According to new research, being physically active can reduce the incidence of type 2 diabetes even in persons who have a high hereditary risk of having the disease.
According to a new study, some persons with motor neuron disease (MND) and frontotemporal dementia (FTD) share the same rare genetic diseases that cause other neurodegenerative illnesses.
One in every 5,000 boys born suffers from the crippling muscle-wasting illness DMD, which is known to be caused by mutations of the dystrophin gene. Typically, those who have the illness only survive into their 20s or 30s.
Most proteins localize to distinct protein-rich droplets in cells, also known as "cellular condensates". Such proteins contain sequence features that function as address labels, telling the protein which condensate to move into. When the labels get screwed up, proteins may end up in the wron
Vidisha Superintendent of Police Umashankar Bhargava on Thursday said that a former BJP corporator who died by suicide, took the extreme step as he could not save his children suffering from a genetic disease, treatment for which isn't available.
Researchers at UCL Great Ormond Street Institute of Child Health (UCL GOS ICH) have grown 'mini eyes', which make it possible to study and better understand the development of blindness in a rare genetic disease called Usher syndrome for the first time.
Washington [US], October 18 (ANI): In an analysis of the metabolic profiles of healthy American babies, researchers found surprising differences among ethnic groups which may help make screening for inherited metabolic disorders, cystic fibrosis, or hypothyroidism much more accurate than tra
Hyderabad (Telangana) [India], July 14 (ANI): Emphasising on preventive measures to address the huge burden of genetic diseases, Vice President M. Venkaiah Naidu on Thursday said providing quality and affordable healthcare is a shared responsibility of the public and private sector.
Washington [US], July 3 (ANI): According to a recent study, a group of scientists have stepped closer to understanding the unsolved Mendelian diseases. They have found that Mendelian diseases are inherited from either parent due to gene mutations in the developing egg or sperm by studying th
Washington [US], June 30 (ANI): Scientists have discovered a new way to interpret unsolved Mendelian diseases which are inherited from either parent due to gene mutations in the developing egg or sperm through studying the inheritance of a protein known as SMCHD1 which is coded by the SMCHD1
Washington [US], June 24 (ANI): During a recent study, scientists identified a new genetic disease, which causes some children's brains to develop abnormally, resulting in delayed intellectual development.
Dublin [Ireland], June 14 (ANI): A new study at the RCSI University of Medicine and Health Sciences, which investigates population genetics across Europe, analyzed the clear ancestors of people living in the United Kingdom. This knowledge may be useful for future health research on the genet