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Proceedings of the National Academy of Sciences of the United States of America|June 9, 2005
Cytoplasmic LEK1 is a regulator of microtubule function through its interaction with the LIS1 pathwayVictor Soukoulis, Samyukta Reddy, Ryan D Pooley, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|May 23, 2002
Mapping of the mouse hyh gene to a YAC/BAC contig on proximal Chromosome 7Teresa H Chae, Kristina M Allen, Muriel T Davisson, et al.
The Journal of Comparative Neurology|April 11, 2003
Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brainRussell J Ferland, Timothy J Cherry, Patricia O Preware, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 6, 2007
Both doublecortin and doublecortin-like kinase play a role in cortical interneuron migrationGaëlle Friocourt, Judy S Liu, Mary Antypa, et al.
American Journal of Medical Genetics. Part A|January 28, 2003
Cryptic t(1;12)(q44;p13.3) translocation in a previously described syndrome with polymicrogyria, segregating as an apparently X-linked traitMarcella Zollino, Cesare Colosimo, Orsetta Zuffardi, et al.
Nucleic Acids Research|April 18, 2012
Impact of PNKP mutations associated with microcephaly, seizures and developmental delay on enzyme activity and DNA strand break repairJohn J Reynolds, Alexandra K Walker, Edward C Gilmore, et al.
Human Molecular Genetics|May 13, 2008
Lis1-Nde1-dependent neuronal fate control determines cerebral cortical size and laminationAshley S Pawlisz, Christopher Mutch, Anthony Wynshaw-Boris, et al.
Human Molecular Genetics|October 24, 2002
Filamin A and Filamin B are co-expressed within neurons during periods of neuronal migration and can physically interactVolney L Sheen, Yuanyi Feng, Donna Graham, et al.
Langmuir : the ACS Journal of Surfaces and Colloids|November 1, 2006
Nanostructured biosensors built by layer-by-layer electrostatic assembly of enzyme-coated single-walled carbon nanotubes and redox polymersYoudan Wang, Pratixa P Joshi, Kevin L Hobbs, et al.
American Journal of Medical Genetics. Part A|March 16, 2012
Expanding the spectrum of rearrangements involving chromosome 19: a mild phenotype associated with a 19p13.12-p13.13 deletionGiuseppe Marangi, Daniela Orteschi, Federico Vigevano, et al.
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