(Q24311431)

protein import into peroxisome matrix

GOA release 2020-03-11

1 reference

Peroxisomal biogenesis factor 7

GOA release 2020-03-11

1 reference

rhizomelic chondrodysplasia punctata

GOA release 2020-03-11

1 reference

6

S J Gould

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author name string

N Braverman

1

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G Steel

2

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C Obie

3

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A Moser

4

0 references

H Moser

5

0 references

D Valle

A unified nomenclature for peroxisome biogenesis factors

7

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language of work or name

English

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publication date

April 1997

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published in

Nature Genetics

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volume

15

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issue

4

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page(s)

369-76

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cites work

1 reference

https://api.crossref.org/works/10.1038/NG0497-369

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

20 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0497-369

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

20 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0497-369

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

20 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0497-369

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

20 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0497-369

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.

20 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0497-369

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

20 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0497-369

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

20 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0497-369

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.

20 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0497-369

The ancient regulatory-protein family of WD-repeat proteins

20 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0497-369

FAN, a novel WD-repeat protein, couples the p55 TNF-receptor to neutral sphingomyelinase

20 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0497-369

The Cockayne syndrome group A gene encodes a WD repeat protein that interacts with CSB protein and a subunit of RNA polymerase II TFIIH

20 April 2017

1 reference

https://api.crossref.org/works/10.1038/NG0497-369

Basic local alignment search tool

20 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

A conserved tripeptide sorts proteins to peroxisomes

20 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

Two complementary approaches to study peroxisome biogenesis in Saccharomyces cerevisiae: forward and reversed genetics

20 April 2017

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

How proteins penetrate peroxisomes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

The gene for the peroxisomal targeting signal import receptor (PXR1) is located on human chromosome 12p13, flanked by TPI1 and D12S1089.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

Peroxisomes of normal morphology but deficient in 3-oxoacyl-CoA thiolase in Rhizomelic Chondrodysplasia Punctata fibroblasts

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

Differential protein import deficiencies in human peroxisome assembly disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

The structure of the G protein heterotrimer Gi alpha 1 beta 1 gamma 2

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

The TPR snap helix: a novel protein repeat motif from mitosis to transcription

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

Isolation of monoclonal antibodies specific for human c-myc proto-oncogene product

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

Identification of a peroxisomal targeting signal at the carboxy terminus of firefly luciferase

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

Functional dissection of the yeast Cyc8–Tupl transcriptional co-repressor complex

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

7 January 2021

Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groups

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

7 January 2021

Biochemical abnormalities in rhizomelic chondrodysplasia punctata

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

7 January 2021

Rhizomelic chondrodysplasia punctata. Deficiency of 3-oxoacyl-coenzyme A thiolase in peroxisomes and impaired processing of the enzyme

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

7 January 2021

A new type of chondrodysplasia punctata associated with peroxisomal dysfunction

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

7 January 2021

Rhizomelic chondrodysplasia punctata — A new clinical variant

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

7 January 2021

Chondrodysplasia punctata with a mild clinical course

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

7 January 2021

Variant rhizomelic chondrodysplasia punctata (RCDP) with normal plasma phytanic acid: clinico-biochemical delineation of a subtype and complementation studies

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

7 January 2021

Bone dysplasia associated with phytanic acid accumulation and deficient plasmalogen synthesis: a peroxisomal entity amenable to plasmapheresis

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

7 January 2021

Congenital rubella syndrome associated with calcific epiphyseal stippling and peroxisomal dysfunction

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

7 January 2021

Non-rhizomelic and rhizomelic chondrodysplasia punctata within a single complementation group

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

7 January 2021

Human dihydroxyacetonephosphate acyltransferase deficiency: a new peroxisomal disorder

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

7 January 2021

Human alkyldihydroxyacetonephosphate synthase deficiency: a new peroxisomal disorder

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

7 January 2021

Development of the yeast Pichia pastoris as a model organism for a genetic and molecular analysis of peroxisome assembly

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

7 January 2021

Protein import into peroxisomes and biogenesis of the organelle

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

7 January 2021

Mutational analysis of the N-terminal topogenic signal of watermelon glyoxysomal malate dehydrogenase using the heterologous host Hansenula polymorpha

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

7 January 2021

The N-terminus of amine oxidase of Hansenula polymorpha contains a peroxisomal targeting signal

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

7 January 2021

A human gene responsible for Zellweger syndrome that affects peroxisome assembly

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

7 January 2021

The peroxisome biogenesis disorder group 4 gene, PXAAA1, encodes a cytoplasmic ATPase required for stability of the PTS1 receptor

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

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%2FNG0497-369

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%2FNG0497-369

7 January 2021

From expressed sequence tags to peroxisome biogenesis disorder genes

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

7 January 2021

The yeast genome--a common currency

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

7 January 2021

Regulation of translation in eukaryotic systems

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

7 January 2021

Repetitive segmental structure of the transducin beta subunit: homology with the CDC4 gene and identification of related mRNAs

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

7 January 2021

The skipping of constitutive exons in vivo induced by nonsense mutations

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

7 January 2021

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

7 January 2021

Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNG0497-369

7 January 2021