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Hung-Lun Chiang

Showing results (1-10 of 9) with videos related to

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Human Genomics|November 11, 2017
Identification of functional single nucleotide polymorphisms in the branchpoint siteHung-Lun Chiang, Jer-Yuarn Wu, Yuan-Tsong Chen
Pharmacogenomics|March 18, 2009
Novel DNA sequence variations of cytochrome P450 genes in the Han Chinese populationHui-Hung Wang, Yie-Wen Liao, Hung-Lun Chiang, et al.
Journal of Visualized Experiments : Jove|September 29, 2025
Massively Parallel Splicing Assay to Examine Splicing Errors Caused by Disease-Related Intronic VariantsHung-Lun Chiang, Ang-Chu Huang, Shao-Wei Pan, et al.
Nature Structural & Molecular Biology|October 27, 2022
Mechanism and modeling of human disease-associated near-exon intronic variants that perturb RNA splicingHung-Lun Chiang, Yi-Ting Chen, Jia-Ying Su, et al.
BMC Genomics|June 14, 2024
SpliceAPP: an interactive web server to predict splicing errors arising from human mutationsAng-Chu Huang, Jia-Ying Su, Yu-Jen Hung, et al.
Human Mutation|July 12, 2020
De novo mutation and skewed X-inactivation in girl with BCAP31-related syndromeHsiao-Jung Kao, Hung-Lun Chiang, Hsiao-Huei Chen, et al.
Molecular Genetics and Metabolism|April 6, 2017
Genetic epidemiological study doesn't support GLA IVS4+919G>A variant is a significant mutation in Fabry diseaseHung-Lun Chiang, Nana Hsiang-Hua Wang, I-Wen Song, et al.
The EMBO Journal|September 9, 2025
Nuclear paxillin functions as a molecular switch for alternative splicing in neurons during a critical period of brain developmentChien-Hsin Chu, Guan-Zhu Pan, Ching-Yen Tsai, et al.
Plos One|April 6, 2012
Genome-wide association study of treatment refractory schizophrenia in Han ChineseYing-Jay Liou, Hui-Hung Wang, Ming-Ta Michael Lee, et al.
Pageof 1

Showing results (1-10 of 9) with videos related to

Sort By:
Pageof 1
Human Genomics|November 11, 2017
Identification of functional single nucleotide polymorphisms in the branchpoint siteHung-Lun Chiang, Jer-Yuarn Wu, Yuan-Tsong Chen
Pharmacogenomics|March 18, 2009
Novel DNA sequence variations of cytochrome P450 genes in the Han Chinese populationHui-Hung Wang, Yie-Wen Liao, Hung-Lun Chiang, et al.
Journal of Visualized Experiments : Jove|September 29, 2025
Massively Parallel Splicing Assay to Examine Splicing Errors Caused by Disease-Related Intronic VariantsHung-Lun Chiang, Ang-Chu Huang, Shao-Wei Pan, et al.
Nature Structural & Molecular Biology|October 27, 2022
Mechanism and modeling of human disease-associated near-exon intronic variants that perturb RNA splicingHung-Lun Chiang, Yi-Ting Chen, Jia-Ying Su, et al.
BMC Genomics|June 14, 2024
SpliceAPP: an interactive web server to predict splicing errors arising from human mutationsAng-Chu Huang, Jia-Ying Su, Yu-Jen Hung, et al.
Human Mutation|July 12, 2020
De novo mutation and skewed X-inactivation in girl with BCAP31-related syndromeHsiao-Jung Kao, Hung-Lun Chiang, Hsiao-Huei Chen, et al.
Molecular Genetics and Metabolism|April 6, 2017
Genetic epidemiological study doesn't support GLA IVS4+919G>A variant is a significant mutation in Fabry diseaseHung-Lun Chiang, Nana Hsiang-Hua Wang, I-Wen Song, et al.
The EMBO Journal|September 9, 2025
Nuclear paxillin functions as a molecular switch for alternative splicing in neurons during a critical period of brain developmentChien-Hsin Chu, Guan-Zhu Pan, Ching-Yen Tsai, et al.
Plos One|April 6, 2012
Genome-wide association study of treatment refractory schizophrenia in Han ChineseYing-Jay Liou, Hui-Hung Wang, Ming-Ta Michael Lee, et al.
Pageof 1