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5. Septin-microtubule association via a motif unique to isoform 1 of septin 9 tunes stress fibers. Kuzmić M; Castro Linares G; Leischner Fialová J; Iv F; Salaün D; Llewellyn A; Gomes M; Belhabib M; Liu Y; Asano K; Rodrigues M; Isnardon D; Tachibana T; Koenderink GH; Badache A; Mavrakis M; Verdier-Pinard P J Cell Sci; 2022 Jan; 135(1):. PubMed ID: 34854883 [TBL] [Abstract][Full Text] [Related]
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 Hum Mutat; 2007 Oct; 28(10):1005-13. PubMed ID: 17546647 [TBL] [Abstract][Full Text] [Related]
7. Hereditary neuralgic amyotrophy in childhood caused by duplication within the SEPT9 gene: A family study. Neubauer K; Boeckelmann D; Koehler U; Kracht J; Kirschner J; Pendziwiat M; Zieger B Cytoskeleton (Hoboken); 2019 Jan; 76(1):131-136. PubMed ID: 30019529 [TBL] [Abstract][Full Text] [Related]
9. Inherited focal, episodic neuropathies: hereditary neuropathy with liability to pressure palsies and hereditary neuralgic amyotrophy. Chance PF Neuromolecular Med; 2006; 8(1-2):159-74. PubMed ID: 16775374 [TBL] [Abstract][Full Text] [Related]
10. 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 Hum Mol Genet; 2009 Apr; 18(7):1200-8. PubMed ID: 19139049 [TBL] [Abstract][Full Text] [Related]
11. Regulation of microtubule plus end dynamics by septin 9. Nakos K; Rosenberg M; Spiliotis ET Cytoskeleton (Hoboken); 2019 Jan; 76(1):83-91. PubMed ID: 30144301 [TBL] [Abstract][Full Text] [Related]
12. 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 Clin Genet; 2008 Sep; 74(3):279-83. PubMed ID: 18492087 [TBL] [Abstract][Full Text] [Related]
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18. Mammalian SEPT9 isoforms direct microtubule-dependent arrangements of septin core heteromers. Sellin ME; Stenmark S; Gullberg M Mol Biol Cell; 2012 Nov; 23(21):4242-55. PubMed ID: 22956766 [TBL] [Abstract][Full Text] [Related]
19. Mutation analysis of 4 candidate genes for hereditary neuralgic amyotrophy (HNA). Meuleman J; Kuhlenbäumer G; Audenaert D; Hünermund G; Hor H; Young P; Stögbauer F; Ringelstein EB; Van Broeckhoven C; De Jonghe P; Timmerman V Hum Genet; 2001 May; 108(5):390-3. PubMed ID: 11409865 [TBL] [Abstract][Full Text] [Related]
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