Steven D. Cappell, Ph.D.

Affiliations: 
2010 Pharmacology University of North Carolina, Chapel Hill, Chapel Hill, NC 
Area:
Pharmacology, Biochemistry
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Henrik G. Dohlman grad student 2010 UNC Chapel Hill
 (Systematic analysis of essential genes reveals new regulators of G protein signaling.)
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Publications

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Cornwell JA, Crncec A, Afifi MM, et al. (2024) Author Correction: Loss of CDK4/6 activity in S/G2 phase leads to cell cycle reversal. Nature
Lang F, Cornwell JA, Kaur K, et al. (2023) Abrogation of the G2/M checkpoint as a chemo sensitization approach for alkylating agents. Neuro-Oncology
Cornwell JA, Crncec A, Afifi MM, et al. (2023) Loss of CDK4/6 activity in S/G2 phase leads to cell cycle reversal. Nature
Awadia S, Sitto M, Ram S, et al. (2023) The adapter protein FADD provides an alternate pathway for entry into the cell cycle by regulating APC/C-Cdh1 E3 ubiquitin ligase activity. The Journal of Biological Chemistry. 104786
Nathans JF, Cornwell JA, Afifi MM, et al. (2021) Cell cycle inertia underlies a bifurcation in cell fates after DNA damage. Science Advances. 7
Yang HW, Cappell SD, Jaimovich A, et al. (2020) Stress-mediated exit to quiescence restricted by increasing persistence in CDK4/6 activation. Elife. 9
Chung M, Liu C, Yang HW, et al. (2019) Transient Hysteresis in CDK4/6 Activity Underlies Passage of the Restriction Point in G1. Molecular Cell
Cappell SD, Mark KG, Garbett D, et al. (2018) EMI1 switches from being a substrate to an inhibitor of APC/C to start the cell cycle. Nature
Cappell SD, Chung M, Jaimovich A, et al. (2016) Irreversible APC(Cdh1) Inactivation Underlies the Point of No Return for Cell-Cycle Entry. Cell. 166: 167-180
Spencer SL, Cappell SD, Tsai FC, et al. (2013) The proliferation-quiescence decision is controlled by a bifurcation in CDK2 activity at mitotic exit. Cell. 155: 369-83
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