Vincenzo Nigro
Vincenzo Nigro
Università della Campania "Luigi Vanvitelli" Dipartimento di Medicina di Precisione, and TIGEM
Verified email at unicampania.it
TitleCited byYear
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
5901993
Autosomal recessive limbgirdle muscular dystrophy, LGMD2F, is caused by a mutation in the δ–sarcoglycan gene
V Nigro, E de Sá Moreira, G Piluso, M Vainzof, A Belsito, L Politano, ...
Nature genetics 14 (2), 195, 1996
4891996
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
3421989
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, 1996
3101996
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
2901991
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
2831997
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
2111996
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
1981996
Genetic basis of limb-girdle muscular dystrophies: the 2014 update
V Nigro, M Savarese
Acta Myologica 33 (1), 1, 2014
1962014
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
1962003
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
1881996
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
1761994
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
1541995
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
1372005
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
1342001
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
1322000
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 (5), 538-547, 2005
1262005
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
1251995
Mutation of dystrophin gene and cardiomyopathy
G Nigro, L Politano, V Nigro, VR Petretta, LI Comi
Neuromuscular Disorders 4 (4), 371-379, 1994
1171994
Low frequency of melanocortin-4 receptor (MC4R) mutations in a Mediterranean population with early-onset obesity
EM Del Giudice, G Cirillo, V Nigro, N Santoro, L D'urso, P Raimondo, ...
International journal of obesity 26 (5), 647, 2002
1132002
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