相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。Systemic Radical Scavenger Treatment of a Mouse Model of Rett Syndrome: Merits and Limitations of the Vitamin E Derivative Trolox
Oliwia A. Janc et al.
FRONTIERS IN CELLULAR NEUROSCIENCE (2016)
Mitochondrial free radical overproduction due to respiratory chain impairment in the brain of a mouse model of Rett syndrome: protective effect of CNF1
Bianca De Filippis et al.
FREE RADICAL BIOLOGY AND MEDICINE (2015)
Dysregulation of Glutamine Transporter SNAT1 in Rett Syndrome Microglia: A Mechanism for Mitochondrial Dysfunction and Neurotoxicity
Lee-Way Jin et al.
JOURNAL OF NEUROSCIENCE (2015)
The Changing Face of Survival in Rett Syndrome and MECP2-Related Disorders
Daniel C. Tarquinio et al.
PEDIATRIC NEUROLOGY (2015)
Foxg1 localizes to mitochondria and coordinates cell differentiation and bioenergetics
Laura Pancrazi et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2015)
Aberrant redox homoeostasis and mitochondrial dysfunction in Rett syndrome
Michael Mueller et al.
BIOCHEMICAL SOCIETY TRANSACTIONS (2014)
Transcriptional regulation in pluripotent stem cells by methyl CpG-binding protein 2 (MeCP2)
Yoshiaki Tanaka et al.
HUMAN MOLECULAR GENETICS (2014)
Mitochondrial dysfunction in the skeletal muscle of a mouse model of Rett syndrome (RTT): Implications for the disease phenotype
W. A. Gold et al.
MITOCHONDRION (2014)
Oxidative brain damage in Mecp2-mutant murine models of Rett syndrome
Claudio De Felice et al.
NEUROBIOLOGY OF DISEASE (2014)
Improvement of the Rett Syndrome Phenotype in a Mecp2 Mouse Model Upon Treatment with Levodopa and a Dopa-Decarboxylase Inhibitor
Karolina Szczesna et al.
NEUROPSYCHOPHARMACOLOGY (2014)
Redox Imbalance and Morphological Changes in Skin Fibroblasts in Typical Rett Syndrome
Cinzia Signorini et al.
OXIDATIVE MEDICINE AND CELLULAR LONGEVITY (2014)
Anaplerotic Triheptanoin Diet Enhances Mitochondrial Substrate Use to Remodel the Metabolome and Improve Lifespan, Motor Function, and Sociability in MeCP2-Null Mice
Min Jung Park et al.
PLOS ONE (2014)
The free radical scavengerTrolox dampens neuronal hyperexcitability, reinstates synaptic plasticity, and improves hypoxia tolerance in a mouse model of Rett syndrome
Oliwia A. Janc et al.
FRONTIERS IN CELLULAR NEUROSCIENCE (2014)
Global Transcriptional and Translational Repression in Human-Embryonic-Stem-Cell-Derived Rett Syndrome Neurons
Yun Li et al.
CELL STEM CELL (2013)
Oligodendrocyte Lineage Cells Contribute Unique Features to Rett Syndrome Neuropathology
Minh Vu Chuong Nguyen et al.
JOURNAL OF NEUROSCIENCE (2013)
Genes Related to Mitochondrial Functions, Protein Degradation, and Chromatin Folding Are Differentially Expressed in Lymphomonocytes of Rett Syndrome Patients
Alessandra Pecorelli et al.
MEDIATORS OF INFLAMMATION (2013)
Morphological changes and oxidative damage in Rett Syndrome erythrocytes
Lucia Ciccoli et al.
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS (2012)
Partial rescue of Rett syndrome by ω-3 polyunsaturated fatty acids (PUFAs) oil
Claudio De Felice et al.
GENES AND NUTRITION (2012)
What comes first, misshape or dysfunction? The view from metabolic excess
Chad A. Galloway et al.
JOURNAL OF GENERAL PHYSIOLOGY (2012)
Mitochondrial proteomics-a tool for the study of metabolic disorders
Niels Gregersen et al.
JOURNAL OF INHERITED METABOLIC DISEASE (2012)
Brain Activity Mapping in Mecp2 Mutant Mice Reveals Functional Deficits in Forebrain Circuits, Including Key Nodes in the Default Mode Network, that are Reversed with Ketamine Treatment
Miriam Kron et al.
JOURNAL OF NEUROSCIENCE (2012)
Oxidative burden and mitochondrial dysfunction in a mouse model of Rett syndrome
Emanuel Grosser et al.
NEUROBIOLOGY OF DISEASE (2012)
Mitochondrial proticity and ROS signaling: lessons from the uncoupling proteins
Ryan J. Mailloux et al.
TRENDS IN ENDOCRINOLOGY AND METABOLISM (2012)
Subclinical myocardial dysfunction in Rett syndrome
Claudio De Felice et al.
EUROPEAN HEART JOURNAL-CARDIOVASCULAR IMAGING (2012)
Assessing mitochondrial dysfunction in cells
Martin D. Brand et al.
BIOCHEMICAL JOURNAL (2011)
Increased levels of 4HNE-protein plasma adducts in Rett syndrome
Alessandra Pecorelli et al.
CLINICAL BIOCHEMISTRY (2011)
F2-dihomo-isoprostanes as potential early biomarkers of lipid oxidative damage in Rett syndrome
Claudio De Felice et al.
JOURNAL OF LIPID RESEARCH (2011)
A role for glia in the progression of Rett's syndrome
Daniel T. Lioy et al.
NATURE (2011)
Oxidative stress in Rett syndrome: Natural history, genotype, and variants
Silvia Leoncini et al.
REDOX REPORT (2011)
Downstream targets of methyl CpG binding protein 2 and their abnormal expression in the frontal cortex of the human Rett syndrome brain
Joanne H. Gibson et al.
BMC NEUROSCIENCE (2010)
MOLECULAR GENETICS OF MITOCHONDRIAL DISORDERS
Lee-Jun C. Wong
DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS (2010)
Mitochondrial proton and electron leaks
Martin Jastroch et al.
ESSAYS IN BIOCHEMISTRY: MITOCHONDRIAL FUNCTION (2010)
The MeCP2/YY1 interaction regulates ANT1 expression at 4q35: novel hints for Rett syndrome pathogenesis
Greta Forlani et al.
HUMAN MOLECULAR GENETICS (2010)
Neuronal MeCP2 Is Expressed at Near Histone-Octamer Levels and Globally Alters the Chromatin State
Peter J. Skene et al.
MOLECULAR CELL (2010)
Systemic oxidative stress in classic Rett syndrome
Claudio De Felice et al.
FREE RADICAL BIOLOGY AND MEDICINE (2009)
Widespread Changes in Dendritic and Axonal Morphology in Mecp2-Mutant Mouse Models of Rett Syndrome: Evidence for Disruption of Neuronal Networks
Pavel V. Belichenko et al.
JOURNAL OF COMPARATIVE NEUROLOGY (2009)
FOXG1 is responsible for the congenital variant of Rett syndrome
Francesca Ariani et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
Mecp2-Null Mice Provide New Neuronal Targets for Rett Syndrome
Rocio G. Urdinguio et al.
PLOS ONE (2008)
MeCP2, a key contributor to neurological disease, activates and represses transcription
Maria Chahrour et al.
SCIENCE (2008)
Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes
Dag H. Yasui et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2007)
Gene expression analysis exposes mitochondrial abnormalities in a mouse model of Rett syndrome
Skirmantas Kriaucionis et al.
MOLECULAR AND CELLULAR BIOLOGY (2006)
Brain magnetic resonance study of Mecp2 deletion effects on anatomy and metabolism
W Saywell et al.
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS (2006)
The basal proton conductance of mitochondria depends on adenine nucleotide translocase content
MD Brand et al.
BIOCHEMICAL JOURNAL (2005)
Reduced cortical activity due to a shift in the balance between excitation and inhibition in a mouse model of Rett Syndrome
VS Dani et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2005)
Rett syndrome: A prototypical neurodevelopmental disorder
JL Neul et al.
NEUROSCIENTIST (2004)
Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation
LS Weaving et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2004)
Mitochondria
PF Chinnery et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2003)
Chromatin compaction by human MeCP2 - Assembly of novel secondary chromatin structures in the absence of DNA methylation
PT Georgel et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2003)
Neuronal degeneration and mitochondrial dysfunction
EA Schon et al.
JOURNAL OF CLINICAL INVESTIGATION (2003)
Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation
MD Shahbazian et al.
HUMAN MOLECULAR GENETICS (2002)
Oxidative stress in Rett syndrome
C Sierra et al.
BRAIN & DEVELOPMENT (2001)
Neurobiology of Rett syndrome: a genetic disorder of synapse development
MV Johnston et al.
BRAIN & DEVELOPMENT (2001)
A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome
J Guy et al.
NATURE GENETICS (2001)
Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice
RZ Chen et al.
NATURE GENETICS (2001)
Comparative sequence analysis of the MECP2-locus in human and mouse reveals new transcribed regions
K Reichwald et al.
MAMMALIAN GENOME (2000)