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A Nonredundant Role for the TRPM6 Channel in Neural Tube Closure

In humans, germline mutations in Trpm6 cause autosomal dominant hypomagnesemia with secondary hypocalcemia disorder. Loss of Trpm6 in mice also perturbs cellular magnesium homeostasis but additionally results in early embryonic lethality and neural tube closure defects. To define the mechanisms by w...

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Dades bibliogràfiques
Publicat a:Sci Rep
Autors principals: Komiya, Yuko, Bai, Zhiyong, Cai, Na, Lou, Liping, Al-Saadi, Namariq, Mezzacappa, Courtney, Habas, Raymond, Runnels, Loren W.
Format: Artigo
Idioma:Inglês
Publicat: Nature Publishing Group UK 2017
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC5688082/
https://ncbi.nlm.nih.gov/pubmed/29142255
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-017-15855-y
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