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Walhan Alshaer

Researcher at University of Jordan

Publications -  81
Citations -  1524

Walhan Alshaer is an academic researcher from University of Jordan. The author has contributed to research in topics: Medicine & Chemistry. The author has an hindex of 12, co-authored 51 publications receiving 640 citations. Previous affiliations of Walhan Alshaer include Université Paris-Saclay & Max Delbrück Center for Molecular Medicine.

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Aptamers Chemistry: Chemical Modifications and Conjugation Strategies.

TL;DR: Aptamers are short single-stranded RNA or DNA oligonucleotides capable of folding into complex 3D structures, enabling them to bind to a large variety of targets ranging from small ions to an entire organism, and they are superior regarding a longer shelf life, simple production and chemical modification.
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Functionalizing Liposomes with anti-CD44 Aptamer for Selective Targeting of Cancer Cells

TL;DR: 2'-F-pyrimidine-containing RNA aptamer (Apt1), previously selected against CD44, was successfully conjugated to the surface of PEGylated liposomes using the thiol-maleimide click reaction, demonstrating a promising potency of Apt1-Lip as a specific drug delivery system.
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Comprehensive Structural and Molecular Comparison of Spike Proteins of SARS-CoV-2, SARS-CoV and MERS-CoV, and Their Interactions with ACE2.

TL;DR: This review comprehensively addresses in detail the variations in S protein, its receptor-binding characteristics and detailed structural interactions, the process of cleavage involved in priming, as well as other differences between coronaviruses.
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Aptamer-guided nanomedicines for anticancer drug delivery

TL;DR: The current advances in the use of aptamers as targeting moieties for the delivery of therapeutic and imaging agents to tumors by conjugation to organic and inorganic nanocarriers are described.
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Aptamer-guided siRNA-loaded nanomedicines for systemic gene silencing in CD-44 expressing murine triple-negative breast cancer model.

TL;DR: A liposome‐based siRNA delivery system with a core composed of siRNA:protamine complex and a shell designed for the active targeting of CD44‐expressing cells using for the first time the anti‐CD44 aptamer (named Apt1) as targeting ligand is described.