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- Deka, Jürgen; Herter, Peter; Sprenger-Haußels, Markus et al.
- The APC protein binds to A/T rich DNA sequences
- Oncogene. Bd. 18. H. 41. Springer Science and Business Media LLC 1999 S. 5654 - 5661
- Herter, Peter; Kuhnen, Cornelius; Müller, Klaus-Michael et al.
- Intracellular distribution of β-catenin in colorectal adenomas, carcinomas and Peutz-Jeghers polyps
- Journal of Cancer Research and Clinical Oncology. Bd. 125. H. 5. Springer 1999 S. 297 - 304
- Winde, Guenther; Lügering, Norbert; Glodny, Bernhard et al.
- Decreased HER-2 tyrosine kinase expression in rectal mucosa of FAP patients following low-dose sulindac chemoprevention
- Cancer Letters. Bd. 134. H. 2. Elsevier B.V. 1998 S. 201 - 207
- Müller, O.; Kuhnen, C.; Herter, P. et al.
- Intracellular distribution of beta-catenin in soft tissue tumors
- Verhandlungen der deutschen Gesellschaft für Pathologie. Bd. 82. 1998 S. 322 - 326
- Herrmann, Christian; Block, Christoph; Geisen, Christoph et al.
- Sulindac sulfide inhibits Ras signaling
- Oncogene. Bd. 17. H. 14. Springer Science and Business Media LLC 1998 S. 1769 - 1776
- Deka, Jurgen; Kuhlmann, Jurgen; Muller, Oliver
- A domain within the tumor suppressor protein APC shows very similar biochemical properties as the microtubule-associated protein tau
- European Journal of Biochemistry. Bd. 253. H. 3. Wiley 1998 S. 591 - 597
- Müller, O.; Nimmrich, I.; Finke, U. et al.
- A beta-catenin mutation in a sporadic colorectal tumor of the RER phenotype and absence of beta-catenin germline mutations in FAP patients
- Genes Chromosomes and Cancer. Bd. 22. 1998 S. 37 - 41
- Müller, O.; Deuter, R.
- Detection of APC mutations in stool DNA of patients with colorectal cancer by HD‐PCR
- Human Mutation. Bd. 11. 1998 S. 84 - 89
- Jenne, Dieter E.; Reomann, Heike; Nezu, Jun-ichi et al.
- Peutz-Jeghers syndrome is caused by mutations in a novel serine threoninekinase
- Nature Genetics. Bd. 18. H. 1. Springer Science and Business Media LLC 1998 S. 38 - 43
- Nimmrich, Inko; Friedl, Waltraut; Kruse, Roland et al.
- Loss of the PLA2G2A gene in a sporadic colorectal tumor of a patient with a PLA2G2A germline mutation and absence of PLA2G2A germline alterations in patients with FAP
- Human Genetics. Bd. 100. H. 3-4. Springer Science and Business Media LLC 1997 S. 345 - 349