(Q40482584)

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Inhibition of peroxisomal functions due to oxidative imbalance induced by mistargeting of catalase to cytoplasm is restored by vitamin E treatment in skin fibroblasts from Zellweger syndrome-like patients.

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Europe PubMed Central

PubMed publication ID

20 September 2017

Inhibition of peroxisomal functions due to oxidative imbalance induced by mistargeting of catalase to cytoplasm is restored by vitamin E treatment in skin fibroblasts from Zellweger syndrome-like patients. (English)

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Europe PubMed Central

PubMed publication ID

20 September 2017

author name string

Yasusada Kawada

1

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20 September 2017

Mushfiquddin Khan

2

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20 September 2017

Ashish K Sharma

3

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Europe PubMed Central

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20 September 2017

Dinath B Ratnayake

4

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Europe PubMed Central

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20 September 2017

Kazushige Dobashi

5

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Europe PubMed Central

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20 September 2017

Kohtaro Asayama

6

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Europe PubMed Central

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20 September 2017

Hugo W Moser

7

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20 September 2017

Miguel A Contreras

8

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20 September 2017

Inderjit Singh

9

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20 September 2017

publication date

1 December 2004

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20 September 2017

Molecular Genetics and Metabolism

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20 September 2017

83

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20 September 2017

4

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20 September 2017

297-305

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20 September 2017

Peroxisomal disorders: clinical, biochemical, and molecular aspects

1 reference

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Biochemistry of peroxisomes in health and disease

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Biochemical features of a patient with Zellweger-like syndrome with normal PTS-1 and PTS-2 peroxisomal protein import systems: a new peroxisomal disease.

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Abnormality in catalase import into peroxisomes leads to severe neurological disorder

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A conserved tripeptide sorts proteins to peroxisomes

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Peroxisomal membrane ghosts in Zellweger syndrome--aberrant organelle assembly

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Catalase-less peroxisomes. Implication in the milder forms of peroxisome biogenesis disorder

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Functional heterogeneity of C-terminal peroxisome targeting signal 1 in PEX5-defective patients

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Prooxidant-initiated lipid peroxidation in isolated rat hepatocytes: detection of 4-hydroxynonenal- and malondialdehyde-protein adducts

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Formation of isoprostane-like compounds (neuroprostanes) in vivo from docosahexaenoic acid.

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Oxidative injury of synapse and alteration of antioxidative defense systems in rats, and its prevention by vitamin E.

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Antioxidant effects of lovastatin and vitamin E on experimental atherosclerosis in rabbits

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Peroxisomal fatty acid oxidation and cellular redox

1 reference

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Tissue fractionation studies. 17. Intracellular distribution of monoamine oxidase, aspartate aminotransferase, alanine aminotransferase, D-amino acid oxidase and catalase in rat-liver tissue

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A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding

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Lipid and fatty acid composition of brain tissue from adrenoleukodystrophy patients

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Inducible nitric oxide synthase in the central nervous system of patients with X-adrenoleukodystrophy.

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Components involved in peroxisome import, biogenesis, proliferation, turnover, and movement

1 reference

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7 January 2021

Targeting of human catalase to peroxisomes is dependent upon a novel COOH-terminal peroxisomal targeting sequence

1 reference

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7 January 2021

The pas8 mutant of Pichia pastoris exhibits the peroxisomal protein import deficiencies of Zellweger syndrome cells--the PAS8 protein binds to the COOH-terminal tripeptide peroxisomal targeting signal, and is a member of the TPR protein family

1 reference

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7 January 2021

An isoform of pex5p, the human PTS1 receptor, is required for the import of PTS2 proteins into peroxisomes

1 reference

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7 January 2021

Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata

1 reference

https://api.crossref.org/works/10.1016%2FJ.YMGME.2004.07.012

7 January 2021

A proposed model for the PEX5-peroxisomal targeting signal-1 recognition complex

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7 January 2021

Mutation analysis of PEX7 in 60 probands with rhizomelic chondrodysplasia punctata and functional correlations of genotype with phenotype

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Peroxisome targeting signal type 1 (PTS1) receptor is involved in import of both PTS1 and PTS2: studies with PEX5-defective CHO cell mutants

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Different intracellular localization of peroxisomal proteins in fibroblasts from patients with aberrant peroxisome assembly

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Zellweger syndrome: diagnostic assays, syndrome delineation, and potential therapy.

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Dietary ether lipid incorporation into tissue plasmalogens of humans and rodents

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Oral bile acid treatment and the patient with zellweger syndrome

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Therapeutic effects of docosahexaenoic acid ethyl ester in patients with generalized peroxisomal disorders

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Plasmalogens as endogenous antioxidants: somatic cell mutants reveal the importance of the vinyl ether

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Docosahexaenoic acid abundance in the brain: a biodevice to combat oxidative stress

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Dietary intake of antioxidants and risk of Alzheimer disease

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Temperature sensitivity in peroxisome assembly processes characterizes milder forms of peroxisome biogenesis disorders

1 reference

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7 January 2021

Temperature-sensitive phenotypes of peroxisome-assembly processes represent the milder forms of human peroxisome-biogenesis disorders

1 reference

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The effect of vitamin E on the structure of membrane lipid assemblies

1 reference

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7 January 2021

Identifiers

10.1016/J.YMGME.2004.07.012

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

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