Univ.-Prof. Dr. Bernhard Zabel
FB 04 - Universitätsmedizin, Johannes Gutenberg-Universität Mainz
- 06131/17-6826
- 06131/17-5528
Wagner, T.; Wirth, J.; Meyer, J. et al.
Autosomal Sex Reversal and Campomelic Dysplasia Are Caused by Mutations in and around the SRY-Related Gene SOX9Cell. Bd. 79. H. 6. Cambridge, Mass.: Cell Press 1994
Bardeesy, Nabeel; Zabel, Bernhard; Schmitt, Klaus et al.
Brief Report: WT1 Mutations Associated with Incomplete Denys-Drash Syndrome Define a Domain Predicted to Behave in a Dominant-Negative FashionGenomics. internat. journal of gene mapping and nucleotide sequencing ; emphasizing analyses of the human and other complex genomes. Bd. 21. H. 3. San Diego, Calif. [u.a.]: Elsevier 1994 S. 663 - 664
Troster, Helmut; Metzger, Thomas E.; Semsei, Imre et al.
One gene, two transcripts: isolation of an alternative transcript encoding for the autoantigen La-SS-B from a cDNA library of a patient with primary Sjögrens' syndromeThe journal of experimental medicine. JEM. Bd. 180. H. 6. New York, NY: Rockefeller Univ. Press 1994 S. 2059 - 2068
Bardeesy, N.; Falkoff, D.; Petruzzi, M. - J. et al.
P53 gene mutations are a rare event in Wilms'tumors and associated with poor prognosisNature Genetics. Bd. Nature Genetics. 1994 S. 91-97
Winterpacht, A.; Hilbert, M.; Schwarze, U. et al.
Kniest and Stickler dysplasia phenotypes caused by collagen type II gene (COL2A1) defectNature genetics. Bd. 3. H. 4. New York, NY: Nature America 1993 S. 323 - 326
Zabel, Bernhard
Nuclear localization of the protein encoded by the Wilms' tumor gene WT1 in embryonic and adult tissuesDevelopment. Bd. 119. H. 4. Cambridge: The Company of Biologists 1993 S. 1329 - 1341
Davis, M.; Zabel, B.; Senger, G. et al.
A tumor chromosome rearrangement further defines the 11p13 Wilms'tumor locusGenomics. Bd. Genomics. 1991 S. 588-592