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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Detalles Bibliográficos
Autores principales: Karakus, Emre, Wannowius, Marie, Müller, Simon Franz, Leiting, Silke, Leidolf, Regina, Noppes, Saskia, Oswald, Stefan, Diener, Martin, Geyer, Joachim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7190670/
https://www.ncbi.nlm.nih.gov/pubmed/32350310
http://dx.doi.org/10.1038/s41598-020-64006-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7190670/
https://www.ncbi.nlm.nih.gov/pubmed/32350310
http://dx.doi.org/10.1038/s41598-020-64006-3

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