Cargando…
Axonemal Symmetry Break, a New Ultrastructural Diagnostic Tool for Primary Ciliary Dyskinesia?
Diagnosis testing for primary ciliary dyskinesia (PCD) requires a combination of investigations that includes study of ciliary beat pattern by high-speed video-microscopy, genetic testing and assessment of the ciliary ultrastructure by transmission electron microscopy (TEM). Historically, TEM was co...
Autores principales: | Blanco-Máñez, Rosana, Armengot-Carceller, Miguel, Jaijo, Teresa, Vera-Sempere, Francisco |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8774754/ https://www.ncbi.nlm.nih.gov/pubmed/35054295 http://dx.doi.org/10.3390/diagnostics12010129 |
Ejemplares similares
-
Understanding Primary Ciliary Dyskinesia: Experience From a Mediterranean Diagnostic Reference Centre
por: Armengot-Carceller, Miguel, et al.
Publicado: (2020) -
Mutations in axonemal dynein assembly factor DNAAF3 cause primary ciliary dyskinesia
por: Mitchison, Hannah M., et al.
Publicado: (2012) -
Ciliary beat pattern is associated with specific ultrastructural defects in primary ciliary dyskinesia()
por: Chilvers, Mark A, et al.
Publicado: (2003) -
X-linked primary ciliary dyskinesia due to mutations in the cytoplasmic axonemal dynein assembly factor PIH1D3
por: Olcese, Chiara, et al.
Publicado: (2017) -
The Drosophila orthologue of the primary ciliary dyskinesia-associated gene, DNAAF3, is required for axonemal dynein assembly
por: zur Lage, Petra, et al.
Publicado: (2021)