Transcriptomic Signatures of Single-Suture Craniosynostosis Phenotypes

Transcriptomic Signatures of Single-Suture Craniosynostosis Phenotypes

Craniosynostosis is a birth defect where calvarial sutures close prematurely, as part of a genetic syndrome or independently, with unknown cause. This study aimed to identify differences in gene expression in primary calvarial cell lines derived from patients with four phenotypes of single-suture cr...

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Bibliographic Details
Main Authors: Samantha Lapehn, Jonas A. Gustafson, Andrew E. Timms, Michael L. Cunningham, Alison G. Paquette
Format: Article
Language:English
Published: MDPI AG 2023-03-01
Series:International Journal of Molecular Sciences
Subjects:
craniosynostosis
RNA sequencing
homeobox
transcriptome
Online Access:https://www.mdpi.com/1422-0067/24/6/5353

Internet

https://www.mdpi.com/1422-0067/24/6/5353

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