A new cellular model of dyskeratosis congenita will help to understand the disease and evaluate new therapies. - BioInn
A new cellular model of dyskeratosis congenita will help to understand the disease and evaluate new therapies.
A study led by Guillermo Güenechea, researcher at the U710 CIBERER at CIEMAT / IIS-FJD, and Rosario Perona, from the U757 CIBERER at the Alberto Sols Biomedical Research Institute (CSIC / UAM), has managed to develop a new cellular model of X-linked dyskeratosis congenita in progenitors and hematopoietic stem cells. For more information, consult the following news:
2021
CIEMAT participates in the XVI Congress of the Spanish Society of Laboratory Animal Sciences (SECAL)
2020
Un proyecto de terapia génica para la trombastenia de Glanzmann, dotado con 50.000 euros de la EAHAD
2019