Results 71 to 80 of about 260,635 (281)

Lentiviral transduction v1

open access: yes
Lentiviral transduction of primary neurons
Bishal Basak, Erika Holzbaur
openaire   +1 more source

Remote Activation of Wnt Signaling and Cell Proliferation by E‐Cadherin Magnetomechanical Stimulation

open access: yesAdvanced Functional Materials, EarlyView.
A pioneering magnetogenetic toolkit enables non‐invasive, precise spatiotemporal modulation of intracellular Wnt/β‐catenin signaling. Functionalized magnetic nanoparticles (MNPs@E/EC15) target cellular E‐cadherins to generate localized magnetomechanical forces under low‐intensity magnetic fields.
Christian Castro‐Hinojosa   +7 more
wiley   +1 more source

High efficiency closed-system gene transfer using automated spinoculation

open access: yesJournal of Translational Medicine, 2021
Background Gene transfer is an important tool for cellular therapies. Lentiviral vectors are most effectively transferred into lymphocytes or hematopoietic progenitor cells using spinoculation.
Victoria Ann Remley   +11 more
doaj   +1 more source

Lentiviral vectors for gene therapy of Gaucher disease [PDF]

open access: yes, 2015
Gaucher disease (GD), a recessive disorder characterised by hepatosplenomegaly, pancytopenia and skeletal complications, is caused by deficiency of the enzyme glucocerebrosidase (GC).
Aitchison, KL
core  

Rescue of lentiviral vector transduction by artificial LEDGF-hybrids.

open access: yes, 2016
LEDGF-fusions were evaluated for their ability to support lentiviral vector transduction. LEDGF-depleted HelaP4-based cell lines stably complemented with LEDGF-hybrids were challenged with a VSV-G pseudo-typed lentiviral reporter vector encoding enhanced
Lenard S. Vranckx (3278832)   +3 more
core   +1 more source

Apoptosis mediated by lentiviral TRAIL transfer involves transduction-dependent and -independent effects [PDF]

open access: yes, 2007
Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) is a promising anticancer agent, which selectively induces apoptosis in many transformed cells without apparent toxic side effects in normal tissue.
Haas, T. L.
core   +1 more source

A methodological scheme illustrates the culture of CD34+ cells, lentiviral transduction conditions, erythroid differentiation protocols, and timeframes for gene expression, morphology, and HPLC studies.

open access: yes, 2023
A methodological scheme illustrates the culture of CD34+ cells, lentiviral transduction conditions, erythroid differentiation protocols, and timeframes for gene expression, morphology, and HPLC studies.
Sukanya Chumchuen (14761903)   +4 more
core   +1 more source

Dual Role of Tamoxifen in Enhancing STING and CEACAM1 Expression to Prime a Favorable Tumor Microenvironment for Anti‐TIM3 Immunotherapy

open access: yesAdvanced Science, EarlyView.
Anti‐PD‐1/PD‐L1 blockade has revolutionized cancer immunotherapy, but is ineffective against endocrine‐treated (i.e., Tamoxifen), relapsed ER+ breast cancer (BC) patients. This study provides insight into the sub‐optimal response of ER+BCs to anti‐PD‐1/PD‐L1 blockade – highlighting the induction of STING and the CEACAM1/TIM3 axis after chronic ...
Marvin Angelo E Aberin   +20 more
wiley   +1 more source

Toward Tightly Tuned Gene Expression Following Lentiviral Vector Transduction

open access: yesViruses, 2020
Lentiviral vectors are versatile tools for gene delivery purposes. While in the earlier versions of retroviral vectors, transgene expression was controlled by the long terminal repeats (LTRs), the latter generations of vectors, including those derived ...
Audrey Page   +2 more
doaj   +1 more source

Lentiviral transduction and establishment of transgenic hNPCs.

open access: yes, 2015
(A) Schematic representation of the experimental procedure. (B) Immunofluorescence labeling of undifferentiated (day 0) and differentiated (day 14) hNPCs, following lentiviral transduction.
Jennifer Richardson (125536)   +9 more
core   +1 more source

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