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Lars Tebbe

Showing results (1-10 of 17) with videos related to

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Advances in Experimental Medicine and Biology|February 10, 2025
A Knockin Model with the Mouse Equivalent to the c.2299delG Mutation in Usherin Exhibits Early-Onset Hearing Loss and Progressive Retinal DegenerationLars Tebbe, Muayyad R Al-Ubaidi, Muna I Naash
Frontiers in Pharmacology|July 25, 2022
The Neuroprotective Role of Retbindin, a Metabolic Regulator in the Neural RetinaXue Zhao, Lars Tebbe, Muna I Naash, et al.
Frontiers in Cellular Neuroscience|May 27, 2024
The role of syntaxins in retinal function and healthLars Tebbe, Mashal Kakakhel, Muayyad R Al-Ubaidi, et al.
Cells|March 28, 2020
The Interplay between Peripherin 2 Complex Formation and Degenerative Retinal DiseasesLars Tebbe, Mashal Kakakhel, Mustafa S Makia, et al.
Communications Biology|September 12, 2023
Expression of the human usherin c.2299delG mutation leads to early-onset auditory loss and stereocilia disorganizationRyan Crane, Lars Tebbe, Maggie L Mwoyosvi, et al.
Neurobiology of Disease|May 20, 2015
A novel function of Huntingtin in the cilium and retinal ciliopathy in Huntington's disease miceAlice Karam, Lars Tebbe, Chantal Weber, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|November 12, 2025
Syntaxin 3B Mediates Light-Dependent Interactions with STXBP1 and Arrestin 4: Distinct Roles in Rods and ConesLars Tebbe, Larissa Ikelle, Mustafa S Makia, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 28, 2022
Prph2 disease mutations lead to structural and functional defects in the RPELars Tebbe, Haarthi Sakthivel, Mustafa S Makia, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 12, 2020
Syntaxin 3 is essential for photoreceptor outer segment protein trafficking and survivalMashal Kakakhel, Lars Tebbe, Mustafa S Makia, et al.
Nature Communications|February 22, 2023
The usherin mutation c.2299delG leads to its mislocalization and disrupts interactions with whirlin and VLGR1Lars Tebbe, Maggie L Mwoyosvi, Ryan Crane, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Advances in Experimental Medicine and Biology|February 10, 2025
A Knockin Model with the Mouse Equivalent to the c.2299delG Mutation in Usherin Exhibits Early-Onset Hearing Loss and Progressive Retinal DegenerationLars Tebbe, Muayyad R Al-Ubaidi, Muna I Naash
Frontiers in Pharmacology|July 25, 2022
The Neuroprotective Role of Retbindin, a Metabolic Regulator in the Neural RetinaXue Zhao, Lars Tebbe, Muna I Naash, et al.
Frontiers in Cellular Neuroscience|May 27, 2024
The role of syntaxins in retinal function and healthLars Tebbe, Mashal Kakakhel, Muayyad R Al-Ubaidi, et al.
Cells|March 28, 2020
The Interplay between Peripherin 2 Complex Formation and Degenerative Retinal DiseasesLars Tebbe, Mashal Kakakhel, Mustafa S Makia, et al.
Communications Biology|September 12, 2023
Expression of the human usherin c.2299delG mutation leads to early-onset auditory loss and stereocilia disorganizationRyan Crane, Lars Tebbe, Maggie L Mwoyosvi, et al.
Neurobiology of Disease|May 20, 2015
A novel function of Huntingtin in the cilium and retinal ciliopathy in Huntington's disease miceAlice Karam, Lars Tebbe, Chantal Weber, et al.
Advanced Science (Weinheim, Baden-Wurttemberg, Germany)|November 12, 2025
Syntaxin 3B Mediates Light-Dependent Interactions with STXBP1 and Arrestin 4: Distinct Roles in Rods and ConesLars Tebbe, Larissa Ikelle, Mustafa S Makia, et al.
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|March 28, 2022
Prph2 disease mutations lead to structural and functional defects in the RPELars Tebbe, Haarthi Sakthivel, Mustafa S Makia, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 12, 2020
Syntaxin 3 is essential for photoreceptor outer segment protein trafficking and survivalMashal Kakakhel, Lars Tebbe, Mustafa S Makia, et al.
Nature Communications|February 22, 2023
The usherin mutation c.2299delG leads to its mislocalization and disrupts interactions with whirlin and VLGR1Lars Tebbe, Maggie L Mwoyosvi, Ryan Crane, et al.
Pageof 2