RGB marking with lentiviral vectors for multicolor clonal cell tracking
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Michael Thomaschewski | Kristoffer Weber | Boris Fehse | Daniel Benten | B. Fehse | M. Thomaschewski | D. Benten | K. Weber
[1] M. Malim,et al. Human Immunodeficiency Virus Type 1 Spinoculation Enhances Infection through Virus Binding , 2000, Journal of Virology.
[2] R. Tsien,et al. Improved monomeric red, orange and yellow fluorescent proteins derived from Discosoma sp. red fluorescent protein , 2004, Nature Biotechnology.
[3] B. Fehse,et al. Lentiviral gene ontology (LeGO) vectors equipped with novel drug-selectable fluorescent proteins: new building blocks for cell marking and multi-gene analysis , 2010, Gene Therapy.
[4] Michael Thomaschewski,et al. RGB marking facilitates multicolor clonal cell tracking , 2011, Nature Medicine.
[5] David A. Williams,et al. Rapid lentiviral transduction preserves the engraftment potential of Fanca(-/-) hematopoietic stem cells. , 2008, Molecular therapy : the journal of the American Society of Gene Therapy.
[6] V. Baekelandt,et al. Comparison of lentiviral vector titration methods , 2006, BMC biotechnology.
[7] David A. Williams,et al. Lentiviral vectors pseudotyped with murine ecotropic envelope: increased biosafety and convenience in preclinical research. , 2006, Experimental hematology.
[8] B. Fehse,et al. A multicolor panel of novel lentiviral "gene ontology" (LeGO) vectors for functional gene analysis. , 2008, Molecular Therapy.
[9] R. W. Draft,et al. Transgenic strategies for combinatorial expression of fluorescent proteins in the nervous system , 2007, Nature.
[10] R. Tsien,et al. The Fluorescent Toolbox for Assessing Protein Location and Function , 2006, Science.
[11] T. Schumacher,et al. Mapping the life histories of T cells , 2010, Nature Reviews Immunology.
[12] Mark A Rizzo,et al. An improved cyan fluorescent protein variant useful for FRET , 2004, Nature Biotechnology.
[13] C. Dunbar,et al. Contributions of gene marking to cell and gene therapies. , 2011, Human gene therapy.
[14] C. von Kalle,et al. Leukemias following retroviral transfer of multidrug resistance 1 (MDR1) are driven by combinatorial insertional mutagenesis. , 2005, Blood.
[15] M. Bock,et al. Epidermal growth factor improves lentivirus vector gene transfer into primary mouse hepatocytes , 2011, Gene Therapy.
[16] I. Verma,et al. Production and purification of lentiviral vectors , 2006, Nature Protocols.
[17] F. Cosset,et al. Characterization of HIV-1 vectors with gammaretrovirus envelope glycoproteins produced from stable packaging cells , 2004, Gene Therapy.
[18] N. Chaffey. Red fluorescent protein , 2001 .
[19] L. Naldini,et al. Short-term culture of human CD34+ cells for lentiviral gene transfer. , 2009, Methods in molecular biology.
[20] Takeharu Nagai,et al. Shift anticipated in DNA microarray market , 2002, Nature Biotechnology.
[21] Frederic D. Bushman,et al. Dynamics of gene-modified progenitor cells analyzed by tracking retroviral integration sites in a human SCID-X1 gene therapy trial. , 2010, Blood.
[22] B. Fehse,et al. Pois(s)on – It's a Question of Dose… , 2004, Gene Therapy.
[23] Nathan C Shaner,et al. A guide to choosing fluorescent proteins , 2005, Nature Methods.
[24] R. Kutner,et al. Production, concentration and titration of pseudotyped HIV-1-based lentiviral vectors , 2009, Nature Protocols.