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Distinct translatome changes in specific neural populations precede electroencephalographic changes in prion-infected mice

PLoS pathogens, 2022-08, Vol.18 (8), p.e1010747-e1010747

2022

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Selective vulnerability to neurodegenerative disease: the curious case of Prion Protein

Disease models & mechanisms, 2014-01, Vol.7 (1), p.21-29

Jackson, Walker S

2014

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Etiology matters: genetic and acquired prion diseases engage different mechanisms at a presymptomatic stage

Neural regeneration research, 2023-12, Vol.18 (12), p.2707-2708

Jackson, Walker

2023

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Memory trace interference impairs recall in a mouse model of Alzheimer's disease

Nature neuroscience, 2020-08, Vol.23 (8), p.952-958

2020

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Epigenetic alterations in longevity regulators, reduced life span, and exacerbated aging-related pathology in old father offspring mice

Proceedings of the National Academy of Sciences - PNAS, 2018-03, Vol.115 (10), p.E2348-E2357

2018

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Anti-prion drugs do not improve survival in novel knock-in models of inherited prion disease

PLoS pathogens, 2024-04, Vol.20 (4), p.e1012087-e1012087

2024

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Manipulating the Prion Protein Gene Sequence and Expression Levels with CRISPR/Cas9

PloS one, 2016-04, Vol.11 (4), p.e0154604

2016

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The natural Disc1-deletion present in several inbred mouse strains does not affect sleep

Scientific reports, 2017-07, Vol.7 (1), p.5665-12, Article 5665

2017

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Slc1a3-2A-CreERT2 mice reveal unique features of Bergmann glia and augment a growing collection of Cre drivers and effectors in the 129S4 genetic background

Scientific reports, 2021-03, Vol.11 (1), p.5412-5412, Article 5412

2021

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Intraflagellar transport is essential for endochondral bone formation

Development (Cambridge), 2007-01, Vol.134 (2), p.307-316

2007

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Selective Vulnerability to Neurodegenerative Disease: Insights from Cell Type-Specific Translatome Studies

Biology (Basel, Switzerland), 2024, Vol.13 (2), p.67

2024

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CalDAG-GEFI mediates striatal cholinergic modulation of dendritic excitability, synaptic plasticity and psychomotor behaviors

Neurobiology of disease, 2021-10, Vol.158, p.105473-105473, Article 105473

2021

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Structural and mechanistic aspects influencing the ADAM10-mediated shedding of the prion protein

Molecular neurodegeneration, 2018-04, Vol.13 (1), p.18-18, Article 18

2018

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Cerebellar granule neurons induce Cyclin D1 before the onset of motor symptoms in Huntington's disease mice

Acta neuropathologica communications, 2023-01, Vol.11 (1), p.17-17, Article 17

2023

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Spontaneous Generation of Prion Infectivity in Fatal Familial Insomnia Knockin Mice

Neuron (Cambridge, Mass.), 2009-08, Vol.63 (4), p.438-450

2009

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power of automated high-resolution behavior analysis revealed by its application to mouse models of Huntington's and prion diseases

Proceedings of the National Academy of Sciences - PNAS, 2007-02, Vol.104 (6), p.1983-1988

2007

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Peculiarities of prion diseases

PLoS pathogens, 2014-11, Vol.10 (11), p.e1004451-e1004451

2014

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Requirements for Mutant and Wild-Type Prion Protein Misfolding In Vitro

Biochemistry (Easton), 2015-02, Vol.54 (5), p.1180-1187

2015

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Profoundly different prion diseases in knock-in mice carrying single PrP codon substitutions associated with human diseases

Proceedings of the National Academy of Sciences - PNAS, 2013-09, Vol.110 (36), p.14759-14764

2013

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Translation of the prion protein mRNA is robust in astrocytes but does not amplify during reactive astrocytosis in the mouse brain

PloS one, 2014-04, Vol.9 (4), p.e95958-e95958

2014

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Heat shock factor 1 regulates lifespan as distinct from disease onset in prion disease

Proceedings of the National Academy of Sciences - PNAS, 2008-09, Vol.105 (36), p.13626-13631

2008

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Application of a RiboTag‐based approach to generate and analyze mRNA from enteric neural cells

Neurogastroenterology and motility, 2022-07, Vol.34 (7), p.e14309-n/a

2022

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Stroke target identification guided by astrocyte transcriptome analysis

Glia, 2019-04, Vol.67 (4), p.619-633

2019

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Convergent generation of atypical prions in knockin mouse models of genetic prion disease

The Journal of clinical investigation, 2024-08, Vol.134 (15), p.1-15

2024

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Therapeutic Trial of anle138b in Mouse Models of Genetic Prion Disease

Journal of virology, 2023-02, Vol.97 (2), p.e0167222-e0167222

2023

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Distinct translatome changes in specific neural populations precede electroencephalographic changes in prion-infected mice

Selective vulnerability to neurodegenerative disease: the curious case of Prion Protein

Etiology matters: genetic and acquired prion diseases engage different mechanisms at a presymptomatic stage

Memory trace interference impairs recall in a mouse model of Alzheimer's disease

Epigenetic alterations in longevity regulators, reduced life span, and exacerbated aging-related pathology in old father offspring mice

Anti-prion drugs do not improve survival in novel knock-in models of inherited prion disease

Manipulating the Prion Protein Gene Sequence and Expression Levels with CRISPR/Cas9

The natural Disc1-deletion present in several inbred mouse strains does not affect sleep

Slc1a3-2A-CreERT2 mice reveal unique features of Bergmann glia and augment a growing collection of Cre drivers and effectors in the 129S4 genetic background

Intraflagellar transport is essential for endochondral bone formation

Selective Vulnerability to Neurodegenerative Disease: Insights from Cell Type-Specific Translatome Studies

CalDAG-GEFI mediates striatal cholinergic modulation of dendritic excitability, synaptic plasticity and psychomotor behaviors

Structural and mechanistic aspects influencing the ADAM10-mediated shedding of the prion protein

Cerebellar granule neurons induce Cyclin D1 before the onset of motor symptoms in Huntington's disease mice

Spontaneous Generation of Prion Infectivity in Fatal Familial Insomnia Knockin Mice

power of automated high-resolution behavior analysis revealed by its application to mouse models of Huntington's and prion diseases

Peculiarities of prion diseases

Requirements for Mutant and Wild-Type Prion Protein Misfolding In Vitro

Profoundly different prion diseases in knock-in mice carrying single PrP codon substitutions associated with human diseases

Translation of the prion protein mRNA is robust in astrocytes but does not amplify during reactive astrocytosis in the mouse brain

Heat shock factor 1 regulates lifespan as distinct from disease onset in prion disease

Application of a RiboTag‐based approach to generate and analyze mRNA from enteric neural cells

Stroke target identification guided by astrocyte transcriptome analysis

Convergent generation of atypical prions in knockin mouse models of genetic prion disease

Therapeutic Trial of anle138b in Mouse Models of Genetic Prion Disease

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