Histological characterization of orphan transporter MCT14 (SLC16A14) shows abundant expression in mouse CNS and kidney-Reference-Cited by-同舟云学术

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Histological characterization of orphan transporter MCT14 (SLC16A14) shows abundant expression in mouse CNS and kidney

Published:2016-07-01 Issue:1 Volume:17 Page:
ISSN:1471-2202
Container-title:BMC Neuroscience
language:en
Short-container-title:BMC Neurosci

Author:

Roshanbin Sahar,Lindberg Frida A.,Lekholm Emilia,Eriksson Mikaela M.,Perland Emelie,Åhlund Johan,Raine Amanda,Fredriksson Robert

Funder

Vetenskapsrådet

Novo Nordisk

Åhlén-stiftelsen (SE)

Magnus Bergvalls Stiftelse

Hjärnfonden

svenska sällskapet för medicinsk forskning

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,General Neuroscience

Link

http://link.springer.com/content/pdf/10.1186/s12868-016-0274-7

Reference58 articles.

1. Cesar-Razquin A, Snijder B, Frappier-Brinton T, Isserlin R, Gyimesi G, Bai X, Reithmeier RA, Hepworth D, Hediger MA, Edwards AM, et al. A call for systematic research on solute carriers. Cell. 2015;162(3):478–87.

2. He L, Vasiliou K, Nebert DW. Analysis and update of the human solute carrier (SLC) gene superfamily. Hum Genomics. 2009;3(2):195–206.

3. Hediger MA, Romero MF, Peng JB, Rolfs A, Takanaga H, Bruford EA. The ABCs of solute carriers: physiological, pathological and therapeutic implications of human membrane transport proteins. Pflug Arch. 2004;447(5):465–8.

4. Hediger MA, Clemencon B, Burrier RE, Bruford EA. The ABCs of membrane transporters in health and disease (SLC series): introduction. Mol Asp Med. 2013;34(2–3):95–107.

5. Höglund PJ, Nordström KJ, Schiöth HB, Fredriksson R. The solute carrier families have a remarkably long evolutionary history with the majority of the human families present before divergence of Bilaterian species. Mol Biol Evol. 2011;28(4):1531–41.

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