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You searched for subject:(Endocytosis). Showing records 1 – 30 of 532 total matches.

[1] [2] [3] [4] [5] … [18]

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Rutgers University

1. Santiana, Marianita, 1973-. Host cellular cholesterol distribution and dynamics during enteroviral infection.

Degree: PhD, Biology, 2015, Rutgers University

Many RNA viruses, including enteroviruses, remodel host ER membranes to form platforms with unique lipid components to assemble replication complexes and synthesize new viral RNA.… (more)

Subjects/Keywords: Endocytosis; Enteroviruses

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APA (6th Edition):

Santiana, Marianita, 1. (2015). Host cellular cholesterol distribution and dynamics during enteroviral infection. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/47709/

Chicago Manual of Style (16th Edition):

Santiana, Marianita, 1973-. “Host cellular cholesterol distribution and dynamics during enteroviral infection.” 2015. Doctoral Dissertation, Rutgers University. Accessed March 29, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/47709/.

MLA Handbook (7th Edition):

Santiana, Marianita, 1973-. “Host cellular cholesterol distribution and dynamics during enteroviral infection.” 2015. Web. 29 Mar 2020.

Vancouver:

Santiana, Marianita 1. Host cellular cholesterol distribution and dynamics during enteroviral infection. [Internet] [Doctoral dissertation]. Rutgers University; 2015. [cited 2020 Mar 29]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/47709/.

Council of Science Editors:

Santiana, Marianita 1. Host cellular cholesterol distribution and dynamics during enteroviral infection. [Doctoral Dissertation]. Rutgers University; 2015. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/47709/


Hong Kong University of Science and Technology

2. Lin, Ran. Study of single-cell electroendocytosis using bio-MEMS technology.

Degree: 2011, Hong Kong University of Science and Technology

 Electroendocytosis (EED), i.e. electric-field-induced endocytosis-like process, is a technique to facilitate molecules delivery to cells using a pulsed electric field train (PEF). PEF enhances the… (more)

Subjects/Keywords: BioMEMS ; Endocytosis

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APA (6th Edition):

Lin, R. (2011). Study of single-cell electroendocytosis using bio-MEMS technology. (Thesis). Hong Kong University of Science and Technology. Retrieved from http://repository.ust.hk/ir/Record/1783.1-7299 ; https://doi.org/10.14711/thesis-b1155683 ; http://repository.ust.hk/ir/bitstream/1783.1-7299/1/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):

Lin, Ran. “Study of single-cell electroendocytosis using bio-MEMS technology.” 2011. Thesis, Hong Kong University of Science and Technology. Accessed March 29, 2020. http://repository.ust.hk/ir/Record/1783.1-7299 ; https://doi.org/10.14711/thesis-b1155683 ; http://repository.ust.hk/ir/bitstream/1783.1-7299/1/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):

Lin, Ran. “Study of single-cell electroendocytosis using bio-MEMS technology.” 2011. Web. 29 Mar 2020.

Vancouver:

Lin R. Study of single-cell electroendocytosis using bio-MEMS technology. [Internet] [Thesis]. Hong Kong University of Science and Technology; 2011. [cited 2020 Mar 29]. Available from: http://repository.ust.hk/ir/Record/1783.1-7299 ; https://doi.org/10.14711/thesis-b1155683 ; http://repository.ust.hk/ir/bitstream/1783.1-7299/1/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:

Lin R. Study of single-cell electroendocytosis using bio-MEMS technology. [Thesis]. Hong Kong University of Science and Technology; 2011. Available from: http://repository.ust.hk/ir/Record/1783.1-7299 ; https://doi.org/10.14711/thesis-b1155683 ; http://repository.ust.hk/ir/bitstream/1783.1-7299/1/th_redirect.html

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


Penn State University

3. Jiang, Min. FUNCTIONAL CHARACTERIZATION OF A NOVEL CLATHRIN-INDEPENDENT ENDOCYTOSIS IN ASTROCYTES.

Degree: PhD, Biology, 2008, Penn State University

Endocytosis plays a fundamental role in regulating cell signaling, protein and lipid trafficking, and uptake of nutrients and pathogens in all eukaryotic cells. In astrocytes,… (more)

Subjects/Keywords: astrocytes; endocytosis; clathrin

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APA (6th Edition):

Jiang, M. (2008). FUNCTIONAL CHARACTERIZATION OF A NOVEL CLATHRIN-INDEPENDENT ENDOCYTOSIS IN ASTROCYTES. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/8546

Chicago Manual of Style (16th Edition):

Jiang, Min. “FUNCTIONAL CHARACTERIZATION OF A NOVEL CLATHRIN-INDEPENDENT ENDOCYTOSIS IN ASTROCYTES.” 2008. Doctoral Dissertation, Penn State University. Accessed March 29, 2020. https://etda.libraries.psu.edu/catalog/8546.

MLA Handbook (7th Edition):

Jiang, Min. “FUNCTIONAL CHARACTERIZATION OF A NOVEL CLATHRIN-INDEPENDENT ENDOCYTOSIS IN ASTROCYTES.” 2008. Web. 29 Mar 2020.

Vancouver:

Jiang M. FUNCTIONAL CHARACTERIZATION OF A NOVEL CLATHRIN-INDEPENDENT ENDOCYTOSIS IN ASTROCYTES. [Internet] [Doctoral dissertation]. Penn State University; 2008. [cited 2020 Mar 29]. Available from: https://etda.libraries.psu.edu/catalog/8546.

Council of Science Editors:

Jiang M. FUNCTIONAL CHARACTERIZATION OF A NOVEL CLATHRIN-INDEPENDENT ENDOCYTOSIS IN ASTROCYTES. [Doctoral Dissertation]. Penn State University; 2008. Available from: https://etda.libraries.psu.edu/catalog/8546


University of California – Berkeley

4. Cheng, Aaron T. Investigation of Clathrin-Mediated Endocytosis Using Genome Editing in Somatic and Pluripotent Human Cells.

Degree: Molecular & Cell Biology, 2013, University of California – Berkeley

 Clathrin-mediated endocytosis (CME) is the best-studied and predominant pathway by which portions of the plasma membrane and extracellular material are internalized. Traditional methods using ectopically… (more)

Subjects/Keywords: Cellular biology; endocytosis

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APA (6th Edition):

Cheng, A. T. (2013). Investigation of Clathrin-Mediated Endocytosis Using Genome Editing in Somatic and Pluripotent Human Cells. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/23442017

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, Aaron T. “Investigation of Clathrin-Mediated Endocytosis Using Genome Editing in Somatic and Pluripotent Human Cells.” 2013. Thesis, University of California – Berkeley. Accessed March 29, 2020. http://www.escholarship.org/uc/item/23442017.

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

MLA Handbook (7th Edition):

Cheng, Aaron T. “Investigation of Clathrin-Mediated Endocytosis Using Genome Editing in Somatic and Pluripotent Human Cells.” 2013. Web. 29 Mar 2020.

Vancouver:

Cheng AT. Investigation of Clathrin-Mediated Endocytosis Using Genome Editing in Somatic and Pluripotent Human Cells. [Internet] [Thesis]. University of California – Berkeley; 2013. [cited 2020 Mar 29]. Available from: http://www.escholarship.org/uc/item/23442017.

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

Council of Science Editors:

Cheng AT. Investigation of Clathrin-Mediated Endocytosis Using Genome Editing in Somatic and Pluripotent Human Cells. [Thesis]. University of California – Berkeley; 2013. Available from: http://www.escholarship.org/uc/item/23442017

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


Cornell University

5. Ray, Gregory. Arabidopsis Thaliana Syta As A Model To Address Whether Synaptotagmin Proteins Function As Dimers Or Tetramers .

Degree: 2014, Cornell University

 The Arabidopsis thaliana synaptotagmin SYTA (AT2G20990) regulates endocytosis at the plasma membrane and virus movement protein-mediated cellto-cell movement. As with all synaptotagmin proteins, SYTA is… (more)

Subjects/Keywords: Synaptotagmin; Endocytosis; SYTA

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APA (6th Edition):

Ray, G. (2014). Arabidopsis Thaliana Syta As A Model To Address Whether Synaptotagmin Proteins Function As Dimers Or Tetramers . (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/37059

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):

Ray, Gregory. “Arabidopsis Thaliana Syta As A Model To Address Whether Synaptotagmin Proteins Function As Dimers Or Tetramers .” 2014. Thesis, Cornell University. Accessed March 29, 2020. http://hdl.handle.net/1813/37059.

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

MLA Handbook (7th Edition):

Ray, Gregory. “Arabidopsis Thaliana Syta As A Model To Address Whether Synaptotagmin Proteins Function As Dimers Or Tetramers .” 2014. Web. 29 Mar 2020.

Vancouver:

Ray G. Arabidopsis Thaliana Syta As A Model To Address Whether Synaptotagmin Proteins Function As Dimers Or Tetramers . [Internet] [Thesis]. Cornell University; 2014. [cited 2020 Mar 29]. Available from: http://hdl.handle.net/1813/37059.

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

Council of Science Editors:

Ray G. Arabidopsis Thaliana Syta As A Model To Address Whether Synaptotagmin Proteins Function As Dimers Or Tetramers . [Thesis]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/37059

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


University of Texas Southwestern Medical Center

6. Umlauf, Benjamin J. Methods for Identifying Subcellular Targeting Ligands and Selected Applications.

Degree: 2015, University of Texas Southwestern Medical Center

 Subcellular localization plays an essential role in targeting drug therapies as generally the pro-drug or linker relies on physical conditions of a particular subcellular compartment… (more)

Subjects/Keywords: Endocytosis; Lysosomes; Peptides

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APA (6th Edition):

Umlauf, B. J. (2015). Methods for Identifying Subcellular Targeting Ligands and Selected Applications. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4228

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):

Umlauf, Benjamin J. “Methods for Identifying Subcellular Targeting Ligands and Selected Applications.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed March 29, 2020. http://hdl.handle.net/2152.5/4228.

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

MLA Handbook (7th Edition):

Umlauf, Benjamin J. “Methods for Identifying Subcellular Targeting Ligands and Selected Applications.” 2015. Web. 29 Mar 2020.

Vancouver:

Umlauf BJ. Methods for Identifying Subcellular Targeting Ligands and Selected Applications. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2020 Mar 29]. Available from: http://hdl.handle.net/2152.5/4228.

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

Council of Science Editors:

Umlauf BJ. Methods for Identifying Subcellular Targeting Ligands and Selected Applications. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4228

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


Rutgers University

7. Shi, Anbing, 1974-. Regulation of endocytic recycling in Caenorhabditis elegans.

Degree: PhD, Microbiology and Molecular Genetics, 2010, Rutgers University

Eukaryotic endocytic pathway is important for the uptake, sorting, and the subsequential recycling or degradation processes of various cargos. It has been shown that the… (more)

Subjects/Keywords: Endocytosis; Caenorhabditis elegans

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APA (6th Edition):

Shi, Anbing, 1. (2010). Regulation of endocytic recycling in Caenorhabditis elegans. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000053159

Chicago Manual of Style (16th Edition):

Shi, Anbing, 1974-. “Regulation of endocytic recycling in Caenorhabditis elegans.” 2010. Doctoral Dissertation, Rutgers University. Accessed March 29, 2020. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000053159.

MLA Handbook (7th Edition):

Shi, Anbing, 1974-. “Regulation of endocytic recycling in Caenorhabditis elegans.” 2010. Web. 29 Mar 2020.

Vancouver:

Shi, Anbing 1. Regulation of endocytic recycling in Caenorhabditis elegans. [Internet] [Doctoral dissertation]. Rutgers University; 2010. [cited 2020 Mar 29]. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000053159.

Council of Science Editors:

Shi, Anbing 1. Regulation of endocytic recycling in Caenorhabditis elegans. [Doctoral Dissertation]. Rutgers University; 2010. Available from: http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.000053159


Rutgers University

8. Gleason, Adenrele Madeline, 1982-. Endocytic recycling in Caenorhabditis elegans.

Degree: PhD, Cell and Developmental Biology, 2016, Rutgers University

The power of conservation is exemplified in the C. elegans intestinal epithelia. As a model to study endocytic recycling, molecular transport regulators have been characterized… (more)

Subjects/Keywords: Caenorhabditis elegans; Endocytosis

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APA (6th Edition):

Gleason, Adenrele Madeline, 1. (2016). Endocytic recycling in Caenorhabditis elegans. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/51295/

Chicago Manual of Style (16th Edition):

Gleason, Adenrele Madeline, 1982-. “Endocytic recycling in Caenorhabditis elegans.” 2016. Doctoral Dissertation, Rutgers University. Accessed March 29, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/51295/.

MLA Handbook (7th Edition):

Gleason, Adenrele Madeline, 1982-. “Endocytic recycling in Caenorhabditis elegans.” 2016. Web. 29 Mar 2020.

Vancouver:

Gleason, Adenrele Madeline 1. Endocytic recycling in Caenorhabditis elegans. [Internet] [Doctoral dissertation]. Rutgers University; 2016. [cited 2020 Mar 29]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/51295/.

Council of Science Editors:

Gleason, Adenrele Madeline 1. Endocytic recycling in Caenorhabditis elegans. [Doctoral Dissertation]. Rutgers University; 2016. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/51295/


University of Southern California

9. Ji, Man. Entry and intracellular trafficking of measles virus glycoprotein pseudotyping lentivector for transduction in target cells.

Degree: MS, Biochemistry and Molecular Biology, 2013, University of Southern California

 Measles virus, enveloped RNA virus, infects lungs, airways, lymphocytes and multiple organs, causing respiratory disease and immune suppression. Due to the specificity of measles virus… (more)

Subjects/Keywords: measles; lentiviral vectors; endocytosis; microtubules

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APA (6th Edition):

Ji, M. (2013). Entry and intracellular trafficking of measles virus glycoprotein pseudotyping lentivector for transduction in target cells. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/356286/rec/2393

Chicago Manual of Style (16th Edition):

Ji, Man. “Entry and intracellular trafficking of measles virus glycoprotein pseudotyping lentivector for transduction in target cells.” 2013. Masters Thesis, University of Southern California. Accessed March 29, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/356286/rec/2393.

MLA Handbook (7th Edition):

Ji, Man. “Entry and intracellular trafficking of measles virus glycoprotein pseudotyping lentivector for transduction in target cells.” 2013. Web. 29 Mar 2020.

Vancouver:

Ji M. Entry and intracellular trafficking of measles virus glycoprotein pseudotyping lentivector for transduction in target cells. [Internet] [Masters thesis]. University of Southern California; 2013. [cited 2020 Mar 29]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/356286/rec/2393.

Council of Science Editors:

Ji M. Entry and intracellular trafficking of measles virus glycoprotein pseudotyping lentivector for transduction in target cells. [Masters Thesis]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/356286/rec/2393


University of Southern California

10. Chen, Chun-Kan. Minibrain kinase enhances synaptojanin activity to facilitate endocytosis during synaptic activity.

Degree: MS, Biochemistry and Molecular Biology, 2015, University of Southern California

 Protein phosphorylation by kinases plays an important role in regulating synaptic development and function. During synaptic activity, coordinated phosphorylation and dephosphorylation of endocytic proteins dynamically… (more)

Subjects/Keywords: synaptic transmission; endocytosis; kinase

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APA (6th Edition):

Chen, C. (2015). Minibrain kinase enhances synaptojanin activity to facilitate endocytosis during synaptic activity. (Masters Thesis). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/285458/rec/4080

Chicago Manual of Style (16th Edition):

Chen, Chun-Kan. “Minibrain kinase enhances synaptojanin activity to facilitate endocytosis during synaptic activity.” 2015. Masters Thesis, University of Southern California. Accessed March 29, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/285458/rec/4080.

MLA Handbook (7th Edition):

Chen, Chun-Kan. “Minibrain kinase enhances synaptojanin activity to facilitate endocytosis during synaptic activity.” 2015. Web. 29 Mar 2020.

Vancouver:

Chen C. Minibrain kinase enhances synaptojanin activity to facilitate endocytosis during synaptic activity. [Internet] [Masters thesis]. University of Southern California; 2015. [cited 2020 Mar 29]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/285458/rec/4080.

Council of Science Editors:

Chen C. Minibrain kinase enhances synaptojanin activity to facilitate endocytosis during synaptic activity. [Masters Thesis]. University of Southern California; 2015. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/285458/rec/4080


Penn State University

11. Wu, Juan. Investigating the roles of beta Heavy-spectrin in epidermal growth factor receptor signaling activity in Drosophila melanogaster.

Degree: MS, Biochemistry, Microbiology, and Molecular Biology, 2011, Penn State University

 The spectrin-based membrane skeleton (SBMS) is a flexible and multifunctional scaffold involved in a wide spectrum of cellular processes including the generation of specialized membrane… (more)

Subjects/Keywords: Trafficking; Spectrin; EGFR; Endocytosis

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APA (6th Edition):

Wu, J. (2011). Investigating the roles of beta Heavy-spectrin in epidermal growth factor receptor signaling activity in Drosophila melanogaster. (Masters Thesis). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/11687

Chicago Manual of Style (16th Edition):

Wu, Juan. “Investigating the roles of beta Heavy-spectrin in epidermal growth factor receptor signaling activity in Drosophila melanogaster.” 2011. Masters Thesis, Penn State University. Accessed March 29, 2020. https://etda.libraries.psu.edu/catalog/11687.

MLA Handbook (7th Edition):

Wu, Juan. “Investigating the roles of beta Heavy-spectrin in epidermal growth factor receptor signaling activity in Drosophila melanogaster.” 2011. Web. 29 Mar 2020.

Vancouver:

Wu J. Investigating the roles of beta Heavy-spectrin in epidermal growth factor receptor signaling activity in Drosophila melanogaster. [Internet] [Masters thesis]. Penn State University; 2011. [cited 2020 Mar 29]. Available from: https://etda.libraries.psu.edu/catalog/11687.

Council of Science Editors:

Wu J. Investigating the roles of beta Heavy-spectrin in epidermal growth factor receptor signaling activity in Drosophila melanogaster. [Masters Thesis]. Penn State University; 2011. Available from: https://etda.libraries.psu.edu/catalog/11687


University of Sydney

12. Collett, Michael. An allosteric network within dynamin .

Degree: 2016, University of Sydney

 Dynamins are large enzymes that catalyse the hydrolysis of GTP (GTPase activity). They assemble through oligomerisation into helical polymers during endocytosis to facilitate membrane scission… (more)

Subjects/Keywords: Dynamin; Allostery; Endocytosis; Enzyme; Kinetics

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APA (6th Edition):

Collett, M. (2016). An allosteric network within dynamin . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/15871

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):

Collett, Michael. “An allosteric network within dynamin .” 2016. Thesis, University of Sydney. Accessed March 29, 2020. http://hdl.handle.net/2123/15871.

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

MLA Handbook (7th Edition):

Collett, Michael. “An allosteric network within dynamin .” 2016. Web. 29 Mar 2020.

Vancouver:

Collett M. An allosteric network within dynamin . [Internet] [Thesis]. University of Sydney; 2016. [cited 2020 Mar 29]. Available from: http://hdl.handle.net/2123/15871.

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

Council of Science Editors:

Collett M. An allosteric network within dynamin . [Thesis]. University of Sydney; 2016. Available from: http://hdl.handle.net/2123/15871

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

13. Paolucci, Clara. Role of nitric oxide in the maturation process of human dendritic cells.

Degree: PhD, 2003, Open University

 Nitric oxide (NO) generated by phagocytes at inflammation sites contributes to regulate immune responses through both autocrine and paracrine actions on bystander cells. Among the… (more)

Subjects/Keywords: 571; Endocytosis

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APA (6th Edition):

Paolucci, C. (2003). Role of nitric oxide in the maturation process of human dendritic cells. (Doctoral Dissertation). Open University. Retrieved from http://oro.open.ac.uk/63250/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.273309

Chicago Manual of Style (16th Edition):

Paolucci, Clara. “Role of nitric oxide in the maturation process of human dendritic cells.” 2003. Doctoral Dissertation, Open University. Accessed March 29, 2020. http://oro.open.ac.uk/63250/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.273309.

MLA Handbook (7th Edition):

Paolucci, Clara. “Role of nitric oxide in the maturation process of human dendritic cells.” 2003. Web. 29 Mar 2020.

Vancouver:

Paolucci C. Role of nitric oxide in the maturation process of human dendritic cells. [Internet] [Doctoral dissertation]. Open University; 2003. [cited 2020 Mar 29]. Available from: http://oro.open.ac.uk/63250/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.273309.

Council of Science Editors:

Paolucci C. Role of nitric oxide in the maturation process of human dendritic cells. [Doctoral Dissertation]. Open University; 2003. Available from: http://oro.open.ac.uk/63250/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.273309


Vanderbilt University

14. Vijayakrishnan, Niranjana. Cellular Role Of The Drosophila EFR3, Rolling Blackout (RBO) In Synaptic Transmission.

Degree: PhD, Neuroscience, 2010, Vanderbilt University

 Rolling Blackout (RBO), a Drosophila EFR3 homolog, is an integral membrane protein predicted to be a lipase. A conditional temperature-sensitive (TS) mutant (rbots) displays paralysis… (more)

Subjects/Keywords: Drosophila; endocytosis; garland cell

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APA (6th Edition):

Vijayakrishnan, N. (2010). Cellular Role Of The Drosophila EFR3, Rolling Blackout (RBO) In Synaptic Transmission. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu//available/etd-03292010-133228/ ;

Chicago Manual of Style (16th Edition):

Vijayakrishnan, Niranjana. “Cellular Role Of The Drosophila EFR3, Rolling Blackout (RBO) In Synaptic Transmission.” 2010. Doctoral Dissertation, Vanderbilt University. Accessed March 29, 2020. http://etd.library.vanderbilt.edu//available/etd-03292010-133228/ ;.

MLA Handbook (7th Edition):

Vijayakrishnan, Niranjana. “Cellular Role Of The Drosophila EFR3, Rolling Blackout (RBO) In Synaptic Transmission.” 2010. Web. 29 Mar 2020.

Vancouver:

Vijayakrishnan N. Cellular Role Of The Drosophila EFR3, Rolling Blackout (RBO) In Synaptic Transmission. [Internet] [Doctoral dissertation]. Vanderbilt University; 2010. [cited 2020 Mar 29]. Available from: http://etd.library.vanderbilt.edu//available/etd-03292010-133228/ ;.

Council of Science Editors:

Vijayakrishnan N. Cellular Role Of The Drosophila EFR3, Rolling Blackout (RBO) In Synaptic Transmission. [Doctoral Dissertation]. Vanderbilt University; 2010. Available from: http://etd.library.vanderbilt.edu//available/etd-03292010-133228/ ;


University of Texas Southwestern Medical Center

15. Fine, Michael Jon. How to Mend a Broken Heart: Massive Endocytosis and the Role of Lipidic Forces in Membrane Trafficking.

Degree: 2012, University of Texas Southwestern Medical Center

 Novel forms of membrane internalization defined as massive endocytosis (MEND) were characterized for mechanism and physiological significance in isolated cells and intact cardiac tissue. These… (more)

Subjects/Keywords: Membrane Microdomains; Cell Membrane; Endocytosis

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APA (6th Edition):

Fine, M. J. (2012). How to Mend a Broken Heart: Massive Endocytosis and the Role of Lipidic Forces in Membrane Trafficking. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/1024

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):

Fine, Michael Jon. “How to Mend a Broken Heart: Massive Endocytosis and the Role of Lipidic Forces in Membrane Trafficking.” 2012. Thesis, University of Texas Southwestern Medical Center. Accessed March 29, 2020. http://hdl.handle.net/2152.5/1024.

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

MLA Handbook (7th Edition):

Fine, Michael Jon. “How to Mend a Broken Heart: Massive Endocytosis and the Role of Lipidic Forces in Membrane Trafficking.” 2012. Web. 29 Mar 2020.

Vancouver:

Fine MJ. How to Mend a Broken Heart: Massive Endocytosis and the Role of Lipidic Forces in Membrane Trafficking. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2012. [cited 2020 Mar 29]. Available from: http://hdl.handle.net/2152.5/1024.

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

Council of Science Editors:

Fine MJ. How to Mend a Broken Heart: Massive Endocytosis and the Role of Lipidic Forces in Membrane Trafficking. [Thesis]. University of Texas Southwestern Medical Center; 2012. Available from: http://hdl.handle.net/2152.5/1024

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


University of Kentucky

16. Banerjee, Meenakshi. PLATELET ENDOCYTOSIS: ROLES IN HEMOSTASIS AND INNATE IMMUNITY.

Degree: 2017, University of Kentucky

Endocytosis is key to fibrinogen (Fg) uptake, receptor trafficking of integrins (αIIbβ3, αvβ3) and purinergic receptors (P2Y1, P2Y12), and thereby for normal platelet function. However,… (more)

Subjects/Keywords: platelets; endocytosis; innate immunity; Biochemistry

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APA (6th Edition):

Banerjee, M. (2017). PLATELET ENDOCYTOSIS: ROLES IN HEMOSTASIS AND INNATE IMMUNITY. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/biochem_etds/32

Chicago Manual of Style (16th Edition):

Banerjee, Meenakshi. “PLATELET ENDOCYTOSIS: ROLES IN HEMOSTASIS AND INNATE IMMUNITY.” 2017. Doctoral Dissertation, University of Kentucky. Accessed March 29, 2020. https://uknowledge.uky.edu/biochem_etds/32.

MLA Handbook (7th Edition):

Banerjee, Meenakshi. “PLATELET ENDOCYTOSIS: ROLES IN HEMOSTASIS AND INNATE IMMUNITY.” 2017. Web. 29 Mar 2020.

Vancouver:

Banerjee M. PLATELET ENDOCYTOSIS: ROLES IN HEMOSTASIS AND INNATE IMMUNITY. [Internet] [Doctoral dissertation]. University of Kentucky; 2017. [cited 2020 Mar 29]. Available from: https://uknowledge.uky.edu/biochem_etds/32.

Council of Science Editors:

Banerjee M. PLATELET ENDOCYTOSIS: ROLES IN HEMOSTASIS AND INNATE IMMUNITY. [Doctoral Dissertation]. University of Kentucky; 2017. Available from: https://uknowledge.uky.edu/biochem_etds/32


Virginia Tech

17. Mitra, Sharmistha. Ubiquitin Modulates Tollip's PtdIns(3)P Binding and Dissociates the Dimeric State of C-Terminal Cue Domain.

Degree: PhD, Biological Sciences, 2013, Virginia Tech

 Ubiquitylation is a highly controlled post-translational modification of proteins, in which proteins are conjugated either with monoubiquitin or polyubiquitin chains. Ubiquitin modifications on target proteins… (more)

Subjects/Keywords: Tollip; phosphoinositides; ubiquitin; endocytosis

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APA (6th Edition):

Mitra, S. (2013). Ubiquitin Modulates Tollip's PtdIns(3)P Binding and Dissociates the Dimeric State of C-Terminal Cue Domain. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/51151

Chicago Manual of Style (16th Edition):

Mitra, Sharmistha. “Ubiquitin Modulates Tollip's PtdIns(3)P Binding and Dissociates the Dimeric State of C-Terminal Cue Domain.” 2013. Doctoral Dissertation, Virginia Tech. Accessed March 29, 2020. http://hdl.handle.net/10919/51151.

MLA Handbook (7th Edition):

Mitra, Sharmistha. “Ubiquitin Modulates Tollip's PtdIns(3)P Binding and Dissociates the Dimeric State of C-Terminal Cue Domain.” 2013. Web. 29 Mar 2020.

Vancouver:

Mitra S. Ubiquitin Modulates Tollip's PtdIns(3)P Binding and Dissociates the Dimeric State of C-Terminal Cue Domain. [Internet] [Doctoral dissertation]. Virginia Tech; 2013. [cited 2020 Mar 29]. Available from: http://hdl.handle.net/10919/51151.

Council of Science Editors:

Mitra S. Ubiquitin Modulates Tollip's PtdIns(3)P Binding and Dissociates the Dimeric State of C-Terminal Cue Domain. [Doctoral Dissertation]. Virginia Tech; 2013. Available from: http://hdl.handle.net/10919/51151


University of Toronto

18. Tjia, Jason Alexander. Journey into C. albicans Biofilms: Proteomic and functional genomic approaches to uncovering mechanisms of adherence.

Degree: 2016, University of Toronto

Candida albicans is an opportunistic fungal human pathogen that naturally forms biofilms, which are a community of yeast and filamentous cells surrounded by an extracellular… (more)

Subjects/Keywords: Adherence; Biofilms; Candida; Endocytosis; 0410

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APA (6th Edition):

Tjia, J. A. (2016). Journey into C. albicans Biofilms: Proteomic and functional genomic approaches to uncovering mechanisms of adherence. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/72808

Chicago Manual of Style (16th Edition):

Tjia, Jason Alexander. “Journey into C. albicans Biofilms: Proteomic and functional genomic approaches to uncovering mechanisms of adherence.” 2016. Masters Thesis, University of Toronto. Accessed March 29, 2020. http://hdl.handle.net/1807/72808.

MLA Handbook (7th Edition):

Tjia, Jason Alexander. “Journey into C. albicans Biofilms: Proteomic and functional genomic approaches to uncovering mechanisms of adherence.” 2016. Web. 29 Mar 2020.

Vancouver:

Tjia JA. Journey into C. albicans Biofilms: Proteomic and functional genomic approaches to uncovering mechanisms of adherence. [Internet] [Masters thesis]. University of Toronto; 2016. [cited 2020 Mar 29]. Available from: http://hdl.handle.net/1807/72808.

Council of Science Editors:

Tjia JA. Journey into C. albicans Biofilms: Proteomic and functional genomic approaches to uncovering mechanisms of adherence. [Masters Thesis]. University of Toronto; 2016. Available from: http://hdl.handle.net/1807/72808


University of Manchester

19. Monticone, Giulia. Consequences of EGF-module mutations on Notch signalling and trafficking.

Degree: 2018, University of Manchester

 The Notch pathway is evolutionary conserved and involved in several key cellular functions that ensure tissue homeostasis in the adult organism. Such an important pathway… (more)

Subjects/Keywords: Notch; endocytosis; cancer; Drosophila

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APA (6th Edition):

Monticone, G. (2018). Consequences of EGF-module mutations on Notch signalling and trafficking. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:317234

Chicago Manual of Style (16th Edition):

Monticone, Giulia. “Consequences of EGF-module mutations on Notch signalling and trafficking.” 2018. Doctoral Dissertation, University of Manchester. Accessed March 29, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:317234.

MLA Handbook (7th Edition):

Monticone, Giulia. “Consequences of EGF-module mutations on Notch signalling and trafficking.” 2018. Web. 29 Mar 2020.

Vancouver:

Monticone G. Consequences of EGF-module mutations on Notch signalling and trafficking. [Internet] [Doctoral dissertation]. University of Manchester; 2018. [cited 2020 Mar 29]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:317234.

Council of Science Editors:

Monticone G. Consequences of EGF-module mutations on Notch signalling and trafficking. [Doctoral Dissertation]. University of Manchester; 2018. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:317234


Boston University

20. Ho, Nhu Quynh. Studies on the structure of aldolase bound to F-actin and its role in endocytosis.

Degree: PhD, Biology, 2019, Boston University

 Fructose 1,6-bisphosphate aldolase, or simply aldolase, is a key enzyme involved in the glucose and fructose metabolic pathways. Vertebrate aldolases exists in nature as extremely… (more)

Subjects/Keywords: Biochemistry; Actin; Aldolase; Endocytosis

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APA (6th Edition):

Ho, N. Q. (2019). Studies on the structure of aldolase bound to F-actin and its role in endocytosis. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/39562

Chicago Manual of Style (16th Edition):

Ho, Nhu Quynh. “Studies on the structure of aldolase bound to F-actin and its role in endocytosis.” 2019. Doctoral Dissertation, Boston University. Accessed March 29, 2020. http://hdl.handle.net/2144/39562.

MLA Handbook (7th Edition):

Ho, Nhu Quynh. “Studies on the structure of aldolase bound to F-actin and its role in endocytosis.” 2019. Web. 29 Mar 2020.

Vancouver:

Ho NQ. Studies on the structure of aldolase bound to F-actin and its role in endocytosis. [Internet] [Doctoral dissertation]. Boston University; 2019. [cited 2020 Mar 29]. Available from: http://hdl.handle.net/2144/39562.

Council of Science Editors:

Ho NQ. Studies on the structure of aldolase bound to F-actin and its role in endocytosis. [Doctoral Dissertation]. Boston University; 2019. Available from: http://hdl.handle.net/2144/39562


University of Manchester

21. Monticone, Giulia. Consequences of EGF-module mutations on Notch signalling and trafficking.

Degree: PhD, 2019, University of Manchester

 The Notch pathway is evolutionary conserved and involved in several key cellular functions that ensure tissue homeostasis in the adult organism. Such an important pathway… (more)

Subjects/Keywords: Notch; endocytosis; cancer; Drosophila

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APA (6th Edition):

Monticone, G. (2019). Consequences of EGF-module mutations on Notch signalling and trafficking. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/consequences-of-egfmodule-mutations-on-notch-signalling-and-trafficking(ebbcc017-651b-4b42-9ea4-b2a85d91fdcc).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.799310

Chicago Manual of Style (16th Edition):

Monticone, Giulia. “Consequences of EGF-module mutations on Notch signalling and trafficking.” 2019. Doctoral Dissertation, University of Manchester. Accessed March 29, 2020. https://www.research.manchester.ac.uk/portal/en/theses/consequences-of-egfmodule-mutations-on-notch-signalling-and-trafficking(ebbcc017-651b-4b42-9ea4-b2a85d91fdcc).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.799310.

MLA Handbook (7th Edition):

Monticone, Giulia. “Consequences of EGF-module mutations on Notch signalling and trafficking.” 2019. Web. 29 Mar 2020.

Vancouver:

Monticone G. Consequences of EGF-module mutations on Notch signalling and trafficking. [Internet] [Doctoral dissertation]. University of Manchester; 2019. [cited 2020 Mar 29]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/consequences-of-egfmodule-mutations-on-notch-signalling-and-trafficking(ebbcc017-651b-4b42-9ea4-b2a85d91fdcc).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.799310.

Council of Science Editors:

Monticone G. Consequences of EGF-module mutations on Notch signalling and trafficking. [Doctoral Dissertation]. University of Manchester; 2019. Available from: https://www.research.manchester.ac.uk/portal/en/theses/consequences-of-egfmodule-mutations-on-notch-signalling-and-trafficking(ebbcc017-651b-4b42-9ea4-b2a85d91fdcc).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.799310


Colorado State University

22. Farrell, Kristen. Investigating new protein components of the endocytic machinery in Saccharomyces cerevisiae.

Degree: PhD, Cell and Molecular Biology, 2016, Colorado State University

 Clathrin-mediated endocytosis is an essential eukaryotic process which allows cells to control membrane lipid and protein content, signaling processes, and uptake of nutrients among other… (more)

Subjects/Keywords: GFP; Ubx3; endocytosis; yeast; Tda2

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APA (6th Edition):

Farrell, K. (2016). Investigating new protein components of the endocytic machinery in Saccharomyces cerevisiae. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/173369

Chicago Manual of Style (16th Edition):

Farrell, Kristen. “Investigating new protein components of the endocytic machinery in Saccharomyces cerevisiae.” 2016. Doctoral Dissertation, Colorado State University. Accessed March 29, 2020. http://hdl.handle.net/10217/173369.

MLA Handbook (7th Edition):

Farrell, Kristen. “Investigating new protein components of the endocytic machinery in Saccharomyces cerevisiae.” 2016. Web. 29 Mar 2020.

Vancouver:

Farrell K. Investigating new protein components of the endocytic machinery in Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. Colorado State University; 2016. [cited 2020 Mar 29]. Available from: http://hdl.handle.net/10217/173369.

Council of Science Editors:

Farrell K. Investigating new protein components of the endocytic machinery in Saccharomyces cerevisiae. [Doctoral Dissertation]. Colorado State University; 2016. Available from: http://hdl.handle.net/10217/173369


University of Windsor

23. Xhabija, Besa. MYOTUBULARIN RELATED - 2 REGULATES RECEPTOR MEDIATED ENDOCYTOSIS - 8, A NOVEL PI (3) P BINDING PROTEIN THAT CONTROLS EARLY ENDOSOMAL CLATHRIN DYNAMICS AND ENDOSOMAL RETROGRADE TRANSPORT PATHWAY THROUGH ITS N-TERMINAL PHOSPHOINOSITIDE BINDING MOTIF.

Degree: PhD, Chemistry and Biochemistry, 2016, University of Windsor

  Myotubularin related protein 2 (MTMR2) is a member of the myotubularin family of phosphoinositide lipid phosphatases whose subcellular localization is regulated by a phosphorylation… (more)

Subjects/Keywords: Endocytosis; Myotubilarin; Parkinson; Receptor Mediated Endocytosis 8; Retrograde; Signalling

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APA (6th Edition):

Xhabija, B. (2016). MYOTUBULARIN RELATED - 2 REGULATES RECEPTOR MEDIATED ENDOCYTOSIS - 8, A NOVEL PI (3) P BINDING PROTEIN THAT CONTROLS EARLY ENDOSOMAL CLATHRIN DYNAMICS AND ENDOSOMAL RETROGRADE TRANSPORT PATHWAY THROUGH ITS N-TERMINAL PHOSPHOINOSITIDE BINDING MOTIF. (Doctoral Dissertation). University of Windsor. Retrieved from http://scholar.uwindsor.ca/etd/5693

Chicago Manual of Style (16th Edition):

Xhabija, Besa. “MYOTUBULARIN RELATED - 2 REGULATES RECEPTOR MEDIATED ENDOCYTOSIS - 8, A NOVEL PI (3) P BINDING PROTEIN THAT CONTROLS EARLY ENDOSOMAL CLATHRIN DYNAMICS AND ENDOSOMAL RETROGRADE TRANSPORT PATHWAY THROUGH ITS N-TERMINAL PHOSPHOINOSITIDE BINDING MOTIF.” 2016. Doctoral Dissertation, University of Windsor. Accessed March 29, 2020. http://scholar.uwindsor.ca/etd/5693.

MLA Handbook (7th Edition):

Xhabija, Besa. “MYOTUBULARIN RELATED - 2 REGULATES RECEPTOR MEDIATED ENDOCYTOSIS - 8, A NOVEL PI (3) P BINDING PROTEIN THAT CONTROLS EARLY ENDOSOMAL CLATHRIN DYNAMICS AND ENDOSOMAL RETROGRADE TRANSPORT PATHWAY THROUGH ITS N-TERMINAL PHOSPHOINOSITIDE BINDING MOTIF.” 2016. Web. 29 Mar 2020.

Vancouver:

Xhabija B. MYOTUBULARIN RELATED - 2 REGULATES RECEPTOR MEDIATED ENDOCYTOSIS - 8, A NOVEL PI (3) P BINDING PROTEIN THAT CONTROLS EARLY ENDOSOMAL CLATHRIN DYNAMICS AND ENDOSOMAL RETROGRADE TRANSPORT PATHWAY THROUGH ITS N-TERMINAL PHOSPHOINOSITIDE BINDING MOTIF. [Internet] [Doctoral dissertation]. University of Windsor; 2016. [cited 2020 Mar 29]. Available from: http://scholar.uwindsor.ca/etd/5693.

Council of Science Editors:

Xhabija B. MYOTUBULARIN RELATED - 2 REGULATES RECEPTOR MEDIATED ENDOCYTOSIS - 8, A NOVEL PI (3) P BINDING PROTEIN THAT CONTROLS EARLY ENDOSOMAL CLATHRIN DYNAMICS AND ENDOSOMAL RETROGRADE TRANSPORT PATHWAY THROUGH ITS N-TERMINAL PHOSPHOINOSITIDE BINDING MOTIF. [Doctoral Dissertation]. University of Windsor; 2016. Available from: http://scholar.uwindsor.ca/etd/5693


University of Newcastle

24. MacGregor, Kylie Anne. Disruption of clathrin-mediated endocytosis through small molecule inhibition of dynamin and clathrin.

Degree: PhD, 2012, University of Newcastle

Research Doctorate - Doctor of Philosophy (PhD)

Since the first evidence of clathrin-mediated endocytosis was reported almost 50 years ago, extensive research has been devoted… (more)

Subjects/Keywords: clathrin-mediated endocytosis; endocytosis; inhibitors; targeted therapeutic agents; dynamin; 1,4-benzoquinone

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APA (6th Edition):

MacGregor, K. A. (2012). Disruption of clathrin-mediated endocytosis through small molecule inhibition of dynamin and clathrin. (Doctoral Dissertation). University of Newcastle. Retrieved from http://hdl.handle.net/1959.13/935828

Chicago Manual of Style (16th Edition):

MacGregor, Kylie Anne. “Disruption of clathrin-mediated endocytosis through small molecule inhibition of dynamin and clathrin.” 2012. Doctoral Dissertation, University of Newcastle. Accessed March 29, 2020. http://hdl.handle.net/1959.13/935828.

MLA Handbook (7th Edition):

MacGregor, Kylie Anne. “Disruption of clathrin-mediated endocytosis through small molecule inhibition of dynamin and clathrin.” 2012. Web. 29 Mar 2020.

Vancouver:

MacGregor KA. Disruption of clathrin-mediated endocytosis through small molecule inhibition of dynamin and clathrin. [Internet] [Doctoral dissertation]. University of Newcastle; 2012. [cited 2020 Mar 29]. Available from: http://hdl.handle.net/1959.13/935828.

Council of Science Editors:

MacGregor KA. Disruption of clathrin-mediated endocytosis through small molecule inhibition of dynamin and clathrin. [Doctoral Dissertation]. University of Newcastle; 2012. Available from: http://hdl.handle.net/1959.13/935828


University of Utah

25. Ott, Elizabeth Mary. The multivesicular body pathway and the endosomal sorting complexes required for transports: escrt -II recruitment and cargo sorting mechanisms.

Degree: PhD, Biology, 2011, University of Utah

 The ESCRT (endosomal sorting complexes required for transport) proteincomplexes are required for the sorting of proteins into the MVB (multivesicularbody) pathway, a protein trafficking pathway… (more)

Subjects/Keywords: Endocytosis; Endosome; ESCRT; Multivesicular body; Vacuole

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APA (6th Edition):

Ott, E. M. (2011). The multivesicular body pathway and the endosomal sorting complexes required for transports: escrt -II recruitment and cargo sorting mechanisms. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/3508/rec/2609

Chicago Manual of Style (16th Edition):

Ott, Elizabeth Mary. “The multivesicular body pathway and the endosomal sorting complexes required for transports: escrt -II recruitment and cargo sorting mechanisms.” 2011. Doctoral Dissertation, University of Utah. Accessed March 29, 2020. http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/3508/rec/2609.

MLA Handbook (7th Edition):

Ott, Elizabeth Mary. “The multivesicular body pathway and the endosomal sorting complexes required for transports: escrt -II recruitment and cargo sorting mechanisms.” 2011. Web. 29 Mar 2020.

Vancouver:

Ott EM. The multivesicular body pathway and the endosomal sorting complexes required for transports: escrt -II recruitment and cargo sorting mechanisms. [Internet] [Doctoral dissertation]. University of Utah; 2011. [cited 2020 Mar 29]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/3508/rec/2609.

Council of Science Editors:

Ott EM. The multivesicular body pathway and the endosomal sorting complexes required for transports: escrt -II recruitment and cargo sorting mechanisms. [Doctoral Dissertation]. University of Utah; 2011. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/3508/rec/2609


Victoria University of Wellington

26. Joshi, Praneta. The Effects of Microtubule Stabilizing Drugs on Macrophage Immune-Mediated Endocytosis.

Degree: 2010, Victoria University of Wellington

 Microtubule stabilizing drugs (MSD) bind and stabilize microtubules, thus inhibiting their normal function. MSD exhibit anti-mitotic effects which makes them attractive as cancer chemotherapeutics and… (more)

Subjects/Keywords: Peloruside A; Macrophage endocytosis; Microtubule stabilizers

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APA (6th Edition):

Joshi, P. (2010). The Effects of Microtubule Stabilizing Drugs on Macrophage Immune-Mediated Endocytosis. (Masters Thesis). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/1447

Chicago Manual of Style (16th Edition):

Joshi, Praneta. “The Effects of Microtubule Stabilizing Drugs on Macrophage Immune-Mediated Endocytosis.” 2010. Masters Thesis, Victoria University of Wellington. Accessed March 29, 2020. http://hdl.handle.net/10063/1447.

MLA Handbook (7th Edition):

Joshi, Praneta. “The Effects of Microtubule Stabilizing Drugs on Macrophage Immune-Mediated Endocytosis.” 2010. Web. 29 Mar 2020.

Vancouver:

Joshi P. The Effects of Microtubule Stabilizing Drugs on Macrophage Immune-Mediated Endocytosis. [Internet] [Masters thesis]. Victoria University of Wellington; 2010. [cited 2020 Mar 29]. Available from: http://hdl.handle.net/10063/1447.

Council of Science Editors:

Joshi P. The Effects of Microtubule Stabilizing Drugs on Macrophage Immune-Mediated Endocytosis. [Masters Thesis]. Victoria University of Wellington; 2010. Available from: http://hdl.handle.net/10063/1447


University of Hong Kong

27. Chew, Sze-lun. Genomic organization and expression of EEN-B2, a member of EEN (endophilin) family involved in endocytosis.

Degree: M. Phil., 1999, University of Hong Kong

published_or_final_version

Pathology

Master

Master of Philosophy

Advisors/Committee Members: Sham, MH, Chan, LC, Chung, SK.

Subjects/Keywords: Endocytosis.; Proteins.; Genetics.

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APA (6th Edition):

Chew, S. (1999). Genomic organization and expression of EEN-B2, a member of EEN (endophilin) family involved in endocytosis. (Masters Thesis). University of Hong Kong. Retrieved from Chew, S. [趙士麟]. (1999). Genomic organization and expression of EEN-B2, a member of EEN (endophilin) family involved in endocytosis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3122238 ; http://dx.doi.org/10.5353/th_b3122238 ; http://hdl.handle.net/10722/33688

Chicago Manual of Style (16th Edition):

Chew, Sze-lun. “Genomic organization and expression of EEN-B2, a member of EEN (endophilin) family involved in endocytosis.” 1999. Masters Thesis, University of Hong Kong. Accessed March 29, 2020. Chew, S. [趙士麟]. (1999). Genomic organization and expression of EEN-B2, a member of EEN (endophilin) family involved in endocytosis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3122238 ; http://dx.doi.org/10.5353/th_b3122238 ; http://hdl.handle.net/10722/33688.

MLA Handbook (7th Edition):

Chew, Sze-lun. “Genomic organization and expression of EEN-B2, a member of EEN (endophilin) family involved in endocytosis.” 1999. Web. 29 Mar 2020.

Vancouver:

Chew S. Genomic organization and expression of EEN-B2, a member of EEN (endophilin) family involved in endocytosis. [Internet] [Masters thesis]. University of Hong Kong; 1999. [cited 2020 Mar 29]. Available from: Chew, S. [趙士麟]. (1999). Genomic organization and expression of EEN-B2, a member of EEN (endophilin) family involved in endocytosis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3122238 ; http://dx.doi.org/10.5353/th_b3122238 ; http://hdl.handle.net/10722/33688.

Council of Science Editors:

Chew S. Genomic organization and expression of EEN-B2, a member of EEN (endophilin) family involved in endocytosis. [Masters Thesis]. University of Hong Kong; 1999. Available from: Chew, S. [趙士麟]. (1999). Genomic organization and expression of EEN-B2, a member of EEN (endophilin) family involved in endocytosis. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b3122238 ; http://dx.doi.org/10.5353/th_b3122238 ; http://hdl.handle.net/10722/33688


University of Rochester

28. Shi, Shujie. Identification of Human Gene Products Containing Pro-Pro-x-Tyr (PY) Motifs That Enhance Glutathione and Endocytotic Markers Uptake in Yeast.

Degree: PhD, 2010, University of Rochester

 Glutathione (GSH) plays essential roles in many cellular processes, and disturbances in its homeostasis are associated with a number of human diseases. GSH export from… (more)

Subjects/Keywords: GSH; Py; Endocytosis; Yeast; Membrane Turnover; Transporters

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APA (6th Edition):

Shi, S. (2010). Identification of Human Gene Products Containing Pro-Pro-x-Tyr (PY) Motifs That Enhance Glutathione and Endocytotic Markers Uptake in Yeast. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/10503

Chicago Manual of Style (16th Edition):

Shi, Shujie. “Identification of Human Gene Products Containing Pro-Pro-x-Tyr (PY) Motifs That Enhance Glutathione and Endocytotic Markers Uptake in Yeast.” 2010. Doctoral Dissertation, University of Rochester. Accessed March 29, 2020. http://hdl.handle.net/1802/10503.

MLA Handbook (7th Edition):

Shi, Shujie. “Identification of Human Gene Products Containing Pro-Pro-x-Tyr (PY) Motifs That Enhance Glutathione and Endocytotic Markers Uptake in Yeast.” 2010. Web. 29 Mar 2020.

Vancouver:

Shi S. Identification of Human Gene Products Containing Pro-Pro-x-Tyr (PY) Motifs That Enhance Glutathione and Endocytotic Markers Uptake in Yeast. [Internet] [Doctoral dissertation]. University of Rochester; 2010. [cited 2020 Mar 29]. Available from: http://hdl.handle.net/1802/10503.

Council of Science Editors:

Shi S. Identification of Human Gene Products Containing Pro-Pro-x-Tyr (PY) Motifs That Enhance Glutathione and Endocytotic Markers Uptake in Yeast. [Doctoral Dissertation]. University of Rochester; 2010. Available from: http://hdl.handle.net/1802/10503


University of Southern California

29. Rajapaksa, Thejani Evenia. Characterization of the role of LIM and SH3 protein (LASP-1) in endocytosis and actin cytoskeleton remodeling.

Degree: PhD, Pharmaceutical Sciences, 2008, University of Southern California

 LIM and SH3 protein (lasp-1) is a multidomain-containing protein found to be overexpressed in several breast cancer cell lines. Lasp-1 co-localizes with F-actin and the… (more)

Subjects/Keywords: endocytosis; lasp-1

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

APA (6th Edition):

Rajapaksa, T. E. (2008). Characterization of the role of LIM and SH3 protein (LASP-1) in endocytosis and actin cytoskeleton remodeling. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/85710/rec/1311

Chicago Manual of Style (16th Edition):

Rajapaksa, Thejani Evenia. “Characterization of the role of LIM and SH3 protein (LASP-1) in endocytosis and actin cytoskeleton remodeling.” 2008. Doctoral Dissertation, University of Southern California. Accessed March 29, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/85710/rec/1311.

MLA Handbook (7th Edition):

Rajapaksa, Thejani Evenia. “Characterization of the role of LIM and SH3 protein (LASP-1) in endocytosis and actin cytoskeleton remodeling.” 2008. Web. 29 Mar 2020.

Vancouver:

Rajapaksa TE. Characterization of the role of LIM and SH3 protein (LASP-1) in endocytosis and actin cytoskeleton remodeling. [Internet] [Doctoral dissertation]. University of Southern California; 2008. [cited 2020 Mar 29]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/85710/rec/1311.

Council of Science Editors:

Rajapaksa TE. Characterization of the role of LIM and SH3 protein (LASP-1) in endocytosis and actin cytoskeleton remodeling. [Doctoral Dissertation]. University of Southern California; 2008. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/85710/rec/1311


University of Edinburgh

30. Abdelhameed, Taher. Role of src splice variants in nerve terminal function.

Degree: 2010, University of Edinburgh

 Src is a 60 kDa tyrosine kinase that is expressed in most of animal tissues. Src has three splice variants, C-src, which is ubiquitously expressed,… (more)

Subjects/Keywords: 573.8; src; nerve terminal; endocytosis; exocytosis

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

APA (6th Edition):

Abdelhameed, T. (2010). Role of src splice variants in nerve terminal function. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/4485

Chicago Manual of Style (16th Edition):

Abdelhameed, Taher. “Role of src splice variants in nerve terminal function.” 2010. Doctoral Dissertation, University of Edinburgh. Accessed March 29, 2020. http://hdl.handle.net/1842/4485.

MLA Handbook (7th Edition):

Abdelhameed, Taher. “Role of src splice variants in nerve terminal function.” 2010. Web. 29 Mar 2020.

Vancouver:

Abdelhameed T. Role of src splice variants in nerve terminal function. [Internet] [Doctoral dissertation]. University of Edinburgh; 2010. [cited 2020 Mar 29]. Available from: http://hdl.handle.net/1842/4485.

Council of Science Editors:

Abdelhameed T. Role of src splice variants in nerve terminal function. [Doctoral Dissertation]. University of Edinburgh; 2010. Available from: http://hdl.handle.net/1842/4485

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