Complementation study of peroxisome-deficient disorders by immunofluorescence staining and characterization of fused cells (Q41637765)

5 October 2017

title

Complementation study of peroxisome-deficient disorders by immunofluorescence staining and characterization of fused cells (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1372585

immunofluorescence microscopy

19 September 2022

main subject

1 reference

S. Yajima

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1372585

19 September 2022

Y. Suzuki

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1372585

19 September 2022

N. Shimozawa

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1372585

19 September 2022

S. Yamaguchi

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1372585

19 September 2022

T. Orii

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1372585

19 September 2022

Y. Fujiki

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1372585

19 September 2022

T. Osumi

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1372585

19 September 2022

T. Hashimoto

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1372585

19 September 2022

H. W. Moser

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1372585

19 September 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1372585

19 September 2022

publication date

1 March 1992

1 reference

5 October 2017

1 reference

5 October 2017

1 reference

5 October 2017

1 reference

5 October 2017

page(s)

491-499

1 reference

Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis

5 October 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FBF00219334

Peroxisomal beta-oxidation enzyme proteins in adrenoleukodystrophy: distinction between X-linked adrenoleukodystrophy and neonatal adrenoleukodystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00219334

Deficiency of enzymes catalyzing the biosynthesis of glycerol-ether lipids in Zellweger syndrome. A new category of metabolic disease involving the absence of peroxisomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00219334

Synthesis of a major integral membrane polypeptide of rat liver peroxisomes on free polysomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00219334

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00219334

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00219334

Peroxisomal disorders: complementation analysis using beta-oxidation of very long chain fatty acids

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00219334

Phytanic acid alpha-oxidation and complementation analysis of classical Refsum and peroxisomal disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00219334

Genetic and phenotypic heterogeneity in disorders of peroxisome biogenesis--a complementation study involving cell lines from 19 patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00219334

Infantile phytanic acid storage disease, a possible variant of Refsum's disease: three cases, including ultrastructural studies of the liver

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00219334

Biosynthesis and maturation of peroxisomal beta-oxidation enzymes in fibroblasts in relation to the Zellweger syndrome and infantile Refsum disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00219334

Deficient activities and proteins of peroxisomal beta-oxidation enzymes in infants with Zellweger syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00219334

Zellweger-like syndrome with detectable hepatic peroxisomes: a variant form of peroxisomal disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00219334

Effects of sodium 2-[5-(4-chlorophenyl)pentyl]-oxirane-2-carboxylate (POCA) on fatty acid oxidation in fibroblasts from patients with peroxisomal diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00219334

Adrenoleukodystrophy. Preliminary report of a connatal case. Light- and electron microscopical, immunohistochemical and biochemical findings

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00219334

Isolation of animal cell mutants deficient in plasmalogen biosynthesis and peroxisome assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00219334

Biochemical abnormalities in rhizomelic chondrodysplasia punctata

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FBF00219334

Molecular analysis of peroxisomal beta-oxidation enzymes in infants with Zellweger syndrome and Zellweger-like syndrome: further heterogeneity of the peroxisomal disorder

21 January 2018

1 reference

12 December 2020

A prenatal test for the cerebro-hepato-renal (Zellweger) syndrome by demonstration of the absence of catalase-containing particles (peroxisomes) in cultured amniotic fluid cells

1 reference

12 December 2020

Peroxisomal membrane ghosts in Zellweger syndrome--aberrant organelle assembly

1 reference

12 December 2020

Presence of peroxisomal membrane proteins in liver and fibroblasts from patients with the Zellweger syndrome and related disorders: evidence for the existence of peroxisomal ghosts

1 reference

12 December 2020

Chinese hamster ovary cell mutants defective in peroxisome biogenesis. Comparison to Zellweger syndrome

1 reference

12 December 2020

A possible role for plasmalogens in protecting animal cells against photosensitized killing

1 reference

12 December 2020

Peroxisomal beta-oxidation enzyme proteins in the Zellweger syndrome

1 reference

12 December 2020

A FAMILIAL SYNDROME OF MULTIPLE CONGENITAL DEFECTS

1 reference

12 December 2020

Neonatal adrenoleukodystrophy. Impaired plasmalogen biosynthesis and peroxisomal beta-oxidation due to a deficiency of catalase-containing particles (peroxisomes) in cultured skin fibroblasts

1 reference

12 December 2020

Protein measurement with the Folin phenol reagent

1 reference

12 December 2020

Kinetics of the assembly of peroxisomes after fusion of complementary cell lines from patients with the cerebro-hepato-renal (Zellweger) syndrome and related disorders

1 reference

12 December 2020

Infantile Refsum disease: deficiency of catalase-containing particles (peroxisomes), alkyldihydroxyacetone phosphate synthase and peroxisomal beta-oxidation enzyme proteins

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00219334

1 reference

Dimensions Publication ID

5 October 2017

1003521077

0 references

1 reference