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The Subtype of GluN2 C-terminal Domain Determines the Response to Excitotoxic Insults

Neuron (Cambridge, Mass.), 2012-05, Vol.74 (3), p.543-556

2012

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Reactive astrocytes acquire neuroprotective as well as deleterious signatures in response to Tau and Aß pathology

Nature communications, 2022-01, Vol.13 (1), p.135-135, Article 135

2022

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Medial septal GABAergic neurons reduce seizure duration upon optogenetic closed-loop stimulation

Brain (London, England : 1878), 2021-06, Vol.144 (5), p.1576-1589

2021

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NMDA Receptor C-Terminal Domain Signalling in Development, Maturity, and Disease

International journal of molecular sciences, 2022-09, Vol.23 (19), p.11392

2022

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Excess ribosomal protein production unbalances translation in a model of Fragile X Syndrome

Nature communications, 2022-06, Vol.13 (1), p.3236-3236, Article 3236

2022

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Cellular and synaptic phenotypes lead to disrupted information processing in Fmr1-KO mouse layer 4 barrel cortex

Nature communications, 2019-10, Vol.10 (1), p.4814-18, Article 4814

2019

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Sustained correction of associative learning deficits after brief, early treatment in a rat model of Fragile X Syndrome

Science translational medicine, 2019-05, Vol.11 (494)

2019

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Altered dendritic spine function and integration in a mouse model of fragile X syndrome

Nature communications, 2019-10, Vol.10 (1), p.4813-14, Article 4813

2019

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Characterisation of CDKL5 Transcript Isoforms in Human and Mouse

PloS one, 2016-06, Vol.11 (6), p.e0157758-e0157758

2016

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Cell-Type-Specific Translation Profiling Reveals a Novel Strategy for Treating Fragile X Syndrome

Neuron (Cambridge, Mass.), 2017-08, Vol.95 (3), p.550-563.e5

2017

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Stimulated emission depletion (STED) microscopy reveals nanoscale defects in the developmental trajectory of dendritic spine morphogenesis in a mouse model of fragile X syndrome

The Journal of neuroscience, 2014-04, Vol.34 (18), p.6405-6412

2014

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Input-Output Relationship of CA1 Pyramidal Neurons Reveals Intact Homeostatic Mechanisms in a Mouse Model of Fragile X Syndrome

Cell reports (Cambridge), 2020-08, Vol.32 (6), p.107988-107988, Article 107988

2020

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Maturation and electrophysiological properties of human pluripotent stem cell‐derived oligodendrocytes

Stem cells (Dayton, Ohio), 2016-04, Vol.34 (4), p.1040-1053

2016

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Astrocytes mediate cell non-autonomous correction of aberrant firing in human FXS neurons

Cell reports (Cambridge), 2023-04, Vol.42 (4), p.112344-112344, Article 112344

2023

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Cerebellar contributions to fear-based emotional processing: relevance to understanding the neural circuits involved in autism

Frontiers in systems neuroscience, 2023, Vol.17, p.1229627-1229627

2023

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Sexually dimorphic patterns in electroencephalography power spectrum and autism-related behaviors in a rat model of fragile X syndrome

Neurobiology of disease, 2020-12, Vol.146, p.105118-105118, Article 105118

2020

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Altered maturation of the primary somatosensory cortex in a mouse model of fragile X syndrome

Human molecular genetics, 2012-05, Vol.21 (10), p.2143-2156

2012

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Identifying foetal forebrain interneurons as a target for monogenic autism risk factors and the polygenic 16p11.2 microdeletion

BMC neuroscience, 2023-01, Vol.24 (1), p.5-5, Article 5

2023

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Experience-dependent changes in hippocampal spatial activity and hippocampal circuit function are disrupted in a rat model of Fragile X Syndrome

Molecular autism, 2022-12, Vol.13 (1), p.49-49, Article 49

2022

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Expression of mRNA Encoding Mcu and Other Mitochondrial Calcium Regulatory Genes Depends on Cell Type, Neuronal Subtype, and Ca2+ Signaling

PloS one, 2016-02, Vol.11 (2), p.e0148164-e0148164

2016

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The Developmental Shift of NMDA Receptor Composition Proceeds Independently of GluN2 Subunit-Specific GluN2 C-Terminal Sequences

Cell reports (Cambridge), 2018-10, Vol.25 (4), p.841-851.e4

2018

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Enhanced hippocampal LTP but normal NMDA receptor and AMPA receptor function in a rat model of CDKL5 deficiency disorder

Molecular autism, 2024-06, Vol.15 (1), p.28-21

2024

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A sex difference in the response of the rodent postsynaptic density to synGAP haploinsufficiency

eLife, 2020-01, Vol.9

2020

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CDKL5 deficiency disorder: a pathophysiology of neural maintenance

The Journal of clinical investigation, 2021-11, Vol.131 (21)

2021

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Delayed recruitment of activity‐dependent bulk endocytosis in Fmr1 knockout neurons

Journal of neurochemistry, 2024-07

2024

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The Subtype of GluN2 C-terminal Domain Determines the Response to Excitotoxic Insults

Reactive astrocytes acquire neuroprotective as well as deleterious signatures in response to Tau and Aß pathology

Medial septal GABAergic neurons reduce seizure duration upon optogenetic closed-loop stimulation

NMDA Receptor C-Terminal Domain Signalling in Development, Maturity, and Disease

Excess ribosomal protein production unbalances translation in a model of Fragile X Syndrome

Cellular and synaptic phenotypes lead to disrupted information processing in Fmr1-KO mouse layer 4 barrel cortex

Sustained correction of associative learning deficits after brief, early treatment in a rat model of Fragile X Syndrome

Altered dendritic spine function and integration in a mouse model of fragile X syndrome

Characterisation of CDKL5 Transcript Isoforms in Human and Mouse

Cell-Type-Specific Translation Profiling Reveals a Novel Strategy for Treating Fragile X Syndrome

Stimulated emission depletion (STED) microscopy reveals nanoscale defects in the developmental trajectory of dendritic spine morphogenesis in a mouse model of fragile X syndrome

Input-Output Relationship of CA1 Pyramidal Neurons Reveals Intact Homeostatic Mechanisms in a Mouse Model of Fragile X Syndrome

Maturation and electrophysiological properties of human pluripotent stem cell‐derived oligodendrocytes

Astrocytes mediate cell non-autonomous correction of aberrant firing in human FXS neurons

Cerebellar contributions to fear-based emotional processing: relevance to understanding the neural circuits involved in autism

Sexually dimorphic patterns in electroencephalography power spectrum and autism-related behaviors in a rat model of fragile X syndrome

Altered maturation of the primary somatosensory cortex in a mouse model of fragile X syndrome

Identifying foetal forebrain interneurons as a target for monogenic autism risk factors and the polygenic 16p11.2 microdeletion

Experience-dependent changes in hippocampal spatial activity and hippocampal circuit function are disrupted in a rat model of Fragile X Syndrome

Expression of mRNA Encoding Mcu and Other Mitochondrial Calcium Regulatory Genes Depends on Cell Type, Neuronal Subtype, and Ca2+ Signaling

The Developmental Shift of NMDA Receptor Composition Proceeds Independently of GluN2 Subunit-Specific GluN2 C-Terminal Sequences

Enhanced hippocampal LTP but normal NMDA receptor and AMPA receptor function in a rat model of CDKL5 deficiency disorder

A sex difference in the response of the rodent postsynaptic density to synGAP haploinsufficiency

CDKL5 deficiency disorder: a pathophysiology of neural maintenance

Delayed recruitment of activity‐dependent bulk endocytosis in Fmr1 knockout neurons

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