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Results: 1 to 20 of 146

Similar articles for PubMed (Select 23495356)

1.

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.

2.

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
3.

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.

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.

5.

[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
6.

The dynamics of neuronal migration.

Wu Q, Liu J, Fang A, Li R, Bai Y, Kriegstein AR, Wang X.

Adv Exp Med Biol. 2014;800:25-36. doi: 10.1007/978-94-007-7687-6_2. Review.

PMID:
24243098
7.
8.

Inhibition of calpain increases LIS1 expression and partially rescues in vivo phenotypes in a mouse model of lissencephaly.

Yamada M, Yoshida Y, Mori D, Takitoh T, Kengaku M, Umeshima H, Takao K, Miyakawa T, Sato M, Sorimachi H, Wynshaw-Boris A, Hirotsune S.

Nat Med. 2009 Oct;15(10):1202-7. doi: 10.1038/nm.2023. Epub 2009 Sep 6.

9.

Human lissencephaly with cerebellar hypoplasia due to mutations in TUBA1A: expansion of the foetal neuropathological phenotype.

Lecourtois M, Poirier K, Friocourt G, Jaglin X, Goldenberg A, Saugier-Veber P, Chelly J, Laquerrière A.

Acta Neuropathol. 2010 Jun;119(6):779-89. doi: 10.1007/s00401-010-0684-z. Epub 2010 Apr 8.

PMID:
20376468
10.

Global developmental gene expression and pathway analysis of normal brain development and mouse models of human neuronal migration defects.

Pramparo T, Libiger O, Jain S, Li H, Youn YH, Hirotsune S, Schork NJ, Wynshaw-Boris A.

PLoS Genet. 2011 Mar;7(3):e1001331. doi: 10.1371/journal.pgen.1001331. Epub 2011 Mar 10.

11.

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.

12.

Multiple dose-dependent effects of Lis1 on cerebral cortical development.

Gambello MJ, Darling DL, Yingling J, Tanaka T, Gleeson JG, Wynshaw-Boris A.

J Neurosci. 2003 Mar 1;23(5):1719-29.

13.

Role of cytoskeletal abnormalities in the neuropathology and pathophysiology of type I lissencephaly.

Friocourt G, Marcorelles P, Saugier-Veber P, Quille ML, Marret S, Laquerrière A.

Acta Neuropathol. 2011 Feb;121(2):149-70. doi: 10.1007/s00401-010-0768-9. Epub 2010 Nov 3. Review.

14.

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
15.

Murine modelling of classical lissencephaly.

Gambello MJ, Hirotsune S, Wynshaw-Boris A.

Neurogenetics. 1999 Apr;2(2):77-86. Review.

PMID:
10369882
16.

The location and type of mutation predict malformation severity in isolated lissencephaly caused by abnormalities within the LIS1 gene.

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

Hum Mol Genet. 2000 Dec 12;9(20):3019-28.

17.

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
18.

Lis1 reduction causes tangential migratory errors in mouse spinal cord.

Moore KD, Chen R, Cilluffo M, Golden JA, Phelps PE.

J Comp Neurol. 2012 Apr 15;520(6):1198-211. doi: 10.1002/cne.22768.

19.

Protein-protein interactions, cytoskeletal regulation and neuronal migration.

Feng Y, Walsh CA.

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

PMID:
11389474
20.

Disregulated RhoGTPases and actin cytoskeleton contribute to the migration defect in Lis1-deficient neurons.

Kholmanskikh SS, Dobrin JS, Wynshaw-Boris A, Letourneau PC, Ross ME.

J Neurosci. 2003 Sep 24;23(25):8673-81.

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