Intrabody applications in neurological disorders: progress and future prospects (Q33217378)

24 July 2017

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title

Intrabody applications in neurological disorders: progress and future prospects (English)

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24 July 2017

Todd W Miller

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24 July 2017

Anne Messer

series ordinal

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24 July 2017

publication date

1 September 2005

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24 July 2017

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24 July 2017

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24 July 2017

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24 July 2017

page(s)

394-401

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Intrabodies: production and promise

24 July 2017

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Prevention of scrapie pathogenesis by transgenic expression of anti-prion protein antibodies

7 January 2021

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Conversion of PrP to a self-perpetuating PrPSc-like conformation in the cytosol

7 January 2021

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Neurotoxicity and neurodegeneration when PrP accumulates in the cytosol

7 January 2021

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Molecular mechanisms of neurotoxicity of pathological prion protein

7 January 2021

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Scrapie-specific neuronal lesions are independent of neuronal PrP expression

7 January 2021

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Role of the prion protein in copper turnover in astrocytes

7 January 2021

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Extended half-life and elevated steady-state level of a single-chain Fv intrabody are critical for specific intracellular retargeting of its antigen, caspase-7.

7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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Huntingtin interacts with a family of WW domain proteins

7 January 2021

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Expansion of polyglutamine repeat in huntingtin leads to abnormal protein interactions involving calmodulin

7 January 2021

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Proteasomal-dependent aggregate reversal and absence of cell death in a conditional mouse model of Huntington's disease.

7 January 2021

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Reversal of neuropathology and motor dysfunction in a conditional model of Huntington's disease

7 January 2021

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7 January 2021

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7 January 2021

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7 January 2021

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Generation of beta-amyloid in the secretory pathway in neuronal and nonneuronal cells

7 January 2021

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Normal cellular processing of the beta-amyloid precursor protein results in the secretion of the amyloid beta peptide and related molecules

7 January 2021

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Production of the Alzheimer amyloid beta protein by normal proteolytic processing

7 January 2021

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Neuropathological stageing of Alzheimer-related changes

7 January 2021

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A strategy for designing inhibitors of alpha-synuclein aggregation and toxicity as a novel treatment for Parkinson's disease and related disorders

7 January 2021

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Zeroing in on the pathogenic form of alpha-synuclein and its mechanism of neurotoxicity in Parkinson's disease

7 January 2021

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Scrapie protein degradation by cysteine proteases in CD11c+ dendritic cells and GT1-1 neuronal cells

7 January 2021

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Molecular biology of prion diseases

7 January 2021

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Conversion of alpha-helices into beta-sheets features in the formation of the scrapie prion proteins

7 January 2021

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Secondary structure analysis of the scrapie-associated protein PrP 27-30 in water by infrared spectroscopy

7 January 2021

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Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant allele

7 January 2021

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Nitration of tau protein is linked to neurodegeneration in tauopathies

7 January 2021

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Tau phosphorylation, tangles, and neurodegeneration: the chicken or the egg?

7 January 2021

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Abnormal tau-containing filaments in neurodegenerative diseases

7 January 2021

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USP7, a ubiquitin-specific protease, interacts with ataxin-1, the SCA1 gene product

7 January 2021

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Serine 776 of ataxin-1 is critical for polyglutamine-induced disease in SCA1 transgenic mice

7 January 2021

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alpha-Synuclein is phosphorylated in synucleinopathy lesions

7 January 2021

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Hyperphosphorylation and insolubility of alpha-synuclein in transgenic mouse oligodendrocytes

7 January 2021

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Phosphorylated alpha-synuclein is ubiquitinated in alpha-synucleinopathy lesions

7 January 2021

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Widespread nitration of pathological inclusions in neurodegenerative synucleinopathies

7 January 2021

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Dityrosine cross-linking promotes formation of stable alpha -synuclein polymers. Implication of nitrative and oxidative stress in the pathogenesis of neurodegenerative synucleinopathies

7 January 2021

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Tyrosine 125 of alpha-synuclein plays a critical role for dimerization following nitrative stress.

7 January 2021

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The precursor of Alzheimer's disease amyloid A4 protein resembles a cell-surface receptor

7 January 2021

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Distinct cleavage patterns of normal and pathologic forms of alpha-synuclein by calpain I in vitro

7 January 2021

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Human alpha-synuclein-harboring familial Parkinson's disease-linked Ala-53 --> Thr mutation causes neurodegenerative disease with alpha-synuclein aggregation in transgenic mice

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YMTHE.2005.04.003

Protein aggregation and neurodegenerative disease

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YMTHE.2005.04.003

Conformation-dependent antibodies target diseases of protein misfolding

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YMTHE.2005.04.003

Abnormal isoform of prion protein accumulates in follicular dendritic cells in mice with Creutzfeldt-Jakob disease

7 January 2021

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10.1016/J.YMTHE.2005.04.003

7 January 2021

Identifiers

DOI

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24 July 2017

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