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SF3A1
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An Error has occured retrieving Wikidata item for infobox SF3A1 (Splicing factor 3a subunit 1) هوَ بروتين يُشَفر بواسطة جين SF3A1 في الإنسان.[1][2][1]
الوظيفة
![[أيقونة]](/%D9%85%D9%84%D9%81:Crystal_xedit.svg){kind=small} | هذا القسم فارغ أو غير مكتمل. ساهم في توسيعه. (يوليو 2018) |
الأهمية السريرية
| هذا القسم فارغ أو غير مكتمل. ساهم في توسيعه. (يوليو 2018) |
المراجع
- ^ أ ب "Entrez Gene: SF3A1 splicing factor 3a, subunit 1, 120kDa". مؤرشف من الأصل في 2010-12-05.
- ^ Kramer A؛ Mulhauser F؛ Wersig C؛ Groning K؛ Bilbe G (يناير 1996). "Mammalian splicing factor SF3a120 represents a new member of the SURP family of proteins and is homologous to the essential splicing factor PRP21p of Saccharomyces cerevisiae". RNA. ج. 1 ع. 3: 260–72. PMC:1369079. PMID:7489498.
قراءة متعمقة
- Chiara MD، Champion-Arnaud P، Buvoli M، وآخرون (1994). "Specific protein-protein interactions between the essential mammalian spliceosome-associated proteins SAP 61 and SAP 114". Proc. Natl. Acad. Sci. U.S.A. ج. 91 ع. 14: 6403–7. Bibcode:1994PNAS...91.6403C. DOI:10.1073/pnas.91.14.6403. PMC:44210. PMID:8022796.
- Rain JC؛ Tartakoff AM؛ Krämer A؛ Legrain P (1996). "Essential domains of the PRP21 splicing factor are implicated in the binding to PRP9 and PRP11 proteins and are conserved through evolution". RNA. ج. 2 ع. 6: 535–50. PMC:1369393. PMID:8718683.
- Neubauer G، King A، Rappsilber J، وآخرون (1998). "Mass spectrometry and EST-database searching allows characterization of the multi-protein spliceosome complex". Nat. Genet. ج. 20 ع. 1: 46–50. DOI:10.1038/1700. PMID:9731529.
- "Toward a complete human genome sequence". Genome Res. ج. 8 ع. 11: 1097–108. 1999. DOI:10.1101/gr.8.11.1097. PMID:9847074.
- Krämer A؛ Grüter P؛ Gröning K؛ Kastner B (1999). "Combined biochemical and electron microscopic analyses reveal the architecture of the mammalian U2 snRNP". J. Cell Biol. ج. 145 ع. 7: 1355–68. DOI:10.1083/jcb.145.7.1355. PMC:2133165. PMID:10385517.
- Dunham I، Shimizu N، Roe BA، وآخرون (1999). "The DNA sequence of human chromosome 22". Nature. ج. 402 ع. 6761: 489–95. Bibcode:1999Natur.402..489D. DOI:10.1038/990031. PMID:10591208.
- Das R؛ Zhou Z؛ Reed R (2000). "Functional association of U2 snRNP with the ATP-independent spliceosomal complex E.". Mol. Cell. ج. 5 ع. 5: 779–87. DOI:10.1016/S1097-2765(00)80318-4. PMID:10882114.
- Gunther M؛ Laithier M؛ Brison O (2000). "A set of proteins interacting with transcription factor Sp1 identified in a two-hybrid screening". Mol. Cell. Biochem. ج. 210 ع. 1–2: 131–42. DOI:10.1023/A:1007177623283. PMID:10976766.
- Ajuh P، Kuster B، Panov K، وآخرون (2001). "Functional analysis of the human CDC5L complex and identification of its components by mass spectrometry". EMBO J. ج. 19 ع. 23: 6569–81. DOI:10.1093/emboj/19.23.6569. PMC:305846. PMID:11101529.
- Suzuki Y، Tsunoda T، Sese J، وآخرون (2001). "Identification and characterization of the potential promoter regions of 1031 kinds of human genes". Genome Res. ج. 11 ع. 5: 677–84. DOI:10.1101/gr.gr-1640r. PMC:311086. PMID:11337467.
- Will CL، Schneider C، MacMillan AM، وآخرون (2001). "A novel U2 and U11/U12 snRNP protein that associates with the pre-mRNA branch site". EMBO J. ج. 20 ع. 16: 4536–46. DOI:10.1093/emboj/20.16.4536. PMC:125580. PMID:11500380.
- Nesic D؛ Krämer A (2001). "Domains in human splicing factors SF3a60 and SF3a66 required for binding to SF3a120, assembly of the 17S U2 snRNP, and prespliceosome formation". Mol. Cell. Biol. ج. 21 ع. 19: 6406–17. DOI:10.1128/MCB.21.19.6406-6417.2001. PMC:99788. PMID:11533230.
- Jurica MS، Licklider LJ، Gygi SR، وآخرون (2002). "Purification and characterization of native spliceosomes suitable for three-dimensional structural analysis". RNA. ج. 8 ع. 4: 426–39. DOI:10.1017/S1355838202021088. PMC:1370266. PMID:11991638.
- Will CL، Urlaub H، Achsel T، وآخرون (2002). "Characterization of novel SF3b and 17S U2 snRNP proteins, including a human Prp5p homologue and an SF3b DEAD-box protein". EMBO J. ج. 21 ع. 18: 4978–88. DOI:10.1093/emboj/cdf480. PMC:126279. PMID:12234937.
- 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. Bibcode:2002PNAS...9916899M. DOI:10.1073/pnas.242603899. PMC:139241. PMID:12477932.
- Beausoleil SA، Jedrychowski M، Schwartz D، وآخرون (2004). "Large-scale characterization of HeLa cell nuclear phosphoproteins". Proc. Natl. Acad. Sci. U.S.A. ج. 101 ع. 33: 12130–5. Bibcode:2004PNAS..10112130B. DOI:10.1073/pnas.0404720101. PMC:514446. PMID:15302935.
- Nesic D؛ Tanackovic G؛ Krämer A (2005). "A role for Cajal bodies in the final steps of U2 snRNP biogenesis". J. Cell Sci. ج. 117 ع. Pt 19: 4423–33. DOI:10.1242/jcs.01308. PMID:15316075.
- Lin KT؛ Lu RM؛ Tarn WY (2004). "The WW domain-containing proteins interact with the early spliceosome and participate in pre-mRNA splicing in vivo". Mol. Cell. Biol. ج. 24 ع. 20: 9176–85. DOI:10.1128/MCB.24.20.9176-9185.2004. PMC:517884. PMID:15456888.
- Collins JE، Wright CL، Edwards CA، وآخرون (2005). "A genome annotation-driven approach to cloning the human ORFeome". Genome Biol. ج. 5 ع. 10: R84. DOI:10.1186/gb-2004-5-10-r84. PMC:545604. PMID:15461802.
