Inversin relays Frizzled-8 signals to promote proximal pronephros development

Mutations of inversin cause type II nephronophthisis, an infantile autosomal recessive disease characterized by cystic kidney disease and developmental defects. Inversin regulates Wnt signaling and is required for convergent extension movements during early embryogenesis. We now show that Inversin i...

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Detaylı Bibliyografya
Asıl Yazarlar: Lienkamp, Soeren, Ganner, Athina, Boehlke, Christopher, Schmidt, Thorsten, Arnold, Sebastian J., Schäfer, Tobias, Romaker, Daniel, Schuler, Julia, Hoff, Sylvia, Powelske, Christian, Eifler, Annekathrin, Krönig, Corinna, Bullerkotte, Axel, Nitschke, Roland, Kuehn, E. Wolfgang, Kim, Emily, Burkhardt, Hans, Brox, Thomas, Ronneberger, Olaf, Gloy, Joachim, Walz, Gerd
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: National Academy of Sciences 2010
Konular:
Biological Sciences
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2996658/
https://ncbi.nlm.nih.gov/pubmed/21059920
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1013070107
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