Jin-Wu Tsai, Ph.D.
Affiliations: | Institute of Brain Science | National Yang-Ming University, Allendale Charter Township, Taipei City, Taiwan |
Area:
Neural developmentWebsite:
http://bml.ym.edu.tw/ibs/brain/TsaiLab/index.htmlGoogle:
"Jin-Wu Tsai"Mean distance: 13.65 (cluster 11) | S | N | B | C | P |
Parents
Sign in to add mentor| Chi-Hung Lin | grad student | 1998-2000 | National Yang-Ming University | |
| Arnold R. Kriegstein | grad student | 2003-2004 | Columbia | |
| Richard B. Vallee | grad student | 2002-2008 | Columbia | |
| (Roles for cytoplasmic dynein and the lissencephaly gene LIS1 in brain development and disease.) | ||||
| Wen-Biao Gan | post-doc | 2008-2009 | NYU | |
BETA: Related publications
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Publications
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| Tsai MH, Ke HC, Lin WC, et al. (2024) Novel lissencephaly-associated NDEL1 variant reveals distinct roles of NDE1 and NDEL1 in nucleokinesis and human cortical malformations. Acta Neuropathologica. 147: 13 |
| Tsai MH, Lin WC, Chen SY, et al. (2023) Lissencephaly-associated BAIAP2 variant causes defects in neuronal migration during brain development. Development (Cambridge, England) |
| Huang CW, Lee KY, Lin PT, et al. (2023) Muscleblind-Like 2 knockout shifts adducin 1 isoform expression and alters dendritic spine dynamics of cortical neurons during brain development. Neuropathology and Applied Neurobiology. e12890 |
| Cheng HY, Nian FS, Ou YW, et al. (2023) Assessment of Dynein-Mediated Nuclear Migration in the Developing Cortex by Live-Tissue Microscopy. Methods in Molecular Biology (Clifton, N.J.). 2623: 61-71 |
| Tsai MH, Cheng HY, Nian FS, et al. (2020) Impairment in dynein-mediated nuclear translocation by BICD2 C-terminal truncation leads to neuronal migration defect and human brain malformation. Acta Neuropathologica Communications. 8: 106 |
| Chang CY, Liang MZ, Wu CC, et al. (2020) WNT3A Promotes Neuronal Regeneration upon Traumatic Brain Injury. International Journal of Molecular Sciences. 21 |
| Chang HY, Cheng HY, Tsao AN, et al. (2019) Multiple Functions of KBP in Neural Development Underlie Brain Anomalies in Goldberg-Shprintzen Syndrome. Frontiers in Molecular Neuroscience. 12: 265 |
| Nian FS, Li LL, Cheng CY, et al. (2019) 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. Molecular Neurobiology |
| Chang CH, Zanini M, Shirvani H, et al. (2019) Atoh1 Controls Primary Cilia Formation to Allow for SHH-Triggered Granule Neuron Progenitor Proliferation. Developmental Cell. 48: 184-199.e5 |
| Chen YA, Lu IL, Tsai JW. (2018) Contactin-1/F3 Regulates Neuronal Migration and Morphogenesis Through Modulating RhoA Activity. Frontiers in Molecular Neuroscience. 11: 422 |