A mouse model to test the in vivo efficacy of chemical chaperones (Q77910842)

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9 December 2019

title

A mouse model to test the in vivo efficacy of chemical chaperones (English)

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9 December 2019

author name string

C Bai

1

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9 December 2019

J Biwersi

2

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9 December 2019

A S Verkman

3

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9 December 2019

M A Matthay

4

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9 December 2019

publication date

1 July 1998

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Journal of Pharmacological and Toxicological Methods

9 December 2019

published in

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9 December 2019

volume

40

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9 December 2019

issue

1

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9 December 2019

page(s)

39-45

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The relative importance of N-oxidation and N-demethylation in the metabolism of trimethylamine in man.

9 December 2019

cites work

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Double-blind randomised trial of intravenous glycerol in acute stroke

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Chemical chaperones correct the mutant phenotype of the ΔF508 cystic fibrosis transmembrane conductance regulator protein

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Correcting temperature-sensitive protein folding defects

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Metabolism of trimethylamines in kelp bass (Paralabrax clathratus) and marine and freshwater pink salmon (Oncorhynchus gorbuscha).

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7 January 2021

Glycerol: a review of its pharmacology, pharmacokinetics, adverse reactions, and clinical use.

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Mechanism of protein stabilization by glycerol: preferential hydration in glycerol-water mixtures

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Generation and phenotype of a transgenic knockout mouse lacking the mercurial-insensitive water channel aquaporin-4.

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Severely impaired urinary concentrating ability in transgenic mice lacking aquaporin-1 water channels

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Glycerol-assisted Restorative Adjustment of Flavoenzyme Conformation Perturbed by Site-directed Mutagenesis

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Glycerol reverses the misfolding phenotype of the most common cystic fibrosis mutation.

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Transgenic mice expressing hamster prion protein produce species-specific scrapie infectivity and amyloid plaques.

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Defective aquaporin-2 trafficking in nephrogenic diabetes insipidus and correction by chemical chaperones

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Influence of molecular and chemical chaperones on protein folding

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Treatment of acute cortical infarct with intravenous glycerol. A double-blind, placebo-controlled randomized trial

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A mouse model for the delta F508 allele of cystic fibrosis.

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7 January 2021

10.1016/S1056-8719(98)00034-3

Identifiers

DOI

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9 December 2019

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