Concepedia

Loss of Syntaxin 3 Causes Variant Microvillus Inclusion Disease

Caroline L. Wiegerinck, Andreas Janecke, Kerstin Schneeberger, Georg F. Vogel, Désirée Y. van Haaften–Visser, Johanna C. Escher, Rüdiger Adam, Cornelia E. Thöni, Kristian Pfaller, Alexander J. Jordan,

Gastroenterology · 2014 · 174 citations · 15 references

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References

15

Single Lgr5 stem cells build crypt-villus structures in vitro without a mesenchymal niche

Toshiro Sato, Robert G.J. Vries, Hugo J.G. Snippert et al. · Nature · 2009 · 7.2K citations

, , +14

A functional CFTR assay using primary cystic fibrosis intestinal organoids

Johanna F. Dekkers, Caroline L. Wiegerinck, Hugo R. de Jonge et al. · Nature Medicine · 2013 · 997 citations

, , +8

Exome Capture Reveals ZNF423 and CEP164 Mutations, Linking Renal Ciliopathies to DNA Damage Response Signaling

Moumita Chaki, Rannar Airik, Amiya K. Ghosh et al. · Cell · 2012 · 391 citations · Full text

, , +16

MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity

Thomas Müller, Michael W. Hess, Natalia Schiefermeier-Mach et al. · Nature Genetics · 2008 · 377 citations

, , +10

Dominant missense mutations in ABCC9 cause Cantú syndrome

Magdaléna Harakaľová, J. J. T. van Harssel, Stef van Lieshout et al. · Nature Genetics · 2012 · 200 citations

, , +9