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Systemic lupus erythematosus: Molecular cloning and analysis of recombinant DNase monoclonal kappa light chain NGK-1 recombinant monoclonal antibody light chains (MLChs) capable of binding DNA were isolated by affinity

DOCKING PROBLEMS: PROTEIN-LIGAND LOW ENERGY MINIMA ANALYSIS-DOCKING PROBLEMS: PROTEIN-LIGAND LOW ENERGY MINIMA ANALYSIS-

Does pandemic A/H1N1 virus have the potential to become more pathogenic? and polymerase acidic protein L295P) that conferred a more virulent phenotype, both in cell cultures

Isolation and purification of staphylococcus aureus hibernationpromoting factor inactivating of the ribosome aureus hibernation-promoting factor (SaHPF) binds to ribosomes depleting translation and turning

Insights into the binding interaction mechanism of 12,12-dihydrochromeno[2,3-c]isoquinolin-5-amine in bovine serum albumin and prostaglandin H2 synthase-1: A biophysical approach-amine (drug) molecule binding interaction mechanism with bovine serum albumin (BSA) and prostaglandin H2

NMR screening of potential inhibitors of methionine γ-lyase from Citrobacter freundii of this enzyme in mammals allows us consider it to be a promising target for rational antibacterial drug design

The interaction of chlorin photosensitizers for photodynamic therapy with blood transport proteins much higher selectivity of tumor targeting during PDT can be achieved by the PS binding to appropriate

Pathway enrichment analysis of virus-host interactome and prioritization of novel compounds targeting the spike glycoprotein receptor binding domain–human angiotensin-converting enzyme 2 interface to combat SARS-CoV-2 drugs for treatment of the disease has caused its rapid spread on a global scale. Similarly to the SARS

Effects of testosterone supplementation on markers of the metabolic syndrome and inflammation in hypogonadal men with the metabolic syndrome: The double-blinded placebo-controlled Moscow study, high-density lipoprotein cholesterol, low-density lipoprotein cholesterol, C-reactive protein (CRP

Compounds identified by virtual docking to a tetrameric EGFR extracellular domain can modulate Grb2 internalization potential target for drug discovery. Methods: Our focus is on the prone EGFR tetramer, which contains a

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