Cargando…
Loss of Ift74 Leads to Slow Photoreceptor Degeneration and Ciliogenesis Defects in Zebrafish
Cilia are microtubule-based structures projecting from the cell surface that perform diverse biological functions. Ciliary defects can cause a wide range of genetic disorders known collectively as ciliopathies. Intraflagellar transport (IFT) proteins are essential for the assembly and maintenance of...
Autores principales: | Zhu, Panpan, Xu, Jingjin, Wang, Yadong, Zhao, Chengtian |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8431285/ https://www.ncbi.nlm.nih.gov/pubmed/34502236 http://dx.doi.org/10.3390/ijms22179329 |
Ejemplares similares
-
Robust interaction of IFT70 with IFT52–IFT88 in the IFT-B complex is required for ciliogenesis
por: Takei, Ryota, et al.
Publicado: (2018) -
Deletion of CEP164 in mouse photoreceptors post-ciliogenesis interrupts ciliary intraflagellar transport (IFT)
por: Reed, Michelle, et al.
Publicado: (2022) -
Functional exploration of the IFT-A complex in intraflagellar transport and ciliogenesis
por: Zhu, Bing, et al.
Publicado: (2017) -
Knockdown of ttc26 disrupts ciliogenesis of the photoreceptor cells and the pronephros in zebrafish
por: Zhang, Qi, et al.
Publicado: (2012) -
Novel IFT122 mutation associated with impaired ciliogenesis and cranioectodermal dysplasia
por: Alazami, Anas M, et al.
Publicado: (2014)