Fang-shin Nian
TPQ, Taiwan
Last Updated: 09/26/2026
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Found 16 publications
Recessive TMEM167A variants cause neonatal diabetes, microcephaly, and epilepsy syndrome.
Journal: The Journal of clinical investigation
Published: May 21, 2025
Epilepsy-associated FOXJ3 variants link a transcriptional program of the PTEN-mTOR pathway to neuronal specification and cortical lamination.
Journal: Nature communications
Published: January 24, 2025
Novel lissencephaly-associated NDEL1 variant reveals distinct roles of NDE1 and NDEL1 in nucleokinesis and human cortical malformations.
Journal: Acta neuropathologica
Published: October 23, 2023
Oscillatory DeltaC Expression in Neural Progenitors Primes the Prototype of Forebrain Development.
Journal: Molecular neurobiology
Published: June 25, 2023
A lissencephaly-associated BAIAP2 variant causes defects in neuronal migration during brain development.
Journal: Development (Cambridge, England)
Published: April 26, 2023
Assessment of Dynein-Mediated Nuclear Migration in the Developing Cortex by Live-Tissue Microscopy.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: January 05, 2023
Evolving Roles of Notch Signaling in Cortical Development.
Journal: Frontiers in neuroscience
Published: December 28, 2021
Muscleblind-like 2 knockout shifts adducin 1 isoform expression and alters dendritic spine dynamics of cortical neurons during brain development.
Journal: Neuropathology and applied neurobiology
Published: September 15, 2021
Impairment in dynein-mediated nuclear translocation by BICD2 C-terminal truncation leads to neuronal migration defect and human brain malformation.
Journal: Acta neuropathologica communications
Published: April 29, 2020
Muscle atrophy-related myotube-derived exosomal microRNA in neuronal dysfunction: Targeting both coding and long noncoding RNAs.
Journal: Aging cell
Published: September 04, 2019
Last Updated: 09/26/2026