| scholarly article | Q13442814 |
| P356 | DOI | 10.1038/MT.2014.173 |
| P8608 | Fatcat ID | release_blsp42ebkfdjjdbxr4fesmdwku |
| P932 | PMC publication ID | 4426797 |
| P698 | PubMed publication ID | 25189742 |
| P5875 | ResearchGate publication ID | 265377392 |
| P50 | author | Kerstin B Kaufmann | Q38326220 |
| Hubert Serve | Q39186141 | ||
| P2093 | author name string | Manuel Grez | |
| Tobias Abel | |||
| Christian J Buchholz | |||
| Sabrina Kneissl | |||
| Martijn Brugman | |||
| Hana Kunkel | |||
| Uta Müller-Kuller | |||
| Joachim Schwäble | |||
| Linping Chen-Wichmann | |||
| Benjamin Goebel | |||
| Christian Brendel | |||
| Leonid Bystrykh | |||
| Abriss Daniela | |||
| P2860 | cites work | Mutations in the H, F, or M Proteins Can Facilitate Resistance of Measles Virus to Neutralizing Human Anti-MV Sera. | Q41972771 |
| Selection based on CD133 and high aldehyde dehydrogenase activity isolates long-term reconstituting human hematopoietic stem cells | Q42741832 | ||
| Specific gene transfer to neurons, endothelial cells and hematopoietic progenitors with lentiviral vectors | Q42863043 | ||
| Mystery solved: VSV-G-LVs do not allow efficient gene transfer into unstimulated T cells, B cells, and HSCs because they lack the LDL receptor. | Q43944919 | ||
| Novel lentiviral vectors displaying "early-acting cytokines" selectively promote survival and transduction of NOD/SCID repopulating human hematopoietic stem cells. | Q44120659 | ||
| Highly efficient lentiviral gene transfer in CD34+ and CD34+/38-/lin- cells from mobilized peripheral blood after cytokine prestimulation | Q44495581 | ||
| Maximal lentivirus-mediated gene transfer and sustained transgene expression in human hematopoietic primitive cells and their progeny | Q44772246 | ||
| Cytokine-facilitated transduction leads to low-level engraftment in nonablated hosts | Q45295243 | ||
| Transduction of human CD34+ cells that mediate long-term engraftment of NOD/SCID mice by HIV vectors | Q45855831 | ||
| Immature human cord blood progenitors engraft and proliferate to high levels in severe combined immunodeficient mice | Q45866157 | ||
| Distinct classes of human stem cells that differ in proliferative and self-renewal potential | Q45873643 | ||
| AC133+ G0 cells from cord blood show a high incidence of long-term culture-initiating cells and a capacity for more than 100 million-fold amplification of colony-forming cells in vitro | Q45877579 | ||
| Gene therapy matures in the clinic | Q45880394 | ||
| Molecular evidence for stem cell function of the slow-dividing fraction among human hematopoietic progenitor cells by genome-wide analysis | Q47749134 | ||
| Cytokines, including stem cell factor alone, enhance lentiviral transduction in nondividing human LTCIC and NOD/SCID repopulating cells | Q48001966 | ||
| A novel five-transmembrane hematopoietic stem cell antigen: isolation, characterization, and molecular cloning | Q48041391 | ||
| Isolation of single human hematopoietic stem cells capable of long-term multilineage engraftment. | Q50676184 | ||
| Isolation and characterization of human CD34(-)Lin(-) and CD34(+)Lin(-) hematopoietic stem cells using cell surface markers AC133 and CD7. | Q51081344 | ||
| Individual stem cells with highly variable proliferation and self-renewal properties comprise the human hematopoietic stem cell compartment. | Q52005673 | ||
| Large-scale isolation of CD133+ progenitor cells from G-CSF mobilized peripheral blood stem cells. | Q54785700 | ||
| Cytokine stimulation of multilineage hematopoiesis from immature human cells engrafted in SCID mice | Q67532844 | ||
| Cell cycle-related changes in repopulating capacity of human mobilized peripheral blood CD34(+) cells in non-obese diabetic/severe combined immune-deficient mice | Q77380979 | ||
| Comparison of various envelope proteins for their ability to pseudotype lentiviral vectors and transduce primitive hematopoietic cells from human blood | Q77684631 | ||
| Comparative analysis of proliferative potential and clonogenicity of MACS-immunomagnetic isolated CD34+ and CD133+ blood stem cells derived from a single donor | Q80005254 | ||
| Adherens junction protein nectin-4 is the epithelial receptor for measles virus | Q24295305 | ||
| Foamy virus biology and its application for vector development | Q26864134 | ||
| Gene therapy on the move | Q27007012 | ||
| AC133, a novel marker for human hematopoietic stem and progenitor cells | Q28115893 | ||
| LDL receptor and its family members serve as the cellular receptors for vesicular stomatitis virus | Q28118448 | ||
| Human hematopoietic stem cells stimulated to proliferate in vitro lose engraftment potential during their S/G(2)/M transit and do not reenter G(0). | Q33181506 | ||
| Transplantation of a combination of CD133+ and CD34+ selected progenitor cells from alternative donors | Q33358178 | ||
| Dynamics of HSPC repopulation in nonhuman primates revealed by a decade-long clonal-tracking study | Q33563393 | ||
| Lentiviral hematopoietic stem cell gene therapy in patients with Wiskott-Aldrich syndrome. | Q34356904 | ||
| Lentiviral hematopoietic stem cell gene therapy benefits metachromatic leukodystrophy | Q34356914 | ||
| Measles virus glycoprotein-based lentiviral targeting vectors that avoid neutralizing antibodies | Q34447329 | ||
| DARPins: an efficient targeting domain for lentiviral vectors | Q34757199 | ||
| The replication rate of human hematopoietic stem cells in vivo | Q34997694 | ||
| Hematopoietic stem cell gene therapy with a lentiviral vector in X-linked adrenoleukodystrophy | Q35011497 | ||
| Lentiviral vectors displaying modified measles virus gp overcome pre-existing immunity in in vivo-like transduction of human T and B cells. | Q36220659 | ||
| Purification of primitive human hematopoietic cells capable of repopulating immune-deficient mice. | Q36772601 | ||
| Measles virus receptors | Q37386883 | ||
| Lentiviral vectors with measles virus glycoproteins - dream team for gene transfer? | Q37425507 | ||
| Phenotypes of stem cells from diverse origin | Q37660233 | ||
| CD133(+) cells isolated from various sources and their role in future clinical perspectives | Q37798837 | ||
| CD133 as a biomarker for putative cancer stem cells in solid tumours: limitations, problems and challenges | Q38035206 | ||
| Haematopoietic stem cell differentiation promotes the release of prominin-1/CD133-containing membrane vesicles--a role of the endocytic-exocytic pathway | Q38984604 | ||
| Transduction of human progenitor hematopoietic stem cells by human immunodeficiency virus type 1-based vectors is cell cycle dependent. | Q39550293 | ||
| RD114 envelope proteins provide an effective and versatile approach to pseudotype lentiviral vectors | Q39650863 | ||
| A novel lentiviral vector targets gene transfer into human hematopoietic stem cells in marrow from patients with bone marrow failure syndrome and in vivo in humanized mice. | Q39683011 | ||
| Molecular evidence of lentiviral vector-mediated gene transfer into human self-renewing, multi-potent, long-term NOD/SCID repopulating hematopoietic cells | Q40693301 | ||
| Absence of a relationship between immunophenotypic and colony enumeration analysis of endothelial progenitor cells in clinical haematopoietic cell sources | Q41944621 | ||
| P433 | issue | 1 | |
| P304 | page(s) | 63-70 | |
| P577 | publication date | 2014-09-05 | |
| P1433 | published in | Molecular Therapy | Q15762400 |
| P1476 | title | CD133-targeted gene transfer into long-term repopulating hematopoietic stem cells | |
| P478 | volume | 23 |
| Q41899254 | CD105 is a surface marker for receptor-targeted gene transfer into human long-term repopulating hematopoietic stem cells |
| Q40228003 | Chemoprotection of murine hematopoietic cells by combined gene transfer of cytidine deaminase (CDD) and multidrug resistance 1 gene (MDR1). |
| Q91841922 | Gene therapy of hematological disorders: current challenges |
| Q36596865 | Genetic treatment of a molecular disorder: gene therapy approaches to sickle cell disease |
| Q40045829 | In Vivo Hematopoietic Stem Cell Transduction. |
| Q37395719 | Lineage-specific BCL11A knockdown circumvents toxicities and reverses sickle phenotype |
| Q38815488 | Optimizing autologous cell grafts to improve stem cell gene therapy |
| Q26750586 | Production of lentiviral vectors |
| Q38672557 | Single-cell analyses to reveal hematopoietic stem cell fate decisions |
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