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You searched for subject:(Metabolic Labeling). Showing records 1 – 16 of 16 total matches.

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University of Illinois – Urbana-Champaign

1. Kim, Raehyun. Investigating sphingolipid behavior and function using metabolic labeling.

Degree: PhD, Chemical Engineering, 2016, University of Illinois – Urbana-Champaign

 The past few decades of research have accumulated a body of evidence that membrane lipids are far more than merely the structural components of biological… (more)

Subjects/Keywords: Sphingolipids; Lipids; Isotope labeling; Metabolic labeling

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APA (6th Edition):

Kim, R. (2016). Investigating sphingolipid behavior and function using metabolic labeling. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/93059

Chicago Manual of Style (16th Edition):

Kim, Raehyun. “Investigating sphingolipid behavior and function using metabolic labeling.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed December 07, 2019. http://hdl.handle.net/2142/93059.

MLA Handbook (7th Edition):

Kim, Raehyun. “Investigating sphingolipid behavior and function using metabolic labeling.” 2016. Web. 07 Dec 2019.

Vancouver:

Kim R. Investigating sphingolipid behavior and function using metabolic labeling. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Dec 07]. Available from: http://hdl.handle.net/2142/93059.

Council of Science Editors:

Kim R. Investigating sphingolipid behavior and function using metabolic labeling. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/93059


University of Windsor

2. Rizzo, Christina Marisa. Model Systems to Explore CPB2 Pre-mRNA Splicing.

Degree: MS, Chemistry and Biochemistry, 2014, University of Windsor

  Thrombin Activatable Fibrinolysis Inhibitor (TAFI), encoded by CPB2, cleaves carboxyl-terminal lysine residues from partially degraded fibrin, thus assisting in the attenuation of fibrinolysis. The… (more)

Subjects/Keywords: Alternative Splicing; CPB2; Metabolic Labeling; Minigene; Real Time RT-PCR; TAFI

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APA (6th Edition):

Rizzo, C. M. (2014). Model Systems to Explore CPB2 Pre-mRNA Splicing. (Masters Thesis). University of Windsor. Retrieved from http://scholar.uwindsor.ca/etd/5176

Chicago Manual of Style (16th Edition):

Rizzo, Christina Marisa. “Model Systems to Explore CPB2 Pre-mRNA Splicing.” 2014. Masters Thesis, University of Windsor. Accessed December 07, 2019. http://scholar.uwindsor.ca/etd/5176.

MLA Handbook (7th Edition):

Rizzo, Christina Marisa. “Model Systems to Explore CPB2 Pre-mRNA Splicing.” 2014. Web. 07 Dec 2019.

Vancouver:

Rizzo CM. Model Systems to Explore CPB2 Pre-mRNA Splicing. [Internet] [Masters thesis]. University of Windsor; 2014. [cited 2019 Dec 07]. Available from: http://scholar.uwindsor.ca/etd/5176.

Council of Science Editors:

Rizzo CM. Model Systems to Explore CPB2 Pre-mRNA Splicing. [Masters Thesis]. University of Windsor; 2014. Available from: http://scholar.uwindsor.ca/etd/5176


University of Windsor

3. Rizzo, Christina Marisa. Model Systems to Explore CPB2 Pre-mRNA Splicing.

Degree: MS, Chemistry and Biochemistry, 2014, University of Windsor

  Thrombin Activatable Fibrinolysis Inhibitor (TAFI), encoded by CPB2, cleaves carboxyl-terminal lysine residues from partially degraded fibrin, thus assisting in the attenuation of fibrinolysis. The… (more)

Subjects/Keywords: Alternative Splicing; CPB2; Metabolic Labeling; Minigene; Real Time RT-PCR; TAFI

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APA (6th Edition):

Rizzo, C. M. (2014). Model Systems to Explore CPB2 Pre-mRNA Splicing. (Masters Thesis). University of Windsor. Retrieved from https://scholar.uwindsor.ca/etd/5176

Chicago Manual of Style (16th Edition):

Rizzo, Christina Marisa. “Model Systems to Explore CPB2 Pre-mRNA Splicing.” 2014. Masters Thesis, University of Windsor. Accessed December 07, 2019. https://scholar.uwindsor.ca/etd/5176.

MLA Handbook (7th Edition):

Rizzo, Christina Marisa. “Model Systems to Explore CPB2 Pre-mRNA Splicing.” 2014. Web. 07 Dec 2019.

Vancouver:

Rizzo CM. Model Systems to Explore CPB2 Pre-mRNA Splicing. [Internet] [Masters thesis]. University of Windsor; 2014. [cited 2019 Dec 07]. Available from: https://scholar.uwindsor.ca/etd/5176.

Council of Science Editors:

Rizzo CM. Model Systems to Explore CPB2 Pre-mRNA Splicing. [Masters Thesis]. University of Windsor; 2014. Available from: https://scholar.uwindsor.ca/etd/5176


ETH Zürich

4. Liphardt, Thomas. Efficient computational methods for sampling-based metabolic flux analysis.

Degree: 2018, ETH Zürich

 The aim of metabolic flux analysis is to determine the rates at which the processes in metabolism take place. Stationary isotopomer labeling experiments are the… (more)

Subjects/Keywords: Sampling methods; Metabolic Flux Analysis; Isotopomer labeling experiments; MCMC methods

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APA (6th Edition):

Liphardt, T. (2018). Efficient computational methods for sampling-based metabolic flux analysis. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/271574

Chicago Manual of Style (16th Edition):

Liphardt, Thomas. “Efficient computational methods for sampling-based metabolic flux analysis.” 2018. Doctoral Dissertation, ETH Zürich. Accessed December 07, 2019. http://hdl.handle.net/20.500.11850/271574.

MLA Handbook (7th Edition):

Liphardt, Thomas. “Efficient computational methods for sampling-based metabolic flux analysis.” 2018. Web. 07 Dec 2019.

Vancouver:

Liphardt T. Efficient computational methods for sampling-based metabolic flux analysis. [Internet] [Doctoral dissertation]. ETH Zürich; 2018. [cited 2019 Dec 07]. Available from: http://hdl.handle.net/20.500.11850/271574.

Council of Science Editors:

Liphardt T. Efficient computational methods for sampling-based metabolic flux analysis. [Doctoral Dissertation]. ETH Zürich; 2018. Available from: http://hdl.handle.net/20.500.11850/271574


University of Toronto

5. Lugowski, Andrew Robert. Transcriptome-wide Measurements of mRNA Stability.

Degree: 2017, University of Toronto

Numerous regulatory processes work at the level of RNA to ensure proper control of gene expression. Of these, transcription and decay are particularly important as… (more)

Subjects/Keywords: 4-thiouridine; DRUID; introns; metabolic labeling; RNA degradation; transcription inhibition; 0307

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APA (6th Edition):

Lugowski, A. R. (2017). Transcriptome-wide Measurements of mRNA Stability. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/79302

Chicago Manual of Style (16th Edition):

Lugowski, Andrew Robert. “Transcriptome-wide Measurements of mRNA Stability.” 2017. Masters Thesis, University of Toronto. Accessed December 07, 2019. http://hdl.handle.net/1807/79302.

MLA Handbook (7th Edition):

Lugowski, Andrew Robert. “Transcriptome-wide Measurements of mRNA Stability.” 2017. Web. 07 Dec 2019.

Vancouver:

Lugowski AR. Transcriptome-wide Measurements of mRNA Stability. [Internet] [Masters thesis]. University of Toronto; 2017. [cited 2019 Dec 07]. Available from: http://hdl.handle.net/1807/79302.

Council of Science Editors:

Lugowski AR. Transcriptome-wide Measurements of mRNA Stability. [Masters Thesis]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/79302


Northeastern University

6. Quijada, Jeniffer del Valle. Tunable Intact Protein Mass Increases (TIPMI) as a simple and affordable method for relative intact protein quantitation and intact protein turnover rate optimized for Top-Down Liquid Chromatography-Mass Spectrometry (LC-MS) approach.

Degree: PhD, Department of Chemistry and Chemical Biology, 2017, Northeastern University

 Mass spectrometry studies of most proteins is preceded by their endoproteinase digestion into peptides. This experimental step is a vestige of a time when mass… (more)

Subjects/Keywords: intact protein; mass spectrometry; metabolic labeling; relative quantitation; turnover rate

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APA (6th Edition):

Quijada, J. d. V. (2017). Tunable Intact Protein Mass Increases (TIPMI) as a simple and affordable method for relative intact protein quantitation and intact protein turnover rate optimized for Top-Down Liquid Chromatography-Mass Spectrometry (LC-MS) approach. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/D20248916

Chicago Manual of Style (16th Edition):

Quijada, Jeniffer del Valle. “Tunable Intact Protein Mass Increases (TIPMI) as a simple and affordable method for relative intact protein quantitation and intact protein turnover rate optimized for Top-Down Liquid Chromatography-Mass Spectrometry (LC-MS) approach.” 2017. Doctoral Dissertation, Northeastern University. Accessed December 07, 2019. http://hdl.handle.net/2047/D20248916.

MLA Handbook (7th Edition):

Quijada, Jeniffer del Valle. “Tunable Intact Protein Mass Increases (TIPMI) as a simple and affordable method for relative intact protein quantitation and intact protein turnover rate optimized for Top-Down Liquid Chromatography-Mass Spectrometry (LC-MS) approach.” 2017. Web. 07 Dec 2019.

Vancouver:

Quijada JdV. Tunable Intact Protein Mass Increases (TIPMI) as a simple and affordable method for relative intact protein quantitation and intact protein turnover rate optimized for Top-Down Liquid Chromatography-Mass Spectrometry (LC-MS) approach. [Internet] [Doctoral dissertation]. Northeastern University; 2017. [cited 2019 Dec 07]. Available from: http://hdl.handle.net/2047/D20248916.

Council of Science Editors:

Quijada JdV. Tunable Intact Protein Mass Increases (TIPMI) as a simple and affordable method for relative intact protein quantitation and intact protein turnover rate optimized for Top-Down Liquid Chromatography-Mass Spectrometry (LC-MS) approach. [Doctoral Dissertation]. Northeastern University; 2017. Available from: http://hdl.handle.net/2047/D20248916


Iowa State University

7. Truong, Quyen Xuan. 13C-Metabolic flux analysis of soybean somatic embryos for identification of metabolic control points in developing seed.

Degree: 2012, Iowa State University

 Of the world's major agronomic food crops soybeans rank highest in protein content (~40% Dwt) while also containing significant quantities of oil (~20% Dwt). Based… (more)

Subjects/Keywords: carbon labeling; metabolic engineering; metabolic flux analysis; oil; protein; soybean; Agricultural Science; Agriculture; Biochemistry; Chemical Engineering; Plant Sciences

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APA (6th Edition):

Truong, Q. X. (2012). 13C-Metabolic flux analysis of soybean somatic embryos for identification of metabolic control points in developing seed. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/13274

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):

Truong, Quyen Xuan. “13C-Metabolic flux analysis of soybean somatic embryos for identification of metabolic control points in developing seed.” 2012. Thesis, Iowa State University. Accessed December 07, 2019. https://lib.dr.iastate.edu/etd/13274.

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

MLA Handbook (7th Edition):

Truong, Quyen Xuan. “13C-Metabolic flux analysis of soybean somatic embryos for identification of metabolic control points in developing seed.” 2012. Web. 07 Dec 2019.

Vancouver:

Truong QX. 13C-Metabolic flux analysis of soybean somatic embryos for identification of metabolic control points in developing seed. [Internet] [Thesis]. Iowa State University; 2012. [cited 2019 Dec 07]. Available from: https://lib.dr.iastate.edu/etd/13274.

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

Council of Science Editors:

Truong QX. 13C-Metabolic flux analysis of soybean somatic embryos for identification of metabolic control points in developing seed. [Thesis]. Iowa State University; 2012. Available from: https://lib.dr.iastate.edu/etd/13274

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


Iowa State University

8. Fu, Xinyu. Compartment-specific metabolism associated with acetyl-CoA and acyl carrier protein.

Degree: 2019, Iowa State University

 A characteristic feature of plant cells is the subcellular compartmentation of metabolism. Duplicated enzymes or cofactors occur in the same or distinct compartments, posing a… (more)

Subjects/Keywords: acetate; acetyl-CoA; acyl carrier protein; metabolic compartmentaion; metabolic flux; stable isotope labeling; Agriculture; Biochemistry; Plant Sciences

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APA (6th Edition):

Fu, X. (2019). Compartment-specific metabolism associated with acetyl-CoA and acyl carrier protein. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/17448

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):

Fu, Xinyu. “Compartment-specific metabolism associated with acetyl-CoA and acyl carrier protein.” 2019. Thesis, Iowa State University. Accessed December 07, 2019. https://lib.dr.iastate.edu/etd/17448.

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

MLA Handbook (7th Edition):

Fu, Xinyu. “Compartment-specific metabolism associated with acetyl-CoA and acyl carrier protein.” 2019. Web. 07 Dec 2019.

Vancouver:

Fu X. Compartment-specific metabolism associated with acetyl-CoA and acyl carrier protein. [Internet] [Thesis]. Iowa State University; 2019. [cited 2019 Dec 07]. Available from: https://lib.dr.iastate.edu/etd/17448.

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

Council of Science Editors:

Fu X. Compartment-specific metabolism associated with acetyl-CoA and acyl carrier protein. [Thesis]. Iowa State University; 2019. Available from: https://lib.dr.iastate.edu/etd/17448

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


University of Washington

9. Basisty, Natan. Proteome Turnover in Mouse Aging: In Vivo Studies by Stable Isotope Mass Spectrometry.

Degree: PhD, 2016, University of Washington

 Introduction: Maintenance of proper protein homeostasis (proteostasis) is essential to cellular and organismal health. A wealth of research has shown that age-related diseases and conditions… (more)

Subjects/Keywords: Longevity; Mass Spectrometry; Metabolic Labeling; Mitochondria; Protein Homeostasis; Reactive Oxygen Species; Aging; Biology; Gerontology; pathology

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APA (6th Edition):

Basisty, N. (2016). Proteome Turnover in Mouse Aging: In Vivo Studies by Stable Isotope Mass Spectrometry. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/35291

Chicago Manual of Style (16th Edition):

Basisty, Natan. “Proteome Turnover in Mouse Aging: In Vivo Studies by Stable Isotope Mass Spectrometry.” 2016. Doctoral Dissertation, University of Washington. Accessed December 07, 2019. http://hdl.handle.net/1773/35291.

MLA Handbook (7th Edition):

Basisty, Natan. “Proteome Turnover in Mouse Aging: In Vivo Studies by Stable Isotope Mass Spectrometry.” 2016. Web. 07 Dec 2019.

Vancouver:

Basisty N. Proteome Turnover in Mouse Aging: In Vivo Studies by Stable Isotope Mass Spectrometry. [Internet] [Doctoral dissertation]. University of Washington; 2016. [cited 2019 Dec 07]. Available from: http://hdl.handle.net/1773/35291.

Council of Science Editors:

Basisty N. Proteome Turnover in Mouse Aging: In Vivo Studies by Stable Isotope Mass Spectrometry. [Doctoral Dissertation]. University of Washington; 2016. Available from: http://hdl.handle.net/1773/35291


Vanderbilt University

10. Jazmin, Lara Jeline. Mapping Photoautotrophic Metabolism of Cyanobacterial and Plant Systems with Isotopically Nonstationary 13C Metabolic Flux Analysis.

Degree: PhD, Chemical Engineering, 2015, Vanderbilt University

 Photoautotrophic metabolism represents the primary source of all food on earth as well as raw materials for bio-based production of fuels and chemicals. Therefore, improving… (more)

Subjects/Keywords: metabolic flux analysis; arabidopsis thaliana; cyanobacteria; INST-MFA; 13C labeling experiments; photoautotrophic metabolism

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APA (6th Edition):

Jazmin, L. J. (2015). Mapping Photoautotrophic Metabolism of Cyanobacterial and Plant Systems with Isotopically Nonstationary 13C Metabolic Flux Analysis. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-11232015-165833/ ;

Chicago Manual of Style (16th Edition):

Jazmin, Lara Jeline. “Mapping Photoautotrophic Metabolism of Cyanobacterial and Plant Systems with Isotopically Nonstationary 13C Metabolic Flux Analysis.” 2015. Doctoral Dissertation, Vanderbilt University. Accessed December 07, 2019. http://etd.library.vanderbilt.edu/available/etd-11232015-165833/ ;.

MLA Handbook (7th Edition):

Jazmin, Lara Jeline. “Mapping Photoautotrophic Metabolism of Cyanobacterial and Plant Systems with Isotopically Nonstationary 13C Metabolic Flux Analysis.” 2015. Web. 07 Dec 2019.

Vancouver:

Jazmin LJ. Mapping Photoautotrophic Metabolism of Cyanobacterial and Plant Systems with Isotopically Nonstationary 13C Metabolic Flux Analysis. [Internet] [Doctoral dissertation]. Vanderbilt University; 2015. [cited 2019 Dec 07]. Available from: http://etd.library.vanderbilt.edu/available/etd-11232015-165833/ ;.

Council of Science Editors:

Jazmin LJ. Mapping Photoautotrophic Metabolism of Cyanobacterial and Plant Systems with Isotopically Nonstationary 13C Metabolic Flux Analysis. [Doctoral Dissertation]. Vanderbilt University; 2015. Available from: http://etd.library.vanderbilt.edu/available/etd-11232015-165833/ ;


University of Minnesota

11. Fan, Kai-Ting. Analysis of Proteome-scale Protein Turnover in Arabidopsis thaliana Seedlings and Its Application to the Plant Heat Stress Response.

Degree: PhD, Plant Biological Sciences, 2015, University of Minnesota

 Protein turnover, the balance between protein synthesis and degradation, is an important aspect of the regulation of cellular processes for organisms as they respond to… (more)

Subjects/Keywords: Arabidopsis thaliana; heat stress; metabolic labeling; protein turnover rates; proteome dynamics; stable isotope

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APA (6th Edition):

Fan, K. (2015). Analysis of Proteome-scale Protein Turnover in Arabidopsis thaliana Seedlings and Its Application to the Plant Heat Stress Response. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/182834

Chicago Manual of Style (16th Edition):

Fan, Kai-Ting. “Analysis of Proteome-scale Protein Turnover in Arabidopsis thaliana Seedlings and Its Application to the Plant Heat Stress Response.” 2015. Doctoral Dissertation, University of Minnesota. Accessed December 07, 2019. http://hdl.handle.net/11299/182834.

MLA Handbook (7th Edition):

Fan, Kai-Ting. “Analysis of Proteome-scale Protein Turnover in Arabidopsis thaliana Seedlings and Its Application to the Plant Heat Stress Response.” 2015. Web. 07 Dec 2019.

Vancouver:

Fan K. Analysis of Proteome-scale Protein Turnover in Arabidopsis thaliana Seedlings and Its Application to the Plant Heat Stress Response. [Internet] [Doctoral dissertation]. University of Minnesota; 2015. [cited 2019 Dec 07]. Available from: http://hdl.handle.net/11299/182834.

Council of Science Editors:

Fan K. Analysis of Proteome-scale Protein Turnover in Arabidopsis thaliana Seedlings and Its Application to the Plant Heat Stress Response. [Doctoral Dissertation]. University of Minnesota; 2015. Available from: http://hdl.handle.net/11299/182834


Université de Grenoble

12. Pegeot, Mathieu. Etudes structurales par RMN des profils Saccharidiques d'Héparanes sulfates et de leur régulation cellulaire : Mise en place d'un protocole de marquage, de purification et d'analyse de chaines entières : Structural studies of heparan sulfate profiles and their cellular regulation by nmr : set up of a labeling and purification protocol for full-length chains analysis.

Degree: Docteur es, Biologie structurale et nanobiologie, 2014, Université de Grenoble

Les glycosaminoglycanes (GAG) forment une famille de polysaccharides linéaires retrouvés dans tous les tissus, au niveau des matrices extracellulaires et des surfaces cellulaires. Les héparanes… (more)

Subjects/Keywords: Héparane Sulfate; Résonance Magnétique Nucléaire; Sulfatation; Epimérisation; Purification; Marquage Métabolique; Heparan Sulfate; Nuclear Magnetic Resonance; Sulfation; Epimerization; Purification; Metabolic Labeling; 570

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APA (6th Edition):

Pegeot, M. (2014). Etudes structurales par RMN des profils Saccharidiques d'Héparanes sulfates et de leur régulation cellulaire : Mise en place d'un protocole de marquage, de purification et d'analyse de chaines entières : Structural studies of heparan sulfate profiles and their cellular regulation by nmr : set up of a labeling and purification protocol for full-length chains analysis. (Doctoral Dissertation). Université de Grenoble. Retrieved from http://www.theses.fr/2014GRENV056

Chicago Manual of Style (16th Edition):

Pegeot, Mathieu. “Etudes structurales par RMN des profils Saccharidiques d'Héparanes sulfates et de leur régulation cellulaire : Mise en place d'un protocole de marquage, de purification et d'analyse de chaines entières : Structural studies of heparan sulfate profiles and their cellular regulation by nmr : set up of a labeling and purification protocol for full-length chains analysis.” 2014. Doctoral Dissertation, Université de Grenoble. Accessed December 07, 2019. http://www.theses.fr/2014GRENV056.

MLA Handbook (7th Edition):

Pegeot, Mathieu. “Etudes structurales par RMN des profils Saccharidiques d'Héparanes sulfates et de leur régulation cellulaire : Mise en place d'un protocole de marquage, de purification et d'analyse de chaines entières : Structural studies of heparan sulfate profiles and their cellular regulation by nmr : set up of a labeling and purification protocol for full-length chains analysis.” 2014. Web. 07 Dec 2019.

Vancouver:

Pegeot M. Etudes structurales par RMN des profils Saccharidiques d'Héparanes sulfates et de leur régulation cellulaire : Mise en place d'un protocole de marquage, de purification et d'analyse de chaines entières : Structural studies of heparan sulfate profiles and their cellular regulation by nmr : set up of a labeling and purification protocol for full-length chains analysis. [Internet] [Doctoral dissertation]. Université de Grenoble; 2014. [cited 2019 Dec 07]. Available from: http://www.theses.fr/2014GRENV056.

Council of Science Editors:

Pegeot M. Etudes structurales par RMN des profils Saccharidiques d'Héparanes sulfates et de leur régulation cellulaire : Mise en place d'un protocole de marquage, de purification et d'analyse de chaines entières : Structural studies of heparan sulfate profiles and their cellular regulation by nmr : set up of a labeling and purification protocol for full-length chains analysis. [Doctoral Dissertation]. Université de Grenoble; 2014. Available from: http://www.theses.fr/2014GRENV056

13. Fourmois, Laura. Marquage métabolique de glycanes : diagnostic et approches thérapeutiques : Metabolic labeling of glycans : diagnostic and therapeutic approaches.

Degree: Docteur es, Chimie, 2016, Paris Saclay

 Cette thèse porte sur la méthode de marquage métabolique de glycanes. Elle consiste à utiliser des monosaccharides modifiés pouvant être métaboliquement introduits sur la membrane… (more)

Subjects/Keywords: Marquage métabolique; Glycanes; Chimie click; Molécules recrutant les anticorps; Chimie organique; Metabolic labeling; Glycans; Click chemistry; Antibody recruiting molecules; Organic chemistry

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APA (6th Edition):

Fourmois, L. (2016). Marquage métabolique de glycanes : diagnostic et approches thérapeutiques : Metabolic labeling of glycans : diagnostic and therapeutic approaches. (Doctoral Dissertation). Paris Saclay. Retrieved from http://www.theses.fr/2016SACLS262

Chicago Manual of Style (16th Edition):

Fourmois, Laura. “Marquage métabolique de glycanes : diagnostic et approches thérapeutiques : Metabolic labeling of glycans : diagnostic and therapeutic approaches.” 2016. Doctoral Dissertation, Paris Saclay. Accessed December 07, 2019. http://www.theses.fr/2016SACLS262.

MLA Handbook (7th Edition):

Fourmois, Laura. “Marquage métabolique de glycanes : diagnostic et approches thérapeutiques : Metabolic labeling of glycans : diagnostic and therapeutic approaches.” 2016. Web. 07 Dec 2019.

Vancouver:

Fourmois L. Marquage métabolique de glycanes : diagnostic et approches thérapeutiques : Metabolic labeling of glycans : diagnostic and therapeutic approaches. [Internet] [Doctoral dissertation]. Paris Saclay; 2016. [cited 2019 Dec 07]. Available from: http://www.theses.fr/2016SACLS262.

Council of Science Editors:

Fourmois L. Marquage métabolique de glycanes : diagnostic et approches thérapeutiques : Metabolic labeling of glycans : diagnostic and therapeutic approaches. [Doctoral Dissertation]. Paris Saclay; 2016. Available from: http://www.theses.fr/2016SACLS262


Rice University

14. Thomas, Emily Elizabeth. Post-Translational Control over Metabolic Labeling of Newly Synthesized Proteins.

Degree: PhD, Natural Sciences, 2018, Rice University

 A variety of aminoacyl-tRNA synthetases (aaRSs) have had their substrate specificities altered through protein engineering to create mutant aaRSs that can charge tRNA with noncanonical… (more)

Subjects/Keywords: amino acyl tRNA synthetase; domain insertion; metabolic labeling; noncanonical amino acid; protein engineering; protein fragment complementation; protein−protein interaction

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APA (6th Edition):

Thomas, E. E. (2018). Post-Translational Control over Metabolic Labeling of Newly Synthesized Proteins. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/105569

Chicago Manual of Style (16th Edition):

Thomas, Emily Elizabeth. “Post-Translational Control over Metabolic Labeling of Newly Synthesized Proteins.” 2018. Doctoral Dissertation, Rice University. Accessed December 07, 2019. http://hdl.handle.net/1911/105569.

MLA Handbook (7th Edition):

Thomas, Emily Elizabeth. “Post-Translational Control over Metabolic Labeling of Newly Synthesized Proteins.” 2018. Web. 07 Dec 2019.

Vancouver:

Thomas EE. Post-Translational Control over Metabolic Labeling of Newly Synthesized Proteins. [Internet] [Doctoral dissertation]. Rice University; 2018. [cited 2019 Dec 07]. Available from: http://hdl.handle.net/1911/105569.

Council of Science Editors:

Thomas EE. Post-Translational Control over Metabolic Labeling of Newly Synthesized Proteins. [Doctoral Dissertation]. Rice University; 2018. Available from: http://hdl.handle.net/1911/105569


Delft University of Technology

15. Suarez-Mendez, C.A. Dynamics of Storage Carbohydrates Metabolism in Saccharomyces cerevisiae.

Degree: 2015, Delft University of Technology

 Production of chemicals via biotechnological routes are becoming rapidly an alternative to oil-based processes. Several microorganisms including yeast, bacteria, fungi and algae can transform feedstocks… (more)

Subjects/Keywords: Trehalose and Glycogen metabolism; Dynamic fluxes; 13C labeling; Saccharomyces cerevisiae; Metabolic robustness

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

APA (6th Edition):

Suarez-Mendez, C. A. (2015). Dynamics of Storage Carbohydrates Metabolism in Saccharomyces cerevisiae. (Doctoral Dissertation). Delft University of Technology. Retrieved from http://resolver.tudelft.nl/uuid:2504bd76-9811-4d3c-a66b-3aae7fbb40b5 ; urn:NBN:nl:ui:24-uuid:2504bd76-9811-4d3c-a66b-3aae7fbb40b5 ; urn:NBN:nl:ui:24-uuid:2504bd76-9811-4d3c-a66b-3aae7fbb40b5 ; http://resolver.tudelft.nl/uuid:2504bd76-9811-4d3c-a66b-3aae7fbb40b5

Chicago Manual of Style (16th Edition):

Suarez-Mendez, C A. “Dynamics of Storage Carbohydrates Metabolism in Saccharomyces cerevisiae.” 2015. Doctoral Dissertation, Delft University of Technology. Accessed December 07, 2019. http://resolver.tudelft.nl/uuid:2504bd76-9811-4d3c-a66b-3aae7fbb40b5 ; urn:NBN:nl:ui:24-uuid:2504bd76-9811-4d3c-a66b-3aae7fbb40b5 ; urn:NBN:nl:ui:24-uuid:2504bd76-9811-4d3c-a66b-3aae7fbb40b5 ; http://resolver.tudelft.nl/uuid:2504bd76-9811-4d3c-a66b-3aae7fbb40b5.

MLA Handbook (7th Edition):

Suarez-Mendez, C A. “Dynamics of Storage Carbohydrates Metabolism in Saccharomyces cerevisiae.” 2015. Web. 07 Dec 2019.

Vancouver:

Suarez-Mendez CA. Dynamics of Storage Carbohydrates Metabolism in Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. Delft University of Technology; 2015. [cited 2019 Dec 07]. Available from: http://resolver.tudelft.nl/uuid:2504bd76-9811-4d3c-a66b-3aae7fbb40b5 ; urn:NBN:nl:ui:24-uuid:2504bd76-9811-4d3c-a66b-3aae7fbb40b5 ; urn:NBN:nl:ui:24-uuid:2504bd76-9811-4d3c-a66b-3aae7fbb40b5 ; http://resolver.tudelft.nl/uuid:2504bd76-9811-4d3c-a66b-3aae7fbb40b5.

Council of Science Editors:

Suarez-Mendez CA. Dynamics of Storage Carbohydrates Metabolism in Saccharomyces cerevisiae. [Doctoral Dissertation]. Delft University of Technology; 2015. Available from: http://resolver.tudelft.nl/uuid:2504bd76-9811-4d3c-a66b-3aae7fbb40b5 ; urn:NBN:nl:ui:24-uuid:2504bd76-9811-4d3c-a66b-3aae7fbb40b5 ; urn:NBN:nl:ui:24-uuid:2504bd76-9811-4d3c-a66b-3aae7fbb40b5 ; http://resolver.tudelft.nl/uuid:2504bd76-9811-4d3c-a66b-3aae7fbb40b5

16. Kovatcheva, P.P. Analyzing the functionality of the human intestinal microbiota by stable isotope probing.

Degree: 2010, NARCIS

  Key words: gut bacteria, dietary carbohydrates, digestion, RNA-SIP, TIM-2, HITChip, human trial The human gastro-intestinal (GI) tract comprises a series of complex and dynamic… (more)

Subjects/Keywords: darmmicro-organismen; koolhydraatmetabolisme; isotopenlabelling; Metabole processen; intestinal microorganisms; carbohydrate metabolism; isotope labeling; Metabolic Processes

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

APA (6th Edition):

Kovatcheva, P. P. (2010). Analyzing the functionality of the human intestinal microbiota by stable isotope probing. (Doctoral Dissertation). NARCIS. Retrieved from http://library.wur.nl/WebQuery/wurpubs/392958 ; urn:nbn:nl:ui:32-392958 ; urn:nbn:nl:ui:32-392958 ; http://library.wur.nl/WebQuery/wurpubs/392958

Chicago Manual of Style (16th Edition):

Kovatcheva, P P. “Analyzing the functionality of the human intestinal microbiota by stable isotope probing.” 2010. Doctoral Dissertation, NARCIS. Accessed December 07, 2019. http://library.wur.nl/WebQuery/wurpubs/392958 ; urn:nbn:nl:ui:32-392958 ; urn:nbn:nl:ui:32-392958 ; http://library.wur.nl/WebQuery/wurpubs/392958.

MLA Handbook (7th Edition):

Kovatcheva, P P. “Analyzing the functionality of the human intestinal microbiota by stable isotope probing.” 2010. Web. 07 Dec 2019.

Vancouver:

Kovatcheva PP. Analyzing the functionality of the human intestinal microbiota by stable isotope probing. [Internet] [Doctoral dissertation]. NARCIS; 2010. [cited 2019 Dec 07]. Available from: http://library.wur.nl/WebQuery/wurpubs/392958 ; urn:nbn:nl:ui:32-392958 ; urn:nbn:nl:ui:32-392958 ; http://library.wur.nl/WebQuery/wurpubs/392958.

Council of Science Editors:

Kovatcheva PP. Analyzing the functionality of the human intestinal microbiota by stable isotope probing. [Doctoral Dissertation]. NARCIS; 2010. Available from: http://library.wur.nl/WebQuery/wurpubs/392958 ; urn:nbn:nl:ui:32-392958 ; urn:nbn:nl:ui:32-392958 ; http://library.wur.nl/WebQuery/wurpubs/392958

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