Publications by authors named "Francesca Gullotta"

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Design, Construction and Validation of Targeted BAC Array-Based CGH Test for Detecting the Most Commons Chromosomal Abnormalities.
Stefano Gambardella, Erika Ciabattoni, Francesca Motta, Giusy Stoico, Francesca Gullotta

Genomics Insights· August 2015

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Deletion of REXO1L1 locus in a patient with malabsorption syndrome, growth retardation, and dysmorphic features: a novel recognizable microdeletion syndrome?
Maria Rosaria D'Apice, Antonio Novelli, Alessandra di Masi, Michela Biancolella, Antonio Antoccia, Francesca Gullotta

BMC Med Genet· April 2015

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CO metabolism, sensing, and signaling.
Francesca Gullotta, Alessandra di Masi, Massimo Coletta, Paolo Ascenzi

Biofactors· June 2012

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Carbon monoxide: an unusual drug.
Francesca Gullotta, Alessandra di Masi, Paolo Ascenzi

IUBMB Life· May 2012

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Evidence for pH-dependent multiple conformers in iron(II) heme-human serum albumin: spectroscopic and kinetic investigation of carbon monoxide binding.
Yu Cao, Francesco P Nicoletti, Giampiero De Sanctis, Alessio Bocedi, Chiara Ciaccio, Francesca Gullotta

J Biol Inorg Chem· January 2012

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Cancer predisposing mutations in BRCT domains.
Alessandra di Masi, Francesca Gullotta, Valentina Cappadonna, Loris Leboffe, Paolo Ascenzi

IUBMB Life· July 2011

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O2-mediated oxidation of ferrous nitrosylated human serum heme-albumin is limited by nitrogen monoxide dissociation.
Paolo Ascenzi, Francesca Gullotta, Magda Gioia, Massimo Coletta, Mauro Fasano

Biochem Biophys Res Commun· March 2011

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Ibuprofen binding to secondary sites allosterically modulates the spectroscopic and catalytic properties of human serum heme-albumin.
Alessandra di Masi, Francesca Gullotta, Alessandro Bolli, Gabriella Fanali, Mauro Fasano

FEBS J· February 2011

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Targeting the DNA double strand breaks repair for cancer therapy.
Francesca Gullotta, Elisabetta De Marinis, Paolo Ascenzi, Alessandra di Masi

Curr Med Chem· October 2010

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New PRSS1 and common CFTR mutations in a child with acute recurrent pancreatitis, could be considered an "Hereditary" form of pancreatitis ?
Vito D Corleto, Stefano Gambardella, Francesca Gullotta, Maria R D'Apice, Matteo Piciucchi

BMC Gastroenterol· October 2010

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Drug binding to Sudlow's site I impairs allosterically human serum heme-albumin-catalyzed peroxynitrite detoxification.
Paolo Ascenzi, Alessandro Bolli, Francesca Gullotta, Gabriella Fanali, Mauro Fasano

IUBMB Life· October 2010

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Reductive nitrosylation of ferric human serum heme-albumin.
Paolo Ascenzi, Yu Cao, Alessandra di Masi, Francesca Gullotta, Giampiero De Sanctis

FEBS J· June 2010

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Determination of antituberculosis drug concentration in human plasma by MALDI-TOF/TOF.
Stefania Notari, Carmine Mancone, Manuel Sergi, Francesca Gullotta, Nazzario Bevilacqua

IUBMB Life· May 2010

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Premature ovarian failure, absence of pubic and axillary hair with de novo 46,X,t(X;15)(q24;q26.3).
Claudio Giacomozzi, Francesca Gullotta, Giovanni Federico, Isabella Colapietro, Anna Maria Nardone

Am J Med Genet A· May 2010

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Reductive nitrosylation of ferric cyanide horse heart myoglobin is limited by cyanide dissociation.
Paolo Ascenzi, Alessandra di Masi, Francesca Gullotta, Marco Mattu, Chiara Ciaccio

Biochem Biophys Res Commun· March 2010

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Hyperproliferation in nasal polyposis tissues is not associated with somatic genomic instability.
Carlo Corradini, Francesca Gullotta, Silvia Ciacci, Giampiero Palmieri, Leila Baghernajad Salehi

J Otolaryngol Head Neck Surg· August 2008

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Deletion 2q37: an identifiable clinical syndrome with mental retardation and autism.
Cinzia Galasso, Adriana Lo-Castro, Cristina Lalli, Anna Maria Nardone, Francesca Gullotta

J Child Neurol· July 2008

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Compound heterozygosity for mutations in LMNA in a patient with a myopathic and lipodystrophic mandibuloacral dysplasia type A phenotype.
Francesca Lombardi, Francesca Gullotta, Marta Columbaro, Antonio Filareto, Monica D'Adamo

J Clin Endocrinol Metab· November 2007

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Prenatal diagnosis of genomic disorders and chromosome abnormalities using array-based comparative genomic hybridization.
Francesca Gullotta, Michela Biancolella, Elena Costa, Isabella Colapietro, Anna Maria Nardone

J Prenat Med· January 2007

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Effect of the [CCTG]n repeat expansion on ZNF9 expression in myotonic dystrophy type II (DM2).
Annalisa Botta, Sara Caldarola, Laura Vallo, Emanuela Bonifazi, Doriana Fruci, Francesca Gullotta

Biochim Biophys Acta· March 2006

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Use of RNA fluorescence in situ hybridization in the prenatal molecular diagnosis of myotonic dystrophy type I.
Emanuela Bonifazi, Francesca Gullotta, Laura Vallo, Raniero Iraci, Anna Maria Nardone

Clin Chem· February 2006

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Alterations of nuclear envelope and chromatin organization in mandibuloacral dysplasia, a rare form of laminopathy.
Ilaria Filesi, Francesca Gullotta, Giovanna Lattanzi, Maria Rosaria D'Apice, Cristina Capanni

Physiol Genomics· October 2005

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Use of chromosome painting for detecting stable chromosome aberrations induced by melphalan in mice.
Antonella Sgura, Laura Stronati, Francesca Gullotta, Andrea Pecis, Serena Cinelli

Environ Mol Mutagen· June 2005

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