All Stories

  1. Identity, lineage and fates of a temporally distinct progenitor population in the embryonic olfactory epithelium
  2. Ranbp1 modulates morphogenesis of the craniofacial midline in mouse models of 22q11.2 deletion syndrome
  3. Lineage, Identity, and Fate of Distinct Progenitor Populations in the Embryonic Olfactory Epithelium
  4. Selective disruption of trigeminal sensory neurogenesis and differentiation in a mouse model of 22q11.2 deletion syndrome
  5. Aberrant early growth of individual trigeminal sensory and motor axons in a series of mouse genetic models of 22q11.2 deletion syndrome
  6. Variations in maternal vitamin A intake modifies phenotypes in a mouse model of 22q11.2 deletion syndrome
  7. Suckling, Feeding, and Swallowing: Behaviors, Circuits, and Targets for Neurodevelopmental Pathology
  8. Transcriptional dysregulation in developing trigeminal sensory neurons in the LgDel mouse model of DiGeorge 22q11.2 deletion syndrome
  9. Persistent Feeding and Swallowing Deficits in a Mouse Model of 22q11.2 Deletion Syndrome
  10. In the line-up: deleted genes associated with DiGeorge/22q11.2 deletion syndrome: are they all suspects?
  11. Mitochondrial Dysfunction Leads to Cortical Under-Connectivity and Cognitive Impairment
  12. Foxd4 is essential for establishing neural cell fate and for neuronal differentiation
  13. Oxidative stress-driven parvalbumin interneuron impairment as a common mechanism in models of schizophrenia
  14. Balancing Act: Maintaining Amino Acid Levels in the Autistic Brain
  15. A cellular and molecular mosaic establishes growth and differentiation states for cranial sensory neurons
  16. Functional Divergence of the Nuclear Receptor NR2C1 as a Modulator of Pluripotentiality During Hominid Evolution
  17. Neural transcription factors bias cleavage stage blastomeres to give rise to neural ectoderm
  18. MicroRNAs Are Involved in the Development of Morphine-Induced Analgesic Tolerance and Regulate Functionally Relevant Changes in Serpini1
  19. Hard to swallow: Developmental biological insights into pediatric dysphagia
  20. Testicular receptor 2, Nr2c1, is associated with stem cells in the developing olfactory epithelium and other cranial sensory and skeletal structures
  21. Progressive Differentiation and Instructive Capacities of Amniotic Fluid and Cerebrospinal Fluid Proteomes following Neural Tube Closure
  22. Modeling a model: Mouse genetics, 22q11.2 Deletion Syndrome, and disorders of cortical circuit development
  23. 22q11 Deletion Syndrome
  24. Microarray identification of novel genes downstream of Six1, a critical factor in cranial placode, somite, and kidney development
  25. Ranbp1, Deleted in DiGeorge/22q11.2 Deletion Syndrome, is a Microcephaly Gene That Selectively Disrupts Layer 2/3 Cortical Projection Neuron Generation
  26. Hectd1 is required for development of the junctional zone of the placenta
  27. Dysphagia and disrupted cranial nerve development in a mouse model of DiGeorge (22q11) deletion syndrome
  28. Cognitive Ability is Associated with Altered Medial Frontal Cortical Circuits in the LgDel Mouse Model of 22q11.2DS
  29. 22q11 Gene dosage establishes an adaptive range for sonic hedgehog and retinoic acid signaling during early development
  30. Cxcr4 regulation of interneuron migration is disrupted in 22q11.2 deletion syndrome
  31. Exome Sequencing and Functional Validation in Zebrafish Identify GTDC2 Mutations as a Cause of Walker-Warburg Syndrome
  32. Three phases of DiGeorge/22q11 deletion syndrome pathogenesis during brain development: Patterning, proliferation, and mitochondrial functions of 22q11 genes
  33. The Cerebrospinal Fluid Provides a Proliferative Niche for Neural Progenitor Cells
  34. Comt1 genotype and expression predicts anxiety and nociceptive sensitivity in inbred strains of mice
  35. Proliferative and transcriptional identity of distinct classes of neural precursors in the mammalian olfactory epithelium
  36. Specific mesenchymal/epithelial induction of olfactory receptor, vomeronasal, and gonadotropin-releasing hormone (GnRH) neurons
  37. Developmental and degenerative features in a complicated spastic paraplegia
  38. Diminished dosage of 22q11 genes disrupts neurogenesis and cortical development in a mouse model of 22q11 deletion/DiGeorge syndrome
  39. Mitochondrial localization and function of a subset of 22q11 deletion syndrome candidate genes
  40. Gene dosage in the developing and adult brain in a mouse model of 22q11 deletion syndrome
  41. No evidence for parental imprinting of mouse 22q11 gene orthologs
  42. Limited influence of olanzapine on adult forebrain neural precursors in vitro
  43. A comprehensive analysis of 22q11 gene expression in the developing and adult brain
  44. Mesenchymal/epithelial regulation of retinoic acid signaling in the olfactory placode
  45. Retinoic acid signaling at sites of plasticity in the mature central nervous system
  46. 22q11 DS: genomic mechanisms and gene function in DiGeorge/velocardiofacial syndrome
  47. RanBP1, a velocardiofacial/DiGeorge syndrome candidate gene, is expressed at sites of mesenchymal/epithelial induction
  48. High-resolution mapping of the Gli3 mutation Extra-toesJ reveals a 51.5-kb deletion
  49. Neural Development, Cell-Cell Signaling, and the "Two-Hit" Hypothesis of Schizophrenia
  50. Avian transitin expression mirrors glial cell fate restrictions during neural crest development
  51. NUMB Localizes in the Basal Cortex of Mitotic Avian Neuroepithelial Cells and Modulates Neuronal Differentiation by Binding to NOTCH-1
  52. Glial domains and axonal reordering in the chiasmatic region of the developing ferret