13. Piao Z., Wang W., Wei Y., Zonta F., Wan C., Bai J., Wu S., Wang X., Fang J.*, Characterization of an acetohydroxy acid synthase mutant conferring tolerance to imidazolinone herbicides in rice (Oryza sativa). Planta, 2017 Nov 18. doi: 10.1007/s00425-017-2817-2

12. Crispino G., Galindo Ramirez F., Campioni M., Zorzi V., Praetorius M., Di Pasquale G., Chiorini J., Mammano F*., In vivo genetic manipulation of inner ear connexin expression by bovine adeno-associated viral vectors. Scientific Reports, 7(1): 6567. DOI: 10.1038/s41598-017-06759-y PMID: 28779115 IF: 4,259 (2016)

11. Zorzi V., Paciello F., Ziraldo G., Peres C., Mazzarda F., Nardin C., Pasquini M., Chiani F., Raspa M., Scavizzi F., Carrer A., Crispino G., Ciubotaru CD., Monyer H., Fetoni AR., Salvatore AM., Mammano F*., Mouse Panx1 is dispensable for hearing acquisition and auditory function. Frontiers in Molecular Neuroscience, 10, 298. Received: 02 Oct 2017; Accepted: 30 Oct 2017. In Press. DOI: doi: 10.3389/fnmol.2017.00379 IF: 5,076 (2016)

10. Carrer A., Leparulo A., Crispino G., Ciubotaru CD., Marin O., Zonta F., Bortolozzi M., Cx32 hemichannel opening by cytosolic Ca2+ is inhibited by the R220X mutation that causes Charcot-Marie-Tooth disease. Hum Mol Genet. 2017 Oct 25. doi: 10.1093/hmg/ddx386. [Epub ahead of print] PMID: 29077882

9. Xu L., Carrer A., Zonta F., Ma P, Qu Z., Li S., Buratto D., Ceriani F., Crispino G., Zorzi V., Ziraldo G., Bruno F., Nardin C., Peres C., Mazzarda .F, Salvatore A., Raspa M., Scavizzi F., Chu Y, Xie S., Liao J., Liu X., Wang W., Wang S., Yang G., Lerner R. and Mammano F.. Design and characterization of a human monoclonal antibody that modulates mutant  connexin 26 hemichannels implicated in deafness and skin disorders. Front. Mol. Neurosci. | doi: 10.3389/fnmol.2017.00298

8. Vicario M., Calì T., Cieri D., Vallese F., Bortolotto R., Lopreiato R., Zonta F., Nardella M., Micalizzi A., Lefeber D., Valente E., Bertini E., Zanotti G., Zanni G., Brini M., Carafoli E.. Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease, (in press). A novel PMCA3 mutation in an ataxic patient with hypomorphic phosphomannomutase 2 (PMM2) heterozygote mutations: Biochemical characterization of the pump defect. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease doi: 10.1016/j.bbadis.2017.08.006

7. Ceriani F., Pozzan T., and Mammano F. (2016) Critical role of ATP-induced ATP release for Ca2+ signaling in nonsensory cell networks of the developing cochlea. Proc Natl Acad Sci U S A 113(46):E7194-E7201 doi: 10.1073/pnas.1616061113.

6. Cali T., Frizzarin M., Luoni L., Zonta F., Pantano S., Cruz C., Bonza M.C., Bertipaglia I., Ruzzene M., De Michelis M.I., Damiano N., Marin O., Zanni G., Zanotti G., Brini M., Lopreiato R., and Carafoli E. (2016) The ataxia related G1107D mutation of the plasma membrane Ca2+ ATPase isoform 3 affects its interplay with calmodulin and the autoinhibition process. Biochim Biophys Acta 1863(1):165-173 doi: 10.1016/j.bbadis.2016.09.007.

5. Orlandini E.*, Baiesi M., Zonta F. (2016) How Local Flexibility Affects Knot Positioning in Ring Polymers. Macromolecules (online) doi: 10.1021/acs.macromol.6b00712.

4. A Folda, Citta A, Scalcon V, Cali T, Zonta F, Scutari G, Bindoli A and Rigobello M P. Mitochondrial Thioredoxin System as a Modulator of Cyclophilin D Redox State. Sci Rep 6, 23071, doi:10.1038/srep23071 (2016).

3. Cianci, M., Folli, C., Zonta, F., Florio, P., Berni, R. & Zanotti, G. (2015). Structural evidence for asymmetric ligand binding to transthyretin. Acta Cryst. D71 doi:10.1107/S1399004715010585.

2. Zhao X., Qu Z., Tickner J., Xu J., Dai K., and Zhang X. (2014) The role of SATB2 in skeletogenesis and human disease. Cytokine Growth Factor Rev 25(1):35-44 doi: 10.1016/j.cytogfr.2013.12.010.

1. Yea K., Zhang H., Xie J., Jones T.M., Yang G., Song B.D., and Lerner R.A. (2013) Converting stem cells to dendritic cells by agonist antibodies from unbiased morphogenic selections. Proc Natl Acad Sci U S A 110(37):14966-14971 doi: 10.1073/pnas.1313671110.