Cargando…
Gpr63 is a modifier of microcephaly in Ttc21b mouse mutants
The primary cilium is a signaling center critical for proper embryonic development. Previous studies have demonstrated that mice lacking Ttc21b have impaired retrograde trafficking within the cilium and multiple organogenesis phenotypes, including microcephaly. Interestingly, the severity of the mic...
Autores principales: | Snedeker, John, Gibbons, William J., Paulding, David F., Abdelhamed, Zakia, Prows, Daniel R., Stottmann, Rolf W. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6881074/ https://www.ncbi.nlm.nih.gov/pubmed/31730647 http://dx.doi.org/10.1371/journal.pgen.1008467 |
Ejemplares similares
-
Ttc21b Is Required in Bergmann Glia for Proper Granule Cell Radial Migration
por: Driver, Ashley M., et al.
Publicado: (2017) -
A novel hypomorphic allele of Spag17 causes primary ciliary dyskinesia phenotypes in mice
por: Abdelhamed, Zakia, et al.
Publicado: (2020) -
Correction: A novel hypomorphic allele of Spag17 causes primary ciliary dyskinesia phenotypes in mice
por: Abdelhamed, Zakia, et al.
Publicado: (2021) -
Heart disease in a mutant mouse model of spontaneous eosinophilic myocarditis maps to three loci
por: Zimmermann, Nives, et al.
Publicado: (2019) -
TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum
por: Davis, Erica E., et al.
Publicado: (2011)