Pak1ip1 Loss-of-Function Leads to Cell Cycle Arrest, Loss of Neural Crest Cells, and Craniofacial Abnormalities.
Pak1ip1
development
mouse
neural crest
orofacial clefts
ribosomopathies
Journal
Frontiers in cell and developmental biology
ISSN: 2296-634X
Titre abrégé: Front Cell Dev Biol
Pays: Switzerland
ID NLM: 101630250
Informations de publication
Date de publication:
2020
2020
Historique:
received:
05
11
2019
accepted:
13
08
2020
entrez:
28
9
2020
pubmed:
29
9
2020
medline:
29
9
2020
Statut:
epublish
Résumé
Neural crest cells (NCCs) comprise a transient progenitor cell population of neuroepithelial origin that contributes to a variety of cell types throughout vertebrate embryos including most mesenchymal cells of the cranial and facial structures. Consequently, abnormal NCC development underlies a variety of craniofacial defects including orofacial clefts, which constitute some of the most common birth defects. We previously reported the generation of
Identifiants
pubmed: 32984348
doi: 10.3389/fcell.2020.510063
pmc: PMC7490522
doi:
Types de publication
Journal Article
Langues
eng
Pagination
510063Subventions
Organisme : NIDCR NIH HHS
ID : R01 DE022830
Pays : United States
Informations de copyright
Copyright © 2020 Panoutsopoulos, De Crescenzo, Lee, Lu, Ross, Borodinsky, Marcucio, Trainor and Zarbalis.
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