171 related articles for article (PubMed ID: 11262729)
1. Cerebral gyral dysplasias: molecular genetics and cell biology.
Clark GD
Curr Opin Neurol; 2001 Apr; 14(2):157-62. PubMed ID: 11262729
[TBL] [Abstract][Full Text] [Related]
2. 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. PubMed ID: 12390976
[TBL] [Abstract][Full Text] [Related]
3. Lissencephaly and the molecular basis of neuronal migration.
Kato M; Dobyns WB
Hum Mol Genet; 2003 Apr; 12 Spec No 1():R89-96. PubMed ID: 12668601
[TBL] [Abstract][Full Text] [Related]
4. Lissencephaly with cerebellar hypoplasia (LCH): a heterogeneous group of cortical malformations.
Ross ME; Swanson K; Dobyns WB
Neuropediatrics; 2001 Oct; 32(5):256-63. PubMed ID: 11748497
[TBL] [Abstract][Full Text] [Related]
5. 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; 69(5):442-7. PubMed ID: 17664403
[TBL] [Abstract][Full Text] [Related]
6. Genotype-phenotype correlation in lissencephaly and subcortical band heterotopia: the key questions answered.
Leventer RJ
J Child Neurol; 2005 Apr; 20(4):307-12. PubMed ID: 15921231
[TBL] [Abstract][Full Text] [Related]
7. 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. PubMed ID: 11899256
[TBL] [Abstract][Full Text] [Related]
8. Selective expression of doublecortin and LIS1 in developing human cortex suggests unique modes of neuronal movement.
Meyer G; Perez-Garcia CG; Gleeson JG
Cereb Cortex; 2002 Dec; 12(12):1225-36. PubMed ID: 12427674
[TBL] [Abstract][Full Text] [Related]
9. Molecular genetics of neuronal migration disorders.
Liu JS
Curr Neurol Neurosci Rep; 2011 Apr; 11(2):171-8. PubMed ID: 21222180
[TBL] [Abstract][Full Text] [Related]
10. 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; 23(5):1719-29. PubMed ID: 12629176
[TBL] [Abstract][Full Text] [Related]
11. 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
Nat Genet; 2003 Nov; 35(3):270-6. PubMed ID: 14578885
[TBL] [Abstract][Full Text] [Related]
12. Missense mutations resulting in type 1 lissencephaly.
Reiner O; Coquelle FM
Cell Mol Life Sci; 2005 Feb; 62(4):425-34. PubMed ID: 15719169
[TBL] [Abstract][Full Text] [Related]
13. Reelin mutations in mouse and man: from reeler mouse to schizophrenia, mood disorders, autism and lissencephaly.
Fatemi SH
Mol Psychiatry; 2001 Mar; 6(2):129-33. PubMed ID: 11317213
[No Abstract] [Full Text] [Related]
14. 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
Neurology; 2004 Mar; 62(5):799-802. PubMed ID: 15007136
[TBL] [Abstract][Full Text] [Related]
15. 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. PubMed ID: 12764037
[TBL] [Abstract][Full Text] [Related]
16. Reelin mouse mutants as models of cortical development disorders.
D'Arcangelo G
Epilepsy Behav; 2006 Feb; 8(1):81-90. PubMed ID: 16266828
[TBL] [Abstract][Full Text] [Related]
17. 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; 30(8):3002-12. PubMed ID: 20181597
[TBL] [Abstract][Full Text] [Related]
18. The multipolar stage and disruptions in neuronal migration.
LoTurco JJ; Bai J
Trends Neurosci; 2006 Jul; 29(7):407-413. PubMed ID: 16713637
[TBL] [Abstract][Full Text] [Related]
19. Smooth mosaics: genotype and phenotype in lissencephaly.
Jung HH
Neurology; 2007 Jul; 69(5):425-6. PubMed ID: 17664400
[No Abstract] [Full Text] [Related]
20. LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation.
Pilz DT; Matsumoto N; Minnerath S; Mills P; Gleeson JG; Allen KM; Walsh CA; Barkovich AJ; Dobyns WB; Ledbetter DH; Ross ME
Hum Mol Genet; 1998 Dec; 7(13):2029-37. PubMed ID: 9817918
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]