehrlich ascites cell).[ncbi.nlm.nih.gov] Excretion of orotic acid and orotidine were 8.24 and 0.52 mmol/mol of creatinine.[ncbi.nlm.nih.gov] US6900298 Patent ID Date Patent Title US7807654 2010-10-05 Compositions and methods for treatment of mitochondrial diseases US2010222296 2010-09-02 PYRIMIDINES, SUCH AS URIDINE[drugapprovalsint.com]

  • Disorder of Purine Metabolism

    The phosphate group is usually joined to the OH group of the NUCLEOSIDE i.e on the SUGAR E.g ADENOSINE-51 MONOPHOSPHATE(AMP) DE OXYTHMIDINE-3 1- MONOPHOSPHATE (DTMP) 8 NUCLIEC[powershow.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] Retrieved 2008-05-07.[en.wikipedia.org] Uridine monophosphate is the enzyme that catalyzes orotate phosphoribosyltransferase and orotidine-5 ′ -monophosphate decarboxylase reactions.[msdmanuals.com]

  • Hyperammonemia Type 3

    phosphate is produced.[en.wikipedia.org] Disorders in tyrosine metabolism,チロシン代謝異常 1. tyrosinemia type I,チロシン血症Ⅰ型 98% 2. tyrosinemia type II,チロシン血症Ⅱ型 98% 3. tyrosinemia type III,チロシン血症Ⅲ型 98% 4. aromatic amino acid decarboxylase[jc-metabolomics.com] […] aisbell 's version from 2013-12-22 19:07 Section 1 Question Answer inability to convert orotic acid to UMP due to defect in either orotic acid phophoribosyltransferase or orotidine[memorize.com] カテゴリ 先天代謝異常症 階層分類 ヒト疾患 [BR: jp08402 ] 先天性代謝異常症 先天性アミノ酸代謝異常症 H01400 二次性高アンモニア血症 ICD-11 による疾患分類 [BR: jp08403 ] 05 Endocrine, nutritional or metabolic diseases Metabolic disorders[genome.jp]

  • Disorder of Ornithine Metabolism

    Creatine is then utilized in the cellular pool of creatine/creatine-phosphate, which together with creatine kinase and ATP/ADP provides a high energy phosphate buffering system[mhmedical.com] Allopurinol inhibits orotidine monophosphate decarboxylase and, when given to OTC carriers (who may have normal orotic acid excretion), can cause increased excretion of orotic[mayomedicallaboratories.com] カテゴリ 先天代謝異常症; 眼疾患 階層分類 ヒト疾患 [BR: jp08402 ] 先天性代謝異常症 先天性アミノ酸代謝異常症 H00189 高オルニチン血症 ICD-11 による疾患分類 [BR: jp08403 ] 05 Endocrine, nutritional or metabolic diseases Metabolic disorders[kegg.jp] Disorders in tyrosine metabolism,チロシン代謝異常 1. tyrosinemia type I,チロシン血症Ⅰ型 98% 2. tyrosinemia type II,チロシン血症Ⅱ型 98% 3. tyrosinemia type III,チロシン血症Ⅲ型 98% 4. aromatic amino acid decarboxylase[jc-metabolomics.com]

  • Aromatic L-Amino Acid Decarboxylase Deficiency

    Pyridoxal 5'-phosphate could have advantages as a treatment instead of pyridoxine.[ncbi.nlm.nih.gov] Simplified assays for human plasma L-dopa decarboxylase and liver L-dopa and 5-hydroxytryptophan decarboxylase, used to demonstrate the enzyme deficiency, are also reported[ncbi.nlm.nih.gov] Nervous system diseases Other nervous and sensory system diseases H01161 Aromatic L-amino acid decarboxylase deficiency Human diseases in ICD-11 classification [BR: br08403 ] 05[genome.jp] In: Neurology, 2010, vol. 75, n 1, p. 64-71. 216 hits 0 download Update Deposited on : 2012-05-23 Export document Format : Citation style :[archive-ouverte.unige.ch]

    Missing: OROTIDINE
  • Disorder of Pyrimidine Metabolism

    900000000000508004 ACCEPTABILITYID 900000000000548007 6011000124106 MAPGROUP 1 6011000124106 MAPADVICE IF DIHYDROURACIL DEHYDROGENASE (NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE[purl.bioontology.org] Uridine monophosphate is the enzyme that catalyzes orotate phosphoribosyltransferase and orotidine-5 ′ -monophosphate decarboxylase reactions.[merckmanuals.com] Both purines and pyrimidines may be synthesized de novo from ribose-5-phosphate and carbamyl phosphate, respectively, as shown in Figs. 391.1 and 391.2.[musculoskeletalkey.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]

    Missing: 05
  • Urea Cycle Disorder

    Abstract Carbamoyl phosphate synthetase 1 (CPS1) deficiency (CPS1D) is a rare autosomal recessive urea cycle disorder (UCD), which can lead to life-threatening hyperammonemia[ncbi.nlm.nih.gov] (OMP decarboxylase) with allopurinol (fig 2 ).[adc.bmj.com] カテゴリ 先天代謝異常症; 神経系疾患 階層分類 ヒト疾患 [BR: jp08402 ] 先天性代謝異常症 先天性アミノ酸代謝異常症 H00186 高アルギニン血症 ICD-11 による疾患分類 [BR: jp08403 ] 05 Endocrine, nutritional or metabolic diseases Metabolic[genome.jp] To enter the cycle, ammonia is converted to carbamoyl phosphate.[en.wikipedia.org]

  • Refractory Megaloblastic Anemia

    This book discusses as well the chemistry, absorption, and metabolic functions of pyridoxal phosphate and cobalamin.[books.google.de] Either orotate phosphoribosyl transferase and orotidylate decarboxylase both are defective, or the decarboxylase alone is defective (figure).[usmle.biochemistryformedics.com] Born 27 May 1975 (1975 05 27) (age 36) Kolar, Karnataka, India Education Bangalore Medical College Karnataka Years active 1999 present … Wikipedia Paroxysmal nocturnal hemoglobinuria[translate.academic.ru] Keywords orotic aciduria - orotidine - megaloblastic anemia[thieme-connect.com]

  • Glycogen Storage Disease due to GLUT2 Deficiency

    Vitamin D and phosphate supplements are essential for preventing hypophosphatemic rickets.[orpha.net] Glutamate decarboxylase deficiency[?] Glutamate-aspartate transport defect[?] Glutaricaciduria I[?] Glutaricaciduria II[?] Glutaryl-CoA dehydrogenase deficiency[?][encyclopedia.kids.net.au] Orotic aciduria type I S Uridine monophosphate synthase deficiency Orotic aciduria type II S Orotidine - 5 -phosphate decarboxylase deficiency Pyrimidine - 5 - nucleotidase[studyres.com] […] deficiency Pyruvate dehydrogenase phosphatase deficiency Tricarboxylic acid cycle disorder Fumaric aciduria Infantile cerebellar-retinal degeneration Oxoglutaricaciduria 05[repository.innermed.eu]

  • Adrenal Insufficiency

    SGPL1 executes the final decisive step of the sphingolipid breakdown pathway, mediating the irreversible cleavage of the lipid-signaling molecule sphingosine-1-phosphate ([ncbi.nlm.nih.gov] Nicolas Kluger, Martta Jokinen, Anu Lintulahti, Kai Krohn and Annamari Ranki , Gastrointestinal immunity against tryptophan hydroxylase-1, aromatic L-amino-acid decarboxylase[doi.org] […] and cumulative ICS doses were significantly related to serum cortisol levels 60 minutes after taking adrenocorticotrophic hormone (r -0.300 and -0.287, respectively; P .05[ncbi.nlm.nih.gov] BACKGROUND: Congenital sphingosine-1-phosphate (S1P) lyase deficiency due to biallelic mutations in SGPL1 gene has recently been described in association with primary adrenal[ncbi.nlm.nih.gov]

    Missing: OROTIDINE