Gerardo García Díaz-Barriga

A FBN1 3'UTR mutation variant is associated with endoplasmic reticulum stress in aortic aneurysm in Marfan syndrome.

S. Heath, Anna-Maria Siegert, G. Egea, 2019, Biochimica et biophysica acta. Molecular basis of disease.

Myeloid C/EBPβ deficiency reshapes microglial gene expression and is protective in experimental autoimmune encephalomyelitis

A. Valledor, J. Serratosa, J. Saura, 2017, Journal of Neuroinflammation.

Myeloid C/EBPβ deficiency reshapes microglial gene expression and is protective in experimental autoimmune encephalomyelitis

A. Valledor, J. Serratosa, J. Saura, 2017, Journal of Neuroinflammation.