Mostrar 181 - 200 resultats de 788 per cerca '"malaria parasite"', hora de la petició: 0.07sec Refinar resultats
  1. 181

    Long-term storage limits PCR-based analyses of malaria parasites in archival dried blood spots. per Hwang, J, Jaroensuk, J, Leimanis, M, Russell, B, McGready, R, Day, N, Snounou, G, Nosten, F, Imwong, M

    Publicat 2012
    “…BACKGROUND: Blood samples collected in epidemiological and clinical investigations and then stored, often at room temperature, as blood spots dried on a filter paper have become one of the most popular source of material for further molecular analyses of malaria parasites. The dried blood spots are often archived so that they can be used for further retrospective investigations of parasite prevalence, or as new genetic markers come to the fore. …”
    Journal article
  2. 182
  3. 183
  4. 184
  5. 185
  6. 186

    A malaria parasite cross reveals genetic determinants of Plasmodium falciparum growth in different culture media per Kumar, S, Li, X, McDew-White, M, Reyes, A, Delgado, E, Sayeed, A, Haile, MT, Abatiyow, BA, Kennedy, SY, Camargo, N, Checkley, LA, Brenneman, KV, Button-Simons, KA, Duraisingh, MT, Cheeseman, IH, Kappe, SHI, Nosten, F, Ferdig, MT, Vaughan, AM, Anderson, TJC

    Publicat 2022
    “…What genes determine in vitro growth and nutrient utilization in asexual blood-stage malaria parasites? Competition experiments between NF54, clone 3D7, a lab-adapted African parasite, and a recently isolated Asian parasite (NHP4026) reveal contrasting outcomes in different media: 3D7 outcompetes NHP4026 in media containing human serum, while NHP4026 outcompetes 3D7 in media containing AlbuMAX, a commercial lipid-rich bovine serum formulation. …”
    Journal article
  7. 187

    A putative homologue of CDC20/CDH1 in the malaria parasite is essential for male gamete development per Guttery, D, Ferguson, D, Poulin, B, Xu, Z, Straschil, U, Klop, O, Solyakov, L, Sandrini, S, Brady, D, Nieduszynski, C, Janse, C, Holder, A, Tobin, AB, Tewari, R

    Publicat 2012
    “…Two major regulators are cell-division cycle protein 20 (CDC20) and its homologue, CDC20 homologue 1 (CDH1), which activate the anaphase-promoting complex/cyclosome (APC/C) in mitosis, and facilitate degradation of mitotic APC/C substrates. The malaria parasite, Plasmodium, is a haploid organism which, during its life-cycle undergoes two stages of mitosis; one associated with asexual multiplication and the other with male gametogenesis. …”
    Journal article
  8. 188

    Comparative folate metabolism in humans and malaria parasites (part II): activities as yet untargeted or specific to Plasmodium. per Nzila, A, Ward, SA, Marsh, K, Sims, P, Hyde, J

    Publicat 2005
    “…The folate pathway represents a powerful target for combating rapidly dividing systems such as cancer cells, bacteria and malaria parasites. Whereas folate metabolism in mammalian cells and bacteria has been studied extensively, it is understood less well in malaria parasites. …”
    Journal article
  9. 189

    Reconstitution of the core of the malaria parasite glideosome with recombinant Plasmodium class XIV myosin A and Plasmodium actin per Bookwalter, CS, Tay, CL, McCrorie, R, Previs, MJ, Lu, H, Krementsova, EB, Fagnant, PM, Baum, J, Trybus, KM

    Publicat 2017
    “…Motility of the apicomplexan malaria parasite Plasmodium falciparum is enabled by a multiprotein glideosome complex, whose core is the class XIV myosin motor, PfMyoA, and a divergent Plasmodium actin (PfAct1). …”
    Journal article
  10. 190

    Pooled sequencing and rare variant association tests for identifying the determinants of emerging drug resistance in malaria parasites. per Cheeseman, I, McDew-White, M, Phyo, A, Sriprawat, K, Nosten, F, Anderson, T

    Publicat 2014
    “…We explored the potential of pooled sequencing to swiftly and economically identify selective sweeps due to emerging artemisinin (ART) resistance in a South-East Asian malaria parasite population. ART resistance is defined by slow parasite clearance from the blood of ART-treated patients and mutations in the kelch gene (chr. 13) have been strongly implicated to play a role. …”
    Journal article
  11. 191
  12. 192

    Identification of malaria parasite-infected red blood cell surface aptamers by inertial microfluidic SELEX (I-SELEX) per Birch, Christina M., Hou, Han Wei, Han, Jongyoon, Niles, Jacquin

    Publicat 2015
    “…Plasmodium falciparum malaria parasites invade and remodel human red blood cells (RBCs) by trafficking parasite-synthesized proteins to the RBC surface. …”
    Obtenir text complet
    Obtenir text complet
    Obtenir text complet
    Article
  13. 193

    Multiple stiffening effects of nanoscale knobs on human red blood cells infected with Plasmodium falciparum malaria parasite per Zhang, Yao, Huang, Changjin, Kim, Sangtae, Golkaram, Mahdi, Dixon, Matthew W. A., Tilley, Leann, Li, Ju, Zhang, Sulin, Suresh, Subra

    Publicat 2016
    “…During its asexual development within the red blood cell (RBC), Plasmodium falciparum (Pf), the most virulent human malaria parasite, exports proteins that modify the host RBC membrane. …”
    Obtenir text complet
    Obtenir text complet
    Obtenir text complet
    Article
  14. 194
  15. 195
  16. 196
  17. 197
  18. 198

    Comparative gene expression profiling of P. falciparum malaria parasites exposed to three different histone deacetylase inhibitors per Andrews, Katherine T., Gupta, Archna P., Tran, Thanh N., Fairlie, David P., Gobert, Geoffrey N., Bozdech, Zbynek

    Publicat 2013
    “…This dataset represents an important contribution to our understanding of how HDAC inhibitors act on malaria parasites and identifies alpha tubulin II as a potential transcriptional marker of HDAC inhibition in malaria parasites that may be able to be exploited for future development of HDAC inhibitors as new antimalarial agents.…”
    Obtenir text complet
    Obtenir text complet
    Journal Article
  19. 199
  20. 200