Phosphate dependent and independent neurofilament epitopes in the axonal swellings of patients with motor neuron disease and controls.
about
Overexpression of the human NFM subunit in transgenic mice modifies the level of endogenous NFL and the phosphorylation state of NFH subunitsThe fluorescent Congo red derivative, (trans, trans)-1-bromo-2,5-bis-(3-hydroxycarbonyl-4-hydroxy)styrylbenzene (BSB), labels diverse beta-pleated sheet structures in postmortem human neurodegenerative disease brainsEpitope map of neurofilament protein domains in cortical and peripheral nervous system Lewy bodies.Alzheimer disease tangles share immunological similarities with multiphosphorylation repeats in the two large neurofilament proteinsA mutation affecting the sodium/proton exchanger, SLC9A6, causes mental retardation with tau deposition.A simple test to monitor the motor dysfunction in a transgenic mouse model of amyotrophic lateral sclerosisThe cytoskeleton in neurodegenerative diseases.alpha-internexin is present in the pathological inclusions of neuronal intermediate filament inclusion disease.Tau and alpha-synuclein pathology in amygdala of Parkinsonism-dementia complex patients of GuamPesticide exposure exacerbates alpha-synucleinopathy in an A53T transgenic mouse modelPurification and characterization of Lewy bodies from the brains of patients with diffuse Lewy body disease.The neuroendocrine and neural profiles of neuroblastomas, ganglioneuroblastomas, and ganglioneuromas.Relative abundance of tau and neurofilament epitopes in hippocampal neurofibrillary tangles.Phosphate-dependent and independent neurofilament protein epitopes are expressed throughout the cell cycle in human medulloblastoma (D283 MED) cells.Phenotypic and genotypic analysis of a human medulloblastoma cell line and transplantable xenograft (D341 Med) demonstrating amplification of c-mycFragmentation of the Golgi apparatus of motor neurons in amyotrophic lateral sclerosisFragmentation of the Golgi apparatus of motor neurons in amyotrophic lateral sclerosis (ALS). Clinical studies in ALS of Guam and experimental studies in deafferented neurons and in beta,beta'-iminodipropionitrile axonopathy.Clinical and neuropathologic variation in neuronal intermediate filament inclusion diseaseNeurofilaments and orthograde transport are reduced in ventral root axons of transgenic mice that express human SOD1 with a G93A mutationalpha-Internexin aggregates are abundant in neuronal intermediate filament inclusion disease (NIFID) but rare in other neurodegenerative diseasesTransgenic mice carrying a human mutant superoxide dismutase transgene develop neuronal cytoskeletal pathology resembling human amyotrophic lateral sclerosis lesions.Nerve growth factor receptor expression in peripheral and central neuroectodermal tumors, other pediatric brain tumors, and during development of the adrenal gland.
P2860
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P2860
Phosphate dependent and independent neurofilament epitopes in the axonal swellings of patients with motor neuron disease and controls.
description
1987 nî lūn-bûn
@nan
1987 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
1987 թվականի մարտին հրատարակված գիտական հոդված
@hy
1987年の論文
@ja
1987年論文
@yue
1987年論文
@zh-hant
1987年論文
@zh-hk
1987年論文
@zh-mo
1987年論文
@zh-tw
1987年论文
@wuu
name
Phosphate dependent and indepe ...... r neuron disease and controls.
@ast
Phosphate dependent and indepe ...... r neuron disease and controls.
@en
type
label
Phosphate dependent and indepe ...... r neuron disease and controls.
@ast
Phosphate dependent and indepe ...... r neuron disease and controls.
@en
prefLabel
Phosphate dependent and indepe ...... r neuron disease and controls.
@ast
Phosphate dependent and indepe ...... r neuron disease and controls.
@en
P2093
P1476
Phosphate dependent and indepe ...... r neuron disease and controls.
@en
P2093
Schmidt ML
Trojanowski JQ
P304
P577
1987-03-01T00:00:00Z