Author

A. S. Ng

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· 1 Cancer Biology· 1 Immunology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1 Organism:E. coli· 1 Organism:mouse· 1

Frequent Co-Authors

A. Apostoli· 1 shared A. Rising· 1 shared A. WEE· 1 shared B. MICKELSON· 1 shared B. Raught· 1 shared B. Vojtesek· 1 shared C. BALL· 1 shared C. CAI· 1 shared

Activity by Year

2021-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 13 mutual co-author links

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1 shared paperCancer Biology

A. Apostoli

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

PRMT1 is a critical dependency in clear cell renal cell carcinoma through its role in post-transcriptional regulation of DNA damage response genes

J. Walton, A. S. Ng, K. Arevalo, A. Apostoli, J. Meens, C. Karamboulas, J. St-Germain, P. Prinos, J. Dmytryshyn, E. Chen, C. H. Arrowsmith, B. Raught, L. Ailles

bioRxiv · Mar 30, 2023Cancer Biology

Angiopoietin-like 4 shapes the intrahepatic T-cell landscape via eIF2α signalingduring steatohepatitis in diet-induced NAFLD.

Z. S. LOW, D. CHUA, H. S. CHENG, R. TEE, W. R. TAN, C. BALL, N. B. E. SAHIB, S. S. NG, J. QU, Y. LIU, H. HONG, C. CAI, N. C. L. RAO, A. WEE, M. D. MUTHIAH, , W. WAHLI

The paper identifies Angptl4's role in shaping intrahepatic T-cell activation via eIF2α signaling during fibrosis in diet-induced NAFLD.

bioRxiv · Jan 10, 2023 · PreprintImmunology

A spindle and thread-mechanism unblocks translation of N-terminally disordered proteins

M. Kaldmae, T. Vosselman, X. Zhong, D. Lama, G. Chen, M. Saluri, N. Kronqvist, J. W. Siau, A. S. Ng, F. J. Ghadessy, P. Sabatier, B. Vojtesek, M. Sarr, C. Sahin, N. Osterlund, , M. Landreh

This study shows that fusing disordered proteins to an engineered spider silk domain improves their translation efficiency and activity in cells.

bioRxiv · Feb 22, 2021 · PreprintBiochemistry