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Author Details

Jin-Wu Tsai
Brain Research Center, National Yang Ming Chiao Tung University
1995
44
18
Antoine Forget (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
36602679Assessment of Dynein-Mediated Nuclear Migration in the Developing Cortex by Live-Tissue Microscopy.Methods Mol Biol2023
36765387Muscleblind-like 2 knockout shifts adducin 1 isoform expression and alters dendritic spine dynamics of cortical neurons during brain development.Neuropathol Appl Neurobiol2023
35213059Novel lissencephaly-associated DCX variants in the C-terminal DCX domain affect microtubule binding and dynamics.Epilepsia2022
36449334Thymic macrophages consist of two populations with distinct localization and origin.Elife2022
34565360Clinical and functional characterization of a novel STUB1 frameshift mutation in autosomal dominant spinocerebellar ataxia type 48 (SCA48).J Biomed Sci2021
34685646An Emerging Role of PRRT2 in Regulating Growth Cone Morphology.Cells2021
32233025Muscle atrophy-related myotube-derived exosomal microRNA in neuronal dysfunction: Targeting both coding and long noncoding RNAs.Aging Cell2020
31728576Cellular secretion and cytotoxicity of transthyretin mutant proteins underlie late-onset amyloidosis and neurodegeneration.Cell Mol Life Sci2020
32098078WNT3A Promotes Neuronal Regeneration upon Traumatic Brain Injury.Int J Mol Sci2020
32097630Pathogenic Variants in CEP85L Cause Sporadic and Familial Posterior Predominant Lissencephaly.Neuron2020
32665036Impairment in dynein-mediated nuclear translocation by BICD2 C-terminal truncation leads to neuronal migration defect and human brain malformation.Acta Neuropathol Commun2020
32775487Efficient in Utero Gene Transfer to the Mammalian Inner Ears by the Synthetic Adeno-Associated Viral Vector Anc80L65.Mol Ther Methods Clin Dev2020
29342244Gli2 Rescues Delays in Brain Development Induced by Kif3a Dysfunction.Cereb Cortex2019
31736709Multiple Functions of KBP in Neural Development Underlie Brain Anomalies in Goldberg-Shprintzen Syndrome.Front Mol Neurosci2019
29912316Constitutive Inactivation of the PRRT2 Gene Alters Short-Term Synaptic Plasticity and Promotes Network Hyperexcitability in Hippocampal Neurons.Cereb Cortex2019
30980674PRRT2 missense mutations cluster near C-terminus and frequently lead to protein mislocalization.Epilepsia2019
31001136Contributions of Animal Models to the Mechanisms and Therapies of Transthyretin Amyloidosis.Front Physiol2019
30721447Rab18 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.Mol Neurobiol2019
30695697Atoh1 Controls Primary Cilia Formation to Allow for SHH-Triggered Granule Neuron Progenitor Proliferation.Dev Cell2019
29470990Lis1 dysfunction leads to traction force reduction and cytoskeletal disorganization during cell migration.Biochem Biophys Res Commun2018
29950674Identification of genes associated with cortical malformation using a transposon-mediated somatic mutagenesis screen in mice.Nat Commun2018
30463852Gli2 modulates cell cycle re-entry through autophagy-mediated regulation of the length of primary cilia.J Cell Sci2018
30515076Contactin-1/F3 Regulates Neuronal Migration and Morphogenesis Through Modulating RhoA Activity.Front Mol Neurosci2018
30478281A rare human CEP290 variant disrupts the molecular integrity of the primary cilium and impairs Sonic Hedgehog machinery.Sci Rep2018
27073218Cdk12 Regulates Neurogenesis and Late-Arising Neuronal Migration in the Developing Cerebral Cortex.Cereb Cortex2017
28276447Ascl1 promotes tangential migration and confines migratory routes by induction of Ephb2 in the telencephalon.Sci Rep2017
29209088Inhibitory effects of curcumin and cyclocurcumin in 1-methyl-4-phenylpyridinium (MPP<sup>+</sup>) induced neurotoxicity in differentiated PC12 cells.Sci Rep2017
26058471Long-term stability of axonal boutons in the mouse barrel cortex.Dev Neurobiol2016
27172900PRRT2 mutations lead to neuronal dysfunction and neurodevelopmental defects.Oncotarget2016
27292316A novel DCX missense mutation in a family with X-linked lissencephaly and subcortical band heterotopia syndrome inherited from a low-level somatic mosaic mother: Genetic and functional studies.Eur J Paediatr Neurol2016
26758390Quantification of the Metabolic State in Cell-Model of Parkinson's Disease by Fluorescence Lifetime Imaging Microscopy.Sci Rep2016
26033635Experience-dependent plasticity of dendritic spines of layer 2/3 pyramidal neurons in the mouse cortex.Dev Neurobiol2016
25779931ENU mutagenesis identifies mice modeling Warburg Micro Syndrome with sensory axon degeneration caused by a deletion in Rab18.Exp Neurol2015
21478886A new subtype of progenitor cell in the mouse embryonic neocortex.Nat Neurosci2011
21618088Live microscopy of neural stem cell migration in brain slices.Methods Mol Biol2011
21037580Kinesin 3 and cytoplasmic dynein mediate interkinetic nuclear migration in neural stem cells.Nat Neurosci2010
19524440Emerging roles for myosin II and cytoplasmic dynein in migrating neurons and growth cones.Trends Cell Biol2009
19829375Asymmetric centrosome inheritance maintains neural progenitors in the neocortex.Nature2009
17618279Dual subcellular roles for LIS1 and dynein in radial neuronal migration in live brain tissue.Nat Neurosci2007
16751177The cellular roles of the lissencephaly gene LIS1, and what they tell us about brain development.Genes Dev2006
16793773Stepped changes of monovalent ligand-binding force during ligand-induced clustering of integrin alphaIIB beta3.J Biol Chem2006
16144905LIS1 RNA interference blocks neural stem cell division, morphogenesis, and motility at multiple stages.J Cell Biol2005
10462382Targeting of aminopeptidase N to bile canaliculi correlates with secretory activities of the developing canalicular domain.Hepatology1999
7770551Assessment of heart wall motion: modified spatial modulation of magnetization for MR imaging.Proc Natl Sci Counc Repub China B1995
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Collaborators

Chia-Hsiang Chang
Institute of Biomedical Sciences
Co-authored papers 5
Chun-Hung Wang
University of Central Florida
Co-authored papers 4
Won-Jing Wang
Institute of Biochemistry and Molecular Biology, National Yang Ming University
Co-authored papers 3
Jia-Shing Cheng
Institute of Brain Science, National Yang-Ming University
Co-authored papers 3
Arnold R Kriegstein
University of California san francisco
Co-authored papers 3
I-Lin Lu
Institute of Biomedical Sciences
Co-authored papers 3
Ingrid E Scheffer
Co-authored papers 1
Hua Yu
Guangzhou University
Co-authored papers 1
Ghayda M Mirzaa
Seattle Children's Hospital.
Co-authored papers 1
Chih-Hsin Feng
Institute of Brain Science, National Yang-Ming University
Co-authored papers 1
Audrey L Mercier
Institut Curie, CNRS UMR 3306, INSERM U1005, Centre Universitaire
Co-authored papers 1
Antoine Forget (CM4AI)
University of California San Francisco
Co-authored papers 1
Shiue-Yu Hung
National Yang-Ming University
Co-authored papers 1
Nathalie Spassky
Ecole Normale Superieure, Institut de Biologie de l'ENS, France CNRS, France INSERM
Co-authored papers 1
Martial Ruat
CNRS, Institut des Neurosciences Paris-Saclay, Universite Paris-Saclay
Co-authored papers 1
Hamasseh Shirvani
Institut Roche
Co-authored papers 1
William B Dobyns
University of Minnesota
Co-authored papers 1
Michael S Hildebrand
Co-authored papers 1
Olivier Ayrault
Institut Curie, PSL Research University, CNRS UMR, INSERM
Co-authored papers 1
Wei-Yi Chen
College of Biomedical Engineering, Taiyuan University of Technology
Co-authored papers 1
Sophie Leboucher
Institut Curie, Universite PSL, CNRS UMR8
Co-authored papers 1
Cheng-Fu Kao
Institute of Cellular and Organismic Biology
Co-authored papers 1
Sara Maria Cigna
Institut Curie, CNRS UMR 3306, INSERM U1005, Centre Universitaire
Co-authored papers 1
Marco Zanini
Institut Curie, PSL Research University, CNRS UMR, INSERM
Co-authored papers 1
Shu Chien
and Institute of Engineering in Medicine, University of California
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