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You searched for subject:(mitosis). Showing records 1 – 30 of 505 total matches.

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Universidad de Cantabria

1. Alonso Lecue, Pilar. Alteraciones del control mitosis-diferenciación en el carcinoma de piel.

Degree: 2015, Universidad de Cantabria

 RESUMEN: El cáncer de piel no melanocítico es el tipo de cáncer más común en sus dos formas predominantes: carcinoma Basocelular (BCC) y carcinoma escamoso… (more)

Subjects/Keywords: Mitosis

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APA (6th Edition):

Alonso Lecue, P. (2015). Alteraciones del control mitosis-diferenciación en el carcinoma de piel. (Doctoral Dissertation). Universidad de Cantabria. Retrieved from http://hdl.handle.net/10902/7812

Chicago Manual of Style (16th Edition):

Alonso Lecue, Pilar. “Alteraciones del control mitosis-diferenciación en el carcinoma de piel.” 2015. Doctoral Dissertation, Universidad de Cantabria. Accessed January 23, 2021. http://hdl.handle.net/10902/7812.

MLA Handbook (7th Edition):

Alonso Lecue, Pilar. “Alteraciones del control mitosis-diferenciación en el carcinoma de piel.” 2015. Web. 23 Jan 2021.

Vancouver:

Alonso Lecue P. Alteraciones del control mitosis-diferenciación en el carcinoma de piel. [Internet] [Doctoral dissertation]. Universidad de Cantabria; 2015. [cited 2021 Jan 23]. Available from: http://hdl.handle.net/10902/7812.

Council of Science Editors:

Alonso Lecue P. Alteraciones del control mitosis-diferenciación en el carcinoma de piel. [Doctoral Dissertation]. Universidad de Cantabria; 2015. Available from: http://hdl.handle.net/10902/7812

2. 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 (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 23, 2021. 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. 23 Jan 2021.

Vancouver:

Bennett A. Exploiting mitosis to improve anti-cancer strategies. [Internet] [Doctoral dissertation]. University of Manchester; 2017. [cited 2021 Jan 23]. 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

3. 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 23, 2021. 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. 23 Jan 2021.

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 2021 Jan 23]. 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


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 23, 2021. 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. 23 Jan 2021.

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 2021 Jan 23]. 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


Georgia Tech

5. 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 23, 2021. 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. 23 Jan 2021.

Vancouver:

Koza RW. A study of hypotheses on the role of electrical forces in mitosis. [Internet] [Masters thesis]. Georgia Tech; 1948. [cited 2021 Jan 23]. 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


Columbia University

6. 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 23, 2021. https://doi.org/10.7916/D8KH0NMD.

MLA Handbook (7th Edition):

Wynne, Caitlin Lazar. “Molecular Dissection of Nde1's Role in Mitosis.” 2016. Web. 23 Jan 2021.

Vancouver:

Wynne CL. Molecular Dissection of Nde1's Role in Mitosis. [Internet] [Doctoral dissertation]. Columbia University; 2016. [cited 2021 Jan 23]. 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


Vanderbilt University

7. Gayek, Anna Sophia. Not Just for Pulling Chromosomes: The Role of Kinetochore-Microtubules in Enforcing Bipolarity of the Human Mitotic Spindle.

Degree: PhD, Cell and Developmental Biology, 2016, Vanderbilt University

 Two processes influence the success of mitosis, the process by which eukaryotic cells divide their replicated genome into two new daughter cells. First, the cell… (more)

Subjects/Keywords: microtubule; kinetochore; mitosis

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APA (6th Edition):

Gayek, A. S. (2016). Not Just for Pulling Chromosomes: The Role of Kinetochore-Microtubules in Enforcing Bipolarity of the Human Mitotic Spindle. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/11635

Chicago Manual of Style (16th Edition):

Gayek, Anna Sophia. “Not Just for Pulling Chromosomes: The Role of Kinetochore-Microtubules in Enforcing Bipolarity of the Human Mitotic Spindle.” 2016. Doctoral Dissertation, Vanderbilt University. Accessed January 23, 2021. http://hdl.handle.net/1803/11635.

MLA Handbook (7th Edition):

Gayek, Anna Sophia. “Not Just for Pulling Chromosomes: The Role of Kinetochore-Microtubules in Enforcing Bipolarity of the Human Mitotic Spindle.” 2016. Web. 23 Jan 2021.

Vancouver:

Gayek AS. Not Just for Pulling Chromosomes: The Role of Kinetochore-Microtubules in Enforcing Bipolarity of the Human Mitotic Spindle. [Internet] [Doctoral dissertation]. Vanderbilt University; 2016. [cited 2021 Jan 23]. Available from: http://hdl.handle.net/1803/11635.

Council of Science Editors:

Gayek AS. Not Just for Pulling Chromosomes: The Role of Kinetochore-Microtubules in Enforcing Bipolarity of the Human Mitotic Spindle. [Doctoral Dissertation]. Vanderbilt University; 2016. Available from: http://hdl.handle.net/1803/11635


Boston College

8. 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 23, 2021. 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. 23 Jan 2021.

Vancouver:

Farrell MC. Deciphering the Role of Kinetochores and Microtubules During Interphase and Mitosis in Toxoplasma Gondii. [Internet] [Doctoral dissertation]. Boston College; 2014. [cited 2021 Jan 23]. 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

9. 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 (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 23, 2021. 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. 23 Jan 2021.

Vancouver:

Bennett A. Exploiting mitosis to improve anti-cancer strategies. [Internet] [Doctoral dissertation]. University of Manchester; 2017. [cited 2021 Jan 23]. 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 Melbourne

10. Kim, Ji Hun. Condensin: a dynamic organizer of vertebrate chromosome structure: analysis of condensin binding sites and function in vertebrates.

Degree: 2013, University of Melbourne

 Condensin is essential for the packaging of chromatin into condensed chromosomes in all eukaryotes. It is a multi-subunit protein complex consisting of two core subunits… (more)

Subjects/Keywords: condensin; chromosome; mitosis

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APA (6th Edition):

Kim, J. H. (2013). Condensin: a dynamic organizer of vertebrate chromosome structure: analysis of condensin binding sites and function in vertebrates. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/38707

Chicago Manual of Style (16th Edition):

Kim, Ji Hun. “Condensin: a dynamic organizer of vertebrate chromosome structure: analysis of condensin binding sites and function in vertebrates.” 2013. Doctoral Dissertation, University of Melbourne. Accessed January 23, 2021. http://hdl.handle.net/11343/38707.

MLA Handbook (7th Edition):

Kim, Ji Hun. “Condensin: a dynamic organizer of vertebrate chromosome structure: analysis of condensin binding sites and function in vertebrates.” 2013. Web. 23 Jan 2021.

Vancouver:

Kim JH. Condensin: a dynamic organizer of vertebrate chromosome structure: analysis of condensin binding sites and function in vertebrates. [Internet] [Doctoral dissertation]. University of Melbourne; 2013. [cited 2021 Jan 23]. Available from: http://hdl.handle.net/11343/38707.

Council of Science Editors:

Kim JH. Condensin: a dynamic organizer of vertebrate chromosome structure: analysis of condensin binding sites and function in vertebrates. [Doctoral Dissertation]. University of Melbourne; 2013. Available from: http://hdl.handle.net/11343/38707


University of New South Wales

11. 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 23, 2021. 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. 23 Jan 2021.

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 2021 Jan 23]. 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


Mississippi State University

12. 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 23, 2021. 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. 23 Jan 2021.

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 2021 Jan 23]. 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/ ;


University of Alberta

13. 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 23, 2021. https://era.library.ualberta.ca/files/fx719n183.

MLA Handbook (7th Edition):

Heit, Ryan. “Epigenetic Regulation of Centromere Formation and Kinetochore Function.” 2009. Web. 23 Jan 2021.

Vancouver:

Heit R. Epigenetic Regulation of Centromere Formation and Kinetochore Function. [Internet] [Masters thesis]. University of Alberta; 2009. [cited 2021 Jan 23]. 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

14. 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 23, 2021. 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. 23 Jan 2021.

Vancouver:

Pennings C. Molecular composition and function of the kinetochore-microtubule interface in chromosome segregation. [Internet] [Masters thesis]. Universiteit Utrecht; 2014. [cited 2021 Jan 23]. 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


Vanderbilt University

15. 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://hdl.handle.net/1803/12304

Chicago Manual of Style (16th Edition):

Dumas, Megan Elissa. “Regulation and Pharmacology of the Mitotic Kinesin Kif15.” 2019. Doctoral Dissertation, Vanderbilt University. Accessed January 23, 2021. http://hdl.handle.net/1803/12304.

MLA Handbook (7th Edition):

Dumas, Megan Elissa. “Regulation and Pharmacology of the Mitotic Kinesin Kif15.” 2019. Web. 23 Jan 2021.

Vancouver:

Dumas ME. Regulation and Pharmacology of the Mitotic Kinesin Kif15. [Internet] [Doctoral dissertation]. Vanderbilt University; 2019. [cited 2021 Jan 23]. Available from: http://hdl.handle.net/1803/12304.

Council of Science Editors:

Dumas ME. Regulation and Pharmacology of the Mitotic Kinesin Kif15. [Doctoral Dissertation]. Vanderbilt University; 2019. Available from: http://hdl.handle.net/1803/12304


University of Texas Southwestern Medical Center

16. 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 January 23, 2021. 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. 23 Jan 2021.

Vancouver:

Chaudhary J. Function And Recruitment Of Centromeric Heterochromatin Protein 1. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2011. [cited 2021 Jan 23]. 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

17. 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 23, 2021. 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. 23 Jan 2021.

Vancouver:

Weil LM. Regulation of the Cytoskeleton by Kinesins. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2013. [cited 2021 Jan 23]. 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

18. 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 23, 2021. 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. 23 Jan 2021.

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 2021 Jan 23]. 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


Boston College

19. 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 (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 23, 2021. 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. 23 Jan 2021.

Vancouver:

Meyer LF. Meiosis-Specific Regulation of Centromeric Chromatin and Chromosome Segregation by a Transposase-Derived Protein. [Internet] [Doctoral dissertation]. Boston College; 2016. [cited 2021 Jan 23]. 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

20. 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 (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 23, 2021. 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. 23 Jan 2021.

Vancouver:

Liu C. Cytoskeletal Regulation of Centromere Maintenance and Function in the Mammalian Cell Cycle. [Internet] [Doctoral dissertation]. Columbia University; 2016. [cited 2021 Jan 23]. 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


Hong Kong University of Science and Technology

21. 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 23, 2021. 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. 23 Jan 2021.

Vancouver:

Zhao YL. Functional study of GAS2L1 in mitosis. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2015. [cited 2021 Jan 23]. 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

22. 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 23, 2021. 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. 23 Jan 2021.

Vancouver:

Xu KL. Molecular regulation of mitotic slippage. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2016. [cited 2021 Jan 23]. 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

23. 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 23, 2021. 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. 23 Jan 2021.

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 2021 Jan 23]. 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

24. 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 (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 23, 2021. 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. 23 Jan 2021.

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 2021 Jan 23]. 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 Edinburgh

25. 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 23, 2021. http://hdl.handle.net/1842/8734.

MLA Handbook (7th Edition):

Martin, Carol-Anne. “Role of microcephalin at mitosis.” 2011. Web. 23 Jan 2021.

Vancouver:

Martin C. Role of microcephalin at mitosis. [Internet] [Doctoral dissertation]. University of Edinburgh; 2011. [cited 2021 Jan 23]. 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 Manchester

26. 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 (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 23, 2021. 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. 23 Jan 2021.

Vancouver:

Sloss O. The functional role of Mcl-1 in the dynamics of mitotic cell fate. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2021 Jan 23]. 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


Osaka University

27. 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 23, 2021. 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. 23 Jan 2021.

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 2021 Jan 23]. 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 Pennsylvania

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

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 23, 2021. 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. 23 Jan 2021.

Vancouver:

Palozola K. Global Mitotic Transcription And Reactivation During Mitotic Exit: A Potential Epigenetic Mechanism. [Internet] [Thesis]. University of Pennsylvania; 2017. [cited 2021 Jan 23]. 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


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 23, 2021. 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. 23 Jan 2021.

Vancouver:

Shtylla B. Mathematical models of chromosome motility during mitosis. [Internet] [Doctoral dissertation]. University of Utah; 2011. [cited 2021 Jan 23]. 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 23, 2021. 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. 23 Jan 2021.

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 2021 Jan 23]. 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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