Mostrando 1,521 - 1,540 Resultados de 13,225 Para Buscar 'Tranqueras~', tiempo de consulta: 5.05s Limitar resultados
  1. 1521
    “…Both NRPSs and PKSs harbor carrier domains that are primed for acceptance of secondary metabolic building blocks by a phosphopantetheinyl transferase (P-pant). The A. fumigatus P-pant PptA has been shown to prime the putative NRPS Pes1 in vitro and has an independent role in lysine biosynthesis; however, its role in global secondary metabolism and its impact on virulence has not been described. …”
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  2. 1522
    “…One approach to reversing epigenetic suppression of tumor suppressor genes is to inhibit DNA methyl transferase. 5-aza-2′,2′-diflurorodeoxycytidine (NUC013) is a novel DNA methyl transferase and ribonucleotide reductase inhibitor that is a more potent inhibitor of growth than decitabine in the NCI 60 cancer cell line panel. …”
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  3. 1523
    “…The current study aims to investigate serum biomarkers of glucose and lipid metabolism and gamma-glutamyl transferase (GGT) measured prior to PCa diagnosis and their association with the occurrence of SDPTS. …”
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  4. 1524
  5. 1525
  6. 1526
    “…Potential synergism among 5 heterocyclic amines at low doses in the induction of glutathione S–transferase placental form (GST–P)–positive liver cell foci was examined in an 8–week experiment using male rats initially given diethylnitrosamine (200 mg/kg, ip). …”
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  7. 1527
    “…Initiating potential was assayed on the basis of significant increase in values of preneoplastic placental form glutathione S‐transferase‐positive (GST‐P(+)) foci of more than 3 cells in cross section at week 10. …”
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  8. 1528
    “…The biphasic modifying effects of indole‐3‐carbinol (I3C), a naturally occurring constituent of edible cruciferous vegetables, on the development of glutathione S‐transferase placental form (GST‐P)‐positive liver cell foci were investigated by using a medium‐term liver bioassay system and a newborn rat hepatocarcinogenesis system. …”
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  9. 1529
    “…The aim of our study was to assess: (1) the oxidative stress/antioxidative defense markers such as malondialdehyde (MDA), oxidative glutathione (GSH) and glutathione S-transferase (GST), (2) inflammation [C-reactive protein (CRP)], and (3) nitrate/nitrite levels (NOx) and its substrate L-arginine level. …”
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  10. 1530
  11. 1531
  12. 1532
  13. 1533
    “…AIM OF THE STUDY: Among the key genes involved in the development of non-alcoholic fatty liver disease (NAFLD) are genes encoding the synthesis of glutathione S-transferase (GST). MATERIAL AND METHODS: Deletion polymorphism of GSTT1 and GSTM1 genes was investigated in 104 NAFLD patients and 45 healthy individuals. …”
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  14. 1534
    “…We show that, by downregulating the metabolism of lipids through the key molecule carnitine palmitoyl transferase 1 (CPT1), it is possible to reverse or slowdown disease progression in experimental models of autoimmune encephalomyelitis-, SOD1(G93A) and rotenone models, mimicking these CNS diseases in humans. …”
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  15. 1535
    “…BACKGROUND: The multidrug resistance (MDR) of cancer cells is a major obstacle to cancer treatment. Glutathione S-transferase Pi (GSTP1-1) catalyzes the conjugation of glutathione with anticancer drugs and therefore reduces their efficacy. …”
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  16. 1536
  17. 1537
    “…O-linked β-N-acetyl-D-glucosamine (O-GlcNAc) transferase (OGT) is an essential enzyme in many cellular physiological catalytic reactions that regulates protein O-GlcNAcylation. …”
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  18. 1538
    por Cao, Yaochen, Chen, Xin, Sun, Hongming
    Publicado 2021
    “…This study identifies a molecular mechanism of the O-linked N-acetylglucosamine transferase (OGT)-mediated enhancer of zeste homolog 2 (EZH2)/krüppel-like factor 2 (KLF2)/chemokine (C-X-C motif) ligand 1 (CXCL1) axis underlying the hypercalcemia-induced nerve injury in renal failure. …”
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  19. 1539
    “…We investigate the impact of this dysregulated miRNA and its protein target O-GlcNAc-transferase (OGT) to better understand the mechanisms behind aggressive stage I ccRCC. …”
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  20. 1540
    “…Nicotinamide-nucleotide adenylyl transferase (Rv2421c) was selected as a potential drug target, because it has been shown, in vitro, to be essential for Mycobacterium tuberculosis growth. …”
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