[cite web | title = Entrez Gene: PEX6 peroxisomal biogenesis factor 6| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=5190| accessdate = ] ] PBB_Summary
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References
Further reading
PBB_Further_reading
citations =
*cite journal | author=Maruyama K, Sugano S |title=Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides. |journal=Gene |volume=138 |issue= 1-2 |pages= 171–4 |year= 1994 |pmid= 8125298 |doi=
*cite journal | author=Yahraus T, Braverman N, Dodt G, "et al." |title=The peroxisome biogenesis disorder group 4 gene, PXAAA1, encodes a cytoplasmic ATPase required for stability of the PTS1 receptor. |journal=EMBO J. |volume=15 |issue= 12 |pages= 2914–23 |year= 1996 |pmid= 8670792 |doi=
*cite journal | author=Fukuda S, Shimozawa N, Suzuki Y, "et al." |title=Human peroxisome assembly factor-2 (PAF-2): a gene responsible for group C peroxisome biogenesis disorder in humans. |journal=Am. J. Hum. Genet. |volume=59 |issue= 6 |pages= 1210–20 |year= 1997 |pmid= 8940266 |doi=
*cite journal | author=Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, "et al." |title=Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library. |journal=Gene |volume=200 |issue= 1-2 |pages= 149–56 |year= 1997 |pmid= 9373149 |doi=
*cite journal | author=Tamura S, Shimozawa N, Suzuki Y, "et al." |title=A cytoplasmic AAA family peroxin, Pex1p, interacts with Pex6p. |journal=Biochem. Biophys. Res. Commun. |volume=245 |issue= 3 |pages= 883–6 |year= 1998 |pmid= 9588209 |doi= 10.1006/bbrc.1998.8522
*cite journal | author=Geisbrecht BV, Collins CS, Reuber BE, Gould SJ |title=Disruption of a PEX1-PEX6 interaction is the most common cause of the neurologic disorders Zellweger syndrome, neonatal adrenoleukodystrophy, and infantile Refsum disease. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=95 |issue= 15 |pages= 8630–5 |year= 1998 |pmid= 9671729 |doi=
*cite journal | author=Zhang Z, Suzuki Y, Shimozawa N, "et al." |title=Genomic structure and identification of 11 novel mutations of the PEX6 (peroxisome assembly factor-2) gene in patients with peroxisome biogenesis disorders. |journal=Hum. Mutat. |volume=13 |issue= 6 |pages= 487–96 |year= 1999 |pmid= 10408779 |doi= 10.1002/(SICI)1098-1004(1999)13:6<487::AID-HUMU9>3.0.CO;2-T |doilabel=10.1002/(SICI)1098-1004(1999)13:6487::AID-HUMU93.0.CO;2-T
*cite journal | author=Matsumoto N, Tamura S, Moser A, "et al." |title=The peroxin Pex6p gene is impaired in peroxisomal biogenesis disorders of complementation group 6. |journal=J. Hum. Genet. |volume=46 |issue= 5 |pages= 273–7 |year= 2001 |pmid= 11355018 |doi=
*cite journal | author=Tamura S, Matsumoto N, Imamura A, "et al." |title=Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction. |journal=Biochem. J. |volume=357 |issue= Pt 2 |pages= 417–26 |year= 2001 |pmid= 11439091 |doi=
*cite journal | author=Raas-Rothschild A, Wanders RJ, Mooijer PA, "et al." |title=A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parents. |journal=Am. J. Hum. Genet. |volume=70 |issue= 4 |pages= 1062–8 |year= 2002 |pmid= 11873320 |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=Matsumoto N, Tamura S, Fujiki Y |title=The pathogenic peroxin Pex26p recruits the Pex1p-Pex6p AAA ATPase complexes to peroxisomes. |journal=Nat. Cell Biol. |volume=5 |issue= 5 |pages= 454–60 |year= 2003 |pmid= 12717447 |doi= 10.1038/ncb982
*cite journal | author=Warner DR, Roberts EA, Greene RM, Pisano MM |title=Identification of novel Smad binding proteins. |journal=Biochem. Biophys. Res. Commun. |volume=312 |issue= 4 |pages= 1185–90 |year= 2004 |pmid= 14651998 |doi=
*cite journal | author=Colland F, Jacq X, Trouplin V, "et al." |title=Functional proteomics mapping of a human signaling pathway. |journal=Genome Res. |volume=14 |issue= 7 |pages= 1324–32 |year= 2004 |pmid= 15231748 |doi= 10.1101/gr.2334104
*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=Furuki S, Tamura S, Matsumoto N, "et al." |title=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. |journal=J. Biol. Chem. |volume=281 |issue= 3 |pages= 1317–23 |year= 2006 |pmid= 16257970 |doi= 10.1074/jbc.M510044200
*cite journal | author=Tamura S, Yasutake S, Matsumoto N, Fujiki Y |title=Dynamic and functional assembly of the AAA peroxins, Pex1p and Pex6p, and their membrane receptor Pex26p. |journal=J. Biol. Chem. |volume=281 |issue= 38 |pages= 27693–704 |year= 2006 |pmid= 16854980 |doi= 10.1074/jbc.M605159200
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