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You searched for subject:(Cell cycle ). Showing records 1 – 30 of 1449 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 October 15, 2019. 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. 15 Oct 2019.

Vancouver:

Burbage CD. Picocyanobacterial cellular physiology and trophic interaction with a heterotrophic nanoflagellate. [Internet] [Doctoral dissertation]. University of Georgia; 2007. [cited 2019 Oct 15]. 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 October 15, 2019. 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. 15 Oct 2019.

Vancouver:

Baxter SA. Mechanisms of PROX1 mediated regulation of the lymphatic endothelial cell cycle. [Internet] [Masters thesis]. University of Manitoba; 2010. [cited 2019 Oct 15]. 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


University of Hong Kong

3. 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 October 15, 2019. 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. 15 Oct 2019.

Vancouver:

Ruan Y. Investigating the regulation of UHRF1 in cell cycle. [Internet] [Masters thesis]. University of Hong Kong; 2015. [cited 2019 Oct 15]. 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

4. 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 October 15, 2019. 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. 15 Oct 2019.

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 2019 Oct 15]. 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.


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 October 15, 2019. 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. 15 Oct 2019.

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 2019 Oct 15]. 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 October 15, 2019. 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. 15 Oct 2019.

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 2019 Oct 15]. 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


Case Western Reserve University

7. 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 October 15, 2019. 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. 15 Oct 2019.

Vancouver:

Wang L. CELL CYCLE REGULATION IN THE POST-MITOTIC NEURONAL CELLS. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2007. [cited 2019 Oct 15]. 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

8. 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 October 15, 2019. 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. 15 Oct 2019.

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 2019 Oct 15]. 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

9. 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 October 15, 2019. 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. 15 Oct 2019.

Vancouver:

Worthington DH. Hydroxyurea : physiological effects on Tetrahymena pyriformis and use in cell cycle analysis. [Internet] [Doctoral dissertation]. Oregon State University; 1973. [cited 2019 Oct 15]. 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


McMaster University

10. Almawi, Ahmad. Protein-protein interactions that mediate cell cycle events.

Degree: PhD, 2018, McMaster University

Molecular recognition is at the core of all biological processes whereby protein-protein interactions (PPI) relay messages to drive signaling events. However, many regulatory responses are… (more)

Subjects/Keywords: Cell cycle; crystallography; protein interactions.

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APA (6th Edition):

Almawi, A. (2018). Protein-protein interactions that mediate cell cycle events. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/24282

Chicago Manual of Style (16th Edition):

Almawi, Ahmad. “Protein-protein interactions that mediate cell cycle events.” 2018. Doctoral Dissertation, McMaster University. Accessed October 15, 2019. http://hdl.handle.net/11375/24282.

MLA Handbook (7th Edition):

Almawi, Ahmad. “Protein-protein interactions that mediate cell cycle events.” 2018. Web. 15 Oct 2019.

Vancouver:

Almawi A. Protein-protein interactions that mediate cell cycle events. [Internet] [Doctoral dissertation]. McMaster University; 2018. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/11375/24282.

Council of Science Editors:

Almawi A. Protein-protein interactions that mediate cell cycle events. [Doctoral Dissertation]. McMaster University; 2018. Available from: http://hdl.handle.net/11375/24282


Hong Kong University of Science and Technology

11. 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 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 October 15, 2019. 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. 15 Oct 2019.

Vancouver:

Qin YL. The role of hNOC3 in human DNA replication. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2013. [cited 2019 Oct 15]. Available from: 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: 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

12. 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 (6th Edition):

Zhao, Y. L. (2015). Functional study of GAS2L1 in mitosis. (Thesis). Hong Kong University of Science and Technology. Retrieved from 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 October 15, 2019. 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. 15 Oct 2019.

Vancouver:

Zhao YL. Functional study of GAS2L1 in mitosis. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2015. [cited 2019 Oct 15]. Available from: 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: 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


Vanderbilt University

13. 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 October 15, 2019. 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. 15 Oct 2019.

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 2019 Oct 15]. 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/ ;


University of New Mexico

14. Quintana, Anita. Changes in c-Myb activity during proliferation.

Degree: Biomedical Sciences Graduate Program, 2010, University of New Mexico

 c-myb encodes a transcription factor and is the cellular parent of the v-myb oncogene, which causes acute myeloid leukemia in chickens and mice. Truncation or… (more)

Subjects/Keywords: c-myb; cell cycle

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APA (6th Edition):

Quintana, A. (2010). Changes in c-Myb activity during proliferation. (Doctoral Dissertation). University of New Mexico. Retrieved from https://digitalrepository.unm.edu/biom_etds/20

Chicago Manual of Style (16th Edition):

Quintana, Anita. “Changes in c-Myb activity during proliferation.” 2010. Doctoral Dissertation, University of New Mexico. Accessed October 15, 2019. https://digitalrepository.unm.edu/biom_etds/20.

MLA Handbook (7th Edition):

Quintana, Anita. “Changes in c-Myb activity during proliferation.” 2010. Web. 15 Oct 2019.

Vancouver:

Quintana A. Changes in c-Myb activity during proliferation. [Internet] [Doctoral dissertation]. University of New Mexico; 2010. [cited 2019 Oct 15]. Available from: https://digitalrepository.unm.edu/biom_etds/20.

Council of Science Editors:

Quintana A. Changes in c-Myb activity during proliferation. [Doctoral Dissertation]. University of New Mexico; 2010. Available from: https://digitalrepository.unm.edu/biom_etds/20


University of Texas Southwestern Medical Center

15. 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 (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 October 15, 2019. 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. 15 Oct 2019.

Vancouver:

Chaudhary J. Function And Recruitment Of Centromeric Heterochromatin Protein 1. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2011. [cited 2019 Oct 15]. 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

16. 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 October 15, 2019. 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. 15 Oct 2019.

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 2019 Oct 15]. 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


University of Sydney

17. 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 October 15, 2019. 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. 15 Oct 2019.

Vancouver:

Dokumcu KA. Non-encoded Mechanisms of Stress Adaptation in Cancer . [Internet] [Thesis]. University of Sydney; 2019. [cited 2019 Oct 15]. 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 Hong Kong

18. 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 (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 October 15, 2019. 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. 15 Oct 2019.

Vancouver:

Zheng F. Molecular mechanisms regulating bipolar spindle formation and microtubule depolymerization. [Internet] [Doctoral dissertation]. University of Hong Kong; 2015. [cited 2019 Oct 15]. 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


Washington University in St. Louis

19. 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 October 15, 2019. 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. 15 Oct 2019.

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 2019 Oct 15]. 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


University of Tennessee – Knoxville

20. 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 October 15, 2019. 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. 15 Oct 2019.

Vancouver:

Stutts DK. Role of the mitotic cyclin Clb2 in mitotic regulation. [Internet] [Thesis]. University of Tennessee – Knoxville; 2010. [cited 2019 Oct 15]. 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


University of Notre Dame

21. 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 October 15, 2019. 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. 15 Oct 2019.

Vancouver:

Jeffrey R. Effects of the Anti-Androgen Bicalutamide on Prostate Cancer Cells</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2012. [cited 2019 Oct 15]. 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


IUPUI

22. 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 October 15, 2019. 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. 15 Oct 2019.

Vancouver:

Rohrabaugh SL. Effects of Altering Cell Proliferation on Hematopoietic Stem and Progenitor Cell Function. [Internet] [Thesis]. IUPUI; 2011. [cited 2019 Oct 15]. 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


University of Illinois – Urbana-Champaign

23. Sridharan, Santhipriyadar. The role of conexin 43 in murine sertoli cell development.

Degree: PhD, 0357, 2010, University of Illinois – Urbana-Champaign

 Sertoli cells are the only somatic cell type present within the seminiferous tubules of the testis. The support of these somatic cells is essential for… (more)

Subjects/Keywords: Sertoli cell; gap junctions; Connexin 43; Sertoli cell development; cell cycle; cell cycle regulators

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APA (6th Edition):

Sridharan, S. (2010). The role of conexin 43 in murine sertoli cell development. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/16108

Chicago Manual of Style (16th Edition):

Sridharan, Santhipriyadar. “The role of conexin 43 in murine sertoli cell development.” 2010. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed October 15, 2019. http://hdl.handle.net/2142/16108.

MLA Handbook (7th Edition):

Sridharan, Santhipriyadar. “The role of conexin 43 in murine sertoli cell development.” 2010. Web. 15 Oct 2019.

Vancouver:

Sridharan S. The role of conexin 43 in murine sertoli cell development. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2010. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/2142/16108.

Council of Science Editors:

Sridharan S. The role of conexin 43 in murine sertoli cell development. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2010. Available from: http://hdl.handle.net/2142/16108


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 October 15, 2019. 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. 15 Oct 2019.

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 2019 Oct 15]. 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

25. 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 October 15, 2019. 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. 15 Oct 2019.

Vancouver:

Keifenheim DL. Cell Size Control in the Fission Yeast Schizosaccharomyces pombe: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2015. [cited 2019 Oct 15]. 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

26. 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 October 15, 2019. 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. 15 Oct 2019.

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 2019 Oct 15]. 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

27. 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 (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 October 15, 2019. 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. 15 Oct 2019.

Vancouver:

Collins ML. DHFR RNA metabolism during the cell cycle : a critical review. [Internet] [Doctoral dissertation]. The Ohio State University; 1983. [cited 2019 Oct 15]. 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

28. 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 October 15, 2019. 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. 15 Oct 2019.

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 2019 Oct 15]. 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

29. 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 October 15, 2019. http://hdl.handle.net/10222/15490.

MLA Handbook (7th Edition):

O'Brien, Michael. “CHARACTERIZATION OF A NOVEL ISOFORM OF NOS1AP: NOS1APc.” 2012. Web. 15 Oct 2019.

Vancouver:

O'Brien M. CHARACTERIZATION OF A NOVEL ISOFORM OF NOS1AP: NOS1APc. [Internet] [Masters thesis]. Dalhousie University; 2012. [cited 2019 Oct 15]. 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

30. MORITA, HIROSHI. Characterization of phosphodiesterase 2A in human malignant melanoma PMP cells.

Degree: 博士(医学), 2017, Mie University / 三重大学

The prognosis for malignant melanoma is poor; therefore, new diagnostic methods and treatment strategies are urgently needed. Phosphodiesterase 2 (PDE2) is one of 21 phosphodiesterases,… (more)

Subjects/Keywords: malignant melanoma; phosphodiesterase 2A; cell cycle

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APA (6th Edition):

MORITA, H. (2017). Characterization of phosphodiesterase 2A in human malignant melanoma PMP cells. (Thesis). Mie University / 三重大学. Retrieved from http://hdl.handle.net/10076/13987

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):

MORITA, HIROSHI. “Characterization of phosphodiesterase 2A in human malignant melanoma PMP cells.” 2017. Thesis, Mie University / 三重大学. Accessed October 15, 2019. http://hdl.handle.net/10076/13987.

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

MLA Handbook (7th Edition):

MORITA, HIROSHI. “Characterization of phosphodiesterase 2A in human malignant melanoma PMP cells.” 2017. Web. 15 Oct 2019.

Vancouver:

MORITA H. Characterization of phosphodiesterase 2A in human malignant melanoma PMP cells. [Internet] [Thesis]. Mie University / 三重大学; 2017. [cited 2019 Oct 15]. Available from: http://hdl.handle.net/10076/13987.

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

Council of Science Editors:

MORITA H. Characterization of phosphodiesterase 2A in human malignant melanoma PMP cells. [Thesis]. Mie University / 三重大学; 2017. Available from: http://hdl.handle.net/10076/13987

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

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