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11,205 Possible Causes for C, deacetoxycephalosporin, hydroxylase

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  • Penicillin G

    These results provide new insight regarding molecular activities that accompany persistence of C. psittaci, which may play important roles in the pathogenesis of C. psittaci[] ABBREVIATIONS DAOG , deacetoxycephalosporin G ; 6-APA , 6-aminopenicillanic acid Accepted August 6, 1998.[] METHODS: Collagen metabolism of cultured dermal fibroblasts was studied by Northern hybridisation for mRNA of collagen I, proline-4-hydroxylase, lysyl hydroxylase, matrix[]

  • Endocrine Dysfunction

    (a) elevated concentrations of total serum estradiol and serum estradiol not bound to sex hormone-binding globulin, (b) impaired spermatogenesis and sperm motility, and (c)[] We present a case of a myelolipoma in conjunction with congenital adrenal hyperplasia secondary to 21-hydroxylase deficiency.[] Antonelli A, Ferri C, Ferrari SM, Colaci M, Sansonno D, Fallahi P. Endocrine manifestations of hepatitis C virus infection.[]

    Missing: deacetoxycephalosporin
  • Adrenal Insufficiency

    RATIONALE: Adrenal incidentaloma is sometimes complicated with 21-hydroxylase deficiency (21-OHD). Latent nonclassical 21-OHD in incidentaloma is difficult to diagnose.[] We describe a novel missense mutation c.814A C (p. T272P) in NR5A1 gene which had not previously been reported.[] Of the synthesis problems, congenital adrenal hyperplasia is the most common (in various forms: 21-hydroxylase , 17α-hydroxylase , 11β-hydroxylase and 3β-hydroxysteroid dehydrogenase[]

    Missing: deacetoxycephalosporin
  • Mitomycin

    . – Likely via cytochrome P450 monooxygenase or benzoate hydroxylase O-Methylation at C-9a – Likely via SAM dependent methyltransferase Oxidation at C-5 and C8 – Unknown Intramolecular[] Abstract Mitomycin C (MC), a commonly used anticancer drug, induces DNA damage via DNA alkylation.[] We do not know whether the use of Mitomycin C will reduce scar formation.[]

    Missing: deacetoxycephalosporin
  • Eucalyptus

    Aniline hydroxylase activity was significantly increased, with levels of 2.95 and 1.43 nmol min(-1) mg(-1) microsomal protein in the test and control animals, respectively[] Macrocarpals A-C were isolated from Eucalyptus globulus through activity-guided fractionation and shown to be DPP-4 inhibitors.[] In this study, hepatic levels of microsomal lauric acid hydroxylase and peroxisomal cyanide-intensive palmitoyl coenzyme A oxidative activities were examined in livers of[]

    Missing: deacetoxycephalosporin
  • Adenovirus

    Aspartate- β -hydroxylase (AAH), an overexpressed tumor-associated cell surface protein, is considered as a promising biomarker and therapeutic target for HCC.[] KEYWORDS: C-terminus; E1A; adenovirus[] The HAdV species identified included B (184 samples), C (51 samples), and E (39 samples).[]

    Missing: deacetoxycephalosporin
  • Insulin Resistance

    Taken together, vitamin C is essential for preventing and improving insulin resistance, and the supplementing with vitamin C may be an effective therapeutic intervention for[] Context: Dopamine β-hydroxylase (DBH) deficiency is a rare genetic disorder characterized by failure to convert dopamine to norepinephrine.[] OBJECTIVE: This study aims to estimate the prevalence of insulin resistance (IR) among chronic hepatitis C (CHC) patients and their related laboratory and demographic data[]

    Missing: deacetoxycephalosporin
  • Dopamine Beta-Hydroxylase Deficiency

    Dopamine beta-hydroxylase deficiency (DBHD) is a congenital disorder caused by mutations in the DBH gene.[] The affected individuals were a c.339 2T C homozygote, a c.806G T homozygote, and compound heterozygotes for c.[339 2T C];[617delA] and for c.[339 2T C];[1667A G].[] Dopamine-beta-hydroxylase deficiency should be suspected also in infants presenting with delayed eye opening, hypoglycemia, hypothermia, or hypotension.[]

    Missing: deacetoxycephalosporin
  • Birth

    We report a 24-year-old Japanese woman with primary amenorrhea who was diagnosed as partial 17α-hydroxylase deficiency caused by homozygous 3 bp deletion in exon 1 of 17α-hydroxylase[] Abstract We report on the first PGD performed for the m.14487 T C mitochondrial DNA (mtDNA) mutation in the MT-ND6 gene, associated with Leigh syndrome.[] , Tolino M , Torres R , Varela C , Robilar D , Filippini V , De Medeiros C , Junquera S , Bernadelle Y , Durigotti C , Legarreta M , Sauan SB , Glereas C , Koch G , Acuña[]

    Missing: deacetoxycephalosporin
  • Melatonin

    The patient was an XX male, had classic simple virilizing form of 21-hydroxylase deficiency, which led to a masculine phenotype.[] […] activation of mammalian target of rapamycin (mTOR), AMP-activated protein kinase (AMPK), mitogen-activated protein kinase (MAPK) and Nuclear factor of activated T-cells (NFAT) c-[] […] that PrP C could be a key molecule in oxaliplatin resistance of colorectal cancer cells.[]

    Missing: deacetoxycephalosporin