| YEAR | FIRST AUTHOR | JOURNAL | TITLE |
|---|---|---|---|
| 2008 | Takashi Matsuzaki | J. Cell Biol. | The peroxisomal membrane protein import receptor Pex3p is directly transported to peroxisomes by a novel Pex19p- and Pex16p-dependent pathway.[Pubmed] |
| 2007 | Sashko Cooper | Dev. Dyn. | Peroxisome biogenesis occurs in late dorsal-anterior structures in the development of Xenopus laevis.[Pubmed] |
| 2007 | Tong Guo | J. Cell Biol. | A signal from inside the peroxisome initiates its division by promoting the remodeling of the peroxisomal membrane.[Pubmed] |
| 2007 | Kazumasa Nito | Plant Cell Physiol. | Functional classification of Arabidopsis peroxisome biogenesis factors proposed from analyses of knockdown mutants.[Pubmed] |
| 2006 | Clara Pinto | J. Biol. Chem. | The import competence of a peroxisomal membrane protein is determined by Pex19p before the docking step.[Pubmed] |
| 2005 | Christopher Brocard | Traffic | Requirement for microtubules and dynein motors in the earliest stages of peroxisome biogenesis.[Pubmed] |
| 2005 | Karnik Karnik | Plant Physiol. | Arabidopsis peroxin 16 coexists at steady state in peroxisomes and endoplasmic reticulum.[Pubmed] |
| 2004 | Hiroyuki Shibata | J. Biol. Chem. | Domain architecture and activity of human Pex19p, a chaperone-like protein for intracellular trafficking of peroxisomal membrane proteins.[Pubmed] |
| 2003 | Sietske Hogenboom | Mol. Genet. Metab. | Cholesterol biosynthesis is not defective in peroxisome biogenesis defective fibroblasts.[Pubmed] |
| 2002 | Masanori Honsho | J. Biol. Chem. | The membrane biogenesis peroxin Pex16p. Topogenesis and functional roles in peroxisomal membrane assembly.[Pubmed] |
| 2002 | Nobuyuki Shimozawa | Biochem. Biophys. Res. Commun. | A novel aberrant splicing mutation of the PEX16 gene in two patients with Zellweger syndrome.[Pubmed] |
| 2001 | M Fransen | Mol. Cell. Biol. | Human pex19p binds peroxisomal integral membrane proteins at regions distinct from their sorting sequences.[Pubmed] |
| 2001 | Y Suzuki | J. Inherit. Metab. Dis. | Clinical, biochemical and genetic aspects and neuronal migration in peroxisome biogenesis disorders.[Pubmed] |
| 2001 | T Voorn-Brouwer | J. Cell. Sci. | Peroxisomal membrane proteins are properly targeted to peroxisomes in the absence of COPI- and COPII-mediated vesicular transport.[Pubmed] |
| 1999 | Y Lin | Science | The Pex16p homolog SSE1 and storage organelle formation in Arabidopsis seeds.[Pubmed] |
| 1999 | South South | J. Cell Biol. | Peroxisome synthesis in the absence of preexisting peroxisomes.[Pubmed] |
| 1998 | M Honsho | Am. J. Hum. Genet. | Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.[Pubmed] |
| 1998 | Titorenko Titorenko | Mol. Cell. Biol. | Mutants of the yeast Yarrowia lipolytica defective in protein exit from the endoplasmic reticulum are also defective in peroxisome biogenesis.[Pubmed] |
| 1997 | Titorenko Titorenko | Mol. Cell. Biol. | Four distinct secretory pathways serve protein secretion, cell surface growth, and peroxisome biogenesis in the yeast Yarrowia lipolytica.[Pubmed] |
| 1997 | Eitzen Eitzen | J. Cell Biol. | Enlarged peroxisomes are present in oleic acid-grown Yarrowia lipolytica overexpressing the PEX16 gene encoding an intraperoxisomal peripheral membrane peroxin.[Pubmed] |