Comprehensive analysis to explain reduced or increased SOD1 enzymatic activity in ALS patients and their relatives-Reference-Cited by-同舟云学术

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Comprehensive analysis to explain reduced or increased SOD1 enzymatic activity in ALS patients and their relatives

Published:2017-03-21 Issue:5-6 Volume:18 Page:457-463
ISSN:2167-8421
Container-title:Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
language:en
Short-container-title:Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration

Author:

Keskin Isil¹,Birve Anna¹,Berdynski Mariusz¹²,Hjertkvist Karin³,Rofougaran Reza¹,Nilsson Torbjörn K.³,Glass Jonathan D.⁴,Marklund Stefan L.³,Andersen Peter M.¹

Affiliation:

1. Department of Pharmacology and Clinical Neurosciences, Umeå University, Umeå, Sweden,

2. Department of Neurodegenerative Disorders, Mossakowski Medical Research Centre, Polish Academy of Sciences, Warsaw, Poland,

3. Department of Medical Biosciences, Clinical Chemistry, Umeå University, Umeå, Sweden, and

4. Department of Neurology, Emory University School of Medicine, Atlanta, GA, USA

Funder

Swedish Research Council

Knut and Alice Wallenberg Foundation

Bertil Hållsten Foundation

Torsten and Ragnar Söderberg Foundation

Swedish Brain Fund

Stratneuro Initiative, Västerbotten County Council

Kempe Foundations

Publisher

Informa UK Limited

Subject

Neurology (clinical),Neurology

Link

https://www.tandfonline.com/doi/pdf/10.1080/21678421.2017.1301481

Reference30 articles.

1. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

2. Clinical genetics of amyotrophic lateral sclerosis: what do we really know?

3. Minute quantities of misfolded mutant superoxide dismutase‐1 cause amyotrophic lateral sclerosis

4. Disulphide-reduced superoxide dismutase-1 in CNS of transgenic amyotrophic lateral sclerosis models

5. Identification of three novel mutations in the gene for CuZn superoxide dismutase in patients with familial amyotrophic lateral sclerosis

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1. SOD1 Enzymatic Activity in CSF from ALS patients with and withoutSOD1mutations;2024-06-16

2. Molecular dynamics analysis of superoxide dismutase 1 mutations suggests decoupling between mechanisms underlying ALS onset and progression;Computational and Structural Biotechnology Journal;2023

3. The motor system is exceptionally vulnerable to absence of the ubiquitously expressed superoxide dismutase-1;Brain Communications;2022-12-29

4. Molecular dynamics analysis of Superoxide Dismutase 1 mutations suggests decoupling between mechanisms underlying ALS onset and progression;2022-12-05

5. Alteration of Mitochondrial Integrity as Upstream Event in the Pathophysiology of SOD1-ALS;Cells;2022-04-06

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