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Vincenzo Nigro

Research Profile

Disorders

Chemicals & Drugs

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Molecular Sequence Data

Physiology

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DNA Mutational Analysis

Genes & Molecular Sequences

Amino Acid Sequences

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Annalaura Torella; Corrado Angelini; Francesca Del Vecchio Blanco; Marina Fanin; Arcomaria Garofalo; Lucia Morandi; Margherita Mutarelli; Enrico Peterle; Giulio Piluso; Giulia Ricci; Rossella Rispoli; Marco Savarese; Gabriele Siciliano; Vincenzo Nigro
Next-Generation Sequencing Identifies Transportin 3 as the Causative Gene for LGMD1F.
Ivana Peluso; Mariateresa Pizzo; Francesca Simonelli; Francesco Testa; Carmela Ziviello; Anna Maria Barbarulo; Sara Barbato; Rob W J Collin; Ivan Conte; Gopuraja Dharmalingam; Mariarosa A B Melone; Nicola Meola; Margherita Mutarelli; Vincenzo Nigro; Sandro Banfi
The ADAMTS18 gene is responsible for autosomal recessive early onset severe retinal dystrophy.
Vincenzo Nigro; Giulio Piluso
Next generation sequencing (NGS) strategies for the genetic testing of myopathies.

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All Publications

2013: Annalaura Torella; Corrado Angelini; Francesca Del Vecchio Blanco; Marina Fanin; Arcomaria Garofalo; Lucia Morandi; Margherita Mutarelli; Enrico Peterle; Giulio Piluso; Giulia Ricci; Rossella Rispoli; Marco Savarese; Gabriele Siciliano; Vincenzo Nigro
Next-Generation Sequencing Identifies Transportin 3 as the Causative Gene for LGMD1F.
PloS one 2013;8(5):e63536.
2013: Ivana Peluso; Mariateresa Pizzo; Francesca Simonelli; Francesco Testa; Carmela Ziviello; Anna Maria Barbarulo; Sara Barbato; Rob W J Collin; Ivan Conte; Gopuraja Dharmalingam; Mariarosa A B Melone; Nicola Meola; Margherita Mutarelli; Vincenzo Nigro; Sandro Banfi
The ADAMTS18 gene is responsible for autosomal recessive early onset severe retinal dystrophy.
Orphanet journal of rare diseases 2013;8():16.
2012: Vincenzo Nigro; Giulio Piluso
Next generation sequencing (NGS) strategies for the genetic testing of myopathies.
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology / edited by the Gaetano Conte Academy for the study of striated muscle diseases 2012;31(3):196-200.
2012: Luca Bello; Enrico Bertini; Adele D'Amico; Bruno F Gavassini; Emanuela Leonardi; Paola Melacini; Vincenzo Nigro; Arianna Palmieri; raffaele pezzani; Luisa Piva; Gessica Smaniotto; Gianni Soraru; Annalaura Torella; Silvio C E Tosatto; Andrea Vianello; Corrado Angelini; Elena Pegoraro
Cardiomyopathy in patients with POMT1-related congenital and limb-girdle muscular dystrophy.
European journal of human genetics : EJHG 2012;20(12):1234-9.
2012: Vincenzo Nigro
Improving the course of muscular dystrophy?
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology / edited by the Gaetano Conte Academy for the study of striated muscle diseases 2012;31(2):109.
2012: Marco Savarese; Annalaura Torella; Marcella Zollino; Daniela Orteschi; Giulio Piluso; Francesca del Vecchio Blanco; Giuseppina Di Fruscio; Manuela Dionisi; Teresa Giugliano; Michele Iacomino; Giovanni Neri; Vincenzo Nigro
Enhancer chip: detecting human copy number variations in regulatory elements.
PloS one 2012;7(12):e52264.
2011: Corrado Angelini; Wolfgang Grisold; Vincenzo Nigro
Diagnosis by protein analysis of dysferlinopathy in two patients mistaken as polymyositis.
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology / edited by the Gaetano Conte Academy for the study of striated muscle diseases 2011;30(3):185-7.
2011: Alessio Lancioni; Ida Luisa Rotundo; Yvonne Monique Kobayashi; Gerardo Nigro; Dario Acampora; Stefania Aurino; Mafalda Cacciottolo; Kevin P Campbell; Luca D'Orsi; Giulio Piluso; Vincenzo Nigro
Combined deficiency of alpha and epsilon sarcoglycan disrupts the cardiac dystrophin complex.
Human molecular genetics 2011;20(23):4644-54.
2011: Giulio Piluso; Luisa Politano; Filippo Maria Santorelli; Marco Savarese; Alessandra Terracciano; Annalaura Torella; Mariz Vainzof; Stefania Aurino; Enrico Bertini; Carlo Casali; Chiara Criscuolo; Francesca Del Vecchio Blanco; Manuela Dionisi; Teresa Giugliano; Vincenzo Nigro
Motor chip: a comparative genomic hybridization microarray for copy-number mutations in 245 neuromuscular disorders.
Clinical chemistry 2011;57(11):1584-96.
2011: Roberta Roncarati; Annalaura Torella; Massimo Volpe; Stefania Aurino; Camillo Autore; Marie-Louise Bang; Gloria Saccani Jotti; Michael V G Latronico; Beatrice Musumeci; Vincenzo Nigro; Annibale A Puca; Gianluigi Condorelli
Unexpectedly low mutation rates in beta-myosin heavy chain and cardiac myosin binding protein genes in Italian patients with hypertrophic cardiomyopathy.
Journal of cellular physiology 2011;226(11):2894-900.
2011: Vincenzo Nigro; Stefania Aurino; Giulio Piluso
Limb girdle muscular dystrophies: update on genetic diagnosis and therapeutic approaches.
Current opinion in neurology 2011;24(5):429-36.
2011: Mafalda Cacciottolo; Imma Rosaria Caserta; Marina Fanin; Carlo Minetti; Gelsomina Numitone; Giulio Piluso; Luisa Politano; Enzo Ricci; Corrado Angelini; Stefania Aurino; Vincenzo Nigro
Muscular dystrophy with marked Dysferlin deficiency is consistently caused by primary dysferlin gene mutations.
European journal of human genetics : EJHG 2011;19(9):974-80.
2011: A Tammaro; Antonietta Di Martino; A Bracco; Santolo Cozzolino; G Savoia; B Andria; A Cannavo; M Spagnuolo; Giulio Piluso; Stefania Aurino; Vincenzo Nigro
Novel missense mutations and unexpected multiple changes of RYR1 gene in 75 malignant hyperthermia families.
Clinical genetics 2011;79(5):438-47.
2011: Ida Luisa Rotundo; Fabio Russo; Vincenzo Russo; Carmen Vitiello; Giulio Piluso; Alberto Auricchio; Sigismondo Castaldo; Elvira De Leonibus; Daniele Di Napoli; Stefania Faraso; Alessio Lancioni; Gerardo Nigro; Vincenzo Nigro
Worsening of cardiomyopathy using deflazacort in an animal model rescued by gene therapy.
PloS one 2011;6(9):e24729.
2010: Raoul Jean Pierre Bonnal; Marco Severgnini; Alessandra Castaldi; Roberta Bordoni; Michele Iacono; Amelia Trimarco; Annalaura Torella; Giulio Piluso; Stefania Aurino; Gianluigi Condorelli; De Bellis Gianluca; Vincenzo Nigro
Reliable resequencing of the human dystrophin locus by universal long polymerase chain reaction and massive pyrosequencing.
Analytical biochemistry 2010;406(2):176-84.
2010: Giulio Piluso; I L Rotundo; A Torella; Stefania Aurino; M Cacciottolo; F Del Vecchio Blanco; A Lancioni; Vincenzo Nigro
Mendelian bases of myopathies, cardiomyopathies, and neuromyopathies.
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology / edited by the Gaetano Conte Academy for the study of striated muscle diseases 2010;29(1):1-20.
2010: Lucio Santoro; Maria Nolano; Stefania Faraso; Chiara Fiorillo; Carmen Vitiello; Vincenzo Provitera; Stefania Aurino; Vincenzo Nigro
Perioral skin biopsy to study skeletal muscle protein expression.
Muscle & nerve 2010;41(3):392-8.
2010: Gerardo Nigro; Vincenzo Russo; Vega Maria Ventriglia; Nadia Della Cioppa; A Palladino; Vincenzo Nigro; Raffaele Calabrò; Giovanni Nigro; Luisa Politano
Early onset of cardiomyopathy and primary prevention of sudden death in X-linked Emery-Dreifuss muscular dystrophy.
Neuromuscular disorders : NMD 2010;20(3):174-7.
2010: Annalaura Torella; Amelia Trimarco; Francesca Del Vecchio Blanco; Anna Cuomo; Stefania Aurino; Giulio Piluso; Carlo Minetti; Luisa Politano; Vincenzo Nigro
One hundred twenty-one dystrophin point mutations detected from stored DNA samples by combinatorial denaturing high-performance liquid chromatography.
The Journal of molecular diagnostics : JMD 2010;12(1):65-73.
2009: Marina Fanin; Anna Chiara Nascimbeni; S Aurino; E Tasca; Elena Pegoraro; Vincenzo Nigro; Corrado Angelini
Frequency of LGMD gene mutations in Italian patients with distinct clinical phenotypes.
Neurology 2009;72(16):1432-5.
2009: Giulio Piluso; Francesca D'Amico; Valentina Saccone; Ettore Bismuto; Ida Luisa Rotundo; Marina Di Domenico; Stefania Aurino; Charles E Schwartz; Giovanni Neri; Vincenzo Nigro
A missense mutation in CASK causes FG syndrome in an Italian family.
American journal of human genetics 2009;84(2):162-77.
2009: Carmen Vitiello; Stefania Faraso; Nicolina Cristina Sorrentino; Giovanni Di Salvo; Edoardo Nusco; Gerardo Nigro; Luisa Cutillo; Raffaele Calabrò; Alberto Auricchio; Vincenzo Nigro
Disease rescue and increased lifespan in a model of cardiomyopathy and muscular dystrophy by combined AAV treatments.
PloS one 2009;4(3):e5051.
2008: S Aurino; Giulio Piluso; V Saccone; M Cacciottolo; F D'Amico; M Dionisi; A Totaro; A Belsito; Umberto Di Vicino; Vincenzo Nigro
Candidate-gene testing for orphan limb-girdle muscular dystrophies.
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology / edited by the Gaetano Conte Academy for the study of striated muscle diseases 2008;27():90-7.
2008: Valentina Saccone; Michela Palmieri; Luigia Passamano; Giulio Piluso; Germana Meroni; Luisa Politano; Vincenzo Nigro
Mutations that impair interaction properties of TRIM32 associated with limb-girdle muscular dystrophy 2H.
Human mutation 2008;29(2):240-7.
2006: Lucio Santoro; Fiore Manganelli; Roberta Lanzillo; Alessandra Tessa; Fabrizio Barbieri; F Pierelli; G Di Giacinto; Vincenzo Nigro; Filippo M Santorelli
A new POLG1 mutation with peo and severe axonal and demyelinating sensory-motor neuropathy.
Journal of neurology 2006;253(7):869-74.
2006: Stefania Aurino; Vincenzo Nigro
Readthrough strategies for stop codons in Duchenne muscular dystrophy.
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology / edited by the Gaetano Conte Academy for the study of striated muscle diseases 2006;25(1):5-12.
2006: Burcu Balci; Stefania Aurino; Göknur Haliloglu; Beril Talim; Sevim Erdem; Zuhal Akcören; Ersin Tan; Melda Caglar; Isabelle Richard; Vincenzo Nigro; Haluk Topaloglu; Pervin Dincer
Calpain-3 mutations in Turkey.
European journal of pediatrics 2006;165(5):293-8.
2006: Roberta Lanzillo; Stefania Aurino; Marina Fanin; M Aguennoz; F Vitale; Chiara Fiorillo; Emanuele Miraglia del Giudice; Vincenzo Nigro; Lucio Santoro
Early onset calpainopathy with normal non-functional calpain 3 level.
Developmental medicine and child neurology 2006;48(4):304-6.
2005: Giulio Piluso; Luisa Politano; Stefania Aurino; Marina Fanin; Enzo Ricci; V M Ventriglia; A Belsito; A Totaro; V Saccone; Haluk Topaloglu; Anna Chiara Nascimbeni; Luigi Fulizio; A Broccolini; Nina Canki-Klain; Lucia I Comi; Ge Nigro; Corrado Angelini; Vincenzo Nigro
Extensive scanning of the calpain-3 gene broadens the spectrum of LGMD2A phenotypes.
Journal of medical genetics 2005;42(9):686-93.
2005: Dirk Fischer; Maggie C Walter; Kristina Kesper; Jens A Petersen; Stefania Aurino; Vincenzo Nigro; Christian Kubisch; Thomas Meindl; Hanns Lochmüller; Kai Wilhelm; Horst Urbach; Rolf Schröder
Diagnostic value of muscle MRI in differentiating LGMD2I from other LGMDs.
Journal of neurology 2005;252(5):538-47.
2005: Eugenio Mercuri; Kate Bushby; Enzo Ricci; Daniel Birchall; Marika Pane; Maria Kinali; Joanna M Allsop; Vincenzo Nigro; Amets Sáenz; Anna Chiara Nascimbeni; Luigi Fulizio; Corrado Angelini; Francesco Muntoni
Muscle MRI findings in patients with limb girdle muscular dystrophy with calpain 3 deficiency (LGMD2A) and early contractures.
Neuromuscular disorders : NMD 2005;15(2):164-71.
2005: Luigi Fulizio; Anna Chiara Nascimbeni; Marina Fanin; Giulio Piluso; Luisa Politano; Vincenzo Nigro; Corrado Angelini
Molecular and muscle pathology in a series of caveolinopathy patients.
Human mutation 2005;25(1):82-9.
2004: Burcu Balci; E Wilichowski; G Haliloğlu; Beril Talim; Stefania Aurino; E Kremer; F Ebinger; Nesrin Senbil; Banu Anlar; Gülsev Kale; Vincenzo Nigro; H Topaloğlu; C Bonnemann; Pervin Dinçer
Beta-sarcoglycan gene mutations in Turkey.
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology / edited by the Gaetano Conte Academy for the study of striated muscle diseases 2004;23(3):154-8.
2004: Marina Fanin; Luigi Fulizio; Anna Chiara Nascimbeni; Marco Spinazzi; Giulio Piluso; V M Ventriglia; G Ruzza; Gabriele Siciliano; Carlo Pietro Trevisan; Luisa Politano; Vincenzo Nigro; Corrado Angelini
Molecular diagnosis in LGMD2A: mutation analysis or protein testing?
Human mutation 2004;24(1):52-62.
2003: Dirk Fischer; Stefania Aurino; Vincenzo Nigro; Rolf Schröder
On symptomatic heterozygous alpha-sarcoglycan gene mutation carriers.
Annals of neurology 2003;54(5):674-8.
2003: Vincenzo Nigro
Molecular bases of autosomal recessive limb-girdle muscular dystrophies.
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology / edited by the Gaetano Conte Academy for the study of striated muscle diseases 2003;22(2):35-42.
2003: Luisa Politano; Ge Nigro; Vincenzo Nigro; Giulio Piluso; Serenella Papparella; Orlando Paciello; Lucia I Comi
Gentamicin administration in Duchenne patients with premature stop codon. Preliminary results.
Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology / edited by the Gaetano Conte Academy for the study of striated muscle diseases 2003;22(1):15-21.
2003: Angela Tammaro; Adele Bracco; Santolo Cozzolino; Maria Esposito; Antonietta Di Martino; Gennaro Savoia; Laura Zeuli; Giulio Piluso; Stefania Aurino; Vincenzo Nigro
Scanning for mutations of the ryanodine receptor (RYR1) gene by denaturing HPLC: detection of three novel malignant hyperthermia alleles.
Clinical chemistry 2003;49(5):761-8.
2003: Giulio Piluso; Massimo Carella; Michele D'Avanzo; Raffaele Santinelli; Elena Maria Carrano; Angelo D'Avanzo; Adamo Pio D'Adamo; Paolo Gasparini; Vincenzo Nigro
Genetic heterogeneity of FG syndrome: a fourth locus (FGS4) maps to Xp11.4-p11.3 in an Italian family.
Human genetics 2003;112(2):124-30.
2002: Carlo Nobile; Luisa Toffolatti; Francesca Rizzi; Barbara Simionati; Vincenzo Nigro; Barbara Cardazzo; Tomaso Patarnello; Giorgio Valle; Gian Antonio Danieli
Analysis of 22 deletion breakpoints in dystrophin intron 49.
Human genetics 2002;110(5):418-21.
2001: Luisa Politano; Vincenzo Nigro; Luigia Passamano; Vito R Petretta; Lucia I Comi; Serenella Papparella; Ge Nigro; Pier Francesco Rambaldi; P Raia; Antonella Pini; Marina Mora; M A Giugliano; M G Esposito; G Nigro
Evaluation of cardiac and respiratory involvement in sarcoglycanopathies.
Neuromuscular disorders : NMD 2001;11(2):178-85.
2000: Pervin Dinçer; C G Bönnemann; O Erdir Aker; Z Akçoren; Vincenzo Nigro; Louis Kunkel; H Topalolu
A homozygous nonsense mutation in delta-sarcoglycan exon 3 in a case of LGMD2F.
Neuromuscular disorders : NMD 2000;10(4-5):247-50.
2000: Giulio Piluso; Massimiliano Mirabella; Enzo Ricci; A Belsito; Ciro Abbondanza; Serenella Servidei; AA Puca; P Tonali; Giovanni Alfredo Puca; Vincenzo Nigro
Gamma1- and gamma2-syntrophins, two novel dystrophin-binding proteins localized in neuronal cells.
The Journal of biological chemistry 2000;275(21):15851-60.
2000: Anna Maria Molinari; Paola Bontempo; Ettore Mariano Schiavone; V Tortora; M A Verdicchio; M Napolitano; E Nola; Bruno Moncharmont; Nicola Medici; Vincenzo Nigro; I Armetta; Ciro Abbondanza; Giovanni Alfredo Puca
Estradiol induces functional inactivation of p53 by intracellular redistribution.
Cancer research 2000;60(10):2594-7.
2000: Ciro Abbondanza; Nicola Medici; Vincenzo Nigro; V Rossi; L Gallo; Giulio Piluso; A Belsito; A Roscigno; Paola Bontempo; AA Puca; Anna Maria Molinari; Bruno Moncharmont; Giovanni Alfredo Puca
The retinoblastoma-interacting zinc-finger protein RIZ is a downstream effector of estrogen action.
Proceedings of the National Academy of Sciences of the United States of America 2000;97(7):3130-5.
1999: Nicola Medici; Ciro Abbondanza; Vincenzo Nigro; V Rossi; Giulio Piluso; A Belsito; L Gallo; A Roscigno; Paola Bontempo; AA Puca; Anna Maria Molinari; Bruno Moncharmont; Giovanni Alfredo Puca
Identification of a DNA binding protein cooperating with estrogen receptor as RIZ (retinoblastoma interacting zinc finger protein).
Biochemical and biophysical research communications 1999;264(3):983-9.
1999: Simone Sampaolo; AA Puca; Vincenzo Nigro; V Cappa; Vincenzo Sannino; G Sanges; Vincenzo Bonavita; Giuseppe Di Iorio
Lack of sodium channel mutation in an Italian family with paramyotonia congenita.
Neurology 1999;53(7):1549-55.
1998: Ciro Abbondanza; V Rossi; A Roscigno; L Gallo; A Belsito; Giulio Piluso; Nicola Medici; Vincenzo Nigro; Anna Maria Molinari; Bruno Moncharmont; Giovanni Alfredo Puca
Interaction of vault particles with estrogen receptor in the MCF-7 breast cancer cell.
The Journal of cell biology 1998;141(6):1301-10.
1998: AA Puca; Vincenzo Nigro; Giulio Piluso; A Belsito; Simone Sampaolo; NA Quaderi; E Rossi; Giuseppe Di Iorio; Andrea Ballabio; Brunella Franco
Identification and characterization of a novel member of the dystrobrevin gene family.
FEBS letters 1998;425(1):7-13.
1997: Carlo Nobile; J Marchi; Vincenzo Nigro; Roland Roberts; Gian Antonio Danieli
Exon-intron organization of the human dystrophin gene.
Genomics 1997;45(2):421-4.
1997: Marina Mora; Luca Cartegni; Claudia Di Blasi; Rita Barresi; Silvia Bione; Marina Raffaele di Barletta; Lucia Morandi; Luciano Merlini; Vincenzo Nigro; Luisa Politano; Maria Alice Donati; Ferdinando Cornelio; Fabio Cobianchi; Daniela Toniolo
X-linked Emery-Dreifuss muscular dystrophy can be diagnosed from skin biopsy or blood sample.
Annals of neurology 1997;42(2):249-53.
1997: Vincenzo Nigro; Yasushi Okazaki; A Belsito; Giulio Piluso; Y Matsuda; Luisa Politano; Ge Nigro; C Ventura; Ciro Abbondanza; Anna Maria Molinari; D Acampora; M Nishimura; Y Hayashizaki; Giovanni Alfredo Puca
Identification of the Syrian hamster cardiomyopathy gene.
Human molecular genetics 1997;6(4):601-7.
1997: Mikiharu Yoshida; Satoru Noguchi; E Wakabayashi; Giulio Piluso; A Belsito; Vincenzo Nigro; Eijiro Ozawa
The fourth component of the sarcoglycan complex.
FEBS letters 1997;403(2):143-8.
1996: Mariz Vainzof; Maria Rita Passos-Bueno; M Canovas; Eloisa S Moreira; Rita C M Pavanello; Suely K N Marie; Louise V B Anderson; C G Bonnemann; Elizabeth McNally; Vincenzo Nigro; Louis Kunkel; Mayana Zatz
The sarcoglycan complex in the six autosomal recessive limb-girdle muscular dystrophies.
Human molecular genetics 1996;5(12):1963-9.
1996: A Micali; Nicola Medici; A Sottile; M Venza; I Venza; Vincenzo Nigro; Giovanni Alfredo Puca; Diana Teti
Prostaglandin E2 induction of binding activity to CRE and AP-2 elements in human T lymphocytes.
Cellular immunology 1996;174(1):99-105.
1996: Vincenzo Nigro; E de Sá Moreira; Giulio Piluso; Mariz Vainzof; A Belsito; Luisa Politano; AA Puca; Maria Rita Passos-Bueno; Mayana Zatz
Autosomal recessive limb-girdle muscular dystrophy, LGMD2F, is caused by a mutation in the delta-sarcoglycan gene.
Nature genetics 1996;14(2):195-8.
1996: Vincenzo Nigro; Giulio Piluso; A Belsito; Luisa Politano; AA Puca; Serenella Papparella; E Rossi; G Viglietto; M G Esposito; Ciro Abbondanza; Nicola Medici; Anna Maria Molinari; Ge Nigro; Giovanni Alfredo Puca
Identification of a novel sarcoglycan gene at 5q33 encoding a sarcolemmal 35 kDa glycoprotein.
Human molecular genetics 1996;5(8):1179-86.
1996: Luisa Politano; Vincenzo Nigro; Ge Nigro; Vito R Petretta; L Passamano; Serenella Papparella; S Di Somma; L I Comi
Development of cardiomyopathy in female carriers of Duchenne and Becker muscular dystrophies.
JAMA : the journal of the American Medical Association 1996;275(17):1335-8.
1996: S Brunelli; Antonio Faiella; V Capra; Vincenzo Nigro; A Simeone; Armando Cama; Edoardo Boncinelli
Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly.
Nature genetics 1996;12(1):94-6.
1995: Vincenzo Nigro; P Bruni; Alfredo Ciccodicola; Luisa Politano; Ge Nigro; Giulio Piluso; V Cappa; A E Covone; G Romeo; Michele D'Urso
SSCP detection of novel mutations in patients with Emery-Dreifuss muscular dystrophy: definition of a small C-terminal region required for emerin function.
Human molecular genetics 1995;4(10):2003-4.
1995: A Simeone; V Avantaggiato; M C Moroni; F Mavilio; C Arra; F Cotelli; Vincenzo Nigro; Dario Acampora
Retinoic acid induces stage-specific antero-posterior transformation of rostral central nervous system.
Mechanisms of development 1995;51(1):83-98.
1995: Ge Nigro; L I Comi; Luisa Politano; F M Limongelli; Vincenzo Nigro; M L De Rimini; M A Giugliano; Vito R Petretta; L Passamano; Brunella Restucci
Evaluation of the cardiomyopathy in Becker muscular dystrophy.
Muscle & nerve 1995;18(3):283-91.
1995: Ge Nigro; L I Comi; Luisa Politano; Vincenzo Nigro
Dilated cardiomyopathy of muscular dystrophy: a multifaceted approach to management.
Seminars in neurology 1995;15(1):90-2.
1994: Vincenzo Nigro; Ge Nigro; M G Esposito; L I Comi; Anna Maria Molinari; Giovanni Alfredo Puca; Luisa Politano
Novel small mutations along the DMD/BMD gene associated with different phenotypes.
Human molecular genetics 1994;3(10):1907-8.
1994: Ge Nigro; Luisa Politano; Vincenzo Nigro; Vito R Petretta; L I Comi
Mutation of dystrophin gene and cardiomyopathy.
Neuromuscular disorders : NMD 1994;4(4):371-9.
1994: A Simeone; M R D'Apice; Vincenzo Nigro; J Casanova; Franco Graziani; Dario Acampora; V Avantaggiato
Orthopedia, a novel homeobox-containing gene expressed in the developing CNS of both mouse and Drosophila.
Neuron 1994;13(1):83-101.
1994: Vincenzo Nigro; M Napolitano; Ciro Abbondanza; Nicola Medici; AA Puca; M Schiavulli; I Armetta; Bruno Moncharmont; Giovanni Alfredo Puca; Anna Maria Molinari
A novel p53 mutant in human breast cancer revealed by multiple SSCP analysis.
Cancer letters 1994;79(1):73-5.
1993: A Simeone; Dario Acampora; Antonello Mallamaci; A Stornaiuolo; M R D'Apice; Vincenzo Nigro; Edoardo Boncinelli
A vertebrate gene related to orthodenticle contains a homeodomain of the bicoid class and demarcates anterior neuroectoderm in the gastrulating mouse embryo.
The EMBO journal 1993;12(7):2735-47.
1993: Ciro Abbondanza; A de Falco; Vincenzo Nigro; Nicola Medici; I Armetta; Anna Maria Molinari; Bruno Moncharmont; Giovanni Alfredo Puca
Characterization and epitope mapping of a new panel of monoclonal antibodies to estradiol receptor.
Steroids 1993;58(1):4-12.
1992: Vincenzo Nigro; Luisa Politano; Ge Nigro; S C Romano; Anna Maria Molinari; Giovanni Alfredo Puca
Detection of a nonsense mutation in the dystrophin gene by multiple SSCP.
Human molecular genetics 1992;1(7):517-20.
1992: Vincenzo Nigro; Anna Maria Molinari; I Armetta; A de Falco; Ciro Abbondanza; Nicola Medici; Giovanni Alfredo Puca
Purified estrogen receptor enhances in vitro transcription.
Biochemical and biophysical research communications 1992;186(2):803-10.
1991: Anna Maria Molinari; Ciro Abbondanza; I Armetta; Nicola Medici; S Minucci; Bruno Moncharmont; Vincenzo Nigro; Giovanni Alfredo Puca
Proteolytic activity of the purified hormone-binding subunit in the estrogen receptor.
Proceedings of the National Academy of Sciences of the United States of America 1991;88(10):4463-7.
1991: Nicola Medici; Vincenzo Nigro; Ciro Abbondanza; Bruno Moncharmont; Anna Maria Molinari; Giovanni Alfredo Puca
In vitro binding of the purified hormone-binding subunit of the estrogen receptor to oligonucleotides containing natural or modified sequences of an estrogen-responsive element.
Molecular endocrinology (Baltimore, Md.) 1991;5(4):555-63.
1991: A Simeone; Dario Acampora; Vincenzo Nigro; Antonio Faiella; Maurizio D'Esposito; A Stornaiuolo; F Mavilio; Edoardo Boncinelli
Differential regulation by retinoic acid of the homeobox genes of the four HOX loci in human embryonal carcinoma cells.
Mechanisms of development 1991;33(3):215-27.
1990: A Stornaiuolo; Dario Acampora; M Pannese; Maurizio D'Esposito; F Morelli; E Migliaccio; M Rambaldi; Antonio Faiella; Vincenzo Nigro; A Simeone
Human HOX genes are differentially activated by retinoic acid in embryonal carcinoma cells according to their position within the four loci.
Cell differentiation and development : the official journal of the International Society of Developmental Biologists 1990;31(2):119-27.
1990: Vincenzo Nigro; Nicola Medici; Ciro Abbondanza; S Minucci; Bruno Moncharmont; Anna Maria Molinari; Giovanni Alfredo Puca
An aprotinin binding site localized in the hormone binding domain of the estrogen receptor from calf uterus.
Biochemical and biophysical research communications 1990;170(2):930-6.
1989: Dario Acampora; Maurizio D'Esposito; Antonio Faiella; M Pannese; E Migliaccio; F Morelli; A Stornaiuolo; Vincenzo Nigro; A Simeone; Edoardo Boncinelli
The human HOX gene family.
Nucleic acids research 1989;17(24):10385-402.
1989: Vincenzo Nigro; Nicola Medici; Ciro Abbondanza; S Minucci; Anna Maria Molinari; Giovanni Alfredo Puca
Aprotinin inhibits the hormone binding of the estrogen receptor from calf uterus.
Biochemical and biophysical research communications 1989;164(3):1206-11.
1989: Nicola Medici; S Minucci; Vincenzo Nigro; Ciro Abbondanza; I Armetta; Anna Maria Molinari; Giovanni Alfredo Puca
Metal binding sites of the estradiol receptor from calf uterus and their possible role in the regulation of receptor function.
Biochemistry 1989;28(1):212-9.
1986: Giovanni Alfredo Puca; Ciro Abbondanza; Vincenzo Nigro; I Armetta; Nicola Medici; Anna Maria Molinari
Estradiol receptor has proteolytic activity that is responsible for its own transformation.
Proceedings of the National Academy of Sciences of the United States of America 1986;83(15):5367-71.
1986: Giovanni Alfredo Puca; Nicola Medici; I Armetta; Vincenzo Nigro; Bruno Moncharmont; Anna Maria Molinari
Interaction between estrogen receptor and subcellular structures of target cells: nuclear localization of unoccupied receptor and its modification induced by estradiol.
Annals of the New York Academy of Sciences 1986;464():168-89.
1985: Anna Maria Molinari; Nicola Medici; I Armetta; Vincenzo Nigro; Bruno Moncharmont; Giovanni Alfredo Puca
Particulate nature of the unoccupied uterine estrogen receptor.
Biochemical and biophysical research communications 1985;128(2):634-42.