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Systematic multi-level analysis of an organelle proteome reveals new peroxisomal functions

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A novel PEX12 mutation identified as the cause of a peroxisomal biogenesis disorder with mild clinical phenotype, mild biochemical abnormalities in fibroblasts and a mosaic catalase immunofluorescence pattern, even at 40 °C

Determining the targeting specificity of the selective peroxisomal targeting factor Pex9

Zebrafish model of human Zellweger syndrome reveals organ specific accumulation of distinct fatty acid species and widespread gene expression changes

Systems-level organization of yeast methylotrophic lifestyle. - Abstract - Europe PMC

Systems-level organization of yeast methylotrophic lifestyle, BMC Biology

PDF) Systems-level organization of yeast methylotrophic lifestyle