Precision nanomedicine: Shaping cellulose nanocrystals
The invention consists of a smart, inexpensive and biocompatible nanomaterial with custom-designed bioactivity.
The invention consists of a smart, inexpensive and biocompatible nanomaterial with custom-designed bioactivity.
The extracorporeal clearance precision measurement system allows clearance rate of extracorporeal treatments to be measured in real time and adjusted to patients’ needs.
The invention consists of a nanofunctionalized device that enables the quantitative determination of a specific biomarker, the FKBP12 protein, involved in many diseases.
The patent application protects nontoxic small molecules (glycomimetics), easily obtained from natural compounds (carbohydrates), which can be used for personalized treatment of glycan-related diseases
The molecular Oncology Lab is focalized on single-cell high resolution transcriptomics and cell lines and murine models follow up to drug treatment
The invention relates to a 'Clustered Regularly Interspersed Short Palindromic Repeat (CRISPR) CRISPR associated (Cas)’ (CRISPR-Cas) system targeting a genome sequence in a eukaryotic cell, i.e. a system useful for making modifications within the cell genome.
The invention consists of a method and related device for evaluating and diagnosing allergic-type reactions in a patient by analysing in vitro impedance changes detected by contacting the patient's serum with a given allergen
The invention refers to the use of an engineered 'Clustered Regularly Interspersed Short Palindromic Repeat (CRISPR)-CRISPR associated (Cas)’ (CRISPR-Cas) technology targeting a sequence mutated at one or more loci in the genome of a given eukaryotic cell
The compounds of the present invention are pyrazole[4,3-b]pyridin-6-carboxamide derivatives characterised by direct antibacterial activity against several Gram-positive bacteria
The present invention represents an in vitro implementable method and related kit for assessing the response to immune tolerance restoration therapy by evaluating the expression of specific microRNAs (miRNAs) as biomarkers of residual beta-cell function