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Items: 1 to 20 of 58

1.

Novel embryonic neuronal migration and proliferation defects in Dcx mutant mice are exacerbated by Lis1 reduction.

Pramparo T, Youn YH, Yingling J, Hirotsune S, Wynshaw-Boris A.

J Neurosci. 2010 Feb 24;30(8):3002-12. doi: 10.1523/JNEUROSCI.4851-09.2010.

2.
3.

LIS1 functions in normal development and disease.

Reiner O, Sapir T.

Curr Opin Neurobiol. 2013 Dec;23(6):951-6. doi: 10.1016/j.conb.2013.08.001. Epub 2013 Aug 23. Review.

PMID:
23973156
4.

Lissencephaly: mechanistic insights from animal models and potential therapeutic strategies.

Wynshaw-Boris A, Pramparo T, Youn YH, Hirotsune S.

Semin Cell Dev Biol. 2010 Oct;21(8):823-30. doi: 10.1016/j.semcdb.2010.07.008. Epub 2010 Aug 3. Review.

5.

Cytoskeleton in action: lissencephaly, a neuronal migration disorder.

Moon HM, Wynshaw-Boris A.

Wiley Interdiscip Rev Dev Biol. 2013 Mar-Apr;2(2):229-45. Review.

6.

LIS-less neurons don't even make it to the starting gate.

Hatten ME.

J Cell Biol. 2005 Sep 12;170(6):867-71. Review.

7.

[Molecular mechanism of lissencephaly--how LIS1 and NDEL1 regulate cytoplasmic dynein?].

Hirotsune S.

Brain Nerve. 2008 Apr;60(4):375-81. Review. Japanese.

PMID:
18421979
8.

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
9.

Protein-protein interactions, cytoskeletal regulation and neuronal migration.

Feng Y, Walsh CA.

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

PMID:
11389474
10.

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
11.

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
12.

Functional analyses of lissencephaly-related proteins in Dictyostelium.

Meyer I, Kuhnert O, Gräf R.

Semin Cell Dev Biol. 2011 Feb;22(1):89-96. doi: 10.1016/j.semcdb.2010.10.007. Epub 2010 Oct 27. Review.

PMID:
21034843
13.

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
14.

Missense mutations resulting in type 1 lissencephaly.

Reiner O, Coquelle FM.

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

PMID:
15719169
15.

[Genetic and clinical aspects of lissencephaly].

Verloes A, Elmaleh M, Gonzales M, Laquerrière A, Gressens P.

Rev Neurol (Paris). 2007 May;163(5):533-47. Review. French.

PMID:
17571022
16.

Genetic control of neuronal migrations in human cortical development.

Meyer G.

Adv Anat Embryol Cell Biol. 2007;189:1 p preceding 1, 1-111. Review.

PMID:
17212070
17.

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
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.

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
20.

Cerebral gyral dysplasias: molecular genetics and cell biology.

Clark GD.

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

PMID:
11262729

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