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

par Ekstrøm, Per Olaf, Nakken, Sigve, Johansen, Morten, Hovig, Eivind
Publié dans BMC Res Notes (2015)

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

par Refinetti, Paulo, Arstad, Christian, Thilly, William G., Morgenthaler, Stephan, Ekstrøm, Per Olaf
Publié dans BMC Clin Pathol (2017)

Ten modifiers of BRCA1 penetrance validated in a Norwegian series

par Heramb, Cecilie, Ekstrøm, Per Olaf, Tharmaratnam, Kukatharmini, Hovig, Eivind, Møller, Pål, Mæhle, Lovise
Publié dans Hered Cancer Clin Pract (2015)

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

par Arstad, Christian, Refinetti, Paulo, Kristensen, Annette Torgunrud, Giercksky, Karl-Erik, Ekstrøm, Per Olaf
Publié dans BMC Cancer (2017)

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

par Arstad, Christian, Taskén, Kristin, Refinetti, Paulo, Axcrona, Ulrika, Giercksky, Karl-Erik, Ekstrøm, Per Olaf
Publié dans Prostate Cancer (2020)

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

par Sørensen, Olaf, Andersen, Anders, Olsen, Harald, Alexandr, Kristian, Ekstrøm, Per Olaf, Giercksky, Karl-Erik, Flatmark, Kjersti
Publié 2010

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

par FRIIS-OTTESSEN, MARIANN, BURUM-AUENSEN, ESPEN, SCHJØLBERG, AASA R., EKSTRØM, PER OLAF, ANDERSEN, SOLVEIG N., CLAUSEN, OLE PETTER, DE ANGELIS, PAULA M.
Publié dans Int J Mol Med (2015)

Identification of genetic variants for clinical management of familial colorectal tumors

par 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
Publié dans BMC Med Genet (2018)

Genetic variants of prospectively demonstrated phenocopies in BRCA1/2 kindreds

par 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
Publié dans Hered Cancer Clin Pract (2018)

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

par 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
Publié dans Sci Rep (2019)