(Q28145786)

English

Developmental and pathological expression of peroxisomal enzymes: their relationship of D-bifunctional protein deficiency and Zellweger syndrome

scientific article (publication date: 6 March 2000)

In more languages

Statements

scholarly article

0 references

Developmental and pathological expression of peroxisomal enzymes: their relationship of D-bifunctional protein deficiency and Zellweger syndrome (English)

0 references

Zellweger syndrome

1 reference

based on heuristic

inferred from title

D-bifunctional protein deficiency

1 reference

based on heuristic

inferred from title

protein deficiency

1 reference

based on heuristic

inferred from title

author name string

M Itoh

1

0 references

Y Suzuki

2

0 references

S Akaboshi

3

0 references

Z Zhang

4

0 references

S Miyabara

5

0 references

S Takashima

6

0 references

language of work or name

0 references

publication date

6 March 2000

0 references

0 references

858

0 references

1

0 references

40-7

0 references

Peroxisomal bifunctional enzyme deficiency: serial neurophysiological examinations of a case

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2902423-3

7 January 2021

Biochemical and immunological identity of the hepatic peroxisomal and microsomal trans-2-enoyl CoA hydratase bifunctional protein

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2902423-3

7 January 2021

Molecular analysis of peroxisomal beta-oxidation enzymes in infants with peroxisomal disorders indicates heterogeneity of the primary defect

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2902423-3

7 January 2021

cDNA cloning of the human peroxisomal enoyl-CoA hydratase: 3-hydroxyacyl-CoA dehydrogenase bifunctional enzyme and localization to chromosome 3q26.3-3q28: a free left Alu Arm is inserted in the 3' noncoding region

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2902423-3

7 January 2021

Developmental immunohistochemistry of catalase in the human brain

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2902423-3

7 January 2021

Immunohistochemical expression of peroxisomal enzymes in developing human brain

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2902423-3

7 January 2021

Developmental immunohistochemistry of bifunctional protein in human brain

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2902423-3

7 January 2021

Immunohistochemistry for a bifunctional protein in patients with peroxisomal disorders

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2902423-3

7 January 2021

A novel peroxisomal enzyme, D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein: its expression in the developing human brain

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2902423-3

7 January 2021

Purification and properties of human D-3-hydroxyacyl-CoA dehydratase: medium-chain enoyl-CoA hydratase is D-3-hydroxyacyl-CoA dehydratase

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2902423-3

7 January 2021

Structure of D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2902423-3

7 January 2021

Physiological role of D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2902423-3

7 January 2021

Peroxisomal disorders in children: immunohistochemistry and neuropathology.

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2902423-3

7 January 2021

Neuronal migration abnormality in peroxisomal bifunctional enzyme defect.

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2902423-3

7 January 2021

A pathological study of a peripheral nerve in a case of neonatal adrenoleukodystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2902423-3

7 January 2021

A case of pseudo-Zellweger syndrome with a possible bifunctional enzyme deficiency but detectable enzyme protein. Comparison of two cases of Zellweger syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2902423-3

7 January 2021

Fetal cerebrohepatorenal (Zellweger) syndrome: dysmorphic, radiologic, biochemical, and pathologic findings in four affected fetuses.

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2902423-3

7 January 2021

Peroxisomal disorders: genotype, phenotype, major neuropathologic lesions, and pathogenesis.

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2902423-3

7 January 2021

Peroxisomal membrane ghosts in Zellweger syndrome--aberrant organelle assembly

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2902423-3

7 January 2021

D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency: a newly identified peroxisomal disorder

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2902423-3

7 January 2021

Prenatal diagnosis of peroxisomal D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2902423-3

7 January 2021

Bile acid profiles in a peroxisomal D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2902423-3

7 January 2021

Peroxisomal bifunctional protein deficiency revisited: resolution of its true enzymatic and molecular basis

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2902423-3

7 January 2021

Enoyl-CoA hydratase deficiency: identification of a new type of D-bifunctional protein deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2902423-3

7 January 2021

Bifunctional enzyme deficiency: identification of a new type of peroxisomal disorder in a patient with an impairment in peroxisomal beta-oxidation of unknown aetiology by means of complementation analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2902423-3

7 January 2021

Peroxisomal bifunctional enzyme deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2902423-3

7 January 2021

Distinction between peroxisomal bifunctional enzyme and acyl-CoA oxidase deficiencies

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2902423-3

7 January 2021

Cortical cytoarchitectural and immunohistochemical studies on Zellweger syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0006-8993%2899%2902423-3

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0006-8993(99)02423-3

0 references

PubMed publication ID

0 references

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=Q28145786&oldid=1614913035"