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You searched for subject:(Fluorescence Lifetime Imaging Microscopy). Showing records 1 – 30 of 24768 total matches.

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McMaster University

1. Hirmiz, Nehad. DEVELOPMENT OF A MULTIPLEXED CONFOCAL FLUORESCENCE LIFETIME IMAGING MICROSCOPE FOR SCREENING APPLICATIONS.

Degree: 2019, McMaster University

Protein-protein interactions are important for biological processes. Therefore, many small molecules target a specific protein or interaction in the cell to have biological consequence. While… (more)

Subjects/Keywords: Fluorescence Microscopy; Confocal Microsopy; Fluorescence Lifetime; Rapid Imaging; Drug Screening

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

APA (6th Edition):

Hirmiz, N. (2019). DEVELOPMENT OF A MULTIPLEXED CONFOCAL FLUORESCENCE LIFETIME IMAGING MICROSCOPE FOR SCREENING APPLICATIONS. (Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/25137

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):

Hirmiz, Nehad. “DEVELOPMENT OF A MULTIPLEXED CONFOCAL FLUORESCENCE LIFETIME IMAGING MICROSCOPE FOR SCREENING APPLICATIONS.” 2019. Thesis, McMaster University. Accessed November 26, 2020. http://hdl.handle.net/11375/25137.

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

MLA Handbook (7th Edition):

Hirmiz, Nehad. “DEVELOPMENT OF A MULTIPLEXED CONFOCAL FLUORESCENCE LIFETIME IMAGING MICROSCOPE FOR SCREENING APPLICATIONS.” 2019. Web. 26 Nov 2020.

Vancouver:

Hirmiz N. DEVELOPMENT OF A MULTIPLEXED CONFOCAL FLUORESCENCE LIFETIME IMAGING MICROSCOPE FOR SCREENING APPLICATIONS. [Internet] [Thesis]. McMaster University; 2019. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/11375/25137.

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

Council of Science Editors:

Hirmiz N. DEVELOPMENT OF A MULTIPLEXED CONFOCAL FLUORESCENCE LIFETIME IMAGING MICROSCOPE FOR SCREENING APPLICATIONS. [Thesis]. McMaster University; 2019. Available from: http://hdl.handle.net/11375/25137

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


Texas A&M University

2. Hinsdale, Taylor A. Enhanced Early Detection of Oral Squamous Cell Carcinoma via Structured Illumination Fluorescence Lifetime Imaging.

Degree: PhD, Biomedical Engineering, 2018, Texas A&M University

 The early diagnosis of oral carcinoma has proven to be a difficult task. Fully developed oral squamous cell carcinomas can be easily recognized by trained… (more)

Subjects/Keywords: Fluorescence Lifetime; Cancer; Imaging; Microscopy; Structured Illumination Microscopy; Optical Sectioning

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APA (6th Edition):

Hinsdale, T. A. (2018). Enhanced Early Detection of Oral Squamous Cell Carcinoma via Structured Illumination Fluorescence Lifetime Imaging. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/173411

Chicago Manual of Style (16th Edition):

Hinsdale, Taylor A. “Enhanced Early Detection of Oral Squamous Cell Carcinoma via Structured Illumination Fluorescence Lifetime Imaging.” 2018. Doctoral Dissertation, Texas A&M University. Accessed November 26, 2020. http://hdl.handle.net/1969.1/173411.

MLA Handbook (7th Edition):

Hinsdale, Taylor A. “Enhanced Early Detection of Oral Squamous Cell Carcinoma via Structured Illumination Fluorescence Lifetime Imaging.” 2018. Web. 26 Nov 2020.

Vancouver:

Hinsdale TA. Enhanced Early Detection of Oral Squamous Cell Carcinoma via Structured Illumination Fluorescence Lifetime Imaging. [Internet] [Doctoral dissertation]. Texas A&M University; 2018. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1969.1/173411.

Council of Science Editors:

Hinsdale TA. Enhanced Early Detection of Oral Squamous Cell Carcinoma via Structured Illumination Fluorescence Lifetime Imaging. [Doctoral Dissertation]. Texas A&M University; 2018. Available from: http://hdl.handle.net/1969.1/173411


Texas A&M University

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

Degree: MS, Electrical Engineering, 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. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/153669

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. Masters Thesis, Texas A&M University. Accessed November 26, 2020. http://hdl.handle.net/1969.1/153669.

MLA Handbook (7th Edition):

Lee, Joohyung. “Supervised Machine Learning Algorithms for Early Detection of Oral Epithelial Cancer Using Fluorescence Lifetime Imaging Microscopy.” 2014. Web. 26 Nov 2020.

Vancouver:

Lee J. Supervised Machine Learning Algorithms for Early Detection of Oral Epithelial Cancer Using Fluorescence Lifetime Imaging Microscopy. [Internet] [Masters thesis]. Texas A&M University; 2014. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1969.1/153669.

Council of Science Editors:

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


University of California – Irvine

4. Trinh, Andrew Long. Fluorescence and Phosphorescence Lifetime Imaging Microscopy for Spatial Mapping of Tumor Behavior.

Degree: Biomedical Engineering, 2018, University of California – Irvine

Fluorescence intensity measurements in cellular microscopy have become a valuable tool for resolving cellular structures and quantifying protein dynamics. Furthermore, the fluorescence lifetime can reveal… (more)

Subjects/Keywords: Biomedical engineering; Biophysics; Cellular biology; Cancer; Fluorescence; Fluorescence Lifetime Imaging; FRET; Microscopy; Oxygen Sensing

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APA (6th Edition):

Trinh, A. L. (2018). Fluorescence and Phosphorescence Lifetime Imaging Microscopy for Spatial Mapping of Tumor Behavior. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/64v3w28q

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):

Trinh, Andrew Long. “Fluorescence and Phosphorescence Lifetime Imaging Microscopy for Spatial Mapping of Tumor Behavior.” 2018. Thesis, University of California – Irvine. Accessed November 26, 2020. http://www.escholarship.org/uc/item/64v3w28q.

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

MLA Handbook (7th Edition):

Trinh, Andrew Long. “Fluorescence and Phosphorescence Lifetime Imaging Microscopy for Spatial Mapping of Tumor Behavior.” 2018. Web. 26 Nov 2020.

Vancouver:

Trinh AL. Fluorescence and Phosphorescence Lifetime Imaging Microscopy for Spatial Mapping of Tumor Behavior. [Internet] [Thesis]. University of California – Irvine; 2018. [cited 2020 Nov 26]. Available from: http://www.escholarship.org/uc/item/64v3w28q.

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

Council of Science Editors:

Trinh AL. Fluorescence and Phosphorescence Lifetime Imaging Microscopy for Spatial Mapping of Tumor Behavior. [Thesis]. University of California – Irvine; 2018. Available from: http://www.escholarship.org/uc/item/64v3w28q

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


University of Minnesota

5. Geppert, Sarah. Benzoxazole and Benzothiazole Derivatives as Potential Fluorescence Imaging Agents.

Degree: MS, Chemistry, 2019, University of Minnesota

 Abstract: Substituted Benzoxazole (1-hydroxy-2-naphthoic benzoxazole and 2-hydroxy- 3-naphthoic benzoxazole) and benzothiazole (1-hydroxy-2-naphthoic benzoxazole and 2- hydroxy-3-naphthoic benzothiazole) derivatives previously complexed with Boroncontaining fragments in our… (more)

Subjects/Keywords: Benzothiazole; Benzoxazole; Excited State Intermolecular Proton Transfer; Fluorescence; Fluorescence Lifetime Imaging Microscopy

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APA (6th Edition):

Geppert, S. (2019). Benzoxazole and Benzothiazole Derivatives as Potential Fluorescence Imaging Agents. (Masters Thesis). University of Minnesota. Retrieved from http://hdl.handle.net/11299/208926

Chicago Manual of Style (16th Edition):

Geppert, Sarah. “Benzoxazole and Benzothiazole Derivatives as Potential Fluorescence Imaging Agents.” 2019. Masters Thesis, University of Minnesota. Accessed November 26, 2020. http://hdl.handle.net/11299/208926.

MLA Handbook (7th Edition):

Geppert, Sarah. “Benzoxazole and Benzothiazole Derivatives as Potential Fluorescence Imaging Agents.” 2019. Web. 26 Nov 2020.

Vancouver:

Geppert S. Benzoxazole and Benzothiazole Derivatives as Potential Fluorescence Imaging Agents. [Internet] [Masters thesis]. University of Minnesota; 2019. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/11299/208926.

Council of Science Editors:

Geppert S. Benzoxazole and Benzothiazole Derivatives as Potential Fluorescence Imaging Agents. [Masters Thesis]. University of Minnesota; 2019. Available from: http://hdl.handle.net/11299/208926


Vanderbilt University

6. Sharick, Joseph Thomas. Fluorescence Lifetime Imaging of NAD(P)H Distinguishes Pathways of Metabolic Inhibition.

Degree: MS, Biomedical Engineering, 2016, Vanderbilt University

Fluorescence lifetime imaging microscopy (FLIM) of the metabolic co-enzyme nicotinamide adenine dinucleotide (NAD(P)H) non-invasively probes metabolic protein-binding dynamics without the need for exogenous dyes. FLIM… (more)

Subjects/Keywords: cancer; optical imaging; NAD(P)H; microscopy; fluorescence lifetime imaging; multiphoton; FAD; metabolism

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APA (6th Edition):

Sharick, J. T. (2016). Fluorescence Lifetime Imaging of NAD(P)H Distinguishes Pathways of Metabolic Inhibition. (Thesis). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/11627

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):

Sharick, Joseph Thomas. “Fluorescence Lifetime Imaging of NAD(P)H Distinguishes Pathways of Metabolic Inhibition.” 2016. Thesis, Vanderbilt University. Accessed November 26, 2020. http://hdl.handle.net/1803/11627.

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

MLA Handbook (7th Edition):

Sharick, Joseph Thomas. “Fluorescence Lifetime Imaging of NAD(P)H Distinguishes Pathways of Metabolic Inhibition.” 2016. Web. 26 Nov 2020.

Vancouver:

Sharick JT. Fluorescence Lifetime Imaging of NAD(P)H Distinguishes Pathways of Metabolic Inhibition. [Internet] [Thesis]. Vanderbilt University; 2016. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1803/11627.

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

Council of Science Editors:

Sharick JT. Fluorescence Lifetime Imaging of NAD(P)H Distinguishes Pathways of Metabolic Inhibition. [Thesis]. Vanderbilt University; 2016. Available from: http://hdl.handle.net/1803/11627

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


Texas A&M University

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

Degree: PhD, Biomedical Engineering, 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. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/155617

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. Doctoral Dissertation, Texas A&M University. Accessed November 26, 2020. http://hdl.handle.net/1969.1/155617.

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. 26 Nov 2020.

Vancouver:

Shrestha S. Development of Dual-Modality Optical Imaging Systems Consisting of Optical Coherence Tomography and Fluorescence Lifetime Imaging Microscopy. [Internet] [Doctoral dissertation]. Texas A&M University; 2015. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1969.1/155617.

Council of Science Editors:

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

8. 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 November 26, 2020. 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. 26 Nov 2020.

Vancouver:

Burton MG. Imaging the interactions of antimicrobial peptides with model and living cellular membrane systems. [Internet] [Doctoral dissertation]. University of Melbourne; 2016. [cited 2020 Nov 26]. 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


Texas A&M University

9. Hwang, Dae Yon. Detection of In vivo Oral Epithelial Cancer using Fluorescence Lifetime Imaging.

Degree: MS, Electrical Engineering, 2016, Texas A&M University

 Endogenous fluorescence lifetime imaging microscopy (FLIM) provides a nondestructive means to interrogate the biochemical composition of biological tissues. Therefore, it has the potential to identify… (more)

Subjects/Keywords: endogenous fluorescence lifetime imaging microscopy; FLIM; oral cancer; classification; LDA; KNN; SVM

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APA (6th Edition):

Hwang, D. Y. (2016). Detection of In vivo Oral Epithelial Cancer using Fluorescence Lifetime Imaging. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/187406

Chicago Manual of Style (16th Edition):

Hwang, Dae Yon. “Detection of In vivo Oral Epithelial Cancer using Fluorescence Lifetime Imaging.” 2016. Masters Thesis, Texas A&M University. Accessed November 26, 2020. http://hdl.handle.net/1969.1/187406.

MLA Handbook (7th Edition):

Hwang, Dae Yon. “Detection of In vivo Oral Epithelial Cancer using Fluorescence Lifetime Imaging.” 2016. Web. 26 Nov 2020.

Vancouver:

Hwang DY. Detection of In vivo Oral Epithelial Cancer using Fluorescence Lifetime Imaging. [Internet] [Masters thesis]. Texas A&M University; 2016. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1969.1/187406.

Council of Science Editors:

Hwang DY. Detection of In vivo Oral Epithelial Cancer using Fluorescence Lifetime Imaging. [Masters Thesis]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/187406


Texas A&M University

10. Hwang, Dae Yon. Detection of In vivo Oral Epithelial Cancer using Fluorescence Lifetime Imaging.

Degree: MS, Electrical Engineering, 2016, Texas A&M University

 Endogenous fluorescence lifetime imaging microscopy (FLIM) provides a nondestructive means to interrogate the biochemical composition of biological tissues. Therefore, it has the potential to identify… (more)

Subjects/Keywords: endogenous fluorescence lifetime imaging microscopy; FLIM; oral cancer; classification; LDA; KNN; SVM

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

APA (6th Edition):

Hwang, D. Y. (2016). Detection of In vivo Oral Epithelial Cancer using Fluorescence Lifetime Imaging. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/187405

Chicago Manual of Style (16th Edition):

Hwang, Dae Yon. “Detection of In vivo Oral Epithelial Cancer using Fluorescence Lifetime Imaging.” 2016. Masters Thesis, Texas A&M University. Accessed November 26, 2020. http://hdl.handle.net/1969.1/187405.

MLA Handbook (7th Edition):

Hwang, Dae Yon. “Detection of In vivo Oral Epithelial Cancer using Fluorescence Lifetime Imaging.” 2016. Web. 26 Nov 2020.

Vancouver:

Hwang DY. Detection of In vivo Oral Epithelial Cancer using Fluorescence Lifetime Imaging. [Internet] [Masters thesis]. Texas A&M University; 2016. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1969.1/187405.

Council of Science Editors:

Hwang DY. Detection of In vivo Oral Epithelial Cancer using Fluorescence Lifetime Imaging. [Masters Thesis]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/187405


University of Cambridge

11. Collins, Súil. The identification and development of small molecule inhibitors of amyloid β aggregation.

Degree: PhD, 2017, University of Cambridge

 Amyloid β (1-42) (Aβ42) is a seminal neuropathic agent in Alzheimer’s disease (AD), a multifaceted neurodegenerative disorder for which no preventative measures or disease modifying… (more)

Subjects/Keywords: 612.8; amyloid beta; aggregation inhibitiors; protein aggregation; fluorescence lifetime imaging microscopy; microfluidic screening; drug screening

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APA (6th Edition):

Collins, S. (2017). The identification and development of small molecule inhibitors of amyloid β aggregation. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.23088 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.745047

Chicago Manual of Style (16th Edition):

Collins, Súil. “The identification and development of small molecule inhibitors of amyloid β aggregation.” 2017. Doctoral Dissertation, University of Cambridge. Accessed November 26, 2020. https://doi.org/10.17863/CAM.23088 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.745047.

MLA Handbook (7th Edition):

Collins, Súil. “The identification and development of small molecule inhibitors of amyloid β aggregation.” 2017. Web. 26 Nov 2020.

Vancouver:

Collins S. The identification and development of small molecule inhibitors of amyloid β aggregation. [Internet] [Doctoral dissertation]. University of Cambridge; 2017. [cited 2020 Nov 26]. Available from: https://doi.org/10.17863/CAM.23088 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.745047.

Council of Science Editors:

Collins S. The identification and development of small molecule inhibitors of amyloid β aggregation. [Doctoral Dissertation]. University of Cambridge; 2017. Available from: https://doi.org/10.17863/CAM.23088 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.745047


University of Melbourne

12. Soleimaninejad, Hamid. Time-resolved and polarised fluorescence studies of polymeric and biological systems.

Degree: 2018, University of Melbourne

 Understanding the dynamics of energy migration for disordered complex systems such as polymeric solar cells is crucial for optimizing the charge transport process and obtaining… (more)

Subjects/Keywords: energy migration; polymeric solar cells; Fluorescence anisotropy; fluorescence depolarisation; fluorescence anisotropy imaging microscopy; fluorescence lifetime imaging; conjugated polymers; total internal reflection fluorescence anisotropy measurements

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APA (6th Edition):

Soleimaninejad, H. (2018). Time-resolved and polarised fluorescence studies of polymeric and biological systems. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/214485

Chicago Manual of Style (16th Edition):

Soleimaninejad, Hamid. “Time-resolved and polarised fluorescence studies of polymeric and biological systems.” 2018. Doctoral Dissertation, University of Melbourne. Accessed November 26, 2020. http://hdl.handle.net/11343/214485.

MLA Handbook (7th Edition):

Soleimaninejad, Hamid. “Time-resolved and polarised fluorescence studies of polymeric and biological systems.” 2018. Web. 26 Nov 2020.

Vancouver:

Soleimaninejad H. Time-resolved and polarised fluorescence studies of polymeric and biological systems. [Internet] [Doctoral dissertation]. University of Melbourne; 2018. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/11343/214485.

Council of Science Editors:

Soleimaninejad H. Time-resolved and polarised fluorescence studies of polymeric and biological systems. [Doctoral Dissertation]. University of Melbourne; 2018. Available from: http://hdl.handle.net/11343/214485

13. 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

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 : 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 November 26, 2020. 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. 26 Nov 2020.

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 2020 Nov 26]. 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

14. 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 November 26, 2020. 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. 26 Nov 2020.

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 2020 Nov 26]. 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


University of Notre Dame

15. Yide Zhang. Super-Sensitivity and Super-Resolution Quantitative Multiphoton Microscopy</h1>.

Degree: Electrical Engineering, 2019, University of Notre Dame

  Multiphoton microscopy (MPM) combined with frequency-domain fluorescence lifetime imaging microscopy (FD-FLIM) has enabled three-dimensional quantitative molecular microscopy in vivo. The integrated MPM-FD-FLIM imaging system… (more)

Subjects/Keywords: Multiphoton microscopy; Super-resolution; Stepwise optical saturation; Fluorescence lifetime imaging microscopy; Fluorescence microscopy; Deep learning; Signal-to-noise ratio; K-means clustering; Denoising; Super-sensitivity

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APA (6th Edition):

Zhang, Y. (2019). Super-Sensitivity and Super-Resolution Quantitative Multiphoton Microscopy</h1>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/0k225b02b9b

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, Yide. “Super-Sensitivity and Super-Resolution Quantitative Multiphoton Microscopy</h1>.” 2019. Thesis, University of Notre Dame. Accessed November 26, 2020. https://curate.nd.edu/show/0k225b02b9b.

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

MLA Handbook (7th Edition):

Zhang, Yide. “Super-Sensitivity and Super-Resolution Quantitative Multiphoton Microscopy</h1>.” 2019. Web. 26 Nov 2020.

Vancouver:

Zhang Y. Super-Sensitivity and Super-Resolution Quantitative Multiphoton Microscopy</h1>. [Internet] [Thesis]. University of Notre Dame; 2019. [cited 2020 Nov 26]. Available from: https://curate.nd.edu/show/0k225b02b9b.

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

Council of Science Editors:

Zhang Y. Super-Sensitivity and Super-Resolution Quantitative Multiphoton Microscopy</h1>. [Thesis]. University of Notre Dame; 2019. Available from: https://curate.nd.edu/show/0k225b02b9b

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


University of Michigan

16. 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 November 26, 2020. 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. 26 Nov 2020.

Vancouver:

Chen L. Label-Free Optical Imaging and Quantitative Algorithms to Assess Living Biological Systems. [Internet] [Doctoral dissertation]. University of Michigan; 2014. [cited 2020 Nov 26]. 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 California – Irvine

17. Murata, Michael. Analyses of the Cellular Signaling Responses to DNA Damage and DNA Repair Factor Recruitment Using Fluorescence Lifetimes and Fluctuations.

Degree: Biomedical Engineering, 2018, University of California – Irvine

 Genome integrity is continually challenged by threats including DNA replication errors, toxic metabolic byproducts, and exposure to exogenous genotoxins. Responding to and repairing damaged DNA… (more)

Subjects/Keywords: Biomedical engineering; Biophysics; Cellular biology; Cellular metabolism; DNA damage; Fluorescence lifetime imaging microscopy; Microirradiation; Pair correlation function analysis

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APA (6th Edition):

Murata, M. (2018). Analyses of the Cellular Signaling Responses to DNA Damage and DNA Repair Factor Recruitment Using Fluorescence Lifetimes and Fluctuations. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/6f23d2j6

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):

Murata, Michael. “Analyses of the Cellular Signaling Responses to DNA Damage and DNA Repair Factor Recruitment Using Fluorescence Lifetimes and Fluctuations.” 2018. Thesis, University of California – Irvine. Accessed November 26, 2020. http://www.escholarship.org/uc/item/6f23d2j6.

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

MLA Handbook (7th Edition):

Murata, Michael. “Analyses of the Cellular Signaling Responses to DNA Damage and DNA Repair Factor Recruitment Using Fluorescence Lifetimes and Fluctuations.” 2018. Web. 26 Nov 2020.

Vancouver:

Murata M. Analyses of the Cellular Signaling Responses to DNA Damage and DNA Repair Factor Recruitment Using Fluorescence Lifetimes and Fluctuations. [Internet] [Thesis]. University of California – Irvine; 2018. [cited 2020 Nov 26]. Available from: http://www.escholarship.org/uc/item/6f23d2j6.

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

Council of Science Editors:

Murata M. Analyses of the Cellular Signaling Responses to DNA Damage and DNA Repair Factor Recruitment Using Fluorescence Lifetimes and Fluctuations. [Thesis]. University of California – Irvine; 2018. Available from: http://www.escholarship.org/uc/item/6f23d2j6

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


Texas A&M University

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

Degree: MS, Biomedical Engineering, 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 (6th Edition):

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

Chicago Manual of Style (16th Edition):

Thomas, Patrick A. “Detection of Atherosclerotic Coronary Plaques by Fluorescence Lifetime Imaging Angioscopy.” 2010. Masters Thesis, Texas A&M University. Accessed November 26, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8299.

MLA Handbook (7th Edition):

Thomas, Patrick A. “Detection of Atherosclerotic Coronary Plaques by Fluorescence Lifetime Imaging Angioscopy.” 2010. Web. 26 Nov 2020.

Vancouver:

Thomas PA. Detection of Atherosclerotic Coronary Plaques by Fluorescence Lifetime Imaging Angioscopy. [Internet] [Masters thesis]. Texas A&M University; 2010. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8299.

Council of Science Editors:

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


University of California – Irvine

19. Li, Xuan. Microfluidic Single-Cell Analysis from Phenotype to Genotype.

Degree: Biomedical Engineering, 2019, University of California – Irvine

 Single-cell analysis is of critical importance in revealing population heterogeneity, identifying minority sub-populations of interest, as well as discovering unique characteristics of individual cells. Conventional… (more)

Subjects/Keywords: Biomedical engineering; Cell-Cell Interaction; Dielectrophoretic Nanotweezers; Fluorescence Lifetime Imaging Microscopy; Microfluidics; Single-Cell Analysis; Transfection

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APA (6th Edition):

Li, X. (2019). Microfluidic Single-Cell Analysis from Phenotype to Genotype. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/4x14p4mb

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, Xuan. “Microfluidic Single-Cell Analysis from Phenotype to Genotype.” 2019. Thesis, University of California – Irvine. Accessed November 26, 2020. http://www.escholarship.org/uc/item/4x14p4mb.

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

MLA Handbook (7th Edition):

Li, Xuan. “Microfluidic Single-Cell Analysis from Phenotype to Genotype.” 2019. Web. 26 Nov 2020.

Vancouver:

Li X. Microfluidic Single-Cell Analysis from Phenotype to Genotype. [Internet] [Thesis]. University of California – Irvine; 2019. [cited 2020 Nov 26]. Available from: http://www.escholarship.org/uc/item/4x14p4mb.

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

Council of Science Editors:

Li X. Microfluidic Single-Cell Analysis from Phenotype to Genotype. [Thesis]. University of California – Irvine; 2019. Available from: http://www.escholarship.org/uc/item/4x14p4mb

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


University of California – Irvine

20. Ma, Ning. Assessment of Embryo Health and Circulating Tumor Cell Metabolism Using the Phasor-FLIM Approach.

Degree: Biomedical Engineering, 2019, University of California – Irvine

 Cellular functional and structural changes associated with metabolism are essential for understanding healthy tissue development and the progression of numerous diseases. Quantitatively monitoring of metabolic… (more)

Subjects/Keywords: Developmental biology; Biophysics; Oncology; Distance Algorithm; Fluorescence lifetime Imaging Microscopy; Human embryonic stem cells; Microfluidic systems; Phasor; Pre-implantation embryos

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APA (6th Edition):

Ma, N. (2019). Assessment of Embryo Health and Circulating Tumor Cell Metabolism Using the Phasor-FLIM Approach. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/6bv0234w

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):

Ma, Ning. “Assessment of Embryo Health and Circulating Tumor Cell Metabolism Using the Phasor-FLIM Approach.” 2019. Thesis, University of California – Irvine. Accessed November 26, 2020. http://www.escholarship.org/uc/item/6bv0234w.

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

MLA Handbook (7th Edition):

Ma, Ning. “Assessment of Embryo Health and Circulating Tumor Cell Metabolism Using the Phasor-FLIM Approach.” 2019. Web. 26 Nov 2020.

Vancouver:

Ma N. Assessment of Embryo Health and Circulating Tumor Cell Metabolism Using the Phasor-FLIM Approach. [Internet] [Thesis]. University of California – Irvine; 2019. [cited 2020 Nov 26]. Available from: http://www.escholarship.org/uc/item/6bv0234w.

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

Council of Science Editors:

Ma N. Assessment of Embryo Health and Circulating Tumor Cell Metabolism Using the Phasor-FLIM Approach. [Thesis]. University of California – Irvine; 2019. Available from: http://www.escholarship.org/uc/item/6bv0234w

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


University of Edinburgh

21. 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 November 26, 2020. 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. 26 Nov 2020.

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 2020 Nov 26]. 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


Delft University of Technology

22. Zhao, Q. Solid-State Camera System for Fluorescence Lifetime Microscopy.

Degree: 2014, Delft University of Technology

Fluorescence microscopy is a well-established platform for biology and biomedical research (Chapter 2). Based on this platform, fluorescence lifetime imaging microscopy (FLIM) has been developed… (more)

Subjects/Keywords: fluorescence lifetime imaging microscopy; camera; modulated; frequency-domain

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APA (6th Edition):

Zhao, Q. (2014). Solid-State Camera System for Fluorescence Lifetime Microscopy. (Doctoral Dissertation). Delft University of Technology. Retrieved from http://resolver.tudelft.nl/uuid:d6d0698c-8961-414e-9818-220ee08647e6 ; urn:NBN:nl:ui:24-uuid:d6d0698c-8961-414e-9818-220ee08647e6 ; urn:NBN:nl:ui:24-uuid:d6d0698c-8961-414e-9818-220ee08647e6 ; http://resolver.tudelft.nl/uuid:d6d0698c-8961-414e-9818-220ee08647e6

Chicago Manual of Style (16th Edition):

Zhao, Q. “Solid-State Camera System for Fluorescence Lifetime Microscopy.” 2014. Doctoral Dissertation, Delft University of Technology. Accessed November 26, 2020. http://resolver.tudelft.nl/uuid:d6d0698c-8961-414e-9818-220ee08647e6 ; urn:NBN:nl:ui:24-uuid:d6d0698c-8961-414e-9818-220ee08647e6 ; urn:NBN:nl:ui:24-uuid:d6d0698c-8961-414e-9818-220ee08647e6 ; http://resolver.tudelft.nl/uuid:d6d0698c-8961-414e-9818-220ee08647e6.

MLA Handbook (7th Edition):

Zhao, Q. “Solid-State Camera System for Fluorescence Lifetime Microscopy.” 2014. Web. 26 Nov 2020.

Vancouver:

Zhao Q. Solid-State Camera System for Fluorescence Lifetime Microscopy. [Internet] [Doctoral dissertation]. Delft University of Technology; 2014. [cited 2020 Nov 26]. Available from: http://resolver.tudelft.nl/uuid:d6d0698c-8961-414e-9818-220ee08647e6 ; urn:NBN:nl:ui:24-uuid:d6d0698c-8961-414e-9818-220ee08647e6 ; urn:NBN:nl:ui:24-uuid:d6d0698c-8961-414e-9818-220ee08647e6 ; http://resolver.tudelft.nl/uuid:d6d0698c-8961-414e-9818-220ee08647e6.

Council of Science Editors:

Zhao Q. Solid-State Camera System for Fluorescence Lifetime Microscopy. [Doctoral Dissertation]. Delft University of Technology; 2014. Available from: http://resolver.tudelft.nl/uuid:d6d0698c-8961-414e-9818-220ee08647e6 ; urn:NBN:nl:ui:24-uuid:d6d0698c-8961-414e-9818-220ee08647e6 ; urn:NBN:nl:ui:24-uuid:d6d0698c-8961-414e-9818-220ee08647e6 ; http://resolver.tudelft.nl/uuid:d6d0698c-8961-414e-9818-220ee08647e6


University of Cambridge

23. Woodhams, Philippa. Graphene microelectrode arrays to combine electrophysiology with fluorescence imaging of amyloid proteins.

Degree: PhD, 2020, University of Cambridge

 Alzheimer's disease (AD) and Parkinson's diseases (PD) are neurodegenerative diseases that affect ~ 60 million people worldwide. Both diseases are linked to the misfolding of… (more)

Subjects/Keywords: Graphene; Microelectrode array; electrophysiology; amyloid; Parkinson's disease; electrochemical impedance spectroscopy; alpha synuclein; Fourier transform infrared spectroscopy; equivalent circuit model; PMMA; neuron; neuroscience; impedance; fluorescence lifetime imaging microscopy; fluorescence imaging

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APA (6th Edition):

Woodhams, P. (2020). Graphene microelectrode arrays to combine electrophysiology with fluorescence imaging of amyloid proteins. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.48700 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.801703

Chicago Manual of Style (16th Edition):

Woodhams, Philippa. “Graphene microelectrode arrays to combine electrophysiology with fluorescence imaging of amyloid proteins.” 2020. Doctoral Dissertation, University of Cambridge. Accessed November 26, 2020. https://doi.org/10.17863/CAM.48700 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.801703.

MLA Handbook (7th Edition):

Woodhams, Philippa. “Graphene microelectrode arrays to combine electrophysiology with fluorescence imaging of amyloid proteins.” 2020. Web. 26 Nov 2020.

Vancouver:

Woodhams P. Graphene microelectrode arrays to combine electrophysiology with fluorescence imaging of amyloid proteins. [Internet] [Doctoral dissertation]. University of Cambridge; 2020. [cited 2020 Nov 26]. Available from: https://doi.org/10.17863/CAM.48700 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.801703.

Council of Science Editors:

Woodhams P. Graphene microelectrode arrays to combine electrophysiology with fluorescence imaging of amyloid proteins. [Doctoral Dissertation]. University of Cambridge; 2020. Available from: https://doi.org/10.17863/CAM.48700 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.801703


University of Cambridge

24. Woodhams, Philippa. Graphene Microelectrode Arrays to Combine Electrophysiology with Fluorescence Imaging of Amyloid Proteins.

Degree: PhD, 2020, University of Cambridge

 Alzheimer's disease (AD) and Parkinson's diseases (PD) are neurodegenerative diseases that affect ∼60\,million people worldwide. Both diseases are linked to the misfolding of proteins from… (more)

Subjects/Keywords: Graphene; Microelectrode array; electrophysiology; amyloid; Parkinson's disease; electrochemical impedance spectroscopy; alpha synuclein; Fourier transform infrared spectroscopy; equivalent circuit model; PMMA; neuron; neuroscience; impedance; fluorescence lifetime imaging microscopy; fluorescence imaging

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APA (6th Edition):

Woodhams, P. (2020). Graphene Microelectrode Arrays to Combine Electrophysiology with Fluorescence Imaging of Amyloid Proteins. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/301630

Chicago Manual of Style (16th Edition):

Woodhams, Philippa. “Graphene Microelectrode Arrays to Combine Electrophysiology with Fluorescence Imaging of Amyloid Proteins.” 2020. Doctoral Dissertation, University of Cambridge. Accessed November 26, 2020. https://www.repository.cam.ac.uk/handle/1810/301630.

MLA Handbook (7th Edition):

Woodhams, Philippa. “Graphene Microelectrode Arrays to Combine Electrophysiology with Fluorescence Imaging of Amyloid Proteins.” 2020. Web. 26 Nov 2020.

Vancouver:

Woodhams P. Graphene Microelectrode Arrays to Combine Electrophysiology with Fluorescence Imaging of Amyloid Proteins. [Internet] [Doctoral dissertation]. University of Cambridge; 2020. [cited 2020 Nov 26]. Available from: https://www.repository.cam.ac.uk/handle/1810/301630.

Council of Science Editors:

Woodhams P. Graphene Microelectrode Arrays to Combine Electrophysiology with Fluorescence Imaging of Amyloid Proteins. [Doctoral Dissertation]. University of Cambridge; 2020. Available from: https://www.repository.cam.ac.uk/handle/1810/301630


University of Utah

25. 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 November 26, 2020. 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. 26 Nov 2020.

Vancouver:

Cooper JT. Single-molecule fluorescence microscopy of molecular interactions at reversed-phase chromatographic interfaces. [Internet] [Doctoral dissertation]. University of Utah; 2014. [cited 2020 Nov 26]. 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


Georgia State University

26. Goolsby, Demesheka. Optical Property Enhancement And Characterization Of Fluorescent Protein Based Intracellular Calcium Probes.

Degree: MS, Chemistry, 2016, Georgia State University

  Calcium (Ca2+), a crucial effector for many biological systems, has been associated with diseases such as cardiovascular disease, Alzheimer’s, Parkinson’s, cancer, and osteoporosis. It… (more)

Subjects/Keywords: Fluorescence; mCherry; EGFP; Calcium imaging; Fluorescence spectroscopy; Fluorescence lifetime

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APA (6th Edition):

Goolsby, D. (2016). Optical Property Enhancement And Characterization Of Fluorescent Protein Based Intracellular Calcium Probes. (Thesis). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_theses/91

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):

Goolsby, Demesheka. “Optical Property Enhancement And Characterization Of Fluorescent Protein Based Intracellular Calcium Probes.” 2016. Thesis, Georgia State University. Accessed November 26, 2020. https://scholarworks.gsu.edu/chemistry_theses/91.

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

MLA Handbook (7th Edition):

Goolsby, Demesheka. “Optical Property Enhancement And Characterization Of Fluorescent Protein Based Intracellular Calcium Probes.” 2016. Web. 26 Nov 2020.

Vancouver:

Goolsby D. Optical Property Enhancement And Characterization Of Fluorescent Protein Based Intracellular Calcium Probes. [Internet] [Thesis]. Georgia State University; 2016. [cited 2020 Nov 26]. Available from: https://scholarworks.gsu.edu/chemistry_theses/91.

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

Council of Science Editors:

Goolsby D. Optical Property Enhancement And Characterization Of Fluorescent Protein Based Intracellular Calcium Probes. [Thesis]. Georgia State University; 2016. Available from: https://scholarworks.gsu.edu/chemistry_theses/91

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


University of Edinburgh

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

Degree: PhD, 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 · Chicago · MLA · Vancouver · CSE | Export to Zotero / EndNote / Reference Manager

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 November 26, 2020. 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. 26 Nov 2020.

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 2020 Nov 26]. 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

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

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 November 26, 2020. 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. 26 Nov 2020.

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 2020 Nov 26]. 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


Texas A&M University

29. Rico Jimenez, Jose de Jesus. Computational Tools for Image Processing, Integration, and Visualization of Simultaneous OCT-FLIM Images of Tissue.

Degree: PhD, Biomedical Engineering, 2016, Texas A&M University

 Multimodal imaging systems have emerged as robust methods for the characterization of atherosclerotic plaques and early diagnosis of oral cancer. Multispectral wide-field Fluorescence Lifetime Imaging(more)

Subjects/Keywords: Fluorescence Lifetime Imaging Microscopy; Optical coherence tomography; Atherosclerosis; oral cancer; macrophage density; Tissue characterization; Medical and biological imaging; Image analysis; Pattern recognition; Visualization

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

APA (6th Edition):

Rico Jimenez, J. d. J. (2016). Computational Tools for Image Processing, Integration, and Visualization of Simultaneous OCT-FLIM Images of Tissue. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/187323

Chicago Manual of Style (16th Edition):

Rico Jimenez, Jose de Jesus. “Computational Tools for Image Processing, Integration, and Visualization of Simultaneous OCT-FLIM Images of Tissue.” 2016. Doctoral Dissertation, Texas A&M University. Accessed November 26, 2020. http://hdl.handle.net/1969.1/187323.

MLA Handbook (7th Edition):

Rico Jimenez, Jose de Jesus. “Computational Tools for Image Processing, Integration, and Visualization of Simultaneous OCT-FLIM Images of Tissue.” 2016. Web. 26 Nov 2020.

Vancouver:

Rico Jimenez JdJ. Computational Tools for Image Processing, Integration, and Visualization of Simultaneous OCT-FLIM Images of Tissue. [Internet] [Doctoral dissertation]. Texas A&M University; 2016. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1969.1/187323.

Council of Science Editors:

Rico Jimenez JdJ. Computational Tools for Image Processing, Integration, and Visualization of Simultaneous OCT-FLIM Images of Tissue. [Doctoral Dissertation]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/187323


University of Cambridge

30. Sims, Ruth Rebecca. Volumetric Imaging Across Spatiotemporal Scales in Biology with Fluorescence Microscopy.

Degree: PhD, 2019, University of Cambridge

 Quantitative three dimensional maps of cellular structure, activity and function provide the key to answering many prevalent questions in modern biological research. Fluorescence microscopy has… (more)

Subjects/Keywords: Fluorescence microscopy; Computational imaging; Volumetric imaging

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

APA (6th Edition):

Sims, R. R. (2019). Volumetric Imaging Across Spatiotemporal Scales in Biology with Fluorescence Microscopy. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/289719

Chicago Manual of Style (16th Edition):

Sims, Ruth Rebecca. “Volumetric Imaging Across Spatiotemporal Scales in Biology with Fluorescence Microscopy.” 2019. Doctoral Dissertation, University of Cambridge. Accessed November 26, 2020. https://www.repository.cam.ac.uk/handle/1810/289719.

MLA Handbook (7th Edition):

Sims, Ruth Rebecca. “Volumetric Imaging Across Spatiotemporal Scales in Biology with Fluorescence Microscopy.” 2019. Web. 26 Nov 2020.

Vancouver:

Sims RR. Volumetric Imaging Across Spatiotemporal Scales in Biology with Fluorescence Microscopy. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2020 Nov 26]. Available from: https://www.repository.cam.ac.uk/handle/1810/289719.

Council of Science Editors:

Sims RR. Volumetric Imaging Across Spatiotemporal Scales in Biology with Fluorescence Microscopy. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/289719

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