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You searched for subject:(associated cycle). Showing records 1 – 18 of 18 total matches.

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Université de Grenoble

1. Paez, Claudia. Etude fonctionnelle de la protéine associée aux microtubules XMAP215/ch-TOG : Fonctional study of microtubule associated protein XMAP215/ch-TOG.

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

Résumé Les protéines XMAP215/ch-TOG appartiennent à une famille de protéines associées aux microtubules (MAPs), bien conservée tout au long de l'évolution, la famille XMAP215/Dis1. Cette… (more)

Subjects/Keywords: Microtubule Associated Proteins (MAPs); Microtubules; Cicle cellulaire; Microtubule Associated Proteins (MAPS); Microtubules; Cell cycle; Microtubules

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APA (6th Edition):

Paez, C. (2011). Etude fonctionnelle de la protéine associée aux microtubules XMAP215/ch-TOG : Fonctional study of microtubule associated protein XMAP215/ch-TOG. (Doctoral Dissertation). Université de Grenoble. Retrieved from http://www.theses.fr/2011GRENV014

Chicago Manual of Style (16th Edition):

Paez, Claudia. “Etude fonctionnelle de la protéine associée aux microtubules XMAP215/ch-TOG : Fonctional study of microtubule associated protein XMAP215/ch-TOG.” 2011. Doctoral Dissertation, Université de Grenoble. Accessed September 30, 2020. http://www.theses.fr/2011GRENV014.

MLA Handbook (7th Edition):

Paez, Claudia. “Etude fonctionnelle de la protéine associée aux microtubules XMAP215/ch-TOG : Fonctional study of microtubule associated protein XMAP215/ch-TOG.” 2011. Web. 30 Sep 2020.

Vancouver:

Paez C. Etude fonctionnelle de la protéine associée aux microtubules XMAP215/ch-TOG : Fonctional study of microtubule associated protein XMAP215/ch-TOG. [Internet] [Doctoral dissertation]. Université de Grenoble; 2011. [cited 2020 Sep 30]. Available from: http://www.theses.fr/2011GRENV014.

Council of Science Editors:

Paez C. Etude fonctionnelle de la protéine associée aux microtubules XMAP215/ch-TOG : Fonctional study of microtubule associated protein XMAP215/ch-TOG. [Doctoral Dissertation]. Université de Grenoble; 2011. Available from: http://www.theses.fr/2011GRENV014


University of Toledo Health Science Campus

2. Bevington, Joyce M. Cellular Response to Adenovirus and Adeno- Associated Virus Coinfection.

Degree: PhD, College of Medicine, 2009, University of Toledo Health Science Campus

 Adeno-associated virus (AAV) is a small single-stranded linear DNA virus thatrequires a helper-virus to efficiently replicate inside a host cell. The cellular effects of anAAV… (more)

Subjects/Keywords: Virology; Adeno-Associated Virus; Nucleophosmin; Cell cycle; Adenovirus; DNA Damage Repair Response; Host-Virus Interaction

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APA (6th Edition):

Bevington, J. M. (2009). Cellular Response to Adenovirus and Adeno- Associated Virus Coinfection. (Doctoral Dissertation). University of Toledo Health Science Campus. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=mco1242921394

Chicago Manual of Style (16th Edition):

Bevington, Joyce M. “Cellular Response to Adenovirus and Adeno- Associated Virus Coinfection.” 2009. Doctoral Dissertation, University of Toledo Health Science Campus. Accessed September 30, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=mco1242921394.

MLA Handbook (7th Edition):

Bevington, Joyce M. “Cellular Response to Adenovirus and Adeno- Associated Virus Coinfection.” 2009. Web. 30 Sep 2020.

Vancouver:

Bevington JM. Cellular Response to Adenovirus and Adeno- Associated Virus Coinfection. [Internet] [Doctoral dissertation]. University of Toledo Health Science Campus; 2009. [cited 2020 Sep 30]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1242921394.

Council of Science Editors:

Bevington JM. Cellular Response to Adenovirus and Adeno- Associated Virus Coinfection. [Doctoral Dissertation]. University of Toledo Health Science Campus; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1242921394


University of Illinois – Chicago

3. Kwan, Jennifer M. Akt Regulation of Adipogenesis: Implications for Skp2 Involvement.

Degree: 2013, University of Illinois – Chicago

 Amongst the backdrop of a worldwide obesity epidemic and its increased risk for heart disease, diabetes, stroke, and a wide range of cancers, including breast,… (more)

Subjects/Keywords: adipogenesis; cell cycle; tumorigenesis; insulin; akt; S-phase kinase-associated protein 2 (Skp2); protein translation

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APA (6th Edition):

Kwan, J. M. (2013). Akt Regulation of Adipogenesis: Implications for Skp2 Involvement. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/10047

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):

Kwan, Jennifer M. “Akt Regulation of Adipogenesis: Implications for Skp2 Involvement.” 2013. Thesis, University of Illinois – Chicago. Accessed September 30, 2020. http://hdl.handle.net/10027/10047.

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

MLA Handbook (7th Edition):

Kwan, Jennifer M. “Akt Regulation of Adipogenesis: Implications for Skp2 Involvement.” 2013. Web. 30 Sep 2020.

Vancouver:

Kwan JM. Akt Regulation of Adipogenesis: Implications for Skp2 Involvement. [Internet] [Thesis]. University of Illinois – Chicago; 2013. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/10027/10047.

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

Council of Science Editors:

Kwan JM. Akt Regulation of Adipogenesis: Implications for Skp2 Involvement. [Thesis]. University of Illinois – Chicago; 2013. Available from: http://hdl.handle.net/10027/10047

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

4. Housley, Matthew. Polynomial representations and associated cycles for indefinite unitary groups.

Degree: PhD, Mathematics, 2011, University of Utah

 The associated variety is a geometric invariant attached to each Harish-Chandra module of a real reductive Lie group. The associated cycle is a ner invariant… (more)

Subjects/Keywords: Associated cycle; Unitary groups; Polynomial representations

…These polynomials are building blocks for associated cycle polynomials via results of Chang… …have known for some time that associated cycle polynomials are equal to certain fiber… …main results of this paper give closed formulas for associated cycle polynomials in three… …broad cases: Theorem 29 gives a closed formula for the associated cycle polynomial for any… …variety. This extends associated cycle polynomial calculations to another large family of… 

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APA (6th Edition):

Housley, M. (2011). Polynomial representations and associated cycles for indefinite unitary groups. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/270/rec/1915

Chicago Manual of Style (16th Edition):

Housley, Matthew. “Polynomial representations and associated cycles for indefinite unitary groups.” 2011. Doctoral Dissertation, University of Utah. Accessed September 30, 2020. http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/270/rec/1915.

MLA Handbook (7th Edition):

Housley, Matthew. “Polynomial representations and associated cycles for indefinite unitary groups.” 2011. Web. 30 Sep 2020.

Vancouver:

Housley M. Polynomial representations and associated cycles for indefinite unitary groups. [Internet] [Doctoral dissertation]. University of Utah; 2011. [cited 2020 Sep 30]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/270/rec/1915.

Council of Science Editors:

Housley M. Polynomial representations and associated cycles for indefinite unitary groups. [Doctoral Dissertation]. University of Utah; 2011. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/270/rec/1915


Freie Universität Berlin

5. Krämer, Anika. Immunohistochemical studies of cell cycle-associated protein expression in different subtypes of invasive breast cancer.

Degree: 2013, Freie Universität Berlin

 Invasive breast cancer is the most frequent cancer in women, with a mortality rate still beeing high. Although a multitude of studies have been performed,… (more)

Subjects/Keywords: immunohistochemical; cell cycle-associated protein; subtypes; invasive breast cancer; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit

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APA (6th Edition):

Krämer, A. (2013). Immunohistochemical studies of cell cycle-associated protein expression in different subtypes of invasive breast cancer. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-11828

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):

Krämer, Anika. “Immunohistochemical studies of cell cycle-associated protein expression in different subtypes of invasive breast cancer.” 2013. Thesis, Freie Universität Berlin. Accessed September 30, 2020. http://dx.doi.org/10.17169/refubium-11828.

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

MLA Handbook (7th Edition):

Krämer, Anika. “Immunohistochemical studies of cell cycle-associated protein expression in different subtypes of invasive breast cancer.” 2013. Web. 30 Sep 2020.

Vancouver:

Krämer A. Immunohistochemical studies of cell cycle-associated protein expression in different subtypes of invasive breast cancer. [Internet] [Thesis]. Freie Universität Berlin; 2013. [cited 2020 Sep 30]. Available from: http://dx.doi.org/10.17169/refubium-11828.

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

Council of Science Editors:

Krämer A. Immunohistochemical studies of cell cycle-associated protein expression in different subtypes of invasive breast cancer. [Thesis]. Freie Universität Berlin; 2013. Available from: http://dx.doi.org/10.17169/refubium-11828

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


Georgia Tech

6. Ganesh, Sangita. Environmental niche partitioning of microbial community genomic diversity, gene expression, and metabolism in a marine oxygen minimum zone.

Degree: PhD, Biology, 2016, Georgia Tech

 Oxygen Minimum Zones (OMZs) serve as habitats to diverse assemblages of microorganisms that play an important role in mediating global biogeochemical cycles. OMZ microbial communities… (more)

Subjects/Keywords: OMZ; Marine; Metagenomics; Metatranscriptomics; Single cell genomics; Nitrogen cycle; Size fraction; Particle associated; Microbial community; Process rates

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APA (6th Edition):

Ganesh, S. (2016). Environmental niche partitioning of microbial community genomic diversity, gene expression, and metabolism in a marine oxygen minimum zone. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/59164

Chicago Manual of Style (16th Edition):

Ganesh, Sangita. “Environmental niche partitioning of microbial community genomic diversity, gene expression, and metabolism in a marine oxygen minimum zone.” 2016. Doctoral Dissertation, Georgia Tech. Accessed September 30, 2020. http://hdl.handle.net/1853/59164.

MLA Handbook (7th Edition):

Ganesh, Sangita. “Environmental niche partitioning of microbial community genomic diversity, gene expression, and metabolism in a marine oxygen minimum zone.” 2016. Web. 30 Sep 2020.

Vancouver:

Ganesh S. Environmental niche partitioning of microbial community genomic diversity, gene expression, and metabolism in a marine oxygen minimum zone. [Internet] [Doctoral dissertation]. Georgia Tech; 2016. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/1853/59164.

Council of Science Editors:

Ganesh S. Environmental niche partitioning of microbial community genomic diversity, gene expression, and metabolism in a marine oxygen minimum zone. [Doctoral Dissertation]. Georgia Tech; 2016. Available from: http://hdl.handle.net/1853/59164


University of Texas Southwestern Medical Center

7. Brulotte, Melissa Lynn. Spindle Checkpoint Silencing by TRIP13.

Degree: 2017, University of Texas Southwestern Medical Center

 The spindle checkpoint is important for maintaining genomic stability and preventing aneuploidy, a hallmark of cancer. The checkpoint ensures that chromosome segregation does not occur… (more)

Subjects/Keywords: Adaptor Proteins, Signal Transducing; ATPases Associated with Diverse Cellular Activities; Cdc20 Proteins; Cell Cycle Proteins; M Phase Cell Cycle Checkpoints; Mad2 Proteins; Nuclear Proteins

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APA (6th Edition):

Brulotte, M. L. (2017). Spindle Checkpoint Silencing by TRIP13. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/7734

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):

Brulotte, Melissa Lynn. “Spindle Checkpoint Silencing by TRIP13.” 2017. Thesis, University of Texas Southwestern Medical Center. Accessed September 30, 2020. http://hdl.handle.net/2152.5/7734.

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

MLA Handbook (7th Edition):

Brulotte, Melissa Lynn. “Spindle Checkpoint Silencing by TRIP13.” 2017. Web. 30 Sep 2020.

Vancouver:

Brulotte ML. Spindle Checkpoint Silencing by TRIP13. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2017. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/2152.5/7734.

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

Council of Science Editors:

Brulotte ML. Spindle Checkpoint Silencing by TRIP13. [Thesis]. University of Texas Southwestern Medical Center; 2017. Available from: http://hdl.handle.net/2152.5/7734

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

8. Ji, Zhejian. Safeguard of Mitosis: The Spindle Checkpoint.

Degree: 2016, University of Texas Southwestern Medical Center

 In mitosis, the kinetochore-microtubule attachment is under surveillance by the spindle checkpoint to ensure the fidelity of chromosome segregation. Defects in the checkpoint could lead… (more)

Subjects/Keywords: Cell Cycle Checkpoints; Cell Cycle Proteins; Microtubule-Associated Proteins; Nuclear Proteins; Protein Processing, Post-Translational; Protein-Serine-Threonine Kinases; Protein-Tyrosine Kinases; Signal Transduction

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APA (6th Edition):

Ji, Z. (2016). Safeguard of Mitosis: The Spindle Checkpoint. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/6144

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):

Ji, Zhejian. “Safeguard of Mitosis: The Spindle Checkpoint.” 2016. Thesis, University of Texas Southwestern Medical Center. Accessed September 30, 2020. http://hdl.handle.net/2152.5/6144.

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

MLA Handbook (7th Edition):

Ji, Zhejian. “Safeguard of Mitosis: The Spindle Checkpoint.” 2016. Web. 30 Sep 2020.

Vancouver:

Ji Z. Safeguard of Mitosis: The Spindle Checkpoint. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2016. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/2152.5/6144.

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

Council of Science Editors:

Ji Z. Safeguard of Mitosis: The Spindle Checkpoint. [Thesis]. University of Texas Southwestern Medical Center; 2016. Available from: http://hdl.handle.net/2152.5/6144

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

9. Straker, Geburah. Characterization of the FHA domain involved in Saccharomyces cerevisiae dNTP regulation.

Degree: 2018, University of Waterloo

 Over 2000 Forkhead-associated (FHA) domain-containing proteins exhibiting diverse functions, such as kinases, phosphatases, and transcription factors, have been identified to date in both eukaryotic and… (more)

Subjects/Keywords: Forkhead-associated domain; Saccharomyces cerevisiae; dNTP regulation; cell cycle

…squares represent associated cyclins (adapted from Morgan, 1997). 1.1.3 Cell Cycle… …List of Figures Figure 1.1: Eukaryotic Cell Cycle and Saccharomyces cerevisiae… …5 Figure 1.2: Cyclin-CDK Complexes and S. cerevisiae Cell Cycle Phase Progression… …28 ix List of Abbreviations Cdc: Cell division cycle CDK: Cyclin dependent kinase DDK… …Dithiothreitol EDTA: Ethylenediaminetetraacetic acid FHA: Forkhead-associated FL: Full-length GAL/RAF… 

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APA (6th Edition):

Straker, G. (2018). Characterization of the FHA domain involved in Saccharomyces cerevisiae dNTP regulation. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/13182

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):

Straker, Geburah. “Characterization of the FHA domain involved in Saccharomyces cerevisiae dNTP regulation.” 2018. Thesis, University of Waterloo. Accessed September 30, 2020. http://hdl.handle.net/10012/13182.

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

MLA Handbook (7th Edition):

Straker, Geburah. “Characterization of the FHA domain involved in Saccharomyces cerevisiae dNTP regulation.” 2018. Web. 30 Sep 2020.

Vancouver:

Straker G. Characterization of the FHA domain involved in Saccharomyces cerevisiae dNTP regulation. [Internet] [Thesis]. University of Waterloo; 2018. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/10012/13182.

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

Council of Science Editors:

Straker G. Characterization of the FHA domain involved in Saccharomyces cerevisiae dNTP regulation. [Thesis]. University of Waterloo; 2018. Available from: http://hdl.handle.net/10012/13182

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


University of Vienna

10. Levy, Johanna. ER-associated degradation of glycoproteins in a glucosylation-deficient Chinese hamster fibroblast cell line.

Degree: 2010, University of Vienna

Die Qualitätskontrolle im endoplasmatischen Retikulum (ER) stellt einen wichtigen Mechanismus zur Sicherstellung der korrekten Faltung und des richtigen Zusammenbaus von neusynthetisierten Proteinen dar. Viele Proteine,… (more)

Subjects/Keywords: 42.13 Molekularbiologie; ER / ER-assoziierter Abbau / Calnexin/Calreticulin Zyklus / N-Glykan / Qualitätskontrolle; ER / ER-associated degradation / Calnexin/Calreticulin cycle / N-glycan / Quality control

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APA (6th Edition):

Levy, J. (2010). ER-associated degradation of glycoproteins in a glucosylation-deficient Chinese hamster fibroblast cell line. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/8891/

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):

Levy, Johanna. “ER-associated degradation of glycoproteins in a glucosylation-deficient Chinese hamster fibroblast cell line.” 2010. Thesis, University of Vienna. Accessed September 30, 2020. http://othes.univie.ac.at/8891/.

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

MLA Handbook (7th Edition):

Levy, Johanna. “ER-associated degradation of glycoproteins in a glucosylation-deficient Chinese hamster fibroblast cell line.” 2010. Web. 30 Sep 2020.

Vancouver:

Levy J. ER-associated degradation of glycoproteins in a glucosylation-deficient Chinese hamster fibroblast cell line. [Internet] [Thesis]. University of Vienna; 2010. [cited 2020 Sep 30]. Available from: http://othes.univie.ac.at/8891/.

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

Council of Science Editors:

Levy J. ER-associated degradation of glycoproteins in a glucosylation-deficient Chinese hamster fibroblast cell line. [Thesis]. University of Vienna; 2010. Available from: http://othes.univie.ac.at/8891/

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


Vrije Universiteit Amsterdam

11. Yergeau, E. Effects of global warming on Antarctic soil microorganisms and associated functions .

Degree: 2008, Vrije Universiteit Amsterdam

Subjects/Keywords: Effects of global warming on antarctic soil microorganisms and associated functions; Antarctica; Global warming; Soil microorganisms; Carbon cycle; Nitrogen cycle; Molecular analyses

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APA (6th Edition):

Yergeau, E. (2008). Effects of global warming on Antarctic soil microorganisms and associated functions . (Doctoral Dissertation). Vrije Universiteit Amsterdam. Retrieved from http://hdl.handle.net/1871/13118

Chicago Manual of Style (16th Edition):

Yergeau, E. “Effects of global warming on Antarctic soil microorganisms and associated functions .” 2008. Doctoral Dissertation, Vrije Universiteit Amsterdam. Accessed September 30, 2020. http://hdl.handle.net/1871/13118.

MLA Handbook (7th Edition):

Yergeau, E. “Effects of global warming on Antarctic soil microorganisms and associated functions .” 2008. Web. 30 Sep 2020.

Vancouver:

Yergeau E. Effects of global warming on Antarctic soil microorganisms and associated functions . [Internet] [Doctoral dissertation]. Vrije Universiteit Amsterdam; 2008. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/1871/13118.

Council of Science Editors:

Yergeau E. Effects of global warming on Antarctic soil microorganisms and associated functions . [Doctoral Dissertation]. Vrije Universiteit Amsterdam; 2008. Available from: http://hdl.handle.net/1871/13118

12. Parial, Shaon Badhan. Novel Interaction, Regulation of Phosphorylation and Mitotic Localization of Cell Division Cycle Associated Protein 7 (CDCA7).

Degree: MSc -MS, Biology, 2018, York University

 Cell Division Cycle Associated Protein 7 (CDCA7) is a novel protein with poorly defined physiological significance. The proximity labeling method known as Biotin Identification (BioID)… (more)

Subjects/Keywords: Biology; Molecular biology; Cellular Biology; Biochemistry; Cancer; Tumorigenesis; Cell Division Cycle Associated Protein 7; CDCA7; Target Protein for Xenopus centrosomal kinesin-like protein 2; TPX2; Aurora A Kinase; Transfection; Western Blot; Immunoprecipitation; Cell cycle synchronization; Flow cytometry; Microscopy; Proximity Dependent Biotin Identification; BioID; Mass spectrometry; Protein-protein interaction; Evolutionarily Conserved DNA sequences; Phosphorylation; Kinase Inhibitor; Localization; Colocalization; Proposed Model

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APA (6th Edition):

Parial, S. B. (2018). Novel Interaction, Regulation of Phosphorylation and Mitotic Localization of Cell Division Cycle Associated Protein 7 (CDCA7). (Masters Thesis). York University. Retrieved from http://hdl.handle.net/10315/35017

Chicago Manual of Style (16th Edition):

Parial, Shaon Badhan. “Novel Interaction, Regulation of Phosphorylation and Mitotic Localization of Cell Division Cycle Associated Protein 7 (CDCA7).” 2018. Masters Thesis, York University. Accessed September 30, 2020. http://hdl.handle.net/10315/35017.

MLA Handbook (7th Edition):

Parial, Shaon Badhan. “Novel Interaction, Regulation of Phosphorylation and Mitotic Localization of Cell Division Cycle Associated Protein 7 (CDCA7).” 2018. Web. 30 Sep 2020.

Vancouver:

Parial SB. Novel Interaction, Regulation of Phosphorylation and Mitotic Localization of Cell Division Cycle Associated Protein 7 (CDCA7). [Internet] [Masters thesis]. York University; 2018. [cited 2020 Sep 30]. Available from: http://hdl.handle.net/10315/35017.

Council of Science Editors:

Parial SB. Novel Interaction, Regulation of Phosphorylation and Mitotic Localization of Cell Division Cycle Associated Protein 7 (CDCA7). [Masters Thesis]. York University; 2018. Available from: http://hdl.handle.net/10315/35017

13. Jurczyk, Agata. Centrosomes in Cytokinesis, Cell Cycle Progression and Ciliogenesis: a Dissertation.

Degree: Interdisciplinary Graduate Program, Molecular Medicine, 2004, U of Massachusetts : Med

  The work presented here describes novel functions for centrosome proteins, specifically for pericentrin and centriolin. The first chapter describes the involvement of pericentrin in… (more)

Subjects/Keywords: Cell Cycle Proteins; Cell Division; Centrosome; Cilia; Cytokinesis; Microtubule-Associated Proteins; Amino Acids, Peptides, and Proteins; Cells

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APA (6th Edition):

Jurczyk, A. (2004). Centrosomes in Cytokinesis, Cell Cycle Progression and Ciliogenesis: a Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/73

Chicago Manual of Style (16th Edition):

Jurczyk, Agata. “Centrosomes in Cytokinesis, Cell Cycle Progression and Ciliogenesis: a Dissertation.” 2004. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 30, 2020. https://escholarship.umassmed.edu/gsbs_diss/73.

MLA Handbook (7th Edition):

Jurczyk, Agata. “Centrosomes in Cytokinesis, Cell Cycle Progression and Ciliogenesis: a Dissertation.” 2004. Web. 30 Sep 2020.

Vancouver:

Jurczyk A. Centrosomes in Cytokinesis, Cell Cycle Progression and Ciliogenesis: a Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2004. [cited 2020 Sep 30]. Available from: https://escholarship.umassmed.edu/gsbs_diss/73.

Council of Science Editors:

Jurczyk A. Centrosomes in Cytokinesis, Cell Cycle Progression and Ciliogenesis: a Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2004. Available from: https://escholarship.umassmed.edu/gsbs_diss/73

14. MA JIAJUN. Two Topics on Local Theta Correspondence.

Degree: 2012, National University of Singapore

Subjects/Keywords: Representation theory of classical groups; local theta correspondence; invariant theory; transfer of K-type; associated cycle; highest weight module

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APA (6th Edition):

JIAJUN, M. (2012). Two Topics on Local Theta Correspondence. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/36425

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):

JIAJUN, MA. “Two Topics on Local Theta Correspondence.” 2012. Thesis, National University of Singapore. Accessed September 30, 2020. http://scholarbank.nus.edu.sg/handle/10635/36425.

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

MLA Handbook (7th Edition):

JIAJUN, MA. “Two Topics on Local Theta Correspondence.” 2012. Web. 30 Sep 2020.

Vancouver:

JIAJUN M. Two Topics on Local Theta Correspondence. [Internet] [Thesis]. National University of Singapore; 2012. [cited 2020 Sep 30]. Available from: http://scholarbank.nus.edu.sg/handle/10635/36425.

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

Council of Science Editors:

JIAJUN M. Two Topics on Local Theta Correspondence. [Thesis]. National University of Singapore; 2012. Available from: http://scholarbank.nus.edu.sg/handle/10635/36425

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

15. Rosa, Jack. Perturbation and Modulation of Microtubule Cytoskeletal Elements in Response to the Potentially Oncogenic Molecules, Survivin and P53, and Cytokinesis: A Dissertation.

Degree: Interdisciplinary Graduate Program, Molecular Medicine, 2006, U of Massachusetts : Med

  A complex network of protein filaments collectively known as the cytoskeleton carries out several crucial cellular processes. These functions include, but are not limited… (more)

Subjects/Keywords: Microtubules; Cytoskeleton; Microtubule-Associated Proteins; Cell Cycle Proteins; Neoplasm Proteins; Tumor Suppressor Protein p53; Protein-Serine-Threonine Kinases; Cytokinesisl; Centrosome; Amino Acids, Peptides, and Proteins; Cells; Neoplasms

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APA (6th Edition):

Rosa, J. (2006). Perturbation and Modulation of Microtubule Cytoskeletal Elements in Response to the Potentially Oncogenic Molecules, Survivin and P53, and Cytokinesis: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/280

Chicago Manual of Style (16th Edition):

Rosa, Jack. “Perturbation and Modulation of Microtubule Cytoskeletal Elements in Response to the Potentially Oncogenic Molecules, Survivin and P53, and Cytokinesis: A Dissertation.” 2006. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 30, 2020. https://escholarship.umassmed.edu/gsbs_diss/280.

MLA Handbook (7th Edition):

Rosa, Jack. “Perturbation and Modulation of Microtubule Cytoskeletal Elements in Response to the Potentially Oncogenic Molecules, Survivin and P53, and Cytokinesis: A Dissertation.” 2006. Web. 30 Sep 2020.

Vancouver:

Rosa J. Perturbation and Modulation of Microtubule Cytoskeletal Elements in Response to the Potentially Oncogenic Molecules, Survivin and P53, and Cytokinesis: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2006. [cited 2020 Sep 30]. Available from: https://escholarship.umassmed.edu/gsbs_diss/280.

Council of Science Editors:

Rosa J. Perturbation and Modulation of Microtubule Cytoskeletal Elements in Response to the Potentially Oncogenic Molecules, Survivin and P53, and Cytokinesis: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2006. Available from: https://escholarship.umassmed.edu/gsbs_diss/280

16. Abramo, Kristin N. Building the Interphase Nucleus: A study on the kinetics of 3D chromosome formation, temporal relation to active transcription, and the role of nuclear RNAs.

Degree: Interdisciplinary Graduate Program, Program in Systems Biology, 2020, U of Massachusetts : Med

  Following the discovery of the one-dimensional sequence of human DNA, much focus has been directed on microscopy and molecular techniques to learn about the… (more)

Subjects/Keywords: chromatin; Hi-C; transcription; RNA; telophase; kinetics; cell cycle; mitosis; interphase; chromosome conformation capture; CTCF; condensin; cohesin; TAD; topologically associated domain; loop extrusion; microphase separation; NCAPH; Rad21; NCAPH2; synchronization; G1 entry; triptolide; DRB; RNase A; Bioinformatics; Cell Biology; Computational Biology; Genomics; Laboratory and Basic Science Research; Molecular Biology; Molecular Genetics; Systems Biology

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APA (6th Edition):

Abramo, K. N. (2020). Building the Interphase Nucleus: A study on the kinetics of 3D chromosome formation, temporal relation to active transcription, and the role of nuclear RNAs. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/1099

Chicago Manual of Style (16th Edition):

Abramo, Kristin N. “Building the Interphase Nucleus: A study on the kinetics of 3D chromosome formation, temporal relation to active transcription, and the role of nuclear RNAs.” 2020. Doctoral Dissertation, U of Massachusetts : Med. Accessed September 30, 2020. https://escholarship.umassmed.edu/gsbs_diss/1099.

MLA Handbook (7th Edition):

Abramo, Kristin N. “Building the Interphase Nucleus: A study on the kinetics of 3D chromosome formation, temporal relation to active transcription, and the role of nuclear RNAs.” 2020. Web. 30 Sep 2020.

Vancouver:

Abramo KN. Building the Interphase Nucleus: A study on the kinetics of 3D chromosome formation, temporal relation to active transcription, and the role of nuclear RNAs. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2020. [cited 2020 Sep 30]. Available from: https://escholarship.umassmed.edu/gsbs_diss/1099.

Council of Science Editors:

Abramo KN. Building the Interphase Nucleus: A study on the kinetics of 3D chromosome formation, temporal relation to active transcription, and the role of nuclear RNAs. [Doctoral Dissertation]. U of Massachusetts : Med; 2020. Available from: https://escholarship.umassmed.edu/gsbs_diss/1099

17. 川本, 幸寛. Mucosa-associated lymphoid tissue 1(MALT1)による口腔癌細胞のケラチン発現と増殖能の変化について : Alterations of Keratin Expression and Proliferation of Oral Carcinoma Cells in Response to Mucosa-Associated Lymphoid Tissue 1 (MALT1).

Degree: 博士(歯学), 2014, Meikai University / 明海大学

2013

Subjects/Keywords: MALT1; 口腔扁平上皮癌|ケラチン|細胞増殖|細胞周期; Mucosa-associated lymphoid tissue 1; Oral squamous cell carcinoma; Keratin; Cell proliferation; Cell cycle

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APA (6th Edition):

川本, . (2014). Mucosa-associated lymphoid tissue 1(MALT1)による口腔癌細胞のケラチン発現と増殖能の変化について : Alterations of Keratin Expression and Proliferation of Oral Carcinoma Cells in Response to Mucosa-Associated Lymphoid Tissue 1 (MALT1). (Thesis). Meikai University / 明海大学. Retrieved from http://id.nii.ac.jp/1216/00000022/

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):

川本, 幸寛. “Mucosa-associated lymphoid tissue 1(MALT1)による口腔癌細胞のケラチン発現と増殖能の変化について : Alterations of Keratin Expression and Proliferation of Oral Carcinoma Cells in Response to Mucosa-Associated Lymphoid Tissue 1 (MALT1).” 2014. Thesis, Meikai University / 明海大学. Accessed September 30, 2020. http://id.nii.ac.jp/1216/00000022/.

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

MLA Handbook (7th Edition):

川本, 幸寛. “Mucosa-associated lymphoid tissue 1(MALT1)による口腔癌細胞のケラチン発現と増殖能の変化について : Alterations of Keratin Expression and Proliferation of Oral Carcinoma Cells in Response to Mucosa-Associated Lymphoid Tissue 1 (MALT1).” 2014. Web. 30 Sep 2020.

Vancouver:

川本 . Mucosa-associated lymphoid tissue 1(MALT1)による口腔癌細胞のケラチン発現と増殖能の変化について : Alterations of Keratin Expression and Proliferation of Oral Carcinoma Cells in Response to Mucosa-Associated Lymphoid Tissue 1 (MALT1). [Internet] [Thesis]. Meikai University / 明海大学; 2014. [cited 2020 Sep 30]. Available from: http://id.nii.ac.jp/1216/00000022/.

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

Council of Science Editors:

川本 . Mucosa-associated lymphoid tissue 1(MALT1)による口腔癌細胞のケラチン発現と増殖能の変化について : Alterations of Keratin Expression and Proliferation of Oral Carcinoma Cells in Response to Mucosa-Associated Lymphoid Tissue 1 (MALT1). [Thesis]. Meikai University / 明海大学; 2014. Available from: http://id.nii.ac.jp/1216/00000022/

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

18. Buckalew, Richard L. Mathematical Models in Cell Cycle Biology and Pulmonary Immunity.

Degree: PhD, Mathematics (Arts and Sciences), 2014, Ohio University

 Mathematical models are used to study two biological systems: pulmonary innate immunity and autonomous oscillation in yeast. In order to better understand the dynamics of… (more)

Subjects/Keywords: Applied Mathematics; Cellular Biology; Immunology; mathematical biology; cell cycle; pulmonary innate immunity; immunity; ODE model; PDE model; couples oscillators; VAP; ventilator associated pneumonia; autonomous oscillation; S cerevisiae; quorum sensing; cell cycle clustering; dynamical systems

…Lavage CDC · Cell Division Cycle HCH · Hygroscopic Condenser Humidifier IVP · Initial… …Partial Differential Equation PMN · Polymorphonuclear Leukocyte VAP · Ventilator Associated… …risk of developing ventilator associated pneumonia (VAP), an infection of the lungs… …unwieldy for calculations by hand. 31 3 Response / Signaling Models of Cell Cycle Feedback… …division cycle (CDC) because of the latter’s segmentation into distinct phases. The… 

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

APA (6th Edition):

Buckalew, R. L. (2014). Mathematical Models in Cell Cycle Biology and Pulmonary Immunity. (Doctoral Dissertation). Ohio University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1395242276

Chicago Manual of Style (16th Edition):

Buckalew, Richard L. “Mathematical Models in Cell Cycle Biology and Pulmonary Immunity.” 2014. Doctoral Dissertation, Ohio University. Accessed September 30, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1395242276.

MLA Handbook (7th Edition):

Buckalew, Richard L. “Mathematical Models in Cell Cycle Biology and Pulmonary Immunity.” 2014. Web. 30 Sep 2020.

Vancouver:

Buckalew RL. Mathematical Models in Cell Cycle Biology and Pulmonary Immunity. [Internet] [Doctoral dissertation]. Ohio University; 2014. [cited 2020 Sep 30]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1395242276.

Council of Science Editors:

Buckalew RL. Mathematical Models in Cell Cycle Biology and Pulmonary Immunity. [Doctoral Dissertation]. Ohio University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ohiou1395242276

.