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Methods in Molecular Biology (Clifton, N.J.)
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December 1, 2017
Design and In Vitro Use of Antisense Oligonucleotides to Correct Pre-mRNA Splicing Defects in Inherited Retinal Dystrophies
Alejandro Garanto, Rob W J Collin
Current Opinion in Ophthalmology
|
February 3, 2017
Applications of antisense oligonucleotides for the treatment of inherited retinal diseases
Rob W J Collin, Alejandro Garanto
Genes
|
February 9, 2020
Preface of Special Issue "Molecular Therapies for Inherited Retinal Diseases"
Rob W J Collin, Alejandro Garanto
Molecular and Cellular Neurosciences
|
September 13, 2005
The amyloid-beta precursor-like protein APLP2 and its relative APP are differentially regulated during neuroendocrine cell activation
Rob W J Collin, Gerard J M Martens
Brain Research
|
April 22, 2006
The coding sequence of amyloid-beta precursor protein APP contains a neural-specific promoter element
Rob W J Collin, Gerard J M Martens
International Journal of Molecular Sciences
|
March 12, 2015
Species-dependent splice recognition of a cryptic exon resulting from a recurrent intronic CEP290 mutation that causes congenital blindness
Alejandro Garanto, Lonneke Duijkers, Rob W J Collin
Molecular Aspects of Medicine
|
October 2, 2025
Antisense oligonucleotides for inherited retinal diseases: a comprehensive review
Hossein D Banadaki, Alejandro Garanto, Rob W J Collin
Genes
|
August 31, 2019
Molecular Therapies for Inherited Retinal Diseases-Current Standing, Opportunities and Challenges
Irene Vázquez-Domínguez, Alejandro Garanto, Rob W J Collin
Nucleic Acid Therapeutics
|
March 11, 2024
Understanding and Rescuing the Splicing Defect Caused by the Frequent <i>ABCA4</i> Variant c.4253+43G>A Underlying Stargardt Disease
Nuria Suárez-Herrera, Alejandro Garanto, Rob W J Collin
Advances in Experimental Medicine and Biology
|
October 3, 2015
Antisense Oligonucleotide Therapy for Inherited Retinal Dystrophies
Xavier Gerard, Alejandro Garanto, Jean-Michel Rozet, et al.
Page
of 15
Search research articles
Search
Showing results (1-10 of 149) with videos related to
Sort By:
Page
of 15
Methods in Molecular Biology (Clifton, N.J.)
|
December 1, 2017
Design and In Vitro Use of Antisense Oligonucleotides to Correct Pre-mRNA Splicing Defects in Inherited Retinal Dystrophies
Alejandro Garanto, Rob W J Collin
Current Opinion in Ophthalmology
|
February 3, 2017
Applications of antisense oligonucleotides for the treatment of inherited retinal diseases
Rob W J Collin, Alejandro Garanto
Genes
|
February 9, 2020
Preface of Special Issue "Molecular Therapies for Inherited Retinal Diseases"
Rob W J Collin, Alejandro Garanto
Molecular and Cellular Neurosciences
|
September 13, 2005
The amyloid-beta precursor-like protein APLP2 and its relative APP are differentially regulated during neuroendocrine cell activation
Rob W J Collin, Gerard J M Martens
Brain Research
|
April 22, 2006
The coding sequence of amyloid-beta precursor protein APP contains a neural-specific promoter element
Rob W J Collin, Gerard J M Martens
International Journal of Molecular Sciences
|
March 12, 2015
Species-dependent splice recognition of a cryptic exon resulting from a recurrent intronic CEP290 mutation that causes congenital blindness
Alejandro Garanto, Lonneke Duijkers, Rob W J Collin
Molecular Aspects of Medicine
|
October 2, 2025
Antisense oligonucleotides for inherited retinal diseases: a comprehensive review
Hossein D Banadaki, Alejandro Garanto, Rob W J Collin
Genes
|
August 31, 2019
Molecular Therapies for Inherited Retinal Diseases-Current Standing, Opportunities and Challenges
Irene Vázquez-Domínguez, Alejandro Garanto, Rob W J Collin
Nucleic Acid Therapeutics
|
March 11, 2024
Understanding and Rescuing the Splicing Defect Caused by the Frequent <i>ABCA4</i> Variant c.4253+43G>A Underlying Stargardt Disease
Nuria Suárez-Herrera, Alejandro Garanto, Rob W J Collin
Advances in Experimental Medicine and Biology
|
October 3, 2015
Antisense Oligonucleotide Therapy for Inherited Retinal Dystrophies
Xavier Gerard, Alejandro Garanto, Jean-Michel Rozet, et al.
Page
of 15