FXYD2 and Na,K-ATPase Expression in Isolated Human Proximal Tubular Cells: Disturbed Upregulation on Renal Hypomagnesemia?

Autosomal dominant renal hypomagnesemia (OMIM 154020), associated with hypocalciuria, has been linked to a 121G to A mutation in the FXYD2 gene. To gain insight into the molecular mechanisms linking this mutation to the clinical phenotype, we studied isolated proximal tubular cells from urine of a p...

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Detalles Bibliográficos
Autores principales: Cairo, Edinio R., Swarts, Herman G. P., Wilmer, Martijn J. G., Willems, Peter H. G. M., Levtchenko, Elena N., De Pont, Jan Joep H. H. M., Koenderink, Jan B.
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2009
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2776943/
https://www.ncbi.nlm.nih.gov/pubmed/19865785
http://dx.doi.org/10.1007/s00232-009-9210-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2776943/
https://www.ncbi.nlm.nih.gov/pubmed/19865785
http://dx.doi.org/10.1007/s00232-009-9210-4

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