Mohamed N. Seleem

Construction of a high-efficiency shuttle vector for Histophilus somni.

Vectors for enhanced gene expression and protein purification in Salmonella.

Reporter genes for real-time in vive monitoring of Ochrobactrum anthropi infection.

Activity of native vs. synthetic promoters in Brucella.

Brucella abortus strain RB51 leucine auxotroph as an environmentally safe vaccine for plasmid maintenance and antigen overexpression.

Targeting Brucella melitensis with polymeric nanoparticles containing streptomycin and doxycycline.

Plasmid-based system for high-level gene expression and antisense gene knockdown in Bartonella henselae.

Brucellosis: a re-emerging zoonosis.

Silica-antibiotic hybrid nanoparticles for targeting intracellular pathogens.

Tightly regulated expression vectors for Ochrobactrum anthropi.

Effect of entF deletion on iron acquisition and erythritol metabolism by Brucella abortus 2308.

Peptide nucleic acids inhibit growth of Brucella suis in pure culture and in infected murine macrophages.

Development of Biphenylthiazoles Exhibiting Improved Pharmacokinetics and Potent Activity Against Intracellular .

Ultrapotent Inhibitor of Growth, Which Suppresses Recurrence .

Repurposing the Veterinary Antiprotozoal Drug Ronidazole for the Treatment of Clostridioides difficile Infection.

Potent Synergistic Interactions between Lopinavir and Azole Antifungal Drugs against Emerging Multidrug-Resistant Candida auris.

Discovery of Prenyltransferase Inhibitors with and Antibacterial Activity.

Aprepitant, an antiemetic agent, interferes with metal ion homeostasis of and displays potent synergistic interactions with azole drugs.

Antibacterial Activity of Acetazolamide.

Evaluation of ebselen in resolving a methicillin-resistant Staphylococcus aureus infection of pressure ulcers in obese and diabetic mice.

-(1,3,4-Oxadiazol-2-yl)Benzamides as Antibacterial Agents against .

Structure-Activity Relationship Studies of Acetazolamide-Based Carbonic Anhydrase Inhibitors with Activity against .

In vivo efficacy of auranofin in a hamster model of Clostridioides difficile infection.

Sheep as a Potential Model of Intradiscal Infection by the Bacterium .

In vitro and in vivo activities of the carbonic anhydrase inhibitor, dorzolamide, against vancomycin-resistant enterococci.

High-throughput screening identifies a novel natural product-inspired scaffold capable of inhibiting Clostridioides difficile in vitro.

Investigating auranofin for the treatment of infected diabetic pressure ulcers in mice and dermal toxicity in pigs.

Nanocapsules modify membrane interaction of polymyxin B to enable safe systemic therapy of Gram-negative sepsis.

RNA-seq-based transcriptome analysis of a cefquinome-treated, highly resistant, and virulent MRSA strain.

Evaluation of bisphenylthiazoles as a promising class for combating multidrug-resistant fungal infections.

Dithiocarbamates effectively inhibit the α-carbonic anhydrase from .

Repurposing FDA-approved sulphonamide carbonic anhydrase inhibitors for treatment of .

Flexible Microneedle Array Patch for Chronic Wound Oxygenation and Biofilm Eradication.