Imbrici P - Search Results

1

Dapagliflozin protects the kidney in a non-diabetic model of cardiorenal syndrome.

Urbanek K, Cappetta D, Bellocchio G, Coppola MA, Imbrici P, Telesca M, Donniacuo M, Riemma MA, Mele E, Cianflone E, Naviglio S, Conte E, Camerino GM, Mele M, Bucci M, Castaldo G, De Luca A, Rossi F, Berrino L, Liantonio A, De Angelis A. Urbanek K, et al. Among authors: imbrici p. Pharmacol Res. 2023 Feb;188:106659. doi: 10.1016/j.phrs.2023.106659. Epub 2023 Jan 14. Pharmacol Res. 2023. PMID: 36646190 Free article.

2

Role of receptor protein tyrosine phosphatase alpha (RPTPalpha) and tyrosine phosphorylation in the serotonergic inhibition of voltage-dependent potassium channels.

Imbrici P, Tucker SJ, D'Adamo MC, Pessia M. Imbrici P, et al. Pflugers Arch. 2000 Dec;441(2-3):257-62. doi: 10.1007/s004240000406. Pflugers Arch. 2000. PMID: 11211111

3

Episodic ataxia type 1 mutations in the KCNA1 gene impair the fast inactivation properties of the human potassium channels Kv1.4-1.1/Kvbeta1.1 and Kv1.4-1.1/Kvbeta1.2.

Imbrici P, D'Adamo MC, Kullmann DM, Pessia M. Imbrici P, et al. Eur J Neurosci. 2006 Dec;24(11):3073-83. doi: 10.1111/j.1460-9568.2006.05186.x. Eur J Neurosci. 2006. PMID: 17156368

4

Episodic ataxia type 1 mutation F184C alters Zn2+-induced modulation of the human K+ channel Kv1.4-Kv1.1/Kvbeta1.1.

Imbrici P, D'Adamo MC, Cusimano A, Pessia M. Imbrici P, et al. Am J Physiol Cell Physiol. 2007 Feb;292(2):C778-87. doi: 10.1152/ajpcell.00259.2006. Epub 2006 Sep 6. Am J Physiol Cell Physiol. 2007. PMID: 16956965 Free article.

5

Functional characterization of an episodic ataxia type-1 mutation occurring in the S1 segment of hKv1.1 channels.

Imbrici P, Cusimano A, D'Adamo MC, De Curtis A, Pessia M. Imbrici P, et al. Pflugers Arch. 2003 Jun;446(3):373-9. doi: 10.1007/s00424-002-0962-2. Epub 2002 Nov 26. Pflugers Arch. 2003. PMID: 12799903

6

Premature stop codons in a facilitating EF-hand splice variant of CaV2.1 cause episodic ataxia type 2.

Graves TD, Imbrici P, Kors EE, Terwindt GM, Eunson LH, Frants RR, Haan J, Ferrari MD, Goadsby PJ, Hanna MG, van den Maagdenberg AM, Kullmann DM. Graves TD, et al. Among authors: imbrici p. Neurobiol Dis. 2008 Oct;32(1):10-5. doi: 10.1016/j.nbd.2008.06.002. Epub 2008 Jun 19. Neurobiol Dis. 2008. PMID: 18606230

7

Andersen-Tawil syndrome: new potassium channel mutations and possible phenotypic variation.

Davies NP, Imbrici P, Fialho D, Herd C, Bilsland LG, Weber A, Mueller R, Hilton-Jones D, Ealing J, Boothman BR, Giunti P, Parsons LM, Thomas M, Manzur AY, Jurkat-Rott K, Lehmann-Horn F, Chinnery PF, Rose M, Kullmann DM, Hanna MG. Davies NP, et al. Among authors: imbrici p. Neurology. 2005 Oct 11;65(7):1083-9. doi: 10.1212/01.wnl.0000178888.03767.74. Neurology. 2005. PMID: 16217063

8

A large cohort of myotonia congenita probands: novel mutations and a high-frequency mutation region in exons 4 and 5 of the CLCN1 gene.

Brugnoni R, Kapetis D, Imbrici P, Pessia M, Canioni E, Colleoni L, de Rosbo NK, Morandi L, Cudia P, Gashemi N, Bernasconi P, Desaphy JF, Conte D, Mantegazza R. Brugnoni R, et al. Among authors: imbrici p. J Hum Genet. 2013 Sep;58(9):581-7. doi: 10.1038/jhg.2013.58. Epub 2013 Jun 6. J Hum Genet. 2013. PMID: 23739125

9

Genetic inactivation of Kcnj16 identifies Kir5.1 as an important determinant of neuronal PCO2/pH sensitivity.

D'Adamo MC, Shang L, Imbrici P, Brown SD, Pessia M, Tucker SJ. D'Adamo MC, et al. Among authors: imbrici p. J Biol Chem. 2011 Jan 7;286(1):192-8. doi: 10.1074/jbc.M110.189290. Epub 2010 Nov 3. J Biol Chem. 2011. PMID: 21047793 Free PMC article.

10

Coexistence of CLCN1 and SCN4A mutations in one family suffering from myotonia.

Maggi L, Ravaglia S, Farinato A, Brugnoni R, Altamura C, Imbrici P, Camerino DC, Padovani A, Mantegazza R, Bernasconi P, Desaphy JF, Filosto M. Maggi L, et al. Among authors: imbrici p. Neurogenetics. 2017 Dec;18(4):219-225. doi: 10.1007/s10048-017-0525-5. Epub 2017 Oct 9. Neurogenetics. 2017. PMID: 28993909

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