Lysosomal storage disease upon disruption of the neuronal chloride transport protein ClC-6

Mammalian CLC proteins function as Cl(−) channels or as electrogenic Cl(−)/H(+) exchangers and are present in the plasma membrane and intracellular vesicles. We now show that the ClC-6 protein is almost exclusively expressed in neurons of the central and peripheral nervous systems, with a particular...

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Detaylı Bibliyografya
Asıl Yazarlar: Poët, Mallorie, Kornak, Uwe, Schweizer, Michaela, Zdebik, Anselm A., Scheel, Olaf, Hoelter, Sabine, Wurst, Wolfgang, Schmitt, Anja, Fuhrmann, Jens C., Planells-Cases, Rosa, Mole, Sara E., Hübner, Christian A., Jentsch, Thomas J.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: National Academy of Sciences 2006
Konular:
Biological Sciences
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1564226/
https://ncbi.nlm.nih.gov/pubmed/16950870
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.0606137103
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