Protective gene found to preserve mitochondria during kidney disease progression
Research led by Children's Hospital of Fudan University in China has found that a gene called pancreatic progenitor cell ...
WBUR16h
16 people died of ALS in a tiny Alpine village. Was a mushroom to blame?
Recent research shows that only 5% to 10% of patients have a family member diagnosed with the disease, and there are only a handful of known genetic mutations. So, what's causing the other 90% of ...
DNA mutations that contribute to spina bifida during embryogenesis open the door to potential treatments
Scientists at Rady Children's Institute for Genomic Medicine, and the Department of Neurosciences and Pediatrics at the ...
Baylor College of Medicine20h
Mutated blood cells define clinical risks in Langerhans cell histiocytosis, paving the way for better diagnosis and treatment
A nationwide team led by researchers at Baylor College of Medicine, Texas Children’s Hospital and UPMC Children's Hospital of ...
News-Medical.Net on MSN6h
Scientists make breakthrough in understanding the causes of spina bifida
Scientists at Rady Children's Institute for Genomic Medicine, and the Department of Neurosciences and Pediatrics at the University of California, San Diego, have made a significant breakthrough in ...
AHA/ASA Journals23h
Lymphatic Endothelial Branched-Chain Amino Acid Catabolic Defects Undermine Cardiac Lymphatic Integrity and Drive HFpEF
BACKGROUND: Heart failure with preserved ejection fraction (HFpEF) has become the most prevalent type of heart failure, but ...
Open Access Government23h
Tracing evolution’s blueprint: Minimal genome life and the engineering of synthetic endosymbiosis
Roksana Riddle and Christopher H. Contag from Michigan State University discuss the concept of endosymbiosis, how it has ...