ZFIN ID: ZDB-PERS-110304-13
Vettori, Andrea
Email: andrea.vettori@univr.it
URL:
Affiliation:
Address: Department of Biotechnology University of Verona Strada Le Grazie 15 Ca Vignal 1 Verona 37134 Italy
Country: Italy
Phone:
Fax:
ORCID ID: 0000-0003-4958-0619


BIOGRAPHY AND RESEARCH INTERESTS


PUBLICATIONS
Facchinello, N., Laquatra, C., Locatello, L., Beffagna, G., Brañas Casas, R., Fornetto, C., Dinarello, A., Martorano, L., Vettori, A., Risato, G., Celeghin, R., Meneghetti, G., Santoro, M.M., Delahodde, A., Vanzi, F., Rasola, A., Dalla Valle, L., Rasotto, M.B., Lodi, T., Baruffini, E., Argenton, F., Tiso, N. (2021) Efficient clofilium tosylate-mediated rescue of POLG-related disease phenotypes in zebrafish. Cell Death & Disease. 12:100
Ambrosini, G., Dalla Pozza, E., Fanelli, G., Di Carlo, C., Vettori, A., Cannino, G., Cavallini, C., Carmona-Carmona, C.A., Brandi, J., Rinalducci, S., Scupoli, M.T., Rasola, A., Cecconi, D., Palmieri, M., Dando, I. (2020) Progressively De-Differentiated Pancreatic Cancer Cells Shift from Glycolysis to Oxidative Metabolism and Gain a Quiescent Stem State. Cells. 9(7):
Peron, M., Dinarello, A., Meneghetti, G., Martorano, L., Facchinello, N., Vettori, A., Licciardello, G., Tiso, N., Argenton, F. (2020) The stem-like STAT3-responsive cells of zebrafish intestine are WNT/β-catenin dependent. Development (Cambridge, England). 147(12):
Schaeffer, C., Izzi, C., Vettori, A., Pasqualetto, E., Cittaro, D., Lazarevic, D., Caridi, G., Gnutti, B., Mazza, C., Jovine, L., Scolari, F., Rampoldi, L. (2019) Autosomal Dominant Tubulointerstitial Kidney Disease with Adult Onset due to a Novel Renin Mutation Mapping in the Mature Protein. Scientific Reports. 9:11601
Astone, M., Lai, J.K.H., Dupont, S., Stainier, D.Y.R., Argenton, F., Vettori, A. (2018) Zebrafish mutants and TEAD reporters reveal essential functions for Yap and Taz in posterior cardinal vein development. Scientific Reports. 8:10189
Diquigiovanni, C., Bergamini, C., Evangelisti, C., Isidori, F., Vettori, A., Tiso, N., Argenton, F., Costanzini, A., Iommarini, L., Anbunathan, H., Pagotto, U., Repaci, A., Babbi, G., Casadio, R., Lenaz, G., Rhoden, K.J., Porcelli, A.M., Fato, R., Bowcock, A., Seri, M., Romeo, G., Bonora, E. (2018) Mutant MYO1F alters the mitochondrial network and induces tumor proliferation in thyroid cancer. International Journal of Cancer. 143(7):1706-1719
Giuliodori, A., Beffagna, G., Marchetto, G., Fornetto, C., Vanzi, F., Toppo, S., Facchinello, N., Santimaria, M., Vettori, A., Rizzo, S., Della Barbera, M., Pilichou, K., Argenton, F., Thiene, G., Tiso, N., Basso, C. (2018) Loss of cardiac Wnt/β-catenin signalling in Desmoplakin-deficient AC8 zebrafish models is rescuable by genetic and pharmacological intervention. Cardiovascular research. 114(8):1082-1097
Vettori, A., Greenald, D., Wilson, G.K., Peron, M., Facchinello, N., Markham, E., Sinnakaruppan, M., Matthews, L.C., McKeating, J.A., Argenton, F., van Eeden, F.J.M. (2017) Glucocorticoids promote Von Hippel Lindau degradation and Hif-1α stabilization. Proceedings of the National Academy of Sciences of the United States of America. 114(37):9948-9953
Turrini, L., Fornetto, C., Marchetto, G., Müllenbroich, M.C., Tiso, N., Vettori, A., Resta, F., Masi, A., Mannaioni, G., Pavone, F.S., Vanzi, F. (2017) Optical mapping of neuronal activity during seizures in zebrafish. Scientific Reports. 7:3025
Kim, H.R., Greenald, D., Vettori, A., Markham, E., Santhakumar, K., Argenton, F., van Eeden, F. (2017) Zebrafish as a model for von Hippel Lindau and hypoxia-inducible factor signaling. Methods in cell biology. 138:497-523
Facchinello, N., Schiavone, M., Vettori, A., Argenton, F., Tiso, N. (2016) Monitoring Wnt Signaling in Zebrafish Using Fluorescent Biosensors. Methods in molecular biology (Clifton, N.J.). 1481:81-94
Astone, M., Pizzi, M., Peron, M., Domenichini, A., Guzzardo, V., Töchterle, S., Tiso, N., Rugge, M., Meyer, D., Argenton, F., Vettori, A. (2015) A GFP-Tagged Gross Deletion on Chromosome 1 Causes Malignant Peripheral Nerve Sheath Tumors and Carcinomas in Zebrafish. PLoS One. 10:e0145178
Casari, A., Schiavone, M., Facchinello, N., Vettori, A., Meyer, D., Tiso, N., Moro, E., Argenton, F. (2014) A Smad3 transgenic reporter reveals TGF-beta control of zebrafish spinal cord development. Developmental Biology. 396(1):81-93
Moro, E., Vettori, A., Porazzi, P., Schiavone, M., Rampazzo, E., Casari, A., Ek, O., Facchinello, N., Astone, M., Zancan, I., Milanetto, M., Tiso, N., and Argenton, F. (2013) Generation and application of signaling pathway reporter lines in zebrafish. Molecular genetics and genomics : MGG. 288(5-6):231-242

NON-ZEBRAFISH PUBLICATIONS
Boaretto F*, Vettori A*, Casarin A,Vazza G, Muglia M, Rossetto MG, Cavallaro T, Rizzuto N, Carelli V, Salviati L, Mostacciuolo ML, Martinuzzi A. Severe CMT type 2 with fatal encephalopathy associated with a novel mfn2 splicing mutation. Neurology. 2010 Jun 8;74(23):1919-21.

Millino C, Fanin M, Vettori A, Laveder P, Mostacciuolo ML, Angelini C, Lanfranchi G. Different atrophy-hypertrophy transcription pathways in muscles affected by severe and mild spinal muscular atrophy. BMC Med. 2009 Apr 7;7:14.

Bovo G, Diani E, Bisulli F, Di Bonaventura C, Striano P, Gambardella A, Ferlazzo E, Egeo G, Mecarelli O, Elia M, Bianchi A, Bortoluzzi S, Vettori A, Aguglia U, Binelli S, De Falco A, Coppola G, Gobbi G, Sofia V, Striano S, Tinuper P, Giallonardo AT, Michelucci R, Nobile C. Analysis of LGI1 promoter sequence, PDYN and GABBR1 polymorphisms in sporadic and familial lateral temporal lobe epilepsy. Neurosci Lett. 2008 May 2;436(1):23-6.

Vazza G, Bertolin C, Scudellaro E, Vettori A, Boaretto F, Rampinelli S, De Sanctis G, Perini G, Peruzzi P, Mostacciuolo ML. Genome-wide scan supports the existence of a susceptibility locus for schizophrenia and bipolar disorder on chromosome 15q26. Mol Psychiatry. 2007 Jan;12(1):87-93.

Simonati A, Boaretto F, Vettori A, Dabrilli P, Criscuolo L, Rizzuto N, Mostacciuolo ML. A novel missense mutation in the l1cam gene in a boy with L1 disease. Neurol Sci. 2006 Jun;27(2):114-7.

Pilichou K, Nava A, Basso A, Beffagna A, Bauce B, Lorenzon A, Frigo G, Vettori A, Valente M, Towbin J, Thiene G, Danieli GA, Ramazzo A. Mutations in desmoglein-2 gene cause arrhythmogenic right ventricular cardiomyopathy. Circulation. 2006 Mar 7;113(9):1171-9.

Velayos-Baeza A* Vettori A* Copley RR, Dobson-Stone C, Monaco AP. Analysis of the human VSP13 gene family. Genomics. 2004 Sep; 84(3):536-49.

Opocher G, Schiavi F, Vettori A, Pampinella F, Vitiello L, Murgia A, Martella M, Taccaliti A, Mantero F, Mostacciuolo M.L. Fine analysis of the short arm of chromosome 1 in sporadic and familial pheochromocytoma. Clin Endocrino (Oxf). 2003 Dec; 59(6): 707-715.

Pegoraro E, Vettori A, Valentino ML, Molon A, Mostacciuolo ML, Howell N, Carelli V. X-Inactivation pattern in multiple tissues from two leber's hereditary optic neuropathy (LHON) patients. Am J Med Genet. 2003 May; 15,119A(1):37-40.

Soragna D*, Vettori A*, Carraro G, Marchioni E, Vazza G, Bellini S, Tupler R, Savoldi F, Mostacciuolo ML. A locus for migraine without aura maps on chromosome 14q21.2-q22.3. Am J Hum Genet. 2003 Jan; 72(1):161-167.

Zortea M, Vettori A, Trevisan CP, Bellini S, Vazza G, Armani M, Simonati A, Mostacciuolo ML. Genetic mapping of a susceptibility locus for disc herniation and spastic paraplegia on 6q23.3-q24.1. J Med Genet. 2002 Jun; 39(6):387-90.