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You searched for subject:(Assay methods). Showing records 1 – 26 of 26 total matches.

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University of Gothenburg / Göteborgs Universitet

1. Berg, Walter, 1918-. Plasminogen and urokinase determination based on the lysis time method : purification of the substrates - kinetic and methodological studies.

Degree: 1967, University of Gothenburg / Göteborgs Universitet

Subjects/Keywords: Biological assay: methods; Plasminogen: analysis

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APA (6th Edition):

Berg, Walter, 1. (1967). Plasminogen and urokinase determination based on the lysis time method : purification of the substrates - kinetic and methodological studies. (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/13859

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):

Berg, Walter, 1918-. “Plasminogen and urokinase determination based on the lysis time method : purification of the substrates - kinetic and methodological studies.” 1967. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed May 09, 2021. http://hdl.handle.net/2077/13859.

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

MLA Handbook (7th Edition):

Berg, Walter, 1918-. “Plasminogen and urokinase determination based on the lysis time method : purification of the substrates - kinetic and methodological studies.” 1967. Web. 09 May 2021.

Vancouver:

Berg, Walter 1. Plasminogen and urokinase determination based on the lysis time method : purification of the substrates - kinetic and methodological studies. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 1967. [cited 2021 May 09]. Available from: http://hdl.handle.net/2077/13859.

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

Council of Science Editors:

Berg, Walter 1. Plasminogen and urokinase determination based on the lysis time method : purification of the substrates - kinetic and methodological studies. [Thesis]. University of Gothenburg / Göteborgs Universitet; 1967. Available from: http://hdl.handle.net/2077/13859

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


Virginia Tech

2. Zhou, Rui. FITSelect: An Invention to Select Microbial Strains Maximizing Product Formation from a Single Culture Without High-Throughput Screening.

Degree: MS, Biological Systems Engineering, 2011, Virginia Tech

 In metabolic engineering of prokaryotes, combinatorial approaches have developed recently that induce random genetic perturbations to achieve a desired cell phenotype. A screening strategy follows… (more)

Subjects/Keywords: synthetic biology; growth competition assay; combinatorial methods; metabolic engineering

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APA (6th Edition):

Zhou, R. (2011). FITSelect: An Invention to Select Microbial Strains Maximizing Product Formation from a Single Culture Without High-Throughput Screening. (Masters Thesis). Virginia Tech. Retrieved from http://hdl.handle.net/10919/76843

Chicago Manual of Style (16th Edition):

Zhou, Rui. “FITSelect: An Invention to Select Microbial Strains Maximizing Product Formation from a Single Culture Without High-Throughput Screening.” 2011. Masters Thesis, Virginia Tech. Accessed May 09, 2021. http://hdl.handle.net/10919/76843.

MLA Handbook (7th Edition):

Zhou, Rui. “FITSelect: An Invention to Select Microbial Strains Maximizing Product Formation from a Single Culture Without High-Throughput Screening.” 2011. Web. 09 May 2021.

Vancouver:

Zhou R. FITSelect: An Invention to Select Microbial Strains Maximizing Product Formation from a Single Culture Without High-Throughput Screening. [Internet] [Masters thesis]. Virginia Tech; 2011. [cited 2021 May 09]. Available from: http://hdl.handle.net/10919/76843.

Council of Science Editors:

Zhou R. FITSelect: An Invention to Select Microbial Strains Maximizing Product Formation from a Single Culture Without High-Throughput Screening. [Masters Thesis]. Virginia Tech; 2011. Available from: http://hdl.handle.net/10919/76843

3. S. Lauria. THE ENDOCANNABINOID ENZYME MONOACYLGLYCEROL LIPASE: DEVELOPMENT OF A NEW FLUORESCENT ASSAY AND NOVEL INHIBITORS.

Degree: 2015, Università degli Studi di Milano

 The endocannabinoid system (ECS), comprising CB1/CB2 receptors, endocannabinoids (ECs) and their metabolic enzymes, FAAH (fatty acid amide hydrolase) and MAGL (monoacylglycerol lipase), is responsible for… (more)

Subjects/Keywords: Endocannabinoid system; Monoacylglycerol Lipase; inhibitors; activity assay; fluyorescent methods; molecular modelling; Settore BIO/10 - Biochimica

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APA (6th Edition):

Lauria, S. (2015). THE ENDOCANNABINOID ENZYME MONOACYLGLYCEROL LIPASE: DEVELOPMENT OF A NEW FLUORESCENT ASSAY AND NOVEL INHIBITORS. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/336675

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):

Lauria, S.. “THE ENDOCANNABINOID ENZYME MONOACYLGLYCEROL LIPASE: DEVELOPMENT OF A NEW FLUORESCENT ASSAY AND NOVEL INHIBITORS.” 2015. Thesis, Università degli Studi di Milano. Accessed May 09, 2021. http://hdl.handle.net/2434/336675.

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

MLA Handbook (7th Edition):

Lauria, S.. “THE ENDOCANNABINOID ENZYME MONOACYLGLYCEROL LIPASE: DEVELOPMENT OF A NEW FLUORESCENT ASSAY AND NOVEL INHIBITORS.” 2015. Web. 09 May 2021.

Vancouver:

Lauria S. THE ENDOCANNABINOID ENZYME MONOACYLGLYCEROL LIPASE: DEVELOPMENT OF A NEW FLUORESCENT ASSAY AND NOVEL INHIBITORS. [Internet] [Thesis]. Università degli Studi di Milano; 2015. [cited 2021 May 09]. Available from: http://hdl.handle.net/2434/336675.

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

Council of Science Editors:

Lauria S. THE ENDOCANNABINOID ENZYME MONOACYLGLYCEROL LIPASE: DEVELOPMENT OF A NEW FLUORESCENT ASSAY AND NOVEL INHIBITORS. [Thesis]. Università degli Studi di Milano; 2015. Available from: http://hdl.handle.net/2434/336675

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

4. Junqueira, César Alexandre. Determinação de pureza de fármacos por meio de métodos diretos e indiretos : vantagens e desvantagens.

Degree: 2012, Brazil

Pureza é um dos principais atributos de qualidade de matérias-primas farmacêuticas, já que a identificação e determinação quantitativa de impurezas podem ajudar a controlar/minimizar o… (more)

Subjects/Keywords: Impurezas; Nifedipino; Diazepam; Glibenclamida; Estavudina; Controle de qualidade; Impurities; Mass balance; Assay methods

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APA (6th Edition):

Junqueira, C. A. (2012). Determinação de pureza de fármacos por meio de métodos diretos e indiretos : vantagens e desvantagens. (Masters Thesis). Brazil. Retrieved from http://hdl.handle.net/10183/143686

Chicago Manual of Style (16th Edition):

Junqueira, César Alexandre. “Determinação de pureza de fármacos por meio de métodos diretos e indiretos : vantagens e desvantagens.” 2012. Masters Thesis, Brazil. Accessed May 09, 2021. http://hdl.handle.net/10183/143686.

MLA Handbook (7th Edition):

Junqueira, César Alexandre. “Determinação de pureza de fármacos por meio de métodos diretos e indiretos : vantagens e desvantagens.” 2012. Web. 09 May 2021.

Vancouver:

Junqueira CA. Determinação de pureza de fármacos por meio de métodos diretos e indiretos : vantagens e desvantagens. [Internet] [Masters thesis]. Brazil; 2012. [cited 2021 May 09]. Available from: http://hdl.handle.net/10183/143686.

Council of Science Editors:

Junqueira CA. Determinação de pureza de fármacos por meio de métodos diretos e indiretos : vantagens e desvantagens. [Masters Thesis]. Brazil; 2012. Available from: http://hdl.handle.net/10183/143686

5. Cook, Matthew Tyler. Hybrid K-edge Densitometry as a Method for Materials Accountancy Measurements in Pyrochemical Reprocessing.

Degree: 2015, University of Tennessee – Knoxville

 Pyrochemical reprocessing is a proven method to recover useful fissile material from spent nuclear fuel. The process requires high temperatures and an inert atmosphere thus… (more)

Subjects/Keywords: pyrochemical reprocessing; Monte Carlo methods; MCNP; nuclear safeguards; non-destructive assay; Nuclear Engineering

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APA (6th Edition):

Cook, M. T. (2015). Hybrid K-edge Densitometry as a Method for Materials Accountancy Measurements in Pyrochemical Reprocessing. (Doctoral Dissertation). University of Tennessee – Knoxville. Retrieved from https://trace.tennessee.edu/utk_graddiss/3329

Chicago Manual of Style (16th Edition):

Cook, Matthew Tyler. “Hybrid K-edge Densitometry as a Method for Materials Accountancy Measurements in Pyrochemical Reprocessing.” 2015. Doctoral Dissertation, University of Tennessee – Knoxville. Accessed May 09, 2021. https://trace.tennessee.edu/utk_graddiss/3329.

MLA Handbook (7th Edition):

Cook, Matthew Tyler. “Hybrid K-edge Densitometry as a Method for Materials Accountancy Measurements in Pyrochemical Reprocessing.” 2015. Web. 09 May 2021.

Vancouver:

Cook MT. Hybrid K-edge Densitometry as a Method for Materials Accountancy Measurements in Pyrochemical Reprocessing. [Internet] [Doctoral dissertation]. University of Tennessee – Knoxville; 2015. [cited 2021 May 09]. Available from: https://trace.tennessee.edu/utk_graddiss/3329.

Council of Science Editors:

Cook MT. Hybrid K-edge Densitometry as a Method for Materials Accountancy Measurements in Pyrochemical Reprocessing. [Doctoral Dissertation]. University of Tennessee – Knoxville; 2015. Available from: https://trace.tennessee.edu/utk_graddiss/3329


Wayne State University

6. Krishnoji Rao, Vidhya Bai. Quantification Of Antimicrobial Resistance Genes In Urban Agricultural Soil.

Degree: MS, Nutrition and Food Science, 2018, Wayne State University

  The increased dissemination of antibiotic resistance genes and their acquisition by clinically relevant microbes in the environmental setting is becoming a global alarming issue.… (more)

Subjects/Keywords: Antibiotic Resistant Genes (ARGs); 16S rRNA identification; Resistance Gene Copy Number Analysis in Environmental Samples; Soil DNA sequence analysis; Molecular cloning; qPCR assay methods; Statistical Analysis; Genetics; Microbiology; Molecular Biology

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APA (6th Edition):

Krishnoji Rao, V. B. (2018). Quantification Of Antimicrobial Resistance Genes In Urban Agricultural Soil. (Masters Thesis). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_theses/680

Chicago Manual of Style (16th Edition):

Krishnoji Rao, Vidhya Bai. “Quantification Of Antimicrobial Resistance Genes In Urban Agricultural Soil.” 2018. Masters Thesis, Wayne State University. Accessed May 09, 2021. https://digitalcommons.wayne.edu/oa_theses/680.

MLA Handbook (7th Edition):

Krishnoji Rao, Vidhya Bai. “Quantification Of Antimicrobial Resistance Genes In Urban Agricultural Soil.” 2018. Web. 09 May 2021.

Vancouver:

Krishnoji Rao VB. Quantification Of Antimicrobial Resistance Genes In Urban Agricultural Soil. [Internet] [Masters thesis]. Wayne State University; 2018. [cited 2021 May 09]. Available from: https://digitalcommons.wayne.edu/oa_theses/680.

Council of Science Editors:

Krishnoji Rao VB. Quantification Of Antimicrobial Resistance Genes In Urban Agricultural Soil. [Masters Thesis]. Wayne State University; 2018. Available from: https://digitalcommons.wayne.edu/oa_theses/680

7. Pedroso, Tahisa Marcela [UNESP]. Desenvolvimento e validação de métodos analíticos para caracterização e quantificação de ertapenem sódico em pó liofilizado para solução injetável.

Degree: 2017, Universidade Estadual Paulista (UNESP)

Submitted by TAHISA MARCELA PEDROSO null ([email protected]) on 2017-10-10T17:48:16Z No. of bitstreams: 1 Tese - Tahisa Marcela Pedroso.pdf: 4038010 bytes, checksum: 692c5c994a95d2ac8244a0bf6901330b (MD5)

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Subjects/Keywords: Ertapenem sódico; Controle de qualidade; Métodos analíticos; Validação; Espectrofotometria; CLAE; Ensaio microbiológico; Eletroforese capilar; Sodium ertapenem; Analytical methods; Capillary electrophoresis; HPLC; Microbiological assay; Quality control; Spectroscopy; Validation

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APA (6th Edition):

Pedroso, T. M. [. (2017). Desenvolvimento e validação de métodos analíticos para caracterização e quantificação de ertapenem sódico em pó liofilizado para solução injetável. (Doctoral Dissertation). Universidade Estadual Paulista (UNESP). Retrieved from http://hdl.handle.net/11449/151897

Chicago Manual of Style (16th Edition):

Pedroso, Tahisa Marcela [UNESP]. “Desenvolvimento e validação de métodos analíticos para caracterização e quantificação de ertapenem sódico em pó liofilizado para solução injetável.” 2017. Doctoral Dissertation, Universidade Estadual Paulista (UNESP). Accessed May 09, 2021. http://hdl.handle.net/11449/151897.

MLA Handbook (7th Edition):

Pedroso, Tahisa Marcela [UNESP]. “Desenvolvimento e validação de métodos analíticos para caracterização e quantificação de ertapenem sódico em pó liofilizado para solução injetável.” 2017. Web. 09 May 2021.

Vancouver:

Pedroso TM[. Desenvolvimento e validação de métodos analíticos para caracterização e quantificação de ertapenem sódico em pó liofilizado para solução injetável. [Internet] [Doctoral dissertation]. Universidade Estadual Paulista (UNESP); 2017. [cited 2021 May 09]. Available from: http://hdl.handle.net/11449/151897.

Council of Science Editors:

Pedroso TM[. Desenvolvimento e validação de métodos analíticos para caracterização e quantificação de ertapenem sódico em pó liofilizado para solução injetável. [Doctoral Dissertation]. Universidade Estadual Paulista (UNESP); 2017. Available from: http://hdl.handle.net/11449/151897


Swedish University of Agricultural Sciences

8. Dernfalk, Johanna. Multiplex flow cytometric assays for markers of inflammation.

Degree: 2008, Swedish University of Agricultural Sciences

 The aim of this thesis was to develop new techniques for quantification of bovine pro-inflammatory markers, with emphasis on cytokines and acute phase proteins, and… (more)

Subjects/Keywords: dairy cows; bovine mastitis; cow milk; blood composition; cytokines; inflammation; immunological techniques; immunity; antibodies; animal diseases; laboratory diagnosis; analytical methods; biochemistry; bovine; multiplex particle based flow cytometry; immunoassay; suspension array; biomarkers; pro-inflammatory cytokines; acute phase proteins; mastitis; whole blood stimulation assay; milk; blood

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APA (6th Edition):

Dernfalk, J. (2008). Multiplex flow cytometric assays for markers of inflammation. (Doctoral Dissertation). Swedish University of Agricultural Sciences. Retrieved from http://pub.epsilon.slu.se/1696/

Chicago Manual of Style (16th Edition):

Dernfalk, Johanna. “Multiplex flow cytometric assays for markers of inflammation.” 2008. Doctoral Dissertation, Swedish University of Agricultural Sciences. Accessed May 09, 2021. http://pub.epsilon.slu.se/1696/.

MLA Handbook (7th Edition):

Dernfalk, Johanna. “Multiplex flow cytometric assays for markers of inflammation.” 2008. Web. 09 May 2021.

Vancouver:

Dernfalk J. Multiplex flow cytometric assays for markers of inflammation. [Internet] [Doctoral dissertation]. Swedish University of Agricultural Sciences; 2008. [cited 2021 May 09]. Available from: http://pub.epsilon.slu.se/1696/.

Council of Science Editors:

Dernfalk J. Multiplex flow cytometric assays for markers of inflammation. [Doctoral Dissertation]. Swedish University of Agricultural Sciences; 2008. Available from: http://pub.epsilon.slu.se/1696/

9. Evandro Antônio Bentes de Oliveira Júnior. Alpha Glutationa S Transferase: marcador de lesão hepática em pacientes com hepatite pelo vírus C?.

Degree: 2005, University of São Paulo

INTRODUÇÃO E OBJETIVOS: A a-Glutathiona-S-transferase (aGST) vem sendo proposta como um marcador sensível e não-invasivo de lesão hepática em pacientes com Hepatite pelo vírus C.… (more)

Subjects/Keywords: Elisa/métodos; Glutationa transferase/análise; Hepatite C/patologia; Enzyme-linked immunosorbent assay/methods; Glutathione transferase/analys; Hepatitis C/pathology

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APA (6th Edition):

Júnior, E. A. B. d. O. (2005). Alpha Glutationa S Transferase: marcador de lesão hepática em pacientes com hepatite pelo vírus C?. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5144/tde-19032007-101313/

Chicago Manual of Style (16th Edition):

Júnior, Evandro Antônio Bentes de Oliveira. “Alpha Glutationa S Transferase: marcador de lesão hepática em pacientes com hepatite pelo vírus C?.” 2005. Doctoral Dissertation, University of São Paulo. Accessed May 09, 2021. http://www.teses.usp.br/teses/disponiveis/5/5144/tde-19032007-101313/.

MLA Handbook (7th Edition):

Júnior, Evandro Antônio Bentes de Oliveira. “Alpha Glutationa S Transferase: marcador de lesão hepática em pacientes com hepatite pelo vírus C?.” 2005. Web. 09 May 2021.

Vancouver:

Júnior EABdO. Alpha Glutationa S Transferase: marcador de lesão hepática em pacientes com hepatite pelo vírus C?. [Internet] [Doctoral dissertation]. University of São Paulo; 2005. [cited 2021 May 09]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5144/tde-19032007-101313/.

Council of Science Editors:

Júnior EABdO. Alpha Glutationa S Transferase: marcador de lesão hepática em pacientes com hepatite pelo vírus C?. [Doctoral Dissertation]. University of São Paulo; 2005. Available from: http://www.teses.usp.br/teses/disponiveis/5/5144/tde-19032007-101313/

10. Andrea Glezer. "Estudo da atividade biológica da macroprolactina humana em células Nb2 e em células Ba/F-03 transfectadas com o receptor de prolactina humano forma longa".

Degree: 2006, University of São Paulo

A macroprolactinemia é condição freqüente na hiperprolactinemia e em geral, sem impacto clínico. Os dados sobre a atividade biológica da macroprolactina (bbPRL) são controversos e… (more)

Subjects/Keywords: Bioensaios/métodos; Hiperprolactinemia; Isoformas de proteínas; Prolactina; Prolactinoma; Receptores da prolactina; Biological assay/methods; Hyperprolactinemia; Prolactin; Prolactinoma; Protein Isoforms; Receptors Prolactin

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APA (6th Edition):

Glezer, A. (2006). "Estudo da atividade biológica da macroprolactina humana em células Nb2 e em células Ba/F-03 transfectadas com o receptor de prolactina humano forma longa". (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5135/tde-12042006-085305/

Chicago Manual of Style (16th Edition):

Glezer, Andrea. “"Estudo da atividade biológica da macroprolactina humana em células Nb2 e em células Ba/F-03 transfectadas com o receptor de prolactina humano forma longa".” 2006. Doctoral Dissertation, University of São Paulo. Accessed May 09, 2021. http://www.teses.usp.br/teses/disponiveis/5/5135/tde-12042006-085305/.

MLA Handbook (7th Edition):

Glezer, Andrea. “"Estudo da atividade biológica da macroprolactina humana em células Nb2 e em células Ba/F-03 transfectadas com o receptor de prolactina humano forma longa".” 2006. Web. 09 May 2021.

Vancouver:

Glezer A. "Estudo da atividade biológica da macroprolactina humana em células Nb2 e em células Ba/F-03 transfectadas com o receptor de prolactina humano forma longa". [Internet] [Doctoral dissertation]. University of São Paulo; 2006. [cited 2021 May 09]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5135/tde-12042006-085305/.

Council of Science Editors:

Glezer A. "Estudo da atividade biológica da macroprolactina humana em células Nb2 e em células Ba/F-03 transfectadas com o receptor de prolactina humano forma longa". [Doctoral Dissertation]. University of São Paulo; 2006. Available from: http://www.teses.usp.br/teses/disponiveis/5/5135/tde-12042006-085305/

11. Belavenuto, Eliane Gandolpho Tótoli [UNESP]. Análise químico-farmacêutica e estudos microbiológico e de estabilidade de preparações injetáveis de daptomicina.

Degree: 2016, Universidade Estadual Paulista (UNESP)

Submitted by ELIANE GANDOLPHO TÓTOLI BELAVENUTO null ([email protected]) on 2016-10-31T14:11:54Z No. of bitstreams: 1 Eliane_Belavenuto_Tese.pdf: 5620592 bytes, checksum: abddf0c57a2b88094afa708c6937b575 (MD5)

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Subjects/Keywords: CLAE; Controle de qualidade; Daptomicina; Eletroforese capilar; Espectrofotometria; Estabilidade; Estudo microbiológico; Método turbidimétrico; Métodos analíticos; Sinergia; Analytical methods; Capillary electrophoresis; Daptomycin; HPLC; Microbiological study; Quality control; Spectrophotometry; Stability; Synergy; Turbidimetric assay

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APA (6th Edition):

Belavenuto, E. G. T. [. (2016). Análise químico-farmacêutica e estudos microbiológico e de estabilidade de preparações injetáveis de daptomicina. (Doctoral Dissertation). Universidade Estadual Paulista (UNESP). Retrieved from http://hdl.handle.net/11449/144528

Chicago Manual of Style (16th Edition):

Belavenuto, Eliane Gandolpho Tótoli [UNESP]. “Análise químico-farmacêutica e estudos microbiológico e de estabilidade de preparações injetáveis de daptomicina.” 2016. Doctoral Dissertation, Universidade Estadual Paulista (UNESP). Accessed May 09, 2021. http://hdl.handle.net/11449/144528.

MLA Handbook (7th Edition):

Belavenuto, Eliane Gandolpho Tótoli [UNESP]. “Análise químico-farmacêutica e estudos microbiológico e de estabilidade de preparações injetáveis de daptomicina.” 2016. Web. 09 May 2021.

Vancouver:

Belavenuto EGT[. Análise químico-farmacêutica e estudos microbiológico e de estabilidade de preparações injetáveis de daptomicina. [Internet] [Doctoral dissertation]. Universidade Estadual Paulista (UNESP); 2016. [cited 2021 May 09]. Available from: http://hdl.handle.net/11449/144528.

Council of Science Editors:

Belavenuto EGT[. Análise químico-farmacêutica e estudos microbiológico e de estabilidade de preparações injetáveis de daptomicina. [Doctoral Dissertation]. Universidade Estadual Paulista (UNESP); 2016. Available from: http://hdl.handle.net/11449/144528

12. Rodrigues, Danilo Fernando [UNESP]. Análise químico-farmacêutica de cloridrato de cefepima em pó liofilizado para solução injetável.

Degree: 2017, Universidade Estadual Paulista (UNESP)

Submitted by DANILO FERNANDO RODRIGUES null ([email protected]) on 2017-06-14T12:36:45Z No. of bitstreams: 1 Tese de Doutorado Danilo Fernando Rodrigues.pdf: 4388842 bytes, checksum: 6975b0a3885b46d10797a9d801f7f969 (MD5)

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Subjects/Keywords: CLAE; Cloridrato de cefepima; Controle de qualidade; Ensaio microbiológico; Espectrofotometria; Estabilidade; Métodos analíticos; Produtos de degradação; Validação; Analytical methods; Cefepime hydrochloride; Degradation products; HPLC; Microbiological assay; Quality control; Spectrophotometry; Stability; Validation

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APA (6th Edition):

Rodrigues, D. F. [. (2017). Análise químico-farmacêutica de cloridrato de cefepima em pó liofilizado para solução injetável. (Doctoral Dissertation). Universidade Estadual Paulista (UNESP). Retrieved from http://hdl.handle.net/11449/150909

Chicago Manual of Style (16th Edition):

Rodrigues, Danilo Fernando [UNESP]. “Análise químico-farmacêutica de cloridrato de cefepima em pó liofilizado para solução injetável.” 2017. Doctoral Dissertation, Universidade Estadual Paulista (UNESP). Accessed May 09, 2021. http://hdl.handle.net/11449/150909.

MLA Handbook (7th Edition):

Rodrigues, Danilo Fernando [UNESP]. “Análise químico-farmacêutica de cloridrato de cefepima em pó liofilizado para solução injetável.” 2017. Web. 09 May 2021.

Vancouver:

Rodrigues DF[. Análise químico-farmacêutica de cloridrato de cefepima em pó liofilizado para solução injetável. [Internet] [Doctoral dissertation]. Universidade Estadual Paulista (UNESP); 2017. [cited 2021 May 09]. Available from: http://hdl.handle.net/11449/150909.

Council of Science Editors:

Rodrigues DF[. Análise químico-farmacêutica de cloridrato de cefepima em pó liofilizado para solução injetável. [Doctoral Dissertation]. Universidade Estadual Paulista (UNESP); 2017. Available from: http://hdl.handle.net/11449/150909

13. Corrêa, Josilene Chaves Ruela [UNESP]. Desenvolvimento de métodos analíticos para estudos de estabilidade para fluconazol cápsulas.

Degree: 2011, Universidade Estadual Paulista (UNESP)

Made available in DSpace on 2014-06-11T19:25:27Z (GMT). No. of bitstreams: 0 Previous issue date: 2011-01-21Bitstream added on 2014-06-13T19:32:33Z : No. of bitstreams: 1 correa_jcr_me_arafcf.pdf: 630725… (more)

Subjects/Keywords: Medicamentos - Formas farmaceuticas; Fluconazol; Estudo de estabiblidade; Fluconazole; Stability studies; Validation of analytical methods; Microbiological assay; Dissolution

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APA (6th Edition):

Corrêa, J. C. R. [. (2011). Desenvolvimento de métodos analíticos para estudos de estabilidade para fluconazol cápsulas. (Masters Thesis). Universidade Estadual Paulista (UNESP). Retrieved from http://hdl.handle.net/11449/91697

Chicago Manual of Style (16th Edition):

Corrêa, Josilene Chaves Ruela [UNESP]. “Desenvolvimento de métodos analíticos para estudos de estabilidade para fluconazol cápsulas.” 2011. Masters Thesis, Universidade Estadual Paulista (UNESP). Accessed May 09, 2021. http://hdl.handle.net/11449/91697.

MLA Handbook (7th Edition):

Corrêa, Josilene Chaves Ruela [UNESP]. “Desenvolvimento de métodos analíticos para estudos de estabilidade para fluconazol cápsulas.” 2011. Web. 09 May 2021.

Vancouver:

Corrêa JCR[. Desenvolvimento de métodos analíticos para estudos de estabilidade para fluconazol cápsulas. [Internet] [Masters thesis]. Universidade Estadual Paulista (UNESP); 2011. [cited 2021 May 09]. Available from: http://hdl.handle.net/11449/91697.

Council of Science Editors:

Corrêa JCR[. Desenvolvimento de métodos analíticos para estudos de estabilidade para fluconazol cápsulas. [Masters Thesis]. Universidade Estadual Paulista (UNESP); 2011. Available from: http://hdl.handle.net/11449/91697


Monash University

14. PARAMASIVAM, RAGUL. Development of recombinant multiepitope proteins-based point of care test diagnosis for multiple sexual transmitted diseases in humans.

Degree: Science, 2020, Monash University

 This research aims to performed systematic review to assess the diagnostic accuracy of all reported recombinant antigens and multiple point-of-care rapid assay platforms for Chlamydia,… (more)

Subjects/Keywords: Applied Immunology (incl. Antibody Engineering, Xenotransplantation and T-cell Therapies); Immunological and Bioassay Methods; Proteins and Peptides; Medical Biotechnology Diagnostics (incl. Biosensors); Sexually Transmitted Diseases; HIV; AIDS; Syphilis; Herpes; gonorrhea; Chlamydia; Hepatitis B; Assay Development; Serological; Ethiopia

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APA (6th Edition):

PARAMASIVAM, R. (2020). Development of recombinant multiepitope proteins-based point of care test diagnosis for multiple sexual transmitted diseases in humans. (Thesis). Monash University. Retrieved from https://doi.org/10.26180/5e429eaccb67c

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):

PARAMASIVAM, RAGUL. “Development of recombinant multiepitope proteins-based point of care test diagnosis for multiple sexual transmitted diseases in humans.” 2020. Thesis, Monash University. Accessed May 09, 2021. https://doi.org/10.26180/5e429eaccb67c.

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

MLA Handbook (7th Edition):

PARAMASIVAM, RAGUL. “Development of recombinant multiepitope proteins-based point of care test diagnosis for multiple sexual transmitted diseases in humans.” 2020. Web. 09 May 2021.

Vancouver:

PARAMASIVAM R. Development of recombinant multiepitope proteins-based point of care test diagnosis for multiple sexual transmitted diseases in humans. [Internet] [Thesis]. Monash University; 2020. [cited 2021 May 09]. Available from: https://doi.org/10.26180/5e429eaccb67c.

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

Council of Science Editors:

PARAMASIVAM R. Development of recombinant multiepitope proteins-based point of care test diagnosis for multiple sexual transmitted diseases in humans. [Thesis]. Monash University; 2020. Available from: https://doi.org/10.26180/5e429eaccb67c

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

15. Ashley, Jason Waid. Significance and regulation of CD68 expression in the osteoclast.

Degree: PhD, 2011, University of Alabama – Birmingham

The mucin-like Lysosome Associated Membrane Protein (LAMP) family member CD68 is a primarily myeloid lineage restricted transmembrane protein that is expressed in macrophages and osteoclasts.… (more)

Subjects/Keywords: Antigens, CD  – genetics<; br>; Antigens, Differentiation, Myelomonocytic  – genetics<; br>; Biological Assay  – methods<; br>; Bone and Bones<; br>; Drug Evaluation, Preclinical  – methods<; br>; Gene Deletion<; br>; High-Throughput Screening Assays  – methods<; br>; Macrophages  – drug effects<; br>; Osteoclasts<; br>; Receptor Activator of Nuclear Factor-kappa B  – metabolism<; br>; Signal Transduction  – physiology

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APA (6th Edition):

Ashley, J. W. (2011). Significance and regulation of CD68 expression in the osteoclast. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1033

Chicago Manual of Style (16th Edition):

Ashley, Jason Waid. “Significance and regulation of CD68 expression in the osteoclast.” 2011. Doctoral Dissertation, University of Alabama – Birmingham. Accessed May 09, 2021. http://contentdm.mhsl.uab.edu/u?/etd,1033.

MLA Handbook (7th Edition):

Ashley, Jason Waid. “Significance and regulation of CD68 expression in the osteoclast.” 2011. Web. 09 May 2021.

Vancouver:

Ashley JW. Significance and regulation of CD68 expression in the osteoclast. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2011. [cited 2021 May 09]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1033.

Council of Science Editors:

Ashley JW. Significance and regulation of CD68 expression in the osteoclast. [Doctoral Dissertation]. University of Alabama – Birmingham; 2011. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1033

16. Κωνσταντινίδης, Αθανάσιος. Αξιολόγηση της ορολογικής μεθόδου φθορίζουσας πόλωσης του φωτός (Fluorescence Polarization Assay - FPA) στη διάγνωση της βρουκέλλωσης του ανθρώπου.

Degree: 2007, University of Thessaly (UTH); Πανεπιστήμιο Θεσσαλίας

Brucellosis is an important zoonosis in many parts of the world. Many serological methods such as SAT, RBT and ELISA, are used in diagnosis of… (more)

Subjects/Keywords: Βρουκέλλωση; Ορολογική διάγνωση βρουκέλλωσης; Φθορίζουσα πόλωση του φωτός; Σύγκριση ορολογικών μεθόδων; Human brucellosis; Serology; Fluorescence polarization assay; FPA; Comparison of FPA with other serological methods

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APA (6th Edition):

Κωνσταντινίδης, . . (2007). Αξιολόγηση της ορολογικής μεθόδου φθορίζουσας πόλωσης του φωτός (Fluorescence Polarization Assay - FPA) στη διάγνωση της βρουκέλλωσης του ανθρώπου. (Thesis). University of Thessaly (UTH); Πανεπιστήμιο Θεσσαλίας. Retrieved from http://hdl.handle.net/10442/hedi/17211

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):

Κωνσταντινίδης, Αθανάσιος. “Αξιολόγηση της ορολογικής μεθόδου φθορίζουσας πόλωσης του φωτός (Fluorescence Polarization Assay - FPA) στη διάγνωση της βρουκέλλωσης του ανθρώπου.” 2007. Thesis, University of Thessaly (UTH); Πανεπιστήμιο Θεσσαλίας. Accessed May 09, 2021. http://hdl.handle.net/10442/hedi/17211.

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

MLA Handbook (7th Edition):

Κωνσταντινίδης, Αθανάσιος. “Αξιολόγηση της ορολογικής μεθόδου φθορίζουσας πόλωσης του φωτός (Fluorescence Polarization Assay - FPA) στη διάγνωση της βρουκέλλωσης του ανθρώπου.” 2007. Web. 09 May 2021.

Vancouver:

Κωνσταντινίδης . Αξιολόγηση της ορολογικής μεθόδου φθορίζουσας πόλωσης του φωτός (Fluorescence Polarization Assay - FPA) στη διάγνωση της βρουκέλλωσης του ανθρώπου. [Internet] [Thesis]. University of Thessaly (UTH); Πανεπιστήμιο Θεσσαλίας; 2007. [cited 2021 May 09]. Available from: http://hdl.handle.net/10442/hedi/17211.

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

Council of Science Editors:

Κωνσταντινίδης . Αξιολόγηση της ορολογικής μεθόδου φθορίζουσας πόλωσης του φωτός (Fluorescence Polarization Assay - FPA) στη διάγνωση της βρουκέλλωσης του ανθρώπου. [Thesis]. University of Thessaly (UTH); Πανεπιστήμιο Θεσσαλίας; 2007. Available from: http://hdl.handle.net/10442/hedi/17211

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


Swedish University of Agricultural Sciences

17. Spjuth, Linda. Di(2-ethylhexyl) phthalate and semen quality in boars.

Degree: 2006, Swedish University of Agricultural Sciences

 Di(2-ethylhexyl) phthalate (DEHP), a plasticizer used in polyvinyl chloride (PVC) products, has been reported to have toxic effects on animal reproduction. However, these reports come… (more)

Subjects/Keywords: boars; semen; spermatozoa; freezing; thawing; viability; movement; animal morphology; chemical contamination; analytical methods; spermatozoa; di(2-ethylhexyl) phthalate (DEHP); sperm motility; computer-assisted sperm analysis (CASA); sperm morphology; plasma membrane integrity (PMI); freezing; capacitation; acrosome reaction (AR); sperm chromatin structure assay (SCSA); in vitro penetration assay; boar

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APA (6th Edition):

Spjuth, L. (2006). Di(2-ethylhexyl) phthalate and semen quality in boars. (Doctoral Dissertation). Swedish University of Agricultural Sciences. Retrieved from http://pub.epsilon.slu.se/1273/

Chicago Manual of Style (16th Edition):

Spjuth, Linda. “Di(2-ethylhexyl) phthalate and semen quality in boars.” 2006. Doctoral Dissertation, Swedish University of Agricultural Sciences. Accessed May 09, 2021. http://pub.epsilon.slu.se/1273/.

MLA Handbook (7th Edition):

Spjuth, Linda. “Di(2-ethylhexyl) phthalate and semen quality in boars.” 2006. Web. 09 May 2021.

Vancouver:

Spjuth L. Di(2-ethylhexyl) phthalate and semen quality in boars. [Internet] [Doctoral dissertation]. Swedish University of Agricultural Sciences; 2006. [cited 2021 May 09]. Available from: http://pub.epsilon.slu.se/1273/.

Council of Science Editors:

Spjuth L. Di(2-ethylhexyl) phthalate and semen quality in boars. [Doctoral Dissertation]. Swedish University of Agricultural Sciences; 2006. Available from: http://pub.epsilon.slu.se/1273/


University of Windsor

18. Annett, Robert G. I. Assay methods for the keto-enol tautomerization of oxalacetic acid. II. Purification and characterization of oxalacetate keto-enol tautomerase.

Degree: PhD, Chemistry and Biochemistry, 1968, University of Windsor

Subjects/Keywords: ACID; ASSAY; CHARACTERIZATION; ENOL; I; II; KETO; KETO-ENOL TAUTOMERIZATION; Keto-enol tautomerization; METHODS; OXALACETATE; OXALACETATE KETO-ENOL TAUTOMERASE; OXALACETIC; OXALACETIC ACID; Oxalacetate keto-enol tautomerase; Oxalacetic acid; PURIFICATION; TAUTOMERASE; TAUTOMERIZATION

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APA (6th Edition):

Annett, R. G. (1968). I. Assay methods for the keto-enol tautomerization of oxalacetic acid. II. Purification and characterization of oxalacetate keto-enol tautomerase. (Doctoral Dissertation). University of Windsor. Retrieved from https://scholar.uwindsor.ca/etd/6052

Chicago Manual of Style (16th Edition):

Annett, Robert G. “I. Assay methods for the keto-enol tautomerization of oxalacetic acid. II. Purification and characterization of oxalacetate keto-enol tautomerase.” 1968. Doctoral Dissertation, University of Windsor. Accessed May 09, 2021. https://scholar.uwindsor.ca/etd/6052.

MLA Handbook (7th Edition):

Annett, Robert G. “I. Assay methods for the keto-enol tautomerization of oxalacetic acid. II. Purification and characterization of oxalacetate keto-enol tautomerase.” 1968. Web. 09 May 2021.

Vancouver:

Annett RG. I. Assay methods for the keto-enol tautomerization of oxalacetic acid. II. Purification and characterization of oxalacetate keto-enol tautomerase. [Internet] [Doctoral dissertation]. University of Windsor; 1968. [cited 2021 May 09]. Available from: https://scholar.uwindsor.ca/etd/6052.

Council of Science Editors:

Annett RG. I. Assay methods for the keto-enol tautomerization of oxalacetic acid. II. Purification and characterization of oxalacetate keto-enol tautomerase. [Doctoral Dissertation]. University of Windsor; 1968. Available from: https://scholar.uwindsor.ca/etd/6052

19. Iara Terezinha Queiroz Pereira dos Santos. "Avaliação da atividade clastogênica do resíduo catalítico industrial, por meio do bioensaio de micronúcleos com Tradescantia pallida cv. Purpurea".

Degree: 2004, University of São Paulo

O objetivo deste estudo foi aumentar o banco de dados em relação a resíduos (cake) e efluentes (licor) industriais e o seu nível de clastogenicidade.… (more)

Subjects/Keywords: BIOENSAIOS/métodos; MICRONÚCLEOS/química; MUTAGÊNESE/química; POLUENTES INDUSTRIAIS; POLUENTES QUÍMICOS; RESÍDUOS INDUSTRIAIS/análise; TRADESCANTIA/toxicidade; BIOLOGICAL ASSAY/methods; CHEMICAL POLLUTANTS; INDUSTRIAL POLLUTANTS; INDUSTRIAL WASTE/analysis; MICRONUCLEI/chemistry; MUTAGENESIS/chemistry; MUTAGENESIS/toxicity; TRADESCANTIA/toxicity

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APA (6th Edition):

Santos, I. T. Q. P. d. (2004). "Avaliação da atividade clastogênica do resíduo catalítico industrial, por meio do bioensaio de micronúcleos com Tradescantia pallida cv. Purpurea". (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5160/tde-04082005-131203/

Chicago Manual of Style (16th Edition):

Santos, Iara Terezinha Queiroz Pereira dos. “"Avaliação da atividade clastogênica do resíduo catalítico industrial, por meio do bioensaio de micronúcleos com Tradescantia pallida cv. Purpurea".” 2004. Doctoral Dissertation, University of São Paulo. Accessed May 09, 2021. http://www.teses.usp.br/teses/disponiveis/5/5160/tde-04082005-131203/.

MLA Handbook (7th Edition):

Santos, Iara Terezinha Queiroz Pereira dos. “"Avaliação da atividade clastogênica do resíduo catalítico industrial, por meio do bioensaio de micronúcleos com Tradescantia pallida cv. Purpurea".” 2004. Web. 09 May 2021.

Vancouver:

Santos ITQPd. "Avaliação da atividade clastogênica do resíduo catalítico industrial, por meio do bioensaio de micronúcleos com Tradescantia pallida cv. Purpurea". [Internet] [Doctoral dissertation]. University of São Paulo; 2004. [cited 2021 May 09]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5160/tde-04082005-131203/.

Council of Science Editors:

Santos ITQPd. "Avaliação da atividade clastogênica do resíduo catalítico industrial, por meio do bioensaio de micronúcleos com Tradescantia pallida cv. Purpurea". [Doctoral Dissertation]. University of São Paulo; 2004. Available from: http://www.teses.usp.br/teses/disponiveis/5/5160/tde-04082005-131203/

20. Celia Regina Furucho Yamamoto. "Diagnóstico da doença de Chagas em bancos de sangue: linfoproliferação, detecção de anticorpos e estudo epidemiológico em indivíduos com provas sorológicas inconclusivas".

Degree: 2006, University of São Paulo

O objetivo deste estudo foi avaliar a contribuição de linfoproliferação (1 parâmetro) em associação a provas sorológicas de alto desempenho (4 parâmetros), estudo epidemiológico (1)… (more)

Subjects/Keywords: Bancos de sangue/métodos; Doença de Chagas/diagnóstico; Doença de Chagas/epidemiologia; Elisa/métodos; Linfócitos; Testes sorológicos; Trypanosoma cruzi/imunologia; Western blotting; Blood banks/methods; Blotting Western; Chagas disease/diagnosis; Chagas disease/epidemiology; Enzyme-linked immunosorbent assay/methods; Lymphocytes; Serologic tests; Trypanosoma cruzi/immunology

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APA (6th Edition):

Yamamoto, C. R. F. (2006). "Diagnóstico da doença de Chagas em bancos de sangue: linfoproliferação, detecção de anticorpos e estudo epidemiológico em indivíduos com provas sorológicas inconclusivas". (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5134/tde-03052006-133432/

Chicago Manual of Style (16th Edition):

Yamamoto, Celia Regina Furucho. “"Diagnóstico da doença de Chagas em bancos de sangue: linfoproliferação, detecção de anticorpos e estudo epidemiológico em indivíduos com provas sorológicas inconclusivas".” 2006. Masters Thesis, University of São Paulo. Accessed May 09, 2021. http://www.teses.usp.br/teses/disponiveis/5/5134/tde-03052006-133432/.

MLA Handbook (7th Edition):

Yamamoto, Celia Regina Furucho. “"Diagnóstico da doença de Chagas em bancos de sangue: linfoproliferação, detecção de anticorpos e estudo epidemiológico em indivíduos com provas sorológicas inconclusivas".” 2006. Web. 09 May 2021.

Vancouver:

Yamamoto CRF. "Diagnóstico da doença de Chagas em bancos de sangue: linfoproliferação, detecção de anticorpos e estudo epidemiológico em indivíduos com provas sorológicas inconclusivas". [Internet] [Masters thesis]. University of São Paulo; 2006. [cited 2021 May 09]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5134/tde-03052006-133432/.

Council of Science Editors:

Yamamoto CRF. "Diagnóstico da doença de Chagas em bancos de sangue: linfoproliferação, detecção de anticorpos e estudo epidemiológico em indivíduos com provas sorológicas inconclusivas". [Masters Thesis]. University of São Paulo; 2006. Available from: http://www.teses.usp.br/teses/disponiveis/5/5134/tde-03052006-133432/

21. Fabiana Maria de Souza Leoratti. "Resposta imune humoral na malária humana: quantidade e qualidade de anticorpos anti-Plasmodium falciparum".

Degree: 2004, University of São Paulo

Neste estudo avaliamos a resposta imune humoral de indivíduos naturalmente expostos à malária em áreas endêmicas no Brasil. Os anticorpos IgG, IgG1, IgG2, IgG3, IgG4,… (more)

Subjects/Keywords: AFINIDADE DE ANTICORPOS/imunologia; ELISA/métodos; FORMAÇÃO DE ANTICORPOS/imunologia; IGE/imunologia; IGG/imunologia; MALÁRIA/epidemiologia; MALÁRIA/imunologia; PLASMODIUM FALCIPARUM/imunologia; ANTIBODY AFFINITY/immunology; ANTIBODY FORMATION/immunology; BLACKWATER FEVER/epidemiology; BLACKWATER FEVER/immunology; ENZYME-LINKED IMMUNOSORBENT ASSAY/methods; IMMUNOGLOBULIN E/immunology; IMMUNOGLOBULIN G/immunology; PLASMODIUM FALCIPARUM/immunology

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APA (6th Edition):

Leoratti, F. M. d. S. (2004). "Resposta imune humoral na malária humana: quantidade e qualidade de anticorpos anti-Plasmodium falciparum". (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5160/tde-04102005-144150/

Chicago Manual of Style (16th Edition):

Leoratti, Fabiana Maria de Souza. “"Resposta imune humoral na malária humana: quantidade e qualidade de anticorpos anti-Plasmodium falciparum".” 2004. Masters Thesis, University of São Paulo. Accessed May 09, 2021. http://www.teses.usp.br/teses/disponiveis/5/5160/tde-04102005-144150/.

MLA Handbook (7th Edition):

Leoratti, Fabiana Maria de Souza. “"Resposta imune humoral na malária humana: quantidade e qualidade de anticorpos anti-Plasmodium falciparum".” 2004. Web. 09 May 2021.

Vancouver:

Leoratti FMdS. "Resposta imune humoral na malária humana: quantidade e qualidade de anticorpos anti-Plasmodium falciparum". [Internet] [Masters thesis]. University of São Paulo; 2004. [cited 2021 May 09]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5160/tde-04102005-144150/.

Council of Science Editors:

Leoratti FMdS. "Resposta imune humoral na malária humana: quantidade e qualidade de anticorpos anti-Plasmodium falciparum". [Masters Thesis]. University of São Paulo; 2004. Available from: http://www.teses.usp.br/teses/disponiveis/5/5160/tde-04102005-144150/

22. Maury Massani Tanji. Resposta imune celular a diferentes antígenos micobacterianos em indivíduos infectados por Mycobacterium tuberculosis: avaliação por elispot, elisa e linfoproliferação.

Degree: 2005, University of São Paulo

A tuberculose é uma doença crônica granulomatosa caracterizada por um déficit de imunidade antígeno específica do hospedeiro, cuja resposta imune é ativamente regulada por citocinas.… (more)

Subjects/Keywords: Citocinas/análise; Elisa/métodos; Interleucina-S/análise; Leucócitos mononucleares/imunologia; Micobacteriose/imunologia; Mycobacterium tuberculosis/imunologia; Tuberculose/imunologia; Cytokines/analysis; Enzyme-linked immunosorbent assay/methods; Interleukin-5/analysis; Leukocytes mononuclear/immunology; Mycobacterium infections/immunology; Mycobacterium tuberculosis/immunology; Tuberculosis/immunology

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APA (6th Edition):

Tanji, M. M. (2005). Resposta imune celular a diferentes antígenos micobacterianos em indivíduos infectados por Mycobacterium tuberculosis: avaliação por elispot, elisa e linfoproliferação. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5160/tde-31102006-113056/

Chicago Manual of Style (16th Edition):

Tanji, Maury Massani. “Resposta imune celular a diferentes antígenos micobacterianos em indivíduos infectados por Mycobacterium tuberculosis: avaliação por elispot, elisa e linfoproliferação.” 2005. Doctoral Dissertation, University of São Paulo. Accessed May 09, 2021. http://www.teses.usp.br/teses/disponiveis/5/5160/tde-31102006-113056/.

MLA Handbook (7th Edition):

Tanji, Maury Massani. “Resposta imune celular a diferentes antígenos micobacterianos em indivíduos infectados por Mycobacterium tuberculosis: avaliação por elispot, elisa e linfoproliferação.” 2005. Web. 09 May 2021.

Vancouver:

Tanji MM. Resposta imune celular a diferentes antígenos micobacterianos em indivíduos infectados por Mycobacterium tuberculosis: avaliação por elispot, elisa e linfoproliferação. [Internet] [Doctoral dissertation]. University of São Paulo; 2005. [cited 2021 May 09]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5160/tde-31102006-113056/.

Council of Science Editors:

Tanji MM. Resposta imune celular a diferentes antígenos micobacterianos em indivíduos infectados por Mycobacterium tuberculosis: avaliação por elispot, elisa e linfoproliferação. [Doctoral Dissertation]. University of São Paulo; 2005. Available from: http://www.teses.usp.br/teses/disponiveis/5/5160/tde-31102006-113056/


Georgia Tech

23. Jones, Christina Michele. Applications and challenges in mass spectrometry-based untargeted metabolomics.

Degree: PhD, Chemistry and Biochemistry, 2015, Georgia Tech

 Metabolomics is the methodical scientific study of biochemical processes associated with the metabolome—which comprises the entire collection of metabolites in any biological entity. Metabolome changes… (more)

Subjects/Keywords: Metabolomics; Untargeted metabolomics; Metabolite profiling; Metabolite fingerprinting; Mass spectrometry; Oncometabolomics; Ecometabolomics; Serum metabolomics; Systems biology; Proteomics; Cancer detection; Early detection; Biomarkers; Prostate cancer; Prostate cancer detection; Machine learning methods; Support vector machines; In vitro diagnostic multivariate index assay; IVDMIA; Ovarian cancer; Ovarian cancer detection; Mouse models; DKO mouse model; Early stage cancer detection; Chemically mediated interactions; Chemical ecology; Karenia brevis; Allelopathy; Red tide; Ambient mass spectrometry; Ultra performance liquid chromatography; Direct analysis in real time; DART; Transmission mode DART; Probe mode DART; Traveling wave ion mobility-mass spectrometry; TWIMS; Exhaled breath condensate; Cystic fibrosis

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

APA (6th Edition):

Jones, C. M. (2015). Applications and challenges in mass spectrometry-based untargeted metabolomics. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/54830

Chicago Manual of Style (16th Edition):

Jones, Christina Michele. “Applications and challenges in mass spectrometry-based untargeted metabolomics.” 2015. Doctoral Dissertation, Georgia Tech. Accessed May 09, 2021. http://hdl.handle.net/1853/54830.

MLA Handbook (7th Edition):

Jones, Christina Michele. “Applications and challenges in mass spectrometry-based untargeted metabolomics.” 2015. Web. 09 May 2021.

Vancouver:

Jones CM. Applications and challenges in mass spectrometry-based untargeted metabolomics. [Internet] [Doctoral dissertation]. Georgia Tech; 2015. [cited 2021 May 09]. Available from: http://hdl.handle.net/1853/54830.

Council of Science Editors:

Jones CM. Applications and challenges in mass spectrometry-based untargeted metabolomics. [Doctoral Dissertation]. Georgia Tech; 2015. Available from: http://hdl.handle.net/1853/54830

24. Marco Antonio Arap. Estudo da proteína de choque térmico GRP78 para o desenvolvimento de um sistema de receptor-ligante para o câncer de próstata.

Degree: 2003, University of São Paulo

Introdução: Apesar dos avanços nas técnicas de diagnóstico e tratamento, o câncer de próstata avançado ainda é uma condição letal. Terapêuticas mais eficazes são necessárias… (more)

Subjects/Keywords: Bacteriófagos/crescimento & desenvolvimento; Bacteriófagos/genética; Camundongos nus; Elisa/métodos; Estadiamento de neoplasias; Expressão gênica/genética; Imunohistoquímica/métodos; Ligantes; Marcadores biológicos de tumor/análise; Metástase neoplásica; Neoplasias prostáticas/diagnóstico; Neoplasias prostáticas/genética; Sítios de ligação (microbiologia)/genética; Attachment sites microbiological/genetics; Bacteriophages/genetics; Bacteriophages/growth & development; Biological markers/analysis; Enzyme-linked immunosorbent assay/methods; Gene expression/genetics; Immunohistochemistry/methods; Ligands; Mice nude; Neoplasm metastasis; Neoplasm staging; Prostatic neoplasms/diagnosis; Prostatic neoplasms/genetics

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

APA (6th Edition):

Arap, M. A. (2003). Estudo da proteína de choque térmico GRP78 para o desenvolvimento de um sistema de receptor-ligante para o câncer de próstata. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5153/tde-31052007-122749/

Chicago Manual of Style (16th Edition):

Arap, Marco Antonio. “Estudo da proteína de choque térmico GRP78 para o desenvolvimento de um sistema de receptor-ligante para o câncer de próstata.” 2003. Doctoral Dissertation, University of São Paulo. Accessed May 09, 2021. http://www.teses.usp.br/teses/disponiveis/5/5153/tde-31052007-122749/.

MLA Handbook (7th Edition):

Arap, Marco Antonio. “Estudo da proteína de choque térmico GRP78 para o desenvolvimento de um sistema de receptor-ligante para o câncer de próstata.” 2003. Web. 09 May 2021.

Vancouver:

Arap MA. Estudo da proteína de choque térmico GRP78 para o desenvolvimento de um sistema de receptor-ligante para o câncer de próstata. [Internet] [Doctoral dissertation]. University of São Paulo; 2003. [cited 2021 May 09]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5153/tde-31052007-122749/.

Council of Science Editors:

Arap MA. Estudo da proteína de choque térmico GRP78 para o desenvolvimento de um sistema de receptor-ligante para o câncer de próstata. [Doctoral Dissertation]. University of São Paulo; 2003. Available from: http://www.teses.usp.br/teses/disponiveis/5/5153/tde-31052007-122749/

25. Barker, Megan. Structural Investigation of Processing α-Glucosidase I from Saccharomyces cerevisiae.

Degree: 2010, University of Toronto

N-glycosylation is the most common eukaryotic post-translational modification, impacting on protein stability, folding, and protein-protein interactions. More broadly, N-glycans play biological roles in reaction kinetics… (more)

Subjects/Keywords: Biomolecular structure; Eukaryotic glycosylation; glycosylation; N-glycan; N-linked glycosylation; Carbohydrate; biochemistry; Inhibitor; antiviral therapeutic; Structure-based drug design; glucosidase; glycosidase; glycoside hydrolase; post-translational modification; enzyme; enzyme mechanism; inverting mechanism; structural biology; protein structure; 6xHis tag; Crystal packing; sugar; substrate; X-ray crystallography; single anomalous dispersion; PHENIX; heavy-atom phasing; docking; autodock; autodock vina; biophysical methods; tryptophan fluorescence; glucose oxidase; activity assay; enzyme inhibition; Protein expression; Protein purification; Pichia pastoris; Saccharomyces cerevisiae; fondue; AOX1 promoter; glycoside hydrolysis; substrate binding model; molecular dynamics; molecular dynamics; Binding site; Active site cleft; Endoplasmic reticulum; Glycan processing; Glycan trimming; protein-protein interactions; cell-cell communication; X-ray diffraction; crystallization; secreted protein; substrate selectivity; kojibiose; glucotriose; miglitol; deoxynojirimycin; Glc3Man9GlcNAc2; free oligosaccharide species; GluI; Cwh41; Cwh41p; Cwht1p; 0306; 0307; 0760

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

APA (6th Edition):

Barker, M. (2010). Structural Investigation of Processing α-Glucosidase I from Saccharomyces cerevisiae. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/32660

Chicago Manual of Style (16th Edition):

Barker, Megan. “Structural Investigation of Processing α-Glucosidase I from Saccharomyces cerevisiae.” 2010. Doctoral Dissertation, University of Toronto. Accessed May 09, 2021. http://hdl.handle.net/1807/32660.

MLA Handbook (7th Edition):

Barker, Megan. “Structural Investigation of Processing α-Glucosidase I from Saccharomyces cerevisiae.” 2010. Web. 09 May 2021.

Vancouver:

Barker M. Structural Investigation of Processing α-Glucosidase I from Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. University of Toronto; 2010. [cited 2021 May 09]. Available from: http://hdl.handle.net/1807/32660.

Council of Science Editors:

Barker M. Structural Investigation of Processing α-Glucosidase I from Saccharomyces cerevisiae. [Doctoral Dissertation]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/32660


University of Waterloo

26. 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 May 09, 2021. 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. 09 May 2021.

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 2021 May 09]. 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

.