Vincenzo Nigro
Vincenzo Nigro
Universitą della Campania "Luigi Vanvitelli" Dipartimento di Medicina di Precisione, and TIGEM
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A vertebrate gene related to orthodenticle contains a homeodomain of the bicoid class and demarcates anterior neuroectoderm in the gastrulating mouse embryo.
A Simeone, D Acampora, A Mallamaci, A Stornaiuolo, MR D'Apice, ...
The EMBO journal 12 (7), 2735-2747, 1993
Autosomal recessive limbgirdle muscular dystrophy, LGMD2F, is caused by a mutation in the δ–sarcoglycan gene
V Nigro, ES Moreira, G Piluso, M Vainzof, A Belsito, L Politano, AA Puca, ...
Nature genetics 14 (2), 195-198, 1996
The human HOX gene family
D Acampora, M D'Esposito, A Faiella, M Pannese, E Migliaccio, F Morelli, ...
Nucleic acids research 17 (24), 10385-10402, 1989
Differential regulation by retinoic acid of the homeobox genes of the four HOX loci in human embryonal carcinoma cells
A Simeone, D Acampora, V Nigro, A Faiella, M D'Esposito, A Stornaiuolo, ...
Mechanisms of development 33 (3), 215-227, 1991
Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly
S Brunelli, A Faiella, V Capra, V Nigro, A Simeone, A Cama, E Boncinelli
Nature genetics 12 (1), 94-96, 1996
Genetic basis of limb-girdle muscular dystrophies: the 2014 update
V Nigro, M Savarese
Acta Myologica 33 (1), 1, 2014
Identification of the Syrian hamster cardiomyopathy gene
V Nigro, Y Okazaki, A Belsito, G Piluso, Y Matsuda, L Politano, G Nigro, ...
Human molecular genetics 6 (4), 601-607, 1997
229th ENMC international workshop: Limb girdle muscular dystrophies–Nomenclature and reformed classification Naarden, the Netherlands, 17–19 March 2017
V Straub, A Murphy, B Udd, A Corrado, S Aymé, C Bönneman, ...
Neuromuscular Disorders 28 (8), 702-710, 2018
ACE2 gene variants may underlie interindividual variability and susceptibility to COVID-19 in the Italian population
E Benetti, R Tita, O Spiga, A Ciolfi, G Birolo, A Bruselles, G Doddato, ...
European Journal of Human Genetics 28 (11), 1602-1614, 2020
Gentamicin administration in Duchenne patients with premature stop codon. Preliminary results.
L Politano, G Nigro, V Nigro, G Piluso, S Papparella, O Paciello, LI Comi
Acta Myologica: Myopathies and Cardiomyopathies: Official Journal of the …, 2003
Development of cardiomyopathy in female carriers of Duchenne and Becker muscular dystrophies
L Politano, V Nigro, G Nigro, VR Petretta, L Passamano, S Papparella, ...
Jama 275 (17), 1335-1338, 1996
Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein
V Nigro, G Piluso, A Belsito, L Politano, AA Puca, S Papparella, E Rossi, ...
Human molecular genetics 5 (8), 1179-1186, 1996
The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies
M Vainzof, MR Passos-Bueno, M Canovas, ES Moreira, RCM Pavanello, ...
Human molecular genetics 5 (12), 1963-1969, 1996
Orthopedia, a novel homeobox-containing gene expressed in the developing CNS of both mouse and Drosophila
A Simeone, MR D'Apice, V Nigro, J Casanova, F Graziani, D Acampora, ...
Neuron 13 (1), 83-101, 1994
Muscle MRI findings in patients with limb girdle muscular dystrophy with calpain 3 deficiency (LGMD2A) and early contractures
E Mercuri, K Bushby, E Ricci, D Birchall, M Pane, M Kinali, J Allsop, ...
Neuromuscular Disorders 15 (2), 164-171, 2005
Evaluation of cardiac and respiratory involvement in sarcoglycanopathies
L Politano, V Nigro, L Passamano, V Petretta, LI Comi, S Papparella, ...
Neuromuscular disorders 11 (2), 178-185, 2001
Retinoic acid induces stage-specific antero-posterior transformation of rostral central nervous system
A Simeone, V Avantaggiato, MC Moroni, F Mavilio, C Arra, F Cotelli, ...
Mechanisms of development 51 (1), 83-98, 1995
γ1-and γ2-syntrophins, two novel dystrophin-binding proteins localized in neuronal cells
G Piluso, M Mirabella, E Ricci, A Belsito, C Abbondanza, S Servidei, ...
Journal of Biological Chemistry 275 (21), 15851-15860, 2000
Diagnostic value of muscle MRI in differentiating LGMD2I from other LGMDs
D Fischer, MC Walter, K Kesper, JA Petersen, S Aurino, V Nigro, ...
Journal of neurology 252, 538-547, 2005
Evaluation of the cardiomyopathy in Becker muscular dystrophy
G Nigro, LI Comi, L Politano, FM Limongelli, V Nigro, ML De Rimini, ...
Muscle & Nerve: Official Journal of the American Association of …, 1995
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