The stabilization of G-Quadruplex DNA structures by ligands is a promising strategy for telomerase inhibition in cancer therapy since this enzyme is responsible for the unlimited proliferation of cancer cells. To assess the potential of a compound as a telomerase inhibitor. selectivity for quadruplex over duplex DNA is a fundamental attribute. as the drug must be able to recognize qua... https://bursgaers.shop/product-category/laptop-sleeves/
Multicharged Phthalocyanines as Selective Ligands for G-Quadruplex DNA Structures
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