Cargando…
Multiomics Analysis of a DNAH5-Mutated PCD Organoid Model Revealed the Key Role of the TGF-β/BMP and Notch Pathways in Epithelial Differentiation and the Immune Response in DNAH5-Mutated Patients
Dynein axonemal heavy chain 5 (DNAH5) is the most mutated gene in primary ciliary dyskinesia (PCD), leading to abnormal cilia ultrastructure and function. Few studies have revealed the genetic characteristics and pathogenetic mechanisms of PCD caused by DNAH5 mutation. Here, we established a child P...
Autores principales: | Yang, Wenhao, Chen, Lina, Guo, Juncen, Shi, Fang, Yang, Qingxin, Xie, Liang, Lu, Danli, Li, Yingna, Luo, Jiaxin, Wang, Li, Qiu, Li, Chen, Ting, Li, Yan, Zhang, Rui, Chen, Lu, Xu, Wenming, Liu, Hanmin |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9776854/ https://www.ncbi.nlm.nih.gov/pubmed/36552777 http://dx.doi.org/10.3390/cells11244013 |
Ejemplares similares
-
Dnah9 mutant mice and organoid models recapitulate the clinical features of patients with PCD and provide an excellent platform for drug screening
por: Zheng, Rui, et al.
Publicado: (2022) -
Novel homozygous mutations of DNAH5 in Kartagener syndrome
por: Cheng, Xian-Dong, et al.
Publicado: (2021) -
Co-occurrence of Moyamoya syndrome and Kartagener syndrome caused by the mutation of DNAH5 and DNAH11: a case report
por: Zhang, Lili, et al.
Publicado: (2020) -
DNAH6 and Its Interactions with PCD Genes in Heterotaxy and Primary Ciliary Dyskinesia
por: Li, You, et al.
Publicado: (2016) -
A Japanese Case of Primary Ciliary Dyskinesia with DNAH5 Mutations
por: Orimo, Mami, et al.
Publicado: (2019)