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Rogier M Vos

Showing results (1-10 of 18) with videos related to

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Molecular Therapy. Methods & Clinical Development|February 12, 2021
AAV-<i>CRB2</i> protects against vision loss in an inducible <i>CRB1</i> retinitis pigmentosa mouse modelThilo M Buck, Rogier M Vos, C Henrique Alves, et al.
Methods in Molecular Biology (Clifton, N.J.)|December 1, 2017
AAV Serotype Testing on Cultured Human Donor Retinal ExplantsThilo M Buck, Lucie P Pellissier, Rogier M Vos, et al.
Molecular and Cellular Neurosciences|February 24, 2009
PSD95beta regulates plasma membrane Ca2+ pump localization at the photoreceptor synapseWendy M Aartsen, Jean-Pierre Arsanto, Jean-Paul Chauvin, et al.
Human Molecular Genetics|February 22, 2015
Gene therapy into photoreceptors and Müller glial cells restores retinal structure and function in CRB1 retinitis pigmentosa mouse modelsLucie P Pellissier, Peter M Quinn, C Henrique Alves, et al.
Molecular Therapy. Methods & Clinical Development|May 28, 2015
Specific tools for targeting and expression in Müller glial cellsLucie P Pellissier, Robert M Hoek, Rogier M Vos, et al.
Plos One|December 11, 2013
Microarray and morphological analysis of early postnatal CRB2 mutant retinas on a pure C57BL/6J genetic backgroundCelso Henrique Alves, Koen Bossers, Rogier M Vos, et al.
Atherosclerosis|August 30, 2006
Macrophage-specific inhibition of NF-kappaB activation reduces foam-cell formationValérie Ferreira, Ko Willems van Dijk, Albert K Groen, et al.
Glia|August 21, 2007
Crb1 is a determinant of retinal apical Müller glia cell featuresSerge A van de Pavert, Alicia Sanz Sanz, Wendy M Aartsen, et al.
Human Molecular Genetics|February 26, 2014
CRB2 acts as a modifying factor of CRB1-related retinal dystrophies in miceLucie P Pellissier, Ditte M S Lundvig, Naoyuki Tanimoto, et al.
International Journal of Molecular Sciences|April 3, 2021
Defining Phenotype, Tropism, and Retinal Gene Therapy Using Adeno-Associated Viral Vectors (AAVs) in New-Born Brown Norway Rats with a Spontaneous Mutation in <i>Crb1</i>Nanda Boon, C Henrique Alves, Aat A Mulder, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Molecular Therapy. Methods & Clinical Development|February 12, 2021
AAV-<i>CRB2</i> protects against vision loss in an inducible <i>CRB1</i> retinitis pigmentosa mouse modelThilo M Buck, Rogier M Vos, C Henrique Alves, et al.
Methods in Molecular Biology (Clifton, N.J.)|December 1, 2017
AAV Serotype Testing on Cultured Human Donor Retinal ExplantsThilo M Buck, Lucie P Pellissier, Rogier M Vos, et al.
Molecular and Cellular Neurosciences|February 24, 2009
PSD95beta regulates plasma membrane Ca2+ pump localization at the photoreceptor synapseWendy M Aartsen, Jean-Pierre Arsanto, Jean-Paul Chauvin, et al.
Human Molecular Genetics|February 22, 2015
Gene therapy into photoreceptors and Müller glial cells restores retinal structure and function in CRB1 retinitis pigmentosa mouse modelsLucie P Pellissier, Peter M Quinn, C Henrique Alves, et al.
Molecular Therapy. Methods & Clinical Development|May 28, 2015
Specific tools for targeting and expression in Müller glial cellsLucie P Pellissier, Robert M Hoek, Rogier M Vos, et al.
Plos One|December 11, 2013
Microarray and morphological analysis of early postnatal CRB2 mutant retinas on a pure C57BL/6J genetic backgroundCelso Henrique Alves, Koen Bossers, Rogier M Vos, et al.
Atherosclerosis|August 30, 2006
Macrophage-specific inhibition of NF-kappaB activation reduces foam-cell formationValérie Ferreira, Ko Willems van Dijk, Albert K Groen, et al.
Glia|August 21, 2007
Crb1 is a determinant of retinal apical Müller glia cell featuresSerge A van de Pavert, Alicia Sanz Sanz, Wendy M Aartsen, et al.
Human Molecular Genetics|February 26, 2014
CRB2 acts as a modifying factor of CRB1-related retinal dystrophies in miceLucie P Pellissier, Ditte M S Lundvig, Naoyuki Tanimoto, et al.
International Journal of Molecular Sciences|April 3, 2021
Defining Phenotype, Tropism, and Retinal Gene Therapy Using Adeno-Associated Viral Vectors (AAVs) in New-Born Brown Norway Rats with a Spontaneous Mutation in <i>Crb1</i>Nanda Boon, C Henrique Alves, Aat A Mulder, et al.
Pageof 2