Necdin shapes serotonergic development and SERT activity modulating breathing in a mouse model for Prader-Willi syndrome

Prader-Willi syndrome (PWS) is a genetic neurodevelopmental disorder that presents with hypotonia and respiratory distress in neonates. The Necdin-deficient mouse is the only model that reproduces the respiratory phenotype of PWS (central apnea and blunted response to respiratory challenges). Here,...

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Principais autores:	Valéry Matarazzo, Laura Caccialupi, Fabienne Schaller, Yuri Shvarev, Nazim Kourdougli, Alessandra Bertoni, Clément Menuet, Nicolas Voituron, Evan Deneris, Patricia Gaspar, Laurent Bezin, Pascale Durbec, Gérard Hilaire, Françoise Muscatelli
פורמט:	Artigo
שפה:	Inglês
יצא לאור:	eLife Sciences Publications Ltd 2017-10-01
סדרה:	eLife
נושאים:	serotonin necdin Prader-Willi Syndrome respiration apnea neurodevelopment
גישה מקוונת:	https://elifesciences.org/articles/32640
תגים:	הוספת תג אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!