An <i>in situ</i> and <i>in vitro</i> investigation of cytoplasmic TDP-43 inclusions reveals the absence of a clear amyloid signature-Reference-Cited by-同舟云学术

An in situ and in vitro investigation of cytoplasmic TDP-43 inclusions reveals the absence of a clear amyloid signature

Published:2022-12-10 Issue:1 Volume:55 Page:72-88
ISSN:0785-3890
Container-title:Annals of Medicine
language:en
Short-container-title:Annals of Medicine

Author:

Cascella Roberta¹^ORCID,Banchelli Martina²^ORCID,Abolghasem Ghadami Seyyed³^ORCID,Ami Diletta⁴⁵^ORCID,Gagliani Maria Cristina⁶^ORCID,Bigi Alessandra¹^ORCID,Staderini Tommaso¹^ORCID,Tampellini Davide⁷⁸^ORCID,Cortese Katia⁶^ORCID,Cecchi Cristina¹^ORCID,Natalello Antonino⁴⁵^ORCID,Adibi Hadi⁹^ORCID,Matteini Paolo²^ORCID,Chiti Fabrizio¹^ORCID

Affiliation:

1. Department of Experimental and Clinical Biomedical Sciences “Mario Serio”, University of Florence, Florence, Italy

2. Institute of Applied Physics “Nello Carrara”, National Research Council, Sesto Fiorentino, Italy

3. Department of Biotechnology, Faculty of Biological Sciences, Alzahra University, Tehran, Iran

4. Department of Biotechnologies and Biosciences, University of Milano-Bicocca, Milan, Italy

5. Milan Center of Neuroscience (NeuroMI), Milan, Italy

6. Cellular Electron Microscopy Laboratory, Department of Experimental Medicine, University of Genova, Genoa, Italy

7. U 1195 INSERM-Université Paris-Saclay, Paris, France

8. Institut Professeur Baulieu, Paris, France

9. Pharmaceutical Sciences Research Center, Health Institute, Kermanshah University of Medical Sciences, Kermanshah, Iran

Funder

Fondazione Italiana di Ricerca per la Sclerosi Laterale Amiotrofica

Università di Firenze-Fondazione Cassa di Risparmio di Firenze

University of Florence

University of Genoa

Hitachi

Grant Heavy Equipment

Publisher

Informa UK Limited

Subject

General Medicine

Link

https://www.tandfonline.com/doi/pdf/10.1080/07853890.2022.2148734

Reference87 articles.

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

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

3. Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis withSOD1 mutations

4. TDP-43 immunoreactivity in neuronal inclusions in familial amyotrophic lateral sclerosis with or without SOD1 gene mutation

5. Stages of pTDP-43 pathology in amyotrophic lateral sclerosis

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