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Genetic and phenotypic differences between sexes in congenital hypogonadotropic hypogonadism (CHH): Large cohort analysis from a single tertiary centre.
Federici S, Cangiano B, Goggi G, Messetti D, Munari EV, Amer M, Giovanelli L, Hrvat F, Vezzoli V, Persani L, Bonomi M. Federici S, et al. Among authors: vezzoli v. Front Endocrinol (Lausanne). 2022 Dec 2;13:965074. doi: 10.3389/fendo.2022.965074. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 36531499 Free PMC article.
A new gene-finding tool: using the Caenorhabditis elegans operons for identifying functional partner proteins in human cells.
Eichmüller S, Vezzoli V, Bazzini C, Ritter M, Fürst J, Jakab M, Ravasio A, Chwatal S, Dossena S, Bottà G, Meyer G, Maier B, Valenti G, Lang F, Paulmichl M. Eichmüller S, et al. Among authors: vezzoli v. J Biol Chem. 2004 Feb 20;279(8):7136-46. doi: 10.1074/jbc.M307347200. Epub 2003 Nov 13. J Biol Chem. 2004. PMID: 14615488 Free article.
The expression of wild-type pendrin (SLC26A4) in human embryonic kidney (HEK 293 Phoenix) cells leads to the activation of cationic currents.
Dossena S, Maccagni A, Vezzoli V, Bazzini C, Garavaglia ML, Meyer G, Fürst J, Ritter M, Fugazzola L, Persani L, Zorowka P, Storelli C, Beck-Peccoz P, Bottà G, Paulmichl M. Dossena S, et al. Among authors: vezzoli v. Eur J Endocrinol. 2005 Nov;153(5):693-9. doi: 10.1530/eje.1.02018. Eur J Endocrinol. 2005. PMID: 16260428 Free article.
Germline prokineticin receptor 2 (PROKR2) variants associated with central hypogonadism cause differental modulation of distinct intracellular pathways.
Libri DV, Kleinau G, Vezzoli V, Busnelli M, Guizzardi F, Sinisi AA, Pincelli AI, Mancini A, Russo G, Beck-Peccoz P, Loche S, Crivellaro C, Maghnie M, Krausz C, Persani L, Bonomi M; Italian Study Group on Idiopathic Central Hypogonadism (ICH). Libri DV, et al. Among authors: vezzoli v. J Clin Endocrinol Metab. 2014 Mar;99(3):E458-63. doi: 10.1210/jc.2013-2431. Epub 2013 Nov 25. J Clin Endocrinol Metab. 2014. PMID: 24276467 Free article.
45 results