Author

K. Suda

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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Cancer Biology· 1 Cell Biology· 1 Pathology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:human· 3 Research Focus:host-pathogen & immune response· 2 Assay:proteomics· 2 Research Focus:cell type annotation· 1 Research Focus:development & morphogenesis· 1 Research Focus:differential expression· 1 Assay:imaging· 1

Frequent Co-Authors

B. Dome· 1 shared C. Rivard· 1 shared D. Dora· 1 shared F. R. Hirsch· 1 shared H. Barbee· 1 shared H. Nakaoka· 1 shared H. Takase· 1 shared H. Ueda· 1 shared

Activity by Year

2020-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 17 mutual co-author links

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1 shared paperCancer Biology

B. Dome

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Plasma membrane damage limits replicative lifespan in yeast and induces premature senescence in human fibroblasts

K. Suda, Y. Moriyama, Y. Masukagami, N. B. Razali, Y. Chiu, K. Nishimura, H. Barbee, H. Takase, S. Sugiyama, Y. Sato, T. Higashiyama, Y. Johmura, M. Nakanishi, K. Kono

This study shows plasma membrane damage limits replicative lifespan in yeast and induces premature senescence in human fibroblasts through the ESCRT pathway and Ca2+-p53 axis.

bioRxiv · Mar 26, 2021Cell Biology

Three-dimensional understanding of the morphological complexity of the human uterine endometrium

M. Yamaguchi, K. Yoshihara, K. Suda, H. Nakaoka, N. Yachida, H. Ueda, K. Sugino, Y. Mori, K. Yamawaki, R. Tamura, T. Ishiguro, T. Motoyama, Y. Watanabe, S. Okuda, K. Tainaka, T. Enomoto

This study uses 3D imaging to reveal the complex morphology of human endometrial glands and their pathological features in adenomyosis.

bioRxiv · May 29, 2020Pathology

Small Cell Lung Cancer Neuroendocrine Subtypes are Associated with Different Immune Microenvironment and Checkpoint Molecule Distribution

D. Dora, C. Rivard, H. Yu, P. Bunn, K. Suda, S. Ren, S. L. Pickard, V. Laszlo, T. Harko, Z. Megyesfalvi, J. Moldvay, F. R. Hirsch, B. Dome, Z. Lohinai

This study shows that NE-low SCLC tumors have more immune cell infiltration and higher expression of IDO and PVR compared to NE-high tumors, suggesting these as potential immunotherapy targets.

bioRxiv · Feb 2, 2020Cancer Biology