Heinrich Schrewe
Max Planck Institute for Molecular Genetics(DE)
Publications by Year
Research Areas
Retinal Development and Disorders, TGF-β signaling in diseases, Cell Adhesion Molecules Research, RNA Research and Splicing, Monoclonal and Polyclonal Antibodies Research
Most-Cited Works
- → Inactivation of the murine X-linked juvenile retinoschisis gene, Rs1h, suggests a role of retinoschisin in retinal cell layer organisation and synaptic structure(2002)213 cited
- → Activin receptor patterning of foregut organogenesis(2000)213 cited
- → The Type II Activin Receptors Are Essential for Egg Cylinder Growth, Gastrulation, and Rostral Head Development in Mice(1999)194 cited
- → Cloning of the complete gene for carcinoembryonic antigen: analysis of its promoter indicates a region conveying cell type-specific expression.(1990)161 cited
- → Med12 is essential for early mouse development and for canonical Wnt and Wnt/PCP signaling(2010)160 cited
- → Bestrophin 1 is indispensable for volume regulation in human retinal pigment epithelium cells(2015)120 cited
- → Somatic MED12 mutations in uterine leiomyosarcoma and colorectal cancer(2012)114 cited
- → Conditional inactivation of Sox9: A mouse model for campomelic dysplasia(2002)108 cited
- → MED12 Regulates HSC-Specific Enhancers Independently of Mediator Kinase Activity to Control Hematopoiesis(2016)107 cited
- → Nuclear factor I-B (Nfib) deficient mice have severe lung hypoplasia(2002)105 cited