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Items: 18


The ERP correlates of self-knowledge: Are assessments of one's past, present, and future traits closer to semantic or episodic memory?

Tanguay AN, Benton L, Romio L, Sievers C, Davidson PSR, Renoult L.

Neuropsychologia. 2018 Feb;110:65-83. doi: 10.1016/j.neuropsychologia.2017.10.024. Epub 2017 Nov 10.


Centriolar satellites are assembly points for proteins implicated in human ciliopathies, including oral-facial-digital syndrome 1.

Lopes CA, Prosser SL, Romio L, Hirst RA, O'Callaghan C, Woolf AS, Fry AM.

J Cell Sci. 2011 Feb 15;124(Pt 4):600-12. doi: 10.1242/jcs.077156. Epub 2011 Jan 25.


Primary cilia of odontoblasts: possible role in molar morphogenesis.

Thivichon-Prince B, Couble ML, Giamarchi A, Delmas P, Franco B, Romio L, Struys T, Lambrichts I, Ressnikoff D, Magloire H, Bleicher F.

J Dent Res. 2009 Oct;88(10):910-5. doi: 10.1177/0022034509345822.


Nephrin deficiency activates NF-kappaB and promotes glomerular injury.

Hussain S, Romio L, Saleem M, Mathieson P, Serrano M, Moscat J, Diaz-Meco M, Scambler P, Koziell A.

J Am Soc Nephrol. 2009 Aug;20(8):1733-43. doi: 10.1681/ASN.2008111219. Epub 2009 Jun 4.


Mutations in radial spoke head protein genes RSPH9 and RSPH4A cause primary ciliary dyskinesia with central-microtubular-pair abnormalities.

Castleman VH, Romio L, Chodhari R, Hirst RA, de Castro SC, Parker KA, Ybot-Gonzalez P, Emes RD, Wilson SW, Wallis C, Johnson CA, Herrera RJ, Rutman A, Dixon M, Shoemark A, Bush A, Hogg C, Gardiner RM, Reish O, Greene ND, O'Callaghan C, Purton S, Chung EM, Mitchison HM.

Am J Hum Genet. 2009 Feb;84(2):197-209. doi: 10.1016/j.ajhg.2009.01.011. Epub 2009 Feb 5.


Convergent extension movements and ciliary function are mediated by ofd1, a zebrafish orthologue of the human oral-facial-digital type 1 syndrome gene.

Ferrante MI, Romio L, Castro S, Collins JE, Goulding DA, Stemple DL, Woolf AS, Wilson SW.

Hum Mol Genet. 2009 Jan 15;18(2):289-303. doi: 10.1093/hmg/ddn356. Epub 2008 Oct 29.


OFD1 is a centrosomal/basal body protein expressed during mesenchymal-epithelial transition in human nephrogenesis.

Romio L, Fry AM, Winyard PJ, Malcolm S, Woolf AS, Feather SA.

J Am Soc Nephrol. 2004 Oct;15(10):2556-68.


OFD1, the gene mutated in oral-facial-digital syndrome type 1, is expressed in the metanephros and in human embryonic renal mesenchymal cells.

Romio L, Wright V, Price K, Winyard PJ, Donnai D, Porteous ME, Franco B, Giorgio G, Malcolm S, Woolf AS, Feather SA.

J Am Soc Nephrol. 2003 Mar;14(3):680-9.


Correction of G551D-CFTR transport defect in epithelial monolayers by genistein but not by CPX or MPB-07.

Zegarra-Moran O, Romio L, Folli C, Caci E, Becq F, Vierfond JM, Mettey Y, Cabrini G, Fanen P, Galietta LJ.

Br J Pharmacol. 2002 Oct;137(4):504-12.


Molecular characterization and expression analysis of Mtmr2, mouse homologue of MTMR2, the Myotubularin-related 2 gene, mutated in CMT4B.

Bolino A, Marigo V, Ferrera F, Loader J, Romio L, Leoni A, Di Duca M, Cinti R, Cecchi C, Feltri ML, Wrabetz L, Ravazzolo R, Monaco AP.

Gene. 2002 Jan 23;283(1-2):17-26.


IL-4 is a potent modulator of ion transport in the human bronchial epithelium in vitro.

Galietta LJ, Pagesy P, Folli C, Caci E, Romio L, Costes B, Nicolis E, Cabrini G, Goossens M, Ravazzolo R, Zegarra-Moran O.

J Immunol. 2002 Jan 15;168(2):839-45.


Regulation of taurine transport in murine macrophages.

Romio L, Zegarra-Moran, Varesio L, Galietta LJV.

Amino Acids. 2001;21(2):151-60.


Activation of G551D CFTR channel with MPB-91: regulation by ATPase activity and phosphorylation.

Dérand R, Bulteau-Pignoux L, Mettey Y, Zegarra-Moran O, Howell LD, Randak C, Galietta LJ, Cohn JA, Norez C, Romio L, Vierfond JM, Joffre M, Becq F.

Am J Physiol Cell Physiol. 2001 Nov;281(5):C1657-66.


Mutational germline analysis of hMSH2 and hMLH1 genes in early onset colorectal cancer patients.

Montera M, Resta N, Simone C, Guanti G, Marchese C, Civitelli S, Mancini A, Pozzi S, De Salvo L, Bruzzone D, Donadini A, Romio L, Mareni C.

J Med Genet. 2000 Jul;37(7):E7. No abstract available. Erratum in: J Med Genet. 2003 Jun;40(6):472.


Characterization of a murine gene homologous to the bovine CaCC chloride channel.

Romio L, Musante L, Cinti R, Seri M, Moran O, Zegarra-Moran O, Galietta LJ.

Gene. 1999 Mar 4;228(1-2):181-8.


An electrogenic amino acid transporter in the apical membrane of cultured human bronchial epithelial cells.

Galietta LJ, Musante L, Romio L, Caruso U, Fantasia A, Gazzolo A, Romano L, Sacco O, Rossi GA, Varesio L, Zegarra-Moran O.

Am J Physiol. 1998 Nov;275(5):L917-23. doi: 10.1152/ajplung.1998.275.5.L917.


Clinical findings in a family with familial adenomatous polyposis and a missense mutation of the adenomatous polyposis coli gene.

Marchese CA, Bertolino F, Ceccopieri B, Vanzetti M, Scaglione D, Locatelli L, Montera M, Romio L, Resta N, Stella A, Guanti G, Mareni C.

Scand J Gastroenterol. 1996 Sep;31(9):917-20.


Four novel mutations of the APC (adenomatous polyposis coli) gene in FAP patients.

Stella A, Montera M, Resta N, Marchese C, Susca F, Gentile M, Romio L, Pilia S, Prete F, Mareni C, et al.

Hum Mol Genet. 1994 Sep;3(9):1687-8. No abstract available. Erratum in: Hum Mol Genet 1994 Oct;3(10):1918.


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