Search Results - "KORSINCZKY, M"

  • Showing 1 - 5 results of 5
Refine Results
  1. 1

    Mutations in Plasmodium falciparum cytochrome b that are associated with Atovaquone resistance are located at a putative drug-binding site by KORSINCZKY, M, NANHUA CHEN, KOTECKA, B, SAUL, A, RIECKMANN, K, QIN CHENG

    Published in Antimicrobial agents and chemotherapy (01-08-2000)
    “…Atovaquone is the major active component of the new antimalarial drug Malarone. Considerable evidence suggests that malaria parasites become resistant to…”
    Get full text
    Journal Article
  2. 2

    Sulfadoxine Resistance in Plasmodium vivax Is Associated with a Specific Amino Acid in Dihydropteroate Synthase at the Putative Sulfadoxine-Binding Site by Korsinczky, Michael, Fischer, Katja, Chen, Nanhua, Baker, Joanne, Rieckmann, Karl, Cheng, Qin

    Published in Antimicrobial Agents and Chemotherapy (01-06-2004)
    “…Classifications Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit…”
    Get full text
    Journal Article
  3. 3

    Mutations in Cytochrome b Resulting in Atovaquone Resistance Are Associated with Loss of Fitness in Plasmodium falciparum by PETERS, Jennifer M, NANHUA CHEN, GATTON, Michelle, KORSINCZKY, Michael, FOWLER, Elizabeth V, MANZETTI, Sergio, SAUL, Allan, QIN CHENG

    Published in Antimicrobial Agents and Chemotherapy (01-08-2002)
    “…Classifications Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit…”
    Get full text
    Journal Article
  4. 4

    Purple acid phosphatases from bacteria: similarities to mammalian and plant enzymes by Schenk, Gerhard, Korsinczky, Michael L.J., Hume, David A., Hamilton, Susan, DeJersey, John

    Published in Gene (19-09-2000)
    “…Mammalian and plant purple acid phosphatases have similar active site structures despite low sequence identity (<20%). Although no bacterial enzyme has been…”
    Get full text
    Journal Article
  5. 5

    Solution structures by 1H NMR of the novel cyclic trypsin inhibitor SFTI-1 from sunflower seeds and an acyclic permutant by Korsinczky, M L, Schirra, H J, Rosengren, K J, West, J, Condie, B A, Otvos, L, Anderson, M A, Craik, D J

    Published in Journal of molecular biology (17-08-2001)
    “…SFTI-1 is a recently discovered cyclic peptide trypsin inhibitor from sunflower seeds comprising 14 amino acid residues. It is the most potent known…”
    Get full text
    Journal Article