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You searched for subject:(Structural Biology). Showing records 1 – 30 of 1431 total matches.

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University of Helsinki

1. Manole, Violeta. Structural studies on viral receptor-binding proteins.

Degree: Department of Biosciences; Institute of Biotechnology, 2012, University of Helsinki

Structure. Almost everything around us has it. But why? What is it needed for? Since the early days of human enquiry people have tried to… (more)

Subjects/Keywords: structural Biology; structural Biology

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APA (6th Edition):

Manole, V. (2012). Structural studies on viral receptor-binding proteins. (Doctoral Dissertation). University of Helsinki. Retrieved from http://hdl.handle.net/10138/36701

Chicago Manual of Style (16th Edition):

Manole, Violeta. “Structural studies on viral receptor-binding proteins.” 2012. Doctoral Dissertation, University of Helsinki. Accessed July 08, 2020. http://hdl.handle.net/10138/36701.

MLA Handbook (7th Edition):

Manole, Violeta. “Structural studies on viral receptor-binding proteins.” 2012. Web. 08 Jul 2020.

Vancouver:

Manole V. Structural studies on viral receptor-binding proteins. [Internet] [Doctoral dissertation]. University of Helsinki; 2012. [cited 2020 Jul 08]. Available from: http://hdl.handle.net/10138/36701.

Council of Science Editors:

Manole V. Structural studies on viral receptor-binding proteins. [Doctoral Dissertation]. University of Helsinki; 2012. Available from: http://hdl.handle.net/10138/36701

2. Liu, Zhen. Understanding and Targeting Lipid Metabolism of Mycobacterium tuberculosis.

Degree: 2013, Texas Digital Library

 Mycobacterium tuberculosis (M. tuberculosis) contains a wide array of genes responsible for the synthesis and secretion of a variety of bioactive lipids. The genes represent… (more)

Subjects/Keywords: Structural biology

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APA (6th Edition):

Liu, Z. (2013). Understanding and Targeting Lipid Metabolism of Mycobacterium tuberculosis. (Thesis). Texas Digital Library. Retrieved from http://hdl.handle.net/1969; http://hdl.handle.net/2249.1/66543

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):

Liu, Zhen. “Understanding and Targeting Lipid Metabolism of Mycobacterium tuberculosis.” 2013. Thesis, Texas Digital Library. Accessed July 08, 2020. http://hdl.handle.net/1969; http://hdl.handle.net/2249.1/66543.

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

MLA Handbook (7th Edition):

Liu, Zhen. “Understanding and Targeting Lipid Metabolism of Mycobacterium tuberculosis.” 2013. Web. 08 Jul 2020.

Vancouver:

Liu Z. Understanding and Targeting Lipid Metabolism of Mycobacterium tuberculosis. [Internet] [Thesis]. Texas Digital Library; 2013. [cited 2020 Jul 08]. Available from: http://hdl.handle.net/1969; http://hdl.handle.net/2249.1/66543.

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

Council of Science Editors:

Liu Z. Understanding and Targeting Lipid Metabolism of Mycobacterium tuberculosis. [Thesis]. Texas Digital Library; 2013. Available from: http://hdl.handle.net/1969; http://hdl.handle.net/2249.1/66543

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

3. Koveal, Dorothy Marie. Structural and functional investigation of protein phosphatases and scaffolds that regulate phosphorylation.

Degree: PhD, Molecular Biology, Cell Biology, and Biochemistry, 2013, Brown University

 Phosphorylation is an essential cellular regulatory mechanism that is conserved from invertebrates to mammals. Despite the simplicity of adding or subtracting a single phosphate molecule,… (more)

Subjects/Keywords: structural biology

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APA (6th Edition):

Koveal, D. M. (2013). Structural and functional investigation of protein phosphatases and scaffolds that regulate phosphorylation. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:320556/

Chicago Manual of Style (16th Edition):

Koveal, Dorothy Marie. “Structural and functional investigation of protein phosphatases and scaffolds that regulate phosphorylation.” 2013. Doctoral Dissertation, Brown University. Accessed July 08, 2020. https://repository.library.brown.edu/studio/item/bdr:320556/.

MLA Handbook (7th Edition):

Koveal, Dorothy Marie. “Structural and functional investigation of protein phosphatases and scaffolds that regulate phosphorylation.” 2013. Web. 08 Jul 2020.

Vancouver:

Koveal DM. Structural and functional investigation of protein phosphatases and scaffolds that regulate phosphorylation. [Internet] [Doctoral dissertation]. Brown University; 2013. [cited 2020 Jul 08]. Available from: https://repository.library.brown.edu/studio/item/bdr:320556/.

Council of Science Editors:

Koveal DM. Structural and functional investigation of protein phosphatases and scaffolds that regulate phosphorylation. [Doctoral Dissertation]. Brown University; 2013. Available from: https://repository.library.brown.edu/studio/item/bdr:320556/


University of Cape Town

4. Dent,Kyle Clayton. Architecture and assembly of maize streak virus: insights from 3D electron microscopy.

Degree: Image, Molecular and Cell Biology, 2014, University of Cape Town

 Maize streak virus (MSV), circular single stranded DNA (ssDNA) virus (~2.7kb), is the causative agent of Maize streak disease, and is a devastating pathogen that… (more)

Subjects/Keywords: Structural Biology

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APA (6th Edition):

Clayton, D. (2014). Architecture and assembly of maize streak virus: insights from 3D electron microscopy. (Thesis). University of Cape Town. Retrieved from http://hdl.handle.net/11427/13389

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):

Clayton, Dent,Kyle. “Architecture and assembly of maize streak virus: insights from 3D electron microscopy.” 2014. Thesis, University of Cape Town. Accessed July 08, 2020. http://hdl.handle.net/11427/13389.

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

MLA Handbook (7th Edition):

Clayton, Dent,Kyle. “Architecture and assembly of maize streak virus: insights from 3D electron microscopy.” 2014. Web. 08 Jul 2020.

Vancouver:

Clayton D. Architecture and assembly of maize streak virus: insights from 3D electron microscopy. [Internet] [Thesis]. University of Cape Town; 2014. [cited 2020 Jul 08]. Available from: http://hdl.handle.net/11427/13389.

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

Council of Science Editors:

Clayton D. Architecture and assembly of maize streak virus: insights from 3D electron microscopy. [Thesis]. University of Cape Town; 2014. Available from: http://hdl.handle.net/11427/13389

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

5. Soufari-Rouba, Heddy. Etude structurale et fonctionnelle du facteur d'épissage alternatif tissu spécifique MEC-8 chez C.elegans : Structural and functional study of the tissue specific alternative splicing factor MEC-8 from C.elegans.

Degree: Docteur es, Biochimie, 2015, Bordeaux

Chez les organismes multicellulaires la diversité protéique dans chaque cellule et chaque tissu est obtenue initialement en régulant l’expression d’une partie des gènes d’un génome.… (more)

Subjects/Keywords: Epissage alternatif; Biologie structurale; ARN; Alternative splicing; Structural biology; RNA

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APA (6th Edition):

Soufari-Rouba, H. (2015). Etude structurale et fonctionnelle du facteur d'épissage alternatif tissu spécifique MEC-8 chez C.elegans : Structural and functional study of the tissue specific alternative splicing factor MEC-8 from C.elegans. (Doctoral Dissertation). Bordeaux. Retrieved from http://www.theses.fr/2015BORD0406

Chicago Manual of Style (16th Edition):

Soufari-Rouba, Heddy. “Etude structurale et fonctionnelle du facteur d'épissage alternatif tissu spécifique MEC-8 chez C.elegans : Structural and functional study of the tissue specific alternative splicing factor MEC-8 from C.elegans.” 2015. Doctoral Dissertation, Bordeaux. Accessed July 08, 2020. http://www.theses.fr/2015BORD0406.

MLA Handbook (7th Edition):

Soufari-Rouba, Heddy. “Etude structurale et fonctionnelle du facteur d'épissage alternatif tissu spécifique MEC-8 chez C.elegans : Structural and functional study of the tissue specific alternative splicing factor MEC-8 from C.elegans.” 2015. Web. 08 Jul 2020.

Vancouver:

Soufari-Rouba H. Etude structurale et fonctionnelle du facteur d'épissage alternatif tissu spécifique MEC-8 chez C.elegans : Structural and functional study of the tissue specific alternative splicing factor MEC-8 from C.elegans. [Internet] [Doctoral dissertation]. Bordeaux; 2015. [cited 2020 Jul 08]. Available from: http://www.theses.fr/2015BORD0406.

Council of Science Editors:

Soufari-Rouba H. Etude structurale et fonctionnelle du facteur d'épissage alternatif tissu spécifique MEC-8 chez C.elegans : Structural and functional study of the tissue specific alternative splicing factor MEC-8 from C.elegans. [Doctoral Dissertation]. Bordeaux; 2015. Available from: http://www.theses.fr/2015BORD0406

6. Romoli, Filippo. Méthodes de cristallographie communes par rayons X et neutrons pour l'étude de réactions enzymatiques : Joint X-ray and neutron crystallography methods for the study of enzymatic reactions.

Degree: Docteur es, Chimie Physique Moléculaire et Structurale, 2015, Université Grenoble Alpes (ComUE)

 L'importance des techniques de diffraction aux rayons-X pour la détermination de structures macromoléculaires en rapport à la fonction biologique peut être facilement comprise lorsque l'on… (more)

Subjects/Keywords: Biologie structuralles; Rayons x; Neutrons; Structural Biology; X ray; Neutrons; 570

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APA (6th Edition):

Romoli, F. (2015). Méthodes de cristallographie communes par rayons X et neutrons pour l'étude de réactions enzymatiques : Joint X-ray and neutron crystallography methods for the study of enzymatic reactions. (Doctoral Dissertation). Université Grenoble Alpes (ComUE). Retrieved from http://www.theses.fr/2015GREAV062

Chicago Manual of Style (16th Edition):

Romoli, Filippo. “Méthodes de cristallographie communes par rayons X et neutrons pour l'étude de réactions enzymatiques : Joint X-ray and neutron crystallography methods for the study of enzymatic reactions.” 2015. Doctoral Dissertation, Université Grenoble Alpes (ComUE). Accessed July 08, 2020. http://www.theses.fr/2015GREAV062.

MLA Handbook (7th Edition):

Romoli, Filippo. “Méthodes de cristallographie communes par rayons X et neutrons pour l'étude de réactions enzymatiques : Joint X-ray and neutron crystallography methods for the study of enzymatic reactions.” 2015. Web. 08 Jul 2020.

Vancouver:

Romoli F. Méthodes de cristallographie communes par rayons X et neutrons pour l'étude de réactions enzymatiques : Joint X-ray and neutron crystallography methods for the study of enzymatic reactions. [Internet] [Doctoral dissertation]. Université Grenoble Alpes (ComUE); 2015. [cited 2020 Jul 08]. Available from: http://www.theses.fr/2015GREAV062.

Council of Science Editors:

Romoli F. Méthodes de cristallographie communes par rayons X et neutrons pour l'étude de réactions enzymatiques : Joint X-ray and neutron crystallography methods for the study of enzymatic reactions. [Doctoral Dissertation]. Université Grenoble Alpes (ComUE); 2015. Available from: http://www.theses.fr/2015GREAV062

7. Nedeljkovic, Marko. Caractérisation structurale d'un complexe de défense bactérienne : Structural characterization of bacterial defense complex.

Degree: Docteur es, Biologie structurale et nanobiologie, 2017, Université Grenoble Alpes (ComUE)

 De nos jours, la résistance aux antibiotiques développée par des pathogènes bactériens est de plus en plus répandue, et en conséquent il devient primordial de… (more)

Subjects/Keywords: Infection; Bacterie; Biologie structurale; Défense; Infection; Bacteria; Structural biology; Defense; 570

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APA (6th Edition):

Nedeljkovic, M. (2017). Caractérisation structurale d'un complexe de défense bactérienne : Structural characterization of bacterial defense complex. (Doctoral Dissertation). Université Grenoble Alpes (ComUE). Retrieved from http://www.theses.fr/2017GREAV067

Chicago Manual of Style (16th Edition):

Nedeljkovic, Marko. “Caractérisation structurale d'un complexe de défense bactérienne : Structural characterization of bacterial defense complex.” 2017. Doctoral Dissertation, Université Grenoble Alpes (ComUE). Accessed July 08, 2020. http://www.theses.fr/2017GREAV067.

MLA Handbook (7th Edition):

Nedeljkovic, Marko. “Caractérisation structurale d'un complexe de défense bactérienne : Structural characterization of bacterial defense complex.” 2017. Web. 08 Jul 2020.

Vancouver:

Nedeljkovic M. Caractérisation structurale d'un complexe de défense bactérienne : Structural characterization of bacterial defense complex. [Internet] [Doctoral dissertation]. Université Grenoble Alpes (ComUE); 2017. [cited 2020 Jul 08]. Available from: http://www.theses.fr/2017GREAV067.

Council of Science Editors:

Nedeljkovic M. Caractérisation structurale d'un complexe de défense bactérienne : Structural characterization of bacterial defense complex. [Doctoral Dissertation]. Université Grenoble Alpes (ComUE); 2017. Available from: http://www.theses.fr/2017GREAV067


University of Oxford

8. Sabaratnam, Keshalini. The interaction between the Marek's Disease Virus (MDV) neurovirulence factor pp14 and the host transcription factor, CREB3.

Degree: PhD, 2017, University of Oxford

 Marek's Disease Virus (MDV) induces a wide range of neurological syndromes in susceptible hosts; however, the mechanisms behind the MDV-induced neuropathology are still poorly understood.… (more)

Subjects/Keywords: Structural Biology; Virology

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APA (6th Edition):

Sabaratnam, K. (2017). The interaction between the Marek's Disease Virus (MDV) neurovirulence factor pp14 and the host transcription factor, CREB3. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:d2fc6bd4-bc3a-4a37-924b-86881096a9b5 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.748883

Chicago Manual of Style (16th Edition):

Sabaratnam, Keshalini. “The interaction between the Marek's Disease Virus (MDV) neurovirulence factor pp14 and the host transcription factor, CREB3.” 2017. Doctoral Dissertation, University of Oxford. Accessed July 08, 2020. http://ora.ox.ac.uk/objects/uuid:d2fc6bd4-bc3a-4a37-924b-86881096a9b5 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.748883.

MLA Handbook (7th Edition):

Sabaratnam, Keshalini. “The interaction between the Marek's Disease Virus (MDV) neurovirulence factor pp14 and the host transcription factor, CREB3.” 2017. Web. 08 Jul 2020.

Vancouver:

Sabaratnam K. The interaction between the Marek's Disease Virus (MDV) neurovirulence factor pp14 and the host transcription factor, CREB3. [Internet] [Doctoral dissertation]. University of Oxford; 2017. [cited 2020 Jul 08]. Available from: http://ora.ox.ac.uk/objects/uuid:d2fc6bd4-bc3a-4a37-924b-86881096a9b5 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.748883.

Council of Science Editors:

Sabaratnam K. The interaction between the Marek's Disease Virus (MDV) neurovirulence factor pp14 and the host transcription factor, CREB3. [Doctoral Dissertation]. University of Oxford; 2017. Available from: http://ora.ox.ac.uk/objects/uuid:d2fc6bd4-bc3a-4a37-924b-86881096a9b5 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.748883


University of Victoria

9. Gregg, Katie Jean. Carbohydrate processing by bacterial pathogens: structural and functional analyses of glycoside hydrolases.

Degree: Dept. of Biochemistry and Microbiology, 2011, University of Victoria

 Carbohydrates are important in a large number of cellular, physiological, and pathological processes. Carbohydrates often function as the human host’s first line of defence against… (more)

Subjects/Keywords: Biochemistry; Structural Biology

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APA (6th Edition):

Gregg, K. J. (2011). Carbohydrate processing by bacterial pathogens: structural and functional analyses of glycoside hydrolases. (Thesis). University of Victoria. Retrieved from http://hdl.handle.net/1828/3726

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):

Gregg, Katie Jean. “Carbohydrate processing by bacterial pathogens: structural and functional analyses of glycoside hydrolases.” 2011. Thesis, University of Victoria. Accessed July 08, 2020. http://hdl.handle.net/1828/3726.

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

MLA Handbook (7th Edition):

Gregg, Katie Jean. “Carbohydrate processing by bacterial pathogens: structural and functional analyses of glycoside hydrolases.” 2011. Web. 08 Jul 2020.

Vancouver:

Gregg KJ. Carbohydrate processing by bacterial pathogens: structural and functional analyses of glycoside hydrolases. [Internet] [Thesis]. University of Victoria; 2011. [cited 2020 Jul 08]. Available from: http://hdl.handle.net/1828/3726.

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

Council of Science Editors:

Gregg KJ. Carbohydrate processing by bacterial pathogens: structural and functional analyses of glycoside hydrolases. [Thesis]. University of Victoria; 2011. Available from: http://hdl.handle.net/1828/3726

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


University of Melbourne

10. Periasamy, Agalya. Investigation of the mitochondrial translocase of the outer membrane (TOM) of Drosophila melanogaster.

Degree: 2018, University of Melbourne

 The macromolecular protein translocation machinery of the outer mitochondrial membrane, TOM, mediates the import of nuclear-encoded mitochondria-bound precursor proteins. Moreover, a demonstrated role in importing… (more)

Subjects/Keywords: Biochemistry; Structural Biology

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APA (6th Edition):

Periasamy, A. (2018). Investigation of the mitochondrial translocase of the outer membrane (TOM) of Drosophila melanogaster. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/214490

Chicago Manual of Style (16th Edition):

Periasamy, Agalya. “Investigation of the mitochondrial translocase of the outer membrane (TOM) of Drosophila melanogaster.” 2018. Doctoral Dissertation, University of Melbourne. Accessed July 08, 2020. http://hdl.handle.net/11343/214490.

MLA Handbook (7th Edition):

Periasamy, Agalya. “Investigation of the mitochondrial translocase of the outer membrane (TOM) of Drosophila melanogaster.” 2018. Web. 08 Jul 2020.

Vancouver:

Periasamy A. Investigation of the mitochondrial translocase of the outer membrane (TOM) of Drosophila melanogaster. [Internet] [Doctoral dissertation]. University of Melbourne; 2018. [cited 2020 Jul 08]. Available from: http://hdl.handle.net/11343/214490.

Council of Science Editors:

Periasamy A. Investigation of the mitochondrial translocase of the outer membrane (TOM) of Drosophila melanogaster. [Doctoral Dissertation]. University of Melbourne; 2018. Available from: http://hdl.handle.net/11343/214490


University of California – Berkeley

11. Zhang, Elisa Tiannuo. Structural and Biochemical Characterization of the XPC DNA Repair and Stem Cell Coactivator Complex.

Degree: Molecular & Cell Biology, 2015, University of California – Berkeley

 The regulation of eukaryotic gene expression is critical for proper cell homeostasis and development and relies largely on appropriate initiation of transcription. Transcriptional regulators, such… (more)

Subjects/Keywords: Molecular biology; Biochemistry; Structural biology

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APA (6th Edition):

Zhang, E. T. (2015). Structural and Biochemical Characterization of the XPC DNA Repair and Stem Cell Coactivator Complex. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/08k0g39d

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

Chicago Manual of Style (16th Edition):

Zhang, Elisa Tiannuo. “Structural and Biochemical Characterization of the XPC DNA Repair and Stem Cell Coactivator Complex.” 2015. Thesis, University of California – Berkeley. Accessed July 08, 2020. http://www.escholarship.org/uc/item/08k0g39d.

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

MLA Handbook (7th Edition):

Zhang, Elisa Tiannuo. “Structural and Biochemical Characterization of the XPC DNA Repair and Stem Cell Coactivator Complex.” 2015. Web. 08 Jul 2020.

Vancouver:

Zhang ET. Structural and Biochemical Characterization of the XPC DNA Repair and Stem Cell Coactivator Complex. [Internet] [Thesis]. University of California – Berkeley; 2015. [cited 2020 Jul 08]. Available from: http://www.escholarship.org/uc/item/08k0g39d.

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

Council of Science Editors:

Zhang ET. Structural and Biochemical Characterization of the XPC DNA Repair and Stem Cell Coactivator Complex. [Thesis]. University of California – Berkeley; 2015. Available from: http://www.escholarship.org/uc/item/08k0g39d

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

12. Lin, Yi. Structural and Functional Studies of Urea Amidolyase.

Degree: 2014, Marquette University

 Urea amidolyase (UAL) is a key virulence factor that regulates the yeast to hyphae switch in the opportunistic pathogen, Candida albicans. UAL is a multi-domain… (more)

Subjects/Keywords: Enzymology; Genetics; Structural biology; Biology

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APA (6th Edition):

Lin, Y. (2014). Structural and Functional Studies of Urea Amidolyase. (Thesis). Marquette University. Retrieved from https://epublications.marquette.edu/dissertations_mu/381

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):

Lin, Yi. “Structural and Functional Studies of Urea Amidolyase.” 2014. Thesis, Marquette University. Accessed July 08, 2020. https://epublications.marquette.edu/dissertations_mu/381.

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

MLA Handbook (7th Edition):

Lin, Yi. “Structural and Functional Studies of Urea Amidolyase.” 2014. Web. 08 Jul 2020.

Vancouver:

Lin Y. Structural and Functional Studies of Urea Amidolyase. [Internet] [Thesis]. Marquette University; 2014. [cited 2020 Jul 08]. Available from: https://epublications.marquette.edu/dissertations_mu/381.

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

Council of Science Editors:

Lin Y. Structural and Functional Studies of Urea Amidolyase. [Thesis]. Marquette University; 2014. Available from: https://epublications.marquette.edu/dissertations_mu/381

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


Université Paris-Sud – Paris XI

13. Nogaret, Sophie. Etude par RMN de macromolécules biologiques : étude structurale de la protéine CGC-19 impliquée dans la biosynthèse d’un métabolite secondaire, la congocidine chez Streptomyces Ambofaciens. Développement d’inhibiteurs des Bcl-2, protéines modulatrices de l’apoptose : NMR study of biological macromolecules : structural study of CGC-19, a single domain protein involved in the biosynthesis of congocidine, a secondary metabolite from Streptomyces Ambofaciens, NMR contribution to anti-apoptotic protein ligand development.

Degree: Docteur es, Ingénierie des protéines, 2011, Université Paris-Sud – Paris XI

 Ma thèse comporte deux volets: d’une part, le développement de ligands ciblant les protéines antiapoptotiques et d’autre part, l’étude par RMN des protéines CGC impliquées… (more)

Subjects/Keywords: Biologie structurale; Métabolisme secondaire; Interaction protéine ligand; Structural biology; Secondary metabolism; Protein ligand interaction

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APA (6th Edition):

Nogaret, S. (2011). Etude par RMN de macromolécules biologiques : étude structurale de la protéine CGC-19 impliquée dans la biosynthèse d’un métabolite secondaire, la congocidine chez Streptomyces Ambofaciens. Développement d’inhibiteurs des Bcl-2, protéines modulatrices de l’apoptose : NMR study of biological macromolecules : structural study of CGC-19, a single domain protein involved in the biosynthesis of congocidine, a secondary metabolite from Streptomyces Ambofaciens, NMR contribution to anti-apoptotic protein ligand development. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2011PA114848

Chicago Manual of Style (16th Edition):

Nogaret, Sophie. “Etude par RMN de macromolécules biologiques : étude structurale de la protéine CGC-19 impliquée dans la biosynthèse d’un métabolite secondaire, la congocidine chez Streptomyces Ambofaciens. Développement d’inhibiteurs des Bcl-2, protéines modulatrices de l’apoptose : NMR study of biological macromolecules : structural study of CGC-19, a single domain protein involved in the biosynthesis of congocidine, a secondary metabolite from Streptomyces Ambofaciens, NMR contribution to anti-apoptotic protein ligand development.” 2011. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed July 08, 2020. http://www.theses.fr/2011PA114848.

MLA Handbook (7th Edition):

Nogaret, Sophie. “Etude par RMN de macromolécules biologiques : étude structurale de la protéine CGC-19 impliquée dans la biosynthèse d’un métabolite secondaire, la congocidine chez Streptomyces Ambofaciens. Développement d’inhibiteurs des Bcl-2, protéines modulatrices de l’apoptose : NMR study of biological macromolecules : structural study of CGC-19, a single domain protein involved in the biosynthesis of congocidine, a secondary metabolite from Streptomyces Ambofaciens, NMR contribution to anti-apoptotic protein ligand development.” 2011. Web. 08 Jul 2020.

Vancouver:

Nogaret S. Etude par RMN de macromolécules biologiques : étude structurale de la protéine CGC-19 impliquée dans la biosynthèse d’un métabolite secondaire, la congocidine chez Streptomyces Ambofaciens. Développement d’inhibiteurs des Bcl-2, protéines modulatrices de l’apoptose : NMR study of biological macromolecules : structural study of CGC-19, a single domain protein involved in the biosynthesis of congocidine, a secondary metabolite from Streptomyces Ambofaciens, NMR contribution to anti-apoptotic protein ligand development. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2011. [cited 2020 Jul 08]. Available from: http://www.theses.fr/2011PA114848.

Council of Science Editors:

Nogaret S. Etude par RMN de macromolécules biologiques : étude structurale de la protéine CGC-19 impliquée dans la biosynthèse d’un métabolite secondaire, la congocidine chez Streptomyces Ambofaciens. Développement d’inhibiteurs des Bcl-2, protéines modulatrices de l’apoptose : NMR study of biological macromolecules : structural study of CGC-19, a single domain protein involved in the biosynthesis of congocidine, a secondary metabolite from Streptomyces Ambofaciens, NMR contribution to anti-apoptotic protein ligand development. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2011. Available from: http://www.theses.fr/2011PA114848

14. Cannella, Sara Elisabetta. Effect of CyaA acylation on its folding and membrane properties : Effet de l’acylation de CyaA sur son repliement et son interaction avec les membranes.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie. Biophysique et Biochimie, 2016, Sorbonne Paris Cité

L’Adénylate cyclase (CyaA), produite par B. pertussis, agent responsable de la coqueluche, est un des principaux facteurs de virulence de la bactérie. La toxine est… (more)

Subjects/Keywords: Interaction protéine membrane; Biologie structurale; RTX; Protein-membrane interaction; Structural biology; RTX

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APA (6th Edition):

Cannella, S. E. (2016). Effect of CyaA acylation on its folding and membrane properties : Effet de l’acylation de CyaA sur son repliement et son interaction avec les membranes. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2016USPCC198

Chicago Manual of Style (16th Edition):

Cannella, Sara Elisabetta. “Effect of CyaA acylation on its folding and membrane properties : Effet de l’acylation de CyaA sur son repliement et son interaction avec les membranes.” 2016. Doctoral Dissertation, Sorbonne Paris Cité. Accessed July 08, 2020. http://www.theses.fr/2016USPCC198.

MLA Handbook (7th Edition):

Cannella, Sara Elisabetta. “Effect of CyaA acylation on its folding and membrane properties : Effet de l’acylation de CyaA sur son repliement et son interaction avec les membranes.” 2016. Web. 08 Jul 2020.

Vancouver:

Cannella SE. Effect of CyaA acylation on its folding and membrane properties : Effet de l’acylation de CyaA sur son repliement et son interaction avec les membranes. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2016. [cited 2020 Jul 08]. Available from: http://www.theses.fr/2016USPCC198.

Council of Science Editors:

Cannella SE. Effect of CyaA acylation on its folding and membrane properties : Effet de l’acylation de CyaA sur son repliement et son interaction avec les membranes. [Doctoral Dissertation]. Sorbonne Paris Cité; 2016. Available from: http://www.theses.fr/2016USPCC198

15. Brasseur, Laurent. Caractérisations biochimiques des protéines à répétitions de dipeptides et de leurs assemblages : Biochemical Caracterisations of Dipeptides Repeat Proteins and their Assemblies.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2019, Université Paris-Saclay (ComUE)

Résumé : La répétition de l’hexanucléotide GGGGCC est le facteur génétique le plus présent chez les patients atteints de démence fronto-temporale (DFT) et de sclérose… (more)

Subjects/Keywords: Démence fronto temporale; Biologie Structurelle; Aggrégation protéique; Protein aggregation; Frontotemporal demantia; Structural Biology

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APA (6th Edition):

Brasseur, L. (2019). Caractérisations biochimiques des protéines à répétitions de dipeptides et de leurs assemblages : Biochemical Caracterisations of Dipeptides Repeat Proteins and their Assemblies. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2019SACLS538

Chicago Manual of Style (16th Edition):

Brasseur, Laurent. “Caractérisations biochimiques des protéines à répétitions de dipeptides et de leurs assemblages : Biochemical Caracterisations of Dipeptides Repeat Proteins and their Assemblies.” 2019. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed July 08, 2020. http://www.theses.fr/2019SACLS538.

MLA Handbook (7th Edition):

Brasseur, Laurent. “Caractérisations biochimiques des protéines à répétitions de dipeptides et de leurs assemblages : Biochemical Caracterisations of Dipeptides Repeat Proteins and their Assemblies.” 2019. Web. 08 Jul 2020.

Vancouver:

Brasseur L. Caractérisations biochimiques des protéines à répétitions de dipeptides et de leurs assemblages : Biochemical Caracterisations of Dipeptides Repeat Proteins and their Assemblies. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2019. [cited 2020 Jul 08]. Available from: http://www.theses.fr/2019SACLS538.

Council of Science Editors:

Brasseur L. Caractérisations biochimiques des protéines à répétitions de dipeptides et de leurs assemblages : Biochemical Caracterisations of Dipeptides Repeat Proteins and their Assemblies. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2019. Available from: http://www.theses.fr/2019SACLS538

16. Cabanettes, Aurore. Caractérisation et modification de lectines fongiques pour la reconnaissance spécifique de motifs glucidiques principalement associés aux cancers : Characterization and modification of fungal lectins for specific binding to carbohydrates patterns mainly involved in cancers.

Degree: Docteur es, Chimie biologie, 2019, Université Grenoble Alpes (ComUE)

Les lectines sont des protéines ubiquitaires qui se lient spécifiquement et de manière réversible aux sucres sans les modifier. Elles peuvent déchiffrer le glycocode :… (more)

Subjects/Keywords: Biomarqueurs; Champignon; Cancer; Biologie structurale; Lectins; Biomarkers; Mushroom; Cancer; Structural biology; 570

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APA (6th Edition):

Cabanettes, A. (2019). Caractérisation et modification de lectines fongiques pour la reconnaissance spécifique de motifs glucidiques principalement associés aux cancers : Characterization and modification of fungal lectins for specific binding to carbohydrates patterns mainly involved in cancers. (Doctoral Dissertation). Université Grenoble Alpes (ComUE). Retrieved from http://www.theses.fr/2019GREAV021

Chicago Manual of Style (16th Edition):

Cabanettes, Aurore. “Caractérisation et modification de lectines fongiques pour la reconnaissance spécifique de motifs glucidiques principalement associés aux cancers : Characterization and modification of fungal lectins for specific binding to carbohydrates patterns mainly involved in cancers.” 2019. Doctoral Dissertation, Université Grenoble Alpes (ComUE). Accessed July 08, 2020. http://www.theses.fr/2019GREAV021.

MLA Handbook (7th Edition):

Cabanettes, Aurore. “Caractérisation et modification de lectines fongiques pour la reconnaissance spécifique de motifs glucidiques principalement associés aux cancers : Characterization and modification of fungal lectins for specific binding to carbohydrates patterns mainly involved in cancers.” 2019. Web. 08 Jul 2020.

Vancouver:

Cabanettes A. Caractérisation et modification de lectines fongiques pour la reconnaissance spécifique de motifs glucidiques principalement associés aux cancers : Characterization and modification of fungal lectins for specific binding to carbohydrates patterns mainly involved in cancers. [Internet] [Doctoral dissertation]. Université Grenoble Alpes (ComUE); 2019. [cited 2020 Jul 08]. Available from: http://www.theses.fr/2019GREAV021.

Council of Science Editors:

Cabanettes A. Caractérisation et modification de lectines fongiques pour la reconnaissance spécifique de motifs glucidiques principalement associés aux cancers : Characterization and modification of fungal lectins for specific binding to carbohydrates patterns mainly involved in cancers. [Doctoral Dissertation]. Université Grenoble Alpes (ComUE); 2019. Available from: http://www.theses.fr/2019GREAV021

17. Engilberge, Sylvain. Nouveaux développements en biologie structurale basés sur des complexes de lanthanide : New developments in structural biology based on lanthanide complexes.

Degree: Docteur es, Physique pour les sciences du vivant, 2017, Université Grenoble Alpes (ComUE)

Depuis les premières structures de protéines déterminées dans les années 1950, la cristallographie aux rayons X s’est imposée comme une méthode de choix pour l’obtention… (more)

Subjects/Keywords: Biologie structurale; Complexes de lanthanides; Diffusion anomale; Structural biology; Lanthanide complexes; Anomalous scattering; 530; 570

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

APA (6th Edition):

Engilberge, S. (2017). Nouveaux développements en biologie structurale basés sur des complexes de lanthanide : New developments in structural biology based on lanthanide complexes. (Doctoral Dissertation). Université Grenoble Alpes (ComUE). Retrieved from http://www.theses.fr/2017GREAY094

Chicago Manual of Style (16th Edition):

Engilberge, Sylvain. “Nouveaux développements en biologie structurale basés sur des complexes de lanthanide : New developments in structural biology based on lanthanide complexes.” 2017. Doctoral Dissertation, Université Grenoble Alpes (ComUE). Accessed July 08, 2020. http://www.theses.fr/2017GREAY094.

MLA Handbook (7th Edition):

Engilberge, Sylvain. “Nouveaux développements en biologie structurale basés sur des complexes de lanthanide : New developments in structural biology based on lanthanide complexes.” 2017. Web. 08 Jul 2020.

Vancouver:

Engilberge S. Nouveaux développements en biologie structurale basés sur des complexes de lanthanide : New developments in structural biology based on lanthanide complexes. [Internet] [Doctoral dissertation]. Université Grenoble Alpes (ComUE); 2017. [cited 2020 Jul 08]. Available from: http://www.theses.fr/2017GREAY094.

Council of Science Editors:

Engilberge S. Nouveaux développements en biologie structurale basés sur des complexes de lanthanide : New developments in structural biology based on lanthanide complexes. [Doctoral Dissertation]. Université Grenoble Alpes (ComUE); 2017. Available from: http://www.theses.fr/2017GREAY094


Université de Grenoble

18. Benoit, Matthieu. Etudes biophysiques de l'interaction entre la protéine humaine TRBP et un précurseur de microARN oncogène : Biophysical studies of the interaction between the human protein TRBP and an oncogenic microRNA precursor.

Degree: Docteur es, Sciences de la vie, 2013, Université de Grenoble

Les microARNs sont une classe de petits ARNs non codants qui régulent l'expression des gènes via un mecanisme d'interference par ARN. Les microARNs humains sont… (more)

Subjects/Keywords: MicroARN; TRBP; Dicer; Cancers; RMN; Biologie structurale; MicroRNA; TRBP; Dicer; Cancers; NMR; Structural biology

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APA (6th Edition):

Benoit, M. (2013). Etudes biophysiques de l'interaction entre la protéine humaine TRBP et un précurseur de microARN oncogène : Biophysical studies of the interaction between the human protein TRBP and an oncogenic microRNA precursor. (Doctoral Dissertation). Université de Grenoble. Retrieved from http://www.theses.fr/2013GRENV015

Chicago Manual of Style (16th Edition):

Benoit, Matthieu. “Etudes biophysiques de l'interaction entre la protéine humaine TRBP et un précurseur de microARN oncogène : Biophysical studies of the interaction between the human protein TRBP and an oncogenic microRNA precursor.” 2013. Doctoral Dissertation, Université de Grenoble. Accessed July 08, 2020. http://www.theses.fr/2013GRENV015.

MLA Handbook (7th Edition):

Benoit, Matthieu. “Etudes biophysiques de l'interaction entre la protéine humaine TRBP et un précurseur de microARN oncogène : Biophysical studies of the interaction between the human protein TRBP and an oncogenic microRNA precursor.” 2013. Web. 08 Jul 2020.

Vancouver:

Benoit M. Etudes biophysiques de l'interaction entre la protéine humaine TRBP et un précurseur de microARN oncogène : Biophysical studies of the interaction between the human protein TRBP and an oncogenic microRNA precursor. [Internet] [Doctoral dissertation]. Université de Grenoble; 2013. [cited 2020 Jul 08]. Available from: http://www.theses.fr/2013GRENV015.

Council of Science Editors:

Benoit M. Etudes biophysiques de l'interaction entre la protéine humaine TRBP et un précurseur de microARN oncogène : Biophysical studies of the interaction between the human protein TRBP and an oncogenic microRNA precursor. [Doctoral Dissertation]. Université de Grenoble; 2013. Available from: http://www.theses.fr/2013GRENV015

19. Schweke, Hugo. Développement d’une méthode in silico pour caractériser le potentiel d’interaction des surfaces protéiques dans un environnement encombré : Development of an in silico method to characterize the interaction potential of protein surfaces in a crowded environment.

Degree: Docteur es, Biochimie et biologie structurale, 2018, Université Paris-Saclay (ComUE)

Dans la cellule, les protéines évoluent dans un environnement très dense et interagissent ainsi avec un grand nombre de partenaires spécifiques et non-spécifiques qui entrent… (more)

Subjects/Keywords: Biologie structurale; Amarrage moléculaire; Interactions protéine-protéine; Structural biology; Molecular docking; Protein-protein interactions

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APA (6th Edition):

Schweke, H. (2018). Développement d’une méthode in silico pour caractériser le potentiel d’interaction des surfaces protéiques dans un environnement encombré : Development of an in silico method to characterize the interaction potential of protein surfaces in a crowded environment. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2018SACLS554

Chicago Manual of Style (16th Edition):

Schweke, Hugo. “Développement d’une méthode in silico pour caractériser le potentiel d’interaction des surfaces protéiques dans un environnement encombré : Development of an in silico method to characterize the interaction potential of protein surfaces in a crowded environment.” 2018. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed July 08, 2020. http://www.theses.fr/2018SACLS554.

MLA Handbook (7th Edition):

Schweke, Hugo. “Développement d’une méthode in silico pour caractériser le potentiel d’interaction des surfaces protéiques dans un environnement encombré : Development of an in silico method to characterize the interaction potential of protein surfaces in a crowded environment.” 2018. Web. 08 Jul 2020.

Vancouver:

Schweke H. Développement d’une méthode in silico pour caractériser le potentiel d’interaction des surfaces protéiques dans un environnement encombré : Development of an in silico method to characterize the interaction potential of protein surfaces in a crowded environment. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2018. [cited 2020 Jul 08]. Available from: http://www.theses.fr/2018SACLS554.

Council of Science Editors:

Schweke H. Développement d’une méthode in silico pour caractériser le potentiel d’interaction des surfaces protéiques dans un environnement encombré : Development of an in silico method to characterize the interaction potential of protein surfaces in a crowded environment. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2018. Available from: http://www.theses.fr/2018SACLS554

20. Barad, Benjamin Asher. Maximizing Interpretability from Complex Experiments in Structural Biology and Biochemistry.

Degree: Biophysics, 2019, University of California – San Francisco

 Proteins are complex macromolecules whose structure informs their function and regulation in difficult to predict ways. Understanding their shape, dynamics, and regulation all pose major… (more)

Subjects/Keywords: Biophysics; Biochemistry; Quantitative Biology; Structural Biology; Time Resolved Structural Biology

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APA (6th Edition):

Barad, B. A. (2019). Maximizing Interpretability from Complex Experiments in Structural Biology and Biochemistry. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/8t7048v8

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):

Barad, Benjamin Asher. “Maximizing Interpretability from Complex Experiments in Structural Biology and Biochemistry.” 2019. Thesis, University of California – San Francisco. Accessed July 08, 2020. http://www.escholarship.org/uc/item/8t7048v8.

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

MLA Handbook (7th Edition):

Barad, Benjamin Asher. “Maximizing Interpretability from Complex Experiments in Structural Biology and Biochemistry.” 2019. Web. 08 Jul 2020.

Vancouver:

Barad BA. Maximizing Interpretability from Complex Experiments in Structural Biology and Biochemistry. [Internet] [Thesis]. University of California – San Francisco; 2019. [cited 2020 Jul 08]. Available from: http://www.escholarship.org/uc/item/8t7048v8.

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

Council of Science Editors:

Barad BA. Maximizing Interpretability from Complex Experiments in Structural Biology and Biochemistry. [Thesis]. University of California – San Francisco; 2019. Available from: http://www.escholarship.org/uc/item/8t7048v8

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


McMaster University

21. Sugiman-Marangos, Seiji N. Structural Analysis of DdrB from Deinococcus radiodurans: Insight into the Mechanism of Protein Mediated Single-Stranded DNA Annealing.

Degree: PhD, 2013, McMaster University

Bacteria of the genus Deinococcus are perhaps the most resilient life forms ever discovered, demonstrating extreme resistance to ionizing radiation, ultraviolet radiation, desiccation, and… (more)

Subjects/Keywords: DdrB; Deinococcus radiodurans; single-stranded DNA annealing; structural biology; Structural Biology; Structural Biology

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APA (6th Edition):

Sugiman-Marangos, S. N. (2013). Structural Analysis of DdrB from Deinococcus radiodurans: Insight into the Mechanism of Protein Mediated Single-Stranded DNA Annealing. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/15263

Chicago Manual of Style (16th Edition):

Sugiman-Marangos, Seiji N. “Structural Analysis of DdrB from Deinococcus radiodurans: Insight into the Mechanism of Protein Mediated Single-Stranded DNA Annealing.” 2013. Doctoral Dissertation, McMaster University. Accessed July 08, 2020. http://hdl.handle.net/11375/15263.

MLA Handbook (7th Edition):

Sugiman-Marangos, Seiji N. “Structural Analysis of DdrB from Deinococcus radiodurans: Insight into the Mechanism of Protein Mediated Single-Stranded DNA Annealing.” 2013. Web. 08 Jul 2020.

Vancouver:

Sugiman-Marangos SN. Structural Analysis of DdrB from Deinococcus radiodurans: Insight into the Mechanism of Protein Mediated Single-Stranded DNA Annealing. [Internet] [Doctoral dissertation]. McMaster University; 2013. [cited 2020 Jul 08]. Available from: http://hdl.handle.net/11375/15263.

Council of Science Editors:

Sugiman-Marangos SN. Structural Analysis of DdrB from Deinococcus radiodurans: Insight into the Mechanism of Protein Mediated Single-Stranded DNA Annealing. [Doctoral Dissertation]. McMaster University; 2013. Available from: http://hdl.handle.net/11375/15263


Carnegie Mellon University

22. Dykstra, Kaitlyn M. Yip1A structures the mammalian endoplasmic reticulum.

Degree: 2012, Carnegie Mellon University

 The mammalian endoplasmic reticulum (ER) is the largest organelle in the cell, extending from the nuclear envelope throughout the cell periphery. The ER houses a… (more)

Subjects/Keywords: Biochemistry; Biophysics; and Structural Biology

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APA (6th Edition):

Dykstra, K. M. (2012). Yip1A structures the mammalian endoplasmic reticulum. (Thesis). Carnegie Mellon University. Retrieved from http://repository.cmu.edu/dissertations/140

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):

Dykstra, Kaitlyn M. “Yip1A structures the mammalian endoplasmic reticulum.” 2012. Thesis, Carnegie Mellon University. Accessed July 08, 2020. http://repository.cmu.edu/dissertations/140.

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

MLA Handbook (7th Edition):

Dykstra, Kaitlyn M. “Yip1A structures the mammalian endoplasmic reticulum.” 2012. Web. 08 Jul 2020.

Vancouver:

Dykstra KM. Yip1A structures the mammalian endoplasmic reticulum. [Internet] [Thesis]. Carnegie Mellon University; 2012. [cited 2020 Jul 08]. Available from: http://repository.cmu.edu/dissertations/140.

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

Council of Science Editors:

Dykstra KM. Yip1A structures the mammalian endoplasmic reticulum. [Thesis]. Carnegie Mellon University; 2012. Available from: http://repository.cmu.edu/dissertations/140

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

23. Vickery, Christopher R. Posttranslational modification of natural product biosynthetic enzymes in bacteria and plants.

Degree: Chemistry, 2016, University of California – San Diego

 Carrier proteins (CPs) are essential proteins for many biosynthetic pathways responsible for coordinating the biosynthesis of natural products. However, the CP must be posttranslationally modified… (more)

Subjects/Keywords: Biochemistry; Biochemistry; Bioinformatics; Structural Biology

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APA (6th Edition):

Vickery, C. R. (2016). Posttranslational modification of natural product biosynthetic enzymes in bacteria and plants. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/02s8d2zp

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):

Vickery, Christopher R. “Posttranslational modification of natural product biosynthetic enzymes in bacteria and plants.” 2016. Thesis, University of California – San Diego. Accessed July 08, 2020. http://www.escholarship.org/uc/item/02s8d2zp.

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

MLA Handbook (7th Edition):

Vickery, Christopher R. “Posttranslational modification of natural product biosynthetic enzymes in bacteria and plants.” 2016. Web. 08 Jul 2020.

Vancouver:

Vickery CR. Posttranslational modification of natural product biosynthetic enzymes in bacteria and plants. [Internet] [Thesis]. University of California – San Diego; 2016. [cited 2020 Jul 08]. Available from: http://www.escholarship.org/uc/item/02s8d2zp.

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

Council of Science Editors:

Vickery CR. Posttranslational modification of natural product biosynthetic enzymes in bacteria and plants. [Thesis]. University of California – San Diego; 2016. Available from: http://www.escholarship.org/uc/item/02s8d2zp

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


University of California – Merced

24. Mallios, Ronna Reuben. An iterative strategy combining biophysical criteria and duration hidden Markov models for structural predictions of Chlamydia trachomatis σ66 promoters.

Degree: Quantitative Systems Biology, 2010, University of California – Merced

 Promoter identification is crucial for understanding gene regulation in bacteria. It has been demonstrated that the initiation of bacterial transcription depends upon the stability and… (more)

Subjects/Keywords: Biology; Chlamydia trachomatis; structural predictions

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APA (6th Edition):

Mallios, R. R. (2010). An iterative strategy combining biophysical criteria and duration hidden Markov models for structural predictions of Chlamydia trachomatis σ66 promoters. (Thesis). University of California – Merced. Retrieved from http://www.escholarship.org/uc/item/916228ks

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):

Mallios, Ronna Reuben. “An iterative strategy combining biophysical criteria and duration hidden Markov models for structural predictions of Chlamydia trachomatis σ66 promoters.” 2010. Thesis, University of California – Merced. Accessed July 08, 2020. http://www.escholarship.org/uc/item/916228ks.

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

MLA Handbook (7th Edition):

Mallios, Ronna Reuben. “An iterative strategy combining biophysical criteria and duration hidden Markov models for structural predictions of Chlamydia trachomatis σ66 promoters.” 2010. Web. 08 Jul 2020.

Vancouver:

Mallios RR. An iterative strategy combining biophysical criteria and duration hidden Markov models for structural predictions of Chlamydia trachomatis σ66 promoters. [Internet] [Thesis]. University of California – Merced; 2010. [cited 2020 Jul 08]. Available from: http://www.escholarship.org/uc/item/916228ks.

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

Council of Science Editors:

Mallios RR. An iterative strategy combining biophysical criteria and duration hidden Markov models for structural predictions of Chlamydia trachomatis σ66 promoters. [Thesis]. University of California – Merced; 2010. Available from: http://www.escholarship.org/uc/item/916228ks

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

25. Liu, Dan. Mitsunobu Reactions of Bulky Phenols and Lignin Model Dimer Synthesis & Decomposition.

Degree: MS, Chemistry and Biochemistry, 2015, South Dakota State University

  This thesis is divided into two parts: investigation of the Mitsunobu reaction of bulky phenols and aliphatic alcohols to improve yield, and studies of… (more)

Subjects/Keywords: Biochemistry; Biophysics; and Structural Biology

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APA (6th Edition):

Liu, D. (2015). Mitsunobu Reactions of Bulky Phenols and Lignin Model Dimer Synthesis & Decomposition. (Masters Thesis). South Dakota State University. Retrieved from http://openprairie.sdstate.edu/etd/1808

Chicago Manual of Style (16th Edition):

Liu, Dan. “Mitsunobu Reactions of Bulky Phenols and Lignin Model Dimer Synthesis & Decomposition.” 2015. Masters Thesis, South Dakota State University. Accessed July 08, 2020. http://openprairie.sdstate.edu/etd/1808.

MLA Handbook (7th Edition):

Liu, Dan. “Mitsunobu Reactions of Bulky Phenols and Lignin Model Dimer Synthesis & Decomposition.” 2015. Web. 08 Jul 2020.

Vancouver:

Liu D. Mitsunobu Reactions of Bulky Phenols and Lignin Model Dimer Synthesis & Decomposition. [Internet] [Masters thesis]. South Dakota State University; 2015. [cited 2020 Jul 08]. Available from: http://openprairie.sdstate.edu/etd/1808.

Council of Science Editors:

Liu D. Mitsunobu Reactions of Bulky Phenols and Lignin Model Dimer Synthesis & Decomposition. [Masters Thesis]. South Dakota State University; 2015. Available from: http://openprairie.sdstate.edu/etd/1808


University of Louisville

26. Clark, Jennifer. Enzyme kinetics : 6-phosphofructo-2-kinase/2,6-bisphosphatase.

Degree: MS, 2014, University of Louisville

  Altered energy metabolism is an established hallmark of cancer cells. Fructose-2,6-bisphosphate is an allosteric activator of glycolysis and its concentration in a cell is… (more)

Subjects/Keywords: Biochemistry; Biophysics; and Structural Biology

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APA (6th Edition):

Clark, J. (2014). Enzyme kinetics : 6-phosphofructo-2-kinase/2,6-bisphosphatase. (Masters Thesis). University of Louisville. Retrieved from 10.18297/etd/1720 ; https://ir.library.louisville.edu/etd/1720

Chicago Manual of Style (16th Edition):

Clark, Jennifer. “Enzyme kinetics : 6-phosphofructo-2-kinase/2,6-bisphosphatase.” 2014. Masters Thesis, University of Louisville. Accessed July 08, 2020. 10.18297/etd/1720 ; https://ir.library.louisville.edu/etd/1720.

MLA Handbook (7th Edition):

Clark, Jennifer. “Enzyme kinetics : 6-phosphofructo-2-kinase/2,6-bisphosphatase.” 2014. Web. 08 Jul 2020.

Vancouver:

Clark J. Enzyme kinetics : 6-phosphofructo-2-kinase/2,6-bisphosphatase. [Internet] [Masters thesis]. University of Louisville; 2014. [cited 2020 Jul 08]. Available from: 10.18297/etd/1720 ; https://ir.library.louisville.edu/etd/1720.

Council of Science Editors:

Clark J. Enzyme kinetics : 6-phosphofructo-2-kinase/2,6-bisphosphatase. [Masters Thesis]. University of Louisville; 2014. Available from: 10.18297/etd/1720 ; https://ir.library.louisville.edu/etd/1720


McMaster University

27. Brown, Christopher, M. CHARACTERIZATION OF THE END BRIDGING COMPLEX OF NON-HOMOLOGOUS END JOINING REPAIR OF DNA DOUBLE STRAND BREAKS.

Degree: PhD, 2018, McMaster University

DNA double strand breaks represent the single most dangerous type of damage that can afflict the genome. Given the severity of such a lesion, higher… (more)

Subjects/Keywords: Structural biology; DNA repair

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APA (6th Edition):

Brown, Christopher, M. (2018). CHARACTERIZATION OF THE END BRIDGING COMPLEX OF NON-HOMOLOGOUS END JOINING REPAIR OF DNA DOUBLE STRAND BREAKS. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/22876

Chicago Manual of Style (16th Edition):

Brown, Christopher, M. “CHARACTERIZATION OF THE END BRIDGING COMPLEX OF NON-HOMOLOGOUS END JOINING REPAIR OF DNA DOUBLE STRAND BREAKS.” 2018. Doctoral Dissertation, McMaster University. Accessed July 08, 2020. http://hdl.handle.net/11375/22876.

MLA Handbook (7th Edition):

Brown, Christopher, M. “CHARACTERIZATION OF THE END BRIDGING COMPLEX OF NON-HOMOLOGOUS END JOINING REPAIR OF DNA DOUBLE STRAND BREAKS.” 2018. Web. 08 Jul 2020.

Vancouver:

Brown, Christopher M. CHARACTERIZATION OF THE END BRIDGING COMPLEX OF NON-HOMOLOGOUS END JOINING REPAIR OF DNA DOUBLE STRAND BREAKS. [Internet] [Doctoral dissertation]. McMaster University; 2018. [cited 2020 Jul 08]. Available from: http://hdl.handle.net/11375/22876.

Council of Science Editors:

Brown, Christopher M. CHARACTERIZATION OF THE END BRIDGING COMPLEX OF NON-HOMOLOGOUS END JOINING REPAIR OF DNA DOUBLE STRAND BREAKS. [Doctoral Dissertation]. McMaster University; 2018. Available from: http://hdl.handle.net/11375/22876

28. Verma, Nupur. Targeting Trehalose and Methylglucose Lipopolysaccharide Biosynthetic Pathways in M. tuberculosis - Structural and Functional Characterisation, and Early-Stage Drug Discovery of OtsA and Rv3030.

Degree: PhD, 2016, University of Cambridge

 Mycobacterium tuberculosis, the causative agent of tuberculosis in humans, is one of the most successful pathogens, with much of its virulence predominantly associated with its… (more)

Subjects/Keywords: OtsA; Rv3030; structural biology

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APA (6th Edition):

Verma, N. (2016). Targeting Trehalose and Methylglucose Lipopolysaccharide Biosynthetic Pathways in M. tuberculosis - Structural and Functional Characterisation, and Early-Stage Drug Discovery of OtsA and Rv3030. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/267830

Chicago Manual of Style (16th Edition):

Verma, Nupur. “Targeting Trehalose and Methylglucose Lipopolysaccharide Biosynthetic Pathways in M. tuberculosis - Structural and Functional Characterisation, and Early-Stage Drug Discovery of OtsA and Rv3030.” 2016. Doctoral Dissertation, University of Cambridge. Accessed July 08, 2020. https://www.repository.cam.ac.uk/handle/1810/267830.

MLA Handbook (7th Edition):

Verma, Nupur. “Targeting Trehalose and Methylglucose Lipopolysaccharide Biosynthetic Pathways in M. tuberculosis - Structural and Functional Characterisation, and Early-Stage Drug Discovery of OtsA and Rv3030.” 2016. Web. 08 Jul 2020.

Vancouver:

Verma N. Targeting Trehalose and Methylglucose Lipopolysaccharide Biosynthetic Pathways in M. tuberculosis - Structural and Functional Characterisation, and Early-Stage Drug Discovery of OtsA and Rv3030. [Internet] [Doctoral dissertation]. University of Cambridge; 2016. [cited 2020 Jul 08]. Available from: https://www.repository.cam.ac.uk/handle/1810/267830.

Council of Science Editors:

Verma N. Targeting Trehalose and Methylglucose Lipopolysaccharide Biosynthetic Pathways in M. tuberculosis - Structural and Functional Characterisation, and Early-Stage Drug Discovery of OtsA and Rv3030. [Doctoral Dissertation]. University of Cambridge; 2016. Available from: https://www.repository.cam.ac.uk/handle/1810/267830


East Tennessee State University

29. Yan, Hui. Regulation of Acute and Chronic Immune Responses by β-Arrestin2.

Degree: PhD, Biomedical Sciences, 2016, East Tennessee State University

  β-arrestin2, previously recognized as a facilitator for G-protein associated 7 TMR desensitization/ internalization, has now been appreciated as an independent signal transducer that regulates… (more)

Subjects/Keywords: Biochemistry; Biophysics; and Structural Biology

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APA (6th Edition):

Yan, H. (2016). Regulation of Acute and Chronic Immune Responses by β-Arrestin2. (Doctoral Dissertation). East Tennessee State University. Retrieved from https://dc.etsu.edu/etd/3049

Chicago Manual of Style (16th Edition):

Yan, Hui. “Regulation of Acute and Chronic Immune Responses by β-Arrestin2.” 2016. Doctoral Dissertation, East Tennessee State University. Accessed July 08, 2020. https://dc.etsu.edu/etd/3049.

MLA Handbook (7th Edition):

Yan, Hui. “Regulation of Acute and Chronic Immune Responses by β-Arrestin2.” 2016. Web. 08 Jul 2020.

Vancouver:

Yan H. Regulation of Acute and Chronic Immune Responses by β-Arrestin2. [Internet] [Doctoral dissertation]. East Tennessee State University; 2016. [cited 2020 Jul 08]. Available from: https://dc.etsu.edu/etd/3049.

Council of Science Editors:

Yan H. Regulation of Acute and Chronic Immune Responses by β-Arrestin2. [Doctoral Dissertation]. East Tennessee State University; 2016. Available from: https://dc.etsu.edu/etd/3049


UCLA

30. Macdonald, Ramsay. Structural and Mechanistic Insights into Iron Acquisition from Human Hemoglobin by Gram-positive Pathogens with a Focus on Two Organisms: Streptococcus pyogenes and Staphylococcus aureus.

Degree: Biochemistry & Molecular Biology, 2018, UCLA

 Staphylococcus aureus and other clinically important species of Gram-positive bacteria have acquired resistance to commonly used antibiotics. This underscores the need for new therapeutics and… (more)

Subjects/Keywords: Biochemistry; bacterial pathogenesis; structural biology

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

APA (6th Edition):

Macdonald, R. (2018). Structural and Mechanistic Insights into Iron Acquisition from Human Hemoglobin by Gram-positive Pathogens with a Focus on Two Organisms: Streptococcus pyogenes and Staphylococcus aureus. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/06h0b7r2

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):

Macdonald, Ramsay. “Structural and Mechanistic Insights into Iron Acquisition from Human Hemoglobin by Gram-positive Pathogens with a Focus on Two Organisms: Streptococcus pyogenes and Staphylococcus aureus.” 2018. Thesis, UCLA. Accessed July 08, 2020. http://www.escholarship.org/uc/item/06h0b7r2.

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

MLA Handbook (7th Edition):

Macdonald, Ramsay. “Structural and Mechanistic Insights into Iron Acquisition from Human Hemoglobin by Gram-positive Pathogens with a Focus on Two Organisms: Streptococcus pyogenes and Staphylococcus aureus.” 2018. Web. 08 Jul 2020.

Vancouver:

Macdonald R. Structural and Mechanistic Insights into Iron Acquisition from Human Hemoglobin by Gram-positive Pathogens with a Focus on Two Organisms: Streptococcus pyogenes and Staphylococcus aureus. [Internet] [Thesis]. UCLA; 2018. [cited 2020 Jul 08]. Available from: http://www.escholarship.org/uc/item/06h0b7r2.

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

Council of Science Editors:

Macdonald R. Structural and Mechanistic Insights into Iron Acquisition from Human Hemoglobin by Gram-positive Pathogens with a Focus on Two Organisms: Streptococcus pyogenes and Staphylococcus aureus. [Thesis]. UCLA; 2018. Available from: http://www.escholarship.org/uc/item/06h0b7r2

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

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