Piazza V - Search Results

1

Purinergic signalling and intercellular Ca2+ wave propagation in the organ of Corti.

Piazza V, Ciubotaru CD, Gale JE, Mammano F. Piazza V, et al. Cell Calcium. 2007 Jan;41(1):77-86. doi: 10.1016/j.ceca.2006.05.005. Epub 2006 Jul 7. Cell Calcium. 2007. PMID: 16828497

2

A mechanism for sensing noise damage in the inner ear.

Gale JE, Piazza V, Ciubotaru CD, Mammano F. Gale JE, et al. Among authors: piazza v. Curr Biol. 2004 Mar 23;14(6):526-9. doi: 10.1016/j.cub.2004.03.002. Curr Biol. 2004. PMID: 15043820 Free article.

3

Impaired permeability to Ins(1,4,5)P3 in a mutant connexin underlies recessive hereditary deafness.

Beltramello M, Piazza V, Bukauskas FF, Pozzan T, Mammano F. Beltramello M, et al. Among authors: piazza v. Nat Cell Biol. 2005 Jan;7(1):63-9. doi: 10.1038/ncb1205. Epub 2004 Dec 12. Nat Cell Biol. 2005. PMID: 15592461

4

Permeability and gating properties of human connexins 26 and 30 expressed in HeLa cells.

Beltramello M, Bicego M, Piazza V, Ciubotaru CD, Mammano F, D'Andrea P. Beltramello M, et al. Among authors: piazza v. Biochem Biophys Res Commun. 2003 Jun 13;305(4):1024-33. doi: 10.1016/s0006-291x(03)00868-4. Biochem Biophys Res Commun. 2003. PMID: 12767933

5

ATP-mediated cell-cell signaling in the organ of Corti: the role of connexin channels.

Majumder P, Crispino G, Rodriguez L, Ciubotaru CD, Anselmi F, Piazza V, Bortolozzi M, Mammano F. Majumder P, et al. Among authors: piazza v. Purinergic Signal. 2010 Jun;6(2):167-87. doi: 10.1007/s11302-010-9192-9. Epub 2010 Jun 17. Purinergic Signal. 2010. PMID: 20806010 Free PMC article.

6

Functional analysis of R75Q mutation in the gene coding for Connexin 26 identified in a family with nonsyndromic hearing loss.

Piazza V, Beltramello M, Menniti M, Colao E, Malatesta P, Argento R, Chiarella G, Gallo LV, Catalano M, Perrotti N, Mammano F, Cassandro E. Piazza V, et al. Clin Genet. 2005 Aug;68(2):161-6. doi: 10.1111/j.1399-0004.2005.00468.x. Clin Genet. 2005. PMID: 15996214

7

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: piazza v. 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.

8

MRI Features in a Rat Model of H-ABC Tubulinopathy.

Garduno-Robles A, Alata M, Piazza V, Cortes C, Eguibar JR, Pantano S, Hernandez VH. Garduno-Robles A, et al. Among authors: piazza v. Front Neurosci. 2020 Jun 3;14:555. doi: 10.3389/fnins.2020.00555. eCollection 2020. Front Neurosci. 2020. PMID: 32581692 Free PMC article.

9

Auditory impairment in H-ABC tubulinopathy.

Lopez-Juarez A, Gonzalez-Vega A, Kleinert-Altamirano A, Piazza V, Garduno-Robles A, Alata M, Villaseñor-Mora C, Eguibar JR, Cortes C, Padierna LC, Hernandez VH. Lopez-Juarez A, et al. Among authors: piazza v. J Comp Neurol. 2021 Apr 1;529(5):957-968. doi: 10.1002/cne.24990. Epub 2020 Aug 22. J Comp Neurol. 2021. PMID: 32681585

10

Longitudinal Evaluation of Cerebellar Signs of H-ABC Tubulinopathy in a Patient and in the taiep Model.

Alata M, González-Vega A, Piazza V, Kleinert-Altamirano A, Cortes C, Ahumada-Juárez JC, Eguibar JR, López-Juárez A, Hernandez VH. Alata M, et al. Among authors: piazza v. Front Neurol. 2021 Jul 14;12:702039. doi: 10.3389/fneur.2021.702039. eCollection 2021. Front Neurol. 2021. PMID: 34335454 Free PMC article.

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