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Neuron-specific inactivation of Wt1 alters locomotion in mice and changes interneuron composition in the spinal cord

Danny Schnerwitzki, Sharn Perry, Anna Ivanova, View ORCID ProfileFabio V Caixeta, Paul Cramer, View ORCID ProfileSven Günther, View ORCID ProfileKathrin Weber, Atieh Tafreshiha, View ORCID ProfileLore Becker, Ingrid L Vargas Panesso, Thomas Klopstock, Martin Hrabe de Angelis, Manuela Schmidt, Klas Kullander, View ORCID ProfileChristoph Englert  Correspondence email
Danny Schnerwitzki
1Molecular Genetics Lab, Leibniz Institute on Aging—Fritz Lipmann Institute, Jena, Germany
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Sharn Perry
2Department of Neuroscience, Uppsala University, Uppsala, Sweden
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Anna Ivanova
1Molecular Genetics Lab, Leibniz Institute on Aging—Fritz Lipmann Institute, Jena, Germany
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Fabio V Caixeta
2Department of Neuroscience, Uppsala University, Uppsala, Sweden
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  • ORCID record for Fabio V Caixeta
Paul Cramer
1Molecular Genetics Lab, Leibniz Institute on Aging—Fritz Lipmann Institute, Jena, Germany
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Sven Günther
1Molecular Genetics Lab, Leibniz Institute on Aging—Fritz Lipmann Institute, Jena, Germany
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  • ORCID record for Sven Günther
Kathrin Weber
1Molecular Genetics Lab, Leibniz Institute on Aging—Fritz Lipmann Institute, Jena, Germany
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  • ORCID record for Kathrin Weber
Atieh Tafreshiha
2Department of Neuroscience, Uppsala University, Uppsala, Sweden
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Lore Becker
3German Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany
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  • ORCID record for Lore Becker
Ingrid L Vargas Panesso
3German Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany
6Department of Neurology, Friedrich-Baur-Institut, Ludwig Maximilian University Munich, Munich, Germany
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Thomas Klopstock
6Department of Neurology, Friedrich-Baur-Institut, Ludwig Maximilian University Munich, Munich, Germany
7German Center for Neurodegenerative Diseases, Munich, Germany
8Munich Cluster for Systems Neurology, Adolf-Butenandt-Institut, Ludwig Maximilian University Munich, Munich, Germany
9German Center for Vertigo and Balance Disorders, University Hospital Munich, Campus Grosshadern, Munich, Germany
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Martin Hrabe de Angelis
3German Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, German Research Center for Environmental Health, Neuherberg, Germany
10Chair of Experimental Genetics, School of Life Science Weihenstephan, Technical University of Munich, Freising, Germany
11German Center for Diabetes Research, Neuherberg, Germany
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Manuela Schmidt
4Institute of Systematic Zoology and Evolutionary Biology with Phyletic Museum, Friedrich Schiller University Jena, Jena, Germany
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Klas Kullander
2Department of Neuroscience, Uppsala University, Uppsala, Sweden
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Christoph Englert
1Molecular Genetics Lab, Leibniz Institute on Aging—Fritz Lipmann Institute, Jena, Germany
5Institute of Biochemistry and Biophysics, Friedrich-Schiller-University Jena, Jena, Germany
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  • ORCID record for Christoph Englert
  • For correspondence: Christoph.englert@leibniz-fli.de
Published 16 August 2018. DOI: 10.26508/lsa.201800106
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Neuron-specific inactivation of Wt1 alters locomotion in mice and changes interneuron composition in the spinal cord
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Wt1 inactivation alters dl6 neurons and locomotion
Danny Schnerwitzki, Sharn Perry, Anna Ivanova, Fabio V Caixeta, Paul Cramer, Sven Günther, Kathrin Weber, Atieh Tafreshiha, Lore Becker, Ingrid L Vargas Panesso, Thomas Klopstock, Martin Hrabe de Angelis, Manuela Schmidt, Klas Kullander, Christoph Englert
Life Science Alliance Aug 2018, 1 (4) e201800106; DOI: 10.26508/lsa.201800106

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Wt1 inactivation alters dl6 neurons and locomotion
Danny Schnerwitzki, Sharn Perry, Anna Ivanova, Fabio V Caixeta, Paul Cramer, Sven Günther, Kathrin Weber, Atieh Tafreshiha, Lore Becker, Ingrid L Vargas Panesso, Thomas Klopstock, Martin Hrabe de Angelis, Manuela Schmidt, Klas Kullander, Christoph Englert
Life Science Alliance Aug 2018, 1 (4) e201800106; DOI: 10.26508/lsa.201800106
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Volume 1, No. 4
August 2018
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Cited By...

  • Cell-type-specific origins of locomotor rhythmicity at different speeds in larval zebrafish
  • Characterization of a novel Lbx1 mouse loss of function strain
  • Behavioral Characterization of dmrt3a Mutant Zebrafish Reveals Crucial Aspects of Vertebrate Locomotion through Phenotypes Related to Acceleration
  • Wt1 positive neurons in the hindbrain are essential for respiration
  • Characterization of Dmrt3-Derived Neurons Suggest a Role within Locomotor Circuits
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