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You searched for subject:(peptide structure). Showing records 1 – 30 of 173 total matches.

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University of Alberta

1. Binazadeh, Mojtaba. Effect of Secondary Structure on Surface Adsorption of Peptides.

Degree: PhD, Department of Chemical and Materials Engineering, 2013, University of Alberta

 Protein adsorption at the biomaterial-tissue interface has several detrimental consequences which undermines the widespread application of engineered materials. Herein, it was asked what role protein… (more)

Subjects/Keywords: Peptide; Surface Adsorption; Secondary Structure

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APA (6th Edition):

Binazadeh, M. (2013). Effect of Secondary Structure on Surface Adsorption of Peptides. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/jh343v004

Chicago Manual of Style (16th Edition):

Binazadeh, Mojtaba. “Effect of Secondary Structure on Surface Adsorption of Peptides.” 2013. Doctoral Dissertation, University of Alberta. Accessed October 17, 2019. https://era.library.ualberta.ca/files/jh343v004.

MLA Handbook (7th Edition):

Binazadeh, Mojtaba. “Effect of Secondary Structure on Surface Adsorption of Peptides.” 2013. Web. 17 Oct 2019.

Vancouver:

Binazadeh M. Effect of Secondary Structure on Surface Adsorption of Peptides. [Internet] [Doctoral dissertation]. University of Alberta; 2013. [cited 2019 Oct 17]. Available from: https://era.library.ualberta.ca/files/jh343v004.

Council of Science Editors:

Binazadeh M. Effect of Secondary Structure on Surface Adsorption of Peptides. [Doctoral Dissertation]. University of Alberta; 2013. Available from: https://era.library.ualberta.ca/files/jh343v004


University of Adelaide

2. Horsfall, Aimee Jade. The synthesis of bimane constrained peptides and their fluorescent and structural properties.

Degree: 2017, University of Adelaide

 Aberrant protein-protein interactions often result in disease, and as such, effective protein-protein interaction inhibitors are needed to mitigate the disease state. These interaction interfaces often… (more)

Subjects/Keywords: bromobimane; peptide; constrained peptides; fluorescence; secondary structure; solid-phase peptide synthesis

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APA (6th Edition):

Horsfall, A. J. (2017). The synthesis of bimane constrained peptides and their fluorescent and structural properties. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/104675

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):

Horsfall, Aimee Jade. “The synthesis of bimane constrained peptides and their fluorescent and structural properties.” 2017. Thesis, University of Adelaide. Accessed October 17, 2019. http://hdl.handle.net/2440/104675.

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

MLA Handbook (7th Edition):

Horsfall, Aimee Jade. “The synthesis of bimane constrained peptides and their fluorescent and structural properties.” 2017. Web. 17 Oct 2019.

Vancouver:

Horsfall AJ. The synthesis of bimane constrained peptides and their fluorescent and structural properties. [Internet] [Thesis]. University of Adelaide; 2017. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/2440/104675.

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

Council of Science Editors:

Horsfall AJ. The synthesis of bimane constrained peptides and their fluorescent and structural properties. [Thesis]. University of Adelaide; 2017. Available from: http://hdl.handle.net/2440/104675

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

3. Lee, Youngshim. Peptide Nanoparticles As CXCR4 Chemokine Receptor Antagonists.

Degree: 2012, University of Illinois – Chicago

 CXCR4 is a chemokine receptor that induces cell migration upon binding its ligand CXCL12 that is also known as the stromal derived factor 1 (SDF1α).… (more)

Subjects/Keywords: Peptide structure

structure of X4-2-6 peptide derivatives. The X4-2-9 peptide has identical primary structure to… …a conical topology, the X4-2-9 peptide has a cylindrical structure. It is known that… …and Sparky, respectively (66). 2.2.5. Peptide structure calculations NOEs and… …x29;. 2.3.3. Structure determination of X4-2-1 and X4-2-9 peptide monomers The amino acid… …that the peptide structure with PEG is similar to the structure without PEG. NMR chemical… 

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APA (6th Edition):

Lee, Y. (2012). Peptide Nanoparticles As CXCR4 Chemokine Receptor Antagonists. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/9211

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):

Lee, Youngshim. “Peptide Nanoparticles As CXCR4 Chemokine Receptor Antagonists.” 2012. Thesis, University of Illinois – Chicago. Accessed October 17, 2019. http://hdl.handle.net/10027/9211.

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

MLA Handbook (7th Edition):

Lee, Youngshim. “Peptide Nanoparticles As CXCR4 Chemokine Receptor Antagonists.” 2012. Web. 17 Oct 2019.

Vancouver:

Lee Y. Peptide Nanoparticles As CXCR4 Chemokine Receptor Antagonists. [Internet] [Thesis]. University of Illinois – Chicago; 2012. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10027/9211.

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

Council of Science Editors:

Lee Y. Peptide Nanoparticles As CXCR4 Chemokine Receptor Antagonists. [Thesis]. University of Illinois – Chicago; 2012. Available from: http://hdl.handle.net/10027/9211

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


Kansas State University

4. Yu, Jing. Structure determination, mechanistic study, and safe delivery of an anti-cancer peptide.

Degree: PhD, Department of Chemistry, 2018, Kansas State University

 The therapeutic peptide sequence D-K₆L₉: LKLLKKLLKKLLKLL-NH₂ was developed for treating bacterial infections and solid tumors. It is effective against both conditions, because it is capable… (more)

Subjects/Keywords: Peptide; Cancer; Structure; Mechanism; Drug delivery

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APA (6th Edition):

Yu, J. (2018). Structure determination, mechanistic study, and safe delivery of an anti-cancer peptide. (Doctoral Dissertation). Kansas State University. Retrieved from http://hdl.handle.net/2097/39032

Chicago Manual of Style (16th Edition):

Yu, Jing. “Structure determination, mechanistic study, and safe delivery of an anti-cancer peptide.” 2018. Doctoral Dissertation, Kansas State University. Accessed October 17, 2019. http://hdl.handle.net/2097/39032.

MLA Handbook (7th Edition):

Yu, Jing. “Structure determination, mechanistic study, and safe delivery of an anti-cancer peptide.” 2018. Web. 17 Oct 2019.

Vancouver:

Yu J. Structure determination, mechanistic study, and safe delivery of an anti-cancer peptide. [Internet] [Doctoral dissertation]. Kansas State University; 2018. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/2097/39032.

Council of Science Editors:

Yu J. Structure determination, mechanistic study, and safe delivery of an anti-cancer peptide. [Doctoral Dissertation]. Kansas State University; 2018. Available from: http://hdl.handle.net/2097/39032


Iowa State University

5. Su, Yongchao. Structure and dynamics of membrane peptides from solid-state NMR.

Degree: 2011, Iowa State University

 Solid-state NMR is among the most important analytical techniques to provide atomic-level structural and dynamic information of chemical and biological systems. Due to the insoluble… (more)

Subjects/Keywords: antimicrobial peptide; cell-penetrating peptide; lipid; membrane protein; NMR; structure and dynamics; Chemistry

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APA (6th Edition):

Su, Y. (2011). Structure and dynamics of membrane peptides from solid-state NMR. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/10197

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):

Su, Yongchao. “Structure and dynamics of membrane peptides from solid-state NMR.” 2011. Thesis, Iowa State University. Accessed October 17, 2019. https://lib.dr.iastate.edu/etd/10197.

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

MLA Handbook (7th Edition):

Su, Yongchao. “Structure and dynamics of membrane peptides from solid-state NMR.” 2011. Web. 17 Oct 2019.

Vancouver:

Su Y. Structure and dynamics of membrane peptides from solid-state NMR. [Internet] [Thesis]. Iowa State University; 2011. [cited 2019 Oct 17]. Available from: https://lib.dr.iastate.edu/etd/10197.

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

Council of Science Editors:

Su Y. Structure and dynamics of membrane peptides from solid-state NMR. [Thesis]. Iowa State University; 2011. Available from: https://lib.dr.iastate.edu/etd/10197

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


University of California – San Francisco

6. Barkan, David Tennent. Computational Identification of Protein-Peptide Interaction Specificity.

Degree: Biological and Medical Informatics, 2011, University of California – San Francisco

 Evolution is the uniting concept of biology and life. At its fundamental level, it operates by sampling amino acid residues in proteins to optimize stability… (more)

Subjects/Keywords: Bioinformatics; Biophysics; Host-Pathogen Interactions; Peptide Docking; Peptide Specificity; Protein Structure Prediction

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APA (6th Edition):

Barkan, D. T. (2011). Computational Identification of Protein-Peptide Interaction Specificity. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/3g3952kq

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):

Barkan, David Tennent. “Computational Identification of Protein-Peptide Interaction Specificity.” 2011. Thesis, University of California – San Francisco. Accessed October 17, 2019. http://www.escholarship.org/uc/item/3g3952kq.

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

MLA Handbook (7th Edition):

Barkan, David Tennent. “Computational Identification of Protein-Peptide Interaction Specificity.” 2011. Web. 17 Oct 2019.

Vancouver:

Barkan DT. Computational Identification of Protein-Peptide Interaction Specificity. [Internet] [Thesis]. University of California – San Francisco; 2011. [cited 2019 Oct 17]. Available from: http://www.escholarship.org/uc/item/3g3952kq.

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

Council of Science Editors:

Barkan DT. Computational Identification of Protein-Peptide Interaction Specificity. [Thesis]. University of California – San Francisco; 2011. Available from: http://www.escholarship.org/uc/item/3g3952kq

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


Texas A&M University

7. McLean, Janel Renee. Biophysical studies of anhydrous peptide structure.

Degree: 2009, Texas A&M University

 Defining the intrinsic properties of amino acids which dictate the formation of helices, the most common protein secondary structure element, is an essential part of… (more)

Subjects/Keywords: ion mobility; ion structure; alpha-helices; alanine-based peptides; anhydrous peptide structure

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APA (6th Edition):

McLean, J. R. (2009). Biophysical studies of anhydrous peptide structure. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-1437

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):

McLean, Janel Renee. “Biophysical studies of anhydrous peptide structure.” 2009. Thesis, Texas A&M University. Accessed October 17, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-1437.

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

MLA Handbook (7th Edition):

McLean, Janel Renee. “Biophysical studies of anhydrous peptide structure.” 2009. Web. 17 Oct 2019.

Vancouver:

McLean JR. Biophysical studies of anhydrous peptide structure. [Internet] [Thesis]. Texas A&M University; 2009. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1437.

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

Council of Science Editors:

McLean JR. Biophysical studies of anhydrous peptide structure. [Thesis]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1437

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


Universiteit Utrecht

8. Mihalca, R. Structural and conformational aspects of gas phase peptides probed by electron capture dissociation.

Degree: 2007, Universiteit Utrecht

 Mass spectrometry (MS) is a major player in the field of structural characterization of peptides and proteins. MS-based proteomics is nowadays routinely carried out at… (more)

Subjects/Keywords: Scheikunde; ECD; IRMPD; SORI-CID; peptide; protein; structure; conformation; metals

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APA (6th Edition):

Mihalca, R. (2007). Structural and conformational aspects of gas phase peptides probed by electron capture dissociation. (Doctoral Dissertation). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/20339

Chicago Manual of Style (16th Edition):

Mihalca, R. “Structural and conformational aspects of gas phase peptides probed by electron capture dissociation.” 2007. Doctoral Dissertation, Universiteit Utrecht. Accessed October 17, 2019. http://dspace.library.uu.nl:8080/handle/1874/20339.

MLA Handbook (7th Edition):

Mihalca, R. “Structural and conformational aspects of gas phase peptides probed by electron capture dissociation.” 2007. Web. 17 Oct 2019.

Vancouver:

Mihalca R. Structural and conformational aspects of gas phase peptides probed by electron capture dissociation. [Internet] [Doctoral dissertation]. Universiteit Utrecht; 2007. [cited 2019 Oct 17]. Available from: http://dspace.library.uu.nl:8080/handle/1874/20339.

Council of Science Editors:

Mihalca R. Structural and conformational aspects of gas phase peptides probed by electron capture dissociation. [Doctoral Dissertation]. Universiteit Utrecht; 2007. Available from: http://dspace.library.uu.nl:8080/handle/1874/20339


University of Manchester

9. Gibbons, Jonathan. Manipulating the structural and mechanical properties of ionic-complementary peptide hydrogels.

Degree: PhD, 2015, University of Manchester

 Hydrogels based on self-assembling peptides are believed to have potential for use in a wide range of biomedical and biodiagnostic applications. For many of these,… (more)

Subjects/Keywords: 660; self-assembling, peptide, hydrogel, ionic-complementary, fibre, fibril, structure, mesh

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APA (6th Edition):

Gibbons, J. (2015). Manipulating the structural and mechanical properties of ionic-complementary peptide hydrogels. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/manipulating-the-structural-and-mechanical-properties-of-ioniccomplementary-peptide-hydrogels(66d0379c-290a-4903-866a-a12fffb6eae0).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644459

Chicago Manual of Style (16th Edition):

Gibbons, Jonathan. “Manipulating the structural and mechanical properties of ionic-complementary peptide hydrogels.” 2015. Doctoral Dissertation, University of Manchester. Accessed October 17, 2019. https://www.research.manchester.ac.uk/portal/en/theses/manipulating-the-structural-and-mechanical-properties-of-ioniccomplementary-peptide-hydrogels(66d0379c-290a-4903-866a-a12fffb6eae0).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644459.

MLA Handbook (7th Edition):

Gibbons, Jonathan. “Manipulating the structural and mechanical properties of ionic-complementary peptide hydrogels.” 2015. Web. 17 Oct 2019.

Vancouver:

Gibbons J. Manipulating the structural and mechanical properties of ionic-complementary peptide hydrogels. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2019 Oct 17]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/manipulating-the-structural-and-mechanical-properties-of-ioniccomplementary-peptide-hydrogels(66d0379c-290a-4903-866a-a12fffb6eae0).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644459.

Council of Science Editors:

Gibbons J. Manipulating the structural and mechanical properties of ionic-complementary peptide hydrogels. [Doctoral Dissertation]. University of Manchester; 2015. Available from: https://www.research.manchester.ac.uk/portal/en/theses/manipulating-the-structural-and-mechanical-properties-of-ioniccomplementary-peptide-hydrogels(66d0379c-290a-4903-866a-a12fffb6eae0).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.644459


University of Washington

10. Jones, Alisha. Development and evaluation of peptide mimetic inhibitors of HIV-1 replication. Structure of the conserved core region of the lincRNA Cyrano.

Degree: PhD, 2015, University of Washington

 Abstract 1: An estimated 1.2 million people in the United States are living with the human immunodeficiency virus (HIV), as reported by the Center for… (more)

Subjects/Keywords: HIV-1; inhibitor; lincRNA; peptide; structure; Chemistry; chemistry

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APA (6th Edition):

Jones, A. (2015). Development and evaluation of peptide mimetic inhibitors of HIV-1 replication. Structure of the conserved core region of the lincRNA Cyrano. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/33649

Chicago Manual of Style (16th Edition):

Jones, Alisha. “Development and evaluation of peptide mimetic inhibitors of HIV-1 replication. Structure of the conserved core region of the lincRNA Cyrano.” 2015. Doctoral Dissertation, University of Washington. Accessed October 17, 2019. http://hdl.handle.net/1773/33649.

MLA Handbook (7th Edition):

Jones, Alisha. “Development and evaluation of peptide mimetic inhibitors of HIV-1 replication. Structure of the conserved core region of the lincRNA Cyrano.” 2015. Web. 17 Oct 2019.

Vancouver:

Jones A. Development and evaluation of peptide mimetic inhibitors of HIV-1 replication. Structure of the conserved core region of the lincRNA Cyrano. [Internet] [Doctoral dissertation]. University of Washington; 2015. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/1773/33649.

Council of Science Editors:

Jones A. Development and evaluation of peptide mimetic inhibitors of HIV-1 replication. Structure of the conserved core region of the lincRNA Cyrano. [Doctoral Dissertation]. University of Washington; 2015. Available from: http://hdl.handle.net/1773/33649


University of New South Wales

11. Wahyudi, Hendra. Development of lead structures that are cytotoxic and are derived from macrocycle natural products.

Degree: Chemistry, 2014, University of New South Wales

 This thesis describes the development of lead structures from two macrocyclic peptide-based natural products: Sansalvamide A (San A) and Sanguinamide B (San B). San A,… (more)

Subjects/Keywords: Natural Product; Macrocycle; Structure-Activity Relationship; Cytotoxic; Macrocyclic Peptide

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APA (6th Edition):

Wahyudi, H. (2014). Development of lead structures that are cytotoxic and are derived from macrocycle natural products. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/53751 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12446/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Wahyudi, Hendra. “Development of lead structures that are cytotoxic and are derived from macrocycle natural products.” 2014. Doctoral Dissertation, University of New South Wales. Accessed October 17, 2019. http://handle.unsw.edu.au/1959.4/53751 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12446/SOURCE02?view=true.

MLA Handbook (7th Edition):

Wahyudi, Hendra. “Development of lead structures that are cytotoxic and are derived from macrocycle natural products.” 2014. Web. 17 Oct 2019.

Vancouver:

Wahyudi H. Development of lead structures that are cytotoxic and are derived from macrocycle natural products. [Internet] [Doctoral dissertation]. University of New South Wales; 2014. [cited 2019 Oct 17]. Available from: http://handle.unsw.edu.au/1959.4/53751 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12446/SOURCE02?view=true.

Council of Science Editors:

Wahyudi H. Development of lead structures that are cytotoxic and are derived from macrocycle natural products. [Doctoral Dissertation]. University of New South Wales; 2014. Available from: http://handle.unsw.edu.au/1959.4/53751 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:12446/SOURCE02?view=true


Purdue University

12. Tabatabaei Ghomi, Hamed. COMPUTATIONAL MODELLING OF PROTEIN FIBRILLATION WITH APPLICATION TO GLUCAGON.

Degree: PhD, Medicinal Chemistry and Molecular Pharmacology, 2015, Purdue University

 A computational method to model the steric zipper of amyloid fibrils (FibPreditor) is developed. The method generates an ensemble of structures for the steric zipper… (more)

Subjects/Keywords: Amyloid fibril; Fibrilation; Glucogon; Peptide formulation; Protein structure; Statistical potential

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APA (6th Edition):

Tabatabaei Ghomi, H. (2015). COMPUTATIONAL MODELLING OF PROTEIN FIBRILLATION WITH APPLICATION TO GLUCAGON. (Doctoral Dissertation). Purdue University. Retrieved from https://docs.lib.purdue.edu/open_access_dissertations/1321

Chicago Manual of Style (16th Edition):

Tabatabaei Ghomi, Hamed. “COMPUTATIONAL MODELLING OF PROTEIN FIBRILLATION WITH APPLICATION TO GLUCAGON.” 2015. Doctoral Dissertation, Purdue University. Accessed October 17, 2019. https://docs.lib.purdue.edu/open_access_dissertations/1321.

MLA Handbook (7th Edition):

Tabatabaei Ghomi, Hamed. “COMPUTATIONAL MODELLING OF PROTEIN FIBRILLATION WITH APPLICATION TO GLUCAGON.” 2015. Web. 17 Oct 2019.

Vancouver:

Tabatabaei Ghomi H. COMPUTATIONAL MODELLING OF PROTEIN FIBRILLATION WITH APPLICATION TO GLUCAGON. [Internet] [Doctoral dissertation]. Purdue University; 2015. [cited 2019 Oct 17]. Available from: https://docs.lib.purdue.edu/open_access_dissertations/1321.

Council of Science Editors:

Tabatabaei Ghomi H. COMPUTATIONAL MODELLING OF PROTEIN FIBRILLATION WITH APPLICATION TO GLUCAGON. [Doctoral Dissertation]. Purdue University; 2015. Available from: https://docs.lib.purdue.edu/open_access_dissertations/1321


Australian National University

13. Rouse, Charlotte Kirsty. Supramolecular Devices and Materials .

Degree: 2016, Australian National University

 This thesis describes work towards the development of a range of supramolecular devices and materials based on cyclodextrin host-guest interactions, and/or short peptide structures. The… (more)

Subjects/Keywords: supramolecular; host-guest; self assembly; cyclodextrin; peptide structure; gel; molecular switch

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APA (6th Edition):

Rouse, C. K. (2016). Supramolecular Devices and Materials . (Thesis). Australian National University. Retrieved from http://hdl.handle.net/1885/112505

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):

Rouse, Charlotte Kirsty. “Supramolecular Devices and Materials .” 2016. Thesis, Australian National University. Accessed October 17, 2019. http://hdl.handle.net/1885/112505.

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

MLA Handbook (7th Edition):

Rouse, Charlotte Kirsty. “Supramolecular Devices and Materials .” 2016. Web. 17 Oct 2019.

Vancouver:

Rouse CK. Supramolecular Devices and Materials . [Internet] [Thesis]. Australian National University; 2016. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/1885/112505.

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

Council of Science Editors:

Rouse CK. Supramolecular Devices and Materials . [Thesis]. Australian National University; 2016. Available from: http://hdl.handle.net/1885/112505

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


University of Melbourne

14. BALAKRISHNAN NAIR, VINOJINI. Human Relaxin-2: design, synthesis and development of novel RXFP1 agonists and antagonists.

Degree: 2014, University of Melbourne

 The ten members of the human insulin-relaxin superfamily comprise insulin, IGFs 1 and 2, relaxin-1, 2 and 3, and INSL3, 4, 5 and 6. Members… (more)

Subjects/Keywords: peptides; structure-activity relationships; relaxin; peptide chemistry; disulfide bond formations; cysteine; RXFP1; agonist; antagonist; peptide mimetics

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APA (6th Edition):

BALAKRISHNAN NAIR, V. (2014). Human Relaxin-2: design, synthesis and development of novel RXFP1 agonists and antagonists. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/44216

Chicago Manual of Style (16th Edition):

BALAKRISHNAN NAIR, VINOJINI. “Human Relaxin-2: design, synthesis and development of novel RXFP1 agonists and antagonists.” 2014. Doctoral Dissertation, University of Melbourne. Accessed October 17, 2019. http://hdl.handle.net/11343/44216.

MLA Handbook (7th Edition):

BALAKRISHNAN NAIR, VINOJINI. “Human Relaxin-2: design, synthesis and development of novel RXFP1 agonists and antagonists.” 2014. Web. 17 Oct 2019.

Vancouver:

BALAKRISHNAN NAIR V. Human Relaxin-2: design, synthesis and development of novel RXFP1 agonists and antagonists. [Internet] [Doctoral dissertation]. University of Melbourne; 2014. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/11343/44216.

Council of Science Editors:

BALAKRISHNAN NAIR V. Human Relaxin-2: design, synthesis and development of novel RXFP1 agonists and antagonists. [Doctoral Dissertation]. University of Melbourne; 2014. Available from: http://hdl.handle.net/11343/44216


University of Melbourne

15. Rimmer, Kieran. Structural perspectives on mitochondrial import across the outer membrane.

Degree: 2010, University of Melbourne

 The mitochondrion is an essential organelle in the eukaryotic cell, mediating functions as diverse as oxidative phosphorylation and apoptosis. The mitochondrion, which was once a… (more)

Subjects/Keywords: NMR; nuclear magnetic resonance; protein structure; mitochondrial import; import; peptide expression; peptide purification; peptide structure; spin label; paramagnetic; protein-peptide interactions; cyanogen bromide; CNBr; Tom20; Tom22; presequence; preprotein; mitochondrial outer membrane; Translocase

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APA (6th Edition):

Rimmer, K. (2010). Structural perspectives on mitochondrial import across the outer membrane. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/35457

Chicago Manual of Style (16th Edition):

Rimmer, Kieran. “Structural perspectives on mitochondrial import across the outer membrane.” 2010. Doctoral Dissertation, University of Melbourne. Accessed October 17, 2019. http://hdl.handle.net/11343/35457.

MLA Handbook (7th Edition):

Rimmer, Kieran. “Structural perspectives on mitochondrial import across the outer membrane.” 2010. Web. 17 Oct 2019.

Vancouver:

Rimmer K. Structural perspectives on mitochondrial import across the outer membrane. [Internet] [Doctoral dissertation]. University of Melbourne; 2010. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/11343/35457.

Council of Science Editors:

Rimmer K. Structural perspectives on mitochondrial import across the outer membrane. [Doctoral Dissertation]. University of Melbourne; 2010. Available from: http://hdl.handle.net/11343/35457


University of California – Riverside

16. Tao, Yuanqi. Mass Spectrometry Based Characterization of Protein Structure and Peptide Isomerization.

Degree: Chemistry, 2014, University of California – Riverside

Structure is the key factor in protein function. Mass spectrometry has been shown to be a powerful technique for exploring protein structures and post translational… (more)

Subjects/Keywords: Analytical chemistry; Biochemistry; Isomerization; LC-MS; mass spectrometry; Peptide; Protein structure; proteomics

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APA (6th Edition):

Tao, Y. (2014). Mass Spectrometry Based Characterization of Protein Structure and Peptide Isomerization. (Thesis). University of California – Riverside. Retrieved from http://www.escholarship.org/uc/item/9sn806r9

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):

Tao, Yuanqi. “Mass Spectrometry Based Characterization of Protein Structure and Peptide Isomerization.” 2014. Thesis, University of California – Riverside. Accessed October 17, 2019. http://www.escholarship.org/uc/item/9sn806r9.

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

MLA Handbook (7th Edition):

Tao, Yuanqi. “Mass Spectrometry Based Characterization of Protein Structure and Peptide Isomerization.” 2014. Web. 17 Oct 2019.

Vancouver:

Tao Y. Mass Spectrometry Based Characterization of Protein Structure and Peptide Isomerization. [Internet] [Thesis]. University of California – Riverside; 2014. [cited 2019 Oct 17]. Available from: http://www.escholarship.org/uc/item/9sn806r9.

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

Council of Science Editors:

Tao Y. Mass Spectrometry Based Characterization of Protein Structure and Peptide Isomerization. [Thesis]. University of California – Riverside; 2014. Available from: http://www.escholarship.org/uc/item/9sn806r9

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


University of California – Irvine

17. Kreutzer, Adam George. Elucidating the Structures of Oligomers Formed by Macrocyclic β-Hairpin Mimics: Insights into Alzheimer’s Disease.

Degree: Chemistry, 2017, University of California – Irvine

 Chapter 1 provides an overview of the field of amyloid structural biology and provides context for the work described in this dissertation. In the more… (more)

Subjects/Keywords: Chemistry; Organic chemistry; Biochemistry; Alzheimer's; Amyloid; Oligomer; Peptide; Structure; X-ray crystallogrpahy

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APA (6th Edition):

Kreutzer, A. G. (2017). Elucidating the Structures of Oligomers Formed by Macrocyclic β-Hairpin Mimics: Insights into Alzheimer’s Disease. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/8w27p4c7

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):

Kreutzer, Adam George. “Elucidating the Structures of Oligomers Formed by Macrocyclic β-Hairpin Mimics: Insights into Alzheimer’s Disease.” 2017. Thesis, University of California – Irvine. Accessed October 17, 2019. http://www.escholarship.org/uc/item/8w27p4c7.

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

MLA Handbook (7th Edition):

Kreutzer, Adam George. “Elucidating the Structures of Oligomers Formed by Macrocyclic β-Hairpin Mimics: Insights into Alzheimer’s Disease.” 2017. Web. 17 Oct 2019.

Vancouver:

Kreutzer AG. Elucidating the Structures of Oligomers Formed by Macrocyclic β-Hairpin Mimics: Insights into Alzheimer’s Disease. [Internet] [Thesis]. University of California – Irvine; 2017. [cited 2019 Oct 17]. Available from: http://www.escholarship.org/uc/item/8w27p4c7.

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

Council of Science Editors:

Kreutzer AG. Elucidating the Structures of Oligomers Formed by Macrocyclic β-Hairpin Mimics: Insights into Alzheimer’s Disease. [Thesis]. University of California – Irvine; 2017. Available from: http://www.escholarship.org/uc/item/8w27p4c7

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


University of California – Berkeley

18. Dube, Nikhil. 3-Helix Micelles as Drug Nanocarriers.

Degree: Materials Science & Engineering, 2014, University of California – Berkeley

 3-Helix Micelles as Drug NanocarriersControl over particle size, cargo loading, encapsulation stability, and drug release is critical to optimize the safety and efficacy of drug… (more)

Subjects/Keywords: Materials Science; Nanotechnology; Pharmaceutical sciences; Drug delivery; Micelles; Peptide; Polymer; Stability; Structure

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APA (6th Edition):

Dube, N. (2014). 3-Helix Micelles as Drug Nanocarriers. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/2j24x74f

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):

Dube, Nikhil. “3-Helix Micelles as Drug Nanocarriers.” 2014. Thesis, University of California – Berkeley. Accessed October 17, 2019. http://www.escholarship.org/uc/item/2j24x74f.

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

MLA Handbook (7th Edition):

Dube, Nikhil. “3-Helix Micelles as Drug Nanocarriers.” 2014. Web. 17 Oct 2019.

Vancouver:

Dube N. 3-Helix Micelles as Drug Nanocarriers. [Internet] [Thesis]. University of California – Berkeley; 2014. [cited 2019 Oct 17]. Available from: http://www.escholarship.org/uc/item/2j24x74f.

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

Council of Science Editors:

Dube N. 3-Helix Micelles as Drug Nanocarriers. [Thesis]. University of California – Berkeley; 2014. Available from: http://www.escholarship.org/uc/item/2j24x74f

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


Université Laval

19. Dorion, Geneviève. Mécanismes et structures impliqués dans l'effet anti-inflammatoire et bronchorelaxant du 1,1-diméthylphényl1-4pipérazinium.

Degree: 2005, Université Laval

 Le 1,1-dimethylphenyl1-4piperazinium (DMPP), un agoniste nicotinique, a un effet anti-inflammatoire et bronchorelaxant. Afin de comprendre ces effets, les sous-unités alpha-3, alpha-4 et alpha-7 du récepteur… (more)

Subjects/Keywords: Diméthylphénylpipérazinium  – Relations structure-activité; VIP (Peptide)

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APA (6th Edition):

Dorion, G. (2005). Mécanismes et structures impliqués dans l'effet anti-inflammatoire et bronchorelaxant du 1,1-diméthylphényl1-4pipérazinium. (Thesis). Université Laval. Retrieved from http://hdl.handle.net/20.500.11794/18098

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):

Dorion, Geneviève. “Mécanismes et structures impliqués dans l'effet anti-inflammatoire et bronchorelaxant du 1,1-diméthylphényl1-4pipérazinium.” 2005. Thesis, Université Laval. Accessed October 17, 2019. http://hdl.handle.net/20.500.11794/18098.

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

MLA Handbook (7th Edition):

Dorion, Geneviève. “Mécanismes et structures impliqués dans l'effet anti-inflammatoire et bronchorelaxant du 1,1-diméthylphényl1-4pipérazinium.” 2005. Web. 17 Oct 2019.

Vancouver:

Dorion G. Mécanismes et structures impliqués dans l'effet anti-inflammatoire et bronchorelaxant du 1,1-diméthylphényl1-4pipérazinium. [Internet] [Thesis]. Université Laval; 2005. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/20.500.11794/18098.

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

Council of Science Editors:

Dorion G. Mécanismes et structures impliqués dans l'effet anti-inflammatoire et bronchorelaxant du 1,1-diméthylphényl1-4pipérazinium. [Thesis]. Université Laval; 2005. Available from: http://hdl.handle.net/20.500.11794/18098

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


University of Adelaide

20. Marshall, Andrew Craig. Structural and biochemical studies on three Aspergillus fumigatus proteins that present as targets for novel antifungal drugs.

Degree: 2018, University of Adelaide

 The increasing use of aggressive immunosuppressive regimes over the last half-century has been accompanied by an increased incidence of opportunistic invasive fungal infections, with Aspergillus… (more)

Subjects/Keywords: Research by publication; X-ray crystallography; protein structure; antifungal drugs; enzymes; catalysis; protein-peptide interactions

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APA (6th Edition):

Marshall, A. C. (2018). Structural and biochemical studies on three Aspergillus fumigatus proteins that present as targets for novel antifungal drugs. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/115176

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):

Marshall, Andrew Craig. “Structural and biochemical studies on three Aspergillus fumigatus proteins that present as targets for novel antifungal drugs.” 2018. Thesis, University of Adelaide. Accessed October 17, 2019. http://hdl.handle.net/2440/115176.

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

MLA Handbook (7th Edition):

Marshall, Andrew Craig. “Structural and biochemical studies on three Aspergillus fumigatus proteins that present as targets for novel antifungal drugs.” 2018. Web. 17 Oct 2019.

Vancouver:

Marshall AC. Structural and biochemical studies on three Aspergillus fumigatus proteins that present as targets for novel antifungal drugs. [Internet] [Thesis]. University of Adelaide; 2018. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/2440/115176.

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

Council of Science Editors:

Marshall AC. Structural and biochemical studies on three Aspergillus fumigatus proteins that present as targets for novel antifungal drugs. [Thesis]. University of Adelaide; 2018. Available from: http://hdl.handle.net/2440/115176

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


ETH Zürich

21. Müller, Alex T. De Novo Design of Antimicrobial Peptides: From Sequence Templates to Artificial Intelligence.

Degree: 2018, ETH Zürich

 Bacterial resistance, eradicating the efficiency of many antibiotics, is globally increasing and poses a threat to public health. In parallel, an all-time low number of… (more)

Subjects/Keywords: Antibiotic resistance; Machine learning; Recurrent neural networks; Peptide design; Structure-activity relationship; Artificial intelligence

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

APA (6th Edition):

Müller, A. T. (2018). De Novo Design of Antimicrobial Peptides: From Sequence Templates to Artificial Intelligence. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/267218

Chicago Manual of Style (16th Edition):

Müller, Alex T. “De Novo Design of Antimicrobial Peptides: From Sequence Templates to Artificial Intelligence.” 2018. Doctoral Dissertation, ETH Zürich. Accessed October 17, 2019. http://hdl.handle.net/20.500.11850/267218.

MLA Handbook (7th Edition):

Müller, Alex T. “De Novo Design of Antimicrobial Peptides: From Sequence Templates to Artificial Intelligence.” 2018. Web. 17 Oct 2019.

Vancouver:

Müller AT. De Novo Design of Antimicrobial Peptides: From Sequence Templates to Artificial Intelligence. [Internet] [Doctoral dissertation]. ETH Zürich; 2018. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/20.500.11850/267218.

Council of Science Editors:

Müller AT. De Novo Design of Antimicrobial Peptides: From Sequence Templates to Artificial Intelligence. [Doctoral Dissertation]. ETH Zürich; 2018. Available from: http://hdl.handle.net/20.500.11850/267218

22. Vignaud, Hélène. Étude de la toxicité du peptide amyloïde beta Aß42 dans la levure Saccharomyces cerevisiae : Toxicity study of beta amyloid peptide Aß42 in Saccharomyces cerevisiae.

Degree: Docteur es, Sciences, technologie, santé. Génétique, 2013, Université de Bordeaux Segalen

La maladie d’Alzheimer est la maladie neurodégénérative la plus fréquente chez l’Homme et constitue un enjeu économique et de santé publique majeur. Les cerveaux de… (more)

Subjects/Keywords: Levure; Peptide Aß; Toxicité; Étude structure-toxicité; Oligomères antiparallèles; Trafic intracellulaire; Yeast; ; Toxicity; Structure-toxicity study; Antiparallel oligomers; Intracellular trafficking

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APA (6th Edition):

Vignaud, H. (2013). Étude de la toxicité du peptide amyloïde beta Aß42 dans la levure Saccharomyces cerevisiae : Toxicity study of beta amyloid peptide Aß42 in Saccharomyces cerevisiae. (Doctoral Dissertation). Université de Bordeaux Segalen. Retrieved from http://www.theses.fr/2013BOR22068

Chicago Manual of Style (16th Edition):

Vignaud, Hélène. “Étude de la toxicité du peptide amyloïde beta Aß42 dans la levure Saccharomyces cerevisiae : Toxicity study of beta amyloid peptide Aß42 in Saccharomyces cerevisiae.” 2013. Doctoral Dissertation, Université de Bordeaux Segalen. Accessed October 17, 2019. http://www.theses.fr/2013BOR22068.

MLA Handbook (7th Edition):

Vignaud, Hélène. “Étude de la toxicité du peptide amyloïde beta Aß42 dans la levure Saccharomyces cerevisiae : Toxicity study of beta amyloid peptide Aß42 in Saccharomyces cerevisiae.” 2013. Web. 17 Oct 2019.

Vancouver:

Vignaud H. Étude de la toxicité du peptide amyloïde beta Aß42 dans la levure Saccharomyces cerevisiae : Toxicity study of beta amyloid peptide Aß42 in Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. Université de Bordeaux Segalen; 2013. [cited 2019 Oct 17]. Available from: http://www.theses.fr/2013BOR22068.

Council of Science Editors:

Vignaud H. Étude de la toxicité du peptide amyloïde beta Aß42 dans la levure Saccharomyces cerevisiae : Toxicity study of beta amyloid peptide Aß42 in Saccharomyces cerevisiae. [Doctoral Dissertation]. Université de Bordeaux Segalen; 2013. Available from: http://www.theses.fr/2013BOR22068


University of Florida

23. Yu, Long. Infrared Spectroscopy of Peptide Fragment Structures Parameterization, Conformational Searching and Frequency Calculation.

Degree: MS, Chemistry, 2010, University of Florida

 The structures of b2 and b5 product ions from oligoglycine peptide fragmentation by collision-induced dissociation (CID) are studied through comparison between experimental infrared multiple-photon dissociation… (more)

Subjects/Keywords: Amides; Annealing; Electronic structure; Electronics; Energy; Geometry; Ions; Molecular structure; Molecules; Photons; conformational, infrared, parameterization, peptide

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APA (6th Edition):

Yu, L. (2010). Infrared Spectroscopy of Peptide Fragment Structures Parameterization, Conformational Searching and Frequency Calculation. (Masters Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0042229

Chicago Manual of Style (16th Edition):

Yu, Long. “Infrared Spectroscopy of Peptide Fragment Structures Parameterization, Conformational Searching and Frequency Calculation.” 2010. Masters Thesis, University of Florida. Accessed October 17, 2019. http://ufdc.ufl.edu/UFE0042229.

MLA Handbook (7th Edition):

Yu, Long. “Infrared Spectroscopy of Peptide Fragment Structures Parameterization, Conformational Searching and Frequency Calculation.” 2010. Web. 17 Oct 2019.

Vancouver:

Yu L. Infrared Spectroscopy of Peptide Fragment Structures Parameterization, Conformational Searching and Frequency Calculation. [Internet] [Masters thesis]. University of Florida; 2010. [cited 2019 Oct 17]. Available from: http://ufdc.ufl.edu/UFE0042229.

Council of Science Editors:

Yu L. Infrared Spectroscopy of Peptide Fragment Structures Parameterization, Conformational Searching and Frequency Calculation. [Masters Thesis]. University of Florida; 2010. Available from: http://ufdc.ufl.edu/UFE0042229


Université de Montréal

24. Beauregard, Kim. Développement de peptidomimétiques antagonistes du récepteur de l’interleukine-1β .

Degree: 2012, Université de Montréal

 Dans ce mémoire, je présente mes études sur la synthèse, la caractérisation et l’évaluation biologique de différentes séries d’analogues du D-heptapeptide appelé 101.10, un modulateur… (more)

Subjects/Keywords: Inflammation; Inflammation; Interleukine-1 bêta; Interleukin-1 beta; Mime peptidique; Peptide mimic; Amino-gamma-lactame; Amino-gamma-lactam; Indolizidinone; Indolizidinone; Structure secondaire de peptide; Peptide secondary structure; Repliement bêta; Beta turn; Prolifération de thymocyte; Thymocyte proliferation; Contre-anion; Counter-anion

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APA (6th Edition):

Beauregard, K. (2012). Développement de peptidomimétiques antagonistes du récepteur de l’interleukine-1β . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/8460

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):

Beauregard, Kim. “Développement de peptidomimétiques antagonistes du récepteur de l’interleukine-1β .” 2012. Thesis, Université de Montréal. Accessed October 17, 2019. http://hdl.handle.net/1866/8460.

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

MLA Handbook (7th Edition):

Beauregard, Kim. “Développement de peptidomimétiques antagonistes du récepteur de l’interleukine-1β .” 2012. Web. 17 Oct 2019.

Vancouver:

Beauregard K. Développement de peptidomimétiques antagonistes du récepteur de l’interleukine-1β . [Internet] [Thesis]. Université de Montréal; 2012. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/1866/8460.

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

Council of Science Editors:

Beauregard K. Développement de peptidomimétiques antagonistes du récepteur de l’interleukine-1β . [Thesis]. Université de Montréal; 2012. Available from: http://hdl.handle.net/1866/8460

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

25. Santos, Fellipe Bronze dos. Análise bioquímica e estrutural das proteínas dermicidina-1L e sua splice variante em sistema biomimético.

Degree: Mestrado, Farmacologia, 2014, University of São Paulo

Dermicidina (DCD) é um gene mapeado no cromossomo 12, lócus 12q13.1, e codifica uma proteína de 110 aminoácidos, que sofre um processamento proteolítico, gerando peptídeos… (more)

Subjects/Keywords: Antimicrobial peptide; Biomimetic system; Dermicidin; Dermicidina; Estrutura de proteínas; Peptídeo antimicrobiano; Protein structure; Sistema biomimético; Splice variant; Splice variante

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APA (6th Edition):

Santos, F. B. d. (2014). Análise bioquímica e estrutural das proteínas dermicidina-1L e sua splice variante em sistema biomimético. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/42/42136/tde-26062014-170711/ ;

Chicago Manual of Style (16th Edition):

Santos, Fellipe Bronze dos. “Análise bioquímica e estrutural das proteínas dermicidina-1L e sua splice variante em sistema biomimético.” 2014. Masters Thesis, University of São Paulo. Accessed October 17, 2019. http://www.teses.usp.br/teses/disponiveis/42/42136/tde-26062014-170711/ ;.

MLA Handbook (7th Edition):

Santos, Fellipe Bronze dos. “Análise bioquímica e estrutural das proteínas dermicidina-1L e sua splice variante em sistema biomimético.” 2014. Web. 17 Oct 2019.

Vancouver:

Santos FBd. Análise bioquímica e estrutural das proteínas dermicidina-1L e sua splice variante em sistema biomimético. [Internet] [Masters thesis]. University of São Paulo; 2014. [cited 2019 Oct 17]. Available from: http://www.teses.usp.br/teses/disponiveis/42/42136/tde-26062014-170711/ ;.

Council of Science Editors:

Santos FBd. Análise bioquímica e estrutural das proteínas dermicidina-1L e sua splice variante em sistema biomimético. [Masters Thesis]. University of São Paulo; 2014. Available from: http://www.teses.usp.br/teses/disponiveis/42/42136/tde-26062014-170711/ ;


University of Southern California

26. Schiewe, Alexandra J. Structural prediction of MHC-peptide-TCR interactions: potential for vaccine design.

Degree: PhD, Pharmaceutical Sciences, 2007, University of Southern California

 Major histocompatibility complex (MHC) molecules are cell surface glycoproteins that bind short peptide fragments and present them to T lymphocytes. The MHC presentation mechanism is… (more)

Subjects/Keywords: MHC-peptide; T cell receptor; structure prediction

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APA (6th Edition):

Schiewe, A. J. (2007). Structural prediction of MHC-peptide-TCR interactions: potential for vaccine design. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/12635/rec/6116

Chicago Manual of Style (16th Edition):

Schiewe, Alexandra J. “Structural prediction of MHC-peptide-TCR interactions: potential for vaccine design.” 2007. Doctoral Dissertation, University of Southern California. Accessed October 17, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/12635/rec/6116.

MLA Handbook (7th Edition):

Schiewe, Alexandra J. “Structural prediction of MHC-peptide-TCR interactions: potential for vaccine design.” 2007. Web. 17 Oct 2019.

Vancouver:

Schiewe AJ. Structural prediction of MHC-peptide-TCR interactions: potential for vaccine design. [Internet] [Doctoral dissertation]. University of Southern California; 2007. [cited 2019 Oct 17]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/12635/rec/6116.

Council of Science Editors:

Schiewe AJ. Structural prediction of MHC-peptide-TCR interactions: potential for vaccine design. [Doctoral Dissertation]. University of Southern California; 2007. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/12635/rec/6116


University of Saskatchewan

27. Chowdhury, Somenath. Controlling the structure of peptide using ferrocene as a molecular scaffold.

Degree: 2007, University of Saskatchewan

 The de novo design of peptides is a central area of research in chemical biology. Although it is now possible to design helical peptide structures… (more)

Subjects/Keywords: Beta-barrel; Ferrocene; Structure Design; Beta-helix; Peptide

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APA (6th Edition):

Chowdhury, S. (2007). Controlling the structure of peptide using ferrocene as a molecular scaffold. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/etd-06142007-063338

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):

Chowdhury, Somenath. “Controlling the structure of peptide using ferrocene as a molecular scaffold.” 2007. Thesis, University of Saskatchewan. Accessed October 17, 2019. http://hdl.handle.net/10388/etd-06142007-063338.

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

MLA Handbook (7th Edition):

Chowdhury, Somenath. “Controlling the structure of peptide using ferrocene as a molecular scaffold.” 2007. Web. 17 Oct 2019.

Vancouver:

Chowdhury S. Controlling the structure of peptide using ferrocene as a molecular scaffold. [Internet] [Thesis]. University of Saskatchewan; 2007. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/10388/etd-06142007-063338.

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

Council of Science Editors:

Chowdhury S. Controlling the structure of peptide using ferrocene as a molecular scaffold. [Thesis]. University of Saskatchewan; 2007. Available from: http://hdl.handle.net/10388/etd-06142007-063338

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


University of Gothenburg / Göteborgs Universitet

28. Yatsyna, Vasyl. Structure-Specific Vibrational Modes of Isolated Biomolecules Studied with Mid- and Far-Infrared Laser Spectroscopy.

Degree: 2019, University of Gothenburg / Göteborgs Universitet

 Biomolecular structure elucidation is crucial for our detailed understanding of various biological processes, since there is an intimate relationship between the biomolecular function and structure.… (more)

Subjects/Keywords: far-infrared gas-phase spectroscopy; conformers; vibrational anharmonicity; infrared multiple photon dissociation; peptide structure; folded and extended peptides; hydrogen bonding

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

APA (6th Edition):

Yatsyna, V. (2019). Structure-Specific Vibrational Modes of Isolated Biomolecules Studied with Mid- and Far-Infrared Laser Spectroscopy. (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/58138

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):

Yatsyna, Vasyl. “Structure-Specific Vibrational Modes of Isolated Biomolecules Studied with Mid- and Far-Infrared Laser Spectroscopy.” 2019. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed October 17, 2019. http://hdl.handle.net/2077/58138.

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

MLA Handbook (7th Edition):

Yatsyna, Vasyl. “Structure-Specific Vibrational Modes of Isolated Biomolecules Studied with Mid- and Far-Infrared Laser Spectroscopy.” 2019. Web. 17 Oct 2019.

Vancouver:

Yatsyna V. Structure-Specific Vibrational Modes of Isolated Biomolecules Studied with Mid- and Far-Infrared Laser Spectroscopy. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 2019. [cited 2019 Oct 17]. Available from: http://hdl.handle.net/2077/58138.

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

Council of Science Editors:

Yatsyna V. Structure-Specific Vibrational Modes of Isolated Biomolecules Studied with Mid- and Far-Infrared Laser Spectroscopy. [Thesis]. University of Gothenburg / Göteborgs Universitet; 2019. Available from: http://hdl.handle.net/2077/58138

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

29. Mihalca, R. Structural and conformational aspects of gas phase peptides probed by electron capture dissociation.

Degree: 2007, University Utrecht

 Mass spectrometry (MS) is a major player in the field of structural characterization of peptides and proteins. MS-based proteomics is nowadays routinely carried out at… (more)

Subjects/Keywords: ECD; IRMPD; SORI-CID; peptide; protein; structure; conformation; metals

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

APA (6th Edition):

Mihalca, R. (2007). Structural and conformational aspects of gas phase peptides probed by electron capture dissociation. (Doctoral Dissertation). University Utrecht. Retrieved from http://dspace.library.uu.nl/handle/1874/20339 ; URN:NBN:NL:UI:10-1874-20339 ; URN:NBN:NL:UI:10-1874-20339 ; http://dspace.library.uu.nl/handle/1874/20339

Chicago Manual of Style (16th Edition):

Mihalca, R. “Structural and conformational aspects of gas phase peptides probed by electron capture dissociation.” 2007. Doctoral Dissertation, University Utrecht. Accessed October 17, 2019. http://dspace.library.uu.nl/handle/1874/20339 ; URN:NBN:NL:UI:10-1874-20339 ; URN:NBN:NL:UI:10-1874-20339 ; http://dspace.library.uu.nl/handle/1874/20339.

MLA Handbook (7th Edition):

Mihalca, R. “Structural and conformational aspects of gas phase peptides probed by electron capture dissociation.” 2007. Web. 17 Oct 2019.

Vancouver:

Mihalca R. Structural and conformational aspects of gas phase peptides probed by electron capture dissociation. [Internet] [Doctoral dissertation]. University Utrecht; 2007. [cited 2019 Oct 17]. Available from: http://dspace.library.uu.nl/handle/1874/20339 ; URN:NBN:NL:UI:10-1874-20339 ; URN:NBN:NL:UI:10-1874-20339 ; http://dspace.library.uu.nl/handle/1874/20339.

Council of Science Editors:

Mihalca R. Structural and conformational aspects of gas phase peptides probed by electron capture dissociation. [Doctoral Dissertation]. University Utrecht; 2007. Available from: http://dspace.library.uu.nl/handle/1874/20339 ; URN:NBN:NL:UI:10-1874-20339 ; URN:NBN:NL:UI:10-1874-20339 ; http://dspace.library.uu.nl/handle/1874/20339

30. SHIVA KUMAR. Crystal structure of PacIR Extracelluar Domain: Insights of Hormone Recognition.

Degree: 2010, National University of Singapore

Subjects/Keywords: Crystal structure; GPCR; PAC1R; PACAP; Membrane protein; peptide hormone

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

APA (6th Edition):

KUMAR, S. (2010). Crystal structure of PacIR Extracelluar Domain: Insights of Hormone Recognition. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/25819

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

Chicago Manual of Style (16th Edition):

KUMAR, SHIVA. “Crystal structure of PacIR Extracelluar Domain: Insights of Hormone Recognition.” 2010. Thesis, National University of Singapore. Accessed October 17, 2019. http://scholarbank.nus.edu.sg/handle/10635/25819.

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

MLA Handbook (7th Edition):

KUMAR, SHIVA. “Crystal structure of PacIR Extracelluar Domain: Insights of Hormone Recognition.” 2010. Web. 17 Oct 2019.

Vancouver:

KUMAR S. Crystal structure of PacIR Extracelluar Domain: Insights of Hormone Recognition. [Internet] [Thesis]. National University of Singapore; 2010. [cited 2019 Oct 17]. Available from: http://scholarbank.nus.edu.sg/handle/10635/25819.

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

Council of Science Editors:

KUMAR S. Crystal structure of PacIR Extracelluar Domain: Insights of Hormone Recognition. [Thesis]. National University of Singapore; 2010. Available from: http://scholarbank.nus.edu.sg/handle/10635/25819

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

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