Peter Heinz‐Erian

MYO5B mutations cause microvillus inclusion disease and disrupt epithelial cell polarity

Thomas Müller, Michael W. Hess, Natalia Schiefermeier-Mach et al. · Nature Genetics · 2008 · 370 citations

Disease Mechanism, Pathogenesis, Pathology +10

Sex- and Age-Specific Reference Curves for Serum Markers of Bone Turnover in Healthy Children from 2 Months to 18 Years

Markus Rauchenzauner, Andrea Schmid, Peter Heinz‐Erian et al. · The Journal of Clinical Endocrinology & Metabolism · 2006 · 275 citations

Probing peptide backbone function in bombesin. A reduced peptide bond analogue with potent and specific receptor antagonist activity.

D.H. Coy, Peter Heinz‐Erian, Ning Jiang et al. · Journal of Biological Chemistry · 1988 · 210 citations · Full text

Protein Chemistry, Val10-gly11 Replacement, Medicinal Chemistry +14

Reduced sodium/proton exchanger NHE3 activity causes congenital sodium diarrhea

Andreas Janecke, Peter Heinz‐Erian, Jianyi Yin et al. · Human Molecular Genetics · 2015 · 131 citations · Full text

Engineering, Genetics, Genetic Epidemiology +17

Loss-of-function of MYO5B is the main cause of microvillus inclusion disease: 15 novel mutations and a CaCo-2 RNAi cell model

Frank M. Ruemmele, Thomas Müller, Natalia Schiefermeier-Mach et al. · Human Mutation · 2010 · 129 citations · Full text