Month: August 2021

IDIBELL scientists identify the PI4KA gene as the cause of a new neurological disease

The study has identified mutations of this gene in ten families and biochemical studies in the laboratory have confirmed that these variants are responsible for the symptoms. Possible treatments have already been tested through massive drug analyzes, which will then be tested in mini-brains generated from cells of the patients.

The Spanish State at the forefront of Europe in young waterpipe tobacco smokers

A study in which IDIBELL and ICO professionals have participated confirms that 90% of electronic cigarette smokers also consume conventional cigarettes and warns that social networks are becoming a channel of promotion, covertly or indirectly, of tobacco products banned by the European Tobacco Products Directive (TPD).

An international study with IDIBELL participation associates new genetic and immunological defects with severe COVID-19

TLR7 gene is essential for shaping response mechanisms to the virus and having deficiencies can lead to severe cases of SARS-CoV-2 in young people. The presence of autoantibodies against type I interferons increases with age and it is confirmed that it would increase the severity of COVID-19 in people older than 70 years.

Dr. Sebastiano Biondo obtains the position of Professor of Surgery at the University of Barcelona

Dr. Sebastiano Biondo, head of the Digestive Tube Pathology research group at IDIBELL and the Bellvitge University Hospital, has obtained the position of Professor of Surgery at the University of Barcelona in the competition held on July 20.

Pancreatic beta-cell boost in mice paves way for future diabetes treatments

A research team from IDIBELL, CRG and UB has uncovered the role of a gene that is critical to boosting the number of insulin-producing cells during the early development of the pancreas. The findings could bolster diabetes research efforts and eventually lead to new replacement therapies for the disease.

Identified two new genes implicated in developmental brain diseases

Two studies with the participation of IDIBELL and the University of Barcelona have identified mutations in the CLCN3 gene, encoding a chloride transporter in endosomes, and the CHRM1 gene, corresponding to the M1 muscarinic neuronal receptor, as responsible for defects in brain development.

Scroll to Top