Direkt zum Inhalt

Entries of Amann, T. on the publication server

Up a level
Export as
[feed] Atom [feed] RSS 1.0 [feed] RSS 2.0
Group by: Date | Item type | No Grouping
Jump to: 2010 | 2008 | 2007 | 2006 | 1996 | 1995
Number of items: 7.

2010

Kirovski, G., Amann, T., Bosserhoff, A. and Hellerbrand, C. (2010) 559 ANALYSIS OF A PROMOTER POLYMORPHISM OF THE GLUT1 GENE IN PATIENTS WITH HEPATOCELLULAR CARCINOMA. Journal of Hepatology 52, S222-S223. Fulltext not available.

Valletta, D., Amann, T., Bosserhoff, A.K. and Hellerbrand, C. (2010) 904 INCREASED EXPRESSION OF FAT1 IN HEPATOCELLULAR CARCINOMA PROMOTES TUMORIGENICITY. Journal of Hepatology 52, S351. Fulltext not available.

2008

Amann, T., Maegdefrau, U., Kreuz, M., Hartmann, A., Schoelmerich, J., Bosserhoff, A.K. and Hellerbrand, C. (2008) 318 GLUT1 EXPRESSION IS INCREASED IN HEPATOCELLULAR CARCINOMA AND PROMOTES TUMORIGENESIS. Journal of Hepatology 48, S126. Fulltext not available.

2007

Amann, T., Spruss, T., Bataille, F., Liedtke, C., Muhlbauer, M., Trautwein, C., Bosserhoff, A.K. and Hellerbrand, C. (2007) [69] IDENTIFICATION OF FIBROBLAST GROWTH FACTOR RECEPTOR 2IIIB (FGFR2IIIB) AS TUMOR SUPPRESSOR IN HEPATOCANCEROGENESIS. Journal of Hepatology 46, S31. Fulltext not available.

2006

Hellerbrand, C., Amann, T., Schlegel, J., Spruss, T., Bataille, F., Hartmann, A., Mühlbauer, M., Schölmerich, J. and Bosserhoff, A.K. (2006) 98 The novel gene MIA2 promotes progression of hepatocellular carcinoma. Journal of Hepatology 44, S43. Fulltext not available.

1996

Felbor, U., Stöhr, H., Amann, T., Schönherr, U., Apfelstedt-Sylla, E. and Weber, Bernhard H. F. (1996) A second independent Tyr168Cys mutation in the tissue inhibitor of metalloproteinases-3 (TIMP3) in Sorsby's fundus dystrophy. Journal of Medical Genetics 33 (3), pp. 233-236. Fulltext not available.

1995

Felbor, U., Stöhr, H., Amann, T., Schönherr, U. and Weber, Bernhard H. F. (1995) A novel Ser156Cys mutation in the tissue inhibitor of metalloproteinases-3 (TIMP3) in Sorsby's fundus dystrophy with unusual clinical features. Human Molecular Genetics 4 (12), pp. 2415-2416. Fulltext not available.

This list was generated on Tue Jun 9 18:32:57 2026 CEST.
nach oben