PubMed for id: 116256489

Year	Number of Results
1993	1
1997	1
1999	2
2001	1
2003	1
2007	1
2008	1
2012	1
2023	2
2024	1

1

Septin9 DNA methylation is associated with breast cancer recurrence or metastasis.

Zhang SL, Yu HJ, Lian ZQ, Wan J, Xie SM, Lei W, Chen QP, Zhang L, Wang Q. Zhang SL, et al. J Int Med Res. 2024 Jan;52(1):3000605231220827. doi: 10.1177/03000605231220827. J Int Med Res. 2024. PMID: 38180895 Free PMC article.

2

SEPT9, H4C6, and RASSF1A methylation in nasopharyngeal swabs: A reflection of potential minimally invasive biomarkers for early screening of nasopharyngeal cancer.

Qian T, Zhou Z, Zhang Q, Liou YL, Zhou H. Qian T, et al. Medicine (Baltimore). 2023 Dec 15;102(50):e36583. doi: 10.1097/MD.0000000000036583. Medicine (Baltimore). 2023. PMID: 38115290 Free PMC article.

3

Septin 9 Orients the Apico-Basal Polarity Axis and Controls Plasticity Signals.

Cai T, Peng J, Omrane M, Benzoubir N, Samuel D, Gassama-Diagne A. Cai T, et al. Cells. 2023 Jul 9;12(14):1815. doi: 10.3390/cells12141815. Cells. 2023. PMID: 37508480 Free PMC article.

4

Hereditary Neuralgic Amyotrophy – RETIRED CHAPTER, FOR HISTORICAL REFERENCE ONLY.

van Alfen N, Hannibal MC, Chance PF, van Engelen BGM. van Alfen N, et al. 2008 Feb 27 [updated 2012 Dec 6]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2008 Feb 27 [updated 2012 Dec 6]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301569 Free Books & Documents. Review.

5

Translational control of SEPT9 isoforms is perturbed in disease.

McDade SS, Hall PA, Russell SE. McDade SS, et al. Hum Mol Genet. 2007 Apr 1;16(7):742-52. doi: 10.1093/hmg/ddm003. Hum Mol Genet. 2007. PMID: 17468182 Free article.

6

Altered expression of the septin gene, SEPT9, in ovarian neoplasia.

Burrows JF, Chanduloy S, McIlhatton MA, Nagar H, Yeates K, Donaghy P, Price J, Godwin AK, Johnston PG, Russell SE. Burrows JF, et al. J Pathol. 2003 Dec;201(4):581-8. doi: 10.1002/path.1484. J Pathol. 2003. PMID: 14648661

7

Genomic organization, complex splicing pattern and expression of a human septin gene on chromosome 17q25.3.

McIlhatton MA, Burrows JF, Donaghy PG, Chanduloy S, Johnston PG, Russell SE. McIlhatton MA, et al. Oncogene. 2001 Sep 13;20(41):5930-9. doi: 10.1038/sj.onc.1204752. Oncogene. 2001. PMID: 11593400

8

AF17q25, a putative septin family gene, fuses the MLL gene in acute myeloid leukemia with t(11;17)(q23;q25).

Taki T, Ohnishi H, Shinohara K, Sako M, Bessho F, Yanagisawa M, Hayashi Y. Taki T, et al. Cancer Res. 1999 Sep 1;59(17):4261-5. Cancer Res. 1999. PMID: 10485469

9

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).

Osaka M, Rowley JD, Zeleznik-Le NJ. Osaka M, et al. Proc Natl Acad Sci U S A. 1999 May 25;96(11):6428-33. doi: 10.1073/pnas.96.11.6428. Proc Natl Acad Sci U S A. 1999. PMID: 10339604 Free PMC article.

10

Hereditary neuralgic amyotrophy: evidence for genetic homogeneity and mapping to chromosome 17q25.

Pellegrino JE, George RA, Biegel J, Farlow MR, Gardner K, Caress J, Brown MJ, Rebbeck TR, Bird TD, Chance PF. Pellegrino JE, et al. Hum Genet. 1997 Dec;101(3):277-83. doi: 10.1007/s004390050629. Hum Genet. 1997. PMID: 9439655

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