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专题专栏

  • Genetic architecture of amyotrophic lateral sclerosis: a comprehensive review
  • ATPase-deficient CHD7 disease variant disrupts neural development via chromatin dysregulation
  • Spatiotemporal dynamics of neuron differentiation and migration in the developing human spinal cord
  • Deep sequencing reveals SLC35A2 somatic variants in MOGHE: molecular and clinical insights
  • Recapitulation of key phenotypes and pathological features of primary familial brain calcification (PFBC) in a mouse Slc20a2S602W/S602W model
  • Postnatal critical-period brain plasticity and neurodevelopmental disorders: revisited circuit mechanisms
  • Biallelic MED16 variants disrupt neural development and lead to an intellectual disability syndrome
  • Diverse functions of sex determination gene doublesex on sexually dimorphic neuronal development and behaviors
  • The phospholipid scramblase PLSCR5 is regulated by POU4F3 and required for hair cell stereocilia homeostasis and auditory functions
  • Coordinated regulation of cortical astrocyte maturation by OLIG1 and OLIG2 through BMP7 signaling modulation
  • Varying Bifidobacterium species in the maternal-infant gut microbiota correlate with distinct early neurodevelopmental outcomes
  • Massively parallel characterization of non-coding de novo mutations in autism spectrum disorder
  • Rapamycin alleviates neurodegeneration in a Drosophila model of spinocerebellar ataxia type 51