Moving Successful Virus-specific T-cell Therapy for Hematopoietic Stem Cell Recipients to Late Phase Clinical Trials.
about
Genetically modified T cells in cancer therapy: opportunities and challengesPan-viral-microRNA screening identifies interferon inhibition as a common function of diverse viruses.Identification and HLA-tetramer-validation of human CD4+ and CD8+ T cell responses against HCMV proteins IE1 and IE2.Antiviral cell therapy: is this the future?Adoptive T-cell therapy in the treatment of viral and opportunistic fungal infections.Treatment of CMV infection after allogeneic hematopoietic stem cell transplantation.
P2860
Moving Successful Virus-specific T-cell Therapy for Hematopoietic Stem Cell Recipients to Late Phase Clinical Trials.
description
2012 nî lūn-bûn
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2012年学术文章
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name
Moving Successful Virus-specif ...... to Late Phase Clinical Trials.
@ast
Moving Successful Virus-specif ...... to Late Phase Clinical Trials.
@en
type
label
Moving Successful Virus-specif ...... to Late Phase Clinical Trials.
@ast
Moving Successful Virus-specif ...... to Late Phase Clinical Trials.
@en
prefLabel
Moving Successful Virus-specif ...... to Late Phase Clinical Trials.
@ast
Moving Successful Virus-specif ...... to Late Phase Clinical Trials.
@en
P2860
P356
P1476
Moving Successful Virus-specif ...... to Late Phase Clinical Trials.
@en
P2093
Cliona Rooney
P2860
P356
10.1038/MTNA.2012.49
P577
2012-11-13T00:00:00Z