Author

S. Sampattavanich

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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Cell Biology· 1 Pharmacology & Toxicology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell-cell communication· 2 Approach:experimental assay· 2 Assay:bulk RNA-seq· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Organism:human· 1 Organism:mouse· 1

Frequent Co-Authors

C. Promptmas· 1 shared E. W.- F. Lam· 1 shared K. Phongkitkarun· 1 shared M. Kamkaew· 1 shared M. Saelim· 1 shared P. Buraphat· 1 shared P. Chusorn· 1 shared P. Kanchanapiboon· 1 shared

Activity by Year

2023-2023 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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1 shared paperCell Biology

C. Promptmas

Mutual co-authors in cluster

Author profile →

2 papers

Recent·Most cited

Chemically Tunable FOXM1-D Sensor Revealed FOXM1 Direct Influence on Cell Cycle

K. Phongkitkarun, P. Chusorn, M. Kamkaew, E. W.- F. Lam, C. Promptmas, S. Sampattavanich

The paper develops a tunable FOXM1-D sensor to study FOXM1 dynamics during the cell cycle and shows that overproduction of FOXM1 causes cell cycle arrest.

bioRxiv · Mar 1, 2023Cell Biology

Keratinocyte-derived paracrine factors regulate stress response of melanocytes to UVB

S. Jeayeng, M. Saelim, P. Muanjumpon, P. Buraphat, P. Kanchanapiboon, S. Sampattavanich, U. Panich

This study identifies G-CSF and CCL20 as paracrine factors from keratinocytes that protect melanocytes from UVB-induced stress by reducing apoptosis and ROS and enhancing melanogenesis.

bioRxiv · Jan 13, 2023 · PreprintPharmacology & Toxicology