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Antisense technology: an overview and prospectus

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405 Most patients with severe thalassemia experience complications of iron overload due to blood transfusions, which promote oxidative damage to various organs, leading to endocrine and ultimately organ dysfunction

Abnormal blood vessel development and lethality in embryos lacking a single VEGF allele

Combined with the analysis of HOMO and LUMO for GSH dimer and their complexes, possible specific sensing mechanism has been offered in the following

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