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Characterization of PKD Protein-Positive Exosome-Like Vesicles

Proteins associated with autosomal dominant and autosomal recessive polycystic kidney disease (polycystin-1, polycystin-2, and fibrocystin) localize to various subcellular compartments, but their functional site is thought to be on primary cilia. PC1+ vesicles surround cilia in Pkhd1(del2/del2) mice...

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Detalhes bibliográficos
Main Authors: Hogan, Marie C., Manganelli, Luca, Woollard, John R., Masyuk, Anatoliy I., Masyuk, Tatyana V., Tammachote, Rachaneekorn, Huang, Bing Q., Leontovich, Alexey A., Beito, Thomas G., Madden, Benjamin J., Charlesworth, M. Cristine, Torres, Vicente E., LaRusso, Nicholas F., Harris, Peter C., Ward, Christopher J.
Formato: Artigo
Idioma:Inglês
Publicado em: American Society of Nephrology 2009
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2637052/
https://ncbi.nlm.nih.gov/pubmed/19158352
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1681/ASN.2008060564
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