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3,266 Possible Causes for Plastoquinol plastocyanin, reductase

  • Influenza

    Immune-mediated necrotizing myopathy may be associated with myositis-specific autoantibodies including anti-single recognition particle and anti-3-hydroxy-3- methylglutaryl-coenzyme A reductase[] Michele Tonelli, Lieve Naesens, Sabrina Gazzarrini, Matteo Santucci, Elena Cichero, Bruno Tasso, Anna Moroni, Maria Paola Costi and Roberta Loddo , Host dihydrofolate reductase[]

    Missing: Plastoquinol plastocyanin
  • Urinary Tract Infection

    […] management of LUTS therefore aims to decrease PVR and TQ while increasing Qmax [5] , [8] , [11] – [15] , which can be reached pharmacologically with use of alpha-blockers and 5α-reductase[]

    Missing: Plastoquinol plastocyanin
  • Sunburn

    Regulation of lipid peroxidation of glutathione and lipoic acid: involvement of liver microsomal vitamin E free radical reductase . In: , editors.[]

    Missing: Plastoquinol plastocyanin
  • Dementia

    We used the search terms: statin OR statins OR "Hydroxymethylglutaryl‐CoA Reductase Inhibitors".[] […] absorption across the small intestine is passive diffusion ( Rosenberg 1985 ), but absorption is influenced by genotypic variation in the enzyme methylenetetrahydrofolate reductase[] HMG‐CoA reductase is the rate‐limiting enzyme in the cascade of cellular cholesterol biosynthesis.[]

    Missing: Plastoquinol plastocyanin
  • Osteoporosis

    This process involves two enzymes, γ-glutamyl carboxylase and vitamin K epoxide reductase (VKORC1).[] Miyao M, Morita H, Hosoi T, Kurihara H, Inoue S, Hoshino S, Shiraki M, Yazaki Y, Ouchi Y (2000) Association of methylenetetrahydrofolate reductase (MTHFR) polymorphism with[] […] use and subsequent fracture supports the role of vitamin K in normal bone formation. 23 It also suggests that patients who are more likely to have lower vitamin K epoxide reductase[]

    Missing: Plastoquinol plastocyanin
  • Isolated CoQ-Cytochrome C Reductase Deficiency

    Other names in common use include: coenzyme Q-cytochrome c reductase, dihydrocoenzyme Q-cytochrome c reductase, reduced ubiquinone-cytochrome c reductase, complex III, (mitochondrial[] Plastoquinone-plastocyanin reductase (b6f complex), present in cyanobacteria and the chloroplasts of plants, catalyses the oxidoreduction of plastoquinol and cytochrome f.[] […] hereditary optic neuropathy Leigh syndrome with nephrotic syndrome Björnstad syndrome GRACILE syndrome Renal tubulopathy - encephalopathy - liver failure Isolated NADH-CoQ reductase[]

  • Pneumonia

    Mutations of Pneumocystis jirovecii dihydrofolate reductase associated with failure of prophylaxis. Antimicrob Agents Chemother 2004 ;48: 4301 –4305.[] Genetic characterization of the dihydrofolate reductase gene of Pneumocystis jirovecii isolates from Portugal. J Antimicrob Chemother 2006 ;58: 1246 –1249.[] Pneumocystis carinii dihydropteroate synthase but not dihydrofolate reductase gene mutations correlate with prior trimethoprim-sulfamethoxazole or dapsone use.[]

    Missing: Plastoquinol plastocyanin
  • Endocrine Dysfunction

    Thioredoxin Reductase 2 ( TXNRD2 ) mutation associated with familial glucocorticoid deficiency (FGD) . J. Clin. Endocrinol. Metab. 99 , E1556–E1563 (2014). 118.[]

    Missing: Plastoquinol plastocyanin
  • Connective Tissue Disease

    Treatment: Aggressive treatment of intercurrent illness, carnitine, Protein, lysine, and tryptophan restriction Saccharopinuria (268700) α -Aminoadipic semialdehyde-glutamate reductase[] Metabolism Disorders Disease (OMIM Number) Defective Proteins or Enzymes Defective Gene or Genes (Chromosomal Location) Comments Hyperlysinemia (238700) Lysine: α -ketoglutarate reductase[]

    Missing: Plastoquinol plastocyanin
  • Adrenal Insufficiency

    […] protein ( StAR ) and CYP11A1 mutations have been described; and more recently novel mutations in genes such as nicotinamide nucleotide transhydrogenase ( NNT ) and thioredoxin reductase[]

    Missing: Plastoquinol plastocyanin

Further symptoms