Stefania Bellesso

FGF signaling deregulation is associated with early developmental skeletal defects in animal models for mucopolysaccharidosis type II (MPSII)

R. Tomanin, M. Filocamo, P. Braghetta, 2018, Human molecular genetics.

A transcriptional and post-transcriptional dysregulation of Dishevelled 1 and 2 underlies the Wnt signaling impairment in type I Gaucher disease experimental models.

M. Filocamo, R. Costa, S. Lualdi, 2019, Human molecular genetics.

The epg5 knockout zebrafish line: a model to study Vici syndrome

F. Cecconi, M. Chrisam, P. Bonaldo, 2019, Autophagy.

Glucocerebrosidase deficiency in zebrafish affects primary bone ossification through increased oxidative stress and reduced Wnt/β-catenin signaling.

M. Filocamo, R. Costa, F. Argenton, 2015, Human molecular genetics.

Perturbations in cell signaling elicit early cardiac defects in mucopolysaccharidosis type II

R. Tomanin, A. Urbani, M. Filocamo, 2017, Human molecular genetics.

Evaluation of Coaguchek®Pro II coagulation testing device performance to assess direct oral anticoagulant action. The DOAC-CHECK study

A. Tosetto, S. Testa, I. Nichele, 2022, Bleeding Thrombosis and Vascular Biology.

Glucocerebrosidase deficiency in zebrafish affects primary bone ossification through increased oxidative stress and reduced Wnt/β-catenin signaling.

M. Filocamo, R. Costa, F. Argenton, 2015, Human molecular genetics.