Beta-amyloid (1-42) peptide impairs blood-brain barrier function after intracarotid infusion in rats. (Q48375855)

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5 December 2019

title

Beta-amyloid (1-42) peptide impairs blood-brain barrier function after intracarotid infusion in rats (English)

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5 December 2019

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8

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Péter Sántha

3

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5 December 2019

author name string

G Jancsó

1

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5 December 2019

F Domoki

2

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J Varga

4

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5 December 2019

J Fischer

5

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K Orosz

6

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B Penke

7

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M Dux

9

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L Tóth

10

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language of work or name

English

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publication date

1 September 1998

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5 December 2019

number of pages

3

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inferred from page(s)

published in

Neuroscience Letters

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volume

253

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issue

2

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page(s)

139-141

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Demonstration of poly-N-acetyl lactosamine residues in ameboid and ramified microglial cells in rat brain by tomato lectin binding

5 December 2019

cites work

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Amyloid beta-peptide induces cell monolayer albumin permeability, impairs glucose transport, and induces apoptosis in vascular endothelial cells.

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Pathological alterations of the cerebral microvasculature in Alzheimer's disease and related dementing disorders

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Cholinotoxic effects of beta-amyloid (1-42) peptide on cortical projections of the rat nucleus basalis magnocellularis

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Cerebrovascular degeneration is related to amyloid-beta protein deposition in Alzheimer's disease

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Passage of human amyloid beta-protein 1-40 across the murine blood-brain barrier

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Lectin histochemistry of cerebral microvessels in ageing, Alzheimer's disease and Down's syndrome

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Blood-brain barrier uptake of the 40 and 42 amino acid sequences of circulating Alzheimer's amyloid beta in guinea pigs

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Altered blood-brain-barrier function in Alzheimer's disease?

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Microvascular pathology and vascular basement membrane components in Alzheimer's disease

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Evans blue fluorescence: quantitative and morphological evaluation of vascular permeability in animal tissues

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Isolation and quantification of soluble Alzheimer's beta-peptide from biological fluids

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Intracarotid infusions of protamine sulfate disrupt the blood-brain barrier of rabbits

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Identifiers

DOI

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5 December 2019

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