(Q73196394)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9090374%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

title

PEX genes on the rise (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9090374%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

author name string

Subramani S

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9090374%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

publication date

1 April 1997

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9090374%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9090374%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

volume

15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9090374%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

issue

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9090374%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

page(s)

331-333

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9090374%20AND%20SRC:MED&resulttype=core&format=json

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

2 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-331

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-331

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-331

7 January 2021

Isolation of the human PEX12 gene, mutated in group 3 of the peroxisome biogenesis disorders

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-331

7 January 2021

Protein import deficiencies in human peroxisomal disorders.

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-331

7 January 2021

How proteins penetrate peroxisomes

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-331

7 January 2021

The sorting sequence of the peroxisomal integral membrane protein PMP47 is contained within a short hydrophilic loop

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-331

7 January 2021

Transport of microinjected proteins into peroxisomes of mammalian cells: inability of Zellweger cell lines to import proteins with the SKL tripeptide peroxisomal targeting signal

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-331

7 January 2021

Presence of cytoplasmic factors functional in peroxisomal protein import implicates organelle-associated defects in several human peroxisomal disorders

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-331

7 January 2021

Differential protein import deficiencies in human peroxisome assembly disorders

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-331

7 January 2021

Convergence of model systems for peroxisome biogenesis

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-331

7 January 2021

A unified nomenclature for peroxisome biogenesis factors

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-331

7 January 2021

The pas8 mutant of Pichia pastoris exhibits the peroxisomal protein import deficiencies of Zellweger syndrome cells--the PAS8 protein binds to the COOH-terminal tripeptide peroxisomal targeting signal, and is a member of the TPR protein family

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-331

7 January 2021

PAS10 is a tetratricopeptide-repeat protein that is essential for the import of most matrix proteins into peroxisomes of Saccharomyces cerevisiae

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-331

7 January 2021

PAS7 encodes a novel yeast member of the WD-40 protein family essential for import of 3-oxoacyl-CoA thiolase, a PTS2-containing protein, into peroxisomes

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-331

7 January 2021

PEB1 (PAS7) in Saccharomyces cerevisiae encodes a hydrophilic, intra-peroxisomal protein that is a member of the WD repeat family and is essential for the import of thiolase into peroxisomes

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-331

7 January 2021

Peb1p (Pas7p) is an intraperoxisomal receptor for the NH2-terminal, type 2, peroxisomal targeting sequence of thiolase: Peb1p itself is targeted to peroxisomes by an NH2-terminal peptide.

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-331

7 January 2021

The import receptor for the peroxisomal targeting signal 2 (PTS2) in Saccharomyces cerevisiae is encoded by the PAS7 gene.

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-331

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-331

7 January 2021

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/10.1038%2FNG0497-331

7 January 2021

Restoration by a 35K membrane protein of peroxisome assembly in a peroxisome-deficient mammalian cell mutant

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-331

7 January 2021

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/10.1038%2FNG0497-331

7 January 2021

The SH3 domain of the Saccharomyces cerevisiae peroxisomal membrane protein Pex13p functions as a docking site for Pex5p, a mobile receptor for the import PTS1-containing proteins.

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-331

7 January 2021

Identification of Pex13p a peroxisomal membrane receptor for the PTS1 recognition factor

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-331

7 January 2021

Pex13p is an SH3 protein of the peroxisome membrane and a docking factor for the predominantly cytoplasmic PTs1 receptor

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-331

7 January 2021

The Hansenula polymorpha PEX14 gene encodes a novel peroxisomal membrane protein essential for peroxisome biogenesis

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-331

7 January 2021

Identifiers

DOI

10.1038/NG0497-331

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9090374%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

1 reference