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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Detaylı Bibliyografya
Asıl Yazarlar: 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.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: American Society of Nephrology 2009
Konular:
Basic Research
Online Erişim: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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