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Monica Miozzo

Showing results (21-30 of 100) with videos related to

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Endocrine|December 8, 2017
MassARRAY-based simultaneous detection of hotspot somatic mutations and recurrent fusion genes in papillary thyroid carcinoma: the PTC-MA assayChiara Pesenti, Marina Muzza, Carla Colombo, et al.
Plos One|July 8, 2014
Genetic polymorphisms and sepsis in premature neonatesSusanna Esposito, Alberto Zampiero, Lorenza Pugni, et al.
Pediatric Research|June 4, 2013
SNAT2 expression and regulation in human growth-restricted placentasChiara Mandò, Silvia Tabano, Paola Pileri, et al.
Hepatology (Baltimore, Md.)|July 31, 2007
Preferential X chromosome loss but random inactivation characterize primary biliary cirrhosisMonica Miozzo, Carlo Selmi, Barbara Gentilin, et al.
International Journal of Cancer|September 25, 2003
Mapping of candidate region for chordoma development to 1p36.13 by LOH analysisPaola Riva, Francesca Crosti, Francesca Orzan, et al.
Scientific Reports|May 20, 2020
Profound alterations of the chromatin architecture at chromosome 11p15.5 in cells from Beckwith-Wiedemann and Silver-Russell syndromes patientsDavide Rovina, Marta La Vecchia, Alice Cortesi, et al.
American Journal of Medical Genetics. Part A|November 1, 2017
STAR syndrome plus: The first description of a female patient with the lethal formMaria F Bedeschi, Sara Giangiobbe, Leda Paganini, et al.
Clinical and Translational Science|February 6, 2025
Pharmacogenetic Information on Drug Labels of the Italian Agency of Medicines (AIFA): Actionability and Comparison Across Other Regulatory AgenciesAntonino Moschella, Soumaya Mourou, Samantha Perfler, et al.
Life (Basel, Switzerland)|July 27, 2022
A Targeted Next-Generation Sequencing Panel to Genotype GliomasMaria Guarnaccia, Laura Guarnaccia, Valentina La Cognata, et al.
Plos One|May 15, 2009
Misbehaviour of XIST RNA in breast cancer cellsSilvia M Sirchia, Silvia Tabano, Laura Monti, et al.
Pageof 10

Showing results (21-30 of 100) with videos related to

Sort By:
Pageof 10
Endocrine|December 8, 2017
MassARRAY-based simultaneous detection of hotspot somatic mutations and recurrent fusion genes in papillary thyroid carcinoma: the PTC-MA assayChiara Pesenti, Marina Muzza, Carla Colombo, et al.
Plos One|July 8, 2014
Genetic polymorphisms and sepsis in premature neonatesSusanna Esposito, Alberto Zampiero, Lorenza Pugni, et al.
Pediatric Research|June 4, 2013
SNAT2 expression and regulation in human growth-restricted placentasChiara Mandò, Silvia Tabano, Paola Pileri, et al.
Hepatology (Baltimore, Md.)|July 31, 2007
Preferential X chromosome loss but random inactivation characterize primary biliary cirrhosisMonica Miozzo, Carlo Selmi, Barbara Gentilin, et al.
International Journal of Cancer|September 25, 2003
Mapping of candidate region for chordoma development to 1p36.13 by LOH analysisPaola Riva, Francesca Crosti, Francesca Orzan, et al.
Scientific Reports|May 20, 2020
Profound alterations of the chromatin architecture at chromosome 11p15.5 in cells from Beckwith-Wiedemann and Silver-Russell syndromes patientsDavide Rovina, Marta La Vecchia, Alice Cortesi, et al.
American Journal of Medical Genetics. Part A|November 1, 2017
STAR syndrome plus: The first description of a female patient with the lethal formMaria F Bedeschi, Sara Giangiobbe, Leda Paganini, et al.
Clinical and Translational Science|February 6, 2025
Pharmacogenetic Information on Drug Labels of the Italian Agency of Medicines (AIFA): Actionability and Comparison Across Other Regulatory AgenciesAntonino Moschella, Soumaya Mourou, Samantha Perfler, et al.
Life (Basel, Switzerland)|July 27, 2022
A Targeted Next-Generation Sequencing Panel to Genotype GliomasMaria Guarnaccia, Laura Guarnaccia, Valentina La Cognata, et al.
Plos One|May 15, 2009
Misbehaviour of XIST RNA in breast cancer cellsSilvia M Sirchia, Silvia Tabano, Laura Monti, et al.
Pageof 10