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Mashal Kakakhel

Showing results (1-10 of 11) with videos related to

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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.
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.
Frontiers in Cellular Neuroscience|May 16, 2020
Photoreceptor Disc Enclosure Occurs in the Absence of Normal Peripherin-2/rds OligomerizationTylor R Lewis, Mustafa S Makia, Mashal Kakakhel, 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.
Human Molecular Genetics|July 28, 2020
ROM1 contributes to phenotypic heterogeneity in PRPH2-associated retinal diseaseDaniel Strayve, Mustafa S Makia, Mashal Kakakhel, et al.
Redox Biology|June 23, 2022
Riboflavin deficiency leads to irreversible cellular changes in the RPE and disrupts retinal function through alterations in cellular metabolic homeostasisTirthankar Sinha, Larissa Ikelle, 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.
Cellular and Molecular Life Sciences : CMLS|July 19, 2023
Comparative study of PRPH2 D2 loop mutants reveals divergent disease mechanism in rods and conesLarissa Ikelle, Mustafa Makia, Tylor Lewis, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
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.
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.
Frontiers in Cellular Neuroscience|May 16, 2020
Photoreceptor Disc Enclosure Occurs in the Absence of Normal Peripherin-2/rds OligomerizationTylor R Lewis, Mustafa S Makia, Mashal Kakakhel, 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.
Human Molecular Genetics|July 28, 2020
ROM1 contributes to phenotypic heterogeneity in PRPH2-associated retinal diseaseDaniel Strayve, Mustafa S Makia, Mashal Kakakhel, et al.
Redox Biology|June 23, 2022
Riboflavin deficiency leads to irreversible cellular changes in the RPE and disrupts retinal function through alterations in cellular metabolic homeostasisTirthankar Sinha, Larissa Ikelle, 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.
Cellular and Molecular Life Sciences : CMLS|July 19, 2023
Comparative study of PRPH2 D2 loop mutants reveals divergent disease mechanism in rods and conesLarissa Ikelle, Mustafa Makia, Tylor Lewis, et al.
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