Cargando…

The landscape of cognitive impairment in superoxide dismutase 1-amyotrophic lateral sclerosis

Although mutations in the superoxide dismutase 1 gene account for only a minority of total amyotrophic lateral sclerosis cases, the discovery of this gene has been crucial for amyotrophic lateral sclerosis research. Since the identification of superoxide dismutase 1 in 1993, the field of amyotrophic...

Descripción completa

Detalles Bibliográficos
Autores principales:	Martinelli, Ilaria, Zucchi, Elisabetta, Simonini, Cecilia, Gianferrari, Giulia, Zamboni, Giovanna, Pinti, Marcello, Mandrioli, Jessica
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer - Medknow 2022
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10075107/ https://www.ncbi.nlm.nih.gov/pubmed/36571338 http://dx.doi.org/10.4103/1673-5374.361535

Ejemplares similares

Effect of tauroursodeoxycholic acid on survival and safety in amyotrophic lateral sclerosis: a retrospective population-based cohort study
por: Zucchi, Elisabetta, et al.
Publicado: (2023)

Mitochondrial and Endoplasmic Reticulum Alterations in a Case of Amyotrophic Lateral Sclerosis Caused by TDP-43 A382T Mutation
por: Zanini, Giada, et al.
Publicado: (2022)

Young Onset Alzheimer’s Disease Associated with C9ORF72 Hexanucleotide Expansion: Further Evidence for a Still Unsolved Association
por: Vinceti, Giulia, et al.
Publicado: (2023)

Randomized, double-blind, placebo-controlled trial of rapamycin in amyotrophic lateral sclerosis
por: Mandrioli, Jessica, et al.
Publicado: (2023)

Case report: p.Glu134del SOD1 mutation in two apparently unrelated ALS patients with mirrored phenotype
por: Gianferrari, Giulia, et al.
Publicado: (2023)

Protein kinetics of superoxide dismutase‐1 in familial and sporadic amyotrophic lateral sclerosis
por: Ly, Cindy V., et al.
Publicado: (2023)

Pathological Roles of Wild-Type Cu, Zn-Superoxide Dismutase in Amyotrophic Lateral Sclerosis
por: Furukawa, Yoshiaki
Publicado: (2012)

A seeded propagation of Cu, Zn-superoxide dismutase aggregates in amyotrophic lateral sclerosis
por: Ogawa, Mariko, et al.
Publicado: (2014)

Psychiatric Symptoms in Amyotrophic Lateral Sclerosis: Beyond a Motor Neuron Disorder
por: Zucchi, Elisabetta, et al.
Publicado: (2019)

Glial nuclear aggregates of superoxide dismutase-1 are regularly present in patients with amyotrophic lateral sclerosis
por: Forsberg, Karin, et al.
Publicado: (2011)

Immunochemical characterization on pathological oligomers of mutant Cu/Zn-superoxide dismutase in amyotrophic lateral sclerosis
por: Tokuda, Eiichi, et al.
Publicado: (2017)

The Role of Metal Binding in the Amyotrophic Lateral Sclerosis-Related Aggregation of Copper-Zinc Superoxide Dismutase
por: Sirangelo, Ivana, et al.
Publicado: (2017)

Mutant superoxide dismutase aggregates from human spinal cord transmit amyotrophic lateral sclerosis
por: Ekhtiari Bidhendi, Elaheh, et al.
Publicado: (2018)

CSF Heavy Neurofilament May Discriminate and Predict Motor Neuron Diseases with Upper Motor Neuron Involvement
por: Simonini, Cecilia, et al.
Publicado: (2021)

A Variant in TBCD Associated with Motoneuronopathy and Corpus Callosum Hypoplasia: A Case Report
por: Caputo, Maria, et al.
Publicado: (2023)

Italian version of the Rasch-Built Overall Amyotrophic Lateral Sclerosis Disability Scale (ROADS): validation and longitudinal performance
por: Fortuna, Andrea, et al.
Publicado: (2022)

Anticipation and Phenotypic Heterogeneity in Korean Familial Amyotrophic Lateral Sclerosis with Superoxide Dismutase 1 Gene Mutation
por: Kim, Woojun, et al.
Publicado: (2007)

Glutathionylation potentiates benign superoxide dismutase 1 variants to the toxic forms associated with amyotrophic lateral sclerosis
por: McAlary, Luke, et al.
Publicado: (2013)

Does wild-type Cu/Zn-superoxide dismutase have pathogenic roles in amyotrophic lateral sclerosis?
por: Furukawa, Yoshiaki, et al.
Publicado: (2020)

Wild-type Cu/Zn-superoxide dismutase is misfolded in cerebrospinal fluid of sporadic amyotrophic lateral sclerosis
por: Tokuda, Eiichi, et al.
Publicado: (2019)

Insights on the Multifaceted Roles of Wild-Type and Mutated Superoxide Dismutase 1 in Amyotrophic Lateral Sclerosis Pathogenesis
por: Rubino, Valentina, et al.
Publicado: (2023)

Correction to: Italian version of the Rasch-Built Overall Amyotrophic Lateral Sclerosis Disability Scale (ROADS): validation and longitudinal performance
por: Fortuna, Andrea, et al.
Publicado: (2023)

Structural properties and neuronal toxicity of amyotrophic lateral sclerosis–associated Cu/Zn superoxide dismutase 1 aggregates
por: Matsumoto, Gen, et al.
Publicado: (2005)

Finding Inhibitors of Mutant Superoxide Dismutase-1 for Amyotrophic Lateral Sclerosis Therapy from Traditional Chinese Medicine
por: Huang, Hung-Jin, et al.
Publicado: (2014)

A pathological link between dysregulated copper binding in Cu/Zn-superoxide dismutase and amyotrophic lateral sclerosis
por: Furukawa, Yoshiaki
Publicado: (2022)

Selenoprotein P Concentrations in the Cerebrospinal Fluid and Serum of Individuals Affected by Amyotrophic Lateral Sclerosis, Mild Cognitive Impairment and Alzheimer’s Dementia
por: Urbano, Teresa, et al.
Publicado: (2022)

Neutrophils-to-Lymphocyte Ratio Is Associated with Progression and Overall Survival in Amyotrophic Lateral Sclerosis
por: Leone, Maurizio A., et al.
Publicado: (2022)

The association between lifelong personality and clinical phenotype in the FTD-ALS spectrum
por: Vinceti, Giulia, et al.
Publicado: (2023)

Redox environment is an intracellular factor to operate distinct pathways for aggregation of Cu,Zn-superoxide dismutase in amyotrophic lateral sclerosis
por: Furukawa, Yoshiaki
Publicado: (2013)

Screening of Drugs Inhibiting In vitro Oligomerization of Cu/Zn-Superoxide Dismutase with a Mutation Causing Amyotrophic Lateral Sclerosis
por: Anzai, Itsuki, et al.
Publicado: (2016)

Comprehensive in silico analysis and molecular dynamics of the superoxide dismutase 1 (SOD1) variants related to amyotrophic lateral sclerosis
por: Pereira, Gabriel Rodrigues Coutinho, et al.
Publicado: (2021)

Superoxide Dismutase 1 Folding Stability as a Target for Molecular Tweezers in SOD1‐Related Amyotrophic Lateral Sclerosis
por: Samanta, Nirnay, et al.
Publicado: (2022)

In Silico Analyses of a Promising Drug Candidate for the Treatment of Amyotrophic Lateral Sclerosis Targeting Superoxide Dismutase I Protein
por: Pereira, Gabriel Rodrigues Coutinho, et al.
Publicado: (2023)

Modification of Superoxide Dismutase 1 (SOD1) Properties by a GFP Tag – Implications for Research into Amyotrophic Lateral Sclerosis (ALS)
por: Stevens, James C., et al.
Publicado: (2010)

Experimental Mutations in Superoxide Dismutase 1 Provide Insight into Potential Mechanisms Involved in Aberrant Aggregation in Familial Amyotrophic Lateral Sclerosis
por: Crown, Anthony M., et al.
Publicado: (2019)

Pyrimethamine significantly lowers cerebrospinal fluid Cu/Zn superoxide dismutase in amyotrophic lateral sclerosis patients with SOD1 mutations
por: Lange, Dale J., et al.
Publicado: (2017)

Expression of a Cu,Zn superoxide dismutase typical for familial amyotrophic lateral sclerosis increases the vulnerability of neuroblastoma cells to infectious injury
por: Goos, Miriam, et al.
Publicado: (2007)

An Allosteric Pathway in Copper, Zinc Superoxide Dismutase Unravels the Molecular Mechanism of the G93A Amyotrophic Lateral Sclerosis-Linked Mutation
por: Souza, Paulo C. T., et al.
Publicado: (2019)

Atypical Familial Amyotrophic Lateral Sclerosis Secondary to Superoxide Dismutase 1 Gene Mutation With Coexistent Axonal Polyneuropathy: A Challenging Diagnosis
por: Makkawi, Seraj, et al.
Publicado: (2022)

Autophagic induction of amyotrophic lateral sclerosis-linked Cu/Zn superoxide dismutase 1 G93A mutant in NSC34 cells
por: Wei, Yanming
Publicado: (2014)

Cannot write session to /tmp/vufind_sessions/sess_j1smla6b12rr57kfc3pm5v78qc