Author

S.-J. Lin

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Biochemistry· 2 Bioengineering· 1 Cell Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 4 Research Focus:cell type annotation· 2 Research Focus:development & morphogenesis· 2 Research Focus:host-pathogen & immune response· 2 Assay:proteomics· 2 Research Focus:cell signaling & trafficking· 1 Organism:human· 1 Assay:imaging· 1

Frequent Co-Authors

B. Groth· 1 shared C. James Theoga Raj· 1 shared C. Petree· 1 shared G. K. Varshney· 1 shared J.-B. Hong· 1 shared K. Huang· 1 shared L. O. Sti Dahl· 1 shared L.-A. Chu· 1 shared

Activity by Year

2019-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 13 mutual co-author links

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1 shared paperBiochemistry

B. Groth

Mutual co-authors in cluster

Author profile →

4 papers

Recent·Most cited

Naa80 is required for actin N-terminal acetylation and normal hearing in zebrafish

R. Ree, S.-J. Lin, L. O. Sti Dahl, K. Huang, C. Petree, G. K. Varshney, T. Arnesen

This study shows that zebrafish Naa80 acetylates actins and is essential for normal hearing, but not for muscle development or viability.

bioRxiv · Mar 17, 2024Biochemistry

Expansion microscopy for super-resolution imaging of collagen-abundant tissues

Y.-H. Chuang, Y.-F. Wu, Y.-H. Lin, Y.-X. Zhou, S.-C. Hsu, S.-J. Lin, L.-A. Chu

This paper introduces ColExM, a method for expanding collagen-abundant tissues to enable super-resolution imaging of nanoscale structures.

bioRxiv · Feb 28, 2024 · PreprintBioengineering

Prostaglandin E2 prevents radiotherapy-induced alopecia by attenuating transit amplifying cell apoptosis through promoting G1 arrest

S.-f. Lai, W.-Y. Huang, W.-H. Wang, J.-B. Hong, S.-H. Kuo, S.-J. Lin

This study shows that PGE2 pretreatment prevents radiotherapy-induced alopecia by protecting transit amplifying cells through G1 arrest, promoting hair follicle regeneration.

bioRxiv · Nov 24, 2022Cell Biology

N-terminal protein acetylation by NatB modulates the levels of Nmnats, the NAD+ biosynthetic enzymes in Saccharomyces cerevisiae

T. Croft, P. Venkatakrishnan, C. James Theoga Raj, B. Groth, T. Cater, S.-J. Lin

This study shows that N-terminal acetylation by NatB regulates Nmnat protein levels in yeast, affecting NAD+ homeostasis through co-translational degradation.

bioRxiv · Oct 29, 2019Biochemistry