171 related articles for article (PubMed ID: 11262729)
21. Aberrant dentate gyrus cytoarchitecture and fiber lamination in Lis1 mutant mice.
Wang Y; Baraban SC
Hippocampus; 2008; 18(8):758-65. PubMed ID: 18446829
[TBL] [Abstract][Full Text] [Related]
22. Lissencephaly and subcortical band heterotopia: molecular basis and diagnosis.
Leventer RJ; Pilz DT; Matsumoto N; Ledbetter DH; Dobyns WB
Mol Med Today; 2000 Jul; 6(7):277-84. PubMed ID: 10859564
[TBL] [Abstract][Full Text] [Related]
23. Smooth, rough and upside-down neocortical development.
Olson EC; Walsh CA
Curr Opin Genet Dev; 2002 Jun; 12(3):320-7. PubMed ID: 12076676
[TBL] [Abstract][Full Text] [Related]
24. Classical lissencephaly and double cortex (subcortical band heterotopia): LIS1 and doublecortin.
Gleeson JG
Curr Opin Neurol; 2000 Apr; 13(2):121-5. PubMed ID: 10987567
[TBL] [Abstract][Full Text] [Related]
25. Protein-protein interactions, cytoskeletal regulation and neuronal migration.
Feng Y; Walsh CA
Nat Rev Neurosci; 2001 Jun; 2(6):408-16. PubMed ID: 11389474
[TBL] [Abstract][Full Text] [Related]
26. Cytoskeleton in action: lissencephaly, a neuronal migration disorder.
Moon HM; Wynshaw-Boris A
Wiley Interdiscip Rev Dev Biol; 2013; 2(2):229-45. PubMed ID: 23495356
[TBL] [Abstract][Full Text] [Related]
27. 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; 165(5):709-21. PubMed ID: 15173193
[TBL] [Abstract][Full Text] [Related]
28. 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. PubMed ID: 21423666
[TBL] [Abstract][Full Text] [Related]
29. The doublecortin gene family and disorders of neuronal structure.
Dijkmans TF; van Hooijdonk LW; Fitzsimons CP; Vreugdenhil E
Cent Nerv Syst Agents Med Chem; 2010 Mar; 10(1):32-46. PubMed ID: 20236041
[TBL] [Abstract][Full Text] [Related]
30. 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
Neurology; 2003 Oct; 61(8):1042-6. PubMed ID: 14581661
[TBL] [Abstract][Full Text] [Related]
31. Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations.
Hong SE; Shugart YY; Huang DT; Shahwan SA; Grant PE; Hourihane JO; Martin ND; Walsh CA
Nat Genet; 2000 Sep; 26(1):93-6. PubMed ID: 10973257
[TBL] [Abstract][Full Text] [Related]
32. Mitotic impairment by doublecortin is diminished by doublecortin mutations found in patients.
Couillard-Despres S; Uyanik G; Ploetz S; Karl C; Koch H; Winkler J; Aigner L
Neurogenetics; 2004 Jun; 5(2):83-93. PubMed ID: 15045646
[TBL] [Abstract][Full Text] [Related]
33. [Neurosurgical Embryology. Part 2: Recent data on normal and pathological development of the cortex].
Catala M
Neurochirurgie; 2003 Sep; 49(4):431-40. PubMed ID: 14526254
[TBL] [Abstract][Full Text] [Related]
34. The Pafah1b complex interacts with the reelin receptor VLDLR.
Zhang G; Assadi AH; McNeil RS; Beffert U; Wynshaw-Boris A; Herz J; Clark GD; D'Arcangelo G
PLoS One; 2007 Feb; 2(2):e252. PubMed ID: 17330141
[TBL] [Abstract][Full Text] [Related]
35. Lissencephaly type I.
Leventer R
Handb Clin Neurol; 2008; 87():205-18. PubMed ID: 18809027
[No Abstract] [Full Text] [Related]
36. Alternative transcripts of Dclk1 and Dclk2 and their expression in doublecortin knockout mice.
Tuy FP; Saillour Y; Kappeler C; Chelly J; Francis F
Dev Neurosci; 2008; 30(1-3):171-86. PubMed ID: 18075264
[TBL] [Abstract][Full Text] [Related]
37. Lissencephaly: Expanded imaging and clinical classification.
Di Donato N; Chiari S; Mirzaa GM; Aldinger K; Parrini E; Olds C; Barkovich AJ; Guerrini R; Dobyns WB
Am J Med Genet A; 2017 Jun; 173(6):1473-1488. PubMed ID: 28440899
[TBL] [Abstract][Full Text] [Related]
38. C-Terminal Region Truncation of RELN Disrupts an Interaction with VLDLR, Causing Abnormal Development of the Cerebral Cortex and Hippocampus.
Ha S; Tripathi PP; Mihalas AB; Hevner RF; Beier DR
J Neurosci; 2017 Jan; 37(4):960-971. PubMed ID: 28123028
[TBL] [Abstract][Full Text] [Related]
39. Epileptogenic brain malformations: clinical presentation, malformative patterns and indications for genetic testing.
Guerrini R; Carrozzo R
Seizure; 2002 Apr; 11 Suppl A():532-43; quiz 544-7. PubMed ID: 12185771
[TBL] [Abstract][Full Text] [Related]
40. Genotypically defined lissencephalies show distinct pathologies.
Forman MS; Squier W; Dobyns WB; Golden JA
J Neuropathol Exp Neurol; 2005 Oct; 64(10):847-57. PubMed ID: 16215456
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
