Establishment of urinary exosome-like vesicles isolation protocol for FHHNC patients and evaluation of different exosomal RNA extraction methods

BACKGROUND: Molecular and cellular pathophysiological events occurring in the majority of rare kidney diseases remain to be elucidated. Familial hypomagnesemia with hypercalciuria and nephrocalcinosis (FHHNC) is a rare autosomal recessive disorder caused by mutations in either CLDN16 or CLDN19 genes...

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Detalles Bibliográficos
Autores principales: Vall-Palomar, M., Arévalo, J., Ariceta, G., Meseguer, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Methodology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6180391/
https://www.ncbi.nlm.nih.gov/pubmed/30305086
http://dx.doi.org/10.1186/s12967-018-1651-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6180391/
https://www.ncbi.nlm.nih.gov/pubmed/30305086
http://dx.doi.org/10.1186/s12967-018-1651-z

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