ZMYM2

ZMYM2

Zinc finger, MYM-type 2, also known as ZMYM2, is a human gene.cite web | title = Entrez Gene: ZMYM2 zinc finger, MYM-type 2| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=7750| accessdate = ]

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References

Further reading

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*cite journal | author=Bonaldo MF, Lennon G, Soares MB |title=Normalization and subtraction: two approaches to facilitate gene discovery. |journal=Genome Res. |volume=6 |issue= 9 |pages= 791–806 |year= 1997 |pmid= 8889548 |doi=
*cite journal | author=Xiao S, Nalabolu SR, Aster JC, "et al." |title=FGFR1 is fused with a novel zinc-finger gene, ZNF198, in the t(8;13) leukaemia/lymphoma syndrome. |journal=Nat. Genet. |volume=18 |issue= 1 |pages= 84–7 |year= 1998 |pmid= 9425908 |doi= 10.1038/ng0198-84
*cite journal | author=Smedley D, Hamoudi R, Clark J, "et al." |title=The t(8;13)(p11;q11-12) rearrangement associated with an atypical myeloproliferative disorder fuses the fibroblast growth factor receptor 1 gene to a novel gene RAMP. |journal=Hum. Mol. Genet. |volume=7 |issue= 4 |pages= 637–42 |year= 1998 |pmid= 9499416 |doi=
*cite journal | author=Popovici C, Adélaïde J, Ollendorff V, "et al." |title=Fibroblast growth factor receptor 1 is fused to FIM in stem-cell myeloproliferative disorder with t(8;13). |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=95 |issue= 10 |pages= 5712–7 |year= 1998 |pmid= 9576949 |doi=
*cite journal | author=Still IH, Cowell JK |title=The t(8;13) atypical myeloproliferative disorder: further analysis of the ZNF198 gene and lack of evidence for multiple genes disrupted on chromosome 13. |journal=Blood |volume=92 |issue= 4 |pages= 1456–8 |year= 1998 |pmid= 9694738 |doi=
*cite journal | author=Reiter A, Sohal J, Kulkarni S, "et al." |title=Consistent fusion of ZNF198 to the fibroblast growth factor receptor-1 in the t(8;13)(p11;q12) myeloproliferative syndrome. |journal=Blood |volume=92 |issue= 5 |pages= 1735–42 |year= 1998 |pmid= 9716603 |doi=
*cite journal | author=Kulkarni S, Reiter A, Smedley D, "et al." |title=The genomic structure of ZNF198 and location of breakpoints in the t(8;13) myeloproliferative syndrome. |journal=Genomics |volume=55 |issue= 1 |pages= 118–21 |year= 1999 |pmid= 9889006 |doi= 10.1006/geno.1998.5634
*cite journal | author=Ollendorff V, Guasch G, Isnardon D, "et al." |title=Characterization of FIM-FGFR1, the fusion product of the myeloproliferative disorder-associated t(8;13) translocation. |journal=J. Biol. Chem. |volume=274 |issue= 38 |pages= 26922–30 |year= 1999 |pmid= 10480903 |doi=
*cite journal | author=Matsumoto K, Morita K, Takada S, "et al." |title=A chronic myelogenous leukemia-like myeloproliferative disorder accompanied by T-cell lymphoblastic lymphoma with chromosome translocation t(8;13)(p11;q12): a Japanese case. |journal=Int. J. Hematol. |volume=70 |issue= 4 |pages= 278–82 |year= 2000 |pmid= 10643154 |doi=
*cite journal | author=Hartley JL, Temple GF, Brasch MA |title=DNA cloning using in vitro site-specific recombination. |journal=Genome Res. |volume=10 |issue= 11 |pages= 1788–95 |year= 2001 |pmid= 11076863 |doi=
*cite journal | author=Wiemann S, Weil B, Wellenreuther R, "et al." |title=Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs. |journal=Genome Res. |volume=11 |issue= 3 |pages= 422–35 |year= 2001 |pmid= 11230166 |doi= 10.1101/gr.154701
*cite journal | author=Simpson JC, Wellenreuther R, Poustka A, "et al." |title=Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing. |journal=EMBO Rep. |volume=1 |issue= 3 |pages= 287–92 |year= 2001 |pmid= 11256614 |doi= 10.1093/embo-reports/kvd058
*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=Hakimi MA, Dong Y, Lane WS, "et al." |title=A candidate X-linked mental retardation gene is a component of a new family of histone deacetylase-containing complexes. |journal=J. Biol. Chem. |volume=278 |issue= 9 |pages= 7234–9 |year= 2003 |pmid= 12493763 |doi= 10.1074/jbc.M208992200
*cite journal | author=Baumann H, Kunapuli P, Tracy E, Cowell JK |title=The oncogenic fusion protein-tyrosine kinase ZNF198/fibroblast growth factor receptor-1 has signaling function comparable with interleukin-6 cytokine receptors. |journal=J. Biol. Chem. |volume=278 |issue= 18 |pages= 16198–208 |year= 2003 |pmid= 12594223 |doi= 10.1074/jbc.M300018200
*cite journal | author=Kunapuli P, Somerville R, Still IH, Cowell JK |title=ZNF198 protein, involved in rearrangement in myeloproliferative disease, forms complexes with the DNA repair-associated HHR6A/6B and RAD18 proteins. |journal=Oncogene |volume=22 |issue= 22 |pages= 3417–23 |year= 2003 |pmid= 12776193 |doi= 10.1038/sj.onc.1206408
*cite journal | author=Warner DR, Roberts EA, Greene RM, Pisano MM |title=Identification of novel Smad binding proteins. |journal=Biochem. Biophys. Res. Commun. |volume=312 |issue= 4 |pages= 1185–90 |year= 2004 |pmid= 14651998 |doi=
*cite journal | author=Dunham A, Matthews LH, Burton J, "et al." |title=The DNA sequence and analysis of human chromosome 13. |journal=Nature |volume=428 |issue= 6982 |pages= 522–8 |year= 2004 |pmid= 15057823 |doi= 10.1038/nature02379
*cite journal | author=Colland F, Jacq X, Trouplin V, "et al." |title=Functional proteomics mapping of a human signaling pathway. |journal=Genome Res. |volume=14 |issue= 7 |pages= 1324–32 |year= 2004 |pmid= 15231748 |doi= 10.1101/gr.2334104
*cite journal | author=Beausoleil SA, Jedrychowski M, Schwartz D, "et al." |title=Large-scale characterization of HeLa cell nuclear phosphoproteins. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=101 |issue= 33 |pages= 12130–5 |year= 2004 |pmid= 15302935 |doi= 10.1073/pnas.0404720101

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