Cell-cycle control in aging, cancer, and homeostasis

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Abstract/Contents

Abstract
Mammalian development and homeostasis require precise control of cellular proliferation. Excess cellular proliferation causes cancer, while insufficient cellular proliferation is associated with aging. The work presented herein details specific mechanisms of cell-cycle regulation and how they contribute to homeostasis, aging, and cancer. The first study reveals how a lack of coordination between major proliferation signaling pathways contributes to cellular aging. In the second study, an unexpected mechanism of action is revealed for an important class of cancer therapeutics targeting the core cell-cycle machinery. The final study describes how cells navigate the inherently stressful process of genome duplication. Taken together, these studies contribute novel insights to our understanding of the mechanisms and importance of cell-cycle regulation

Description

Type of resource text
Form electronic resource; remote; computer; online resource
Extent 1 online resource
Place California
Place [Stanford, California]
Publisher [Stanford University]
Copyright date 2020; ©2020
Publication date 2020; 2020
Issuance monographic
Language English

Creators/Contributors

Author Daigh, Leighton Harrison
Degree supervisor Meyer, Tobias
Thesis advisor Meyer, Tobias
Thesis advisor Ferrell, James Ellsworth
Thesis advisor Sage, Julien
Degree committee member Ferrell, James Ellsworth
Degree committee member Sage, Julien
Associated with Stanford University, Department of Chemical and Systems Biology.

Subjects

Genre Theses
Genre Text

Bibliographic information

Statement of responsibility Leighton H. Daigh
Note Submitted to the Department of Chemical and Systems Biology
Thesis Thesis Ph.D. Stanford University 2020
Location electronic resource

Access conditions

Copyright
© 2020 by Leighton Harrison Daigh
License
This work is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported license (CC BY-NC).

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