MODULO Facoltà di Medicina e Chirurgia Data di nascita 14 ...
MODULO Facoltà di Medicina e Chirurgia Data di nascita 14 ...
MODULO Facoltà di Medicina e Chirurgia Data di nascita 14 ...
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Facoltà <strong>di</strong> Me<strong>di</strong>cinae <strong>Chirurgia</strong><strong>MODULO</strong>SCHEDE PERSONALI DOCENTITEC. LAB. BIO.<strong>Data</strong><strong>14</strong>.10.2008 Pag. 12 <strong>di</strong> 54J Cyst Fibros. 2008 Jul;7(4):292-4.5.Mattioli E, Columbaro M, Capanni C, Santi S, Maral<strong>di</strong> NM, D'Apice MR, Novelli G, Riccio M, Squarzoni S, Foisner R,Lattanzi G.Drugs affecting prelamin A processing: effects on heterochromatin organization.Exp Cell Res. 2008 Feb 1;3<strong>14</strong>(3):453-62.6.Lombar<strong>di</strong> F, Gullotta F, Columbaro M, Filareto A, D'Adamo M, Vielle A, Guglielmi V, Nardone AM, Azzolini V, GrossoE, Lattanzi G, D'Apice MR, Masala S, Maral<strong>di</strong> NM, Sbraccia P, Novelli G.Compound heterozygosity for mutations in LMNA in a patient with a myopathic andlipodystrophic man<strong>di</strong>buloacral dysplasia type A phenotype.J Clin Endocrinol Metab. 2007 Nov;92(11):4467-71. Epub 2007 Sep 11.7.Filesi I, Gullotta F, Lattanzi G, D'Apice MR, Capanni C, Nardone AM, Columbaro M, Scarano G, Mattioli E, Sabatelli P,Maral<strong>di</strong> NM, Biocca S, Novelli G.Alterations of nuclear envelope and chromatin organization in man<strong>di</strong>buloacral dysplasia, a rareform of laminopathy.Physiol Genomics. 2005 Oct 17;23(2):150-8. Epub 2005 Jul 26.8.D'Apice MR, Gambardella S, Bengala M, Russo S, Nardone AM, Luci<strong>di</strong> V, Sangiuolo F, Novelli G.Molecular analysis using DHPLC of cystic fibrosis: increase of the mutation detection rate amongthe affected population in Central Italy.BMC Med Genet. 2004 Apr <strong>14</strong>;5:8.9.Novelli G, Muchir A, Sangiuolo F, Helbling-Leclerc A, D'Apice MR, Massart C, Capon F, Sbraccia P, Federici M, LauroR, Tu<strong>di</strong>sco C, Pallotta R, Scarano G, Dallapiccola B, Merlini L, Bonne G.Man<strong>di</strong>buloacral dysplasia is caused by a mutation in LMNA-enco<strong>di</strong>ng lamin A/C.Am J Hum Genet. 2002 Aug;71(2):426-31. Epub 2002 Jun 19.10.Flex E, De Luca A, D'Apice MR, Buccino A, Dallapiccola B, Novelli G.Rapid scanning of myotubularin (MTM1) gene by denaturing high-performance liquidchromatography (DHPLC).Neuromuscul Disord. 2002 Jun;12(5):501-5.
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