Research Article

Open Access
Concomitant gain and loss of function pathomechanisms in C9ORF72 amyotrophic lateral sclerosis
Arun Pal, Benedikt Kretner, Masin Abo-Rady, Hannes Glaβ, View ORCID ProfileBanaja P Dash, Marcel Naumann, Julia Japtok, Nicole Kreiter, Ashutosh Dhingra, Peter Heutink, Tobias M Böckers, René Günther, View ORCID ProfileJared Sterneckert, View ORCID ProfileAndreas Hermann Correspondence email
Arun Pal
1Division of Neurodegenerative Diseases, Department of Neurology, Technische Universität Dresden, Dresden, Germany
Benedikt Kretner
1Division of Neurodegenerative Diseases, Department of Neurology, Technische Universität Dresden, Dresden, Germany
2Center for Regenerative Therapies TU Dresden (CRTD), Technische Universität Dresden, Dresden, Germany
Masin Abo-Rady
2Center for Regenerative Therapies TU Dresden (CRTD), Technische Universität Dresden, Dresden, Germany
Hannes Glaβ
3Translational Neurodegeneration Section “Albrecht-Kossel,” Department of Neurology, and Center for Transdisciplinary Neuroscience (CTNR), University Medical Center Rostock, University of Rostock, Rostock, Germany
Banaja P Dash
3Translational Neurodegeneration Section “Albrecht-Kossel,” Department of Neurology, and Center for Transdisciplinary Neuroscience (CTNR), University Medical Center Rostock, University of Rostock, Rostock, Germany
Marcel Naumann
3Translational Neurodegeneration Section “Albrecht-Kossel,” Department of Neurology, and Center for Transdisciplinary Neuroscience (CTNR), University Medical Center Rostock, University of Rostock, Rostock, Germany
Julia Japtok
1Division of Neurodegenerative Diseases, Department of Neurology, Technische Universität Dresden, Dresden, Germany
Nicole Kreiter
1Division of Neurodegenerative Diseases, Department of Neurology, Technische Universität Dresden, Dresden, Germany
Ashutosh Dhingra
6German Center for Neurodegenerative Diseases (DZNE), Genome Biology of Neurodegenerative Diseases, Tübingen, Germany
Peter Heutink
6German Center for Neurodegenerative Diseases (DZNE), Genome Biology of Neurodegenerative Diseases, Tübingen, Germany
7Department for Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany
Tobias M Böckers
5Institute for Anatomy and Cell Biology, Ulm University, Ulm, Germany
René Günther
1Division of Neurodegenerative Diseases, Department of Neurology, Technische Universität Dresden, Dresden, Germany
8German Center for Neurodegenerative Diseases (DZNE) Dresden, Dresden, Germany
Jared Sterneckert
2Center for Regenerative Therapies TU Dresden (CRTD), Technische Universität Dresden, Dresden, Germany
Andreas Hermann
3Translational Neurodegeneration Section “Albrecht-Kossel,” Department of Neurology, and Center for Transdisciplinary Neuroscience (CTNR), University Medical Center Rostock, University of Rostock, Rostock, Germany
4German Center for Neurodegenerative Diseases (DZNE) Rostock/Greifswald, Rostock, Germany
Published 22 February 2021. DOI: 10.26508/lsa.202000764
Distinct axonopathy in C9ORF72 ALS
Arun Pal, Benedikt Kretner, Masin Abo-Rady, Hannes Glaβ, Banaja P Dash, Marcel Naumann, Julia Japtok, Nicole Kreiter, Ashutosh Dhingra, Peter Heutink, Tobias M Böckers, René Günther, Jared Sterneckert, Andreas Hermann
Life Science Alliance Feb 2021, 4 (4) e202000764; DOI: 10.26508/lsa.202000764
Distinct axonopathy in C9ORF72 ALS
Arun Pal, Benedikt Kretner, Masin Abo-Rady, Hannes Glaβ, Banaja P Dash, Marcel Naumann, Julia Japtok, Nicole Kreiter, Ashutosh Dhingra, Peter Heutink, Tobias M Böckers, René Günther, Jared Sterneckert, Andreas Hermann
Life Science Alliance Feb 2021, 4 (4) e202000764; DOI: 10.26508/lsa.202000764
In this Issue
Volume 4, No. 4
April 2021
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