Fully human monoclonal antibodies block PCSK9 binding to LDL receptors, restoring cellular uptake and reducing circulating LDL-C concentrations.
A virus-like particle immunogen elicits antibody responses against angiopoietin-like polypeptides to inhibit lipoprotein lipase activity.
Segmenting ACAT isoforms preserves cholesterol homeostasis while treating obesity.
S-nitrosylating agents restore VLCAD enzymatic activity, reducing liver triglycerides and treating very long-chain acyl-CoA dehydrogenase deficiency.
Recombinant adeno-associated viral vectors deliver the GLA gene to target tissues, enabling sustained alpha-GAL enzyme production.
Intrathecal recombinant iduronate-2-sulfatase administration delivers therapeutic enzyme directly to the central nervous system.
Mutating residues 24, 25, and 27 in glucagon analogs prevents fibrillation and deamidation at physiological pH.
Chimeric trigonal agonists merge exendin-4 with glucagon sequences to enhance solubility, stability, and multi-receptor activation efficacy.
Withholding valine in parenteral or enteral formulas eliminates hematopoietic stem cells without radiation-induced tissue damage.
A molecular probe targets pancreatic islets via GLP-1R binding for PET or SPECT imaging.
Monoclonal antibodies neutralize ANGPTL3 activity to lower serum lipid concentrations, addressing underlying metabolic dysfunction in hypertriglyceridemia.
Aromatic-cationic peptides treat metabolic syndrome by improving lipid metabolism and blood sugar levels.
Hydroquinone ansamycins resolve low solubility and hepatotoxicity of geldanamycin by adding hydroxyl groups to improve delivery.
Novel glucagon analogue peptides act as dual agonists for glucagon and GLP-1 receptors to modulate metabolic functions.
Lactobacillus plantarum LP10 reduces body fat without adverse effects by mediating lipid metabolism at dosages exceeding 3×10^10 CFU daily.
Agglomerated amphiphilic polymer microparticles prevent initial burst and sustain release of hydrophilic drugs via controlled degradation.
Anti-PCSK9 antibodies target pathological protein activity to lower serum LDL cholesterol levels in patients with autosomal dominant hypercholesterolemia.
Cardiosphere-derived exosomes reduce inflammation and fibrosis, addressing limited efficacy of corticosteroids in chronic GVHD.
Negative modulator antibody fragments block insulin-receptor binding to prevent recurrent hypoglycemia and improve glycemic control.
Liver-targeting nanoparticles deliver SHP2 inhibitors to alleviate insulin resistance while minimizing off-target toxicity.
Amino acid modifications in GLP-1 polypeptides resolve the trade-off between glucose lowering and cardiorenal protection.
64Zn-enriched zinc reduces liver inflammation and fat accumulation while minimizing toxic side effects associated with traditional therapies.
Segmenting CB1 receptors via large molecule antibodies blocks peripheral signaling without CNS penetration, reducing adverse effects.