Author

D. Colby

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 Cell Biology· 1

Signature Assays, Organisms & Methods

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Organism:mouse· 2 Approach:biophysical modeling· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:development & morphogenesis· 1 Approach:experimental assay· 1 Approach:microscopy & imaging analysis· 1 Assay:proteomics· 1

Frequent Co-Authors

I. Chambers· 2 shared N. Mullin· 2 shared A. Corsinotti· 1 shared D. Kelly· 1 shared E. Hall-Ponsele· 1 shared E. S. Mirfazeli· 1 shared F. C. Wong· 1 shared F. Halbritter· 1 shared

Activity by Year

2017-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 33 mutual co-author links

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2 shared papersBiochemistry

I. Chambers

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2 papers

Recent·Most cited

Analysis of pluripotency transcription factor interactions reveals preferential binding of NANOG to SOX2 rather than NANOG or OCT4

T. K. Mistri, D. Kelly, J. Mak, D. Colby, N. Mullin, I. Chambers

This study investigates the interactions of pluripotency transcription factors Nanog, Sox2, and Oct4, revealing Nanog's preferential binding to Sox2 over Oct4 and its ability to form homomultimers.

bioRxiv · Jun 24, 2020 · PreprintBiochemistry

Distinct SoxB1 networks are required for naïve and primed pluripotency

A. Corsinotti, F. C. Wong, T. Tatar, I. Szczerbinska, F. Halbritter, D. Colby, S. Gogolok, R. Pantier, K. Liggat, E. S. Mirfazeli, E. Hall-Ponsele, N. Mullin, V. Wilson, I. Chambers

The paper shows that distinct SoxB1 networks support naïve and primed pluripotency, with different expression balances of Sox2 and Sox3 in ESCs and EpiSCs.

bioRxiv · Dec 6, 2017Cell Biology