Cargando…
The Axenfeld–Rieger Syndrome Gene FOXC1 Contributes to Left–Right Patterning
Precise spatiotemporal expression of the Nodal-Lefty-Pitx2 cascade in the lateral plate mesoderm establishes the left–right axis, which provides vital cues for correct organ formation and function. Mutations of one cascade constituent PITX2 and, separately, the Forkhead transcription factor FOXC1 in...
Autores principales: | Chrystal, Paul W., French, Curtis R., Jean, Francesca, Havrylov, Serhiy, van Baarle, Suey, Peturson, Ann-Marie, Xu, Pengfei, Crump, J. Gage, Pilgrim, David B., Lehmann, Ordan J., Waskiewicz, Andrew J. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7912076/ https://www.ncbi.nlm.nih.gov/pubmed/33530637 http://dx.doi.org/10.3390/genes12020170 |
Ejemplares similares
-
Mechanistic Insights into Axenfeld–Rieger Syndrome from Zebrafish foxc1 and pitx2 Mutants
por: French, Curtis R.
Publicado: (2021) -
Novel mutations in the FOXC1 gene in Japanese patients with Axenfeld-Rieger syndrome
por: Fuse, Nobuo, et al.
Publicado: (2007) -
A novel variant in FOXC1 associated with atypical Axenfeld-Rieger syndrome
por: Wang, Rui, et al.
Publicado: (2021) -
A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma
por: Micheal, Shazia, et al.
Publicado: (2016) -
Gene‐specific facial dysmorphism in Axenfeld‐Rieger syndrome caused by FOXC1 and PITX2 variants
por: Souzeau, Emmanuelle, et al.
Publicado: (2020)