Hung-lun Chiang
TPQ, Taiwan
Last Updated: 09/26/2026
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Found 8 publications
Massively Parallel Splicing Assay to Examine Splicing Errors Caused by Disease-Related Intronic Variants.
Journal: Journal of visualized experiments : JoVE
Published: September 29, 2025
Nuclear paxillin functions as a molecular switch for alternative splicing in neurons during a critical period of brain development.
Journal: The EMBO journal
Published: March 10, 2025
SpliceAPP: an interactive web server to predict splicing errors arising from human mutations.
Journal: BMC genomics
Published: March 01, 2024
Mechanism and modeling of human disease-associated near-exon intronic variants that perturb RNA splicing.
Journal: Nature structural & molecular biology
Published: September 06, 2021
De novo mutation and skewed X-inactivation in girl with BCAP31-related syndrome.
Journal: Human mutation
Published: May 05, 2020
Identification of functional single nucleotide polymorphisms in the branchpoint site.
Journal: Human genomics
Published: August 21, 2017
Genetic epidemiological study doesn't support GLA IVS4+919G>A variant is a significant mutation in Fabry disease.
Journal: Molecular genetics and metabolism
Published: February 02, 2017
Genome-wide association study of treatment refractory schizophrenia in Han Chinese.
Journal: PloS one
Published: October 10, 2011
Showing 1-8 of 8
Last Updated: 09/26/2026