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10.1111/j.0031-9317.2005.00582.x 83 TamuraK.StecherG.PetersonD.FilipskiA.KumarS

Patients were divided into a high-risk group (high expression of TXN and TXNRD and low expression of TXNIP) and a low-risk group (low expression of TXN and TXNRD and high expression of TXNIP) for analysis

A key advantage of in situ cancer vaccines lies in their ability to harness the full antigenic repertoire of the tumor, including shared TAAs, neoantigens generated by somatic mutations, post-translationally modified epitopes, viral antigens (e.g., human papillomavirus (HPV), EpsteinBarr virus (EBV)), and oncofetal proteins

Linossi was already an independent clinician when she arrived in Cambridge but, she says, EMI has given me the guidance and support to set up my own early-phase trials, ask relevant research questions and help me answer them