Author

S. J. Kinston

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· 2 Physiology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 3 Organism:mouse· 3 Approach:deep learning· 2 Assay:scRNA-seq· 2 Approach:statistical model· 2 Research Focus:cell signaling & trafficking· 1 Research Focus:cell-cell communication· 1 Assay:CITE-seq· 1

Frequent Co-Authors

B. Gottgens· 2 shared A. E. Adriaenssens· 1 shared A. Kumanogoh· 1 shared A. Pradeep· 1 shared A. Scialdone· 1 shared B. Göttgens· 1 shared B. U. Phillips· 1 shared C. A. Smith· 1 shared

Activity by Year

2021-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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2 shared papersCell Biology

B. Gottgens

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Author profile →

3 papers

Recent·Most cited

A time and single-cell resolved model of hematopoiesis

I. Kucinski, J. Campos, M. Barile, F. Severi, N. Bohin, P. N. Moreira, L. Allen, H. Lawson, M. L. R. Haltalli, S. J. Kinston, D. O'Carroll, K. R. Kranc, B. Göttgens

The paper builds a real-time, quantitative model of hematopoiesis using time-series single-cell RNA-Seq and persistent labeling, revealing lineage-specific self-renewal and differentiation properties.

bioRxiv · Sep 7, 2022 · PreprintCell Biology

Myeloid-biased HSC require Semaphorin 4A from the bone marrow niche for self-renewal under stress and life-long persistence

D. Toghani, S. Zeng, E. Mahammadov, E. I. Crosse, N. Seyedhassantehrani, C. Burns, D. Gravano, S. Radtke, H.-P. Kiem, S. Rodriguez, N. Carlesso, A. Pradeep, N. K. Wilson, S. J. Kinston, B. Gottgens, , L. Silberstein

This study identifies Sema4A as a critical niche factor required for myeloid-biased HSC self-renewal and long-term persistence under stress.

bioRxiv · Jan 12, 2022 · PreprintCell Biology

Relaxin/insulin-like family peptide receptor 4 (Rxfp4) expressing hypothalamic neurons modulate food intake and preference in mice

J. E. Lewis, O. R. Woodward, D. Nuzzaci, C. A. Smith, A. E. Adriaenssens, L. Billing, C. Brighton, B. U. Phillips, J. A. Tadross, S. J. Kinston, E. Ciabatti, B. Gottgens, M. Tripodi, D. Hornigold, D. Baker, , F. Reimann

This study identifies Rxfp4-expressing hypothalamic neurons as regulators of food intake and preference in mice through genetic and pharmacological manipulations.

bioRxiv · Jun 26, 2021Physiology