Anja Bjolgerud

Oslo, Norway

Last Updated: 09/26/2026

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Found 8 publications

Effects of Anthocyanins on CAG Repeat Instability and Behaviour in Huntington's Disease R6/1 Mice.

Effects of Anthocyanins on CAG Repeat Instability and Behaviour in Huntington's Disease R6/1 Mice.

Journal: PLoS currents
Published: August 20, 2016

The multiple sclerosis susceptibility genes TAGAP and IL2RA are regulated by vitamin D in CD4+ T cells.

The multiple sclerosis susceptibility genes TAGAP and IL2RA are regulated by vitamin D in CD4+ T cells.

Journal: Genes and immunity
Published: May 05, 2015

Multiple Sclerosis Risk Allele in CLEC16A Acts as an Expression Quantitative Trait Locus for CLEC16A and SOCS1 in CD4+ T Cells.

Multiple Sclerosis Risk Allele in CLEC16A Acts as an Expression Quantitative Trait Locus for CLEC16A and SOCS1 in CD4+ T Cells.

Journal: PloS one
Published: March 24, 2015

Genome-wide DNA methylation profiles indicate CD8+ T cell hypermethylation in multiple sclerosis.

Genome-wide DNA methylation profiles indicate CD8+ T cell hypermethylation in multiple sclerosis.

Journal: PloS one
Published: July 21, 2014

Environmental exposures and the risk of multiple sclerosis investigated in a Norwegian case-control study.

Environmental exposures and the risk of multiple sclerosis investigated in a Norwegian case-control study.

Journal: BMC neurology
Published: July 05, 2014

No association between multiple sclerosis and periodontitis after adjusting for smoking habits.

No association between multiple sclerosis and periodontitis after adjusting for smoking habits.

Journal: European journal of neurology
Published: January 02, 2014

Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles.

Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles.

Journal: PloS one
Published: September 20, 2012

Neil1 is a genetic modifier of somatic and germline CAG trinucleotide repeat instability in R6/1 mice.

Neil1 is a genetic modifier of somatic and germline CAG trinucleotide repeat instability in R6/1 mice.

Journal: Human molecular genetics
Published: August 24, 2012
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Last Updated: 09/26/2026