Search Results 461-470 of 49201 for Genetic

1. Longitudinal Characterization and Genetic Analysis of Pediatric-Onset Morphea - Mayo Clinic

   About this study. The purpose of this project is to determine the genetic causes of disease and establish accurate clinical indicators and biomarkers of ...

2. Congenital myasthenic syndromes - Diagnosis and treatment - Mayo Clinic

   Genetic testing can reveal changes, sometimes called mutations, in genes that cause congenital myasthenic syndromes. Genetic testing may also be recommended for ...

3. Mayo researchers earn NIH award to study use of genetic risk scores for heart disease in diverse populations

   In recognition of their high impact work of advancing the field of genetic risk profiling for disease risk stratification, the National Institutes of Health ...

4. Science Saturday: Novel suppression-replacement preclinical gene therapy study shows promise in long and short QT syndromes - Mayo Clinic News Network

   ... genes in various genetic disorders. Funding This publication was supported by the Mayo Clinic Windland Smith Rice Comprehensive Sudden Cardiac Death Program ...

5. Disease Specific IPS Lines From Patients With a Genetic or Developmental Basis for Their Renal Disease - Mayo Clinic

   The purpose of this study is to derive disease specific iPS lines from patients with a genetic or developmental basis for their renal disease. Participation ...

6. 20-year Mayo Clinic study suggests return to play is manageable for athletes with most genetic heart diseases

   ... genetic heart diseases that predisposed them to disease-triggered sudden cardiac arrest. Of these athletes, 495 had long QT syndrome, a genetic heart ...

7. Tuberous sclerosis - Symptoms and causes - Mayo Clinic

   Tuberous sclerosis is a genetic disorder caused by gene changes — sometimes called mutations — in either the TSC1 or the TSC2 gene. These genes are thought ...

8. DiGeorge syndrome (22q11.2 deletion syndrome) - Symptoms and causes - Mayo Clinic

   The deletion of genes from chromosome 22 usually occurs as a random event in the father's sperm or in the mother's egg. Or it may occur early when the baby is ...

9. Gene variants may increase susceptibility to accumulate Alzheimer's protein tau, study shows - Mayo Clinic News Network

   Researchers studied the participants' genetic profiles and used positron emission tomography (PET) scans to look for tau proteins in their brains. The study ...

10. Education - Genetics of Alzheimer's Disease and Endophenotypes Laboratory - Mayo Clinic Research

    See educational opportunities and alumni in Nilufer Ertekin-Taner's Genetics of Alzheimer's Disease and Endophenotypes lab at Mayo Clinic.