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Differential susceptibility of human motor neurons to infection with Usutu and West Nile virus

Journal of neuroinflammation, 2024-09, Vol.21 (1), p.236-13, Article 236

2024

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In vitro and in vivo differences in neurovirulence between D614G, Delta And Omicron BA.1 SARS-CoV-2 variants

Acta neuropathologica communications, 2022-09, Vol.10 (1), p.124-124, Article 124

2022

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Replication Kinetics, Cell Tropism, and Associated Immune Responses in SARS-CoV-2- and H5N1 Virus-Infected Human Induced Pluripotent Stem Cell-Derived Neural Models

mSphere, 2021-06, Vol.6 (3), p.e0027021-e0027021

2021

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Phenotypic Differences between Asian and African Lineage Zika Viruses in Human Neural Progenitor Cells

mSphere, 2017-07, Vol.2 (4), p.e00292-17

2017

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An expandable embryonic stem cell-derived Purkinje neuron progenitor population that exhibits in vivo maturation in the adult mouse cerebellum

Scientific reports, 2017-08, Vol.7 (1), p.8863-19, Article 8863

2017

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Loss of nuclear UBE3A causes electrophysiological and behavioral deficits in mice and is associated with Angelman syndrome

Nature neuroscience, 2019-08, Vol.22 (8), p.1235-1247

2019

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A novel fragile X syndrome mutation reveals a conserved role for the carboxy‐terminus in FMRP localization and function

EMBO molecular medicine, 2015-04, Vol.7 (4), p.423-437

2015

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Subregion-specific dendritic spine abnormalities in the hippocampus of Fmr1 KO mice

Neurobiology of learning and memory, 2011-05, Vol.95 (4), p.467-472

2011

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A functional variant in the miR‐142 promoter modulating its expression and conferring risk of Alzheimer disease

Human mutation, 2019-11, Vol.40 (11), p.2131-2145

2019

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The neuroinvasiveness, neurotropism, and neurovirulence of SARS-CoV-2

Trends in neurosciences (Regular ed.), 2022-05, Vol.45 (5), p.358-368

2022

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A simplified protocol for the generation of cortical brain organoids

Frontiers in cellular neuroscience, 2023-04, Vol.17, p.1114420-1114420

2023

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Dose-dependent inhibition of proteasome activity by a mutant ubiquitin associated with neurodegenerative disease

Journal of cell science, 2007-05, Vol.120 (9), p.1615-1623

2007

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The SAC1 domain in synaptojanin is required for autophagosome maturation at presynaptic terminals

The EMBO journal, 2017-05, Vol.36 (10), p.1392-1411

2017

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Mutant Ubiquitin Found in Neurodegenerative Disorders Is a Ubiquitin Fusion Degradation Substrate That Blocks Proteasomal Degradation

The Journal of cell biology, 2002-04, Vol.157 (3), p.417-427

2002

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Hepatitis E Virus Infects Neurons and Brains

The Journal of infectious diseases, 2017-04, Vol.215 (8), p.1197-1206

2017

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iPSC-derived healthy human astrocytes selectively load miRNAs targeting neuronal genes into extracellular vesicles

Molecular and cellular neuroscience, 2024-06, Vol.129, p.103933-103933, Article 103933

2024

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Conserved UBE3A subcellular distribution between human and mice is facilitated by non-homologous isoforms

Human molecular genetics, 2020-11, Vol.29 (18), p.3032-3043

2020

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Rescue of behavioral phenotype and neuronal protrusion morphology in Fmr1 KO mice

Neurobiology of disease, 2008-07, Vol.31 (1), p.127-132

2008

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Potential therapeutic interventions for fragile X syndrome

Trends in molecular medicine, 2010-11, Vol.16 (11), p.516-527

2010

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AFQ056, a new mGluR5 antagonist for treatment of fragile X syndrome

Neurobiology of disease, 2011-06, Vol.42 (3), p.311-317

2011

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Epigenetic Characterization of the FMR1 Promoter in Induced Pluripotent Stem Cells from Human Fibroblasts Carrying an Unmethylated Full Mutation

Stem cell reports, 2014-10, Vol.3 (4), p.548-555

2014

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ACO2 homozygous missense mutation associated with complicated hereditary spastic paraplegia

Neurology. Genetics, 2018-04, Vol.4 (2), p.e223-e223

2018

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Ultrastructural analysis of the functional domains in FMRP using primary hippocampal mouse neurons

Neurobiology of disease, 2009-08, Vol.35 (2), p.241-250

2009

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Differential susceptibility of human motor neurons to infection with Usutu and West Nile virus

In vitro and in vivo differences in neurovirulence between D614G, Delta And Omicron BA.1 SARS-CoV-2 variants

Replication Kinetics, Cell Tropism, and Associated Immune Responses in SARS-CoV-2- and H5N1 Virus-Infected Human Induced Pluripotent Stem Cell-Derived Neural Models

Phenotypic Differences between Asian and African Lineage Zika Viruses in Human Neural Progenitor Cells

An expandable embryonic stem cell-derived Purkinje neuron progenitor population that exhibits in vivo maturation in the adult mouse cerebellum

Loss of nuclear UBE3A causes electrophysiological and behavioral deficits in mice and is associated with Angelman syndrome

A novel fragile X syndrome mutation reveals a conserved role for the carboxy‐terminus in FMRP localization and function

Subregion-specific dendritic spine abnormalities in the hippocampus of Fmr1 KO mice

A functional variant in the miR‐142 promoter modulating its expression and conferring risk of Alzheimer disease

The neuroinvasiveness, neurotropism, and neurovirulence of SARS-CoV-2

A simplified protocol for the generation of cortical brain organoids

Dose-dependent inhibition of proteasome activity by a mutant ubiquitin associated with neurodegenerative disease

Standardizing designed and emergent quantitative features in microphysiological systems

The SAC1 domain in synaptojanin is required for autophagosome maturation at presynaptic terminals

Mutant Ubiquitin Found in Neurodegenerative Disorders Is a Ubiquitin Fusion Degradation Substrate That Blocks Proteasomal Degradation

Hepatitis E Virus Infects Neurons and Brains

iPSC-derived healthy human astrocytes selectively load miRNAs targeting neuronal genes into extracellular vesicles

Conserved UBE3A subcellular distribution between human and mice is facilitated by non-homologous isoforms

Rescue of behavioral phenotype and neuronal protrusion morphology in Fmr1 KO mice

Potential therapeutic interventions for fragile X syndrome

AFQ056, a new mGluR5 antagonist for treatment of fragile X syndrome

Second-tier trio exome sequencing after negative solo clinical exome sequencing: an efficient strategy to increase diagnostic yield and decipher molecular bases in undiagnosed developmental disorders

Epigenetic Characterization of the FMR1 Promoter in Induced Pluripotent Stem Cells from Human Fibroblasts Carrying an Unmethylated Full Mutation

ACO2 homozygous missense mutation associated with complicated hereditary spastic paraplegia

Ultrastructural analysis of the functional domains in FMRP using primary hippocampal mouse neurons

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