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You searched for subject:(Cell receptors). Showing records 1 – 30 of 600 total matches.

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Oregon State University

1. Venkataraman, Anand. In vitro and in vivo approaches for the functional characterization of the scaffold protein, GRASP.

Degree: PhD, Molecular and Cellular Biology, 2009, Oregon State University

 Studies using the pluripotent embryonic carcinoma cell line, P19, as a retinoic acid (RA)-responsive model system have been instrumental towards our understanding of the RA-dependent… (more)

Subjects/Keywords: Trafficking; Cell receptors

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APA (6th Edition):

Venkataraman, A. (2009). In vitro and in vivo approaches for the functional characterization of the scaffold protein, GRASP. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/13654

Chicago Manual of Style (16th Edition):

Venkataraman, Anand. “In vitro and in vivo approaches for the functional characterization of the scaffold protein, GRASP.” 2009. Doctoral Dissertation, Oregon State University. Accessed March 07, 2021. http://hdl.handle.net/1957/13654.

MLA Handbook (7th Edition):

Venkataraman, Anand. “In vitro and in vivo approaches for the functional characterization of the scaffold protein, GRASP.” 2009. Web. 07 Mar 2021.

Vancouver:

Venkataraman A. In vitro and in vivo approaches for the functional characterization of the scaffold protein, GRASP. [Internet] [Doctoral dissertation]. Oregon State University; 2009. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1957/13654.

Council of Science Editors:

Venkataraman A. In vitro and in vivo approaches for the functional characterization of the scaffold protein, GRASP. [Doctoral Dissertation]. Oregon State University; 2009. Available from: http://hdl.handle.net/1957/13654


University of Aberdeen

2. Dorning, Ashley J. The pharmacology, signalling and expression of the lipid-sensing receptor GPR92.

Degree: PhD, 2013, University of Aberdeen

 G protein-coupled receptors (GPCRs) are 7 transmembrane domain proteins capable of initiating cellular responses following ligand binding. GPR92 is expressed in the central nervous system… (more)

Subjects/Keywords: 610; Cell receptors

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APA (6th Edition):

Dorning, A. J. (2013). The pharmacology, signalling and expression of the lipid-sensing receptor GPR92. (Doctoral Dissertation). University of Aberdeen. Retrieved from https://abdn.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12152684420005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.582731

Chicago Manual of Style (16th Edition):

Dorning, Ashley J. “The pharmacology, signalling and expression of the lipid-sensing receptor GPR92.” 2013. Doctoral Dissertation, University of Aberdeen. Accessed March 07, 2021. https://abdn.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12152684420005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.582731.

MLA Handbook (7th Edition):

Dorning, Ashley J. “The pharmacology, signalling and expression of the lipid-sensing receptor GPR92.” 2013. Web. 07 Mar 2021.

Vancouver:

Dorning AJ. The pharmacology, signalling and expression of the lipid-sensing receptor GPR92. [Internet] [Doctoral dissertation]. University of Aberdeen; 2013. [cited 2021 Mar 07]. Available from: https://abdn.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12152684420005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.582731.

Council of Science Editors:

Dorning AJ. The pharmacology, signalling and expression of the lipid-sensing receptor GPR92. [Doctoral Dissertation]. University of Aberdeen; 2013. Available from: https://abdn.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12152684420005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.582731


Hong Kong University of Science and Technology

3. He, Wei. Single-particle tracking of acetylcholine receptors and ganglioside GM1 on live cell membranes.

Degree: 2015, Hong Kong University of Science and Technology

 Single-particle tracking was used to monitor 2 highly expressed molecules in live Xenopus muscle cells: the transmembrane ion channel acetylcholine receptor (AChR) and the outer-leaflet… (more)

Subjects/Keywords: Cell membranes ; Nicotinic receptors ; Acetylcholine ; Receptors ; Gangliosides

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APA (6th Edition):

He, W. (2015). Single-particle tracking of acetylcholine receptors and ganglioside GM1 on live cell membranes. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-83591 ; https://doi.org/10.14711/thesis-b1477557 ; http://repository.ust.hk/ir/bitstream/1783.1-83591/1/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):

He, Wei. “Single-particle tracking of acetylcholine receptors and ganglioside GM1 on live cell membranes.” 2015. Thesis, Hong Kong University of Science and Technology. Accessed March 07, 2021. http://repository.ust.hk/ir/Record/1783.1-83591 ; https://doi.org/10.14711/thesis-b1477557 ; http://repository.ust.hk/ir/bitstream/1783.1-83591/1/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):

He, Wei. “Single-particle tracking of acetylcholine receptors and ganglioside GM1 on live cell membranes.” 2015. Web. 07 Mar 2021.

Vancouver:

He W. Single-particle tracking of acetylcholine receptors and ganglioside GM1 on live cell membranes. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2015. [cited 2021 Mar 07]. Available from: http://repository.ust.hk/ir/Record/1783.1-83591 ; https://doi.org/10.14711/thesis-b1477557 ; http://repository.ust.hk/ir/bitstream/1783.1-83591/1/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:

He W. Single-particle tracking of acetylcholine receptors and ganglioside GM1 on live cell membranes. [Thesis]. Hong Kong University of Science and Technology; 2015. Available from: http://repository.ust.hk/ir/Record/1783.1-83591 ; https://doi.org/10.14711/thesis-b1477557 ; http://repository.ust.hk/ir/bitstream/1783.1-83591/1/th_redirect.html

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


North Carolina State University

4. Shah, Radhika. Evaluation of Zebrafish Novel Immune-Type Receptor 9 (NITR9).

Degree: PhD, Immunology, 2009, North Carolina State University

 Natural killer (NK) cells are lymphocytes of the innate immune system that express several cell surface receptors including both activating and inhibitory forms. The natural… (more)

Subjects/Keywords: NK cell receptors; teleost; NITR

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APA (6th Edition):

Shah, R. (2009). Evaluation of Zebrafish Novel Immune-Type Receptor 9 (NITR9). (Doctoral Dissertation). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/3864

Chicago Manual of Style (16th Edition):

Shah, Radhika. “Evaluation of Zebrafish Novel Immune-Type Receptor 9 (NITR9).” 2009. Doctoral Dissertation, North Carolina State University. Accessed March 07, 2021. http://www.lib.ncsu.edu/resolver/1840.16/3864.

MLA Handbook (7th Edition):

Shah, Radhika. “Evaluation of Zebrafish Novel Immune-Type Receptor 9 (NITR9).” 2009. Web. 07 Mar 2021.

Vancouver:

Shah R. Evaluation of Zebrafish Novel Immune-Type Receptor 9 (NITR9). [Internet] [Doctoral dissertation]. North Carolina State University; 2009. [cited 2021 Mar 07]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/3864.

Council of Science Editors:

Shah R. Evaluation of Zebrafish Novel Immune-Type Receptor 9 (NITR9). [Doctoral Dissertation]. North Carolina State University; 2009. Available from: http://www.lib.ncsu.edu/resolver/1840.16/3864


Queen Mary, University of London

5. Farren, Timothy william. The role of the NK cell receptor CD160 in the diagnosis, differentiation and function of chronic B-cell malignancies.

Degree: PhD, 2013, Queen Mary, University of London

 Chronic Lymphocytic Leukaemia (CLL) remains the most abundant leukaemia in those aged over 65 years. It is characterised by the expansion of malignant monoclonal B-lymphocytes… (more)

Subjects/Keywords: 616.99; Leukaemia; NK cell receptors

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APA (6th Edition):

Farren, T. w. (2013). The role of the NK cell receptor CD160 in the diagnosis, differentiation and function of chronic B-cell malignancies. (Doctoral Dissertation). Queen Mary, University of London. Retrieved from http://qmro.qmul.ac.uk/xmlui/handle/123456789/9011 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.667236

Chicago Manual of Style (16th Edition):

Farren, Timothy william. “The role of the NK cell receptor CD160 in the diagnosis, differentiation and function of chronic B-cell malignancies.” 2013. Doctoral Dissertation, Queen Mary, University of London. Accessed March 07, 2021. http://qmro.qmul.ac.uk/xmlui/handle/123456789/9011 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.667236.

MLA Handbook (7th Edition):

Farren, Timothy william. “The role of the NK cell receptor CD160 in the diagnosis, differentiation and function of chronic B-cell malignancies.” 2013. Web. 07 Mar 2021.

Vancouver:

Farren Tw. The role of the NK cell receptor CD160 in the diagnosis, differentiation and function of chronic B-cell malignancies. [Internet] [Doctoral dissertation]. Queen Mary, University of London; 2013. [cited 2021 Mar 07]. Available from: http://qmro.qmul.ac.uk/xmlui/handle/123456789/9011 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.667236.

Council of Science Editors:

Farren Tw. The role of the NK cell receptor CD160 in the diagnosis, differentiation and function of chronic B-cell malignancies. [Doctoral Dissertation]. Queen Mary, University of London; 2013. Available from: http://qmro.qmul.ac.uk/xmlui/handle/123456789/9011 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.667236


University of Aberdeen

6. Dorning, Ashley J. The pharmacology, signalling and expression of the lipid-sensing receptor GPR92.

Degree: School of Medical Sciences., 2013, University of Aberdeen

Subjects/Keywords: Cell receptors.

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APA (6th Edition):

Dorning, A. J. (2013). The pharmacology, signalling and expression of the lipid-sensing receptor GPR92. (Doctoral Dissertation). University of Aberdeen. Retrieved from http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=201860 ; http://digitool.abdn.ac.uk:1801/webclient/DeliveryManager?pid=201860&custom_att_2=simple_viewer

Chicago Manual of Style (16th Edition):

Dorning, Ashley J. “The pharmacology, signalling and expression of the lipid-sensing receptor GPR92.” 2013. Doctoral Dissertation, University of Aberdeen. Accessed March 07, 2021. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=201860 ; http://digitool.abdn.ac.uk:1801/webclient/DeliveryManager?pid=201860&custom_att_2=simple_viewer.

MLA Handbook (7th Edition):

Dorning, Ashley J. “The pharmacology, signalling and expression of the lipid-sensing receptor GPR92.” 2013. Web. 07 Mar 2021.

Vancouver:

Dorning AJ. The pharmacology, signalling and expression of the lipid-sensing receptor GPR92. [Internet] [Doctoral dissertation]. University of Aberdeen; 2013. [cited 2021 Mar 07]. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=201860 ; http://digitool.abdn.ac.uk:1801/webclient/DeliveryManager?pid=201860&custom_att_2=simple_viewer.

Council of Science Editors:

Dorning AJ. The pharmacology, signalling and expression of the lipid-sensing receptor GPR92. [Doctoral Dissertation]. University of Aberdeen; 2013. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=201860 ; http://digitool.abdn.ac.uk:1801/webclient/DeliveryManager?pid=201860&custom_att_2=simple_viewer


University of Hong Kong

7. 葉慈灃. Characterization of an orphan receptor : sub-cellular localization, ligand identification and cellular events for signaling activation of toll-like receptor 10.

Degree: 2015, University of Hong Kong

 Toll-like receptors (TLRs) play key roles in innate immune recognition of pathogen-associated molecular patterns (PAMPs) of invading microbes. Among the ten TLR family members identified… (more)

Subjects/Keywords: Cell receptors

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APA (6th Edition):

葉慈灃. (2015). Characterization of an orphan receptor : sub-cellular localization, ligand identification and cellular events for signaling activation of toll-like receptor 10. (Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/223025

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

Chicago Manual of Style (16th Edition):

葉慈灃. “Characterization of an orphan receptor : sub-cellular localization, ligand identification and cellular events for signaling activation of toll-like receptor 10.” 2015. Thesis, University of Hong Kong. Accessed March 07, 2021. http://hdl.handle.net/10722/223025.

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

MLA Handbook (7th Edition):

葉慈灃. “Characterization of an orphan receptor : sub-cellular localization, ligand identification and cellular events for signaling activation of toll-like receptor 10.” 2015. Web. 07 Mar 2021.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

葉慈灃. Characterization of an orphan receptor : sub-cellular localization, ligand identification and cellular events for signaling activation of toll-like receptor 10. [Internet] [Thesis]. University of Hong Kong; 2015. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/10722/223025.

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

Council of Science Editors:

葉慈灃. Characterization of an orphan receptor : sub-cellular localization, ligand identification and cellular events for signaling activation of toll-like receptor 10. [Thesis]. University of Hong Kong; 2015. Available from: http://hdl.handle.net/10722/223025

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


University of Aberdeen

8. Kalogeropoulos, Michail. Novel mechanisms of dendritic cell regulation by leukocyte immunoglobulin-like receptor B1.

Degree: PhD, 2014, University of Aberdeen

 Dendritic cells play an essential role in activating immune responses upon recognition of pathogens. This results in maturation and migration to the lymph nodes, where… (more)

Subjects/Keywords: 616.07; Dendritic cells; Cell receptors

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APA (6th Edition):

Kalogeropoulos, M. (2014). Novel mechanisms of dendritic cell regulation by leukocyte immunoglobulin-like receptor B1. (Doctoral Dissertation). University of Aberdeen. Retrieved from https://abdn.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12153524600005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.600118

Chicago Manual of Style (16th Edition):

Kalogeropoulos, Michail. “Novel mechanisms of dendritic cell regulation by leukocyte immunoglobulin-like receptor B1.” 2014. Doctoral Dissertation, University of Aberdeen. Accessed March 07, 2021. https://abdn.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12153524600005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.600118.

MLA Handbook (7th Edition):

Kalogeropoulos, Michail. “Novel mechanisms of dendritic cell regulation by leukocyte immunoglobulin-like receptor B1.” 2014. Web. 07 Mar 2021.

Vancouver:

Kalogeropoulos M. Novel mechanisms of dendritic cell regulation by leukocyte immunoglobulin-like receptor B1. [Internet] [Doctoral dissertation]. University of Aberdeen; 2014. [cited 2021 Mar 07]. Available from: https://abdn.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12153524600005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.600118.

Council of Science Editors:

Kalogeropoulos M. Novel mechanisms of dendritic cell regulation by leukocyte immunoglobulin-like receptor B1. [Doctoral Dissertation]. University of Aberdeen; 2014. Available from: https://abdn.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12153524600005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.600118


University of Delaware

9. McNeely, Patrick M. Receptor-receptor, ligand, and membrane interactions of the adenosine A2A receptor.

Degree: PhD, University of Delaware, Department of Chemical and Biomolecular Engineering, 2016, University of Delaware

 G Protein-Coupled Receptors (GPCRs) comprise the largest superfamily of membrane proteins in the human genome, with ~800 GPCRs identified. These receptors are responsible for many… (more)

Subjects/Keywords: Adenosine.; Cell receptors.; Cell membranes.; Ligands (Biochemistry)

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APA (6th Edition):

McNeely, P. M. (2016). Receptor-receptor, ligand, and membrane interactions of the adenosine A2A receptor. (Doctoral Dissertation). University of Delaware. Retrieved from http://udspace.udel.edu/handle/19716/20568

Chicago Manual of Style (16th Edition):

McNeely, Patrick M. “Receptor-receptor, ligand, and membrane interactions of the adenosine A2A receptor.” 2016. Doctoral Dissertation, University of Delaware. Accessed March 07, 2021. http://udspace.udel.edu/handle/19716/20568.

MLA Handbook (7th Edition):

McNeely, Patrick M. “Receptor-receptor, ligand, and membrane interactions of the adenosine A2A receptor.” 2016. Web. 07 Mar 2021.

Vancouver:

McNeely PM. Receptor-receptor, ligand, and membrane interactions of the adenosine A2A receptor. [Internet] [Doctoral dissertation]. University of Delaware; 2016. [cited 2021 Mar 07]. Available from: http://udspace.udel.edu/handle/19716/20568.

Council of Science Editors:

McNeely PM. Receptor-receptor, ligand, and membrane interactions of the adenosine A2A receptor. [Doctoral Dissertation]. University of Delaware; 2016. Available from: http://udspace.udel.edu/handle/19716/20568


Rutgers University

10. Gutierrez, Natasha C., 1987-. Contact localized β-actin translation drives epithelial adherens junction assembly.

Degree: PhD, Biology, 2014, Rutgers University

Adherens junctions are multi-protein adhesion complexes that anchor to the actin cytoskeleton at cell-cell contact sites to stimulate tissue assembly and thereby regulate barrier maintenance,… (more)

Subjects/Keywords: Actin; Cell adhesion molecules; Cell receptors

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APA (6th Edition):

Gutierrez, Natasha C., 1. (2014). Contact localized β-actin translation drives epithelial adherens junction assembly. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/45628/

Chicago Manual of Style (16th Edition):

Gutierrez, Natasha C., 1987-. “Contact localized β-actin translation drives epithelial adherens junction assembly.” 2014. Doctoral Dissertation, Rutgers University. Accessed March 07, 2021. https://rucore.libraries.rutgers.edu/rutgers-lib/45628/.

MLA Handbook (7th Edition):

Gutierrez, Natasha C., 1987-. “Contact localized β-actin translation drives epithelial adherens junction assembly.” 2014. Web. 07 Mar 2021.

Vancouver:

Gutierrez, Natasha C. 1. Contact localized β-actin translation drives epithelial adherens junction assembly. [Internet] [Doctoral dissertation]. Rutgers University; 2014. [cited 2021 Mar 07]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/45628/.

Council of Science Editors:

Gutierrez, Natasha C. 1. Contact localized β-actin translation drives epithelial adherens junction assembly. [Doctoral Dissertation]. Rutgers University; 2014. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/45628/


Michigan State University

11. Hubbs, Natalia Barbara. Hijacking the cell : how bacteriophage Sf6 uses Shigella flexneri outer membrane proteins for infection.

Degree: 2017, Michigan State University

"Viral infections cause problems worldwide and result in a multitude of human diseases ranging in severity from influenza to HIV. Most viruses infect their respective… (more)

Subjects/Keywords: Viruses – Receptors; Cell receptors; Bacteriophages; Cell membranes; Shigella flexneri; Virology; Microbiology

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APA (6th Edition):

Hubbs, N. B. (2017). Hijacking the cell : how bacteriophage Sf6 uses Shigella flexneri outer membrane proteins for infection. (Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:4824

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):

Hubbs, Natalia Barbara. “Hijacking the cell : how bacteriophage Sf6 uses Shigella flexneri outer membrane proteins for infection.” 2017. Thesis, Michigan State University. Accessed March 07, 2021. http://etd.lib.msu.edu/islandora/object/etd:4824.

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

MLA Handbook (7th Edition):

Hubbs, Natalia Barbara. “Hijacking the cell : how bacteriophage Sf6 uses Shigella flexneri outer membrane proteins for infection.” 2017. Web. 07 Mar 2021.

Vancouver:

Hubbs NB. Hijacking the cell : how bacteriophage Sf6 uses Shigella flexneri outer membrane proteins for infection. [Internet] [Thesis]. Michigan State University; 2017. [cited 2021 Mar 07]. Available from: http://etd.lib.msu.edu/islandora/object/etd:4824.

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

Council of Science Editors:

Hubbs NB. Hijacking the cell : how bacteriophage Sf6 uses Shigella flexneri outer membrane proteins for infection. [Thesis]. Michigan State University; 2017. Available from: http://etd.lib.msu.edu/islandora/object/etd:4824

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


University of Alberta

12. Moran, Catherine Marie. Characterization of Verocytotoxin-2 resistant Vero and Hela 229 cells.

Degree: MS, Department of Medical Microbiology and Infectious Diseases, 1989, University of Alberta

Subjects/Keywords: Toxins – Receptors.; Cell receptors.

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APA (6th Edition):

Moran, C. M. (1989). Characterization of Verocytotoxin-2 resistant Vero and Hela 229 cells. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/kh04ds02j

Chicago Manual of Style (16th Edition):

Moran, Catherine Marie. “Characterization of Verocytotoxin-2 resistant Vero and Hela 229 cells.” 1989. Masters Thesis, University of Alberta. Accessed March 07, 2021. https://era.library.ualberta.ca/files/kh04ds02j.

MLA Handbook (7th Edition):

Moran, Catherine Marie. “Characterization of Verocytotoxin-2 resistant Vero and Hela 229 cells.” 1989. Web. 07 Mar 2021.

Vancouver:

Moran CM. Characterization of Verocytotoxin-2 resistant Vero and Hela 229 cells. [Internet] [Masters thesis]. University of Alberta; 1989. [cited 2021 Mar 07]. Available from: https://era.library.ualberta.ca/files/kh04ds02j.

Council of Science Editors:

Moran CM. Characterization of Verocytotoxin-2 resistant Vero and Hela 229 cells. [Masters Thesis]. University of Alberta; 1989. Available from: https://era.library.ualberta.ca/files/kh04ds02j


Hong Kong University of Science and Technology

13. Siow, Lam. ATP and P2Y1 nucleotide receptor in cortical neurons : localization, signal transduction and transcriptional regulation.

Degree: 2006, Hong Kong University of Science and Technology

 In vertebrate nervous system, adenosine 5'-triphosphate (ATP) is co-stored and co-released at central and peripheral cholinergic and bioaminergic neuronal synapses. At the neuromuscular junctions, ATP… (more)

Subjects/Keywords: Cell receptors ; Neurotransmitter receptors ; Neurons

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APA (6th Edition):

Siow, L. (2006). ATP and P2Y1 nucleotide receptor in cortical neurons : localization, signal transduction and transcriptional regulation. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-2862 ; https://doi.org/10.14711/thesis-b938092 ; http://repository.ust.hk/ir/bitstream/1783.1-2862/1/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):

Siow, Lam. “ATP and P2Y1 nucleotide receptor in cortical neurons : localization, signal transduction and transcriptional regulation.” 2006. Thesis, Hong Kong University of Science and Technology. Accessed March 07, 2021. http://repository.ust.hk/ir/Record/1783.1-2862 ; https://doi.org/10.14711/thesis-b938092 ; http://repository.ust.hk/ir/bitstream/1783.1-2862/1/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):

Siow, Lam. “ATP and P2Y1 nucleotide receptor in cortical neurons : localization, signal transduction and transcriptional regulation.” 2006. Web. 07 Mar 2021.

Vancouver:

Siow L. ATP and P2Y1 nucleotide receptor in cortical neurons : localization, signal transduction and transcriptional regulation. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2006. [cited 2021 Mar 07]. Available from: http://repository.ust.hk/ir/Record/1783.1-2862 ; https://doi.org/10.14711/thesis-b938092 ; http://repository.ust.hk/ir/bitstream/1783.1-2862/1/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:

Siow L. ATP and P2Y1 nucleotide receptor in cortical neurons : localization, signal transduction and transcriptional regulation. [Thesis]. Hong Kong University of Science and Technology; 2006. Available from: http://repository.ust.hk/ir/Record/1783.1-2862 ; https://doi.org/10.14711/thesis-b938092 ; http://repository.ust.hk/ir/bitstream/1783.1-2862/1/th_redirect.html

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


University of Toronto

14. Darvish-Ghane, Soroush. Dopaminergic Modulation of Excitatory Transmission in the Anterior Cingulate Cortex of Adult Mice.

Degree: 2016, University of Toronto

Bath application of dopamine (DA) (50 μM) caused a significant, rapid and reversible inhibition of evoked AMPA receptor mediated EPSCs (eEPSC). This inhibitory effect is… (more)

Subjects/Keywords: ACC; AMPA; Dopamine; receptors; Whole-cell; 0317

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

APA (6th Edition):

Darvish-Ghane, S. (2016). Dopaminergic Modulation of Excitatory Transmission in the Anterior Cingulate Cortex of Adult Mice. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/79696

Chicago Manual of Style (16th Edition):

Darvish-Ghane, Soroush. “Dopaminergic Modulation of Excitatory Transmission in the Anterior Cingulate Cortex of Adult Mice.” 2016. Masters Thesis, University of Toronto. Accessed March 07, 2021. http://hdl.handle.net/1807/79696.

MLA Handbook (7th Edition):

Darvish-Ghane, Soroush. “Dopaminergic Modulation of Excitatory Transmission in the Anterior Cingulate Cortex of Adult Mice.” 2016. Web. 07 Mar 2021.

Vancouver:

Darvish-Ghane S. Dopaminergic Modulation of Excitatory Transmission in the Anterior Cingulate Cortex of Adult Mice. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1807/79696.

Council of Science Editors:

Darvish-Ghane S. Dopaminergic Modulation of Excitatory Transmission in the Anterior Cingulate Cortex of Adult Mice. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/79696

15. Boyce, Andrew Kenneth Jameson. Regulation of pannexin 1 trafficking by adenosine triphosphate.

Degree: Program: Neuroscience, 2017, University of Victoria

 The ubiquitously expressed pannexin 1 (Panx1) ion- and metabolite-permeable channel is capable of mediating ATP release in a multitude of cells and tissues. This leads… (more)

Subjects/Keywords: Cell receptors; Ion channels; Ion-permeable membranes

Page 1

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APA (6th Edition):

Boyce, A. K. J. (2017). Regulation of pannexin 1 trafficking by adenosine triphosphate. (Thesis). University of Victoria. Retrieved from https://dspace.library.uvic.ca//handle/1828/8444

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):

Boyce, Andrew Kenneth Jameson. “Regulation of pannexin 1 trafficking by adenosine triphosphate.” 2017. Thesis, University of Victoria. Accessed March 07, 2021. https://dspace.library.uvic.ca//handle/1828/8444.

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

MLA Handbook (7th Edition):

Boyce, Andrew Kenneth Jameson. “Regulation of pannexin 1 trafficking by adenosine triphosphate.” 2017. Web. 07 Mar 2021.

Vancouver:

Boyce AKJ. Regulation of pannexin 1 trafficking by adenosine triphosphate. [Internet] [Thesis]. University of Victoria; 2017. [cited 2021 Mar 07]. Available from: https://dspace.library.uvic.ca//handle/1828/8444.

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

Council of Science Editors:

Boyce AKJ. Regulation of pannexin 1 trafficking by adenosine triphosphate. [Thesis]. University of Victoria; 2017. Available from: https://dspace.library.uvic.ca//handle/1828/8444

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


Hong Kong University of Science and Technology

16. Chen, Li LIFS. Mutations in TED1 and DCR2, two glycosylphosphatidylinositol anchored protein remodelases, activate the spindle assembly checkpoint in budding yeast cells.

Degree: 2017, Hong Kong University of Science and Technology

 Herein I describe a genetic study that employed a temperature-sensitive allele encoding the Golgi glycosyltransferase sorting receptor VPS74. Through characterizing genes that act as dosage… (more)

Subjects/Keywords: Yeast ; Genetics ; Growth ; Proteins ; Cell receptors

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APA (6th Edition):

Chen, L. L. (2017). Mutations in TED1 and DCR2, two glycosylphosphatidylinositol anchored protein remodelases, activate the spindle assembly checkpoint in budding yeast cells. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-105622 ; https://doi.org/10.14711/thesis-991012564169103412 ; http://repository.ust.hk/ir/bitstream/1783.1-105622/1/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):

Chen, Li LIFS. “Mutations in TED1 and DCR2, two glycosylphosphatidylinositol anchored protein remodelases, activate the spindle assembly checkpoint in budding yeast cells.” 2017. Thesis, Hong Kong University of Science and Technology. Accessed March 07, 2021. http://repository.ust.hk/ir/Record/1783.1-105622 ; https://doi.org/10.14711/thesis-991012564169103412 ; http://repository.ust.hk/ir/bitstream/1783.1-105622/1/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):

Chen, Li LIFS. “Mutations in TED1 and DCR2, two glycosylphosphatidylinositol anchored protein remodelases, activate the spindle assembly checkpoint in budding yeast cells.” 2017. Web. 07 Mar 2021.

Vancouver:

Chen LL. Mutations in TED1 and DCR2, two glycosylphosphatidylinositol anchored protein remodelases, activate the spindle assembly checkpoint in budding yeast cells. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2017. [cited 2021 Mar 07]. Available from: http://repository.ust.hk/ir/Record/1783.1-105622 ; https://doi.org/10.14711/thesis-991012564169103412 ; http://repository.ust.hk/ir/bitstream/1783.1-105622/1/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:

Chen LL. Mutations in TED1 and DCR2, two glycosylphosphatidylinositol anchored protein remodelases, activate the spindle assembly checkpoint in budding yeast cells. [Thesis]. Hong Kong University of Science and Technology; 2017. Available from: http://repository.ust.hk/ir/Record/1783.1-105622 ; https://doi.org/10.14711/thesis-991012564169103412 ; http://repository.ust.hk/ir/bitstream/1783.1-105622/1/th_redirect.html

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


Montana State University

17. Kohler, Maria Renata. Production and purification of formyl peptide receptor : explorations of protein-protein interactions.

Degree: MS, College of Agriculture, 1997, Montana State University

Subjects/Keywords: Neutrophils.; Cell receptors.

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APA (6th Edition):

Kohler, M. R. (1997). Production and purification of formyl peptide receptor : explorations of protein-protein interactions. (Masters Thesis). Montana State University. Retrieved from https://scholarworks.montana.edu/xmlui/handle/1/7752

Chicago Manual of Style (16th Edition):

Kohler, Maria Renata. “Production and purification of formyl peptide receptor : explorations of protein-protein interactions.” 1997. Masters Thesis, Montana State University. Accessed March 07, 2021. https://scholarworks.montana.edu/xmlui/handle/1/7752.

MLA Handbook (7th Edition):

Kohler, Maria Renata. “Production and purification of formyl peptide receptor : explorations of protein-protein interactions.” 1997. Web. 07 Mar 2021.

Vancouver:

Kohler MR. Production and purification of formyl peptide receptor : explorations of protein-protein interactions. [Internet] [Masters thesis]. Montana State University; 1997. [cited 2021 Mar 07]. Available from: https://scholarworks.montana.edu/xmlui/handle/1/7752.

Council of Science Editors:

Kohler MR. Production and purification of formyl peptide receptor : explorations of protein-protein interactions. [Masters Thesis]. Montana State University; 1997. Available from: https://scholarworks.montana.edu/xmlui/handle/1/7752


Drexel University

18. Judy, Renae. Analysis of the Process of N-region addition in V(D)J Recombination through Diversity Identification of the CDR3 Region of B and T Cells.

Degree: 2013, Drexel University

A diverse and adaptable population of antigen receptors is an essential characteristic of a strong immune system. One way of generating this diversity is through… (more)

Subjects/Keywords: Biomedical engineering; Immune system; Cell receptors

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APA (6th Edition):

Judy, R. (2013). Analysis of the Process of N-region addition in V(D)J Recombination through Diversity Identification of the CDR3 Region of B and T Cells. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/4241

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):

Judy, Renae. “Analysis of the Process of N-region addition in V(D)J Recombination through Diversity Identification of the CDR3 Region of B and T Cells.” 2013. Thesis, Drexel University. Accessed March 07, 2021. http://hdl.handle.net/1860/4241.

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

MLA Handbook (7th Edition):

Judy, Renae. “Analysis of the Process of N-region addition in V(D)J Recombination through Diversity Identification of the CDR3 Region of B and T Cells.” 2013. Web. 07 Mar 2021.

Vancouver:

Judy R. Analysis of the Process of N-region addition in V(D)J Recombination through Diversity Identification of the CDR3 Region of B and T Cells. [Internet] [Thesis]. Drexel University; 2013. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1860/4241.

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

Council of Science Editors:

Judy R. Analysis of the Process of N-region addition in V(D)J Recombination through Diversity Identification of the CDR3 Region of B and T Cells. [Thesis]. Drexel University; 2013. Available from: http://hdl.handle.net/1860/4241

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


Drexel University

19. Zhang, Bochao. Tools for the analysis of B-cell clonal diversity in immune repertoires.

Degree: 2018, Drexel University

 The lymphocytes of an organism harbor a diverse collection or repertoire of antigen receptors (antibodies (Ab) on B cells and T cell receptors (TCR) on… (more)

Subjects/Keywords: Medical sciences; Immunology; Cell receptors; B cells

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APA (6th Edition):

Zhang, B. (2018). Tools for the analysis of B-cell clonal diversity in immune repertoires. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:7716

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, Bochao. “Tools for the analysis of B-cell clonal diversity in immune repertoires.” 2018. Thesis, Drexel University. Accessed March 07, 2021. http://hdl.handle.net/1860/idea:7716.

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

MLA Handbook (7th Edition):

Zhang, Bochao. “Tools for the analysis of B-cell clonal diversity in immune repertoires.” 2018. Web. 07 Mar 2021.

Vancouver:

Zhang B. Tools for the analysis of B-cell clonal diversity in immune repertoires. [Internet] [Thesis]. Drexel University; 2018. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1860/idea:7716.

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

Council of Science Editors:

Zhang B. Tools for the analysis of B-cell clonal diversity in immune repertoires. [Thesis]. Drexel University; 2018. Available from: http://hdl.handle.net/1860/idea:7716

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


Drexel University

20. Schwartz, Gregory W. Diversity analysis of B cell receptors - novel tools for repertoire comparisons.

Degree: 2016, Drexel University

The adaptive immune system provides the body the ability to mount a targeted defense against pathogens. This process depends not on a single cell but… (more)

Subjects/Keywords: Biomedical engineering; B cells; Cell receptors

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APA (6th Edition):

Schwartz, G. W. (2016). Diversity analysis of B cell receptors - novel tools for repertoire comparisons. (Thesis). Drexel University. Retrieved from http://hdl.handle.net/1860/idea:6774

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):

Schwartz, Gregory W. “Diversity analysis of B cell receptors - novel tools for repertoire comparisons.” 2016. Thesis, Drexel University. Accessed March 07, 2021. http://hdl.handle.net/1860/idea:6774.

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

MLA Handbook (7th Edition):

Schwartz, Gregory W. “Diversity analysis of B cell receptors - novel tools for repertoire comparisons.” 2016. Web. 07 Mar 2021.

Vancouver:

Schwartz GW. Diversity analysis of B cell receptors - novel tools for repertoire comparisons. [Internet] [Thesis]. Drexel University; 2016. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1860/idea:6774.

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

Council of Science Editors:

Schwartz GW. Diversity analysis of B cell receptors - novel tools for repertoire comparisons. [Thesis]. Drexel University; 2016. Available from: http://hdl.handle.net/1860/idea:6774

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


University of Aberdeen

21. Clark, Alexandra Elsie. Characterisation of the C-type lectin-like receptor 1 (CLEC-1).

Degree: PhD, 2013, University of Aberdeen

Subjects/Keywords: Immunology; Cell receptors

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APA (6th Edition):

Clark, A. E. (2013). Characterisation of the C-type lectin-like receptor 1 (CLEC-1). (Doctoral Dissertation). University of Aberdeen. Retrieved from https://abdn.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12153524540005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.600104

Chicago Manual of Style (16th Edition):

Clark, Alexandra Elsie. “Characterisation of the C-type lectin-like receptor 1 (CLEC-1).” 2013. Doctoral Dissertation, University of Aberdeen. Accessed March 07, 2021. https://abdn.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12153524540005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.600104.

MLA Handbook (7th Edition):

Clark, Alexandra Elsie. “Characterisation of the C-type lectin-like receptor 1 (CLEC-1).” 2013. Web. 07 Mar 2021.

Vancouver:

Clark AE. Characterisation of the C-type lectin-like receptor 1 (CLEC-1). [Internet] [Doctoral dissertation]. University of Aberdeen; 2013. [cited 2021 Mar 07]. Available from: https://abdn.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12153524540005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.600104.

Council of Science Editors:

Clark AE. Characterisation of the C-type lectin-like receptor 1 (CLEC-1). [Doctoral Dissertation]. University of Aberdeen; 2013. Available from: https://abdn.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12153524540005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.600104


University of Aberdeen

22. Kerscher, Berhard Gerhard Richard. Characterisation of the C-type lectin receptor Clecsf8.

Degree: PhD, 2016, University of Aberdeen

 C-type lectin-like receptors (CTLRs) play critical roles in immunity and homeostasis by recognising a variety of microbial or endogenous ligands. Clecsf8 is a member of… (more)

Subjects/Keywords: 572; Lectins; Cell receptors; Immune response

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APA (6th Edition):

Kerscher, B. G. R. (2016). Characterisation of the C-type lectin receptor Clecsf8. (Doctoral Dissertation). University of Aberdeen. Retrieved from https://abdn.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12152477460005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.698845

Chicago Manual of Style (16th Edition):

Kerscher, Berhard Gerhard Richard. “Characterisation of the C-type lectin receptor Clecsf8.” 2016. Doctoral Dissertation, University of Aberdeen. Accessed March 07, 2021. https://abdn.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12152477460005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.698845.

MLA Handbook (7th Edition):

Kerscher, Berhard Gerhard Richard. “Characterisation of the C-type lectin receptor Clecsf8.” 2016. Web. 07 Mar 2021.

Vancouver:

Kerscher BGR. Characterisation of the C-type lectin receptor Clecsf8. [Internet] [Doctoral dissertation]. University of Aberdeen; 2016. [cited 2021 Mar 07]. Available from: https://abdn.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12152477460005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.698845.

Council of Science Editors:

Kerscher BGR. Characterisation of the C-type lectin receptor Clecsf8. [Doctoral Dissertation]. University of Aberdeen; 2016. Available from: https://abdn.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12152477460005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.698845


University of Aberdeen

23. Lee, Po-Tsang. Identification and characterisation of toll-like receptors (TLRs) and the TLR accessory molecule UNC93B1 in Atlantic salmon (Salmo salar).

Degree: PhD, 2015, University of Aberdeen

 Aquaculture is known as a major food-producing industry and Atlantic salmon (Salmo salar) and rainbow trout (Oncorhynchus mykiss) are the major cultured species in Scotland.… (more)

Subjects/Keywords: 590; Atlantic salmon; Cell receptors; Immune response

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APA (6th Edition):

Lee, P. (2015). Identification and characterisation of toll-like receptors (TLRs) and the TLR accessory molecule UNC93B1 in Atlantic salmon (Salmo salar). (Doctoral Dissertation). University of Aberdeen. Retrieved from https://abdn.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12152989930005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.655677

Chicago Manual of Style (16th Edition):

Lee, Po-Tsang. “Identification and characterisation of toll-like receptors (TLRs) and the TLR accessory molecule UNC93B1 in Atlantic salmon (Salmo salar).” 2015. Doctoral Dissertation, University of Aberdeen. Accessed March 07, 2021. https://abdn.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12152989930005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.655677.

MLA Handbook (7th Edition):

Lee, Po-Tsang. “Identification and characterisation of toll-like receptors (TLRs) and the TLR accessory molecule UNC93B1 in Atlantic salmon (Salmo salar).” 2015. Web. 07 Mar 2021.

Vancouver:

Lee P. Identification and characterisation of toll-like receptors (TLRs) and the TLR accessory molecule UNC93B1 in Atlantic salmon (Salmo salar). [Internet] [Doctoral dissertation]. University of Aberdeen; 2015. [cited 2021 Mar 07]. Available from: https://abdn.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12152989930005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.655677.

Council of Science Editors:

Lee P. Identification and characterisation of toll-like receptors (TLRs) and the TLR accessory molecule UNC93B1 in Atlantic salmon (Salmo salar). [Doctoral Dissertation]. University of Aberdeen; 2015. Available from: https://abdn.alma.exlibrisgroup.com/view/delivery/44ABE_INST/12152989930005941 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.655677


University of Cambridge

24. Gürel, Meltem. Intratumoral B and T cell receptors: reconstruction and analysis.

Degree: PhD, 2019, University of Cambridge

 When cells divide, mistakes happen. However, an intricate surveillance system has evolved to detect and eliminate anomalous cells before they become detrimental to the host… (more)

Subjects/Keywords: computational immunology; single-cell RNA sequencing; B and T cell receptors

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APA (6th Edition):

Gürel, M. (2019). Intratumoral B and T cell receptors: reconstruction and analysis. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/313326

Chicago Manual of Style (16th Edition):

Gürel, Meltem. “Intratumoral B and T cell receptors: reconstruction and analysis.” 2019. Doctoral Dissertation, University of Cambridge. Accessed March 07, 2021. https://www.repository.cam.ac.uk/handle/1810/313326.

MLA Handbook (7th Edition):

Gürel, Meltem. “Intratumoral B and T cell receptors: reconstruction and analysis.” 2019. Web. 07 Mar 2021.

Vancouver:

Gürel M. Intratumoral B and T cell receptors: reconstruction and analysis. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2021 Mar 07]. Available from: https://www.repository.cam.ac.uk/handle/1810/313326.

Council of Science Editors:

Gürel M. Intratumoral B and T cell receptors: reconstruction and analysis. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/313326


University of Cambridge

25. Gürel, Meltem. Intratumoral B and T cell receptors : reconstruction and analysis.

Degree: PhD, 2019, University of Cambridge

 When cells divide, mistakes happen. However, an intricate surveillance system has evolved to detect and eliminate anomalous cells before they become detrimental to the host… (more)

Subjects/Keywords: computational immunology; single-cell RNA sequencing; B and T cell receptors

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APA (6th Edition):

Gürel, M. (2019). Intratumoral B and T cell receptors : reconstruction and analysis. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.60433 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.821525

Chicago Manual of Style (16th Edition):

Gürel, Meltem. “Intratumoral B and T cell receptors : reconstruction and analysis.” 2019. Doctoral Dissertation, University of Cambridge. Accessed March 07, 2021. https://doi.org/10.17863/CAM.60433 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.821525.

MLA Handbook (7th Edition):

Gürel, Meltem. “Intratumoral B and T cell receptors : reconstruction and analysis.” 2019. Web. 07 Mar 2021.

Vancouver:

Gürel M. Intratumoral B and T cell receptors : reconstruction and analysis. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2021 Mar 07]. Available from: https://doi.org/10.17863/CAM.60433 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.821525.

Council of Science Editors:

Gürel M. Intratumoral B and T cell receptors : reconstruction and analysis. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://doi.org/10.17863/CAM.60433 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.821525


Northeastern University

26. Honavar, Siddhi. Conformationally constrained analogs of Org27569 as allosteric modulators of CB1 cannabinoid receptor.

Degree: MS, School of Pharmacy, 2016, Northeastern University

 The Cannabinoid receptors have become the focus of research due to their importance as targets for treating a number of disorders. These receptors which are… (more)

Subjects/Keywords: cannabinoid receptors; CB<; sub>; 1<; /sub>; receptors; negative allosteric modulators; Cannabinoids; Receptors; Allosteric regulation; G proteins; Receptors; Cell receptors; Ligand binding (Biochemistry)

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APA (6th Edition):

Honavar, S. (2016). Conformationally constrained analogs of Org27569 as allosteric modulators of CB1 cannabinoid receptor. (Masters Thesis). Northeastern University. Retrieved from http://hdl.handle.net/2047/D20196974

Chicago Manual of Style (16th Edition):

Honavar, Siddhi. “Conformationally constrained analogs of Org27569 as allosteric modulators of CB1 cannabinoid receptor.” 2016. Masters Thesis, Northeastern University. Accessed March 07, 2021. http://hdl.handle.net/2047/D20196974.

MLA Handbook (7th Edition):

Honavar, Siddhi. “Conformationally constrained analogs of Org27569 as allosteric modulators of CB1 cannabinoid receptor.” 2016. Web. 07 Mar 2021.

Vancouver:

Honavar S. Conformationally constrained analogs of Org27569 as allosteric modulators of CB1 cannabinoid receptor. [Internet] [Masters thesis]. Northeastern University; 2016. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/2047/D20196974.

Council of Science Editors:

Honavar S. Conformationally constrained analogs of Org27569 as allosteric modulators of CB1 cannabinoid receptor. [Masters Thesis]. Northeastern University; 2016. Available from: http://hdl.handle.net/2047/D20196974


University of Illinois – Urbana-Champaign

27. Soto, Carolina. Adoptive cell therapy using primary T lymphocytes with genetically engineered T cell receptors against melanoma and glioma.

Degree: PhD, 0323, 2013, University of Illinois – Urbana-Champaign

 Over the past few decades, our knowledge of tumor immunology and the role antitumor immune responses play in tumor recognition and eradication has greatly increased… (more)

Subjects/Keywords: Cancer Immunotherapy; Tumor Targeting; T cell receptors (TCR); T cell; Melanoma; Adoptive Cell Therapy; Glioma

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

APA (6th Edition):

Soto, C. (2013). Adoptive cell therapy using primary T lymphocytes with genetically engineered T cell receptors against melanoma and glioma. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/42476

Chicago Manual of Style (16th Edition):

Soto, Carolina. “Adoptive cell therapy using primary T lymphocytes with genetically engineered T cell receptors against melanoma and glioma.” 2013. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed March 07, 2021. http://hdl.handle.net/2142/42476.

MLA Handbook (7th Edition):

Soto, Carolina. “Adoptive cell therapy using primary T lymphocytes with genetically engineered T cell receptors against melanoma and glioma.” 2013. Web. 07 Mar 2021.

Vancouver:

Soto C. Adoptive cell therapy using primary T lymphocytes with genetically engineered T cell receptors against melanoma and glioma. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2013. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/2142/42476.

Council of Science Editors:

Soto C. Adoptive cell therapy using primary T lymphocytes with genetically engineered T cell receptors against melanoma and glioma. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2013. Available from: http://hdl.handle.net/2142/42476


University of Alberta

28. Clark, Clifford G. Characterization of receptors for pertussis toxin.

Degree: PhD, Department of Medical Microbiology and Infectious Diseases, 1992, University of Alberta

Subjects/Keywords: Toxins – Receptors.; Cell receptors.; Pertussis toxin.

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APA (6th Edition):

Clark, C. G. (1992). Characterization of receptors for pertussis toxin. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/m326m367z

Chicago Manual of Style (16th Edition):

Clark, Clifford G. “Characterization of receptors for pertussis toxin.” 1992. Doctoral Dissertation, University of Alberta. Accessed March 07, 2021. https://era.library.ualberta.ca/files/m326m367z.

MLA Handbook (7th Edition):

Clark, Clifford G. “Characterization of receptors for pertussis toxin.” 1992. Web. 07 Mar 2021.

Vancouver:

Clark CG. Characterization of receptors for pertussis toxin. [Internet] [Doctoral dissertation]. University of Alberta; 1992. [cited 2021 Mar 07]. Available from: https://era.library.ualberta.ca/files/m326m367z.

Council of Science Editors:

Clark CG. Characterization of receptors for pertussis toxin. [Doctoral Dissertation]. University of Alberta; 1992. Available from: https://era.library.ualberta.ca/files/m326m367z


University of Toronto

29. Sokolina, Ekaterina. Human GPCR Interactome and Investigation of the KCTD/beta2-adrenergic Receptor Interactions.

Degree: 2014, University of Toronto

G-protein-coupled receptors (GPCRs) are the largest family of transmembrane receptors with key roles in regulating signaling pathways targeted by therapeutics. To identify novel components of… (more)

Subjects/Keywords: cell signalling; G-protein coupled receptors; interactome; KCTDs; protein-protein interactions; receptors; 0487

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

APA (6th Edition):

Sokolina, E. (2014). Human GPCR Interactome and Investigation of the KCTD/beta2-adrenergic Receptor Interactions. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/70192

Chicago Manual of Style (16th Edition):

Sokolina, Ekaterina. “Human GPCR Interactome and Investigation of the KCTD/beta2-adrenergic Receptor Interactions.” 2014. Masters Thesis, University of Toronto. Accessed March 07, 2021. http://hdl.handle.net/1807/70192.

MLA Handbook (7th Edition):

Sokolina, Ekaterina. “Human GPCR Interactome and Investigation of the KCTD/beta2-adrenergic Receptor Interactions.” 2014. Web. 07 Mar 2021.

Vancouver:

Sokolina E. Human GPCR Interactome and Investigation of the KCTD/beta2-adrenergic Receptor Interactions. [Internet] [Masters thesis]. University of Toronto; 2014. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/1807/70192.

Council of Science Editors:

Sokolina E. Human GPCR Interactome and Investigation of the KCTD/beta2-adrenergic Receptor Interactions. [Masters Thesis]. University of Toronto; 2014. Available from: http://hdl.handle.net/1807/70192


Universitat de Barcelona

30. Mineo, Alessandro. Mechanisms of restricted activation of the Torso receptor: from the eggshell to the embryo.

Degree: Departament de Genètica, 2016, Universitat de Barcelona

 El eje antero-posterior del embrión de Drosophila se especifica por acción de tres sistemas maternos: el sistema anterior, el sistema posterior y el sistema terminal.… (more)

Subjects/Keywords: Receptors cel·lulars; Receptores celulares; Cell receptors; Embriologia; Embriología; Embryology; Ciències Experimentals i Matemàtiques; 575

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

APA (6th Edition):

Mineo, A. (2016). Mechanisms of restricted activation of the Torso receptor: from the eggshell to the embryo. (Thesis). Universitat de Barcelona. Retrieved from http://hdl.handle.net/10803/402625

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):

Mineo, Alessandro. “Mechanisms of restricted activation of the Torso receptor: from the eggshell to the embryo.” 2016. Thesis, Universitat de Barcelona. Accessed March 07, 2021. http://hdl.handle.net/10803/402625.

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

MLA Handbook (7th Edition):

Mineo, Alessandro. “Mechanisms of restricted activation of the Torso receptor: from the eggshell to the embryo.” 2016. Web. 07 Mar 2021.

Vancouver:

Mineo A. Mechanisms of restricted activation of the Torso receptor: from the eggshell to the embryo. [Internet] [Thesis]. Universitat de Barcelona; 2016. [cited 2021 Mar 07]. Available from: http://hdl.handle.net/10803/402625.

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

Council of Science Editors:

Mineo A. Mechanisms of restricted activation of the Torso receptor: from the eggshell to the embryo. [Thesis]. Universitat de Barcelona; 2016. Available from: http://hdl.handle.net/10803/402625

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

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