PEX13

PEX13

Peroxisome biogenesis factor 13, also known as PEX13, is a human gene.cite web | title = Entrez Gene: PEX13 peroxisome biogenesis factor 13| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=5194| accessdate = ]

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References

Further reading

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*cite journal | author=Gould SJ, Kalish JE, Morrell JC, "et al." |title=Pex13p is an SH3 protein of the peroxisome membrane and a docking factor for the predominantly cytoplasmic PTs1 receptor. |journal=J. Cell Biol. |volume=135 |issue= 1 |pages= 85–95 |year= 1996 |pmid= 8858165 |doi=
*cite journal | author=Albertini M, Rehling P, Erdmann R, "et al." |title=Pex14p, a peroxisomal membrane protein binding both receptors of the two PTS-dependent import pathways. |journal=Cell |volume=89 |issue= 1 |pages= 83–92 |year= 1997 |pmid= 9094717 |doi=
*cite journal | author=Fransen M, Terlecky SR, Subramani S |title=Identification of a human PTS1 receptor docking protein directly required for peroxisomal protein import. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=95 |issue= 14 |pages= 8087–92 |year= 1998 |pmid= 9653144 |doi=
*cite journal | author=Björkman J, Stetten G, Moore CS, "et al." |title=Genomic structure of PEX13, a candidate peroxisome biogenesis disorder gene. |journal=Genomics |volume=54 |issue= 3 |pages= 521–8 |year= 1999 |pmid= 9878256 |doi= 10.1006/geno.1998.5520
*cite journal | author=Girzalsky W, Rehling P, Stein K, "et al." |title=Involvement of Pex13p in Pex14p localization and peroxisomal targeting signal 2-dependent protein import into peroxisomes. |journal=J. Cell Biol. |volume=144 |issue= 6 |pages= 1151–62 |year= 1999 |pmid= 10087260 |doi=
*cite journal | author=Shimozawa N, Suzuki Y, Zhang Z, "et al." |title=Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders. |journal=Hum. Mol. Genet. |volume=8 |issue= 6 |pages= 1077–83 |year= 1999 |pmid= 10332040 |doi=
*cite journal | author=Toyama R, Mukai S, Itagaki A, "et al." |title=Isolation, characterization and mutation analysis of PEX13-defective Chinese hamster ovary cell mutants. |journal=Hum. Mol. Genet. |volume=8 |issue= 9 |pages= 1673–81 |year= 2000 |pmid= 10441330 |doi=
*cite journal | author=Liu Y, Björkman J, Urquhart A, "et al." |title=PEX13 is mutated in complementation group 13 of the peroxisome-biogenesis disorders. |journal=Am. J. Hum. Genet. |volume=65 |issue= 3 |pages= 621–34 |year= 1999 |pmid= 10441568 |doi=
*cite journal | author=Sacksteder KA, Jones JM, South ST, "et al." |title=PEX19 binds multiple peroxisomal membrane proteins, is predominantly cytoplasmic, and is required for peroxisome membrane synthesis. |journal=J. Cell Biol. |volume=148 |issue= 5 |pages= 931–44 |year= 2000 |pmid= 10704444 |doi=
*cite journal | author=Fransen M, Wylin T, Brees C, "et al." |title=Human pex19p binds peroxisomal integral membrane proteins at regions distinct from their sorting sequences. |journal=Mol. Cell. Biol. |volume=21 |issue= 13 |pages= 4413–24 |year= 2001 |pmid= 11390669 |doi= 10.1128/MCB.21.13.4413-4424.2001
*cite journal | author=Jones JM, Morrell JC, Gould SJ |title=Multiple distinct targeting signals in integral peroxisomal membrane proteins. |journal=J. Cell Biol. |volume=153 |issue= 6 |pages= 1141–50 |year= 2001 |pmid= 11402059 |doi=
*cite journal | author=Otera H, Setoguchi K, Hamasaki M, "et al." |title=Peroxisomal targeting signal receptor Pex5p interacts with cargoes and import machinery components in a spatiotemporally differentiated manner: conserved Pex5p WXXXF/Y motifs are critical for matrix protein import. |journal=Mol. Cell. Biol. |volume=22 |issue= 6 |pages= 1639–55 |year= 2002 |pmid= 11865044 |doi=
*cite journal | author=Fransen M, Brees C, Ghys K, "et al." |title=Analysis of mammalian peroxin interactions using a non-transcription-based bacterial two-hybrid assay. |journal=Mol. Cell Proteomics |volume=1 |issue= 3 |pages= 243–52 |year= 2002 |pmid= 12096124 |doi=
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Fransen M, Vastiau I, Brees C, "et al." |title=Potential role for Pex19p in assembly of PTS-receptor docking complexes. |journal=J. Biol. Chem. |volume=279 |issue= 13 |pages= 12615–24 |year= 2004 |pmid= 14715663 |doi= 10.1074/jbc.M304941200
*cite journal | author=Gerhard DS, Wagner L, Feingold EA, "et al." |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504
*cite journal | author=Hashimoto K, Kato Z, Nagase T, "et al." |title=Molecular mechanism of a temperature-sensitive phenotype in peroxisomal biogenesis disorder. |journal=Pediatr. Res. |volume=58 |issue= 2 |pages= 263–9 |year= 2005 |pmid= 16006427 |doi= 10.1203/01.PDR.0000169984.89199.69
*cite journal | author=Nguyen T, Bjorkman J, Paton BC, Crane DI |title=Failure of microtubule-mediated peroxisome division and trafficking in disorders with reduced peroxisome abundance. |journal=J. Cell. Sci. |volume=119 |issue= Pt 4 |pages= 636–45 |year= 2006 |pmid= 16449325 |doi= 10.1242/jcs.02776

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