Automated amplicon design suitable for analysis of DNA variants by melting techniques

Por Ekstrøm, Per Olaf, Nakken, Sigve, Johansen, Morten, Hovig, Eivind
Publicado no BMC Res Notes (2015)

Mapping mitochondrial heteroplasmy in a Leydig tumor by laser capture micro-dissection and cycling temperature capillary electrophoresis

Por Refinetti, Paulo, Arstad, Christian, Thilly, William G., Morgenthaler, Stephan, Ekstrøm, Per Olaf
Publicado no BMC Clin Pathol (2017)

Ten modifiers of BRCA1 penetrance validated in a Norwegian series

Por Heramb, Cecilie, Ekstrøm, Per Olaf, Tharmaratnam, Kukatharmini, Hovig, Eivind, Møller, Pål, Mæhle, Lovise
Publicado no Hered Cancer Clin Pract (2015)

Is detection of intraperitoneal exfoliated tumor cells after surgical resection of rectal cancer a prognostic factor of survival?

Por Arstad, Christian, Refinetti, Paulo, Kristensen, Annette Torgunrud, Giercksky, Karl-Erik, Ekstrøm, Per Olaf
Publicado no BMC Cancer (2017)

Somatic Mitochondrial DNA Point Mutations Used as Biomarkers to Demonstrate Genomic Heterogeneity in Primary Prostate Cancer

Por Arstad, Christian, Taskén, Kristin, Refinetti, Paulo, Axcrona, Ulrika, Giercksky, Karl-Erik, Ekstrøm, Per Olaf
Publicado no Prostate Cancer (2020)

Validation and use of microdialysis for determination of pharmacokinetic properties of the chemotherapeutic agent mitomycin C - an experimental study

Por Sørensen, Olaf, Andersen, Anders, Olsen, Harald, Alexandr, Kristian, Ekstrøm, Per Olaf, Giercksky, Karl-Erik, Flatmark, Kjersti
Publicado em 2010

TP53/p53 alterations and Aurora A expression in progressor and non-progressor colectomies from patients with longstanding ulcerative colitis

Por FRIIS-OTTESSEN, MARIANN, BURUM-AUENSEN, ESPEN, SCHJØLBERG, AASA R., EKSTRØM, PER OLAF, ANDERSEN, SOLVEIG N., CLAUSEN, OLE PETTER, DE ANGELIS, PAULA M.
Publicado no Int J Mol Med (2015)

Identification of genetic variants for clinical management of familial colorectal tumors

Por Dominguez-Valentin, Mev, Nakken, Sigve, Tubeuf, Hélène, Vodak, Daniel, Ekstrøm, Per Olaf, Nissen, Anke M., Morak, Monika, Holinski-Feder, Elke, Martins, Alexandra, Møller, Pål, Hovig, Eivind
Publicado no BMC Med Genet (2018)

Genetic variants of prospectively demonstrated phenocopies in BRCA1/2 kindreds

Por Dominguez-Valentin, Mev, Evans, D. Gareth R., Nakken, Sigve, Tubeuf, Hélène, Vodak, Daniel, Ekstrøm, Per Olaf, Nissen, Anke M., Morak, Monika, Holinski-Feder, Elke, Martins, Alexandra, Møller, Pål, Hovig, Eivind
Publicado no Hered Cancer Clin Pract (2018)

Results of multigene panel testing in familial cancer cases without genetic cause demonstrated by single gene testing

Por Dominguez-Valentin, Mev, Nakken, Sigve, Tubeuf, Hélène, Vodak, Daniel, Ekstrøm, Per Olaf, Nissen, Anke M., Morak, Monika, Holinski-Feder, Elke, Holth, Arild, Capella, Gabriel, Davidson, Ben, Evans, D. Gareth, Martins, Alexandra, Møller, Pål, Hovig, Eivind
Publicado no Sci Rep (2019)