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Showing 201 - 205 results of 205 for search '((bill OR mild) OR (all OR full)) (((dmugo OR bmugo) OR drugs) OR drag)*', query time: 0.14s Refine Results
  1. 201
  2. 202

    The effect of regularly dosed paracetamol versus no paracetamol on renal function in Plasmodium knowlesi malaria (PACKNOW) : study protocol for a randomised controlled trial by Cooper, Daniel J., Plewes, Katherine, Grigg, Matthew J., Rajahram, Giri S., Piera, Kim A., William, Timothy, Chatfield, Mark D., Yeo, Tsin Wen, Dondorp, Arjen M., Anstey, Nicholas M., Barber, Bridget E.

    Published 2018
    “…The inexpensive and widely available drug paracetamol inhibits CFHb-induced lipid peroxidation via reduction of ferryl haem to the less toxic Fe3+ state, and has been shown to reduce oxidative damage and improve renal function in patients with sepsis complicated by haemolysis as well as in falciparum malaria. …”
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    Journal Article
  3. 203

    Metformin degradation with combined Ozone/UV/H2O2 process by Fujinami, Shoko Carissa

    Published 2020
    “…As our bodies are unable to fully metabolise all Metformin, a significant amount of Metformin is excreted unchanged into water bodies and studies have found that Metformin is an endocrine disruptor compound (EDC) which can interfere with reproduction system. …”
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    Final Year Project (FYP)
  4. 204

    RES.LL-005 D4M: Signal Processing on Databases, Fall 2012 by Kepner, Jeremy

    Published 2020
    “…Search, social media, ad placement, mapping, tracking, spam filtering, fraud detection, wireless communication, drug discovery, and bioinformatics all attempt to find items of interest in vast quantities of data. …”
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    Learning Object
  5. 205

    Synthesis, biological evaluation, and stability studies of raloxifene mono- and bis-sulfamates as dual-targeting agents by Zaraei, S-O, Dohle, W, Anbar, HS, El-Gamal, R, Leblond, B, Foster, PA, Al-Tel, TH, Potter, BVL, El-Gamal, MI

    Published 2024
    “…All three possible sulfamate derivatives of the selective estrogen receptor modulator Raloxifene (bis-sulfamate 7 and two mono-sulfamates 8–9) were synthesized and evaluated as inhibitors of the clinical drug target steroid sulfatase (STS), both in cell-free and in cell-based assays, and also as estrogen receptor (ER) modulators. …”
    Journal article