(Q42426495)

31 October 2017

title

Isoprenoid biosynthesis is not compromised in a Zellweger syndrome mouse model (English)

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31 October 2017

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1

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31 October 2017

M Baes

2

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31 October 2017

P E Declercq

series ordinal

3

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31 October 2017

publication date

1 May 2001

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31 October 2017

number of pages

9

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Biochimica et Biophysica Acta

inferred from page(s)

published in

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31 October 2017

volume

1532

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31 October 2017

issue

1-2

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31 October 2017

page(s)

28-36

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Peroxisomal and mitochondrial defects in the cerebro-hepato-renal syndrome

31 October 2017

cites work

1 reference

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7 January 2021

Cell compartmentalization of cholesterol biosynthesis

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7 January 2021

Molecular cloning of human phosphomevalonate kinase and identification of a consensus peroxisomal targeting sequence

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7 January 2021

Cloning and subcellular localization of hamster and rat isopentenyl diphosphate dimethylallyl diphosphate isomerase. A PTS1 motif targets the enzyme to peroxisomes

1 reference

https://api.crossref.org/works/10.1016%2FS1388-1981%2801%2900108-1

7 January 2021

Infantile Refsum disease: an inherited peroxisomal disorder. Comparison with Zellweger syndrome and neonatal adrenoleukodystrophy.

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7 January 2021

A sibship with a mild variant of Zellweger syndrome

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7 January 2021

Plasma and skin fibroblast C26 fatty acids in infantile Refsum's disease

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7 January 2021

Differential deficiency of mevalonate kinase and phosphomevalonate kinase in patients with distinct defects in peroxisome biogenesis: evidence for a major role of peroxisomes in cholesterol biosynthesis

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https://api.crossref.org/works/10.1016%2FS1388-1981%2801%2900108-1

7 January 2021

Normal cholesterol synthesis in human cells requires functional peroxisomes

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7 January 2021

Cholesterol biosynthesis in dermal fibroblasts from patients with metabolic disorders of peroxisomal origin

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7 January 2021

Synthesis of mevalonate pathway lipids in fibroblasts from Zellweger and X-linked ALD patients

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7 January 2021

A mouse model for Zellweger syndrome

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7 January 2021

C-terminal tripeptide Ser-Asn-Leu (SNL) of human D-aspartate oxidase is a functional peroxisome-targeting signal

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7 January 2021

Docosahexaenoic acid deficit is not a major pathogenic factor in peroxisome-deficient mice

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7 January 2021

Improved high-performance liquid chromatographic method for the determination of coenzyme Q10 in plasma

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7 January 2021

Leigh syndrome: clinical features and biochemical and DNA abnormalities.

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7 January 2021

Influence of peroxisome proliferator-activated receptor alpha on ubiquinone biosynthesis

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7 January 2021

Impaired cholesterol synthesis rate in fibroblasts and reduced cellular uptake of LDLs derived from peroxisome-deficient patients cause cellular cholesterol deficiency in peroxisome-deficient fibroblasts

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7 January 2021

Placental transfer of cholesterol into the human fetus

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7 January 2021

Sterol synthesis and low density lipoprotein clearance in vivo in the pregnant rat, placenta, and fetus. Sources for tissue cholesterol during fetal development

1 reference

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7 January 2021

Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groups

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7 January 2021

Cholesterol biosynthesis in Zellweger syndrome: normal activity of mevalonate kinase, mevalonate-5'-pyrophosphate decarboxylase and IPP-isomerase in patients' fibroblasts but deficient mevalonate kinase activity in liver

1 reference

https://api.crossref.org/works/10.1016%2FS1388-1981%2801%2900108-1

7 January 2021

10.1016/S1388-1981(01)00108-1

Identifiers

DOI

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31 October 2017

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