33 results on '"Lieber, Andre"'
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2. In vitro and in vivo expansion of CD33/HBG promoter-edited HSPCs with Mylotarg
3. A simplified G-CSF–free procedure allows for in vivo HSC gene therapy of sickle cell disease in a mouse model
4. HDAd6/35++ - A new helper-dependent adenovirus vector platform for in vivo transduction of hematopoietic stem cells
5. In vivo HSC prime editing rescues sickle cell disease in a mouse model
6. Stable HIV decoy receptor expression after in vivo HSC transduction in mice and NHPs: Safety and efficacy in protection from SHIV
7. In vivo HSC transduction in rhesus macaques with an HDAd5/3+ vector targeting desmoglein 2 and transiently overexpressing cxcr4
8. Autoantibodies against desmoglein 2 are not pathogenic in pemphigus
9. Single-dose MGTA-145/plerixafor leads to efficient mobilization and in vivo transduction of HSCs with thalassemia correction in mice
10. In vivo HSPC gene therapy with base editors allows for efficient reactivation of fetal γ-globin in β-YAC mice
11. High-level protein production in erythroid cells derived from in vivo transduced hematopoietic stem cells
12. Disassembling a cancer puzzle: Cell junctions and plasma membrane as targets for anticancer therapy
13. Reactivation of γ-globin in adult β-YAC mice after ex vivo and in vivo hematopoietic stem cell genome editing
14. Junction opener protein increases nanoparticle accumulation in solid tumors
15. In vivo transduction of primitive mobilized hematopoietic stem cells after intravenous injection of integrating adenovirus vectors
16. P317: Gene therapy base editors reshape single-molecule chromatin architecture of γ-globin promoters
17. The transduction of Coxsackie and Adenovirus Receptor-negative cells and protection against neutralizing antibodies by HPMA- co-oligolysine copolymer-coated adenovirus
18. Biodistribution and retargeting of FX-binding ablated adenovirus serotype 5 vectors
19. A recombinant adenovirus type 35 fiber knob protein sensitizes lymphoma cells to rituximab therapy
20. Toward a stem cell gene therapy for breast cancer
21. Potent inhibition of OKT3-induced T cell proliferation and suppression of CD147 cell surface expression in HeLa cells by scFv-M6-1B9
22. Prospects and challenges of in vivo hematopoietic stem cell genome editing for hemoglobinopathies
23. Stable HIV decoy receptor expression after in vivo HSC transduction in mice and NHPs: Safety and efficacy in protection from SHIV
24. The complete nucleotide sequence, genome organization, and origin of human adenovirus type 11
25. 16 - Mgta-145 and Plerixafor-Mediated HSC Mobilization Along with HDAd5/35++ Vector into Mice Allows for Efficient In Vivo HSC Transduction and Stable Gene Marking in Peripheral Blood Cells
26. In Vivo HSC Gene Therapy with Base Editors Allows for Efficient Reactivation of Fetal Globin in Beta-Yac Mice
27. Mgta-145 / Plerixafor-Mediated HSC Mobilization and Intravenous HDAd5/35++ Vector Injection into Mice Allows for Efficient In Vivo HSC Transduction and Stable Gene Marking in Peripheral Blood Cells of CD46-Transgenic and Thalassemia Mice
28. In Vivo HSC Gene Therapy for Hemoglobinopathies: A Proof of Concept Evaluation in Rhesus Macaques
29. Thalassemia Gene Therapy By In Vivo Transduction of Mobilized Hematopoietic Stem Cells (HSCs) with an Integrating Hybrid Adenovirus Vector System
30. Introduction of Two Simultaneous Mutations By Genome Editing Greatly Enhances the Accumulation of the Endogenous Fetal Hemoglobin in Human Normal Erythroid Cells
31. A novel in vivo chemoselection strategy for genetically modified hematopoietic stem cells
32. Targeted integration of adenovirus vectors in hematopoietic stem cells
33. Production of recombinant antibodies in lymphoid and non-lymphoid cells
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