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Christopher Baum

Showing results (111-120 of 143) with videos related to

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Genes, Chromosomes & Cancer|January 24, 2013
Histone methyltransferase Suv39h1 deficiency prevents Myc-induced chromosomal instability in murine myeloid leukemiasBeate Vajen, Ute Modlich, Andrea Schienke, et al.
Nature Medicine|October 26, 2006
LEF-1 is crucial for neutrophil granulocytopoiesis and its expression is severely reduced in congenital neutropeniaJulia Skokowa, Gunnar Cario, Murat Uenalan, et al.
Human Gene Therapy|March 10, 2009
Protein scaffold and expression level determine antiviral activity of membrane-anchored antiviral peptidesFelix G Hermann, Holger Martinius, Marc Egelhofer, et al.
Nucleic Acids Research|May 26, 2011
Avoiding cytotoxicity of transposases by dose-controlled mRNA deliveryMelanie Galla, Axel Schambach, Christine S Falk, et al.
Stem Cells and Development|July 8, 2011
Efficient hematopoietic redifferentiation of induced pluripotent stem cells derived from primitive murine bone marrow cellsNils Pfaff, Nico Lachmann, Saskia Kohlscheen, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 3, 2011
Lentiviral vector design and imaging approaches to visualize the early stages of cellular reprogrammingEva Warlich, Johannes Kuehle, Tobias Cantz, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 9, 2008
Self-inactivating gammaretroviral vectors for gene therapy of X-linked severe combined immunodeficiencySusannah I Thornhill, Axel Schambach, Steven J Howe, et al.
British Journal of Haematology|September 22, 2005
Expression of the p75 neurotrophin receptor in acute leukaemiaGernot Beutel, Johann Meyer, Liping Ma, et al.
Nucleic Acids Research|January 1, 2013
Sleeping Beauty transposon-based system for cellular reprogramming and targeted gene insertion in induced pluripotent stem cellsIvana Grabundzija, Jichang Wang, Attila Sebe, et al.
Molecular Pharmaceutics|August 20, 2011
Development of novel efficient SIN vectors with improved safety features for Wiskott-Aldrich syndrome stem cell based gene therapyInés Avedillo Díez, Daniela Zychlinski, Emanuele G Coci, et al.
Pageof 15

Showing results (111-120 of 143) with videos related to

Sort By:
Pageof 15
Genes, Chromosomes & Cancer|January 24, 2013
Histone methyltransferase Suv39h1 deficiency prevents Myc-induced chromosomal instability in murine myeloid leukemiasBeate Vajen, Ute Modlich, Andrea Schienke, et al.
Nature Medicine|October 26, 2006
LEF-1 is crucial for neutrophil granulocytopoiesis and its expression is severely reduced in congenital neutropeniaJulia Skokowa, Gunnar Cario, Murat Uenalan, et al.
Human Gene Therapy|March 10, 2009
Protein scaffold and expression level determine antiviral activity of membrane-anchored antiviral peptidesFelix G Hermann, Holger Martinius, Marc Egelhofer, et al.
Nucleic Acids Research|May 26, 2011
Avoiding cytotoxicity of transposases by dose-controlled mRNA deliveryMelanie Galla, Axel Schambach, Christine S Falk, et al.
Stem Cells and Development|July 8, 2011
Efficient hematopoietic redifferentiation of induced pluripotent stem cells derived from primitive murine bone marrow cellsNils Pfaff, Nico Lachmann, Saskia Kohlscheen, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|February 3, 2011
Lentiviral vector design and imaging approaches to visualize the early stages of cellular reprogrammingEva Warlich, Johannes Kuehle, Tobias Cantz, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 9, 2008
Self-inactivating gammaretroviral vectors for gene therapy of X-linked severe combined immunodeficiencySusannah I Thornhill, Axel Schambach, Steven J Howe, et al.
British Journal of Haematology|September 22, 2005
Expression of the p75 neurotrophin receptor in acute leukaemiaGernot Beutel, Johann Meyer, Liping Ma, et al.
Nucleic Acids Research|January 1, 2013
Sleeping Beauty transposon-based system for cellular reprogramming and targeted gene insertion in induced pluripotent stem cellsIvana Grabundzija, Jichang Wang, Attila Sebe, et al.
Molecular Pharmaceutics|August 20, 2011
Development of novel efficient SIN vectors with improved safety features for Wiskott-Aldrich syndrome stem cell based gene therapyInés Avedillo Díez, Daniela Zychlinski, Emanuele G Coci, et al.
Pageof 15