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Author Details
Full Name
Leslie M Thompson
Affiliation
ORCID
Career Start Year
1980
Papers
143
H Index
59
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36864071
Author Correction: Gene expression and functional deficits underlie TREM2-knockout microglia responses in human models of Alzheimer's disease.
Nat Commun
2023
37961595
Aberrant splicing in Huntington's disease via disrupted TDP-43 activity accompanied by altered m6A RNA modification.
2023
37863037
HD and SCA1: Tales from two 30-year journeys since gene discovery.
2023
36510111
An RNA-targeting CRISPR-Cas13d system alleviates disease-related phenotypes in Huntington's disease models.
Nat Neurosci
2023
36764301
Large-scale differentiation of iPSC-derived motor neurons from ALS and control subjects.
Neuron
2023
36547263
An altered extracellular matrix-integrin interface contributes to Huntington's disease-associated CNS dysfunction in glial and vascular cells.
Hum Mol Genet
2023
35262656
Translating cell therapies for neurodegenerative diseases: Huntington's disease as a model disorder.
Brain
2022
36590162
Single-nuclei transcriptome analysis of Huntington disease iPSC and mouse astrocytes implicates maturation and functional deficits.
iScience
2022
36543778
Huntington disease oligodendrocyte maturation deficits revealed by single-nucleus RNAseq are rescued by thiamine-biotin supplementation.
Nat Commun
2022
34982109
Isoform-dependent lysosomal degradation and internalization of apolipoprotein E requires autophagy proteins.
Journal of Cell Science
2022
35253772
Diminished LC3-Associated Phagocytosis by Huntington's Disease Striatal Astrocytes.
Journal of Huntington's disease
2022
35115730
Answer ALS, a large-scale resource for sporadic and familial ALS combining clinical and multi-omics data from induced pluripotent cell lines.
Nat Neurosci
2022
34935438
Microglia Do Not Restrict SARS-CoV-2 Replication following Infection of the Central Nervous System of K18-Human ACE2 Transgenic Mice.
Journal of Virology
2022
34816260
Microglia do not restrict SARS-CoV-2 replication following infection of the central nervous system of K18-hACE2 transgenic mice.
2021
33749919
Cell Therapy for Huntington's Disease: Learning from Failure.
Mov Disord
2021
33945510
Huntington's disease mice and human brain tissue exhibit increased G3BP1 granules and TDP43 mislocalization.
J Clin Invest
2021
34866144
A Scoping Review of Dietary Factors Conferring Risk or Protection for Cognitive Decline in APOE ε4 Carriers.
Journal of Nutrition, Health and Aging
2021
34786551
Cooperation of cell adhesion and autophagy in the brain: Functional roles in development and neurodegenerative disease.
Matrix Biology Plus
2021
32984268
Calcium Dynamics in Astrocytes During Cell Injury.
Frontiers in Bioengineering and Biotechnology
2020
31696228
Treatment with JQ1, a BET bromodomain inhibitor, is selectively detrimental to R6/2 Huntington's disease mice.
Human Molecular Genetics
2020
31848580
Microglial depletion prevents extracellular matrix changes and striatal volume reduction in a model of Huntington's disease.
Brain
2020
32109367
Aberrant Development Corrected in Adult-Onset Huntington's Disease iPSC-Derived Neuronal Cultures via WNT Signaling Modulation.
Stem Cell Reports
2020
30994454
Mutant huntingtin impairs PNKP and ATXN3, disrupting DNA repair and transcription.
Elife
2019
31612586
A short note for Mike.
Journal of Neuroscience Research
2019
31088970
IKKβ slows Huntington's disease progression in R6/1 mice.
Proc Natl Acad Sci U S A
2019
29843246
Striatal Mutant Huntingtin Protein Levels Decline with Age in Homozygous Huntington's Disease Knock-In Mouse Models.
Journal of Huntington's disease
2018
28986324
The ubiquitin conjugating enzyme Ube2W regulates solubility of the Huntington's disease protein, huntingtin.
Neurobiol Dis
2018
30452420
Longitudinal Biochemical Assay Analysis of Mutant Huntingtin Exon 1 Protein in R6/2 Mice.
Journal of Huntington's disease
2018
29856014
Cellular Models: HD Patient-Derived Pluripotent Stem Cells.
Methods in Molecular Biology
2018
29311338
Faulty neuronal determination and cell polarization are reverted by modulating HD early phenotypes.
Proceedings of the National Academy of Sciences of the United States of America
2018
29566793
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene.
Neuron
2018
29553509
Fractionation for Resolution of Soluble and Insoluble Huntingtin Species.
Journal of Visualized Experiments
2018
29512295
Therapeutic effects of stem cells in rodent models of Huntington's disease: Review and electrophysiological findings.
CNS Neuroscience and Therapeutics
2018
29199020
The Library of Integrated Network-Based Cellular Signatures NIH Program: System-Level Cataloging of Human Cells Response to Perturbations.
Cell Syst
2018
29233555
Human Neural Stem Cell Transplantation Rescues Functional Deficits in R6/2 and Q140 Huntington's Disease Mice.
Stem Cell Reports
2018
28225193
Human Neural Progenitor Transplantation Rescues Behavior and Reduces α-Synuclein in a Transgenic Model of Dementia with Lewy Bodies.
Stem cells translational medicine
2017
28384479
Mutant Huntingtin Disrupts the Nuclear Pore Complex.
Neuron
2017
28533375
KEAP1-modifying small molecule reveals muted NRF2 signaling responses in neural stem cells from Huntington's disease patients.
Proc Natl Acad Sci U S A
2017
28526555
Modeling Psychomotor Retardation using iPSCs from MCT8-Deficient Patients Indicates a Prominent Role for the Blood-Brain Barrier.
Cell Stem Cell
2017
28968246
Introducing the "Clinical Trials Corner".
Journal of Huntington's disease
2017
28514657
Huntington's Disease iPSC-Derived Brain Microvascular Endothelial Cells Reveal WNT-Mediated Angiogenic and Blood-Brain Barrier Deficits.
Cell Reports
2017
29116112
A Comparison of mRNA Sequencing with Random Primed and 3'-Directed Libraries.
Sci Rep
2017
27601642
TRiC subunits enhance BDNF axonal transport and rescue striatal atrophy in Huntington's disease.
Proc Natl Acad Sci U S A
2016
27427231
SIRT2- and NRF2-Targeting Thiazole-Containing Compound with Therapeutic Activity in Huntington's Disease Models.
Cell Chem Biol
2016
27146268
PIAS1 Regulates Mutant Huntingtin Accumulation and Huntington's Disease-Associated Phenotypes In Vivo.
Neuron
2016
26100538
Huntington's disease cerebrospinal fluid seeds aggregation of mutant huntingtin.
Mol Psychiatry
2015
25398943
Disruption of the nuclear membrane by perinuclear inclusions of mutant huntingtin causes cell-cycle re-entry and striatal cell death in mouse and cell models of Huntington's disease.
Human Molecular Genetics
2015
25556834
Reinstating aberrant mTORC1 activity in Huntington's disease mice improves disease phenotypes.
Neuron
2015
24466111
Fibroblast growth factor receptor 3 interacts with and activates TGFβ-activated kinase 1 tyrosine phosphorylation and NFκB signaling in multiple myeloma and bladder cancer.
PLoS ONE
2014
25575954
Comparison of phosphodiesterase 10A, dopamine receptors D1 and D2 and dopamine transporter ligand binding in the striatum of the R6/2 and BACHD mouse models of Huntington's disease.
Journal of Huntington's disease
2014
1 - 50 of 143
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