Ester Boix

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Universitat Autònoma de Barcelona (UAB)

Spain

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Recent Grants

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An RNase-based drug to target antimicrobial resistance

Open Date: 2022-10-01

Close Date: 2024-05-01

Grant: Close

Escisión de RNAs no codificantes durante la respuesta inmunitaria a procesos infecciosos.

Open Date: 2020-06-01

Close Date: 2023-05-01

Grant: Close

Human RNases to combat antimicrobial resistance.

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A human derived peptide (hECP-5P36) as an novel antimicrobial agent to fight bacterial resistance

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Grant: Close

Pattern recognition of non-coding RNAs to search for novel therapeutic targets in the fight against bacterial antimicrobial resistance

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Articles (15)

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2024

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2022

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2022

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2022

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2021

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2021

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2021

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2021

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2021

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2020

Collaborators (4)

M. Angeles Jimenez

SPAIN

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Sanjib Bhakta

Professor of Molecular Microbiology and Biochemistry

Birkbeck University of London

UNITED KINGDOM

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David Andreu

Universitat Pompeu Fabra

SPAIN

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Marc Torrent

Associate professor

Universitat Autònoma de Barcelona Facultat de Medicina

SPAIN

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Ester Boix

Research Interests

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Recent Grants

Articles (15)

Structural determinants for tRNA selective cleavage by RNase 2/EDN

A Common Polymorphism in RNASE6 Impacts Its Antimicrobial Activity toward Uropathogenic Escherichia coli

Ancestral ribonucleases back in motion for evolutionary-dynamics guided protein design

Murine Ribonuclease 6 Limits Bacterial Dissemination During Experimental Urinary Tract Infection

Human Ribonuclease 6 Has a Protective Role during Experimental Urinary Tract Infection

Exploring the RNase A scaffold to combine catalytic and antimicrobial activities. Structural characterization of RNase 3/1 chimeras

Essential Role of Enzymatic Activity in the Leishmanicidal Mechanism of the Eosinophil Cationic Protein (RNase 3)

Selective cleavage of ncRNA and antiviral activity by RNase2/EDN in THP1-induced macrophages

In Vivo Evaluation of ECP Peptide Analogues for the Treatment of Acinetobacter baumannii Infection

Host Defence RNases as Antiviral Agents against Enveloped Single Stranded RNA Viruses

Structure-Based Design of an RNase Chimera for Antimicrobial Therapy

Rationally Modified Antimicrobial Peptides from the N-Terminal Domain of Human RNase 3 Show Exceptional Serum Stability

Human RNase3 immune modulation by catalytic-dependent and independent modes in a macrophage-cell line infection model

Weighted Gene Co-Expression Network Analysis Identifies Key Modules and Hub Genes Associated with Mycobacterial Infection of Human Macrophages

Magnetite Nanoparticles Functionalized with RNases against Intracellular Infection of Pseudomonas aeruginosa

Collaborators (4)

M. Angeles Jimenez

Sanjib Bhakta

David Andreu

Marc Torrent

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