Benutzerspezifische Werkzeuge

Publications - 2003

Martinez,R., Schackert,H.K., von Kannen,S., Lichter,P., Joos,S., and Schackert,G. (2003). Independent molecular development of metachronous glioblastomas with extended intervening recurrence-free interval. Brain Pathol. 13, 598-607.

Krex,D., Mohr,B., Appelt,H., Schackert,H.K., and Schackert,G. (2003). Genetic analysis of a multifocal glioblastoma multiforme: a suitable tool to gain new aspects in glioma development. Neurosurgery 53, 1377-1384.

Krex,D., Rohl,H., Konig,I.R., Ziegler,A., Schackert,H.K., and Schackert,G. (2003). Tissue inhibitor of metalloproteinases-1, -2, and -3 polymorphisms in a white population with intracranial aneurysms. Stroke 34, 2817-2821.

Fitze,G., Appelt,H., Konig,I.R., Gorgens,H., Stein,U., Walther,W., Gossen,M., Schreiber,M., Ziegler,A., Roesner,D., and Schackert,H.K. (2003). Functional haplotypes of the RET proto-oncogene promoter are associated with Hirschsprung disease (HSCR). Hum. Mol. Genet. 12, 3207-3214.

Pistorius,S., Plaschke,J., Kruppa,C., Ruschoff,J., Nagel,M., Saeger,H.D., and Schackert,H.K. (1998). [Molecular diagnosis and clinical consequences in families with HNPCC syndrome]. Langenbecks Arch. Chir Suppl Kongressbd. 115, 293-297.

Hampl,M., Plaschke,J., Burgemeister,R., Schwarz,P., Saeger,H.D., and Schackert,H.K. (1998). [Sequence analysis of BRCA1 gene in young breast cancer patients and/or positive family history]. Langenbecks Arch. Chir Suppl Kongressbd. 115, 267-272.

Krex,D., Ziegler,A., Konig,I.R., Schackert,H.K., and Schackert,G. (2003). Polymorphisms of the NADPH oxidase P22PHOX gene in a Caucasian population with intracranial aneurysms. Cerebrovasc. Dis. 16, 363-368.

Fitze,G., Cramer,J., Serra,A., Schreiber,M., Roesner,D., and Schackert,H.K. (2003). Within-gene interaction between c.135 G/A genotypes and RET proto-oncogene germline mutations in HSCR families. Eur. J. Pediatr. Surg. 13, 152-157.

Plaschke,J., Ruschoff,J., and Schackert,H.K. (2003). Genomic rearrangements of hMSH6 contribute to the genetic predisposition in suspected hereditary non-polyposis colorectal cancer syndrome. J. Med. Genet. 40, 597-600.

Gorgens,H., Schwarz,P., Schulze,J., and Schackert,H.K. (2003). LightCycler assay in the analysis of haplotypes of the type 2 diabetes susceptibility gene CAPN10. Clin. Chem. 49, 1405-1408.

Fitze,G., Schierz,M., Kuhlisch,E., Schreiber,M., Ziegler,A., Roesner,D., and Schackert,H.K. (2003). Novel intronic polymorphisms in the RET proto-oncogene and their association with Hirschsprung disease. Hum. Mutat. 22, 177.

Weilemann,F., Steinmetz,A., Kirsch,M., Buttler,A., Kunze,S., Kuhlisch,E., Schackert,H.K., and Schackert,G. (2003). Prevention of brain metastasis formation by local expression of interleukin-4 or hemagglutinin antigen. Zentralbl. Neurochir. 64, 65-70.

Hofmann,W., Gorgens,H., John,A., Horn,D., Huttner,C., Arnold,N., Scherneck,S., and Schackert,H.K. (2003). Screening for large rearrangements of the BRCA1 gene in German breast or ovarian cancer families using semi-quantitative multiplex PCR method. Hum. Mutat. 22, 103-104.

Moslein,G., Pistorius,S., Saeger,H.D., and Schackert,H.K. (2003). Preventive surgery for colon cancer in familial adenomatous polyposis and hereditary nonpolyposis colorectal cancer syndrome. Langenbecks Arch. Surg. 388, 9-16.

Seitz,S., Wassmuth,P., Plaschke,J., Schackert,H.K., Karsten,U., Santibanez-Koref,M.F., Schlag,P.M., and Scherneck,S. (2003). Identification of microsatellite instability and mismatch repair gene mutations in breast cancer cell lines. Genes Chromosomes. Cancer 37, 29-35.

Kruger,S., Plaschke,J., Jeske,B., Gorgens,H., Pistorius,S.R., Bier,A., Kreuz,F.R., Theissig,F., Aust,D.E., Saeger,H.D., and Schackert,H.K. (2003). Identification of six novel MSH2 and MLH1 germline mutations in HNPCC. Hum. Mutat. 21, 445-446.

Plaschke,J., Schwanebeck,U., Pistorius,S., Saeger,H.D., and Schackert,H.K. (2003). Methylenetetrahydrofolate reductase polymorphisms and risk of sporadic and hereditary colorectal cancer with or without microsatellite instability. Cancer Lett. 191, 179-185.

Fitze,G., Paditz,E., Schlafke,M., Kuhlisch,E., Roesner,D., and Schackert,H.K. (2003). Association of germline mutations and polymorphisms of the RET proto-oncogene with idiopathic congenital central hypoventilation syndrome in 33 patients. J. Med. Genet. 40, E10.