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You searched for subject:(Centrosome). Showing records 1 – 30 of 119 total matches.

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Université de Montréal

1. Javadi Esfehani, Yalda. CEP78, a novel centrosomal protein .

Degree: 2014, Université de Montréal

 Contexte: Le centrosome est un petit organite bien connu pour son rôle dans l'établissement du fuseau bipolaire pendant la division cellulaire. Les déficiences de la… (more)

Subjects/Keywords: CEP78; Centrosome; CEP170; Microtubules

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

APA (6th Edition):

Javadi Esfehani, Y. (2014). CEP78, a novel centrosomal protein . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/11029

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):

Javadi Esfehani, Yalda. “CEP78, a novel centrosomal protein .” 2014. Thesis, Université de Montréal. Accessed November 19, 2019. http://hdl.handle.net/1866/11029.

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

MLA Handbook (7th Edition):

Javadi Esfehani, Yalda. “CEP78, a novel centrosomal protein .” 2014. Web. 19 Nov 2019.

Vancouver:

Javadi Esfehani Y. CEP78, a novel centrosomal protein . [Internet] [Thesis]. Université de Montréal; 2014. [cited 2019 Nov 19]. Available from: http://hdl.handle.net/1866/11029.

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

Council of Science Editors:

Javadi Esfehani Y. CEP78, a novel centrosomal protein . [Thesis]. Université de Montréal; 2014. Available from: http://hdl.handle.net/1866/11029

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


EPFL

2. Kohlmaier, Gregor. Functional characterization of the SAS-4-related protein CPAP in centrosome biology of human cells.

Degree: 2009, EPFL

 The centrosome is an organelle that resides at the center of most animal cells and comprises two microtubule-based centriole cylinders surrounded by pericentriolar material (PCM).… (more)

Subjects/Keywords: centrosome; centriole; cell division; cancer

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APA (6th Edition):

Kohlmaier, G. (2009). Functional characterization of the SAS-4-related protein CPAP in centrosome biology of human cells. (Thesis). EPFL. Retrieved from http://infoscience.epfl.ch/record/140340

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):

Kohlmaier, Gregor. “Functional characterization of the SAS-4-related protein CPAP in centrosome biology of human cells.” 2009. Thesis, EPFL. Accessed November 19, 2019. http://infoscience.epfl.ch/record/140340.

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

MLA Handbook (7th Edition):

Kohlmaier, Gregor. “Functional characterization of the SAS-4-related protein CPAP in centrosome biology of human cells.” 2009. Web. 19 Nov 2019.

Vancouver:

Kohlmaier G. Functional characterization of the SAS-4-related protein CPAP in centrosome biology of human cells. [Internet] [Thesis]. EPFL; 2009. [cited 2019 Nov 19]. Available from: http://infoscience.epfl.ch/record/140340.

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

Council of Science Editors:

Kohlmaier G. Functional characterization of the SAS-4-related protein CPAP in centrosome biology of human cells. [Thesis]. EPFL; 2009. Available from: http://infoscience.epfl.ch/record/140340

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


University of Ottawa

3. Pundir, Sheetal. The Characterization of the Novel Chloroquine Derivative VR23 for its Anticancer Properties .

Degree: 2015, University of Ottawa

 Since Bortezomib®, a proteasome inhibitor, was approved by US FDA for the treatment of multiple myeloma in 2003, proteasome is recognized as one of the… (more)

Subjects/Keywords: Proteasome; Centrosome; Chloroquine; Anticancer

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APA (6th Edition):

Pundir, S. (2015). The Characterization of the Novel Chloroquine Derivative VR23 for its Anticancer Properties . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/32405

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):

Pundir, Sheetal. “The Characterization of the Novel Chloroquine Derivative VR23 for its Anticancer Properties .” 2015. Thesis, University of Ottawa. Accessed November 19, 2019. http://hdl.handle.net/10393/32405.

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

MLA Handbook (7th Edition):

Pundir, Sheetal. “The Characterization of the Novel Chloroquine Derivative VR23 for its Anticancer Properties .” 2015. Web. 19 Nov 2019.

Vancouver:

Pundir S. The Characterization of the Novel Chloroquine Derivative VR23 for its Anticancer Properties . [Internet] [Thesis]. University of Ottawa; 2015. [cited 2019 Nov 19]. Available from: http://hdl.handle.net/10393/32405.

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

Council of Science Editors:

Pundir S. The Characterization of the Novel Chloroquine Derivative VR23 for its Anticancer Properties . [Thesis]. University of Ottawa; 2015. Available from: http://hdl.handle.net/10393/32405

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


University of California – San Francisco

4. Citron, Yemima Rose. The Small Conserved CM2 Domain in Centrosomin is a Multi-functional Binding Domain that Drives Protein Organization in the Centrosome.

Degree: Biophysics, 2018, University of California – San Francisco

 The centrosome serves as the main microtubule-organizing center in metazoan cells, yet despite its functional importance, little is known mechanistically about the structure and organizational… (more)

Subjects/Keywords: Biophysics; Centrosome; Centrosomin; Self-Assembly

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APA (6th Edition):

Citron, Y. R. (2018). The Small Conserved CM2 Domain in Centrosomin is a Multi-functional Binding Domain that Drives Protein Organization in the Centrosome. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/9f2803zr

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):

Citron, Yemima Rose. “The Small Conserved CM2 Domain in Centrosomin is a Multi-functional Binding Domain that Drives Protein Organization in the Centrosome.” 2018. Thesis, University of California – San Francisco. Accessed November 19, 2019. http://www.escholarship.org/uc/item/9f2803zr.

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

MLA Handbook (7th Edition):

Citron, Yemima Rose. “The Small Conserved CM2 Domain in Centrosomin is a Multi-functional Binding Domain that Drives Protein Organization in the Centrosome.” 2018. Web. 19 Nov 2019.

Vancouver:

Citron YR. The Small Conserved CM2 Domain in Centrosomin is a Multi-functional Binding Domain that Drives Protein Organization in the Centrosome. [Internet] [Thesis]. University of California – San Francisco; 2018. [cited 2019 Nov 19]. Available from: http://www.escholarship.org/uc/item/9f2803zr.

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

Council of Science Editors:

Citron YR. The Small Conserved CM2 Domain in Centrosomin is a Multi-functional Binding Domain that Drives Protein Organization in the Centrosome. [Thesis]. University of California – San Francisco; 2018. Available from: http://www.escholarship.org/uc/item/9f2803zr

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


Universidade Nova

5. Dores, Katharina Santos das. How do cancer cells cope with supernumerary centrosomes?.

Degree: 2015, Universidade Nova

 Cancer kills one in five people each year in western societies, therefore clinicians are eager to find novel diagnostic, prognostic and therapeutic tools to predict… (more)

Subjects/Keywords: Centrosome amplification; Cancer; Mitosis; Clustering; Centrosome extrusion; Centrosome inactivation; Domínio/Área Científica::Engenharia e Tecnologia::Engenharia Química

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APA (6th Edition):

Dores, K. S. d. (2015). How do cancer cells cope with supernumerary centrosomes?. (Thesis). Universidade Nova. Retrieved from https://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/31886

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):

Dores, Katharina Santos das. “How do cancer cells cope with supernumerary centrosomes?.” 2015. Thesis, Universidade Nova. Accessed November 19, 2019. https://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/31886.

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

MLA Handbook (7th Edition):

Dores, Katharina Santos das. “How do cancer cells cope with supernumerary centrosomes?.” 2015. Web. 19 Nov 2019.

Vancouver:

Dores KSd. How do cancer cells cope with supernumerary centrosomes?. [Internet] [Thesis]. Universidade Nova; 2015. [cited 2019 Nov 19]. Available from: https://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/31886.

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

Council of Science Editors:

Dores KSd. How do cancer cells cope with supernumerary centrosomes?. [Thesis]. Universidade Nova; 2015. Available from: https://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/31886

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


University of Toledo

6. Wang, Yongheng. The role of Sas-4 in ciliogenesis and centriole biogenesis in Drosophila.

Degree: MS, Biology (Cell-Molecular Biology), 2016, University of Toledo

 The centrosome is an organelle essential for microtubule nucleation, cell division and cilia formation. A centrosome consists of a pair of centrioles surrounded by pericentriolar… (more)

Subjects/Keywords: Biology; Sas-4, ciliogenesis, centrosome biogenesis

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APA (6th Edition):

Wang, Y. (2016). The role of Sas-4 in ciliogenesis and centriole biogenesis in Drosophila. (Masters Thesis). University of Toledo. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=toledo1461074141

Chicago Manual of Style (16th Edition):

Wang, Yongheng. “The role of Sas-4 in ciliogenesis and centriole biogenesis in Drosophila.” 2016. Masters Thesis, University of Toledo. Accessed November 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1461074141.

MLA Handbook (7th Edition):

Wang, Yongheng. “The role of Sas-4 in ciliogenesis and centriole biogenesis in Drosophila.” 2016. Web. 19 Nov 2019.

Vancouver:

Wang Y. The role of Sas-4 in ciliogenesis and centriole biogenesis in Drosophila. [Internet] [Masters thesis]. University of Toledo; 2016. [cited 2019 Nov 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1461074141.

Council of Science Editors:

Wang Y. The role of Sas-4 in ciliogenesis and centriole biogenesis in Drosophila. [Masters Thesis]. University of Toledo; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1461074141


University of Colorado

7. Daez, Carolina. Localization and Interactions of γ-Tubulin Tether Spc110 C-Terminus in Yeast Centrosome.

Degree: PhD, 2017, University of Colorado

  Centrosomes are essential components of the cell-cycle machinery of eukaryotic cells; dysfunction of centrosomes is thus linked to cell-cycle misregulation, aneuploidy and tumorigenesis. A… (more)

Subjects/Keywords: centrosome; yeast; γ-tubulin; Molecular Biology

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APA (6th Edition):

Daez, C. (2017). Localization and Interactions of γ-Tubulin Tether Spc110 C-Terminus in Yeast Centrosome. (Doctoral Dissertation). University of Colorado. Retrieved from http://scholar.colorado.edu/mcdb_gradetds/68

Chicago Manual of Style (16th Edition):

Daez, Carolina. “Localization and Interactions of γ-Tubulin Tether Spc110 C-Terminus in Yeast Centrosome.” 2017. Doctoral Dissertation, University of Colorado. Accessed November 19, 2019. http://scholar.colorado.edu/mcdb_gradetds/68.

MLA Handbook (7th Edition):

Daez, Carolina. “Localization and Interactions of γ-Tubulin Tether Spc110 C-Terminus in Yeast Centrosome.” 2017. Web. 19 Nov 2019.

Vancouver:

Daez C. Localization and Interactions of γ-Tubulin Tether Spc110 C-Terminus in Yeast Centrosome. [Internet] [Doctoral dissertation]. University of Colorado; 2017. [cited 2019 Nov 19]. Available from: http://scholar.colorado.edu/mcdb_gradetds/68.

Council of Science Editors:

Daez C. Localization and Interactions of γ-Tubulin Tether Spc110 C-Terminus in Yeast Centrosome. [Doctoral Dissertation]. University of Colorado; 2017. Available from: http://scholar.colorado.edu/mcdb_gradetds/68

8. Pannu, Vaishali. Conduits of Intratumor Heterogeneity: Centrosome Amplification, Centrosome Clustering and Mitotic Frequency.

Degree: PhD, Biology, 2014, Georgia State University

  Tumor initiation and progression is dependent on the acquisition and accumulation of multiple driver mutations that acti­vate and fuel oncogenic pathways and deactivate tumor… (more)

Subjects/Keywords: Mitotic frequency; Intratumoral heterogeneity; Metastasis; Centrosome amplification

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

APA (6th Edition):

Pannu, V. (2014). Conduits of Intratumor Heterogeneity: Centrosome Amplification, Centrosome Clustering and Mitotic Frequency. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/biology_diss/153

Chicago Manual of Style (16th Edition):

Pannu, Vaishali. “Conduits of Intratumor Heterogeneity: Centrosome Amplification, Centrosome Clustering and Mitotic Frequency.” 2014. Doctoral Dissertation, Georgia State University. Accessed November 19, 2019. https://scholarworks.gsu.edu/biology_diss/153.

MLA Handbook (7th Edition):

Pannu, Vaishali. “Conduits of Intratumor Heterogeneity: Centrosome Amplification, Centrosome Clustering and Mitotic Frequency.” 2014. Web. 19 Nov 2019.

Vancouver:

Pannu V. Conduits of Intratumor Heterogeneity: Centrosome Amplification, Centrosome Clustering and Mitotic Frequency. [Internet] [Doctoral dissertation]. Georgia State University; 2014. [cited 2019 Nov 19]. Available from: https://scholarworks.gsu.edu/biology_diss/153.

Council of Science Editors:

Pannu V. Conduits of Intratumor Heterogeneity: Centrosome Amplification, Centrosome Clustering and Mitotic Frequency. [Doctoral Dissertation]. Georgia State University; 2014. Available from: https://scholarworks.gsu.edu/biology_diss/153


Universiteit Utrecht

9. Tas, R.P. The role of the centrosome in mitotic spindle formation.

Degree: 2014, Universiteit Utrecht

 During cell division, correct chromosome segregation between the two daughter cells is important to maintain the genetic balance in the organism. A bipolar mitotic spindle… (more)

Subjects/Keywords: Centrosome; non-centrosomal; microtubule; spindle formation; review

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APA (6th Edition):

Tas, R. P. (2014). The role of the centrosome in mitotic spindle formation. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/296987

Chicago Manual of Style (16th Edition):

Tas, R P. “The role of the centrosome in mitotic spindle formation.” 2014. Masters Thesis, Universiteit Utrecht. Accessed November 19, 2019. http://dspace.library.uu.nl:8080/handle/1874/296987.

MLA Handbook (7th Edition):

Tas, R P. “The role of the centrosome in mitotic spindle formation.” 2014. Web. 19 Nov 2019.

Vancouver:

Tas RP. The role of the centrosome in mitotic spindle formation. [Internet] [Masters thesis]. Universiteit Utrecht; 2014. [cited 2019 Nov 19]. Available from: http://dspace.library.uu.nl:8080/handle/1874/296987.

Council of Science Editors:

Tas RP. The role of the centrosome in mitotic spindle formation. [Masters Thesis]. Universiteit Utrecht; 2014. Available from: http://dspace.library.uu.nl:8080/handle/1874/296987


University of Cambridge

10. Quarantotti, Valentina. Towards the understanding of pericentriolar satellite biology.

Degree: PhD, 2018, University of Cambridge

 Pericentriolar satellites (PS) are electron dense granules surrounding the centrosome, the major microtubule-organizing centre in eukaryotic cells. In cycling cells the centrosome promotes spindle assembly… (more)

Subjects/Keywords: centrosome; centriole; pericentriolar satellite; PCM1; proteomic composition

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APA (6th Edition):

Quarantotti, V. (2018). Towards the understanding of pericentriolar satellite biology. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/274539 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744654

Chicago Manual of Style (16th Edition):

Quarantotti, Valentina. “Towards the understanding of pericentriolar satellite biology.” 2018. Doctoral Dissertation, University of Cambridge. Accessed November 19, 2019. https://www.repository.cam.ac.uk/handle/1810/274539 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744654.

MLA Handbook (7th Edition):

Quarantotti, Valentina. “Towards the understanding of pericentriolar satellite biology.” 2018. Web. 19 Nov 2019.

Vancouver:

Quarantotti V. Towards the understanding of pericentriolar satellite biology. [Internet] [Doctoral dissertation]. University of Cambridge; 2018. [cited 2019 Nov 19]. Available from: https://www.repository.cam.ac.uk/handle/1810/274539 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744654.

Council of Science Editors:

Quarantotti V. Towards the understanding of pericentriolar satellite biology. [Doctoral Dissertation]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/274539 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.744654


University of Cambridge

11. Quarantotti, Valentina. Towards the understanding of pericentriolar satellite biology .

Degree: 2018, University of Cambridge

 Pericentriolar satellites (PS) are electron dense granules surrounding the centrosome, the major microtubule-organizing centre in eukaryotic cells. In cycling cells the centrosome promotes spindle assembly… (more)

Subjects/Keywords: centrosome; centriole; pericentriolar satellite; PCM1; proteomic composition

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

APA (6th Edition):

Quarantotti, V. (2018). Towards the understanding of pericentriolar satellite biology . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/274539

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):

Quarantotti, Valentina. “Towards the understanding of pericentriolar satellite biology .” 2018. Thesis, University of Cambridge. Accessed November 19, 2019. https://www.repository.cam.ac.uk/handle/1810/274539.

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

MLA Handbook (7th Edition):

Quarantotti, Valentina. “Towards the understanding of pericentriolar satellite biology .” 2018. Web. 19 Nov 2019.

Vancouver:

Quarantotti V. Towards the understanding of pericentriolar satellite biology . [Internet] [Thesis]. University of Cambridge; 2018. [cited 2019 Nov 19]. Available from: https://www.repository.cam.ac.uk/handle/1810/274539.

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

Council of Science Editors:

Quarantotti V. Towards the understanding of pericentriolar satellite biology . [Thesis]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/274539

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


University of Sydney

12. Lui, Christina Ka-Wing. Characterisation of APC localisation, dynamics and functions at the centrosome .

Degree: 2014, University of Sydney

 Adenomatous polyposis coli (APC) is a tumour suppressor protein and regulator of the wnt signalling pathway. APC is mutated in >90% of colorectal tumours and… (more)

Subjects/Keywords: APC; centrosome; localisation; microtubule; nucleation; dynamics

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APA (6th Edition):

Lui, C. K. (2014). Characterisation of APC localisation, dynamics and functions at the centrosome . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/12507

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):

Lui, Christina Ka-Wing. “Characterisation of APC localisation, dynamics and functions at the centrosome .” 2014. Thesis, University of Sydney. Accessed November 19, 2019. http://hdl.handle.net/2123/12507.

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

MLA Handbook (7th Edition):

Lui, Christina Ka-Wing. “Characterisation of APC localisation, dynamics and functions at the centrosome .” 2014. Web. 19 Nov 2019.

Vancouver:

Lui CK. Characterisation of APC localisation, dynamics and functions at the centrosome . [Internet] [Thesis]. University of Sydney; 2014. [cited 2019 Nov 19]. Available from: http://hdl.handle.net/2123/12507.

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

Council of Science Editors:

Lui CK. Characterisation of APC localisation, dynamics and functions at the centrosome . [Thesis]. University of Sydney; 2014. Available from: http://hdl.handle.net/2123/12507

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


University of Cincinnati

13. BENNETT, RICHARD A. The p53-p21-Cyclin E Pathway in Centrosome Amplification and Chromosome Instability.

Degree: PhD, Medicine : Cell and Molecular Biology, 2007, University of Cincinnati

 Cancer is characterized by cells that have many genetic mutations. Chromosome instability is a hallmark of cancer, because it promotes the acquisition of the many… (more)

Subjects/Keywords: Centrosome; Chromosome Instability; p53; p21; Cyclin E; Cancer; Centrosome amplification; Mitosis; Anticancer drugs

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APA (6th Edition):

BENNETT, R. A. (2007). The p53-p21-Cyclin E Pathway in Centrosome Amplification and Chromosome Instability. (Doctoral Dissertation). University of Cincinnati. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ucin1189188730

Chicago Manual of Style (16th Edition):

BENNETT, RICHARD A. “The p53-p21-Cyclin E Pathway in Centrosome Amplification and Chromosome Instability.” 2007. Doctoral Dissertation, University of Cincinnati. Accessed November 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1189188730.

MLA Handbook (7th Edition):

BENNETT, RICHARD A. “The p53-p21-Cyclin E Pathway in Centrosome Amplification and Chromosome Instability.” 2007. Web. 19 Nov 2019.

Vancouver:

BENNETT RA. The p53-p21-Cyclin E Pathway in Centrosome Amplification and Chromosome Instability. [Internet] [Doctoral dissertation]. University of Cincinnati; 2007. [cited 2019 Nov 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1189188730.

Council of Science Editors:

BENNETT RA. The p53-p21-Cyclin E Pathway in Centrosome Amplification and Chromosome Instability. [Doctoral Dissertation]. University of Cincinnati; 2007. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ucin1189188730

14. Gaume, Xavier. Localisation et fonctions de la nucléoline au centrosome : Localisation and functions of nucleolin at the centrosome.

Degree: Docteur es, Sciences de la Vie, 2014, Lyon, École normale supérieure

La nucléoline est une des protéines les plus abondantes des nucléoles. Ses fonctions ne sont cependant pas restreintes à la biogénèse des ribosomes. En absence… (more)

Subjects/Keywords: Nucléoline; Centrosome; Microtubules; Centriole mature; Ancrage; Nucléation; Nucleolin; Centrosome; Microtubules; Mature centriole; Anchoring; Nucleation

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APA (6th Edition):

Gaume, X. (2014). Localisation et fonctions de la nucléoline au centrosome : Localisation and functions of nucleolin at the centrosome. (Doctoral Dissertation). Lyon, École normale supérieure. Retrieved from http://www.theses.fr/2014ENSL0890

Chicago Manual of Style (16th Edition):

Gaume, Xavier. “Localisation et fonctions de la nucléoline au centrosome : Localisation and functions of nucleolin at the centrosome.” 2014. Doctoral Dissertation, Lyon, École normale supérieure. Accessed November 19, 2019. http://www.theses.fr/2014ENSL0890.

MLA Handbook (7th Edition):

Gaume, Xavier. “Localisation et fonctions de la nucléoline au centrosome : Localisation and functions of nucleolin at the centrosome.” 2014. Web. 19 Nov 2019.

Vancouver:

Gaume X. Localisation et fonctions de la nucléoline au centrosome : Localisation and functions of nucleolin at the centrosome. [Internet] [Doctoral dissertation]. Lyon, École normale supérieure; 2014. [cited 2019 Nov 19]. Available from: http://www.theses.fr/2014ENSL0890.

Council of Science Editors:

Gaume X. Localisation et fonctions de la nucléoline au centrosome : Localisation and functions of nucleolin at the centrosome. [Doctoral Dissertation]. Lyon, École normale supérieure; 2014. Available from: http://www.theses.fr/2014ENSL0890

15. Bouhlel Bougdhira, Imen. The centrin-binding protein Sfi1 : functions in fission yeast and human : Fonctions de la protéine centrosomale Sfi1 chez la levure et l'homme.

Degree: Docteur es, Sciences de la vie et de la santé, 2017, Paris Saclay

Le centrosome est le centre organisateur des microtubules dans les cellules animales, il nucléé les microtubules interphasiques ainsi que le fuseau mitotique. Les centrosomes sont… (more)

Subjects/Keywords: Mitose; Centrosome; Spb; Division cellulaire; Centriole; Centrine; Mitosis; Centrosome; Spb; Cell division; Centriole; Centrin

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APA (6th Edition):

Bouhlel Bougdhira, I. (2017). The centrin-binding protein Sfi1 : functions in fission yeast and human : Fonctions de la protéine centrosomale Sfi1 chez la levure et l'homme. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2017SACLS465

Chicago Manual of Style (16th Edition):

Bouhlel Bougdhira, Imen. “The centrin-binding protein Sfi1 : functions in fission yeast and human : Fonctions de la protéine centrosomale Sfi1 chez la levure et l'homme.” 2017. Doctoral Dissertation, Paris Saclay. Accessed November 19, 2019. http://www.theses.fr/2017SACLS465.

MLA Handbook (7th Edition):

Bouhlel Bougdhira, Imen. “The centrin-binding protein Sfi1 : functions in fission yeast and human : Fonctions de la protéine centrosomale Sfi1 chez la levure et l'homme.” 2017. Web. 19 Nov 2019.

Vancouver:

Bouhlel Bougdhira I. The centrin-binding protein Sfi1 : functions in fission yeast and human : Fonctions de la protéine centrosomale Sfi1 chez la levure et l'homme. [Internet] [Doctoral dissertation]. Paris Saclay; 2017. [cited 2019 Nov 19]. Available from: http://www.theses.fr/2017SACLS465.

Council of Science Editors:

Bouhlel Bougdhira I. The centrin-binding protein Sfi1 : functions in fission yeast and human : Fonctions de la protéine centrosomale Sfi1 chez la levure et l'homme. [Doctoral Dissertation]. Paris Saclay; 2017. Available from: http://www.theses.fr/2017SACLS465


National University of Ireland – Galway

16. Adesanya, Yetunde. Centrobin functions in centriole duplication, primary ciliogenesis and genome maintenance.

Degree: 2018, National University of Ireland – Galway

 The centrosome is composed of numerous proteins that make up its core structure. Other proteins also transiently localise and interact with centrosomal proteins for functional… (more)

Subjects/Keywords: Centrobin; Daughter centriole; Centrosome; DNA damage; Primary ciliogenesis; Primary cilia; Centrosome duplication; Biochemistry; Natural sciences

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APA (6th Edition):

Adesanya, Y. (2018). Centrobin functions in centriole duplication, primary ciliogenesis and genome maintenance. (Thesis). National University of Ireland – Galway. Retrieved from http://hdl.handle.net/10379/7187

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):

Adesanya, Yetunde. “Centrobin functions in centriole duplication, primary ciliogenesis and genome maintenance.” 2018. Thesis, National University of Ireland – Galway. Accessed November 19, 2019. http://hdl.handle.net/10379/7187.

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

MLA Handbook (7th Edition):

Adesanya, Yetunde. “Centrobin functions in centriole duplication, primary ciliogenesis and genome maintenance.” 2018. Web. 19 Nov 2019.

Vancouver:

Adesanya Y. Centrobin functions in centriole duplication, primary ciliogenesis and genome maintenance. [Internet] [Thesis]. National University of Ireland – Galway; 2018. [cited 2019 Nov 19]. Available from: http://hdl.handle.net/10379/7187.

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

Council of Science Editors:

Adesanya Y. Centrobin functions in centriole duplication, primary ciliogenesis and genome maintenance. [Thesis]. National University of Ireland – Galway; 2018. Available from: http://hdl.handle.net/10379/7187

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

17. Ribe-Pinachyan, Emilie. Des Polycystines au centrosome, une enzyme clef : la calcium/calmoduline dependent kinase 2 : From polycystins to centrosomes, a key enzyme : the calcium/calmodulin dependant kinase 2.

Degree: Docteur es, Pathologie humaine, 2010, Aix-Marseille 2

La polykystose rénale autosomique dominante (ADPKD) est la maladie monogéniquehumaine la plus fréquente (prévalence 1/800). Les gènes responsables de cette maladie sont PKD1(codant pour PC1)… (more)

Subjects/Keywords: Polykystose rénale autosomique dominante; Centrosome; CaMKII; Polycystine; Cil primaire; Aneuploïdie; Modèles animaux d'ADPKD; Fibroblastes; Polycystin-2; Mitosis; Polycystic kidney disease; Centrosome

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APA (6th Edition):

Ribe-Pinachyan, E. (2010). Des Polycystines au centrosome, une enzyme clef : la calcium/calmoduline dependent kinase 2 : From polycystins to centrosomes, a key enzyme : the calcium/calmodulin dependant kinase 2. (Doctoral Dissertation). Aix-Marseille 2. Retrieved from http://www.theses.fr/2010AIX20715

Chicago Manual of Style (16th Edition):

Ribe-Pinachyan, Emilie. “Des Polycystines au centrosome, une enzyme clef : la calcium/calmoduline dependent kinase 2 : From polycystins to centrosomes, a key enzyme : the calcium/calmodulin dependant kinase 2.” 2010. Doctoral Dissertation, Aix-Marseille 2. Accessed November 19, 2019. http://www.theses.fr/2010AIX20715.

MLA Handbook (7th Edition):

Ribe-Pinachyan, Emilie. “Des Polycystines au centrosome, une enzyme clef : la calcium/calmoduline dependent kinase 2 : From polycystins to centrosomes, a key enzyme : the calcium/calmodulin dependant kinase 2.” 2010. Web. 19 Nov 2019.

Vancouver:

Ribe-Pinachyan E. Des Polycystines au centrosome, une enzyme clef : la calcium/calmoduline dependent kinase 2 : From polycystins to centrosomes, a key enzyme : the calcium/calmodulin dependant kinase 2. [Internet] [Doctoral dissertation]. Aix-Marseille 2; 2010. [cited 2019 Nov 19]. Available from: http://www.theses.fr/2010AIX20715.

Council of Science Editors:

Ribe-Pinachyan E. Des Polycystines au centrosome, une enzyme clef : la calcium/calmoduline dependent kinase 2 : From polycystins to centrosomes, a key enzyme : the calcium/calmodulin dependant kinase 2. [Doctoral Dissertation]. Aix-Marseille 2; 2010. Available from: http://www.theses.fr/2010AIX20715

18. Burute, Mithila. Régulation de l'organisation des microtubules par les adhérences cellulaires au cours de la morphogenèse épithéliale : Interplay between microtubule organization and cell adhesions during epithelial morphogenesis.

Degree: Docteur es, Physique pour les sciences du vivant, 2016, Grenoble Alpes

 Au cours de son développement depuis la cellule unique jusqu’à la forme adulte, l’embryon passe par de nombreuses étapes de morphogenèse. L'harmonie entre les cellules… (more)

Subjects/Keywords: Centrosome et microutubule; Adhérence cellulaire; Polarité cellulaire; Micropatterning; Centrosome and microbules; Cell adhesion; Cell polarity; Micropatterning; 570

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APA (6th Edition):

Burute, M. (2016). Régulation de l'organisation des microtubules par les adhérences cellulaires au cours de la morphogenèse épithéliale : Interplay between microtubule organization and cell adhesions during epithelial morphogenesis. (Doctoral Dissertation). Grenoble Alpes. Retrieved from http://www.theses.fr/2016GREAY035

Chicago Manual of Style (16th Edition):

Burute, Mithila. “Régulation de l'organisation des microtubules par les adhérences cellulaires au cours de la morphogenèse épithéliale : Interplay between microtubule organization and cell adhesions during epithelial morphogenesis.” 2016. Doctoral Dissertation, Grenoble Alpes. Accessed November 19, 2019. http://www.theses.fr/2016GREAY035.

MLA Handbook (7th Edition):

Burute, Mithila. “Régulation de l'organisation des microtubules par les adhérences cellulaires au cours de la morphogenèse épithéliale : Interplay between microtubule organization and cell adhesions during epithelial morphogenesis.” 2016. Web. 19 Nov 2019.

Vancouver:

Burute M. Régulation de l'organisation des microtubules par les adhérences cellulaires au cours de la morphogenèse épithéliale : Interplay between microtubule organization and cell adhesions during epithelial morphogenesis. [Internet] [Doctoral dissertation]. Grenoble Alpes; 2016. [cited 2019 Nov 19]. Available from: http://www.theses.fr/2016GREAY035.

Council of Science Editors:

Burute M. Régulation de l'organisation des microtubules par les adhérences cellulaires au cours de la morphogenèse épithéliale : Interplay between microtubule organization and cell adhesions during epithelial morphogenesis. [Doctoral Dissertation]. Grenoble Alpes; 2016. Available from: http://www.theses.fr/2016GREAY035

19. Sedjai, Fatima. Caractérisation d'une nouvelle protéine impliquée dans la ciliogenèse, FOR20 : Hadron and light quark masses in lattice quantum chromodynamics.

Degree: Docteur es, Pathologie Humaine, 2011, Aix-Marseille 2

Les cils/flagelles sont des organites conservés au cours de l’évolution qui peuvent permettre le mouvement de fluide, la locomotion ainsi que la chimiosensation, mécanosensation et… (more)

Subjects/Keywords: For20; Pcm1; Primary cilium; Satellites péricentriolaires; Centrosome; Microtubules; For20; Pcm1; Primary cilium; Pericentriolar satellites; Centrosome; Microtubules

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APA (6th Edition):

Sedjai, F. (2011). Caractérisation d'une nouvelle protéine impliquée dans la ciliogenèse, FOR20 : Hadron and light quark masses in lattice quantum chromodynamics. (Doctoral Dissertation). Aix-Marseille 2. Retrieved from http://www.theses.fr/2011AIX20670

Chicago Manual of Style (16th Edition):

Sedjai, Fatima. “Caractérisation d'une nouvelle protéine impliquée dans la ciliogenèse, FOR20 : Hadron and light quark masses in lattice quantum chromodynamics.” 2011. Doctoral Dissertation, Aix-Marseille 2. Accessed November 19, 2019. http://www.theses.fr/2011AIX20670.

MLA Handbook (7th Edition):

Sedjai, Fatima. “Caractérisation d'une nouvelle protéine impliquée dans la ciliogenèse, FOR20 : Hadron and light quark masses in lattice quantum chromodynamics.” 2011. Web. 19 Nov 2019.

Vancouver:

Sedjai F. Caractérisation d'une nouvelle protéine impliquée dans la ciliogenèse, FOR20 : Hadron and light quark masses in lattice quantum chromodynamics. [Internet] [Doctoral dissertation]. Aix-Marseille 2; 2011. [cited 2019 Nov 19]. Available from: http://www.theses.fr/2011AIX20670.

Council of Science Editors:

Sedjai F. Caractérisation d'une nouvelle protéine impliquée dans la ciliogenèse, FOR20 : Hadron and light quark masses in lattice quantum chromodynamics. [Doctoral Dissertation]. Aix-Marseille 2; 2011. Available from: http://www.theses.fr/2011AIX20670


Kyoto University / 京都大学

20. Sano(Hamasaki), Mayumi. Pregnenoloneは分裂期のcentriole engagementを制御する.

Degree: 博士(生命科学), 2015, Kyoto University / 京都大学

新制・課程博士

甲第18703号

生博第322号

Subjects/Keywords: centrosome; pregnenolone; centriole engagement

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APA (6th Edition):

Sano(Hamasaki), M. (2015). Pregnenoloneは分裂期のcentriole engagementを制御する. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/195989 ; http://dx.doi.org/10.14989/doctor.k18703

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):

Sano(Hamasaki), Mayumi. “Pregnenoloneは分裂期のcentriole engagementを制御する.” 2015. Thesis, Kyoto University / 京都大学. Accessed November 19, 2019. http://hdl.handle.net/2433/195989 ; http://dx.doi.org/10.14989/doctor.k18703.

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

MLA Handbook (7th Edition):

Sano(Hamasaki), Mayumi. “Pregnenoloneは分裂期のcentriole engagementを制御する.” 2015. Web. 19 Nov 2019.

Vancouver:

Sano(Hamasaki) M. Pregnenoloneは分裂期のcentriole engagementを制御する. [Internet] [Thesis]. Kyoto University / 京都大学; 2015. [cited 2019 Nov 19]. Available from: http://hdl.handle.net/2433/195989 ; http://dx.doi.org/10.14989/doctor.k18703.

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

Council of Science Editors:

Sano(Hamasaki) M. Pregnenoloneは分裂期のcentriole engagementを制御する. [Thesis]. Kyoto University / 京都大学; 2015. Available from: http://hdl.handle.net/2433/195989 ; http://dx.doi.org/10.14989/doctor.k18703

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


University of Toledo

21. Hynek, Sarah E. A Visual Screen for Centrosome Mutants in <i>Drosophila melanogaster</i>.

Degree: MS, Biology (Cell-Molecular Biology), 2015, University of Toledo

 Centrosomes are highly conserved organelles that are composed of two microtubule-based centrioles surrounded by an amorphous protein cloud of pericentriolar material (PCM), which is able… (more)

Subjects/Keywords: Biology; Cellular Biology; Developmental Biology; Drosophila; spermatogenesis; centrosome

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APA (6th Edition):

Hynek, S. E. (2015). A Visual Screen for Centrosome Mutants in <i>Drosophila melanogaster</i>. (Masters Thesis). University of Toledo. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=toledo1430408862

Chicago Manual of Style (16th Edition):

Hynek, Sarah E. “A Visual Screen for Centrosome Mutants in <i>Drosophila melanogaster</i>.” 2015. Masters Thesis, University of Toledo. Accessed November 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1430408862.

MLA Handbook (7th Edition):

Hynek, Sarah E. “A Visual Screen for Centrosome Mutants in <i>Drosophila melanogaster</i>.” 2015. Web. 19 Nov 2019.

Vancouver:

Hynek SE. A Visual Screen for Centrosome Mutants in <i>Drosophila melanogaster</i>. [Internet] [Masters thesis]. University of Toledo; 2015. [cited 2019 Nov 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1430408862.

Council of Science Editors:

Hynek SE. A Visual Screen for Centrosome Mutants in <i>Drosophila melanogaster</i>. [Masters Thesis]. University of Toledo; 2015. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1430408862


Université de Montréal

22. Barbelanne, Marine. Études fonctionnelles de deux nouvelles protéines centrosomales, NPHP5 et Cep76, et leurs implications dans les maladies humaines .

Degree: 2016, Université de Montréal

 Les centrosomes sont de petits organites qui régulent divers processus cellulaires comme la polarité ou la mitose dans les cellules de mammifères. Ils sont composés… (more)

Subjects/Keywords: Cil; NPHP5; Cep76; cycle cellulaire; Cep290; BBSome; Cell cycle; Cilia; Centrosome

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APA (6th Edition):

Barbelanne, M. (2016). Études fonctionnelles de deux nouvelles protéines centrosomales, NPHP5 et Cep76, et leurs implications dans les maladies humaines . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/13530

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):

Barbelanne, Marine. “Études fonctionnelles de deux nouvelles protéines centrosomales, NPHP5 et Cep76, et leurs implications dans les maladies humaines .” 2016. Thesis, Université de Montréal. Accessed November 19, 2019. http://hdl.handle.net/1866/13530.

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

MLA Handbook (7th Edition):

Barbelanne, Marine. “Études fonctionnelles de deux nouvelles protéines centrosomales, NPHP5 et Cep76, et leurs implications dans les maladies humaines .” 2016. Web. 19 Nov 2019.

Vancouver:

Barbelanne M. Études fonctionnelles de deux nouvelles protéines centrosomales, NPHP5 et Cep76, et leurs implications dans les maladies humaines . [Internet] [Thesis]. Université de Montréal; 2016. [cited 2019 Nov 19]. Available from: http://hdl.handle.net/1866/13530.

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

Council of Science Editors:

Barbelanne M. Études fonctionnelles de deux nouvelles protéines centrosomales, NPHP5 et Cep76, et leurs implications dans les maladies humaines . [Thesis]. Université de Montréal; 2016. Available from: http://hdl.handle.net/1866/13530

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


NSYSU

23. Chou , Chia-hua. Characterize the molecular mechanisms of mitochondrial GSK3beta-Drp1 and centrosomal Ninein-AIBp-Aurora A/ Plk1 protein-protein interactions.

Degree: PhD, Biological Sciences, 2015, NSYSU

 Glycogen synthase kinase-3beta (GSK3beta) has been reported to participate in several signaling pathways and crucial for cell development, metabolic homeostasis, neuronal growth and differentiation, cell… (more)

Subjects/Keywords: hNinein; GSK3beta; mitochondria; AIBp; Drp1; centrosome; Aurora A; Plk1

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APA (6th Edition):

Chou , C. (2015). Characterize the molecular mechanisms of mitochondrial GSK3beta-Drp1 and centrosomal Ninein-AIBp-Aurora A/ Plk1 protein-protein interactions. (Doctoral Dissertation). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0608115-114035

Chicago Manual of Style (16th Edition):

Chou , Chia-hua. “Characterize the molecular mechanisms of mitochondrial GSK3beta-Drp1 and centrosomal Ninein-AIBp-Aurora A/ Plk1 protein-protein interactions.” 2015. Doctoral Dissertation, NSYSU. Accessed November 19, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0608115-114035.

MLA Handbook (7th Edition):

Chou , Chia-hua. “Characterize the molecular mechanisms of mitochondrial GSK3beta-Drp1 and centrosomal Ninein-AIBp-Aurora A/ Plk1 protein-protein interactions.” 2015. Web. 19 Nov 2019.

Vancouver:

Chou C. Characterize the molecular mechanisms of mitochondrial GSK3beta-Drp1 and centrosomal Ninein-AIBp-Aurora A/ Plk1 protein-protein interactions. [Internet] [Doctoral dissertation]. NSYSU; 2015. [cited 2019 Nov 19]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0608115-114035.

Council of Science Editors:

Chou C. Characterize the molecular mechanisms of mitochondrial GSK3beta-Drp1 and centrosomal Ninein-AIBp-Aurora A/ Plk1 protein-protein interactions. [Doctoral Dissertation]. NSYSU; 2015. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0608115-114035


National University of Ireland – Galway

24. Wang, Yifan Jr. Reverse Genetic Analysis of Pericentrin Functions .

Degree: 2012, National University of Ireland – Galway

 The centrosome is a subcellular organelle that organises the mitotic spindle microtubules to ensure accurate segregation of chromosomes during cell division. Most animal centrosomes comprise… (more)

Subjects/Keywords: Pericentrin; Centrosome; DNA damage response; Mitosis; Chromosome Biology; Natural Sciences

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APA (6th Edition):

Wang, Y. J. (2012). Reverse Genetic Analysis of Pericentrin Functions . (Thesis). National University of Ireland – Galway. Retrieved from http://hdl.handle.net/10379/3112

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):

Wang, Yifan Jr. “Reverse Genetic Analysis of Pericentrin Functions .” 2012. Thesis, National University of Ireland – Galway. Accessed November 19, 2019. http://hdl.handle.net/10379/3112.

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

MLA Handbook (7th Edition):

Wang, Yifan Jr. “Reverse Genetic Analysis of Pericentrin Functions .” 2012. Web. 19 Nov 2019.

Vancouver:

Wang YJ. Reverse Genetic Analysis of Pericentrin Functions . [Internet] [Thesis]. National University of Ireland – Galway; 2012. [cited 2019 Nov 19]. Available from: http://hdl.handle.net/10379/3112.

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

Council of Science Editors:

Wang YJ. Reverse Genetic Analysis of Pericentrin Functions . [Thesis]. National University of Ireland – Galway; 2012. Available from: http://hdl.handle.net/10379/3112

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


National University of Ireland – Galway

25. Inanc, Burcu. The control of centrosome duplication after genotoxic stress .

Degree: 2011, National University of Ireland – Galway

 The centrosome is the major microtubule organising center in animal cells. Following DNA damage, centrosome amplification can occur, which in turn can result in the… (more)

Subjects/Keywords: Centrosome; DNA damage response; Cell cycle; Checkpoint; Ionizing radiation; Cep135.

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APA (6th Edition):

Inanc, B. (2011). The control of centrosome duplication after genotoxic stress . (Thesis). National University of Ireland – Galway. Retrieved from http://hdl.handle.net/10379/2862

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):

Inanc, Burcu. “The control of centrosome duplication after genotoxic stress .” 2011. Thesis, National University of Ireland – Galway. Accessed November 19, 2019. http://hdl.handle.net/10379/2862.

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

MLA Handbook (7th Edition):

Inanc, Burcu. “The control of centrosome duplication after genotoxic stress .” 2011. Web. 19 Nov 2019.

Vancouver:

Inanc B. The control of centrosome duplication after genotoxic stress . [Internet] [Thesis]. National University of Ireland – Galway; 2011. [cited 2019 Nov 19]. Available from: http://hdl.handle.net/10379/2862.

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

Council of Science Editors:

Inanc B. The control of centrosome duplication after genotoxic stress . [Thesis]. National University of Ireland – Galway; 2011. Available from: http://hdl.handle.net/10379/2862

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

26. Farache, Dorian. Etude des fonctions de GCP4, 5 et 6 dans l'assemblage du complexe de nucléation des microtubules : Investigating the function of GCPs 4, 5, 6 in the Gamma-tubulin ring complex assembly.

Degree: Docteur es, Biologie cellulaire et moléculaire, 2016, Université Toulouse III – Paul Sabatier

Les microtubules sont des composants hautement dynamiques du cytosquelette. La tubuline gamma est localisée au centrosome. Elle y forme le complexe de nucléation des microtubules,… (more)

Subjects/Keywords: Tubuline; Mitose; Microtubule; Fuceau mitotique; Nucléation; Centrosome; Gamma complex proteins

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APA (6th Edition):

Farache, D. (2016). Etude des fonctions de GCP4, 5 et 6 dans l'assemblage du complexe de nucléation des microtubules : Investigating the function of GCPs 4, 5, 6 in the Gamma-tubulin ring complex assembly. (Doctoral Dissertation). Université Toulouse III – Paul Sabatier. Retrieved from http://www.theses.fr/2016TOU30231

Chicago Manual of Style (16th Edition):

Farache, Dorian. “Etude des fonctions de GCP4, 5 et 6 dans l'assemblage du complexe de nucléation des microtubules : Investigating the function of GCPs 4, 5, 6 in the Gamma-tubulin ring complex assembly.” 2016. Doctoral Dissertation, Université Toulouse III – Paul Sabatier. Accessed November 19, 2019. http://www.theses.fr/2016TOU30231.

MLA Handbook (7th Edition):

Farache, Dorian. “Etude des fonctions de GCP4, 5 et 6 dans l'assemblage du complexe de nucléation des microtubules : Investigating the function of GCPs 4, 5, 6 in the Gamma-tubulin ring complex assembly.” 2016. Web. 19 Nov 2019.

Vancouver:

Farache D. Etude des fonctions de GCP4, 5 et 6 dans l'assemblage du complexe de nucléation des microtubules : Investigating the function of GCPs 4, 5, 6 in the Gamma-tubulin ring complex assembly. [Internet] [Doctoral dissertation]. Université Toulouse III – Paul Sabatier; 2016. [cited 2019 Nov 19]. Available from: http://www.theses.fr/2016TOU30231.

Council of Science Editors:

Farache D. Etude des fonctions de GCP4, 5 et 6 dans l'assemblage du complexe de nucléation des microtubules : Investigating the function of GCPs 4, 5, 6 in the Gamma-tubulin ring complex assembly. [Doctoral Dissertation]. Université Toulouse III – Paul Sabatier; 2016. Available from: http://www.theses.fr/2016TOU30231


Case Western Reserve University

27. Montanez-Wiscovich, Marjorie E. Discerning the Role of LMO4 as a Global Modulator of G2/M Cell Cycle Progression and Centrosome Cycle in Breast Cancer Cells.

Degree: PhD, Pharmacology, 2010, Case Western Reserve University

 A woman’s lifetime risk of developing breast cancer in the United States is 1 in 8 (12.3%). Of these women, 15% will die from this… (more)

Subjects/Keywords: Molecular Biology; Oncology; Pharmacology; LMO4; gene expression; ErbB2/HER2/Neu; centrosome

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APA (6th Edition):

Montanez-Wiscovich, M. E. (2010). Discerning the Role of LMO4 as a Global Modulator of G2/M Cell Cycle Progression and Centrosome Cycle in Breast Cancer Cells. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1259899890

Chicago Manual of Style (16th Edition):

Montanez-Wiscovich, Marjorie E. “Discerning the Role of LMO4 as a Global Modulator of G2/M Cell Cycle Progression and Centrosome Cycle in Breast Cancer Cells.” 2010. Doctoral Dissertation, Case Western Reserve University. Accessed November 19, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1259899890.

MLA Handbook (7th Edition):

Montanez-Wiscovich, Marjorie E. “Discerning the Role of LMO4 as a Global Modulator of G2/M Cell Cycle Progression and Centrosome Cycle in Breast Cancer Cells.” 2010. Web. 19 Nov 2019.

Vancouver:

Montanez-Wiscovich ME. Discerning the Role of LMO4 as a Global Modulator of G2/M Cell Cycle Progression and Centrosome Cycle in Breast Cancer Cells. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2010. [cited 2019 Nov 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1259899890.

Council of Science Editors:

Montanez-Wiscovich ME. Discerning the Role of LMO4 as a Global Modulator of G2/M Cell Cycle Progression and Centrosome Cycle in Breast Cancer Cells. [Doctoral Dissertation]. Case Western Reserve University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1259899890


Penn State University

28. Gao, Zhizhen. DEPLETION OF NUCLEAR ENVELOPE COMPONENTS CAUSES A NOVEL CENTROSOME ATTACHMENT DEFECT.

Degree: MS, Biochemistry, Microbiology, and Molecular Biology, 2008, Penn State University

 The attachment of the centrosome to the nucleus is essential for C. elegans development. Two genes, zyg-12 and sun-1, are essential for centrosome attachment; zyg-12… (more)

Subjects/Keywords: Lamin-binding proteins; Nuclear lamins; Nuclear size; Centrosome attachment; Nuclear Pores

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APA (6th Edition):

Gao, Z. (2008). DEPLETION OF NUCLEAR ENVELOPE COMPONENTS CAUSES A NOVEL CENTROSOME ATTACHMENT DEFECT. (Masters Thesis). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/8654

Chicago Manual of Style (16th Edition):

Gao, Zhizhen. “DEPLETION OF NUCLEAR ENVELOPE COMPONENTS CAUSES A NOVEL CENTROSOME ATTACHMENT DEFECT.” 2008. Masters Thesis, Penn State University. Accessed November 19, 2019. https://etda.libraries.psu.edu/catalog/8654.

MLA Handbook (7th Edition):

Gao, Zhizhen. “DEPLETION OF NUCLEAR ENVELOPE COMPONENTS CAUSES A NOVEL CENTROSOME ATTACHMENT DEFECT.” 2008. Web. 19 Nov 2019.

Vancouver:

Gao Z. DEPLETION OF NUCLEAR ENVELOPE COMPONENTS CAUSES A NOVEL CENTROSOME ATTACHMENT DEFECT. [Internet] [Masters thesis]. Penn State University; 2008. [cited 2019 Nov 19]. Available from: https://etda.libraries.psu.edu/catalog/8654.

Council of Science Editors:

Gao Z. DEPLETION OF NUCLEAR ENVELOPE COMPONENTS CAUSES A NOVEL CENTROSOME ATTACHMENT DEFECT. [Masters Thesis]. Penn State University; 2008. Available from: https://etda.libraries.psu.edu/catalog/8654


Penn State University

29. Nguyen, Michelle Marie. Why Move It When You Can Make It? Drosophila Neuronal Microtubule Polarity Requires Local Microtubule Nucleation.

Degree: PhD, Biochemistry, Microbiology, and Molecular Biology, 2013, Penn State University

 The polarization of neurons into axons and dendrites is essential in building functional neuronal circuits. The arrangement of microtubules is an important factor in neuronal… (more)

Subjects/Keywords: microtubules; neuronal polarity; Golgi; axon initial segment; Drosophila; centrosome; ankyrin

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APA (6th Edition):

Nguyen, M. M. (2013). Why Move It When You Can Make It? Drosophila Neuronal Microtubule Polarity Requires Local Microtubule Nucleation. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/19744

Chicago Manual of Style (16th Edition):

Nguyen, Michelle Marie. “Why Move It When You Can Make It? Drosophila Neuronal Microtubule Polarity Requires Local Microtubule Nucleation.” 2013. Doctoral Dissertation, Penn State University. Accessed November 19, 2019. https://etda.libraries.psu.edu/catalog/19744.

MLA Handbook (7th Edition):

Nguyen, Michelle Marie. “Why Move It When You Can Make It? Drosophila Neuronal Microtubule Polarity Requires Local Microtubule Nucleation.” 2013. Web. 19 Nov 2019.

Vancouver:

Nguyen MM. Why Move It When You Can Make It? Drosophila Neuronal Microtubule Polarity Requires Local Microtubule Nucleation. [Internet] [Doctoral dissertation]. Penn State University; 2013. [cited 2019 Nov 19]. Available from: https://etda.libraries.psu.edu/catalog/19744.

Council of Science Editors:

Nguyen MM. Why Move It When You Can Make It? Drosophila Neuronal Microtubule Polarity Requires Local Microtubule Nucleation. [Doctoral Dissertation]. Penn State University; 2013. Available from: https://etda.libraries.psu.edu/catalog/19744


Penn State University

30. Chen, Yi. IDENTIFYING ADDITIONAL CENTROSOME ATTACHMENT GENES AND CHARACTERIZING CENTROSOMAL LOCALIZATION OF ZYG-12.

Degree: MS, Genetics, 2008, Penn State University

 The association between the centrosome and the nucleus is crucial for mitosis in the early Caenorhabditis elegans embryo. Four components are essential for this association:… (more)

Subjects/Keywords: zyg-12; zyg-1; centrosome attachment; suppressor screen

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

APA (6th Edition):

Chen, Y. (2008). IDENTIFYING ADDITIONAL CENTROSOME ATTACHMENT GENES AND CHARACTERIZING CENTROSOMAL LOCALIZATION OF ZYG-12. (Masters Thesis). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/8651

Chicago Manual of Style (16th Edition):

Chen, Yi. “IDENTIFYING ADDITIONAL CENTROSOME ATTACHMENT GENES AND CHARACTERIZING CENTROSOMAL LOCALIZATION OF ZYG-12.” 2008. Masters Thesis, Penn State University. Accessed November 19, 2019. https://etda.libraries.psu.edu/catalog/8651.

MLA Handbook (7th Edition):

Chen, Yi. “IDENTIFYING ADDITIONAL CENTROSOME ATTACHMENT GENES AND CHARACTERIZING CENTROSOMAL LOCALIZATION OF ZYG-12.” 2008. Web. 19 Nov 2019.

Vancouver:

Chen Y. IDENTIFYING ADDITIONAL CENTROSOME ATTACHMENT GENES AND CHARACTERIZING CENTROSOMAL LOCALIZATION OF ZYG-12. [Internet] [Masters thesis]. Penn State University; 2008. [cited 2019 Nov 19]. Available from: https://etda.libraries.psu.edu/catalog/8651.

Council of Science Editors:

Chen Y. IDENTIFYING ADDITIONAL CENTROSOME ATTACHMENT GENES AND CHARACTERIZING CENTROSOMAL LOCALIZATION OF ZYG-12. [Masters Thesis]. Penn State University; 2008. Available from: https://etda.libraries.psu.edu/catalog/8651

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