W. Ballhausen

发表

Three novel types of splicing aberrations in the tuberous sclerosis TSC2 gene caused by mutations apart from splice consensus sequences.

K. Mayer, W. Ballhausen, W. Leistner, 2000, Biochimica et biophysica acta.

Constitutive APC exon 14 skipping in early‐onset familial adenomatous polyposis reveals a dramatic quantitative distortion of APC gene‐specific isoforms

S. Bala, W. Ballhausen, Z. Šuleková, 1997, Human mutation.

Genetic screening for Peutz–Jeghers syndrome

K. Günther, W. Ballhausen, 2003, Expert review of molecular diagnostics.

Ectopic activation of lymphoid high mobility group‐box transcription factor TCF‐1 and overexpression in colorectal cancer cells

H. Clevers, K. Mayer, W. Ballhausen, 1997, International journal of cancer.

Mutation screening of the entire coding regions of the TSC1 and the TSC2 gene with the protein truncation test (PTT) identifies frequent splicing defects

K. Mayer, W. Ballhausen, H. Rott, 1999, Human mutation.

Distinction between natural and pathological autoantibodies by immunoblotting and densitometric subtraction: liver-kidney microsomal antibody (LKM) positive sera identify multiple antigens in human liver tissue.

M. Manns, G. Gerken, A. Lohse, 1987, Clinical and Experimental Immunology.

Genetic Testing for Germline Mutations of the APC Gene in Patients With Apparently Sporadic Desmoid Tumors but a Family History of Colorectal Carcinoma

W. Hohenberger, E. Hahn, K. Günther, 2005, Diseases of the colon and rectum.

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)

W. Hohenberger, K. Günther, C. Kraus, 2001, Human mutation.

DHPLC mutation analysis of the hereditary nonpolyposis colon cancer (HNPCC) genes hMLH1 and hMSH2.

T. Meitinger, H. Schackert, W. Ballhausen, 2001, Journal of biochemical and biophysical methods.

T cell tolerance to Mlsa encoded antigens in T cell receptor V beta 8.1 chain transgenic mice.

H. Pircher, R. Zinkernagel, T. Mak, 1989, The EMBO journal.

Epigenetic silencing contributes to frequent loss of the fragile histidine triad tumour suppressor in basal cell carcinomas

P. Helmbold, W. Ballhausen, C. Rummelt, 2006, The British journal of dermatology.

Acquisition of an additional antigen specificity after mouse CD4 gene transfer into a T helper hybridoma

T. Mak, P. Ohashi, A. Reske-Kunz, 1988, The Journal of experimental medicine.

P. Helmbold, H. Holzhausen, R. Dammann, 2007, Journal of hepatology.

T cell function and expression are dramatically altered in T cell receptor Vγ1.1Jγ4Cγ4 transgenic mice

H. Pircher, T. Mak, A. Iwamoto, 1989, Cell.

The invariant chains of mouse class II antigens: biochemical properties and molecular relationship

D. Linder, W. Ballhausen, S. Stirm, 1984, European journal of immunology.

Childhood hepatocellular adenoma in familial adenomatous polyposis: mutations in adenomatous polyposis coli gene and p53.

S. Bala, W. Ballhausen, P. Wünsch, 1997, Gastroenterology.

Yeast artificial chromosomes for the molecular analysis of the familial polyposis APC gene region.

D. Sheer, E. Solomon, T. Jones, 1992, Proceedings of the National Academy of Sciences of the United States of America.

Synthesis and expression of MHC class II molecules in the absence of attached invariant chains by recombinant interferon‐γ‐activated bone marrow‐derived macrophages

P. Steinlein, W. Ballhausen, K. Reske, 1987, European journal of immunology.

Identification of an alternative 5′ untranslated region of the adenomatous polyposis coli gene

W. Ballhausen, S. Lambertz, 1993, Human Genetics.

The human high mobility group (HMG)-box transcription factor TCF-1: novel isoforms due to alternative splicing and usage of a new exon IXA.

H. Clevers, K. Mayer, W. Ballhausen, 1995, Biochimica et biophysica acta.

Detection of APC region-specific signals by nonisotopic chromosomal in situ suppression (CISS)-hybridization using a microdissection library as a probe

G. Senger, U. Claussen, W. Ballhausen, 1991, Human Genetics.

Identification of lymphocyte cell-specific protein-tyrosine kinase (LCK) as a driver for invasion and migration of oral cancer by tumor heterogeneity exploitation

M. Kappler, Tony Gutschner, A. Eckert, 2021, Molecular Cancer.

Frequency and clinical features of visceral malignancy in a consecutive case series of patients with periocular sebaceous gland carcinoma

L. Holbach, W. Ballhausen, R. Conway, 2004, Graefe's Archive for Clinical and Experimental Ophthalmology.

Regional mapping of 22 microclones around the adenomatous polyposis coli (APC) locus on chromosome 5q

W. Bodmer, E. Solomon, W. Ballhausen, 1991, Human Genetics.

Genetic Testing for Familial Adenomatous Polyposis

W. Ballhausen, 2000, Annals of the New York Academy of Sciences.

Forced expression of deltaN-TCF-1B in colon cancer derived cell lines is accompanied by the induction of CEACAM5/6 and mesothelin.

S. Burdach, T. Brabletz, W. Ballhausen, 2005, Cancer letters.

MSH2 deficient mice are viable and susceptible to lymphoid tumours

H. Griesser, T. Mak, P. Waterhouse, 1995, Nature Genetics.

Subcellular localization and expression pattern of the neurofibromatosis type 2 protein merlin/schwannomin.

W. Ballhausen, M. Kressel, B. Schmucker, 1997, European journal of cell biology.

Multiple products in the protein truncation test due to alternative splicing in the adenomatous polyposis coli (APC) gene

S. Bala, J. Wijnen, C. Kraus, 1996, Human Genetics.

Loss of fragile histidine triad (FHIT) expression and microsatellite instability in periocular sebaceous gland carcinoma in patients with Muir-Torre syndrome.

L. Holbach, W. Ballhausen, A. Jünemann, 2002, American journal of ophthalmology.

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 mutation

W. Ballhausen, R. Pfeiffer, B. Schmucker, 1996, Human Genetics.

Two intragenic polymorphisms of the APC-gene detected by PCR and enzymatic digestion

C. Kraus, W. Ballhausen, 1992, Human Genetics.

Alteration of the fragile histidine triad gene in intrahepatic cholangiocarcinoma

A. Tannapfel, W. Ballhausen, W. Fiedler, 2003, European journal of gastroenterology & hepatology.

Multiple APC messenger RNA isoforms encoding exon 15 short open reading frames are expressed in the context of a novel exon 10A‐derived sequence

W. Ballhausen, Z. Šuleková, Julio Reina‐Sanchez, 1995, International journal of cancer.

A novel coding exon of the human adenomatous polyposis coli gene

W. Ballhausen, Z. Šuleková, 1995, Human Genetics.

Expression of a T cell receptor gamma-chain (V gamma 1.1J gamma 4C gamma 4) transgene in mice influences T cell receptor ontogeny and thymic architecture during development.

J. Bluestone, J. Allison, W. Ballhausen, 1990, Journal of Immunology.

Different genetic pathways in the development of periocular sebaceous gland carcinomas in presumptive Muir‐Torre syndrome patients

L. Holbach, W. Ballhausen, W. Ballhausen, 2006, Human mutation.

Localization of the human beta-catenin gene (CTNNB1) to 3p21: a region implicated in tumor development.

K. Grzeschik, W. Birchmeier, T. Liehr, 1994, Genomics.

Novel exon connections of the brain‐specific (BS) exon of the adenomatous polyposis coli gene

W. Ballhausen, Z. Šuleková, J. Bardos, 1997, International journal of cancer.

Immunochemical identification of novel high‐molecular‐weight protein isoforms of the adenomatous polyposis coli (APC) gene

C. Kraus, W. Ballhausen, Julio Reina‐Sanchez, 1996, International journal of cancer.

T cell function and expression are dramatically altered in T cell receptor V gamma 1.1J gamma 4C gamma 4 transgenic mice.

H. Pircher, T. Mak, A. Iwamoto, 1989, Cell.

Freezing of isolated cells provides free mRNA for RT-PCR amplification.

W. Ballhausen, F. von Eggeling, 1995, BioTechniques.