Role of the Benzodioxole Group in the Interactions between the Natural Alkaloids Chelerythrine and Coptisine and the Human Telomeric G-Quadruplex DNA. A Multiapproach Investigation | Journal of Natural Products
IJMS | Free Full-Text | Targeting Lipocalin-2 in Inflammatory Breast Cancer Cells with Small Interference RNA and Small Molecule Inhibitors
Subcellular distribution and mechanism of action of AL906, a novel and potent EGFR inhibitor rationally designed to be green fluorescent | SpringerLink
PHF3 regulates neuronal gene expression through the Pol II CTD reader domain SPOC | Nature Communications
Understanding G-NAF and Australian addresses | PPT
Total Licensing Autumn Fall 2023 by Total Licensing - Issuu
Lanthanide Doped Near Infrared Active Upconversion Nanophosphors: Fundamental Concepts, Synthesis Strategies, and Technological Applications - Lingeshwar Reddy - 2018 - Small - Wiley Online Library
PDF) Targeting Lipocalin-2 in Inflammatory Breast Cancer Cells with Small Interference RNA and Small Molecule Inhibitors
IJMS | Free Full-Text | Molecular Alterations in Sporadic and SOD1-ALS Immortalized Lymphocytes: Towards a Personalized Therapy
IJMS | Free Full-Text | Molecular Alterations in Sporadic and SOD1-ALS Immortalized Lymphocytes: Towards a Personalized Therapy
Covor NAF NAF CODE 12254-S | BioKarpet
IJMS | Free Full-Text | Targeting Lipocalin-2 in Inflammatory Breast Cancer Cells with Small Interference RNA and Small Molecule Inhibitors
Slides2 | PPT
Liste des codes NAF
Structure-Based Drug Design and Synthesis of Novel N-Aryl-2,4-bithiazole-2-amine CYP1B1-Selective Inhibitors in Overcoming Taxol Resistance in A549 Cells | Journal of Medicinal Chemistry
Nafamostat is a Potent Human Diamine Oxidase Inhibitor Possibly Augmenting Hypersensitivity Reactions during Nafamostat Administration | Journal of Pharmacology and Experimental Therapeutics
Fluoride Bridges as Structure-Directing Motifs in 3d-4f Cluster Chemistry | Inorganic Chemistry
Breast cancer tumorigenicity is dependent on high expression levels of NAF-1 and the lability of its Fe-S clusters | PNAS
Tumor suppressor mediated ubiquitylation of hnRNPK is a barrier to oncogenic translation | Nature Communications
4-(3-Phenyl-4-(3,4,5-trimethoxybenzoyl)-1H-pyrrol-1-yl)benzenesulfonamide, a Novel Carbonic Anhydrase and Wnt/β-Catenin Signaling Pathway Dual-Targeting Inhibitor with Potent Activity against Multidrug Resistant Cancer Cells
Nafamostat is a Potent Human Diamine Oxidase Inhibitor Possibly Augmenting Hypersensitivity Reactions during Nafamostat Administration | Journal of Pharmacology and Experimental Therapeutics
Full article: Exploring the functionalization of Ti-6Al-4V alloy with the novel antimicrobial peptide JIChis-2 via plasma polymerization