Entries of Krämer, F. on the publication server

Nanda, I., Krämer, F., Weber, Bernhard H. F. , Schempp, W. and Schmid, M. (2005) Comparative mapping of human claudin-1 (CLDN1) in great apes. Cytogenetic and Genome Research 108 (1-3), pp. 229-233. Fulltext not available.

Stöhr, H., Molday, L. L., Molday, R. S., Weber, Bernhard H. F. , Biedermann, B., Reichenbach, A. and Krämer, F. (2005) Membrane-associated guanylate kinase proteins MPP4 and MPP5 associate with Veli3 at distinct intercellular junctions of the neurosensory retina. The Journal of Comparative Neurology 481 (1), pp. 31-41.

Krämer, F., Stöhr, H. and Weber, Bernhard H. F. (2004) Cloning and characterization of the murine Vmd2 RFP-TM gene family. Cytogenetic and Genome Research 105 (1), pp. 107-114. Fulltext not available.

Bendig, I., Mohr, N., Krämer, F. and Weber, Bernhard H. F. (2004) Identification of novel TP53 mutations in familial and sporadic cancer cases of German and Swiss origin. Cancer Genetics and Cytogenetics 154 (1), pp. 22-26. Fulltext not available.

Krämer, F., Mohr, N., Kellner, U., Rudolph, G. and Weber, Bernhard H. F. (2003) Ten novel mutations in VMD2 associated with Best macular dystrophy (BMD). Human Mutation 22 (5), p. 418. Fulltext not available.

Krämer, F., White, K., Kubbies, M., Swisshelm, K. and Weber, Bernhard H. F. (2000) Genomic organization of claudin-1 and its assessment in hereditary and sporadic breast cancer. Human Genetics 107 (3), pp. 249-256. Fulltext not available.

Krämer, F., White, K., Pauleikhoff, D., Gehrig, A., Passmore, L., Rivera, A., Rudolph, G., Kellner, U., Andrassi, M., Lorenz, B., Rohrschneider, K., Blankenagel, A., Jurklies, B., Schilling, H., Schütt, F., Holz, F. G. and Weber, Bernhard H. F. (2000) Mutations in the VMD2 gene are associated with juvenile-onset vitelliform macular dystrophy (Best disease) and adult vitelliform macular dystrophy but not age-related macular degeneration. European Journal of Human Genetics 8 (4), pp. 286-292. Fulltext not available.