Dr. Rex
used gene delivery to provide long - term production of a modified form of erythropoietin (EPO), a hormone that induces red blood cell production but is also a neuroprotective cytokine.
Not exact matches
Gene therapy involves the delivery, using a modified virus, of a healthy copy of a gene to make up for one that's deficient in a way that causes dise
Gene therapy involves the
delivery,
using a modified virus, of a healthy copy of a
gene to make up for one that's deficient in a way that causes dise
gene to make up for one that's deficient in a way that causes disease.
To
use viruses as
delivery vehicles for
gene therapy, researchers take all the harmful and replicative
genes out of the virus and put in the therapeutic
genes they want to deliver.
Muscle biologists Qi Long Lu and Terence Partridge at the Medical Research Council Clinical Sciences Centre in London, U.K., and their colleagues decided to combined the antisense strategy with a chemical often
used in
gene therapy because it is known to improve
delivery of DNA into cells.
«To date, this type of system has only been
used in humans with viral methods of
gene delivery, of which the safety profiles are still heavily in debate,» says Betty Tyler, associate professor of neurosurgery at Johns Hopkins.
Dr Wenxin Wang is trying to uncover therapies for diseases such as diabetic ulcers and Epidermolysis Bullosa, which causes chronic skin conditions: «We are currently investigating the
use of these new materials for biomedical applications such as drug /
gene delivery, cross linkable hydrogel materials and skin adhesives.
Using molecular scissors wrapped in a greasy
delivery package, researchers have disrupted a
gene variant that leads to deafness in mice.
Yehoash Raphael, an auditory neuroscientist at the University of Michigan, Ann Arbor, says the findings provide a new
delivery model for researchers trying to
use developmental
genes to restore lost hearing.
Lombardo A, Genovese P, Beausejour CM, Colleoni S, Lee YL, Kim KA, Ando D, Urnov FD, Galli C, Gregory PD, Holmes MC, Naldini L.
Gene editing in human stem cells
using zinc finger nucleases and integrase - defective lentiviral vector
delivery.
Request a custom bibliography search or select from our list of citations available on - line: Select one Agents Administered Biotechnology / Protein & Peptide
Delivery Cancer Research Cardiovascular Research Endocrinology
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Use Nude Mice Neonates
New
delivery technique
used to create a glowing adult mouse potentially opens the door for in vivo
gene therapy
To
use viruses as
delivery vehicles for the
gene therapy, the researchers took all the harmful
genes out of the virus and put in the beneficial
genes in.
The variety of new tools available for genetic manipulation now include lentiviral - based
gene delivery, and
gene editing
using CRISPR / Cas9, zinc finger nucleases (ZFNs) or transcription activator - like effector nucleases (TALENs).
We have demonstrated that our liposomes can mediate in vivo target mRNA
delivery as well as
gene disruption
using an entirely RNA - based approach.
By eliminating HIV's ability to replicate (a feat accomplished in the mid 90s), Dr. Verma's group created a vector, or carrier, that is now
used worldwide for
gene delivery.
LA JOLLA, CA —
Using a
gene therapy
delivery system developed in the laboratory of Inder Verma at the Salk Institute for Biological Studies, an international team of researchers successfully treated two...
Dr. Verma's group created a vector, or carrier, that is now
used worldwide for
gene delivery.
Nanoparticles conjugated with two active ligands, one for its effective uptake and the other for it's binding or
use to
gene delivery agents to deliver drug inside cells.
Because of their unique properties such as monodispersity, large surface area and high drug loading efficiency, silica nanoparticles (SiNPs) have been developed for a vast array of biomedical
uses such as optical imaging, cancer therapy, targeted drug
delivery and controlled drug release for
genes and proteins.
Meanwhile,
gene delivery systems other than retro - or lenti - viral ones, such as repeated transfection with plasmids and
use of a non-integration virus, have been successfully applied in generation of iPS cells [8], [9].
The
use of viral vector for mouse mutagenesis and / or for
delivery of
gene editing by nuclease (F. Piguet, IGBMC)
Particle bombardment, also known as
gene - gun or ballistic
gene delivery,
uses heavy - metal particles to propel naked DNA plasmids into target cells.
These alternate strategies include
using small - molecule drugs that affect RNA metabolism or protein stability, as well as administering modified viruses for therapeutic
gene delivery (see «Getting a fix on SMA»).
The Magnetofection Method:
Using Magnetic Force to Enhance
Gene Delivery.
The image shows green fluorescent protein (GFP) in the mouse cerebellum after
delivery of the GFP
gene using AAV - PHP.
Duan also provided significant expertise from a long history of work on
gene therapy for neuromuscular disorders.To
use viruses as
delivery vehicles for
gene therapy, researchers take all the harmful and replicative
genes out of the virus and put in the therapeutic
genes they want to deliver.
Mooney
uses the results from these studies to design and synthesize new biomaterials that regulate the
gene expression of interacting cells for a variety of tissue engineering and drug
delivery projects.