C. Skjelbred

发表

Influence of DNA repair gene polymorphisms of hOGG1, XRCC1, XRCC3, ERCC2 and the folate metabolism gene MTHFR on chromosomal aberration frequencies.

M. Svendsen, C. Skjelbred, Marit Svendsen, 2006, Mutation research.

Single-track sequencing for genotyping of multiple SNPs in the N-acetyltransferase 1 (NAT1) gene

V. Kristensen, T. Kristensen, P. Souček, 2004, BMC biotechnology.

Meat, vegetables and genetic polymorphisms and the risk of colorectal carcinomas and adenomas

G. Hoff, E. Kure, K. Tveit, 2007, BMC Cancer.

Repair of cyclobutane pyrimidine dimers in the O6-methylguanine-DNA methyltransferase (MGMT) gene of MGMT proficient and deficient human cell lines and comparison with the repair of other genes and a repressed X-chromosomal locus.

F. Skorpen, H. Krokan, S. Schønberg, 1998, Mutation research.

The ratio of Matriptase/HAI-1 mRNA is higher in colorectal cancer adenomas and carcinomas than corresponding tissue from control individuals

U. Vogel, E. Kure, M. Sæbø, 2006, BMC Cancer.

Paracetamol increases sensitivity to ultraviolet (UV) irradiation, delays repair of the UNG-gene and recovery of RNA synthesis in HaCaT cells.

F. Skorpen, H. Krokan, P. A. Aas, 1998, Chemico-biological interactions.

Properties and functions of human uracil-DNA glycosylase from the UNG gene.

F. Skorpen, H. Nilsen, M. Otterlei, 2001, Progress in nucleic acid research and molecular biology.

GPX Pro198Leu and OGG1 Ser326Cys polymorphisms and risk of development of colorectal adenomas and colorectal cancer.

U. Vogel, E. Kure, B. Nexø, 2005, Cancer letters.

A single nucleotide polymorphism in BMP15 is associated with high response to ovarian stimulation.

T. Tanbo, C. Skjelbred, H. I. Hanevik, 2011, Reproductive biomedicine online.

Single nucleotide polymorphisms in the anti-Müllerian hormone signalling pathway do not determine high or low response to ovarian stimulation.

T. Tanbo, C. Skjelbred, H. I. Hanevik, 2010, Reproductive biomedicine online.

Expression of NDRG2 is down-regulated in high-risk adenomas and colorectal carcinoma

G. Hoff, E. Kure, T. Ikdahl, 2007, BMC Cancer.

Copy Number Variations in a Population-Based Study of Charcot-Marie-Tooth Disease

M. Russell, G. Braathen, H. Høyer, 2015, BioMed research international.

Uracil-DNA glycosylase (UNG)-deficient mice reveal a primary role of the enzyme during DNA replication.

T. Lindahl, D. Barnes, H. Nilsen, 2000, Molecular cell.

Human Uracil-DNA Glycosylase

F. Skorpen, H. Nilsen, M. Otterlei, 1999 .

Increased mRNA expression levels of ERCC1, OGG1 and RAI in colorectal adenomas and carcinomas

U. Vogel, H. Wallin, E. Kure, 2006, BMC Cancer.

Polymorphisms of the XRCC 1 , XRCC 3 and XPD genes and risk of colorectal adenoma and carcinoma , in a Norwegian cohort : a case control study

H. Wallin, E. Kure, B. Nexø, 2006 .

Polymorphisms of the XRCC1, XRCC3 and XPD genes and risk of colorectal adenoma and carcinoma, in a Norwegian cohort: a case control study

U. Vogel, H. Wallin, E. Kure, 2006, BMC Cancer.

Variants in the genes DCTN2,DNAH10,LRIG3, and MYO1A are associated with intermediate Charcot–Marie–Tooth disease in a Norwegian family

M. Russell, G. Braathen, H. Høyer, 2015, Acta neurologica Scandinavica.

Genetic Diagnosis of Charcot-Marie-Tooth Disease in a Population by Next-Generation Sequencing

M. Russell, L. Strand, G. Braathen, 2014, BioMed research international.

Effects of polymorphisms in ERCC1, ASE-1 and RAI on the risk of colorectal carcinomas and adenomas: a case control study

U. Vogel, H. Wallin, E. Kure, 2006, BMC Cancer.

Clinical exome sequencing – Norwegian findings.

L. Strand, G. Braathen, H. Høyer, 2015, Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke.

Charcot-Marie-Tooth caused by a copy number variation in myelin protein zero.

M. Russell, G. Braathen, H. Høyer, 2011, European journal of medical genetics.

Association between cigarette smoking, APC mutations and the risk of developing sporadic colorectal adenomas and carcinomas

E. Kure, M. Sæbø, I. Lothe, 2006, BMC Cancer.

Influence of GSTM1, GSTT1, GSTP1, NAT1, NAT2, EPHX1, MTR and MTHFR polymorphism on chromosomal aberration frequencies in human lymphocytes.

H. Norppa, J. Tuimala, E. Kure, 2011, Carcinogenesis.

Hereditary peripheral neuropathies diagnosed by next-generation sequencing.

M. Russell, L. Strand, G. Braathen, 2015, Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke.

Regulation of expression of nuclear and mitochondrial forms of human uracil-DNA glycosylase.

F. Skorpen, H. Krokan, T. Haug, 1998, Nucleic acids research.

Association between Frequency of Chromosomal Aberrations and Cancer Risk Is Not Influenced by Genetic Polymorphisms in GSTM1 and GSTT1

H. Norppa, S. Bonassi, R. Barale, 2008, Environmental health perspectives.

CYP 1 A 2 164 A C Polymorphism , Cigarette Smoking , Consumption of Well-done Red Meat and Risk of Developing Colorectal Adenomas and Carcinomas

E. Kure, K. Tveit, I. Lothe, 2009 .

CYP1A2 164 A-->C polymorphism, cigarette smoking, consumption of well-done red meat and risk of developing colorectal adenomas and carcinomas.

E. Kure, K. Tveit, C. Skjelbred, 2008, Anticancer research.

S H O R T C O M M U N I C a T I O N Open Access

T. Tanbo, C. Skjelbred, H. I. Hanevik, 2022 .

A gel electrophoresis method for detection of mitochondrial DNA mutation (3243 tRNALeu (UUR)) applied to a Norwegian family with diabetes mellitus and hearing loss

H. Krokan, C. Skjelbred, I. Følling, 2004, Scandinavian journal of clinical and laboratory investigation.

Erratum to “Influence of DNA repair gene polymorphisms of hOGG1, XRCC1, XRCC3, ERCC2 and the folate metabolism gene MTHFR on chromosomal aberration frequencies” [Mut. Res. 602 (2006) 151–162]

M. Svendsen, C. Skjelbred, Marit Svendsen, 2007 .

Repair of chromosomal abasic sites in vivo involves at least three different repair pathways

M. Otterlei, H. Krokan, S. Bharati, 2000, The EMBO journal.

Increased risk of ovarian hyperstimulation syndrome following controlled ovarian hyperstimulation in patients with vascular endothelial growth factor +405 cc genotype

T. Tanbo, C. Skjelbred, H. I. Hanevik, 2012, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.