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Research ArticleNew Research, Disorders of the Nervous System

Non-Cell-Autonomous Regulation of Retrograde Motoneuronal Axonal Transport in an SBMA Mouse Model

Katherine Halievski, Michael Q. Kemp, S. Marc Breedlove, Kyle E. Miller and Cynthia L. Jordan
eNeuro 21 July 2016, 3 (4) ENEURO.0062-16.2016; https://doi.org/10.1523/ENEURO.0062-16.2016
Katherine Halievski
1Neuroscience Program, Michigan State University, East Lansing, Michigan 48824-1115
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Michael Q. Kemp
1Neuroscience Program, Michigan State University, East Lansing, Michigan 48824-1115
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S. Marc Breedlove
1Neuroscience Program, Michigan State University, East Lansing, Michigan 48824-1115
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Kyle E. Miller
1Neuroscience Program, Michigan State University, East Lansing, Michigan 48824-1115
2Department of Integrative Biology, Michigan State University, East Lansing, Michigan 48824-1115
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Cynthia L. Jordan
1Neuroscience Program, Michigan State University, East Lansing, Michigan 48824-1115
3Department of Physiology, Michigan State University, East Lansing, Michigan 48824-1115
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Article Information

DOI 
https://doi.org/10.1523/ENEURO.0062-16.2016
PubMed 
27517091
Published By 
Society for Neuroscience
History 
  • Received March 15, 2016
  • Revision received June 23, 2016
  • Accepted July 14, 2016
  • Published online July 21, 2016.
Copyright & Usage 
Copyright © 2016 Halievski et al. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.

Author Information

  1. Katherine Halievski1,
  2. Michael Q. Kemp1,
  3. S. Marc Breedlove1,
  4. Kyle E. Miller1,2 and
  5. Cynthia L. Jordan1,3
  1. 1Neuroscience Program, Michigan State University, East Lansing, Michigan 48824-1115
  2. 2Department of Integrative Biology, Michigan State University, East Lansing, Michigan 48824-1115
  3. 3Department of Physiology, Michigan State University, East Lansing, Michigan 48824-1115
  1. Correspondence should be addressed to Cynthia L. Jordan, Neuroscience Program and Physiology Department, 108 Giltner Hall, Michigan State University, East Lansing, MI 48824. E-mail: jordancy{at}msu.edu.
View Full Text

Author contributions

  1. Author contributions: M.Q.K., S.M.B., K.E.M., and C.L.J. designed research; M.Q.K., S.M.B., K.E.M., and C.L.J. performed research; S.M.B., K.E.M., and C.L.J. contributed unpublished reagents/analytic tools; K.H., M.Q.K., S.M.B., K.E.M., and C.L.J. analyzed data; K.H., M.Q.K., S.M.B., K.E.M., and C.L.J. wrote the paper.

Disclosures

  • The authors declare no competing financial interests.

  • This research was supported National Institutes of Health (NIH) Grant NS045195 (to C.L.J.), a Ruth L. Kirchstein National Research Service Award 1F32AR055848-01 (to M.Q.K.), a Ruth L. Kirchstein National Institutional Research Service Award T32-MH-070343 (M.Q.K.), NIH Grant 1R01-MH-094607-01A1 (to K.E.M.), and National Science Foundation Grant IOS_0951019 (to K.E.M.).

Funding

  • National Institute of Health

    NS045195
  • Ruth L. Kirchstein National Research Service Award

    1F32AR055848-01
  • Ruth L. Kirchstein National Institutional Research Service Award

    T32-MH070343
  • NIH

    1R01MH094607-01A1
  • NSF

    IOS_0951019

Other Version

  • You are viewing the most recent version of this article.
  • previous version (July 21, 2016).
  • previous version (July 21, 2016).

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Non-Cell-Autonomous Regulation of Retrograde Motoneuronal Axonal Transport in an SBMA Mouse Model
Katherine Halievski, Michael Q. Kemp, S. Marc Breedlove, Kyle E. Miller, Cynthia L. Jordan
eNeuro 21 July 2016, 3 (4) ENEURO.0062-16.2016; DOI: 10.1523/ENEURO.0062-16.2016

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Non-Cell-Autonomous Regulation of Retrograde Motoneuronal Axonal Transport in an SBMA Mouse Model
Katherine Halievski, Michael Q. Kemp, S. Marc Breedlove, Kyle E. Miller, Cynthia L. Jordan
eNeuro 21 July 2016, 3 (4) ENEURO.0062-16.2016; DOI: 10.1523/ENEURO.0062-16.2016
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Keywords

  • androgen
  • Androgen Receptor
  • Kennedy’s disease
  • neuromuscular disease
  • skeletal muscle
  • testicular feminization mutation

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