Sentences with phrase «identify multiple disease»
«Innovative genetic, cellular techniques help identify multiple disease targets: CRISPR - Cas9 and iPSC advances hold treatment promise for schizophrenia, addiction, Zika infection and other diseases.»
https://www.sciencedaily.com/
American Humane Association's Animal Welfare Research Institute has identified multiple diseases and disorders that afflict both animals and children, to include cancer, diabetes, respiratory syncytial virus, asthma, food borne illnesses, obesity, neurological disorders and tuberculosis.
Not exact matches
Through talking to experts in the field over the past year, Gates said he had identified five areas of need: Understanding better how Alzheimer's unfolds, detecting and diagnosing it earlier, pursuing multiple approaches to trying to halt the disease, making it easier for people to take part in clinical trials of potential new medicines, and using data better.
Multiple genetic markers have been identified for celiac disease, but many genetically susceptible individuals tolerate gluten and never develop symptoms, leading to speculation about other risk factors, including early childhood nutrition.
Jaenisch says that the method that identified the single point mutation in SNCA's enhancer could be used to pinpoint additional pathogenic genes for sporadic PD and sift through the GWAS hits for other diseases, including Alzheimer's disease, cancer, diabetes, and multiple sclerosis.
The team identified 345 regions of the genome where they could pinpoint the likely molecular causes underlying a person's predisposition to immune - related diseases such as inflammatory bowel disease, type 1 diabetes and multiple sclerosis.
«The compounds identified in this study, when administered orally, both reduced the inflammation that is a hallmark of multiple sclerosis and protected against the nerve cell damage seen in mouse models of the disease,» said Jeffery Haines, PhD, a post-doctoral fellow at Mount Sinai and the study's lead author.
«Once this has been achieved,» he explains, «we will be seeing a new era of pre-implantation genetic diagnosis aimed at, identifying disease - free blastocysts, identifying developmentally competent blastocysts among a cohort developing in vitro and achieving single blastocyst transfer in order to avoid multiple births.»
«Research team first to identify AF1q protein associated with multiple myeloma, extramedullary disease.»
«We wanted to identify some potential therapeutic targets that are common not just to one but to multiple forms of retinitis pigmentosa at late - stage disease, when it is more likely to be clinically diagnosed in a patient population.»
Researchers in the Jacobs School of Medicine and Biomedical Sciences at UB are continuing to study cerebral microbleeds, identified in the image above, as indicators of disease progression in multiple sclerosis.
«Our discovery proposes a new and alternative way to conduct research into multiple sclerosis, by, for the first time, identifying a clear link to other neurodegenerative diseases.
Identifying these factors is relevant for further understanding Parkinson's disease and multiple system atrophy,» adds Elias Bechara, CRG researcher and one of the authors of the article.
Because disease organisms mutate quickly to overcome crop resistance controlled by single genes, researchers are rushing to identify new resistance genes and to incorporate multiple genes into high - yielding varieties, according to Ravi Singh, CIMMYT wheat scientist who participated in the reported study.
A UC San Francisco - led research team has identified the likely genetic mechanism that causes some patients with multiple sclerosis (MS) to progress more quickly than others to a debilitating stage of the disease.
One of its priorities is to develop relevant strategies to decipher multiple forms of neuromuscular diseases, identify new therapeutic targets and foster novel strategies for innovative treatments.
«We are currently working to identify the relationship between the circadian clock, metabolism and the immune system, so that one day we could develop therapies to treat diseases influenced by circadian clock disruption — including not only obesity and diabetes, but also potentially multiple sclerosis and even Alzheimer's disease.»
Our scientists have also pointed the way to a new therapeutic strategy for multiple sclerosis and other neurological diseases by identifying that a blood protein, fibrinogen, plays a causal role in damaging the central nervous system.
Whole - exome sequencing has identified the causes of several Mendelian diseases by analyzing multiple unrelated cases, but it is more challenging to resolve the cause of extremely rare and suspected Mendelian diseases from individual families.
A novel GWAS has identified multiple genomic links between clinical laboratory measurements and several complex diseases in a Japanese population.
«Our research on the role of blood proteins in brain functions has identified new targets for therapeutic intervention in multiple sclerosis and other neurological diseases,» said Dr. Akassoglou.
Performing genetic studies in multiple human populations can identify disease risk alleles that are common in one population but rare in others, with the potential to illuminate pathophysiology, health disparities, and the population genetic origins of disease alleles.
Identifying a reliable biomarker may accelerate diagnosis of multiple sclerosis (MS) and lead to early management of the disease.
As with most technologic methods, we expect multiple replicate analyses of the highly fractionated samples would result in a reduction of the number of seemingly unique proteins identified for each disease group [33].
In instances of one of the more common autoimmune diseases, multiple sclerosis, or MS, this means identifying potential triggers and working with individuals to develop a lifestyle that is conducive to avoiding the worsening of symptomology.
The goal was to determine the ability of multiple biomarkers to identify and assess, and hopefully correlate to, the degree of heart disease in cats.
There are multiple causes of kidney disease and one of the very frustrating things about this disease is that often by the time it is identified, the cause itself is no longer present and is no longer treatable.
With this panel, we can identify, or rule out, multiple diseases inherited in Labradors, such as hip dysplasia, ruptured anterior (cranial) cruciate ligament, mast cell tumor, T and B - cell lymphoma, posterior polar cataracts, liver disease, laryngeal paralysis, degenerative myelopathy, epilepsy, tricuspid valve dysplasia and obesity.