S1PR2 variants associated with auditory function in humans and endocochlear potential decline in mouse-Reference-Cited by-同舟云学术

S1PR2 variants associated with auditory function in humans and endocochlear potential decline in mouse

Published:2016-07-07 Issue:1 Volume:6 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Ingham Neil J.,Carlisle Francesca,Pearson Selina,Lewis Morag A.,Buniello Annalisa,Chen Jing,Isaacson Rivka L.,Pass Johanna,White Jacqueline K.,Dawson Sally J.,Steel Karen P.

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/srep28964.pdf

Reference48 articles.

1. Chen, J. et al. Spinster homolog 2 (Spns2) deficiency causes early onset progressive hearing loss. PLoS Genet. 30, e1004688 (2014).

2. MacLennan, A. et al. The S1P2 sphingosine 1-phosphate receptor is essential for auditory and vestibular function. Hear. Res. 220, 38–48 (2006).

3. Kono, M. et al. Deafness and Stria Vascularis Defects in S1P2 Receptor-null mice. J. Biol. Chem. 282, 10690–10696 (2007).

4. Herr, D. R. et al. Sphingosine 1-Phosphate (S1P) Signaling Is Required for Maintenance of Hair Cells Mainly via Activation of S1P2. J. Neurosci. 27, 1474–1478 (2007).

5. Fyrst, H. & Saba, J. D. An update on sphingosine-1-phosphate and other sphingolipid mediators. Nat. Chem. Biol. 6, 489–497 (2010).

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