Efficient transduction of healthy and malignant plasma cells by lentiviral vectors pseudotyped with measles virus glycoproteins
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Title
Efficient transduction of healthy and malignant plasma cells by lentiviral vectors pseudotyped with measles virus glycoproteins
Authors
Keywords
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Journal
LEUKEMIA
Volume 26, Issue 7, Pages 1663-1670
Publisher
Springer Nature
Online
2012-02-09
DOI
10.1038/leu.2012.36
References
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Related references
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- A high-risk signature for patients with multiple myeloma established from the molecular classification of human myeloma cell lines
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- Proliferation is a central independent prognostic factor and target for personalized and risk-adapted treatment in multiple myeloma
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- Mobilization of plasma cells in healthy individuals treated with granulocyte colony-stimulating factor for haematopoietic stem cell collection
- (2010) Anouk Caraux et al. IMMUNOLOGY
- An in vitro model of differentiation of memory B cells into plasmablasts and plasma cells including detailed phenotypic and molecular characterization
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- (2009) C. Frecha et al. BLOOD
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- (2009) H.-D. Hummel et al. JOURNAL OF GENERAL VIROLOGY
- High-risk myeloma: a gene expression based risk-stratification model for newly diagnosed multiple myeloma treated with high-dose therapy is predictive of outcome in relapsed disease treated with single-agent bortezomib or high-dose dexamethasone
- (2008) F. Zhan et al. BLOOD
- Stable transduction of quiescent T cells without induction of cycle progression by a novel lentiviral vector pseudotyped with measles virus glycoproteins
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- Oncolytic virotherapy for multiple myeloma
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- Report of the European Myeloma Network on multiparametric flow cytometry in multiple myeloma and related disorders
- (2008) A. C. Rawstron et al. HAEMATOLOGICA
- Prediction of Survival in Multiple Myeloma Based on Gene Expression Profiles Reveals Cell Cycle and Chromosomal Instability Signatures in High-Risk Patients and Hyperdiploid Signatures in Low-Risk Patients: A Study of the Intergroupe Francophone du Myélome
- (2008) Olivier Decaux et al. JOURNAL OF CLINICAL ONCOLOGY
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