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Items: 1 to 20 of 32

1.

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
2.

Lissencephaly and the molecular basis of neuronal migration.

Kato M, Dobyns WB.

Hum Mol Genet. 2003 Apr 1;12 Spec No 1:R89-96. Review.

PMID:
12668601
3.

Doublecortin functions at the extremities of growing neuronal processes.

Friocourt G, Koulakoff A, Chafey P, Boucher D, Fauchereau F, Chelly J, Francis F.

Cereb Cortex. 2003 Jun;13(6):620-6. Review.

PMID:
12764037
4.

The doublecortin gene family and disorders of neuronal structure.

Dijkmans TF, van Hooijdonk LW, Fitzsimons CP, Vreugdenhil E.

Cent Nerv Syst Agents Med Chem. 2010 Mar;10(1):32-46. Review.

PMID:
20236041
5.

Neuronal migration disorders.

Guerrini R, Parrini E.

Neurobiol Dis. 2010 May;38(2):154-66. doi: 10.1016/j.nbd.2009.02.008. Epub 2009 Feb 23. Review.

PMID:
19245832
6.

Genetic mechanisms underlying abnormal neuronal migration in classical lissencephaly.

Kerjan G, Gleeson JG.

Trends Genet. 2007 Dec;23(12):623-30. Epub 2007 Nov 8. Review.

PMID:
17997185
7.

Missense mutations resulting in type 1 lissencephaly.

Reiner O, Coquelle FM.

Cell Mol Life Sci. 2005 Feb;62(4):425-34. Review.

PMID:
15719169
8.

Neuronal migration.

Lambert de Rouvroit C, Goffinet AM.

Mech Dev. 2001 Jul;105(1-2):47-56. Review.

9.

Genes that regulate neuronal migration in the cerebral cortex.

Allen KM, Walsh CA.

Epilepsy Res. 1999 Sep;36(2-3):143-54. Review.

PMID:
10515162
10.

Lissencephaly and subcortical band heterotopia: molecular basis and diagnosis.

Leventer RJ, Pilz DT, Matsumoto N, Ledbetter DH, Dobyns WB.

Mol Med Today. 2000 Jul;6(7):277-84. Review.

PMID:
10859564
11.

Molecular genetics of neuronal migration disorders.

Liu JS.

Curr Neurol Neurosci Rep. 2011 Apr;11(2):171-8. doi: 10.1007/s11910-010-0176-5. Review.

PMID:
21222180
12.

Molecular mechanisms of neuronal migration disorders, quo vadis?

Couillard-Despres S, Winkler J, Uyanik G, Aigner L.

Curr Mol Med. 2001 Dec;1(6):677-88. Review.

PMID:
11899256
13.

Cerebral gyral dysplasias: molecular genetics and cell biology.

Clark GD.

Curr Opin Neurol. 2001 Apr;14(2):157-62. Review.

PMID:
11262729
14.

Neuronal migration, cerebral cortical development, and cerebral cortical anomalies.

Pilz D, Stoodley N, Golden JA.

J Neuropathol Exp Neurol. 2002 Jan;61(1):1-11. Review.

PMID:
11829339
15.

Protein-protein interactions, cytoskeletal regulation and neuronal migration.

Feng Y, Walsh CA.

Nat Rev Neurosci. 2001 Jun;2(6):408-16. Review.

PMID:
11389474
16.

The multipolar stage and disruptions in neuronal migration.

LoTurco JJ, Bai J.

Trends Neurosci. 2006 Jul;29(7):407-13. Epub 2006 May 19. Review.

PMID:
16713637
17.
18.

The unfolding story of two lissencephaly genes and brain development.

Reiner O.

Mol Neurobiol. 1999 Oct-Dec;20(2-3):143-56. Review.

PMID:
10966119
19.

[Subcortical band heterotopia].

Takeuchi Y.

Ryoikibetsu Shokogun Shirizu. 2002;(37 Pt 6):133-6. Review. Japanese. No abstract available.

PMID:
12483846
20.

DCX's phosphorylation by not just another kinase (JNK).

Reiner O, Gdalyahu A, Ghosh I, Levy T, Sapoznik S, Nir R, Sapir T.

Cell Cycle. 2004 Jun;3(6):747-51. Epub 2004 Jun 6. Review.

PMID:
15118415

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