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1,972 Possible Causes for hydrolases

  • Influenza

    IDV HEF shares a conserved esterase pocket with ICV HEF The E domain of IDV HEF, harboring the receptor-destroying enzyme (RDE) activity, has a hydrolase fold that is highly[] , [Web of Science ] , [Google Scholar] The esterase domain is the structurally most conserved part of HEF; the position of the catalytic triad characteristic for serine hydrolases[] […] the structure of an acetyl esterase, HerE, and its complex with the inhibitor dimethylarsinic acid, and illustrated the mechanism of the broad scope inhibition of serine hydrolases[]

  • Acute Bronchitis

    They are metabolized by cytochrome P450 enzymes and epoxide hydrolases, which are polymorphic among the human population.[] Association between polymorphism in gene for microsomal epoxide hydrolase and susceptibility to emphysema. Lancet 1997 ;350: 630 –633. 35. U.S. Surgeon General.[]

  • Dementia

    Alkayed , Role of soluble epoxide hydrolase in age-related vascular cognitive decline , Prostaglandins & Other Lipid Mediators , 113-115 , (30) , (2014) . Stephen W.[]

  • Pneumonia

    Patients who suffer from lung and skin toxicities may be deficient in a bleomycin hydrolase enzyme [ 5 ].[]

  • Idiopathic Pulmonary Fibrosis

    Protein binding and hydrolase activity were respectively enriched with 36 and 20 proteins.[]

  • Meningitis

    Leukotriene A4 hydrolase (LTA4H) has been implicated in the pathogenesis of mycobacterial infection through its effect on the equilibrium between pro‐ and anti‐inflammatory[]

  • Tuberculosis

    […] with these immature characteristics, this organelle lacks the late endosomal and lysosomal markers Rab7 and CD63, as well as mature and active forms of various lysosomal hydrolases[]

  • Tyrosinemia Type 1

    Hereditary tyrosinemia type 1 (HT1) is an autosomal recessive disease caused by a deficiency of the enzyme involved in the last step of tyrosine degradation, fumarylacetoacetate hydrolase[] Abstract The complete fumarylacetoacetate hydrolase (FAH) genotype of probands of thirteen unrelated families with hereditary tyrosinemia type 1 (HT 1) was established.[] Abstract Hereditary tyrosinemia type 1 (HT1) is a severe autosomal recessive metabolic disease associated with point mutations in the human fumarylacetoacetate hydrolase ([]

  • Tyrosinemia

    Abstract Tyrosinemia type I is an autosomal recessive inborn error of metabolism caused by deficiency of the enzyme fumaryl acetoacetate hydrolase (FAH, EC[] BACKGROUND: Tyrosinemia type I, the most severe disease of the tyrosine catabolic pathway is caused by a deficiency in fumarylacetoacetate hydrolase (FAH).[] Classical tyrosinemia type I arises from a deficiency of fumarylacetoacetate hydrolase while the variant tyrosinemia type Ib results from a deficiency of maleylacetoacetate[]

  • Bile Salt

    Finally, gel-forming abilities of bifidobacteria exhibiting bile salt hydrolase activity were analyzed.[] ., 20-704, Lublin, Poland. [email protected] Abstract This study analyzes the application of degenerative primers for the screening of bile salt hydrolase-encoding genes[] KEYWORDS: Bile salt hydrolase; Co-precipitation of cholesterol; SBA-15[]

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