Identification of lymphocyte cell-specific protein-tyrosine kinase (LCK) as a driver for invasion and migration of oral cancer by tumor heterogeneity exploitation von Weisse, Jonas, Rosemann, Julia, Muller, Lisa, Kappler, Matthias, Eckert, Alexander W., Glass, Markus, Misiak, Danny, Huttelmaier, Stefan, Ballhausen, Wolfgang G., Hatzfeld, Mechthild, Haemmerle, Monika, Gutschner, Tony

Volltext

Correction: Identification of lymphocyte cell-specific protein-tyrosine kinase (LCK) as a driver for invasion and migration of oral cancer by tumor heterogeneity exploitation von Weiße, Jonas, Rosemann, Julia, Müller, Lisa, Kappler, Matthias, Eckert, Alexander W, Glaß, Markus, Misiak, Danny, Hüttelmaier, Stefan, Ballhausen, Wolfgang G, Hatzfeld, Mechthild, Haemmerle, Monika, Gutschner, Tony

Volltext

Epigenetic changes in the promoter of the fragile histidine triad (FHIT) gene in human sebocytes under the influence of in vitro culture von Jotzo, Magdalena, Zouboulis, Christos C, Ballhausen, Wolfgang G

Volltext

Epigenetische Veränderungen am Promotor des fragilen Histidin-Trias(FHIT)-Gens in menschlichen Sebozyten unter dem Einfluss der In-vitro-Kultur von Jotzo, Magdalena, Zouboulis, Christos C., Ballhausen, Wolfgang G.

Volltext

Prospero -related homeobox 1 ( PROX1 ) is frequently inactivated by genomic deletions and epigenetic silencing in carcinomas of the bilary system von Laerm, Antonia, Helmbold, Peter, Goldberg, Martina, Dammann, Reinhard, Holzhausen, Hans-Jürgen, Ballhausen, Wolfgang Gerhard

Volltext

Genetic Testing for Germline Mutations of the APC Gene in Patients With Apparently Sporadic Desmoid Tumors but a Family History of Colorectal Carcinoma von Brueckl, Wolfgang M, Ballhausen, Wolfgang G, Förtsch, Thomas, Günther, Klaus, Fiedler, Wolfgang, Gentner, Bernhard, Croner, Roland, Boxberger, Frank, Kirchner, Thomas, Hahn, Eckhart G, Hohenberger, Werner, Wein, Axel

Volltext

Erratum to: Epigenetic changes in the promoter of the fragile histidine triad (FHIT) gene in human sebocytes under the influence of in vitro culture von Jotzo, Magdalena, Zouboulis, Christos C, Ballhausen, Wolfgang G

Volltext

Genetic screening for Peutz-Jeghers syndrome von Ballhausen, Wolfgang G, Günther, Klaus

Volltext

Mutation screening at the RNA level of the STK11/LKB1 gene in Peutz-Jeghers syndrome reveals complex splicing abnormalities and a novel mRNA isoform (STK11 c.597⁁598insIVS4) von Abed, Abdalla A., Günther, Klaus, Kraus, Cornelia, Hohenberger, Werner, Ballhausen, Wolfgang G.

Volltext

Alteration of the fragile histidine triad gene in intrahepatic cholangiocarcinoma von Koch, Eileen, Fiedler, Wolfgang, Tannapfel, Andrea, Ballhausen, Wolfgang G

Volltext

Loss of Fragile Histidine Triad (FHIT) expression and microsatellite instability in periocular sebaceous gland carcinoma in patients with Muir-Torre syndrome von HOLBACH, Leonard M, VON MOLLER, Alexander, DECKER, Carsten, JÜNEMANN, Anselm G. M, RUMMELT-HOFMANN, Carmen, BALLHAUSEN, Wolfgang G

Volltext

Erratum zu: Epigenetische Veränderungen am Promotor des fragilen Histidin-Trias(FHIT)-Gens in menschlichen Sebozyten unter dem Einfluss der In-vitro-Kultur von Jotzo, Magdalena, Zouboulis, Christos C., Ballhausen, Wolfgang G.

Volltext

Constitutive APC exon 14 skipping in early-onset familial adenomatous polyposis reveals a dramatic quantitative distortion of APC gene-specific isoforms von Bala, Shashi, Sulekova, Zora, Ballhausen, Wolfgang G.

Volltext

Different genetic pathways in the development of periocular sebaceous gland carcinomas in presumptive Muir-Torre syndrome patients von Goldberg, M., Rummelt, C., Foja, S., Holbach, L.M., Ballhausen, W.G.

Volltext

Promoter methylation and loss of coding exons of the fragile histidine triad (FHIT) gene in intrahepatic cholangiocarcinomas von Foja, S., Goldberg, M., Schagdarsurengin, U., Dammann, R., Tannapfel, A., Ballhausen, W. G.

Volltext

Mosaicism of a microdeletion of 486 bp involving the CGG repeat of the FMR1 gene due to misalignment of GTT tandem repeats at chi-like elements flanking both breakpoints and a full... von Schmucker, B, Ballhausen, W G, Pfeiffer, R A

Volltext

Genetic Testing for Familial Adenomatous Polyposis von BALLHAUSEN, WOLFGANG G.

Volltext

Forced expression of ΔN-TCF-1B in colon cancer derived cell lines is accompanied by the induction of CEACAM5/6 and mesothelin von Liebig, Beate, Brabletz, Thomas, Staege, Martin S., Wulfänger, Jens, Riemann, Dagmar, Burdach, Stefan, Ballhausen, Wolfgang G.

Volltext

Three novel types of splicing aberrations in the tuberous sclerosis TSC2 gene caused by mutations apart from splice consensus sequences von Mayer, Karin, Ballhausen, Wolfgang, Leistner, Werner, Rott, Hans-Dieter

Volltext

Localization of the Human β-Catenin Gene (CTNNB1) to 3p21: A Region Implicated in Tumor Development von Kraus, Cornelia, Liehr, Thomas, Hülsken, Jörg, Behrens, Jürgen, Birchmeier, Walter, Grzeschik, Karl-Heinz, Ballhausen, Wolfgang G.

Volltext