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Francesca Gullotta

Showing results (11-20 of 23) with videos related to

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Environmental and Molecular Mutagenesis|February 3, 2005
Use of chromosome painting for detecting stable chromosome aberrations induced by melphalan in miceAntonella Sgura, Laura Stronati, Francesca Gullotta, et al.
Clinical Chemistry|February 2, 2006
Use of RNA fluorescence in situ hybridization in the prenatal molecular diagnosis of myotonic dystrophy type IEmanuela Bonifazi, Francesca Gullotta, Laura Vallo, et al.
Biochimica Et Biophysica Acta|December 27, 2005
Effect of the [CCTG]n repeat expansion on ZNF9 expression in myotonic dystrophy type II (DM2)Annalisa Botta, Sara Caldarola, Laura Vallo, et al.
The FEBS Journal|May 12, 2010
Reductive nitrosylation of ferric human serum heme-albuminPaolo Ascenzi, Yu Cao, Alessandra di Masi, et al.
Journal of Otolaryngology - Head & Neck Surgery = Le Journal D'Oto-Rhino-Laryngologie Et De Chirurgie Cervico-Faciale|January 9, 2009
Hyperproliferation in nasal polyposis tissues is not associated with somatic genomic instabilityCarlo Corradini, Francesca Gullotta, Silvia Ciacci, et al.
BMC Gastroenterology|October 19, 2010
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, et al.
Journal of Prenatal Medicine|April 4, 2012
Prenatal diagnosis of genomic disorders and chromosome abnormalities using array-based comparative genomic hybridizationFrancesca Gullotta, Michela Biancolella, Elena Costa, et al.
Genomics Insights|August 18, 2015
Design, Construction and Validation of Targeted BAC Array-Based CGH Test for Detecting the Most Commons Chromosomal AbnormalitiesStefano Gambardella, Erika Ciabattoni, Francesca Motta, et al.
IUBMB Life|March 23, 2010
Determination of antituberculosis drug concentration in human plasma by MALDI-TOF/TOFStefania Notari, Carmine Mancone, Manuel Sergi, et al.
Physiological Genomics|July 28, 2005
Alterations of nuclear envelope and chromatin organization in mandibuloacral dysplasia, a rare form of laminopathyIlaria Filesi, Francesca Gullotta, Giovanna Lattanzi, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Environmental and Molecular Mutagenesis|February 3, 2005
Use of chromosome painting for detecting stable chromosome aberrations induced by melphalan in miceAntonella Sgura, Laura Stronati, Francesca Gullotta, et al.
Clinical Chemistry|February 2, 2006
Use of RNA fluorescence in situ hybridization in the prenatal molecular diagnosis of myotonic dystrophy type IEmanuela Bonifazi, Francesca Gullotta, Laura Vallo, et al.
Biochimica Et Biophysica Acta|December 27, 2005
Effect of the [CCTG]n repeat expansion on ZNF9 expression in myotonic dystrophy type II (DM2)Annalisa Botta, Sara Caldarola, Laura Vallo, et al.
The FEBS Journal|May 12, 2010
Reductive nitrosylation of ferric human serum heme-albuminPaolo Ascenzi, Yu Cao, Alessandra di Masi, et al.
Journal of Otolaryngology - Head & Neck Surgery = Le Journal D'Oto-Rhino-Laryngologie Et De Chirurgie Cervico-Faciale|January 9, 2009
Hyperproliferation in nasal polyposis tissues is not associated with somatic genomic instabilityCarlo Corradini, Francesca Gullotta, Silvia Ciacci, et al.
BMC Gastroenterology|October 19, 2010
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, et al.
Journal of Prenatal Medicine|April 4, 2012
Prenatal diagnosis of genomic disorders and chromosome abnormalities using array-based comparative genomic hybridizationFrancesca Gullotta, Michela Biancolella, Elena Costa, et al.
Genomics Insights|August 18, 2015
Design, Construction and Validation of Targeted BAC Array-Based CGH Test for Detecting the Most Commons Chromosomal AbnormalitiesStefano Gambardella, Erika Ciabattoni, Francesca Motta, et al.
IUBMB Life|March 23, 2010
Determination of antituberculosis drug concentration in human plasma by MALDI-TOF/TOFStefania Notari, Carmine Mancone, Manuel Sergi, et al.
Physiological Genomics|July 28, 2005
Alterations of nuclear envelope and chromatin organization in mandibuloacral dysplasia, a rare form of laminopathyIlaria Filesi, Francesca Gullotta, Giovanna Lattanzi, et al.
Pageof 3