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Highlights: New multicenter study helps understand how a single mutation in splicing factor gene SF3B1 is the cause of several cancers This mutation is the cause of m...
An association between a genetic mutation, flu and heart irregularities that might one day improve the care of flu patients has been discovered. The study, led by Jacob Yount at The Ohio Sta...
Low levels of bilirubin lead to more chances of brain damage, suggesting that bilirubin protects brain cells from superoxide reactions. In studies in mice, Johns Hopkins Medicine rese...
Mutations in ABHD5 gene associated with non-alcoholic fatty liver disease have been reported by researchers led by Jouni Uitto, MD, PhD, Professor of Dermatology and Cutaneous Biology at Tho...
Newly developed CRISPR-powered device can help identify genetic mutations in a matter of minutes. The findings of the study are published in the journal Nature Biomedical Engineering . ...
Molecular abnormalities that make people vulnerable to mycobacterial infections have been discovered by researchers. The findings of the study published in Science Immunology point strategie...
Genetic mutation and the faulty development process it triggers, causing a debilitating brain-based disorder in children has been discovered by Ashleigh Schaffer, PhD, assistant professor of...
Genetic mutations in appendix cancer are different from those found in colon cancer and mutations in the genes TP53 and GNAS are good predictors of survival among people with appendix cancer...
An artificial intelligence tool called ExPecto, developed by Simons Foundation, shows how gene mutations affect the body. Using the method, its creators at the Flatiron Institute's Center...
New study has identified 63 new genetic variations that could indicate higher risk of prostate cancer in men of European descent. The study is the result of a six-year long research process ...
Mitochondrial dysfunction can alter activity of serotonergic neurons in bipolar disorder, and this is the first time these two lines of evidence have been linked, revealed Tadafumi Kato, res...
Bilirubin, a yellow-orange pigment which is formed after the breakdown of red blood cells (RBC) and is excreted by the liver may improve cardiovascular health, reveals a new study. The findi...
A model that can predict the effect of a genetic variant on a person's cognitive traits has been developed by research teams at CHU Sainte-Justine, the Université de Montréal and the Institu...
The molecular consequences of a previously undefined genetic mutation have been discovered by a new study. The study was led by Dr. Nora Vögtle, head of an Emmy Noether junior research group...
Genetic mutations in Parkinson's disease can be linked to the formation of fatty plaques in the brain that characterize the disease by the destruction of motor neurons, finds a new study. Th...
Gilbert’s syndrome is a common, mild liver disease in which a liver enzyme required to process bilirubin is abnormal. Treatment is unnecessary.
Biliary atresia is a serious condition that occurs due to the obstruction of bile ducts and results in cirrhosis of liver in infants.
A careful history in women with a breast lump includes: The precise location of the lump, whether there is any accompanying nipple discharge, whether the lump has changed in size.
Crigler-Najjar syndrome arises due to the lack or deficiency of the enzyme uridine diphosphate glucuronosyl transferase. Type 1 and type 2 forms of the disease have been described.
Yellow colouring of skin in newborns, a condition called Neonatal jaundice. , Neonatal jaundice is caused by presence of excessive serum bilirubin.
Home remedies offers you herbal and natural method to treat jaundice effectively. Jaundice treatment at home is done using basic household ingredients and dosage to cure jaundice.
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