Benutzerspezifische Werkzeuge

Publikationen - 2008

Kruger,S., Kinzel,M., Walldorf,C., Gottschling,S., Bier,A., Tinschert,S., von Stackelberg,A., Henn,W., Gorgens,H., Boue,S., Kolble,K., Buttner,R., and Schackert,H.K. (2008). Homozygous PMS2 germline mutations in two families with early-onset haematological malignancy, brain tumours, HNPCC-associated tumours, and signs of neurofibromatosis type 1. Eur. J. Hum. Genet. 16, 62-72.
Morak,M., Schackert,H.K., Rahner,N., Betz,B., Ebert,M., Walldorf,C., Royer-Pokora,B., Schulmann,K., Knebel-Doeberitz,M., Dietmaier,W., Keller,G., Kerker,B., Leitner,G., and Holinski-Feder,E. (2008). Further evidence for heritability of an epimutation in one of 12 cases with MLH1 promoter methylation in blood cells clinically displaying HNPCC. Eur. J. Hum. Genet. 16 , 804-811.
Noack,B., Gorgens,H., Schacher,B., Puklo,M., Eickholz,P., Hoffmann,T., and Schackert,H.K. (2008). Functional Cathepsin C mutations cause different Papillon-Lefevre syndrome phenotypes. J. Clin. Periodontol. 35, 311-316.
Pilarsky,C., Ammerpohl,O., Sipos,B., Dahl,E., Hartmann,A., Wellmann,A., Braunschweig,T., Lohr,M., Jesnowski,R., Friess,H., Wente,M.N., Kristiansen,G., Jahnke,B., Denz,A., Ruckert,F., Schackert,H.K., Kloppel,G., Kalthoff,H., Saeger,H.D., and Grutzmann,R. (2008). Activation of Wnt signalling in stroma from pancreatic cancer identified by gene expression profiling. J. Cell Mol. Med. 12, 2823-2835.
Steinke,V., Rahner,N., Morak,M., Keller,G., Schackert,H.K., Gorgens,H., Schmiegel,W., Royer-Pokora,B., Dietmaier,W., Kloor,M., Engel,C., Propping,P., and Aretz,S. (2008). No association between MUTYH and MSH6 germline mutations in 64 HNPCC patients. Eur. J. Hum. Genet. 16, 587-592.
Fitze,G., Konig,I.R., Paditz,E., Serra,A., Schlafke,M., Roesner,D., Ziegler,A., and Schackert,H.K. (2008). Compound effect of PHOX2B and RET gene variants in congenital central hypoventilation syndrome combined with Hirschsprung disease. Am. J. Med. Genet. A 146A, 1486-1489.
Frank,B., Burwinkel,B., Bermejo,J.L., Forsti,A., Hemminki,K., Houlston,R., Mangold,E., Rahner,N., Friedl,W., Friedrichs,N., Buettner,R., Engel,C., Loeffler,M., Holinski-Feder,E., Morak,M., Keller,G., Schackert,H.K., Kruger,S., Goecke,T., Moeslein,G., Kloor,M., Gebert,J., Kunstmann,E., Schulmann,K., Ruschoff,J., and Propping,P. (2008). Ten recently identified associations between nsSNPs and colorectal cancer could not be replicated in German families. Cancer Lett. 271, 153-157.
Muller,A., Zielinski,D., Friedrichs,N., Oberschmid,B., Merkelbach-Bruse,S., Schackert,H.K., Linnebacher,M., von Knebel,D.M., Buttner,R., and Ruschoff,J. (2008). Reduced mRNA expression in paraffin-embedded tissue identifies. Virchows Arch. 453, 9-16.
Papaemmanuil,E., Carvajal-Carmona,L., Sellick,G.S., Kemp,Z., Webb,E., Spain,S., Sullivan,K., Barclay,E., Lubbe,S., Jaeger,E., Vijayakrishnan,J., Broderick,P., Gorman,M., Martin,L., Lucassen,A., Bishop,D.T., Evans,D.G., Maher,E.R., Steinke,V., Rahner,N., Schackert,H.K., Goecke,T.O., Holinski-Feder,E., Propping,P., Van Wezel,T., Wijnen,J., Cazier,J.B., Thomas,H., Houlston,R.S., and Tomlinson,I. (2008). Deciphering the genetics of hereditary non-syndromic colorectal cancer. Eur. J. Hum. Genet. 16, 1477-1486.
Noack,B., Gorgens,H., Lorenz,K., Ziegler,A., Hoffmann,T., and Schackert,H.K. (2008). TLR4 and IL-18 gene variants in aggressive periodontitis. J. Clin. Periodontol. 35, 1020-1026.
Noack,B., Gorgens,H., Hempel,U., Fanghanel,J., Hoffmann,T., Ziegler,A., and Schackert,H.K. (2008). Cathepsin C gene variants in aggressive periodontitis. J. Dent. Res. 87, 958-963.
Serra,A., Haberle,B., Konig,I.R., Kappler,R., Suttorp,M., Schackert,H.K., Roesner,D., and Fitze,G. (2008). Rare occurrence of PHOX2b mutations in sporadic neuroblastomas. J. Pediatr. Hematol. Oncol. 30, 728-732.
Koy,S., Plaschke,J., Luksch,H., Friedrich,K., Kuhlisch,E., Eckelt,U., and Martinez,R. (2008). Microsatellite instability and loss of heterozygosity in squamous cell carcinoma of the head and neck. Head Neck 30, 1105-1113.
Schulte,T.L., Liljenqvist,U., Gorgens,H., Hackenberg,L., Bullmann,V., and Tinschert,S. (2008). Hemihyperplasia-multiple lipomatosis syndrome (HHML): a challenge in spinal care. Acta Orthop. Belg. 74, 714-719.