243 related articles for article (PubMed ID: 24120883)
1. CFEOM1-associated kinesin KIF21A is a cortical microtubule growth inhibitor.
van der Vaart B; van Riel WE; Doodhi H; Kevenaar JT; Katrukha EA; Gumy L; Bouchet BP; Grigoriev I; Spangler SA; Yu KL; Wulf PS; Wu J; Lansbergen G; van Battum EY; Pasterkamp RJ; Mimori-Kiyosue Y; Demmers J; Olieric N; Maly IV; Hoogenraad CC; Akhmanova A
Dev Cell; 2013 Oct; 27(2):145-160. PubMed ID: 24120883
[TBL] [Abstract][Full Text] [Related]
2. Structural basis for misregulation of kinesin KIF21A autoinhibition by CFEOM1 disease mutations.
Bianchi S; van Riel WE; Kraatz SH; Olieric N; Frey D; Katrukha EA; Jaussi R; Missimer J; Grigoriev I; Olieric V; Benoit RM; Steinmetz MO; Akhmanova A; Kammerer RA
Sci Rep; 2016 Aug; 6():30668. PubMed ID: 27485312
[TBL] [Abstract][Full Text] [Related]
3. A major mutation of KIF21A associated with congenital fibrosis of the extraocular muscles type 1 (CFEOM1) enhances translocation of Kank1 to the membrane.
Kakinuma N; Kiyama R
Biochem Biophys Res Commun; 2009 Sep; 386(4):639-44. PubMed ID: 19559006
[TBL] [Abstract][Full Text] [Related]
4. Structural analyses of key features in the KANK1·KIF21A complex yield mechanistic insights into the cross-talk between microtubules and the cell cortex.
Weng Z; Shang Y; Yao D; Zhu J; Zhang R
J Biol Chem; 2018 Jan; 293(1):215-225. PubMed ID: 29158259
[TBL] [Abstract][Full Text] [Related]
5. Human CFEOM1 mutations attenuate KIF21A autoinhibition and cause oculomotor axon stalling.
Cheng L; Desai J; Miranda CJ; Duncan JS; Qiu W; Nugent AA; Kolpak AL; Wu CC; Drokhlyansky E; Delisle MM; Chan WM; Wei Y; Propst F; Reck-Peterson SL; Fritzsch B; Engle EC
Neuron; 2014 Apr; 82(2):334-49. PubMed ID: 24656932
[TBL] [Abstract][Full Text] [Related]
6. Structural basis for the recognition of kinesin family member 21A (KIF21A) by the ankyrin domains of KANK1 and KANK2 proteins.
Guo Q; Liao S; Zhu Z; Li Y; Li F; Xu C
J Biol Chem; 2018 Jan; 293(2):557-566. PubMed ID: 29183992
[TBL] [Abstract][Full Text] [Related]
7. Magnetic resonance imaging evidence for widespread orbital dysinnervation in congenital fibrosis of extraocular muscles due to mutations in KIF21A.
Demer JL; Clark RA; Engle EC
Invest Ophthalmol Vis Sci; 2005 Feb; 46(2):530-9. PubMed ID: 15671279
[TBL] [Abstract][Full Text] [Related]
8. Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1).
Yamada K; Andrews C; Chan WM; McKeown CA; Magli A; de Berardinis T; Loewenstein A; Lazar M; O'Keefe M; Letson R; London A; Ruttum M; Matsumoto N; Saito N; Morris L; Del Monte M; Johnson RH; Uyama E; Houtman WA; de Vries B; Carlow TJ; Hart BL; Krawiecki N; Shoffner J; Vogel MC; Katowitz J; Goldstein SM; Levin AV; Sener EC; Ozturk BT; Akarsu AN; Brodsky MC; Hanisch F; Cruse RP; Zubcov AA; Robb RM; Roggenkäemper P; Gottlob I; Kowal L; Battu R; Traboulsi EI; Franceschini P; Newlin A; Demer JL; Engle EC
Nat Genet; 2003 Dec; 35(4):318-21. PubMed ID: 14595441
[TBL] [Abstract][Full Text] [Related]
9. Three novel mutations in KIF21A highlight the importance of the third coiled-coil stalk domain in the etiology of CFEOM1.
Chan WM; Andrews C; Dragan L; Fredrick D; Armstrong L; Lyons C; Geraghty MT; Hunter DG; Yazdani A; Traboulsi EI; Pott JW; Gutowski NJ; Ellard S; Young E; Hanisch F; Koc F; Schnall B; Engle EC
BMC Genet; 2007 May; 8():26. PubMed ID: 17511870
[TBL] [Abstract][Full Text] [Related]
10. Novel and recurrent KIF21A mutations in congenital fibrosis of the extraocular muscles type 1 and 3.
Lu S; Zhao C; Zhao K; Li N; Larsson C
Arch Ophthalmol; 2008 Mar; 126(3):388-94. PubMed ID: 18332320
[TBL] [Abstract][Full Text] [Related]
11. Spatiotemporal expression pattern of KIF21A during normal embryonic development and in congenital fibrosis of the extraocular muscles type 1 (CFEOM1).
Desai J; Velo MP; Yamada K; Overman LM; Engle EC
Gene Expr Patterns; 2012; 12(5-6):180-8. PubMed ID: 22465342
[TBL] [Abstract][Full Text] [Related]
12. A rare case of congenital fibrosis of extraocular muscle type 1A due to KIF21A mutation with Marcus Gunn jaw-winking phenomenon.
Kaçar Bayram A; Per H; Quon J; Canpolat M; Ülgen E; Doğan H; Gumus H; Kumandas S; Bayram N; Bilguvar K; Çağlayan AO
Eur J Paediatr Neurol; 2015 Nov; 19(6):743-6. PubMed ID: 26190014
[TBL] [Abstract][Full Text] [Related]
13. Identification of KIF21A mutations as a rare cause of congenital fibrosis of the extraocular muscles type 3 (CFEOM3).
Yamada K; Chan WM; Andrews C; Bosley TM; Sener EC; Zwaan JT; Mullaney PB; Oztürk BT; Akarsu AN; Sabol LJ; Demer JL; Sullivan TJ; Gottlob I; Roggenkäemper P; Mackey DA; De Uzcategui CE; Uzcategui N; Ben-Zeev B; Traboulsi EI; Magli A; de Berardinis T; Gagliardi V; Awasthi-Patney S; Vogel MC; Rizzo JF; Engle EC
Invest Ophthalmol Vis Sci; 2004 Jul; 45(7):2218-23. PubMed ID: 15223798
[TBL] [Abstract][Full Text] [Related]
14. A novel KIF21A mutation in a patient with congenital fibrosis of the extraocular muscles and Marcus Gunn jaw-winking phenomenon.
Yamada K; Hunter DG; Andrews C; Engle EC
Arch Ophthalmol; 2005 Sep; 123(9):1254-9. PubMed ID: 16157808
[TBL] [Abstract][Full Text] [Related]
15. Congenital fibrosis of extraocular muscle type 1A due to KIF21A mutation: first case report from Hong Kong.
Luk HM; Lo IF; Lai CW; Ma LC; Tong TM; Chan DH; Lam ST
Hong Kong Med J; 2013 Apr; 19(2):182-5. PubMed ID: 23535681
[TBL] [Abstract][Full Text] [Related]
16. Ocular congenital cranial dysinnervation disorders (CCDDs): insights into axon growth and guidance.
Whitman MC; Engle EC
Hum Mol Genet; 2017 Aug; 26(R1):R37-R44. PubMed ID: 28459979
[TBL] [Abstract][Full Text] [Related]
17. Recurrent mutation of the KIF21A gene in Japanese patients with congenital fibrosis of the extraocular muscles.
Shimizu S; Okinaga A; Maruo T
Jpn J Ophthalmol; 2005; 49(6):443-447. PubMed ID: 16365788
[TBL] [Abstract][Full Text] [Related]
18. CLASPs attach microtubule plus ends to the cell cortex through a complex with LL5beta.
Lansbergen G; Grigoriev I; Mimori-Kiyosue Y; Ohtsuka T; Higa S; Kitajima I; Demmers J; Galjart N; Houtsmuller AB; Grosveld F; Akhmanova A
Dev Cell; 2006 Jul; 11(1):21-32. PubMed ID: 16824950
[TBL] [Abstract][Full Text] [Related]
19. Congenital fibrosis of extraocular muscles type 1 with progression of ophthalmoplegia.
Hanisch F; Bau V; Zierz S
Eur J Med Res; 2005 Aug; 10(8):366-8. PubMed ID: 16131480
[TBL] [Abstract][Full Text] [Related]
20. Effects of brefeldin A-inhibited guanine nucleotide-exchange (BIG) 1 and KANK1 proteins on cell polarity and directed migration during wound healing.
Li CC; Kuo JC; Waterman CM; Kiyama R; Moss J; Vaughan M
Proc Natl Acad Sci U S A; 2011 Nov; 108(48):19228-33. PubMed ID: 22084092
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
