171 related articles for article (PubMed ID: 11262729)
41. Normal and abnormal neuronal migration in the developing cerebral cortex.
Sun XZ; Takahashi S; Cui C; Zhang R; Sakata-Haga H; Sawada K; Fukui Y
J Med Invest; 2002 Aug; 49(3-4):97-110. PubMed ID: 12323012
[TBL] [Abstract][Full Text] [Related]
42. The location and type of mutation predict malformation severity in isolated lissencephaly caused by abnormalities within the LIS1 gene.
Cardoso C; Leventer RJ; Matsumoto N; Kuc JA; Ramocki MB; Mewborn SK; Dudlicek LL; May LF; Mills PL; Das S; Pilz DT; Dobyns WB; Ledbetter DH
Hum Mol Genet; 2000 Dec; 9(20):3019-28. PubMed ID: 11115846
[TBL] [Abstract][Full Text] [Related]
43. Epilepsy and genetic malformations of the cerebral cortex.
Guerrini R; Carrozzo R
Am J Med Genet; 2001; 106(2):160-73. PubMed ID: 11579436
[TBL] [Abstract][Full Text] [Related]
44. Lissencephaly and LIS1: insights into the molecular mechanisms of neuronal migration and development.
Wynshaw-Boris A
Clin Genet; 2007 Oct; 72(4):296-304. PubMed ID: 17850624
[TBL] [Abstract][Full Text] [Related]
45. Genetic mechanisms underlying abnormal neuronal migration in classical lissencephaly.
Kerjan G; Gleeson JG
Trends Genet; 2007 Dec; 23(12):623-30. PubMed ID: 17997185
[TBL] [Abstract][Full Text] [Related]
46. Lissencephaly: mechanistic insights from animal models and potential therapeutic strategies.
Wynshaw-Boris A; Pramparo T; Youn YH; Hirotsune S
Semin Cell Dev Biol; 2010 Oct; 21(8):823-30. PubMed ID: 20688183
[TBL] [Abstract][Full Text] [Related]
47. Epileptogenic brain malformations: clinical presentation, malformative patterns and indications for genetic testing.
Guerrini R; Carrozzo R
Seizure; 2001 Oct; 10(7):532-43; quiz 544-7. PubMed ID: 11749114
[TBL] [Abstract][Full Text] [Related]
48. Lissencephaly and band heterotopia: LIS1, TUBA1A, and DCX mutations in Hungary.
Mokánszki A; Körhegyi I; Szabó N; Bereg E; Gergev G; Balogh E; Bessenyei B; Sümegi A; Morris-Rosendahl DJ; Sztriha L; Oláh E
J Child Neurol; 2012 Dec; 27(12):1534-40. PubMed ID: 22408144
[TBL] [Abstract][Full Text] [Related]
49. Malformations of cortical development.
Pang T; Atefy R; Sheen V
Neurologist; 2008 May; 14(3):181-91. PubMed ID: 18469675
[TBL] [Abstract][Full Text] [Related]
50. So-called 'cryptogenic' partial seizures resulting from a subtle cortical dysgenesis due to a doublecortin gene mutation.
des Portes V; Abaoub L; Joannard A; Souville I; Francis F; Pinard JM; Chelly J; Beldjord C; Jouk PS
Seizure; 2002 Jun; 11(4):273-7. PubMed ID: 12027577
[TBL] [Abstract][Full Text] [Related]
51. Postnatal shifts of interneuron position in the neocortex of normal and reeler mice: evidence for inward radial migration.
Hevner RF; Daza RA; Englund C; Kohtz J; Fink A
Neuroscience; 2004; 124(3):605-18. PubMed ID: 14980731
[TBL] [Abstract][Full Text] [Related]
52. [Development and developmental disorders of the human brain. III. Neuronal migration disorders of the cerebrum].
ten Donkelaar HJ; Lammens M; Wesseling P; Thijssen HO; Renier WO; Gabreëls FJ
Ned Tijdschr Geneeskd; 2001 Mar; 145(10):466-74. PubMed ID: 11268908
[TBL] [Abstract][Full Text] [Related]
53. Neuronal migration, cerebral cortical development, and cerebral cortical anomalies.
Pilz D; Stoodley N; Golden JA
J Neuropathol Exp Neurol; 2002 Jan; 61(1):1-11. PubMed ID: 11829339
[TBL] [Abstract][Full Text] [Related]
54. Molecular pathways controlling the sequential steps of cortical projection neuron migration.
Hippenmeyer S
Adv Exp Med Biol; 2014; 800():1-24. PubMed ID: 24243097
[TBL] [Abstract][Full Text] [Related]
55. [Molecular genetics of lissencephaly and microcephaly].
Mochida GH
Brain Nerve; 2008 Apr; 60(4):437-44. PubMed ID: 18421985
[TBL] [Abstract][Full Text] [Related]
56. [Molecular mechanism of lissencephaly--how LIS1 and NDEL1 regulate cytoplasmic dynein?].
Hirotsune S
Brain Nerve; 2008 Apr; 60(4):375-81. PubMed ID: 18421979
[TBL] [Abstract][Full Text] [Related]
57. Identification of DCX gene mutation in lissencephaly spectrum with subcortical band heterotopia using whole exome sequencing.
Jang MA; Woo HI; Kim JW; Lee J; Ki CS
Pediatr Neurol; 2013 May; 48(5):411-4. PubMed ID: 23583063
[TBL] [Abstract][Full Text] [Related]
58. 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; 520(6):1198-211. PubMed ID: 21935943
[TBL] [Abstract][Full Text] [Related]
59. Reelin and human nodular heterotopia.
Thom M; Garbelli R; Spreafico R
Epilepsia; 2011 Mar; 52(3):650-2. PubMed ID: 21395570
[No Abstract] [Full Text] [Related]
60. Subcortical band heterotopia in rare affected males can be caused by missense mutations in DCX (XLIS) or LIS1.
Pilz DT; Kuc J; Matsumoto N; Bodurtha J; Bernadi B; Tassinari CA; Dobyns WB; Ledbetter DH
Hum Mol Genet; 1999 Sep; 8(9):1757-60. PubMed ID: 10441340
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]