Anja R. Oldenburg
Oslo, Norway
Last Updated: 09/26/2026
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Found 13 publications
Preclinical assessment of MAGE-A4-specific TCR-NK cells against solid tumors.
Journal: Immunotherapy advances
Published: June 11, 2025
The lipodystrophic hotspot lamin A p.R482W mutation deregulates the mesodermal inducer T/Brachyury and early vascular differentiation gene networks.
Journal: Human molecular genetics
Published: January 18, 2018
A lipodystrophy-causing lamin A mutant alters conformation and epigenetic regulation of the anti-adipogenic MIR335 locus.
Journal: The Journal of cell biology
Published: January 05, 2017
Chrom3D: three-dimensional genome modeling from Hi-C and nuclear lamin-genome contacts.
Journal: Genome biology
Published: October 02, 2016
Mapping Nuclear Lamin-Genome Interactions by Chromatin Immunoprecipitation of Nuclear Lamins.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: May 06, 2016
Distinct features of lamin A-interacting chromatin domains mapped by ChIP-sequencing from sonicated or micrococcal nuclease-digested chromatin.
Journal: Nucleus (Austin, Tex.)
Published: January 21, 2015
The p.R482W substitution in A-type lamins deregulates SREBP1 activity in Dunnigan-type familial partial lipodystrophy.
Journal: Human molecular genetics
Published: December 20, 2014
Closing the (nuclear) envelope on the genome: how nuclear lamins interact with promoters and modulate gene expression.
Journal: BioEssays : news and reviews in molecular, cellular and developmental biology
Published: November 26, 2013
Deregulation of Fragile X-related protein 1 by the lipodystrophic lamin A p.R482W mutation elicits a myogenic gene expression program in preadipocytes.
Journal: Human molecular genetics
Published: October 11, 2013
Last Updated: 09/26/2026