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Open questions on the nature of Parkinson's disease: from triggers to spreading pathology

Journal of medical genetics, 2020-02, Vol.57 (2), p.73-81

2020

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D159 and S167 are protective residues in the prion protein from dog and horse, two prion-resistant animals

Neurobiology of disease, 2018-11, Vol.119, p.1-12

2018

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Intrinsic determinants of prion protein neurotoxicity in Drosophila: from sequence to (dys)function

Frontiers in molecular neuroscience, 2023-08, Vol.16, p.1231079-1231079

2023

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Conformational dynamics as an intrinsic determinant of prion protein misfolding and neurotoxicity

Neural regeneration research, 2024-10, Vol.19 (10), p.2095-2096

2024

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Insight From Animals Resistant to Prion Diseases: Deciphering the Genotype – Morphotype – Phenotype Code for the Prion Protein

Frontiers in cellular neuroscience, 2020-08, Vol.14, p.254-254

2020

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Stress and viral insults do not trigger E200K PrP conversion in human cerebral organoids

PloS one, 2022-10, Vol.17 (10), p.e0277051-e0277051

2022

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Fingolimod phosphate attenuates oligomeric amyloid β-induced neurotoxicity via increased brain-derived neurotrophic factor expression in neurons

PloS one, 2013-04, Vol.8 (4), p.e61988

2013

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Hybrid 2-[18F] FDG PET/MRI in premanifest Huntington’s disease gene-expansion carriers: The significance of partial volume correction

PloS one, 2021-06, Vol.16 (6), p.e0252683-e0252683

2021

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Genetics of Parkinson’s disease and related disorders

Journal of medical genetics, 2018-02, Vol.55 (2), p.73-80

2018

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Loss of the Spinocerebellar Ataxia type 3 disease protein ATXN3 alters transcription of multiple signal transduction pathways

PloS one, 2018-09, Vol.13 (9), p.e0204438-e0204438

2018

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A 1 bp deletion in HACE1 causes ataxia in Norwegian elkhound, black

PloS one, 2022-01, Vol.17 (1), p.e0261845

2022

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Drosophila models of proteinopathies: the little fly that could

Current pharmaceutical design, 2012-03, Vol.18 (8), p.1108-1122

2012

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Linking aβ42-induced hyperexcitability to neurodegeneration, learning and motor deficits, and a shorter lifespan in an Alzheimer's model

PLoS genetics, 2015-03, Vol.11 (3), p.e1005025-e1005025

2015

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Etersalate prevents the formations of 6Aβ16-22 oligomer: An in silico study

PloS one, 2018-09, Vol.13 (9), p.e0204026

2018

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Repeat Associated Non-AUG Translation (RAN Translation) Dependent on Sequence Downstream of the ATXN2 CAG Repeat

PloS one, 2015-06, Vol.10 (6), p.e0128769

2015

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GSK3β inhibition promotes synaptogenesis in Drosophila and mammalian neurons

PloS one, 2015-03, Vol.10 (3), p.e0118475-e0118475

2015

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New Drosophila models to uncover the intrinsic and extrinsic factors that mediate the toxicity of the human prion protein

Disease models & mechanisms, 2022-04, Vol.15 (4)

2022

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Improved high sensitivity screen for Huntington disease using a one-step triplet-primed PCR and melting curve assay

PloS one, 2017-07, Vol.12 (7), p.e0180984-e0180984

2017

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Characterization of the structural and functional determinants of MANF/CDNF in Drosophila in vivo model

PloS one, 2013-09, Vol.8 (9), p.e73928-e73928

2013

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Neuron-type specific functions of DNT1, DNT2 and Spz at the Drosophila neuromuscular junction

PloS one, 2013-10, Vol.8 (10), p.e75902-e75902

2013

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β-glucuronidase use as a single internal control gene may confound analysis in FMR1 mRNA toxicity studies

PloS one, 2018-02, Vol.13 (2), p.e0192151

2018

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Activation of JNK signaling mediates amyloid-ß-dependent cell death

PloS one, 2011-09, Vol.6 (9), p.e24361

2011

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FRET-assisted determination of CLN3 membrane topology

PloS one, 2014-07, Vol.9 (7), p.e102593-e102593

2014

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The pathogenic aβ43 is enriched in familial and sporadic Alzheimer disease

PloS one, 2013, Vol.8 (2), p.e55847

2013

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Pharmacological inhibition of CXCR2 chemokine receptors modulates paraquat-induced intoxication in rats

PloS one, 2014-08, Vol.9 (8), p.e105740

2014

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Open questions on the nature of Parkinson's disease: from triggers to spreading pathology

D159 and S167 are protective residues in the prion protein from dog and horse, two prion-resistant animals

Intrinsic determinants of prion protein neurotoxicity in Drosophila: from sequence to (dys)function

Conformational dynamics as an intrinsic determinant of prion protein misfolding and neurotoxicity

Insight From Animals Resistant to Prion Diseases: Deciphering the Genotype – Morphotype – Phenotype Code for the Prion Protein

Stress and viral insults do not trigger E200K PrP conversion in human cerebral organoids

Fingolimod phosphate attenuates oligomeric amyloid β-induced neurotoxicity via increased brain-derived neurotrophic factor expression in neurons

Hybrid 2-[18F] FDG PET/MRI in premanifest Huntington’s disease gene-expansion carriers: The significance of partial volume correction

Genetics of Parkinson’s disease and related disorders

Loss of the Spinocerebellar Ataxia type 3 disease protein ATXN3 alters transcription of multiple signal transduction pathways

A 1 bp deletion in HACE1 causes ataxia in Norwegian elkhound, black

Drosophila models of proteinopathies: the little fly that could

Linking aβ42-induced hyperexcitability to neurodegeneration, learning and motor deficits, and a shorter lifespan in an Alzheimer's model

Etersalate prevents the formations of 6Aβ16-22 oligomer: An in silico study

Repeat Associated Non-AUG Translation (RAN Translation) Dependent on Sequence Downstream of the ATXN2 CAG Repeat

GSK3β inhibition promotes synaptogenesis in Drosophila and mammalian neurons

New Drosophila models to uncover the intrinsic and extrinsic factors that mediate the toxicity of the human prion protein

Improved high sensitivity screen for Huntington disease using a one-step triplet-primed PCR and melting curve assay

Characterization of the structural and functional determinants of MANF/CDNF in Drosophila in vivo model

Neuron-type specific functions of DNT1, DNT2 and Spz at the Drosophila neuromuscular junction

β-glucuronidase use as a single internal control gene may confound analysis in FMR1 mRNA toxicity studies

Activation of JNK signaling mediates amyloid-ß-dependent cell death

FRET-assisted determination of CLN3 membrane topology

The pathogenic aβ43 is enriched in familial and sporadic Alzheimer disease

Pharmacological inhibition of CXCR2 chemokine receptors modulates paraquat-induced intoxication in rats

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