Benutzerspezifische Werkzeuge

Publikationen - 2006

Noack,B., Gorgens,H., Hoffmann,T., and Schackert,H.K. (2006). CARD15 gene variants in aggressive periodontitis. J. Clin. Periodontol. 33, 779-783.
Goecke,T., Schulmann,K., Engel,C., Holinski-Feder,E., Pagenstecher,C., Schackert,H.K., Kloor,M., Kunstmann,E., Vogelsang,H., Keller,G., Dietmaier,W., Mangold,E., Friedrichs,N., Propping,P., Kruger,S., Gebert,J., Schmiegel,W., Rueschoff,J., Loeffler,M., and Moeslein,G. (2006). Genotype-phenotype comparison of German MLH1 and MSH2 mutation carriers clinically affected with Lynch syndrome: a report by the German HNPCC Consortium. J. Clin. Oncol. 24, 4285-4292.
Kruger,S., Engel,C., Bier,A., Mangold,E., Pagenstecher,C., Doeberitz,M.K., Holinski-Feder,E., Moeslein,G., Keller,G., Kunstmann,E., Friedl,W., Plaschke,J., Ruschoff,J., and Schackert,H.K. (2006). Absence of association between cyclin D1 (CCND1) G870A polymorphism and age of onset in hereditary nonpolyposis colorectal cancer. Cancer Lett. 236, 191-197.
Gorgens,H., Kruger,S., Kuhlisch,E., Pagenstecher,C., Hohl,R., Schackert,H.K., and Muller,A. (2006). Microsatellite stable colorectal cancers in clinically suspected hereditary nonpolyposis colorectal cancer patients without vertical transmission of disease are unlikely to be caused by biallelic germline mutations in MYH. J. Mol. Diagn. 8, 178-182.
Pistorius,S., Kruger,S., Hohl,R., Plaschke,J., Distler,W., Saeger,H.D., and Schackert,H.K. (2006). Occult endometrial cancer and decision making for prophylactic hysterectomy in hereditary nonpolyposis colorectal cancer patients. Gynecol. Oncol. 102, 189-194.
Krex,D., Fortun,S., Kuhlisch,E., Schackert,H.K., and Schackert,G. (2006). The role of endothelial nitric oxide synthase (eNOS) genetic variants in European patients with intracranial aneurysms. J. Cereb. Blood Flow Metab 26, 1250-1255.
Plaschke,J., Linnebacher,M., Kloor,M., Gebert,J., Cremer,F.W., Tinschert,S., Aust,D.E., von Knebel,D.M., and Schackert,H.K. (2006). Compound heterozygosity for two MSH6 mutations in a patient with early onset of HNPCC-associated cancers, but without hematological malignancy and brain tumor. Eur. J. Hum. Genet. 14, 561-566.
Muller,A., Schackert,H.K., Lange,B., Ruschoff,J., Fuzesi,L., Willert,J., Burfeind,P., Shah,P., Becker,H., Epplen,J.T., and Stemmler,S. (2006). A novel MSH2 germline mutation in homozygous state in two brothers with colorectal cancers diagnosed at the age of 11 and 12 years. Am. J. Med. Genet. A 140, 195-199.
Pistorius,S., Gorgens,H., Kruger,S., Engel,C., Mangold,E., Pagenstecher,C., Holinski-Feder,E., Moeslein,G., von Knebel,D.M., Ruschoff,J., Karner-Hanusch,J., Saeger,H.D., and Schackert,H.K. (2006). N-acetyltransferase (NAT) 2 acetylator status and age of onset in patients with hereditary nonpolyposis colorectal cancer (HNPCC). Cancer Lett. 241, 150-157.
Kruger,S., Emig,M., Lohse,P., Ehninger,G., Hochhaus,A., and Schackert,H.K. (2006). The c-kit (CD117) sequence variation M541L, but not N564K, is frequent in the general population, and is not associated with CML in Caucasians. Leukemia 20, 354-355.
Engel,C., Forberg,J., Holinski-Feder,E., Pagenstecher,C., Plaschke,J., Kloor,M., Poremba,C., Pox,C.P., Ruschoff,J., Keller,G., Dietmaier,W., Rummele,P., Friedrichs,N., Mangold,E., Buettner,R., Schackert,H.K., Kienle,P., Stemmler,S., Moeslein,G., and Loeffler,M. (2006). Novel strategy for optimal sequential application of clinical criteria, immunohistochemistry and microsatellite analysis in the diagnosis of hereditary nonpolyposis colorectal cancer. Int. J. Cancer 118, 115-122.
Aretz,S., Uhlhaas,S., Goergens,H., Siberg,K., Vogel,M., Pagenstecher,C., Mangold,E., Caspari,R., Propping,P., and Friedl,W. (2006). MUTYH-associated polyposis: 70 of 71 patients with biallelic mutations present with an attenuated or atypical phenotype. Int. J. Cancer 119, 807-814.