PABPN1
PABPN1 (Poly(A) binding protein nuclear 1) هوَ بروتين يُشَفر بواسطة جين PABPN1 في الإنسان.[1][2]
المراجع
- "The oculopharyngeal muscular dystrophy locus maps to the region of the cardiac alpha and beta myosin heavy chain genes on chromosome 14q11.2-q13"، Hum Mol Genet، 4 (3): 429–34، أغسطس 1995، doi:10.1093/hmg/4.3.429، PMID 7795598.
- "Entrez Gene: PABPN1 poly(A) binding protein, nuclear 1"، مؤرشف من الأصل في 06 مارس 2010.
قراءة متعمقة
- "Short GCG expansions in the PABP2 gene cause oculopharyngeal muscular dystrophy"، Nat. Genet.، 18 (2): 164–7، 1998، doi:10.1038/ng0298-164، PMID 9462747.
- "Influenza A virus NS1 protein targets poly(A)-binding protein II of the cellular 3'-end processing machinery"، EMBO J.، 18 (8): 2273–83، 1999، doi:10.1093/emboj/18.8.2273، PMC 1171310، PMID 10205180.
- "Unusual sites of arginine methylation in Poly(A)-binding protein II and in vitro methylation by protein arginine methyltransferases PRMT1 and PRMT3"، J. Biol. Chem.، 274 (19): 13229–34، 1999، doi:10.1074/jbc.274.19.13229، PMID 10224081.
- "The eukaryotic polypeptide chain releasing factor (eRF3/GSPT) carrying the translation termination signal to the 3'-Poly(A) tail of mRNA. Direct association of erf3/GSPT with polyadenylate-binding protein"، J. Biol. Chem.، 274 (24): 16677–80، 1999، doi:10.1074/jbc.274.24.16677، PMID 10358005.
- "Chromosomal localization of three human poly(A)-binding protein genes and four related pseudogenes"، Hum. Genet.، 105 (4): 347–53، 1999، doi:10.1007/s004390051113، PMC 1865476، PMID 10543404.
- "Deciphering the cellular pathway for transport of poly(A)-binding protein II"، RNA، 6 (2): 245–56، 2000، doi:10.1017/S1355838200991908، PMC 1369910، PMID 10688363.
- "Nuclear inclusions in oculopharyngeal muscular dystrophy consist of poly(A) binding protein 2 aggregates which sequester poly(A) RNA"، Hum. Mol. Genet.، 9 (15): 2321–8، 2001، doi:10.1093/oxfordjournals.hmg.a018924، PMID 11001936.
- "The product of an oculopharyngeal muscular dystrophy gene, poly(A)-binding protein 2, interacts with SKIP and stimulates muscle-specific gene expression"، Hum. Mol. Genet.، 10 (11): 1129–39، 2001، doi:10.1093/hmg/10.11.1129، PMID 11371506.
- "Oligomerization of polyalanine expanded PABPN1 facilitates nuclear protein aggregation that is associated with cell death"، Hum. Mol. Genet.، 10 (21): 2341–51، 2002، doi:10.1093/hmg/10.21.2341، PMID 11689481.
- "Oculopharyngeal muscular dystrophy (OPMD) due to a small duplication in the PABPN1 gene"، Hum. Mutat.، 21 (5): 553، 2003، doi:10.1002/humu.9138، PMID 12673802.
- "HnRNP A1 and A/B interaction with PABPN1 in oculopharyngeal muscular dystrophy"، The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques، 30 (3): 244–51، 2003، doi:10.1017/s0317167100002675، PMID 12945950.
- "An aggregate-prone conformational epitope in trinucleotide repeat diseases"، NeuroReport، 14 (18): 2331–5، 2004، doi:10.1097/01.wnr.0000089568.45990.3d، PMID 14663186.
- "The composition of Staufen-containing RNA granules from human cells indicates their role in the regulated transport and translation of messenger RNAs"، Nucleic Acids Res.، 32 (8): 2411–20، 2004، doi:10.1093/nar/gkh552، PMC 419443، PMID 15121898.
- "Distinct sequence motifs within the 68-kDa subunit of cleavage factor Im mediate RNA binding, protein-protein interactions, and subcellular localization"، J. Biol. Chem.، 279 (34): 35788–97، 2005، doi:10.1074/jbc.M403927200، PMID 15169763.
- "(GCG)11 founder mutation in the PABPN1 gene of OPMD Uruguayan families"، Neuromuscul. Disord.، 15 (2): 185–90، 2005، doi:10.1016/j.nmd.2004.10.012، PMID 15694141.
- "Oculopharyngeal muscular dystrophy with PABPN1 mutation in a Chinese Malaysian woman"، Neuromuscul. Disord.، 15 (3): 262–4، 2005، doi:10.1016/j.nmd.2004.10.016، PMID 15725589.
- "Transgenic expression of an expanded (GCG)13 repeat PABPN1 leads to weakness and coordination defects in mice"، Neurobiol. Dis.، 18 (3): 528–36، 2005، doi:10.1016/j.nbd.2004.09.021، PMID 15755680.
بوابة طب
بوابة الكيمياء الحيوية
بوابة علم الأحياء الخلوي والجزيئي
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