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Ruxandra Bachmann

Showing results (21-30 of 51) with videos related to

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Scientific Reports|February 4, 2018
The ciliopathy protein TALPID3/KIAA0586 acts upstream of Rab8 activation in zebrafish photoreceptor outer segment formation and maintenanceIrene Ojeda Naharros, Flavia B Cristian, Jingjing Zang, et al.
Plos Genetics|December 28, 2017
Loss-of-function of the ciliopathy protein Cc2d2a disorganizes the vesicle fusion machinery at the periciliary membrane and indirectly affects Rab8-trafficking in zebrafish photoreceptorsIrene Ojeda Naharros, Matthias Gesemann, José M Mateos, et al.
Journal of Cell Science|June 22, 2021
Genetic compensation for cilia defects in cep290 mutants by upregulation of cilia-associated small GTPasesMagdalena Cardenas-Rodriguez, Christina Austin-Tse, Judith G M Bergboer, et al.
Journal of Visualized Experiments : Jove|November 21, 2017
Correlative Super-resolution and Electron Microscopy to Resolve Protein Localization in Zebrafish RetinaJosé M Mateos, Gery Barmettler, Jana Doehner, et al.
Frontiers in Cell and Developmental Biology|April 28, 2025
Differences in neuronal ciliation rate and ciliary content revealed by systematic imaging-based analysis of hiPSC-derived models across protocolsWalther Haenseler, Melanie Eschment, Beth Evans, et al.
Biorxiv : the Preprint Server for Biology|October 10, 2024
Pythia: Non-random DNA repair allows predictable CRISPR/Cas9 integration and gene editingThomas Naert, Taiyo Yamamoto, Shuting Han, et al.
Nature Communications|March 12, 2022
Loss of the Bardet-Biedl protein Bbs1 alters photoreceptor outer segment protein and lipid compositionMarkus Masek, Christelle Etard, Claudia Hofmann, et al.
Journal of Cell Science|October 9, 2025
CEP290 deficiency disrupts ciliary axonemal architecture in human iPSC-derived brain organoidsMelanie Eschment, Olivier Mercey, Ellen M Aarts, et al.
Human Mutation|June 23, 2015
KIAA0586 is Mutated in Joubert SyndromeRuxandra Bachmann-Gagescu, Ian G Phelps, Jennifer C Dempsey, et al.
Nature Biotechnology|August 12, 2025
Precise, predictable genome integrations by deep-learning-assisted design of microhomology-based templatesThomas Naert, Taiyo Yamamoto, Shuting Han, et al.
Pageof 6

Showing results (21-30 of 51) with videos related to

Sort By:
Pageof 6
Scientific Reports|February 4, 2018
The ciliopathy protein TALPID3/KIAA0586 acts upstream of Rab8 activation in zebrafish photoreceptor outer segment formation and maintenanceIrene Ojeda Naharros, Flavia B Cristian, Jingjing Zang, et al.
Plos Genetics|December 28, 2017
Loss-of-function of the ciliopathy protein Cc2d2a disorganizes the vesicle fusion machinery at the periciliary membrane and indirectly affects Rab8-trafficking in zebrafish photoreceptorsIrene Ojeda Naharros, Matthias Gesemann, José M Mateos, et al.
Journal of Cell Science|June 22, 2021
Genetic compensation for cilia defects in cep290 mutants by upregulation of cilia-associated small GTPasesMagdalena Cardenas-Rodriguez, Christina Austin-Tse, Judith G M Bergboer, et al.
Journal of Visualized Experiments : Jove|November 21, 2017
Correlative Super-resolution and Electron Microscopy to Resolve Protein Localization in Zebrafish RetinaJosé M Mateos, Gery Barmettler, Jana Doehner, et al.
Frontiers in Cell and Developmental Biology|April 28, 2025
Differences in neuronal ciliation rate and ciliary content revealed by systematic imaging-based analysis of hiPSC-derived models across protocolsWalther Haenseler, Melanie Eschment, Beth Evans, et al.
Biorxiv : the Preprint Server for Biology|October 10, 2024
Pythia: Non-random DNA repair allows predictable CRISPR/Cas9 integration and gene editingThomas Naert, Taiyo Yamamoto, Shuting Han, et al.
Nature Communications|March 12, 2022
Loss of the Bardet-Biedl protein Bbs1 alters photoreceptor outer segment protein and lipid compositionMarkus Masek, Christelle Etard, Claudia Hofmann, et al.
Journal of Cell Science|October 9, 2025
CEP290 deficiency disrupts ciliary axonemal architecture in human iPSC-derived brain organoidsMelanie Eschment, Olivier Mercey, Ellen M Aarts, et al.
Human Mutation|June 23, 2015
KIAA0586 is Mutated in Joubert SyndromeRuxandra Bachmann-Gagescu, Ian G Phelps, Jennifer C Dempsey, et al.
Nature Biotechnology|August 12, 2025
Precise, predictable genome integrations by deep-learning-assisted design of microhomology-based templatesThomas Naert, Taiyo Yamamoto, Shuting Han, et al.
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