[cite web | title = Entrez Gene: SEPT9 septin 9| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=10801| accessdate = ] ] PBB_Summary
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References
Further reading
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*cite journal | author=Pellegrino JE, George RA, Biegel J, "et al." |title=Hereditary neuralgic amyotrophy: evidence for genetic homogeneity and mapping to chromosome 17q25. |journal=Hum. Genet. |volume=101 |issue= 3 |pages= 277–83 |year= 1998 |pmid= 9439655 |doi=
*cite journal | author=Nagase T, Ishikawa K, Suyama M, "et al." |title=Prediction of the coding sequences of unidentified human genes. XIII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro. |journal=DNA Res. |volume=6 |issue= 1 |pages= 63–70 |year= 1999 |pmid= 10231032 |doi=
*cite journal | author=Osaka M, Rowley JD, Zeleznik-Le NJ |title=MSF (MLL septin-like fusion), a fusion partner gene of MLL, in a therapy-related acute myeloid leukemia with a t(11;17)(q23;q25). |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=96 |issue= 11 |pages= 6428–33 |year= 1999 |pmid= 10339604 |doi=
*cite journal | author=Taki T, Ohnishi H, Shinohara K, "et al." |title=AF17q25, a putative septin family gene, fuses the MLL gene in acute myeloid leukemia with t(11;17)(q23;q25). |journal=Cancer Res. |volume=59 |issue= 17 |pages= 4261–5 |year= 1999 |pmid= 10485469 |doi=
*cite journal | author=Medina M, Marinescu RC, Overhauser J, Kosik KS |title=Hemizygosity of delta-catenin (CTNND2) is associated with severe mental retardation in cri-du-chat syndrome. |journal=Genomics |volume=63 |issue= 2 |pages= 157–64 |year= 2000 |pmid= 10673328 |doi= 10.1006/geno.1999.6090
*cite journal | author=Kalikin LM, Sims HL, Petty EM |title=Genomic and expression analyses of alternatively spliced transcripts of the MLL septin-like fusion gene (MSF) that map to a 17q25 region of loss in breast and ovarian tumors. |journal=Genomics |volume=63 |issue= 2 |pages= 165–72 |year= 2000 |pmid= 10673329 |doi= 10.1006/geno.1999.6077
*cite journal | author=Russell SE, McIlhatton MA, Burrows JF, "et al." |title=Isolation and mapping of a human septin gene to a region on chromosome 17q, commonly deleted in sporadic epithelial ovarian tumors. |journal=Cancer Res. |volume=60 |issue= 17 |pages= 4729–34 |year= 2000 |pmid= 10987277 |doi=
*cite journal | author=McIlhatton MA, Burrows JF, Donaghy PG, "et al." |title=Genomic organization, complex splicing pattern and expression of a human septin gene on chromosome 17q25.3. |journal=Oncogene |volume=20 |issue= 41 |pages= 5930–9 |year= 2001 |pmid= 11593400 |doi= 10.1038/sj.onc.1204752
*cite journal | author=Yamamoto K, Shibata F, Yamaguchi M, Miura O |title=Fusion of MLL and MSF in adult de novo acute myelomonocytic leukemia (M4) with t(11;17)(q23;q25). |journal=Int. J. Hematol. |volume=75 |issue= 5 |pages= 503–7 |year= 2003 |pmid= 12095151 |doi=
*cite journal | author=Surka MC, Tsang CW, Trimble WS |title=The mammalian septin MSF localizes with microtubules and is required for completion of cytokinesis. |journal=Mol. Biol. Cell |volume=13 |issue= 10 |pages= 3532–45 |year= 2003 |pmid= 12388755 |doi= 10.1091/mbc.E02-01-0042
*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=Nagata K, Kawajiri A, Matsui S, "et al." |title=Filament formation of MSF-A, a mammalian septin, in human mammary epithelial cells depends on interactions with microtubules. |journal=J. Biol. Chem. |volume=278 |issue= 20 |pages= 18538–43 |year= 2003 |pmid= 12626509 |doi= 10.1074/jbc.M205246200
*cite journal | author=Ota T, Suzuki Y, Nishikawa T, "et al." |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285
*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
*cite journal | author=Nagata K, Asano T, Nozawa Y, Inagaki M |title=Biochemical and cell biological analyses of a mammalian septin complex, Sept7/9b/11. |journal=J. Biol. Chem. |volume=279 |issue= 53 |pages= 55895–904 |year= 2005 |pmid= 15485874 |doi= 10.1074/jbc.M406153200
*cite journal | author=Gerhard DS, Wagner L, Feingold EA, "et al." |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504
*cite journal | author=Scott M, Hyland PL, McGregor G, "et al." |title=Multimodality expression profiling shows SEPT9 to be overexpressed in a wide range of human tumours. |journal=Oncogene |volume=24 |issue= 29 |pages= 4688–700 |year= 2005 |pmid= 15782116 |doi= 10.1038/sj.onc.1208574
*cite journal | author=Ito H, Iwamoto I, Morishita R, "et al." |title=Possible role of Rho/Rhotekin signaling in mammalian septin organization. |journal=Oncogene |volume=24 |issue= 47 |pages= 7064–72 |year= 2005 |pmid= 16007136 |doi= 10.1038/sj.onc.1208862
*cite journal | author=Scott M, McCluggage WG, Hillan KJ, "et al." |title=Altered patterns of transcription of the septin gene, SEPT9, in ovarian tumorigenesis. |journal=Int. J. Cancer |volume=118 |issue= 5 |pages= 1325–9 |year= 2006 |pmid= 16161048 |doi= 10.1002/ijc.21486
*cite journal | author=Kuhlenbäumer G, Hannibal MC, Nelis E, "et al." |title=Mutations in SEPT9 cause hereditary neuralgic amyotrophy. |journal=Nat. Genet. |volume=37 |issue= 10 |pages= 1044–6 |year= 2005 |pmid= 16186812 |doi= 10.1038/ng1649
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