Insights Gained From Zebrafish Models for the Ciliopathy Joubert Syndrome
Cilia are quasi-ubiquitous microtubule-based sensory organelles, which play vital roles in signal transduction during development and cell homeostasis. Dysfunction of cilia leads to a group of Mendelian disorders called ciliopathies, divided into different diagnoses according to clinical phenotype c...
Main Authors: | Tamara D. S. Rusterholz, Claudia Hofmann, Ruxandra Bachmann-Gagescu |
---|---|
Format: | Article |
Language: | English |
Published: |
Frontiers Media S.A.
2022-06-01
|
Series: | Frontiers in Genetics |
Subjects: | |
Online Access: | https://www.frontiersin.org/articles/10.3389/fgene.2022.939527/full |
Similar Items
-
TMEM218 dysfunction causes ciliopathies, including Joubert and Meckel syndromes
by: Julie C. Van De Weghe, et al.
Published: (2021-01-01) -
Novel Compound Heterozygous Variants in MKS1 Leading to Joubert Syndrome
by: Minna Luo, et al.
Published: (2020-10-01) -
CPLANE Complex and Ciliopathies
by: Jesús Eduardo Martín-Salazar, et al.
Published: (2022-06-01) -
Ciliopathies in pediatric endocrinology
by: Ilenia Cicolini, et al.
Published: (2023-03-01) -
The role of cilia during organogenesis in zebrafish
by: Junjun Liu, et al.
Published: (2023-12-01)