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Roberto Díez-Martínez

Researcher at Spanish National Research Council

Publications -  16
Citations -  710

Roberto Díez-Martínez is an academic researcher from Spanish National Research Council. The author has contributed to research in topics: Streptococcus pneumoniae & Lysin. The author has an hindex of 11, co-authored 16 publications receiving 534 citations. Previous affiliations of Roberto Díez-Martínez include Carlos III Health Institute.

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Novel Phage Lysin Capable of Killing the Multidrug-Resistant Gram-Negative Bacterium Acinetobacter baumannii in a Mouse Bacteremia Model

TL;DR: PlyF307 represents the first highly active therapeutic lysin specific for Gram-negative organisms in an array of native lysins found in Acinetobacter phage and rescued mice from lethal A. baumannii bacteremia.
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Zebrafish: Speeding Up the Cancer Drug Discovery Process

TL;DR: This review provides a comprehensive overview of zebrafish in the cancer drug discovery process, from approaches to induce malignant tumors, techniques to monitor cancer progression, and strategies for compound administration to a compilation of the 355 existing case studies showing the impact ofZebrafish models on cancer drug Discovery.
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A novel chimeric phage lysin with high in vitro and in vivo bactericidal activity against Streptococcus pneumoniae

TL;DR: Cpl-711, the most powerful endolysin against pneumococci, offers a promising therapeutic perspective for the treatment of multiresistant pneumococcal infections and domain swapping among phage lysins allows the construction of new chimeric enzymes with high bactericidal activity and a different substrate range.
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Improving the Lethal Effect of Cpl-7, a Pneumococcal Phage Lysozyme with Broad Bactericidal Activity, by Inverting the Net Charge of Its Cell Wall-Binding Module

TL;DR: These findings provide a strategy to improve the lytic activity of phage endolysins based on facilitating their pass through the negatively charged bacterial envelope, and thereby their interaction with the cell wall target, by modulating the net charge of thecell wall-binding modules.