Publikationen von Heinrich Schrewe

Althoff, G. E. M.; Wolfer, D. P.; Timmesfeld, N.; Kanzler, B.; Schrewe, H.; Axel, P.: Long-Term Expression of Tissue-Inhibitor of Matrix Metalloproteinase-1 in the Murine Central Nervous System Does Not Alter the Morphological and Behavioral Phenotype but Alleviates the Course of Experimental Allergic Encephalomyelitis. The American Journal of Pathology 177 (2), S. 840 - 853 (2010)

Althoff, G. E. M.; Wolfer, D. P.; Timmesfeld, N.; Kanzler, B.; Schrewe, H.; Axel, P.: Long-Term Expression of Tissue-Inhibitor of Matrix Metalloproteinase-1 in the Murine Central Nervous System Does Not Alter the Morphological and Behavioral Phenotype but Alleviates the Course of Experimental Allergic Encephalomyelitis. The American Journal of Pathology 177 (2), S. 840 - 853 (2010)

Soboleva, G.; Geis, B.; Schrewe, H.; Weber, B. H. F.: Sorsby Fundus Dystrophy Mutation Timp3^S156C Affects the Morphological and Biochemical Phenotype But Not Metalloproteinase Homeostasis. Journal of Cellular Physiology 197 (1), S. 149 - 156 (2003)

Finkenzeller, D.; Fischer, B.; Lutz, S.; Schrewe, H.; Shimizu, T.; Zimmermann, W.: Carcinoembryonic Antigen-Related Cell Adhesion Molecule 10 Expressed Specifically Early in Pregnancy in the Decidua is Dispensable for Normal Murine Development. Molecular and Cellular Biology 23 (1), S. 272 - 279 (2003)

Oh, S. P.; Yeo, C.-Y.; Lee, Y.; Schrewe, H.; Whitman, M.; Li, E.: Activin type IIA and IIB receptors mediate Gdf11 signaling in axial vertebral patterning. Genes & Development 16 (21), S. 2749 - 2754 (2002)

Weber, B. H. F.; Lin, B. Y.; White, K.; Kohler, K.; Soboleva, G.; Herterich, S.; Seeliger, M. W.; Jaissle, G. B.; Grimm, C.; Reme, C. et al.; Wenzel, A.; Asan, E.; Schrewe, H.: A Mouse Model for Sorsby Fundus Dystrophy. Investigative Ophthalmology & Visual Science 43 (8), S. 2732 - 2740 (2002)

Weber, B. H. F.; Schrewe, H.; Molday, L. L.; Gehrig, A.; White, K. L.; Seeliger, M. W.; Jaissle, G. B.; Friedburg, C.; Tamm, E.; Molday, R. S.: Inactivation of the murine X-linked juvenile retinoschisis gene, Rs1h, suggests a role of retinoschisin in retinal cell layer organization and synaptic structure. Proceedings of the National Academy of Sciences of the United States of America 99 (9), S. 6222 - 6227 (2002)

Gründer, A.; Ebel, T. T.; Mallo, M.; Schwarzkopf, G.; Shimizu, T.; Sippel, A. E.; Schrewe, H.: Nuclear factor I-B (Nfib) deficient mice have severe lung hypoplasia. Mechanisms of Development 112 (1-2), S. 69 - 77 (2002)

Kist, R.; Schrewe, H.; Balling, R.; Scherer, G.: Conditional Inactivation of Sox9: A Mouse Model for Campomelic Dysplasia. Genesis 32 (2 Sp. Iss. SI), S. 121 - 123 (2002)