«Commonalities in late stages of inherited blinding
diseases suggest targets for therapy.»
Not exact matches
Clinically important findings
suggest that
targeting the epidermal growth factor receptor (EGFR) and the fibroblast growth factor receptor (FGFR) cellular pathways may benefit thousands of patients with this
disease, according to the study published today in the journal PLOS Genetics.
The work
suggests that changing levels of the PIAS1 protein and
targeting this pathway could have a benefit to
disease.
«What we found was, if we block mGluR5, which is the glutamate receptor we're interested in, the mice become hyper locomotive so they become able to move better than wild type mice
suggesting glutamate receptors might be a good
target for treating movement disorders such as Parkinson's
disease.
But the new Salk research, published in the journal eLife,
suggests that rapamycin could also
target the neural damage associated with Leigh syndrome, a rare genetic
disease, and potentially other forms of neurodegeneration as well.
«Our data
suggests that
targeting specific immune cell subsets at defined stages of
disease may represent a better approach to therapeutic immunomodulation to improve heart failure.»
«Inflammation is associated with bone growth: A study using induced pluripotent stem cells
suggests that a molecule for inflammation could be a good drug
target to prevent
diseased bone growth.»
Although that marker, called IL21, had not previously been associated with autoimmune
diseases, the gene that produces it sits right in the stretch of DNA known to make these mice vulnerable to diabetes,
suggesting that IL21 might make a drug
target, says Sarvetnick.Furthermore, by giving the animals a shot of dead bacteria — similar to an immunization in humans — when they were newborns, Sarvetnick and her colleagues prevented a surfeit of CD4 + and CD8 + cells.
Overall the findings
suggest that granzyme A could serve as a potential drug
target for anti-inflammatory treatments for chikungunya — and perhaps also for other inflammatory
diseases.
«Our findings
suggest that PRMT5 is a possible prognostic factor and therapeutic
target for glioblastoma, and they provide a rationale for developing agents that
target PRMT5 in this deadly
disease,» says co-corresponding author Robert A. Baiocchi, MD, PhD, associate professor of medicine and a hematologist at the OSUCCC — James who is also collaborating on an Ohio State effort to develop a PMRT5 inhibitor.
Already, researchers have linked noncoding DNA to Crohn
disease, heart
disease, multiple sclerosis, and other disorders,
suggesting that enhancers could be
targets for medical manipulation.
Not only does it
suggest new
targets for drug development, but it also puts forward new behavioral changes that may be taken on the part of the infected individual in order to decrease the chances of developing a major
disease and increase longevity.
That's an important lesson, Tolar says; it
suggests that future attempts to correct genetic skin
diseases should focus on culture conditions that nourish these stem cells, and potentially even
target them for modification.
«Although it's still early days for this line of research, these findings provoke the hypothesis that MHCII + innate lymphoid cells may be an important pathway to therapeutically
target in the treatment of some chronic inflammatory
diseases,»
suggests Sonnenberg.
Based on these results, researchers
suggest that «if post-2000 trends continue, the chance of meeting the global
target of UN on this
disease is lower than 1 % for males and 1 % for females worldwide.
Now a scientist reports that mice engineered to make extra follistatin, which deactivates myostatin, have four times the muscle of regular mice,
suggesting a new
target for drugs to fight muscle - wasting
diseases such as muscular dystrophy.
The study is investigator led and has therefore focused on clinical need,
targeting patients with progressive multiple sclerosis in whom most disability is incurred... The study also reports a predominant effect on neurodegenerative rather than inflammatory outcomes,
suggesting a novel mechanism of action that might be suitable as combination treatment with immunomodulatory treatments... Further phase 3 studies to measure the effect of simvastatin on sustained disability, particularly in patients with non-relapsing secondary progressive and primary progressive multiple sclerosis, are clearly needed, but this trial represents a promising point from which to develop trials of progressive
disease.»
The study
suggests that attacking those subsets with
targeted drugs may degrade the
disease's ability to spread throughout the bone marrow of affected patients, the authors say.
The results
suggest that, theoretically, delivering
targeted, selective, and specific brain stimulation might improve some of the cognitive aspects of losing dopamine in Parkinson's
disease.»
«PINK1 protein crucial for removing broken - down energy reactors: Study
suggests potential new pathway to
target for treating ALS, other
diseases.»
Our research
suggests that we may also need to think about
targeting the brain to treat non-alcoholic fatty liver
disease.»
This similarity
suggests that researchers should
target the underlying process in the different varieties of the
disease, he says, for example by developing a drug to prevent dystrophin from breaking down.
«Our results
suggest that heart failure would be better addressed by treatments that shut down immune cells that are both sources and
targets of cytokines in the spleen and heart, instead of
targeting any one cytokine,» said Sumanth Prabhu, M.D., director of the Division of Cardiovascular
Disease within the UAB School of Medicine and study leader.
The finding, published in The Journal of Clinical Investigation, validates a similar discovery made by the scientists in mice two years ago and
suggests a
target for future therapies to treat the devastating eye
disease that currently has no cure.
«While we need to better understand how these abnormally regulated metabolites activate oncogenic proteins, our intriguing discovery
suggests novel therapeutic
targets for this
disease,» says principal investigator and study leader Arnab Chakravarti, MD, chair and professor of Radiation Oncology and co-director of the Brain Tumor Program at the OSUCCC — James.
The findings challenge the long - held theory that leukemia cells simply outperform healthy cells by living longer and
suggest that
targeting this «death factor» may be a viable way of combating the
disease.
«These events predict a worse outcome in TNBC patients
suggesting that the LINK - A pathway plays a critical role in this
disease and may provide wide - ranging therapeutic treatment
targets.»
«This
suggests a mechanism by which drugs that
target certain other neurological
diseases may be effective.»
The research
suggests that
targeting the protein called GLUT1 could help prevent or slow the effects of Alzheimer's, especially among those at risk for the
disease.
«Following the exciting discovery that dengue virus NS1 protein can directly cause vascular leak, the hallmark of severe dengue
disease, we have now succeeded in disentangling the mechanisms responsible,
suggesting new drug
targets for inhibiting severe dengue,» says Dr. Eva Harris, the senior investigator.
One third of the
target genes for which they had patient data - 32 out of 97 - were also linked to survival in women with oestrogen receptor - positive breast cancer,
suggesting they play an important role in the
disease.
While some are
suggesting the failure of these BACE1 trials indicate that the amyloid plaque hypothesis for Alzheimer's
disease may in fact be wrong, other recent research still
suggests more
targeted methods of inhibiting the enzyme could result in positive outcomes.
In our latest work, for example, we have found evidence of a potentially clinically useful connection of complement in mesenchymal stem cell - based therapies,
suggesting that complement is a valid
target for improving the viability and function of mesenchymal stem cells, which are under extensive evaluation in clinical trials for treating many inflammatory and degenerative
diseases.
Their findings on telomeres, the stretches of DNA at the ends of chromosomes that protect our genetic code and make it possible for cells to divide,
suggest a potential
target for preventive measures against cancer, aging and other
diseases.
These findings
suggested two things: that if a person naturally carried a similar mutation in their MSH3 gene, they might also have reduced CAG repeat instability, and hence a better
disease prognosis, and secondly, that making drugs to
target MSH3 could be valuable for the treatment of Huntington's
disease, assuming that instability is important.
«Usually that's useless because they are already inactive in that state, but this finding
suggests we might be able to find new therapeutic approaches to
target these
diseases.»
«In this study, we found two genes that control levels of lipids with anti-diabetic and anti-inflammatory activity,
suggesting exciting
targets for diabetes and inflammatory
diseases,» said co-senior author Alan Saghatelian, who holds the Dr. Frederik Paulsen Chair at the Salk Institute.
This finding
suggests new
targets for drugs designed to treat inflammatory
diseases.
The study
suggests a potential treatment
target for
diseases such as Crohn's
disease and ulcerative colitis.
In the case of Influenza A, the loss of RNA exosome activity severely compromises viral infectivity, but also manifests in human neurodegeneration
suggesting that viruses
target essential proteins implicated in rare
disease in order to ensure continual adaptation.
The high selectivity, and the potency with which some of these receptors promote flavivirus infection,
suggest only a small number of receptors might be effectively
targeted to treat these
diseases.
The new research, along with an accompanying editorial by Martin C. Michel of Johannes Gutenberg University in Mainz, Germany, and Paul A. Insel of the University of California at San Diego,
suggest new contributors to this near - universal problem and potential
targets to treat more serious problems that affect blood vessels in the cold, such as in Raynaud's
disease.
Exciting new research from the Francis Crick Institute and King's College London
suggests novel
targets for cancer and inflammatory
diseases.
Emerging studies
suggest that miRs are novel therapeutic
targets for complex
diseases.
In the meantime, our experience to date
suggests that precise genome editing of putative
targets in primary cell systems is possible, offering more human
disease relevant systems than conventional cell lines.
This study leads to a better understanding of macrophage responses to infection, provides insight into
disease development, and
suggests targets for therapeutic intervention.
The findings, published today in Translational Psychiatry,
suggest leptin deficiency may contribute to physical health problems associated with early life stress, and provide a possible
target in
disease prevention.
Researchers at Karolinska Institutet in Sweden now demonstrate in a paper published in Nature that a well - known family of enzymes can prevent the inflammation and thus constitute a potential
target for drugs.Research
suggests that microglial cells — the nerve system's primary immune cells — play a critical part in neurodegenerative
diseases, such as Alzheimer's and Parkinson's.
The Centers for
Disease Control and Prevention
suggests setting a
target weight loss goal of 1 to 2 lbs.