Sentences with phrase «identify common diseases»

The vet will do the routine tests that usually identify common diseases of older cats.

Our main goal is to keep your pet healthy by identifying some common diseases and conditions before they become serious or life threatening.

This stage focuses on identifying different breeds of dogs and cats, recognizing normal and abnormal behavior in dogs and cats, identifying common diseases and medical conditions, and properly caring for the hospitalized patient in your charge.

Not exact matches

That number needn't be so low, as many carriers offer online programs to help identify risk factors for common chronic diseases (e.g.: diabetes, congestive heart failure, asthma, obesity, cancer) and offer prevention programs.

PoopMD and PoopMD + use a validated stool color analyzer to identify a life threatening disease that is the most common cause of liver failure in children.

A joint work by EPFL, ETH Zürich and the CHUV has identified a pathological process that takes place in both mice and humans towards one of the most common diseases that people face in the industrialized world: type 2 diabetes.

A large - scale genetic analysis in PSP patients, however, identified a common tau sequence that increases by 5.5 times a person's chances of developing the disease, making this variant a stronger risk factor for PSP than one copy of the apolipoprotein E-ε4 variant is for Alzheimer's.

Researchers have identified a common variant in a non-coding RNA that may contribute to the intestinal inflammation that occurs in people with celiac disease.

A COMMON dye used to identify the tangles of proteins that accompany ageing also helps to prevent protein misfolding — one of the hallmarks of Alzheimer's disease.

Scientists have identified unique genetic signatures strongly associated with a long and healthy life, findings that could help to further the understanding of how certain genes may offer protection from common age - related diseases like cancer, dementia and cardiovascular disease.

In an extended analysis, the team identified an additional 33 genetic regions that are also involved in several common immune - mediated conditions (celiac disease, Crohn's disease, ulcerative colitis, type 1 diabetes, rheumatoid arthritis, sarcoidosis and psoriasis).

«The iPS cells may also help us identify treatments for more common diseases, such as atherosclerosis and vascular calcification, because the same bone morphogenetic protein pathways are involved in these medical conditions.»

As a common cause of early mortality, public health officials carefully count when heart disease is identified as the underlying cause on death certificates.

«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.»

Published September 15 in Genome Biology, the study relied on new software for researchers that identifies connections between seemingly unrelated human diseases and traits through the tiny, risk - conferring genetic variations they have in common.

«Future research should focus on identifying common genes, immune responses and environmental exposures that may link these two diseases,» says first author Lauren Dalvin, M.D., a Mayo Foundation Scholar in Ocular Oncology.

MS is a relatively rare disease, but the peptides identified by Wucherpfennig and Strominger come from viruses and a bacterium that are very common.

Ovarian cancer researchers have identified a protein biomarker expressed on the surface of tumour cells in high - grade serous ovarian cancer, the most common and lethal subtype of the disease.

It is particularly useful when clinicians want to identify an illness or gene mutation involving a single patient or the patient and two or three other family members, which is the most common clinical situation for undiagnosed diseases.

Scientists at Icahn School of Medicine at Mount Sinai, along with collaborators at institutions in India, Italy, and Japan, have identified the first gene linked to childhood - onset familial dilated cardiomyopathy (DCM), one of the most common heart muscle diseases in children.

Published online ahead of print in the leading microbiology journal Molecular Microbiology, the researchers have identified a building block common to many types of bacterial «virulence factors» (the bacterial proteins which act as weapons to cause disease, such as toxins or degrading enzymes).

«In genetics, it's common to identify a gene that is the source of a disease.

«With TEK, we know exactly what's going wrong, which means we've identified a pathway that could be a great new therapeutic target for severe glaucoma and even more common forms of the disease.»

Of the dozen of these metabolites that were measured in cohorts from the longitudinal Framingham Heart Study (the long - term 1948 study to identify the common contributive factors of cardiovascular disease by following its development in a large subject group) levels of glycerol turned out to be «significantly correlated» with resting heart rate, another indicator of fitness, as measured in the study.

In 2009, the islands also launched a public effort to identify people afflicted with carnitine transporter deficiency (CTD), a disease that can lead to sudden death in young adults and is a hundred times more common among the isolated Faroese population than elsewhere.

Identifying the origin could lead to targeted therapies for these very common diseases.»

Scientists have identified the molecular mechanism that leads to the death of neurons in amyotrophic lateral sclerosis (also known as ALS or motor neurone disease) and a common form of frontotemporal dementia.

Other medical sequencing projects will use DNA sequencing to: discover new genes that are involved in common diseases; identify the genes responsible for dozens of relatively rare, single - gene (autosomal Mendelian) diseases; sequence all of the genes on the X chromosome from affected individuals to identify those involved in sex - linked diseases; and survey the range of variants in genes known to contribute to certain common diseases.

To identify the characteristics that are most helpful in screening for cancer, the team created hand - crafted pyramid features (basic components of recognition systems)-- as well as investigated the performance of a common deep learning framework known as convolutional neural networks (CNN) for cervical disease classification.

He's identified several families with a strong hereditary pattern of the disease and has begun searching for common genetic markers.

Scientists have confirmed one gene variant and have identified several others that may be risk factors for late - onset Alzheimer's disease, the most common form of the disorder.

Some are at a basic research level, where investigators study genetic variation to identify pathways that can be targets for common diseases, such as diabetes and common birth defects.

This unprecedented analysis led to the discovery of the first identified common genetic variant shown to predispose Latin American populations to the disease.

A study in the Jan. 19 issue of Cancer Cell reports on researchers who believe they have identified where the most common form of breast cancer originates, which may offer a hope for better targeting drugs at the disease's Achilles» heel.

deCODE has identified key variations in the sequence of the genome conferring increased risk of major public health challenges from cardiovascular disease to cancer, and employs its gene discovery engine to develop DNA - based tests to assess individual risk of common diseases; to license its tests and intellectual property to partners; and to provide comprehensive, leading - edge contract services to companies and research institutions around the globe.

deCODE's landmark study in the genetics of stroke, identifying the first gene ever linked to common forms of the disease, has been published in the online edition of Nature Genetics.

The Swedish Genomes Program will focus on identifying genetic causes of common human diseases.

Researchers have newly identified three genetic regions associated with primary biliary cirrhosis (PBC), the most common autoimmune liver disease, increasing...

Scientists from the Centers for Disease Control and Prevention have identified a puzzling and unsettling new cancer - like condition in a 41 - year - old man, who is believed to have become ill through a common stomach bug.

Four years ago, researchers identified a genetic mutation associated with spinal muscular atrophy (SMA), an inherited neuromuscular disease that is the most common genetic cause of infant mortality...

For many human diseases, large - scale genomic studies have identified common genetic variants that occur more frequently in people with cardiovascular, autoimmune, inflammatory and infectious diseases, diabetes and asthma than in those without these diseases.

Potential projects include identifying common pathways that modify retinal degenerative disease from a large collection of actively maintained mouse models; determining molecular networks implicated in pathological disruption of the retinal pigment epithelium; identifying molecular pathways that regulate postnatal ocular growth; and using mouse models to assess the pathogenic role of gene variants that increase the risk of age - related macular degeneration as identified by human genome - wide association studies.

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.

St. Jude Children's Research Hospital scientists studying two rare, inherited childhood neurodegenerative disorders have identified a new, possibly common source of DNA damage that may play a role in other neurodegenerative diseases, cancer and aging.

Another common theme identified in the analysis revealed that students did not fully understand concepts related to heredity and patterns of inheritance (14 %); these essays reflected studentsâ $ ™ belief that single genes are the cause of traits and inherited diseases.

These mutant kinases are attractive therapeutic targets, as demonstrated by the efficacy of imatinib in BCR - ABL — positive chronic myelogenous leukemia (CML), 5 as well as in MPD associated with activating alleles involving PDGFRA or PDGFRB.2, 6,7 In addition, activating mutations in the FLT3 receptor tyrosine kinase are the most common genetic event in acute myeloid leukemia (AML), and specific inhibitors of the FMS - like tyrosine kinase 3 (FLT3) have entered late - stage clinical trials.8 Although mutations in tyrosine kinases and in other genes have been identified in a subset of MPD and AML, in many cases the genetic events that contribute to the molecular pathogenesis of these diseases remain unknown.

These types of studies usually contain small sample sizes and focus on identifying large, rare variants in the genome rather than smaller, more common variants that may also drive disease pathology.

Family health history risk assessment has long been recognized as standard of care in preventative medicine, and is a useful tool for identifying risks of common diseases such as diabetes and cardiovascular disease, in addition to hereditary risks.

Such work has become increasingly important given the expansion of genome - wide association studies identifying genetic risk factors for common diseases and corresponding efforts to commercialize genetic testing using these markers.

The Broad Institute and its collaborating institutions have received two major grants from the National Human Genome Research Institute (NHGRI) that will support the use of genome sequencing and analysis to identify the genes and genetic variation that underlie both rare and common diseases.