Concepedia

Rhizomelic chondrodysplasia punctata is a peroxisomal protein targeting disease caused by a non-functional PTS2 receptor

Alison M. Motley, Ewald H. Hettema, Eveline M. Hogenhout, Pedro Brites, Anneloor L.M.A. ten Asbroek, Frits A. Wijburg, Frank Baas, Hugo S.A. Heijmans, Henk F. Tabak, Ronald J. A. Wanders,

Nature Genetics · 1997 · 272 citations · 25 references

DOI

Concepts

References

25

A novel, cleavable peroxisomal targeting signal at the amino‐terminus of the rat 3‐ketoacyl‐CoA thiolase.

Bart W. Swinkels, Stephen J. Gould, Andrea Bodnár et al. · The EMBO Journal · 1991 · 626 citations · Full text

, , +11

Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders

Gabriele Dodt, Nancy Braverman, C Wong et al. · Nature Genetics · 1995 · 426 citations

, , +12

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.

Gabriele Dodt, S. J. GOULD · The Journal of Cell Biology · 1996 · 319 citations · Full text

, , +12

PAS7 encodes a novel yeast member of the WD‐40 protein family essential for import of 3‐oxoacyl‐CoA thiolase, a PTS2‐containing protein, into peroxisomes.

Martina Marzioch, Ralf Erdmann, Marten Veenhuis et al. · The EMBO Journal · 1994 · 294 citations · Full text

, , +6

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

Toshiro Tsukamoto, Satoshi Miura, Yukio Fujiki · Nature · 1991 · 251 citations

, , +15