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Françoise Mathieu-Daudé

Researcher at Institut de recherche pour le développement

Publications -  38
Citations -  1240

Françoise Mathieu-Daudé is an academic researcher from Institut de recherche pour le développement. The author has contributed to research in topics: Differential display & Trypanosoma cruzi. The author has an hindex of 16, co-authored 37 publications receiving 1173 citations. Previous affiliations of Françoise Mathieu-Daudé include Torrey Pines Institute for Molecular Studies.

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RNA fingerprinting and differential display using arbitrarily primed PCR

TL;DR: RNA fingerprinting by arbitrarily primed PCR can be used to detect and clone transcripts that are differentially expressed between cells that have been subject to different environments or developmental programs.
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DNA Rehybridization During PCR: The ‘Cot Effect’ and Its Consequences

TL;DR: In some applications, where the object is to stochiometrically amplify a mixture of nucleic acids, the bias against abundant PCR products can be partly overcome by limiting the number of PCR cycles and, thus, the concentration of the products.
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Advances and perspectives in Leishmania cell based drug-screening procedures.

TL;DR: This review will focus on available methodologies for direct drug screening purposes against the mammalian stage of the parasite, with emphasis on the future developments that could improve sensitivity, reliability, versatility and the throughput of the intracellular model screening.
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Socio-economic and Climate Factors Associated with Dengue Fever Spatial Heterogeneity: A Worked Example in New Caledonia.

TL;DR: This study presents a methodology that can be used as a step by step guide to model dengue spatial heterogeneity in other countries and modelled and estimated the future evolution of d Dengue incidence rates using a regional downscaling of future climate projections.
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Screening of Differentially Amplified cDNA Products from RNA Arbitrarily Primed PCR Fingerprints Using Single Strand Conformation Polymorphism (SSCP) Gels

TL;DR: This screen should save considerable effort now wasted on directly cloning unsuitable products from RNA fingerprinting experiments, and an example is presented of cloning a gene differentially expressed in Trypanosoma brucei life cycle.