All Stories

  1. Patient-derived iPSCs show premature neural differentiation and neuron type-specific phenotypes relevant to neurodevelopment
  2. Reverse Pathway Genetic Approach Identifies Epistasis in Autism Spectrum Disorders
  3. If genetic variation could talk: What genomic data may teach us about the importance of gene expression regulation in the genetics of autism
  4. Human iPS Cell-Derived Neurons Uncover the Impact of Increased Ras Signaling in Costello Syndrome
  5. Novel Molecular Pathways Elicited by Mutant FGFR2 May Account for Brain Abnormalities in Apert Syndrome
  6. Wnt/β-catenin signaling and Msx1 promote outgrowth of the maxillary prominences
  7. FGFR2 Mutation Confers a Less Drastic Gain of Function in Mesenchymal Stem Cells Than in Fibroblasts
  8. Deletion of the Basement Membrane Heparan Sulfate Proteoglycan Type XVIII Collagen Causes Hypertriglyceridemia in Mice and Humans
  9. Genetics of Craniosynostosis: Genes, Syndromes, Mutations and Genotype-Phenotype Correlations
  10. Functional Vascular Endothelial Growth Factor -634G>C SNP Is Associated With Proliferative Diabetic Retinopathy: A case-control study in a Brazilian population of European ancestry
  11. Effect of polymorphisms of the MTHFR and APOE genes on susceptibility to diabetes and severity of diabetic retinopathy in Brazilian patients
  12. Estudo da contribuição molecular e celular do periósteo na craniossinostose da síndrome de Apert