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TK1 expression influences pathogenicity by cell cycle progression, cellular migration, and cellular survival in HCC 1806 breast cancer cells
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Eliza E. Bitter,
Roles Conceptualization, Formal analysis, Writing – original draft, Writing – review & editing
Affiliations Department of Microbiology and Molecular Biology, Brigham Young University, Provo, Utah, United States of America, Thunder Biotech Inc., Provo, Utah, United States of America
⨯ -
Jonathan Skidmore,
Roles Methodology, Writing – review & editing
Affiliation Department of Microbiology and Molecular Biology, Brigham Young University, Provo, Utah, United States of America
⨯ - Carolyn I. Allen,
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Rachel I. Erickson,
Roles Data curation, Methodology
Affiliation Department of Microbiology and Molecular Biology, Brigham Young University, Provo, Utah, United States of America
⨯ - Rachel M. Morris,
- Toni Mortimer,
- Audrey Meade,
- Rachel Brog,
- Tim Phares,
- Michelle Townsend,
- Brett E. Pickett,
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Kim L. O’Neill
Roles Conceptualization, Formal analysis, Methodology, Project administration, Resources, Writing – original draft, Writing – review & editing
* E-mail: kim_oneill@byu.edu
Affiliation Department of Microbiology and Molecular Biology, Brigham Young University, Provo, Utah, United States of America
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https://orcid.org/0000-0001-5339-2544
TK1 expression influences pathogenicity by cell cycle progression, cellular migration, and cellular survival in HCC 1806 breast cancer cells
- Eliza E. Bitter,
- Jonathan Skidmore,
- Carolyn I. Allen,
- Rachel I. Erickson,
- Rachel M. Morris,
- Toni Mortimer,
- Audrey Meade,
- Rachel Brog,
- Tim Phares,
- Michelle Townsend
- Published: November 30, 2023
- https://doi.org/10.1371/journal.pone.0293128