Solrun
Steine
Chief Engineer
Visit Address:
Haukeland Universitetssykehus Laboratoriebygget, 7. etg. Heis øst
5021 Bergen
Postal Address:
Postboks 7804
5021 Bergen
Phone:
+47 55 97 32 01
E-mail:
Journal articles
- 2013. Melanoma prone families with CDK4 germline mutation: phenotypic profile and associations with MC1R variants. Journal of Medical Genetics. 50: 264-U82. doi: 10.1136/jmedgenet-2012-101455
- 2009. pRb2/p130 protein expression and RBL2 mutation analysis in Burkitt lymphoma from Uganda. BMC Clinical Pathology. 9. Published 2009-08-19. doi: 10.1186/1472-6890-9-6
- 2009. Mutasjonsdiagnostikk ved syndromer knyttet til RAS/MAPK-signalveien. Tidsskrift for Den norske legeforening. 129: 2358-2361.
- 2008. Population-based prevalence of CDKN2A and CDK4 mutations in patients with multiple primary melanomas. Genes, Chromosomes and Cancer. 47: 175-184. doi: 10.1002/gcc.20518
- 2008. Clinicopathological characteristics and non-adhesive organ culture of insulinomas. Scandinavian Journal of Surgery. 97: 42-49.
- 2007. De novo HRAS and KRAS mutations in two siblings with short stature and neuro-cardio-facio-cutaneous features. Journal of Medical Genetics. 44. 6 pages. doi: 10.1136/jmg.2007.049361
- 2007. Circadian variation in Clock Gene Expression of Human Bone Marrow CD34+ Cells. Journal of Biological Rhythms. 22: 140-150. doi: 10.1177/0748730406299078
- 2006. AKT phosphorylation and PIK3CA amplification are common in cervical neoplasia. Laboratory Investigation. 86: 172A-172A.
- 2006. Molecular analysis of the PI3K-AKT pathway in uterine cervical neoplasia: Frequent PIK3CA amplification and AKT phosphorylation. International Journal of Cancer. 118: 1877-1883. doi: 10.1002/ijc.21461
- 2006. AKT phosphorylation and PIK3CA amplification are common in cervical neoplasia. Modern Pathology. 19: 172A-172A.
- 2006. Molecular analysis of the EGFR-RAS-RAF pathway in pancreatic ductal adenocarcinomas: lack of mutations in the BRAF and EGFR genes. Virchows Archiv. 448: 788-796. doi: 10.1007/s00428-006-0191-8
- 2005. A large Norwegian family with inherited malignant melanoma, multiple atypical nevi, and CDK4 mutation. Genes, Chromosomes and Cancer. 44: 10-18. doi: 10.1002/gcc.20202
- 2000. Enhanced detection of mutations in BRCA1 exon 11 using restricion endonuclease-fingerprinting SSCP. Journal of Molecular Medicine. 78: 580-587.
- 1999. Identification of suspectibility genes in Sjögren's syndrome. Norsk Biokjemisk Selskaps 30 års jubileumsmøte. 1.
Reports and theses
- 1996. PCR-based sequenced analysis of <I>c-kit</I> in formaldehyde fixed melanoma tissue (cand. scient. avhandling i bioteknologi). UiB. 62 pages.
More information in national current research information system (CRIStin)
