Cargando…
A Complex of BBS1 and NPHP7 Is Required for Cilia Motility in Zebrafish
Bardet-Biedl syndrome (BBS) and nephronophthisis (NPH) are hereditary autosomal recessive disorders, encoded by two families of diverse genes. BBS and NPH display several overlapping phenotypes including cystic kidney disease, retinitis pigmentosa, liver fibrosis, situs inversus and cerebellar defec...
Autores principales: | Kim, Yun Hee, Epting, Daniel, Slanchev, Krasimir, Engel, Christina, Walz, Gerd, Kramer-Zucker, Albrecht |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3771994/ https://www.ncbi.nlm.nih.gov/pubmed/24069149 http://dx.doi.org/10.1371/journal.pone.0072549 |
Ejemplares similares
-
Microridge-like structures anchor motile cilia
por: Yasunaga, Takayuki, et al.
Publicado: (2022) -
Clock genes rescue nphp mutations in zebrafish
por: Kayser, Nicolas, et al.
Publicado: (2022) -
The C175R mutation alters nuclear localization and transcriptional activity of the nephronophthisis NPHP7 gene product
por: Ramachandran, Haribaskar, et al.
Publicado: (2016) -
USP9X counteracts differential ubiquitination of NPHP5 by MARCH7 and BBS11 to regulate ciliogenesis
por: Das, Arindam, et al.
Publicado: (2017) -
BBS7–SHH Signaling Activity Regulates Primary Cilia for Periodontal Homeostasis
por: Chang, Pi En, et al.
Publicado: (2021)