4.3 Article

Deciphering the Impact of Parameters Influencing Transgene Expression Kinetics after Repeated Cell Transduction with Integration-Deficient Retroviral Vectors

Related references

Note: Only part of the references are listed.
Article Biochemistry & Molecular Biology

Improved retroviral episome transfer of transcription factors enables sustained cell fate modification

J. W. Schott et al.

GENE THERAPY (2014)

Article Multidisciplinary Sciences

Non-integrating gamma-retroviral vectors as a versatile tool for transient zinc-finger nuclease delivery

Sylwia Bobis-Wozowicz et al.

SCIENTIFIC REPORTS (2014)

Review Cell & Tissue Engineering

Direct Reprogramming of Adult Somatic Cells Into Other Lineages: Past Evidence and Future Perspectives

Monica Nizzardo et al.

CELL TRANSPLANTATION (2013)

Review Biotechnology & Applied Microbiology

Biosafety Features of Lentiviral Vectors

Axel Schambach et al.

HUMAN GENE THERAPY (2013)

Review Biotechnology & Applied Microbiology

Mechanisms of Retroviral Integration and Mutagenesis

Alessia Cavazza et al.

HUMAN GENE THERAPY (2013)

Article Genetics & Heredity

Viral and Non-Viral Approaches for Transient Delivery of mRNA and Proteins

Juliane W. Schott et al.

CURRENT GENE THERAPY (2012)

Article Biochemical Research Methods

RGB marking with lentiviral vectors for multicolor clonal cell tracking

Kristoffer Weber et al.

NATURE PROTOCOLS (2012)

Review Biochemistry & Molecular Biology

Regulation of FOXO protein stability via ubiquitination and proteasome degradation

Haojie Huang et al.

BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH (2011)

Article Biochemistry & Molecular Biology

Avoiding cytotoxicity of transposases by dose-controlled mRNA delivery

Melanie Galla et al.

NUCLEIC ACIDS RESEARCH (2011)

Review Virology

Gammaretroviral Vectors: Biology, Technology and Application

Tobias Maetzig et al.

VIRUSES-BASEL (2011)

Article Biochemistry & Molecular Biology

A General Chemical Method to Regulate Protein Stability in the Mammalian Central Nervous System

Mari Iwamoto et al.

CHEMISTRY & BIOLOGY (2010)

Review Biochemistry & Molecular Biology

Integrase-defective lentiviral vectors: progress and applications

M. B. Banasik et al.

GENE THERAPY (2010)

Review Biochemistry & Molecular Biology

Identification, analysis, and prediction of protein ubiquitination sites

Predrag Radivojac et al.

PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS (2010)

Article Immunology

Raltegravir: The First HIV Type 1 Integrase Inhibitor

Charles Hicks et al.

CLINICAL INFECTIOUS DISEASES (2009)

Review Biotechnology & Applied Microbiology

Integration-deficient Lentiviral Vectors: A Slow Coming of Age

Klaus Wanisch et al.

MOLECULAR THERAPY (2009)

Review Multidisciplinary Sciences

Forcing cells to change lineages

Thomas Graf et al.

NATURE (2009)

Article Medicine, Research & Experimental

Insertional mutagenesis combined with acquired somatic mutations causes leukemogenesis following gene therapy of SCID-X1 patients

Steven J. Howe et al.

JOURNAL OF CLINICAL INVESTIGATION (2008)

Article Medicine, Research & Experimental

Insertional oncogenesis in 4 patients after retrovirus-mediated gene therapy of SCID-X1

Salima Hacein-Bey-Abina et al.

JOURNAL OF CLINICAL INVESTIGATION (2008)

Article Multidisciplinary Sciences

Lentiviral vectors with a defective integrase allow efficient and sustained transgene expression in vitro and in vivo

Stephanie Philippe et al.

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)

Article Biotechnology & Applied Microbiology

Transient gene expression by nonintegrating lentiviral vectors

Sarah J. Nightingale et al.

MOLECULAR THERAPY (2006)

Review Biotechnology & Applied Microbiology

Retrovirus vectors: Toward the plentivirus?

Christopher Baum et al.

MOLECULAR THERAPY (2006)

Letter Medicine, General & Internal

A serious adverse event after successful gene therapy for X-linked severe combined immunodeficiency

S Hacein-Bey-Abina et al.

NEW ENGLAND JOURNAL OF MEDICINE (2003)

Review Biochemistry & Molecular Biology

Lentiviral vectors: turning a deadly foe into a therapeutic agent

D Trono

GENE THERAPY (2000)