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Items: 1 to 20 of 127

1.

Doublecortin mutations cluster in evolutionarily conserved functional domains.

Sapir T, Horesh D, Caspi M, Atlas R, Burgess HA, Wolf SG, Francis F, Chelly J, Elbaum M, Pietrokovski S, Reiner O.

Hum Mol Genet. 2000 Mar 22;9(5):703-12. Erratum in: Hum Mol Genet 2000 May 22;9(9):1461.

PMID:
10749977
2.

Identification of a novel human doublecortin-domain-containing gene (DCDC1) expressed mainly in testis.

Zeng L, Gu S, Li Y, Zhao E, Xu J, Ye X, Wu Q, Wang L, Xie Y, Mao Y.

J Hum Genet. 2003;48(7):393-6. Epub 2003 Jun 18.

PMID:
12820024
3.

The DCX-domain tandems of doublecortin and doublecortin-like kinase.

Kim MH, Cierpicki T, Derewenda U, Krowarsch D, Feng Y, Devedjiev Y, Dauter Z, Walsh CA, Otlewski J, Bushweller JH, Derewenda ZS.

Nat Struct Biol. 2003 May;10(5):324-33.

PMID:
12692530
4.

Patient mutations in doublecortin define a repeated tubulin-binding domain.

Taylor KR, Holzer AK, Bazan JF, Walsh CA, Gleeson JG.

J Biol Chem. 2000 Nov 3;275(44):34442-50.

5.

The location of DCX mutations predicts malformation severity in X-linked lissencephaly.

Leger PL, Souville I, Boddaert N, Elie C, Pinard JM, Plouin P, Moutard ML, des Portes V, Van Esch H, Joriot S, Renard JL, Chelly J, Francis F, Beldjord C, Bahi-Buisson N.

Neurogenetics. 2008 Oct;9(4):277-85. doi: 10.1007/s10048-008-0141-5. Epub 2008 Aug 7.

PMID:
18685874
6.

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.

PMID:
10770842
7.

Interaction between LIS1 and doublecortin, two lissencephaly gene products.

Caspi M, Atlas R, Kantor A, Sapir T, Reiner O.

Hum Mol Genet. 2000 Sep 22;9(15):2205-13.

PMID:
11001923
8.

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. Epub 2004 Mar 25.

PMID:
15045646
9.

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.

PMID:
9668176
10.

Genetic alteration of the DCX gene in Japanese patients with subcortical laminar heterotopia or isolated lissencephaly sequence.

Sakamoto M, Ono J, Okada S, Nakamura Y, Kurahashi H.

J Hum Genet. 2000;45(3):167-70.

PMID:
10807542
11.

Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia.

Matsumoto N, Leventer RJ, Kuc JA, Mewborn SK, Dudlicek LL, Ramocki MB, Pilz DT, Mills PL, Das S, Ross ME, Ledbetter DH, Dobyns WB.

Eur J Hum Genet. 2001 Jan;9(1):5-12.

12.

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.

PMID:
10441340
13.

Expression of doublecortin (DCX) and doublecortin-like kinase (DCLK) within the developing chick brain.

Capes-Davis A, Tolhurst O, Dunn JM, Jeffrey PL.

Dev Dyn. 2005 Feb;232(2):457-67.

14.

Doublecortin-like kinase is associated with microtubules in neuronal growth cones.

Burgess HA, Reiner O.

Mol Cell Neurosci. 2000 Nov;16(5):529-41.

PMID:
11083916
15.

Doublecortin, a stabilizer of microtubules.

Horesh D, Sapir T, Francis F, Wolf SG, Caspi M, Elbaum M, Chelly J, Reiner O.

Hum Mol Genet. 1999 Sep;8(9):1599-610.

PMID:
10441322
16.

The DC-module of doublecortin: dynamics, domain boundaries, and functional implications.

Cierpicki T, Kim MH, Cooper DR, Derewenda U, Bushweller JH, Derewenda ZS.

Proteins. 2006 Sep 1;64(4):874-82.

PMID:
16835924
17.

LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation.

Pilz DT, Matsumoto N, Minnerath S, Mills P, Gleeson JG, Allen KM, Walsh CA, Barkovich AJ, Dobyns WB, Ledbetter DH, Ross ME.

Hum Mol Genet. 1998 Dec;7(13):2029-37.

PMID:
9817918
18.

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.

PMID:
12390976
19.

Doublecortin interacts with the ubiquitin protease DFFRX, which associates with microtubules in neuronal processes.

Friocourt G, Kappeler C, Saillour Y, Fauchereau F, Rodriguez MS, Bahi N, Vinet MC, Chafey P, Poirier K, Taya S, Wood SA, Dargemont C, Francis F, Chelly J.

Mol Cell Neurosci. 2005 Jan;28(1):153-64.

PMID:
15607950
20.

Expression and chromosomal localization of KIAA0369, a putative kinase structurally related to Doublecortin.

Omori Y, Suzuki M, Ozaki K, Harada Y, Nakamura Y, Takahashi E, Fujiwara T.

J Hum Genet. 1998;43(3):169-77.

PMID:
9747029

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