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Molecular Medicine (Cambridge, Mass.)|May 19, 2026
PHOX2B defects alter protein folding, cell-cycle, and mitochondrial pathways in an in vitro model of CCHSChiara Africano, Tiziana Bachetti, Eleonora Di Zanni, et al.
Glia|February 24, 2021
Amphioxus neuroglia: Molecular characterization and evidence for early compartmentalization of the developing nerve cordMatteo Bozzo, Thurston C Lacalli, Valentina Obino, et al.
American Journal of Respiratory and Critical Care Medicine|June 10, 2006
Brainstem anomalies in two patients affected by congenital central hypoventilation syndromeTiziana Bachetti, Angela Robbiano, Sara Parodi, et al.
Pharmacological Research|March 8, 2005
Effects of endotoxic shock on neuronal NOS and calcium transients in rat cardiac myocytesLaura Comini, Antonella Boraso, Tiziana Bachetti, et al.
Journal of Cardiovascular Development and Disease|May 27, 2022
Mechanisms and Clinical Implications of Endothelial Dysfunction in Arterial HypertensionPasquale Ambrosino, Tiziana Bachetti, Silvestro Ennio D'Anna, et al.
Journal of Experimental & Clinical Cancer Research : CR|March 12, 2022
Recent advances in the developmental origin of neuroblastoma: an overviewMirco Ponzoni, Tiziana Bachetti, Maria Valeria Corrias, et al.
Frontiers in Physiology|October 8, 2025
The <i>PHOX2B</i> c.428A>G missense variant affects post-transcriptional regulation and may explain the absence of neural crest-derived tumors in congenital central hypoventilation syndromeTiziana Bachetti, Simona Bagnasco, Giuseppe Santamaria, et al.
European Journal of Human Genetics : EJHG|January 17, 2008
Mild functional effects of a novel GFAP mutant allele identified in a familial case of adult-onset Alexander diseaseTiziana Bachetti, Francesco Caroli, Paola Bocca, et al.
International Journal of Molecular Sciences|June 27, 2024
A Proteomics Approach Identifies RREB1 as a Crucial Molecular Target of Imidazo-Pyrazole Treatment in SKMEL-28 Melanoma CellsErika Iervasi, Gabriela Coronel Vargas, Tiziana Bachetti, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|April 24, 2017
Common PHOX2B poly-alanine contractions impair RET gene transcription, predisposing to Hirschsprung diseaseEleonora Di Zanni, Annalisa Adamo, Elga Belligni, et al.
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