Sentences with phrase «identify genetic»

Applying Systems Biology Methodology To Identify Genetic Factors Possibly Associated with Recovery after Traumatic Brain Injury.

In precision medicine, molecular profiling of an individual patient's tumor is used to identify genetic mutations that drive that...

They believed that in many cases the risk of identification was greater in the research context because researchers may attempt to identify genetic and hereditary conditions of the deceased.

Consequently, these interactions must be considered when attempting to identify the genetic contribution.

Genetic mutations for HCM have been identified in both the Maine Coon and Ragdoll breeds, and researchers hope to soon identify a genetic basis for HCM in the Norwegian Forest Cat.

Texas A&M and Clemson University are currently embarking on Phase II of an EPI research project to try to identify the genetic markers for the disease.

The aim of this study is to identify the genetic basis of HOD in susceptible breeds.

We try to identify genetic markers (single nucleotide polymorphisms) that point to the associated or causal genes and the genes themselves underlying the development of canine hip dysplasia and secondary hip osteoarthritis.

With regard to breeding, it is important to identify genetic carriers of von Willebrand's disease.

We are also available to provide pet - breeding clients with bite evaluations that will help them identify genetic abnormalities in prospective breeding animals.

Grant 1592: Investigation into the Genetics of Scottie Cramp: Sequencing of Associated Chromosomal Regions Dr. Natasha J Olby, VetMB PhD Project Goal: Following up on previous research funded by CHF, the goal of this project is to use deep sequencing techniques to identify genetic mutations associated with Scottie Cramp.

With support from the investigator award, Meurs» research team hopes to identify genetic variants that lead to the development of mitral valve degeneration, and use that information to innovate treatment and prevention plans for dogs with high - risk DNA variants.

While there are other studies currently enrolling deerhounds, I want to make it clear, this project is the only study currently trying to identify genetic risk factors for the development of these health problems in deerhounds.

I have been isolating DNA from deaf dogs for several years, and have just gotten a study funded with a colleague to attempt to identify the genetic defect.

We aim to identify genetic determinants of the disease.

Generally speaking, dog breeders are keen to participate in efforts to identify the genetic causes of disease in their favorite pooches, with the hope of improving the health and quality of life for their animals.

Two genome - wide association studies were conducted to identify a genetic component within the Friesian horse breed that may cause CPL or predispose them to the condition.

These funds will be used in research to try to identify the genetic factors that would enable the development of a genetic marker based risk test for our Yorkshire Terriers along with developing a more effective treatment.

On Saturday, Jan. 15, at TNAVC, Pfizer will participate in a luncheon announcing its financial and scientific support of the Morris Animal Foundation's Canine Lifetime Health Project, the largest and most comprehensive study ever conducted in dogs to identify genetic, environmental and nutritional risk factors for the development of cancer and other diseases.

The American Shih Tzu Club is at the forefront of research to identify a genetic marker for Renal Dysplasia.

Responsible breeders try to identify genetic diseases their dogs might be carrying and to eliminate them by careful breeding.

The Foundation has helped support cancer studies that have led to better treatment for all dogs who have been diagnosed with cancer, have helped with the development of a test that catches lymphoma far earlier than before and also has helped identify genetic causes for lymphoma.

Here, we propose to identify genetic variants that lead to the development of mitral valve degeneration and to use this information to begin to develop treatment and prevention plans for dogs with high - risk DNA variants.

Researchers are working hard to identify the genetic origin of canine diseases so they can be excised from breeding programs by responsible breeders.

The study, published in the current issue of the journal Veterinary Record Case Reports, highlights the need to identify genetic risk factors for rare breeds.

There is evidence this disorder is a complex hereditary trait, but attempts to identify genetic causes have been hampered by assigning an affected or normal phenotype.

There is evidence this disorder is a complex hereditary trait, but attempts to identify genetic causes have been hampered by assigning...

Meanwhile, work is ongoing to identify the genetic basis of this disorder and the team is now also working on a paper about treatment of these cases.

This study will identify genetic, environmental and nutritional risk factors for the development of cancer and other diseases.

The purpose of this study was to characterize this disease with advanced imaging techniques and identify the genetic components.

«The Canine Lifetime Health Project is a groundbreaking, long - term effort to identify genetic, nutritional and environmental risk factors for the development of cancer and other canine diseases,» MAF reports.

Genome - wide association studies use «genechip» technology to identify genetic variants (single gene polymorphisms or «SNPs») that could explain differences in health between individuals.

These disciplines combine statistics, epidemiology, mathematics, molecular genetics and computer science to identify genetic variants responsible for increased susceptibility to disease and variation of phenotypic traits.

Objectives: To identify the genetic aetiology of Chitayat syndrome and identify a unifying cause for this specific form of hyperphalangism.

This includes Genome - Wide Association Studies (GWAS) to identify genetic loci associated with insecticide resistance and population genetic studies to describe population sub-structuring.

Tapscott applies the method to study regulation of gene expression in normal development of muscle tissue, while Olson uses it to identify genetic profiles of brain - cancer development.

Dr. Bailey - Wilson specializes in statistical genetics and genetic epidemiology, which are disciplines of genetics that combine statistics, epidemiology, mathematics, molecular genetics and computer science to identify genetic variants responsible for increased susceptibility to disease and variation of phenotypic traits.

Objectives: To undertake a genome - wide association study (GWAS) to identify genetic predisposing factors for the different clinical phenotypes associated with nevirapine hypersensitivity.

Advancements in medical research over the past 20 years have improved our ability to identify the genetic factors that may lead to higher risk of cancers.

The scale and scope of these data are enabling genotype - phenotype association studies to identify genetic determinants of pathogen virulence and drug / insecticide resistance, and phylogenetic studies to track the origin and spread of disease outbreaks.

The aim of this study is to identify genetic variants associated with PSC disease progression and development of complications.

Their goal is to identify genetic - expression profiles that correlate with the development of oral cancer, a disease with a five - year survival rate of only about 50 percent.

Utilizing data collected from human clinical populations, Dr. Ressler and his team identify genetic traits and neural processes that may contribute to the underlying causes of these illnesses and provide novel targets for animal models research.

Adipose tissue is key For more than 20 years, McNamara and his team have been working to identify genetic factors related to efficient milk production in dairy cattle.

We have addressed adaption to the host, to antibiotics and to vaccine pressure, most recently developing new bacterial genome - wide association approaches to identify genetic determinants responsible for this adaptation.

SciLifeLab is the first IGN partner in Europe and will initiate a national large - scale population sequencing program seeking to identify genetic causes of human diseases.

Objective: To identify genetic factors that, next to APOE - ɛ 4 homozygosity, contribute to the development of AD.

Working from the inside out, researchers have slowly begun to identify genetic variations that, by distorting the brain's information - processing abilities, seem to nudge some individuals toward disease.

Findings underscore deCODE's ability to identify genetic risk factors in the most complex traits, and have been integrated into the deCODEme ™ service Reykjavik, ICELAND, April 29, 2008 — In a paper published today in the New England Journal of Medicine, a team of...

The team will identify genetic and epigenetic features in CAR T cells and / or cancer cells that will help predict which patients will respond to the immunotherapy, with an eventual goal of initiating clinical trials that employ a combination of approaches to therapy.