E2F4
E2F4 (E2F transcription factor 4) هوَ بروتين يُشَفر بواسطة جين E2F4 في الإنسان.[1][2]
المراجع
- "E2F-4, a new member of the E2F transcription factor family, interacts with p107"، Genes Dev، 8 (22): 2665–79، ديسمبر 1994، doi:10.1101/gad.8.22.2665، PMID 7958924.
- "E2F-4 and E2F-5, two members of the E2F family, are expressed in the early phases of the cell cycle"، Proc Natl Acad Sci U S A، 92 (6): 2403–7، أبريل 1995، doi:10.1073/pnas.92.6.2403، PMC 42492، PMID 7892279.
قراءة متعمقة
- "The human melanocyte: a model system to study the complexity of cellular aging and transformation in non-fibroblastic cells."، Exp. Gerontol.، 36 (8): 1265–75، 2001، doi:10.1016/S0531-5565(01)00098-5، PMID 11602203.
- "E2F-4, a new member of the E2F gene family, has oncogenic activity and associates with p107 in vivo."، Genes Dev.، 8 (22): 2680–90، 1994، doi:10.1101/gad.8.22.2680، PMID 7958925.
- "Regulation of the retinoblastoma protein-related protein p107 by G1 cyclin-associated kinases."، Proc. Natl. Acad. Sci. U.S.A.، 93 (10): 4633–7، 1996، doi:10.1073/pnas.93.10.4633، PMC 39330، PMID 8643455.
- "E2F-4 switches from p130 to p107 and pRB in response to cell cycle reentry."، Mol. Cell. Biol.، 16 (4): 1436–49، 1996، PMC 231128، PMID 8657117.
- "Reverse two-hybrid and one-hybrid systems to detect dissociation of protein-protein and DNA-protein interactions."، Proc. Natl. Acad. Sci. U.S.A.، 93 (19): 10315–20، 1996، doi:10.1073/pnas.93.19.10315، PMC 38381، PMID 8816797.
- "The predominant E2F complex in human primary haemopoietic cells and in AML blasts contains E2F-4, DP-1 and p130."، Br. J. Haematol.، 96 (4): 688–96، 1997، doi:10.1046/j.1365-2141.1997.d01-2086.x، PMID 9074408.
- "The subcellular localization of E2F-4 is cell-cycle dependent."، Proc. Natl. Acad. Sci. U.S.A.، 94 (10): 5095–100، 1997، doi:10.1073/pnas.94.10.5095، PMC 24637، PMID 9144196.
- "BRCA1 proteins are transported to the nucleus in the absence of serum and splice variants BRCA1a, BRCA1b are tyrosine phosphoproteins that associate with E2F, cyclins and cyclin dependent kinases."، Oncogene، 15 (2): 143–57، 1997، doi:10.1038/sj.onc.1201252، PMID 9244350.
- "Induction of S-phase entry by E2F transcription factors depends on their nuclear localization."، Mol. Cell. Biol.، 17 (9): 5508–20، 1997، PMC 232399، PMID 9271426.
- "Differential activities of E2F family members: unique functions in regulating transcription."، Mol. Carcinog.، 22 (3): 190–8، 1998، doi:10.1002/(SICI)1098-2744(199807)22:3<190::AID-MC7>3.0.CO;2-P، PMID 9688145.
- "The three members of the pocket proteins family share the ability to repress E2F activity through recruitment of a histone deacetylase."، Proc. Natl. Acad. Sci. U.S.A.، 95 (18): 10493–8، 1998، doi:10.1073/pnas.95.18.10493، PMC 27922، PMID 9724731.
- "C/EBPalpha regulates formation of S-phase-specific E2F-p107 complexes in livers of newborn mice."، Mol. Cell. Biol.، 19 (4): 2936–45، 1999، PMC 84088، PMID 10082561.
- "Structural basis of DNA recognition by the heterodimeric cell cycle transcription factor E2F-DP."، Genes Dev.، 13 (6): 666–74، 1999، doi:10.1101/gad.13.6.666، PMC 316551، PMID 10090723.
- "Transcriptional repression of the E2F-1 gene by interferon-alpha is mediated through induction of E2F-4/pRB and E2F-4/p130 complexes."، Oncogene، 18 (11): 2003–14، 1999، doi:10.1038/sj.onc.1202500، PMID 10208422.
- "Modulation of E2F activity in primary mouse B cells following stimulation via surface IgM and CD40 receptors."، Eur. J. Immunol.، 29 (10): 3380–9، 1999، doi:10.1002/(SICI)1521-4141(199910)29:10<3380::AID-IMMU3380>3.0.CO;2-C، PMID 10540350.
- "Various AGC repeat numbers in the coding region of the human transcription factor gene E2F-4."، Hum. Mutat.، 15 (3): 296–7، 2000، doi:10.1002/(SICI)1098-1004(200003)15:3<296::AID-HUMU18>3.0.CO;2-X، PMID 10679953.
- "Analysis of promoter binding by the E2F and pRB families in vivo: distinct E2F proteins mediate activation and repression."، Genes Dev.، 14 (7): 804–16، 2000، doi:10.1101/gad.14.7.804، PMC 316494، PMID 10766737.
- "Genomic structure and mutation screening of the E2F4 gene in human tumors."، Int. J. Cancer، 86 (5): 672–7، 2000، doi:10.1002/(SICI)1097-0215(20000601)86:5<672::AID-IJC11>3.0.CO;2-X، PMID 10797289.
- بوابة الكيمياء الحيوية
- بوابة طب
- بوابة علم الأحياء الخلوي والجزيئي
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