Markus Moser

E-cadherin integrates mechanotransduction and EGFR signaling to control junctional tissue polarization and tight junction positioning

Carien M. Niessen, Valerie Horsley, Eric R. Dufresne, 2017, Nature Communications.

Leukocyte adhesion deficiency-III is caused by mutations in KINDLIN3 affecting integrin activation

Ian Tomlinson, Mike Fried, N. Hogg, 2009, Nature Medicine.

The Tail of Integrins, Talin, and Kindlins

R. Fässler, M. Moser, K. Legate, 2009, Science.

Inactivation of anoctamin‐6/Tmem16f, a regulator of phosphatidylserine scrambling in osteoblasts, leads to decreased mineral deposition in skeletal tissues

Uwe Kornak, Andrea Vortkamp, U. Kornak, 2013, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Stable Isotope Labeling by Amino Acids in Cell Culture (SILAC) and Proteome Quantitation of Mouse Embryonic Stem Cells to a Depth of 5,111 Proteins*S

Jürgen Cox, Matthias Mann, Johannes Graumann, 2008, Molecular & Cellular Proteomics.

LAD-1/variant syndrome is caused by mutations in FERMT3.

Dirk Roos, Frank Baas, Arthur J Verhoeven, 2009, Blood.

The small RNA expression profile of the developing murine urinary and reproductive systems

Gunter Meister, G. Meister, M. Beitzinger, 2010, FEBS letters.

Spectrum of mutations in the gene for autosomal recessive polycystic kidney disease (ARPKD/PKHD1).

Carsten Bergmann, Sabine Rudnik-Schöneborn, Klaus Zerres, 2003, Journal of the American Society of Nephrology : JASN.

The Transcription Factor TCFAP2C/AP-2γ Cooperates with CDX2 To Maintain Trophectoderm Formation

Hubert Schorle, E. Tolkunova, A. Tomilin, 2010, Molecular and Cellular Biology.

PKHD1 mutations in families requesting prenatal diagnosis for autosomal recessive polycystic kidney disease (ARPKD)

Carsten Bergmann, Sabine Rudnik-Schöneborn, Klaus Zerres, 2004, Human mutation.