Works matching AU Gullotta, Francesca

Results: 18

Hyperproliferation in Nasal Polyposis Tissues Is Not Associated with Somatic Genomic Instability.

Published in:

Journal of Otolaryngology -- Head & Neck Surgery, 2008, v. 37, n. 4, p. 510, doi. 10.2310/7070.2008.0097

By:

Corradini, Carlo;
Gullotta, Francesca;
Ciacci, Silvia;
Palmieri, Giampiero;
Salehi, Leila Baghernajad;
De Corso, Eugenio;
Novelli, Giuseppe;
Gambardella, Stefano

Publication type:

Article

Ibuprofen binding to secondary sites allosterically modulates the spectroscopic and catalytic properties of human serum heme-albumin.

Published in:

FEBS Journal, 2011, v. 278, n. 4, p. 654, doi. 10.1111/j.1742-4658.2010.07986.x

By:

di Masi, Alessandra;
Gullotta, Francesca;
Bolli, Alessandro;
Fanali, Gabriella;
Fasano, Mauro;
Ascenzi, Paolo

Publication type:

Article

Reductive nitrosylation of ferric human serum heme-albumin.

Published in:

FEBS Journal, 2010, v. 277, n. 11, p. 2474, doi. 10.1111/j.1742-4658.2010.07662.x

By:

Ascenzi, Paolo;
Yu Cao;
di Masi, Alessandra;
Gullotta, Francesca;
De Sanctis, Giampiero;
Fanali, Gabriella;
Fasano, Mauro;
Coletta, Massimo

Publication type:

Article

Design, Construction and Validation of Targeted BAC Array-Based CGH Test for Detecting the Most Commons Chromosomal Abnormalities.

Published in:

Genomics Insights, 2010, n. 3, p. 9

By:

Gambardella, Stefano;
Ciabattoni, Erika;
Motta, Francesca;
Stoico, Giusy;
Gullotta, Francesca;
Biancolella, Michela;
Nardone, Anna Maria;
Novelli, Antonio;
Brunetti, Ercole;
Bernardini, Laura;
Novelli, Giuseppe

Publication type:

Article

CO metabolism, sensing, and signaling.

Published in:

Biofactors, 2012, v. 38, n. 1, p. 1, doi. 10.1002/biof.192

By:

Gullotta, Francesca;
di Masi, Alessandra;
Coletta, Massimo;
Ascenzi, Paolo

Publication type:

Article

Use of chromosome painting for detecting stable chromosome aberrations induced by melphalan in mice.

Published in:

Environmental & Molecular Mutagenesis, 2005, v. 45, n. 5, p. 419

By:

Antonella Sgura;
Laura Stronati;
Francesca Gullotta;
Andrea Pecis;
Serena Cinelli;
Antonella Lascialfari;
Caterina Tanzarella;
Francesca Pacchierotti

Publication type:

Article

Compound heterozygosity for mutations in LMNA in a patient with a myopathic and lipodystrophic mandibuloacral dysplasia type A phenotype.

Published in:

2007

By:

Lombardi, Francesca;
Gullotta, Francesca;
Columbaro, Marta;
Filareto, Antonio;
D'Adamo, Monica;
Vielle, Anne;
Guglielmi, Valeria;
Nardone, Anna Maria;
Azzolini, Valeria;
Grosso, Enrico;
Lattanzi, Giovanna;
D'Apice, Maria Rosaria;
Masala, Salvatore;
Maraldi, Nadir Mario;
Sbraccia, Paolo;
Novelli, Giuseppe

Publication type:

journal article

New PRSS1 and common CFTR mutations in a child with acute recurrent pancreatitis, could be considered an "Hereditary" form of pancreatitis ?

Published in:

2010

By:

Corleto, Vito D;
Gambardella, Stefano;
Gullotta, Francesca;
D'Apice, Maria R;
Piciucchi, Matteo;
Galli, Elena;
Lucidi, Vincenzina;
Novelli, Giuseppe;
Delle Fave, Gianfranco

Publication type:

journal article

New PRSS1 and common CFTR mutations in a child with acute recurrent pancreatitis, could be considered an "Hereditary" form of pancreatitis?

Published in:

BMC Gastroenterology, 2010, v. 10, p. 119, doi. 10.1186/1471-230X-10-119

By:

Corleto, Vito D.;
Gambardella, Stefano;
Gullotta, Francesca;
D'Apice, Maria R.;
Piciucchi, Matteo;
Galli, Elena;
Lucidi, Vincenzina;
Novelli, Giuseppe;
Fave, Gianfranco Delle

Publication type:

Article

Carbon monoxide: An unusual drug.

Published in:

IUBMB Life, 2012, v. 64, n. 5, p. 378, doi. 10.1002/iub.1015

By:

Gullotta, Francesca;
Masi, Alessandra di;
Ascenzi, Paolo

Publication type:

Article

Drug binding to sudlow's site i impairs allosterically human serum heme-albumin-catalyzed peroxynitrite detoxification, iubmb life 2010 oct;62(10):776-80.

Published in:

IUBMB Life, 2011, v. 63, n. 12, p. 1116, doi. 10.1002/iub.548

By:

Ascenzi, Paolo;
Bolli, Alessandro;
Gullotta, Francesca;
Fanali, Gabriella;
Fasano, Mauro

Publication type:

Article

Cancer predisposing mutations in BRCT domains.

Published in:

IUBMB Life, 2011, v. 63, n. 7, p. 503, doi. 10.1002/iub.472

By:

di Masi, Alessandra;
Gullotta, Francesca;
Cappadonna, Valentina;
Leboffe, Loris;
Ascenzi, Paolo

Publication type:

Article

Erratum: Drug binding to Sudlow's site I impairs allosterically human serum heme-albumin-catalyzed peroxynitrite detoxification.

Published in:

2010

By:

Ascenzi, Paolo;
Bolli, Alessandro;
Gullotta, Francesca;
Fanali, Gabriella;
Fasano, Mauro

Publication type:

Erratum

Drug binding to Sudlow's site I impairs allosterically human serum heme-albumin-catalyzed peroxynitrite detoxification.

Published in:

IUBMB Life, 2010, v. 62, n. 10, p. 776, doi. 10.1002/iub.381

By:

Ascenzi, Paolo;
Bolli, Alessandro;
Gullotta, Francesca;
Fanali, Gabriella;
Fasano, Mauro

Publication type:

Article

Determination of antituberculosis drug concentration in human plasma by MALDI-TOF/TOF.

Published in:

IUBMB Life, 2010, v. 62, n. 5, p. 387, doi. 10.1002/iub.321

By:

Notari, Stefania;
Mancone, Carmine;
Sergi, Manuel;
Gullotta, Francesca;
Bevilacqua, Nazzario;
Tempestilli, Massimo;
Urso, Rocco;
Lauria, Francesco Nicola;
Pucillo, Leopoldo Paolo;
Tripodi, Marco;
Ascenzi, Paolo

Publication type:

Article

Deletion 2q37: An Identifiable Clinical Syndrome With Mental Retardation and Autism.

Published in:

Journal of Child Neurology, 2008, v. 23, n. 7, p. 802, doi. 10.1177/0883073808314150

By:

Galasso, Cinzia;
Lo-Castro, Adriana;
Lalli, Cristina;
Nardone, Anna Maria;
Gullotta, Francesca;
Curatolo, Paolo

Publication type:

Article

Evidence for pH-dependent multiple conformers in iron(II) heme-human serum albumin: spectroscopic and kinetic investigation of carbon monoxide binding.

Published in:

Journal of Biological Inorganic Chemistry (JBIC), 2012, v. 17, n. 1, p. 133, doi. 10.1007/s00775-011-0837-0

By:

Cao, Yu;
Nicoletti, Francesco;
Sanctis, Giampiero;
Bocedi, Alessio;
Ciaccio, Chiara;
Gullotta, Francesca;
Fanali, Gabriella;
Tundo, Grazia;
Masi, Alessandra;
Fasano, Mauro;
Smulevich, Giulietta;
Ascenzi, Paolo;
Coletta, Massimo

Publication type:

Article

Deletion of REXO1L1 locus in a patient with malabsorption syndrome, growth retardation, and dysmorphic features: a novel recognizable microdeletion syndrome?

Published in:

BMC Medical Genetics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12881-015-0164-3

By:

D'Apice, Maria Rosaria;
Novelli, Antonio;
di Masi, Alessandra;
Biancolella, Michela;
Antoccia, Antonio;
Gullotta, Francesca;
Licata, Norma;
Minella, Daniela;
Testa, Barbara;
Nardone, Anna Maria;
Palmieri, Giampiero;
Calabrese, Emma;
Biancone, Livia;
Tanzarella, Caterina;
Frontali, Marina;
Sangiuolo, Federica;
Novelli, Giuseppe;
Pallone, Francesco

Publication type:

Article