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MetabolomicsSequential lipidomic, metabolomic, and proteomic analyses of serum, liver, and heart tissue specimens from peroxisomal biogenesis factor 11α knockout mice
Peroxisomes are versatile single membrane-enclosed cytoplasmic organelles, involved in reactive oxygen species (ROS) and lipid metabolism and diverse other metabolic processes. Peroxisomal disorders result from mutations in Pex genes-encoded proteins named peroxins (PEX proteins) and single peroxiso...
2022-02-02 | MTBLS1887 | MetaboLights
TranscriptomicsA Drosophila model for the Zellweger spectrum of peroxisome biogenesis disorders
Human peroxisome biogenesis disorders are lethal genetic disease in which abnormal peroxisome assembly compromises overall peroxisome and cellular function. Peroxisomes are ubiquitous membrane-bound organelles involved in several important biochemical processes, notably lipid metabolism and the use ...
ORGANISM(S): Drosophila melanogaster 
2011-07-02 | E-GEOD-30362 | biostudies-arrayexpress
UnknownPeroxisomal biogenesis is genetically and biochemically linked to carbohydrate metabolism in Drosophila and mouse.
Not available
S-EPMC5480855 | biostudies-literature
UnknownThe peroxisomal AAA ATPase complex prevents pexophagy and development of peroxisome biogenesis disorders.
Not available
S-EPMC5446072 | biostudies-literature
ProteomicsA Mitochondria-Driven Quality Control Pathway Eliminates Mislocalized Peroxisomal Membrane Proteins
Protein quality control (PQC) systems are essential for maintaining a healthy proteome by removing aberrant proteins, including mislocalized proteins. However, the mechanisms for eliminating mislocalized Peroxisomal Membrane Proteins (PMPs) have remained elusive. Here, using quantitative proteomics ...
ORGANISM(S): Homo sapiens (Human) 
2026-05-14 | PXD069489 | Pride
Peroxisome Protein degradation March5 E3 ligases Mul1 Ubiquitin Protein quality control Peroxisomal membrane proteins (pmps) 
UnknownPEX6 Mutations in Peroxisomal Biogenesis Disorders: An Usher Syndrome Mimic.
Not available
S-EPMC9559095 | biostudies-literature
UnknownDistinguishing PEX2 and PEX16 gene variant severity for mild, severe and atypical peroxisome biogenesis disorders.
Not available
S-EPMC12352285 | biostudies-literature
UnknownPlasma lipidomics as a diagnostic tool for peroxisomal disorders.
Not available
S-EPMC5959966 | biostudies-literature
UnknownDicarboxylic acylcarnitine biomarkers in peroxisome biogenesis disorders.
Not available
S-EPMC10840807 | biostudies-literature
UnknownContiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disorders.
Not available
S-EPMC419992 | biostudies-literature
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