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Ya-Chu Chang

Researcher at National Tsing Hua University

Publications -  17
Citations -  378

Ya-Chu Chang is an academic researcher from National Tsing Hua University. The author has contributed to research in topics: AAA proteins & Cas9. The author has an hindex of 8, co-authored 15 publications receiving 280 citations. Previous affiliations of Ya-Chu Chang include National Taiwan University & University of Minnesota.

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Deregulated microRNAs in triple-negative breast cancer revealed by deep sequencing

TL;DR: A novel 25-miRNA expression signature was found to effectively distinguish triple-negative breast cancers from surrounding normal tissues in a hierarchical clustering analysis, and implicate a miR-130b-5p-CCNG2 axis that may be involved in the malignant progression of triple- negative breast cancer.
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Pathogenic VCP/TER94 Alleles Are Dominant Actives and Contribute to Neurodegeneration by Altering Cellular ATP Level in a Drosophila IBMPFD Model

TL;DR: It is shown that increasing cellular ATP by independent mechanisms could suppress the phenotypes of TER94 mutants and decreasing cellular ATP would enhance the TER94 mutant phenotypes, making an unexpected link between cellular ATP level and IBMPFD pathogenesis.
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Spatiotemporal manipulation of ciliary glutamylation reveals its roles in intraciliary trafficking and Hedgehog signaling.

TL;DR: A method to rapidly deplete tubulin glutamylation inside the primary cilia, a microtubule-based sensory organelle protruding on the cell surface, by targeting an engineered deglutamylase to the cilia in minutes is developed.
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Sonogenetic Modulation of Cellular Activities Using an Engineered Auditory-Sensing Protein

TL;DR: A sonogenetic approach that can manipulate target cell activities by focused ultrasound stimulation derived from an engineered auditory-sensing protein prestin is reported, which will serve as new strategies for non-invasive therapy in deep tissues.
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MicroRNA-769-3p Down-regulates NDRG1 and Enhances Apoptosis in MCF-7 Cells During Reoxygenation

TL;DR: It is revealed that miR-769-3p can functionally regulate NDRG1 during changes in oxygen concentration, which caused a significant reduction of N DRG1 protein upon reoxygenation.