PEX10

An Error has occured retrieving Wikidata item for infobox PEX10‏ (Peroxisomal biogenesis factor 10) هوَ بروتين يُشَفر بواسطة جين PEX10 في الإنسان.

قراءة متعمقة

• Okumoto K، Itoh R، Shimozawa N، وآخرون (1998). "Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B.". Hum. Mol. Genet. ج. 7 ع. 9: 1399–405. DOI:10.1093/hmg/7.9.1399. PMID:9700193.
• South ST، Gould SJ (1999). "Peroxisome synthesis in the absence of preexisting peroxisomes". J. Cell Biol. ج. 144 ع. 2: 255–66. DOI:10.1083/jcb.144.2.255. PMC:2132891. PMID:9922452.
• Chang CC، Warren DS، Sacksteder KA، Gould SJ (1999). "PEX12 interacts with PEX5 and PEX10 and acts downstream of receptor docking in peroxisomal matrix protein import". J. Cell Biol. ج. 147 ع. 4: 761–74. DOI:10.1083/jcb.147.4.761. PMC:2156163. PMID:10562279.
• Sacksteder KA، Jones JM، South ST، وآخرون (2000). "PEX19 binds multiple peroxisomal membrane proteins, is predominantly cytoplasmic, and is required for peroxisome membrane synthesis". J. Cell Biol. ج. 148 ع. 5: 931–44. DOI:10.1083/jcb.148.5.931. PMC:2174547. PMID:10704444.
• Okumoto K، Abe I، Fujiki Y (2000). "Molecular anatomy of the peroxin Pex12p: ring finger domain is essential for Pex12p function and interacts with the peroxisome-targeting signal type 1-receptor Pex5p and a ring peroxin, Pex10p". J. Biol. Chem. ج. 275 ع. 33: 25700–10. DOI:10.1074/jbc.M003303200. PMID:10837480.
• Warren DS، Wolfe BD، Gould SJ (2000). "Phenotype-genotype relationships in PEX10-deficient peroxisome biogenesis disorder patients". Hum. Mutat. ج. 15 ع. 6: 509–21. DOI:10.1002/1098-1004(200006)15:6<509::AID-HUMU3>3.0.CO;2-#. PMID:10862081.
• Fransen M، Wylin T، Brees C، وآخرون (2001). "Human pex19p binds peroxisomal integral membrane proteins at regions distinct from their sorting sequences". Mol. Cell. Biol. ج. 21 ع. 13: 4413–24. DOI:10.1128/MCB.21.13.4413-4424.2001. PMC:87101. PMID:11390669.
• Fransen M، Brees C، Ghys K، وآخرون (2002). "Analysis of mammalian peroxin interactions using a non-transcription-based bacterial two-hybrid assay". Mol. Cell. Proteomics. ج. 1 ع. 3: 243–52. DOI:10.1074/mcp.M100025-MCP200. PMID:12096124.
• Strausberg RL، Feingold EA، Grouse LH، وآخرون (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. ج. 99 ع. 26: 16899–903. DOI:10.1073/pnas.242603899. PMC:139241. PMID:12477932.
• Ota T، Suzuki Y، Nishikawa T، وآخرون (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. ج. 36 ع. 1: 40–5. DOI:10.1038/ng1285. PMID:14702039.
• Shimozawa N، Nagase T، Takemoto Y، وآخرون (2004). "Genetic heterogeneity in Japanese patients with peroxisome biogenesis disorders and evidence for a founder haplotype for the most common mutation in PEX10 gene". Adv. Exp. Med. Biol. ج. 544: 71. DOI:10.1007/978-1-4419-9072-3_10. PMID:14713216.
• Gerhard DS، Wagner L، Feingold EA، وآخرون (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. ج. 14 ع. 10B: 2121–7. DOI:10.1101/gr.2596504. PMC:528928. PMID:15489334.
• Rual JF، Venkatesan K، Hao T، وآخرون (2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. ج. 437 ع. 7062: 1173–8. DOI:10.1038/nature04209. PMID:16189514.
• Gregory SG، Barlow KF، McLay KE، وآخرون (2006). "The DNA sequence and biological annotation of human chromosome 1". Nature. ج. 441 ع. 7091: 315–21. DOI:10.1038/nature04727. PMID:16710414.