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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 vision
Ludovica 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 coloboma
Ivan 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 Italy
Marianthi 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 diseases
Sabrina 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 clearance
Federica Naso, Daniela Intartaglia, Danila Falanga, et al.
EMBO Molecular Medicine
|
April 14, 2019
miR-181a/b downregulation exerts a protective action on mitochondrial disease models
Alessia 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 heritability
Zelia 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 gastropathy
Pasquale 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 administration
Francesca 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 Study
Francesco Testa, Vittoria Murro, Sabrina Signorini, et al.
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of 14
Search research articles
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Showing results (101-110 of 136) with videos related to
Sort By:
Page
of 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 vision
Ludovica 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 coloboma
Ivan 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 Italy
Marianthi 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 diseases
Sabrina 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 clearance
Federica Naso, Daniela Intartaglia, Danila Falanga, et al.
EMBO Molecular Medicine
|
April 14, 2019
miR-181a/b downregulation exerts a protective action on mitochondrial disease models
Alessia 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 heritability
Zelia 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 gastropathy
Pasquale 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 administration
Francesca 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 Study
Francesco Testa, Vittoria Murro, Sabrina Signorini, et al.
Page
of 14