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A fully atomistic model of the Cx32 connexon.
Pantano S, Zonta F, Mammano F. Pantano S, et al. Among authors: mammano f. PLoS One. 2008 Jul 2;3(7):e2614. doi: 10.1371/journal.pone.0002614. PLoS One. 2008. PMID: 18648547 Free PMC article.
The p.Cys169Tyr variant of connexin 26 is not a polymorphism.
Zonta F, Girotto G, Buratto D, Crispino G, Morgan A, Abdulhadi K, Alkowari M, Badii R, Gasparini P, Mammano F. Zonta F, et al. Among authors: mammano f. Hum Mol Genet. 2015 May 1;24(9):2641-8. doi: 10.1093/hmg/ddv026. Epub 2015 Jan 26. Hum Mol Genet. 2015. PMID: 25628337 Free PMC article.
Pathogenetic role of the deafness-related M34T mutation of Cx26.
Bicego M, Beltramello M, Melchionda S, Carella M, Piazza V, Zelante L, Bukauskas FF, Arslan E, Cama E, Pantano S, Bruzzone R, D'Andrea P, Mammano F. Bicego M, et al. Among authors: mammano f. Hum Mol Genet. 2006 Sep 1;15(17):2569-87. doi: 10.1093/hmg/ddl184. Epub 2006 Jul 18. Hum Mol Genet. 2006. PMID: 16849369 Free PMC article.
A potent antagonist antibody targeting connexin hemichannels alleviates Clouston syndrome symptoms in mutant mice.
Kuang Y, Zorzi V, Buratto D, Ziraldo G, Mazzarda F, Peres C, Nardin C, Salvatore AM, Chiani F, Scavizzi F, Raspa M, Qiang M, Chu Y, Shi X, Li Y, Liu L, Shi Y, Zonta F, Yang G, Lerner RA, Mammano F. Kuang Y, et al. Among authors: mammano f. EBioMedicine. 2020 Jul;57:102825. doi: 10.1016/j.ebiom.2020.102825. Epub 2020 Jun 15. EBioMedicine. 2020. PMID: 32553574 Free PMC article.
193 results