(Q71345327)

English

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

scientific article published on 01 January 1996

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8739963%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

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 (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8739963%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

Zellweger syndrome

1 reference

based on heuristic

inferred from title

author name string

R J Wanders

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8739963%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

G J Romeijn

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8739963%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

publication date

1 January 1996

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8739963%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

Journal of Inherited Metabolic Disease

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8739963%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

19

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8739963%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8739963%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

193-196

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8739963%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

https://scigraph.springernature.com/pub.10.1007/bf01799427

0 references

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8739963

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

3-Hydroxy-3-methylglutaryl-coenzyme A reductase is present in peroxisomes in normal rat liver cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/8739963

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Reduced cellular cholesterol content in peroxisome-deficient fibroblasts is associated with impaired uptake of the patient's low density lipoprotein and with reduced cholesterol synthesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8739963

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Farnesyl-diphosphate synthase is localized in peroxisomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8739963

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of three distinct peroxisomal protein import defects in patients with peroxisome biogenesis disorders.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8739963

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differential protein import deficiencies in human peroxisome assembly disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/8739963

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/8739963

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mevalonate kinase is localized in rat liver peroxisomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8739963

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Control of phosphorylation and decarboxylation of mevalonic acid and its metabolites in cultured human fibroblasts and in rat liver in vivo

1 reference

https://pubmed.ncbi.nlm.nih.gov/8739963

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8739963

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The role of peroxisomes in cholesterol metabolism

1 reference

https://pubmed.ncbi.nlm.nih.gov/8739963

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Normal cholesterol synthesis in human cells requires functional peroxisomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8739963

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Presence of individual enzymes of cholesterol biosynthesis in rat liver peroxisomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8739963

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF01799427

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8739963%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:8739963%20AND%20SRC:MED&resulttype=core&format=json

18 October 2019

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q71345327&oldid=1754197083"