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You searched for subject:(MICROSCOPY FLUORESCENCE methods). Showing records 1 – 11 of 11 total matches.

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University of Oklahoma

1. Zhou, Yongyao. MOBILITY STUDY OF PROTEIN AND DYE MOLECULES WITHIN SILICA HYDROGEL, LIPOSOMES, AND BACTERIA CELLS BY FLUORESCENCE MICROSCOPY.

Degree: PhD, 2010, University of Oklahoma

Fluorescence techniques are very useful for understanding the various processes in biological science. This thesis presents the applications of several fluorescence techniques for studying the… (more)

Subjects/Keywords: Fluorescence microscopy – Methods

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

APA (6th Edition):

Zhou, Y. (2010). MOBILITY STUDY OF PROTEIN AND DYE MOLECULES WITHIN SILICA HYDROGEL, LIPOSOMES, AND BACTERIA CELLS BY FLUORESCENCE MICROSCOPY. (Doctoral Dissertation). University of Oklahoma. Retrieved from http://hdl.handle.net/11244/318648

Chicago Manual of Style (16th Edition):

Zhou, Yongyao. “MOBILITY STUDY OF PROTEIN AND DYE MOLECULES WITHIN SILICA HYDROGEL, LIPOSOMES, AND BACTERIA CELLS BY FLUORESCENCE MICROSCOPY.” 2010. Doctoral Dissertation, University of Oklahoma. Accessed October 27, 2020. http://hdl.handle.net/11244/318648.

MLA Handbook (7th Edition):

Zhou, Yongyao. “MOBILITY STUDY OF PROTEIN AND DYE MOLECULES WITHIN SILICA HYDROGEL, LIPOSOMES, AND BACTERIA CELLS BY FLUORESCENCE MICROSCOPY.” 2010. Web. 27 Oct 2020.

Vancouver:

Zhou Y. MOBILITY STUDY OF PROTEIN AND DYE MOLECULES WITHIN SILICA HYDROGEL, LIPOSOMES, AND BACTERIA CELLS BY FLUORESCENCE MICROSCOPY. [Internet] [Doctoral dissertation]. University of Oklahoma; 2010. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/11244/318648.

Council of Science Editors:

Zhou Y. MOBILITY STUDY OF PROTEIN AND DYE MOLECULES WITHIN SILICA HYDROGEL, LIPOSOMES, AND BACTERIA CELLS BY FLUORESCENCE MICROSCOPY. [Doctoral Dissertation]. University of Oklahoma; 2010. Available from: http://hdl.handle.net/11244/318648


University of Utah

2. Watanabe, Shigeki. Synaptic vesicle cycle at nano-resolution.

Degree: PhD, Biology, 2013, University of Utah

 Electron microscopy can visualize synapses at nanometer resolution, andcan thereby capture the fine structure of these contacts. However, this imagingmethod lacks three key elements: temporal… (more)

Subjects/Keywords: advanced microscopy methods; correlative microscopy; neurotransmission; super-resolution fluorescence microscopy; synaptic vesicle cycle; time-resolved electron microscopy

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APA (6th Edition):

Watanabe, S. (2013). Synaptic vesicle cycle at nano-resolution. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2314/rec/2330

Chicago Manual of Style (16th Edition):

Watanabe, Shigeki. “Synaptic vesicle cycle at nano-resolution.” 2013. Doctoral Dissertation, University of Utah. Accessed October 27, 2020. http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2314/rec/2330.

MLA Handbook (7th Edition):

Watanabe, Shigeki. “Synaptic vesicle cycle at nano-resolution.” 2013. Web. 27 Oct 2020.

Vancouver:

Watanabe S. Synaptic vesicle cycle at nano-resolution. [Internet] [Doctoral dissertation]. University of Utah; 2013. [cited 2020 Oct 27]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2314/rec/2330.

Council of Science Editors:

Watanabe S. Synaptic vesicle cycle at nano-resolution. [Doctoral Dissertation]. University of Utah; 2013. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/2314/rec/2330

3. Rombouts, Koen. Fluorescent labeling of DNA : strategies, pitfalls and necessity for fluorescence microscopy investigations of gene therapy.

Degree: 2016, Ghent University

 Gene therapy is a field of research in which a huge amount of effort has been spent over the last two decades. To succeed, a… (more)

Subjects/Keywords: Biology and Life Sciences; Fluorescence microscopy methods; DNA labeling; Gene therapy

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APA (6th Edition):

Rombouts, K. (2016). Fluorescent labeling of DNA : strategies, pitfalls and necessity for fluorescence microscopy investigations of gene therapy. (Thesis). Ghent University. Retrieved from http://hdl.handle.net/1854/LU-7246373

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):

Rombouts, Koen. “Fluorescent labeling of DNA : strategies, pitfalls and necessity for fluorescence microscopy investigations of gene therapy.” 2016. Thesis, Ghent University. Accessed October 27, 2020. http://hdl.handle.net/1854/LU-7246373.

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

MLA Handbook (7th Edition):

Rombouts, Koen. “Fluorescent labeling of DNA : strategies, pitfalls and necessity for fluorescence microscopy investigations of gene therapy.” 2016. Web. 27 Oct 2020.

Vancouver:

Rombouts K. Fluorescent labeling of DNA : strategies, pitfalls and necessity for fluorescence microscopy investigations of gene therapy. [Internet] [Thesis]. Ghent University; 2016. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/1854/LU-7246373.

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

Council of Science Editors:

Rombouts K. Fluorescent labeling of DNA : strategies, pitfalls and necessity for fluorescence microscopy investigations of gene therapy. [Thesis]. Ghent University; 2016. Available from: http://hdl.handle.net/1854/LU-7246373

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

4. Wang, Ziwei. Developing methods to detect nascent transcripts in single molecule fluorescence experiments.

Degree: 2017, Brandeis University

 Two new methods of detecting nascent transcripts in vitro in single molecule fluorescence experiments were developed in this study. The first method is to utilize… (more)

Subjects/Keywords: Microscopy; Fluorescence models; Methods; Transcription; Protein binding; Oligonucleotide probes

…the GFP fluorescence using wide-field microscopy. Here I applied the PP7 protein-PP7 target… …approach in whole cell extract, a significant portion of the oligo fluorescence signal… …efficiently. Here I applied two methods to detect transcripts with different mechanisms from the… …complementary oligo approach. The long-term goal of developing these new methods is to apply them in… …constructed PP7 target hairpin encoding transcription templates for single molecule fluorescence… 

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APA (6th Edition):

Wang, Z. (2017). Developing methods to detect nascent transcripts in single molecule fluorescence experiments. (Thesis). Brandeis University. Retrieved from http://hdl.handle.net/10192/33913

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

Chicago Manual of Style (16th Edition):

Wang, Ziwei. “Developing methods to detect nascent transcripts in single molecule fluorescence experiments.” 2017. Thesis, Brandeis University. Accessed October 27, 2020. http://hdl.handle.net/10192/33913.

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

MLA Handbook (7th Edition):

Wang, Ziwei. “Developing methods to detect nascent transcripts in single molecule fluorescence experiments.” 2017. Web. 27 Oct 2020.

Vancouver:

Wang Z. Developing methods to detect nascent transcripts in single molecule fluorescence experiments. [Internet] [Thesis]. Brandeis University; 2017. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10192/33913.

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

Council of Science Editors:

Wang Z. Developing methods to detect nascent transcripts in single molecule fluorescence experiments. [Thesis]. Brandeis University; 2017. Available from: http://hdl.handle.net/10192/33913

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


Penn State University

5. Hughes, John. Likelihood Inference for Particle Location in Fluorescence Microscopy .

Degree: 2009, Penn State University

 We introduce a procedure to automatically count and locate the fuorescent particles in a microscopy image. Our procedure employs an approximate likelihood estimator derived from… (more)

Subjects/Keywords: organelle; particle tracking; fluorescence microscopy; Poisson random field; maximum likelihood methods; molecular motor; nanotechnology

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APA (6th Edition):

Hughes, J. (2009). Likelihood Inference for Particle Location in Fluorescence Microscopy . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/9320

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):

Hughes, John. “Likelihood Inference for Particle Location in Fluorescence Microscopy .” 2009. Thesis, Penn State University. Accessed October 27, 2020. https://submit-etda.libraries.psu.edu/catalog/9320.

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

MLA Handbook (7th Edition):

Hughes, John. “Likelihood Inference for Particle Location in Fluorescence Microscopy .” 2009. Web. 27 Oct 2020.

Vancouver:

Hughes J. Likelihood Inference for Particle Location in Fluorescence Microscopy . [Internet] [Thesis]. Penn State University; 2009. [cited 2020 Oct 27]. Available from: https://submit-etda.libraries.psu.edu/catalog/9320.

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

Council of Science Editors:

Hughes J. Likelihood Inference for Particle Location in Fluorescence Microscopy . [Thesis]. Penn State University; 2009. Available from: https://submit-etda.libraries.psu.edu/catalog/9320

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

6. Ambrósio Júnior, Renato. "Estudo laboratorial da cicatrização de córneas humanas após debridamento epitelial".

Degree: PhD, Oftalmologia, 2004, University of São Paulo

Objetivo: Verificar resposta após debridamento epitelial de córneas humanas. Métodos: Córneas normais foram submetidas a debridamento antes da cirurgia de enucleação. Realizou-se histologia, TUNEL, Ki67,… (more)

Subjects/Keywords: APOPTOSE; APOPTOSIS; CORNEAL STROMA/anatomy & histology; CORNEAL STROMA/cytology; CORNEAL STROMA/physiology; EPITÉLIO DA CÓRNEA/anatomia & histologia; EPITÉLIO DA CÓRNEA/cirurgia; EPITÉLIO DA CÓRNEA/crescimento & desenvolvimento; EPITHELIUM CORNEAL/anatomy & histology; EPITHELIUM CORNEAL/growth & development; EPITHELIUM CORNEAL/surgery; ESTROMA CORNEAL/anatomia & histologia; ESTROMA CORNEAL/citologia; ESTROMA CORNEAL/fisiopatologia; IMMUNOHISTOCHEMISTRY/methods; IMUNOHISTOQUÍMICA/métodos; MICROSCOPIA CONFOCAL/métodos; MICROSCOPIA DE FLUORESCÊNCIA/métodos; MICROSCOPIA ELETRÔNICA/métodos; MICROSCOPY CONFOCAL/methods; MICROSCOPY ELECTRON/methods; MICROSCOPY FLUORESCENCE/methods; MITOSE/fisiologia; MITOSIS/physiology

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APA (6th Edition):

Ambrósio Júnior, R. (2004). "Estudo laboratorial da cicatrização de córneas humanas após debridamento epitelial". (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5149/tde-21102005-085247/ ;

Chicago Manual of Style (16th Edition):

Ambrósio Júnior, Renato. “"Estudo laboratorial da cicatrização de córneas humanas após debridamento epitelial".” 2004. Doctoral Dissertation, University of São Paulo. Accessed October 27, 2020. http://www.teses.usp.br/teses/disponiveis/5/5149/tde-21102005-085247/ ;.

MLA Handbook (7th Edition):

Ambrósio Júnior, Renato. “"Estudo laboratorial da cicatrização de córneas humanas após debridamento epitelial".” 2004. Web. 27 Oct 2020.

Vancouver:

Ambrósio Júnior R. "Estudo laboratorial da cicatrização de córneas humanas após debridamento epitelial". [Internet] [Doctoral dissertation]. University of São Paulo; 2004. [cited 2020 Oct 27]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5149/tde-21102005-085247/ ;.

Council of Science Editors:

Ambrósio Júnior R. "Estudo laboratorial da cicatrização de córneas humanas após debridamento epitelial". [Doctoral Dissertation]. University of São Paulo; 2004. Available from: http://www.teses.usp.br/teses/disponiveis/5/5149/tde-21102005-085247/ ;

7. Selig, Bettina. Image segmentation using snakes and stochastic watershed.

Degree: 2015, Swedish University of Agricultural Sciences

 The purpose of computerized image analysis is to extract meaningful information from digital images. To be able to find interesting regions or objects in the… (more)

Subjects/Keywords: image analysis; imagery; methods; eyes; cornea; reaction wood; structures; fluorescence; microscopy; image segmentation; snakes; active contours; stochastic watershed; minimal spanning tree; corneal endothelium; compression wood

methods SW, ESW, RSW and FRSW to a data set of fluorescence microscopy images of nuclei and… …Application: Fluorescence microscopy images of compression wood 35 4.1 Background 35 4.2… …microscopy images of compression wood Figure 15: Fluorescence microscope image of compression wood… …Selig developed the methods, designed and performed the experiments, and wrote the paper… …automatic evaluation of the corneal endothelium from in vivo confocal microscopy”, submitted for… 

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APA (6th Edition):

Selig, B. (2015). Image segmentation using snakes and stochastic watershed. (Doctoral Dissertation). Swedish University of Agricultural Sciences. Retrieved from https://pub.epsilon.slu.se/11891/

Chicago Manual of Style (16th Edition):

Selig, Bettina. “Image segmentation using snakes and stochastic watershed.” 2015. Doctoral Dissertation, Swedish University of Agricultural Sciences. Accessed October 27, 2020. https://pub.epsilon.slu.se/11891/.

MLA Handbook (7th Edition):

Selig, Bettina. “Image segmentation using snakes and stochastic watershed.” 2015. Web. 27 Oct 2020.

Vancouver:

Selig B. Image segmentation using snakes and stochastic watershed. [Internet] [Doctoral dissertation]. Swedish University of Agricultural Sciences; 2015. [cited 2020 Oct 27]. Available from: https://pub.epsilon.slu.se/11891/.

Council of Science Editors:

Selig B. Image segmentation using snakes and stochastic watershed. [Doctoral Dissertation]. Swedish University of Agricultural Sciences; 2015. Available from: https://pub.epsilon.slu.se/11891/

8. Menezes, Luis Fernando Carvalho de. "Análise do padrão de expressão do produto de PKHD1, o gene mutado na doença renal policística autossômica recessiva".

Degree: PhD, Fisiopatologia Experimental, 2004, University of São Paulo

O gene PKHD1, mutado na doença renal policística autossômica recessiva, apresenta um padrão de splicing complexo associado a múltiplos transcritos alternativos. Neste trabalho estudamos o… (more)

Subjects/Keywords: BLOTTING WESTERN/methods; CÍLIOS/patologia; IMMUNOHISTOCHEMISTRY/methods; IMUNOHISTOQUÍMICA/métodos; ISOFORMAS DE PROTEÍNAS/análise; KIDNEY TUBULES COLLECTING/pathology; KIDNEY TUBULES COLLECTING/physiopathology; MEMBRANE PROTEINS/analysis; MICROSCOPIA IMUNOELETRÔNICA/métodos/ MICROSCOPIA DE FLUORESCÊNCIA/méto; MICROSCOPY FLUORESCENCE/methods; MICROSCOPY IMMUNOELECTRON/methods; POLYCYSTIC KIDNEY AUTOSOMAL RECESSIVE/etiology; POLYCYSTIC KIDNEY AUTOSOMAL RECESSIVE/genetics; POLYCYSTIC KIDNEY AUTOSOMAL RECESSIVE/physiopathology; PROTEIN ISOFORMS/analysis; PROTEÍNAS DE MEMBRANA/análise; RIM POLICÍSTICO AUTOSSÔMICO RECESSIVO/etiologia; RIM POLICÍSTICO AUTOSSÔMICO RECESSIVO/fisiopatologia; RIM POLICÍSTICO AUTOSSÔMICO RECESSIVO/genética; TÚBULOS COLETORES RENAIS/fisiopatologia; TÚBULOS COLETORES RENAIS/patologia; WESTERN BLOTTING/métodos

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APA (6th Edition):

Menezes, L. F. C. d. (2004). "Análise do padrão de expressão do produto de PKHD1, o gene mutado na doença renal policística autossômica recessiva". (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5160/tde-04102005-111547/ ;

Chicago Manual of Style (16th Edition):

Menezes, Luis Fernando Carvalho de. “"Análise do padrão de expressão do produto de PKHD1, o gene mutado na doença renal policística autossômica recessiva".” 2004. Doctoral Dissertation, University of São Paulo. Accessed October 27, 2020. http://www.teses.usp.br/teses/disponiveis/5/5160/tde-04102005-111547/ ;.

MLA Handbook (7th Edition):

Menezes, Luis Fernando Carvalho de. “"Análise do padrão de expressão do produto de PKHD1, o gene mutado na doença renal policística autossômica recessiva".” 2004. Web. 27 Oct 2020.

Vancouver:

Menezes LFCd. "Análise do padrão de expressão do produto de PKHD1, o gene mutado na doença renal policística autossômica recessiva". [Internet] [Doctoral dissertation]. University of São Paulo; 2004. [cited 2020 Oct 27]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5160/tde-04102005-111547/ ;.

Council of Science Editors:

Menezes LFCd. "Análise do padrão de expressão do produto de PKHD1, o gene mutado na doença renal policística autossômica recessiva". [Doctoral Dissertation]. University of São Paulo; 2004. Available from: http://www.teses.usp.br/teses/disponiveis/5/5160/tde-04102005-111547/ ;


ETH Zürich

9. Unger, Michael Peter. Interrogating the single cell: computational and experimental methods for optimal live cell experiments.

Degree: 2014, ETH Zürich

Subjects/Keywords: CYTOLOGISCHE METHODEN + CYTOLOGISCHE TECHNIKEN + CYTOLOGISCHE EXPERIMENTE; EXPERIMENTE AN LEBENDEN ZELLEN, METHODEN UND TECHNIKEN; BIOCHEMISCHE UND MOLEKULARBIOLOGISCHE MODELLE; BIOLOGISCHE INFORMATIK UND COMPUTERANWENDUNG IN DER BIOLOGIE; BAYESSCHE THEORIE (WAHRSCHEINLICHKEITSRECHNUNG); FLUORESZENZMIKROSKOPIE (BIOLOGISCHE TECHNIKEN); STOCHASTISCHE MODELLE + STOCHASTISCHE SIMULATION (WAHRSCHEINLICHKEITSRECHNUNG); CYTOLOGICAL METHODS + CYTOLOGICAL TECHNIQUES + CYTOLOGICAL EXPERIMENTS; EXPERIMENTS ON LIVING CELLS, METHODS AND TECHNIQUES; BIOCHEMICAL AND MOLECULAR BIOLOGICAL MODELS; BIOLOGICAL INFORMATICS AND COMPUTER APPLICATIONS IN BIOLOGY; BAYESIAN THEORY (PROBABILITY THEORY); FLUORESCENCE MICROSCOPY (BIOLOGICAL TECHNIQUES); STOCHASTIC MODELS + STOCHASTIC SIMULATION (PROBABILITY THEORY); info:eu-repo/classification/ddc/570; Life sciences

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APA (6th Edition):

Unger, M. P. (2014). Interrogating the single cell: computational and experimental methods for optimal live cell experiments. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/154878

Chicago Manual of Style (16th Edition):

Unger, Michael Peter. “Interrogating the single cell: computational and experimental methods for optimal live cell experiments.” 2014. Doctoral Dissertation, ETH Zürich. Accessed October 27, 2020. http://hdl.handle.net/20.500.11850/154878.

MLA Handbook (7th Edition):

Unger, Michael Peter. “Interrogating the single cell: computational and experimental methods for optimal live cell experiments.” 2014. Web. 27 Oct 2020.

Vancouver:

Unger MP. Interrogating the single cell: computational and experimental methods for optimal live cell experiments. [Internet] [Doctoral dissertation]. ETH Zürich; 2014. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/20.500.11850/154878.

Council of Science Editors:

Unger MP. Interrogating the single cell: computational and experimental methods for optimal live cell experiments. [Doctoral Dissertation]. ETH Zürich; 2014. Available from: http://hdl.handle.net/20.500.11850/154878


ETH Zürich

10. Kumar, Sri Krishna Suresh. Implementation of a Closed-loop Microscopy Pipeline to Stitch and Segment Images of Growing Cell Populations.

Degree: 2013, ETH Zürich

Subjects/Keywords: ZELLPOPULATIONEN + ZELLKOLONIEN (CYTOLOGIE); ZELLMORPHOLOGIE + ZELLSTRUKTUR (CYTOLOGIE); EXPERIMENTE AN LEBENDEN ZELLEN, METHODEN UND TECHNIKEN; FLUORESZENZMIKROSKOPIE (BIOLOGISCHE TECHNIKEN); SYSTEMBIOLOGIE; COMPUTERANWENDUNGEN IN BIOLOGISCHEN EXPERIMENTEN; BIOLOGISCHE INFORMATIK UND COMPUTERANWENDUNG IN DER BIOLOGIE; CELL POPULATIONS + CELL COLONIES (CYTOLOGY); CELL MORPHOLOGY + CELL STRUCTURE (CYTOLOGY); EXPERIMENTS ON LIVING CELLS, METHODS AND TECHNIQUES; FLUORESCENCE MICROSCOPY (BIOLOGICAL TECHNIQUES); SYSTEMS BIOLOGY; COMPUTER APPLICATIONS IN BIOLOGICAL EXPERIMENTS; BIOLOGICAL INFORMATICS AND COMPUTER APPLICATIONS IN BIOLOGY; info:eu-repo/classification/ddc/570; Life sciences

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APA (6th Edition):

Kumar, S. K. S. (2013). Implementation of a Closed-loop Microscopy Pipeline to Stitch and Segment Images of Growing Cell Populations. (Thesis). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/154065

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):

Kumar, Sri Krishna Suresh. “Implementation of a Closed-loop Microscopy Pipeline to Stitch and Segment Images of Growing Cell Populations.” 2013. Thesis, ETH Zürich. Accessed October 27, 2020. http://hdl.handle.net/20.500.11850/154065.

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

MLA Handbook (7th Edition):

Kumar, Sri Krishna Suresh. “Implementation of a Closed-loop Microscopy Pipeline to Stitch and Segment Images of Growing Cell Populations.” 2013. Web. 27 Oct 2020.

Vancouver:

Kumar SKS. Implementation of a Closed-loop Microscopy Pipeline to Stitch and Segment Images of Growing Cell Populations. [Internet] [Thesis]. ETH Zürich; 2013. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/20.500.11850/154065.

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

Council of Science Editors:

Kumar SKS. Implementation of a Closed-loop Microscopy Pipeline to Stitch and Segment Images of Growing Cell Populations. [Thesis]. ETH Zürich; 2013. Available from: http://hdl.handle.net/20.500.11850/154065

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


University of Waterloo

11. McCanna, David. Development of Sensitive In Vitro Assays to Assess the Ocular Toxicity Potential of Chemicals and Ophthalmic Products.

Degree: 2009, University of Waterloo

 The utilization of in vitro tests with a tiered testing strategy for detection of mild ocular irritants can reduce the use of animals for testing,… (more)

Subjects/Keywords: in vitro; Alternative Methods; alamarBlue; rhodamine; tight junctions; bovine lens; viability; toxicity; mitochondria; mitochondria integrity; benzalkonium chloride; sodium dodecyl sulphate; sodium lauryl sulfate; scanning electron microscopy; Draize; Draize maximal average scores; zonula occludens; cosmetic directive; PETA; humane society; animal league; people for the ethical treatment of animals; interagency coordinating committee on the validation of alternative methods; ICCVAM; ECVAM; JaCVAM; BCOP; bovine cornea; ocular irritants; ocular irritation; ocular toxicity; human corneal epithelial cells; vitro; confocal; confocal microscopy; metabolic activity; optical quality; reactive oxygen species; contact lens; contact lens care solutions; barrier function; microbial keratitis; mulitipurpose solutions; tight junction; cell damage; claudin; ZO-1; occludin; MDCK; Madin; Madin-Darby; canine kidney cells; cornea; human cornea; human corneal epithelium; epithelial cell line; human corneal epithelial cell line; sodium fluorescein; sodium fluorescein permeability; fluorescein permeability; ocular surface; cell monolayer; Araki-Sasaki; cell physiology; risk assessment; safety assessment; ScanTox; scanning laser; lens epithelium; corneal cells; in vitro model; ophthalmic formulations; multiple instillation; back vertex; animal testing; rabbit testing; alternatives to animal testing; cultured bovine lens; toxicity of chemicals; irritation; irritants; laser scanner; organ culture; delayed toxicity; toxins; hydrogen peroxide; cornea toxicity; cornea toxicity models; prediction of human toxicity; no observable adverse effect level; lowest observable adverse effect level; NOAEL; LOAEL; toxicity thresholds; safety factors; cornea; uncertainty factors; preservatives; disinfectants; ophthalmic products; preclinical; preclinical testing; epithelial barrier; drug penetration; clinical confocal microscopy; animal rights; rabbit cornea; human cornea; human clinical effects; toxic; animal rights activist; sensitive measures; toxic effect; toxicity threshold; agar overlay; agar diffusion; agar overlay method; agar diffusion method; cytochrome; cytochrome c; apoptosis; necrotic; apoptotic; necrosis; caspase; rhodamine 123; resazuran; resorufin; cell death; cell viability; metabolic dye; microsomal; microsomal enzymes; cytotoxicity; cytotoxic; cytotoxic effect; MTT; XTT; WST-1; plasma membrane; mitochondrial; mitochondrial morphology; ocular toxicity potential; ocular toxicity; human corneal epithelial; cell line; confocal analysis; corneal epithelium; cell fluorescence; alamarBlue assay; rhodamine dye; animal welfare; toxic injury; degraded mitochondria; epithelial monolayer; disinfectants; membrane integrity; eye toxicity; eye; viability dye; toxicity in humans; human toxicity; effects on the mitochondria; mitochondrial toxicity; in vitro battery; in vitro test battery; ophthalmic eye drop; direct contact; product safety; cytotoxicity potential; molecular; molecular biology; refine reduce replace; sensitivity and relevance; sensitivity; relevance; rabbit ocular irritation test; product development; cytotoxicity models; cytotoxicity alternative methods; replacements for animal testing; three r's; beagle; tiered testing; tiered testing strategy; replacements animal testing; mechanistic toxicity; cornea mitochondria; dose response; threshold

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

APA (6th Edition):

McCanna, D. (2009). Development of Sensitive In Vitro Assays to Assess the Ocular Toxicity Potential of Chemicals and Ophthalmic Products. (Thesis). University of Waterloo. Retrieved from http://hdl.handle.net/10012/4338

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):

McCanna, David. “Development of Sensitive In Vitro Assays to Assess the Ocular Toxicity Potential of Chemicals and Ophthalmic Products.” 2009. Thesis, University of Waterloo. Accessed October 27, 2020. http://hdl.handle.net/10012/4338.

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

MLA Handbook (7th Edition):

McCanna, David. “Development of Sensitive In Vitro Assays to Assess the Ocular Toxicity Potential of Chemicals and Ophthalmic Products.” 2009. Web. 27 Oct 2020.

Vancouver:

McCanna D. Development of Sensitive In Vitro Assays to Assess the Ocular Toxicity Potential of Chemicals and Ophthalmic Products. [Internet] [Thesis]. University of Waterloo; 2009. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10012/4338.

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

Council of Science Editors:

McCanna D. Development of Sensitive In Vitro Assays to Assess the Ocular Toxicity Potential of Chemicals and Ophthalmic Products. [Thesis]. University of Waterloo; 2009. Available from: http://hdl.handle.net/10012/4338

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

.