Biology:EVI2B
From HandWiki
 Generic protein structure example |
Protein EVI2B is a protein that in humans is encoded by the EVI2B gene.[1][2]
References
- ↑ "cDNA sequence and genomic structure of EV12B, a gene lying within an intron of the neurofibromatosis type 1 gene". Genomics 9 (3): 446–60. Jun 1991. doi:10.1016/0888-7543(91)90410-G. PMID 1903357.
- ↑ "Entrez Gene: EVI2B ecotropic viral integration site 2B". https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=2124.
Further reading
- "Characterization of human adenylate kinase 3 (AK3) cDNA and mapping of the AK3 pseudogene to an intron of the NF1 gene.". Genomics 13 (3): 537–42. 1992. doi:10.1016/0888-7543(92)90122-9. PMID 1639383.
- "A de novo Alu insertion results in neurofibromatosis type 1.". Nature 353 (6347): 864–6. 1991. doi:10.1038/353864a0. PMID 1719426. Bibcode: 1991Natur.353..864W. https://deepblue.lib.umich.edu/bitstream/2027.42/62641/1/353864a0.pdf.
- "The gene encoding the oligodendrocyte-myelin glycoprotein is embedded within the neurofibromatosis type 1 gene.". Mol. Cell. Biol. 11 (2): 906–12. 1991. doi:10.1128/mcb.11.2.906. PMID 1899288.
- "A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutations.". Cell 62 (1): 193–201. 1990. doi:10.1016/0092-8674(90)90253-B. PMID 2114220.
- "Identification and characterization of transcripts from the neurofibromatosis 1 region: the sequence and genomic structure of EVI2 and mapping of other transcripts.". Genomics 7 (4): 555–65. 1990. doi:10.1016/0888-7543(90)90199-5. PMID 2117566. https://zenodo.org/record/1258573.
- "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. PMID 12477932. Bibcode: 2002PNAS...9916899M.
- "Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes.". Genome Res. 16 (1): 55–65. 2006. doi:10.1101/gr.4039406. PMID 16344560.
- "Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth.". Nat. Genet. 39 (8): 963–5. 2007. doi:10.1038/ng2083. PMID 17632510.
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