213 results on '"Tsai, Jin-Wu"'
Search Results
2. Oscillatory DeltaC Expression in Neural Progenitors Primes the Prototype of Forebrain Development
Catalog
Books, media, physical & digital resources
3. Regulation of primary cilia disassembly through HUWE1-mediated TTBK2 degradation plays a crucial role in cerebellar development and medulloblastoma growth
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.
6. The nucleoporin Nup153 is the anchor for Kif1a during basal nuclear migration in brain progenitor cells
7. Pathogenic SHQ1 variants result in disruptions to neuronal development and the dopaminergic pathway
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
10. Assessment of Dynein-Mediated Nuclear Migration in the Developing Cortex by Live-Tissue Microscopy
11. Efficient In Utero Gene Transfer to the Mammalian Inner Ears by the Synthetic Adeno-Associated Viral Vector Anc80L65
12. Cellular secretion and cytotoxicity of transthyretin mutant proteins underlie late-onset amyloidosis and neurodegeneration
13. Regulation of Primary Cilia Disassembly Through HUWE1-Mediated TTBK2 Degradation Plays a Crucial Role in Cerebellar Development and Medulloblastoma Growth
14. Clinical and functional characterization of a novel STUB1 frameshift mutation in autosomal dominant spinocerebellar ataxia type 48 (SCA48)
15. Atoh1 Controls Primary Cilia Formation to Allow for SHH-Triggered Granule Neuron Progenitor Proliferation
16. Rab18 Collaborates with Rab7 to Modulate Lysosomal and Autophagy Activities in the Nervous System: an Overlapping Mechanism for Warburg Micro Syndrome and Charcot-Marie-Tooth Neuropathy Type 2B
17. LIS1 RNA Interference Blocks Neural Stem Cell Division, Morphogenesis, and Motility at Multiple Stages
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
20. Kinesin family member Kif23 regulates cytokinetic division and maintains neural stem/progenitor cell pool in the developing neocortex
21. Impairment in dynein-mediated nuclear translocation by BICD2 C-terminal truncation leads to neuronal migration defect and human brain malformation
22. ENU mutagenesis identifies mice modeling Warburg Micro Syndrome with sensory axon degeneration caused by a deletion in Rab18
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
25. A rare human CEP290 variant disrupts the molecular integrity of the primary cilium and impairs Sonic Hedgehog machinery
26. Thymic macrophages consist of two populations with distinct localization and origin
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]
28. Author response: Thymic macrophages consist of two populations with distinct localization and origin
29. Cdk12 Regulates Neurogenesis and Late-Arising Neuronal Migration in the Developing Cerebral Cortex
30. Novel lissencephaly‐associated DCX variants in the C‐terminal DCX domain affect microtubule binding and dynamics
31. Experience-dependent plasticity of dendritic spines of layer 2/3 pyramidal neurons in the mouse cortex
32. Long-term stability of axonal boutons in the mouse barrel cortex
33. Quantification of the Metabolic State in Cell-Model of Parkinson’s Disease by Fluorescence Lifetime Imaging Microscopy
34. Emerging roles for myosin II and cytoplasmic dynein in migrating neurons and growth cones
35. Thymic macrophages consist of two populations with distinct localization and origin
36. An Emerging Role of PRRT2 in Regulating Growth Cone Morphology
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)
40. Live Microscopy of Neural Stem Cell Migration in Brain Slices
41. Stepped Changes of Monovalent Ligand-binding Force during Ligand-induced Clustering of Integrin αIIBβ3
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
43. Lis1 dysfunction leads to traction force reduction and cytoskeletal disorganization during cell migration
44. Muscle atrophy‐related myotube‐derived exosomal microRNA in neuronal dysfunction: Targeting both coding and long noncoding RNAs
45. WNT3A Promotes Neuronal Regeneration upon Traumatic Brain Injury
46. Cellular secretion and cytotoxicity of transthyretin mutant proteins underlie late-onset amyloidosis and neurodegeneration
47. Multiple Functions of KBP in Neural Development Underlie Brain Anomalies in Goldberg-Shprintzen Syndrome
48. P3-236: PERIPHERAL TRIGGERING RECEPTOR EXPRESSED ON MYELOID CELLS 2 EXPRESSION IS ASSOCIATED WITH THE COGNITIVE DECLINE IN EARLY DEMENTIA DUE TO ALZHEIMER'S DISEASE
49. PRRT 2missense mutations cluster near C‐terminus and frequently lead to protein mislocalization
50. Contributions of Animal Models to the Mechanisms and Therapies of Transthyretin Amyloidosis
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.