Astroglial-Mediated Remodeling of the Interhemispheric Midline Is Required for the Formation of the Corpus Callosum.

[1]  W. Chung,et al.  Perinatal midline astrocyte development is impaired in fibroblast growth factor 8 hypomorphic mice , 2016, Brain Research.

[2]  L. Richards,et al.  Evolution and development of interhemispheric connections in the vertebrate forebrain , 2014, Front. Hum. Neurosci..

[3]  Laura R. Fenlon,et al.  Balanced Interhemispheric Cortical Activity Is Required for Correct Targeting of the Corpus Callosum , 2014, Neuron.

[4]  N. Salamon,et al.  Microdeletion of 1p32-p31 involving NFIA in a patient with hypoplastic corpus callosum, ventriculomegaly, seizures and urinary tract defects. , 2014, European journal of medical genetics.

[5]  G. Goodhill,et al.  Netrin-DCC signaling regulates corpus callosum formation through attraction of pioneering axons and by modulating Slit2-mediated repulsion. , 2014, Cerebral cortex.

[6]  C. Meldrum,et al.  An intragenic deletion of the NFIA gene in a patient with a hypoplastic corpus callosum, craniofacial abnormalities and urinary tract defects. , 2014, European journal of medical genetics.

[7]  A James Barkovich,et al.  Clinical, genetic and imaging findings identify new causes for corpus callosum development syndromes. , 2014, Brain : a journal of neurology.

[8]  Joseph T. Glessner,et al.  Both Rare and De Novo Copy Number Variants Are Prevalent in Agenesis of the Corpus Callosum but Not in Cerebellar Hypoplasia or Polymicrogyria , 2013, PLoS genetics.

[9]  W. Snider,et al.  MEK Is a Key Regulator of Gliogenesis in the Developing Brain , 2012, Neuron.

[10]  J. Loturco,et al.  A method for stable transgenesis of radial glia lineage in rat neocortex by piggyBac mediated transposition , 2012, Journal of Neuroscience Methods.

[11]  J. Siegenthaler,et al.  A Cascade of Morphogenic Signaling Initiated by the Meninges Controls Corpus Callosum Formation , 2012, Neuron.

[12]  Chih-ping Chen,et al.  Chromosome 1p32-p31 deletion syndrome: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia, and intrauterine growth restriction. , 2011, Taiwanese journal of obstetrics & gynecology.

[13]  E. Puelles,et al.  Novel FGF8 mutations associated with recessive holoprosencephaly, craniofacial defects, and hypothalamo-pituitary dysfunction. , 2011, The Journal of clinical endocrinology and metabolism.

[14]  J. Siegenthaler,et al.  We have got you 'covered': how the meninges control brain development. , 2011, Current opinion in genetics & development.

[15]  P. Bovolenta,et al.  Appropriate Bmp7 levels are required for the differentiation of midline guidepost cells involved in corpus callosum formation , 2011, Developmental neurobiology.

[16]  L. Richards,et al.  Molecular regulation of the developing commissural plate , 2010, The Journal of comparative neurology.

[17]  L. Richards,et al.  NFIA Controls Telencephalic Progenitor Cell Differentiation through Repression of the Notch Effector Hes1 , 2010, The Journal of Neuroscience.

[18]  B. Ertl-Wagner,et al.  A novel 1p31.3p32.2 deletion involving the NFIA gene detected by array CGH in a patient with macrocephaly and hypoplasia of the corpus callosum , 2010, European Journal of Pediatrics.

[19]  Allan R. Jones,et al.  A robust and high-throughput Cre reporting and characterization system for the whole mouse brain , 2009, Nature Neuroscience.

[20]  L. Richards,et al.  Multiple non-cell-autonomous defects underlie neocortical callosal dysgenesis in Nfib-deficient mice , 2009, Neural Development.

[21]  Y. Yanagawa,et al.  Transient Neuronal Populations Are Required to Guide Callosal Axons: A Role for Semaphorin 3C , 2009, PLoS biology.

[22]  J. Kohyama,et al.  Committed neuronal precursors confer astrocytic potential on residual neural precursor cells. , 2009, Developmental cell.

[23]  T. Abe,et al.  Draxin, a Repulsive Guidance Protein for Spinal Cord and Forebrain Commissures , 2009, Science.

[24]  Charles Raybaud,et al.  Brain malformation in syndromic craniosynostoses, a primary disorder of white matter: a review , 2007, Child's Nervous System.

[25]  Ivor Mason,et al.  Initiation to end point: the multiple roles of fibroblast growth factors in neural development , 2007, Nature Reviews Neuroscience.

[26]  C. Walsh,et al.  NFIA Haploinsufficiency Is Associated with a CNS Malformation Syndrome and Urinary Tract Defects , 2007, PLoS genetics.

[27]  R. Adolphs,et al.  Agenesis of the corpus callosum: genetic, developmental and functional aspects of connectivity , 2007, Nature Reviews Neuroscience.

[28]  A James Barkovich,et al.  Anomalies of the corpus callosum: an MR analysis of the phenotypic spectrum of associated malformations. , 2006, AJR. American journal of roentgenology.

[29]  W. Wurst,et al.  Inducible gene deletion in astroglia and radial glia—A valuable tool for functional and lineage analysis , 2006, Glia.

[30]  N. Šestan,et al.  Midline radial glia translocation and corpus callosum formation require FGF signaling , 2006, Nature Neuroscience.

[31]  M. Halford,et al.  The Wnt Receptor Ryk Is Required for Wnt5a-Mediated Axon Guidance on the Contralateral Side of the Corpus Callosum , 2006, The Journal of Neuroscience.

[32]  Salvador Martinez,et al.  Dose-dependent functions of Fgf8 in regulating telencephalic patterning centers , 2006, Development.

[33]  M. Henkemeyer,et al.  Multiple Eph Receptors and B-Class Ephrins Regulate Midline Crossing of Corpus Callosum Fibers in the Developing Mouse Forebrain , 2006, The Journal of Neuroscience.

[34]  M. Gazzaniga.  Forty-five years of split-brain research and still going strong , 2005, Nature Reviews Neuroscience.

[35]  L. Richards,et al.  The Transcription Factor Gene Nfib Is Essential for both Lung Maturation and Brain Development , 2005, Molecular and Cellular Biology.

[36]  S. Itohara,et al.  Dorsal telencephalon‐specific expression of Cre recombinase in PAC transgenic mice , 2004, Genesis.

[37]  L. Richards,et al.  Development of midline glial populations at the corticoseptal boundary. , 2003, Journal of neurobiology.

[38]  F. Speleman,et al.  Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome , 2003, Nature Genetics.

[39]  L. Richards,et al.  Abnormal Development of Forebrain Midline Glia and Commissural Projections in Nfia Knock-Out Mice , 2003, The Journal of Neuroscience.

[40]  W. Halfter,et al.  A Critical Function of the Pial Basement Membrane in Cortical Histogenesis , 2002, The Journal of Neuroscience.

[41]  O. Marín,et al.  Slit Proteins Prevent Midline Crossing and Determine the Dorsoventral Position of Major Axonal Pathways in the Mammalian Forebrain , 2002, Neuron.

[42]  Ralph Weissleder,et al.  In vivo molecular target assessment of matrix metalloproteinase inhibition , 2001, Nature Medicine.

[43]  M. Gonzalès,et al.  Clinical variability in patients with Apert's syndrome. , 1999, Journal of neurosurgery.

[44]  G. Martin,et al.  An Fgf8 mutant allelic series generated by Cre- and Flp-mediated recombination , 1998, Nature Genetics.

[45]  N. Ho,et al.  De novo interstitial deletion of chromosome 1p with absent corpus callosum--a case report. , 1997, Annals of the Academy of Medicine, Singapore.

[46]  A. Barkovich,et al.  Skull base and calvarial deformities: association with intracranial changes in craniofacial syndromes. , 1996, AJNR. American journal of neuroradiology.

[47]  R. Howell,et al.  Developmental delay and dysmorphic features associated with a previously undescribed deletion on chromosome 1. , 1995, Journal of medical genetics.

[48]  W. Reardon,et al.  Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome , 1995, Nature Genetics.

[49]  M. Edwards,et al.  Immunocytochemical demonstration of early appearing astroglial structures that form boundaries and pathways along axon tracts in the fetal brain , 1993, The Journal of comparative neurology.

[50]  D. Wahlsten,et al.  Axonal guidance during development of the great cerebral commissures: Descriptive and experimental studies, in vivo, on the role of preformed glial pathways , 1982, The Journal of comparative neurology.

[51]  P. Rakić,et al.  Development of the corpus callosum and cavum septi in man , 1968, The Journal of comparative neurology.

[52]  Moriz Probst,et al.  Ueber den Bau des vollständig balkenlosen Gross-hirnes sowie über Mikrogyrie und Heterotopie der grauen Substanz , 1901, Archiv für Psychiatrie und Nervenkrankheiten.

[53]  M. A. Basson,et al.  Gli3 controls corpus callosum formation by positioning midline guideposts during telencephalic patterning. , 2014, Cerebral cortex.

[54]  Jean-Pierre Fryns,et al.  Three cases of two unrelated families with a microduplication 22q11.2: developmental skull defects and phenotype variability , 2011 .

[55]  L. Richards,et al.  Neuropilin 1-Sema signaling regulates crossing of cingulate pioneering axons during development of the corpus callosum. , 2009, Cerebral cortex.