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Mostrati risultati da 41 a 60 di 156
Data di pubblicazione Titolo Autore(i) Tipo File
1-ago-2003 108th ENMC International Workshop, 3rd Workshop of the MYO-CLUSTER project: EUROMEN, 7th International Emery-Dreifuss Muscular Dystrophy (EDMD) Workshop, 13-15 September 2002, Naarden, The Netherlands Bonne, G; Yaou, R; Béroud, C; Boriani, G; Brown, S; de Visser, M; Duboc, D; Ellis, J; Hausmanowa Petrusewicz, I; Lattanzi, G; Merlini, L; Morris, G; Muntoni, F; Opolski, G; Pinto, Y; Sangiuolo, Fc; Toniolo, D; Trembath, R; van Berlo, J; van der Kooi, A; Wehnert, M Articolo su rivista
1-set-2003 Analysis of intracellular distribution and apoptosis involvement of the Ufd1l gene product by over-expression studies Amati, F; Condo', I; Conti, E; Sangiuolo, Fc; Dallapiccola, B; Testi, R; Novelli, G Articolo su rivista
1-set-2003 Sequence-specific modification of genomic DNA by small DNA fragments Gruenert, D; Bruscia, E; Novelli, G; Colosimo, A; Dallapiccola, B; Sangiuolo, Fc; Goncz, K Articolo su rivista
1-gen-2004 Prenatal diagnosis of spinal muscular atrophy with respiratory distress (SMARD1) in a twin pregnancy [5] Sangiuolo, Fc; Filareto, A; Giardina, E; Nardone, A; Pilu, G; Pietropolli, A; Bertini, E; Novelli, G Articolo su rivista
1-gen-2004 Sequence-specific modification of mouse genomic DNA mediated by gene targeting techniques Sangiuolo, Fc; Novelli, G Articolo su rivista
1-mar-2004 Expression analysis of the gene encoding for the U-box-type ubiquitin ligase UBE4A in human tissues. Contino, G; Amati, F; Pucci, S; Pontieri, E; Picchiorri, F; Novelli, A; Botta, A; Mango, R; Nardone, A; Sangiuolo, Fc; Citro, G; Spagnoli, Lg; Novelli, G Articolo su rivista
1-apr-2004 Biochemical characterization of two GALK1 mutations in patients with galactokinase deficiency Sangiuolo, Fc; Magnani, M; Stambolian, D; Novelli, G Articolo su rivista
14-apr-2004 Molecular analysis using DHPLC of cystic fibrosis: increase of the mutation detection rate among the affected population in Central Italy D'Apice, M; Gambardella, S; Bengala, M; Russo, S; Nardone, A; Lucidi, V; Sangiuolo, Fc; Novelli, G Articolo su rivista
1-ott-2004 Toward the pharmacogenomics of cystic fibrosis: an update Sangiuolo, Fc; D'Apice, M; Gambardella, S; DI DANIELE, N; Novelli, G Articolo su rivista
1-gen-2005 Oligonucleotide-based gene targeting technologies. Filareto, A; DEL VECCHIO, F; Spitalieri, P; Sangiuolo, Fc; Novelli, G Articolo su rivista
1-gen-2005 Progress in Gene Therapy Research (Horizons in Cancer Research; Vol. 20) Del Vecchio, F; Botta, A; Spitalieri, P; Filareto, A; Sangiuolo, Fc; Novelli, G Contributo in libro
1-gen-2005 Cellular genetic therapy Del Vecchio, F; Filareto, A; Spitalieri, P; Sangiuolo, Fc; Novelli, G Articolo su rivista
1-lug-2005 In vitro restoration of functional SMN protein in human trophoblast cells affected by spinal muscular atrophy by small fragment homologous replacement Sangiuolo, Fc; Filareto, A; Spitalieri, P; Scaldaferri, M; Mango, R; Bruscia, E; Citro, G; Brunetti, E; DE FELICI, M; Novelli, G Articolo su rivista
22-lug-2005 In vivo and in vitro studies support that a new splicing isoform of OLR1 gene is protective against acute myocardial infarction Mango, R; Biocca, S; Del Vecchio, F; Clementi, F; Sangiuolo, Fc; Amati, F; Filareto, A; Grelli, S; Spitalieri, P; Filesi, I; Favalli, C; Lauro, R; Mehta, J; Romeo, F; Novelli, G Articolo su rivista
1-gen-2006 Therapeutic strategies for the treatment of Spinal Muscular Atrophy (SMA) disease Sangiuolo, Fc; Botta, A; Filareto, A; Spitalieri, P; Novelli, G Articolo su rivista
1-dic-2006 Gene expression profile study in CFTR mutated bronchial cell lines Gambardella, S; Biancolella, M; D'Apice, M; Amati, F; Sangiuolo, Fc; Farcomeni, A; Chillemi, G; Bueno, S; Desideri, A; Novelli, G Articolo su rivista
1-gen-2008 Cftr gene targeting in mouse embryonic stem cells mediated by Small Fragment Homologous Replacement (SFHR) Sangiuolo, Fc; Scaldaferri, M; Filareto, A; Spitalieri, P; Guerra, L; Favia, M; Caroppo, R; Mango, R; Bruscia, E; Gruenert, D; Casavola, V; DE FELICI, M; Novelli, G Articolo su rivista
1-gen-2008 Epidemiology and a novel procedure for large scale analysis of CFTR rearrangements in classic and atypical CF patients: A multicentric Italian study. Tomaiuolo, R; Sangiuolo, Fc; Bombieri, C; Bonizzato, A; Cardillo, G; Raia, V; D'Apice, M; Bettin, M; Pignatti, P; Castaldo, G; Novelli, G Articolo su rivista
1-gen-2008 Diagnostic CFTR mutation analysis D’Apice, M; Novelli, G; Sangiuolo, Fc Articolo su rivista
1-gen-2009 Recessive congenital myotonia resulting from maternal isodisomy of chromosome 7: a case report Bulli, C; Battistella, P; Bordignon, M; Bramanti, P; Novelli, G; Sangiuolo, Fc Articolo su rivista
Mostrati risultati da 41 a 60 di 156
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