Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Monica Miozzo

Showing results (31-40 of 100) with videos related to

Pageof 10
Sort By:
BMC Pulmonary Medicine|July 31, 2020
SARS-CoV-2 specific serological pattern in healthcare workers of an Italian COVID-19 forefront hospitalGiovanni Sotgiu, Alessandra Barassi, Monica Miozzo, et al.
Lancet (London, England)|February 21, 2004
Frequency of monosomy X in women with primary biliary cirrhosisPietro Invernizzi, Monica Miozzo, Pier Maria Battezzati, et al.
Genes|April 23, 2022
Preferential X Chromosome Inactivation as a Mechanism to Explain Female Preponderance in Myasthenia GravisVanessa Nicolì, Silvia Maria Tabano, Patrizia Colapietro, et al.
Epigenetics|June 11, 2015
Beckwith-Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villiLeda Paganini, Nicole Carlessi, Laura Fontana, et al.
European Journal of Human Genetics : EJHG|December 16, 2003
Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnanciesFrancesca R Grati, Silvia M Sirchia, Barbara Gentilin, et al.
International Journal of Molecular Sciences|April 13, 2024
Dysfunction in IGF2R Pathway and Associated Perturbations in Autophagy and WNT Processes in Beckwith-Wiedemann Syndrome Cell LinesSilvana Pileggi, Elisa A Colombo, Silvia Ancona, et al.
Plos One|February 16, 2017
Revertant mosaicism for family mutations is not observed in BRCA1/2 phenocopiesJacopo Azzollini, Chiara Pesenti, Luca Ferrari, et al.
Human Genomics|July 10, 2024
Pharmacogenetics in Italy: current landscape and future prospectsMatteo Floris, Antonino Moschella, Myriam Alcalay, et al.
Orphanet Journal of Rare Diseases|January 28, 2012
Preferential expression of mutant ABCD1 allele is common in adrenoleukodystrophy female carriers but unrelated to clinical symptomsEttore Salsano, Silvia Tabano, Silvia M Sirchia, et al.
Cancer Research|March 23, 2005
Loss of the inactive X chromosome and replication of the active X in BRCA1-defective and wild-type breast cancer cellsSilvia M Sirchia, Lisetta Ramoscelli, Francesca R Grati, et al.
Pageof 10

Showing results (31-40 of 100) with videos related to

Sort By:
Pageof 10
BMC Pulmonary Medicine|July 31, 2020
SARS-CoV-2 specific serological pattern in healthcare workers of an Italian COVID-19 forefront hospitalGiovanni Sotgiu, Alessandra Barassi, Monica Miozzo, et al.
Lancet (London, England)|February 21, 2004
Frequency of monosomy X in women with primary biliary cirrhosisPietro Invernizzi, Monica Miozzo, Pier Maria Battezzati, et al.
Genes|April 23, 2022
Preferential X Chromosome Inactivation as a Mechanism to Explain Female Preponderance in Myasthenia GravisVanessa Nicolì, Silvia Maria Tabano, Patrizia Colapietro, et al.
Epigenetics|June 11, 2015
Beckwith-Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villiLeda Paganini, Nicole Carlessi, Laura Fontana, et al.
European Journal of Human Genetics : EJHG|December 16, 2003
Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnanciesFrancesca R Grati, Silvia M Sirchia, Barbara Gentilin, et al.
International Journal of Molecular Sciences|April 13, 2024
Dysfunction in IGF2R Pathway and Associated Perturbations in Autophagy and WNT Processes in Beckwith-Wiedemann Syndrome Cell LinesSilvana Pileggi, Elisa A Colombo, Silvia Ancona, et al.
Plos One|February 16, 2017
Revertant mosaicism for family mutations is not observed in BRCA1/2 phenocopiesJacopo Azzollini, Chiara Pesenti, Luca Ferrari, et al.
Human Genomics|July 10, 2024
Pharmacogenetics in Italy: current landscape and future prospectsMatteo Floris, Antonino Moschella, Myriam Alcalay, et al.
Orphanet Journal of Rare Diseases|January 28, 2012
Preferential expression of mutant ABCD1 allele is common in adrenoleukodystrophy female carriers but unrelated to clinical symptomsEttore Salsano, Silvia Tabano, Silvia M Sirchia, et al.
Cancer Research|March 23, 2005
Loss of the inactive X chromosome and replication of the active X in BRCA1-defective and wild-type breast cancer cellsSilvia M Sirchia, Lisetta Ramoscelli, Francesca R Grati, et al.
Pageof 10