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1. DSCAM gene triplication causes excessive GABAergic synapses in the neocortex in Down syndrome mouse models

2. Symmetric neural progenitor divisions require chromatin-mediated homologous recombination DNA repair by Ino80

3. Robust elimination of genome-damaged cells safeguards against brain somatic aneuploidy following Knl1 deletion

4. A Mouse Model of X-linked Intellectual Disability Associated with Impaired Removal of Histone Methylation

6. Migrating Pyramidal Neurons Require DSCAM to Bypass the Border of the Developing Cortical Plate

7. Robust elimination of genome-damaged cells safeguards against brain somatic aneuploidy following Knl1 deletion

8. Chromatin remodeler Arid1a regulates subplate neuron identity and wiring of cortical connectivity

9. Chromatin remodelerArid1aregulates subplate neuron identity and wiring of cortical connectivity

10. Symmetric neural progenitor divisions require chromatin-mediated homologous recombination DNA repair by Ino80

11. Identification and characterization of occult human-specific LINE-1 insertions using long-read sequencing technology

12. Brain Transcriptome Databases: A User's Guide

13. A Mouse Model of X-linked Intellectual Disability Associated with Impaired Removal of Histone Methylation

14. EphB receptor forward signaling regulates area-specific reciprocal thalamic and cortical axon pathfinding

15. TSHZ3 deletion causes an autism syndrome and defects in cortical projection neurons

16. Cis-regulatory control of corticospinal system development and evolution

17. Species-Dependent Posttranscriptional Regulation of NOS1 by FMRP in the Developing Cerebral Cortex

18. TBR1 directly represses Fezf2 to control the laminar origin and development of the corticospinal tract

19. Axonal ribosomes and mRNAs associate with fragile X granules in adult rodent and human brains

20. Dysregulated nitric oxide signaling as a candidate mechanism of fragile X syndrome and other neuropsychiatric disorders

21. Nitric oxide signaling in the development and evolution of language and cognitive circuits

22. Transcriptional dysregulation of neocortical circuit assembly in ASD

23. Transcriptional co-regulation of neuronal migration and laminar identity in the neocortex

24. Recessive LAMC3 mutations cause malformations of occipital cortical development

25. Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations

26. Selective Depletion of Molecularly Defined Cortical Interneurons in Human Holoprosencephaly with Severe Striatal Hypoplasia

27. SOX5 postmitotically regulates migration, postmigratory differentiation, and projections of subplate and deep-layer neocortical neurons

28. Satb2 is a postmitotic determinant for upper-layer neuron specification in the neocortex

29. Sequence variants in SLITRK1 are associated with Tourette's syndrome

30. Zfp312 is required for subcortical axonal projections and dendritic morphology of deep-layer pyramidal neurons of the cerebral cortex

31. Neurotrophin & synaptogenesis

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