(Q28266235)

https://api.crossref.org/works/10.1002%2FHUMU.20211

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/10.1002%2FHUMU.20211

PEX1 mutations in complementation group 1 of Zellweger spectrum patients correlate with severity of disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

21 January 2018

Peroxisomal disorders

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

Sequence analysis of the AAA protein family

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

The peroxisome biogenesis factors pex4p, pex22p, pex1p, and pex6p act in the terminal steps of peroxisomal matrix protein import

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

A unified nomenclature for peroxisome biogenesis factors

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

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/10.1002%2FHUMU.20211

7 January 2021

PAS1, a yeast gene required for peroxisome biogenesis, encodes a member of a novel family of putative ATPases

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

Zellweger syndrome and associated phenotypes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

Mutations in PEX1 in peroxisome biogenesis disorders: G843D and a mild clinical phenotype

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

Disruption of a PEX1-PEX6 interaction is the most common cause of the neurologic disorders Zellweger syndrome, neonatal adrenoleukodystrophy, and infantile Refsum disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

Peroxisome biogenesis disorders: genetics and cell biology

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

Opinion: peroxisomal-protein import: is it really that complex?

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

Role of the PAS1 gene of Pichia pastoris in peroxisome biogenesis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

Restoration of biochemical function of the peroxisome in the temperature-sensitive mild forms of peroxisome biogenesis disorder in humans

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

Temperature-sensitive mutation of PEX6 in peroxisome biogenesis disorders in complementation group C (CG-C): comparative study of PEX6 and PEX1

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

Interrelationships of the pathways of mRNA decay and translation in eukaryotic cells

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

Hansenula polymorpha Pex1p and Pex6p are peroxisome-associated AAA proteins that functionally and physically interact

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

The pathogenic peroxin Pex26p recruits the Pex1p-Pex6p AAA ATPase complexes to peroxisomes

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

Novel PEX1 mutations and genotype-phenotype correlations in Australasian peroxisome biogenesis disorder patients

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

Novel PEX1 coding mutations and 5' UTR regulatory polymorphisms

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

Phenotype of patients with peroxisomal disorders subdivided into sixteen complementation groups

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

Genotype-phenotype correlations in disorders of peroxisome biogenesis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

Peroxisome biogenesis disorders with prolonged survival: phenotypic expression in a cohort of 31 patients.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

Human PEX1 is mutated in complementation group 1 of the peroxisome biogenesis disorders

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

Two polymorphic mutations (c2331A>C and IVS11+142insAGAAATTTTAAGTCTT) in the human peroxin 1 gene (PEX1).

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

Peroxisome biogenesis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

Peroxisomal membrane ghosts in Zellweger syndrome--aberrant organelle assembly

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

Peroxisomal disorders: a newly recognised group of genetic diseases

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

Structure of the N-terminal domain of PEX1 AAA-ATPase. Characterization of a putative adaptor-binding domain

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

The PEX Gene Screen: molecular diagnosis of peroxisome biogenesis disorders in the Zellweger syndrome spectrum

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

Import of peroxisomal matrix and membrane proteins

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

A cytoplasmic AAA family peroxin, Pex1p, interacts with Pex6p

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

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/10.1002%2FHUMU.20211

7 January 2021

Disorders of peroxisome biogenesis due to mutations in PEX1: phenotypes and PEX1 protein levels

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

7 January 2021

Peroxisome biogenesis disorders

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20211

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/10.1002%2FHUMU.20211

7 January 2021

Identifiers

DOI

10.1002/HUMU.20211

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

16086329

1 reference

Consolidated OpenCitations Corpus – April 2017