(Q28201464)

PEX12, the pathogenic gene of group III Zellweger syndrome: cDNA cloning by functional complementation on a CHO cell mutant, patient analysis, and characterization of PEX12p

21 January 2018

1 reference

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

Snares and Munc18 in synaptic vesicle fusion

21 January 2018

1 reference

A human gene responsible for Zellweger syndrome that affects peroxisome assembly

21 January 2018

1 reference

7 January 2021

The peroxin Pex6p gene is impaired in peroxisomal biogenesis disorders of complementation group 6.

1 reference

7 January 2021

Peroxisome biogenesis and peroxisome biogenesis disorders

1 reference

7 January 2021

PEX3 is the causal gene responsible for peroxisome membrane assembly-defective Zellweger syndrome of complementation group G.

1 reference

7 January 2021

Peroxisome biogenesis disorders: genetics and cell biology

1 reference

7 January 2021

Newly identified Chinese hamster ovary cell mutants defective in peroxisome assembly represent complementation group A of human peroxisome biogenesis disorders and one novel group in mammals

1 reference

7 January 2021

The Pas2 protein essential for peroxisome biogenesis is related to ubiquitin-conjugating enzymes

1 reference

7 January 2021

The Yarrowia lipolytica gene PAY2 encodes a 42-kDa peroxisomal integral membrane protein essential for matrix protein import and peroxisome enlargement but not for peroxisome membrane proliferation

1 reference

7 January 2021

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

7 January 2021

Pex17p of Saccharomyces cerevisiae is a novel peroxin and component of the peroxisomal protein translocation machinery

1 reference

7 January 2021

Pex22p of Pichia pastoris, essential for peroxisomal matrix protein import, anchors the ubiquitin-conjugating enzyme, Pex4p, on the peroxisomal membrane

1 reference

7 January 2021

Isolation and characterization of Chinese hamster ovary cell mutants defective in assembly of peroxisomes

1 reference

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

7 January 2021

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

1 reference

7 January 2021

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

1 reference

7 January 2021

The peroxin Pex14p. cDNA cloning by functional complementation on a Chinese hamster ovary cell mutant, characterization, and functional analysis

1 reference

7 January 2021

Isolation of intracellular membranes by means of sodium carbonate treatment: application to endoplasmic reticulum

1 reference

7 January 2021

PEX12 encodes an integral membrane protein of peroxisomes

1 reference

7 January 2021

A cytoplasmic AAA family peroxin, Pex1p, interacts with Pex6p

1 reference

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

7 January 2021

Import of peroxisomal matrix and membrane proteins

1 reference

7 January 2021

Peroxisome biogenesis

1 reference

7 January 2021

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

1 reference

7 January 2021

Peroxisomes are formed from complex membrane structures in PEX6-deficient CHO cells upon genetic complementation.

1 reference

7 January 2021

The mammalian peroxin Pex5pL, the longer isoform of the mobile peroxisome targeting signal (PTS) type 1 transporter, translocates the Pex7p.PTS2 protein complex into peroxisomes via its initial docking site, Pex14p

1 reference

7 January 2021

Peroxisomal targeting signal receptor Pex5p interacts with cargoes and import machinery components in a spatiotemporally differentiated manner: conserved Pex5p WXXXF/Y motifs are critical for matrix protein import

1 reference

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

7 January 2021

The human peroxisomal targeting signal receptor, Pex5p, is translocated into the peroxisomal matrix and recycled to the cytosol

1 reference

7 January 2021

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

1 reference

7 January 2021

Protein sorting by transport vesicles

1 reference

7 January 2021

Molecular anatomy of the peroxin Pex12p: ring finger domain is essential for Pex12p function and interacts with the peroxisome-targeting signal type 1-receptor Pex5p and a ring peroxin, Pex10p

1 reference

7 January 2021

Intracellular localization, function, and dysfunction of the peroxisome-targeting signal type 2 receptor, Pex7p, in mammalian cells

1 reference

7 January 2021