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DUBAIC M., PESKOVA L., HAMPL M., WEISSOVA K., CELIKER C., SHYLO N., HRUBA E., KAVKOVA M., ZIKMUND T., WEATHERBOO S., KAISER J., BARTA T., BUCHTOVA M.
Original Title
Role of ciliopathy protein TMEM107 in eye development: insights from a mouse model and retinal organoid
Type
journal article in Web of Science
Language
English
Original Abstract
Primary cilia, enriched in receptors and signaling molecules, serve as vital signaling hubs responsive to stimuli and are implicated in human diseases like retinopathies. TMEM107, localized to the transition zone of primary cilia, is linked to conditions such as Joubert and Meckel–Gruber syndromes, and its deficiency hinders cilia formation and early vertebrate eye development in retinal organoids.
Keywords
TMEM107, ciliopathy, eye development, cell biology
Authors
Released
20. 10. 2023
Publisher
Life Science Alliance
ISBN
2575-1077
Periodical
Year of study
6
Number
12
State
United States of America
Pages from
1
Pages to
16
Pages count
URL
https://www.life-science-alliance.org/content/6/12/e202302073
Full text in the Digital Library
http://hdl.handle.net/11012/245089
BibTex
@article{BUT184959, author="Marija {Dubaic} and Lucie {Pešková} and Marek {Hampl} and Kamila {Weissová} and Canan {Celiker} and Natalya A. {Shylo} and Eva {Hrubá} and Michaela {Kavková} and Tomáš {Zikmund} and Scott Donald {Weatherbee} and Jozef {Kaiser} and Tomáš {Bárta} and Marcela {Buchtová}", title="Role of ciliopathy protein TMEM107 in eye development: insights from a mouse model and retinal organoid", journal="Life Science Alliance", year="2023", volume="6", number="12", pages="1--16", doi="10.26508/lsa.202302073", issn="2575-1077", url="https://www.life-science-alliance.org/content/6/12/e202302073" }