Related references
Note: Only part of the references are listed.Novel Embryonic Neuronal Migration and Proliferation Defects in Dcx Mutant Mice Are Exacerbated by Lis1 Reduction
Tiziano Pramparo et al.
JOURNAL OF NEUROSCIENCE (2010)
CHD7 cooperates with PBAF to control multipotent neural crest formation
Ruchi Bajpai et al.
NATURE (2010)
Dixdc1 Is a Critical Regulator of DISC1 and Embryonic Cortical Development
Karun K. Singh et al.
NEURON (2010)
Lissencephaly: Mechanistic insights from animal models and potential therapeutic strategies
Anthony Wynshaw-Boris et al.
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY (2010)
Distinct Dose-Dependent Cortical Neuronal Migration and Neurite Extension Defects in Lis1 and Ndel1 Mutant Mice
Yong Ha Youn et al.
JOURNAL OF NEUROSCIENCE (2009)
SUN1/2 and Syne/Nesprin-1/2 Complexes Connect Centrosome to the Nucleus during Neurogenesis and Neuronal Migration in Mice
Xiaochang Zhang et al.
NEURON (2009)
Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation
Guy Froyen et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2008)
WGCNA: an R package for weighted correlation network analysis
Peter Langfelder et al.
BMC BIOINFORMATICS (2008)
Neuroepithelial stem cell proliferation requires LIS1 for precise spindle orientation and symmetric division
Jessica Yingling et al.
CELL (2008)
Characterization of neuroprogenitor cells expressing the PDGF β-receptor within the subventricular zone of postnatal mice
Yoko Ishii et al.
MOLECULAR AND CELLULAR NEUROSCIENCE (2008)
Cep120 and TACCs control interkinetic nuclear migration and the neural progenitor pool
Zhigang Xie et al.
NEURON (2007)
Lissencephaly and LIS1: insights into the molecular mechanisms of neuronal migration and development
A. Wynshaw-Boris
CLINICAL GENETICS (2007)
Spinophilin facilitates dephosphorylation of doublecortin by PP1 to mediate microtubule bundling at the axonal wrist
Stephanie L. Bielas et al.
CELL (2007)
A functional genomic screen identifies a role for TAO1 kinase in spindle-checkpoint signalling
Viji M. Draviam et al.
NATURE CELL BIOLOGY (2007)
Mutations in the gene encoding the sigma 2 subunit of the adaptor protein 1 complex, AP1S2, cause X-linked mental retardation
Patrick S. Tarpey et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2006)
Doublecortin maintains bipolar shape and nuclear translocation during migration in the adult forebrain
Hiroyuki Koizumi et al.
NATURE NEUROSCIENCE (2006)
Branching and nucleokinesis defects in migrating interneurons derived from doublecortin knockout mice
C Kappeler et al.
HUMAN MOLECULAR GENETICS (2006)
QN1/KIAA1009: a new essential protein for chromosome segregation and mitotic spindle assembly
A Leon et al.
ONCOGENE (2006)
Genetic interactions between doublecortin and doublecortin-like kinase in neuronal migration and axon outgrowth
TAS Deuel et al.
NEURON (2006)
Support for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locus
R Benayed et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2005)
Complete loss of Ndel1 results in neuronal migration defects and early embryonic lethality
S Sasaki et al.
MOLECULAR AND CELLULAR BIOLOGY (2005)
Doublecortin interacts with the ubiquitin protease DFFRX, which associates with microtubules in neuronal processes
G Friocourt et al.
MOLECULAR AND CELLULAR NEUROSCIENCE (2005)
Mutations in the FKRP gene can cause muscle-eye-brain disease and Walker-Warburg syndrome -: art. no. e61
DBV de Bernabé et al.
JOURNAL OF MEDICAL GENETICS (2004)
DCX, a new mediator of the JNK pathway
A Gdalyahu et al.
EMBO JOURNAL (2004)
Nudel functions in membrane traffic mainly through association with Lis1 and cytoplasmic dynein
Y Liang et al.
JOURNAL OF CELL BIOLOGY (2004)
Modulation of T cell development and activation by novel members of the Schlafen (slfn) gene family harbouring an RNA helicase-like motif
P Geserick et al.
INTERNATIONAL IMMUNOLOGY (2004)
Proteomic studies identified a single nucleotide polymorphism in glyoxalase I as autism susceptibility factor
MA Junaid et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2004)
Lis1 and doublecortin function with dynein to mediate coupling of the nucleus to the centrosome in neuronal migration
T Tanaka et al.
JOURNAL OF CELL BIOLOGY (2004)
RNAi reveals doublecortin is required for radial migration in rat neocortex
JL Bai et al.
NATURE NEUROSCIENCE (2003)
14-3-3ε is important for neuronal migration by binding to NUDEL:: a molecular explanation for Miller-Dieker syndrome
K Toyo-oka et al.
NATURE GENETICS (2003)
Lissencephaly and the molecular basis of neuronal migration
M Kato et al.
HUMAN MOLECULAR GENETICS (2003)
Exploration, normalization, and summaries of high density oligonucleotide array probe level data
RA Irizarry et al.
BIOSTATISTICS (2003)
Life is a journey: A genetic look at neocortical development
A Gupta et al.
NATURE REVIEWS GENETICS (2002)
A LIS1/NUDEL/cytoplasmic dynein heavy chain complex in the developing and adult nervous system
S Sasaki et al.
NEURON (2000)
NUDEL is a novel Cdk5 substrate that associates with LIS1 and cytoplasmic dynein
M Niethammer et al.
NEURON (2000)
The retinitis pigmentosa GTPase regulator (RPGR) interacts with novel transport-like proteins in the outer segments of rod photoreceptors
R Roepman et al.
HUMAN MOLECULAR GENETICS (2000)
Share Paper
