Author

A. S. Hammad

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· 3

Signature Assays, Organisms & Methods

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Research Focus:cell signaling & trafficking· 3 Approach:experimental assay· 3 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell type annotation· 1 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:development & morphogenesis· 1 Organism:human· 1 Assay:imaging· 1

Frequent Co-Authors

F. Yu· 3 shared K. Machaca· 3 shared A. A. Elmi· 1 shared A. Elmi· 1 shared E. Alcantara-Adap· 1 shared F. D. Horgen· 1 shared M. Fisher· 1 shared M. Terasaki· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 26 mutual co-author links

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3 shared papersCell Biology

F. Yu

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

ER-Mitochondria Contact Sites expand during mitosis

F. Yu, R. Courjaret, A. Elmi, A. S. Hammad, M. Fisher, M. Terasaki, K. Machaca

The paper shows that ER-mitochondria contact sites expand during mitosis, enhancing Ca2+ coupling and mitochondrial activation to meet increased energy demands.

bioRxiv · Jun 22, 2023Cell Biology

STIM1 signals through NFAT independently of Orai1 and SOCE to regulate breast cancer cell migration

A. S. Hammad, F. Yu, F. D. Horgen, K. Machaca

The paper shows that STIM1 knockout in breast cancer cells increases migration and invasion due to NFATC2 downregulation, independent of SOCE and Ca2+ entry.

bioRxiv · Oct 23, 2022 · PreprintCell Biology

Phosphorylation of STIM1 at ERK/CDK sites is dispensable for cell migration and ER partitioning in mitosis

A. S. Hammad, F. Yu, W. Botheju, A. A. Elmi, E. Alcantara-Adap, K. Machaca

This study shows that STIM1 phosphorylation at ERK/CDK sites is not required for SOCE, cell migration, or ER partitioning during mitosis.

bioRxiv · Jul 6, 2021Cell Biology