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Items: 1 to 20 of 109

1.

ALLN rescues an in vitro excitatory synaptic transmission deficit in Lis1 mutant mice.

Sebe JY, Bershteyn M, Hirotsune S, Wynshaw-Boris A, Baraban SC.

J Neurophysiol. 2013 Jan;109(2):429-36. doi: 10.1152/jn.00431.2012. Epub 2012 Oct 24.

2.

Characterization of inhibitory circuits in the malformed hippocampus of Lis1 mutant mice.

Jones DL, Baraban SC.

J Neurophysiol. 2007 Nov;98(5):2737-46. Epub 2007 Sep 19.

3.

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.

4.

Seizures, enhanced excitation, and increased vesicle number in Lis1 mutant mice.

Greenwood JS, Wang Y, Estrada RC, Ackerman L, Ohara PT, Baraban SC.

Ann Neurol. 2009 Nov;66(5):644-53. doi: 10.1002/ana.21775.

PMID:
19938147
5.

Inhibitory inputs to hippocampal interneurons are reorganized in Lis1 mutant mice.

Jones DL, Baraban SC.

J Neurophysiol. 2009 Aug;102(2):648-58. doi: 10.1152/jn.00392.2009. Epub 2009 Jun 10.

6.

Genetic enhancement of the Lis1+/- phenotype by a heterozygous mutation in the adenomatous polyposis coli gene.

Hebbar S, Guillotte AM, Mesngon MT, Zhou Q, Wynshaw-Boris A, Smith DS.

Dev Neurosci. 2008;30(1-3):157-70.

7.

Aberrant dentate gyrus cytoarchitecture and fiber lamination in Lis1 mutant mice.

Wang Y, Baraban SC.

Hippocampus. 2008;18(8):758-65. doi: 10.1002/hipo.20434.

PMID:
18446829
8.

Post-natal treatment by a blood-brain-barrier permeable calpain inhibitor, SNJ1945 rescued defective function in lissencephaly.

Toba S, Tamura Y, Kumamoto K, Yamada M, Takao K, Hattori S, Miyakawa T, Kataoka Y, Azuma M, Hayasaka K, Amamoto M, Tominaga K, Wynshaw-Boris A, Wanibuchi H, Oka Y, Sato M, Kato M, Hirotsune S.

Sci Rep. 2013;3:1224. doi: 10.1038/srep01224. Epub 2013 Feb 6.

9.

Distinct dose-dependent cortical neuronal migration and neurite extension defects in Lis1 and Ndel1 mutant mice.

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

J Neurosci. 2009 Dec 9;29(49):15520-30. doi: 10.1523/JNEUROSCI.4630-09.2009.

10.

[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
11.

Postnatal alterations of the inhibitory synaptic responses recorded from cortical pyramidal neurons in the Lis1/sLis1 mutant mouse.

Valdés-Sánchez L, Escámez T, Echevarria D, Ballesta JJ, Tabarés-Seisdedos R, Reiner O, Martinez S, Geijo-Barrientos E.

Mol Cell Neurosci. 2007 Jun;35(2):220-9. Epub 2007 Mar 3.

PMID:
17433713
12.

LIS1 deficiency promotes dysfunctional synaptic integration of granule cells generated in the developing and adult dentate gyrus.

Hunt RF, Dinday MT, Hindle-Katel W, Baraban SC.

J Neurosci. 2012 Sep 12;32(37):12862-75. doi: 10.1523/JNEUROSCI.1286-12.2012.

13.
14.

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.

15.

A novel strategy for therapeutic intervention for the genetic disease: preventing proteolytic cleavage using small chemical compound.

Yamada M, Hirotsune S, Wynshaw-Boris A.

Int J Biochem Cell Biol. 2010 Sep;42(9):1401-7. doi: 10.1016/j.biocel.2010.05.017. Epub 2010 Jun 9.

16.

LIS1 controls mitosis and mitotic spindle organization via the LIS1-NDEL1-dynein complex.

Moon HM, Youn YH, Pemble H, Yingling J, Wittmann T, Wynshaw-Boris A.

Hum Mol Genet. 2014 Jan 15;23(2):449-66. doi: 10.1093/hmg/ddt436. Epub 2013 Sep 12.

17.

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.

18.

Impaired learning and motor behavior in heterozygous Pafah1b1 (Lis1) mutant mice.

Paylor R, Hirotsune S, Gambello MJ, Yuva-Paylor L, Crawley JN, Wynshaw-Boris A.

Learn Mem. 1999 Sep-Oct;6(5):521-37.

19.

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.

20.

Lis1 is necessary for normal non-radial migration of inhibitory interneurons.

McManus MF, Nasrallah IM, Pancoast MM, Wynshaw-Boris A, Golden JA.

Am J Pathol. 2004 Sep;165(3):775-84.

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