(Q54242010)

26 May 2018

title

Peroxisomal assembly defects: clinical, pathologic, and biochemical findings in two patients in a newly identified complementation group. (English)

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26 May 2018

author

John Christodoulou

2

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26 May 2018

author name string

Poulos A

1

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26 May 2018

Chow CW

3

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26 May 2018

Goldblatt J

4

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26 May 2018

Paton BC

5

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26 May 2018

Orii T

6

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26 May 2018

Suzuki Y

7

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26 May 2018

Shimozawa N

8

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26 May 2018

language of work or name

English

0 references

publication date

1 October 1995

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26 May 2018

The Journal of Pediatrics

published in

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26 May 2018

volume

127

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26 May 2018

issue

4

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26 May 2018

page(s)

596-599

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26 May 2018

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

cites work

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(95)70121-4

Morphometry of peroxisomes and immunolocalization of peroxisomal proteins in the liver of patients with generalised peroxisomal disorders

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(95)70121-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(95)70121-4

Accumulation of pristanic acid (2, 6, 10, 14 tetramethylpentadecanoic acid) in the plasma of patients with generalised peroxisomal dysfunction

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(95)70121-4

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(95)70121-4

A method for enrichment of hybrid somatic cells: complementation studies in certain lysosomal enzymopathies

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(95)70121-4

The mechanism of arrest of neuronal migration in the Zellweger malformation: An hypothesis based upon cytoarchitectonic analysis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(95)70121-4

A human gene responsible for Zellweger syndrome that affects peroxisome assembly

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(95)70121-4

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(95)70121-4

Mutations in the 70K peroxisomal membrane protein gene in Zellweger syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016/S0022-3476(95)70121-4

10.1016/S0022-3476(95)70121-4

7 January 2021

Identifiers

DOI

1 reference

26 May 2018

1 reference

26 May 2018