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Francesca Di Leva

Showing results (21-30 of 26) with videos related to

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The Journal of Biological Chemistry|September 10, 2010
The novel PMCA2 pump mutation Tommy impairs cytosolic calcium clearance in hair cells and links to deafness in miceMario Bortolozzi, Marisa Brini, Nick Parkinson, et al.
Plos Genetics|November 1, 2008
The novel mouse mutation Oblivion inactivates the PMCA2 pump and causes progressive hearing lossSarah L Spiden, Mario Bortolozzi, Francesca Di Leva, et al.
Plos Genetics|October 13, 2023
CAG repeat expansion in the Huntington's disease gene shapes linear and circular RNAs biogenesisDilara Ayyildiz, Guendalina Bergonzoni, Alan Monziani, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 1, 2025
SINEUP RNA rescues molecular phenotypes associated with CHD8 suppression in autism spectrum disorder model systemsFrancesca Di Leva, Michele Arnoldi, Stefania Santarelli, et al.
Nucleic Acids Research|December 20, 2022
CHD8 suppression impacts on histone H3 lysine 36 trimethylation and alters RNA alternative splicingEmanuela Kerschbamer, Michele Arnoldi, Takshashila Tripathi, et al.
International Journal of Systematic and Evolutionary Microbiology|December 10, 2014
Characterization of 17 strains belonging to the Mycobacterium simiae complex and description of Mycobacterium paraense sp. novAna R Fusco da Costa, Tarcisio Fedrizzi, Maria L Lopes, et al.
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Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
The Journal of Biological Chemistry|September 10, 2010
The novel PMCA2 pump mutation Tommy impairs cytosolic calcium clearance in hair cells and links to deafness in miceMario Bortolozzi, Marisa Brini, Nick Parkinson, et al.
Plos Genetics|November 1, 2008
The novel mouse mutation Oblivion inactivates the PMCA2 pump and causes progressive hearing lossSarah L Spiden, Mario Bortolozzi, Francesca Di Leva, et al.
Plos Genetics|October 13, 2023
CAG repeat expansion in the Huntington's disease gene shapes linear and circular RNAs biogenesisDilara Ayyildiz, Guendalina Bergonzoni, Alan Monziani, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 1, 2025
SINEUP RNA rescues molecular phenotypes associated with CHD8 suppression in autism spectrum disorder model systemsFrancesca Di Leva, Michele Arnoldi, Stefania Santarelli, et al.
Nucleic Acids Research|December 20, 2022
CHD8 suppression impacts on histone H3 lysine 36 trimethylation and alters RNA alternative splicingEmanuela Kerschbamer, Michele Arnoldi, Takshashila Tripathi, et al.
International Journal of Systematic and Evolutionary Microbiology|December 10, 2014
Characterization of 17 strains belonging to the Mycobacterium simiae complex and description of Mycobacterium paraense sp. novAna R Fusco da Costa, Tarcisio Fedrizzi, Maria L Lopes, et al.
Pageof 3