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Scientific Reports
|
June 28, 2018
C2orf71a/pcare1 is important for photoreceptor outer segment morphogenesis and visual function in zebrafish
Julio C Corral-Serrano, Muriël Messchaert, Margo Dona, et al.
Human Genetics
|
June 2, 2016
Identification of a homozygous nonsense mutation in KIAA0556 in a consanguineous family displaying Joubert syndrome
Susanne Roosing, Rasim O Rosti, Basak Rosti, et al.
International Journal of Molecular Sciences
|
September 10, 2021
Efficient Generation of Knock-In Zebrafish Models for Inherited Disorders Using CRISPR-Cas9 Ribonucleoprotein Complexes
Erik de Vrieze, Suzanne E de Bruijn, Janine Reurink, et al.
Molecular Therapy. Nucleic Acids
|
June 14, 2023
A protein domain-oriented approach to expand the opportunities of therapeutic exon skipping for <i>USH2A</i>-associated retinitis pigmentosa
Renske T W Schellens, Sanne Broekman, Theo Peters, et al.
Progress in Retinal and Eye Research
|
May 5, 2015
The pros and cons of vertebrate animal models for functional and therapeutic research on inherited retinal dystrophies
Ralph W N Slijkerman, Fei Song, Galuh D N Astuti, et al.
International Journal of Molecular Sciences
|
September 10, 2021
Zebrafish as a Model to Evaluate a CRISPR/Cas9-Based Exon Excision Approach as a Future Treatment Option for <i>EYS</i>-Associated Retinitis Pigmentosa
Renske Schellens, Erik de Vrieze, Pam Graave, et al.
Molecular Therapy. Nucleic Acids
|
October 2, 2025
Exploring exon excision as a therapeutic intervention strategy for the future treatment of <i>ADGRV1-</i>associated retinitis pigmentosa
Merel Stemerdink, Lucija Malinar, Sanne Broekman, et al.
The Annals of Otology, Rhinology, and Laryngology
|
July 28, 2004
Longitudinal phenotypic analysis in patients with connexin 26 (GJB2) (DFNB1) and connexin 30 (GJB6) mutations
Christel Stinckens, Hannie Kremer, Erwin van Wijk, et al.
American Journal of Physiology. Heart and Circulatory Physiology
|
September 27, 2024
<i>RRAGD</i> variants cause cardiac dysfunction in a zebrafish model
Anastasia Adella, Faris Tengku, Francisco J Arjona, et al.
Plos One
|
July 28, 2018
Eyes shut homolog is important for the maintenance of photoreceptor morphology and visual function in zebrafish
Muriël Messchaert, Margo Dona, Sanne Broekman, et al.
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of 9
Search research articles
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Showing results (11-20 of 82) with videos related to
Sort By:
Page
of 9
Scientific Reports
|
June 28, 2018
C2orf71a/pcare1 is important for photoreceptor outer segment morphogenesis and visual function in zebrafish
Julio C Corral-Serrano, Muriël Messchaert, Margo Dona, et al.
Human Genetics
|
June 2, 2016
Identification of a homozygous nonsense mutation in KIAA0556 in a consanguineous family displaying Joubert syndrome
Susanne Roosing, Rasim O Rosti, Basak Rosti, et al.
International Journal of Molecular Sciences
|
September 10, 2021
Efficient Generation of Knock-In Zebrafish Models for Inherited Disorders Using CRISPR-Cas9 Ribonucleoprotein Complexes
Erik de Vrieze, Suzanne E de Bruijn, Janine Reurink, et al.
Molecular Therapy. Nucleic Acids
|
June 14, 2023
A protein domain-oriented approach to expand the opportunities of therapeutic exon skipping for <i>USH2A</i>-associated retinitis pigmentosa
Renske T W Schellens, Sanne Broekman, Theo Peters, et al.
Progress in Retinal and Eye Research
|
May 5, 2015
The pros and cons of vertebrate animal models for functional and therapeutic research on inherited retinal dystrophies
Ralph W N Slijkerman, Fei Song, Galuh D N Astuti, et al.
International Journal of Molecular Sciences
|
September 10, 2021
Zebrafish as a Model to Evaluate a CRISPR/Cas9-Based Exon Excision Approach as a Future Treatment Option for <i>EYS</i>-Associated Retinitis Pigmentosa
Renske Schellens, Erik de Vrieze, Pam Graave, et al.
Molecular Therapy. Nucleic Acids
|
October 2, 2025
Exploring exon excision as a therapeutic intervention strategy for the future treatment of <i>ADGRV1-</i>associated retinitis pigmentosa
Merel Stemerdink, Lucija Malinar, Sanne Broekman, et al.
The Annals of Otology, Rhinology, and Laryngology
|
July 28, 2004
Longitudinal phenotypic analysis in patients with connexin 26 (GJB2) (DFNB1) and connexin 30 (GJB6) mutations
Christel Stinckens, Hannie Kremer, Erwin van Wijk, et al.
American Journal of Physiology. Heart and Circulatory Physiology
|
September 27, 2024
<i>RRAGD</i> variants cause cardiac dysfunction in a zebrafish model
Anastasia Adella, Faris Tengku, Francisco J Arjona, et al.
Plos One
|
July 28, 2018
Eyes shut homolog is important for the maintenance of photoreceptor morphology and visual function in zebrafish
Muriël Messchaert, Margo Dona, Sanne Broekman, et al.
Page
of 9