Cargando…
Wnt1 Lineage Specific Deletion of Gpr161 Results in Embryonic Midbrain Malformation and Failure of Craniofacial Skeletal Development
Sonic hedgehog (Shh) signaling regulates multiple morphogenetic processes during embryonic neurogenesis and craniofacial skeletal development. Gpr161 is a known negative regulator of Shh signaling. Nullizygous Gpr161 mice are embryonic lethal, presenting with structural defects involving the neural...
Autores principales: | Kim, Sung-Eun, Robles-Lopez, Karla, Cao, Xuanye, Liu, Kristyn, Chothani, Pooja J., Bhavani, Nikitha, Rahman, Lauren, Mukhopadhyay, Saikat, Wlodarczyk, Bogdan J., Finnell, Richard H. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8650154/ https://www.ncbi.nlm.nih.gov/pubmed/34887903 http://dx.doi.org/10.3389/fgene.2021.761418 |
Ejemplares similares
-
Pax3 lineage-specific deletion of Gpr161 is associated with spinal neural tube and craniofacial malformations during embryonic development
por: Kim, Sung-Eun, et al.
Publicado: (2023) -
Ciliary and extraciliary Gpr161 pools repress hedgehog signaling in a tissue-specific manner
por: Hwang, Sun-Hee, et al.
Publicado: (2021) -
Smoothened determines β-arrestin–mediated removal of the G protein–coupled receptor Gpr161 from the primary cilium
por: Pal, Kasturi, et al.
Publicado: (2016) -
Germline GPR161 Mutations Predispose to Pediatric Medulloblastoma
por: Begemann, Matthias, et al.
Publicado: (2020) -
Fuz Regulates Craniofacial Development through Tissue Specific Responses to Signaling Factors
por: Zhang, Zichao, et al.
Publicado: (2011)