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Research Article
The muscle dystrophy-causing ΔK32 lamin A/C mutant does not impair the functions of the nucleoplasmic lamin-A/C–LAP2α complex in mice
Ursula Pilat, Thomas Dechat, Anne T. Bertrand, Nikola Woisetschläger, Ivana Gotic, Rita Spilka, Katarzyna Biadasiewicz, Gisèle Bonne, Roland Foisner
Journal of Cell Science 2013 126: 1753-1762; doi: 10.1242/jcs.115246
Ursula Pilat
1Max F. Perutz Laboratories, Department of Medical Biochemistry, Medical University of Vienna, Dr. Bohr-Gasse 9, A-1030 Vienna, Austria
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Thomas Dechat
1Max F. Perutz Laboratories, Department of Medical Biochemistry, Medical University of Vienna, Dr. Bohr-Gasse 9, A-1030 Vienna, Austria
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Anne T. Bertrand
2Inserm, UMRS_974, Paris F-75013, France
3Université Pierre et Marie Curie-Paris 6, UM76, CNRS, UMR7215, Institut de Myologie, IFR14, Paris F-75013, France
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Nikola Woisetschläger
1Max F. Perutz Laboratories, Department of Medical Biochemistry, Medical University of Vienna, Dr. Bohr-Gasse 9, A-1030 Vienna, Austria
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Ivana Gotic
1Max F. Perutz Laboratories, Department of Medical Biochemistry, Medical University of Vienna, Dr. Bohr-Gasse 9, A-1030 Vienna, Austria
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Rita Spilka
1Max F. Perutz Laboratories, Department of Medical Biochemistry, Medical University of Vienna, Dr. Bohr-Gasse 9, A-1030 Vienna, Austria
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Katarzyna Biadasiewicz
1Max F. Perutz Laboratories, Department of Medical Biochemistry, Medical University of Vienna, Dr. Bohr-Gasse 9, A-1030 Vienna, Austria
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Gisèle Bonne
2Inserm, UMRS_974, Paris F-75013, France
3Université Pierre et Marie Curie-Paris 6, UM76, CNRS, UMR7215, Institut de Myologie, IFR14, Paris F-75013, France
4AP-HP, Groupe Hospitalier Pitié-Salpêtrière, U.F. Cardiogénétique et Myogénétique, Service de Biochimie Métabolique, Paris F-75013, France
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Roland Foisner
1Max F. Perutz Laboratories, Department of Medical Biochemistry, Medical University of Vienna, Dr. Bohr-Gasse 9, A-1030 Vienna, Austria
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  • For correspondence: roland.foisner@meduniwien.ac.at
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Article Information

vol. 126 no. 8, 1753-1762

DOI 
https://doi.org/10.1242/jcs.115246
PubMed 
23444379

Published By 
The Company of Biologists Ltd
Print ISSN 
0021-9533
Online ISSN 
1477-9137
History 
  • Accepted January 26, 2013
  • Published online May 12, 2013.
Posted online 
February 26, 2013
Copyright & Usage 
© 2013. Published by The Company of Biologists Ltd

Article Versions

  • Previous version (February 26, 2013 - 10:24).
  • You are viewing the most recent version of this article.

Author Information

  1. Ursula Pilat1,
  2. Thomas Dechat1,
  3. Anne T. Bertrand2,3,
  4. Nikola Woisetschläger1,
  5. Ivana Gotic1,
  6. Rita Spilka1,
  7. Katarzyna Biadasiewicz1,
  8. Gisèle Bonne2,3,4 and
  9. Roland Foisner1,*
  1. 1Max F. Perutz Laboratories, Department of Medical Biochemistry, Medical University of Vienna, Dr. Bohr-Gasse 9, A-1030 Vienna, Austria
  2. 2Inserm, UMRS_974, Paris F-75013, France
  3. 3Université Pierre et Marie Curie-Paris 6, UM76, CNRS, UMR7215, Institut de Myologie, IFR14, Paris F-75013, France
  4. 4AP-HP, Groupe Hospitalier Pitié-Salpêtrière, U.F. Cardiogénétique et Myogénétique, Service de Biochimie Métabolique, Paris F-75013, France
  1. ↵*Author for correspondence (roland.foisner{at}meduniwien.ac.at)
View Abstract

Article usage

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Usage statistics: February 2013 to December 2020

AbstractFullPdf
Feb 2013115015
Mar 2013238065
Apr 201389030
May 20139492549
Jun 2013138813
Jul 2013411112
Aug 20135856
Sep 201331810
Oct 20132666
Nov 2013352313
Dec 201337218
Total 20131757107227
Jan 2014182310
Feb 201429129
Mar 201413134
Apr 201430135
May 201420167
Jun 2014191415
Jul 201413108
Aug 201413106
Sep 20142673
Oct 20141665
Nov 201410510
Dec 2014144316
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Jan 201532211
Feb 201516716
Mar 20151345
Apr 2015756
May 201512416
Jun 2015737
Jul 2015877
Aug 2015758
Sep 201514413
Oct 2015763
Nov 2015595
Dec 2015789
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Jan 2016101629
Feb 201641211
Mar 2016398
Apr 201661311
May 20165187
Jun 201641940
Jul 201642123
Aug 201612719
Sep 201661514
Oct 20168186
Nov 201651715
Dec 201661112
Total 201662196195
Jan 20172237
Feb 20174226
Mar 20171235
Apr 20170168
May 20174145
Jun 201711415
Jul 20172109
Aug 20170105
Sep 201731111
Oct 20171184
Nov 20171208
Dec 201752715
Total 20172420898
Jan 20185174
Feb 201823710
Mar 201832915
Apr 20183236
May 20181334
Jun 20184297
Jul 201851911
Aug 20180128
Sep 20180269
Oct 20186188
Nov 20180173
Dec 20180163
Total 20182927688
Jan 20194156
Feb 201922320
Mar 20190279
Apr 201931916
May 20192219
Jun 201921315
Jul 20190127
Aug 20193198
Sep 20190194
Oct 201912111
Nov 2019199
Dec 20191114
Total 201919209118
Jan 202041910
Feb 202021919
Mar 202001710
Apr 2020186
May 2020397
Jun 20202113
Jul 202001710
Aug 202071210
Sep 20203248
Oct 2020387
Nov 202011514
Dec 20203138
Total 202029172112
Total224714241042

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Keywords

  • Congenital muscular dystrophy
  • Nuclear envelope
  • Lamin A/C
  • Lamina associated polypeptide 2α
  • Nucleoplasmic lamins

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Research Article
The muscle dystrophy-causing ΔK32 lamin A/C mutant does not impair the functions of the nucleoplasmic lamin-A/C–LAP2α complex in mice
Ursula Pilat, Thomas Dechat, Anne T. Bertrand, Nikola Woisetschläger, Ivana Gotic, Rita Spilka, Katarzyna Biadasiewicz, Gisèle Bonne, Roland Foisner
Journal of Cell Science 2013 126: 1753-1762; doi: 10.1242/jcs.115246
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Research Article
The muscle dystrophy-causing ΔK32 lamin A/C mutant does not impair the functions of the nucleoplasmic lamin-A/C–LAP2α complex in mice
Ursula Pilat, Thomas Dechat, Anne T. Bertrand, Nikola Woisetschläger, Ivana Gotic, Rita Spilka, Katarzyna Biadasiewicz, Gisèle Bonne, Roland Foisner
Journal of Cell Science 2013 126: 1753-1762; doi: 10.1242/jcs.115246

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