Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (2/2 displayed)

  • 2007Resistência à sulfadoxina-pirimetamina em Maputo, Moçambique1citations
  • 2006Co-occurrence of East and West African kdr mutations suggests high levels of resistance to pyrethroid insecticides in Anopheles gambiae from Libreville, Gabon92citations

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Chart of shared publication
Fernandes, Natércia Emília Pedro
1 / 1 shared
Cravo, Pedro
1 / 1 shared
Pinto, Joao
1 / 2 shared
Donnelly, Martin J.
1 / 1 shared
Caccone, A.
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Gentile, Gabriele
1 / 1 shared
Elissa, N.
1 / 1 shared
Lynd, Amy
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Costa, C.
1 / 13 shared
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2007
2006

Co-Authors (by relevance)

  • Fernandes, Natércia Emília Pedro
  • Cravo, Pedro
  • Pinto, Joao
  • Donnelly, Martin J.
  • Caccone, A.
  • Gentile, Gabriele
  • Elissa, N.
  • Lynd, Amy
  • Costa, C.
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article

Resistência à sulfadoxina-pirimetamina em Maputo, Moçambique

  • Rosário, Virgilio Estólio Do
  • Fernandes, Natércia Emília Pedro
  • Cravo, Pedro
Abstract

<p>Foram analisadas a freqüência e distribuição de mutações nos genes dihidrofolato redutase e dihidropteroato sintetase do <i style="font-family: verdana, arial; font-size: 13.192px;">Plasmodium falciparum</i>, usando a metodologia de reação em cadeia da polimerase e polimorfismos de hidrólise por enzimas de restrição, em amostras de sangue infectado proveniente de crianças moçambicanas, residentes em Maputo. A análise foi feita antes e 7 dias após o tratamento com sulfadoxina-pirimetamina (S/P). Os resultados mostraram a ocorrência de mutações pontuais nos genes estudados e a presença de combinações de três alelos em dhfr (51<sup style="font-family: verdana, arial;">Ile</sup>, 59<sup style="font-family: verdana, arial;">Arg</sup> e 108<sup style="font-family: verdana, arial;">Asn</sup>) e do <i style="font-family: verdana, arial; font-size: 13.192px;">quintúplo</i> mutante (<i style="font-family: verdana, arial; font-size: 13.192px;">dhfr</i> 51<sup style="font-family: verdana, arial;">Ile</sup>, 59<sup style="font-family: verdana, arial;">Arg</sup>, 108<sup style="font-family: verdana, arial;">Asn</sup> e <i style="font-family: verdana, arial; font-size: 13.192px;">dhps</i> 437<sup style="font-family: verdana, arial;">Gly</sup>, 540<sup style="font-family: verdana, arial;">Glu</sup>), ambas situações associadas à falha terapêutica no sétimo dia após tratamento com S/P. Esses achados mostram a importância de se estudar a resistência à S/P em Moçambique, e como os marcadores moleculares de resistência aos antimaláricos podem fornecer dados importantes para a política nacional de controlo da malária.</p><p>The frequency and distribution of mutations in Plasmodium falciparum, dihydrofolate reductase and dihydropteroate synthase genes were analyzed, using the polymerase chain reaction and restriction fragment length polymorphism methodology, in infected blood samples from Mozambican children living in Maputo, before and seven days after treatment with sulfadoxine/pyrimethamine (S/P). The results showed the occurrence of point mutations in the genes studied and the presence of combinations of three alleles in dhfr (51Ile, 59Arg and 108Asn) and "quintuple" mutant (dhfr 51Ile, 59Arg, 108Asn and dhps 437Gly, 540Glu). Both of these situations were associated with seven-day therapeutic failure, following treatment with S/P. These findings show the importance of studying S/P resistance in Mozambique, and how molecular markers for antimalarial resistance can provide important data for national malaria control policy.</p>

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