PubMed (OMIM) for id: 10801

Year	Number of Results
1960	1
1961	1
1968	1
1971	1
1972	1
1973	1
1974	1
1983	1
1985	1
1986	1
1993	1
1994	2
1995	1
1996	1
1997	3
1999	2
2000	3
2001	5
2002	2
2004	1
2005	2
2007	2
2008	1
2009	4
2010	1
2024	0

1

Non-recurrent SEPT9 duplications cause hereditary neuralgic amyotrophy.

Collie AM, Landsverk ML, Ruzzo E, Mefford HC, Buysse K, Adkins JR, Knutzen DM, Barnett K, Brown RH Jr, Parry GJ, Yum SW, Simpson DA, Olney RK, Chinnery PF, Eichler EE, Chance PF, Hannibal MC. Collie AM, et al. J Med Genet. 2010 Sep;47(9):601-7. doi: 10.1136/jmg.2009.072348. Epub 2009 Nov 25. J Med Genet. 2010. PMID: 19939853

2

SEPT9 gene sequencing analysis reveals recurrent mutations in hereditary neuralgic amyotrophy.

Hannibal MC, Ruzzo EK, Miller LR, Betz B, Buchan JG, Knutzen DM, Barnett K, Landsverk ML, Brice A, LeGuern E, Bedford HM, Worrall BB, Lovitt S, Appel SH, Andermann E, Bird TD, Chance PF. Hannibal MC, et al. Neurology. 2009 May 19;72(20):1755-9. doi: 10.1212/WNL.0b013e3181a609e3. Neurology. 2009. PMID: 19451530 Free PMC article.

3

SEPT9 mutations and a conserved 17q25 sequence in sporadic and hereditary brachial plexus neuropathy.

Klein CJ, Wu Y, Cunningham JM, Windebank AJ, Dyck PJ, Friedenberg SM, Klein DM, Dyck PJ. Klein CJ, et al. Arch Neurol. 2009 Feb;66(2):238-43. doi: 10.1001/archneurol.2008.585. Arch Neurol. 2009. PMID: 19204161 Free PMC article.

4

Duplication within the SEPT9 gene associated with a founder effect in North American families with hereditary neuralgic amyotrophy.

Landsverk ML, Ruzzo EK, Mefford HC, Buysse K, Buchan JG, Eichler EE, Petty EM, Peterson EA, Knutzen DM, Barnett K, Farlow MR, Caress J, Parry GJ, Quan D, Gardner KL, Hong M, Simmons Z, Bird TD, Chance PF, Hannibal MC. Landsverk ML, et al. Hum Mol Genet. 2009 Apr 1;18(7):1200-8. doi: 10.1093/hmg/ddp014. Epub 2009 Jan 12. Hum Mol Genet. 2009. PMID: 19139049 Free PMC article.

5

Dysmorphic syndrome of hereditary neuralgic amyotrophy associated with a SEPT9 gene mutation--a family study.

Laccone F, Hannibal MC, Neesen J, Grisold W, Chance PF, Rehder H. Laccone F, et al. Clin Genet. 2008 Sep;74(3):279-83. doi: 10.1111/j.1399-0004.2008.01022.x. Epub 2008 May 19. Clin Genet. 2008. PMID: 18492087

6

SEPT9 sequence alternations causing hereditary neuralgic amyotrophy are associated with altered interactions with SEPT4/SEPT11 and resistance to Rho/Rhotekin-signaling.

Sudo K, Ito H, Iwamoto I, Morishita R, Asano T, Nagata K. Sudo K, et al. Hum Mutat. 2007 Oct;28(10):1005-13. doi: 10.1002/humu.20554. Hum Mutat. 2007. PMID: 17546647

7

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.

8

Mutations in SEPT9 cause hereditary neuralgic amyotrophy.

Kuhlenbäumer G, Hannibal MC, Nelis E, Schirmacher A, Verpoorten N, Meuleman J, Watts GD, De Vriendt E, Young P, Stögbauer F, Halfter H, Irobi J, Goossens D, Del-Favero J, Betz BG, Hor H, Kurlemann G, Bird TD, Airaksinen E, Mononen T, Serradell AP, Prats JM, Van Broeckhoven C, De Jonghe P, Timmerman V, Ringelstein EB, Chance PF. Kuhlenbäumer G, et al. Nat Genet. 2005 Oct;37(10):1044-6. doi: 10.1038/ng1649. Epub 2005 Sep 25. Nat Genet. 2005. PMID: 16186812

9

A mitotic septin scaffold required for Mammalian chromosome congression and segregation.

Spiliotis ET, Kinoshita M, Nelson WJ. Spiliotis ET, et al. Science. 2005 Mar 18;307(5716):1781-5. doi: 10.1126/science.1106823. Science. 2005. PMID: 15774761 Free PMC article.

10

Biochemical and cell biological analyses of a mammalian septin complex, Sept7/9b/11.

Nagata K, Asano T, Nozawa Y, Inagaki M. Nagata K, et al. J Biol Chem. 2004 Dec 31;279(53):55895-904. doi: 10.1074/jbc.M406153200. Epub 2004 Oct 12. J Biol Chem. 2004. PMID: 15485874 Free article.

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