(Q40914163)

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Formation of peroxisomes from peroxisomal ghosts in a peroxisome-deficient mammalian cell mutant upon complementation by protein microinjection

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Europe PubMed Central

PubMed publication ID

24 September 2017

Formation of peroxisomes from peroxisomal ghosts in a peroxisome-deficient mammalian cell mutant upon complementation by protein microinjection (English)

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Europe PubMed Central

PubMed publication ID

24 September 2017

author name string

Yamasaki M

1

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Europe PubMed Central

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24 September 2017

Hashiguchi N

2

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Europe PubMed Central

PubMed publication ID

24 September 2017

Fujiwara C

3

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

Imanaka T

4

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Europe PubMed Central

PubMed publication ID

24 September 2017

Tsukamoto T

5

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24 September 2017

Osumi T

6

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24 September 2017

language of work or name

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publication date

1 December 1999

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24 September 2017

Journal of Biological Chemistry

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24 September 2017

274

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24 September 2017

50

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Europe PubMed Central

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24 September 2017

35293-35296

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Europe PubMed Central

PubMed publication ID

24 September 2017

A unified nomenclature for peroxisome biogenesis factors

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.50.35293

21 January 2018

Peroxisomes: Organelles at the crossroads

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.50.35293

21 January 2018

Multiple PEX genes are required for proper subcellular distribution and stability of Pex5p, the PTS1 receptor: evidence that PTS1 protein import is mediated by a cycling receptor

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.50.35293

21 January 2018

Pex14p, a peroxisomal membrane protein binding both receptors of the two PTS-dependent import pathways

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.50.35293

21 January 2018

Two AAA Family Peroxins, PpPex1p and PpPex6p, Interact with Each Other in an ATP-Dependent Manner and Are Associated with Different Subcellular Membranous Structures Distinct from Peroxisomes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.50.35293

21 January 2018

A cytoplasmic AAA family peroxin, Pex1p, interacts with Pex6p

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.50.35293

21 January 2018

Genetic basis of peroxisome-assembly mutants of humans, Chinese hamster ovary cells, and yeast: identification of a new complementation group of peroxisome-biogenesis disorders apparently lacking peroxisomal-membrane ghosts

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.50.35293

21 January 2018

Temperature-sensitive phenotypes of peroxisome-assembly processes represent the milder forms of human peroxisome-biogenesis disorders

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.50.35293

21 January 2018

Temperature-sensitive mutation in PEX1 moderates the phenotypes of peroxisome deficiency disorders

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.50.35293

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.50.35293

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.50.35293

21 January 2018

Identification and characterization of the putative human peroxisomal C-terminal targeting signal import receptor

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.50.35293

21 January 2018

Human peroxisomal targeting signal-1 receptor restores peroxisomal protein import in cells from patients with fatal peroxisomal disorders

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.50.35293

21 January 2018

Peroxisome targeting signal of rat liver acyl-coenzyme A oxidase resides at the carboxy terminus

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.50.35293

21 January 2018

Peroxisome assembly factor-2, a putative ATPase cloned by functional complementation on a peroxisome-deficient mammalian cell mutant

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.50.35293

21 January 2018

Recombinant human peroxisomal targeting signal receptor PEX5. Structural basis for interaction of PEX5 with PEX14.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.50.35293

21 January 2018

Peroxisome biogenesis: back to the endoplasmic reticulum?

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.50.35293

21 January 2018

The Hansenula polymorpha PER9 gene encodes a peroxisomal membrane protein essential for peroxisome assembly and integrity

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.50.35293

21 January 2018

Overexpression of Pex15p, a phosphorylated peroxisomal integral membrane protein required for peroxisome assembly in S.cerevisiae, causes proliferation of the endoplasmic reticulum membrane

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.50.35293

21 January 2018

Four Distinct Secretory Pathways Serve Protein Secretion, Cell Surface Growth, and Peroxisome Biogenesis in the Yeast Yarrowia lipolytica

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.50.35293

21 January 2018

Peroxisome biogenesis: involvement of ARF and coatomer

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.50.35293

21 January 2018

Peroxisome synthesis in the absence of preexisting peroxisomes

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.50.35293

21 January 2018

Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.50.35293

21 January 2018

Newly identified Chinese hamster ovary cell mutants are defective in biogenesis of peroxisomal membrane vesicles (Peroxisomal ghosts), representing a novel complementation group in mammals

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.50.35293

21 January 2018

Human PEX19: cDNA cloning by functional complementation, mutation analysis in a patient with Zellweger syndrome, and potential role in peroxisomal membrane assembly

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.50.35293

21 January 2018

Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders

1 reference

https://api.crossref.org/works/10.1074%2FJBC.274.50.35293

21 January 2018

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10.1074/JBC.274.50.35293

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

24 September 2017

ResearchGate publication ID

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