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  1. 1
    Functional consequences of alterations to Glu309, Glu771, and Asp800 in the Ca(2+)-ATPase of sarcoplasmic reticulum.

    Functional consequences of alterations to Glu309, Glu771, and Asp800 in the Ca(2+)-ATPase of sarcoplasmic reticulum. por Jens Peter Andersen, Bente Vilsen

    Publicado em 1992
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  2. 2
    Structure‐function relationships of cation translocation by Ca<sup>2+</sup>‐ and Na<sup>+</sup>,K<sup>+</sup>‐ATPases studied by site‐directed mutagenesis

    Structure‐function relationships of cation translocation by Ca<sup>2+</sup>‐ and Na<sup>+</sup>,K<sup>+</sup>‐ATPases studied by site‐directed mutagenesis por Jens Peter Anderssen, Bente Vilsen

    Publicado em 1995
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  3. 3
    Mutations Phe785Leu and Thr618Met in Na+,K+-ATPase, Associated with Familial Rapid-onset Dystonia Parkinsonism, Interfere with Na+ Interaction by Distinct Mechanisms

    Mutations Phe785Leu and Thr618Met in Na+,K+-ATPase, Associated with Familial Rapid-onset Dystonia Parkinsonism, Interfere with Na+ Interaction by Distinct Mechanisms por Vivien Rodacker, Mads S. Toustrup-Jensen, Bente Vilsen

    Publicado em 2006
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  4. 4
    Functional consequences of alterations to amino acids located in the hinge domain of the Ca(2+)-ATPase of sarcoplasmic reticulum

    Functional consequences of alterations to amino acids located in the hinge domain of the Ca(2+)-ATPase of sarcoplasmic reticulum por Bente Vilsen, Jens Peter Andersen, David H. MacLennan

    Publicado em 1991
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  5. 5
    Occlusion of 22Na+ and 86Rb+ in membrane-bound and soluble protomeric alpha beta-units of Na,K-ATPase.

    Occlusion of 22Na+ and 86Rb+ in membrane-bound and soluble protomeric alpha beta-units of Na,K-ATPase. por Bente Vilsen, Jens Peter Andersen, Jan Raagaard Petersen, Peter Leth Jørgensen

    Publicado em 1987
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  6. 6
    Functional Consequences of Mutations in the β-Strand Sector of the Ca2+-ATPase of Sarcoplasmic Reticulum

    Functional Consequences of Mutations in the β-Strand Sector of the Ca2+-ATPase of Sarcoplasmic Reticulum por Jens Peter Andersen, Bente Vilsen, Ekkehard Leberer, David H. MacLennan

    Publicado em 1989
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  7. 7
    Functional Consequences of Proline Mutations in the Cytoplasmic and Transmembrane Sectors of the Ca2+-ATPase of Sarcoplasmic Reticulum

    Functional Consequences of Proline Mutations in the Cytoplasmic and Transmembrane Sectors of the Ca2+-ATPase of Sarcoplasmic Reticulum por Bente Vilsen, Jens Peter Andersen, David M. Clarke, David H. MacLennan

    Publicado em 1989
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  8. 8
    Binding of cardiotonic steroids to Na <sup>+</sup> ,K <sup>+</sup> -ATPase in the E2P state

    Binding of cardiotonic steroids to Na <sup>+</sup> ,K <sup>+</sup> -ATPase in the E2P state por R. Kanai, Flemming Cornelius, Haruo Ogawa, K. Motoyama, Bente Vilsen, Chikashi Toyoshima

    Publicado em 2020
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  9. 9
    The Rapid-onset Dystonia Parkinsonism Mutation D923N of the Na+,K+-ATPase α3 Isoform Disrupts Na+ Interaction at the Third Na+ Site

    The Rapid-onset Dystonia Parkinsonism Mutation D923N of the Na+,K+-ATPase α3 Isoform Disrupts Na+ Interaction at the Third Na+ Site por Anja P. Einholm, Mads S. Toustrup-Jensen, Rikke Holm, Jens Peter Andersen, Bente Vilsen

    Publicado em 2010
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  10. 10
    Critical role of a transmembrane lysine in aminophospholipid transport by mammalian photoreceptor P <sub>4</sub> -ATPase ATP8A2

    Critical role of a transmembrane lysine in aminophospholipid transport by mammalian photoreceptor P <sub>4</sub> -ATPase ATP8A2 por Jonathan A. Coleman, Anna L. Vestergaard, Robert S. Molday, Bente Vilsen, Jens Peter Andersen

    Publicado em 2012
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  11. 11
    Dissection of the Functional Differences between Sarco(endo)plasmic Reticulum Ca2+-ATPase (SERCA) 1 and 2 Isoforms and Characterization of Darier Disease (SERCA2) Mutants by Steady-state and Transient Kinetic Analyses

    Dissection of the Functional Differences between Sarco(endo)plasmic Reticulum Ca2+-ATPase (SERCA) 1 and 2 Isoforms and Characterization of Darier Disease (SERCA2) Mutants by Steady... por Leonard Dode, Jens Peter Andersen, Natalie Leslie, Jittima Dhitavat, Bente Vilsen, Alain Hovnanian

    Publicado em 2003
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  12. 12
    Dissection of the Functional Differences between Sarco(endo)plasmic Reticulum Ca2+-ATPase (SERCA) 1 and 3 Isoforms by Steady-state and Transient Kinetic Analyses

    Dissection of the Functional Differences between Sarco(endo)plasmic Reticulum Ca2+-ATPase (SERCA) 1 and 3 Isoforms by Steady-state and Transient Kinetic Analyses por Leonard Dode, Bente Vilsen, Kurt Van Baelen, Frank Wuytack, Johannes D. Clausen, Jens Peter Andersen

    Publicado em 2002
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  13. 13
    The structure of the Na<sup>+</sup>,K<sup>+</sup>-ATPase and mapping of isoform differences and disease-related mutations

    The structure of the Na<sup>+</sup>,K<sup>+</sup>-ATPase and mapping of isoform differences and disease-related mutations por Jens Preben Morth, Hanne Poulsen, Mads S. Toustrup-Jensen, Vivien R. Schack, Jan Egebjerg, Jens Peter Andersen, Bente Vilsen, Poul Nissen

    Publicado em 2008
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  14. 14
    Critical roles of isoleucine-364 and adjacent residues in a hydrophobic gate control of phospholipid transport by the mammalian P4-ATPase ATP8A2

    Critical roles of isoleucine-364 and adjacent residues in a hydrophobic gate control of phospholipid transport by the mammalian P4-ATPase ATP8A2 por Anna L. Vestergaard, Jonathan A. Coleman, Thomas Lemmin, Stine A. Mikkelsen, Laurie L. Molday, Bente Vilsen, Robert S. Molday, Matteo Dal Peraro, Jens Peter Andersen

    Publicado em 2014
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  15. 15
    A C-terminal mutation of ATP1A3 underscores the crucial role of sodium affinity in the pathophysiology of rapid-onset dystonia-parkinsonism

    A C-terminal mutation of ATP1A3 underscores the crucial role of sodium affinity in the pathophysiology of rapid-onset dystonia-parkinsonism por Patricia Blanco, Anja P. Einholm, Hafsa Mamsa, C. Concheiro, Hugo Gutiérrez‐de‐Terán, J. Romero, Mads S. Toustrup-Jensen, Ángel Carracedo, Joanna C. Jen, Bente Vilsen, M.J. Sobrido

    Publicado em 2009
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  16. 16
    Mania-like behavior induced by genetic dysfunction of the neuron-specific Na <sup>+</sup> ,K <sup>+</sup> -ATPase α3 sodium pump

    Mania-like behavior induced by genetic dysfunction of the neuron-specific Na <sup>+</sup> ,K <sup>+</sup> -ATPase α3 sodium pump por Greer S. Kirshenbaum, Steven J. Clapcote, Steven Duffy, Christian R. Burgess, Janne Petersen, Karolina J. Jarowek, Yeni H. Yücel, Miguel A. Cortez, O. Carter Snead, Bente Vilsen, John Peever, Martin R. Ralph, John Roder

    Publicado em 2011
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  17. 17
    P-type ATPases as drug targets: Tools for medicine and science

    P-type ATPases as drug targets: Tools for medicine and science por Laure Yatime, Morten J. Buch-Pedersen, Maria Musgaard, Jens Preben Morth, Anne-Marie Lund Winther, Bjørn Panyella Pedersen, Claus Olesen, Jens Peter Andersen, Bente Vilsen, Birgit Schiøtt, Michael Palmgren, Jesper V. Møller, Poul Nissen, Natalya U. Fedosova

    Publicado em 2009
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  18. 18
    Distinct neurological disorders with ATP1A3 mutations

    Distinct neurological disorders with ATP1A3 mutations por Erin L. Heinzen, Alexis Arzimanoglou, Allison Brashear, Steven J. Clapcote, Fiorella Gurrieri, David B. Goldstein, Sigurður H Jóhannesson, Mohamad A. Mikati, Brian Neville, Sophie Nicole, Laurie J. Ozelius, Hanne Poulsen, Tsveta Schyns, Kathleen J. Sweadner, Arn van den Maagdenberg, Bente Vilsen

    Publicado em 2014
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  19. 19
    Somatic <i>ATP1A1</i> , <i>ATP2B3</i> , and <i>KCNJ5</i> Mutations in Aldosterone-Producing Adenomas

    Somatic <i>ATP1A1</i> , <i>ATP2B3</i> , and <i>KCNJ5</i> Mutations in Aldosterone-Producing Adenomas por Tracy Ann Williams, Silvia Monticone, Vivien R. Schack, Julia Stindl, Jacopo Burrello, Fabrizio Buffolo, Laura Annaratone, Isabella Castellano, Felix Beuschlein, Martín Reincke, Barbara Lucatello, Vanessa Ronconi, Francesco Fallo, Giampaolo Bernini, Mauro Maccario, Gilberta Giacchetti, Franco Veglio, Richard Warth, Bente Vilsen, Paolo Mulatero

    Publicado em 2013
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  20. 20
    Mutation I810N in the α3 isoform of Na <sup>+</sup> ,K <sup>+</sup> -ATPase causes impairments in the sodium pump and hyperexcitability in the CNS

    Mutation I810N in the α3 isoform of Na <sup>+</sup> ,K <sup>+</sup> -ATPase causes impairments in the sodium pump and hyperexcitability in the CNS por Steven J. Clapcote, Steven Duffy, Gang Xie, Greer S. Kirshenbaum, Allison R. Bechard, Vivien R. Schack, Janne Petersen, Laleh Sinai, Bechara J. Saab, Jason P. Lerch, Berge A. Minassian, Cameron Ackerley, John G. Sled, Miguel A. Cortez, Jeffrey T. Henderson, Bente Vilsen, John Roder

    Publicado em 2009
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