FOXJ2
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Species | Human | Mouse | |||||
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Forkhead box protein J2 is a protein that in humans is encoded by the FOXJ2 gene.[1][2][3]
References
- ↑ Perez-Sanchez C, Gomez-Ferreria MA, de La Fuente CA, Granadino B, Velasco G, Esteban-Gamboa A, Rey-Campos J (Jun 2000). "FHX, a novel fork head factor with a dual DNA binding specificity". J Biol Chem. 275 (17): 12909–16. doi:10.1074/jbc.275.17.12909. PMID 10777590.
- ↑ Perez-Sanchez C, Arias-de-la-Fuente C, Gomez-Ferreria MA, Granadino B, Rey-Campos J (Sep 2000). "FHX.L and FHX.S, two isoforms of the human fork-head factor FHX (FOXJ2) with differential activity". J Mol Biol. 301 (4): 795–806. doi:10.1006/jmbi.2000.3999. PMID 10966786.
- ↑ "Entrez Gene: FOXJ2 forkhead box J2".
Further reading
- Andersson B, Wentland MA, Ricafrente JY, et al. (1996). "A "double adaptor" method for improved shotgun library construction". Anal. Biochem. 236 (1): 107–13. doi:10.1006/abio.1996.0138. PMID 8619474.
- Bonaldo MF, Lennon G, Soares MB (1997). "Normalization and subtraction: two approaches to facilitate gene discovery". Genome Res. 6 (9): 791–806. doi:10.1101/gr.6.9.791. PMID 8889548.
- Yu W, Andersson B, Worley KC, et al. (1997). "Large-Scale Concatenation cDNA Sequencing". Genome Res. 7 (4): 353–8. doi:10.1101/gr.7.4.353. PMC 139146. PMID 9110174.
- Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "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. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
- Gómez-Ferrería MA, Rey-Campos J (2003). "Functional domains of FOXJ2". J. Mol. Biol. 329 (4): 631–44. doi:10.1016/S0022-2836(03)00524-2. PMID 12787665.
- Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
- Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
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