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You searched for subject:(MEMBRANE PROTEINS analysis). Showing records 1 – 30 of 35 total matches.

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University of Oxford

1. Newport, Thomas. Tools and resources for molecular simulations of integral membrane proteins.

Degree: PhD, 2017, University of Oxford

 Integral Membrane Proteins (IMPs) are an important and scientifically interesting class of protein which span the lipid bilayer surrounding cells, cell compartments and many viruses.… (more)

Subjects/Keywords: 572; Membrane proteins – Analysis; Molecular dynamics

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APA (6th Edition):

Newport, T. (2017). Tools and resources for molecular simulations of integral membrane proteins. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:b6dc3047-aaf4-4236-8266-7a885fecb5d9 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.740927

Chicago Manual of Style (16th Edition):

Newport, Thomas. “Tools and resources for molecular simulations of integral membrane proteins.” 2017. Doctoral Dissertation, University of Oxford. Accessed October 27, 2020. http://ora.ox.ac.uk/objects/uuid:b6dc3047-aaf4-4236-8266-7a885fecb5d9 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.740927.

MLA Handbook (7th Edition):

Newport, Thomas. “Tools and resources for molecular simulations of integral membrane proteins.” 2017. Web. 27 Oct 2020.

Vancouver:

Newport T. Tools and resources for molecular simulations of integral membrane proteins. [Internet] [Doctoral dissertation]. University of Oxford; 2017. [cited 2020 Oct 27]. Available from: http://ora.ox.ac.uk/objects/uuid:b6dc3047-aaf4-4236-8266-7a885fecb5d9 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.740927.

Council of Science Editors:

Newport T. Tools and resources for molecular simulations of integral membrane proteins. [Doctoral Dissertation]. University of Oxford; 2017. Available from: http://ora.ox.ac.uk/objects/uuid:b6dc3047-aaf4-4236-8266-7a885fecb5d9 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.740927


University of Guelph

2. Coumoundouros, Chelsea. Investigating the Oligomeric State of Osmoregulatory Transporter ProP of Escherichia coli and its Functional Consequences.

Degree: MS, Department of Molecular and Cellular Biology, 2016, University of Guelph

 ProP, an osmoregulatory transporter found in E. coli, is responsible for the accumulation of osmolytes in response to hyperosmotic stress. ProP is able to dimerize… (more)

Subjects/Keywords: E. coli; ProP; Osmoregulation; membrane proteins; protein oligomerization; BN-PAGE; Dominant negative analysis; transport proteins

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APA (6th Edition):

Coumoundouros, C. (2016). Investigating the Oligomeric State of Osmoregulatory Transporter ProP of Escherichia coli and its Functional Consequences. (Masters Thesis). University of Guelph. Retrieved from https://atrium.lib.uoguelph.ca/xmlui/handle/10214/10086

Chicago Manual of Style (16th Edition):

Coumoundouros, Chelsea. “Investigating the Oligomeric State of Osmoregulatory Transporter ProP of Escherichia coli and its Functional Consequences.” 2016. Masters Thesis, University of Guelph. Accessed October 27, 2020. https://atrium.lib.uoguelph.ca/xmlui/handle/10214/10086.

MLA Handbook (7th Edition):

Coumoundouros, Chelsea. “Investigating the Oligomeric State of Osmoregulatory Transporter ProP of Escherichia coli and its Functional Consequences.” 2016. Web. 27 Oct 2020.

Vancouver:

Coumoundouros C. Investigating the Oligomeric State of Osmoregulatory Transporter ProP of Escherichia coli and its Functional Consequences. [Internet] [Masters thesis]. University of Guelph; 2016. [cited 2020 Oct 27]. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/10086.

Council of Science Editors:

Coumoundouros C. Investigating the Oligomeric State of Osmoregulatory Transporter ProP of Escherichia coli and its Functional Consequences. [Masters Thesis]. University of Guelph; 2016. Available from: https://atrium.lib.uoguelph.ca/xmlui/handle/10214/10086


Michigan State University

3. 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 27, 2020. 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. 27 Oct 2020.

Vancouver:

Xie L. Solid state nuclear magnetic resonance studies of structures and membrane locations of peptides. [Internet] [Thesis]. Michigan State University; 2014. [cited 2020 Oct 27]. 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


Michigan State University

4. Mangino, Michael Eugene, 1946-. Electrophoretic and partial chemical characterization of bovine milk fat globule membrane proteins.

Degree: MS, Dept. of Food Science and Human Nutrition, 1973, Michigan State University

Subjects/Keywords: Milkfat; Milk – Analysis; Membrane proteins

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APA (6th Edition):

Mangino, Michael Eugene, 1. (1973). Electrophoretic and partial chemical characterization of bovine milk fat globule membrane proteins. (Masters Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:15470

Chicago Manual of Style (16th Edition):

Mangino, Michael Eugene, 1946-. “Electrophoretic and partial chemical characterization of bovine milk fat globule membrane proteins.” 1973. Masters Thesis, Michigan State University. Accessed October 27, 2020. http://etd.lib.msu.edu/islandora/object/etd:15470.

MLA Handbook (7th Edition):

Mangino, Michael Eugene, 1946-. “Electrophoretic and partial chemical characterization of bovine milk fat globule membrane proteins.” 1973. Web. 27 Oct 2020.

Vancouver:

Mangino, Michael Eugene 1. Electrophoretic and partial chemical characterization of bovine milk fat globule membrane proteins. [Internet] [Masters thesis]. Michigan State University; 1973. [cited 2020 Oct 27]. Available from: http://etd.lib.msu.edu/islandora/object/etd:15470.

Council of Science Editors:

Mangino, Michael Eugene 1. Electrophoretic and partial chemical characterization of bovine milk fat globule membrane proteins. [Masters Thesis]. Michigan State University; 1973. Available from: http://etd.lib.msu.edu/islandora/object/etd:15470

5. Machida, Curtis A. Plasma membrane localization of proteins encoded by murine retroviruses : relationship to viral leukemia.

Degree: PhD, 1982, Oregon Health Sciences University

Subjects/Keywords: Leukemia Virus, Murine; Membrane Proteins  – analysis

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APA (6th Edition):

Machida, C. A. (1982). Plasma membrane localization of proteins encoded by murine retroviruses : relationship to viral leukemia. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M4W66HZ0 ; http://digitalcommons.ohsu.edu/etd/2168

Chicago Manual of Style (16th Edition):

Machida, Curtis A. “Plasma membrane localization of proteins encoded by murine retroviruses : relationship to viral leukemia.” 1982. Doctoral Dissertation, Oregon Health Sciences University. Accessed October 27, 2020. doi:10.6083/M4W66HZ0 ; http://digitalcommons.ohsu.edu/etd/2168.

MLA Handbook (7th Edition):

Machida, Curtis A. “Plasma membrane localization of proteins encoded by murine retroviruses : relationship to viral leukemia.” 1982. Web. 27 Oct 2020.

Vancouver:

Machida CA. Plasma membrane localization of proteins encoded by murine retroviruses : relationship to viral leukemia. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 1982. [cited 2020 Oct 27]. Available from: doi:10.6083/M4W66HZ0 ; http://digitalcommons.ohsu.edu/etd/2168.

Council of Science Editors:

Machida CA. Plasma membrane localization of proteins encoded by murine retroviruses : relationship to viral leukemia. [Doctoral Dissertation]. Oregon Health Sciences University; 1982. Available from: doi:10.6083/M4W66HZ0 ; http://digitalcommons.ohsu.edu/etd/2168


University of St Andrews

6. Huang, Hexian. Regulations of export and chain length of extracellular bacterial polysaccharides.

Degree: PhD, 2013, University of St Andrews

 Many Gram-positive and Gram-negative bacteria produce an additional thick layer of carbohydrate polymers on the cell wall surface. These capsules (capsular polysaccharides; CPS) play critical… (more)

Subjects/Keywords: 572; QR92.P6H8; Microbial polysaccharides – Synthesis; Bacterial cell walls; Membrane proteins – Analysis

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APA (6th Edition):

Huang, H. (2013). Regulations of export and chain length of extracellular bacterial polysaccharides. (Doctoral Dissertation). University of St Andrews. Retrieved from http://hdl.handle.net/10023/4441

Chicago Manual of Style (16th Edition):

Huang, Hexian. “Regulations of export and chain length of extracellular bacterial polysaccharides.” 2013. Doctoral Dissertation, University of St Andrews. Accessed October 27, 2020. http://hdl.handle.net/10023/4441.

MLA Handbook (7th Edition):

Huang, Hexian. “Regulations of export and chain length of extracellular bacterial polysaccharides.” 2013. Web. 27 Oct 2020.

Vancouver:

Huang H. Regulations of export and chain length of extracellular bacterial polysaccharides. [Internet] [Doctoral dissertation]. University of St Andrews; 2013. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10023/4441.

Council of Science Editors:

Huang H. Regulations of export and chain length of extracellular bacterial polysaccharides. [Doctoral Dissertation]. University of St Andrews; 2013. Available from: http://hdl.handle.net/10023/4441


Hong Kong University of Science and Technology

7. Cheng, Yuen Shan. Screening of proteins interacting with the cytoplasmic tail of transmembrane neuregulins.

Degree: 2001, Hong Kong University of Science and Technology

 Neuregulins (NRGs) are a family of growth factors, among which are nerve-derived signaling molecules identified to be important for the formation of the postsynaptic specialization… (more)

Subjects/Keywords: Neuropeptides  – Analysis ; Neurotransmitters  – Analysis ; Membrane proteins  – Analysis

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APA (6th Edition):

Cheng, Y. S. (2001). Screening of proteins interacting with the cytoplasmic tail of transmembrane neuregulins. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-3738 ; https://doi.org/10.14711/thesis-b714010 ; http://repository.ust.hk/ir/bitstream/1783.1-3738/1/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):

Cheng, Yuen Shan. “Screening of proteins interacting with the cytoplasmic tail of transmembrane neuregulins.” 2001. Thesis, Hong Kong University of Science and Technology. Accessed October 27, 2020. http://repository.ust.hk/ir/Record/1783.1-3738 ; https://doi.org/10.14711/thesis-b714010 ; http://repository.ust.hk/ir/bitstream/1783.1-3738/1/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):

Cheng, Yuen Shan. “Screening of proteins interacting with the cytoplasmic tail of transmembrane neuregulins.” 2001. Web. 27 Oct 2020.

Vancouver:

Cheng YS. Screening of proteins interacting with the cytoplasmic tail of transmembrane neuregulins. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2001. [cited 2020 Oct 27]. Available from: http://repository.ust.hk/ir/Record/1783.1-3738 ; https://doi.org/10.14711/thesis-b714010 ; http://repository.ust.hk/ir/bitstream/1783.1-3738/1/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:

Cheng YS. Screening of proteins interacting with the cytoplasmic tail of transmembrane neuregulins. [Thesis]. Hong Kong University of Science and Technology; 2001. Available from: http://repository.ust.hk/ir/Record/1783.1-3738 ; https://doi.org/10.14711/thesis-b714010 ; http://repository.ust.hk/ir/bitstream/1783.1-3738/1/th_redirect.html

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

8. Lochner, Janis Elizabeth. Electrochemical membrane phenomena associated with lymphocyte communication.

Degree: PhD, 1981, Oregon Health Sciences University

Subjects/Keywords: Cell Membrane  – analysis; Cell Membrane  – immunology; Lymphokines; T-Lymphocytes  – immunology; Membrane Proteins; Mice

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APA (6th Edition):

Lochner, J. E. (1981). Electrochemical membrane phenomena associated with lymphocyte communication. (Doctoral Dissertation). Oregon Health Sciences University. Retrieved from doi:10.6083/M42B8W6C ; http://digitalcommons.ohsu.edu/etd/2275

Chicago Manual of Style (16th Edition):

Lochner, Janis Elizabeth. “Electrochemical membrane phenomena associated with lymphocyte communication.” 1981. Doctoral Dissertation, Oregon Health Sciences University. Accessed October 27, 2020. doi:10.6083/M42B8W6C ; http://digitalcommons.ohsu.edu/etd/2275.

MLA Handbook (7th Edition):

Lochner, Janis Elizabeth. “Electrochemical membrane phenomena associated with lymphocyte communication.” 1981. Web. 27 Oct 2020.

Vancouver:

Lochner JE. Electrochemical membrane phenomena associated with lymphocyte communication. [Internet] [Doctoral dissertation]. Oregon Health Sciences University; 1981. [cited 2020 Oct 27]. Available from: doi:10.6083/M42B8W6C ; http://digitalcommons.ohsu.edu/etd/2275.

Council of Science Editors:

Lochner JE. Electrochemical membrane phenomena associated with lymphocyte communication. [Doctoral Dissertation]. Oregon Health Sciences University; 1981. Available from: doi:10.6083/M42B8W6C ; http://digitalcommons.ohsu.edu/etd/2275


University of Alberta

9. Bingle, Wade Hamilton. Regular surface layer of Azotobacter vinelandii.

Degree: PhD, Department of Microbiology, 1987, University of Alberta

Subjects/Keywords: Azotobacter vinelandii.; Membrane proteins – Analysis.; Cell membranes.

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APA (6th Edition):

Bingle, W. H. (1987). Regular surface layer of Azotobacter vinelandii. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/mk61rk367

Chicago Manual of Style (16th Edition):

Bingle, Wade Hamilton. “Regular surface layer of Azotobacter vinelandii.” 1987. Doctoral Dissertation, University of Alberta. Accessed October 27, 2020. https://era.library.ualberta.ca/files/mk61rk367.

MLA Handbook (7th Edition):

Bingle, Wade Hamilton. “Regular surface layer of Azotobacter vinelandii.” 1987. Web. 27 Oct 2020.

Vancouver:

Bingle WH. Regular surface layer of Azotobacter vinelandii. [Internet] [Doctoral dissertation]. University of Alberta; 1987. [cited 2020 Oct 27]. Available from: https://era.library.ualberta.ca/files/mk61rk367.

Council of Science Editors:

Bingle WH. Regular surface layer of Azotobacter vinelandii. [Doctoral Dissertation]. University of Alberta; 1987. Available from: https://era.library.ualberta.ca/files/mk61rk367


Montana State University

10. Adams, Earle Raymond. Solid state and solution NMR studies of model systems for parts of membrane proteins.

Degree: PhD, College of Letters & Science, 1994, Montana State University

Subjects/Keywords: Membrane proteins.; Spectrum analysis.; Bacteriorhodopsin.; Nuclear magnetic resonance.

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APA (6th Edition):

Adams, E. R. (1994). Solid state and solution NMR studies of model systems for parts of membrane proteins. (Doctoral Dissertation). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/7566

Chicago Manual of Style (16th Edition):

Adams, Earle Raymond. “Solid state and solution NMR studies of model systems for parts of membrane proteins.” 1994. Doctoral Dissertation, Montana State University. Accessed October 27, 2020. https://scholarworks.montana.edu/xmlui/handle/1/7566.

MLA Handbook (7th Edition):

Adams, Earle Raymond. “Solid state and solution NMR studies of model systems for parts of membrane proteins.” 1994. Web. 27 Oct 2020.

Vancouver:

Adams ER. Solid state and solution NMR studies of model systems for parts of membrane proteins. [Internet] [Doctoral dissertation]. Montana State University; 1994. [cited 2020 Oct 27]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/7566.

Council of Science Editors:

Adams ER. Solid state and solution NMR studies of model systems for parts of membrane proteins. [Doctoral Dissertation]. Montana State University; 1994. Available from: https://scholarworks.montana.edu/xmlui/handle/1/7566


University of Georgia

11. Hammond, Dorothy Araba. Functional annotation of alternatively spliced isoforms of human G protein-coupled receptors (GPCRs).

Degree: 2015, University of Georgia

 The functional differences that exist between alternatively spliced isoforms of genes can be substantial; it could be variations of the function of the “primary” full-length… (more)

Subjects/Keywords: GPCR; G protein-coupled receptor; RNA-seq; membrane protein; trans-membrane proteins; gene structure; alternative splicing; functional prediction; gene regulation; differential gene expression; next-generation sequencing; transcriptomic data analysis

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APA (6th Edition):

Hammond, D. A. (2015). Functional annotation of alternatively spliced isoforms of human G protein-coupled receptors (GPCRs). (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/31427

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):

Hammond, Dorothy Araba. “Functional annotation of alternatively spliced isoforms of human G protein-coupled receptors (GPCRs).” 2015. Thesis, University of Georgia. Accessed October 27, 2020. http://hdl.handle.net/10724/31427.

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

MLA Handbook (7th Edition):

Hammond, Dorothy Araba. “Functional annotation of alternatively spliced isoforms of human G protein-coupled receptors (GPCRs).” 2015. Web. 27 Oct 2020.

Vancouver:

Hammond DA. Functional annotation of alternatively spliced isoforms of human G protein-coupled receptors (GPCRs). [Internet] [Thesis]. University of Georgia; 2015. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10724/31427.

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

Council of Science Editors:

Hammond DA. Functional annotation of alternatively spliced isoforms of human G protein-coupled receptors (GPCRs). [Thesis]. University of Georgia; 2015. Available from: http://hdl.handle.net/10724/31427

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

12. Huff, Jason D. (Jason D.). Functional determinants of the porin MspA and its role in permeabilizing mycobacterial outer membranes.

Degree: PhD, 2010, University of Alabama – Birmingham

Mycobacterium tuberculosis (Mtb) infects one third of the global population and causes approximately 2,000,000 Tuberculosis-related deaths annually. Mycobacteria are Gram positive organisms but contain a… (more)

Subjects/Keywords: Bacterial Outer Membrane Proteins  – analysis<; br>; Cell Wall  – chemistry<; br>; Membrane Transport Proteins  – analysis<; br>; Mycobacterium smegmatis  – metabolism<; br>; Mycobacterium tuberculosis  – chemistry<; br>; Porins  – chemistry

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APA (6th Edition):

Huff, J. D. (. D. ). (2010). Functional determinants of the porin MspA and its role in permeabilizing mycobacterial outer membranes. (Doctoral Dissertation). University of Alabama – Birmingham. Retrieved from http://contentdm.mhsl.uab.edu/u?/etd,645

Chicago Manual of Style (16th Edition):

Huff, Jason D (Jason D ). “Functional determinants of the porin MspA and its role in permeabilizing mycobacterial outer membranes.” 2010. Doctoral Dissertation, University of Alabama – Birmingham. Accessed October 27, 2020. http://contentdm.mhsl.uab.edu/u?/etd,645.

MLA Handbook (7th Edition):

Huff, Jason D (Jason D ). “Functional determinants of the porin MspA and its role in permeabilizing mycobacterial outer membranes.” 2010. Web. 27 Oct 2020.

Vancouver:

Huff JD(D). Functional determinants of the porin MspA and its role in permeabilizing mycobacterial outer membranes. [Internet] [Doctoral dissertation]. University of Alabama – Birmingham; 2010. [cited 2020 Oct 27]. Available from: http://contentdm.mhsl.uab.edu/u?/etd,645.

Council of Science Editors:

Huff JD(D). Functional determinants of the porin MspA and its role in permeabilizing mycobacterial outer membranes. [Doctoral Dissertation]. University of Alabama – Birmingham; 2010. Available from: http://contentdm.mhsl.uab.edu/u?/etd,645


Indian Institute of Science

13. Gunasekaran, K. Stereochemical Analysis On Protein Structures - Lessons For Design, Engineering And Prediction.

Degree: PhD, Faculty of Science, 2013, Indian Institute of Science

Subjects/Keywords: Stereochemical Analysis; Protiens - Stereochemistry; Biosynthesis; Beta Hairpins; Protein Structures; Protein Motif Analysis; Membrane Proteins; Globular Proteins; Protein Structural Analysis; Biochemistry

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APA (6th Edition):

Gunasekaran, K. (2013). Stereochemical Analysis On Protein Structures - Lessons For Design, Engineering And Prediction. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/2140

Chicago Manual of Style (16th Edition):

Gunasekaran, K. “Stereochemical Analysis On Protein Structures - Lessons For Design, Engineering And Prediction.” 2013. Doctoral Dissertation, Indian Institute of Science. Accessed October 27, 2020. http://etd.iisc.ac.in/handle/2005/2140.

MLA Handbook (7th Edition):

Gunasekaran, K. “Stereochemical Analysis On Protein Structures - Lessons For Design, Engineering And Prediction.” 2013. Web. 27 Oct 2020.

Vancouver:

Gunasekaran K. Stereochemical Analysis On Protein Structures - Lessons For Design, Engineering And Prediction. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2013. [cited 2020 Oct 27]. Available from: http://etd.iisc.ac.in/handle/2005/2140.

Council of Science Editors:

Gunasekaran K. Stereochemical Analysis On Protein Structures - Lessons For Design, Engineering And Prediction. [Doctoral Dissertation]. Indian Institute of Science; 2013. Available from: http://etd.iisc.ac.in/handle/2005/2140


Macquarie University

14. Chick, Joel. Proteomic analysis of liver membranes through an alternative shotgun methodology.

Degree: PhD, 2009, Macquarie University

Bibliography: p. 200-212.

Introduction  – Shotgun proteomic analysis of rat liver membrane proteins  – A combination of immobilised pH gradients improve membrane proteomics  – Affects… (more)

Subjects/Keywords: Proteomics  – Methodology; Proteins  – Separation  – Methodology; Membrane proteins  – Analysis; Membrane proteins  – Structure; Isoelectric focusing; Mass spectrometry; Liver cells  – Molecular aspects; Cancer  – Molecular aspects; immobilised pH gradient; isoelectric focusing; mass spectrometry; shotgun proteomics; membrane proteins

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APA (6th Edition):

Chick, J. (2009). Proteomic analysis of liver membranes through an alternative shotgun methodology. (Doctoral Dissertation). Macquarie University. Retrieved from http://hdl.handle.net/1959.14/42528

Chicago Manual of Style (16th Edition):

Chick, Joel. “Proteomic analysis of liver membranes through an alternative shotgun methodology.” 2009. Doctoral Dissertation, Macquarie University. Accessed October 27, 2020. http://hdl.handle.net/1959.14/42528.

MLA Handbook (7th Edition):

Chick, Joel. “Proteomic analysis of liver membranes through an alternative shotgun methodology.” 2009. Web. 27 Oct 2020.

Vancouver:

Chick J. Proteomic analysis of liver membranes through an alternative shotgun methodology. [Internet] [Doctoral dissertation]. Macquarie University; 2009. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/1959.14/42528.

Council of Science Editors:

Chick J. Proteomic analysis of liver membranes through an alternative shotgun methodology. [Doctoral Dissertation]. Macquarie University; 2009. Available from: http://hdl.handle.net/1959.14/42528


University of Michigan

15. Schneider, Kimberly Ann. Development of multi-dimensional separation schemes for the analysis of membrane proteins.

Degree: PhD, Pure Sciences, 2003, University of Michigan

 The heterogeneity of cellular protein expression has stimulated development of separations targeting smaller groups of related proteins rather than entire proteomes. The following research describes… (more)

Subjects/Keywords: Analysis; Development; Dimensional; Epithelial; Membrane Proteins; Multi; Proteome; Schemes; Separation

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APA (6th Edition):

Schneider, K. A. (2003). Development of multi-dimensional separation schemes for the analysis of membrane proteins. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/123694

Chicago Manual of Style (16th Edition):

Schneider, Kimberly Ann. “Development of multi-dimensional separation schemes for the analysis of membrane proteins.” 2003. Doctoral Dissertation, University of Michigan. Accessed October 27, 2020. http://hdl.handle.net/2027.42/123694.

MLA Handbook (7th Edition):

Schneider, Kimberly Ann. “Development of multi-dimensional separation schemes for the analysis of membrane proteins.” 2003. Web. 27 Oct 2020.

Vancouver:

Schneider KA. Development of multi-dimensional separation schemes for the analysis of membrane proteins. [Internet] [Doctoral dissertation]. University of Michigan; 2003. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/2027.42/123694.

Council of Science Editors:

Schneider KA. Development of multi-dimensional separation schemes for the analysis of membrane proteins. [Doctoral Dissertation]. University of Michigan; 2003. Available from: http://hdl.handle.net/2027.42/123694

16. Bertin, Gwladys. Etude différentielle des protéines membranaires exprimées à la surface de l'hématie infectée par Plasmodium falciparum, en fonction de la symptomatologie : Differential protein expression profiles from Plasmodium falciparum isolates according to clinical forms malaria.

Degree: Docteur es, Biochimie et biologie moléculaire, 2013, Université Paris Descartes – Paris V

La virulence de Plasmodium falciparum est fonction de sa capacité à séquestrer les érythrocytes infectés (iEs) dans les organes profonds de l’hôte. Elle est liée… (more)

Subjects/Keywords: Spectrométrie de masse; RT- qPCR; Paludisme; PfEMP-1; Analyse de clustering; Protéine membranaire; Mass spectrometry; RT- qPCR; Malaria; PfEMP-1; Field isolates; Membrane proteins; Clustering analysis; 616.936 2

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

APA (6th Edition):

Bertin, G. (2013). Etude différentielle des protéines membranaires exprimées à la surface de l'hématie infectée par Plasmodium falciparum, en fonction de la symptomatologie : Differential protein expression profiles from Plasmodium falciparum isolates according to clinical forms malaria. (Doctoral Dissertation). Université Paris Descartes – Paris V. Retrieved from http://www.theses.fr/2013PA05P635

Chicago Manual of Style (16th Edition):

Bertin, Gwladys. “Etude différentielle des protéines membranaires exprimées à la surface de l'hématie infectée par Plasmodium falciparum, en fonction de la symptomatologie : Differential protein expression profiles from Plasmodium falciparum isolates according to clinical forms malaria.” 2013. Doctoral Dissertation, Université Paris Descartes – Paris V. Accessed October 27, 2020. http://www.theses.fr/2013PA05P635.

MLA Handbook (7th Edition):

Bertin, Gwladys. “Etude différentielle des protéines membranaires exprimées à la surface de l'hématie infectée par Plasmodium falciparum, en fonction de la symptomatologie : Differential protein expression profiles from Plasmodium falciparum isolates according to clinical forms malaria.” 2013. Web. 27 Oct 2020.

Vancouver:

Bertin G. Etude différentielle des protéines membranaires exprimées à la surface de l'hématie infectée par Plasmodium falciparum, en fonction de la symptomatologie : Differential protein expression profiles from Plasmodium falciparum isolates according to clinical forms malaria. [Internet] [Doctoral dissertation]. Université Paris Descartes – Paris V; 2013. [cited 2020 Oct 27]. Available from: http://www.theses.fr/2013PA05P635.

Council of Science Editors:

Bertin G. Etude différentielle des protéines membranaires exprimées à la surface de l'hématie infectée par Plasmodium falciparum, en fonction de la symptomatologie : Differential protein expression profiles from Plasmodium falciparum isolates according to clinical forms malaria. [Doctoral Dissertation]. Université Paris Descartes – Paris V; 2013. Available from: http://www.theses.fr/2013PA05P635


University of Texas Southwestern Medical Center

17. Revel, Andrew Thomas. Identification of bptA (bbe16) as an Essential Gene for the Persistence of the Lyme Disease Spirochete, Borrelia Burgdorferi, in its Natural Tick Vector.

Degree: 2005, University of Texas Southwestern Medical Center

 Borrelia burgdorferi (B. burgdorferi), the agent of Lyme disease, is a zoonotic spirochetal bacterium that depends on both arthropod (Ixodes ticks) and ammalian (rodent) hosts… (more)

Subjects/Keywords: Oligonucleotide Array Sequence Analysis; Bacterial Outer Membrane Proteins; Borrelia burgdorferi

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APA (6th Edition):

Revel, A. T. (2005). Identification of bptA (bbe16) as an Essential Gene for the Persistence of the Lyme Disease Spirochete, Borrelia Burgdorferi, in its Natural Tick Vector. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/456

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):

Revel, Andrew Thomas. “Identification of bptA (bbe16) as an Essential Gene for the Persistence of the Lyme Disease Spirochete, Borrelia Burgdorferi, in its Natural Tick Vector.” 2005. Thesis, University of Texas Southwestern Medical Center. Accessed October 27, 2020. http://hdl.handle.net/2152.5/456.

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

MLA Handbook (7th Edition):

Revel, Andrew Thomas. “Identification of bptA (bbe16) as an Essential Gene for the Persistence of the Lyme Disease Spirochete, Borrelia Burgdorferi, in its Natural Tick Vector.” 2005. Web. 27 Oct 2020.

Vancouver:

Revel AT. Identification of bptA (bbe16) as an Essential Gene for the Persistence of the Lyme Disease Spirochete, Borrelia Burgdorferi, in its Natural Tick Vector. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2005. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/2152.5/456.

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

Council of Science Editors:

Revel AT. Identification of bptA (bbe16) as an Essential Gene for the Persistence of the Lyme Disease Spirochete, Borrelia Burgdorferi, in its Natural Tick Vector. [Thesis]. University of Texas Southwestern Medical Center; 2005. Available from: http://hdl.handle.net/2152.5/456

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


University of Illinois – Urbana-Champaign

18. Khvostichenko, Daria. Mesophase-based approaches for on-chip membrane protein crystallization and structure determination.

Degree: PhD, Chemical Engineering, 2012, University of Illinois – Urbana-Champaign

 Transmembrane proteins traverse the lipid bilayers of cell membranes and play a highly important role in many processes in vivo. Malfunctions of membrane proteins have… (more)

Subjects/Keywords: on-chip analysis; membrane proteins; LCP crystallization; in meso crystallization; microfluidics; X-ray diffraction; small-angle X-ray scattering; phase behavior; lipidic mesophases; monoolein

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APA (6th Edition):

Khvostichenko, D. (2012). Mesophase-based approaches for on-chip membrane protein crystallization and structure determination. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/90063

Chicago Manual of Style (16th Edition):

Khvostichenko, Daria. “Mesophase-based approaches for on-chip membrane protein crystallization and structure determination.” 2012. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed October 27, 2020. http://hdl.handle.net/2142/90063.

MLA Handbook (7th Edition):

Khvostichenko, Daria. “Mesophase-based approaches for on-chip membrane protein crystallization and structure determination.” 2012. Web. 27 Oct 2020.

Vancouver:

Khvostichenko D. Mesophase-based approaches for on-chip membrane protein crystallization and structure determination. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2012. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/2142/90063.

Council of Science Editors:

Khvostichenko D. Mesophase-based approaches for on-chip membrane protein crystallization and structure determination. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2012. Available from: http://hdl.handle.net/2142/90063

19. Cao, Liming. Protein Separation with Ion-exchange Membrane Chromatography.

Degree: MS, 2005, Worcester Polytechnic Institute

Membrane chromatography is a promising process for the isolation, purification, and recovery of proteins, enzymes, and nuclear acids. Comparing with traditional beads column chromatography, membrane(more)

Subjects/Keywords: protein separation; Chromatographic analysis; Serum albumin; Proteins; Separation; Membrane chromatography

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APA (6th Edition):

Cao, L. (2005). Protein Separation with Ion-exchange Membrane Chromatography. (Thesis). Worcester Polytechnic Institute. Retrieved from etd-050405-174109 ; https://digitalcommons.wpi.edu/etd-theses/693

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):

Cao, Liming. “Protein Separation with Ion-exchange Membrane Chromatography.” 2005. Thesis, Worcester Polytechnic Institute. Accessed October 27, 2020. etd-050405-174109 ; https://digitalcommons.wpi.edu/etd-theses/693.

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

MLA Handbook (7th Edition):

Cao, Liming. “Protein Separation with Ion-exchange Membrane Chromatography.” 2005. Web. 27 Oct 2020.

Vancouver:

Cao L. Protein Separation with Ion-exchange Membrane Chromatography. [Internet] [Thesis]. Worcester Polytechnic Institute; 2005. [cited 2020 Oct 27]. Available from: etd-050405-174109 ; https://digitalcommons.wpi.edu/etd-theses/693.

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

Council of Science Editors:

Cao L. Protein Separation with Ion-exchange Membrane Chromatography. [Thesis]. Worcester Polytechnic Institute; 2005. Available from: etd-050405-174109 ; https://digitalcommons.wpi.edu/etd-theses/693

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


Brock University

20. Homer-Dixon, Jill A. Pigment orientation changes detected by low temperature linear dichroism spectroscopy: cold-hardening transition in phycobilisome-containing organisms .

Degree: Department of Biological Sciences, 1992, Brock University

 Low temperature (77K) linear dichroism spectroscopy was used to characterize pigment orientation changes accompanying the light state transition in the cyanobacterium, Synechococcus sp. pee 6301,… (more)

Subjects/Keywords: Linear dichroism.; Low temperatures.; Pigments (Biology); Spectrum analysis.; Membrane proteins.

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APA (6th Edition):

Homer-Dixon, J. A. (1992). Pigment orientation changes detected by low temperature linear dichroism spectroscopy: cold-hardening transition in phycobilisome-containing organisms . (Thesis). Brock University. Retrieved from http://hdl.handle.net/10464/2759

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):

Homer-Dixon, Jill A. “Pigment orientation changes detected by low temperature linear dichroism spectroscopy: cold-hardening transition in phycobilisome-containing organisms .” 1992. Thesis, Brock University. Accessed October 27, 2020. http://hdl.handle.net/10464/2759.

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

MLA Handbook (7th Edition):

Homer-Dixon, Jill A. “Pigment orientation changes detected by low temperature linear dichroism spectroscopy: cold-hardening transition in phycobilisome-containing organisms .” 1992. Web. 27 Oct 2020.

Vancouver:

Homer-Dixon JA. Pigment orientation changes detected by low temperature linear dichroism spectroscopy: cold-hardening transition in phycobilisome-containing organisms . [Internet] [Thesis]. Brock University; 1992. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10464/2759.

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

Council of Science Editors:

Homer-Dixon JA. Pigment orientation changes detected by low temperature linear dichroism spectroscopy: cold-hardening transition in phycobilisome-containing organisms . [Thesis]. Brock University; 1992. Available from: http://hdl.handle.net/10464/2759

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


University of Cambridge

21. Sprenger, Teresa. Molecular mechanism of Trypanosoma brucei Aquaglyceroporin 2.

Degree: PhD, 2020, University of Cambridge

 Trypanosoma brucei subspecies cause Human African Trypanosomiasis, which is fatal unless treated. T. brucei Aquaglyceroporin 2 (TbAQP2) is required for the uptake of two of… (more)

Subjects/Keywords: Aquaporin; Trypanosoma brucei; TbAQP2; pentamidine; melarsoprol; cryo-electron microscopy; membrane proteins; SaposinA-lipid nanoparticles; liposomes; uptake/binding assays; genetic modification of Trypanosoma brucei; phylogenetic analysis

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APA (6th Edition):

Sprenger, T. (2020). Molecular mechanism of Trypanosoma brucei Aquaglyceroporin 2. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/309964

Chicago Manual of Style (16th Edition):

Sprenger, Teresa. “Molecular mechanism of Trypanosoma brucei Aquaglyceroporin 2.” 2020. Doctoral Dissertation, University of Cambridge. Accessed October 27, 2020. https://www.repository.cam.ac.uk/handle/1810/309964.

MLA Handbook (7th Edition):

Sprenger, Teresa. “Molecular mechanism of Trypanosoma brucei Aquaglyceroporin 2.” 2020. Web. 27 Oct 2020.

Vancouver:

Sprenger T. Molecular mechanism of Trypanosoma brucei Aquaglyceroporin 2. [Internet] [Doctoral dissertation]. University of Cambridge; 2020. [cited 2020 Oct 27]. Available from: https://www.repository.cam.ac.uk/handle/1810/309964.

Council of Science Editors:

Sprenger T. Molecular mechanism of Trypanosoma brucei Aquaglyceroporin 2. [Doctoral Dissertation]. University of Cambridge; 2020. Available from: https://www.repository.cam.ac.uk/handle/1810/309964


IUPUI

22. Li, Chao. Sphingosine 1-phosphate enhances excitability of sensory neurons through sphingosine 1-phosphate receptors 1 and/or 3.

Degree: 2014, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

Sphingosine 1-phosphate (S1P) is a bioactive sphingolipid that has proven to be an important signaling molecule both as an extracellular… (more)

Subjects/Keywords: sphingosine 1-phosphate; S1P; excitability; sensory neurons; G protein-coupled receptors; Sphingosine  – Physiological effect  – Research  – Evaluation  – Analysis; Sphingolipids  – Research; Excitation (Physiology); Sensory neurons  – Research; Protein kinases; Cellular signal transduction; Phospholipids  – Research; G proteins  – Research; Neurochemistry; Second messengers (Biochemistry); Cell interaction; Neural transmission; Membrane proteins  – Research  – Methodology

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

APA (6th Edition):

Li, C. (2014). Sphingosine 1-phosphate enhances excitability of sensory neurons through sphingosine 1-phosphate receptors 1 and/or 3. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/5970

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, Chao. “Sphingosine 1-phosphate enhances excitability of sensory neurons through sphingosine 1-phosphate receptors 1 and/or 3.” 2014. Thesis, IUPUI. Accessed October 27, 2020. http://hdl.handle.net/1805/5970.

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

MLA Handbook (7th Edition):

Li, Chao. “Sphingosine 1-phosphate enhances excitability of sensory neurons through sphingosine 1-phosphate receptors 1 and/or 3.” 2014. Web. 27 Oct 2020.

Vancouver:

Li C. Sphingosine 1-phosphate enhances excitability of sensory neurons through sphingosine 1-phosphate receptors 1 and/or 3. [Internet] [Thesis]. IUPUI; 2014. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/1805/5970.

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

Council of Science Editors:

Li C. Sphingosine 1-phosphate enhances excitability of sensory neurons through sphingosine 1-phosphate receptors 1 and/or 3. [Thesis]. IUPUI; 2014. Available from: http://hdl.handle.net/1805/5970

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


University of Illinois – Chicago

23. Jimenez-Morales, David. Effects of Physicochemical and Functional Constraints on the Sequence and Structure of Proteins.

Degree: 2013, University of Illinois – Chicago

Proteins carry out essential functions in living organisms. The sequence and structure of proteins are constrained by numerous factors. In this thesis, we use computational… (more)

Subjects/Keywords: beta-barrel membrane protein; pattern of amino acid substitution; beta-barrel Transmembrane Matrices (bbTM); Scoring Matrix; evolutionary analysis of beta-barrel membrane proteins; outer membrane proteins; protein engineering; djm diagrams; bbTM-ST; enzymes; active site; catalytic active site; charge density; charden; craters; post-translational modifications (PTM); lysine carboxylation; lysine carbamylation; prelyscar; predictor of lysine carboxylation; predictor of lysine carbamylation; metal ion center; computational method; bayesian classifier; computational model

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APA (6th Edition):

Jimenez-Morales, D. (2013). Effects of Physicochemical and Functional Constraints on the Sequence and Structure of Proteins. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/10068

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):

Jimenez-Morales, David. “Effects of Physicochemical and Functional Constraints on the Sequence and Structure of Proteins.” 2013. Thesis, University of Illinois – Chicago. Accessed October 27, 2020. http://hdl.handle.net/10027/10068.

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

MLA Handbook (7th Edition):

Jimenez-Morales, David. “Effects of Physicochemical and Functional Constraints on the Sequence and Structure of Proteins.” 2013. Web. 27 Oct 2020.

Vancouver:

Jimenez-Morales D. Effects of Physicochemical and Functional Constraints on the Sequence and Structure of Proteins. [Internet] [Thesis]. University of Illinois – Chicago; 2013. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10027/10068.

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

Council of Science Editors:

Jimenez-Morales D. Effects of Physicochemical and Functional Constraints on the Sequence and Structure of Proteins. [Thesis]. University of Illinois – Chicago; 2013. Available from: http://hdl.handle.net/10027/10068

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

24. Martins, Stephanie Alves. Análise da mobilidade mitocondrial em células vivas do hipocampo, substância negra e locus coeruleus anterior à agregação proteica envolvida  em neurodegeneração.

Degree: Mestrado, Fisiopatologia Experimental, 2013, University of São Paulo

A alteração do tráfego mitocondrial em neurônios leva ao aumento do estresse oxidativo, privação de energia, deficiência da comunicação intercelular e neurodegeneração. Há evidências de… (more)

Subjects/Keywords: Aging/drug effects; Aging/metabolism; Animals models; Doenças neurodegenerativas/fisiopatologia; Envelhecimento/efeitos de drogas; Envelhecimento/metabolismo; Hipocampo/fisiologia; Hippocampus/physiology; Locus cerúleo/fisiologia; Locus coeruleus/physiology; Mitochondrial membrane transport proteins/ physiology; Mitochondrial membrane transport proteins/analysis; Modelos animais; Neurodegenerative diseases/physiopathology; Proteínas de transporte da membrana mitocondrial/análise; Proteínas de transporte da membrana mitocondrial/fisiologia; Ratos endogâmicos Lew; Rats inbred strains; Rotenona/administralçao e dosagem; Rotenone/administration e dosage; Substância negra/fisiologia; Substantia nigra/physiology

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APA (6th Edition):

Martins, S. A. (2013). Análise da mobilidade mitocondrial em células vivas do hipocampo, substância negra e locus coeruleus anterior à agregação proteica envolvida  em neurodegeneração. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/5/5160/tde-07022014-103631/ ;

Chicago Manual of Style (16th Edition):

Martins, Stephanie Alves. “Análise da mobilidade mitocondrial em células vivas do hipocampo, substância negra e locus coeruleus anterior à agregação proteica envolvida  em neurodegeneração.” 2013. Masters Thesis, University of São Paulo. Accessed October 27, 2020. http://www.teses.usp.br/teses/disponiveis/5/5160/tde-07022014-103631/ ;.

MLA Handbook (7th Edition):

Martins, Stephanie Alves. “Análise da mobilidade mitocondrial em células vivas do hipocampo, substância negra e locus coeruleus anterior à agregação proteica envolvida  em neurodegeneração.” 2013. Web. 27 Oct 2020.

Vancouver:

Martins SA. Análise da mobilidade mitocondrial em células vivas do hipocampo, substância negra e locus coeruleus anterior à agregação proteica envolvida  em neurodegeneração. [Internet] [Masters thesis]. University of São Paulo; 2013. [cited 2020 Oct 27]. Available from: http://www.teses.usp.br/teses/disponiveis/5/5160/tde-07022014-103631/ ;.

Council of Science Editors:

Martins SA. Análise da mobilidade mitocondrial em células vivas do hipocampo, substância negra e locus coeruleus anterior à agregação proteica envolvida  em neurodegeneração. [Masters Thesis]. University of São Paulo; 2013. Available from: http://www.teses.usp.br/teses/disponiveis/5/5160/tde-07022014-103631/ ;

25. Glavier, Marie. Études structurales par cryo-microscopie électronique d’un système d’efflux multi-drogues bactérien, impliqué dans la résistance aux antibiotiques : Cryo-electron microscopy structural studies of a bacterial multi-drug efflux pump involved in antibiotic resistance.

Degree: Docteur es, Biochimie, 2018, Bordeaux

 L'apparition croissante de bactéries pathogènes multi-résistantes à la plupart des antibiotiques disponibles apparaît comme un problème mondial de santé publique. Malheureusement, un usage excessif à… (more)

Subjects/Keywords: Cryo-microscopie électronique; Analyse d'image et reconstruction 3D; Système d’efflux tripartite MexA-MexB-OprM; Protéines membranaires; Nanodisques; Cryo-electron microscopy; Single particle analysis; Tripartite efflux system MexA-MexB-OprM; Membrane proteins; Lipid Nanodisc

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APA (6th Edition):

Glavier, M. (2018). Études structurales par cryo-microscopie électronique d’un système d’efflux multi-drogues bactérien, impliqué dans la résistance aux antibiotiques : Cryo-electron microscopy structural studies of a bacterial multi-drug efflux pump involved in antibiotic resistance. (Doctoral Dissertation). Bordeaux. Retrieved from http://www.theses.fr/2018BORD0239

Chicago Manual of Style (16th Edition):

Glavier, Marie. “Études structurales par cryo-microscopie électronique d’un système d’efflux multi-drogues bactérien, impliqué dans la résistance aux antibiotiques : Cryo-electron microscopy structural studies of a bacterial multi-drug efflux pump involved in antibiotic resistance.” 2018. Doctoral Dissertation, Bordeaux. Accessed October 27, 2020. http://www.theses.fr/2018BORD0239.

MLA Handbook (7th Edition):

Glavier, Marie. “Études structurales par cryo-microscopie électronique d’un système d’efflux multi-drogues bactérien, impliqué dans la résistance aux antibiotiques : Cryo-electron microscopy structural studies of a bacterial multi-drug efflux pump involved in antibiotic resistance.” 2018. Web. 27 Oct 2020.

Vancouver:

Glavier M. Études structurales par cryo-microscopie électronique d’un système d’efflux multi-drogues bactérien, impliqué dans la résistance aux antibiotiques : Cryo-electron microscopy structural studies of a bacterial multi-drug efflux pump involved in antibiotic resistance. [Internet] [Doctoral dissertation]. Bordeaux; 2018. [cited 2020 Oct 27]. Available from: http://www.theses.fr/2018BORD0239.

Council of Science Editors:

Glavier M. Études structurales par cryo-microscopie électronique d’un système d’efflux multi-drogues bactérien, impliqué dans la résistance aux antibiotiques : Cryo-electron microscopy structural studies of a bacterial multi-drug efflux pump involved in antibiotic resistance. [Doctoral Dissertation]. Bordeaux; 2018. Available from: http://www.theses.fr/2018BORD0239

26. Karena - Efstathiou, Aikaterini. Δομική και λειτουργική οργάνωση των διαμεμβρανικών ελίκων στους μεταφορείς πουρινών της οικογένειας ΝΑΤ.

Degree: 2014, University of Ioannina; Πανεπιστήμιο Ιωαννίνων

This PHD thesis refers to the research of membrane transport proteins, which (a) constitute a large number of gene products in all species (5-15%), (b)… (more)

Subjects/Keywords: Διαμεμβρανικές πρωτεΐνες μεταφοράς; Νουκλεοτιδικές βάσεις; Πουρίνες; α – έλικα; Οικογένεια ΝΑΤ/NCS2; Μεταφορέας ξανθίνης; Μεταλλαξιγένεση κυστεϊνικής σάρωσης; Κέντρο δέσμευσης; Μοντέλο δομής - μηχανισμού; Membrane transport proteins; Nucleobases; Purines; α – helix; NAT/NCS2 family; Xanthine permease; Cys – scanning analysis; Binding site; Cross – linking; Structure function model

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APA (6th Edition):

Karena - Efstathiou, A. (2014). Δομική και λειτουργική οργάνωση των διαμεμβρανικών ελίκων στους μεταφορείς πουρινών της οικογένειας ΝΑΤ. (Thesis). University of Ioannina; Πανεπιστήμιο Ιωαννίνων. Retrieved from http://hdl.handle.net/10442/hedi/36259

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):

Karena - Efstathiou, Aikaterini. “Δομική και λειτουργική οργάνωση των διαμεμβρανικών ελίκων στους μεταφορείς πουρινών της οικογένειας ΝΑΤ.” 2014. Thesis, University of Ioannina; Πανεπιστήμιο Ιωαννίνων. Accessed October 27, 2020. http://hdl.handle.net/10442/hedi/36259.

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

MLA Handbook (7th Edition):

Karena - Efstathiou, Aikaterini. “Δομική και λειτουργική οργάνωση των διαμεμβρανικών ελίκων στους μεταφορείς πουρινών της οικογένειας ΝΑΤ.” 2014. Web. 27 Oct 2020.

Vancouver:

Karena - Efstathiou A. Δομική και λειτουργική οργάνωση των διαμεμβρανικών ελίκων στους μεταφορείς πουρινών της οικογένειας ΝΑΤ. [Internet] [Thesis]. University of Ioannina; Πανεπιστήμιο Ιωαννίνων; 2014. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10442/hedi/36259.

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

Council of Science Editors:

Karena - Efstathiou A. Δομική και λειτουργική οργάνωση των διαμεμβρανικών ελίκων στους μεταφορείς πουρινών της οικογένειας ΝΑΤ. [Thesis]. University of Ioannina; Πανεπιστήμιο Ιωαννίνων; 2014. Available from: http://hdl.handle.net/10442/hedi/36259

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


Vanderbilt University

27. Zhou, Zheng. EPR and fluorescence studies on erythrocyte membrane skeletal proteins: cdb3 and ankyrin.

Degree: PhD, Molecular Physiology and Biophysics, 2006, Vanderbilt University

 The protein complex composed of the cytoplasmic domain of band 3 (cdb3) and ankyrin forms one of the two major contact sites between the spectrin-based… (more)

Subjects/Keywords: Blood  – Diseases  – Genetic aspects; Protein-protein interactions; Electron paramagnetic resonance spectroscopy; badan; MTSSL; SDSL; ANK repeat; Site directed spin labeling; band 3 Tuscaloosa; Membrane proteins  – Analysis; Blood proteins  – Analysis; Erythrocytes  – Analysis

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APA (6th Edition):

Zhou, Z. (2006). EPR and fluorescence studies on erythrocyte membrane skeletal proteins: cdb3 and ankyrin. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/11954

Chicago Manual of Style (16th Edition):

Zhou, Zheng. “EPR and fluorescence studies on erythrocyte membrane skeletal proteins: cdb3 and ankyrin.” 2006. Doctoral Dissertation, Vanderbilt University. Accessed October 27, 2020. http://hdl.handle.net/1803/11954.

MLA Handbook (7th Edition):

Zhou, Zheng. “EPR and fluorescence studies on erythrocyte membrane skeletal proteins: cdb3 and ankyrin.” 2006. Web. 27 Oct 2020.

Vancouver:

Zhou Z. EPR and fluorescence studies on erythrocyte membrane skeletal proteins: cdb3 and ankyrin. [Internet] [Doctoral dissertation]. Vanderbilt University; 2006. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/1803/11954.

Council of Science Editors:

Zhou Z. EPR and fluorescence studies on erythrocyte membrane skeletal proteins: cdb3 and ankyrin. [Doctoral Dissertation]. Vanderbilt University; 2006. Available from: http://hdl.handle.net/1803/11954


ETH Zürich

28. Petrosyan, Rafayel. Novel single-molecule force spectroscopy approaches to characterize structure and stability of transmembrane proteins.

Degree: 2015, ETH Zürich

Subjects/Keywords: ATOMIC FORCE MICROSCOPES, AFM + ATOMIC FORCE MICROSCOPY; STRUCTURE ANALYSIS OF PROTEINS AND PEPTIDES; STRUKTURANALYSE VON PROTEINEN UND PEPTIDEN; MEMBRANE PROTEIN STRUCTURE; MEMBRANPROTEINSTRUKTUR; RASTERKRAFTMIKROSKOPE, RKM + RASTERKRAFTMIKROSKOPIE; info:eu-repo/classification/ddc/570; Life sciences

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APA (6th Edition):

Petrosyan, R. (2015). Novel single-molecule force spectroscopy approaches to characterize structure and stability of transmembrane proteins. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/109920

Chicago Manual of Style (16th Edition):

Petrosyan, Rafayel. “Novel single-molecule force spectroscopy approaches to characterize structure and stability of transmembrane proteins.” 2015. Doctoral Dissertation, ETH Zürich. Accessed October 27, 2020. http://hdl.handle.net/20.500.11850/109920.

MLA Handbook (7th Edition):

Petrosyan, Rafayel. “Novel single-molecule force spectroscopy approaches to characterize structure and stability of transmembrane proteins.” 2015. Web. 27 Oct 2020.

Vancouver:

Petrosyan R. Novel single-molecule force spectroscopy approaches to characterize structure and stability of transmembrane proteins. [Internet] [Doctoral dissertation]. ETH Zürich; 2015. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/20.500.11850/109920.

Council of Science Editors:

Petrosyan R. Novel single-molecule force spectroscopy approaches to characterize structure and stability of transmembrane proteins. [Doctoral Dissertation]. ETH Zürich; 2015. Available from: http://hdl.handle.net/20.500.11850/109920


ETH Zürich

29. Eichmann, Cédric. NMR studies of large biomolecular systems.

Degree: 2011, ETH Zürich

Subjects/Keywords: KERNRESONANZSPEKTROSKOPIE (BIOLOGISCHE TECHNIKEN); STRUKTURANALYSE VON PROTEINEN UND PEPTIDEN; FALTUNG DER POLYPEPTIDKETTE (PROTEINE, PEPTIDE); STRUKTURÄNDERUNGEN VON PROTEINEN UND PEPTIDEN; MEMBRANPROTEINSTRUKTUR; TRANSLATION (MOLEKULARE GENETIK); RIBOSOMALE PROTEINE (MOLEKULARBIOLOGIE); NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY (BIOLOGICAL TECHNIQUES); STRUCTURE ANALYSIS OF PROTEINS AND PEPTIDES; FOLDING OF POLYPEPTIDE CHAIN (PROTEINS, PEPTIDES); STRUCTURAL CHANGES OF PROTEINS AND PEPTIDES; MEMBRANE PROTEIN STRUCTURE; TRANSLATION (MOLECULAR GENETICS); RIBOSOMAL PROTEINS (MOLECULAR BIOLOGY); info:eu-repo/classification/ddc/570; Life sciences

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APA (6th Edition):

Eichmann, C. (2011). NMR studies of large biomolecular systems. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/152786

Chicago Manual of Style (16th Edition):

Eichmann, Cédric. “NMR studies of large biomolecular systems.” 2011. Doctoral Dissertation, ETH Zürich. Accessed October 27, 2020. http://hdl.handle.net/20.500.11850/152786.

MLA Handbook (7th Edition):

Eichmann, Cédric. “NMR studies of large biomolecular systems.” 2011. Web. 27 Oct 2020.

Vancouver:

Eichmann C. NMR studies of large biomolecular systems. [Internet] [Doctoral dissertation]. ETH Zürich; 2011. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/20.500.11850/152786.

Council of Science Editors:

Eichmann C. NMR studies of large biomolecular systems. [Doctoral Dissertation]. ETH Zürich; 2011. Available from: http://hdl.handle.net/20.500.11850/152786


ETH Zürich

30. Pfreundschuh, Moritz André. High-Resolution Functional Imaging of Native Proteins using Force Distance Curve Based Atomic Force Microscopy.

Degree: 2015, ETH Zürich

Subjects/Keywords: MEMBRANPROTEINSTRUKTUR; MOLEKULARE MOTOREN (BIOCHEMIE UND MOLEKULARBIOLOGIE); RASTERKRAFTMIKROSKOPE, RKM + RASTERKRAFTMIKROSKOPIE; STRUKTURANALYSE VON PROTEINEN UND PEPTIDEN; BIOPHYSIKALISCHE PROTEINCHEMIE; MEMBRANE PROTEIN STRUCTURE; MOLECULAR MOTORS (BIOCHEMISTRY AND MOLECULAR BIOLOGY); ATOMIC FORCE MICROSCOPES, AFM + ATOMIC FORCE MICROSCOPY; STRUCTURE ANALYSIS OF PROTEINS AND PEPTIDES; BIOPHYSICAL PROTEIN CHEMISTRY; info:eu-repo/classification/ddc/570; Life sciences

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Pfreundschuh, M. A. (2015). High-Resolution Functional Imaging of Native Proteins using Force Distance Curve Based Atomic Force Microscopy. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/155241

Chicago Manual of Style (16th Edition):

Pfreundschuh, Moritz André. “High-Resolution Functional Imaging of Native Proteins using Force Distance Curve Based Atomic Force Microscopy.” 2015. Doctoral Dissertation, ETH Zürich. Accessed October 27, 2020. http://hdl.handle.net/20.500.11850/155241.

MLA Handbook (7th Edition):

Pfreundschuh, Moritz André. “High-Resolution Functional Imaging of Native Proteins using Force Distance Curve Based Atomic Force Microscopy.” 2015. Web. 27 Oct 2020.

Vancouver:

Pfreundschuh MA. High-Resolution Functional Imaging of Native Proteins using Force Distance Curve Based Atomic Force Microscopy. [Internet] [Doctoral dissertation]. ETH Zürich; 2015. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/20.500.11850/155241.

Council of Science Editors:

Pfreundschuh MA. High-Resolution Functional Imaging of Native Proteins using Force Distance Curve Based Atomic Force Microscopy. [Doctoral Dissertation]. ETH Zürich; 2015. Available from: http://hdl.handle.net/20.500.11850/155241

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