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In particular, GSTT1-1 and GSTM1-1 null genotypes, as well as GSTP1-1 variants, were studies and showed a positive correlation with cancer risk (Table 1) 24,32,35,36,37,38,39,40,41,42

Figure 7 The disulfide and carba analogues examined demonstrated a relative high stability against proteolysis by metallopeptidases, despite the similarities in the N-terminal to oxytocin 35 and vasopressin 36 that both serve as substrates to IRAP (Alescio-Lautier et al., 2000