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Deer Prion Proteins Modulate the Emergence and Adaptation of Chronic Wasting Disease Strains

Journal of virology, 2015-12, Vol.89 (24), p.12362-12373

2015

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Pathologic tau conformer ensembles induce dynamic, liquid-liquid phase separation events at the nuclear envelope

BMC biology, 2021-09, Vol.19 (1), p.199-199, Article 199

2021

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Quaternary Structure Changes for PrPSc Predate PrPC Downregulation and Neuronal Death During Progression of Experimental Scrapie Disease

Molecular neurobiology, 2021, Vol.58 (1), p.375-390

2021

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Diverse, evolving conformer populations drive distinct phenotypes in frontotemporal lobar degeneration caused by the same MAPT-P301L mutation

Acta neuropathologica, 2020-06, Vol.139 (6), p.1045-1070

2020

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Knockout of the prion protein (PrP)-like Sprn gene does not produce embryonic lethality in combination with PrPc-deficiency

Proceedings of the National Academy of Sciences - PNAS, 2012-06, Vol.109 (23), p.9035-9040

2012

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Substitutions of PrP N-terminal histidine residues modulate scrapie disease pathogenesis and incubation time in transgenic mice

PloS one, 2017-12, Vol.12 (12), p.e0188989-e0188989

2017

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Interactome analyses identify ties of PrP and its mammalian paralogs to oligomannosidic N-glycans and endoplasmic reticulum-derived chaperones

PLoS pathogens, 2009-10, Vol.5 (10), p.e1000608-e1000608

2009

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Correction to: Diverse, evolving conformer populations drive distinct phenotypes in frontotemporal lobar degeneration caused by the same MAPT‑P301L mutation

Acta neuropathologica, 2021-03, Vol.141 (3), p.467-468

2021

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Amyloid beta precursor protein and prion protein have a conserved interaction affecting cell adhesion and CNS development

PloS one, 2012-12, Vol.7 (12), p.e51305

2012

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The CNS in inbred transgenic models of 4-repeat Tauopathy develops consistent tau seeding capacity yet focal and diverse patterns of protein deposition

Molecular neurodegeneration, 2017-10, Vol.12 (1), p.72-72, Article 72

2017

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Mice Treated Subcutaneously with Mouse LPS-Converted PrPres or LPS Alone Showed Brain Gene Expression Profiles Characteristic of Prion Disease

Veterinary sciences, 2021-09, Vol.8 (9), p.200

2021

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Specific inhibition of pathological prion protein accumulation by small interfering RNAs

Journal of cell science, 2003-07, Vol.116 (Pt 13), p.2775-2779

2003

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A Common Phenotype Polymorphism in Mammalian Brains Defined by Concomitant Production of Prolactin and Growth Hormone

PloS one, 2016-02, Vol.11 (2), p.e0149410-e0149410

2016

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Octarepeat region flexibility impacts prion function, endoproteolysis and disease manifestation

EMBO molecular medicine, 2015-03, Vol.7 (3), p.339-356

2015

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Down-Regulation of Shadoo in Prion Infections Traces a Pre-Clinical Event Inversely Related to PrPSc Accumulation

PLoS pathogens, 2011-11, Vol.7 (11), p.e1002391

2011

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Down-regulation of Shadoo in prion infections traces a pre-clinical event inversely related to PrP(Sc) accumulation

PLoS pathogens, 2011-11, Vol.7 (11), p.e1002391-e1002391

2011

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PrPc Does Not Mediate Internalization of PrPSc but Is Required at an Early Stage for De Novo Prion Infection of Rov Cells

Journal of Virology, 2007-10, Vol.81 (19), p.10786-10791

2007

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Frequent Missense and Insertion/Deletion Polymorphisms in the Ovine Shadoo Gene Parallel Species-Specific Variation in PrP

PloS one, 2009-08, Vol.4 (8), p.e6538-e6538

2009

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Biological properties of the PrP-like Shadoo protein

Frontiers in bioscience (Landmark. Print), 2011-01, Vol.16 (4), p.1505

2011

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Application of high-throughput, capillary-based Western analysis to modulated cleavage of the cellular prion protein

The Journal of biological chemistry, 2019-02, Vol.294 (8), p.2642-5291

2019

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Correction to: Diverse, evolving conformer populations drive distinct phenotypes in frontotemporal lobar degeneration caused by the same MAPTâP301L mutation

Acta neuropathologica, 2021-03, Vol.141 (3), p.467

2021

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Prion protein with a mutant N-terminal octarepeat region undergoes cobalamin-dependent assembly into high–molecular weight complexes

The Journal of biological chemistry, 2022-04, Vol.298 (4), p.101770-101770, Article 101770

2022

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Identification of Intermediate Steps in the Conversion of a Mutant Prion Protein to a Scrapie-like Form in Cultured Cells

The Journal of biological chemistry, 1997-04, Vol.272 (17), p.11604-11612

1997

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Shadoo/PrP (Sprn0/0/Prnp0/0) double knockout mice: More than zeroes

Prion, 2012-11, Vol.6 (5), p.420-424

2012

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Deer Prion Proteins Modulate the Emergence and Adaptation of Chronic Wasting Disease Strains

Pathologic tau conformer ensembles induce dynamic, liquid-liquid phase separation events at the nuclear envelope

Quaternary Structure Changes for PrPSc Predate PrPC Downregulation and Neuronal Death During Progression of Experimental Scrapie Disease

Diverse, evolving conformer populations drive distinct phenotypes in frontotemporal lobar degeneration caused by the same MAPT-P301L mutation

Knockout of the prion protein (PrP)-like Sprn gene does not produce embryonic lethality in combination with PrPc-deficiency

Substitutions of PrP N-terminal histidine residues modulate scrapie disease pathogenesis and incubation time in transgenic mice

Interactome analyses identify ties of PrP and its mammalian paralogs to oligomannosidic N-glycans and endoplasmic reticulum-derived chaperones

Correction to: Diverse, evolving conformer populations drive distinct phenotypes in frontotemporal lobar degeneration caused by the same MAPT‑P301L mutation

Amyloid beta precursor protein and prion protein have a conserved interaction affecting cell adhesion and CNS development

The CNS in inbred transgenic models of 4-repeat Tauopathy develops consistent tau seeding capacity yet focal and diverse patterns of protein deposition

A novel Gerstmann-Sträussler-Scheinker disease mutation defines a precursor for amyloidogenic 8 kDa PrP fragments and reveals N-terminal structural changes shared by other GSS alleles

Mice Treated Subcutaneously with Mouse LPS-Converted PrPres or LPS Alone Showed Brain Gene Expression Profiles Characteristic of Prion Disease

Specific inhibition of pathological prion protein accumulation by small interfering RNAs

A Common Phenotype Polymorphism in Mammalian Brains Defined by Concomitant Production of Prolactin and Growth Hormone

Octarepeat region flexibility impacts prion function, endoproteolysis and disease manifestation

Down-Regulation of Shadoo in Prion Infections Traces a Pre-Clinical Event Inversely Related to PrPSc Accumulation

Down-regulation of Shadoo in prion infections traces a pre-clinical event inversely related to PrP(Sc) accumulation

PrPc Does Not Mediate Internalization of PrPSc but Is Required at an Early Stage for De Novo Prion Infection of Rov Cells

Frequent Missense and Insertion/Deletion Polymorphisms in the Ovine Shadoo Gene Parallel Species-Specific Variation in PrP

Biological properties of the PrP-like Shadoo protein

Application of high-throughput, capillary-based Western analysis to modulated cleavage of the cellular prion protein

Correction to: Diverse, evolving conformer populations drive distinct phenotypes in frontotemporal lobar degeneration caused by the same MAPTâP301L mutation

Prion protein with a mutant N-terminal octarepeat region undergoes cobalamin-dependent assembly into high–molecular weight complexes

Identification of Intermediate Steps in the Conversion of a Mutant Prion Protein to a Scrapie-like Form in Cultured Cells

Shadoo/PrP (Sprn0/0/Prnp0/0) double knockout mice: More than zeroes

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