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Results: 1 to 20 of 103

1.

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.

PMID:
21935943
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Evidence for a cell-specific action of Reelin in the spinal cord.

Phelps PE, Rich R, Dupuy-Davies S, Ríos Y, Wong T.

Dev Biol. 2002 Apr 1;244(1):180-98.

PMID:
11900467
[PubMed - indexed for MEDLINE]
Free Article
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.

PMID:
20181597
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

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.

PMID:
12629176
[PubMed - indexed for MEDLINE]
Free Article
5.

Granule cell dispersion and aberrant neurogenesis in the adult hippocampus of an LIS1 mutant mouse.

Wang Y, Baraban SC.

Dev Neurosci. 2007;29(1-2):91-8.

PMID:
17148952
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Lissencephaly and LIS1: insights into the molecular mechanisms of neuronal migration and development.

Wynshaw-Boris A.

Clin Genet. 2007 Oct;72(4):296-304. Review.

PMID:
17850624
[PubMed - indexed for MEDLINE]
7.

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.

PMID:
20007476
[PubMed - indexed for MEDLINE]
Free PMC Article
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.

PMID:
19734909
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

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.

PMID:
14507966
[PubMed - indexed for MEDLINE]
Free Article
10.

Location and type of mutation in the LIS1 gene do not predict phenotypic severity.

Uyanik G, Morris-Rosendahl DJ, Stiegler J, Klapecki J, Gross C, Berman Y, Martin P, Dey L, Spranger S, Korenke GC, Schreyer I, Hertzberg C, Neumann TE, Burkart P, Spaich C, Meng M, Holthausen H, Adès L, Seidel J, Mangold E, Buyse G, Meinecke P, Schara U, Zeschnigk C, Muller D, Helland G, Schulze B, Wright ML, Kortge-Jung S, Hehr A, Bogdahn U, Schuierer G, Kohlhase J, Aigner L, Wolff G, Hehr U, Winkler J.

Neurology. 2007 Jul 31;69(5):442-7.

PMID:
17664403
[PubMed - indexed for MEDLINE]
11.

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.

PMID:
18075263
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Lis1 and doublecortin function with dynein to mediate coupling of the nucleus to the centrosome in neuronal migration.

Tanaka T, Serneo FF, Higgins C, Gambello MJ, Wynshaw-Boris A, Gleeson JG.

J Cell Biol. 2004 Jun 7;165(5):709-21. Epub 2004 Jun 1.

PMID:
15173193
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Migration patterns of sympathetic preganglionic neurons in embryonic rat spinal cord.

Markham JA, Vaughn JE.

J Neurobiol. 1991 Nov;22(8):811-22.

PMID:
1779224
[PubMed - indexed for MEDLINE]
14.

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.

PMID:
23495356
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Complete loss of Ndel1 results in neuronal migration defects and early embryonic lethality.

Sasaki S, Mori D, Toyo-oka K, Chen A, Garrett-Beal L, Muramatsu M, Miyagawa S, Hiraiwa N, Yoshiki A, Wynshaw-Boris A, Hirotsune S.

Mol Cell Biol. 2005 Sep;25(17):7812-27.

PMID:
16107726
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Evidence for tangential migration disturbances in human lissencephaly resulting from a defect in LIS1, DCX and ARX genes.

Marcorelles P, Laquerrière A, Adde-Michel C, Marret S, Saugier-Veber P, Beldjord C, Friocourt G.

Acta Neuropathol. 2010 Oct;120(4):503-15. doi: 10.1007/s00401-010-0692-z. Epub 2010 May 12.

PMID:
20461390
[PubMed - indexed for MEDLINE]
17.

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.

PMID:
15331402
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Subcortical band heterotopia (SBH) in males: clinical, imaging and genetic findings in comparison with females.

D'Agostino MD, Bernasconi A, Das S, Bastos A, Valerio RM, Palmini A, Costa da Costa J, Scheffer IE, Berkovic S, Guerrini R, Dravet C, Ono J, Gigli G, Federico A, Booth F, Bernardi B, Volpi L, Tassinari CA, Guggenheim MA, Ledbetter DH, Gleeson JG, Lopes-Cendes I, Vossler DG, Malaspina E, Franzoni E, Sartori RJ, Mitchell MH, Mercho S, Dubeau F, Andermann F, Dobyns WB, Andermann E.

Brain. 2002 Nov;125(Pt 11):2507-22.

PMID:
12390976
[PubMed - indexed for MEDLINE]
Free Article
19.

Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality.

Hirotsune S, Fleck MW, Gambello MJ, Bix GJ, Chen A, Clark GD, Ledbetter DH, McBain CJ, Wynshaw-Boris A.

Nat Genet. 1998 Aug;19(4):333-9.

PMID:
9697693
[PubMed - indexed for MEDLINE]
20.

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
[PubMed - indexed for MEDLINE]

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