Results 11 to 20 of about 368,855 (303)

ACE2-lentiviral transduction enables mouse SARS-CoV-2 infection and mapping of receptor interactions [PDF]

open access: yesPLoS Pathog, 2021
SARS-CoV-2 uses the human ACE2 (hACE2) receptor for cell attachment and entry, with mouse ACE2 (mACE2) unable to support infection. Herein we describe an ACE2-lentivirus system and illustrate its utility for in vitro and in vivo SARS-CoV-2 infection ...
Rawle DJ   +6 more
europepmc   +3 more sources

Staurosporine Increases Lentiviral Vector Transduction Efficiency of Human Hematopoietic Stem and Progenitor Cells

open access: yesMolecular Therapy - Methods and Clinical Development, 2018
Lentiviral vector (LVV)-mediated transduction of human CD34+ hematopoietic stem and progenitor cells (HSPCs) holds tremendous promise for the treatment of monogenic hematological diseases.
Olivier Negre, Philip Gregory
exaly   +4 more sources

DEAE-Dextran Enhances the Lentiviral Transduction of Primary Human Mesenchymal Stromal Cells from All Major Tissue Sources Without Affecting Their Proliferation and Phenotype. [PDF]

open access: yesMol Biotechnol, 2023
Genetic engineering of mesenchymal stromal cells (MSCs) is a tool widely used to explore MSC properties in vitro and in vivo. Lentiviral infection with the use of polycations as an adjuvant is a method that is commonly used to generate stably transduced ...
Amadeo F, Hanson V, Murray P, Taylor A.
europepmc   +2 more sources

Cellular Proteo-Transcriptomic Changes in the Immediate Early-Phase of Lentiviral Transduction. [PDF]

open access: yesMicroorganisms, 2021
Lentivirus-based vectors derived from human immunodeficiency viruses type 1 and 2 (HIV-1 and 2) are widely used tools in research and may also be utilized in clinical settings.
Linkner TR   +9 more
europepmc   +2 more sources

Lentiviral transduction facilitates RNA interference in the nematode parasite Nippostrongylus brasiliensis. [PDF]

open access: yesPLoS Pathog, 2021
Animal-parasitic nematodes have thus far been largely refractory to genetic manipulation, and methods employed to effect RNA interference (RNAi) have been ineffective or inconsistent in most cases. We describe here a new approach for genetic manipulation
Hagen J, Sarkies P, Selkirk ME.
europepmc   +2 more sources

Efficient lentiviral transduction method to gene modify cord blood CD8<sup>+</sup> T cells for cancer therapy applications. [PDF]

open access: yesMol Ther Methods Clin Dev, 2021
Adoptive T cell therapy utilizing tumor-specific autologous T cells has shown promising results for cancer treatment. However, the limited numbers of autologous tumor-associated antigen (TAA)-specific T cells and the functional aberrancies, due to ...
Lo Presti V   +7 more
europepmc   +2 more sources

CD9 and folate receptor overexpression are not sufficient for VSV-G-independent lentiviral transduction [PDF]

open access: yesPLoS ONE, 2022
Extracellular vesicles have become a research focus for their potential as therapeutic vehicles that carry cargo substances. Extracellular vesicles may origin from the endosomal compartment and share several characteristics with the envelope of ...
Cristina Bellotti   +2 more
doaj   +3 more sources

Process for an efficient lentiviral cell transduction [PDF]

open access: yesBiology Methods and Protocols, 2020
The combination of lentiviruses with techniques such as CRISPR-Cas9 has resulted in efficient and precise processes for targeted genome modification. An often-limiting aspect, however, is the efficiency of cell transduction.
A. Pirona   +3 more
semanticscholar   +3 more sources

A straightforward microfluidic-based approach toward optimizing transduction efficiency of HIV-1-derived lentiviral vectors in BCP-ALL cells

open access: yesBiotechnology Reports (Amsterdam, Netherlands), 2023
Highlights • Lentiviral vectors have a limited half-life, and in order to reach the target, the distance between the target cell and the vector should be minimized.• Microfluidic systems provide a micro-scaled environment in which lentiviral vectors have
Seyed Esmaeil Ahmadi   +2 more
exaly   +2 more sources

Cell-based artificial APC resistant to lentiviral transduction for efficient generation of CAR-T cells from various cell sources. [PDF]

open access: yesJ Immunother Cancer, 2020
Background Adoptive cell therapy with chimeric antigen receptor T cells (CAR-T) has become a standard treatment for patients with certain aggressive B cell malignancies and holds promise to improve the care of patients suffering from numerous other ...
Schmidts A   +17 more
europepmc   +2 more sources

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