PHOX2B in respiratory control: Lessons from congenital central hypoventilation syndrome and its mouse models-Reference-Cited by-同舟云学术

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PHOX2B in respiratory control: Lessons from congenital central hypoventilation syndrome and its mouse models

Published:2009-08 Issue:1-2 Volume:168 Page:125-132
ISSN:1569-9048
Container-title:Respiratory Physiology & Neurobiology
language:en
Short-container-title:Respiratory Physiology & Neurobiology

Author:

Amiel Jeanne,Dubreuil Véronique,Ramanantsoa Nélina,Fortin Gilles,Gallego Jorge,Brunet Jean-François,Goridis Christo

Publisher

Elsevier BV

Subject

Pulmonary and Respiratory Medicine,Physiology,General Neuroscience

Reference75 articles.

1. Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome;Amiel;Nat. Genet.,2003

2. Polyalanine expansions in human;Amiel;Hum. Mol. Genet.,2004

3. Inclusion body formation reduces levels of mutant huntingtin and the risk of neuronal death;Arrasate;Nature,2004

4. Geldanamycin promotes nuclear localisation and clearance of PHOX2B misfolded proteins containing polyalanine expansions;Bachetti;Int. J. Biochem. Cell Biol.,2007

5. PMX2B, a new candidate gene for Hirschsprung's disease;Benailly;Clin. Genet.,2003

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4. Central CO₂ chemosensitivity and CO₂ controller gain independently contribute to daytime Pco₂ in young subjects with congenital central hypoventilation syndrome;Journal of Applied Physiology;2023-08-01

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