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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Published in: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
Language:Inglês
Published: Nature Publishing Group UK 2020
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Online Access: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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