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VITIELLO LIBERO: PUBBLICAZIONI

1 Saad FA, Vitiello L, Merlini L, Mostacciuolo ML, Oliviero S, Danieli GA.
A 3' consensus splice mutation in the human dystrophin gene detected by a screening for intra-exonic deletions.
HUM MOL GENET. Aug 1992; 1(5): 345-6
2 Vitiello L, Mostacciuolo ML, Oliviero S, Schiavon F, Nicoletti L, Angelini C, Danieli GA.
Screening for mutations in the muscle promoter region and for exonic deletions in a series of 115 DMD and BMD patients.
J MED GENET. Feb 1992; 29(2): 127-30
3 Fanin M, Danieli GA, Vitiello L, Senter L, Angelini C.
Prevalence of dystrophin-positive fibers in 85 Duchenne muscular dystrophy patients.
NEUROMUSCULAR DISORD. 1992; 2(1): 41-5
4 Melacini P, Fanin M, Danieli GA, Fasoli G, Villanova C, Angelini C, Vitiello L, Miorelli M, Buja GF, Mostacciuolo ML.
Cardiac involvement in Becker muscular dystrophy.
J AM COLL CARDIOL. Dec 1993; 22(7): 1927-34
5 Saad FA, Busque C, Vitiello L, Danieli GA.
DXS997 localized to intron 48 of dystrophin.
HUM MOL GENET. Dec 1993; 2(12): 2199
6 Saad FA, Vitiello L, Oliviero S, Mostacciuolo ML, Danieli GA.
Detection of unknown gene mutations by multiplex single-strand conformation polymorphism (MSSCP).
PCR METH APPL. Aug 1993; 3(1): 60-2
7 Danieli GA, Mioni F, Müller CR, Vitiello L, Mostacciuolo ML, Grimm T.
Patterns of deletions of the dystrophin gene in different European populations.
HUM GENET. May 1993; 91(4): 342-6
8 Saad FA, Vita G, Mora M, Morandi L, Vitiello L, Oliviero S, Danieli GA.
A novel nonsense mutation in the human dystrophin gene.
HUM MUTAT. 1993; 2(4): 314-6
9 Mostacciuolo ML, Miorin M, Pegoraro E, Fanin M, Schiavon F, Vitiello L, Saad FA, Angelini C, Danieli GA.
Reappraisal of the incidence rate of Duchenne and Becker muscular dystrophies on the basis of molecular diagnosis.
NEUROEPIDEMIOLOGY. 1993; 12(6): 326-30
10 Galvagni F, Saad FA, Danieli GA, Miorin M, Vitiello L, Mostacciuolo ML, Angelini C.
A study on duplications of the dystrophin gene: evidence of a geographical difference in the distribution of breakpoints by intron.
HUM GENET. Jul 1994; 94(1): 83-7
11 Saad FA, Busque C, Vitiello L, Danieli GA.
DXS997 localized to intron 48 of dystrophin.
HUM MOL GENET. Jun 1994; 3(6): 1034
12 Mostacciuolo ML, Miorin M, Vitiello L, Rampazzo A, Fanin M, Angelini C, Danieli GA.
Occurrence of two different intragenic deletions in two male relatives affected with Duchenne muscular dystrophy.
AM J MED GENET. Mar 1994; 50(1): 84-6
13 Mioni F, Danieli GA, Cao A, Cau M, Colonna-romano S, Covone AE, De Leonardis P, De Leo R, Esposito MG, Felicetti L, Et AL, Vitiello L, Zanetti A.
A report on 528 intragenic deletions detected in DMD and BMD patients by an Italian collaborative study.
GENE GEOGR. Apr 1994; 8(1): 35-44
14 Fanin M, Danieli GA, Cadaldini M, Miorin M, Vitiello L, Angelini C.
Dystrophin-positive fibers in Duchenne dystrophy: origin and correlation to clinical course.
MUSCLE NERVE. Oct 1995; 18(10): 1115-20
15 Toscano A, Vitiello L, Comi GP, Galvagni F, Miorin M, Prelle A, Fortunato F, Bardoni A, Mora M, Fiumara A.
Duplication of dystrophin gene and dissimilar clinical phenotype in the same family.
NEUROMUSCULAR DISORD. Nov 1995; 5(6): 475-81
16 Nobile C, Galvagni F, Marchi J, Roberts R, Vitiello L.
Genomic organization of the human dystrophin gene across the major deletion hot spot and the 3' region.
GENOMICS. Jul 1995; 28(1): 97-100
17 Fanin M, Freda MP, Vitiello L, Danieli GA, Pegoraro E, Angelini C.
Duchenne phenotype with in-frame deletion removing major portion of dystrophin rod: threshold effect for deletion size?.
MUSCLE NERVE. Sep 1996; 19(9): 1154-60
18 Vitiello L, Chonn A, Wasserman JD, Duff C, Worton RG.
Condensation of plasmid DNA with polylysine improves liposome-mediated gene transfer into established and primary muscle cells.
GENE THER. May 1996; 3(5): 396-404
19 Miorin M, Todorova A, Vitiello L, Rosa M, Mostacciuolo ML, Danieli GA.
Detection of heterozygotes for intragenic deletions in families with recurrence of Duchenne and Becker muscular dystrophy.
Basic Applied Myology. 1997; 7: 265-269
20 Vitiello L, Bockhold K, Joshi PB, Worton RG.
Transfection of cultured myoblasts in high serum concentration with DODAC:DOPE liposomes.
GENE THER. Oct 1998; 5(10): 1306-13
21 Pampinella F, Pozzobon M, Zanetti E, Gamba PG, Mclachlan I, Cantini M, Vitiello L.
Gene transfer in skeletal muscle by systemic injection of DODAC lipopolyplexes.
NEUROL SCI. 2000; 21(5 Suppl): S967-9
22 Cantini M, Giurisato E, Radu C, Tiozzo S, Pampinella F, Senigaglia D, Zaniolo G, Mazzoleni F, Vitiello L.
Macrophage-secreted myogenic factors: a promising tool for greatly enhancing the proliferative capacity of myoblasts in vitro and in vivo.
NEUROL SCI. Oct 2002; 23(4): 189-94
23 Pampinella F, Lechardeur D, Zanetti E, Maclachlan I, Benharouga M, Lukacs GL, Vitiello L.
Analysis of differential lipofection efficiency in primary and established myoblasts.
MOL THER. Feb 2002; 5(2): 161-9
24 Senigaglia D, Giurisato E, Bon A, Sandri M, Pampinella F, Vitiello L, Cantini M.
Immune-Privileged Sites within Skeletal Muscle: Apoptosis of FasL-Transfected Myoblasts Prevents the Formation of FasL-Expressing Muscle Fibers In Vivo.
Basic Applied Myology. 2002; 12: 101-108
25 Opocher G, Schiavi F, Vettori A, Pampinella F, Vitiello L, Calderan A, Vianello B, Murgia A, Martella M, Taccaliti A, Mantero F, Mostacciuolo ML.
Fine analysis of the short arm of chromosome 1 in sporadic and familial pheochromocytoma.
CLIN ENDOCRINOL. Dec 2003; 59(6): 707-715
26 Vitiello L, Radu C, Malerba A, Segat D, Carraro U, Cantini M, Baroni MD.
Enhancing myoblast proliferation by using myogenic factors: a promising approach for improving fiber regeneration in sport medicine and skeletal muscle diseases.
Basic Applied Myology. 2004; 14(1): 45-51
27 Beffagna G, Occhi G, Nava A, Vitiello L, Ditadi A, Basso C, Bauce B, Carraro G, Thiene G, Towbin JA, Danieli GA, Rampazzo A.
Regulatory mutations in transforming growth factor-beta3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1.
CARDIOVASC RES. Feb 2005; 65(2): 366-73
28 Furlan S, Roncaroli F, Forner F, Vitiello L, Calabria E, Piquer-sirerol S, Valle G, Perez-tur J, Michelucci R, Nobile C.
The LGI1/Epitempin gene encodes two protein isoforms differentially expressed in human brain.
J NEUROCHEM. Jun 2006
29 Boldrin L, Elvassore N, Malerba A, Flaibani M, Cimetta E, Piccoli M, Baroni MD, Gazzola MV, Messina C, Gamba P, Vitiello L, Coppi PD.
Satellite Cells Delivered by Micro-Patterned Scaffolds: A New Strategy for Cell Transplantation in Muscle Diseases.
TISSUE ENG. Dec 2006
30 Fascetti-leon F, Malerba A, Boldrin L, Leone E, Betalli P, Pasut A, Zanon GF, Gamba PG, Vitiello L, De Coppi P.
Murine Muscle Precursor Cells Survived and Integrated in a Cryoinjured Gastroesophageal Junction.
J SURG RES. Jun 2007
31 Boldrin L, Elvassore N, Malerba A, Flaibani M, Cimetta E, Piccoli M, Baroni MD, Gazzola MV, Messina C, Gamba P, Vitiello L, De Coppi P.
Satellite cells delivered by micro-patterned scaffolds: a new strategy for cell transplantation in muscle diseases.
TISSUE ENGINEERING. Feb 2007; 13(2): 253-62
32 Striano P, De Falco A, Diani E, Bovo G, Furlan S, Vitiello L, Pinardi F, Striano S, Michelucci R, De Falco FA, Nobile C.
A Novel Loss-of-Function LGI1 Mutation Linked to Autosomal Dominant Lateral Temporal Epilepsy.
ARCH NEUROL-CHICAGO. Jul 2008; 65(7): 939-42
33 Serena E, Flaibani M, Carnio S, Boldrin L, Vitiello L, De Coppi P, Elvassore N.
Electrophysiologic stimulation improves myogenic potential of muscle precursor cells grown in a 3D collagen scaffold.
NEUROL RES. Mar 2008; 30(2): 207-14
34 Vettor R, Granzotto M, De Stefani D, Trevellin E, Rossato M, Farina MG, Milan G, Pilon C, Nigro A, Federspil G, Vigneri R, Vitiello L, Rizzuto R, Baratta R, Frittitta L.
Loss-of-function mutation of the GPR40 gene associates with abnormal stimulated insulin secretion by acting on intracellular calcium mobilization.
J CLIN ENDOCR METAB. Jun 2008
35 Vitiello L, Bassi N, Campagnolo P, Zaccariotto E, Occhi G, Malerba A, Pigozzo S, Reggiani C, Ausoni S, Zaglia T, Gamba P, Baroni MD, Ditadi AP.
In vivo delivery of naked antisense oligos in aged mdx mice: Analysis of dystrophin restoration in skeletal and cardiac muscle.
NEUROMUSCULAR DISORD. Jul 2008
36 Striano P, De Falco A, Diani E, Bovo G, Furlan S, Vitiello L, Pinardi F, Striano S, Michelucci R, De Falco FA, Nobile C.
A Novel Loss-of-Function LGI1 Mutation Linked to Autosomal Dominant Lateral Temporal Epilepsy.
ARCH NEUROL-CHICAGO. Jul 2008; 65(7): 939-42
37 Boldrin L, Malerba A, Vitiello L, Cimetta E, Piccoli M, Messina C, Gamba PG, Elvassore N, De Coppi P.
Efficient delivery of human single fiber-derived muscle precursor cells via biocompatible scaffold.
CELL TRANSPLANT. 2008; 17(5): 577-84
38 Malerba A, Pasut A, Frigo M, De Coppi P, Baroni MD, Vitiello L.
Macrophage-secreted factors enhance the in vitro expansion of DMD muscle precursor cells while preserving their myogenic potential.
NEUROL RES. Dec 2008
39 Malerba A, Vitiello L, Segat D, Dazzo E, Frigo M, Scambi I, Decoppi P, Boldrin L, Martelli L, Pasut A, Romualdi C, Bellomo G.
Selection of multipotent cells and enhanced muscle reconstruction by myogenic macrophage-secreted factors.
EXP CELL RES. 01 2009; 315(6) Epub: 915-927