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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Detaylı Bibliyografya
Yayımlandı:Sci Rep
Asıl Yazarlar: Karakus, Emre, Wannowius, Marie, Müller, Simon Franz, Leiting, Silke, Leidolf, Regina, Noppes, Saskia, Oswald, Stefan, Diener, Martin, Geyer, Joachim
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Nature Publishing Group UK 2020
Konular:
Article
Online Erişim: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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