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

Massimo Carella

Showing results (101-110 of 207) with videos related to

Pageof 21
Sort By:
BMC Cancer|December 21, 2012
Molecular pathways undergoing dramatic transcriptomic changes during tumor development in the human colonRosalia Maglietta, Vania Cosma Liuzzi, Elisa Cattaneo, et al.
Plos One|November 7, 2013
Genome-wide analysis of differentially expressed genes and splicing isoforms in clear cell renal cell carcinomaAlessio Valletti, Margherita Gigante, Orazio Palumbo, et al.
Seizure|November 5, 2020
The presenting symptoms of Lafora Disease: An electroclinical and genetic study in five Apulian (Southern Italy) familiesGiuseppe d'Orsi, Alessandra Lalla, Orazio Palumbo, et al.
Frontiers in Cardiovascular Medicine|June 7, 2021
Phenotypic Variability of a Pathogenic <i>PKP2</i> Mutation in an Italian Family Affected by Arrhythmogenic Cardiomyopathy and Juvenile Sudden Death: Considerations From Molecular Autopsy to Sport RestrictionMaria Pia Leone, Pietro Palumbo, Johan Saenen, et al.
Frontiers in Cell and Developmental Biology|August 28, 2023
Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism?Laura Pignata, Francesco Cecere, Fabio Acquaviva, et al.
Pancreas|March 9, 2016
Support Vector Machine Based on microRNA Expression Profiles to Predict Histological Origin of Ampullary Carcinoma: Case Report of a Patient Affected From Adenocarcinoma of the Papilla of Vater With Lynch SyndromeFrancesca Tavano, Massimiliano Copetti, Ada Piepoli, et al.
Genes|August 27, 2021
Novel <i>STAG1</i> Frameshift Mutation in a Patient Affected by a Syndromic Form of Neurodevelopmental DisorderEster Di Muro, Pietro Palumbo, Mario Benvenuto, et al.
Human Molecular Genetics|July 20, 2006
Pathogenetic role of the deafness-related M34T mutation of Cx26Massimiliano Bicego, Martina Beltramello, Salvatore Melchionda, et al.
International Journal of Molecular Sciences|July 21, 2017
Functional Implications of MicroRNAs in Crohn's Disease Revealed by Integrating MicroRNA and Messenger RNA Expression ProfilingOrazio Palmieri, Teresa Maria Creanza, Fabrizio Bossa, et al.
NPJ Schizophrenia|June 1, 2017
Decreased free d-aspartate levels are linked to enhanced d-aspartate oxidase activity in the dorsolateral prefrontal cortex of schizophrenia patientsTommaso Nuzzo, Silvia Sacchi, Francesco Errico, et al.
Pageof 21

Showing results (101-110 of 207) with videos related to

Sort By:
Pageof 21
BMC Cancer|December 21, 2012
Molecular pathways undergoing dramatic transcriptomic changes during tumor development in the human colonRosalia Maglietta, Vania Cosma Liuzzi, Elisa Cattaneo, et al.
Plos One|November 7, 2013
Genome-wide analysis of differentially expressed genes and splicing isoforms in clear cell renal cell carcinomaAlessio Valletti, Margherita Gigante, Orazio Palumbo, et al.
Seizure|November 5, 2020
The presenting symptoms of Lafora Disease: An electroclinical and genetic study in five Apulian (Southern Italy) familiesGiuseppe d'Orsi, Alessandra Lalla, Orazio Palumbo, et al.
Frontiers in Cardiovascular Medicine|June 7, 2021
Phenotypic Variability of a Pathogenic <i>PKP2</i> Mutation in an Italian Family Affected by Arrhythmogenic Cardiomyopathy and Juvenile Sudden Death: Considerations From Molecular Autopsy to Sport RestrictionMaria Pia Leone, Pietro Palumbo, Johan Saenen, et al.
Frontiers in Cell and Developmental Biology|August 28, 2023
Co-occurrence of Beckwith-Wiedemann syndrome and pseudohypoparathyroidism type 1B: coincidence or common molecular mechanism?Laura Pignata, Francesco Cecere, Fabio Acquaviva, et al.
Pancreas|March 9, 2016
Support Vector Machine Based on microRNA Expression Profiles to Predict Histological Origin of Ampullary Carcinoma: Case Report of a Patient Affected From Adenocarcinoma of the Papilla of Vater With Lynch SyndromeFrancesca Tavano, Massimiliano Copetti, Ada Piepoli, et al.
Genes|August 27, 2021
Novel <i>STAG1</i> Frameshift Mutation in a Patient Affected by a Syndromic Form of Neurodevelopmental DisorderEster Di Muro, Pietro Palumbo, Mario Benvenuto, et al.
Human Molecular Genetics|July 20, 2006
Pathogenetic role of the deafness-related M34T mutation of Cx26Massimiliano Bicego, Martina Beltramello, Salvatore Melchionda, et al.
International Journal of Molecular Sciences|July 21, 2017
Functional Implications of MicroRNAs in Crohn's Disease Revealed by Integrating MicroRNA and Messenger RNA Expression ProfilingOrazio Palmieri, Teresa Maria Creanza, Fabrizio Bossa, et al.
NPJ Schizophrenia|June 1, 2017
Decreased free d-aspartate levels are linked to enhanced d-aspartate oxidase activity in the dorsolateral prefrontal cortex of schizophrenia patientsTommaso Nuzzo, Silvia Sacchi, Francesco Errico, et al.
Pageof 21