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You searched for subject:(membrane proteins AND peptides). Showing records 1 – 30 of 973 total matches.

[1] [2] [3] [4] [5] … [33]

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University of Limerick

1. Höfer, Nicole. Crystallization and structure determination of gramicidin D and the cytosolic domain of CzrB.

Degree: 2013, University of Limerick

peer-reviewed

Crystallization of membrane proteins and peptides represents a challenge in the field of structural biology. Lipidic cubic phase (LCP) has become an important medium… (more)

Subjects/Keywords: crystallization; membrane proteins and peptides; LCP

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APA (6th Edition):

Höfer, N. (2013). Crystallization and structure determination of gramicidin D and the cytosolic domain of CzrB. (Thesis). University of Limerick. Retrieved from http://hdl.handle.net/10344/3282

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):

Höfer, Nicole. “Crystallization and structure determination of gramicidin D and the cytosolic domain of CzrB.” 2013. Thesis, University of Limerick. Accessed October 18, 2019. http://hdl.handle.net/10344/3282.

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

MLA Handbook (7th Edition):

Höfer, Nicole. “Crystallization and structure determination of gramicidin D and the cytosolic domain of CzrB.” 2013. Web. 18 Oct 2019.

Vancouver:

Höfer N. Crystallization and structure determination of gramicidin D and the cytosolic domain of CzrB. [Internet] [Thesis]. University of Limerick; 2013. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10344/3282.

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

Council of Science Editors:

Höfer N. Crystallization and structure determination of gramicidin D and the cytosolic domain of CzrB. [Thesis]. University of Limerick; 2013. Available from: http://hdl.handle.net/10344/3282

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


University of Texas Southwestern Medical Center

2. Zhang, Yinxin. Sterol Sensing by Two Luminal Loops in Scap.

Degree: 2014, University of Texas Southwestern Medical Center

 SREBP cleavage-activating protein (Scap) is an endoplasmic reticulum (ER) membrane protein that controls cholesterol homeostasis by transporting SREBPs from the ER to the Golgi complex.… (more)

Subjects/Keywords: Cholesterol; Endoplasmic Reticulum; Intracellular Signaling Peptides and Proteins; Membrane Proteins; Sterol Regulatory Element Binding Proteins

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APA (6th Edition):

Zhang, Y. (2014). Sterol Sensing by Two Luminal Loops in Scap. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/3333

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, Yinxin. “Sterol Sensing by Two Luminal Loops in Scap.” 2014. Thesis, University of Texas Southwestern Medical Center. Accessed October 18, 2019. http://hdl.handle.net/2152.5/3333.

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

MLA Handbook (7th Edition):

Zhang, Yinxin. “Sterol Sensing by Two Luminal Loops in Scap.” 2014. Web. 18 Oct 2019.

Vancouver:

Zhang Y. Sterol Sensing by Two Luminal Loops in Scap. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2014. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2152.5/3333.

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

Council of Science Editors:

Zhang Y. Sterol Sensing by Two Luminal Loops in Scap. [Thesis]. University of Texas Southwestern Medical Center; 2014. Available from: http://hdl.handle.net/2152.5/3333

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


University of Miami

3. Kaye, Elena Cortizas. The Function of Outer Membrane Protein A (OmpA) in Yersinia pestis.

Degree: MS, Microbiology and Immunology (Medicine), 2010, University of Miami

 The outer membrane protein OmpA is one of the major outer membrane proteins in many species of bacteria, including the Yersiniae. Our goal was to… (more)

Subjects/Keywords: Bacteria; Outer Membrane Proteins; Bacterial Pathogenesis; Antimicrobial Peptides

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APA (6th Edition):

Kaye, E. C. (2010). The Function of Outer Membrane Protein A (OmpA) in Yersinia pestis. (Thesis). University of Miami. Retrieved from https://scholarlyrepository.miami.edu/oa_theses/58

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):

Kaye, Elena Cortizas. “The Function of Outer Membrane Protein A (OmpA) in Yersinia pestis.” 2010. Thesis, University of Miami. Accessed October 18, 2019. https://scholarlyrepository.miami.edu/oa_theses/58.

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

MLA Handbook (7th Edition):

Kaye, Elena Cortizas. “The Function of Outer Membrane Protein A (OmpA) in Yersinia pestis.” 2010. Web. 18 Oct 2019.

Vancouver:

Kaye EC. The Function of Outer Membrane Protein A (OmpA) in Yersinia pestis. [Internet] [Thesis]. University of Miami; 2010. [cited 2019 Oct 18]. Available from: https://scholarlyrepository.miami.edu/oa_theses/58.

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

Council of Science Editors:

Kaye EC. The Function of Outer Membrane Protein A (OmpA) in Yersinia pestis. [Thesis]. University of Miami; 2010. Available from: https://scholarlyrepository.miami.edu/oa_theses/58

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


Western Washington University

4. Reed, Sierra. Driving Sortase-Mediated Ligations Using Metal-Coordinating Peptides.

Degree: MS, Chemistry, 2018, Western Washington University

  The versatility of sortase-mediated ligations as a protein modification technique has been well demonstrated, but the efficiency of these reactions suffers from inherent reversibility.… (more)

Subjects/Keywords: Chemistry; Membrane proteins; Nickel; Peptides – Synthesis; Ligases; Nucleophilic reactions; masters theses

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APA (6th Edition):

Reed, S. (2018). Driving Sortase-Mediated Ligations Using Metal-Coordinating Peptides. (Masters Thesis). Western Washington University. Retrieved from https://cedar.wwu.edu/wwuet/700

Chicago Manual of Style (16th Edition):

Reed, Sierra. “Driving Sortase-Mediated Ligations Using Metal-Coordinating Peptides.” 2018. Masters Thesis, Western Washington University. Accessed October 18, 2019. https://cedar.wwu.edu/wwuet/700.

MLA Handbook (7th Edition):

Reed, Sierra. “Driving Sortase-Mediated Ligations Using Metal-Coordinating Peptides.” 2018. Web. 18 Oct 2019.

Vancouver:

Reed S. Driving Sortase-Mediated Ligations Using Metal-Coordinating Peptides. [Internet] [Masters thesis]. Western Washington University; 2018. [cited 2019 Oct 18]. Available from: https://cedar.wwu.edu/wwuet/700.

Council of Science Editors:

Reed S. Driving Sortase-Mediated Ligations Using Metal-Coordinating Peptides. [Masters Thesis]. Western Washington University; 2018. Available from: https://cedar.wwu.edu/wwuet/700


Michigan State University

5. Xie, Li. Solid state nuclear magnetic resonance studies of structures and membrane locations of peptides.

Degree: 2014, Michigan State University

Thesis Ph. D. Michigan State University. Chemistry 2014.

Solid state nuclear magnetic resonance (SSNMR) can be used to study the structures of molecules such as… (more)

Subjects/Keywords: Nuclear magnetic resonance spectroscopy; Peptides – Analysis; Membrane proteins – Structure; Chemistry

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APA (6th Edition):

Xie, L. (2014). Solid state nuclear magnetic resonance studies of structures and membrane locations of peptides. (Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:3120

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):

Xie, Li. “Solid state nuclear magnetic resonance studies of structures and membrane locations of peptides.” 2014. Thesis, Michigan State University. Accessed October 18, 2019. http://etd.lib.msu.edu/islandora/object/etd:3120.

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

MLA Handbook (7th Edition):

Xie, Li. “Solid state nuclear magnetic resonance studies of structures and membrane locations of peptides.” 2014. Web. 18 Oct 2019.

Vancouver:

Xie L. Solid state nuclear magnetic resonance studies of structures and membrane locations of peptides. [Internet] [Thesis]. Michigan State University; 2014. [cited 2019 Oct 18]. Available from: http://etd.lib.msu.edu/islandora/object/etd:3120.

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

Council of Science Editors:

Xie L. Solid state nuclear magnetic resonance studies of structures and membrane locations of peptides. [Thesis]. Michigan State University; 2014. Available from: http://etd.lib.msu.edu/islandora/object/etd:3120

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


University of Texas Southwestern Medical Center

6. Faulkner, Rebecca Ann. Utilizing Drosophila S2 Cells as a Model System to Determine Underlying Mechanisms of ER-associated Degradation.

Degree: 2014, University of Texas Southwestern Medical Center

 Proper folding of nascent polypeptides is vital to maintain cellular homeostasis; proteins that adopt aberrant confirmations are selectively degraded through a multi-step process known as… (more)

Subjects/Keywords: Endoplasmic Reticulum-Associated Degradation; Hydroxymethylglutaryl CoA Reductases; Intracellular Signaling Peptides and Proteins; Membrane Proteins

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APA (6th Edition):

Faulkner, R. A. (2014). Utilizing Drosophila S2 Cells as a Model System to Determine Underlying Mechanisms of ER-associated Degradation. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/3312

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):

Faulkner, Rebecca Ann. “Utilizing Drosophila S2 Cells as a Model System to Determine Underlying Mechanisms of ER-associated Degradation.” 2014. Thesis, University of Texas Southwestern Medical Center. Accessed October 18, 2019. http://hdl.handle.net/2152.5/3312.

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

MLA Handbook (7th Edition):

Faulkner, Rebecca Ann. “Utilizing Drosophila S2 Cells as a Model System to Determine Underlying Mechanisms of ER-associated Degradation.” 2014. Web. 18 Oct 2019.

Vancouver:

Faulkner RA. Utilizing Drosophila S2 Cells as a Model System to Determine Underlying Mechanisms of ER-associated Degradation. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2014. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2152.5/3312.

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

Council of Science Editors:

Faulkner RA. Utilizing Drosophila S2 Cells as a Model System to Determine Underlying Mechanisms of ER-associated Degradation. [Thesis]. University of Texas Southwestern Medical Center; 2014. Available from: http://hdl.handle.net/2152.5/3312

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


University of Minnesota

7. Verardi, Raffaello. Biophysical characterization of membrane proteins and antimicrobial peptides by solution and solid-state NMR spectroscopy.

Degree: PhD, 2011, University of Minnesota

Membrane proteins and antimicrobial peptides represent two diverse and challenging classes of macromolecules to characterize at the molecular level. They are linked by the interaction… (more)

Subjects/Keywords: Membrane proteins; Antimicrobial peptides; Lipid bilayers; Phospholamban; Biochemistry, Molecular Bio, and Biophysics

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APA (6th Edition):

Verardi, R. (2011). Biophysical characterization of membrane proteins and antimicrobial peptides by solution and solid-state NMR spectroscopy. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/104629

Chicago Manual of Style (16th Edition):

Verardi, Raffaello. “Biophysical characterization of membrane proteins and antimicrobial peptides by solution and solid-state NMR spectroscopy.” 2011. Doctoral Dissertation, University of Minnesota. Accessed October 18, 2019. http://purl.umn.edu/104629.

MLA Handbook (7th Edition):

Verardi, Raffaello. “Biophysical characterization of membrane proteins and antimicrobial peptides by solution and solid-state NMR spectroscopy.” 2011. Web. 18 Oct 2019.

Vancouver:

Verardi R. Biophysical characterization of membrane proteins and antimicrobial peptides by solution and solid-state NMR spectroscopy. [Internet] [Doctoral dissertation]. University of Minnesota; 2011. [cited 2019 Oct 18]. Available from: http://purl.umn.edu/104629.

Council of Science Editors:

Verardi R. Biophysical characterization of membrane proteins and antimicrobial peptides by solution and solid-state NMR spectroscopy. [Doctoral Dissertation]. University of Minnesota; 2011. Available from: http://purl.umn.edu/104629


University of Oxford

8. Parton, Daniel L. Pushing the boundaries : molecular dynamics simulations of complex biological membranes.

Degree: PhD, 2011, University of Oxford

 A range of simulations have been conducted to investigate the behaviour of a diverse set of complex biological membrane systems. The processes of interest have… (more)

Subjects/Keywords: 616.203019; Computational biochemistry; Biochemistry; Molecular biophysics (biochemistry); Biophysics; molecular dynamics; coarse-grained; Influenza virus; biological membrane; antimicrobial peptides; membrane proteins

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APA (6th Edition):

Parton, D. L. (2011). Pushing the boundaries : molecular dynamics simulations of complex biological membranes. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:7ab91b51-a5ae-46b4-b6dc-3f0dd3f0b477 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.560920

Chicago Manual of Style (16th Edition):

Parton, Daniel L. “Pushing the boundaries : molecular dynamics simulations of complex biological membranes.” 2011. Doctoral Dissertation, University of Oxford. Accessed October 18, 2019. http://ora.ox.ac.uk/objects/uuid:7ab91b51-a5ae-46b4-b6dc-3f0dd3f0b477 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.560920.

MLA Handbook (7th Edition):

Parton, Daniel L. “Pushing the boundaries : molecular dynamics simulations of complex biological membranes.” 2011. Web. 18 Oct 2019.

Vancouver:

Parton DL. Pushing the boundaries : molecular dynamics simulations of complex biological membranes. [Internet] [Doctoral dissertation]. University of Oxford; 2011. [cited 2019 Oct 18]. Available from: http://ora.ox.ac.uk/objects/uuid:7ab91b51-a5ae-46b4-b6dc-3f0dd3f0b477 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.560920.

Council of Science Editors:

Parton DL. Pushing the boundaries : molecular dynamics simulations of complex biological membranes. [Doctoral Dissertation]. University of Oxford; 2011. Available from: http://ora.ox.ac.uk/objects/uuid:7ab91b51-a5ae-46b4-b6dc-3f0dd3f0b477 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.560920


University of Texas Southwestern Medical Center

9. Feramisco, Jamison Derek. SCAP, Insig, and Cholesterol Interactions in Mammalian Cells.

Degree: 2007, University of Texas Southwestern Medical Center

 Cholesterol synthesis in mammalian cells is highly regulated by an end-product feedback mechanism. The transcription of genes necessary for both fatty acid and cholesterol production… (more)

Subjects/Keywords: Lipids; Intracellular Signaling Peptides and Proteins; Membrane Proteins; Cholesterol

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APA (6th Edition):

Feramisco, J. D. (2007). SCAP, Insig, and Cholesterol Interactions in Mammalian Cells. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/386

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):

Feramisco, Jamison Derek. “SCAP, Insig, and Cholesterol Interactions in Mammalian Cells.” 2007. Thesis, University of Texas Southwestern Medical Center. Accessed October 18, 2019. http://hdl.handle.net/2152.5/386.

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

MLA Handbook (7th Edition):

Feramisco, Jamison Derek. “SCAP, Insig, and Cholesterol Interactions in Mammalian Cells.” 2007. Web. 18 Oct 2019.

Vancouver:

Feramisco JD. SCAP, Insig, and Cholesterol Interactions in Mammalian Cells. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2007. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2152.5/386.

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

Council of Science Editors:

Feramisco JD. SCAP, Insig, and Cholesterol Interactions in Mammalian Cells. [Thesis]. University of Texas Southwestern Medical Center; 2007. Available from: http://hdl.handle.net/2152.5/386

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


University of Texas Southwestern Medical Center

10. Hwang, Seonghwan. Regulation of Hepatic Cholesterol Homeostasis Through Accelerated Degradation of HMG CoA Reductase.

Degree: 2017, University of Texas Southwestern Medical Center

 Cholesterol biosynthesis is rigorously controlled by negative feedback regulation. This reaction occurs, in part, through sterol-accelerated degradation of HMG CoA reductase (HMGCR), which catalyzes the… (more)

Subjects/Keywords: Hydroxymethylglutaryl CoA Reductases; Hypoxia-Inducible Factor 1, alpha Subunit; Intracellular Signaling Peptides and Proteins; Liver; Membrane Proteins; Proteolysis; Transcription, Genetic

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APA (6th Edition):

Hwang, S. (2017). Regulation of Hepatic Cholesterol Homeostasis Through Accelerated Degradation of HMG CoA Reductase. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/6612

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):

Hwang, Seonghwan. “Regulation of Hepatic Cholesterol Homeostasis Through Accelerated Degradation of HMG CoA Reductase.” 2017. Thesis, University of Texas Southwestern Medical Center. Accessed October 18, 2019. http://hdl.handle.net/2152.5/6612.

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

MLA Handbook (7th Edition):

Hwang, Seonghwan. “Regulation of Hepatic Cholesterol Homeostasis Through Accelerated Degradation of HMG CoA Reductase.” 2017. Web. 18 Oct 2019.

Vancouver:

Hwang S. Regulation of Hepatic Cholesterol Homeostasis Through Accelerated Degradation of HMG CoA Reductase. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2017. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2152.5/6612.

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

Council of Science Editors:

Hwang S. Regulation of Hepatic Cholesterol Homeostasis Through Accelerated Degradation of HMG CoA Reductase. [Thesis]. University of Texas Southwestern Medical Center; 2017. Available from: http://hdl.handle.net/2152.5/6612

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

11. Gabriel, Luke R. Dynamic Regulation at the Neuronal Plasma Membrane: Novel Endocytic Mechanisms Control Anesthetic-Activated Potassium Channels and Amphetamine-Sensitive Dopamine Transporters: A Dissertation.

Degree: Neuroscience, Psychiatry, 2013, U of Massachusetts : Med

  Endocytic trafficking dynamically regulates neuronal plasma membrane protein presentation and activity, and plays a central role in excitability and plasticity. Over the course of… (more)

Subjects/Keywords: Potassium Channels; Carrier Proteins; Cell Membrane; Dopamine Plasma Membrane Transport Proteins; Dynamins; Membrane Proteins; Neurons; Neurotransmitter Transport Proteins; Tandem Pore Domain Potassium Channels; Protein Kinase C; Amino Acids, Peptides, and Proteins; Molecular and Cellular Neuroscience; Neuroscience and Neurobiology

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APA (6th Edition):

Gabriel, L. R. (2013). Dynamic Regulation at the Neuronal Plasma Membrane: Novel Endocytic Mechanisms Control Anesthetic-Activated Potassium Channels and Amphetamine-Sensitive Dopamine Transporters: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from http://escholarship.umassmed.edu/gsbs_diss/725

Chicago Manual of Style (16th Edition):

Gabriel, Luke R. “Dynamic Regulation at the Neuronal Plasma Membrane: Novel Endocytic Mechanisms Control Anesthetic-Activated Potassium Channels and Amphetamine-Sensitive Dopamine Transporters: A Dissertation.” 2013. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 18, 2019. http://escholarship.umassmed.edu/gsbs_diss/725.

MLA Handbook (7th Edition):

Gabriel, Luke R. “Dynamic Regulation at the Neuronal Plasma Membrane: Novel Endocytic Mechanisms Control Anesthetic-Activated Potassium Channels and Amphetamine-Sensitive Dopamine Transporters: A Dissertation.” 2013. Web. 18 Oct 2019.

Vancouver:

Gabriel LR. Dynamic Regulation at the Neuronal Plasma Membrane: Novel Endocytic Mechanisms Control Anesthetic-Activated Potassium Channels and Amphetamine-Sensitive Dopamine Transporters: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2013. [cited 2019 Oct 18]. Available from: http://escholarship.umassmed.edu/gsbs_diss/725.

Council of Science Editors:

Gabriel LR. Dynamic Regulation at the Neuronal Plasma Membrane: Novel Endocytic Mechanisms Control Anesthetic-Activated Potassium Channels and Amphetamine-Sensitive Dopamine Transporters: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2013. Available from: http://escholarship.umassmed.edu/gsbs_diss/725


Rutgers University

12. Zhang, Yongliang, 1985-. Molecular organization of peptide-based amphiphiles at association colloidal interfaces.

Degree: PhD, Chemistry and Chemical Biology, 2016, Rutgers University

Elucidating proteins/peptides structures at biomembrane interface is a great challenge. We are developing a chemical approach that reveals topological information of peptides at association colloidal… (more)

Subjects/Keywords: Proteins; Peptides; Amphiphiles

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APA (6th Edition):

Zhang, Yongliang, 1. (2016). Molecular organization of peptide-based amphiphiles at association colloidal interfaces. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/51537/

Chicago Manual of Style (16th Edition):

Zhang, Yongliang, 1985-. “Molecular organization of peptide-based amphiphiles at association colloidal interfaces.” 2016. Doctoral Dissertation, Rutgers University. Accessed October 18, 2019. https://rucore.libraries.rutgers.edu/rutgers-lib/51537/.

MLA Handbook (7th Edition):

Zhang, Yongliang, 1985-. “Molecular organization of peptide-based amphiphiles at association colloidal interfaces.” 2016. Web. 18 Oct 2019.

Vancouver:

Zhang, Yongliang 1. Molecular organization of peptide-based amphiphiles at association colloidal interfaces. [Internet] [Doctoral dissertation]. Rutgers University; 2016. [cited 2019 Oct 18]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/51537/.

Council of Science Editors:

Zhang, Yongliang 1. Molecular organization of peptide-based amphiphiles at association colloidal interfaces. [Doctoral Dissertation]. Rutgers University; 2016. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/51537/


McMaster University

13. Sadavarte, Hemant Rahul. MEMBRANE AND TEMPERATURE BASED METHODS FOR PROCESSING AND PURIFYING MONOCLONAL ANTIBODIES.

Degree: MASc, 2013, McMaster University

Monoclonal antibodies (mAbs) as therapeutic proteins have shown great potential in treatment of various human diseases because of their highly specific nature. This has… (more)

Subjects/Keywords: Hydrophobic Interaction Membrane Chromatography; Thermal cycling of Monoclonal Antibodies; Chimeric Heavy Chain Monoclonal Antibody (cHCmAb); Processing and Purification of Monoclonal Antibodies; Membrane Adsorbers; IgG1; EG2.; Amino Acids, Peptides, and Proteins; Biotechnology; Macromolecular Substances; Membrane Science; Other Chemical Engineering; Amino Acids, Peptides, and Proteins

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APA (6th Edition):

Sadavarte, H. R. (2013). MEMBRANE AND TEMPERATURE BASED METHODS FOR PROCESSING AND PURIFYING MONOCLONAL ANTIBODIES. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/12863

Chicago Manual of Style (16th Edition):

Sadavarte, Hemant Rahul. “MEMBRANE AND TEMPERATURE BASED METHODS FOR PROCESSING AND PURIFYING MONOCLONAL ANTIBODIES.” 2013. Masters Thesis, McMaster University. Accessed October 18, 2019. http://hdl.handle.net/11375/12863.

MLA Handbook (7th Edition):

Sadavarte, Hemant Rahul. “MEMBRANE AND TEMPERATURE BASED METHODS FOR PROCESSING AND PURIFYING MONOCLONAL ANTIBODIES.” 2013. Web. 18 Oct 2019.

Vancouver:

Sadavarte HR. MEMBRANE AND TEMPERATURE BASED METHODS FOR PROCESSING AND PURIFYING MONOCLONAL ANTIBODIES. [Internet] [Masters thesis]. McMaster University; 2013. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/11375/12863.

Council of Science Editors:

Sadavarte HR. MEMBRANE AND TEMPERATURE BASED METHODS FOR PROCESSING AND PURIFYING MONOCLONAL ANTIBODIES. [Masters Thesis]. McMaster University; 2013. Available from: http://hdl.handle.net/11375/12863


East Tennessee State University

14. Li, Shuo. Localization of Calbindin-D28k in Extra-Embryonic Membranes of Two Oviparous Scincid Lizards.

Degree: MS, Biomedical Sciences, 2009, East Tennessee State University

  Calbindin-D28K is a cytosolic calcium binding protein found in a variety of cells that transport calcium. The chorioallantoic membrane and yolk sac of oviparous… (more)

Subjects/Keywords: chorioallantoic membrane; calbindin-D28k; yolk sac; Amino Acids, Peptides, and Proteins; Chemicals and Drugs; Medicine and Health Sciences

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APA (6th Edition):

Li, S. (2009). Localization of Calbindin-D28k in Extra-Embryonic Membranes of Two Oviparous Scincid Lizards. (Thesis). East Tennessee State University. Retrieved from https://dc.etsu.edu/etd/1793

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):

Li, Shuo. “Localization of Calbindin-D28k in Extra-Embryonic Membranes of Two Oviparous Scincid Lizards.” 2009. Thesis, East Tennessee State University. Accessed October 18, 2019. https://dc.etsu.edu/etd/1793.

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

MLA Handbook (7th Edition):

Li, Shuo. “Localization of Calbindin-D28k in Extra-Embryonic Membranes of Two Oviparous Scincid Lizards.” 2009. Web. 18 Oct 2019.

Vancouver:

Li S. Localization of Calbindin-D28k in Extra-Embryonic Membranes of Two Oviparous Scincid Lizards. [Internet] [Thesis]. East Tennessee State University; 2009. [cited 2019 Oct 18]. Available from: https://dc.etsu.edu/etd/1793.

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

Council of Science Editors:

Li S. Localization of Calbindin-D28k in Extra-Embryonic Membranes of Two Oviparous Scincid Lizards. [Thesis]. East Tennessee State University; 2009. Available from: https://dc.etsu.edu/etd/1793

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

15. Trueman, Steven F. Insights Into ER Translocation Channel Gating. Structural Regulation of the Transition Between the Closed and Open Channel Conformations: A Dissertation.

Degree: Biochemistry and Molecular Pharmacology, Program in Biochemistry and Molecular Pharmacology, 2011, U of Massachusetts : Med

  The transition between the closed and open conformations of the Sec61 complex permits nascent protein insertion into the translocation channel. A critical event in… (more)

Subjects/Keywords: Protein Transport; Membrane Proteins; Endoplasmic Reticulum; Protein Conformation; Saccharomyces cerevisiae; Amino Acids, Peptides, and Proteins; Biochemistry, Biophysics, and Structural Biology; Cells; Fungi

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APA (6th Edition):

Trueman, S. F. (2011). Insights Into ER Translocation Channel Gating. Structural Regulation of the Transition Between the Closed and Open Channel Conformations: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/576

Chicago Manual of Style (16th Edition):

Trueman, Steven F. “Insights Into ER Translocation Channel Gating. Structural Regulation of the Transition Between the Closed and Open Channel Conformations: A Dissertation.” 2011. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 18, 2019. https://escholarship.umassmed.edu/gsbs_diss/576.

MLA Handbook (7th Edition):

Trueman, Steven F. “Insights Into ER Translocation Channel Gating. Structural Regulation of the Transition Between the Closed and Open Channel Conformations: A Dissertation.” 2011. Web. 18 Oct 2019.

Vancouver:

Trueman SF. Insights Into ER Translocation Channel Gating. Structural Regulation of the Transition Between the Closed and Open Channel Conformations: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2011. [cited 2019 Oct 18]. Available from: https://escholarship.umassmed.edu/gsbs_diss/576.

Council of Science Editors:

Trueman SF. Insights Into ER Translocation Channel Gating. Structural Regulation of the Transition Between the Closed and Open Channel Conformations: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2011. Available from: https://escholarship.umassmed.edu/gsbs_diss/576


Northeastern University

16. Morgan, Christopher R. HIV-1 Nef: from myristoylation to association with biological membranes.

Degree: PhD, Department of Chemistry and Chemical Biology, 2011, Northeastern University

 The HIV-1 accessory protein Nef plays a critical role in HIV/AIDS progression. In order for proper function of Nef, it must be localized to the… (more)

Subjects/Keywords: chemistry; HIV/AIDS; Nef; AIDS; HIV; gamma-glutamyl carboxylase (GGCX); myristoylation; association; HIV (Viruses); Membrane proteins; Nanomedicine; Amino Acids, Peptides, and Proteins; Biochemistry; Nanoscience and Nanotechnology

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APA (6th Edition):

Morgan, C. R. (2011). HIV-1 Nef: from myristoylation to association with biological membranes. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20001053

Chicago Manual of Style (16th Edition):

Morgan, Christopher R. “HIV-1 Nef: from myristoylation to association with biological membranes.” 2011. Doctoral Dissertation, Northeastern University. Accessed October 18, 2019. http://hdl.handle.net/2047/d20001053.

MLA Handbook (7th Edition):

Morgan, Christopher R. “HIV-1 Nef: from myristoylation to association with biological membranes.” 2011. Web. 18 Oct 2019.

Vancouver:

Morgan CR. HIV-1 Nef: from myristoylation to association with biological membranes. [Internet] [Doctoral dissertation]. Northeastern University; 2011. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2047/d20001053.

Council of Science Editors:

Morgan CR. HIV-1 Nef: from myristoylation to association with biological membranes. [Doctoral Dissertation]. Northeastern University; 2011. Available from: http://hdl.handle.net/2047/d20001053


University of Colorado

17. Morton, Leslie Anne. Identifying Peptide Sensors for Highly Curved Membranes and Lipid Components.

Degree: PhD, Chemistry & Biochemistry, 2013, University of Colorado

Membrane curvature is a vital function in several significant biological processes. Indeed, this behavior is critical for activating certain signaling processes, membrane budding for… (more)

Subjects/Keywords: lipids; membranes; peptides; proteins; Biochemistry

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APA (6th Edition):

Morton, L. A. (2013). Identifying Peptide Sensors for Highly Curved Membranes and Lipid Components. (Doctoral Dissertation). University of Colorado. Retrieved from http://scholar.colorado.edu/chem_gradetds/97

Chicago Manual of Style (16th Edition):

Morton, Leslie Anne. “Identifying Peptide Sensors for Highly Curved Membranes and Lipid Components.” 2013. Doctoral Dissertation, University of Colorado. Accessed October 18, 2019. http://scholar.colorado.edu/chem_gradetds/97.

MLA Handbook (7th Edition):

Morton, Leslie Anne. “Identifying Peptide Sensors for Highly Curved Membranes and Lipid Components.” 2013. Web. 18 Oct 2019.

Vancouver:

Morton LA. Identifying Peptide Sensors for Highly Curved Membranes and Lipid Components. [Internet] [Doctoral dissertation]. University of Colorado; 2013. [cited 2019 Oct 18]. Available from: http://scholar.colorado.edu/chem_gradetds/97.

Council of Science Editors:

Morton LA. Identifying Peptide Sensors for Highly Curved Membranes and Lipid Components. [Doctoral Dissertation]. University of Colorado; 2013. Available from: http://scholar.colorado.edu/chem_gradetds/97


University of Hong Kong

18. An, Ke. Conformational studies of hybrid aminoxy peptides & exploration of protein posttranslational modification by medium-chain fatty acid.

Degree: PhD, 2016, University of Hong Kong

 Conformations of aminoxy peptides with a wide range of backbones and substituents have been characterized over the past two decades. It has been discovered that… (more)

Subjects/Keywords: Amino acids; Peptides; Proteins - Analysis

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APA (6th Edition):

An, K. (2016). Conformational studies of hybrid aminoxy peptides & exploration of protein posttranslational modification by medium-chain fatty acid. (Doctoral Dissertation). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/240680

Chicago Manual of Style (16th Edition):

An, Ke. “Conformational studies of hybrid aminoxy peptides & exploration of protein posttranslational modification by medium-chain fatty acid.” 2016. Doctoral Dissertation, University of Hong Kong. Accessed October 18, 2019. http://hdl.handle.net/10722/240680.

MLA Handbook (7th Edition):

An, Ke. “Conformational studies of hybrid aminoxy peptides & exploration of protein posttranslational modification by medium-chain fatty acid.” 2016. Web. 18 Oct 2019.

Vancouver:

An K. Conformational studies of hybrid aminoxy peptides & exploration of protein posttranslational modification by medium-chain fatty acid. [Internet] [Doctoral dissertation]. University of Hong Kong; 2016. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10722/240680.

Council of Science Editors:

An K. Conformational studies of hybrid aminoxy peptides & exploration of protein posttranslational modification by medium-chain fatty acid. [Doctoral Dissertation]. University of Hong Kong; 2016. Available from: http://hdl.handle.net/10722/240680


Hong Kong University of Science and Technology

19. Ma, Chun-Wai. Applications of probabilistic models on peptide MS/MS spectra identification and protein quantification.

Degree: 2014, Hong Kong University of Science and Technology

 Shotgun proteomics, a bottom-up approach for complex protein mixture analysis using mass spectrometry coupled with liquid chromatography (LC-MS), can be viewed as a quasi-random model… (more)

Subjects/Keywords: Proteins; Analysis; Peptides; Mass spectrometry

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APA (6th Edition):

Ma, C. (2014). Applications of probabilistic models on peptide MS/MS spectra identification and protein quantification. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b1274105 ; http://repository.ust.hk/ir/bitstream/1783.1-62754/1/th_redirect.html

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):

Ma, Chun-Wai. “Applications of probabilistic models on peptide MS/MS spectra identification and protein quantification.” 2014. Thesis, Hong Kong University of Science and Technology. Accessed October 18, 2019. https://doi.org/10.14711/thesis-b1274105 ; http://repository.ust.hk/ir/bitstream/1783.1-62754/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Ma, Chun-Wai. “Applications of probabilistic models on peptide MS/MS spectra identification and protein quantification.” 2014. Web. 18 Oct 2019.

Vancouver:

Ma C. Applications of probabilistic models on peptide MS/MS spectra identification and protein quantification. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2014. [cited 2019 Oct 18]. Available from: https://doi.org/10.14711/thesis-b1274105 ; http://repository.ust.hk/ir/bitstream/1783.1-62754/1/th_redirect.html.

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

Council of Science Editors:

Ma C. Applications of probabilistic models on peptide MS/MS spectra identification and protein quantification. [Thesis]. Hong Kong University of Science and Technology; 2014. Available from: https://doi.org/10.14711/thesis-b1274105 ; http://repository.ust.hk/ir/bitstream/1783.1-62754/1/th_redirect.html

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

20. Funk, Adam J. Intracellular signaling abnormalities in schizophrenia.

Degree: PhD, 2011, University of Alabama – Birmingham

The pathophysiology of schizophrenia is complex and diverse, with many classes of receptors, neurotransmitters, and brain regions implicated in this illness. The many hypotheses proposed… (more)

Subjects/Keywords: Carrier Proteins  – metabolism<; br>; GTPase-Activating Proteins  – metabolism<; br>; Gyrus Cinguli  – metabolism<; br>; Intracellular Signaling Peptides and Proteins  – metabolism<; br>; Membrane Proteins  – metabolism<; br>; Prefrontal Cortex  – metabolism<; br>; Schizophrenia  – metabolism

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APA (6th Edition):

Funk, A. J. (2011). Intracellular signaling abnormalities in schizophrenia. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,1151

Chicago Manual of Style (16th Edition):

Funk, Adam J. “Intracellular signaling abnormalities in schizophrenia.” 2011. Doctoral Dissertation, University of Alabama – Birmingham. Accessed October 18, 2019. http://contentdm.mhsl.uab.edu/u?/etd,1151.

MLA Handbook (7th Edition):

Funk, Adam J. “Intracellular signaling abnormalities in schizophrenia.” 2011. Web. 18 Oct 2019.

Vancouver:

Funk AJ. Intracellular signaling abnormalities in schizophrenia. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2011. [cited 2019 Oct 18]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1151.

Council of Science Editors:

Funk AJ. Intracellular signaling abnormalities in schizophrenia. [Doctoral Dissertation]. University of Alabama – Birmingham; 2011. Available from: http://contentdm.mhsl.uab.edu/u?/etd,1151

21. Crowley, Jessica Lynn. Role of Supervillin, a Membrane Raft Protein, in Cytoskeletal Organization and Invadopodia Function.

Degree: Interdisciplinary Graduate Program, Radiology, 2009, U of Massachusetts : Med

  Crucial to a cell’s ability to migrate is the organization of its plasma membrane and associated proteins in a polarized manner to interact with… (more)

Subjects/Keywords: Neoplasm Metastasis; Membrane Proteins; Extracellular Matrix; Microfilament Proteins; Focal Adhesions; Transcription Factors; Adaptor Proteins; Signal Transducing; Actins; Myosin Type II; Amino Acids, Peptides, and Proteins; Cells; Enzymes and Coenzymes; Macromolecular Substances; Neoplasms; Tissues

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APA (6th Edition):

Crowley, J. L. (2009). Role of Supervillin, a Membrane Raft Protein, in Cytoskeletal Organization and Invadopodia Function. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/406

Chicago Manual of Style (16th Edition):

Crowley, Jessica Lynn. “Role of Supervillin, a Membrane Raft Protein, in Cytoskeletal Organization and Invadopodia Function.” 2009. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 18, 2019. https://escholarship.umassmed.edu/gsbs_diss/406.

MLA Handbook (7th Edition):

Crowley, Jessica Lynn. “Role of Supervillin, a Membrane Raft Protein, in Cytoskeletal Organization and Invadopodia Function.” 2009. Web. 18 Oct 2019.

Vancouver:

Crowley JL. Role of Supervillin, a Membrane Raft Protein, in Cytoskeletal Organization and Invadopodia Function. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2009. [cited 2019 Oct 18]. Available from: https://escholarship.umassmed.edu/gsbs_diss/406.

Council of Science Editors:

Crowley JL. Role of Supervillin, a Membrane Raft Protein, in Cytoskeletal Organization and Invadopodia Function. [Doctoral Dissertation]. U of Massachusetts : Med; 2009. Available from: https://escholarship.umassmed.edu/gsbs_diss/406


University of Western Ontario

22. Khamis, Zayn. Producing a Subunit Vaccine for Porcine Epidemic Diarrhea Virus.

Degree: 2016, University of Western Ontario

 Porcine epidemic diarrhea virus (PEDv) causes disease and mortality to piglets worldwide. Most vaccines used to combat the disease have been ineffective live attenuated virus… (more)

Subjects/Keywords: virus-like particle; Nicotiana benthamiana; coronavirus; plant biotechnology; membrane protein; molecular farming; Amino Acids, Peptides, and Proteins; Animal Diseases; Biotechnology; Large or Food Animal and Equine Medicine

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APA (6th Edition):

Khamis, Z. (2016). Producing a Subunit Vaccine for Porcine Epidemic Diarrhea Virus. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/4296

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):

Khamis, Zayn. “Producing a Subunit Vaccine for Porcine Epidemic Diarrhea Virus.” 2016. Thesis, University of Western Ontario. Accessed October 18, 2019. https://ir.lib.uwo.ca/etd/4296.

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

MLA Handbook (7th Edition):

Khamis, Zayn. “Producing a Subunit Vaccine for Porcine Epidemic Diarrhea Virus.” 2016. Web. 18 Oct 2019.

Vancouver:

Khamis Z. Producing a Subunit Vaccine for Porcine Epidemic Diarrhea Virus. [Internet] [Thesis]. University of Western Ontario; 2016. [cited 2019 Oct 18]. Available from: https://ir.lib.uwo.ca/etd/4296.

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

Council of Science Editors:

Khamis Z. Producing a Subunit Vaccine for Porcine Epidemic Diarrhea Virus. [Thesis]. University of Western Ontario; 2016. Available from: https://ir.lib.uwo.ca/etd/4296

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

23. Stone-Hulslander, Judith. Mechanisms of Newcastle Disease Virus-Mediated Membrane Fusion: A Dissertation.

Degree: Molecular Genetics and Microbiology, Microbiology and Physiological Systems, 1999, U of Massachusetts : Med

  For many paramyxoviruses, including Newcastle disease virus (NDV), syncytia formation requires the expression of both surface glycoproteins (HN and F) in the same cell,… (more)

Subjects/Keywords: Newcastle disease virus; Membrane Fusion; Amino Acids, Peptides, and Proteins; Carbohydrates; Viruses

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APA (6th Edition):

Stone-Hulslander, J. (1999). Mechanisms of Newcastle Disease Virus-Mediated Membrane Fusion: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/131

Chicago Manual of Style (16th Edition):

Stone-Hulslander, Judith. “Mechanisms of Newcastle Disease Virus-Mediated Membrane Fusion: A Dissertation.” 1999. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 18, 2019. https://escholarship.umassmed.edu/gsbs_diss/131.

MLA Handbook (7th Edition):

Stone-Hulslander, Judith. “Mechanisms of Newcastle Disease Virus-Mediated Membrane Fusion: A Dissertation.” 1999. Web. 18 Oct 2019.

Vancouver:

Stone-Hulslander J. Mechanisms of Newcastle Disease Virus-Mediated Membrane Fusion: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 1999. [cited 2019 Oct 18]. Available from: https://escholarship.umassmed.edu/gsbs_diss/131.

Council of Science Editors:

Stone-Hulslander J. Mechanisms of Newcastle Disease Virus-Mediated Membrane Fusion: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 1999. Available from: https://escholarship.umassmed.edu/gsbs_diss/131


Tartu University

24. Tali, Carmen. Scavenger receptors as a target for nucleic acid delivery with peptide vectors .

Degree: 2017, Tartu University

 Geeniekspressiooni reguleerimine rakkudesse suunatud nukeiinhapete ja sünteetiliste oligonukleotiidide (ON) abil omab suurt potentsiaali geeniteraapias mitmete haiguste ravil. Suure molekulmassi ning negatiivse laengu tõttu ei ole… (more)

Subjects/Keywords: retseptorid; rakku sisenevad peptiidid; nukleiinhapped; oligonukleotiidid; rakud; rakumembraan; transportvalgud; bioloogiline transport; receptors; cell-penetrating peptides; nucleic acids; oligonucleotides; cells (biology); cell membrane; transport proteins; biological transport

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APA (6th Edition):

Tali, C. (2017). Scavenger receptors as a target for nucleic acid delivery with peptide vectors . (Thesis). Tartu University. Retrieved from http://hdl.handle.net/10062/55680

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):

Tali, Carmen. “Scavenger receptors as a target for nucleic acid delivery with peptide vectors .” 2017. Thesis, Tartu University. Accessed October 18, 2019. http://hdl.handle.net/10062/55680.

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

MLA Handbook (7th Edition):

Tali, Carmen. “Scavenger receptors as a target for nucleic acid delivery with peptide vectors .” 2017. Web. 18 Oct 2019.

Vancouver:

Tali C. Scavenger receptors as a target for nucleic acid delivery with peptide vectors . [Internet] [Thesis]. Tartu University; 2017. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10062/55680.

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

Council of Science Editors:

Tali C. Scavenger receptors as a target for nucleic acid delivery with peptide vectors . [Thesis]. Tartu University; 2017. Available from: http://hdl.handle.net/10062/55680

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

25. Jiang, Ying. Transfer of the Ribosome-Nascent Chain Complex to the Translocon in Cotranslational Translocation: A Thesis.

Degree: Biochemistry and Molecular Pharmacology, Biochemistry & Molecular Pharmacology, 2007, U of Massachusetts : Med

  Cotranslational translocation is initiated by targeting of a ribosome-bound nascent polypeptide chain (RNC) to the endoplasmic reticulum (ER) membrane. The targeting reaction is coordinated… (more)

Subjects/Keywords: Signal Recognition Particle; Protein Transport; Membrane Proteins; Saccharomyces cerevisiae Proteins; Protein Biosynthesis; Amino Acids, Peptides, and Proteins; Cells; Fungi

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APA (6th Edition):

Jiang, Y. (2007). Transfer of the Ribosome-Nascent Chain Complex to the Translocon in Cotranslational Translocation: A Thesis. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/332

Chicago Manual of Style (16th Edition):

Jiang, Ying. “Transfer of the Ribosome-Nascent Chain Complex to the Translocon in Cotranslational Translocation: A Thesis.” 2007. Doctoral Dissertation, U of Massachusetts : Med. Accessed October 18, 2019. https://escholarship.umassmed.edu/gsbs_diss/332.

MLA Handbook (7th Edition):

Jiang, Ying. “Transfer of the Ribosome-Nascent Chain Complex to the Translocon in Cotranslational Translocation: A Thesis.” 2007. Web. 18 Oct 2019.

Vancouver:

Jiang Y. Transfer of the Ribosome-Nascent Chain Complex to the Translocon in Cotranslational Translocation: A Thesis. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2007. [cited 2019 Oct 18]. Available from: https://escholarship.umassmed.edu/gsbs_diss/332.

Council of Science Editors:

Jiang Y. Transfer of the Ribosome-Nascent Chain Complex to the Translocon in Cotranslational Translocation: A Thesis. [Doctoral Dissertation]. U of Massachusetts : Med; 2007. Available from: https://escholarship.umassmed.edu/gsbs_diss/332

26. Flores, Luís Rafael Pereira do Carmo. Membrane-active peptides from structural viral proteins : identifying novel delivery vectors for gene therapy.

Degree: 2014, RCAAP

Péptidos activos em membranas são relevantes em diversos campos da biomedicina. Os péptidos translocadores de membranas (CPPs), em particular, são promissores na administração de fármacos,… (more)

Subjects/Keywords: Proteínas Estruturais de Vírus; Péptidos Translocadores de Membranas; Administração Controlada de Fármacos; Terapia Génica; Péptidos Activos em Membranas; Bioquímica Física; Structural Viral Proteins; Cell-penetrating Peptides; Drug Delivery; Gene Therapy; Membrane-active Peptides; Physical Biochemistry

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APA (6th Edition):

Flores, L. R. P. d. C. (2014). Membrane-active peptides from structural viral proteins : identifying novel delivery vectors for gene therapy. (Thesis). RCAAP. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:repositorio.ucp.pt:10400.14/15011

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):

Flores, Luís Rafael Pereira do Carmo. “Membrane-active peptides from structural viral proteins : identifying novel delivery vectors for gene therapy.” 2014. Thesis, RCAAP. Accessed October 18, 2019. http://www.rcaap.pt/detail.jsp?id=oai:repositorio.ucp.pt:10400.14/15011.

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

MLA Handbook (7th Edition):

Flores, Luís Rafael Pereira do Carmo. “Membrane-active peptides from structural viral proteins : identifying novel delivery vectors for gene therapy.” 2014. Web. 18 Oct 2019.

Vancouver:

Flores LRPdC. Membrane-active peptides from structural viral proteins : identifying novel delivery vectors for gene therapy. [Internet] [Thesis]. RCAAP; 2014. [cited 2019 Oct 18]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:repositorio.ucp.pt:10400.14/15011.

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

Council of Science Editors:

Flores LRPdC. Membrane-active peptides from structural viral proteins : identifying novel delivery vectors for gene therapy. [Thesis]. RCAAP; 2014. Available from: http://www.rcaap.pt/detail.jsp?id=oai:repositorio.ucp.pt:10400.14/15011

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

27. Sarrouj, Hiba. DNP/solid state NMR probehead for the investigation of oriented membranes : Sonde DNP/RMN du solide pour l'étude des protéines membranaires.

Degree: Docteur es, Chimie physique, 2014, Université de Strasbourg

Les protéines membranaires en hélices alpha forment le tiers des protéines codées par notre génome. D’autres protéines membranaires sont formées typiquement de feuillets bêta. Leur… (more)

Subjects/Keywords: Résonnance magnétique nucléaire (RMN); Protéines membranaires; Dynamic nuclear polarisation (DNP); Sonde RMN; Peptides antimicrobiens; PISEMA; Orientation peptidique; Cross polarisation (CP); Nuclear magnetic resonance; Membrane proteins; Dynamic nuclear polarization (DNP); Antimicrobial peptides; Peptide orientation; Cross polarization (CP); 535.8; 572.6

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APA (6th Edition):

Sarrouj, H. (2014). DNP/solid state NMR probehead for the investigation of oriented membranes : Sonde DNP/RMN du solide pour l'étude des protéines membranaires. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2014STRAF005

Chicago Manual of Style (16th Edition):

Sarrouj, Hiba. “DNP/solid state NMR probehead for the investigation of oriented membranes : Sonde DNP/RMN du solide pour l'étude des protéines membranaires.” 2014. Doctoral Dissertation, Université de Strasbourg. Accessed October 18, 2019. http://www.theses.fr/2014STRAF005.

MLA Handbook (7th Edition):

Sarrouj, Hiba. “DNP/solid state NMR probehead for the investigation of oriented membranes : Sonde DNP/RMN du solide pour l'étude des protéines membranaires.” 2014. Web. 18 Oct 2019.

Vancouver:

Sarrouj H. DNP/solid state NMR probehead for the investigation of oriented membranes : Sonde DNP/RMN du solide pour l'étude des protéines membranaires. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2014. [cited 2019 Oct 18]. Available from: http://www.theses.fr/2014STRAF005.

Council of Science Editors:

Sarrouj H. DNP/solid state NMR probehead for the investigation of oriented membranes : Sonde DNP/RMN du solide pour l'étude des protéines membranaires. [Doctoral Dissertation]. Université de Strasbourg; 2014. Available from: http://www.theses.fr/2014STRAF005


Université de Bordeaux I

28. Harmouche, Nicole. Les liposomes biphényles : un nouveau modèle de biomembrane magnétique fluorescent : caractérisation par RMN des solides, microscopies optiques et électroniques et SAXS : Biphenyl liposomes : a new model of fluorescent, magnetic biomembrane : characterisation by Solid State NMR, Optical and Electronic microscopies and SAXS : Perspectives in Vectorisation.

Degree: Docteur es, Physique-chimie, 2013, Université de Bordeaux I

Un nouveau modèle de biomembrane de type liposome a été développé à partir de lipides synthétisés comportant une unité biphényle sur leur chaînes sn2 et… (more)

Subjects/Keywords: Liposomes fluorescents; Unité biphényle; RMN des Solides 31P, 2H, 15N; Déformation membranaire; Diffusion des Rayons X aux Petits Angles (SAXS); Microscopies Optiques et Electroniques; Peptides et Protéines membranaires; Fluorescent liposomes; Biphenyl unit; 31P, 2H, 15N Solid State NMR; Small Angle X-ray Scattering (SAXS); Optical and Electron microscopy; Membrane peptides and proteins.; Membrane Deformation

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

APA (6th Edition):

Harmouche, N. (2013). Les liposomes biphényles : un nouveau modèle de biomembrane magnétique fluorescent : caractérisation par RMN des solides, microscopies optiques et électroniques et SAXS : Biphenyl liposomes : a new model of fluorescent, magnetic biomembrane : characterisation by Solid State NMR, Optical and Electronic microscopies and SAXS : Perspectives in Vectorisation. (Doctoral Dissertation). Université de Bordeaux I. Retrieved from http://www.theses.fr/2013BOR15213

Chicago Manual of Style (16th Edition):

Harmouche, Nicole. “Les liposomes biphényles : un nouveau modèle de biomembrane magnétique fluorescent : caractérisation par RMN des solides, microscopies optiques et électroniques et SAXS : Biphenyl liposomes : a new model of fluorescent, magnetic biomembrane : characterisation by Solid State NMR, Optical and Electronic microscopies and SAXS : Perspectives in Vectorisation.” 2013. Doctoral Dissertation, Université de Bordeaux I. Accessed October 18, 2019. http://www.theses.fr/2013BOR15213.

MLA Handbook (7th Edition):

Harmouche, Nicole. “Les liposomes biphényles : un nouveau modèle de biomembrane magnétique fluorescent : caractérisation par RMN des solides, microscopies optiques et électroniques et SAXS : Biphenyl liposomes : a new model of fluorescent, magnetic biomembrane : characterisation by Solid State NMR, Optical and Electronic microscopies and SAXS : Perspectives in Vectorisation.” 2013. Web. 18 Oct 2019.

Vancouver:

Harmouche N. Les liposomes biphényles : un nouveau modèle de biomembrane magnétique fluorescent : caractérisation par RMN des solides, microscopies optiques et électroniques et SAXS : Biphenyl liposomes : a new model of fluorescent, magnetic biomembrane : characterisation by Solid State NMR, Optical and Electronic microscopies and SAXS : Perspectives in Vectorisation. [Internet] [Doctoral dissertation]. Université de Bordeaux I; 2013. [cited 2019 Oct 18]. Available from: http://www.theses.fr/2013BOR15213.

Council of Science Editors:

Harmouche N. Les liposomes biphényles : un nouveau modèle de biomembrane magnétique fluorescent : caractérisation par RMN des solides, microscopies optiques et électroniques et SAXS : Biphenyl liposomes : a new model of fluorescent, magnetic biomembrane : characterisation by Solid State NMR, Optical and Electronic microscopies and SAXS : Perspectives in Vectorisation. [Doctoral Dissertation]. Université de Bordeaux I; 2013. Available from: http://www.theses.fr/2013BOR15213


Georgia Tech

29. Kirk, Nancy Jo. Effect of microenvironment on the photolysis of tryptophan residues in peptides and proteins.

Degree: PhD, Chemistry, 1984, Georgia Tech

Subjects/Keywords: Peptides; Proteins; Photochemistry

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APA (6th Edition):

Kirk, N. J. (1984). Effect of microenvironment on the photolysis of tryptophan residues in peptides and proteins. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/30303

Chicago Manual of Style (16th Edition):

Kirk, Nancy Jo. “Effect of microenvironment on the photolysis of tryptophan residues in peptides and proteins.” 1984. Doctoral Dissertation, Georgia Tech. Accessed October 18, 2019. http://hdl.handle.net/1853/30303.

MLA Handbook (7th Edition):

Kirk, Nancy Jo. “Effect of microenvironment on the photolysis of tryptophan residues in peptides and proteins.” 1984. Web. 18 Oct 2019.

Vancouver:

Kirk NJ. Effect of microenvironment on the photolysis of tryptophan residues in peptides and proteins. [Internet] [Doctoral dissertation]. Georgia Tech; 1984. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1853/30303.

Council of Science Editors:

Kirk NJ. Effect of microenvironment on the photolysis of tryptophan residues in peptides and proteins. [Doctoral Dissertation]. Georgia Tech; 1984. Available from: http://hdl.handle.net/1853/30303


Hong Kong University of Science and Technology

30. Qiao, Qin. Development and application of advanced modelling algorithms towards a molecular understanding of the aggregation of an intrinsically disordered peptide.

Degree: 2014, Hong Kong University of Science and Technology

 In this thesis, we use molecular dynamic (MD) simulations to study the conformational dynamics of an intrinsically disordered protein, human islet amyloid polypepetide (hIAPP). Meanwhile,… (more)

Subjects/Keywords: Proteins; Structure; Mathematical models; Peptides; Analysis

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APA (6th Edition):

Qiao, Q. (2014). Development and application of advanced modelling algorithms towards a molecular understanding of the aggregation of an intrinsically disordered peptide. (Thesis). Hong Kong University of Science and Technology. Retrieved from https://doi.org/10.14711/thesis-b1432234 ; http://repository.ust.hk/ir/bitstream/1783.1-88754/1/th_redirect.html

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):

Qiao, Qin. “Development and application of advanced modelling algorithms towards a molecular understanding of the aggregation of an intrinsically disordered peptide.” 2014. Thesis, Hong Kong University of Science and Technology. Accessed October 18, 2019. https://doi.org/10.14711/thesis-b1432234 ; http://repository.ust.hk/ir/bitstream/1783.1-88754/1/th_redirect.html.

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

MLA Handbook (7th Edition):

Qiao, Qin. “Development and application of advanced modelling algorithms towards a molecular understanding of the aggregation of an intrinsically disordered peptide.” 2014. Web. 18 Oct 2019.

Vancouver:

Qiao Q. Development and application of advanced modelling algorithms towards a molecular understanding of the aggregation of an intrinsically disordered peptide. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2014. [cited 2019 Oct 18]. Available from: https://doi.org/10.14711/thesis-b1432234 ; http://repository.ust.hk/ir/bitstream/1783.1-88754/1/th_redirect.html.

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

Council of Science Editors:

Qiao Q. Development and application of advanced modelling algorithms towards a molecular understanding of the aggregation of an intrinsically disordered peptide. [Thesis]. Hong Kong University of Science and Technology; 2014. Available from: https://doi.org/10.14711/thesis-b1432234 ; http://repository.ust.hk/ir/bitstream/1783.1-88754/1/th_redirect.html

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

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