(Q40138642)

17 September 2017

title

Amyloid fibrils of mammalian prion protein induce axonal degeneration in NTERA2-derived terminally differentiated neurons (English)

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17 September 2017

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Vera Novitskaya

1

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17 September 2017

Natallia Makarava

2

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17 September 2017

Ian Sylvester

3

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17 September 2017

Igor B Bronstein

4

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17 September 2017

Ilia V Baskakov

5

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17 September 2017

language of work or name

English

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publication date

1 May 2007

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Journal of Neurochemistry

17 September 2017

published in

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17 September 2017

volume

102

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17 September 2017

issue

2

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17 September 2017

page(s)

398-407

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Gene regulation during neuronal and non-neuronal differentiation of NTERA2 human teratocarcinoma-derived stem cells

17 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Retinoic acid induces neuronal differentiation of a cloned human embryonal carcinoma cell line in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Human NT2/D1 cells differentiate into functional astrocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

In vitro conversion of mammalian prion protein into amyloid fibrils displays unusual features

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Folding of prion protein to its native alpha-helical conformation is under kinetic control

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

In vitro conversion of full-length mammalian prion protein produces amyloid form with physical properties of PrP(Sc).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Copper(II) inhibits in vitro conversion of prion protein into amyloid fibrils.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Methionine oxidation interferes with conversion of the prion protein into the fibrillar proteinase K-resistant conformation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Role of microglia and host prion protein in neurotoxicity of a prion protein fragment.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Axonal transport and neurodegenerative disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Bax deletion prevents neuronal loss but not neurological symptoms in a transgenic model of inherited prion disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Synaptic changes characterize early behavioural signs in the ME7 model of murine prion disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Neurochemical diversity of dystrophic neurites in the early and late stages of Alzheimer's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Neurotoxicity of a prion protein fragment

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Neuronal cell death in scrapie-infected mice is due to apoptosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Do disorders of movement cause movement disorders and dementia?

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Disruption of Axonal Transport by Loss of Huntingtin or Expression of Pathogenic PolyQ Proteins in Drosophila

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Functional synapses are formed between human NTera2 (NT2N, hNT) neurons grown on astrocytes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Distinct roles for sodium, chloride, and calcium in excitotoxic dendritic injury and recovery.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Caspase-12 and endoplasmic reticulum stress mediate neurotoxicity of pathological prion protein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Functional and morphological changes induced by transient in vivo ischemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Onset of accumulation of PrPres in murine ME7 scrapie in relation to pathological and PrP immunohistochemical changes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Neurotoxicity and neurodegeneration when PrP accumulates in the cytosol

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Neuritic degeneration in the hippocampus and amygdala in Parkinson's disease in relation to Alzheimer pathology

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Expression of neuronal markers during NTera2/cloneD1 differentiation by cell aggregation method.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Neuronal protein GAP-43 is a member of novel group of brain acid-soluble proteins (BASPs).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Probing the conformation of the prion protein within a single amyloid fibril using a novel immunoconformational assay.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Novel differences between two human prion strains revealed by two-dimensional gel electrophoresis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Axonal transport defects: a common theme in neurodegenerative diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Accumulation of phosphorylated alpha-synuclein in aging human brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Molecular mechanisms of glutamate neurotoxicity in mixed cultures of NT2-derived neurons and astrocytes: protective effects of coenzyme Q10.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

The most infectious prion protein particles.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Prion protein (PrPc) positively regulates neural precursor proliferation during developmental and adult mammalian neurogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Axonopathy and transport deficits early in the pathogenesis of Alzheimer's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Neuritic beading induced by activated microglia is an early feature of neuronal dysfunction toward neuronal death by inhibition of mitochondrial respiration and axonal transport

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Fibrillar amyloid deposition leads to local synaptic abnormalities and breakage of neuronal branches.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

Amyloid Fibrils of Mammalian Prion Protein Are Highly Toxic to Cultured Cells and Primary Neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1471-4159.2007.04537.X

10.1111/J.1471-4159.2007.04537.X

21 January 2018

Identifiers

DOI

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release_b4swk4wagrh2rkimdiongtzchy

17 September 2017

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/b4swk4wagrh2rkimdiongtzchy

mapped directly with Wikidata item

24 November 2022

based on heuristic

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