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

Federica Graziola

Showing results (21-30 of 28) with videos related to

Pageof 3
Sort By:
You have reached the last page of results.This site can display upto 28 results.
International Journal of Molecular Sciences|February 2, 2018
Rings and Bricks: Expression of Cohesin Components is Dynamic during Development and Adult LifeLaura Rachele Bettini, Federica Graziola, Grazia Fazio, et al.
International Journal of Molecular Sciences|June 2, 2021
Novel <i>KCND3</i> Variant Underlying Nonprogressive Congenital Ataxia or SCA19/22 Disrupt K<sub>V</sub>4.3 Protein Expression and K+ Currents with Variable Effects on Channel PropertiesGinevra Zanni, Cheng-Tsung Hsiao, Ssu-Ju Fu, et al.
Journal of Personalized Medicine|January 21, 2022
"Spazio Huntington": Tracing the Early Motor, Cognitive and Behavioral Profiles of Kids with Proven Pediatric Huntington Disease and Expanded Mutations > 80 CAG RepeatsFederica Graziola, Sabrina Maffi, Melissa Grasso, et al.
Journal of Cellular Physiology|July 25, 2015
CyclinD1 Down-Regulation and Increased Apoptosis Are Common Features of CohesinopathiesGrazia Fazio, Carles Gaston-Massuet, Laura Rachele Bettini, et al.
Journal of Medical Genetics|January 5, 2021
Biallelic variants in <i>ZNF526</i> cause a severe neurodevelopmental disorder with microcephaly, bilateral cataract, epilepsy and simplified gyrationMaria Lisa Dentici, Viola Alesi, Mathieu Quinodoz, et al.
Parkinsonism & Related Disorders|January 16, 2019
Phenomenology and clinical course of movement disorder in GNAO1 variants: Results from an analytical reviewTommaso Schirinzi, Giacomo Garone, Lorena Travaglini, et al.
Viruses|April 23, 2022
Subacute Sclerosing Panencephalitis in Children: The Archetype of Non-VaccinationLaura Papetti, Maria Elisa Amodeo, Letizia Sabatini, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 15, 2016
Transcription factor 7-like 1 is involved in hypothalamo-pituitary axis development in mice and humansCarles Gaston-Massuet, Mark J McCabe, Valeria Scagliotti, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
International Journal of Molecular Sciences|February 2, 2018
Rings and Bricks: Expression of Cohesin Components is Dynamic during Development and Adult LifeLaura Rachele Bettini, Federica Graziola, Grazia Fazio, et al.
International Journal of Molecular Sciences|June 2, 2021
Novel <i>KCND3</i> Variant Underlying Nonprogressive Congenital Ataxia or SCA19/22 Disrupt K<sub>V</sub>4.3 Protein Expression and K+ Currents with Variable Effects on Channel PropertiesGinevra Zanni, Cheng-Tsung Hsiao, Ssu-Ju Fu, et al.
Journal of Personalized Medicine|January 21, 2022
"Spazio Huntington": Tracing the Early Motor, Cognitive and Behavioral Profiles of Kids with Proven Pediatric Huntington Disease and Expanded Mutations > 80 CAG RepeatsFederica Graziola, Sabrina Maffi, Melissa Grasso, et al.
Journal of Cellular Physiology|July 25, 2015
CyclinD1 Down-Regulation and Increased Apoptosis Are Common Features of CohesinopathiesGrazia Fazio, Carles Gaston-Massuet, Laura Rachele Bettini, et al.
Journal of Medical Genetics|January 5, 2021
Biallelic variants in <i>ZNF526</i> cause a severe neurodevelopmental disorder with microcephaly, bilateral cataract, epilepsy and simplified gyrationMaria Lisa Dentici, Viola Alesi, Mathieu Quinodoz, et al.
Parkinsonism & Related Disorders|January 16, 2019
Phenomenology and clinical course of movement disorder in GNAO1 variants: Results from an analytical reviewTommaso Schirinzi, Giacomo Garone, Lorena Travaglini, et al.
Viruses|April 23, 2022
Subacute Sclerosing Panencephalitis in Children: The Archetype of Non-VaccinationLaura Papetti, Maria Elisa Amodeo, Letizia Sabatini, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 15, 2016
Transcription factor 7-like 1 is involved in hypothalamo-pituitary axis development in mice and humansCarles Gaston-Massuet, Mark J McCabe, Valeria Scagliotti, et al.
Pageof 3