(Q52828740)

8 May 2018

title

Isolation of Chinese hamster ovary cell pex mutants: two PEX7-defective mutants. (English)

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8 May 2018

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Eiko Yanago

1

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8 May 2018

Takahide Hiromasa

2

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8 May 2018

Tsuyoshi Matsumura

3

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8 May 2018

Naohiko Kinoshita

4

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8 May 2018

Yukio Fujiki

5

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8 May 2018

language of work or name

English

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publication date

1 April 2002

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8 May 2018

Biochemical and Biophysical Research Communications

published in

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8 May 2018

volume

293

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8 May 2018

issue

1

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8 May 2018

page(s)

225-230

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8 May 2018

describes a project that uses

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Biogenesis of peroxisomes

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https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900219-X

Peroxisome biogenesis and molecular defects in peroxisome assembly disorders

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900219-X

Import of peroxisomal matrix and membrane proteins

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900219-X

A conserved tripeptide sorts proteins to peroxisomes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900219-X

Amino-terminal presequence of the precursor of peroxisomal 3-ketoacyl-CoA thiolase is a cleavable signal peptide for peroxisomal targeting.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900219-X

Peroxisome biogenesis and peroxisome biogenesis disorders

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900219-X

Peroxisome biogenesis disorders: genetics and cell biology

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900219-X

The peroxin Pex6p gene is impaired in peroxisomal biogenesis disorders of complementation group 6.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900219-X

A rapid selection for animal cell mutants with defective peroxisomes.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900219-X

PEX3 is the causal gene responsible for peroxisome membrane assembly-defective Zellweger syndrome of complementation group G.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900219-X

Intracellular localization, function, and dysfunction of the peroxisome-targeting signal type 2 receptor, Pex7p, in mammalian cells

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900219-X

The life cycle of the peroxisome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900219-X

Isolation and characterization of Chinese hamster ovary cell mutants defective in assembly of peroxisomes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900219-X

Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group I

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900219-X

Isolation and characterization of novel peroxisome biogenesis-defective Chinese hamster ovary cell mutants using green fluorescent protein

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900219-X

Isolation of a new peroxisome-deficient CHO cell mutant defective in peroxisome targeting signal-1 receptor

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900219-X

Isolation and characterization of peroxisome-deficient Chinese hamster ovary cell mutants representing human complementation group III.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900219-X

Peroxisome targeting signal type 1 (PTS1) receptor is involved in import of both PTS1 and PTS2: studies with PEX5-defective CHO cell mutants

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900219-X

PEX12, the pathogenic gene of group III Zellweger syndrome: cDNA cloning by functional complementation on a CHO cell mutant, patient analysis, and characterization of PEX12p

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900219-X

Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900219-X

Isolation, characterization and mutation analysis of PEX13-defective Chinese hamster ovary cell mutants

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900219-X

Newly identified Chinese hamster ovary cell mutants defective in peroxisome assembly represent complementation group A of human peroxisome biogenesis disorders and one novel group in mammals

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900219-X

PEX7 gene structure, alternative transcripts, and evidence for a founder haplotype for the frequent RCDP allele, L292ter

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900219-X

Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900219-X

Rhizomelic chondrodysplasia punctata is a peroxisomal protein targeting disease caused by a non-functional PTS2 receptor

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900219-X

Rhizomelic chondrodysplasia punctata is caused by deficiency of human PEX7, a homologue of the yeast PTS2 receptor

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-291X%2802%2900219-X

10.1016/S0006-291X(02)00219-X

7 January 2021

Identifiers

DOI

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8 May 2018

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8 May 2018