Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 111

1.

Smooth, rough and upside-down neocortical development.

Olson EC, Walsh CA.

Curr Opin Genet Dev. 2002 Jun;12(3):320-7. Review.

PMID:
12076676
[PubMed - indexed for MEDLINE]
2.

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
[PubMed - indexed for MEDLINE]
3.

Interaction of reelin signaling and Lis1 in brain development.

Assadi AH, Zhang G, Beffert U, McNeil RS, Renfro AL, Niu S, Quattrocchi CC, Antalffy BA, Sheldon M, Armstrong DD, Wynshaw-Boris A, Herz J, D'Arcangelo G, Clark GD.

Nat Genet. 2003 Nov;35(3):270-6. Epub 2003 Oct 26.

PMID:
14578885
[PubMed - indexed for MEDLINE]
4.

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
[PubMed - indexed for MEDLINE]
Free Article
5.

Reelin mouse mutants as models of cortical development disorders.

D'Arcangelo G.

Epilepsy Behav. 2006 Feb;8(1):81-90. Epub 2005 Nov 2. Review.

PMID:
16266828
[PubMed - indexed for MEDLINE]
6.

[Neurosurgical Embryology. Part 2: Recent data on normal and pathological development of the cortex].

Catala M.

Neurochirurgie. 2003 Sep;49(4):431-40. French.

PMID:
14526254
[PubMed - indexed for MEDLINE]
7.

Strange bedfellows: Reelin and Notch signaling interact to regulate cell migration in the developing neocortex.

Gaiano N.

Neuron. 2008 Oct 23;60(2):189-91. doi: 10.1016/j.neuron.2008.10.009. Review.

PMID:
18957210
[PubMed - indexed for MEDLINE]
Free Article
8.

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
[PubMed - indexed for MEDLINE]
9.

Life is a journey: a genetic look at neocortical development.

Gupta A, Tsai LH, Wynshaw-Boris A.

Nat Rev Genet. 2002 May;3(5):342-55. Review.

PMID:
11988760
[PubMed - indexed for MEDLINE]
10.

Lissencephaly with cerebellar hypoplasia (LCH): a heterogeneous group of cortical malformations.

Ross ME, Swanson K, Dobyns WB.

Neuropediatrics. 2001 Oct;32(5):256-63.

PMID:
11748497
[PubMed - indexed for MEDLINE]
11.

Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations.

Hong SE, Shugart YY, Huang DT, Shahwan SA, Grant PE, Hourihane JO, Martin ND, Walsh CA.

Nat Genet. 2000 Sep;26(1):93-6. Erratum in: Nat Genet 2001 Feb;27(2):225.

PMID:
10973257
[PubMed - indexed for MEDLINE]
12.

Neuronal migration.

Lambert de Rouvroit C, Goffinet AM.

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

PMID:
11429281
[PubMed - indexed for MEDLINE]
Free Article
13.

Expression of DISC1 binding partners is reduced in schizophrenia and associated with DISC1 SNPs.

Lipska BK, Peters T, Hyde TM, Halim N, Horowitz C, Mitkus S, Weickert CS, Matsumoto M, Sawa A, Straub RE, Vakkalanka R, Herman MM, Weinberger DR, Kleinman JE.

Hum Mol Genet. 2006 Apr 15;15(8):1245-58. Epub 2006 Mar 1.

PMID:
16510495
[PubMed - indexed for MEDLINE]
Free Article
14.

Cajal-Retzius and subplate neurons: their role in cortical development.

Sarnat HB, Flores-Sarnat L.

Eur J Paediatr Neurol. 2002;6(2):91-7.

PMID:
11995962
[PubMed - indexed for MEDLINE]
15.

Lissencephaly type I.

Leventer R.

Handb Clin Neurol. 2008;87:205-18. doi: 10.1016/S0072-9752(07)87013-8. No abstract available.

PMID:
18809027
[PubMed - indexed for MEDLINE]
16.

Cortical development: receiving reelin.

Gilmore EC, Herrup K.

Curr Biol. 2000 Feb 24;10(4):R162-6. Review.

PMID:
10704405
[PubMed - indexed for MEDLINE]
Free Article
17.

A role of MAP1B in Reelin-dependent neuronal migration.

González-Billault C, Del Río JA, Ureña JM, Jiménez-Mateos EM, Barallobre MJ, Pascual M, Pujadas L, Simó S, Torre AL, Gavin R, Wandosell F, Soriano E, Avila J.

Cereb Cortex. 2005 Aug;15(8):1134-45. Epub 2004 Dec 8.

PMID:
15590913
[PubMed - indexed for MEDLINE]
Free Article
18.

[Molecular genetics of lissencephaly and microcephaly].

Mochida GH.

Brain Nerve. 2008 Apr;60(4):437-44. Review. Japanese.

PMID:
18421985
[PubMed - indexed for MEDLINE]
19.

Selective expression of doublecortin and LIS1 in developing human cortex suggests unique modes of neuronal movement.

Meyer G, Perez-Garcia CG, Gleeson JG.

Cereb Cortex. 2002 Dec;12(12):1225-36.

PMID:
12427674
[PubMed - indexed for MEDLINE]
Free Article
20.

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
[PubMed - indexed for MEDLINE]

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk