Mutant induced pluripotent stem cell lines recapitulate aspects of TDP-43 proteinopathies and reveal cell-specific vulnerability-Reference-Cited by-同舟云学术

Mutant induced pluripotent stem cell lines recapitulate aspects of TDP-43 proteinopathies and reveal cell-specific vulnerability

Published:2012-03-26 Issue:15 Volume:109 Page:5803-5808
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Bilican B.,Serio A.,Barmada S. J.,Nishimura A. L.,Sullivan G. J.,Carrasco M.,Phatnani H. P.,Puddifoot C. A.,Story D.,Fletcher J.,Park I.-H.,Friedman B. A.,Daley G. Q.,Wyllie D. J. A.,Hardingham G. E.,Wilmut I.,Finkbeiner S.,Maniatis T.,Shaw C. E.,Chandran S.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference51 articles.

1. Ubiquitinated TDP-43 in Frontotemporal Lobar Degeneration and Amyotrophic Lateral Sclerosis

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3. TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

4. Concomitant TAR-DNA-Binding Protein 43 Pathology Is Present in Alzheimer Disease and Corticobasal Degeneration but Not in Other Tauopathies

5. TDP-43mutation in familial amyotrophic lateral sclerosis

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