Molecular Genetics of Breast and Ovarian Cancer: Recent Advances and Clinical Implications

per Bogdanova, N, Dörk, T
Publicat 2012

Low prevalence of SPINK1 gene mutations in adult patients with chronic idiopathic pancreatitis

per OCKENGA, J., DORK, T., STUHRMANN, M.
Publicat 2001

A Hinfl polymorphism in the cystic fibrosis gene CFTR

per Dörk, Thilo, Wulbrand, Ulrich, Tümmler, Burkhard
Publicat 1991

Hereditary breast cancer: ever more pieces to the polygenic puzzle

per Bogdanova, Natalia, Helbig, Sonja, Dörk, Thilo
Publicat 2013

Predictability of Precipitation Over the Conterminous U.S. Based on the CMIP5 Multi-Model Ensemble

per Jiang, Mingkai, Felzer, Benjamin S., Sahagian, Dork
Publicat a Sci Rep (2016)

Corrigendum: Predictability of Precipitation Over the Conterminous U.S. Based on the CMIP5 Multi-Model Ensemble

per Jiang, Mingkai, Felzer, Benjamin S., Sahagian, Dork
Publicat a Sci Rep (2016)

Mutation and haplotype analysis of the CFTR gene in atypically mild cystic fibrosis patients from Northern Ireland

per HUGHES, D., DORK, T., STUHRMANN, M., GRAHAM, C.
Publicat 2001

Gene variants associated with obstructive sleep apnea (OSA) in relation to sudden infant death syndrome (SIDS)

per Kerz, J., Schürmann, P., Rothämel, T., Dörk, T., Klintschar, M.
Publicat a Int J Legal Med (2021)

BRCA1 expression is not affected by the intronic 12 bp duplication

per DORK, T., SKAWRAN, B., STUHRMANN, M., BREMER, M., KARSTENS, J.
Publicat 1999

Genetic association study of fatal pulmonary embolism

per Meißner, Lisa, Schürmann, Peter, Dörk, Thilo, Hagemeier, Lars, Klintschar, Michael
Publicat a Int J Legal Med (2020)

Genetic Susceptibility to Endometrial Cancer: Risk Factors and Clinical Management

per Dörk, Thilo, Hillemanns, Peter, Tempfer, Clemens, Breu, Julius, Fleisch, Markus C.
Publicat a Cancers (Basel) (2020)

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 fibrosis.

per Will, K, Dörk, T, Stuhrmann, M, Meitinger, T, Bertele-Harms, R, Tümmler, B, Schmidtke, J
Publicat 1994

Independent origins of cystic fibrosis mutations R334W, R347P, R1162X, and 3849 + 10kbC-->T provide evidence of mutation recurrence in the CFTR gene.

per Morral, N., Llevadot, R., Casals, T., Gasparini, P., Macek, M., Dörk, T., Estivill, X.
Publicat 1994

A Single UDP-galactofuranose Transporter Is Required for Galactofuranosylation in Aspergillus fumigatus

per Engel, Jakob, Schmalhorst, Philipp S., Dörk-Bousset, Thilo, Ferrières, Vincent, Routier, Françoise H.
Publicat 2009

Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping

per Buratti, Emanuele, Dörk, Thilo, Zuccato, Elisabetta, Pagani, Franco, Romano, Maurizio, Baralle, Francisco E.
Publicat 2001

Neuregulin Receptor ErbB4 Functions as a Transcriptional Cofactor for the Expression of Surfactant Protein B in the Fetal Lung

per Zscheppang, Katja, Dörk, Thilo, Schmiedl, Andreas, Jones, Frank E., Dammann, Christiane E. L.
Publicat 2011

Missense mutations but not allelic variants alter the function of ATM by dominant interference in patients with breast cancer

per Scott, Shaun P., Bendix, Regina, Chen, Philip, Clark, Raymond, Dörk, Thilo, Lavin, Martin F.
Publicat 2002

Mutations of the BRCA1 and BRCA2 genes in patients with bilateral breast cancer

per Steinmann, D, Bremer, M, Rades, D, Skawran, B, Siebrands, C, Karstens, J H, Dörk, T
Publicat 2001

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 associa...

per Chillón, M, Dörk, T, Casals, T, Giménez, J, Fonknechten, N, Will, K, Ramos, D, Nunes, V, Estivill, X
Publicat 1995

TOPBP1 missense variant Arg309Cys and breast cancer in a German hospital-based case-control study

per Blaut, Magda A, Bogdanova, Natalia V, Bremer, Michael, Karstens, Johann H, Hillemanns, Peter, Dörk, Thilo
Publicat 2010