275 related articles for article (PubMed ID: 28701917)
1. Distinct Features of Doublecortin as a Marker of Neuronal Migration and Its Implications in Cancer Cell Mobility.
Ayanlaja AA; Xiong Y; Gao Y; Ji G; Tang C; Abdikani Abdullah Z; Gao D
Front Mol Neurosci; 2017; 10():199. PubMed ID: 28701917
[TBL] [Abstract][Full Text] [Related]
2. Novel lissencephaly-associated DCX variants in the C-terminal DCX domain affect microtubule binding and dynamics.
Lin JR; Cheng JF; Liu YT; Hsu TR; Lin KM; Chen C; Lin CL; Tsai MH; Tsai JW
Epilepsia; 2022 May; 63(5):1253-1265. PubMed ID: 35213059
[TBL] [Abstract][Full Text] [Related]
3. Structural studies of the doublecortin family of MAPs.
Fourniol F; Perderiset M; Houdusse A; Moores C
Methods Cell Biol; 2013; 115():27-48. PubMed ID: 23973064
[TBL] [Abstract][Full Text] [Related]
4. Subcortical band heterotopia (SBH) in males: clinical, imaging and genetic findings in comparison with females.
D'Agostino MD; Bernasconi A; Das S; Bastos A; Valerio RM; Palmini A; Costa da Costa J; Scheffer IE; Berkovic S; Guerrini R; Dravet C; Ono J; Gigli G; Federico A; Booth F; Bernardi B; Volpi L; Tassinari CA; Guggenheim MA; Ledbetter DH; Gleeson JG; Lopes-Cendes I; Vossler DG; Malaspina E; Franzoni E; Sartori RJ; Mitchell MH; Mercho S; Dubeau F; Andermann F; Dobyns WB; Andermann E
Brain; 2002 Nov; 125(Pt 11):2507-22. PubMed ID: 12390976
[TBL] [Abstract][Full Text] [Related]
5. Human doublecortin (DCX) and the homologous gene in mouse encode a putative Ca2+-dependent signaling protein which is mutated in human X-linked neuronal migration defects.
Sossey-Alaoui K; Hartung AJ; Guerrini R; Manchester DK; Posar A; Puche-Mira A; Andermann E; Dobyns WB; Srivastava AK
Hum Mol Genet; 1998 Aug; 7(8):1327-32. PubMed ID: 9668176
[TBL] [Abstract][Full Text] [Related]
6. Mitotic impairment by doublecortin is diminished by doublecortin mutations found in patients.
Couillard-Despres S; Uyanik G; Ploetz S; Karl C; Koch H; Winkler J; Aigner L
Neurogenetics; 2004 Jun; 5(2):83-93. PubMed ID: 15045646
[TBL] [Abstract][Full Text] [Related]
7. Pathogenic E2K mutation of doublecortin X (DCX) alters microtubule stabilisation and actin filament association.
Moslehi M; Ng DCH; Bogoyevitch MA
Biochem Biophys Res Commun; 2019 Jun; 513(3):540-545. PubMed ID: 30979500
[TBL] [Abstract][Full Text] [Related]
8. A novel DCX missense mutation in a family with X-linked lissencephaly and subcortical band heterotopia syndrome inherited from a low-level somatic mosaic mother: Genetic and functional studies.
Tsai MH; Kuo PW; Myers CT; Li SW; Lin WC; Fu TY; Chang HY; Mefford HC; Chang YC; Tsai JW
Eur J Paediatr Neurol; 2016 Sep; 20(5):788-94. PubMed ID: 27292316
[TBL] [Abstract][Full Text] [Related]
9. Familial pachygyria in both genders related to a DCX mutation.
Kim YO; Nam TS; Park C; Kim SK; Yoon W; Choi SY; Kim MK; Woo YJ
Brain Dev; 2016 Jun; 38(6):585-9. PubMed ID: 26743950
[TBL] [Abstract][Full Text] [Related]
10. Subcortical band heterotopia in rare affected males can be caused by missense mutations in DCX (XLIS) or LIS1.
Pilz DT; Kuc J; Matsumoto N; Bodurtha J; Bernadi B; Tassinari CA; Dobyns WB; Ledbetter DH
Hum Mol Genet; 1999 Sep; 8(9):1757-60. PubMed ID: 10441340
[TBL] [Abstract][Full Text] [Related]
11. JNK phosphorylates Ser332 of doublecortin and regulates its function in neurite extension and neuronal migration.
Jin J; Suzuki H; Hirai S; Mikoshiba K; Ohshima T
Dev Neurobiol; 2010 Dec; 70(14):929-42. PubMed ID: 20715151
[TBL] [Abstract][Full Text] [Related]
12. An in vitro model of lissencephaly: expanding the role of DCX during neurogenesis.
Shahsavani M; Pronk RJ; Falk R; Lam M; Moslem M; Linker SB; Salma J; Day K; Schuster J; Anderlid BM; Dahl N; Gage FH; Falk A
Mol Psychiatry; 2018 Jul; 23(7):1674-1684. PubMed ID: 28924182
[TBL] [Abstract][Full Text] [Related]
13. Colocalization of doublecortin with the microtubules: an ex vivo colocalization study of mutant doublecortin.
Yoshiura K; Noda Y; Kinoshita A; Niikawa N
J Neurobiol; 2000 May; 43(2):132-9. PubMed ID: 10770842
[TBL] [Abstract][Full Text] [Related]
14. Doublecortin Is Excluded from Growing Microtubule Ends and Recognizes the GDP-Microtubule Lattice.
Ettinger A; van Haren J; Ribeiro SA; Wittmann T
Curr Biol; 2016 Jun; 26(12):1549-1555. PubMed ID: 27238282
[TBL] [Abstract][Full Text] [Related]
15. Doublecortin is widely expressed in the developing and adult retina of sharks.
Sánchez-Farías N; Candal E
Exp Eye Res; 2015 May; 134():90-100. PubMed ID: 25849205
[TBL] [Abstract][Full Text] [Related]
16. Lis1 and doublecortin function with dynein to mediate coupling of the nucleus to the centrosome in neuronal migration.
Tanaka T; Serneo FF; Higgins C; Gambello MJ; Wynshaw-Boris A; Gleeson JG
J Cell Biol; 2004 Jun; 165(5):709-21. PubMed ID: 15173193
[TBL] [Abstract][Full Text] [Related]
17. Dynamic microtubule association of Doublecortin X (DCX) is regulated by its C-terminus.
Moslehi M; Ng DCH; Bogoyevitch MA
Sci Rep; 2017 Jul; 7(1):5245. PubMed ID: 28701724
[TBL] [Abstract][Full Text] [Related]
18. Doublecortin Mutation in an Adolescent Male.
Zare I; Paul D; Moody S
Child Neurol Open; 2019; 6():2329048X19836589. PubMed ID: 31259193
[TBL] [Abstract][Full Text] [Related]
19. Doublecortin X (DCX) serine 28 phosphorylation is a regulatory switch, modulating association of DCX with microtubules and actin filaments.
Moslehi M; Ng DCH; Bogoyevitch MA
Biochim Biophys Acta Mol Cell Res; 2019 Apr; 1866(4):638-649. PubMed ID: 30625347
[TBL] [Abstract][Full Text] [Related]
20. A novel missense mutation of doublecortin: mutation analysis of Korean patients with subcortical band heterotopia.
Kim MK; Park MS; Kim BC; Cho KH; Kim YS; Kim JH; Lee MC; Heo T; Kim EY
J Korean Med Sci; 2005 Aug; 20(4):670-3. PubMed ID: 16100463
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
