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You searched for subject:(Live Cell Imaging). Showing records 1 – 30 of 104 total matches.

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University of Toronto

1. Downie, Kelsey Jean. Live Cell Imaging of CEACAM1 Dynamics and Self-association during Bacterial Binding.

Degree: 2013, University of Toronto

The carcinoembryonic antigen-related cellular adhesion molecule 1 (CEACAM1) is a human receptor that facilitates adhesion with neighbouring cells, as well as with certain pathogens. CEACAM1… (more)

Subjects/Keywords: fluorescence microscopy; CEACAM; live cell imaging; 0541

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APA (6th Edition):

Downie, K. J. (2013). Live Cell Imaging of CEACAM1 Dynamics and Self-association during Bacterial Binding. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/42829

Chicago Manual of Style (16th Edition):

Downie, Kelsey Jean. “Live Cell Imaging of CEACAM1 Dynamics and Self-association during Bacterial Binding.” 2013. Masters Thesis, University of Toronto. Accessed October 13, 2019. http://hdl.handle.net/1807/42829.

MLA Handbook (7th Edition):

Downie, Kelsey Jean. “Live Cell Imaging of CEACAM1 Dynamics and Self-association during Bacterial Binding.” 2013. Web. 13 Oct 2019.

Vancouver:

Downie KJ. Live Cell Imaging of CEACAM1 Dynamics and Self-association during Bacterial Binding. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2019 Oct 13]. Available from: http://hdl.handle.net/1807/42829.

Council of Science Editors:

Downie KJ. Live Cell Imaging of CEACAM1 Dynamics and Self-association during Bacterial Binding. [Masters Thesis]. University of Toronto; 2013. Available from: http://hdl.handle.net/1807/42829


Johannes Gutenberg Universität Mainz

2. Hirsch, Markus. Dynamics of small interfering RNA - FRET based integrity measurements of siRNA in the cuvette & inside cells.

Degree: 2013, Johannes Gutenberg Universität Mainz

RNAi ist ein bedeutendes Werkzeug zur Funktionsanalyse von Genen und hat großes Potential für den Einsatz in der Therapie. Obwohl effiziente Knockdowns in der Zellkultur… (more)

Subjects/Keywords: FRET, siRNA, Integrität, Live cell imaging; FRET, siRNA, integrity, live cell imaging; Life sciences

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APA (6th Edition):

Hirsch, M. (2013). Dynamics of small interfering RNA - FRET based integrity measurements of siRNA in the cuvette & inside cells. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2015/4035/

Chicago Manual of Style (16th Edition):

Hirsch, Markus. “Dynamics of small interfering RNA - FRET based integrity measurements of siRNA in the cuvette & inside cells.” 2013. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed October 13, 2019. http://ubm.opus.hbz-nrw.de/volltexte/2015/4035/.

MLA Handbook (7th Edition):

Hirsch, Markus. “Dynamics of small interfering RNA - FRET based integrity measurements of siRNA in the cuvette & inside cells.” 2013. Web. 13 Oct 2019.

Vancouver:

Hirsch M. Dynamics of small interfering RNA - FRET based integrity measurements of siRNA in the cuvette & inside cells. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2013. [cited 2019 Oct 13]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2015/4035/.

Council of Science Editors:

Hirsch M. Dynamics of small interfering RNA - FRET based integrity measurements of siRNA in the cuvette & inside cells. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2013. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2015/4035/


University of California – San Francisco

3. Thornton, Emily Elizabeth. Lung Surveillance Revealed by Two-Photon Live Imaging.

Degree: Biomedical Sciences, 2012, University of California – San Francisco

 The lung is a complex mucosal organ with the responsibility of oxygenating blood for the entire body. The large surface area of the lung allows… (more)

Subjects/Keywords: Immunology; Biology; Asthma; Dendritic Cell; Immunology; Live Imaging; Lung; T cell

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APA (6th Edition):

Thornton, E. E. (2012). Lung Surveillance Revealed by Two-Photon Live Imaging. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/7ss319j7

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):

Thornton, Emily Elizabeth. “Lung Surveillance Revealed by Two-Photon Live Imaging.” 2012. Thesis, University of California – San Francisco. Accessed October 13, 2019. http://www.escholarship.org/uc/item/7ss319j7.

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

MLA Handbook (7th Edition):

Thornton, Emily Elizabeth. “Lung Surveillance Revealed by Two-Photon Live Imaging.” 2012. Web. 13 Oct 2019.

Vancouver:

Thornton EE. Lung Surveillance Revealed by Two-Photon Live Imaging. [Internet] [Thesis]. University of California – San Francisco; 2012. [cited 2019 Oct 13]. Available from: http://www.escholarship.org/uc/item/7ss319j7.

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

Council of Science Editors:

Thornton EE. Lung Surveillance Revealed by Two-Photon Live Imaging. [Thesis]. University of California – San Francisco; 2012. Available from: http://www.escholarship.org/uc/item/7ss319j7

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


University of New South Wales

4. Li, Jingjing. Cell division tracking by live cell imaging and image processing.

Degree: Graduate School of Biomedical Engineering, 2011, University of New South Wales

 Towards the goal of generating specific tissue from stem or progenitor cells for regenerative medicine, it will be necessary to understand the dynamics of stem… (more)

Subjects/Keywords: Cardiac CFU-F; Live Cell Imaging; Cell lineage tracking; Kaplan Meier

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APA (6th Edition):

Li, J. (2011). Cell division tracking by live cell imaging and image processing. (Masters Thesis). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/51414 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10096/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Li, Jingjing. “Cell division tracking by live cell imaging and image processing.” 2011. Masters Thesis, University of New South Wales. Accessed October 13, 2019. http://handle.unsw.edu.au/1959.4/51414 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10096/SOURCE02?view=true.

MLA Handbook (7th Edition):

Li, Jingjing. “Cell division tracking by live cell imaging and image processing.” 2011. Web. 13 Oct 2019.

Vancouver:

Li J. Cell division tracking by live cell imaging and image processing. [Internet] [Masters thesis]. University of New South Wales; 2011. [cited 2019 Oct 13]. Available from: http://handle.unsw.edu.au/1959.4/51414 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10096/SOURCE02?view=true.

Council of Science Editors:

Li J. Cell division tracking by live cell imaging and image processing. [Masters Thesis]. University of New South Wales; 2011. Available from: http://handle.unsw.edu.au/1959.4/51414 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10096/SOURCE02?view=true


University of California – Berkeley

5. Rodriguez-Rivera, Frances Paola. Probing Bacterial Cell Envelope Structure and Dynamics with Metabolic Reporters.

Degree: Chemistry, 2016, University of California – Berkeley

 The complexity of the bacterial cell envelope along with the clinical implications arising from biological discoveries have produced steady research over the last century. Orchestration… (more)

Subjects/Keywords: Chemistry; bacterial cell envelope; live cell imaging; metabolic reporters

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APA (6th Edition):

Rodriguez-Rivera, F. P. (2016). Probing Bacterial Cell Envelope Structure and Dynamics with Metabolic Reporters. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/62d3q92h

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):

Rodriguez-Rivera, Frances Paola. “Probing Bacterial Cell Envelope Structure and Dynamics with Metabolic Reporters.” 2016. Thesis, University of California – Berkeley. Accessed October 13, 2019. http://www.escholarship.org/uc/item/62d3q92h.

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

MLA Handbook (7th Edition):

Rodriguez-Rivera, Frances Paola. “Probing Bacterial Cell Envelope Structure and Dynamics with Metabolic Reporters.” 2016. Web. 13 Oct 2019.

Vancouver:

Rodriguez-Rivera FP. Probing Bacterial Cell Envelope Structure and Dynamics with Metabolic Reporters. [Internet] [Thesis]. University of California – Berkeley; 2016. [cited 2019 Oct 13]. Available from: http://www.escholarship.org/uc/item/62d3q92h.

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

Council of Science Editors:

Rodriguez-Rivera FP. Probing Bacterial Cell Envelope Structure and Dynamics with Metabolic Reporters. [Thesis]. University of California – Berkeley; 2016. Available from: http://www.escholarship.org/uc/item/62d3q92h

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


University of New South Wales

6. Cornwell, James. Application of time-lapse imaging, single-cell tracking, and competing risks analysis to characterise cardiac stem cell growth dynamics.

Degree: Graduate School of Biomedical Engineering, 2016, University of New South Wales

 Heart failure due to damaged heart muscle is amongst the most common cause of death worldwide. Adult stem cells hold promise for their potential to… (more)

Subjects/Keywords: Single-cell tracking; Cardiac stem cells; Live-cell imaging; Statistics

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APA (6th Edition):

Cornwell, J. (2016). Application of time-lapse imaging, single-cell tracking, and competing risks analysis to characterise cardiac stem cell growth dynamics. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/56173 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:40189/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Cornwell, James. “Application of time-lapse imaging, single-cell tracking, and competing risks analysis to characterise cardiac stem cell growth dynamics.” 2016. Doctoral Dissertation, University of New South Wales. Accessed October 13, 2019. http://handle.unsw.edu.au/1959.4/56173 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:40189/SOURCE02?view=true.

MLA Handbook (7th Edition):

Cornwell, James. “Application of time-lapse imaging, single-cell tracking, and competing risks analysis to characterise cardiac stem cell growth dynamics.” 2016. Web. 13 Oct 2019.

Vancouver:

Cornwell J. Application of time-lapse imaging, single-cell tracking, and competing risks analysis to characterise cardiac stem cell growth dynamics. [Internet] [Doctoral dissertation]. University of New South Wales; 2016. [cited 2019 Oct 13]. Available from: http://handle.unsw.edu.au/1959.4/56173 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:40189/SOURCE02?view=true.

Council of Science Editors:

Cornwell J. Application of time-lapse imaging, single-cell tracking, and competing risks analysis to characterise cardiac stem cell growth dynamics. [Doctoral Dissertation]. University of New South Wales; 2016. Available from: http://handle.unsw.edu.au/1959.4/56173 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:40189/SOURCE02?view=true


University of Illinois – Urbana-Champaign

7. Kim, Tae Jin. Visualization of cellular signaling by fluorescence resonance energy transfer in response to biochemical and mechanical microenvironments.

Degree: PhD, 0323, 2013, University of Illinois – Urbana-Champaign

 Biochemical and mechanical microenvironment have a great impact on a variety of cellular processes including cell adhesion and migration. While substantial progress has been made… (more)

Subjects/Keywords: Fluorescence resonance energy transfer (FRET); Live-cell imaging; Cell Signals; Microenvironment

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APA (6th Edition):

Kim, T. J. (2013). Visualization of cellular signaling by fluorescence resonance energy transfer in response to biochemical and mechanical microenvironments. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/45646

Chicago Manual of Style (16th Edition):

Kim, Tae Jin. “Visualization of cellular signaling by fluorescence resonance energy transfer in response to biochemical and mechanical microenvironments.” 2013. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed October 13, 2019. http://hdl.handle.net/2142/45646.

MLA Handbook (7th Edition):

Kim, Tae Jin. “Visualization of cellular signaling by fluorescence resonance energy transfer in response to biochemical and mechanical microenvironments.” 2013. Web. 13 Oct 2019.

Vancouver:

Kim TJ. Visualization of cellular signaling by fluorescence resonance energy transfer in response to biochemical and mechanical microenvironments. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2013. [cited 2019 Oct 13]. Available from: http://hdl.handle.net/2142/45646.

Council of Science Editors:

Kim TJ. Visualization of cellular signaling by fluorescence resonance energy transfer in response to biochemical and mechanical microenvironments. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2013. Available from: http://hdl.handle.net/2142/45646


Virginia Tech

8. Tavassoly, Iman. Dynamics of Cell Fate Decisions Mediated by the Interplay of Autophagy and Apoptosis in Cancer Cells:  Mathematical Modeling and Experimental Observations    .

Degree: PhD, Animal and Poultry Sciences, 2013, Virginia Tech

 Autophagy is a conserved biological stress response in mammalian cells that is responsible for clearing damaged proteins and organelles from the cytoplasm and recycling their… (more)

Subjects/Keywords: Apoptosis; Autophagy; Cancer; Cell Death; Dynamic Modeling; Live Cell Imaging; Quantitative Fluorescence Microscopy; Single-Cell

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APA (6th Edition):

Tavassoly, I. (2013). Dynamics of Cell Fate Decisions Mediated by the Interplay of Autophagy and Apoptosis in Cancer Cells:  Mathematical Modeling and Experimental Observations    . (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/79557

Chicago Manual of Style (16th Edition):

Tavassoly, Iman. “Dynamics of Cell Fate Decisions Mediated by the Interplay of Autophagy and Apoptosis in Cancer Cells:  Mathematical Modeling and Experimental Observations    .” 2013. Doctoral Dissertation, Virginia Tech. Accessed October 13, 2019. http://hdl.handle.net/10919/79557.

MLA Handbook (7th Edition):

Tavassoly, Iman. “Dynamics of Cell Fate Decisions Mediated by the Interplay of Autophagy and Apoptosis in Cancer Cells:  Mathematical Modeling and Experimental Observations    .” 2013. Web. 13 Oct 2019.

Vancouver:

Tavassoly I. Dynamics of Cell Fate Decisions Mediated by the Interplay of Autophagy and Apoptosis in Cancer Cells:  Mathematical Modeling and Experimental Observations    . [Internet] [Doctoral dissertation]. Virginia Tech; 2013. [cited 2019 Oct 13]. Available from: http://hdl.handle.net/10919/79557.

Council of Science Editors:

Tavassoly I. Dynamics of Cell Fate Decisions Mediated by the Interplay of Autophagy and Apoptosis in Cancer Cells:  Mathematical Modeling and Experimental Observations    . [Doctoral Dissertation]. Virginia Tech; 2013. Available from: http://hdl.handle.net/10919/79557


Penn State University

9. Li, Harvey. THE EFFECTS OF CELL MORPHOLOGY ON NANOPARTICLE UPTAKE AND UPTAKE AT THE LEADING EDGE IN MC3T3 CELLS.

Degree: 2018, Penn State University

 When using the correct material coupled with drugs and specific surface ligands, nanoparticles can have enhanced targeted drug delivery properties. Currently, scientists can alter the… (more)

Subjects/Keywords: cell; cell morphology; nanoparticles; endocytosis; immunostaining; live-cell imaging; MC3T3 cells; microcontact printing; y-27632

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APA (6th Edition):

Li, H. (2018). THE EFFECTS OF CELL MORPHOLOGY ON NANOPARTICLE UPTAKE AND UPTAKE AT THE LEADING EDGE IN MC3T3 CELLS. (Thesis). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/15391hsl5047

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):

Li, Harvey. “THE EFFECTS OF CELL MORPHOLOGY ON NANOPARTICLE UPTAKE AND UPTAKE AT THE LEADING EDGE IN MC3T3 CELLS.” 2018. Thesis, Penn State University. Accessed October 13, 2019. https://etda.libraries.psu.edu/catalog/15391hsl5047.

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

MLA Handbook (7th Edition):

Li, Harvey. “THE EFFECTS OF CELL MORPHOLOGY ON NANOPARTICLE UPTAKE AND UPTAKE AT THE LEADING EDGE IN MC3T3 CELLS.” 2018. Web. 13 Oct 2019.

Vancouver:

Li H. THE EFFECTS OF CELL MORPHOLOGY ON NANOPARTICLE UPTAKE AND UPTAKE AT THE LEADING EDGE IN MC3T3 CELLS. [Internet] [Thesis]. Penn State University; 2018. [cited 2019 Oct 13]. Available from: https://etda.libraries.psu.edu/catalog/15391hsl5047.

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

Council of Science Editors:

Li H. THE EFFECTS OF CELL MORPHOLOGY ON NANOPARTICLE UPTAKE AND UPTAKE AT THE LEADING EDGE IN MC3T3 CELLS. [Thesis]. Penn State University; 2018. Available from: https://etda.libraries.psu.edu/catalog/15391hsl5047

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


University of Edinburgh

10. Altenbach, Kirsten. Development and analysis of recombinant fluorescent probes for use in live cell imaging of filamentous fungi.

Degree: 2010, University of Edinburgh

 The molecular cloning and subsequent engineering of the green fluorescent protein (GFP) of the jellyfish Aequoria victoria allowed a novel approach to the investigation of… (more)

Subjects/Keywords: 571.4; live cell imaging; aspergillus niger; FRET; FLIM; fluorescent probes

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APA (6th Edition):

Altenbach, K. (2010). Development and analysis of recombinant fluorescent probes for use in live cell imaging of filamentous fungi. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/4739

Chicago Manual of Style (16th Edition):

Altenbach, Kirsten. “Development and analysis of recombinant fluorescent probes for use in live cell imaging of filamentous fungi.” 2010. Doctoral Dissertation, University of Edinburgh. Accessed October 13, 2019. http://hdl.handle.net/1842/4739.

MLA Handbook (7th Edition):

Altenbach, Kirsten. “Development and analysis of recombinant fluorescent probes for use in live cell imaging of filamentous fungi.” 2010. Web. 13 Oct 2019.

Vancouver:

Altenbach K. Development and analysis of recombinant fluorescent probes for use in live cell imaging of filamentous fungi. [Internet] [Doctoral dissertation]. University of Edinburgh; 2010. [cited 2019 Oct 13]. Available from: http://hdl.handle.net/1842/4739.

Council of Science Editors:

Altenbach K. Development and analysis of recombinant fluorescent probes for use in live cell imaging of filamentous fungi. [Doctoral Dissertation]. University of Edinburgh; 2010. Available from: http://hdl.handle.net/1842/4739


Cornell University

11. Zobeck, Katie. The Recruitment And Dynamics Of Transcription Factors At The Hsp70 Loci In Living Cells .

Degree: 2011, Cornell University

 Chromatin Immunoprecipitation (ChIP) provides snapshots of the localization of transcription factors on chromatin in cell populations. However, through the development of fluorescent proteins and subsequent… (more)

Subjects/Keywords: Regulation of Transcription; Live Cell Imaging; gfp; Recruitment and Dynamics

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APA (6th Edition):

Zobeck, K. (2011). The Recruitment And Dynamics Of Transcription Factors At The Hsp70 Loci In Living Cells . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/33560

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):

Zobeck, Katie. “The Recruitment And Dynamics Of Transcription Factors At The Hsp70 Loci In Living Cells .” 2011. Thesis, Cornell University. Accessed October 13, 2019. http://hdl.handle.net/1813/33560.

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

MLA Handbook (7th Edition):

Zobeck, Katie. “The Recruitment And Dynamics Of Transcription Factors At The Hsp70 Loci In Living Cells .” 2011. Web. 13 Oct 2019.

Vancouver:

Zobeck K. The Recruitment And Dynamics Of Transcription Factors At The Hsp70 Loci In Living Cells . [Internet] [Thesis]. Cornell University; 2011. [cited 2019 Oct 13]. Available from: http://hdl.handle.net/1813/33560.

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

Council of Science Editors:

Zobeck K. The Recruitment And Dynamics Of Transcription Factors At The Hsp70 Loci In Living Cells . [Thesis]. Cornell University; 2011. Available from: http://hdl.handle.net/1813/33560

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


UCLA

12. Yi, Xiyu. Super resolution of Optical Fluctuation Imaging 2.0 (SOFI-2.0): Towards fast super resolved imaging of live cells.

Degree: Chemistry, 2017, UCLA

 Super resolution Optical Fluctuation Imaging (SOFI) has been widely acknowledged andadvanced over the past years. Comparing to other extensively adopted super resolutiontechniques such as PALM,… (more)

Subjects/Keywords: Chemistry; cumulants; deconvolution; live cell imaging; moments; SOFI; Superresolution

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APA (6th Edition):

Yi, X. (2017). Super resolution of Optical Fluctuation Imaging 2.0 (SOFI-2.0): Towards fast super resolved imaging of live cells. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/5xs5v4qm

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):

Yi, Xiyu. “Super resolution of Optical Fluctuation Imaging 2.0 (SOFI-2.0): Towards fast super resolved imaging of live cells.” 2017. Thesis, UCLA. Accessed October 13, 2019. http://www.escholarship.org/uc/item/5xs5v4qm.

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

MLA Handbook (7th Edition):

Yi, Xiyu. “Super resolution of Optical Fluctuation Imaging 2.0 (SOFI-2.0): Towards fast super resolved imaging of live cells.” 2017. Web. 13 Oct 2019.

Vancouver:

Yi X. Super resolution of Optical Fluctuation Imaging 2.0 (SOFI-2.0): Towards fast super resolved imaging of live cells. [Internet] [Thesis]. UCLA; 2017. [cited 2019 Oct 13]. Available from: http://www.escholarship.org/uc/item/5xs5v4qm.

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

Council of Science Editors:

Yi X. Super resolution of Optical Fluctuation Imaging 2.0 (SOFI-2.0): Towards fast super resolved imaging of live cells. [Thesis]. UCLA; 2017. Available from: http://www.escholarship.org/uc/item/5xs5v4qm

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


University of Southern California

13. Liu, Helene Minyi. The molecular studies of HCV RNA replication and translation.

Degree: PhD, Molecular Microbiology & Immunology, 2010, University of Southern California

 Hepatitis C virus RNA replication requires not only the viral replicase but also the host cytoskeletons, membrane structures, and cellular factors. Several hnRNPs, such as… (more)

Subjects/Keywords: HCV; RNA replication; RNA translation; membrane structures; live cell imaging

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APA (6th Edition):

Liu, H. M. (2010). The molecular studies of HCV RNA replication and translation. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/237010/rec/6993

Chicago Manual of Style (16th Edition):

Liu, Helene Minyi. “The molecular studies of HCV RNA replication and translation.” 2010. Doctoral Dissertation, University of Southern California. Accessed October 13, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/237010/rec/6993.

MLA Handbook (7th Edition):

Liu, Helene Minyi. “The molecular studies of HCV RNA replication and translation.” 2010. Web. 13 Oct 2019.

Vancouver:

Liu HM. The molecular studies of HCV RNA replication and translation. [Internet] [Doctoral dissertation]. University of Southern California; 2010. [cited 2019 Oct 13]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/237010/rec/6993.

Council of Science Editors:

Liu HM. The molecular studies of HCV RNA replication and translation. [Doctoral Dissertation]. University of Southern California; 2010. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/237010/rec/6993


McMaster University

14. Munsie, Lise N. CHARACTERIZING THE FUNCTION OF HUNTINGTIN IN THE CELL STRESS RESPONSE AS A TARGET FOR DRUG DISCOVERY IN HUNTINGTON’S DISEASE.

Degree: PhD, 2012, McMaster University

Huntington’s disease (HD) is a devastating autosomal dominant neurodegenerative disorder for which there are no disease modifying treatments. Owing to this are the multiple… (more)

Subjects/Keywords: Huntington's Disease; FLIM-FRET; cofilin; huntingtin; live cell imaging; Neurosciences; Neurosciences

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APA (6th Edition):

Munsie, L. N. (2012). CHARACTERIZING THE FUNCTION OF HUNTINGTIN IN THE CELL STRESS RESPONSE AS A TARGET FOR DRUG DISCOVERY IN HUNTINGTON’S DISEASE. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/12436

Chicago Manual of Style (16th Edition):

Munsie, Lise N. “CHARACTERIZING THE FUNCTION OF HUNTINGTIN IN THE CELL STRESS RESPONSE AS A TARGET FOR DRUG DISCOVERY IN HUNTINGTON’S DISEASE.” 2012. Doctoral Dissertation, McMaster University. Accessed October 13, 2019. http://hdl.handle.net/11375/12436.

MLA Handbook (7th Edition):

Munsie, Lise N. “CHARACTERIZING THE FUNCTION OF HUNTINGTIN IN THE CELL STRESS RESPONSE AS A TARGET FOR DRUG DISCOVERY IN HUNTINGTON’S DISEASE.” 2012. Web. 13 Oct 2019.

Vancouver:

Munsie LN. CHARACTERIZING THE FUNCTION OF HUNTINGTIN IN THE CELL STRESS RESPONSE AS A TARGET FOR DRUG DISCOVERY IN HUNTINGTON’S DISEASE. [Internet] [Doctoral dissertation]. McMaster University; 2012. [cited 2019 Oct 13]. Available from: http://hdl.handle.net/11375/12436.

Council of Science Editors:

Munsie LN. CHARACTERIZING THE FUNCTION OF HUNTINGTIN IN THE CELL STRESS RESPONSE AS A TARGET FOR DRUG DISCOVERY IN HUNTINGTON’S DISEASE. [Doctoral Dissertation]. McMaster University; 2012. Available from: http://hdl.handle.net/11375/12436


Georgia Tech

15. Wen, Mary Mei. New strategies for tagging quantum dots for dynamic cellular imaging.

Degree: PhD, Biomedical Engineering (Joint GT/Emory Department), 2013, Georgia Tech

 In recent years, semiconductor quantum dots (QDs) have arisen as a new class of fluorescent probes that possess unique optical and electronic properties well-suited for… (more)

Subjects/Keywords: Quantum dots; Live cell imaging; Single molecule imaging; HaloTag; Tagging strategies; Nanotechnology; Bionanotechnology

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APA (6th Edition):

Wen, M. M. (2013). New strategies for tagging quantum dots for dynamic cellular imaging. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/52150

Chicago Manual of Style (16th Edition):

Wen, Mary Mei. “New strategies for tagging quantum dots for dynamic cellular imaging.” 2013. Doctoral Dissertation, Georgia Tech. Accessed October 13, 2019. http://hdl.handle.net/1853/52150.

MLA Handbook (7th Edition):

Wen, Mary Mei. “New strategies for tagging quantum dots for dynamic cellular imaging.” 2013. Web. 13 Oct 2019.

Vancouver:

Wen MM. New strategies for tagging quantum dots for dynamic cellular imaging. [Internet] [Doctoral dissertation]. Georgia Tech; 2013. [cited 2019 Oct 13]. Available from: http://hdl.handle.net/1853/52150.

Council of Science Editors:

Wen MM. New strategies for tagging quantum dots for dynamic cellular imaging. [Doctoral Dissertation]. Georgia Tech; 2013. Available from: http://hdl.handle.net/1853/52150


Georgia Tech

16. Alonas, Eric James. Labeling the human respiratory syncytial virus genomic RNA with exogenous probes for fluorescence and electron microscopy.

Degree: PhD, Biomedical Engineering (Joint GT/Emory Department), 2015, Georgia Tech

 A method for labeling the genomic RNA of the human respiratory syncytial virus, as well as for isolating and examining the labeled filamentous virions was… (more)

Subjects/Keywords: RSV; RNA imaging; Live cell imaging; dSTORM; STED; Cryo-ET; TEM; RNA virus; RNA probes

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APA (6th Edition):

Alonas, E. J. (2015). Labeling the human respiratory syncytial virus genomic RNA with exogenous probes for fluorescence and electron microscopy. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/56173

Chicago Manual of Style (16th Edition):

Alonas, Eric James. “Labeling the human respiratory syncytial virus genomic RNA with exogenous probes for fluorescence and electron microscopy.” 2015. Doctoral Dissertation, Georgia Tech. Accessed October 13, 2019. http://hdl.handle.net/1853/56173.

MLA Handbook (7th Edition):

Alonas, Eric James. “Labeling the human respiratory syncytial virus genomic RNA with exogenous probes for fluorescence and electron microscopy.” 2015. Web. 13 Oct 2019.

Vancouver:

Alonas EJ. Labeling the human respiratory syncytial virus genomic RNA with exogenous probes for fluorescence and electron microscopy. [Internet] [Doctoral dissertation]. Georgia Tech; 2015. [cited 2019 Oct 13]. Available from: http://hdl.handle.net/1853/56173.

Council of Science Editors:

Alonas EJ. Labeling the human respiratory syncytial virus genomic RNA with exogenous probes for fluorescence and electron microscopy. [Doctoral Dissertation]. Georgia Tech; 2015. Available from: http://hdl.handle.net/1853/56173


University of Michigan

17. Siv, Chanrith. Single-Particle Tracking of Proteins in Living Bacteria: From Single Cells to a Mixed Community.

Degree: PhD, Biophysics, 2017, University of Michigan

 Bacteria consist of only a single cell, but these prokaryotes are amazingly complex. Bacteria are among the earliest forms of life that appeared on Earth… (more)

Subjects/Keywords: Single-molecule imaging; Bacterial cell imaging; Cholera; Gut microbiome; Single-particle tracking; Live cell imaging; Science (General); Science

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

APA (6th Edition):

Siv, C. (2017). Single-Particle Tracking of Proteins in Living Bacteria: From Single Cells to a Mixed Community. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/138692

Chicago Manual of Style (16th Edition):

Siv, Chanrith. “Single-Particle Tracking of Proteins in Living Bacteria: From Single Cells to a Mixed Community.” 2017. Doctoral Dissertation, University of Michigan. Accessed October 13, 2019. http://hdl.handle.net/2027.42/138692.

MLA Handbook (7th Edition):

Siv, Chanrith. “Single-Particle Tracking of Proteins in Living Bacteria: From Single Cells to a Mixed Community.” 2017. Web. 13 Oct 2019.

Vancouver:

Siv C. Single-Particle Tracking of Proteins in Living Bacteria: From Single Cells to a Mixed Community. [Internet] [Doctoral dissertation]. University of Michigan; 2017. [cited 2019 Oct 13]. Available from: http://hdl.handle.net/2027.42/138692.

Council of Science Editors:

Siv C. Single-Particle Tracking of Proteins in Living Bacteria: From Single Cells to a Mixed Community. [Doctoral Dissertation]. University of Michigan; 2017. Available from: http://hdl.handle.net/2027.42/138692


University of Pennsylvania

18. Hanby, Hayley. Platelet Dense Granules Mature Within Late Stages Of Megakaryocyte Differentiation By Cargo Delivery.

Degree: 2017, University of Pennsylvania

 Platelet dense granules (DGs) are storage organelles for calcium ions, small organic molecules such as ADP and serotonin, and larger polyphosphates that are secreted upon… (more)

Subjects/Keywords: dense granule; live cell imaging; lysosome-related organelle; megakaryocyte; platelets; proplatelets; Cell Biology

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

APA (6th Edition):

Hanby, H. (2017). Platelet Dense Granules Mature Within Late Stages Of Megakaryocyte Differentiation By Cargo Delivery. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/2837

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):

Hanby, Hayley. “Platelet Dense Granules Mature Within Late Stages Of Megakaryocyte Differentiation By Cargo Delivery.” 2017. Thesis, University of Pennsylvania. Accessed October 13, 2019. https://repository.upenn.edu/edissertations/2837.

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

MLA Handbook (7th Edition):

Hanby, Hayley. “Platelet Dense Granules Mature Within Late Stages Of Megakaryocyte Differentiation By Cargo Delivery.” 2017. Web. 13 Oct 2019.

Vancouver:

Hanby H. Platelet Dense Granules Mature Within Late Stages Of Megakaryocyte Differentiation By Cargo Delivery. [Internet] [Thesis]. University of Pennsylvania; 2017. [cited 2019 Oct 13]. Available from: https://repository.upenn.edu/edissertations/2837.

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

Council of Science Editors:

Hanby H. Platelet Dense Granules Mature Within Late Stages Of Megakaryocyte Differentiation By Cargo Delivery. [Thesis]. University of Pennsylvania; 2017. Available from: https://repository.upenn.edu/edissertations/2837

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


University of Colorado

19. Young, Alexandra Marie. Live Cell Methods to Visualize Translocated Salmonella Effectors and Monitor Ca2+ Transients During Infection.

Degree: PhD, 2017, University of Colorado

 <i>Salmonella</i> species invade and survive within eukaryotic host cells by using a Type Three Secretion System (T3SS) to translocate bacterial effector proteins into the host… (more)

Subjects/Keywords: bacterial effector proteins; host-pathogen interface; live cell imaging; salmonella; split-gfp; Biochemistry; Cell Biology

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

APA (6th Edition):

Young, A. M. (2017). Live Cell Methods to Visualize Translocated Salmonella Effectors and Monitor Ca2+ Transients During Infection. (Doctoral Dissertation). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/279

Chicago Manual of Style (16th Edition):

Young, Alexandra Marie. “Live Cell Methods to Visualize Translocated Salmonella Effectors and Monitor Ca2+ Transients During Infection.” 2017. Doctoral Dissertation, University of Colorado. Accessed October 13, 2019. https://scholar.colorado.edu/chem_gradetds/279.

MLA Handbook (7th Edition):

Young, Alexandra Marie. “Live Cell Methods to Visualize Translocated Salmonella Effectors and Monitor Ca2+ Transients During Infection.” 2017. Web. 13 Oct 2019.

Vancouver:

Young AM. Live Cell Methods to Visualize Translocated Salmonella Effectors and Monitor Ca2+ Transients During Infection. [Internet] [Doctoral dissertation]. University of Colorado; 2017. [cited 2019 Oct 13]. Available from: https://scholar.colorado.edu/chem_gradetds/279.

Council of Science Editors:

Young AM. Live Cell Methods to Visualize Translocated Salmonella Effectors and Monitor Ca2+ Transients During Infection. [Doctoral Dissertation]. University of Colorado; 2017. Available from: https://scholar.colorado.edu/chem_gradetds/279


University of Arizona

20. Vig, Dhruv Kumar. Spanning the Continuum: From Single Cell to Collective Migration .

Degree: 2015, University of Arizona

 A cell's ability to sense and respond to mechanical signals highlights the significance of physical forces in biology; however, to date most biomedical research has… (more)

Subjects/Keywords: collective migration; live-cell imaging; lyme disease; mathematical modeling; Molecular & Cellular Biology; cell motility

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

APA (6th Edition):

Vig, D. K. (2015). Spanning the Continuum: From Single Cell to Collective Migration . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/566259

Chicago Manual of Style (16th Edition):

Vig, Dhruv Kumar. “Spanning the Continuum: From Single Cell to Collective Migration .” 2015. Doctoral Dissertation, University of Arizona. Accessed October 13, 2019. http://hdl.handle.net/10150/566259.

MLA Handbook (7th Edition):

Vig, Dhruv Kumar. “Spanning the Continuum: From Single Cell to Collective Migration .” 2015. Web. 13 Oct 2019.

Vancouver:

Vig DK. Spanning the Continuum: From Single Cell to Collective Migration . [Internet] [Doctoral dissertation]. University of Arizona; 2015. [cited 2019 Oct 13]. Available from: http://hdl.handle.net/10150/566259.

Council of Science Editors:

Vig DK. Spanning the Continuum: From Single Cell to Collective Migration . [Doctoral Dissertation]. University of Arizona; 2015. Available from: http://hdl.handle.net/10150/566259


University of Illinois – Chicago

21. Bang, Chi. The Role of Spectrosome and Centrosome in Asymmetric Stem Cell Division.

Degree: 2015, University of Illinois – Chicago

 Stem cells have remarkable self-renewal ability and differentiation potency, which are critical for tissue repair and tissue homeostasis. Recently it has been found, in many… (more)

Subjects/Keywords: Stem Cell Engineering; Asymmetric Stem Cell Division; Stem Cell Regulation; Tissue Engineering; Sub-cellular Organelle Tracking; Time-Lapse Live-Cell Imaging

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APA (6th Edition):

Bang, C. (2015). The Role of Spectrosome and Centrosome in Asymmetric Stem Cell Division. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/19776

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):

Bang, Chi. “The Role of Spectrosome and Centrosome in Asymmetric Stem Cell Division.” 2015. Thesis, University of Illinois – Chicago. Accessed October 13, 2019. http://hdl.handle.net/10027/19776.

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

MLA Handbook (7th Edition):

Bang, Chi. “The Role of Spectrosome and Centrosome in Asymmetric Stem Cell Division.” 2015. Web. 13 Oct 2019.

Vancouver:

Bang C. The Role of Spectrosome and Centrosome in Asymmetric Stem Cell Division. [Internet] [Thesis]. University of Illinois – Chicago; 2015. [cited 2019 Oct 13]. Available from: http://hdl.handle.net/10027/19776.

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

Council of Science Editors:

Bang C. The Role of Spectrosome and Centrosome in Asymmetric Stem Cell Division. [Thesis]. University of Illinois – Chicago; 2015. Available from: http://hdl.handle.net/10027/19776

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


University of Southern California

22. Lee, Jae Kyoo. Multi-marker real-time optical imaging of live cell population under controlled stress: apoptosis in retinal ganglion cells.

Degree: PhD, Biomedical Engineering, 2011, University of Southern California

 The response of live cells to external stress is regulated and processed through complex and highly-interconnected time-dependent signaling networks. The essential task for the understanding… (more)

Subjects/Keywords: apoptosis; live cell imaging; real-time dynamics; retinal ganglion cell; single molecule imaging; systems biology; mathematical modeling

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APA (6th Edition):

Lee, J. K. (2011). Multi-marker real-time optical imaging of live cell population under controlled stress: apoptosis in retinal ganglion cells. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/662046/rec/4246

Chicago Manual of Style (16th Edition):

Lee, Jae Kyoo. “Multi-marker real-time optical imaging of live cell population under controlled stress: apoptosis in retinal ganglion cells.” 2011. Doctoral Dissertation, University of Southern California. Accessed October 13, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/662046/rec/4246.

MLA Handbook (7th Edition):

Lee, Jae Kyoo. “Multi-marker real-time optical imaging of live cell population under controlled stress: apoptosis in retinal ganglion cells.” 2011. Web. 13 Oct 2019.

Vancouver:

Lee JK. Multi-marker real-time optical imaging of live cell population under controlled stress: apoptosis in retinal ganglion cells. [Internet] [Doctoral dissertation]. University of Southern California; 2011. [cited 2019 Oct 13]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/662046/rec/4246.

Council of Science Editors:

Lee JK. Multi-marker real-time optical imaging of live cell population under controlled stress: apoptosis in retinal ganglion cells. [Doctoral Dissertation]. University of Southern California; 2011. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/662046/rec/4246


University of Colorado

23. Young, Alexandra Marie. Live Cell Methods to Visualize Translocated Salmonella Effectors and Monitor Ca2+ Transients During Infection.

Degree: PhD, 2017, University of Colorado

  Salmonella species invade and survive within eukaryotic host cells by using a Type Three Secretion System (T3SS) to translocate bacterial effector proteins into the… (more)

Subjects/Keywords: Bacterial effector proteins; host-pathogen interface; live cell imaging; salmonella; split-GFP; Biochemistry

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

APA (6th Edition):

Young, A. M. (2017). Live Cell Methods to Visualize Translocated Salmonella Effectors and Monitor Ca2+ Transients During Infection. (Doctoral Dissertation). University of Colorado. Retrieved from http://scholar.colorado.edu/chem_gradetds/209

Chicago Manual of Style (16th Edition):

Young, Alexandra Marie. “Live Cell Methods to Visualize Translocated Salmonella Effectors and Monitor Ca2+ Transients During Infection.” 2017. Doctoral Dissertation, University of Colorado. Accessed October 13, 2019. http://scholar.colorado.edu/chem_gradetds/209.

MLA Handbook (7th Edition):

Young, Alexandra Marie. “Live Cell Methods to Visualize Translocated Salmonella Effectors and Monitor Ca2+ Transients During Infection.” 2017. Web. 13 Oct 2019.

Vancouver:

Young AM. Live Cell Methods to Visualize Translocated Salmonella Effectors and Monitor Ca2+ Transients During Infection. [Internet] [Doctoral dissertation]. University of Colorado; 2017. [cited 2019 Oct 13]. Available from: http://scholar.colorado.edu/chem_gradetds/209.

Council of Science Editors:

Young AM. Live Cell Methods to Visualize Translocated Salmonella Effectors and Monitor Ca2+ Transients During Infection. [Doctoral Dissertation]. University of Colorado; 2017. Available from: http://scholar.colorado.edu/chem_gradetds/209


University of California – Berkeley

24. Kan, Shu. Study of cellular mechanotransduction by visualizing actin and nucleoskeleton dynamics in real-time.

Degree: Comparative Biochemistry, 2015, University of California – Berkeley

 Cellular mechanotransduction, the tight coupling between biochemical and mechanical properties of the cytoskeleton and nucleus, drives a large range of cellular processes including cell mobility,… (more)

Subjects/Keywords: Biogeochemistry; Biomedical engineering; barbed end actin; fluorescent dye; live cell imaging; mechanotransduction

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APA (6th Edition):

Kan, S. (2015). Study of cellular mechanotransduction by visualizing actin and nucleoskeleton dynamics in real-time. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/2fc9s475

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):

Kan, Shu. “Study of cellular mechanotransduction by visualizing actin and nucleoskeleton dynamics in real-time.” 2015. Thesis, University of California – Berkeley. Accessed October 13, 2019. http://www.escholarship.org/uc/item/2fc9s475.

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

MLA Handbook (7th Edition):

Kan, Shu. “Study of cellular mechanotransduction by visualizing actin and nucleoskeleton dynamics in real-time.” 2015. Web. 13 Oct 2019.

Vancouver:

Kan S. Study of cellular mechanotransduction by visualizing actin and nucleoskeleton dynamics in real-time. [Internet] [Thesis]. University of California – Berkeley; 2015. [cited 2019 Oct 13]. Available from: http://www.escholarship.org/uc/item/2fc9s475.

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

Council of Science Editors:

Kan S. Study of cellular mechanotransduction by visualizing actin and nucleoskeleton dynamics in real-time. [Thesis]. University of California – Berkeley; 2015. Available from: http://www.escholarship.org/uc/item/2fc9s475

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


Harvard University

25. Chen, Huiyi. System-Wide Studies of Gene Expression in Escherichia coli by Fluorescence Microscopy and High Throughput Sequencing.

Degree: PhD, Biochemistry, 2011, Harvard University

 Gene expression is a fundamental process in the cell and is made up of two parts – the information flow from DNA to RNA, and… (more)

Subjects/Keywords: bacteria; live-cell imaging; protein noise; quantitative biology; RNA dynamics; single molecule microscopy; biology; biochemistry

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APA (6th Edition):

Chen, H. (2011). System-Wide Studies of Gene Expression in Escherichia coli by Fluorescence Microscopy and High Throughput Sequencing. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:10121974

Chicago Manual of Style (16th Edition):

Chen, Huiyi. “System-Wide Studies of Gene Expression in Escherichia coli by Fluorescence Microscopy and High Throughput Sequencing.” 2011. Doctoral Dissertation, Harvard University. Accessed October 13, 2019. http://nrs.harvard.edu/urn-3:HUL.InstRepos:10121974.

MLA Handbook (7th Edition):

Chen, Huiyi. “System-Wide Studies of Gene Expression in Escherichia coli by Fluorescence Microscopy and High Throughput Sequencing.” 2011. Web. 13 Oct 2019.

Vancouver:

Chen H. System-Wide Studies of Gene Expression in Escherichia coli by Fluorescence Microscopy and High Throughput Sequencing. [Internet] [Doctoral dissertation]. Harvard University; 2011. [cited 2019 Oct 13]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:10121974.

Council of Science Editors:

Chen H. System-Wide Studies of Gene Expression in Escherichia coli by Fluorescence Microscopy and High Throughput Sequencing. [Doctoral Dissertation]. Harvard University; 2011. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:10121974


University of Illinois – Urbana-Champaign

26. Teng, Kai Wen. Intracellular labeling of live cells via transient membrane permeabilization for fluorescence and super resolution microscopy.

Degree: PhD, Biophysics & Computnl Biology, 2016, University of Illinois – Urbana-Champaign

 Fluorescence imaging of intracellular proteins is often achieved by using transfection-induced expression of fluorescent protein. This can potentially impose artifacts such as loss of function… (more)

Subjects/Keywords: Fluorescence Microscopy; Live Cell Imaging; Protein Labeling; Reversible Membrane Permeabilization; Streptolysin O

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APA (6th Edition):

Teng, K. W. (2016). Intracellular labeling of live cells via transient membrane permeabilization for fluorescence and super resolution microscopy. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/95526

Chicago Manual of Style (16th Edition):

Teng, Kai Wen. “Intracellular labeling of live cells via transient membrane permeabilization for fluorescence and super resolution microscopy.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed October 13, 2019. http://hdl.handle.net/2142/95526.

MLA Handbook (7th Edition):

Teng, Kai Wen. “Intracellular labeling of live cells via transient membrane permeabilization for fluorescence and super resolution microscopy.” 2016. Web. 13 Oct 2019.

Vancouver:

Teng KW. Intracellular labeling of live cells via transient membrane permeabilization for fluorescence and super resolution microscopy. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Oct 13]. Available from: http://hdl.handle.net/2142/95526.

Council of Science Editors:

Teng KW. Intracellular labeling of live cells via transient membrane permeabilization for fluorescence and super resolution microscopy. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/95526

27. Kozulic-Pirher, Alja. La visualisation de la transcription en molécules unique révèle de nouvelles caractéristiques des promoteurs cellulaires et viraux : Real time imaging of transcription reveals new features of cellular and viral promoters.

Degree: Docteur es, Biologie Santé, 2018, Montpellier

La transcription est une étape fondamentale dans l'expression des gènes. Cependant, elle reste incomplètement caractérisée dans les cellules vivantes. Pour mieux comprendre la dynamique de… (more)

Subjects/Keywords: Transcription; Promoters; Imagerie; Tat; Cellules vivantes; Vih; Transcription; Promoters; Live cell imaging; Tat; Hiv

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APA (6th Edition):

Kozulic-Pirher, A. (2018). La visualisation de la transcription en molécules unique révèle de nouvelles caractéristiques des promoteurs cellulaires et viraux : Real time imaging of transcription reveals new features of cellular and viral promoters. (Doctoral Dissertation). Montpellier. Retrieved from http://www.theses.fr/2018MONTT080

Chicago Manual of Style (16th Edition):

Kozulic-Pirher, Alja. “La visualisation de la transcription en molécules unique révèle de nouvelles caractéristiques des promoteurs cellulaires et viraux : Real time imaging of transcription reveals new features of cellular and viral promoters.” 2018. Doctoral Dissertation, Montpellier. Accessed October 13, 2019. http://www.theses.fr/2018MONTT080.

MLA Handbook (7th Edition):

Kozulic-Pirher, Alja. “La visualisation de la transcription en molécules unique révèle de nouvelles caractéristiques des promoteurs cellulaires et viraux : Real time imaging of transcription reveals new features of cellular and viral promoters.” 2018. Web. 13 Oct 2019.

Vancouver:

Kozulic-Pirher A. La visualisation de la transcription en molécules unique révèle de nouvelles caractéristiques des promoteurs cellulaires et viraux : Real time imaging of transcription reveals new features of cellular and viral promoters. [Internet] [Doctoral dissertation]. Montpellier; 2018. [cited 2019 Oct 13]. Available from: http://www.theses.fr/2018MONTT080.

Council of Science Editors:

Kozulic-Pirher A. La visualisation de la transcription en molécules unique révèle de nouvelles caractéristiques des promoteurs cellulaires et viraux : Real time imaging of transcription reveals new features of cellular and viral promoters. [Doctoral Dissertation]. Montpellier; 2018. Available from: http://www.theses.fr/2018MONTT080


University of Adelaide

28. Fiches, Guillaume Nicolas. Dynamic imaging of hepatitis C virus RNA localisation and traffic during viral replication.

Degree: 2015, University of Adelaide

 Much of our understanding of the HCV life cycle and host-viral interactions has evolved from the visualisation of fixed images of infected cells. However, the… (more)

Subjects/Keywords: Hepatitis C virus; HCV; RNA; NS5A; Lipid droplets; Live cell imaging; MS2; Traffic

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APA (6th Edition):

Fiches, G. N. (2015). Dynamic imaging of hepatitis C virus RNA localisation and traffic during viral replication. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/97881

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):

Fiches, Guillaume Nicolas. “Dynamic imaging of hepatitis C virus RNA localisation and traffic during viral replication.” 2015. Thesis, University of Adelaide. Accessed October 13, 2019. http://hdl.handle.net/2440/97881.

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

MLA Handbook (7th Edition):

Fiches, Guillaume Nicolas. “Dynamic imaging of hepatitis C virus RNA localisation and traffic during viral replication.” 2015. Web. 13 Oct 2019.

Vancouver:

Fiches GN. Dynamic imaging of hepatitis C virus RNA localisation and traffic during viral replication. [Internet] [Thesis]. University of Adelaide; 2015. [cited 2019 Oct 13]. Available from: http://hdl.handle.net/2440/97881.

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

Council of Science Editors:

Fiches GN. Dynamic imaging of hepatitis C virus RNA localisation and traffic during viral replication. [Thesis]. University of Adelaide; 2015. Available from: http://hdl.handle.net/2440/97881

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


University of Edinburgh

29. Linnik, Volha. Functional analysis of a plant virus replication 'factory' using live cell imaging.

Degree: PhD, 2010, University of Edinburgh

 Plant viruses have developed a number of strategies that enable them to become obligate intracellular parasites of many agricultural crops. Potato virus X (PVX) belongs… (more)

Subjects/Keywords: 579.2; plant viruses; single-stranded plant RNA viruses; live-cell imaging; Pumilio; bimolecular fluorescence

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

APA (6th Edition):

Linnik, V. (2010). Functional analysis of a plant virus replication 'factory' using live cell imaging. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/4639

Chicago Manual of Style (16th Edition):

Linnik, Volha. “Functional analysis of a plant virus replication 'factory' using live cell imaging.” 2010. Doctoral Dissertation, University of Edinburgh. Accessed October 13, 2019. http://hdl.handle.net/1842/4639.

MLA Handbook (7th Edition):

Linnik, Volha. “Functional analysis of a plant virus replication 'factory' using live cell imaging.” 2010. Web. 13 Oct 2019.

Vancouver:

Linnik V. Functional analysis of a plant virus replication 'factory' using live cell imaging. [Internet] [Doctoral dissertation]. University of Edinburgh; 2010. [cited 2019 Oct 13]. Available from: http://hdl.handle.net/1842/4639.

Council of Science Editors:

Linnik V. Functional analysis of a plant virus replication 'factory' using live cell imaging. [Doctoral Dissertation]. University of Edinburgh; 2010. Available from: http://hdl.handle.net/1842/4639


University of Edinburgh

30. Chang, Chia-Chen. Ca2+/Calmodulin signalling during colony initiation in Neurospora crassa.

Degree: PhD, 2015, University of Edinburgh

 The primary research aims of this thesis were to analyse the mechanism of Ca2+/calmodulin (CaM) signalling during conidial germination and conidial anastomosis tube (CAT)-mediated fusion… (more)

Subjects/Keywords: 579.5; calcium signalling; calmodulin; Neurospora crassa.; CAT fusion; proteomis; live-cell imaging

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

APA (6th Edition):

Chang, C. (2015). Ca2+/Calmodulin signalling during colony initiation in Neurospora crassa. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/16176

Chicago Manual of Style (16th Edition):

Chang, Chia-Chen. “Ca2+/Calmodulin signalling during colony initiation in Neurospora crassa.” 2015. Doctoral Dissertation, University of Edinburgh. Accessed October 13, 2019. http://hdl.handle.net/1842/16176.

MLA Handbook (7th Edition):

Chang, Chia-Chen. “Ca2+/Calmodulin signalling during colony initiation in Neurospora crassa.” 2015. Web. 13 Oct 2019.

Vancouver:

Chang C. Ca2+/Calmodulin signalling during colony initiation in Neurospora crassa. [Internet] [Doctoral dissertation]. University of Edinburgh; 2015. [cited 2019 Oct 13]. Available from: http://hdl.handle.net/1842/16176.

Council of Science Editors:

Chang C. Ca2+/Calmodulin signalling during colony initiation in Neurospora crassa. [Doctoral Dissertation]. University of Edinburgh; 2015. Available from: http://hdl.handle.net/1842/16176

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