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International Journal of Molecular Sciences
|
April 1, 2020
In or Out? New Insights on Exon Recognition through Splice-Site Interdependency
Mubeen Khan, Stéphanie S Cornelis, Riccardo Sangermano, et al.
Cell Reports
|
November 11, 2020
The Deubiquitinating Enzyme Ataxin-3 Regulates Ciliogenesis and Phagocytosis in the Retina
Vasileios Toulis, Sílvia García-Monclús, Carlos de la Peña-Ramírez, et al.
Plos Computational Biology
|
August 7, 2023
Comparative Clustering (CompaCt) of eukaryote complexomes identifies novel interactions and sheds light on protein complex evolution
Joeri van Strien, Felix Evers, Madhurya Lutikurti, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
January 20, 2024
Proof-of-concept for multiple AON delivery by a single U7snRNA vector to restore splicing defects in ABCA4
Nuria Suárez-Herrera, Iris B Riswick, Irene Vázquez-Domínguez, et al.
Cells
|
April 12, 2024
Preclinical Development of Antisense Oligonucleotides to Rescue Aberrant Splicing Caused by an Ultrarare <i>ABCA4</i> Variant in a Child with Early-Onset Stargardt Disease
Nuria Suárez-Herrera, Catherina H Z Li, Nico Leijsten, et al.
Genome Research
|
November 23, 2017
<i>ABCA4</i> midigenes reveal the full splice spectrum of all reported noncanonical splice site variants in Stargardt disease
Riccardo Sangermano, Mubeen Khan, Stéphanie S Cornelis, et al.
Human Molecular Genetics
|
September 11, 2021
Systemic complement levels in patients with age-related macular degeneration carrying rare or low-frequency variants in the CFH gene
Sarah de Jong, Anita de Breuk, Elena B Volokhina, et al.
Scientific Reports
|
September 17, 2017
Therapeutic effects of the mitochondrial ROS-redox modulator KH176 in a mammalian model of Leigh Disease
Ria de Haas, Devashish Das, Alejandro Garanto, et al.
Cellular and Molecular Life Sciences : CMLS
|
January 13, 2026
Exploring extracellular vesicle MicroRNAs in Usher syndrome type 1B: Tear-Derived EVs as potential indicators of retinal health
Sander Bervoets, Lonneke Duijkers, Hedwig M Velde, et al.
Molecular Therapy. Methods & Clinical Development
|
June 12, 2023
CRISPR-Cas9 correction of a nonsense mutation in <i>LCA5</i> rescues lebercilin expression and localization in human retinal organoids
Tess A V Afanasyeva, Dimitra Athanasiou, Pedro R L Perdigao, et al.
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of 9
Search research articles
Search
Showing results (51-60 of 82) with videos related to
Sort By:
Page
of 9
International Journal of Molecular Sciences
|
April 1, 2020
In or Out? New Insights on Exon Recognition through Splice-Site Interdependency
Mubeen Khan, Stéphanie S Cornelis, Riccardo Sangermano, et al.
Cell Reports
|
November 11, 2020
The Deubiquitinating Enzyme Ataxin-3 Regulates Ciliogenesis and Phagocytosis in the Retina
Vasileios Toulis, Sílvia García-Monclús, Carlos de la Peña-Ramírez, et al.
Plos Computational Biology
|
August 7, 2023
Comparative Clustering (CompaCt) of eukaryote complexomes identifies novel interactions and sheds light on protein complex evolution
Joeri van Strien, Felix Evers, Madhurya Lutikurti, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
January 20, 2024
Proof-of-concept for multiple AON delivery by a single U7snRNA vector to restore splicing defects in ABCA4
Nuria Suárez-Herrera, Iris B Riswick, Irene Vázquez-Domínguez, et al.
Cells
|
April 12, 2024
Preclinical Development of Antisense Oligonucleotides to Rescue Aberrant Splicing Caused by an Ultrarare <i>ABCA4</i> Variant in a Child with Early-Onset Stargardt Disease
Nuria Suárez-Herrera, Catherina H Z Li, Nico Leijsten, et al.
Genome Research
|
November 23, 2017
<i>ABCA4</i> midigenes reveal the full splice spectrum of all reported noncanonical splice site variants in Stargardt disease
Riccardo Sangermano, Mubeen Khan, Stéphanie S Cornelis, et al.
Human Molecular Genetics
|
September 11, 2021
Systemic complement levels in patients with age-related macular degeneration carrying rare or low-frequency variants in the CFH gene
Sarah de Jong, Anita de Breuk, Elena B Volokhina, et al.
Scientific Reports
|
September 17, 2017
Therapeutic effects of the mitochondrial ROS-redox modulator KH176 in a mammalian model of Leigh Disease
Ria de Haas, Devashish Das, Alejandro Garanto, et al.
Cellular and Molecular Life Sciences : CMLS
|
January 13, 2026
Exploring extracellular vesicle MicroRNAs in Usher syndrome type 1B: Tear-Derived EVs as potential indicators of retinal health
Sander Bervoets, Lonneke Duijkers, Hedwig M Velde, et al.
Molecular Therapy. Methods & Clinical Development
|
June 12, 2023
CRISPR-Cas9 correction of a nonsense mutation in <i>LCA5</i> rescues lebercilin expression and localization in human retinal organoids
Tess A V Afanasyeva, Dimitra Athanasiou, Pedro R L Perdigao, et al.
Page
of 9