Academic article

• Liang, Xiao; Chen, Anbin; Kianian, Atefeh et al. (2024). Activation of Neurotoxic Astrocytes Due to Mitochondrial Dysfunction Triggered by POLG Mutation. (external link)
• Kristiansen, Cecilie Katrin; Furriol, Jessica; Chen, Anbin et al. (2023). Deoxyribonucleoside treatment rescues EtBr-induced mtDNA depletion in iPSC-derived neural stem cells with POLG mutations. (external link)
• Marjan, Sharika; Yangzom, Tsering; Kristiansen, Cecilie Katrin et al. (2023). Application of Flow Cytometric Analysis for Measuring Multiple Mitochondrial Parameters in 3D Brain Organoids. (external link)
• Hong, Yu; Kristiansen, Cecilie Katrin; Chen, Anbin et al. (2023). POLG genotype influences degree of mitochondrial dysfunction in iPSC derived neural progenitors, but not the parent iPSC or derived glia. (external link)
• Kristiansen, Cecilie Katrin; Chen, Anbin; Høyland, Lena Elise et al. (2022). Comparing the mitochondrial signatures in ESCs and iPSCs and their neural derivations. (external link)
• Chen, Anbin; Kristiansen, Cecilie Katrin; Høyland, Lena Elise et al. (2022). POLG mutations lead to abnormal mitochondrial remodeling during neural differentiation of human pluripotent stem cells via SIRT3/AMPK pathway inhibition. (external link)
• Liang, Xiao; Chen, Anbin; Kristiansen, Cecilie Katrin et al. (2021). Flow cytometric analysis of multiple mitochondrial parameters in human induced pluripotent stem cells and their neural and glial derivatives. (external link)
• Chen, Anbin; Kristiansen, Cecilie Katrin; Hong, Yu et al. (2021). Nicotinamide riboside and metformin ameliorate mitophagy defect in induced pluripotent stem cell-derived astrocytes with POLG mutations. (external link)
• Liang, Xiao; Kianian, Atefeh; Chen, Anbin et al. (2021). Stem cell derived astrocytes with POLG mutations and mitochondrial dysfunction including abnormal NAD+ metabolism is toxic for neurons. (external link)
• Liang, Xiao; Vatne, Guro Helén; Kristiansen, Cecilie Katrin et al. (2020). N-acetylcysteine amide ameliorates mitochondrial dysfunction and reduces oxidative stress in hiPSC-derived dopaminergic neurons with POLG mutation. (external link)
• Liang, Xiao; Kristiansen, Cecilie Katrin; Mostafavi, Sepideh et al. (2020). Disease-specific phenotypes in iPSC-derived neural stem cells with POLG mutations. (external link)
• Raasakka, Arne; Ruskamo, Salla; Barker, Robert et al. (2019). Neuropathy-related mutations alter the membrane binding properties of the human myelin protein P0 cytoplasmic tail. (external link)
• Ruskamo, Salla; Nieminen, Tuomo; Kristiansen, Cecilie Katrin et al. (2017). Molecular mechanisms of Charcot-Marie-Tooth neuropathy linked to mutations in human myelin protein P2. (external link)

Academic literature review

• Liang, Xiao; Kristiansen, Cecilie Katrin; Vatne, Guro Helén et al. (2020). Patient-specific neural progenitor cells derived from induced pluripotent stem cells offer a promise of good models for mitochondrial disease. (external link)

Errata

• Ruskamo, Salla; Nieminen, Tuomo; Kristiansen, Cecilie Katrin et al. (2018). Erratum: Publisher Correction: Molecular mechanisms of Charcot-Marie-Tooth neuropathy linked to mutations in human myelin protein P2. (external link)

Masters thesis

• Kristiansen, Cecilie Katrin; Bindoff, Laurence; Liang, Xiao (2018). W748S POLG mutation induced mitochondrial changes in hiPSC-differentiated NSCs. (external link)

See a complete overview of publications in Cristin.