Author

S. A. McKinney

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· 4

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Research Focus:cell type annotation· 2 Research Focus:cell signaling & trafficking· 1 Assay:ChIP-seq· 1 Research Focus:chromatin & epigenetic regulation· 1 Approach:genetic perturbation / CRISPR· 1 Organism:human· 1 Assay:imaging· 1

Frequent Co-Authors

M. McClain· 2 shared A. C. Mok· 1 shared A. Karabulut· 1 shared A. M. Hunn· 1 shared A. S. Gupta· 1 shared A. Sanchez Alvarado· 1 shared B. Rubinstein· 1 shared C. Seidel· 1 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 12 mutual co-author links

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2 shared papersCell Biology

M. McClain

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Author profile →

4 papers

Recent·Most cited

Defining a core configuration for human centromeres during mitosis

A. S. Gupta, C. Seidel, D. Tsuchiya, S. A. McKinney, Z. Yu, S. E. Smith, J. Unruh, J. Gerton

The paper uses ChIP-seq and microscopy to determine the 3D organization of centromere components, revealing a core configuration that explains how centromeres function during mitosis.

bioRxiv · May 10, 2023 · PreprintCell Biology

Retaining pluripotency and exogenous mRNA introduction in planarian stem cell culture

K. Lei, W. Zhang, J. Chen, S. A. McKinney, E. J. Ross, H.-C. Lee, A. Sanchez Alvarado

This study develops methods to culture planarian neoblasts and deliver exogenous mRNAs, demonstrating retained pluripotency and improved yield.

bioRxiv · Jul 9, 2022 · PreprintCell Biology

The architecture and operating mechanism of a cnidarian stinging organelle

A. Karabulut, M. McClain, B. Rubinstein, S. A. McKinney, M. Gibson

This study defines the step-by-step sequence of nematocyst operation in sea anemones using imaging and genetic methods, revealing their biomechanical transformations.

bioRxiv · Sep 9, 2021Cell Biology

The wtf4 meiotic driver utilizes controlled protein aggregation to generate selective cell death

N. L. Nuckolls, A. C. Mok, J. J. Lange, K. Yi, T. S. Kandola, A. M. Hunn, S. McCroskey, J. L. Snyder, M. A. Bravo Nunez, M. McClain, S. A. McKinney, C. Wood, R. Halfmann, S. E. Zanders

This study shows that the wtf4 meiotic driver uses protein aggregation and sequestration to selectively kill cells, revealing a mechanism for meiotic drive.

bioRxiv · Feb 5, 2020Cell Biology