News

Diego Viasus awarded the Extraordinary Doctorate Prize of the Faculty of Medicine of the UB

The PhD thesis of Diego Viasus researcher at Infections of the respiratory tract and in Immunocomproimised Patients research group at IDIBELL has won two awards. On one hand, has received the Extraordinary Doctorate Award from the Faculty of Medicine of the University of Barcelona and on the other, the Gabriel Rufí Prize for the best […]

Leer más about Diego Viasus awarded the Extraordinary Doctorate Prize of the Faculty of Medicine of the UB

José Luis Hernández: ”We have designed two antibodies that block S100 proteins and we’ve observed that slow tumors growth”

The laboratory of José Luis Hernández at the Biomed division, LEITAT Technology Center of Barcelona works in the clinical application of two antibodies designed by them to block proliferative function of extracellular S100 proteins. Hernandez explained his research on April 26 at a conference framed at IDIBELL seminars cycle. “We designed two antibodies that block […]

Leer más about José Luis Hernández: ”We have designed two antibodies that block S100 proteins and we’ve observed that slow tumors growth”

IDIBELL license to Minoryx a patent of a product to treat a rare neurodegenerative disease

IDIBELL has signed a licensing agreement with the Catalan biotechnology company Minoryx of a patent for the treatment of X-linked adrenoleukodystrophy, a rare serious neurodegenerative disease, which has no effective treatment. The Neurometabolic Diseases group led by ICREA researcher Aurora Pujol, has developed an animal model to study this disease. Studies using this model have […]

Leer más about IDIBELL license to Minoryx a patent of a product to treat a rare neurodegenerative disease

‘Dark genome’ is involved in Rett Syndrome

Researchers at the Epigenetics and Cancer Biology Program at IDIBELL led by Manel Esteller, ICREA researcher and professor of genetics at the University of Barcelona, have described alterations in noncoding long chain RNA sequences (lncRNA) in Rett syndrome. These molecules act as supervisor agents responsible of ‘switch on’ or ‘switch off’ other genes in our […]

Leer más about ‘Dark genome’ is involved in Rett Syndrome

Cedric Notredame: “We want to understand under what pressure evolves long noncoding RNA”

According to the ENCODE‘s latest update in the human genome there are about 10,000 long sequences of RNA that do not code for any protein. Cedric Notredame’s lab at the Center for genomic Regulation (CRG) tries to detect these molecules not only in humans but also in other species to understand their functionality. Cedric Notredame […]

Leer más about Cedric Notredame: “We want to understand under what pressure evolves long noncoding RNA”

Piero Crespo: “We look for site-specific inhibitors and that block protein-protein interactions”

The field of study of Piero Crespo at the Institute of Biomedicine and Biotechnology of Cantabria (IBBTEC) is the regulation of Ras-ERK signals. On April 19, explained the latest developments of their research at a conference framed in IDIBELL seminar series. His work focuses on the study of the mechanisms of Ras regulation in particular […]

Leer más about Piero Crespo: “We look for site-specific inhibitors and that block protein-protein interactions”

High school students discover how research at IDIBELL is

On April 16th science students of the French School of Barcelona visited the IDIBELL to see firsthand how a biomedical research center works. Researchers of the neurometabolic diseases group explained to students the research of a rare disease, the X-linked adrenoleukodistrophy, from basic research, to the investigation with animal models and clinical trial patients. The […]

Leer más about High school students discover how research at IDIBELL is

Identified as responsible for breast and ovarian hereditary cancer three BRCA1 mutations

Researchers of the hereditary cancer research group at the Bellvitge Biomedical Research Institute (IDIBELL) and the Catalan Institute of Oncology (ICO) conducted a functional and structural study of seven missense variants of the BRCA1 gene concluding that three of these variants are pathogenic, linked to the risk of suffering breast or ovarian cancer. The study […]

Leer más about Identified as responsible for breast and ovarian hereditary cancer three BRCA1 mutations
Scroll to Top