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4. Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development

5. Thymic macrophages consist of two populations with distinct localization and origin.

8. Novel lissencephaly-associated NDEL1 variant reveals distinct roles of NDE1 and NDEL1 in nucleokinesis and human cortical malformations

9. Equilibrative nucleoside transporter 3 supports microglial functions and protects against the progression of Huntington’s disease in the mouse model

13. Regulation of Primary Cilia Disassembly Through HUWE1-Mediated TTBK2 Degradation Plays a Crucial Role in Cerebellar Development and Medulloblastoma Growth

18. Kinesin 3 and cytoplasmic dynein mediate interkinetic nuclear migration in neural stem cells

19. Lissencephaly-associated BAIAP2 variant causes defects in neuronal migration during brain development

23. Cover Image, Volume 49, Issue 2

24. Muscleblind‐like 2 knockout shifts adducin 1 isoform expression and alters dendritic spine dynamics of cortical neurons during brain development

27. Corrigendum to “Equilibrative nucleoside transporter 3 supports microglial functions and protects against the progression of Huntington’s disease in the mouse model” [Brain Behav. Immun. 120 (2024) 413–429]

37. Pathogenic Variants in CEP85L Cause Sporadic and Familial Posterior Predominant Lissencephaly

38. Asymmetric centrosome inheritance maintains neural progenitors in the neocortex

39. Additional file 1 of Clinical and functional characterization of a novel STUB1 frameshift mutation in autosomal dominant spinocerebellar ataxia type 48 (SCA48)

42. Additional file 1 of Impairment in dynein-mediated nuclear translocation by BICD2 C-terminal truncation leads to neuronal migration defect and human brain malformation

44. Muscle atrophy‐related myotube‐derived exosomal microRNA in neuronal dysfunction: Targeting both coding and long noncoding RNAs