Search Results 311-320 of 50096 for Genetic
Uitti believes CIZ1 is one genetic cause of this disorder, and that other genes will be found. But he is elated that at least one explanation for it has ...
My research focused on understanding a genetic heart disease called hypertrophic cardiomyopathy, or HCM, which causes the heart to become too large and can lead ...
SAN DIEGO — NorthShore University HealthSystem (NorthShore) and Mayo Clinic researchers have partnered on a study that shows genetic and clinical evidence ...
Some genes provide instructions for making proteins, which play many critical roles in the body, including the work in cells that regulate the body's tissues ...
... genes underlie the clinical diversity of these disorders. This will provide an insight into the disease mechanisms, and explore novel mutation screening ...
Genetic variation at the transmembrane protein 106B (TMEM106B) gene has been known to modify disease risk and progression in frontotemporal lobar dementia ...
... genetic testing when prescribing oral P2Y12 inhibitor therapy ... The label notes that CYP2C19 genetic testing can identify people with these genetic variations.
Next, researchers analyzed the remaining 20,000 genes and discovered two new genes ... genetic roots in some patients. They also point to ways that clinicians can ...
The findings come on the heels of previous discoveries by Mayo investigators that the C9ORF72 mutation produces an unusual repetitive genetic sequence that ...
Age. Sporadic CJD tends to develop later in life, usually around age 60. · Genetics. People with familial CJD have genetic changes that cause the disease.
Mayo Clinic does not endorse companies or products. Advertising revenue supports our not-for-profit mission.
Check out these best-sellers and special offers on books and newsletters from Mayo Clinic Press.
Make a gift before July 31 and it can be doubled in impact thanks to a $100,000 Summer Challenge.