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The Journal of Clinical Investigation|April 1, 1994
A novel exon in the cystic fibrosis transmembrane conductance regulator gene activated by the nonsense mutation E92X in airway epithelial cells of patients with cystic fibrosisK Will, T Dörk, M Stuhrmann, et al.
Molecular and Cellular Probes|February 1, 1997
A frequent polymorphism of the gene mutated in ataxia telangiectasiaT Dörk, S Westermann, O Dittrich, et al.
British Journal of Cancer|September 15, 2001
Mutations of the BRCA1 and BRCA2 genes in patients with bilateral breast cancerD Steinmann, M Bremer, D Rades, et al.
Human Genetics|July 8, 1998
Cystic-fibrosis-like disease unrelated to the cystic fibrosis transmembrane conductance regulatorF Mekus, M Ballmann, I Bronsveld, et al.
The American Journal of Gastroenterology|August 19, 2000
Mutations of the cystic fibrosis gene, but not cationic trypsinogen gene, are associated with recurrent or chronic idiopathic pancreatitisJ Ockenga, M Stuhrmann, M Ballmann, et al.
Human Mutation|January 1, 1995
Transcript analysis of CFTR nonsense mutations in lymphocytes and nasal epithelial cells from cystic fibrosis patientsK Will, T Dörk, M Stuhrmann, et al.
Clinical Genetics|June 24, 2010
High frequency and allele-specific differences of BRCA1 founder mutations in breast cancer and ovarian cancer patients from BelarusN V Bogdanova, N N Antonenkova, Y I Rogov, et al.
Human Genetics|August 1, 1991
Cystic fibrosis with three mutations in the cystic fibrosis transmembrane conductance regulator geneT Dörk, U Wulbrand, T Richter, et al.
American Journal of Human Genetics|March 1, 1995
A novel donor splice site in intron 11 of the CFTR gene, created by mutation 1811+1.6kbA-->G, produces a new exon: high frequency in Spanish cystic fibrosis chromosomes and association with severe phenotypeM Chillón, T Dörk, T Casals, et al.
European Journal of Cell Biology|April 1, 1990
Differentiation and retrodifferentiation of U937 cells: reversible induction and suppression of intermediate filament protein synthesisR Hass, G Giese, G Meyer, et al.
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