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You searched for subject:(Cell cycle). Showing records 1 – 30 of 1496 total matches.

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University of Georgia

1. Burbage, Christopher Dieter. Picocyanobacterial cellular physiology and trophic interaction with a heterotrophic nanoflagellate.

Degree: PhD, Marine Sciences, 2007, University of Georgia

 Prochlorococcus and Synechococcus are two closely related picocyanobacteria that together are responsible for a large proportion of the total primary production in open ocean environments.… (more)

Subjects/Keywords: cell cycle

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APA (6th Edition):

Burbage, C. D. (2007). Picocyanobacterial cellular physiology and trophic interaction with a heterotrophic nanoflagellate. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/burbage_christopher_d_200712_phd

Chicago Manual of Style (16th Edition):

Burbage, Christopher Dieter. “Picocyanobacterial cellular physiology and trophic interaction with a heterotrophic nanoflagellate.” 2007. Doctoral Dissertation, University of Georgia. Accessed April 03, 2020. http://purl.galileo.usg.edu/uga_etd/burbage_christopher_d_200712_phd.

MLA Handbook (7th Edition):

Burbage, Christopher Dieter. “Picocyanobacterial cellular physiology and trophic interaction with a heterotrophic nanoflagellate.” 2007. Web. 03 Apr 2020.

Vancouver:

Burbage CD. Picocyanobacterial cellular physiology and trophic interaction with a heterotrophic nanoflagellate. [Internet] [Doctoral dissertation]. University of Georgia; 2007. [cited 2020 Apr 03]. Available from: http://purl.galileo.usg.edu/uga_etd/burbage_christopher_d_200712_phd.

Council of Science Editors:

Burbage CD. Picocyanobacterial cellular physiology and trophic interaction with a heterotrophic nanoflagellate. [Doctoral Dissertation]. University of Georgia; 2007. Available from: http://purl.galileo.usg.edu/uga_etd/burbage_christopher_d_200712_phd


University of Manitoba

2. Baxter, Shannon A. Mechanisms of PROX1 mediated regulation of the lymphatic endothelial cell cycle.

Degree: Biochemistry and Medical Genetics, 2010, University of Manitoba

 The homeobox transcription factor PROX1 is the mammalian ortholog of the Drosophila gene Prospero. Expression of PROX1 in a subset of venous endothelial cells changes… (more)

Subjects/Keywords: Lymphatic endothelial cell; Cell cycle

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APA (6th Edition):

Baxter, S. A. (2010). Mechanisms of PROX1 mediated regulation of the lymphatic endothelial cell cycle. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/14917

Chicago Manual of Style (16th Edition):

Baxter, Shannon A. “Mechanisms of PROX1 mediated regulation of the lymphatic endothelial cell cycle.” 2010. Masters Thesis, University of Manitoba. Accessed April 03, 2020. http://hdl.handle.net/1993/14917.

MLA Handbook (7th Edition):

Baxter, Shannon A. “Mechanisms of PROX1 mediated regulation of the lymphatic endothelial cell cycle.” 2010. Web. 03 Apr 2020.

Vancouver:

Baxter SA. Mechanisms of PROX1 mediated regulation of the lymphatic endothelial cell cycle. [Internet] [Masters thesis]. University of Manitoba; 2010. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/1993/14917.

Council of Science Editors:

Baxter SA. Mechanisms of PROX1 mediated regulation of the lymphatic endothelial cell cycle. [Masters Thesis]. University of Manitoba; 2010. Available from: http://hdl.handle.net/1993/14917


Hong Kong University of Science and Technology

3. Tang, Rui LIFS. Anti-apoptotic functions of BCL-W, MCL-1, and A1 in mitotic cell death.

Degree: 2016, Hong Kong University of Science and Technology

 Anti-microtubule agents activate the spindle-assembly checkpoint by perturbing spindle formation and trapping cells in mitosis. Whether cells undergo mitotic cell death subsequently is an important… (more)

Subjects/Keywords: Cell cycle ; Mitosis ; Cell death

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APA (6th Edition):

Tang, R. L. (2016). Anti-apoptotic functions of BCL-W, MCL-1, and A1 in mitotic cell death. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-100402 ; https://doi.org/10.14711/thesis-b1626285 ; http://repository.ust.hk/ir/bitstream/1783.1-100402/1/th_redirect.html

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Tang, Rui LIFS. “Anti-apoptotic functions of BCL-W, MCL-1, and A1 in mitotic cell death.” 2016. Thesis, Hong Kong University of Science and Technology. Accessed April 03, 2020. http://repository.ust.hk/ir/Record/1783.1-100402 ; https://doi.org/10.14711/thesis-b1626285 ; http://repository.ust.hk/ir/bitstream/1783.1-100402/1/th_redirect.html.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Tang, Rui LIFS. “Anti-apoptotic functions of BCL-W, MCL-1, and A1 in mitotic cell death.” 2016. Web. 03 Apr 2020.

Vancouver:

Tang RL. Anti-apoptotic functions of BCL-W, MCL-1, and A1 in mitotic cell death. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2016. [cited 2020 Apr 03]. Available from: http://repository.ust.hk/ir/Record/1783.1-100402 ; https://doi.org/10.14711/thesis-b1626285 ; http://repository.ust.hk/ir/bitstream/1783.1-100402/1/th_redirect.html.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Tang RL. Anti-apoptotic functions of BCL-W, MCL-1, and A1 in mitotic cell death. [Thesis]. Hong Kong University of Science and Technology; 2016. Available from: http://repository.ust.hk/ir/Record/1783.1-100402 ; https://doi.org/10.14711/thesis-b1626285 ; http://repository.ust.hk/ir/bitstream/1783.1-100402/1/th_redirect.html

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Hong Kong

4. Ruan, Yafei. Investigating the regulation of UHRF1 in cell cycle.

Degree: Master of Medical Sciences, 2015, University of Hong Kong

UHRF1 is a multi-domain protein with multiple functions in mammalian cells including maintenance of DNA methylation, histone modification, DNA damage et al. UHRF1 itself also… (more)

Subjects/Keywords: Cell cycle; Ubiquitin

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APA (6th Edition):

Ruan, Y. (2015). Investigating the regulation of UHRF1 in cell cycle. (Masters Thesis). University of Hong Kong. Retrieved from Ruan, Y. [阮雅菲]. (2015). Investigating the regulation of UHRF1 in cell cycle. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5659412 ; http://hdl.handle.net/10722/221484

Chicago Manual of Style (16th Edition):

Ruan, Yafei. “Investigating the regulation of UHRF1 in cell cycle.” 2015. Masters Thesis, University of Hong Kong. Accessed April 03, 2020. Ruan, Y. [阮雅菲]. (2015). Investigating the regulation of UHRF1 in cell cycle. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5659412 ; http://hdl.handle.net/10722/221484.

MLA Handbook (7th Edition):

Ruan, Yafei. “Investigating the regulation of UHRF1 in cell cycle.” 2015. Web. 03 Apr 2020.

Vancouver:

Ruan Y. Investigating the regulation of UHRF1 in cell cycle. [Internet] [Masters thesis]. University of Hong Kong; 2015. [cited 2020 Apr 03]. Available from: Ruan, Y. [阮雅菲]. (2015). Investigating the regulation of UHRF1 in cell cycle. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5659412 ; http://hdl.handle.net/10722/221484.

Council of Science Editors:

Ruan Y. Investigating the regulation of UHRF1 in cell cycle. [Masters Thesis]. University of Hong Kong; 2015. Available from: Ruan, Y. [阮雅菲]. (2015). Investigating the regulation of UHRF1 in cell cycle. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5659412 ; http://hdl.handle.net/10722/221484


University of Hong Kong

5. Xie, Si. Structural and biochemical study of replication fork protection complex in S-phase checkpoint activation.

Degree: PhD, 2015, University of Hong Kong

 Faithful transmission of genetic information from parent cells to daughter cells is crucial for the survival of all eukaryotic organisms. To achieve high fidelity of… (more)

Subjects/Keywords: Cell cycle; DNA replication

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APA (6th Edition):

Xie, S. (2015). Structural and biochemical study of replication fork protection complex in S-phase checkpoint activation. (Doctoral Dissertation). University of Hong Kong. Retrieved from Xie, S. [谢思]. (2015). Structural and biochemical study of replication fork protection complex in S-phase checkpoint activation. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5576755 ; http://dx.doi.org/10.5353/th_b5576755 ; http://hdl.handle.net/10722/228643

Chicago Manual of Style (16th Edition):

Xie, Si. “Structural and biochemical study of replication fork protection complex in S-phase checkpoint activation.” 2015. Doctoral Dissertation, University of Hong Kong. Accessed April 03, 2020. Xie, S. [谢思]. (2015). Structural and biochemical study of replication fork protection complex in S-phase checkpoint activation. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5576755 ; http://dx.doi.org/10.5353/th_b5576755 ; http://hdl.handle.net/10722/228643.

MLA Handbook (7th Edition):

Xie, Si. “Structural and biochemical study of replication fork protection complex in S-phase checkpoint activation.” 2015. Web. 03 Apr 2020.

Vancouver:

Xie S. Structural and biochemical study of replication fork protection complex in S-phase checkpoint activation. [Internet] [Doctoral dissertation]. University of Hong Kong; 2015. [cited 2020 Apr 03]. Available from: Xie, S. [谢思]. (2015). Structural and biochemical study of replication fork protection complex in S-phase checkpoint activation. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5576755 ; http://dx.doi.org/10.5353/th_b5576755 ; http://hdl.handle.net/10722/228643.

Council of Science Editors:

Xie S. Structural and biochemical study of replication fork protection complex in S-phase checkpoint activation. [Doctoral Dissertation]. University of Hong Kong; 2015. Available from: Xie, S. [谢思]. (2015). Structural and biochemical study of replication fork protection complex in S-phase checkpoint activation. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5576755 ; http://dx.doi.org/10.5353/th_b5576755 ; http://hdl.handle.net/10722/228643


University of Louisville

6. Stallons, Lindsey Jay, 1983-. DNA polymerase iota promotes G2/M checkpoint activation and genetic stability after UV-induced DNA damage.

Degree: PhD, 2011, University of Louisville

 Unrepaired DNA damage poses a serious threat to the genetic stability of a replicating cell. One mechanism of tolerating this damage is translesion DNA synthesis… (more)

Subjects/Keywords: Mutagenesis; Cell cycle; Polymerase iota

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APA (6th Edition):

Stallons, Lindsey Jay, 1. (2011). DNA polymerase iota promotes G2/M checkpoint activation and genetic stability after UV-induced DNA damage. (Doctoral Dissertation). University of Louisville. Retrieved from 10.18297/etd/1369 ; https://ir.library.louisville.edu/etd/1369

Chicago Manual of Style (16th Edition):

Stallons, Lindsey Jay, 1983-. “DNA polymerase iota promotes G2/M checkpoint activation and genetic stability after UV-induced DNA damage.” 2011. Doctoral Dissertation, University of Louisville. Accessed April 03, 2020. 10.18297/etd/1369 ; https://ir.library.louisville.edu/etd/1369.

MLA Handbook (7th Edition):

Stallons, Lindsey Jay, 1983-. “DNA polymerase iota promotes G2/M checkpoint activation and genetic stability after UV-induced DNA damage.” 2011. Web. 03 Apr 2020.

Vancouver:

Stallons, Lindsey Jay 1. DNA polymerase iota promotes G2/M checkpoint activation and genetic stability after UV-induced DNA damage. [Internet] [Doctoral dissertation]. University of Louisville; 2011. [cited 2020 Apr 03]. Available from: 10.18297/etd/1369 ; https://ir.library.louisville.edu/etd/1369.

Council of Science Editors:

Stallons, Lindsey Jay 1. DNA polymerase iota promotes G2/M checkpoint activation and genetic stability after UV-induced DNA damage. [Doctoral Dissertation]. University of Louisville; 2011. Available from: 10.18297/etd/1369 ; https://ir.library.louisville.edu/etd/1369

7. Takatsuka, Hirotomo. Studies on functional roles of CDK-activating kinases in Arabidopsis development : シロイヌナズナの発生におけるCDK活性化キナーゼの機能に関する研究; シロイヌナズナ ノ ハッセイ ニ オケル CDK カッセイ カ キナーゼ ノ キノウ ニ カンスル ケンキュウ.

Degree: Nara Institute of Science and Technology / 奈良先端科学技術大学院大学

Subjects/Keywords: cell cycle

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APA (6th Edition):

Takatsuka, H. (n.d.). Studies on functional roles of CDK-activating kinases in Arabidopsis development : シロイヌナズナの発生におけるCDK活性化キナーゼの機能に関する研究; シロイヌナズナ ノ ハッセイ ニ オケル CDK カッセイ カ キナーゼ ノ キノウ ニ カンスル ケンキュウ. (Thesis). Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Retrieved from http://hdl.handle.net/10061/5706

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Takatsuka, Hirotomo. “Studies on functional roles of CDK-activating kinases in Arabidopsis development : シロイヌナズナの発生におけるCDK活性化キナーゼの機能に関する研究; シロイヌナズナ ノ ハッセイ ニ オケル CDK カッセイ カ キナーゼ ノ キノウ ニ カンスル ケンキュウ.” Thesis, Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Accessed April 03, 2020. http://hdl.handle.net/10061/5706.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Takatsuka, Hirotomo. “Studies on functional roles of CDK-activating kinases in Arabidopsis development : シロイヌナズナの発生におけるCDK活性化キナーゼの機能に関する研究; シロイヌナズナ ノ ハッセイ ニ オケル CDK カッセイ カ キナーゼ ノ キノウ ニ カンスル ケンキュウ.” Web. 03 Apr 2020.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Takatsuka H. Studies on functional roles of CDK-activating kinases in Arabidopsis development : シロイヌナズナの発生におけるCDK活性化キナーゼの機能に関する研究; シロイヌナズナ ノ ハッセイ ニ オケル CDK カッセイ カ キナーゼ ノ キノウ ニ カンスル ケンキュウ. [Internet] [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; [cited 2020 Apr 03]. Available from: http://hdl.handle.net/10061/5706.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Takatsuka H. Studies on functional roles of CDK-activating kinases in Arabidopsis development : シロイヌナズナの発生におけるCDK活性化キナーゼの機能に関する研究; シロイヌナズナ ノ ハッセイ ニ オケル CDK カッセイ カ キナーゼ ノ キノウ ニ カンスル ケンキュウ. [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; Available from: http://hdl.handle.net/10061/5706

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


Case Western Reserve University

8. Wang, Li. CELL CYCLE REGULATION IN THE POST-MITOTIC NEURONAL CELLS.

Degree: PhD, Genetics, 2007, Case Western Reserve University

 A normal cell cycle is essential for cell proliferation in embryonic development. Once the appropriate numbers of cells are generated, however, there are various populations,… (more)

Subjects/Keywords: Cell cycle regulation; E2F1; Cdk5

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APA (6th Edition):

Wang, L. (2007). CELL CYCLE REGULATION IN THE POST-MITOTIC NEURONAL CELLS. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1184254319

Chicago Manual of Style (16th Edition):

Wang, Li. “CELL CYCLE REGULATION IN THE POST-MITOTIC NEURONAL CELLS.” 2007. Doctoral Dissertation, Case Western Reserve University. Accessed April 03, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=case1184254319.

MLA Handbook (7th Edition):

Wang, Li. “CELL CYCLE REGULATION IN THE POST-MITOTIC NEURONAL CELLS.” 2007. Web. 03 Apr 2020.

Vancouver:

Wang L. CELL CYCLE REGULATION IN THE POST-MITOTIC NEURONAL CELLS. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2007. [cited 2020 Apr 03]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1184254319.

Council of Science Editors:

Wang L. CELL CYCLE REGULATION IN THE POST-MITOTIC NEURONAL CELLS. [Doctoral Dissertation]. Case Western Reserve University; 2007. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1184254319


Penn State University

9. MIN, JUNGSOO. Mechanisms of IGF-1 regulation of S and G2/M cell cycle phases in oligodendrocyte progenitor (OP) cells.

Degree: PhD, Molecular Medicine, 2009, Penn State University

 Oligodendrocytes are macroglial cells in the central nervous system (CNS), which myelinate and provide electric insulation for the axons of nerve cells. Oligodendrocyte progenitor (OP)… (more)

Subjects/Keywords: IGF-1; oligodendrocyte; cell cycle

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APA (6th Edition):

MIN, J. (2009). Mechanisms of IGF-1 regulation of S and G2/M cell cycle phases in oligodendrocyte progenitor (OP) cells. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/10077

Chicago Manual of Style (16th Edition):

MIN, JUNGSOO. “Mechanisms of IGF-1 regulation of S and G2/M cell cycle phases in oligodendrocyte progenitor (OP) cells.” 2009. Doctoral Dissertation, Penn State University. Accessed April 03, 2020. https://etda.libraries.psu.edu/catalog/10077.

MLA Handbook (7th Edition):

MIN, JUNGSOO. “Mechanisms of IGF-1 regulation of S and G2/M cell cycle phases in oligodendrocyte progenitor (OP) cells.” 2009. Web. 03 Apr 2020.

Vancouver:

MIN J. Mechanisms of IGF-1 regulation of S and G2/M cell cycle phases in oligodendrocyte progenitor (OP) cells. [Internet] [Doctoral dissertation]. Penn State University; 2009. [cited 2020 Apr 03]. Available from: https://etda.libraries.psu.edu/catalog/10077.

Council of Science Editors:

MIN J. Mechanisms of IGF-1 regulation of S and G2/M cell cycle phases in oligodendrocyte progenitor (OP) cells. [Doctoral Dissertation]. Penn State University; 2009. Available from: https://etda.libraries.psu.edu/catalog/10077


Oregon State University

10. Worthington, David H. Hydroxyurea : physiological effects on Tetrahymena pyriformis and use in cell cycle analysis.

Degree: PhD, Genetics, 1973, Oregon State University

 Hydroxyurea (10mM) blocks the exponential growth of Tetrahymena pyriformis (GL-I) populations by arresting progress through the cell cycle once the cells enter S-phase. Autoradiographic analysis… (more)

Subjects/Keywords: Cell cycle

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APA (6th Edition):

Worthington, D. H. (1973). Hydroxyurea : physiological effects on Tetrahymena pyriformis and use in cell cycle analysis. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/44777

Chicago Manual of Style (16th Edition):

Worthington, David H. “Hydroxyurea : physiological effects on Tetrahymena pyriformis and use in cell cycle analysis.” 1973. Doctoral Dissertation, Oregon State University. Accessed April 03, 2020. http://hdl.handle.net/1957/44777.

MLA Handbook (7th Edition):

Worthington, David H. “Hydroxyurea : physiological effects on Tetrahymena pyriformis and use in cell cycle analysis.” 1973. Web. 03 Apr 2020.

Vancouver:

Worthington DH. Hydroxyurea : physiological effects on Tetrahymena pyriformis and use in cell cycle analysis. [Internet] [Doctoral dissertation]. Oregon State University; 1973. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/1957/44777.

Council of Science Editors:

Worthington DH. Hydroxyurea : physiological effects on Tetrahymena pyriformis and use in cell cycle analysis. [Doctoral Dissertation]. Oregon State University; 1973. Available from: http://hdl.handle.net/1957/44777


Vanderbilt University

11. Talley, Jennell Marie. Exploring the assembly and function of the telomerase accessory proteins Est1 and Est3 in Saccharomyces cerevisiae.

Degree: PhD, Biological Sciences, 2011, Vanderbilt University

 The work presented in this dissertation focuses on a how the telomerase complex assembles both in vivo and in vitro and begins to explore how… (more)

Subjects/Keywords: proteasome; TERT; cell cycle; Telomere

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APA (6th Edition):

Talley, J. M. (2011). Exploring the assembly and function of the telomerase accessory proteins Est1 and Est3 in Saccharomyces cerevisiae. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-07182011-134847/ ;

Chicago Manual of Style (16th Edition):

Talley, Jennell Marie. “Exploring the assembly and function of the telomerase accessory proteins Est1 and Est3 in Saccharomyces cerevisiae.” 2011. Doctoral Dissertation, Vanderbilt University. Accessed April 03, 2020. http://etd.library.vanderbilt.edu/available/etd-07182011-134847/ ;.

MLA Handbook (7th Edition):

Talley, Jennell Marie. “Exploring the assembly and function of the telomerase accessory proteins Est1 and Est3 in Saccharomyces cerevisiae.” 2011. Web. 03 Apr 2020.

Vancouver:

Talley JM. Exploring the assembly and function of the telomerase accessory proteins Est1 and Est3 in Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. Vanderbilt University; 2011. [cited 2020 Apr 03]. Available from: http://etd.library.vanderbilt.edu/available/etd-07182011-134847/ ;.

Council of Science Editors:

Talley JM. Exploring the assembly and function of the telomerase accessory proteins Est1 and Est3 in Saccharomyces cerevisiae. [Doctoral Dissertation]. Vanderbilt University; 2011. Available from: http://etd.library.vanderbilt.edu/available/etd-07182011-134847/ ;


Harvard University

12. Ho, Po-Yi. Models of microbial cell cycles.

Degree: PhD, 2019, Harvard University

Cell division is a fundamental process of life, yet how the timing of cell division is regulated in microorganisms remain unclear. In this dissertation, I… (more)

Subjects/Keywords: Models; microbial cell cycle

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APA (6th Edition):

Ho, P. (2019). Models of microbial cell cycles. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:42029521

Chicago Manual of Style (16th Edition):

Ho, Po-Yi. “Models of microbial cell cycles.” 2019. Doctoral Dissertation, Harvard University. Accessed April 03, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:42029521.

MLA Handbook (7th Edition):

Ho, Po-Yi. “Models of microbial cell cycles.” 2019. Web. 03 Apr 2020.

Vancouver:

Ho P. Models of microbial cell cycles. [Internet] [Doctoral dissertation]. Harvard University; 2019. [cited 2020 Apr 03]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42029521.

Council of Science Editors:

Ho P. Models of microbial cell cycles. [Doctoral Dissertation]. Harvard University; 2019. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42029521


University of Sydney

13. Dokumcu, Kagan Ali. Non-encoded Mechanisms of Stress Adaptation in Cancer .

Degree: 2019, University of Sydney

 Tumour resistance attributed to clonal evolution of neoplastic cells, poses a major challenge for treatment of cancer. Clonality of neoplastic cells is mainly considered to… (more)

Subjects/Keywords: Cancer; Autophagy; Cell Cycle; MicroRNA

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APA (6th Edition):

Dokumcu, K. A. (2019). Non-encoded Mechanisms of Stress Adaptation in Cancer . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/20959

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Dokumcu, Kagan Ali. “Non-encoded Mechanisms of Stress Adaptation in Cancer .” 2019. Thesis, University of Sydney. Accessed April 03, 2020. http://hdl.handle.net/2123/20959.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Dokumcu, Kagan Ali. “Non-encoded Mechanisms of Stress Adaptation in Cancer .” 2019. Web. 03 Apr 2020.

Vancouver:

Dokumcu KA. Non-encoded Mechanisms of Stress Adaptation in Cancer . [Internet] [Thesis]. University of Sydney; 2019. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/2123/20959.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Dokumcu KA. Non-encoded Mechanisms of Stress Adaptation in Cancer . [Thesis]. University of Sydney; 2019. Available from: http://hdl.handle.net/2123/20959

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Texas Southwestern Medical Center

14. Chaudhary, Jaideep. Function And Recruitment Of Centromeric Heterochromatin Protein 1.

Degree: 2011, University of Texas Southwestern Medical Center

 During early mitosis, the sister chromatids are held together by Cohesin, a protein complex composed of Smc3, Smc1, Scc1/Rad21 and Scc3. Cohesin is first released… (more)

Subjects/Keywords: Cell Cycle Proteins; Mitosis; Heterochromatin

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Chaudhary, J. (2011). Function And Recruitment Of Centromeric Heterochromatin Protein 1. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/846

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Chaudhary, Jaideep. “Function And Recruitment Of Centromeric Heterochromatin Protein 1.” 2011. Thesis, University of Texas Southwestern Medical Center. Accessed April 03, 2020. http://hdl.handle.net/2152.5/846.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Chaudhary, Jaideep. “Function And Recruitment Of Centromeric Heterochromatin Protein 1.” 2011. Web. 03 Apr 2020.

Vancouver:

Chaudhary J. Function And Recruitment Of Centromeric Heterochromatin Protein 1. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2011. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/2152.5/846.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Chaudhary J. Function And Recruitment Of Centromeric Heterochromatin Protein 1. [Thesis]. University of Texas Southwestern Medical Center; 2011. Available from: http://hdl.handle.net/2152.5/846

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Texas Southwestern Medical Center

15. Cai, Ling. Insights into the Metabolic Regulation of Growth and Proliferation in Saccharomyces Cerevisiae.

Degree: 2013, University of Texas Southwestern Medical Center

 Cells needs to gauge their capacity to grow based on nutrient availability, and adopt different metabolic strategies for optimal growth and survival. We have investigated… (more)

Subjects/Keywords: Saccharomyces cerevisiae; Cell Cycle; Mitosis

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APA (6th Edition):

Cai, L. (2013). Insights into the Metabolic Regulation of Growth and Proliferation in Saccharomyces Cerevisiae. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/2715

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Cai, Ling. “Insights into the Metabolic Regulation of Growth and Proliferation in Saccharomyces Cerevisiae.” 2013. Thesis, University of Texas Southwestern Medical Center. Accessed April 03, 2020. http://hdl.handle.net/2152.5/2715.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Cai, Ling. “Insights into the Metabolic Regulation of Growth and Proliferation in Saccharomyces Cerevisiae.” 2013. Web. 03 Apr 2020.

Vancouver:

Cai L. Insights into the Metabolic Regulation of Growth and Proliferation in Saccharomyces Cerevisiae. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2013. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/2152.5/2715.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Cai L. Insights into the Metabolic Regulation of Growth and Proliferation in Saccharomyces Cerevisiae. [Thesis]. University of Texas Southwestern Medical Center; 2013. Available from: http://hdl.handle.net/2152.5/2715

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Hong Kong University of Science and Technology

16. Zhao, Yichen LIFS. Functional study of GAS2L1 in mitosis.

Degree: 2015, Hong Kong University of Science and Technology

 Mitosis, as a very important process during the cell cycle, decides chromosome duplication, organelle separation and cell division. During mitosis, metaphase is middle of whole… (more)

Subjects/Keywords: Mitosis ; Cell cycle ; Carrier proteins

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Zhao, Y. L. (2015). Functional study of GAS2L1 in mitosis. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-92284 ; https://doi.org/10.14711/thesis-b1514805 ; http://repository.ust.hk/ir/bitstream/1783.1-92284/1/th_redirect.html

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Zhao, Yichen LIFS. “Functional study of GAS2L1 in mitosis.” 2015. Thesis, Hong Kong University of Science and Technology. Accessed April 03, 2020. http://repository.ust.hk/ir/Record/1783.1-92284 ; https://doi.org/10.14711/thesis-b1514805 ; http://repository.ust.hk/ir/bitstream/1783.1-92284/1/th_redirect.html.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Zhao, Yichen LIFS. “Functional study of GAS2L1 in mitosis.” 2015. Web. 03 Apr 2020.

Vancouver:

Zhao YL. Functional study of GAS2L1 in mitosis. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2015. [cited 2020 Apr 03]. Available from: http://repository.ust.hk/ir/Record/1783.1-92284 ; https://doi.org/10.14711/thesis-b1514805 ; http://repository.ust.hk/ir/bitstream/1783.1-92284/1/th_redirect.html.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Zhao YL. Functional study of GAS2L1 in mitosis. [Thesis]. Hong Kong University of Science and Technology; 2015. Available from: http://repository.ust.hk/ir/Record/1783.1-92284 ; https://doi.org/10.14711/thesis-b1514805 ; http://repository.ust.hk/ir/bitstream/1783.1-92284/1/th_redirect.html

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Hong Kong University of Science and Technology

17. Qin, Yan LIFS. The role of hNOC3 in human DNA replication.

Degree: 2013, Hong Kong University of Science and Technology

 Noc3p (nucleolar complex-associated protein) is highly conserved in eukaryotes, and it plays a critical role in the initiation of DNA replication in budding yeast. Noc3p… (more)

Subjects/Keywords: DNA replication ; Cell cycle

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APA (6th Edition):

Qin, Y. L. (2013). The role of hNOC3 in human DNA replication. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-94452 ; https://doi.org/10.14711/thesis-b1266302 ; http://repository.ust.hk/ir/bitstream/1783.1-94452/1/th_redirect.html

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Qin, Yan LIFS. “The role of hNOC3 in human DNA replication.” 2013. Thesis, Hong Kong University of Science and Technology. Accessed April 03, 2020. http://repository.ust.hk/ir/Record/1783.1-94452 ; https://doi.org/10.14711/thesis-b1266302 ; http://repository.ust.hk/ir/bitstream/1783.1-94452/1/th_redirect.html.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Qin, Yan LIFS. “The role of hNOC3 in human DNA replication.” 2013. Web. 03 Apr 2020.

Vancouver:

Qin YL. The role of hNOC3 in human DNA replication. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2013. [cited 2020 Apr 03]. Available from: http://repository.ust.hk/ir/Record/1783.1-94452 ; https://doi.org/10.14711/thesis-b1266302 ; http://repository.ust.hk/ir/bitstream/1783.1-94452/1/th_redirect.html.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Qin YL. The role of hNOC3 in human DNA replication. [Thesis]. Hong Kong University of Science and Technology; 2013. Available from: http://repository.ust.hk/ir/Record/1783.1-94452 ; https://doi.org/10.14711/thesis-b1266302 ; http://repository.ust.hk/ir/bitstream/1783.1-94452/1/th_redirect.html

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Hong Kong University of Science and Technology

18. Xu, Kaichun LIFS. Molecular regulation of mitotic slippage.

Degree: 2016, Hong Kong University of Science and Technology

 Antimicrotubule drugs are effective chemotherapeutic agents because they can disrupt normal mitotic spindle and activate the spindle-assembly checkpoint (SAC) to arrest cells in mitosis, thereby… (more)

Subjects/Keywords: Cell cycle ; Regulation ; Mitosis

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Xu, K. L. (2016). Molecular regulation of mitotic slippage. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-99847 ; https://doi.org/10.14711/thesis-b1626381 ; http://repository.ust.hk/ir/bitstream/1783.1-99847/1/th_redirect.html

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Xu, Kaichun LIFS. “Molecular regulation of mitotic slippage.” 2016. Thesis, Hong Kong University of Science and Technology. Accessed April 03, 2020. http://repository.ust.hk/ir/Record/1783.1-99847 ; https://doi.org/10.14711/thesis-b1626381 ; http://repository.ust.hk/ir/bitstream/1783.1-99847/1/th_redirect.html.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Xu, Kaichun LIFS. “Molecular regulation of mitotic slippage.” 2016. Web. 03 Apr 2020.

Vancouver:

Xu KL. Molecular regulation of mitotic slippage. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2016. [cited 2020 Apr 03]. Available from: http://repository.ust.hk/ir/Record/1783.1-99847 ; https://doi.org/10.14711/thesis-b1626381 ; http://repository.ust.hk/ir/bitstream/1783.1-99847/1/th_redirect.html.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Xu KL. Molecular regulation of mitotic slippage. [Thesis]. Hong Kong University of Science and Technology; 2016. Available from: http://repository.ust.hk/ir/Record/1783.1-99847 ; https://doi.org/10.14711/thesis-b1626381 ; http://repository.ust.hk/ir/bitstream/1783.1-99847/1/th_redirect.html

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


University of Hong Kong

19. Zheng, Fan. Molecular mechanisms regulating bipolar spindle formation and microtubule depolymerization.

Degree: PhD, 2015, University of Hong Kong

 Microtubules are involved in a wide range of cellular functions including the establishment of cell polarity, organelle trafficking and positioning, and mitotic chromosome segregation. To… (more)

Subjects/Keywords: Spindle (Cell division); Cell cycle; Microtubules

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Zheng, F. (2015). Molecular mechanisms regulating bipolar spindle formation and microtubule depolymerization. (Doctoral Dissertation). University of Hong Kong. Retrieved from Zheng, F. [郑{273c46}]. (2015). Molecular mechanisms regulating bipolar spindle formation and microtubule depolymerization. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5576784 ; http://hdl.handle.net/10722/221095

Chicago Manual of Style (16th Edition):

Zheng, Fan. “Molecular mechanisms regulating bipolar spindle formation and microtubule depolymerization.” 2015. Doctoral Dissertation, University of Hong Kong. Accessed April 03, 2020. Zheng, F. [郑{273c46}]. (2015). Molecular mechanisms regulating bipolar spindle formation and microtubule depolymerization. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5576784 ; http://hdl.handle.net/10722/221095.

MLA Handbook (7th Edition):

Zheng, Fan. “Molecular mechanisms regulating bipolar spindle formation and microtubule depolymerization.” 2015. Web. 03 Apr 2020.

Vancouver:

Zheng F. Molecular mechanisms regulating bipolar spindle formation and microtubule depolymerization. [Internet] [Doctoral dissertation]. University of Hong Kong; 2015. [cited 2020 Apr 03]. Available from: Zheng, F. [郑{273c46}]. (2015). Molecular mechanisms regulating bipolar spindle formation and microtubule depolymerization. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5576784 ; http://hdl.handle.net/10722/221095.

Council of Science Editors:

Zheng F. Molecular mechanisms regulating bipolar spindle formation and microtubule depolymerization. [Doctoral Dissertation]. University of Hong Kong; 2015. Available from: Zheng, F. [郑{273c46}]. (2015). Molecular mechanisms regulating bipolar spindle formation and microtubule depolymerization. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b5576784 ; http://hdl.handle.net/10722/221095


University of Notre Dame

20. Randy Jeffrey. Effects of the Anti-Androgen Bicalutamide on Prostate Cancer Cells</h1>.

Degree: PhD, Biological Sciences, 2012, University of Notre Dame

  The use of anti-androgen therapy for the treatment of invasive and metastatic prostate cancer is common practice. However, after an initial response, the tumor… (more)

Subjects/Keywords: cell death; prostate cancer; cell cycle; bicalutamide

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APA (6th Edition):

Jeffrey, R. (2012). Effects of the Anti-Androgen Bicalutamide on Prostate Cancer Cells</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/qf85n873c5q

Chicago Manual of Style (16th Edition):

Jeffrey, Randy. “Effects of the Anti-Androgen Bicalutamide on Prostate Cancer Cells</h1>.” 2012. Doctoral Dissertation, University of Notre Dame. Accessed April 03, 2020. https://curate.nd.edu/show/qf85n873c5q.

MLA Handbook (7th Edition):

Jeffrey, Randy. “Effects of the Anti-Androgen Bicalutamide on Prostate Cancer Cells</h1>.” 2012. Web. 03 Apr 2020.

Vancouver:

Jeffrey R. Effects of the Anti-Androgen Bicalutamide on Prostate Cancer Cells</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2012. [cited 2020 Apr 03]. Available from: https://curate.nd.edu/show/qf85n873c5q.

Council of Science Editors:

Jeffrey R. Effects of the Anti-Androgen Bicalutamide on Prostate Cancer Cells</h1>. [Doctoral Dissertation]. University of Notre Dame; 2012. Available from: https://curate.nd.edu/show/qf85n873c5q


University of Tennessee – Knoxville

21. Stutts, Dustin K. Role of the mitotic cyclin Clb2 in mitotic regulation.

Degree: MS, Biochemistry and Cellular and Molecular Biology, 2010, University of Tennessee – Knoxville

 In the budding yeast Saccharomyces cerevisiae, the mitotic cell cycle is regulated by the cyclin-dependent kinase (CDK) Cdc28. Cdc28 is activated by binding to one… (more)

Subjects/Keywords: cyclin; mitosis; Clb2; cell cycle; Cell Biology

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APA (6th Edition):

Stutts, D. K. (2010). Role of the mitotic cyclin Clb2 in mitotic regulation. (Thesis). University of Tennessee – Knoxville. Retrieved from https://trace.tennessee.edu/utk_gradthes/752

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Stutts, Dustin K. “Role of the mitotic cyclin Clb2 in mitotic regulation.” 2010. Thesis, University of Tennessee – Knoxville. Accessed April 03, 2020. https://trace.tennessee.edu/utk_gradthes/752.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Stutts, Dustin K. “Role of the mitotic cyclin Clb2 in mitotic regulation.” 2010. Web. 03 Apr 2020.

Vancouver:

Stutts DK. Role of the mitotic cyclin Clb2 in mitotic regulation. [Internet] [Thesis]. University of Tennessee – Knoxville; 2010. [cited 2020 Apr 03]. Available from: https://trace.tennessee.edu/utk_gradthes/752.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Stutts DK. Role of the mitotic cyclin Clb2 in mitotic regulation. [Thesis]. University of Tennessee – Knoxville; 2010. Available from: https://trace.tennessee.edu/utk_gradthes/752

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Washington University in St. Louis

22. Arjes, Heidi Ann. Failsafe Mechanisms Coordinate Cell Division and the Initiation of DNA Replication in Bacteria.

Degree: PhD, Biology and Biomedical Sciences: Molecular Genetics and Genomics, 2014, Washington University in St. Louis

  During the cell cycle, a cell must replicate its DNA, segregate the genome and divide into two identical daughter cells with full chromosomes. This… (more)

Subjects/Keywords: cell cycle; cell division; DNA replication; FtsZ

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APA (6th Edition):

Arjes, H. A. (2014). Failsafe Mechanisms Coordinate Cell Division and the Initiation of DNA Replication in Bacteria. (Doctoral Dissertation). Washington University in St. Louis. Retrieved from https://openscholarship.wustl.edu/etd/1280

Chicago Manual of Style (16th Edition):

Arjes, Heidi Ann. “Failsafe Mechanisms Coordinate Cell Division and the Initiation of DNA Replication in Bacteria.” 2014. Doctoral Dissertation, Washington University in St. Louis. Accessed April 03, 2020. https://openscholarship.wustl.edu/etd/1280.

MLA Handbook (7th Edition):

Arjes, Heidi Ann. “Failsafe Mechanisms Coordinate Cell Division and the Initiation of DNA Replication in Bacteria.” 2014. Web. 03 Apr 2020.

Vancouver:

Arjes HA. Failsafe Mechanisms Coordinate Cell Division and the Initiation of DNA Replication in Bacteria. [Internet] [Doctoral dissertation]. Washington University in St. Louis; 2014. [cited 2020 Apr 03]. Available from: https://openscholarship.wustl.edu/etd/1280.

Council of Science Editors:

Arjes HA. Failsafe Mechanisms Coordinate Cell Division and the Initiation of DNA Replication in Bacteria. [Doctoral Dissertation]. Washington University in St. Louis; 2014. Available from: https://openscholarship.wustl.edu/etd/1280


IUPUI

23. Rohrabaugh, Sara L. Effects of Altering Cell Proliferation on Hematopoietic Stem and Progenitor Cell Function.

Degree: 2011, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

Cell cycle checkpoints guarantee movement through the cell cycle in an appropriate manner. The spindle assembly checkpoint (SAC) ensures the… (more)

Subjects/Keywords: hematopoietic stem cell, hematopoietic progenitor cell, cell cycle; Hematopoietic stem cells; Cell cycle  – Regulation

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APA (6th Edition):

Rohrabaugh, S. L. (2011). Effects of Altering Cell Proliferation on Hematopoietic Stem and Progenitor Cell Function. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/2599

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Rohrabaugh, Sara L. “Effects of Altering Cell Proliferation on Hematopoietic Stem and Progenitor Cell Function.” 2011. Thesis, IUPUI. Accessed April 03, 2020. http://hdl.handle.net/1805/2599.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Rohrabaugh, Sara L. “Effects of Altering Cell Proliferation on Hematopoietic Stem and Progenitor Cell Function.” 2011. Web. 03 Apr 2020.

Vancouver:

Rohrabaugh SL. Effects of Altering Cell Proliferation on Hematopoietic Stem and Progenitor Cell Function. [Internet] [Thesis]. IUPUI; 2011. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/1805/2599.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Rohrabaugh SL. Effects of Altering Cell Proliferation on Hematopoietic Stem and Progenitor Cell Function. [Thesis]. IUPUI; 2011. Available from: http://hdl.handle.net/1805/2599

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


Université de Grenoble

24. Vu Hong, Lien. Les Benzo[e]pyridoindoles, une nouvelle famille d'inhibiteurs de kinase à activité anti-proliférative : Benzo[e]pyridoindole, the novel kinase inhibitor family with antiproliferative activity.

Degree: Docteur es, Biologie cellulaire, 2011, Université de Grenoble

Les Benzo[e]pyridoindoles sont identifiés comme inhibiteurs des kinases Aurora. La molécule la plus active, C1, inhibe efficacement à la fois Aurora B et CHK2. Nous… (more)

Subjects/Keywords: Mitose; Kinase; Cycle cellulaire; Cycle cellulaire; Kinase; Cell cycle; 570

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APA (6th Edition):

Vu Hong, L. (2011). Les Benzo[e]pyridoindoles, une nouvelle famille d'inhibiteurs de kinase à activité anti-proliférative : Benzo[e]pyridoindole, the novel kinase inhibitor family with antiproliferative activity. (Doctoral Dissertation). Université de Grenoble. Retrieved from http://www.theses.fr/2011GRENV049

Chicago Manual of Style (16th Edition):

Vu Hong, Lien. “Les Benzo[e]pyridoindoles, une nouvelle famille d'inhibiteurs de kinase à activité anti-proliférative : Benzo[e]pyridoindole, the novel kinase inhibitor family with antiproliferative activity.” 2011. Doctoral Dissertation, Université de Grenoble. Accessed April 03, 2020. http://www.theses.fr/2011GRENV049.

MLA Handbook (7th Edition):

Vu Hong, Lien. “Les Benzo[e]pyridoindoles, une nouvelle famille d'inhibiteurs de kinase à activité anti-proliférative : Benzo[e]pyridoindole, the novel kinase inhibitor family with antiproliferative activity.” 2011. Web. 03 Apr 2020.

Vancouver:

Vu Hong L. Les Benzo[e]pyridoindoles, une nouvelle famille d'inhibiteurs de kinase à activité anti-proliférative : Benzo[e]pyridoindole, the novel kinase inhibitor family with antiproliferative activity. [Internet] [Doctoral dissertation]. Université de Grenoble; 2011. [cited 2020 Apr 03]. Available from: http://www.theses.fr/2011GRENV049.

Council of Science Editors:

Vu Hong L. Les Benzo[e]pyridoindoles, une nouvelle famille d'inhibiteurs de kinase à activité anti-proliférative : Benzo[e]pyridoindole, the novel kinase inhibitor family with antiproliferative activity. [Doctoral Dissertation]. Université de Grenoble; 2011. Available from: http://www.theses.fr/2011GRENV049


University of Toronto

25. Alexson, Tania O. Redefining Pluripotent Stem Cells: A Cell Cycle Perspective.

Degree: PhD, 2018, University of Toronto

 As it is classically defined, the term stem cell seems at odds with the process of early development where, at least initially, there are no… (more)

Subjects/Keywords: Cell Cycle; Cell Fate; Embryonic Stem Cell; Pluripotency; Stem Cell; 0758

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APA (6th Edition):

Alexson, T. O. (2018). Redefining Pluripotent Stem Cells: A Cell Cycle Perspective. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/89792

Chicago Manual of Style (16th Edition):

Alexson, Tania O. “Redefining Pluripotent Stem Cells: A Cell Cycle Perspective.” 2018. Doctoral Dissertation, University of Toronto. Accessed April 03, 2020. http://hdl.handle.net/1807/89792.

MLA Handbook (7th Edition):

Alexson, Tania O. “Redefining Pluripotent Stem Cells: A Cell Cycle Perspective.” 2018. Web. 03 Apr 2020.

Vancouver:

Alexson TO. Redefining Pluripotent Stem Cells: A Cell Cycle Perspective. [Internet] [Doctoral dissertation]. University of Toronto; 2018. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/1807/89792.

Council of Science Editors:

Alexson TO. Redefining Pluripotent Stem Cells: A Cell Cycle Perspective. [Doctoral Dissertation]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/89792

26. Keifenheim, Daniel L. Cell Size Control in the Fission Yeast Schizosaccharomyces pombe: A Dissertation.

Degree: Interdisciplinary Graduate Program, Biochemistry and Molecular Pharmacology, 2015, U of Massachusetts : Med

  The coordination between cell growth and division is a highly regulated process that is intimately linked to the cell cycle. Efforts to identify an… (more)

Subjects/Keywords: Cell Size; Cell Cycle; Cell Cycle Checkpoints; Cell Division; Schizosaccharomyces; Cell Biology; Cellular and Molecular Physiology

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APA (6th Edition):

Keifenheim, D. L. (2015). Cell Size Control in the Fission Yeast Schizosaccharomyces pombe: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/784

Chicago Manual of Style (16th Edition):

Keifenheim, Daniel L. “Cell Size Control in the Fission Yeast Schizosaccharomyces pombe: A Dissertation.” 2015. Doctoral Dissertation, U of Massachusetts : Med. Accessed April 03, 2020. http://escholarship.umassmed.edu/gsbs_diss/784.

MLA Handbook (7th Edition):

Keifenheim, Daniel L. “Cell Size Control in the Fission Yeast Schizosaccharomyces pombe: A Dissertation.” 2015. Web. 03 Apr 2020.

Vancouver:

Keifenheim DL. Cell Size Control in the Fission Yeast Schizosaccharomyces pombe: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2015. [cited 2020 Apr 03]. Available from: http://escholarship.umassmed.edu/gsbs_diss/784.

Council of Science Editors:

Keifenheim DL. Cell Size Control in the Fission Yeast Schizosaccharomyces pombe: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2015. Available from: http://escholarship.umassmed.edu/gsbs_diss/784


University of Illinois – Chicago

27. Rady, Brian. Transcription Factors E2F Have a Role in Proliferation of Beta-Cells and Development of Type-2 Diabetes.

Degree: 2013, University of Illinois – Chicago

 This work pertains to the search for genetic targets to induce beta-cell proliferation. This proliferation was intended to support the advancement of islet cell transplant… (more)

Subjects/Keywords: Diabetes; cell therapy; beta-cell proliferation; cell-cycle

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APA (6th Edition):

Rady, B. (2013). Transcription Factors E2F Have a Role in Proliferation of Beta-Cells and Development of Type-2 Diabetes. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/10071

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Rady, Brian. “Transcription Factors E2F Have a Role in Proliferation of Beta-Cells and Development of Type-2 Diabetes.” 2013. Thesis, University of Illinois – Chicago. Accessed April 03, 2020. http://hdl.handle.net/10027/10071.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Rady, Brian. “Transcription Factors E2F Have a Role in Proliferation of Beta-Cells and Development of Type-2 Diabetes.” 2013. Web. 03 Apr 2020.

Vancouver:

Rady B. Transcription Factors E2F Have a Role in Proliferation of Beta-Cells and Development of Type-2 Diabetes. [Internet] [Thesis]. University of Illinois – Chicago; 2013. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/10027/10071.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation

Council of Science Editors:

Rady B. Transcription Factors E2F Have a Role in Proliferation of Beta-Cells and Development of Type-2 Diabetes. [Thesis]. University of Illinois – Chicago; 2013. Available from: http://hdl.handle.net/10027/10071

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation


The Ohio State University

28. Collins, Mark Leo. DHFR RNA metabolism during the cell cycle : a critical review.

Degree: PhD, Graduate School, 1983, The Ohio State University

Subjects/Keywords: Chemistry; Cell cycle

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Collins, M. L. (1983). DHFR RNA metabolism during the cell cycle : a critical review. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1487238791269318

Chicago Manual of Style (16th Edition):

Collins, Mark Leo. “DHFR RNA metabolism during the cell cycle : a critical review.” 1983. Doctoral Dissertation, The Ohio State University. Accessed April 03, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487238791269318.

MLA Handbook (7th Edition):

Collins, Mark Leo. “DHFR RNA metabolism during the cell cycle : a critical review.” 1983. Web. 03 Apr 2020.

Vancouver:

Collins ML. DHFR RNA metabolism during the cell cycle : a critical review. [Internet] [Doctoral dissertation]. The Ohio State University; 1983. [cited 2020 Apr 03]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1487238791269318.

Council of Science Editors:

Collins ML. DHFR RNA metabolism during the cell cycle : a critical review. [Doctoral Dissertation]. The Ohio State University; 1983. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1487238791269318


The Ohio State University

29. Evans, David Alan. Modification of the frequency of mitotic crossing in Nicotiana tabacum, Glycine max, and Lycopersicon esculentum using X-rays.

Degree: PhD, Graduate School, 1977, The Ohio State University

Subjects/Keywords: Biology; Cell cycle

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

Evans, D. A. (1977). Modification of the frequency of mitotic crossing in Nicotiana tabacum, Glycine max, and Lycopersicon esculentum using X-rays. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1487064256736819

Chicago Manual of Style (16th Edition):

Evans, David Alan. “Modification of the frequency of mitotic crossing in Nicotiana tabacum, Glycine max, and Lycopersicon esculentum using X-rays.” 1977. Doctoral Dissertation, The Ohio State University. Accessed April 03, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487064256736819.

MLA Handbook (7th Edition):

Evans, David Alan. “Modification of the frequency of mitotic crossing in Nicotiana tabacum, Glycine max, and Lycopersicon esculentum using X-rays.” 1977. Web. 03 Apr 2020.

Vancouver:

Evans DA. Modification of the frequency of mitotic crossing in Nicotiana tabacum, Glycine max, and Lycopersicon esculentum using X-rays. [Internet] [Doctoral dissertation]. The Ohio State University; 1977. [cited 2020 Apr 03]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1487064256736819.

Council of Science Editors:

Evans DA. Modification of the frequency of mitotic crossing in Nicotiana tabacum, Glycine max, and Lycopersicon esculentum using X-rays. [Doctoral Dissertation]. The Ohio State University; 1977. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1487064256736819


Dalhousie University

30. O'Brien, Michael. CHARACTERIZATION OF A NOVEL ISOFORM OF NOS1AP: NOS1APc.

Degree: MS, Department of Pharmacology, 2012, Dalhousie University

 The current study characterizes a novel isoform of the Nitric Oxide Synthase 1 Adaptor Protein (NOS1AP), herein NOS1APc. NOS1APc was identified in a proteomic screen… (more)

Subjects/Keywords: NOS1AP; NOS1APc; Scribble; cerebellum; cell cycle

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APA · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

APA (6th Edition):

O'Brien, M. (2012). CHARACTERIZATION OF A NOVEL ISOFORM OF NOS1AP: NOS1APc. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/15490

Chicago Manual of Style (16th Edition):

O'Brien, Michael. “CHARACTERIZATION OF A NOVEL ISOFORM OF NOS1AP: NOS1APc.” 2012. Masters Thesis, Dalhousie University. Accessed April 03, 2020. http://hdl.handle.net/10222/15490.

MLA Handbook (7th Edition):

O'Brien, Michael. “CHARACTERIZATION OF A NOVEL ISOFORM OF NOS1AP: NOS1APc.” 2012. Web. 03 Apr 2020.

Vancouver:

O'Brien M. CHARACTERIZATION OF A NOVEL ISOFORM OF NOS1AP: NOS1APc. [Internet] [Masters thesis]. Dalhousie University; 2012. [cited 2020 Apr 03]. Available from: http://hdl.handle.net/10222/15490.

Council of Science Editors:

O'Brien M. CHARACTERIZATION OF A NOVEL ISOFORM OF NOS1AP: NOS1APc. [Masters Thesis]. Dalhousie University; 2012. Available from: http://hdl.handle.net/10222/15490

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