Kristine Freude

Kristine Freude

Professor


  1. 2020
  2. Udgivet

    Human induced pluripotent cells in personalized treatment of monogenic epilepsies

    Mohammad, N. A., Freude, Kristine, Haukedal, H., Tümer, Asuman Zeynep & Møller, R. S., 2020, I: Journal of Translational Genetics and Genomics. 2020, 4, s. 238-250

    Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

  3. Udgivet

    Mutation in FTD3 CHMP2B causes impaired autography and distorted energy metabolism cumulating in reactive astrocyte phenotypes

    Chandrasekaran, A., Dittlau, K. S., Corsi, G., Haukedal, H., Doncheva, N. T., Ramakrishna, S., Ambardar, S., Salcedo, C., Schmidt, S. I., Cirera, S., Pihl, M., Schmid, B., Nielsen, T. T., Nielsen, J., Kolko, M., Kobolak, J., Dinnyes, A., Hyttel, P., Palakodeti, D., Gorodkin, J. & 4 flere, Muddashetty, R., Meyer, M., Aldana, Blanca & Freude, Kristine, 2020.

    Publikation: KonferencebidragKonferenceabstrakt til konferenceForskning

  4. Udgivet

    Mutations in FTD3 CHMP2B causes impaired autophagy and distorted energy metabolism cumulating in reactive astrocyte phenotypes

    Chandrasekaran, A., Dittlau, K. S., Corsi, G., Doncheva, N. T., Haukedal, H., Ramakrishna, S., Ambardar, S., Salcedo, C., Schmidt, S. I., Cirera, S., Pihl, M., Schmid, B., Nielsen, T. T., Nielsen, J., Kolko, M., Kobolak, J., Dinnyes, A., Hyttel, P., Palakodeti, D., Gorodkin, J. & 4 flere, Muddashetty, R., Meyer, M., Aldana, Blanca & Freude, Kristine, 2020.

    Publikation: KonferencebidragPosterForskning

  5. 2019
  6. Udgivet

    Patient iPSC-Derived Neurons for Disease Modeling of Familiar Alzheier's Disease with Mutations in Presenilin 1

    Haukedal, H., Poon, A. F., Jensen, P., Aldana, Blanca, Pires, C., Chandrasekaran, Abinaya, Christensen, S. K., Schiønning, P., Vallin, S., Simonsen, A. H., Nielsen, J., Dinnyes, A., Gorodkin, Jan, Ramakrishna, S., Muddashetty, R., Palakodeti, D., Hyttel, P., Waagepetersen, Helle S., Larsen, M. R. & Freude, Kristine, 26 mar. 2019.

    Publikation: KonferencebidragPosterFormidling

  7. Udgivet

    Generation of two isogenic iPSC lines with either a heterozygous or a homozygous E280A mutation in the PSEN1 gene.

    Frederiksen, Henriette Reventlow S, Holst, B., Mau-Holzmann, U. A., Freude, Kristine & Schmid, B., mar. 2019, I: Stem Cell Research. 35, 4 s., 101403.

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

  8. Udgivet

    Generation of two iPSC lines with either a heterozygous V717I or a heterozygous KM670/671NL mutation in the APP gene

    Frederiksen, Henriette Reventlow S, Holst, B., Ramakrishna, S., Muddashetty, R., Schmid, B. & Freude, Kristine, 1 jan. 2019, I: Stem Cell Research. 34, 5 s., 101368.

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

  9. Udgivet

    Cell type specific expression of toll-like receptors in human brains and implications in Alzheimer's disease

    Frederiksen, Henriette Reventlow S, Haukedal, H. & Freude, Kristine, 2019, I: BioMed Research International. 2019, 18 s., 7420189.

    Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

  10. Udgivet

    Dementia, Brain Disorders and Molecular Mechanisms

    Freude, Kristine & Krauss, S., 2019, I: Journal of Molecular Biology. 431, 9, s. 1709-1710

    Publikation: Bidrag til tidsskriftLederForskning

  11. Udgivet

    Genetic protection modifications: Moving beyond the binary distinction between therapy and enhancement for human genome editing

    Mikkelsen, R. C. B., Frederiksen, Henriette Reventlow S, Gjerris, Mickey, Holst, B., Hyttel, P., Luo, Y., Freude, Kristine & Sandøe, Peter, 2019, I: CRISPR Journal. 2, 6, s. 362-369 8 s.

    Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

  12. Udgivet

    Implications of Microglia in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia

    Haukedal, H. & Freude, Kristine, 2019, I: Journal of Molecular Biology. 431, 9, s. 1818-1829

    Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

ID: 38189431