PEX12
PEX12 (Peroxisomal biogenesis factor 12) هوَ بروتين يُشَفر بواسطة جين PEX12 في الإنسان.[1][2]
المراجع
- "Isolation of the human PEX12 gene, mutated in group 3 of the peroxisome biogenesis disorders"، Nat Genet، 15 (4): 385–8، أبريل 1997، doi:10.1038/ng0497-385، PMID 9090384.
- "Entrez Gene: PEX12 peroxisomal biogenesis factor 12"، مؤرشف من الأصل في 05 ديسمبر 2010.
قراءة متعمقة
- "PEX12 encodes an integral membrane protein of peroxisomes"، Nat. Genet.، 17 (3): 265–6، 1997، doi:10.1038/ng1197-265، PMID 9354782.
- "Expression of PEX11beta mediates peroxisome proliferation in the absence of extracellular stimuli"، J. Biol. Chem.، 273 (45): 29607–14، 1998، doi:10.1074/jbc.273.45.29607، PMID 9792670.
- "Phenotype-genotype relationships in complementation group 3 of the peroxisome-biogenesis disorders"، Am. J. Hum. Genet.، 63 (5): 1294–306، 1998، doi:10.1086/302103، PMC 1377540، PMID 9792857.
- "Peroxisome Synthesis in the Absence of Preexisting Peroxisomes"، J. Cell Biol.، 144 (2): 255–66، 1999، doi:10.1083/jcb.144.2.255، PMC 2132891، PMID 9922452.
- "Pex12 Interacts with Pex5 and Pex10 and Acts Downstream of Receptor Docking in Peroxisomal Matrix Protein Import"، J. Cell Biol.، 147 (4): 761–74، 1999، doi:10.1083/jcb.147.4.761، PMC 2156163، PMID 10562279.
- "Pex19 Binds Multiple Peroxisomal Membrane Proteins, Is Predominantly Cytoplasmic, and Is Required for Peroxisome Membrane Synthesis"، J. Cell Biol.، 148 (5): 931–44، 2000، doi:10.1083/jcb.148.5.931، PMC 2174547، PMID 10704444.
- "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.، 275 (33): 25700–10، 2000، doi:10.1074/jbc.M003303200، PMID 10837480.
- "Human Pex19p Binds Peroxisomal Integral Membrane Proteins at Regions Distinct from Their Sorting Sequences"، Mol. Cell. Biol.، 21 (13): 4413–24، 2001، doi:10.1128/MCB.21.13.4413-4424.2001، PMC 87101، PMID 11390669.
- "Analysis of mammalian peroxin interactions using a non-transcription-based bacterial two-hybrid assay"، Mol. Cell. Proteomics، 1 (3): 243–52، 2002، doi:10.1074/mcp.M100025-MCP200، PMID 12096124.
- "PEX5 binds the PTS1 independently of Hsp70 and the peroxin PEX12"، J. Biol. Chem.، 278 (10): 7897–901، 2003، doi:10.1074/jbc.M206651200، PMID 12456682.
- "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences"، Proc. Natl. Acad. Sci. U.S.A.، 99 (26): 16899–903، 2003، doi:10.1073/pnas.242603899، PMC 139241، PMID 12477932.
- "Novel mutations in the PEX12 gene of patients with a peroxisome biogenesis disorder"، Eur. J. Hum. Genet.، 12 (2): 115–20، 2004، doi:10.1038/sj.ejhg.5201090، PMID 14571262.
- "Identification of the molecular defect in patients with peroxisomal mosaicism using a novel method involving culturing of cells at 40 degrees C: implications for other inborn errors of metabolism"، Hum. Mutat.، 24 (2): 130–9، 2004، doi:10.1002/humu.20062، PMID 15241794.
- "The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)"، Genome Res.، 14 (10B): 2121–7، 2004، doi:10.1101/gr.2596504، PMC 528928، PMID 15489334.
- "The Arabidopsis pex12 and pex13 mutants are defective in both PTS1- and PTS2-dependent protein transport to peroxisomes"، Plant J.، 47 (4): 604–18، 2007، doi:10.1111/j.1365-313X.2006.02809.x، PMID 16813573.
- "A novel PEX12 mutation identified as the cause of a peroxisomal biogenesis disorder with mild clinical phenotype, mild biochemical abnormalities in fibroblasts and a mosaic catalase immunofluorescence pattern, even at 40 degrees C"، J. Hum. Genet.، 52 (7): 599–606، 2007، doi:10.1007/s10038-007-0157-y، PMID 17534573.
بوابة طب
بوابة علم الأحياء الخلوي والجزيئي
بوابة الكيمياء الحيوية
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