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U 1: GSTM5; Glutathione S-transferase, omega 1: GSTO1; Glutathione S-transferase, Ya chain (GST class-alpha): GSTA5; Haptoglobin: HP; Hemoglobin subunit alpha: HBA2; Isocitrate dehydrogenase: IDH1; Keratin complex 1, acidic, gene 10: KRT10; Kpnb1 protein b: KPNB1; Lactate dehydrogenase 2, B chain: LDHB; Lysozyme 2:; LYZ; Murinoglobulin-1 precursor: MUG1; Myosin heavy chain IIB: MYH4; Peroxiredoxin
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U 1: GSTM5; Glutathione S-transferase, omega 1: GSTO1; Glutathione S-transferase, Ya chain (GST class-alpha): GSTA5; Haptoglobin: HP; Hemoglobin subunit alpha: HBA2; Isocitrate dehydrogenase: IDH1; Keratin complex 1, acidic, gene 10: KRT10; Kpnb1 protein b: KPNB1; Lactate dehydrogenase 2, B chain: LDHB; Lysozyme 2:; LYZ; Murinoglobulin-1 precursor: MUG1; Myosin heavy chain IIB: MYH4; Peroxiredoxin
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Tion virosomes and virosomal adjuvanted formulations are currently applied in commercialTion virosomes and virosomal adjuvanted formulations are currently applied in commercial vaccines (Hepatitis A vaccines: Epaxal and Epaxal junior; Influenza vaccines: Inflexal V and FluAd). Moreover several promising virosome vaccine candidates , (Malaria, HCV breast cancer HIV Candida vaccines) are , , ,
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R calcium ions or hydroxyapatite was verified by circular dichroism, small angle scattering and vibrational spectroscopy (Figure 4). Based on modeling, the phosphorylated peptide folded differently when associated with a model of type I collagen than did the non-phosphorylated peptide (Figure 5). These changes in conformation associated with post-translational modifications, could facilitate nucle
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R calcium ions or hydroxyapatite was verified by circular dichroism, small angle scattering and vibrational spectroscopy (Figure 4). Based on modeling, the phosphorylated peptide folded differently when associated with a model of type I collagen than did the non-phosphorylated peptide (Figure 5). These changes in conformation associated with post-translational modifications, could facilitate nucle
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And new therapies may possibly be an effective treatment method tactic. From the present get the job done, we've investigated the flexibility of the previously established paclitaxel resistant cell traces (PC-3-TxR and DU145-TxR) to reply to microenvironmental stresses. In addition, the responses of cell lines symbolizing the spectrum of "normal" prostate to metastatic ailment to these microenviro