Results 91 to 100 of about 115,363 (220)

Conformational adaptation of Asian macaque TRIMCyp directs lineage specific antiviral activity [PDF]

open access: yes, 2010
TRIMCyps are anti-retroviral proteins that have arisen independently in New World and Old World primates. All TRIMCyps comprise a CypA domain fused to the tripartite domains of TRIM5α but they have distinct lentiviral specificities, conferring HIV-1 ...
A Katzourakis   +62 more
core   +5 more sources

Development and validation of a droplet digital PCR method for quantifying lentiviral vector infectious titer

open access: yesHeliyon
Lentiviruses, with their high transduction efficiency and gene expression levels, are widely used as gene delivery vectors in the development of chimeric antigen receptor T cells (CAR-T) and other genetically modified cell therapies.
Xueling Wu   +7 more
doaj   +1 more source

Unexpected evolutionarily conserved rapid effects of viral infection on oxytocin receptor and TGF-β/pSmad3

open access: yesSkeletal Muscle, 2017
Background shRNA lentiviral vectors are extensively used for gene knockdowns in mammalian cells, and non-target shRNAs typically are considered the proper experimental control for general changes caused by RNAi.
Yutong Liu, Irina Conboy
doaj   +1 more source

Overexpression of microRNA-16 declines cellular growth, proliferation and induces apoptosis in human breast cancer cells [PDF]

open access: yes, 2015
MicroRNAs (miRNA) are a large family of small single-stranded RNA molecules found in all multicellular organisms. Early studies have been shown that miRNA are involved in cancer development and progression, and this role can be done by working as an ...
Hafizi, M.   +8 more
core   +2 more sources

Transduction of modified factor VIII gene improves lentiviral gene therapy efficacy for hemophilia A

open access: gold, 2021
Jie Gong   +4 more
openalex   +1 more source

Improved Lentiviral Gene Delivery to Mouse Liver by Hydrodynamic Vector Injection through Tail Vein

open access: yesMolecular Therapy: Nucleic Acids, 2018
Delivery of genes to mouse liver is routinely accomplished by tail-vein injections of viral vectors or naked plasmid DNA. While viral vectors are typically injected in a low-pressure and -volume fashion, uptake of naked plasmid DNA to hepatocytes is ...
Trine Dalsgaard   +10 more
doaj   +1 more source

Gene transfer to hepatocellular carcinoma: Transduction efficacy and transgene expression kinetics by using retroviral and lentiviral vectors [PDF]

open access: bronze, 2000
René Gerolami   +6 more
openalex   +1 more source

Lentiviral transduction of CD34(+) cells induces genome-wide epigenetic modifications.

open access: yesPLoS ONE, 2012
Epigenetic modifications may occur during in vitro manipulations of stem cells but these effects have remained unexplored in the context of cell and gene therapy protocols.
Yoshiaki Yamagata   +10 more
doaj   +1 more source

Tal1/Scl Gene Transduction Using a Lentiviral Vector Stimulates Highly Efficient Hematopoietic Cell Differentiation from Common Marmoset ( Callithrix jacchus ) Embryonic Stem Cells [PDF]

open access: bronze, 2006
Ryo Kurita   +14 more
openalex   +1 more source

Home - About - Disclaimer - Privacy