Results 31 to 40 of about 11,612,374 (304)

Internalization of novel non-viral vector TAT-streptavidin into human cells

open access: yesBMC Biotechnology, 2007
Background The cell-penetrating peptide derived from the Human immunodeficiency virus-1 transactivator protein Tat possesses the capacity to promote the effective uptake of various cargo molecules across the plasma membrane in vitro and in vivo.
Kulomaa Markku S   +8 more
doaj   +1 more source

Advances in Nanoparticles as Non-Viral Vectors for Efficient Delivery of CRISPR/Cas9

open access: yesPharmaceutics
The clustered regularly interspaced short palindromic repeat (CRISPR)/Cas9 system is a gene-editing technology. Nanoparticle delivery systems have attracted attention because of the limitations of conventional viral vectors. In this review, we assess the
Minse Kim   +4 more
doaj   +1 more source

Non-viral gene delivery systems for tissue repair and regeneration

open access: yesJournal of Translational Medicine, 2018
Critical tissue defects frequently result from trauma, burns, chronic wounds and/or surgery. The ideal treatment for such tissue loss is autografting, but donor sites are often limited.
Pan Wu   +8 more
doaj   +1 more source

Adenovirus-based gene therapy approaches for hemophilia B [PDF]

open access: yes, 2012
Gene therapy can be used to treat devastating inherited diseases, especially diseases and patients that are not suitable for a conventional cure. The blood clotting disorder hemophilia is one of the most extensively studied monogenetic diseases in gene ...
Zhang, Wenli
core   +1 more source

In vitro permissivity of bovine cells for wild-type and vaccinal myxoma virus strains [PDF]

open access: yes, 2007
Myxoma virus (MYXV), a leporide-specific poxvirus, represents an attractive candidate for the generation of safe, non-replicative vaccine vector for non-host species.
Jean-Luc Duteyrat   +18 more
core   +1 more source

Non Viral Vectors in Gene Therapy- An Overview

open access: yesJOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH, 2015
Non-viral vectors are simple in theory but complex in practice. Apart from intra cellular and extracellular barriers, number of other challenges also needs to be overcome in order to increase the effectiveness of non-viral gene transfer. These barriers are categorized as production, formulation and storage.
Murali Ramamoorth, Aparna Narvekar
openaire   +3 more sources

Cytomegalovirus replicon-based regulation of gene expression in vitro and in vivo [PDF]

open access: yes, 2011
There is increasing evidence for a connection between DNA replication and the expression of adjacent genes. Therefore, this study addressed the question of whether a herpesvirus origin of replication can be used to activate or increase the expression of ...
Mohr, Hermine   +47 more
core   +2 more sources

Degradation of cellular mir-27 by a novel, highly abundant viral transcript is important for efficient virus replication in vivo. [PDF]

open access: yes, 2012
Cytomegaloviruses express large amounts of viral miRNAs during lytic infection, yet, they only modestly alter the cellular miRNA profile. The most prominent alteration upon lytic murine cytomegalovirus (MCMV) infection is the rapid degradation of the ...
Lisnić, V. (V) J. (J)   +98 more
core   +1 more source

Rab14 regulates the transport of human papillomavirus to the trans‐Golgi network for infectious cell entry

open access: yesFEBS Letters, EarlyView.
This study reveals that the small GTPase Rab14 is necessary for human papillomavirus (HPV) infection and plays an essential role in the transport of virions to the trans‐Golgi network (TGN). HPV in the early endosome (EE), which harbors GTP‐bound Rab14, is transported to the TGN through the switch of Rab14 from its GTP‐bound to GDP‐bound form.
Yoshiyuki Ishii, Iwao Kukimoto
wiley   +1 more source

Magselectofection: A novel integrated technology of magnetic separation and genetic modification of target cells [PDF]

open access: yes, 2010
Research applications and cell therapies involving genetically modified cells require reliable, standardized and cost-effective methods for cell manipulation. The goal of this work is to provide a novel methodology that produces, in a single standardized
Sanchez Antequera, Yolanda
core   +1 more source

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