Cargando…
The Joubert syndrome protein CEP41 is excluded from the distal segment of cilia in C. elegans
Rare diseases are a fundamental issue in today’s world, affecting more than 300 million individuals worldwide. According to data from Orphanet and OMIM, about 50-60 new conditions are added to the list of over 6,000 clinically distinct diseases each year, rendering disease diagnosis and treatment ev...
Autores principales: | Cevik, Sebiha, Kaplan, Oktay I. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Caltech Library
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8185565/ https://www.ncbi.nlm.nih.gov/pubmed/34113804 http://dx.doi.org/10.17912/micropub.biology.000406 |
Ejemplares similares
-
Subcellular localization of the voltage-gated K+ channel EGL-36 , a member of the KV3 subfamily, in the ciliated sensory neurons in C. elegans
por: Cevik, Sebiha, et al.
Publicado: (2021) -
A
ccpp-6
deletion mutation does not impair gross cilia integrity in
C. elegans
por: Dominguez, Jessica, et al.
Publicado: (2022) -
CP110 and CEP135 localize near the proximal and distal centrioles of cattle and human spermatozoa
por: Turner, Katerina A., et al.
Publicado: (2023) -
The
C. elegans
deglutamylase CCPP-6 does not operate redundantly with CCPP-1 in gross cilia integrity
por: Klimas, Abigail S, et al.
Publicado: (2023) -
lin-41 controls dauer formation and morphology via lin-29 in C. elegans
por: Cale, Allison R, et al.
Publicado: (2020)