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You searched for subject:(fluorescence lifetime imaging microscopy). Showing records 1 – 30 of 17998 total matches.

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Texas A&M University

1. Thomas, Patrick A. Detection of Atherosclerotic Coronary Plaques by Fluorescence Lifetime Imaging Angioscopy.

Degree: 2010, Texas A&M University

 Vulnerable plaque is a clinically silent condition of atherosclerotic plaque that leaves a large number of patients at risk of a coronary event. A method… (more)

Subjects/Keywords: Fluorescence Lifetime Imaging Microscopy; Atherosclerosis; Vulnerable Plaque

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

APA (6th Edition):

Thomas, P. A. (2010). Detection of Atherosclerotic Coronary Plaques by Fluorescence Lifetime Imaging Angioscopy. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8299

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):

Thomas, Patrick A. “Detection of Atherosclerotic Coronary Plaques by Fluorescence Lifetime Imaging Angioscopy.” 2010. Thesis, Texas A&M University. Accessed June 19, 2018. http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8299.

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

MLA Handbook (7th Edition):

Thomas, Patrick A. “Detection of Atherosclerotic Coronary Plaques by Fluorescence Lifetime Imaging Angioscopy.” 2010. Web. 19 Jun 2018.

Vancouver:

Thomas PA. Detection of Atherosclerotic Coronary Plaques by Fluorescence Lifetime Imaging Angioscopy. [Internet] [Thesis]. Texas A&M University; 2010. [cited 2018 Jun 19]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8299.

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

Council of Science Editors:

Thomas PA. Detection of Atherosclerotic Coronary Plaques by Fluorescence Lifetime Imaging Angioscopy. [Thesis]. Texas A&M University; 2010. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8299

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


University of Edinburgh

2. Ellis, Jonathan. FRET analysis of splicing factors involved in exon and intron definition in living cells.

Degree: 2008, University of Edinburgh

 I have analyzed the interactions between SR proteins and splicing components that are bound at the 5’ or 3’ splice site using fluorescence resonance energy… (more)

Subjects/Keywords: 571.4; FRET; FLIM; fluorescence resonance energy transfer; fluorescence lifetime imaging microscopy

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APA (6th Edition):

Ellis, J. (2008). FRET analysis of splicing factors involved in exon and intron definition in living cells. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/4397

Chicago Manual of Style (16th Edition):

Ellis, Jonathan. “FRET analysis of splicing factors involved in exon and intron definition in living cells.” 2008. Doctoral Dissertation, University of Edinburgh. Accessed June 19, 2018. http://hdl.handle.net/1842/4397.

MLA Handbook (7th Edition):

Ellis, Jonathan. “FRET analysis of splicing factors involved in exon and intron definition in living cells.” 2008. Web. 19 Jun 2018.

Vancouver:

Ellis J. FRET analysis of splicing factors involved in exon and intron definition in living cells. [Internet] [Doctoral dissertation]. University of Edinburgh; 2008. [cited 2018 Jun 19]. Available from: http://hdl.handle.net/1842/4397.

Council of Science Editors:

Ellis J. FRET analysis of splicing factors involved in exon and intron definition in living cells. [Doctoral Dissertation]. University of Edinburgh; 2008. Available from: http://hdl.handle.net/1842/4397


University of Edinburgh

3. Graham, Emmelyn M. The application of fluorescence lifetime imaging microscopy to quantitatively map mixing and temperature in microfluidic systems.

Degree: PhD, 2008, University of Edinburgh

 The technique of Fluorescence Lifetime Imaging Microscopy (FLIM) has been employed to quantitatively and spatially map the fluid composition and temperature within microfluidic systems. A… (more)

Subjects/Keywords: 530.0724; Chemistry; Physical Chemistry; Fluorescence Lifetime Imaging Microscopy

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APA (6th Edition):

Graham, E. M. (2008). The application of fluorescence lifetime imaging microscopy to quantitatively map mixing and temperature in microfluidic systems. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/2432

Chicago Manual of Style (16th Edition):

Graham, Emmelyn M. “The application of fluorescence lifetime imaging microscopy to quantitatively map mixing and temperature in microfluidic systems.” 2008. Doctoral Dissertation, University of Edinburgh. Accessed June 19, 2018. http://hdl.handle.net/1842/2432.

MLA Handbook (7th Edition):

Graham, Emmelyn M. “The application of fluorescence lifetime imaging microscopy to quantitatively map mixing and temperature in microfluidic systems.” 2008. Web. 19 Jun 2018.

Vancouver:

Graham EM. The application of fluorescence lifetime imaging microscopy to quantitatively map mixing and temperature in microfluidic systems. [Internet] [Doctoral dissertation]. University of Edinburgh; 2008. [cited 2018 Jun 19]. Available from: http://hdl.handle.net/1842/2432.

Council of Science Editors:

Graham EM. The application of fluorescence lifetime imaging microscopy to quantitatively map mixing and temperature in microfluidic systems. [Doctoral Dissertation]. University of Edinburgh; 2008. Available from: http://hdl.handle.net/1842/2432


Texas A&M University

4. Lee, Joohyung. Supervised Machine Learning Algorithms for Early Detection of Oral Epithelial Cancer Using Fluorescence Lifetime Imaging Microscopy.

Degree: 2014, Texas A&M University

 In this study, the clinical potential of the endogenous multispectral Fluorescence lifetime imaging microscopy (FLIM) was investigated to objectively detect oral cancer. To this end,… (more)

Subjects/Keywords: Film; Fluorescence Lifetime Imaging Microscopy; Supervised Machine Learning; KNN

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APA (6th Edition):

Lee, J. (2014). Supervised Machine Learning Algorithms for Early Detection of Oral Epithelial Cancer Using Fluorescence Lifetime Imaging Microscopy. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/153669

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):

Lee, Joohyung. “Supervised Machine Learning Algorithms for Early Detection of Oral Epithelial Cancer Using Fluorescence Lifetime Imaging Microscopy.” 2014. Thesis, Texas A&M University. Accessed June 19, 2018. http://hdl.handle.net/1969.1/153669.

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

MLA Handbook (7th Edition):

Lee, Joohyung. “Supervised Machine Learning Algorithms for Early Detection of Oral Epithelial Cancer Using Fluorescence Lifetime Imaging Microscopy.” 2014. Web. 19 Jun 2018.

Vancouver:

Lee J. Supervised Machine Learning Algorithms for Early Detection of Oral Epithelial Cancer Using Fluorescence Lifetime Imaging Microscopy. [Internet] [Thesis]. Texas A&M University; 2014. [cited 2018 Jun 19]. Available from: http://hdl.handle.net/1969.1/153669.

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

Council of Science Editors:

Lee J. Supervised Machine Learning Algorithms for Early Detection of Oral Epithelial Cancer Using Fluorescence Lifetime Imaging Microscopy. [Thesis]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/153669

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


Texas A&M University

5. Shrestha, Sebina. Development of Dual-Modality Optical Imaging Systems Consisting of Optical Coherence Tomography and Fluorescence Lifetime Imaging Microscopy.

Degree: 2015, Texas A&M University

 Both morphological and biochemical changes occur in a diseased tissue. As a result, tissue optical response changes with the progression of disease. A single optical… (more)

Subjects/Keywords: Optical Coherence Tomography; Fluorescence Lifetime Imaging Microscopy; Atherosclerosis; Oral Cancer; dual-modality optical imaging system

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APA (6th Edition):

Shrestha, S. (2015). Development of Dual-Modality Optical Imaging Systems Consisting of Optical Coherence Tomography and Fluorescence Lifetime Imaging Microscopy. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/155617

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):

Shrestha, Sebina. “Development of Dual-Modality Optical Imaging Systems Consisting of Optical Coherence Tomography and Fluorescence Lifetime Imaging Microscopy.” 2015. Thesis, Texas A&M University. Accessed June 19, 2018. http://hdl.handle.net/1969.1/155617.

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

MLA Handbook (7th Edition):

Shrestha, Sebina. “Development of Dual-Modality Optical Imaging Systems Consisting of Optical Coherence Tomography and Fluorescence Lifetime Imaging Microscopy.” 2015. Web. 19 Jun 2018.

Vancouver:

Shrestha S. Development of Dual-Modality Optical Imaging Systems Consisting of Optical Coherence Tomography and Fluorescence Lifetime Imaging Microscopy. [Internet] [Thesis]. Texas A&M University; 2015. [cited 2018 Jun 19]. Available from: http://hdl.handle.net/1969.1/155617.

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

Council of Science Editors:

Shrestha S. Development of Dual-Modality Optical Imaging Systems Consisting of Optical Coherence Tomography and Fluorescence Lifetime Imaging Microscopy. [Thesis]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/155617

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

6. Burton, Matthew Grant. Imaging the interactions of antimicrobial peptides with model and living cellular membrane systems.

Degree: 2016, University of Melbourne

 Since the discovery of penicillin over 80 years, the use of antimicrobial compounds has undoubtedly been one of the greatest contributions to modern science and… (more)

Subjects/Keywords: antimicrobial peptide; fluorescence lifetime imaging microscopy; super-resolution imaging; L-Forms; gram-negative bacteria; giant vesicles; fluorescence; kinetics

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APA (6th Edition):

Burton, M. G. (2016). Imaging the interactions of antimicrobial peptides with model and living cellular membrane systems. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/118417

Chicago Manual of Style (16th Edition):

Burton, Matthew Grant. “Imaging the interactions of antimicrobial peptides with model and living cellular membrane systems.” 2016. Doctoral Dissertation, University of Melbourne. Accessed June 19, 2018. http://hdl.handle.net/11343/118417.

MLA Handbook (7th Edition):

Burton, Matthew Grant. “Imaging the interactions of antimicrobial peptides with model and living cellular membrane systems.” 2016. Web. 19 Jun 2018.

Vancouver:

Burton MG. Imaging the interactions of antimicrobial peptides with model and living cellular membrane systems. [Internet] [Doctoral dissertation]. University of Melbourne; 2016. [cited 2018 Jun 19]. Available from: http://hdl.handle.net/11343/118417.

Council of Science Editors:

Burton MG. Imaging the interactions of antimicrobial peptides with model and living cellular membrane systems. [Doctoral Dissertation]. University of Melbourne; 2016. Available from: http://hdl.handle.net/11343/118417

7. Nozue, Shuho. Functions and differentiations of photosynthetic membranes (thylakoid membranes) in a green alga and nitrogen-fixing filamentous cyanobacteria analyzed by multimodal spectral imaging and fluorescence lifetime imaging .

Degree: 2017, Kyoto University

Subjects/Keywords: cyanobacteria; heterocyst; fluorescence lifetime imaging microscopy; fluorescence spectral microscopy; absorption spectral microscopy

Page 1 Page 2 Page 3

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APA (6th Edition):

Nozue, S. (2017). Functions and differentiations of photosynthetic membranes (thylakoid membranes) in a green alga and nitrogen-fixing filamentous cyanobacteria analyzed by multimodal spectral imaging and fluorescence lifetime imaging . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/226758

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):

Nozue, Shuho. “Functions and differentiations of photosynthetic membranes (thylakoid membranes) in a green alga and nitrogen-fixing filamentous cyanobacteria analyzed by multimodal spectral imaging and fluorescence lifetime imaging .” 2017. Thesis, Kyoto University. Accessed June 19, 2018. http://hdl.handle.net/2433/226758.

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

MLA Handbook (7th Edition):

Nozue, Shuho. “Functions and differentiations of photosynthetic membranes (thylakoid membranes) in a green alga and nitrogen-fixing filamentous cyanobacteria analyzed by multimodal spectral imaging and fluorescence lifetime imaging .” 2017. Web. 19 Jun 2018.

Vancouver:

Nozue S. Functions and differentiations of photosynthetic membranes (thylakoid membranes) in a green alga and nitrogen-fixing filamentous cyanobacteria analyzed by multimodal spectral imaging and fluorescence lifetime imaging . [Internet] [Thesis]. Kyoto University; 2017. [cited 2018 Jun 19]. Available from: http://hdl.handle.net/2433/226758.

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

Council of Science Editors:

Nozue S. Functions and differentiations of photosynthetic membranes (thylakoid membranes) in a green alga and nitrogen-fixing filamentous cyanobacteria analyzed by multimodal spectral imaging and fluorescence lifetime imaging . [Thesis]. Kyoto University; 2017. Available from: http://hdl.handle.net/2433/226758

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


Kyoto University / 京都大学

8. Nozue, Shuho. Functions and differentiations of photosynthetic membranes (thylakoid membranes) in a green alga and nitrogen-fixing filamentous cyanobacteria analyzed by multimodal spectral imaging and fluorescence lifetime imaging : 多角的顕微スペクトル画像及び蛍光寿命画像を用いた緑藻と窒素固定型糸状シアノバクテリアにおける光合成膜の機能と分化の研究.

Degree: 博士(理学), 2017, Kyoto University / 京都大学

新制・課程博士

甲第20604号

理博第4319号

Subjects/Keywords: cyanobacteria; heterocyst; fluorescence lifetime imaging microscopy; fluorescence spectral microscopy; absorption spectral microscopy

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APA (6th Edition):

Nozue, S. (2017). Functions and differentiations of photosynthetic membranes (thylakoid membranes) in a green alga and nitrogen-fixing filamentous cyanobacteria analyzed by multimodal spectral imaging and fluorescence lifetime imaging : 多角的顕微スペクトル画像及び蛍光寿命画像を用いた緑藻と窒素固定型糸状シアノバクテリアにおける光合成膜の機能と分化の研究. (Thesis). Kyoto University / 京都大学. Retrieved from http://hdl.handle.net/2433/226758 ; http://dx.doi.org/10.14989/doctor.k20604

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):

Nozue, Shuho. “Functions and differentiations of photosynthetic membranes (thylakoid membranes) in a green alga and nitrogen-fixing filamentous cyanobacteria analyzed by multimodal spectral imaging and fluorescence lifetime imaging : 多角的顕微スペクトル画像及び蛍光寿命画像を用いた緑藻と窒素固定型糸状シアノバクテリアにおける光合成膜の機能と分化の研究.” 2017. Thesis, Kyoto University / 京都大学. Accessed June 19, 2018. http://hdl.handle.net/2433/226758 ; http://dx.doi.org/10.14989/doctor.k20604.

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

MLA Handbook (7th Edition):

Nozue, Shuho. “Functions and differentiations of photosynthetic membranes (thylakoid membranes) in a green alga and nitrogen-fixing filamentous cyanobacteria analyzed by multimodal spectral imaging and fluorescence lifetime imaging : 多角的顕微スペクトル画像及び蛍光寿命画像を用いた緑藻と窒素固定型糸状シアノバクテリアにおける光合成膜の機能と分化の研究.” 2017. Web. 19 Jun 2018.

Vancouver:

Nozue S. Functions and differentiations of photosynthetic membranes (thylakoid membranes) in a green alga and nitrogen-fixing filamentous cyanobacteria analyzed by multimodal spectral imaging and fluorescence lifetime imaging : 多角的顕微スペクトル画像及び蛍光寿命画像を用いた緑藻と窒素固定型糸状シアノバクテリアにおける光合成膜の機能と分化の研究. [Internet] [Thesis]. Kyoto University / 京都大学; 2017. [cited 2018 Jun 19]. Available from: http://hdl.handle.net/2433/226758 ; http://dx.doi.org/10.14989/doctor.k20604.

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

Council of Science Editors:

Nozue S. Functions and differentiations of photosynthetic membranes (thylakoid membranes) in a green alga and nitrogen-fixing filamentous cyanobacteria analyzed by multimodal spectral imaging and fluorescence lifetime imaging : 多角的顕微スペクトル画像及び蛍光寿命画像を用いた緑藻と窒素固定型糸状シアノバクテリアにおける光合成膜の機能と分化の研究. [Thesis]. Kyoto University / 京都大学; 2017. Available from: http://hdl.handle.net/2433/226758 ; http://dx.doi.org/10.14989/doctor.k20604

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


University of Michigan

9. Chen, Leng-Chun. Label-Free Optical Imaging and Quantitative Algorithms to Assess Living Biological Systems.

Degree: PhD, Biomedical Engineering, 2014, University of Michigan

 Non-perturbing tools that provide reliable, information-rich assessments of living biological systems can inform clinical practice and improve patient health. In this dissertation, we developed label-free… (more)

Subjects/Keywords: Tissue Engineering; Label-free Optical Molecular Imaging; Tissue Viability; Multiphoton Excitation Microscopy; Second Harmonic Generation Imaging; Fluorescence Lifetime Imaging Microscopy; Biomedical Engineering; Engineering

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APA (6th Edition):

Chen, L. (2014). Label-Free Optical Imaging and Quantitative Algorithms to Assess Living Biological Systems. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/108858

Chicago Manual of Style (16th Edition):

Chen, Leng-Chun. “Label-Free Optical Imaging and Quantitative Algorithms to Assess Living Biological Systems.” 2014. Doctoral Dissertation, University of Michigan. Accessed June 19, 2018. http://hdl.handle.net/2027.42/108858.

MLA Handbook (7th Edition):

Chen, Leng-Chun. “Label-Free Optical Imaging and Quantitative Algorithms to Assess Living Biological Systems.” 2014. Web. 19 Jun 2018.

Vancouver:

Chen L. Label-Free Optical Imaging and Quantitative Algorithms to Assess Living Biological Systems. [Internet] [Doctoral dissertation]. University of Michigan; 2014. [cited 2018 Jun 19]. Available from: http://hdl.handle.net/2027.42/108858.

Council of Science Editors:

Chen L. Label-Free Optical Imaging and Quantitative Algorithms to Assess Living Biological Systems. [Doctoral Dissertation]. University of Michigan; 2014. Available from: http://hdl.handle.net/2027.42/108858


University of Utah

10. Cooper, Justin T. Single-molecule fluorescence microscopy of molecular interactions at reversed-phase chromatographic interfaces.

Degree: PhD, Chemistry, 2014, University of Utah

 The development of techniques to probe molecular transport and the dynamics of molecular interactions at interfaces is important for understanding and optimizingsurface-based technologies including surface-enhanced… (more)

Subjects/Keywords: Fluorescence; Microscopy; Single-molecule imaging

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APA (6th Edition):

Cooper, J. T. (2014). Single-molecule fluorescence microscopy of molecular interactions at reversed-phase chromatographic interfaces. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/3354/rec/2197

Chicago Manual of Style (16th Edition):

Cooper, Justin T. “Single-molecule fluorescence microscopy of molecular interactions at reversed-phase chromatographic interfaces.” 2014. Doctoral Dissertation, University of Utah. Accessed June 19, 2018. http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/3354/rec/2197.

MLA Handbook (7th Edition):

Cooper, Justin T. “Single-molecule fluorescence microscopy of molecular interactions at reversed-phase chromatographic interfaces.” 2014. Web. 19 Jun 2018.

Vancouver:

Cooper JT. Single-molecule fluorescence microscopy of molecular interactions at reversed-phase chromatographic interfaces. [Internet] [Doctoral dissertation]. University of Utah; 2014. [cited 2018 Jun 19]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/3354/rec/2197.

Council of Science Editors:

Cooper JT. Single-molecule fluorescence microscopy of molecular interactions at reversed-phase chromatographic interfaces. [Doctoral Dissertation]. University of Utah; 2014. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/3354/rec/2197


Brock University

11. Kefayati, Sarah. Confocal and two-photon microscopy : image enhancement .

Degree: Department of Physics, 2008, Brock University

 Confocal and two-photon microcopy have become essential tools in biological research and today many investigations are not possible without their help. The valuable advantage that… (more)

Subjects/Keywords: Confocal microscopy.; Fluorescence microscopy.; Three-dimensional imaging

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APA (6th Edition):

Kefayati, S. (2008). Confocal and two-photon microscopy : image enhancement . (Thesis). Brock University. Retrieved from http://hdl.handle.net/10464/1619

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):

Kefayati, Sarah. “Confocal and two-photon microscopy : image enhancement .” 2008. Thesis, Brock University. Accessed June 19, 2018. http://hdl.handle.net/10464/1619.

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

MLA Handbook (7th Edition):

Kefayati, Sarah. “Confocal and two-photon microscopy : image enhancement .” 2008. Web. 19 Jun 2018.

Vancouver:

Kefayati S. Confocal and two-photon microscopy : image enhancement . [Internet] [Thesis]. Brock University; 2008. [cited 2018 Jun 19]. Available from: http://hdl.handle.net/10464/1619.

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

Council of Science Editors:

Kefayati S. Confocal and two-photon microscopy : image enhancement . [Thesis]. Brock University; 2008. Available from: http://hdl.handle.net/10464/1619

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

12. Syed, Aleem. Spatial and temporal dynamics of receptor for advanced glycation endproducts, integrins, and actin cytoskeleton as probed with fluorescence-based imaging techniques.

Degree: 2016, Iowa State University

 Systematic spatial and temporal fluctuations are a fundamental part of any biological process. For example, lateral diffusion of membrane proteins is one of the key… (more)

Subjects/Keywords: Cell membrane biophysics; Fluorescence Lifetime Imaging; Fluorescence Recovery after Photobleaching; Single Particle Tracking; Stimulated Emission Depletion Microscopy; Visible light Photocages; Analytical Chemistry; Biophysics; Cell Biology

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APA (6th Edition):

Syed, A. (2016). Spatial and temporal dynamics of receptor for advanced glycation endproducts, integrins, and actin cytoskeleton as probed with fluorescence-based imaging techniques. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/16026

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):

Syed, Aleem. “Spatial and temporal dynamics of receptor for advanced glycation endproducts, integrins, and actin cytoskeleton as probed with fluorescence-based imaging techniques.” 2016. Thesis, Iowa State University. Accessed June 19, 2018. https://lib.dr.iastate.edu/etd/16026.

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

MLA Handbook (7th Edition):

Syed, Aleem. “Spatial and temporal dynamics of receptor for advanced glycation endproducts, integrins, and actin cytoskeleton as probed with fluorescence-based imaging techniques.” 2016. Web. 19 Jun 2018.

Vancouver:

Syed A. Spatial and temporal dynamics of receptor for advanced glycation endproducts, integrins, and actin cytoskeleton as probed with fluorescence-based imaging techniques. [Internet] [Thesis]. Iowa State University; 2016. [cited 2018 Jun 19]. Available from: https://lib.dr.iastate.edu/etd/16026.

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

Council of Science Editors:

Syed A. Spatial and temporal dynamics of receptor for advanced glycation endproducts, integrins, and actin cytoskeleton as probed with fluorescence-based imaging techniques. [Thesis]. Iowa State University; 2016. Available from: https://lib.dr.iastate.edu/etd/16026

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


University of Michigan

13. Chang, Ching-Wei. Improving Accuracy and Precision in Biological Applications of Fluorescence Lifetime Imaging Microscopy.

Degree: PhD, Biomedical Engineering, 2009, University of Michigan

 The quantitative understanding of cellular and molecular responses in living cells is important for many reasons, including identifying potential molecular targets for treatments of diseases… (more)

Subjects/Keywords: Fluorescence Lifetime Imaging Microscopy; Fluorescence Resonance Energy Transfer; Optimal Gating and Fitting; Total Variation Denoising; Molecular Interactions; Live Cells; Biomedical Engineering; Engineering

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APA (6th Edition):

Chang, C. (2009). Improving Accuracy and Precision in Biological Applications of Fluorescence Lifetime Imaging Microscopy. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/63765

Chicago Manual of Style (16th Edition):

Chang, Ching-Wei. “Improving Accuracy and Precision in Biological Applications of Fluorescence Lifetime Imaging Microscopy.” 2009. Doctoral Dissertation, University of Michigan. Accessed June 19, 2018. http://hdl.handle.net/2027.42/63765.

MLA Handbook (7th Edition):

Chang, Ching-Wei. “Improving Accuracy and Precision in Biological Applications of Fluorescence Lifetime Imaging Microscopy.” 2009. Web. 19 Jun 2018.

Vancouver:

Chang C. Improving Accuracy and Precision in Biological Applications of Fluorescence Lifetime Imaging Microscopy. [Internet] [Doctoral dissertation]. University of Michigan; 2009. [cited 2018 Jun 19]. Available from: http://hdl.handle.net/2027.42/63765.

Council of Science Editors:

Chang C. Improving Accuracy and Precision in Biological Applications of Fluorescence Lifetime Imaging Microscopy. [Doctoral Dissertation]. University of Michigan; 2009. Available from: http://hdl.handle.net/2027.42/63765


University of Oklahoma

14. Li, Zheng. HIGH-THROUGHPUT FLUORESCENCE MICROSCOPY FOR AUTOMATED CLINICAL APPLICATIONS.

Degree: PhD, 2017, University of Oklahoma

Fluorescence in situ hybridization (FISH) is a powerful tool for visualizing and detecting genetic abnormalities. Manual scoring FISH analysis is a tedious and labor-and-time-consuming task.… (more)

Subjects/Keywords: Fluorescence Microscopy; Fluorescence in situ hybridization; Microscopic Imaging; Automated Microscopy

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

APA (6th Edition):

Li, Z. (2017). HIGH-THROUGHPUT FLUORESCENCE MICROSCOPY FOR AUTOMATED CLINICAL APPLICATIONS. (Doctoral Dissertation). University of Oklahoma. Retrieved from http://hdl.handle.net/11244/50778

Chicago Manual of Style (16th Edition):

Li, Zheng. “HIGH-THROUGHPUT FLUORESCENCE MICROSCOPY FOR AUTOMATED CLINICAL APPLICATIONS.” 2017. Doctoral Dissertation, University of Oklahoma. Accessed June 19, 2018. http://hdl.handle.net/11244/50778.

MLA Handbook (7th Edition):

Li, Zheng. “HIGH-THROUGHPUT FLUORESCENCE MICROSCOPY FOR AUTOMATED CLINICAL APPLICATIONS.” 2017. Web. 19 Jun 2018.

Vancouver:

Li Z. HIGH-THROUGHPUT FLUORESCENCE MICROSCOPY FOR AUTOMATED CLINICAL APPLICATIONS. [Internet] [Doctoral dissertation]. University of Oklahoma; 2017. [cited 2018 Jun 19]. Available from: http://hdl.handle.net/11244/50778.

Council of Science Editors:

Li Z. HIGH-THROUGHPUT FLUORESCENCE MICROSCOPY FOR AUTOMATED CLINICAL APPLICATIONS. [Doctoral Dissertation]. University of Oklahoma; 2017. Available from: http://hdl.handle.net/11244/50778


University of Tennessee – Knoxville

15. Crawford, Justin Lee. High-sensitivity spectral fluorescence lifetime imaging for resolving spectroscopically overlapping species.

Degree: MS, Physics and Astronomy, 2009, University of Tennessee – Knoxville

 The capability to resolve the contributions from spectroscopically overlapping fluorophores has enabled significant breakthroughs in cellular imaging. However, commercial microscopes for this purpose use analog… (more)

Subjects/Keywords: spectral fluorescence lifetime imaging; maximum likelihood; confocal microscopy; interference filters; spectroscopically overlapping fluorophores; single-photon avalanche detector; Biological and Chemical Physics; Optics

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APA (6th Edition):

Crawford, J. L. (2009). High-sensitivity spectral fluorescence lifetime imaging for resolving spectroscopically overlapping species. (Thesis). University of Tennessee – Knoxville. Retrieved from http://trace.tennessee.edu/utk_gradthes/3

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):

Crawford, Justin Lee. “High-sensitivity spectral fluorescence lifetime imaging for resolving spectroscopically overlapping species.” 2009. Thesis, University of Tennessee – Knoxville. Accessed June 19, 2018. http://trace.tennessee.edu/utk_gradthes/3.

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

MLA Handbook (7th Edition):

Crawford, Justin Lee. “High-sensitivity spectral fluorescence lifetime imaging for resolving spectroscopically overlapping species.” 2009. Web. 19 Jun 2018.

Vancouver:

Crawford JL. High-sensitivity spectral fluorescence lifetime imaging for resolving spectroscopically overlapping species. [Internet] [Thesis]. University of Tennessee – Knoxville; 2009. [cited 2018 Jun 19]. Available from: http://trace.tennessee.edu/utk_gradthes/3.

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

Council of Science Editors:

Crawford JL. High-sensitivity spectral fluorescence lifetime imaging for resolving spectroscopically overlapping species. [Thesis]. University of Tennessee – Knoxville; 2009. Available from: http://trace.tennessee.edu/utk_gradthes/3

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


University of Rochester

16. Shroff, Sapna A. (1981 - ). Structured illumination imaging.

Degree: PhD, 2010, University of Rochester

 The resolution of an imaging system is limited by the wavelength and numerical aperture of the system. Structured illumination imaging has been applied in microscopy(more)

Subjects/Keywords: Optical imaging; Ophthalmoscopy; Microscopy; Fluorescence microscopy; Coherent imaging; Speckle reduction

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APA (6th Edition):

Shroff, S. A. (. -. ). (2010). Structured illumination imaging. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/11379

Chicago Manual of Style (16th Edition):

Shroff, Sapna A (1981 - ). “Structured illumination imaging.” 2010. Doctoral Dissertation, University of Rochester. Accessed June 19, 2018. http://hdl.handle.net/1802/11379.

MLA Handbook (7th Edition):

Shroff, Sapna A (1981 - ). “Structured illumination imaging.” 2010. Web. 19 Jun 2018.

Vancouver:

Shroff SA(-). Structured illumination imaging. [Internet] [Doctoral dissertation]. University of Rochester; 2010. [cited 2018 Jun 19]. Available from: http://hdl.handle.net/1802/11379.

Council of Science Editors:

Shroff SA(-). Structured illumination imaging. [Doctoral Dissertation]. University of Rochester; 2010. Available from: http://hdl.handle.net/1802/11379


NSYSU

17. You, Jr-chi. Spectroscopic characterization of fluorescent nano-diamonds.

Degree: Master, Materials and Optoelectronic Science, 2010, NSYSU

 Fluorescent nano-diamond(FND) is an unique fluorescence bio-labeling materials, which exhibit good fluorescence yield, excellent photostability, and non-toxicity. The emission color of FND is determined by… (more)

Subjects/Keywords: fluorescence lifetime; confocal optical microscopy; fluorescent nano-diamond

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APA (6th Edition):

You, J. (2010). Spectroscopic characterization of fluorescent nano-diamonds. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0210110-104730

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):

You, Jr-chi. “Spectroscopic characterization of fluorescent nano-diamonds.” 2010. Thesis, NSYSU. Accessed June 19, 2018. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0210110-104730.

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

MLA Handbook (7th Edition):

You, Jr-chi. “Spectroscopic characterization of fluorescent nano-diamonds.” 2010. Web. 19 Jun 2018.

Vancouver:

You J. Spectroscopic characterization of fluorescent nano-diamonds. [Internet] [Thesis]. NSYSU; 2010. [cited 2018 Jun 19]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0210110-104730.

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

Council of Science Editors:

You J. Spectroscopic characterization of fluorescent nano-diamonds. [Thesis]. NSYSU; 2010. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0210110-104730

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


West Virginia University

18. Zhang, Yong, 1974-. Lossless compression and neuron structure extraction for fluorescence microscopy confocal neuron images.

Degree: 2006, West Virginia University

 To study the development of nervous systems, biologists are interested in neurite outgrowth, differentiation, synapse formation, and plasticity. High throughput neuron image processing is an… (more)

Subjects/Keywords: Confocal fluorescence microscopy.; Neurons – Imaging.; Image compression.

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APA (6th Edition):

Zhang, Yong, 1. (2006). Lossless compression and neuron structure extraction for fluorescence microscopy confocal neuron images. (Thesis). West Virginia University. Retrieved from http://wvuscholar.wvu.edu:8881/R/?func=dbin-jump-full&object_id=21256

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):

Zhang, Yong, 1974-. “Lossless compression and neuron structure extraction for fluorescence microscopy confocal neuron images.” 2006. Thesis, West Virginia University. Accessed June 19, 2018. http://wvuscholar.wvu.edu:8881/R/?func=dbin-jump-full&object_id=21256.

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

MLA Handbook (7th Edition):

Zhang, Yong, 1974-. “Lossless compression and neuron structure extraction for fluorescence microscopy confocal neuron images.” 2006. Web. 19 Jun 2018.

Vancouver:

Zhang, Yong 1. Lossless compression and neuron structure extraction for fluorescence microscopy confocal neuron images. [Internet] [Thesis]. West Virginia University; 2006. [cited 2018 Jun 19]. Available from: http://wvuscholar.wvu.edu:8881/R/?func=dbin-jump-full&object_id=21256.

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

Council of Science Editors:

Zhang, Yong 1. Lossless compression and neuron structure extraction for fluorescence microscopy confocal neuron images. [Thesis]. West Virginia University; 2006. Available from: http://wvuscholar.wvu.edu:8881/R/?func=dbin-jump-full&object_id=21256

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


University of Toronto

19. 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 June 19, 2018. 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. 19 Jun 2018.

Vancouver:

Downie KJ. Live Cell Imaging of CEACAM1 Dynamics and Self-association during Bacterial Binding. [Internet] [Masters thesis]. University of Toronto; 2013. [cited 2018 Jun 19]. 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


University of Illinois – Urbana-Champaign

20. Chen, Yi-Chun. Fluorescence lifetime-resolved imaging microscopy studies: quantitative image analysis, spectral-FLIM, and photosynthesis.

Degree: PhD, 0408, 2010, University of Illinois – Urbana-Champaign

 Development of instrumentation and image analysis methods for the fluorescence lifetime-resolved imaging microscopy (FLIM) were carried out in this thesis. With the new instrument setup… (more)

Subjects/Keywords: fluorescence lifetime imaging microscopy (FLIM); F??rster resonance energy transfer (FRET); Spectral-FLIM; fluorescence spectrum; linear unmixing; polar plot; Chlorophyll a fluorescence transient; lutein epoxide cycle; non-photochemical quenching; violaxanthin cycle; chlamydomonas reinhardtii

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APA (6th Edition):

Chen, Y. (2010). Fluorescence lifetime-resolved imaging microscopy studies: quantitative image analysis, spectral-FLIM, and photosynthesis. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/17035

Chicago Manual of Style (16th Edition):

Chen, Yi-Chun. “Fluorescence lifetime-resolved imaging microscopy studies: quantitative image analysis, spectral-FLIM, and photosynthesis.” 2010. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed June 19, 2018. http://hdl.handle.net/2142/17035.

MLA Handbook (7th Edition):

Chen, Yi-Chun. “Fluorescence lifetime-resolved imaging microscopy studies: quantitative image analysis, spectral-FLIM, and photosynthesis.” 2010. Web. 19 Jun 2018.

Vancouver:

Chen Y. Fluorescence lifetime-resolved imaging microscopy studies: quantitative image analysis, spectral-FLIM, and photosynthesis. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2010. [cited 2018 Jun 19]. Available from: http://hdl.handle.net/2142/17035.

Council of Science Editors:

Chen Y. Fluorescence lifetime-resolved imaging microscopy studies: quantitative image analysis, spectral-FLIM, and photosynthesis. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2010. Available from: http://hdl.handle.net/2142/17035

21. Mao, Hui. Using Artificial Neural Network Based Algorithm for Data Analysis of Fluorescence Lifetime Imaging .

Degree: 2014, California State University – San Marcos

 The thesis presented here introduces, validates, and implements the artificial neural network (ANN) approach for efficient and accurate analysis of time-resolved fluorescence lifetime image microscopy(more)

Subjects/Keywords: Artificial neural network; Function Approximation; Fluorescence lifetime-resolved imaging

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APA (6th Edition):

Mao, H. (2014). Using Artificial Neural Network Based Algorithm for Data Analysis of Fluorescence Lifetime Imaging . (Thesis). California State University – San Marcos. Retrieved from http://hdl.handle.net/10211.3/120745

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):

Mao, Hui. “Using Artificial Neural Network Based Algorithm for Data Analysis of Fluorescence Lifetime Imaging .” 2014. Thesis, California State University – San Marcos. Accessed June 19, 2018. http://hdl.handle.net/10211.3/120745.

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

MLA Handbook (7th Edition):

Mao, Hui. “Using Artificial Neural Network Based Algorithm for Data Analysis of Fluorescence Lifetime Imaging .” 2014. Web. 19 Jun 2018.

Vancouver:

Mao H. Using Artificial Neural Network Based Algorithm for Data Analysis of Fluorescence Lifetime Imaging . [Internet] [Thesis]. California State University – San Marcos; 2014. [cited 2018 Jun 19]. Available from: http://hdl.handle.net/10211.3/120745.

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

Council of Science Editors:

Mao H. Using Artificial Neural Network Based Algorithm for Data Analysis of Fluorescence Lifetime Imaging . [Thesis]. California State University – San Marcos; 2014. Available from: http://hdl.handle.net/10211.3/120745

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


Vanderbilt University

22. Heaster, Tiffany Marie. Optical imaging of cell cycle-driven tumor heterogeneity.

Degree: MS, Biomedical Engineering, 2016, Vanderbilt University

 Metabolism-driven changes in cell cycle status introduce a high degree of cellular heterogeneity within a tumor, presenting challenges with evasion from drug treatment and increased… (more)

Subjects/Keywords: fluorescence lifetime; tumor dormancy; metabolic imaging; quiescence; cellular heterogeneity; cancer

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APA (6th Edition):

Heaster, T. M. (2016). Optical imaging of cell cycle-driven tumor heterogeneity. (Masters Thesis). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu//available/etd-03282016-155111/ ;

Chicago Manual of Style (16th Edition):

Heaster, Tiffany Marie. “Optical imaging of cell cycle-driven tumor heterogeneity.” 2016. Masters Thesis, Vanderbilt University. Accessed June 19, 2018. http://etd.library.vanderbilt.edu//available/etd-03282016-155111/ ;.

MLA Handbook (7th Edition):

Heaster, Tiffany Marie. “Optical imaging of cell cycle-driven tumor heterogeneity.” 2016. Web. 19 Jun 2018.

Vancouver:

Heaster TM. Optical imaging of cell cycle-driven tumor heterogeneity. [Internet] [Masters thesis]. Vanderbilt University; 2016. [cited 2018 Jun 19]. Available from: http://etd.library.vanderbilt.edu//available/etd-03282016-155111/ ;.

Council of Science Editors:

Heaster TM. Optical imaging of cell cycle-driven tumor heterogeneity. [Masters Thesis]. Vanderbilt University; 2016. Available from: http://etd.library.vanderbilt.edu//available/etd-03282016-155111/ ;

23. Bennet, Mathieu A. Multi-parameter quantitative mapping of microfluidic devices.

Degree: 2011, University of Edinburgh

Fluorescence lifetime imaging microscopy (FLIM) is a powerful technique to non-invasively map the physical and chemical environment within microfluidic devices. In this work FLIM has… (more)

Subjects/Keywords: 620.106; microfluidics; fluorescence; lifetime imaging microscopy; optical trap; particle imaging velocimetry; multimodality imaging

…49 3.3 Wide-field fluorescence lifetime imaging microscopy… …147 7.2.2 Fluorescence lifetime imaging microscopy… …Fluorescence lifetime imaging microscopy of optically trapped microdroplets in the microchannel… …69 PROBING pH IN A MICROFLUIDIC DEVICE USING WIDE-FIELD FLUORESCENCE LIFETIME IMAGING… …117 SIMULTANEOUS USE OF MICRO-PARTICLE IMAGING VELOCIMETRY AND FLUORESCENCE LIFETIME… 

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APA (6th Edition):

Bennet, M. A. (2011). Multi-parameter quantitative mapping of microfluidic devices. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/5739

Chicago Manual of Style (16th Edition):

Bennet, Mathieu A. “Multi-parameter quantitative mapping of microfluidic devices.” 2011. Doctoral Dissertation, University of Edinburgh. Accessed June 19, 2018. http://hdl.handle.net/1842/5739.

MLA Handbook (7th Edition):

Bennet, Mathieu A. “Multi-parameter quantitative mapping of microfluidic devices.” 2011. Web. 19 Jun 2018.

Vancouver:

Bennet MA. Multi-parameter quantitative mapping of microfluidic devices. [Internet] [Doctoral dissertation]. University of Edinburgh; 2011. [cited 2018 Jun 19]. Available from: http://hdl.handle.net/1842/5739.

Council of Science Editors:

Bennet MA. Multi-parameter quantitative mapping of microfluidic devices. [Doctoral Dissertation]. University of Edinburgh; 2011. Available from: http://hdl.handle.net/1842/5739


University of Arizona

24. Lin, Yuxiang. DEVELOPMENT AND ANALYSIS OF OPTICAL PH IMAGING TECHNIQUES .

Degree: 2010, University of Arizona

 The pH of tumors and surrounding tissues is a key biophysical property of the tumor microenvironment that affects how a tumor survives and how it… (more)

Subjects/Keywords: accuracy and precision; error analysis; fluorescence lifetime; optical pH imaging; ratiometric imaging; statistical analysis

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APA (6th Edition):

Lin, Y. (2010). DEVELOPMENT AND ANALYSIS OF OPTICAL PH IMAGING TECHNIQUES . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/193846

Chicago Manual of Style (16th Edition):

Lin, Yuxiang. “DEVELOPMENT AND ANALYSIS OF OPTICAL PH IMAGING TECHNIQUES .” 2010. Doctoral Dissertation, University of Arizona. Accessed June 19, 2018. http://hdl.handle.net/10150/193846.

MLA Handbook (7th Edition):

Lin, Yuxiang. “DEVELOPMENT AND ANALYSIS OF OPTICAL PH IMAGING TECHNIQUES .” 2010. Web. 19 Jun 2018.

Vancouver:

Lin Y. DEVELOPMENT AND ANALYSIS OF OPTICAL PH IMAGING TECHNIQUES . [Internet] [Doctoral dissertation]. University of Arizona; 2010. [cited 2018 Jun 19]. Available from: http://hdl.handle.net/10150/193846.

Council of Science Editors:

Lin Y. DEVELOPMENT AND ANALYSIS OF OPTICAL PH IMAGING TECHNIQUES . [Doctoral Dissertation]. University of Arizona; 2010. Available from: http://hdl.handle.net/10150/193846

25. Elahi, Sakib F. Assessing Molecular Biomarkers in Living Mice Using Fluorescence Microendoscopy and Spectroscopy.

Degree: PhD, Biomedical Engineering, 2014, University of Michigan

 Assessment of molecular biomarkers expressed in cells and tissues can inform scientists and clinicians of physiological and disease processes. Optical techniques can quantitatively and noninvasively… (more)

Subjects/Keywords: Biomedical Optics; Targeted Imaging; Colorectal Cancer; Tissue Engineering; Intravital Imaging; Fluorescence Lifetime; Biomedical Engineering; Engineering

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APA (6th Edition):

Elahi, S. F. (2014). Assessing Molecular Biomarkers in Living Mice Using Fluorescence Microendoscopy and Spectroscopy. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/108845

Chicago Manual of Style (16th Edition):

Elahi, Sakib F. “Assessing Molecular Biomarkers in Living Mice Using Fluorescence Microendoscopy and Spectroscopy.” 2014. Doctoral Dissertation, University of Michigan. Accessed June 19, 2018. http://hdl.handle.net/2027.42/108845.

MLA Handbook (7th Edition):

Elahi, Sakib F. “Assessing Molecular Biomarkers in Living Mice Using Fluorescence Microendoscopy and Spectroscopy.” 2014. Web. 19 Jun 2018.

Vancouver:

Elahi SF. Assessing Molecular Biomarkers in Living Mice Using Fluorescence Microendoscopy and Spectroscopy. [Internet] [Doctoral dissertation]. University of Michigan; 2014. [cited 2018 Jun 19]. Available from: http://hdl.handle.net/2027.42/108845.

Council of Science Editors:

Elahi SF. Assessing Molecular Biomarkers in Living Mice Using Fluorescence Microendoscopy and Spectroscopy. [Doctoral Dissertation]. University of Michigan; 2014. Available from: http://hdl.handle.net/2027.42/108845


Harvard University

26. Lacy, Jessica. Imaging of PARP1/2-Overexpressing Cancers with Novel AZD2281-Derived Probes.

Degree: Doctor of Medicine, 2014, Harvard University

 Poly(ADP-ribose)polymerase-1 and -2 (PARP1/2) are nuclear proteins involved in DNA repair. Tumors with defects in homologous recombination, including BRCA1- and BRCA2-deficient cancers, have been shown… (more)

Subjects/Keywords: PARP; BRCA; PET imaging; PET/CT imaging; fluorescence microscopy

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APA (6th Edition):

Lacy, J. (2014). Imaging of PARP1/2-Overexpressing Cancers with Novel AZD2281-Derived Probes. (Doctoral Dissertation). Harvard University. Retrieved from http://etds.lib.harvard.edu/hms/admin/view/58 ; http://nrs.harvard.edu/urn-3:HUL.InstRepos:12407616

Chicago Manual of Style (16th Edition):

Lacy, Jessica. “Imaging of PARP1/2-Overexpressing Cancers with Novel AZD2281-Derived Probes.” 2014. Doctoral Dissertation, Harvard University. Accessed June 19, 2018. http://etds.lib.harvard.edu/hms/admin/view/58 ; http://nrs.harvard.edu/urn-3:HUL.InstRepos:12407616.

MLA Handbook (7th Edition):

Lacy, Jessica. “Imaging of PARP1/2-Overexpressing Cancers with Novel AZD2281-Derived Probes.” 2014. Web. 19 Jun 2018.

Vancouver:

Lacy J. Imaging of PARP1/2-Overexpressing Cancers with Novel AZD2281-Derived Probes. [Internet] [Doctoral dissertation]. Harvard University; 2014. [cited 2018 Jun 19]. Available from: http://etds.lib.harvard.edu/hms/admin/view/58 ; http://nrs.harvard.edu/urn-3:HUL.InstRepos:12407616.

Council of Science Editors:

Lacy J. Imaging of PARP1/2-Overexpressing Cancers with Novel AZD2281-Derived Probes. [Doctoral Dissertation]. Harvard University; 2014. Available from: http://etds.lib.harvard.edu/hms/admin/view/58 ; http://nrs.harvard.edu/urn-3:HUL.InstRepos:12407616


Indian Institute of Science

27. Purnapatra, Subhajit Banergjee. Spatial Filtering Techniques for Large Penetration Depth and Volume Imaging in Fluorescence Microscopy.

Degree: 2013, Indian Institute of Science

 In the past two decades, Fluorescence microscopy has imparted tremendous impact in Biology and Imaging. Several super-resolution Fluorescence imaging techniques (e.g. PALM, STED, STORM, 4Pi… (more)

Subjects/Keywords: Fluorescence Microscopy; Volume Imaging; Spatial Filtering; Fluorescence Imaging; Point Spread Function and Imaging; Confocal Microscopy; Multi-Photon Microscopy; Light-Sheet Microscopy; Multiple Light-sheet Illumination Microscopy (MLSIM); Instrumentation

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APA (6th Edition):

Purnapatra, S. B. (2013). Spatial Filtering Techniques for Large Penetration Depth and Volume Imaging in Fluorescence Microscopy. (Thesis). Indian Institute of Science. Retrieved from http://etd.iisc.ernet.in/2005/3351 ; http://etd.iisc.ernet.in/abstracts/4217/G25745-Abs.pdf

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):

Purnapatra, Subhajit Banergjee. “Spatial Filtering Techniques for Large Penetration Depth and Volume Imaging in Fluorescence Microscopy.” 2013. Thesis, Indian Institute of Science. Accessed June 19, 2018. http://etd.iisc.ernet.in/2005/3351 ; http://etd.iisc.ernet.in/abstracts/4217/G25745-Abs.pdf.

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

MLA Handbook (7th Edition):

Purnapatra, Subhajit Banergjee. “Spatial Filtering Techniques for Large Penetration Depth and Volume Imaging in Fluorescence Microscopy.” 2013. Web. 19 Jun 2018.

Vancouver:

Purnapatra SB. Spatial Filtering Techniques for Large Penetration Depth and Volume Imaging in Fluorescence Microscopy. [Internet] [Thesis]. Indian Institute of Science; 2013. [cited 2018 Jun 19]. Available from: http://etd.iisc.ernet.in/2005/3351 ; http://etd.iisc.ernet.in/abstracts/4217/G25745-Abs.pdf.

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

Council of Science Editors:

Purnapatra SB. Spatial Filtering Techniques for Large Penetration Depth and Volume Imaging in Fluorescence Microscopy. [Thesis]. Indian Institute of Science; 2013. Available from: http://etd.iisc.ernet.in/2005/3351 ; http://etd.iisc.ernet.in/abstracts/4217/G25745-Abs.pdf

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


UCLA

28. Sherman, Adria Jardeni. Characterization and Optimization of a Normalized Fluorescence Lifetime Imaging System of Biological Samples.

Degree: Biomedical Engineering, 2013, UCLA

Fluorescence lifetime imaging microscopy (FLIM) is a technique that has shown the ability to differentiate malignant from benign tissue in vivo and ex vivo. However,… (more)

Subjects/Keywords: Biomedical engineering; Oncology; Surgery; brain; fluorescence; head and neck; imaging; lifetime; tumors

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

APA (6th Edition):

Sherman, A. J. (2013). Characterization and Optimization of a Normalized Fluorescence Lifetime Imaging System of Biological Samples. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/9276w471

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):

Sherman, Adria Jardeni. “Characterization and Optimization of a Normalized Fluorescence Lifetime Imaging System of Biological Samples.” 2013. Thesis, UCLA. Accessed June 19, 2018. http://www.escholarship.org/uc/item/9276w471.

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

MLA Handbook (7th Edition):

Sherman, Adria Jardeni. “Characterization and Optimization of a Normalized Fluorescence Lifetime Imaging System of Biological Samples.” 2013. Web. 19 Jun 2018.

Vancouver:

Sherman AJ. Characterization and Optimization of a Normalized Fluorescence Lifetime Imaging System of Biological Samples. [Internet] [Thesis]. UCLA; 2013. [cited 2018 Jun 19]. Available from: http://www.escholarship.org/uc/item/9276w471.

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

Council of Science Editors:

Sherman AJ. Characterization and Optimization of a Normalized Fluorescence Lifetime Imaging System of Biological Samples. [Thesis]. UCLA; 2013. Available from: http://www.escholarship.org/uc/item/9276w471

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


Harvard University

29. Hou, Steven Shuyu. Time-Domain Fluorescence Diffuse Optical Tomography: Algorithms and Applications.

Degree: PhD, Engineering and Applied Sciences, 2014, Harvard University

Fluorescence diffuse optical tomography provides non-invasive, in vivo imaging of molecular targets in small animals. While standard fluorescence microscopy is limited to shallow depths and… (more)

Subjects/Keywords: Medical imaging and radiology; Biomedical engineering; Biophysics; diffuse optics; fluorescence; lifetime; reconstruction algorithms; tomography

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

APA (6th Edition):

Hou, S. S. (2014). Time-Domain Fluorescence Diffuse Optical Tomography: Algorithms and Applications. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:13070053

Chicago Manual of Style (16th Edition):

Hou, Steven Shuyu. “Time-Domain Fluorescence Diffuse Optical Tomography: Algorithms and Applications.” 2014. Doctoral Dissertation, Harvard University. Accessed June 19, 2018. http://nrs.harvard.edu/urn-3:HUL.InstRepos:13070053.

MLA Handbook (7th Edition):

Hou, Steven Shuyu. “Time-Domain Fluorescence Diffuse Optical Tomography: Algorithms and Applications.” 2014. Web. 19 Jun 2018.

Vancouver:

Hou SS. Time-Domain Fluorescence Diffuse Optical Tomography: Algorithms and Applications. [Internet] [Doctoral dissertation]. Harvard University; 2014. [cited 2018 Jun 19]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:13070053.

Council of Science Editors:

Hou SS. Time-Domain Fluorescence Diffuse Optical Tomography: Algorithms and Applications. [Doctoral Dissertation]. Harvard University; 2014. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:13070053


Texas A&M University

30. Pande, Paritosh. Algorithms for Fluorescence Lifetime Microscopy and Optical Coherence Tomography Data Analysis: Applications for Diagnosis of Atherosclerosis and Oral Cancer.

Degree: 2014, Texas A&M University

 With significant progress made in the design and instrumentation of optical imaging systems, it is now possible to perform high-resolution tissue imaging in near real-time.… (more)

Subjects/Keywords: Fluorescence Lifetime Imaging; Optical Coherence Tomography; Atherosclerosis; Oral Cancer; Deconvolution; Unmixing; Image Processing

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

APA (6th Edition):

Pande, P. (2014). Algorithms for Fluorescence Lifetime Microscopy and Optical Coherence Tomography Data Analysis: Applications for Diagnosis of Atherosclerosis and Oral Cancer. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/153234

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):

Pande, Paritosh. “Algorithms for Fluorescence Lifetime Microscopy and Optical Coherence Tomography Data Analysis: Applications for Diagnosis of Atherosclerosis and Oral Cancer.” 2014. Thesis, Texas A&M University. Accessed June 19, 2018. http://hdl.handle.net/1969.1/153234.

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

MLA Handbook (7th Edition):

Pande, Paritosh. “Algorithms for Fluorescence Lifetime Microscopy and Optical Coherence Tomography Data Analysis: Applications for Diagnosis of Atherosclerosis and Oral Cancer.” 2014. Web. 19 Jun 2018.

Vancouver:

Pande P. Algorithms for Fluorescence Lifetime Microscopy and Optical Coherence Tomography Data Analysis: Applications for Diagnosis of Atherosclerosis and Oral Cancer. [Internet] [Thesis]. Texas A&M University; 2014. [cited 2018 Jun 19]. Available from: http://hdl.handle.net/1969.1/153234.

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

Council of Science Editors:

Pande P. Algorithms for Fluorescence Lifetime Microscopy and Optical Coherence Tomography Data Analysis: Applications for Diagnosis of Atherosclerosis and Oral Cancer. [Thesis]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/153234

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

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