The orphan solute carrier SLC10A7 is a novel negative regulator of intracellular calcium signaling

SLC10A7 represents an orphan member of the Solute Carrier Family SLC10. Recently, mutations in the human SLC10A7 gene were associated with skeletal dysplasia, amelogenesis imperfecta, and decreased bone mineral density. However, the exact molecular function of SLC10A7 and the mechanisms underlying t...

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Bibliografske podrobnosti
izdano v:Sci Rep
Main Authors: Karakus, Emre, Wannowius, Marie, Müller, Simon Franz, Leiting, Silke, Leidolf, Regina, Noppes, Saskia, Oswald, Stefan, Diener, Martin, Geyer, Joachim
Format: Artigo
Jezik:Inglês
Izdano: Nature Publishing Group UK 2020
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Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC7190670/
https://ncbi.nlm.nih.gov/pubmed/32350310
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-020-64006-3
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