Cecilie Katrin Kristiansen

PhD Candidate

E-mailCecilie.Kristiansen@uib.no
Visitor Address
Haukeland Universitetssykehus Laboratoriebygget, 7. etg. Heis øst

5009 Bergen
Postal Address
Postboks 7804

5020 Bergen

Academic article

Show author(s) (2022). POLG mutations lead to abnormal mitochondrial remodeling during neural differentiation of human pluripotent stem cells via SIRT3/AMPK pathway inhibition. Cell Cycle. 1178-1193.
Show author(s) (2022). Comparing the mitochondrial signatures in ESCs and iPSCs and their neural derivations. Cell Cycle. 2206-2221.

Show author(s) (2021). Stem cell derived astrocytes with POLG mutations and mitochondrial dysfunction including abnormal NAD+ metabolism is toxic for neurons. BioRxiv.
Show author(s) (2021). Nicotinamide riboside and metformin ameliorate mitophagy defect in induced pluripotent stem cell-derived astrocytes with POLG mutations. Frontiers in Cell and Developmental Biology. 1-20.
Show author(s) (2021). Flow cytometric analysis of multiple mitochondrial parameters in human induced pluripotent stem cells and their neural and glial derivatives. Journal of Visualized Experiments.

Show author(s) (2020). N-acetylcysteine amide ameliorates mitochondrial dysfunction and reduces oxidative stress in hiPSC-derived dopaminergic neurons with POLG mutation. Experimental Neurology.
Show author(s) (2020). Disease-specific phenotypes in iPSC-derived neural stem cells with POLG mutations. EMBO Molecular Medicine. 1-26.

Show author(s) (2019). Neuropathy-related mutations alter the membrane binding properties of the human myelin protein P0 cytoplasmic tail. PLOS ONE. 1-24.

Show author(s) (2017). Molecular mechanisms of Charcot-Marie-Tooth neuropathy linked to mutations in human myelin protein P2. Scientific Reports. 1-13.

Masters thesis

Show author(s) (2018). W748S POLG mutation induced mitochondrial changes in hiPSC-differentiated NSCs.

Errata

Show author(s) (2018). Erratum: Publisher Correction: Molecular mechanisms of Charcot-Marie-Tooth neuropathy linked to mutations in human myelin protein P2. Scientific Reports.

Academic literature review

Show author(s) (2020). Patient-specific neural progenitor cells derived from induced pluripotent stem cells offer a promise of good models for mitochondrial disease. Cell and Tissue Research. 15-30.