| scholarly article | Q13442814 |
| review article | Q7318358 |
| P356 | DOI | 10.1016/J.TIBTECH.2009.02.002 |
| P698 | PubMed publication ID | 19327858 |
| P2093 | author name string | Klaus Cichutek | |
| Michael D Mühlebach | |||
| Christian J Buchholz | |||
| P433 | issue | 5 | |
| P921 | main subject | measles | Q79793 |
| vector-borne disease | Q2083837 | ||
| P304 | page(s) | 259-265 | |
| P577 | publication date | 2009-03-25 | |
| P1433 | published in | Trends in Biotechnology | Q2451465 |
| P1476 | title | Lentiviral vectors with measles virus glycoproteins - dream team for gene transfer? | |
| P478 | volume | 27 |
| Q24599954 | A new generation of human artificial chromosomes for functional genomics and gene therapy |
| Q34579790 | A portable BRCA1-HAC (human artificial chromosome) module for analysis of BRCA1 tumor suppressor function. |
| Q38917869 | A scalable method to concentrate lentiviral vectors pseudotyped with measles virus glycoproteins |
| Q59356321 | A simple strategy for retargeting lentiviral vectors to desired cell types via a disulfide-bond-forming protein-peptide pair |
| Q39369916 | A small-molecule-controlled system for efficient pseudotyping of prototype foamy virus vectors |
| Q37782256 | Advances in the field of lentivector-based transduction of T and B lymphocytes for gene therapy |
| Q35198350 | Avoiding cytotoxicity of transposases by dose-controlled mRNA delivery |
| Q38073294 | Biosafety features of lentiviral vectors |
| Q41899254 | CD105 is a surface marker for receptor-targeted gene transfer into human long-term repopulating hematopoietic stem cells |
| Q35238704 | CD133-targeted gene transfer into long-term repopulating hematopoietic stem cells |
| Q42254939 | CD19 and CD20 targeted vectors induce minimal activation of resting B lymphocytes |
| Q41877997 | Cell type specific gene delivery by lentiviral vectors: New options in immunotherapy |
| Q37952177 | Cytoskeletal dynamics: concepts in measles virus replication and immunomodulation |
| Q34757199 | DARPins: an efficient targeting domain for lentiviral vectors |
| Q45872567 | Epidermal growth factor improves lentivirus vector gene transfer into primary mouse hepatocytes |
| Q39707428 | Exploitation of the interaction of measles virus fusogenic envelope proteins with the surface receptor CD46 on human cells for microcell-mediated chromosome transfer |
| Q34223822 | Gammaretroviral vectors: biology, technology and application |
| Q38183464 | Human artificial chromosome-based gene delivery vectors for biomedicine and biotechnology |
| Q35238272 | Human artificial chromosomes for gene delivery and the development of animal models |
| Q40211579 | Immune Modulatory Cell Therapy for Hemophilia B Based on CD20-Targeted Lentiviral Gene Transfer to Primary B Cells. |
| Q33945680 | Immunization of mice with lentiviral vectors targeted to MHC class II+ cells is due to preferential transduction of dendritic cells in vivo |
| Q34447329 | Measles virus glycoprotein-based lentiviral targeting vectors that avoid neutralizing antibodies |
| Q39011184 | Measles virus glycoprotein-pseudotyped lentiviral vector-mediated gene transfer into quiescent lymphocytes requires binding to both SLAM and CD46 entry receptors. |
| Q36607409 | Nipah virus envelope-pseudotyped lentiviruses efficiently target ephrinB2-positive stem cell populations in vitro and bypass the liver sink when administered in vivo |
| Q33842785 | Protein transduction from retroviral Gag precursors |
| Q37678176 | Recent advances in lentiviral vector development and applications |
| Q38906090 | Receptor-targeted lentiviral vectors are exceptionally sensitive toward the biophysical properties of the displayed single-chain Fv. |
| Q26861563 | Recombinant messenger RNA technology and its application in cancer immunotherapy, transcript replacement therapies, pluripotent stem cell induction, and beyond |
| Q45367595 | Resting lymphocyte transduction with measles virus glycoprotein pseudotyped lentiviral vectors relies on CD46 and SLAM. |
| Q42863043 | Specific gene transfer to neurons, endothelial cells and hematopoietic progenitors with lentiviral vectors |
| Q58726929 | Surface-Engineered Lentiviral Vectors for Selective Gene Transfer into Subtypes of Lymphocytes |
| Q45876186 | Targeted lentiviral vectors pseudotyped with the Tupaia paramyxovirus glycoproteins |
| Q38817999 | Transformation-associated recombination (TAR) cloning for genomics studies and synthetic biology |
| Q37945189 | Viral hybrid vectors for somatic integration - are they the better solution? |
Search more.