Organoid models of breathing disorders reveal patterning defect of hindbrain neurons caused by PHOX2B-PARMs
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Developmental Biology,Genetics,Biochemistry
Reference33 articles.
1. SCENIC: single-cell regulatory network inference and clustering;Aibar;Nat. Methods,2017
2. Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome;Amiel;Nat. Genet.,2003
3. Causative and common PHOX2B variants define a broad phenotypic spectrum;Bachetti;Clin. Genet.,2020
4. V2a interneuron differentiation from mouse and human pluripotent stem cells;Butts;Nat. Protoc.,2019
5. A human mutation in Phox2b causes lack of CO2 chemosensitivity, fatal central apnea, and specific loss of parafacial neurons;Dubreuil;Proc. Natl. Acad. Sci. USA,2008
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