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Sandro Banfi

Showing results (101-110 of 136) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|July 20, 2022
Specialization of the photoreceptor transcriptome by <i>Srrm3</i>-dependent microexons is required for outer segment maintenance and visionLudovica Ciampi, Federica Mantica, Laura López-Blanch, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 10, 2015
MiR-204 is responsible for inherited retinal dystrophy associated with ocular colobomaIvan Conte, Kristen D Hadfield, Sara Barbato, et al.
Scientific Reports|December 2, 2022
Genetic epidemiology of inherited retinal diseases in a large patient cohort followed at a single center in ItalyMarianthi Karali, Francesco Testa, Valentina Di Iorio, et al.
EMBO Molecular Medicine|October 4, 2022
miR-181a/b downregulation: a mutation-independent therapeutic approach for inherited retinal diseasesSabrina Carrella, Martina Di Guida, Simona Brillante, et al.
The EMBO Journal|March 11, 2020
Light-responsive microRNA miR-211 targets Ezrin to modulate lysosomal biogenesis and retinal cell clearanceFederica Naso, Daniela Intartaglia, Danila Falanga, et al.
EMBO Molecular Medicine|April 14, 2019
miR-181a/b downregulation exerts a protective action on mitochondrial disease modelsAlessia Indrieri, Sabrina Carrella, Alessia Romano, et al.
HGG Advances|September 14, 2023
Targeted sequencing and in vitro splice assays shed light on ABCA4-associated retinopathies missing heritabilityZelia Corradi, Mubeen Khan, Rebekkah Hitti-Malin, et al.
Human Molecular Genetics|December 26, 2016
MIB2 variants altering NOTCH signalling result in left ventricle hypertrabeculation/non-compaction and are associated with Ménétrier-like gastropathyPasquale Piccolo, Sergio Attanasio, Ilaria Secco, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 3, 2009
Gene therapy for Leber's congenital amaurosis is safe and effective through 1.5 years after vector administrationFrancesca Simonelli, Albert M Maguire, Francesco Testa, et al.
Investigative Ophthalmology & Visual Science|February 7, 2022
RPE65-Associated Retinopathies in the Italian Population: A Longitudinal Natural History StudyFrancesco Testa, Vittoria Murro, Sabrina Signorini, et al.
Pageof 14

Showing results (101-110 of 136) with videos related to

Sort By:
Pageof 14
Proceedings of the National Academy of Sciences of the United States of America|July 20, 2022
Specialization of the photoreceptor transcriptome by <i>Srrm3</i>-dependent microexons is required for outer segment maintenance and visionLudovica Ciampi, Federica Mantica, Laura López-Blanch, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 10, 2015
MiR-204 is responsible for inherited retinal dystrophy associated with ocular colobomaIvan Conte, Kristen D Hadfield, Sara Barbato, et al.
Scientific Reports|December 2, 2022
Genetic epidemiology of inherited retinal diseases in a large patient cohort followed at a single center in ItalyMarianthi Karali, Francesco Testa, Valentina Di Iorio, et al.
EMBO Molecular Medicine|October 4, 2022
miR-181a/b downregulation: a mutation-independent therapeutic approach for inherited retinal diseasesSabrina Carrella, Martina Di Guida, Simona Brillante, et al.
The EMBO Journal|March 11, 2020
Light-responsive microRNA miR-211 targets Ezrin to modulate lysosomal biogenesis and retinal cell clearanceFederica Naso, Daniela Intartaglia, Danila Falanga, et al.
EMBO Molecular Medicine|April 14, 2019
miR-181a/b downregulation exerts a protective action on mitochondrial disease modelsAlessia Indrieri, Sabrina Carrella, Alessia Romano, et al.
HGG Advances|September 14, 2023
Targeted sequencing and in vitro splice assays shed light on ABCA4-associated retinopathies missing heritabilityZelia Corradi, Mubeen Khan, Rebekkah Hitti-Malin, et al.
Human Molecular Genetics|December 26, 2016
MIB2 variants altering NOTCH signalling result in left ventricle hypertrabeculation/non-compaction and are associated with Ménétrier-like gastropathyPasquale Piccolo, Sergio Attanasio, Ilaria Secco, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|December 3, 2009
Gene therapy for Leber's congenital amaurosis is safe and effective through 1.5 years after vector administrationFrancesca Simonelli, Albert M Maguire, Francesco Testa, et al.
Investigative Ophthalmology & Visual Science|February 7, 2022
RPE65-Associated Retinopathies in the Italian Population: A Longitudinal Natural History StudyFrancesco Testa, Vittoria Murro, Sabrina Signorini, et al.
Pageof 14