Anne Nørremølle

Anne Nørremølle

Associate professor, Associate Professor


  1. Published

    Dysfunctional mitochondrial respiration in the striatum of the Huntington's disease transgenic R6/2 mouse model. / Aidt, Frederik Heurlin; Nielsen, Signe Marie Borch; Kanters, Jørgen; Pesta, Dominik; Nielsen, Troels Tolstrup; Nørremølle, Anne; Hasholt, Lis; Christiansen, Michael; Hagen, Christian Munch.

    In: PLoS Currents, Vol. 5, 2013.

    Research output: Contribution to journalJournal articleResearchpeer-review

  2. Published

    Enhanced cerebral branched-chain amino acid metabolism in R6/2 mouse model of Huntington's disease. / Andersen, Jens V.; Skotte, Niels H.; Aldana, Blanca I.; Nørremølle, Anne; Waagepetersen, Helle S.

    In: Cellular and Molecular Life Sciences, Vol. 76, No. 12, 2019, p. 2449-2461.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Published

    DNA analysis of distinct populations suggests multiple origins for the mutation causing Huntington's disease. / Andrew, S.; Theilmann, J.; Almquist, E.; Nørremølle, Anne; Lucotte, G.; Anvret, M.; Sørensen, S.A.; Turpin, J.C.; Hayden, Michael R.

    In: Clinical Genetics, No. 43, 1993, p. 286-294.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Published

    The lrrk2 p.Gly2019Ser mutation is uncommon in a Danish cohort with various neurodegenerative disorders. / Bech, Sara; Nørremølle, Anne; Winge, Kristian; Hasholt, Lis; Tommerup, Niels; Svenstrup, Kirsten; Nielsen, Jørgen E; Hjermind, Lena E.

    In: Parkinsonism & Related Disorders, Vol. 17, No. 5, 01.06.2011, p. 398-9.

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. Published

    Huntington's disease-like and ataxia syndromes: identification of a family with a de novo SCA17/TBP mutation. / Bech, Sara; Petersen, Thor; Nørremølle, Anne; Gjedde, Albert; Ehlers, Lise; Eiberg, Hans; Hjermind, Lena E; Hasholt, Lis; Lundorf, Erik; Nielsen, Jørgen E.

    In: Parkinsonism & Related Disorders, Vol. 16, No. 1, 2010, p. 12-5.

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. Published

    A SNP in the HTT promoter alters NF-κB binding and is a bidirectional genetic modifier of Huntington disease. / Bečanović, Kristina; Nørremølle, Anne; Neal, Scott J; Kay, Chris; Collins, Jennifer A; Arenillas, David; Lilja, Tobias; Gaudenzi, Giulia; Manoharan, Shiana; Doty, Crystal N; Beck, Jessalyn; Lahiri, Nayana; Portales-Casamar, Elodie; Warby, Simon C; Connolly, Colúm; De Souza, Rebecca A G; Tabrizi, Sarah J; Hermanson, Ola; Langbehn, Douglas R; Hayden, Michael R; Wasserman, Wyeth W; Leavitt, Blair R; REGISTRY Investigators of the European Huntington's Disease Network.

    In: Nature Neuroscience, Vol. 18, No. 6, 06.2015, p. 807-816.

    Research output: Contribution to journalJournal articleResearchpeer-review

  7. Published

    Huntington's disease does not appear to increase the risk of diabetes mellitus. / Boesgaard, T W; Nielsen, Troels Tolstrup; Josefsen, Knud Elnegaard; Hansen, T; Jørgensen, T; Pedersen, O; Nørremølle, A; Nielsen, Jørgen Erik; Hasholt, L.

    In: Journal of Neuroendocrinology, Vol. 21, No. 9, 2009, p. 770-6.

    Research output: Contribution to journalJournal articleResearchpeer-review

  8. Published

    MicroRNAs in mammalian brain. / Christensen, M.; Bak, M.; Silahtaroglu, A.; Kloosterman, W.; Skryapin, B.; Nolting, D.; Nørremølle, Anne; Lassen, A.-C.; Halsholm, L.; Brosius, J.; Tommerup, Niels; Plasterk, R.; Kauppinen, Markus Sakari.

    2006. p. 1.

    Research output: Working paperResearch

  9. Published

    Mapping of the human NMDA receptor subunit (NMDAR1) and the proposed NMDA receptor glutamate-binding subunit (NMDARA1) to chromosomes 9q34.3 and chromosome 8, respectively. / Collins, C; Duff, C; Duncan, A M; Planells-Cases, R; Sun, W; Nørremølle, Anne; Michaelis, E; Montal, M; Worton, R; Hayden, M R.

    In: Genomics, Vol. 17, No. 1, 1993, p. 237-9.

    Research output: Contribution to journalJournal articleResearchpeer-review

  10. Published

    Haploinsufficiency of ARHGAP42 is associated with hypertension. / Fjorder, Amanda S.; Rasmussen, Malene B.; Mehrjouy, Mana M.; Nazaryan-Petersen, Lusine; Hansen, Claus; Bak, Mads; Grarup, Niels; Nørremølle, Anne; Larsen, Lars A.; Vestergaard, Henrik; Hansen, Torben; Tommerup, Niels; Bache, Iben.

    In: European Journal of Human Genetics, Vol. 27, No. 8, 2019, p. 1296-1303.

    Research output: Contribution to journalJournal articleResearchpeer-review

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