Peroxisomal disorders I: biochemistry and genetics of peroxisome biogenesis disorders (Q36023724)

11 August 2017

1 reference

title

Peroxisomal disorders I: biochemistry and genetics of peroxisome biogenesis disorders (English)

1 reference

11 August 2017

Wanders RJ

1

1 reference

11 August 2017

Waterham HR

series ordinal

2

1 reference

11 August 2017

publication date

1 February 2005

1 reference

11 August 2017

1 reference

11 August 2017

volume

67

1 reference

11 August 2017

issue

2

1 reference

11 August 2017

page(s)

107-133

1 reference

Import of stably folded proteins into peroxisomes

11 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2004.00329.X

Pex19p interacts with Pex3p and Pex10p and is essential for peroxisome biogenesis in Pichia pastoris

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2004.00329.X

Pex19p, a farnesylated protein essential for peroxisome biogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2004.00329.X

Pex17p is required for import of both peroxisome membrane and lumenal proteins and interacts with Pex19p and the peroxisome targeting signal-receptor docking complex in Pichia pastoris

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2004.00329.X

Identification and characterization of the human peroxin PEX3

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2004.00329.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2004.00329.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2004.00329.X

Global regulatory functions of Oaf1p and Pip2p (Oaf2p), transcription factors that regulate genes encoding peroxisomal proteins in Saccharomyces cerevisiae

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2004.00329.X

Targeted disruption of the alpha isoform of the peroxisome proliferator-activated receptor gene in mice results in abolishment of the pleiotropic effects of peroxisome proliferators

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2004.00329.X

The Candida boidinii peroxisomal membrane protein Pmp30 has a role in peroxisomal proliferation and is functionally homologous to Pmp27 from Saccharomyces cerevisiae

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2004.00329.X

Genetic relation between the Zellweger syndrome, infantile Refsum's disease, and rhizomelic chondrodysplasia punctata

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2004.00329.X

Abnormal profiles of polyunsaturated fatty acids in the brain, liver, kidney and retina of patients with peroxisomal disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2004.00329.X

Mitochondrial alterations caused by defective peroxisomal biogenesis in a mouse model for Zellweger syndrome (PEX5 knockout mouse)

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2004.00329.X

Formation of the peroxisome lumen is abolished by loss of Pichia pastoris Pas7p, a zinc-binding integral membrane protein of the peroxisome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-0004.2004.00329.X

10.1111/J.1399-0004.2004.00329.X

21 January 2018

Identifiers

DOI

1 reference

11 August 2017

1 reference