PubMed (OMIM) for id: 336288

Year	Number of Results
1986	2
1992	2
1993	3
1994	3
1995	1
1997	4
1998	6
1999	3
2000	6
2001	4
2002	2
2003	6
2004	4
2023	0

1

Accelerated evolution of nervous system genes in the origin of Homo sapiens.

Dorus S, Vallender EJ, Evans PD, Anderson JR, Gilbert SL, Mahowald M, Wyckoff GJ, Malcom CM, Lahn BT. Dorus S, et al. Cell. 2004 Dec 29;119(7):1027-40. doi: 10.1016/j.cell.2004.11.040. Cell. 2004. PMID: 15620360 Free article.

2

Coupling PAF signaling to dynein regulation: structure of LIS1 in complex with PAF-acetylhydrolase.

Tarricone C, Perrina F, Monzani S, Massimiliano L, Kim MH, Derewenda ZS, Knapp S, Tsai LH, Musacchio A. Tarricone C, et al. Neuron. 2004 Dec 2;44(5):809-21. doi: 10.1016/j.neuron.2004.11.019. Neuron. 2004. PMID: 15572112 Free article.

3

Ndel1 operates in a common pathway with LIS1 and cytoplasmic dynein to regulate cortical neuronal positioning.

Shu T, Ayala R, Nguyen MD, Xie Z, Gleeson JG, Tsai LH. Shu T, et al. Neuron. 2004 Oct 14;44(2):263-77. doi: 10.1016/j.neuron.2004.09.030. Neuron. 2004. PMID: 15473966 Free article.

4

Mutation screening in a cohort of patients with lissencephaly and subcortical band heterotopia.

Torres FR, Montenegro MA, Marques-De-Faria AP, Guerreiro MM, Cendes F, Lopes-Cendes I. Torres FR, et al. Neurology. 2004 Mar 9;62(5):799-802. doi: 10.1212/01.wnl.0000113725.46254.fd. Neurology. 2004. PMID: 15007136

5

Mosaic mutations of the LIS1 gene cause subcortical band heterotopia.

Sicca F, Kelemen A, Genton P, Das S, Mei D, Moro F, Dobyns WB, Guerrini R. Sicca F, et al. Neurology. 2003 Oct 28;61(8):1042-6. doi: 10.1212/wnl.61.8.1042. Neurology. 2003. PMID: 14581661

6

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. Assadi AH, et al. Nat Genet. 2003 Nov;35(3):270-6. doi: 10.1038/ng1257. Epub 2003 Oct 26. Nat Genet. 2003. PMID: 14578885

7

Previously uncharacterized roles of platelet-activating factor acetylhydrolase 1b complex in mouse spermatogenesis.

Yan W, Assadi AH, Wynshaw-Boris A, Eichele G, Matzuk MM, Clark GD. Yan W, et al. Proc Natl Acad Sci U S A. 2003 Jun 10;100(12):7189-94. doi: 10.1073/pnas.1236145100. Epub 2003 May 29. Proc Natl Acad Sci U S A. 2003. PMID: 12775763 Free PMC article.

8

Lissencephaly and the molecular basis of neuronal migration.

Kato M, Dobyns WB. Kato M, et al. Hum Mol Genet. 2003 Apr 1;12 Spec No 1:R89-96. doi: 10.1093/hmg/ddg086. Hum Mol Genet. 2003. PMID: 12668601 Review.

9

Refinement of a 400-kb critical region allows genotypic differentiation between isolated lissencephaly, Miller-Dieker syndrome, and other phenotypes secondary to deletions of 17p13.3.

Cardoso C, Leventer RJ, Ward HL, Toyo-Oka K, Chung J, Gross A, Martin CL, Allanson J, Pilz DT, Olney AH, Mutchinick OM, Hirotsune S, Wynshaw-Boris A, Dobyns WB, Ledbetter DH. Cardoso C, et al. Am J Hum Genet. 2003 Apr;72(4):918-30. doi: 10.1086/374320. Epub 2003 Mar 5. Am J Hum Genet. 2003. PMID: 12621583 Free PMC article.

10

Somatic mosaicism and variable penetrance in doublecortin-associated migration disorders.

Aigner L, Uyanik G, Couillard-Despres S, Ploetz S, Wolff G, Morris-Rosendahl D, Martin P, Eckel U, Spranger S, Otte J, Woerle H, Holthausen H, Apheshiotis N, Fluegel D, Winkler J. Aigner L, et al. Neurology. 2003 Jan 28;60(2):329-32. doi: 10.1212/01.wnl.0000042091.90361.d2. Neurology. 2003. PMID: 12552055

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