| Edição | 
	Seção | 
        Título | 
	Arquivo | 
											
				| Volume 510, Nº 1 (2023) | 
		Articles | 
		MODULAR NANOTRANSPORTERS CAPABLE OF BINDING WITH SARS-COV-2 VIRUS NUCLEOCAPSID PROTEIN INTO TARGET CELLS | 
		
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				| Volume 509, Nº 1 (2023) | 
		Articles | 
		INTRACELLULAR DELIVERY OF ANTIBODY-LIKE MOLECULE, CAPABLE TO INHIBIT C-MYC | 
		
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				| Volume 509, Nº 1 (2023) | 
		Articles | 
		SELECTION OF AN AMINO ACID SITE WITH ONE OF THE FASTEST CLEAVAGE KINETICS BY THE ENDOSOMAL PROTEASE CATHEPSIN B FOR POTENTIAL USE IN DRUG DELIVERY SYSTEMS | 
		
					 | 
		
												
				| Volume 515, Nº 1 (2024) | 
		Articles | 
		Quantitative description of the N-protein of the SARS-CoV-2 virus degradation in cells stably expressing it under the influence of new modular nanotransporters | 
		
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				| Volume 515, Nº 1 (2024) | 
		Articles | 
		Modular nanotransporters capable of cause intracellular degradation of the N-protein of the SARS-CoV-2 virus in A549 cells with temporary expression of this protein fused with the fluorescent protein mRuby3 | 
		
					 | 
		
												
				| Volume 514, Nº 1 (2024) | 
		Articles | 
		HSPBP1 in complex with the peptide of the innate immunity protein TAG7 is able to lyse tumor cells carrying TNFR1 receptor | 
		
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				| Volume 520, Nº 1 (2025) | 
		Articles | 
		GALA3-containing modular nanotransporters are capable of delivering Keap1 monobody to target cells and inhibiting the formation of reactive oxygen species in the cells | 
		
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				| Volume 521, Nº 1 (2025) | 
		Articles | 
		Optimization of A549 cell transfection efficiency with a plasmid encoding the N-protein of the SARS-COV-2 virus | 
		
					 | 
		
												
				| Volume 521, Nº 1 (2025) | 
		Articles | 
		Increasing the accumulation of modular nanotransporters in mouse tumors by attaching polyethylene glycol to these nanotransporters with the possibility of its release into the tumors | 
		
					 | 
		
												
				| Volume 521, Nº 1 (2025) | 
		Articles | 
		Modular nanotransporters containing Keap1 monobodies are capable of reducing the toxic effect of acetaminophen on the liver of mice | 
		
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