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Clinical Dysmorphology
|
July 1, 1995
Wolcott-Rallison syndrome
L I al-Gazali, S Makia, A Azzam, et al.
Redox Biology
|
July 20, 2025
Developmental riboflavin deficiency results in structural and functional changes in the neural retina and RPE
Xue Zhao, Mustafa S Makia, Muna I Naash, et al.
Cells
|
March 28, 2020
The Interplay between Peripherin 2 Complex Formation and Degenerative Retinal Diseases
Lars 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 Cones
Lars Tebbe, Larissa Ikelle, Mustafa S Makia, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 2, 2021
Absence of retbindin blocks glycolytic flux, disrupts metabolic homeostasis, and leads to photoreceptor degeneration
Tirthankar Sinha, Jianhai Du, Mustafa S Makia, et al.
International Journal of Molecular Sciences
|
November 3, 2020
Retbindin: A riboflavin Binding Protein, Is Critical for Photoreceptor Homeostasis and Survival in Models of Retinal Degeneration
Ayse M Genc, Mustafa S Makia, Tirthankar Sinha, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
March 12, 2021
Photoreceptor Disc Enclosure Is Tightly Controlled by Peripherin-2 Oligomerization
Tylor R Lewis, Mustafa S Makia, Carson M Castillo, et al.
Frontiers in Cellular Neuroscience
|
May 16, 2020
Photoreceptor Disc Enclosure Occurs in the Absence of Normal Peripherin-2/rds Oligomerization
Tylor R Lewis, Mustafa S Makia, Mashal Kakakhel, et al.
Investigative Ophthalmology & Visual Science
|
June 10, 2020
Elimination of a Retinal Riboflavin Binding Protein Exacerbates Degeneration in a Model of Cone-Rod Dystrophy
Ayse M Genc, Mustafa S Makia, Tirthankar Sinha, 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 RPE
Lars Tebbe, Haarthi Sakthivel, Mustafa S Makia, et al.
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of 3
Search research articles
Search
Showing results (1-10 of 28) with videos related to
Sort By:
Page
of 3
Clinical Dysmorphology
|
July 1, 1995
Wolcott-Rallison syndrome
L I al-Gazali, S Makia, A Azzam, et al.
Redox Biology
|
July 20, 2025
Developmental riboflavin deficiency results in structural and functional changes in the neural retina and RPE
Xue Zhao, Mustafa S Makia, Muna I Naash, et al.
Cells
|
March 28, 2020
The Interplay between Peripherin 2 Complex Formation and Degenerative Retinal Diseases
Lars 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 Cones
Lars Tebbe, Larissa Ikelle, Mustafa S Makia, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
February 2, 2021
Absence of retbindin blocks glycolytic flux, disrupts metabolic homeostasis, and leads to photoreceptor degeneration
Tirthankar Sinha, Jianhai Du, Mustafa S Makia, et al.
International Journal of Molecular Sciences
|
November 3, 2020
Retbindin: A riboflavin Binding Protein, Is Critical for Photoreceptor Homeostasis and Survival in Models of Retinal Degeneration
Ayse M Genc, Mustafa S Makia, Tirthankar Sinha, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
March 12, 2021
Photoreceptor Disc Enclosure Is Tightly Controlled by Peripherin-2 Oligomerization
Tylor R Lewis, Mustafa S Makia, Carson M Castillo, et al.
Frontiers in Cellular Neuroscience
|
May 16, 2020
Photoreceptor Disc Enclosure Occurs in the Absence of Normal Peripherin-2/rds Oligomerization
Tylor R Lewis, Mustafa S Makia, Mashal Kakakhel, et al.
Investigative Ophthalmology & Visual Science
|
June 10, 2020
Elimination of a Retinal Riboflavin Binding Protein Exacerbates Degeneration in a Model of Cone-Rod Dystrophy
Ayse M Genc, Mustafa S Makia, Tirthankar Sinha, 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 RPE
Lars Tebbe, Haarthi Sakthivel, Mustafa S Makia, et al.
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of 3