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Showing results (661-670 of 717) with videos related to

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Acta Ophthalmologica|September 26, 2023
Quality of life in patients with CRB1-associated retinal dystrophies: A longitudinal studyJessica S Karuntu, Xuan-Thanh-An Nguyen, Mays Talib, et al.
Human Mutation|November 4, 2014
Heterozygous deep-intronic variants and deletions in ABCA4 in persons with retinal dystrophies and one exonic ABCA4 variantNathalie M Bax, Riccardo Sangermano, Susanne Roosing, et al.
Cardiovascular Research|January 30, 2024
Networks of gut bacteria relate to cardiovascular disease in a multi-ethnic population: the HELIUS studyMoritz V Warmbrunn, Ulrika Boulund, Judith Aron-Wisnewsky, et al.
Clinical & Experimental Ophthalmology|July 11, 2026
CRB1-Associated Inherited Retinal Dystrophies: Prospective Natural History Study With 4 Years of Follow-UpJessica S Karuntu, Xuan-Thanh-An Nguyen, Mays Talib, et al.
Journal of Clinical Medicine|October 10, 2020
Biopsy-Controlled Non-Invasive Quantification of Collagen Type VI in Kidney Transplant Recipients: A Post-Hoc Analysis of the MECANO TrialManuela Yepes-Calderón, Camilo G Sotomayor, Daniel Guldager Kring Rasmussen, et al.
Journal of Medical Genetics|April 27, 2017
Missense mutations in the WD40 domain of <i>AHI1</i> cause non-syndromic retinitis pigmentosaThanh-Minh T Nguyen, Sarah Hull, Ronald Roepman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 29, 2024
Loss-of-function variants in UBAP1L cause autosomal recessive retinal degenerationJi Hoon Han, Kim Rodenburg, Tamar Hayman, et al.
Human Molecular Genetics|August 30, 2014
Mutations in IFT172 cause isolated retinal degeneration and Bardet-Biedl syndromeKinga M Bujakowska, Qi Zhang, Anna M Siemiatkowska, et al.
Nature Genetics|October 3, 1999
Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)A I den Hollander, J B ten Brink, Y J de Kok, et al.
Ophthalmology Science|March 21, 2025
Automated Cone Photoreceptor Detection in Adaptive Optics Flood Illumination OphthalmoscopySander Wooning, Pam A T Heutinck, Kubra Liman, et al.
Pageof 72

Showing results (661-670 of 717) with videos related to

Sort By:
Pageof 72
Acta Ophthalmologica|September 26, 2023
Quality of life in patients with CRB1-associated retinal dystrophies: A longitudinal studyJessica S Karuntu, Xuan-Thanh-An Nguyen, Mays Talib, et al.
Human Mutation|November 4, 2014
Heterozygous deep-intronic variants and deletions in ABCA4 in persons with retinal dystrophies and one exonic ABCA4 variantNathalie M Bax, Riccardo Sangermano, Susanne Roosing, et al.
Cardiovascular Research|January 30, 2024
Networks of gut bacteria relate to cardiovascular disease in a multi-ethnic population: the HELIUS studyMoritz V Warmbrunn, Ulrika Boulund, Judith Aron-Wisnewsky, et al.
Clinical & Experimental Ophthalmology|July 11, 2026
CRB1-Associated Inherited Retinal Dystrophies: Prospective Natural History Study With 4 Years of Follow-UpJessica S Karuntu, Xuan-Thanh-An Nguyen, Mays Talib, et al.
Journal of Clinical Medicine|October 10, 2020
Biopsy-Controlled Non-Invasive Quantification of Collagen Type VI in Kidney Transplant Recipients: A Post-Hoc Analysis of the MECANO TrialManuela Yepes-Calderón, Camilo G Sotomayor, Daniel Guldager Kring Rasmussen, et al.
Journal of Medical Genetics|April 27, 2017
Missense mutations in the WD40 domain of <i>AHI1</i> cause non-syndromic retinitis pigmentosaThanh-Minh T Nguyen, Sarah Hull, Ronald Roepman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 29, 2024
Loss-of-function variants in UBAP1L cause autosomal recessive retinal degenerationJi Hoon Han, Kim Rodenburg, Tamar Hayman, et al.
Human Molecular Genetics|August 30, 2014
Mutations in IFT172 cause isolated retinal degeneration and Bardet-Biedl syndromeKinga M Bujakowska, Qi Zhang, Anna M Siemiatkowska, et al.
Nature Genetics|October 3, 1999
Mutations in a human homologue of Drosophila crumbs cause retinitis pigmentosa (RP12)A I den Hollander, J B ten Brink, Y J de Kok, et al.
Ophthalmology Science|March 21, 2025
Automated Cone Photoreceptor Detection in Adaptive Optics Flood Illumination OphthalmoscopySander Wooning, Pam A T Heutinck, Kubra Liman, et al.
Pageof 72