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Frederico Aires-da-Silva

Researcher at University of Lisbon

Publications -  19
Citations -  324

Frederico Aires-da-Silva is an academic researcher from University of Lisbon. The author has contributed to research in topics: Medicine & Canine Lymphoma. The author has an hindex of 6, co-authored 15 publications receiving 158 citations.

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Journal ArticleDOI

Antibody Approaches To Treat Brain Diseases

TL;DR: Advances in the development and engineering of therapeutic BBB-crossing antibodies and their high potential for treatment of CNS disorders are reviewed.
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Characterization of plasma labile heme in hemolytic conditions.

TL;DR: A panel of heme‐specific single domain antibodies (sdAbs) that neutralize the pro‐oxidant activity of soluble heme in vitro are developed and characterized, suggesting that these maybe used to counter the pathologic effects of labile heme during hemolytic conditions.
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Liposomes as Antibiotic Delivery Systems: A Promising Nanotechnological Strategy against Antimicrobial Resistance.

TL;DR: In this paper, the applicability of antibiotic encapsulated liposomes as an effective therapeutic strategy for bacterial infections is discussed, which holds the potential to overcome antimicrobial resistance and biofilm formation and constituting a promising solution for the treatment of potential fatal multidrug resistant bacterial infections, such as methicillin resistant Staphylococcus aureus.
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Chemokine-Directed Tumor Microenvironment Modulation in Cancer Immunotherapy.

TL;DR: In this article, the authors provide a general overview of chemokine effects on several tumoral processes, as well as a description of the currently available chemokin-directed therapies, highlighting their potential both as monotherapy or in combination with standard chemotherapy or other immunotherapies.
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Novel Peptides Derived from Dengue Virus Capsid Protein Translocate Reversibly the Blood–Brain Barrier through a Receptor-Free Mechanism

TL;DR: It is shown that specific domains of Dengue virus type 2 capsid protein (DEN2C) can be used as trans-BBB peptide vectors and their mechanism of translocation is receptor-independent and consistent with adsorptive-mediated transport (AMT).