Necdin Plays a Role in the Serotonergic Modulation of the Mouse Respiratory Network: Implication for Prader-Willi Syndrome

Prader-Willi syndrome is a neurogenetic disease resulting from the absence of paternal expression of several imprinted genes, including NECDIN. Prader-Willi children and adults have severe breathing defects with irregular rhythm, frequent sleep apneas, and blunted respiratory regulations. For the fi...

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Detalhes bibliográficos
Publicado no:J Neurosci
Main Authors: Zanella, Sébastien, Watrin, Françoise, Mebarek, Saïda, Marly, Fabienne, Roussel, Michel, Gire, Catherine, Diene, Gwenaëlle, Tauber, Maïté, Muscatelli, Françoise, Hilaire, Gérard
Formato: Artigo
Idioma:Inglês
Publicado em: Society for Neuroscience 2008
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6671529/
https://ncbi.nlm.nih.gov/pubmed/18272695
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.4334-07.2008
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