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Published structure-activity relationship (SAR) studies on ipamorelin analogues demonstrate that even single amino-acid substitutions reduce receptor binding affinity by 10- to 100-fold

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OK, fine, I admit that I do feel this paper hides the bodies slightly too effectively, in a way that could mislead people who arent experts or that dont read the paper carefully

Human tumour necrosis factor: precursor structure, expression and homology to lymphotoxin

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