Related references
Note: Only part of the references are listed.Deletion of PDK1 in oligodendrocyte lineage cells causes white matter abnormality and myelination defect in the central nervous system
He Wang et al.
NEUROBIOLOGY OF DISEASE (2021)
Thermosensitive receptors in neural stem cells link stress-induced hyperthermia to impaired neurogenesis via microglial engulfment
Yutaka Hoshi et al.
SCIENCE ADVANCES (2021)
Pen-2 Negatively Regulates the Differentiation of Oligodendrocyte Precursor Cells into Astrocytes in the Central Nervous System
Jinxing Hou et al.
JOURNAL OF NEUROSCIENCE (2021)
Akt Regulates Sox10 Expression to Control Oligodendrocyte Differentiation via Phosphorylating FoxO1
He Wang et al.
JOURNAL OF NEUROSCIENCE (2021)
Overexpressing low-density lipoprotein receptor reduces tau-associated neurodegeneration in relation to apoE-linked mechanisms
Yang Shi et al.
NEURON (2021)
Insights into the mechanisms of epilepsy from structural biology of LGI1-ADAM22
Atsushi Yamagata et al.
CELLULAR AND MOLECULAR LIFE SCIENCES (2020)
Molecular Control of Oligodendrocyte Development
Benayahu Elbaz et al.
TRENDS IN NEUROSCIENCES (2019)
A novel LGI1 missense mutation causes dysfunction in cortical neuronal migration and seizures
Feng Liu et al.
BRAIN RESEARCH (2019)
Amyloid-beta plaques enhance Alzheimer's brain tau-seeded pathologies by facilitating neuritic plaque tau aggregation
Zhuohao He et al.
NATURE MEDICINE (2018)
Structural basis of epilepsy-related ligand-receptor complex LGI1-ADAM22
Atsushi Yamagata et al.
NATURE COMMUNICATIONS (2018)
Leucine-Rich Glioma Inactivated 1 Promotes Oligodendrocyte Differentiation and Myelination via TSC-mTOR Signaling
Ya-Jun Xie et al.
FRONTIERS IN MOLECULAR NEUROSCIENCE (2018)
Enhancing Oligodendrocyte Myelination Rescues Synaptic Loss and Improves Functional Recovery after Chronic Hypoxia
Fei Wang et al.
NEURON (2018)
Impaired Spatial Learning is Associated with Disrupted Integrity of the White Matter in Akt3 Knockout Mice
He Wang et al.
CNS NEUROSCIENCE & THERAPEUTICS (2017)
Conditional Deletion of PDK1 in the Forebrain Causes Neuron Loss and Increased Apoptosis during Cortical Development
Congyu Xu et al.
FRONTIERS IN CELLULAR NEUROSCIENCE (2017)
Dual function of the PI3K-Akt-mTORC1 axis in myelination of the peripheral nervous system
Gianluca Figlia et al.
ELIFE (2017)
Mutation of the 3-Phosphoinositide-Dependent Protein Kinase 1 (PDK1) Substrate-Docking Site in the Developing Brain Causes Microcephaly with Abnormal Brain Morphogenesis Independently of Akt, Leading to Impaired Cognition and Disruptive Behaviors
Lluis Cordon-Barris et al.
MOLECULAR AND CELLULAR BIOLOGY (2016)
Chd7 cooperates with Sox10 and regulates the onset of CNS myelination and remyelination
Danyang He et al.
NATURE NEUROSCIENCE (2016)
Regulation of PERK-eIF2α signalling by tuberous sclerosis complex-1 controls homoeostasis and survival of myelinating oligodendrocytes
Minqing Jiang et al.
NATURE COMMUNICATIONS (2016)
Gliovascular disruption and cognitive deficits in a mouse model with features of small vessel disease
Philip R. Holland et al.
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM (2015)
Physical activity, motor function, and white matter hyperintensity burden in healthy older adults
Debra A. Fleischman et al.
NEUROLOGY (2015)
Essential roles of leucine-rich glioma inactivated 1 in the development of embryonic and postnatal cerebellum
Ya-Jun Xie et al.
SCIENTIFIC REPORTS (2015)
Homozygous Deletion of the LGI1 Gene in Mice Leads to Developmental Abnormalities Resulting in Cortical Dysplasia
Jeane Silva et al.
BRAIN PATHOLOGY (2015)
LGI1 is Involved in the Development of Mouse Brain
Li-Da Su et al.
CEREBELLUM (2015)
Chemical corrector treatment ameliorates increased seizure susceptibility in a mouse model of familial epilepsy
Norihiko Yokoi et al.
NATURE MEDICINE (2015)
Age-dependent neuron loss is associated with impaired adult neurogenesis in forebrain neuron-specific Dicer conditional knockout mice
Shanshan Cheng et al.
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY (2014)
Conditional Ablation of Raptor or Rictor Has Differential Impact on Oligodendrocyte Differentiation and CNS Myelination
Kathryn K. Bercury et al.
JOURNAL OF NEUROSCIENCE (2014)
Mammalian Target of Rapamycin Promotes Oligodendrocyte Differentiation, Initiation and Extent of CNS Myelination
Stacey E. Wahl et al.
JOURNAL OF NEUROSCIENCE (2014)
Balanced mTORC1 Activity in Oligodendrocytes Is Required for Accurate CNS Myelination
Frederic Lebrun-Julien et al.
JOURNAL OF NEUROSCIENCE (2014)
A newly discovered LGI1 mutation in Korean family with autosomal dominant lateral temporal lobe epilepsy
Moon Kyu Lee et al.
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY (2014)
Autoantibodies to Epilepsy-Related LGI1 in Limbic Encephalitis Neutralize LGI1-ADAM22 Interaction and Reduce Synaptic AMPA Receptors
Toshika Ohkawa et al.
JOURNAL OF NEUROSCIENCE (2013)
MYRF Is a Membrane-Associated Transcription Factor That Autoproteolytically Cleaves to Directly Activate Myelin Genes
Helena Bujalka et al.
PLOS BIOLOGY (2013)
The Transcription Factors Sox10 and Myrf Define an Essential Regulatory Network Module in Differentiating Oligodendrocytes
Julia Hornig et al.
PLOS GENETICS (2013)
Olig2-dependent developmental fate switch of NG2 cells
Xiaoqin Zhu et al.
DEVELOPMENT (2012)
Erk1/2 MAPK and mTOR signaling sequentially regulates progression through distinct stages of oligodendrocyte differentiation
Hebe M. Guardiola-Diaz et al.
GLIA (2012)
Frontal white matter integrity is related to psychomotor retardation in major depression
Sebastian Walther et al.
NEUROBIOLOGY OF DISEASE (2012)
Histopathological Correlates of Magnetic Resonance Imaging-Defined Chronic Perinatal White Matter Injury
Art Riddle et al.
ANNALS OF NEUROLOGY (2011)
Axon-glial disruption: the link between vascular disease and Alzheimer's disease?
Karen Horsburgh et al.
BIOCHEMICAL SOCIETY TRANSACTIONS (2011)
The Genetics of White Matter Lesions
Arezoo Assareh et al.
CNS NEUROSCIENCE & THERAPEUTICS (2011)
Rapid Disruption of Axon-Glial Integrity in Response to Mild Cerebral Hypoperfusion
Michell M. Reimer et al.
JOURNAL OF NEUROSCIENCE (2011)
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease
Paul Hollingworth et al.
NATURE GENETICS (2011)
Familial temporal lobe epilepsy with psychic auras associated with a novel LGI1 mutation
P. Striano et al.
NEUROLOGY (2011)
LGI1 Is a Nogo Receptor 1 Ligand that Antagonizes Myelin-Based Growth Inhibition
Rhalena Thomas et al.
JOURNAL OF NEUROSCIENCE (2010)
Homozygous Inactivation of the Lgi1 Gene Results in Hypomyelination in the Peripheral and Central Nervous Systems
Jeane Silva et al.
JOURNAL OF NEUROSCIENCE RESEARCH (2010)
Signals to promote myelin formation and repair
Carla Taveggia et al.
NATURE REVIEWS NEUROLOGY (2010)
Myelin Gene Regulatory Factor Is a Critical Transcriptional Regulator Required for CNS Myelination
Ben Emery et al.
CELL (2009)
LGI1 Mutations in Autosomal Dominant and Sporadic Lateral Temporal Epilepsy
Carlo Nobile et al.
HUMAN MUTATION (2009)
Conditional Forebrain Inactivation of Nicastrin Causes Progressive Memory Impairment and Age-Related Neurodegeneration
Katsuhiko Tabuchi et al.
JOURNAL OF NEUROSCIENCE (2009)
Activation of the Mammalian Target of Rapamycin (mTOR) Is Essential for Oligodendrocyte Differentiation
William A. Tyler et al.
JOURNAL OF NEUROSCIENCE (2009)
Akt Signals through the Mammalian Target of Rapamycin Pathway to Regulate CNS Myelination
S. Priyadarshini Narayanan et al.
JOURNAL OF NEUROSCIENCE (2009)
Arrested oligodendrocyte lineage maturation in chronic perinatal white matter injury
Kristen N. Segovia et al.
ANNALS OF NEUROLOGY (2008)
Constitutively active Akt induces enhanced myelination in the CNS
Ana I. Flores et al.
JOURNAL OF NEUROSCIENCE (2008)
Penetrance of LGI1 mutations in autosomal dominant partial epilepsy with auditory features
Michael J. Rosanoff et al.
NEUROLOGY (2008)
Olig1 and Sox10 interact synergistically to drive Myelin Basic Protein transcription in oligodendrocytes
Huiliang Li et al.
JOURNAL OF NEUROSCIENCE (2007)
Epilepsy-related ligand/receptor complex LGI1 and ADAM22 regulate synaptic transmission
Yuko Fukata et al.
SCIENCE (2006)
ADPEAF mutations reduce levels of secreted LGI1, a putative tumor suppressor protein linked to epilepsy
KR Senechal et al.
HUMAN MOLECULAR GENETICS (2005)
LGI1 mutations in autosomal dominant partial epilepsy with auditory features
R Ottman et al.
NEUROLOGY (2004)
Terminal differentiation of myelin-forming oligodendrocytes depends on the transcription factor Sox10
CC Stolt et al.
GENES & DEVELOPMENT (2002)
Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features
S Kalachikov et al.
NATURE GENETICS (2002)
Share Paper
