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You searched for subject:(mitosis). Showing records 1 – 30 of 457 total matches.

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University of Manchester

1. Bennett, Ailsa. Exploiting mitosis to improve anti-cancer strategies.

Degree: 2017, University of Manchester

 Antimitotics are used in cancer chemotherapy for the treatment of cancers such as breast, ovarian, lung and prostate. Despite the success of agents such as… (more)

Subjects/Keywords: mitosis; apoptosis

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

APA (6th Edition):

Bennett, A. (2017). Exploiting mitosis to improve anti-cancer strategies. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:306798

Chicago Manual of Style (16th Edition):

Bennett, Ailsa. “Exploiting mitosis to improve anti-cancer strategies.” 2017. Doctoral Dissertation, University of Manchester. Accessed January 18, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:306798.

MLA Handbook (7th Edition):

Bennett, Ailsa. “Exploiting mitosis to improve anti-cancer strategies.” 2017. Web. 18 Jan 2020.

Vancouver:

Bennett A. Exploiting mitosis to improve anti-cancer strategies. [Internet] [Doctoral dissertation]. University of Manchester; 2017. [cited 2020 Jan 18]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:306798.

Council of Science Editors:

Bennett A. Exploiting mitosis to improve anti-cancer strategies. [Doctoral Dissertation]. University of Manchester; 2017. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:306798


University of Adelaide

2. John, Ulrik Peter. Isolation and characterisation of three rows, a gene essential for mitotic chromosome disjunction in Drosophila melanogaster / a thesis submiited for the degree of Doctor of Philosophy by Ulrik Peter John.

Degree: 1995, University of Adelaide

Concerns the characterisation of a gene, three throws, whose mutant phenotype of failure of chromosome disjunction in anaphase, is indicative of an essential but unknown function in mitosis. Advisors/Committee Members: Dept. of Genetics (school).

Subjects/Keywords: Mitosis

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APA (6th Edition):

John, U. P. (1995). Isolation and characterisation of three rows, a gene essential for mitotic chromosome disjunction in Drosophila melanogaster / a thesis submiited for the degree of Doctor of Philosophy by Ulrik Peter John. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/18500

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):

John, Ulrik Peter. “Isolation and characterisation of three rows, a gene essential for mitotic chromosome disjunction in Drosophila melanogaster / a thesis submiited for the degree of Doctor of Philosophy by Ulrik Peter John.” 1995. Thesis, University of Adelaide. Accessed January 18, 2020. http://hdl.handle.net/2440/18500.

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

MLA Handbook (7th Edition):

John, Ulrik Peter. “Isolation and characterisation of three rows, a gene essential for mitotic chromosome disjunction in Drosophila melanogaster / a thesis submiited for the degree of Doctor of Philosophy by Ulrik Peter John.” 1995. Web. 18 Jan 2020.

Vancouver:

John UP. Isolation and characterisation of three rows, a gene essential for mitotic chromosome disjunction in Drosophila melanogaster / a thesis submiited for the degree of Doctor of Philosophy by Ulrik Peter John. [Internet] [Thesis]. University of Adelaide; 1995. [cited 2020 Jan 18]. Available from: http://hdl.handle.net/2440/18500.

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

Council of Science Editors:

John UP. Isolation and characterisation of three rows, a gene essential for mitotic chromosome disjunction in Drosophila melanogaster / a thesis submiited for the degree of Doctor of Philosophy by Ulrik Peter John. [Thesis]. University of Adelaide; 1995. Available from: http://hdl.handle.net/2440/18500

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


Georgia Tech

3. Koza, Robert Wayne. A study of hypotheses on the role of electrical forces in mitosis.

Degree: MS, Physics, 1948, Georgia Tech

Subjects/Keywords: Mitosis

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APA (6th Edition):

Koza, R. W. (1948). A study of hypotheses on the role of electrical forces in mitosis. (Masters Thesis). Georgia Tech. Retrieved from http://hdl.handle.net/1853/29437

Chicago Manual of Style (16th Edition):

Koza, Robert Wayne. “A study of hypotheses on the role of electrical forces in mitosis.” 1948. Masters Thesis, Georgia Tech. Accessed January 18, 2020. http://hdl.handle.net/1853/29437.

MLA Handbook (7th Edition):

Koza, Robert Wayne. “A study of hypotheses on the role of electrical forces in mitosis.” 1948. Web. 18 Jan 2020.

Vancouver:

Koza RW. A study of hypotheses on the role of electrical forces in mitosis. [Internet] [Masters thesis]. Georgia Tech; 1948. [cited 2020 Jan 18]. Available from: http://hdl.handle.net/1853/29437.

Council of Science Editors:

Koza RW. A study of hypotheses on the role of electrical forces in mitosis. [Masters Thesis]. Georgia Tech; 1948. Available from: http://hdl.handle.net/1853/29437


Hong Kong University of Science and Technology

4. Wong, Wing Ki. The functions of a short form of shugoshin 1 in mitosis.

Degree: 2012, Hong Kong University of Science and Technology

 Proper chromosome segregation largely relies on the persistence of sister chromatid cohesion until anaphase as well as the correct attachment of microtubules to kinetochores. Premature… (more)

Subjects/Keywords: Mitosis ; Proteins

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APA (6th Edition):

Wong, W. K. (2012). The functions of a short form of shugoshin 1 in mitosis. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-73404 ; https://doi.org/10.14711/thesis-b1190145 ; http://repository.ust.hk/ir/bitstream/1783.1-73404/1/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):

Wong, Wing Ki. “The functions of a short form of shugoshin 1 in mitosis.” 2012. Thesis, Hong Kong University of Science and Technology. Accessed January 18, 2020. http://repository.ust.hk/ir/Record/1783.1-73404 ; https://doi.org/10.14711/thesis-b1190145 ; http://repository.ust.hk/ir/bitstream/1783.1-73404/1/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):

Wong, Wing Ki. “The functions of a short form of shugoshin 1 in mitosis.” 2012. Web. 18 Jan 2020.

Vancouver:

Wong WK. The functions of a short form of shugoshin 1 in mitosis. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2012. [cited 2020 Jan 18]. Available from: http://repository.ust.hk/ir/Record/1783.1-73404 ; https://doi.org/10.14711/thesis-b1190145 ; http://repository.ust.hk/ir/bitstream/1783.1-73404/1/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:

Wong WK. The functions of a short form of shugoshin 1 in mitosis. [Thesis]. Hong Kong University of Science and Technology; 2012. Available from: http://repository.ust.hk/ir/Record/1783.1-73404 ; https://doi.org/10.14711/thesis-b1190145 ; http://repository.ust.hk/ir/bitstream/1783.1-73404/1/th_redirect.html

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


Columbia University

5. Wynne, Caitlin Lazar. Molecular Dissection of Nde1's Role in Mitosis.

Degree: 2016, Columbia University

 Upon entry into G2 and mitosis (G2/M), dynein dissociates from its interphase cargos and forms mitotic-specific interactions that direct dynein to the nuclear envelope, cell-cortex,… (more)

Subjects/Keywords: Mitosis; Cytology; Mitosis – Regulation; Dynein; Biology

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APA (6th Edition):

Wynne, C. L. (2016). Molecular Dissection of Nde1's Role in Mitosis. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8KH0NMD

Chicago Manual of Style (16th Edition):

Wynne, Caitlin Lazar. “Molecular Dissection of Nde1's Role in Mitosis.” 2016. Doctoral Dissertation, Columbia University. Accessed January 18, 2020. https://doi.org/10.7916/D8KH0NMD.

MLA Handbook (7th Edition):

Wynne, Caitlin Lazar. “Molecular Dissection of Nde1's Role in Mitosis.” 2016. Web. 18 Jan 2020.

Vancouver:

Wynne CL. Molecular Dissection of Nde1's Role in Mitosis. [Internet] [Doctoral dissertation]. Columbia University; 2016. [cited 2020 Jan 18]. Available from: https://doi.org/10.7916/D8KH0NMD.

Council of Science Editors:

Wynne CL. Molecular Dissection of Nde1's Role in Mitosis. [Doctoral Dissertation]. Columbia University; 2016. Available from: https://doi.org/10.7916/D8KH0NMD


University of Manchester

6. Bennett, Ailsa. Exploiting mitosis to improve anti-cancer strategies.

Degree: PhD, 2017, University of Manchester

 Antimitotics are used in cancer chemotherapy for the treatment of cancers such as breast, ovarian, lung and prostate. Despite the success of agents such as… (more)

Subjects/Keywords: 616.99; mitosis; apoptosis

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

APA (6th Edition):

Bennett, A. (2017). Exploiting mitosis to improve anti-cancer strategies. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/exploiting-mitosis-to-improve-anticancer-strategies(b29182a1-2f37-47cb-8dc5-cbef76786dd2).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.703036

Chicago Manual of Style (16th Edition):

Bennett, Ailsa. “Exploiting mitosis to improve anti-cancer strategies.” 2017. Doctoral Dissertation, University of Manchester. Accessed January 18, 2020. https://www.research.manchester.ac.uk/portal/en/theses/exploiting-mitosis-to-improve-anticancer-strategies(b29182a1-2f37-47cb-8dc5-cbef76786dd2).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.703036.

MLA Handbook (7th Edition):

Bennett, Ailsa. “Exploiting mitosis to improve anti-cancer strategies.” 2017. Web. 18 Jan 2020.

Vancouver:

Bennett A. Exploiting mitosis to improve anti-cancer strategies. [Internet] [Doctoral dissertation]. University of Manchester; 2017. [cited 2020 Jan 18]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/exploiting-mitosis-to-improve-anticancer-strategies(b29182a1-2f37-47cb-8dc5-cbef76786dd2).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.703036.

Council of Science Editors:

Bennett A. Exploiting mitosis to improve anti-cancer strategies. [Doctoral Dissertation]. University of Manchester; 2017. Available from: https://www.research.manchester.ac.uk/portal/en/theses/exploiting-mitosis-to-improve-anticancer-strategies(b29182a1-2f37-47cb-8dc5-cbef76786dd2).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.703036


University of Notre Dame

7. Colleen Therese Cole. Differential Targeting of Cytoplasmic Dynein During Mitosis by Site Specific Phosphorylation</h1>.

Degree: MS, Biological Sciences, 2011, University of Notre Dame

  The motor protein cytoplasmic dynein has been implicated in mitotic functions that require dynein localization to specific cellular locations. Recent studies in our lab… (more)

Subjects/Keywords: mitosis; phosphorylation; dynein

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APA (6th Edition):

Cole, C. T. (2011). Differential Targeting of Cytoplasmic Dynein During Mitosis by Site Specific Phosphorylation</h1>. (Masters Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/0k225b01f90

Chicago Manual of Style (16th Edition):

Cole, Colleen Therese. “Differential Targeting of Cytoplasmic Dynein During Mitosis by Site Specific Phosphorylation</h1>.” 2011. Masters Thesis, University of Notre Dame. Accessed January 18, 2020. https://curate.nd.edu/show/0k225b01f90.

MLA Handbook (7th Edition):

Cole, Colleen Therese. “Differential Targeting of Cytoplasmic Dynein During Mitosis by Site Specific Phosphorylation</h1>.” 2011. Web. 18 Jan 2020.

Vancouver:

Cole CT. Differential Targeting of Cytoplasmic Dynein During Mitosis by Site Specific Phosphorylation</h1>. [Internet] [Masters thesis]. University of Notre Dame; 2011. [cited 2020 Jan 18]. Available from: https://curate.nd.edu/show/0k225b01f90.

Council of Science Editors:

Cole CT. Differential Targeting of Cytoplasmic Dynein During Mitosis by Site Specific Phosphorylation</h1>. [Masters Thesis]. University of Notre Dame; 2011. Available from: https://curate.nd.edu/show/0k225b01f90


University of Notre Dame

8. James Kasuboski. Mitotic Kinases That Build a Dynein-Binding Platform on Kinetochores</h1>.

Degree: PhD, Biological Sciences, 2011, University of Notre Dame

Mitosis is a series of intricate and complex events that take place during each cell cycle. Regulation of mitosis is especially important at the… (more)

Subjects/Keywords: cell division; mitosis

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APA (6th Edition):

Kasuboski, J. (2011). Mitotic Kinases That Build a Dynein-Binding Platform on Kinetochores</h1>. (Doctoral Dissertation). University of Notre Dame. Retrieved from https://curate.nd.edu/show/8k71ng4715d

Chicago Manual of Style (16th Edition):

Kasuboski, James. “Mitotic Kinases That Build a Dynein-Binding Platform on Kinetochores</h1>.” 2011. Doctoral Dissertation, University of Notre Dame. Accessed January 18, 2020. https://curate.nd.edu/show/8k71ng4715d.

MLA Handbook (7th Edition):

Kasuboski, James. “Mitotic Kinases That Build a Dynein-Binding Platform on Kinetochores</h1>.” 2011. Web. 18 Jan 2020.

Vancouver:

Kasuboski J. Mitotic Kinases That Build a Dynein-Binding Platform on Kinetochores</h1>. [Internet] [Doctoral dissertation]. University of Notre Dame; 2011. [cited 2020 Jan 18]. Available from: https://curate.nd.edu/show/8k71ng4715d.

Council of Science Editors:

Kasuboski J. Mitotic Kinases That Build a Dynein-Binding Platform on Kinetochores</h1>. [Doctoral Dissertation]. University of Notre Dame; 2011. Available from: https://curate.nd.edu/show/8k71ng4715d


Boston College

9. Farrell, Megan Christine. Deciphering the Role of Kinetochores and Microtubules During Interphase and Mitosis in Toxoplasma Gondii.

Degree: PhD, Biology, 2014, Boston College

 The obligate intracellular parasite Toxoplasma gondii exhibits closed mitosis, as chromosome segregation occurs with the confines of the nuclear envelope. Distinct structural changes are absent… (more)

Subjects/Keywords: kinetochore; mitosis; Toxoplasma

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APA (6th Edition):

Farrell, M. C. (2014). Deciphering the Role of Kinetochores and Microtubules During Interphase and Mitosis in Toxoplasma Gondii. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:101634

Chicago Manual of Style (16th Edition):

Farrell, Megan Christine. “Deciphering the Role of Kinetochores and Microtubules During Interphase and Mitosis in Toxoplasma Gondii.” 2014. Doctoral Dissertation, Boston College. Accessed January 18, 2020. http://dlib.bc.edu/islandora/object/bc-ir:101634.

MLA Handbook (7th Edition):

Farrell, Megan Christine. “Deciphering the Role of Kinetochores and Microtubules During Interphase and Mitosis in Toxoplasma Gondii.” 2014. Web. 18 Jan 2020.

Vancouver:

Farrell MC. Deciphering the Role of Kinetochores and Microtubules During Interphase and Mitosis in Toxoplasma Gondii. [Internet] [Doctoral dissertation]. Boston College; 2014. [cited 2020 Jan 18]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101634.

Council of Science Editors:

Farrell MC. Deciphering the Role of Kinetochores and Microtubules During Interphase and Mitosis in Toxoplasma Gondii. [Doctoral Dissertation]. Boston College; 2014. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101634


University of New South Wales

10. Rasouli, Mina. Blocking mitotic exit as a potential target for combination therapy with anti-mitotic drugs.

Degree: Clinical School - St Vincent's Hospital, 2016, University of New South Wales

 Recent efforts in cancer therapy investigations have been focused on developing a rational strategy to specifically target cancer cells to reduce toxic side effects. Uncontrolled… (more)

Subjects/Keywords: Cancer; Mitosis; PP2A

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APA (6th Edition):

Rasouli, M. (2016). Blocking mitotic exit as a potential target for combination therapy with anti-mitotic drugs. (Masters Thesis). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/55846 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:39532/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Rasouli, Mina. “Blocking mitotic exit as a potential target for combination therapy with anti-mitotic drugs.” 2016. Masters Thesis, University of New South Wales. Accessed January 18, 2020. http://handle.unsw.edu.au/1959.4/55846 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:39532/SOURCE02?view=true.

MLA Handbook (7th Edition):

Rasouli, Mina. “Blocking mitotic exit as a potential target for combination therapy with anti-mitotic drugs.” 2016. Web. 18 Jan 2020.

Vancouver:

Rasouli M. Blocking mitotic exit as a potential target for combination therapy with anti-mitotic drugs. [Internet] [Masters thesis]. University of New South Wales; 2016. [cited 2020 Jan 18]. Available from: http://handle.unsw.edu.au/1959.4/55846 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:39532/SOURCE02?view=true.

Council of Science Editors:

Rasouli M. Blocking mitotic exit as a potential target for combination therapy with anti-mitotic drugs. [Masters Thesis]. University of New South Wales; 2016. Available from: http://handle.unsw.edu.au/1959.4/55846 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:39532/SOURCE02?view=true


University of Alberta

11. Heit, Ryan. Epigenetic Regulation of Centromere Formation and Kinetochore Function.

Degree: MS, Department of Oncology, 2009, University of Alberta

 One form of protein regulation is accomplished by post-translational modification (PTM). In order to test the importance one type of PTM, methylation, in chromosome segregation,… (more)

Subjects/Keywords: centromere; methylation; mitosis; histones

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APA (6th Edition):

Heit, R. (2009). Epigenetic Regulation of Centromere Formation and Kinetochore Function. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/fx719n183

Chicago Manual of Style (16th Edition):

Heit, Ryan. “Epigenetic Regulation of Centromere Formation and Kinetochore Function.” 2009. Masters Thesis, University of Alberta. Accessed January 18, 2020. https://era.library.ualberta.ca/files/fx719n183.

MLA Handbook (7th Edition):

Heit, Ryan. “Epigenetic Regulation of Centromere Formation and Kinetochore Function.” 2009. Web. 18 Jan 2020.

Vancouver:

Heit R. Epigenetic Regulation of Centromere Formation and Kinetochore Function. [Internet] [Masters thesis]. University of Alberta; 2009. [cited 2020 Jan 18]. Available from: https://era.library.ualberta.ca/files/fx719n183.

Council of Science Editors:

Heit R. Epigenetic Regulation of Centromere Formation and Kinetochore Function. [Masters Thesis]. University of Alberta; 2009. Available from: https://era.library.ualberta.ca/files/fx719n183


Universiteit Utrecht

12. Pennings, C. Molecular composition and function of the kinetochore-microtubule interface in chromosome segregation.

Degree: 2014, Universiteit Utrecht

 Stable kinetochore-microtubule attachments are essential for equal division of chromosomes among daughter cells. To correctly separate chromosomes in mitosis, kinetochores must capture and bind spindle… (more)

Subjects/Keywords: Mitosis; kinetochore; microtubule; chromosome segregation

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APA (6th Edition):

Pennings, C. (2014). Molecular composition and function of the kinetochore-microtubule interface in chromosome segregation. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/292969

Chicago Manual of Style (16th Edition):

Pennings, C. “Molecular composition and function of the kinetochore-microtubule interface in chromosome segregation.” 2014. Masters Thesis, Universiteit Utrecht. Accessed January 18, 2020. http://dspace.library.uu.nl:8080/handle/1874/292969.

MLA Handbook (7th Edition):

Pennings, C. “Molecular composition and function of the kinetochore-microtubule interface in chromosome segregation.” 2014. Web. 18 Jan 2020.

Vancouver:

Pennings C. Molecular composition and function of the kinetochore-microtubule interface in chromosome segregation. [Internet] [Masters thesis]. Universiteit Utrecht; 2014. [cited 2020 Jan 18]. Available from: http://dspace.library.uu.nl:8080/handle/1874/292969.

Council of Science Editors:

Pennings C. Molecular composition and function of the kinetochore-microtubule interface in chromosome segregation. [Masters Thesis]. Universiteit Utrecht; 2014. Available from: http://dspace.library.uu.nl:8080/handle/1874/292969


University of Edinburgh

13. Martin, Carol-Anne. Role of microcephalin at mitosis.

Degree: PhD, 2011, University of Edinburgh

 A large brain is one of the most distinguishing features of humans compared to other members of the animal kingdom. During mammalian evolution there has… (more)

Subjects/Keywords: 572; Primary microcephaly; MCPH1; Mitosis

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APA (6th Edition):

Martin, C. (2011). Role of microcephalin at mitosis. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/8734

Chicago Manual of Style (16th Edition):

Martin, Carol-Anne. “Role of microcephalin at mitosis.” 2011. Doctoral Dissertation, University of Edinburgh. Accessed January 18, 2020. http://hdl.handle.net/1842/8734.

MLA Handbook (7th Edition):

Martin, Carol-Anne. “Role of microcephalin at mitosis.” 2011. Web. 18 Jan 2020.

Vancouver:

Martin C. Role of microcephalin at mitosis. [Internet] [Doctoral dissertation]. University of Edinburgh; 2011. [cited 2020 Jan 18]. Available from: http://hdl.handle.net/1842/8734.

Council of Science Editors:

Martin C. Role of microcephalin at mitosis. [Doctoral Dissertation]. University of Edinburgh; 2011. Available from: http://hdl.handle.net/1842/8734


University of Pennsylvania

14. Palozola, Katherine. Global Mitotic Transcription And Reactivation During Mitotic Exit: A Potential Epigenetic Mechanism.

Degree: 2017, University of Pennsylvania

 The genome is thought to be transcriptionally silent during mitosis. Decades of studies have used antibody-based detection of proteins in fixed cells to show that… (more)

Subjects/Keywords: epigenetics; mitosis; transcription; Molecular Biology

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APA (6th Edition):

Palozola, K. (2017). Global Mitotic Transcription And Reactivation During Mitotic Exit: A Potential Epigenetic Mechanism. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/2942

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):

Palozola, Katherine. “Global Mitotic Transcription And Reactivation During Mitotic Exit: A Potential Epigenetic Mechanism.” 2017. Thesis, University of Pennsylvania. Accessed January 18, 2020. https://repository.upenn.edu/edissertations/2942.

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

MLA Handbook (7th Edition):

Palozola, Katherine. “Global Mitotic Transcription And Reactivation During Mitotic Exit: A Potential Epigenetic Mechanism.” 2017. Web. 18 Jan 2020.

Vancouver:

Palozola K. Global Mitotic Transcription And Reactivation During Mitotic Exit: A Potential Epigenetic Mechanism. [Internet] [Thesis]. University of Pennsylvania; 2017. [cited 2020 Jan 18]. Available from: https://repository.upenn.edu/edissertations/2942.

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

Council of Science Editors:

Palozola K. Global Mitotic Transcription And Reactivation During Mitotic Exit: A Potential Epigenetic Mechanism. [Thesis]. University of Pennsylvania; 2017. Available from: https://repository.upenn.edu/edissertations/2942

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


Osaka University

15. 陳, 麗晶; Tan, Li Jing. Xeroderma pigmentosum group F protein binds to Eg5 and functions in mitosis : Implications for XP-F : 色素性乾皮症F群蛋白質はキネシンEg5と結合し、細胞分裂に寄与する : XP-F 群患者の病態との関連性; シキソセイ カンピショウ Fグン タンパクシツ ハ キネシンEg5 ト ケツゴウシ サイボウ ブンレツ 二 キヨ スル XP-Fグン カンジャ ノ ビョウタイ トノ カンレンセイ.

Degree: 博士(生命機能学), 2011, Osaka University

This is the author's version of a work that was accepted for publication in Genes to Cells. Changes resulting from the publishing process, such as… (more)

Subjects/Keywords: XPF; Eg5; mitosis; accelerated aging

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APA (6th Edition):

陳, 麗晶; Tan, L. J. (2011). Xeroderma pigmentosum group F protein binds to Eg5 and functions in mitosis : Implications for XP-F : 色素性乾皮症F群蛋白質はキネシンEg5と結合し、細胞分裂に寄与する : XP-F 群患者の病態との関連性; シキソセイ カンピショウ Fグン タンパクシツ ハ キネシンEg5 ト ケツゴウシ サイボウ ブンレツ 二 キヨ スル XP-Fグン カンジャ ノ ビョウタイ トノ カンレンセイ. (Thesis). Osaka University. Retrieved from http://hdl.handle.net/11094/54698

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):

陳, 麗晶; Tan, Li Jing. “Xeroderma pigmentosum group F protein binds to Eg5 and functions in mitosis : Implications for XP-F : 色素性乾皮症F群蛋白質はキネシンEg5と結合し、細胞分裂に寄与する : XP-F 群患者の病態との関連性; シキソセイ カンピショウ Fグン タンパクシツ ハ キネシンEg5 ト ケツゴウシ サイボウ ブンレツ 二 キヨ スル XP-Fグン カンジャ ノ ビョウタイ トノ カンレンセイ.” 2011. Thesis, Osaka University. Accessed January 18, 2020. http://hdl.handle.net/11094/54698.

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

MLA Handbook (7th Edition):

陳, 麗晶; Tan, Li Jing. “Xeroderma pigmentosum group F protein binds to Eg5 and functions in mitosis : Implications for XP-F : 色素性乾皮症F群蛋白質はキネシンEg5と結合し、細胞分裂に寄与する : XP-F 群患者の病態との関連性; シキソセイ カンピショウ Fグン タンパクシツ ハ キネシンEg5 ト ケツゴウシ サイボウ ブンレツ 二 キヨ スル XP-Fグン カンジャ ノ ビョウタイ トノ カンレンセイ.” 2011. Web. 18 Jan 2020.

Vancouver:

陳, 麗晶; Tan LJ. Xeroderma pigmentosum group F protein binds to Eg5 and functions in mitosis : Implications for XP-F : 色素性乾皮症F群蛋白質はキネシンEg5と結合し、細胞分裂に寄与する : XP-F 群患者の病態との関連性; シキソセイ カンピショウ Fグン タンパクシツ ハ キネシンEg5 ト ケツゴウシ サイボウ ブンレツ 二 キヨ スル XP-Fグン カンジャ ノ ビョウタイ トノ カンレンセイ. [Internet] [Thesis]. Osaka University; 2011. [cited 2020 Jan 18]. Available from: http://hdl.handle.net/11094/54698.

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

Council of Science Editors:

陳, 麗晶; Tan LJ. Xeroderma pigmentosum group F protein binds to Eg5 and functions in mitosis : Implications for XP-F : 色素性乾皮症F群蛋白質はキネシンEg5と結合し、細胞分裂に寄与する : XP-F 群患者の病態との関連性; シキソセイ カンピショウ Fグン タンパクシツ ハ キネシンEg5 ト ケツゴウシ サイボウ ブンレツ 二 キヨ スル XP-Fグン カンジャ ノ ビョウタイ トノ カンレンセイ. [Thesis]. Osaka University; 2011. Available from: http://hdl.handle.net/11094/54698

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


University of Manchester

16. Sloss, Olivia. The functional role of Mcl-1 in the dynamics of mitotic cell fate.

Degree: 2015, University of Manchester

Drugs that alter microtubule dynamics are often used in chemotherapy regimes in combination with other agents in order to treat various cancers. Despite the success… (more)

Subjects/Keywords: mitosis; Mcl-1; cell fate

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

APA (6th Edition):

Sloss, O. (2015). The functional role of Mcl-1 in the dynamics of mitotic cell fate. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:291383

Chicago Manual of Style (16th Edition):

Sloss, Olivia. “The functional role of Mcl-1 in the dynamics of mitotic cell fate.” 2015. Doctoral Dissertation, University of Manchester. Accessed January 18, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:291383.

MLA Handbook (7th Edition):

Sloss, Olivia. “The functional role of Mcl-1 in the dynamics of mitotic cell fate.” 2015. Web. 18 Jan 2020.

Vancouver:

Sloss O. The functional role of Mcl-1 in the dynamics of mitotic cell fate. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2020 Jan 18]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:291383.

Council of Science Editors:

Sloss O. The functional role of Mcl-1 in the dynamics of mitotic cell fate. [Doctoral Dissertation]. University of Manchester; 2015. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:291383


Boston College

17. Meyer, Lauren Francis. Meiosis-Specific Regulation of Centromeric Chromatin and Chromosome Segregation by a Transposase-Derived Protein.

Degree: PhD, Biology, 2016, Boston College

 Faithful chromosome segregation is necessary for the successful completion of mitosis and meiosis. The centromere is the site of kinetochore and microtubule attachment during chromosome… (more)

Subjects/Keywords: Centromere; Meiosis; Mitosis; S. pombe

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

APA (6th Edition):

Meyer, L. F. (2016). Meiosis-Specific Regulation of Centromeric Chromatin and Chromosome Segregation by a Transposase-Derived Protein. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:107029

Chicago Manual of Style (16th Edition):

Meyer, Lauren Francis. “Meiosis-Specific Regulation of Centromeric Chromatin and Chromosome Segregation by a Transposase-Derived Protein.” 2016. Doctoral Dissertation, Boston College. Accessed January 18, 2020. http://dlib.bc.edu/islandora/object/bc-ir:107029.

MLA Handbook (7th Edition):

Meyer, Lauren Francis. “Meiosis-Specific Regulation of Centromeric Chromatin and Chromosome Segregation by a Transposase-Derived Protein.” 2016. Web. 18 Jan 2020.

Vancouver:

Meyer LF. Meiosis-Specific Regulation of Centromeric Chromatin and Chromosome Segregation by a Transposase-Derived Protein. [Internet] [Doctoral dissertation]. Boston College; 2016. [cited 2020 Jan 18]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:107029.

Council of Science Editors:

Meyer LF. Meiosis-Specific Regulation of Centromeric Chromatin and Chromosome Segregation by a Transposase-Derived Protein. [Doctoral Dissertation]. Boston College; 2016. Available from: http://dlib.bc.edu/islandora/object/bc-ir:107029


Columbia University

18. Liu, Chenshu. Cytoskeletal Regulation of Centromere Maintenance and Function in the Mammalian Cell Cycle.

Degree: 2016, Columbia University

 Equal partitioning of genetic materials of the chromosomes is key to the mitotic cell cycle, as unequal segregation of chromosomes during mitosis leads to aneuploidy,… (more)

Subjects/Keywords: Mitosis; Cytoskeleton; Centromere; Biology; Cytology

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

APA (6th Edition):

Liu, C. (2016). Cytoskeletal Regulation of Centromere Maintenance and Function in the Mammalian Cell Cycle. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D89S1RBQ

Chicago Manual of Style (16th Edition):

Liu, Chenshu. “Cytoskeletal Regulation of Centromere Maintenance and Function in the Mammalian Cell Cycle.” 2016. Doctoral Dissertation, Columbia University. Accessed January 18, 2020. https://doi.org/10.7916/D89S1RBQ.

MLA Handbook (7th Edition):

Liu, Chenshu. “Cytoskeletal Regulation of Centromere Maintenance and Function in the Mammalian Cell Cycle.” 2016. Web. 18 Jan 2020.

Vancouver:

Liu C. Cytoskeletal Regulation of Centromere Maintenance and Function in the Mammalian Cell Cycle. [Internet] [Doctoral dissertation]. Columbia University; 2016. [cited 2020 Jan 18]. Available from: https://doi.org/10.7916/D89S1RBQ.

Council of Science Editors:

Liu C. Cytoskeletal Regulation of Centromere Maintenance and Function in the Mammalian Cell Cycle. [Doctoral Dissertation]. Columbia University; 2016. Available from: https://doi.org/10.7916/D89S1RBQ


Mississippi State University

19. Clark-Cotton, Manuella. Microtubule dynamics, kinetochore number, and kinetochore distribution in cells undergoing mitosis with unreplicated genomes.

Degree: MS, Biological Sciences, 2014, Mississippi State University

  In cells undergoing mitosis with unreplicated genomes (MUG), anaphase is successfully initiated despite the abundance of kinetochores that are attached to microtubules emanating from… (more)

Subjects/Keywords: mitosis; MUG cells; kinetochores

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APA (6th Edition):

Clark-Cotton, M. (2014). Microtubule dynamics, kinetochore number, and kinetochore distribution in cells undergoing mitosis with unreplicated genomes. (Masters Thesis). Mississippi State University. Retrieved from http://sun.library.msstate.edu/ETD-db/theses/available/etd-03252014-162448/ ;

Chicago Manual of Style (16th Edition):

Clark-Cotton, Manuella. “Microtubule dynamics, kinetochore number, and kinetochore distribution in cells undergoing mitosis with unreplicated genomes.” 2014. Masters Thesis, Mississippi State University. Accessed January 18, 2020. http://sun.library.msstate.edu/ETD-db/theses/available/etd-03252014-162448/ ;.

MLA Handbook (7th Edition):

Clark-Cotton, Manuella. “Microtubule dynamics, kinetochore number, and kinetochore distribution in cells undergoing mitosis with unreplicated genomes.” 2014. Web. 18 Jan 2020.

Vancouver:

Clark-Cotton M. Microtubule dynamics, kinetochore number, and kinetochore distribution in cells undergoing mitosis with unreplicated genomes. [Internet] [Masters thesis]. Mississippi State University; 2014. [cited 2020 Jan 18]. Available from: http://sun.library.msstate.edu/ETD-db/theses/available/etd-03252014-162448/ ;.

Council of Science Editors:

Clark-Cotton M. Microtubule dynamics, kinetochore number, and kinetochore distribution in cells undergoing mitosis with unreplicated genomes. [Masters Thesis]. Mississippi State University; 2014. Available from: http://sun.library.msstate.edu/ETD-db/theses/available/etd-03252014-162448/ ;


Vanderbilt University

20. Dumas, Megan Elissa. Regulation and Pharmacology of the Mitotic Kinesin Kif15.

Degree: PhD, Cell and Developmental Biology, 2019, Vanderbilt University

 The mitotic spindle is the microtubule (MT)-based machine that segregates a replicated set of chromosomes during cell division. Many chemotherapeutics target the mitotic spindle by… (more)

Subjects/Keywords: mitosis; kinesin; oxindole; Kif15; Eg5

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APA (6th Edition):

Dumas, M. E. (2019). Regulation and Pharmacology of the Mitotic Kinesin Kif15. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-05132019-132033/ ;

Chicago Manual of Style (16th Edition):

Dumas, Megan Elissa. “Regulation and Pharmacology of the Mitotic Kinesin Kif15.” 2019. Doctoral Dissertation, Vanderbilt University. Accessed January 18, 2020. http://etd.library.vanderbilt.edu/available/etd-05132019-132033/ ;.

MLA Handbook (7th Edition):

Dumas, Megan Elissa. “Regulation and Pharmacology of the Mitotic Kinesin Kif15.” 2019. Web. 18 Jan 2020.

Vancouver:

Dumas ME. Regulation and Pharmacology of the Mitotic Kinesin Kif15. [Internet] [Doctoral dissertation]. Vanderbilt University; 2019. [cited 2020 Jan 18]. Available from: http://etd.library.vanderbilt.edu/available/etd-05132019-132033/ ;.

Council of Science Editors:

Dumas ME. Regulation and Pharmacology of the Mitotic Kinesin Kif15. [Doctoral Dissertation]. Vanderbilt University; 2019. Available from: http://etd.library.vanderbilt.edu/available/etd-05132019-132033/ ;


University of Texas Southwestern Medical Center

21. 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 January 18, 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. 18 Jan 2020.

Vancouver:

Chaudhary J. Function And Recruitment Of Centromeric Heterochromatin Protein 1. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2011. [cited 2020 Jan 18]. 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

22. Weil, Lauren Melissa. Regulation of the Cytoskeleton by Kinesins.

Degree: 2013, University of Texas Southwestern Medical Center

 Kinesins are motor proteins that associate with microtubules. The position of the motor domain has been linked to kinesin function. While amino-terminal and carboxy-terminal localization… (more)

Subjects/Keywords: Cytoskeleton; Kinesin; Microtubules; Mitosis

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APA (6th Edition):

Weil, L. M. (2013). Regulation of the Cytoskeleton by Kinesins. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/2731

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):

Weil, Lauren Melissa. “Regulation of the Cytoskeleton by Kinesins.” 2013. Thesis, University of Texas Southwestern Medical Center. Accessed January 18, 2020. http://hdl.handle.net/2152.5/2731.

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

MLA Handbook (7th Edition):

Weil, Lauren Melissa. “Regulation of the Cytoskeleton by Kinesins.” 2013. Web. 18 Jan 2020.

Vancouver:

Weil LM. Regulation of the Cytoskeleton by Kinesins. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2013. [cited 2020 Jan 18]. Available from: http://hdl.handle.net/2152.5/2731.

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

Council of Science Editors:

Weil LM. Regulation of the Cytoskeleton by Kinesins. [Thesis]. University of Texas Southwestern Medical Center; 2013. Available from: http://hdl.handle.net/2152.5/2731

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

23. 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 January 18, 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. 18 Jan 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 Jan 18]. 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

24. 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 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 January 18, 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. 18 Jan 2020.

Vancouver:

Zhao YL. Functional study of GAS2L1 in mitosis. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2015. [cited 2020 Jan 18]. 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

25. 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 (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 January 18, 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. 18 Jan 2020.

Vancouver:

Xu KL. Molecular regulation of mitotic slippage. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2016. [cited 2020 Jan 18]. 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


Hong Kong University of Science and Technology

26. 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 January 18, 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. 18 Jan 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 Jan 18]. 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


Hong Kong University of Science and Technology

27. Tsang, Yiu Huen. The identification of phosphatases important for mitosis and replicative stress response.

Degree: 2011, Hong Kong University of Science and Technology

 In every cell division cycle, daughter cells carry the same genomic information as their parental cell. Maintenance of the genomic stability requires several checkpoints that… (more)

Subjects/Keywords: Phosphatases ; DNA replication ; Mitosis

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

APA (6th Edition):

Tsang, Y. H. (2011). The identification of phosphatases important for mitosis and replicative stress response. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-7286 ; https://doi.org/10.14711/thesis-b1160524 ; http://repository.ust.hk/ir/bitstream/1783.1-7286/1/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):

Tsang, Yiu Huen. “The identification of phosphatases important for mitosis and replicative stress response.” 2011. Thesis, Hong Kong University of Science and Technology. Accessed January 18, 2020. http://repository.ust.hk/ir/Record/1783.1-7286 ; https://doi.org/10.14711/thesis-b1160524 ; http://repository.ust.hk/ir/bitstream/1783.1-7286/1/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):

Tsang, Yiu Huen. “The identification of phosphatases important for mitosis and replicative stress response.” 2011. Web. 18 Jan 2020.

Vancouver:

Tsang YH. The identification of phosphatases important for mitosis and replicative stress response. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2011. [cited 2020 Jan 18]. Available from: http://repository.ust.hk/ir/Record/1783.1-7286 ; https://doi.org/10.14711/thesis-b1160524 ; http://repository.ust.hk/ir/bitstream/1783.1-7286/1/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:

Tsang YH. The identification of phosphatases important for mitosis and replicative stress response. [Thesis]. Hong Kong University of Science and Technology; 2011. Available from: http://repository.ust.hk/ir/Record/1783.1-7286 ; https://doi.org/10.14711/thesis-b1160524 ; http://repository.ust.hk/ir/bitstream/1783.1-7286/1/th_redirect.html

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


University of Manchester

28. Sloss, Olivia. The functional role of Mcl-1 in the dynamics of mitotic cell fate.

Degree: PhD, 2015, University of Manchester

 Drugs that alter microtubule dynamics are often used in chemotherapy regimes in combination with other agents in order to treat various cancers. Despite the success… (more)

Subjects/Keywords: 571.8; mitosis; Mcl-1; cell fate

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

APA (6th Edition):

Sloss, O. (2015). The functional role of Mcl-1 in the dynamics of mitotic cell fate. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/the-functional-role-of-mcl1-in-the-dynamics-of-mitotic-cell-fate(d567e84b-3a51-4ec9-8f5c-779704d26bae).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.701101

Chicago Manual of Style (16th Edition):

Sloss, Olivia. “The functional role of Mcl-1 in the dynamics of mitotic cell fate.” 2015. Doctoral Dissertation, University of Manchester. Accessed January 18, 2020. https://www.research.manchester.ac.uk/portal/en/theses/the-functional-role-of-mcl1-in-the-dynamics-of-mitotic-cell-fate(d567e84b-3a51-4ec9-8f5c-779704d26bae).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.701101.

MLA Handbook (7th Edition):

Sloss, Olivia. “The functional role of Mcl-1 in the dynamics of mitotic cell fate.” 2015. Web. 18 Jan 2020.

Vancouver:

Sloss O. The functional role of Mcl-1 in the dynamics of mitotic cell fate. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2020 Jan 18]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/the-functional-role-of-mcl1-in-the-dynamics-of-mitotic-cell-fate(d567e84b-3a51-4ec9-8f5c-779704d26bae).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.701101.

Council of Science Editors:

Sloss O. The functional role of Mcl-1 in the dynamics of mitotic cell fate. [Doctoral Dissertation]. University of Manchester; 2015. Available from: https://www.research.manchester.ac.uk/portal/en/theses/the-functional-role-of-mcl1-in-the-dynamics-of-mitotic-cell-fate(d567e84b-3a51-4ec9-8f5c-779704d26bae).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.701101


University of Utah

29. Shtylla, Blerta. Mathematical models of chromosome motility during mitosis.

Degree: PhD, Mathematics, 2011, University of Utah

 Cell division is a complex process that involves carefully orchestrated chemical and mechanical events. Tight regulation is vital during division, since a breakdown in control… (more)

Subjects/Keywords: Chromosome movement; Jump-diffusion; Mitosis; Molecular motors

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

APA (6th Edition):

Shtylla, B. (2011). Mathematical models of chromosome motility during mitosis. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/292/rec/1537

Chicago Manual of Style (16th Edition):

Shtylla, Blerta. “Mathematical models of chromosome motility during mitosis.” 2011. Doctoral Dissertation, University of Utah. Accessed January 18, 2020. http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/292/rec/1537.

MLA Handbook (7th Edition):

Shtylla, Blerta. “Mathematical models of chromosome motility during mitosis.” 2011. Web. 18 Jan 2020.

Vancouver:

Shtylla B. Mathematical models of chromosome motility during mitosis. [Internet] [Doctoral dissertation]. University of Utah; 2011. [cited 2020 Jan 18]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/292/rec/1537.

Council of Science Editors:

Shtylla B. Mathematical models of chromosome motility during mitosis. [Doctoral Dissertation]. University of Utah; 2011. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/292/rec/1537

30. Cortez, Beatriz de Araujo. Interação da crisotila com células de carcinoma de pulmão humano em cultura: interferência com a mitose utilizando genes repórteres e microscopia em tempo real e estudo do potencial genotóxico.

Degree: Mestrado, Biologia (Genética), 2010, University of São Paulo

Asbesto é um nome geral dado a seis tipos de fibras minerais encontradas naturalmente na crosta terrestre. Estas fibras vêm sendo exploradas industrialmente desde 1970,… (more)

Subjects/Keywords: Aneuploidia; Aneuploidy; Chrysotile; Crisotila; Mitose; Mitosis

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

APA (6th Edition):

Cortez, B. d. A. (2010). Interação da crisotila com células de carcinoma de pulmão humano em cultura: interferência com a mitose utilizando genes repórteres e microscopia em tempo real e estudo do potencial genotóxico. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/41/41131/tde-05042010-134617/ ;

Chicago Manual of Style (16th Edition):

Cortez, Beatriz de Araujo. “Interação da crisotila com células de carcinoma de pulmão humano em cultura: interferência com a mitose utilizando genes repórteres e microscopia em tempo real e estudo do potencial genotóxico.” 2010. Masters Thesis, University of São Paulo. Accessed January 18, 2020. http://www.teses.usp.br/teses/disponiveis/41/41131/tde-05042010-134617/ ;.

MLA Handbook (7th Edition):

Cortez, Beatriz de Araujo. “Interação da crisotila com células de carcinoma de pulmão humano em cultura: interferência com a mitose utilizando genes repórteres e microscopia em tempo real e estudo do potencial genotóxico.” 2010. Web. 18 Jan 2020.

Vancouver:

Cortez BdA. Interação da crisotila com células de carcinoma de pulmão humano em cultura: interferência com a mitose utilizando genes repórteres e microscopia em tempo real e estudo do potencial genotóxico. [Internet] [Masters thesis]. University of São Paulo; 2010. [cited 2020 Jan 18]. Available from: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-05042010-134617/ ;.

Council of Science Editors:

Cortez BdA. Interação da crisotila com células de carcinoma de pulmão humano em cultura: interferência com a mitose utilizando genes repórteres e microscopia em tempo real e estudo do potencial genotóxico. [Masters Thesis]. University of São Paulo; 2010. Available from: http://www.teses.usp.br/teses/disponiveis/41/41131/tde-05042010-134617/ ;

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