Improving human health by enabling safer, more
effective cell and gene medicines through proprietary genomics, bioinformatics and intelligent data driven design
Not exact matches
The Rho - kinase inhibition stimuli under low oxygen conditions (of 5 percent oxygen atmosphere), which is a condition corresponding to conditions in the body's cartilage, produced a more
effective increase in chondrocyte - specific
gene expression
and synthesis of extracellular matrix components by HCS - 2 / 8
cells.
«Techniques to correct defective
genes in «non-reproductive»
cells are already at various stages of clinical development
and promise to be a powerful approach for many human diseases which don't yet have an
effective treatment.
Multiplexed genetic screening for epidermal growth factor receptor (EGFR)
and anaplastic lymphoma kinase (ALK)
gene rearrangements
and subsequent biomarker - guided treatment is cost -
effective compared with standard chemotherapy treatment without any molecular testing in the metastatic non-small
cell lung cancer (NSCLC) setting in the United States.
For example, the study defined cases of pancreatic cancer that are driven by a
gene called BRAF, for which there are FDA - approved drugs,
and showed that such drugs were selectively
effective against BRAF - mutated pancreatic cancer
cells.
«Research into basic workings of immune system points to way of improving therapies for cancer: Differences in wiring of «exhausted»
and effective T
cells indicate possible
gene - editing targets.»
By performing experiments in petri dishes
and with mice, they found that panobinostat, a drug designed to change the way
cells regulate
genes, may be
effective at inhibiting DIPG growth
and extending survival rates.
Intrigued by the ability of certain polymers to mop up DNA
and RNA for
gene transfer, Sullenger
and colleagues tested the idea that these chemical compounds might also be
effective targeting such nucleic acids as they arise in
cell death.
As reported in the new study, the researchers were able to postpone the onset of hearing loss
and associated hair
cell degeneration by about a month, providing enough time to inject normal copies of the Clarin - 1
gene into the ear before the onset of hearing loss to see if the treatment was
effective.
«The problem is cancer
cells are so diverse that even though the drugs, designed to target single cancer driving
genes, often initially are
effective, they eventually stop working
and patients succumb to the disease,» Peter said.
This approach for
gene therapy to treat fatty liver disease, for example, might prove both safer
and more
effective than reengineering
cells in the liver itself.
The scientists took the
genes for the most
effective liver cancer antigen receptors on those T
cells, put those receptors on human T
cells and the resulting engineered human T
cells eradicated the cancer as well, without hurting normal liver
cells, they report in the journal Hepatology.
Interestingly, Rho kinase inhibition under hypoxic conditions produced a more
effective increase in chondrocyte - specific
gene expression
and synthesis of extracellular matrix components by HCS - 2 / 8
cells.
In recent years, scientists have grown new retinal
cells from stem
cells and shown progress in developing an
effective gene therapy.
Since then he has continued to investigate new strategies to overcome the major hurdles to safe
and effective gene transfer, translate then into new therapeutic strategies for genetic disease
and cancer,
and allowed new insights into hematopoietic stem
cell function, induction of immunological tolerance
and tumor angiogenesis.
Adding an extra copy of the azot
gene to increase levels of the azot protein results in more
effective destruction of less fit
cells,
and an increase in life span - in fruit flies at least.
Our team would like to be able to research passenger pigeon
genes for de-extinction while primordial germ
cell cultures are developed,
and an Australian team has developed an
effective way of bypassing
cell cultures for engineering birds by going directly to the primordial germ
cells in the embryo.
The only plausible methods of repairing stochastic nuclear DNA damage look to be the aforementioned advanced molecular nanotechnology, something that lies some decades in the future, or major advances in
gene therapy, to the point at which it could be cost -
effective and safe to scan
and conditionally alter the majority of
genes in the majority of
cells all at once.
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.
Researchers describe how a bacterial infection - based protein delivery strategy can mediate
effective and safe
gene editing in human pluripotent stem
cells.
The Sanger Institute
Gene Trap Resource (SIGTR) mouse ES cell line collection was developed to provide a powerful and cost effective approach using gene trapping to create large numbers of insertional mutations that are immediately accessible to molecular characterizat
Gene Trap Resource (SIGTR) mouse ES
cell line collection was developed to provide a powerful
and cost
effective approach using
gene trapping to create large numbers of insertional mutations that are immediately accessible to molecular characterizat
gene trapping to create large numbers of insertional mutations that are immediately accessible to molecular characterization.
The mission of ACGT is to support the extraordinary potential offered by
cell and gene - based therapies to accelerate
effective and safe treatment of all types of cancer.