EVI2B


EVI2B

Ecotropic viral integration site 2B, also known as EVI2B, is a human gene.cite web | title = Entrez Gene: EVI2B ecotropic viral integration site 2B| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=2124| accessdate = ]

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References

Further reading

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*cite journal | author=Xu G, O'Connell P, Stevens J, White R |title=Characterization of human adenylate kinase 3 (AK3) cDNA and mapping of the AK3 pseudogene to an intron of the NF1 gene. |journal=Genomics |volume=13 |issue= 3 |pages= 537–42 |year= 1992 |pmid= 1639383 |doi=
*cite journal | author=Wallace MR, Andersen LB, Saulino AM, "et al." |title=A de novo Alu insertion results in neurofibromatosis type 1. |journal=Nature |volume=353 |issue= 6347 |pages= 864–6 |year= 1991 |pmid= 1719426 |doi= 10.1038/353864a0
*cite journal | author=Viskochil D, Cawthon R, O'Connell P, "et al." |title=The gene encoding the oligodendrocyte-myelin glycoprotein is embedded within the neurofibromatosis type 1 gene. |journal=Mol. Cell. Biol. |volume=11 |issue= 2 |pages= 906–12 |year= 1991 |pmid= 1899288 |doi=
*cite journal | author=Cawthon RM, Andersen LB, Buchberg AM, "et al." |title=cDNA sequence and genomic structure of EV12B, a gene lying within an intron of the neurofibromatosis type 1 gene. |journal=Genomics |volume=9 |issue= 3 |pages= 446–60 |year= 1991 |pmid= 1903357 |doi=
*cite journal | author=Cawthon RM, Weiss R, Xu GF, "et al." |title=A major segment of the neurofibromatosis type 1 gene: cDNA sequence, genomic structure, and point mutations. |journal=Cell |volume=62 |issue= 1 |pages= 193–201 |year= 1990 |pmid= 2114220 |doi=
*cite journal | author=Cawthon RM, O'Connell P, Buchberg AM, "et al." |title=Identification and characterization of transcripts from the neurofibromatosis 1 region: the sequence and genomic structure of EVI2 and mapping of other transcripts. |journal=Genomics |volume=7 |issue= 4 |pages= 555–65 |year= 1990 |pmid= 2117566 |doi=
*cite journal | author=Strausberg RL, Feingold EA, Grouse LH, "et al." |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899
*cite journal | author=Kimura K, Wakamatsu A, Suzuki Y, "et al." |title=Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes. |journal=Genome Res. |volume=16 |issue= 1 |pages= 55–65 |year= 2006 |pmid= 16344560 |doi= 10.1101/gr.4039406
*cite journal | author=Douglas J, Cilliers D, Coleman K, "et al." |title=Mutations in RNF135, a gene within the NF1 microdeletion region, cause phenotypic abnormalities including overgrowth. |journal=Nat. Genet. |volume=39 |issue= 8 |pages= 963–5 |year= 2007 |pmid= 17632510 |doi= 10.1038/ng2083

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