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  • 1. Eriksson, Johan
    et al.
    Vogel, Edward K.
    Lansner, Anders
    Stockholm University, Faculty of Science, Numerical Analysis and Computer Science (NADA). KTH Royal Institute of Technology, Sweden.
    Bergström, Fredrik
    Nyberg, Lars
    Neurocognitive Architecture of Working Memory2015In: Neuron, ISSN 0896-6273, E-ISSN 1097-4199, Vol. 88, no 1, p. 33-46Article, review/survey (Refereed)
    Abstract [en]

    A crucial role for working memory in temporary information processing and guidance of complex behavior has been recognized for many decades. There is emerging consensus that working-memory maintenance results from the interactions among long-term memory representations and basic processes, including attention, that are instantiated as reentrant loops between frontal and posterior cortical areas, as well as sub-cortical structures. The nature of such interactions can account for capacity limitations, lifespan changes, and restricted transfer after working-memory training. Recent data and models indicate that working memory may also be based on synaptic plasticity and that working memory can operate on non-consciously perceived information.

  • 2. Gharpure, Anant
    et al.
    Teng, Jinfeng
    Zhuang, Yuxuan
    Stockholm University, Faculty of Science, Department of Biochemistry and Biophysics. Stockholm University, Science for Life Laboratory (SciLifeLab).
    Noviello, Colleen M.
    Walsh, Richard M.
    Cabuco, Rico
    Howard, Rebecca J.
    Stockholm University, Faculty of Science, Department of Biochemistry and Biophysics. Stockholm University, Science for Life Laboratory (SciLifeLab).
    Zaveri, Nurulain T.
    Lindahl, Erik
    Stockholm University, Faculty of Science, Department of Biochemistry and Biophysics. Stockholm University, Science for Life Laboratory (SciLifeLab). KTH Royal Institute of Technology, Sweden.
    Hibbs, Ryan E.
    Agonist Selectivity and Ion Permeation in the alpha 3 beta 4 Ganglionic Nicotinic Receptor2019In: Neuron, ISSN 0896-6273, E-ISSN 1097-4199, Vol. 104, no 3, p. 501-511Article in journal (Refereed)
    Abstract [en]

    Nicotinic acetylcholine receptors are pentameric ion channels that mediate fast chemical neurotransmission. The alpha 3 beta 4 nicotinic receptor subtype forms the principal relay between the central and peripheral nervous systems in the autonomic ganglia. This receptor is also expressed focally in brain areas that affect reward circuits and addiction. Here, we present structures of the alpha 3 beta 4 nicotinic receptor in lipidic and detergent environments, using functional reconstitution to define lipids appropriate for structural analysis. The structures of the receptor in complex with nicotine, as well as the alpha 3 beta 4-selective ligand AT-1001, complemented by molecular dynamics, suggest principles of agonist selectivity. The structures further reveal much of the architecture of the intracellular domain, where mutagenesis experiments and simulations define residues governing ion conductance.

  • 3. Milham, Michael P.
    et al.
    Ai, Lei
    Koo, Bonhwang
    Xu, Ting
    Amiez, Celine
    Balezeau, Fabien
    Baxter, Mark G.
    Blezer, Erwin L. A.
    Brochier, Thomas
    Chen, Aihua
    Croxson, Paula L.
    Damatac, Christienne G.
    Dehaene, Stanislas
    Everling, Stefan
    Fair, Damian A.
    Fleysher, Lazar
    Freiwald, Winrich
    Froudist-Walsh, Sean
    Griffiths, Timothy D.
    Guedj, Carole
    Hadj-Bouziane, Fadila
    Ben Hamed, Suliann
    Harel, Noam
    Hiba, Bassem
    Jarraya, Bechir
    Jung, Benjamin
    Kastner, Sabine
    Klink, P. Christiaan
    Kwok, Sze Chai
    Laland, Kevin N.
    Leopold, David A.
    Lindenfors, Patrik
    Stockholm University, Faculty of Humanities, Department of Archaeology and Classical Studies, Centre for Cultural Evolution. Stockholm University, Faculty of Science, Department of Zoology. Institute for Future Studies, Sweden.
    Mars, Rogier B.
    Menon, Ravi S.
    Messinger, Adam
    Meunier, Martine
    Mok, Kelvin
    Morrison, John H.
    Nacef, Jennifer
    Nagy, Jamie
    Ortiz Rios, Michael
    Petkov, Christopher
    Pinsk, Mark
    Poirier, Colline
    Procyk, Emmanuel
    Rajimehr, Reza
    Reader, Simon M.
    Roelfsema, Pieter R.
    Rudko, David A.
    Rushworth, Matthew F. S.
    Russ, Brian E.
    Sallet, Jerome
    Schmid, Michael Christoph
    Schwiedrzik, Caspar M.
    Seidlitz, Jakob
    Sein, Julien
    Shmuel, Amir
    Sullivan, Elinor L.
    Ungerleider, Leslie
    Thiele, Alexander
    Todorov, Orlin S.
    Tsao, Doris
    Wang, Zheng
    Wilson, Charles R. E.
    Yacoub, Essa
    Ye, Frank Q.
    Zarco, Wilbert
    Zhou, Yong-di
    Margulies, Daniel S.
    Schroeder, Charles E.
    An Open Resource for Non-human Primate Imaging2018In: Neuron, ISSN 0896-6273, E-ISSN 1097-4199, Vol. 100, no 1, p. 61-74Article in journal (Refereed)
    Abstract [en]

    Non-human primate neuroimaging is a rapidly growing area of research that promises to transform and scale translational and cross-species comparative neuroscience. Unfortunately, the technological and methodological advances of the past two decades have outpaced the accrual of data, which is particularly challenging given the relatively few centers that have the necessary facilities and capabilities. The PRIMatE Data Exchange (PRIME-DE) addresses this challenge by aggregating independently acquired non-human primate magnetic resonance imaging (MRI) datasets and openly sharing them via the International Neuroimaging Data-sharing Initiative (INDI). Here, we present the rationale, design, and procedures for the PRIME-DE consortium, as well as the initial release, consisting of 25 independent data collections aggregated across 22 sites (total = 217 non-human primates). We also outline the unique pitfalls and challenges that should be considered in the analysis of non-human primate MRI datasets, including providing automated quality assessment of the contributed datasets.

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