Benutzerspezifische Werkzeuge

Publications - 2010

Venkatachalam,R., Ligtenberg,M.J., Hoogerbrugge,N., Schackert,H.K., Gorgens,H., Hahn,M.M., Kamping,E.J., Vreede,L., Hoenselaar,E., van der,L.E., Goossens,M., Churchman,M., Carvajal-Carmona,L., Tomlinson,I.P., de Bruijn,D.R., van Kessel,A.G., and Kuiper,R.P. (2010). Germline epigenetic silencing of the tumor suppressor gene PTPRJ in early-onset familial colorectal cancer. Gastroenterology 139, 2221-2224.

Lascorz,J., Forsti,A., Chen,B., Buch,S., Steinke,V., Rahner,N., Holinski-Feder,E., Morak,M., Schackert,H.K., Gorgens,H., Schulmann,K., Goecke,T., Kloor,M., Engel,C., Buttner,R., Kunkel,N., Weires,M., Hoffmeister,M., Pardini,B., Naccarati,A., Vodickova,L., Novotny,J., Schreiber,S., Krawczak,M., Broring,C.D., Volzke,H., Schafmayer,C., Vodicka,P., Chang-Claude,J., Brenner,H., Burwinkel,B., Propping,P., Hampe,J., and Hemminki,K. (2010). Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility. Carcinogenesis 31, 1612-1619.

Campa,D., Pardini,B., Naccarati,A., Vodickova,L., Novotny,J., Steinke,V., Rahner,N., Holinski-Feder,E., Morak,M., Schackert,H.K., Gorgens,H., Kotting,J., Betz,B., Kloor,M., Engel,C., Buttner,R., Propping,P., Forsti,A., Hemminki,K., Barale,R., Vodicka,P., and Canzian,F. (2010). Polymorphisms of genes coding for ghrelin and its receptor in relation to colorectal cancer risk: a two-step gene-wide case-control study. BMC. Gastroenterol. 10, 112.

Ruckert,F., Dawelbait,G., Winter,C., Hartmann,A., Denz,A., Ammerpohl,O., Schroeder,M., Schackert,H.K., Sipos,B., Kloppel,G., Kalthoff,H., Saeger,H.D., Pilarsky,C., and Grutzmann,R. (2010). Examination of apoptosis signaling in pancreatic cancer by computational signal transduction analysis. PLoS. One. 5, e12243.

Balaz,P., Plaschke,J., Kruger,S., Gorgens,H., and Schackert,H.K. (2010). TCF-3, 4 protein expression correlates with beta-catenin expression in MSS and MSI-H colorectal cancer from HNPCC patients but not in sporadic colorectal cancers. Int. J. Colorectal Dis. 25, 931-939.

Serra,A., Gorgens,H., Alhadad,K., Fitze,G., and Schackert,H.K. (2010). Analysis of RET, ZEB2, EDN3 and GDNF genomic rearrangements in central congenital hyperventilation syndrome patients by multiplex ligation-dependent probe amplification. Ann. Hum. Genet. 74, 369-374.

Khandanpour,C., Thiede,C., Valk,P.J., Sharif-Askari,E., Nuckel,H., Lohmann,D., Horsthemke,B., Siffert,W., Neubauer,A., Grzeschik,K.H., Bloomfield,C.D., Marcucci,G., Maharry,K., Slovak,M.L., van der Reijden,B.A., Jansen,J.H., Schackert,H.K., Afshar,K., Schnittger,S., Peeters,J.K., Kroschinsky,F., Ehninger,G., Lowenberg,B., Duhrsen,U., and Moroy,T. (2010). A variant allele of Growth Factor Independence 1 (GFI1) is associated with acute myeloid leukemia. Blood 115, 2462-2472.

Engel,C., Rahner,N., Schulmann,K., Holinski-Feder,E., Goecke,T.O., Schackert,H.K., Kloor,M., Steinke,V., Vogelsang,H., Moslein,G., Gorgens,H., Dechant,S., von Knebel,D.M., Ruschoff,J., Friedrichs,N., Buttner,R., Loeffler,M., Propping,P., and Schmiegel,W. (2010). Efficacy of annual colonoscopic surveillance in individuals with hereditary nonpolyposis colorectal cancer. Clin. Gastroenterol. Hepatol. 8, 174-182.