| YEAR | FIRST AUTHOR | JOURNAL | TITLE |
|---|---|---|---|
| 2009 | Yik Yik | Hum. Mutat. | Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disorders.[Pubmed] |
| 2008 | Yukio Fujiki | Biochem. Soc. Trans. | Dynamic and functional assembly of the AAA peroxins, Pex1p and Pex6p, and their membrane receptor Pex26p involved in shuttling of the PTS1 receptor Pex5p in peroxisome biogenesis.[Pubmed] |
| 2006 | Shigehiko Tamura | J. Biol. Chem. | Dynamic and functional assembly of the AAA peroxins, Pex1p and Pex6p, and their membrane receptor Pex26p.[Pubmed] |
| 2006 | Satomi Furuki | J. Biol. Chem. | Mutations in the peroxin Pex26p responsible for peroxisome biogenesis disorders of complementation group 8 impair its stability, peroxisomal localization, and interaction with the Pex1p x Pex6p complex.[Pubmed] |
| 2006 | André Halbach | J. Cell. Sci. | Targeting of the tail-anchored peroxisomal membrane proteins PEX26 and PEX15 occurs through C-terminal PEX19-binding sites.[Pubmed] |
| 2005 | Sabine Weller | Am. J. Hum. Genet. | Alternative splicing suggests extended function of PEX26 in peroxisome biogenesis.[Pubmed] |
| 2005 | Non Miyata | Mol. Cell. Biol. | Shuttling mechanism of peroxisome targeting signal type 1 receptor Pex5: ATP-independent import and ATP-dependent export.[Pubmed] |
| 2004 | Steven Steinberg | Mol. Genet. Metab. | The PEX Gene Screen: molecular diagnosis of peroxisome biogenesis disorders in the Zellweger syndrome spectrum.[Pubmed] |
| 2003 | Naomi Matsumoto | Am. J. Hum. Genet. | Mutations in novel peroxin gene PEX26 that cause peroxisome-biogenesis disorders of complementation group 8 provide a genotype-phenotype correlation.[Pubmed] |
| 2003 | Naomi Matsumoto | Nat. Cell Biol. | The pathogenic peroxin Pex26p recruits the Pex1p-Pex6p AAA ATPase complexes to peroxisomes.[Pubmed] |