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Search results for “Huntingtons Disease”

1,000+ results for "Huntingtons Disease"

Gene variant influences chronic kidney disease risk

Researchers identified a single genetic mutation in the CUBN gene linked to albuminuria, a condition indicating kidney disease, in both diabetic and non-diabetic individuals. The study's findings have significant implications for understanding the mechanisms behind kidney disease and potentially leading to novel treatment targets.

SourceJohns Hopkins Bloomberg School of Public Health·JournalJournal of the American Society of Nephrology·DateMar 9, 2011

Mammograms: Detecting more than breast cancer, may help assess heart risk in kidney disease patients

Researchers found mammograms show calcifications in the blood vessels of nearly two-thirds of women with end-stage renal disease, potentially contributing to heart disease risk. The study suggests mammograms may be a useful tool for studying cardiovascular disease progression in kidney patients.

SourceAmerican Society of Nephrology·JournalClinical Journal of the American Society of Nephrology·DateJan 20, 2011

Study identifies promising biomarkers for Huntington's disease that could be used to test disease-modifying treatments

A new study has identified promising biomarkers for Huntington's disease that could be used to track disease progression and test potential disease-modifying treatments. Biomarkers were found in brain imaging techniques, including whole-brain and striatal atrophy, which increased at a higher rate in individuals with the disease.

SourceThe Lancet_DELETED·JournalThe Lancet Neurology·DateDec 1, 2010

Stanford-led study disproves link between genetic variant, risk of coronary artery disease

A massive international study found no association between a genetic marker and the risk of coronary artery disease. The study analyzed data from over 17,000 patients with cardiovascular disease and 40,000 others, concluding that carrying a particular variant of the KIF6 gene does not indicate a greater risk for the disease.

SourceStanford Medicine·JournalJournal of the American College of Cardiology·DateOct 7, 2010

Researchers find gene responsible for neurodegenerative disease in dogs, possibly in humans

A team of researchers discovered a gene responsible for a rare and fatal disease in American Staffordshire terriers. The same gene is believed to cause a similar disease in humans. Genetic analysis led to the identification of an entirely new mutation, which can be tested in human samples to determine its connection to Kufs' disease.

SourceNorth Carolina State University·JournalProceedings of the National Academy of Sciences·DateAug 24, 2010

Premature death less likely than end stage renal disease for African-Americans with kidney disease

African Americans with hypertensive nephrosclerosis have a higher rate of developing end stage renal disease (ESRD) than dying prematurely, according to a new study. The study analyzed data from the African American Study of Kidney Disease and Hypertension (AASK) trial and cohort phase, finding that ESRD rates exceeded mortality rates ...

SourceAmerican Society of Nephrology·JournalJournal of the American Society of Nephrology·DateJul 22, 2010

Virus works with gene to cause Crohn's-like illness

Researchers found that a specific virus interacts with a mutation in the host's genes to trigger disease. In mice, exposure to a damaging chemical and infection with a viral strain caused symptoms similar to human Crohn's disease, suggesting viruses may be key to understanding complex diseases.

SourceWashU Medicine·JournalCell·DateJun 24, 2010

Study sheds light on deadly GI disease in infants born with complex congenital heart disease

A recent study by Nationwide Children's Hospital sheds light on the deadly bowel disease necrotizing enterocolitis (NEC) in infants born with complex congenital heart disease. The research reveals that neonates undergoing the hybrid procedure have a lower risk of NEC compared to those receiving the Norwood procedure.

SourceNationwide Children's Hospital·JournalPediatric Critical Care Medicine·DateMay 26, 2010