Oxidative burden and mitochondrial dysfunction in a mouse model of Rett syndrome. - Wikidata - awgldk - TriplyDB

Oxidative burden and mitochondrial dysfunction in a mouse model of Rett syndrome.

Oxidative burden and mitochondrial dysfunction in a mouse model of Rett syndrome.

http://www.wikidata.org/entity/Q48454183

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Anaplerotic triheptanoin diet enhances mitochondrial substrate use to remodel the metabolome and improve lifespan, motor function, and sociability in MeCP2-null mice Identification and Treatment of Pathophysiological Comorbidities of Autism Spectrum Disorder to Achieve Optimal Outcomes.Reactive Oxygen Species: Physiological and Physiopathological Effects on Synaptic Plasticity Primary Mitochondrial Disease and Secondary Mitochondrial Dysfunction: Importance of Distinction for Diagnosis and Treatment Disturbance of cardiac gene expression and cardiomyocyte structure predisposes Mecp2-null mice to arrhythmias Gastrointestinal dysfunction in autism spectrum disorder: the role of the mitochondria and the enteric microbiome.Redox imbalance and morphological changes in skin fibroblasts in typical Rett syndrome Treatments for biomedical abnormalities associated with autism spectrum disorder.Oxidative brain damage in Mecp2-mutant murine models of Rett syndrome Revealing the complexity of a monogenic disease: rett syndrome exome sequencing Longitudinal course of epilepsy in Rett syndrome and related disorders.Redox Indicator Mice Stably Expressing Genetically Encoded Neuronal roGFP: Versatile Tools to Decipher Subcellular Redox Dynamics in Neuropathophysiology.Systemic Radical Scavenger Treatment of a Mouse Model of Rett Syndrome: Merits and Limitations of the Vitamin E Derivative Trolox The free radical scavenger Trolox dampens neuronal hyperexcitability, reinstates synaptic plasticity, and improves hypoxia tolerance in a mouse model of Rett syndrome.Autism, Mitochondria and Polybrominated Diphenyl Ether Exposure.Mitochondrial abnormalities in temporal lobe of autistic brain Inflammatory lung disease in Rett syndrome.Mitochondrial Dysfunction in the Pathogenesis of Rett Syndrome: Implications for Mitochondria-Targeted Therapies.Aberrant redox homoeostasis and mitochondrial dysfunction in Rett syndrome.Effect of temperature on FAD and NADH-derived signals and neurometabolic coupling in the mouse auditory and motor cortex.Folate metabolism abnormalities in autism: potential biomarkers.CREB Signaling Is Involved in Rett Syndrome Pathogenesis Endogenous Two-Photon Excited Fluorescence Imaging Characterizes Neuron and Astrocyte Metabolic Responses to Manganese Toxicity.Autistic Siblings with Novel Mutations in Two Different Genes: Insight for Genetic Workups of Autistic Siblings and Connection to Mitochondrial Dysfunction.Increased Mitochondrial Mass and Cytosolic Redox Imbalance in Hippocampal Astrocytes of a Mouse Model of Rett Syndrome: Subcellular Changes Revealed by Ratiometric Imaging of JC-1 and roGFP1 Fluorescence.Oxygen exchange and energy metabolism in erythrocytes of Rett syndrome and their relationships with respiratory alterations.Pathophysiological Consequences of Neuronal α-Synuclein Overexpression: Impacts on Ion Homeostasis, Stress Signaling, Mitochondrial Integrity, and Electrical Activity.Rett syndrome from bench to bedside: recent advances.Transcriptome level analysis in Rett syndrome using human samples from different tissues.

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P2860

Oxidative burden and mitochondrial dysfunction in a mouse model of Rett syndrome.

http://www.wikidata.org/entity/Q48454183

description

2012 nî lūn-bûn

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2012年の論文

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2012年学术文章

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2012年学术文章

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2012年学术文章

@zh-cn

2012年学术文章

@zh-hans

2012年学术文章

@zh-my

2012年学术文章

@zh-sg

2012年學術文章

@yue

2012年學術文章

@zh-hant

name

Oxidative burden and mitochondrial dysfunction in a mouse model of Rett syndrome.

@en

Oxidative burden and mitochondrial dysfunction in a mouse model of Rett syndrome.

@nl

type

label

Oxidative burden and mitochondrial dysfunction in a mouse model of Rett syndrome.

@en

Oxidative burden and mitochondrial dysfunction in a mouse model of Rett syndrome.

@nl

prefLabel

Oxidative burden and mitochondrial dysfunction in a mouse model of Rett syndrome.

@en

Oxidative burden and mitochondrial dysfunction in a mouse model of Rett syndrome.

@nl

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J.NBD.2012.06.007

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Neurobiology of Disease

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Oxidative burden and mitochondrial dysfunction in a mouse model of Rett syndrome.

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P2093

Belinda Kempkes

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Christiane Menzfeld

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Emanuel Grosser

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Marc Fischer

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Oliwia A Janc

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Steffen Vogelgesang

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Till U Manzke

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Ursula Hirt

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102-114

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scholarly article

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10.1016/J.NBD.2012.06.007

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1

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48

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Michael Müller

Gabriela Salinas-Riester

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2012-06-30T00:00:00Z

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22750529

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