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1,534 Possible Causes for PG, activity, synthetase

  • Upper Respiratory Infection

    […] in recreational activity.[doi.org] Kusel MM, de Klerk N, Holt PG, Landau LI, Sly PD. Occurrence and management of acute respiratory illnesses in early childhood.[bmj.com] […] are mucolytics, penicillin antibiotics, quinolone antibiotics, tetracycline antibiotics, macrolide antibiotics, lincosamide antibiotics, cephalosporin antibiotics, and RNA synthetase[goodrx.com]

  • Multiple Carboxylase Deficiency

    Furthermore, ACC activity increased six- to eight-fold when cells from these patients were incubated in culture medium containing supplemental biotin.[ncbi.nlm.nih.gov] Abstract The immunoregulatory system has recently been shown to require prostaglandins (PG) for its activation in man.[ncbi.nlm.nih.gov] […] distinct variants at the holocarboxylase synthetase locus.[ncbi.nlm.nih.gov]

  • Tuberculosis

    However, the role of IGRAs for the diagnosis of active tuberculosis (TB) remains unclear.[ncbi.nlm.nih.gov] , 2007 , vol. 60 (pg. 50 - 1 ) 5 Global prevalence of diabetes: estimates for the year 2000 projections for 2030 , Diabetes Care , 2004 , vol. 27 (pg. 1047 - 53 ) 6 World[doi.org] Glickman MS, Cox JS, Jacobs WR (2000) A novel mycolic acid cyclopropane synthetase is required for coding, persistence, and virulence of Mycobacterium tuberculosis .[springerlink.com]

  • Pneumonia

    We examined the role of inflammasome activation in severe infection outcomes.[ncbi.nlm.nih.gov] Park WB 1 , Jun KI 1 , Kim G 2 , Choi JP 3 , Rhee JY 4 , Cheon S 5 , Lee CH 6, 7 , Park JS 8 , Kim Y 2 , Joh JS 9 , Chin BS 2 , Choe PG 1 , Bang JH 1 , Park SW 1 , Kim NJ[ncbi.nlm.nih.gov] […] pneumonia due to anti-synthetase syndrome (ASS).[ncbi.nlm.nih.gov]

  • Endocrine Dysfunction

    Apoptosis, lysosomal activity, insulin secretion were measured after 18 h.[ncbi.nlm.nih.gov] Lankisch, PG ( 2007 ) Chronic pancreatitis. Curr Opin Gastroenterol 23, 502 – 507. 2.[cambridge.org] Mutations in LARS2 , encoding mitochondrial leucyl-tRNA synthetase, lead to premature ovarian failure and hearing loss in Perrault syndrome . Am. J. Hum.[nature.com]

  • 5-Oxoprolinuria

    Primary defects in the gamma-glutamyl cycle were ruled out since glutathione synthase and 5-oxoprolinase activities were normal.[ncbi.nlm.nih.gov] Genomics 30:617–619 Google Scholar Whitbread L, Gali RR, Board PG (1998) The structure of the human glutathione synthetase gene.[doi.org] Abstract 5-Oxoprolinuria (pyroglutamic aciduria) resulting from glutathione synthetase (GSS) deficiency is an inherited autosomal recessive disorder characterized, in its[ncbi.nlm.nih.gov]

  • Carbamoyl Phosphate Synthetase Deficiency

    […] studies in post-mortem liver tissue material revealed a deficiency of carbamoyl-phosphate synthetase (0.9% of the mean value in controls) in combination with an intermediate activity[ncbi.nlm.nih.gov] #1 Rapid Review Biochemistry has carbamoyl phosphate synthetase deficiency (CPS) listed as the cause of orotic acidemia (pg 126).[forums.studentdoctor.net] Mutations in the CPS1 gene cause carbamoyl phosphate synthetase I deficiency .[ghr.nlm.nih.gov]

  • Porphyromonas Gingivalis

    Antimicrobial activity was also observed against P. gingivalis grown on blood agar plates.[ncbi.nlm.nih.gov] Back to the top Contents LPS-PG is provided lyophilized : LPS-PG (Standard): 1 mg of a preparation of lipopolysaccharide from Porphyromonas gingivalis (LPS-PG Standard) 1.5[invivogen.com] […] expression of key enzymes in the glutathione synthesis pathway displayed a marked increase ( p 0.05) in glutamate cysteine ligase (GCL) subunits GCLc and GCLm, glutathione synthetase[ncbi.nlm.nih.gov]

  • Biotin Deficiency

    After biotin supplementation, the skin rash improved and biotinidase activity normalized.[ncbi.nlm.nih.gov] Serum biotin was 332 pg/ml (nl 520 /- 220 pg/ml), and urine biotin was 5.22 ng/mg of creatinine (nl 4.3-95 with a mean of 30.2 ng/mg creatinine).[ncbi.nlm.nih.gov] […] results in a lack of adequate biotin to biotinylate apocarboxylases in the fetus despite the normal expression of genes coding for the apocarboxylases and holocarboxylase synthetase[ncbi.nlm.nih.gov]

  • Hemolytic Anemia due to Deficient Glutathione Synthesis

    Enzyme assays are tests that determine the activity of enzymes in certain cells of the body.[rarediseases.org] (PMID: 8825653) Webb GC … Board PG (Genomics 1995) 2 3 22 60 Sequencing and expression of a cDNA for human glutathione synthetase.[genecards.org] Some people with severe glutathione synthetase deficiency also develop recurrent bacterial infections. Glutathione synthetase deficiency is very rare.[ghr.nlm.nih.gov]