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MALDI imaging MS reveals candidate lipid markers of polycystic kidney disease

Autosomal recessive polycystic kidney disease (ARPKD) is a severe, monogenetically inherited kidney and liver disease. PCK rats carrying the orthologous mutant gene serve as a model of human disease, and alterations in lipid profiles in PCK rats suggest that defined subsets of lipids may be useful a...

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Detalhes bibliográficos
Main Authors: Ruh, Hermelindis, Salonikios, Theresia, Fuchser, Jens, Schwartz, Matthias, Sticht, Carsten, Hochheim, Christina, Wirnitzer, Bernhard, Gretz, Norbert, Hopf, Carsten
Formato: Artigo
Idioma:Inglês
Publicado em: The American Society for Biochemistry and Molecular Biology 2013
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3770091/
https://ncbi.nlm.nih.gov/pubmed/23852700
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1194/jlr.M040014
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