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Converging Mechanisms in ALS and FTD: Disrupted RNA and Protein Homeostasis

Neuron (Cambridge, Mass.), 2013-08, Vol.79 (3), p.416-438

2013

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The Seeds of Neurodegeneration: Prion-like Spreading in ALS

Cell, 2011-10, Vol.147 (3), p.498-508

2011

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Rebuilding Chromosomes After Catastrophe: Emerging Mechanisms of Chromothripsis

Trends in cell biology, 2017-12, Vol.27 (12), p.917-930

2017

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ALS: A Disease of Motor Neurons and Their Nonneuronal Neighbors

Neuron (Cambridge, Mass.), 2006-10, Vol.52 (1), p.39-59

2006

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Understanding the role of TDP-43 and FUS/TLS in ALS and beyond

Current opinion in neurobiology, 2011-12, Vol.21 (6), p.904-919

2011

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Premature polyadenylation-mediated loss of stathmin-2 is a hallmark of TDP-43-dependent neurodegeneration

Nature neuroscience, 2019-02, Vol.22 (2), p.180-190

2019

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Antisense Oligonucleotide Therapies for Neurodegenerative Diseases

Annual review of neuroscience, 2019-07, Vol.42 (1), p.385-406

2019

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Non-cell autonomous toxicity in neurodegenerative disorders: ALS and beyond

The Journal of cell biology, 2009-12, Vol.187 (6), p.761-772

2009

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The Fourth Fermi-GBM Gamma-Ray Burst Catalog: A Decade of Data

The Astrophysical journal, 2020-04, Vol.893 (1), p.46

2020

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The SARS-CoV-2 nucleocapsid phosphoprotein forms mutually exclusive condensates with RNA and the membrane-associated M protein

Nature communications, 2021-01, Vol.12 (1), p.502-502, Article 502

2021

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Sustained Therapeutic Reversal of Huntington's Disease by Transient Repression of Huntingtin Synthesis

Neuron (Cambridge, Mass.), 2012-06, Vol.74 (6), p.1031-1044

2012

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Rethinking ALS: The FUS about TDP-43

Cell, 2009-03, Vol.136 (6), p.1001-1004

2009

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Chromoanagenesis and cancer: mechanisms and consequences of localized, complex chromosomal rearrangements

Nature medicine, 2012-11, Vol.18 (11), p.1630-1638

2012

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Cytoplasmic TDP-43 De-mixing Independent of Stress Granules Drives Inhibition of Nuclear Import, Loss of Nuclear TDP-43, and Cell Death

Neuron (Cambridge, Mass.), 2019-04, Vol.102 (2), p.339-357.e7

2019

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Prion-like spread of protein aggregates in neurodegeneration

The Journal of experimental medicine, 2012-05, Vol.209 (5), p.889-893

2012

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Degeneration and impaired regeneration of gray matter oligodendrocytes in amyotrophic lateral sclerosis

Nature neuroscience, 2013-05, Vol.16 (5), p.571-579

2013

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DNA Sequence-Specific Binding of CENP-B Enhances the Fidelity of Human Centromere Function

Developmental cell, 2015-05, Vol.33 (3), p.314-327

2015

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Losing balance: the origin and impact of aneuploidy in cancer

EMBO reports, 2012-06, Vol.13 (6), p.501-514

2012

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Single-Stranded RNAs Use RNAi to Potently and Allele-Selectively Inhibit Mutant Huntingtin Expression

Cell, 2012-08, Vol.150 (5), p.895-908

2012

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The Fermi-GBM Gamma-Ray Burst Spectral Catalog: 10 yr of Data

The Astrophysical journal, 2021-05, Vol.913 (1), p.60

2021

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Centrosome Amplification Is Sufficient to Promote Spontaneous Tumorigenesis in Mammals

Developmental cell, 2017-02, Vol.40 (3), p.313-322.e5

2017

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Chromothripsis drives the evolution of gene amplification in cancer

Nature (London), 2021-03, Vol.591 (7848), p.137-141

2021

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Inducible, reversible system for the rapid and complete degradation of proteins in mammalian cells

Proceedings of the National Academy of Sciences - PNAS, 2012-12, Vol.109 (49), p.E3350-E3357

2012

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Targeted degradation of sense and antisense C9orf72 RNA foci as therapy for ALS and frontotemporal degeneration

Proceedings of the National Academy of Sciences - PNAS, 2013-11, Vol.110 (47), p.E4530-E4539

2013

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Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43

Nature neuroscience, 2011-04, Vol.14 (4), p.459-468

2011

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Converging Mechanisms in ALS and FTD: Disrupted RNA and Protein Homeostasis

The Seeds of Neurodegeneration: Prion-like Spreading in ALS

Rebuilding Chromosomes After Catastrophe: Emerging Mechanisms of Chromothripsis

ALS: A Disease of Motor Neurons and Their Nonneuronal Neighbors

Understanding the role of TDP-43 and FUS/TLS in ALS and beyond

Premature polyadenylation-mediated loss of stathmin-2 is a hallmark of TDP-43-dependent neurodegeneration

Antisense Oligonucleotide Therapies for Neurodegenerative Diseases

Non-cell autonomous toxicity in neurodegenerative disorders: ALS and beyond

The Fourth Fermi-GBM Gamma-Ray Burst Catalog: A Decade of Data

The SARS-CoV-2 nucleocapsid phosphoprotein forms mutually exclusive condensates with RNA and the membrane-associated M protein

Sustained Therapeutic Reversal of Huntington's Disease by Transient Repression of Huntingtin Synthesis

Rethinking ALS: The FUS about TDP-43

Chromoanagenesis and cancer: mechanisms and consequences of localized, complex chromosomal rearrangements

Cytoplasmic TDP-43 De-mixing Independent of Stress Granules Drives Inhibition of Nuclear Import, Loss of Nuclear TDP-43, and Cell Death

Prion-like spread of protein aggregates in neurodegeneration

Degeneration and impaired regeneration of gray matter oligodendrocytes in amyotrophic lateral sclerosis

DNA Sequence-Specific Binding of CENP-B Enhances the Fidelity of Human Centromere Function

Losing balance: the origin and impact of aneuploidy in cancer

Single-Stranded RNAs Use RNAi to Potently and Allele-Selectively Inhibit Mutant Huntingtin Expression

The Fermi-GBM Gamma-Ray Burst Spectral Catalog: 10 yr of Data

Centrosome Amplification Is Sufficient to Promote Spontaneous Tumorigenesis in Mammals

Chromothripsis drives the evolution of gene amplification in cancer

Inducible, reversible system for the rapid and complete degradation of proteins in mammalian cells

Targeted degradation of sense and antisense C9orf72 RNA foci as therapy for ALS and frontotemporal degeneration

Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43

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