Institut for Molekylærbiologi og Genetik

Aarhus Universitets segl

Neurobiologi

DANDRITE's logo

The Section for Neurobiology is part of the Danish Research Institute of Translational Neuroscience – DANDRITE 

- the Danish node of the Nordic EMBL Partnership for Molecular Medicine, which performs basic and translational research in brain and the nervous system.  

Groups at DANDRITE encompass ambitious research programs that include:

  • Molecular and cellular mechanisms of memory
  • Effort-based decision making
  • Neuronal development and stem cells
  • Motor control
  • Brain processing of vision
  • Neurological and neurodegenerative diseases
  • Psychiatric disorders
  • Neurotrophic receptors, sorting
  • Structural biology of membrane transporters and receptors

Read more about the research at DANDRITE.

Below you see the list of researchers at DANDRITE affiliated with the Department of Molecular Biology and Genetics.

Professor

Lektorer

Tenure Track Adjunkt

Peer-reviewed publikationer

Sortér efter: Dato | Forfatter | Titel

Reinhard (maiden name Schuldt), L., Tidow, H., Clausen, M. J. & Nissen, P. (2013). Na+,K+-ATPase as a docking station: protein-protein complexes of the Na(+),K (+)-ATPase. Cellular and Molecular Life Sciences, 70(2), 205-222. https://doi.org/10.1007/s00018-012-1039-9
Ravishankar, H., Pedersen, M. N., Eklund, M., Sitsel, A., Li, C., Duelli, A., Levantino, M., Wulff, M., Barth, A., Olesen, C., Nissen, P. & Andersson, M. (2020). Tracking Ca2+ ATPase intermediates in real time by x-ray solution scattering. Science Advances, 6(12), Artikel eaaz0981. https://doi.org/10.1126/sciadv.aaz0981
Rafiq, M., Ernst, H. A., Aduri, N. G., Prabhala, B. K., Tufail, S., Rahman, M., Bloch, M. B., Mirza, N., Taylor, N. M. I., Boesen, T., Gajhede, M. & Mirza, O. (2022). Expression, purification and characterization of human proton-coupled oligopeptide transporter 1 hPEPT1. Protein Expression and Purification, 190, Artikel 105990. https://doi.org/10.1016/j.pep.2021.105990
Quistgaard, E. M., Madsen, P., Grøftehauge, M. K., Nissen, P., Petersen, C. M. & Thirup, S. S. (2009). Ligands bind to Sortilin in the tunnel of a ten-bladed beta-propeller domain. Nature Structural and Molecular Biology, 16(1), 96-8. https://doi.org/10.1038/nsmb.1543
Quistgaard, E. M., Grøftehauge, M. K., Madsen, P., Pallesen, L. T., Christensen, B. S., Sørensen, E. S., Nissen, P., Petersen, C. M. & Thirup, S. S. (2014). Revisiting the structure of the Vps10 domain of human sortilin and its interaction with neurotensin. Protein Science, 23(9), 1291-1300. https://doi.org/10.1002/pro.2512
Quistgaard, E. M. H., Nissen, J. D., Hansen, S. & Nissen, P. (2021). Mind the gap: molecular architecture of the axon initial segment – from fold prediction to a mechanistic model of function? Journal of Molecular Biology, 433(20), Artikel 167176. https://doi.org/10.1016/j.jmb.2021.167176
Quick, M., Winther, A.-M. L., Shi, L., Nissen, P., Weinstein, H. & Javitch, J. A. (2009). Binding of an octylglucoside detergent molecule in the second substrate (S2) site of LeuT establishes an inhibitor-bound conformation. Proceedings of the National Academy of Sciences (PNAS), 106(14), 5563-8.
Qin, Q., Wei, P., Usman, S., Ahamefule, C. S., Jin, C., Wang, B., Yan, K., van Aalten, D. M. F. & Fang, W. (2025). Gfa1 (glutamine fructose-6-phosphate aminotransferase) is essential for Aspergillus fumigatus growth and virulence. BMC Biology, 23(1), Artikel 80. https://doi.org/10.1186/s12915-025-02184-0
Pumo, G. M., Kitazawa, T. & Rijli, F. M. (2022). Epigenetic and Transcriptional Regulation of Spontaneous and Sensory Activity Dependent Programs During Neuronal Circuit Development. Frontiers in Neural Circuits, 16, 21. Artikel 911023. https://doi.org/10.3389/fncir.2022.911023
Pravata, V. M., Jiang, H., Ferenbach, A. T., Lamond, A. & van Aalten, D. M. F. (2025). Zscan4 as a Candidate Conveyor of Early Developmental Defects in O-GlcNAc Transferase Intellectual Disability. Molecular & Cellular Proteomics : MCP, 24(11), Artikel 101077. https://doi.org/10.1016/j.mcpro.2025.101077
Poulsen, H., Khandelia, H., Morth, J. P., Bublitz, M., Mouritsen, O. G., Jensen, J. E. & Nissen, P. (2010). Neurological disease mutations compromise a C-terminal ion pathway in the Na(+)/K(+)-ATPas. Nature, 464, 99-102.
Poulsen, H., Morth, J. P., Jensen, J. E. & Nissen, P. (2010). Phosphorylation of the Na+,K+-ATPase and the H+,K+-ATPase. FEBS Letters, 584(12), 2589-2595.

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Revideret 13.11.2025
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Helene Eriksen