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Julio C Corral-Serrano

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Cellular and Molecular Life Sciences : CMLS|August 22, 2021
A look into retinal organoids: methods, analytical techniques, and applicationsTess A V Afanasyeva, Julio C Corral-Serrano, Alejandro Garanto, et al.
Progress in Retinal and Eye Research|February 18, 2024
Pluripotent stem cell-derived models of retinal disease: Elucidating pathogenesis, evaluating novel treatments, and estimating toxicityMarzena Kurzawa-Akanbi, Nikolaos Tzoumas, Julio C Corral-Serrano, et al.
Scientific Reports|June 28, 2018
C2orf71a/pcare1 is important for photoreceptor outer segment morphogenesis and visual function in zebrafishJulio C Corral-Serrano, Muriël Messchaert, Margo Dona, et al.
Human Molecular Genetics|April 24, 2016
In vitro and in vivo rescue of aberrant splicing in CEP290-associated LCA by antisense oligonucleotide deliveryAlejandro Garanto, Daniel C Chung, Lonneke Duijkers, et al.
Plos One|July 28, 2018
Eyes shut homolog is important for the maintenance of photoreceptor morphology and visual function in zebrafishMuriël Messchaert, Margo Dona, Sanne Broekman, et al.
Cells|June 28, 2023
Eupatilin Improves Cilia Defects in Human CEP290 Ciliopathy ModelsJulio C Corral-Serrano, Paul E Sladen, Daniele Ottaviani, et al.
Acta Neuropathologica Communications|February 11, 2025
Small molecule treatment alleviates photoreceptor cilia defects in LCA5-deficient human retinal organoidsDimitra Athanasiou, Tess A V Afanasyeva, Niuzheng Chai, et al.
Molecular Therapy. Nucleic Acids|June 17, 2026
Antisense oligonucleotide allele-specific targeting of EFEMP1 in a patient-derived model of Doyne honeycomb retinal dystrophyFarah O Rezek, Beatriz Sanchez-Pintado, Emily R Eden, et al.
Human Molecular Genetics|March 4, 2025
A novel recurrent ARL3 variant c.209G > A p.(Gly70Glu) causes variable non-syndromic dominant retinal dystrophy with defective lipidated protein transport in human retinal stem cell modelsJulio C Corral-Serrano, Veronika Vaclavik, Stijn Van de Sompele, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 22, 2020
PCARE and WASF3 regulate ciliary F-actin assembly that is required for the initiation of photoreceptor outer segment disk formationJulio C Corral-Serrano, Ideke J C Lamers, Jeroen van Reeuwijk, et al.
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Showing results (1-10 of 11) with videos related to

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Pageof 2
Cellular and Molecular Life Sciences : CMLS|August 22, 2021
A look into retinal organoids: methods, analytical techniques, and applicationsTess A V Afanasyeva, Julio C Corral-Serrano, Alejandro Garanto, et al.
Progress in Retinal and Eye Research|February 18, 2024
Pluripotent stem cell-derived models of retinal disease: Elucidating pathogenesis, evaluating novel treatments, and estimating toxicityMarzena Kurzawa-Akanbi, Nikolaos Tzoumas, Julio C Corral-Serrano, et al.
Scientific Reports|June 28, 2018
C2orf71a/pcare1 is important for photoreceptor outer segment morphogenesis and visual function in zebrafishJulio C Corral-Serrano, Muriël Messchaert, Margo Dona, et al.
Human Molecular Genetics|April 24, 2016
In vitro and in vivo rescue of aberrant splicing in CEP290-associated LCA by antisense oligonucleotide deliveryAlejandro Garanto, Daniel C Chung, Lonneke Duijkers, et al.
Plos One|July 28, 2018
Eyes shut homolog is important for the maintenance of photoreceptor morphology and visual function in zebrafishMuriël Messchaert, Margo Dona, Sanne Broekman, et al.
Cells|June 28, 2023
Eupatilin Improves Cilia Defects in Human CEP290 Ciliopathy ModelsJulio C Corral-Serrano, Paul E Sladen, Daniele Ottaviani, et al.
Acta Neuropathologica Communications|February 11, 2025
Small molecule treatment alleviates photoreceptor cilia defects in LCA5-deficient human retinal organoidsDimitra Athanasiou, Tess A V Afanasyeva, Niuzheng Chai, et al.
Molecular Therapy. Nucleic Acids|June 17, 2026
Antisense oligonucleotide allele-specific targeting of EFEMP1 in a patient-derived model of Doyne honeycomb retinal dystrophyFarah O Rezek, Beatriz Sanchez-Pintado, Emily R Eden, et al.
Human Molecular Genetics|March 4, 2025
A novel recurrent ARL3 variant c.209G > A p.(Gly70Glu) causes variable non-syndromic dominant retinal dystrophy with defective lipidated protein transport in human retinal stem cell modelsJulio C Corral-Serrano, Veronika Vaclavik, Stijn Van de Sompele, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 22, 2020
PCARE and WASF3 regulate ciliary F-actin assembly that is required for the initiation of photoreceptor outer segment disk formationJulio C Corral-Serrano, Ideke J C Lamers, Jeroen van Reeuwijk, et al.
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