All Stories

  1. Proteomic analysis of the developing mammalian brain links PCDH19 to the Wnt/β-catenin signalling pathway
  2. The intracellular domain of the epilepsy-related protein PCDH19 regulates spine density in cortical neurons
  3. Transcriptional control of embryonic and adult neural progenitor activity
  4. Cellular and Behavioral Characterization of Pcdh19 Mutant Mice: subtle Molecular Changes, Increased Exploratory Behavior and an Impact of Social Environment
  5. The placenta protects the fetal circulation from anxiety-driven elevations in maternal serum levels of brain-derived neurotrophic factor
  6. Neuregulin-4 Is Required for Maintaining Soma Size of Pyramidal Neurons in the Motor Cortex
  7. Molecular Mechanisms of Cadherin Function During Cortical Migration
  8. Cellular and behavioral characterization of Pcdh19 mutant mice: subtle molecular changes, increased exploratory behavior and an impact of social environment
  9. Dbx1-Derived Pyramidal Neurons Are Generated Locally in the Developing Murine Neocortex
  10. The neuronal migration hypothesis of dyslexia: A critical evaluation 30 years on
  11. The neuronal migration hypothesis of dyslexia: a critical evaluation thirty years on
  12. Knockout Mice for Dyslexia Susceptibility Gene Homologs KIAA0319 and KIAA0319L have Unaffected Neuronal Migration but Display Abnormal Auditory Processing
  13. A tubulin alpha 8 mouse knockout model indicates a likely role in spermatogenesis but not in brain development
  14. Normal radial migration and lamination are maintained in dyslexia-susceptibility candidate gene homolog Kiaa0319 knockout mice
  15. Cadherin 2/4 signaling via PTP1B and catenins is crucial for nucleokinesis during radial neuronal migration in the neocortex
  16. In Utero Electroporation Methods in the Study of Cerebral Cortical Development
  17. Lineage Tracing Using Cux2-Cre and Cux2-CreERT2 Mice
  18. Cajal-Retzius Cells Instruct Neuronal Migration by Coincidence Signaling between Secreted and Contact-Dependent Guidance Cues
  19. Fate-Restricted Neural Progenitors in the Mammalian Cerebral Cortex
  20. Reelin Regulates Cadherin Function via Dab1/Rap1 to Control Neuronal Migration and Lamination in the Neocortex
  21. VISIONS: the art of science
  22. Duplication of the Williams-Beuren critical region: case report and further delineation of the phenotypic spectrum
  23. Duplication of the Williams-Beuren critical region: case report and further delineation of the phenotypic spectrum
  24. Relationships of Gag-pol Diversity between Ty3/Gypsy and Retroviridae LTR retroelements and the three kings hypothesis
  25. Gypsy endogenous retrovirus maintains potential infectivity in several species of Drosophilids
  26. Duplication of the Williams-Beuren critical region: case report and further delineation of the phenotypic spectrum
  27. Deleción subtelomérica 9qter: definición del síndrome y origen parental en 2 pacientes
  28. A two base pair deletion in the PQBP1 gene is associated with microphthalmia, microcephaly and mental retardation
  29. The novel centrosomal associated protein CEP55 is present in the spindle midzone and the midbody
  30. Localization of MRX82: A new nonsyndromic X-linked mental retardation locus to Xq24-q25 in a Basque family
  31. Folate-sensitive fragile site FRA10A is due to an expansion of a CGG repeat in a novel gene, FRA10AC1, encoding a nuclear protein
  32. Intronic L1 insertion and F268S, novel mutations in RPS6KA3 (RSK2) causing Coffin-Lowry syndrome
  33. Screening for microdeletions of the X-chromosome in non-specific mental retardation
  34. A New Gene Family (FAM9) of Low-Copy Repeats in Xp22.3 Expressed Exclusively in Testis: Implications for Recombinations in This Region
  35. Localization of non-specific X-linked mental retardation gene (MRX73) to Xp22.2