Mitochondrial respiratory chain dysfunction in muscle from patients with amyotrophic lateral sclerosis.
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Peroxisome proliferator-activated receptor γ coactivator 1 (PGC-1)- and estrogen-related receptor (ERR)-induced regulator in muscle 1 (Perm1) is a tissue-specific regulator of oxidative capacity in skeletal muscle cellsSOD1 misplacing and mitochondrial dysfunction in amyotrophic lateral sclerosis pathogenesisMitochondrial dysfunction in amyotrophic lateral sclerosis - a valid pharmacological target?Oxr1 improves pathogenic cellular features of ALS-associated FUS and TDP-43 mutationsClinical perspective on oxidative stress in sporadic amyotrophic lateral sclerosisMitochondrial changes in platelets are not related to those in skeletal muscle during human septic shock.Mitochondria-Derived Damage-Associated Molecular Patterns in Neurodegeneration.New Therapeutics to Modulate Mitochondrial Function in Neurodegenerative Disorders.Caprylic triglyceride as a novel therapeutic approach to effectively improve the performance and attenuate the symptoms due to the motor neuron loss in ALS diseaseMitochondrial network genes in the skeletal muscle of amyotrophic lateral sclerosis patientsMitochondrial abnormalities and low grade inflammation are present in the skeletal muscle of a minority of patients with amyotrophic lateral sclerosis; an observational myopathology study.VAPB/ALS8 MSP ligands regulate striated muscle energy metabolism critical for adult survival in caenorhabditis elegans.Mitochondrial dysfunction in blood cells from amyotrophic lateral sclerosis patients.Secreted VAPB/ALS8 major sperm protein domains modulate mitochondrial localization and morphology via growth cone guidance receptors.Visualization of mitochondrial respiratory function using cytochrome c oxidase/succinate dehydrogenase (COX/SDH) double-labeling histochemistry.Genotype-phenotype relationship in hereditary amyotrophic lateral sclerosis.Triheptanoin Protects Motor Neurons and Delays the Onset of Motor Symptoms in a Mouse Model of Amyotrophic Lateral SclerosisMolecular signatures of amyotrophic lateral sclerosis disease progression in hind and forelimb muscles of an SOD1(G93A) mouse modelA(a)LS: Ammonia-induced amyotrophic lateral sclerosis.ALS and oxidative stress: the neurovascular scenarioA plural role for lipids in motor neuron diseases: energy, signaling and structure.From cholesterogenesis to steroidogenesis: role of riboflavin and flavoenzymes in the biosynthesis of vitamin D.Genome-wide RNA-seq of iPSC-derived motor neurons indicates selective cytoskeletal perturbation in Brown-Vialetto disease that is partially rescued by riboflavin.Emerging drugs for amyotrophic lateral sclerosis.Tetracyclines and neuromuscular disorders.Mitochondrial Disorders May Mimic Amyotrophic Lateral Sclerosis at Onset.Amyotrophic Lateral Sclerosis and Metabolomics: Clinical Implication and Therapeutic Approach.The interplay between metabolic homeostasis and neurodegeneration: insights into the neurometabolic nature of amyotrophic lateral sclerosis.The Role of Skeletal Muscle in Amyotrophic Lateral Sclerosis.New ALS-Related Genes Expand the Spectrum Paradigm of Amyotrophic Lateral Sclerosis.Gene-specific mitochondria dysfunctions in human TARDBP and C9ORF72 fibroblasts.Mitochondrial CHCHD-Containing Proteins: Physiologic Functions and Link with Neurodegenerative Diseases.Energy Homeostasis and Abnormal RNA Metabolism in Amyotrophic Lateral SclerosisCerebrospinal Fluid from Sporadic Amyotrophic Lateral Sclerosis Patients Induces Mitochondrial and Lysosomal Dysfunction.Degeneration of spinal motor neurons by chronic AMPA-induced excitotoxicity in vivo and protection by energy substrates.Spinal muscular atrophy associated with progressive myoclonic epilepsy: A rare condition caused by mutations in ASAH1.Reply: CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosisWhat is "Hyper" in the ALS Hypermetabolism?Reduced exercise capacity in early-stage amyotrophic lateral sclerosis: Role of skeletal muscle.Co-expression Network Approach Reveals Functional Similarities among Diseases Affecting Human Skeletal Muscle.
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Mitochondrial respiratory chain dysfunction in muscle from patients with amyotrophic lateral sclerosis.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on July 2010
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Mitochondrial respiratory chai ...... amyotrophic lateral sclerosis.
@en
Mitochondrial respiratory chai ...... amyotrophic lateral sclerosis.
@nl
type
label
Mitochondrial respiratory chai ...... amyotrophic lateral sclerosis.
@en
Mitochondrial respiratory chai ...... amyotrophic lateral sclerosis.
@nl
prefLabel
Mitochondrial respiratory chai ...... amyotrophic lateral sclerosis.
@en
Mitochondrial respiratory chai ...... amyotrophic lateral sclerosis.
@nl
P2093
P50
P921
P1433
P1476
Mitochondrial respiratory chai ...... amyotrophic lateral sclerosis
@en
P2093
Andreina Bordoni
Costanza Lamperti
Elisa Fassone
Francesco Fortunato
Maurizio Moggio
Salvatore Di Mauro
Valeria Lucchini
Veronica Crugnola
P304
P356
10.1001/ARCHNEUROL.2010.128
P50
P577
2010-07-01T00:00:00Z