A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly Syndrome

This publication has 50 references indexed in Scilit:

• doublecortin, a Brain-Specific Gene Mutated in Human X-Linked Lissencephaly and Double Cortex Syndrome, Encodes a Putative Signaling Protein
  Cell, 1998
• Dominant X linked subcortical laminar heterotopia and lissencephaly syndrome (XSCLH/LIS): evidence for the occurrence of mutation in males and mapping of a potential locus in Xq22.
  Journal of Medical Genetics, 1997
• X-linked malformations of neuronal migration
  Neurology, 1996
• Expression patterns of two human genes coding for different rab GDP-dissociation inhibitors (GDIs), extremely conserved proteins involved in cellular transport
  Human Molecular Genetics, 1995
• A protein related to extracellular matrix proteins deleted in the mouse mutant reeler
  Nature, 1995
• Identification and characterization of the gene causing type 1 spinocerebellar ataxia
  Nature Genetics, 1994
• The Subplate, A Transient Neocortical Structure: Its Role in the Development of Connections between Thalamus and Cortex
  Annual Review of Neuroscience, 1994
• Activation of protein kinase C decreases phosphorylation of c-Jun at sites that negatively regulate its DNA-binding activity
  Cell, 1991
• The agyria-pachygyria complex: A spectrum of cortical malformations
  Brain & Development, 1991
• Illegitimate transcription: transcription of any gene in any cell type.
  Proceedings of the National Academy of Sciences, 1989