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Characterization of five novel vasopressin V2 receptor mutants causing nephrogenic diabetes insipidus reveals a role of tolvaptan for M272R-V2R mutation.
Prosperi F, Suzumoto Y, Marzuillo P, Costanzo V, Jelen S, Iervolino A, Guarino S, La Manna A, Miraglia Del Giudice E, Perna AF, Zacchia M, Cordat E, Capasso G, Trepiccione F. Prosperi F, et al. Among authors: perna af. Sci Rep. 2020 Oct 2;10(1):16383. doi: 10.1038/s41598-020-73089-x. Sci Rep. 2020. PMID: 33009446 Free PMC article.
Renal phenotype in Bardet-Biedl syndrome: a combined defect of urinary concentration and dilution is associated with defective urinary AQP2 and UMOD excretion.
Zacchia M, Zacchia E, Zona E, Capolongo G, Raiola I, Rinaldi L, Trepiccione F, Ingrosso D, Perna A, Di Iorio V, Simonelli F, Moe OW, Capasso G. Zacchia M, et al. Am J Physiol Renal Physiol. 2016 Oct 1;311(4):F686-F694. doi: 10.1152/ajprenal.00224.2016. Epub 2016 Aug 3. Am J Physiol Renal Physiol. 2016. PMID: 27488999 Free PMC article.
MicroRNAs in Renal Diseases: A Potential Novel Therapeutic Target.
Petrillo F, Iervolino A, Zacchia M, Simeoni A, Masella C, Capolongo G, Perna A, Capasso G, Trepiccione F. Petrillo F, et al. Kidney Dis (Basel). 2017 Dec;3(3):111-119. doi: 10.1159/000481730. Epub 2017 Nov 8. Kidney Dis (Basel). 2017. PMID: 29344506 Free PMC article.
193 results