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F Boon

Showing results (91-100 of 292) with videos related to

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Molecular Therapy. Methods & Clinical Development|October 27, 2023
Characterization and AAV-mediated <i>CRB</i> gene augmentation in human-derived <i>CRB1</i><sup>KO</sup> and <i>CRB1</i><sup>KO</sup><i>CRB2</i><sup>+/-</sup> retinal organoidsNanda Boon, Xuefei Lu, Charlotte A Andriessen, et al.
Progress in Retinal and Eye Research|September 14, 2013
Cuticular drusen: stars in the skyCamiel J F Boon, Johannes P H van de Ven, Carel B Hoyng, et al.
Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)|November 17, 2023
NOn-Pachychoroid PEripapillary Schisis (NOPPES) of the Retina: A New Phenotype and its Differential DiagnosisMarc J Sirks, Elon H C van Dijk, Laurenz J B Pauleikhoff, et al.
Retina (Philadelphia, Pa.)|December 31, 2015
BESTROPHINOPATHY: A Spectrum of Ocular Abnormalities Caused by the c.614T>C Mutation in the BEST1 GeneLisa Toto, Camiel J F Boon, Luca Di Antonio, 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.
International Journal of Molecular Sciences|April 28, 2023
Retinitis Pigmentosa: Current Clinical Management and Emerging TherapiesXuan-Thanh-An Nguyen, Lude Moekotte, Astrid S Plomp, et al.
Stem Cell Research|May 1, 2026
Generation of four human induced pluripotent stem cell lines derived from patients with corticosteroid-associated central serous chorioretinopathySekar Galuh, Karine Raymond, Joost Brinks, et al.
Progress in Retinal and Eye Research|April 21, 2009
The spectrum of ocular phenotypes caused by mutations in the BEST1 geneCamiel J F Boon, B Jeroen Klevering, Bart P Leroy, et al.
European Journal of Ophthalmology|May 3, 2016
Chronic central serous chorioretinopathy as a presenting symptom of Cushing syndromeElon H C van Dijk, Greet Dijkman, Nienke R Biermasz, et al.
The British Journal of Ophthalmology|February 13, 2021
<i>CRB1</i>-associated retinal dystrophies in a Belgian cohort: genetic characteristics and long-term clinical follow-upMays Talib, Caroline Van Cauwenbergh, Julie De Zaeytijd, et al.
Pageof 30

Showing results (91-100 of 292) with videos related to

Sort By:
Pageof 30
Molecular Therapy. Methods & Clinical Development|October 27, 2023
Characterization and AAV-mediated <i>CRB</i> gene augmentation in human-derived <i>CRB1</i><sup>KO</sup> and <i>CRB1</i><sup>KO</sup><i>CRB2</i><sup>+/-</sup> retinal organoidsNanda Boon, Xuefei Lu, Charlotte A Andriessen, et al.
Progress in Retinal and Eye Research|September 14, 2013
Cuticular drusen: stars in the skyCamiel J F Boon, Johannes P H van de Ven, Carel B Hoyng, et al.
Asia-Pacific Journal of Ophthalmology (Philadelphia, Pa.)|November 17, 2023
NOn-Pachychoroid PEripapillary Schisis (NOPPES) of the Retina: A New Phenotype and its Differential DiagnosisMarc J Sirks, Elon H C van Dijk, Laurenz J B Pauleikhoff, et al.
Retina (Philadelphia, Pa.)|December 31, 2015
BESTROPHINOPATHY: A Spectrum of Ocular Abnormalities Caused by the c.614T>C Mutation in the BEST1 GeneLisa Toto, Camiel J F Boon, Luca Di Antonio, 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.
International Journal of Molecular Sciences|April 28, 2023
Retinitis Pigmentosa: Current Clinical Management and Emerging TherapiesXuan-Thanh-An Nguyen, Lude Moekotte, Astrid S Plomp, et al.
Stem Cell Research|May 1, 2026
Generation of four human induced pluripotent stem cell lines derived from patients with corticosteroid-associated central serous chorioretinopathySekar Galuh, Karine Raymond, Joost Brinks, et al.
Progress in Retinal and Eye Research|April 21, 2009
The spectrum of ocular phenotypes caused by mutations in the BEST1 geneCamiel J F Boon, B Jeroen Klevering, Bart P Leroy, et al.
European Journal of Ophthalmology|May 3, 2016
Chronic central serous chorioretinopathy as a presenting symptom of Cushing syndromeElon H C van Dijk, Greet Dijkman, Nienke R Biermasz, et al.
The British Journal of Ophthalmology|February 13, 2021
<i>CRB1</i>-associated retinal dystrophies in a Belgian cohort: genetic characteristics and long-term clinical follow-upMays Talib, Caroline Van Cauwenbergh, Julie De Zaeytijd, et al.
Pageof 30