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You searched for +publisher:"Cornell University" +contributor:("Brown, William J"). Showing records 1 – 30 of 30 total matches.

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Cornell University

1. Bechler, Marie. Phospholipase A2 Regulation Of Golgi And Endosome Structure And Function.

Degree: PhD, Molecular and Cell Biology, 2011, Cornell University

 The transport mechanisms of secretory and endocytic pathways are responsible for the coordinated movement of proteins and lipids throughout the cell at the proper time… (more)

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APA (6th Edition):

Bechler, M. (2011). Phospholipase A2 Regulation Of Golgi And Endosome Structure And Function. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/33576

Chicago Manual of Style (16th Edition):

Bechler, Marie. “Phospholipase A2 Regulation Of Golgi And Endosome Structure And Function.” 2011. Doctoral Dissertation, Cornell University. Accessed December 02, 2020. http://hdl.handle.net/1813/33576.

MLA Handbook (7th Edition):

Bechler, Marie. “Phospholipase A2 Regulation Of Golgi And Endosome Structure And Function.” 2011. Web. 02 Dec 2020.

Vancouver:

Bechler M. Phospholipase A2 Regulation Of Golgi And Endosome Structure And Function. [Internet] [Doctoral dissertation]. Cornell University; 2011. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1813/33576.

Council of Science Editors:

Bechler M. Phospholipase A2 Regulation Of Golgi And Endosome Structure And Function. [Doctoral Dissertation]. Cornell University; 2011. Available from: http://hdl.handle.net/1813/33576


Cornell University

2. Ha, Kevin. Investigating Novel Regulators Of Golgi Membrane Tubulation.

Degree: PhD, Biochemistry, 2012, Cornell University

 The Golgi complex serves as a vital organelle from which proteins and membrane lipids are modified, sorted, and trafficked to various destinations. Mutations that cause… (more)

Subjects/Keywords: Golgi; tubules; pace1; dgkg; dagk; rnai

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APA (6th Edition):

Ha, K. (2012). Investigating Novel Regulators Of Golgi Membrane Tubulation. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/31075

Chicago Manual of Style (16th Edition):

Ha, Kevin. “Investigating Novel Regulators Of Golgi Membrane Tubulation.” 2012. Doctoral Dissertation, Cornell University. Accessed December 02, 2020. http://hdl.handle.net/1813/31075.

MLA Handbook (7th Edition):

Ha, Kevin. “Investigating Novel Regulators Of Golgi Membrane Tubulation.” 2012. Web. 02 Dec 2020.

Vancouver:

Ha K. Investigating Novel Regulators Of Golgi Membrane Tubulation. [Internet] [Doctoral dissertation]. Cornell University; 2012. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1813/31075.

Council of Science Editors:

Ha K. Investigating Novel Regulators Of Golgi Membrane Tubulation. [Doctoral Dissertation]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/31075


Cornell University

3. Halaby, Steve. NOVEL REGULATORY MECHANISM OF THE ARF-GEF SEC7 VIA THE N- AND C- TERMINUS.

Degree: PhD, Biochemistry, Molecular and Cell Biology, 2018, Cornell University

 The Golgi complex is the central membrane and protein-sorting station in eukaryotic cells. Activation of Arf (ADP-ribosylation factor) GTPases is essential for vesicle formation via… (more)

Subjects/Keywords: Cellular biology; allosteric regulation; GTPase; Golgi; Biochemistry; ADP ribosylation factor (ARF); Guanine nucleotide exchange factor (GEF); intracellular trafficking

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APA (6th Edition):

Halaby, S. (2018). NOVEL REGULATORY MECHANISM OF THE ARF-GEF SEC7 VIA THE N- AND C- TERMINUS. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/59520

Chicago Manual of Style (16th Edition):

Halaby, Steve. “NOVEL REGULATORY MECHANISM OF THE ARF-GEF SEC7 VIA THE N- AND C- TERMINUS.” 2018. Doctoral Dissertation, Cornell University. Accessed December 02, 2020. http://hdl.handle.net/1813/59520.

MLA Handbook (7th Edition):

Halaby, Steve. “NOVEL REGULATORY MECHANISM OF THE ARF-GEF SEC7 VIA THE N- AND C- TERMINUS.” 2018. Web. 02 Dec 2020.

Vancouver:

Halaby S. NOVEL REGULATORY MECHANISM OF THE ARF-GEF SEC7 VIA THE N- AND C- TERMINUS. [Internet] [Doctoral dissertation]. Cornell University; 2018. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1813/59520.

Council of Science Editors:

Halaby S. NOVEL REGULATORY MECHANISM OF THE ARF-GEF SEC7 VIA THE N- AND C- TERMINUS. [Doctoral Dissertation]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59520


Cornell University

4. Thornlow, Dana. Antibody Bioconjugates for Targeted Therapeutic Delivery.

Degree: PhD, Chemical Engineering, 2019, Cornell University

 Monoclonal antibodies (mAbs) have emerged over the last 20 years as an invaluable biosensing, diagnostic, and therapeutic tool for targeting cancer. With their tight antigen… (more)

Subjects/Keywords: Chemical engineering; Antibody; Antibody drug conjugate; Bioconjugation; LAP tag; Microbial Transglutaminase; siRNA

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APA (6th Edition):

Thornlow, D. (2019). Antibody Bioconjugates for Targeted Therapeutic Delivery. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/67408

Chicago Manual of Style (16th Edition):

Thornlow, Dana. “Antibody Bioconjugates for Targeted Therapeutic Delivery.” 2019. Doctoral Dissertation, Cornell University. Accessed December 02, 2020. http://hdl.handle.net/1813/67408.

MLA Handbook (7th Edition):

Thornlow, Dana. “Antibody Bioconjugates for Targeted Therapeutic Delivery.” 2019. Web. 02 Dec 2020.

Vancouver:

Thornlow D. Antibody Bioconjugates for Targeted Therapeutic Delivery. [Internet] [Doctoral dissertation]. Cornell University; 2019. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1813/67408.

Council of Science Editors:

Thornlow D. Antibody Bioconjugates for Targeted Therapeutic Delivery. [Doctoral Dissertation]. Cornell University; 2019. Available from: http://hdl.handle.net/1813/67408


Cornell University

5. Liu, Wenyu. Characterization Of The Regulation Of Formin Protein Bni1P In Saccharomyces Cerevisiae.

Degree: PhD, Genetics, 2011, Cornell University

 Formins are a family of conserved proteins that assemble unbranched actin filaments. In budding yeast, Saccharomyces cerevisiae, the formin isoforms Bni1p and Bnr1p are vital… (more)

Subjects/Keywords: Formin; Bni1p; Arp1p

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APA (6th Edition):

Liu, W. (2011). Characterization Of The Regulation Of Formin Protein Bni1P In Saccharomyces Cerevisiae. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/30737

Chicago Manual of Style (16th Edition):

Liu, Wenyu. “Characterization Of The Regulation Of Formin Protein Bni1P In Saccharomyces Cerevisiae.” 2011. Doctoral Dissertation, Cornell University. Accessed December 02, 2020. http://hdl.handle.net/1813/30737.

MLA Handbook (7th Edition):

Liu, Wenyu. “Characterization Of The Regulation Of Formin Protein Bni1P In Saccharomyces Cerevisiae.” 2011. Web. 02 Dec 2020.

Vancouver:

Liu W. Characterization Of The Regulation Of Formin Protein Bni1P In Saccharomyces Cerevisiae. [Internet] [Doctoral dissertation]. Cornell University; 2011. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1813/30737.

Council of Science Editors:

Liu W. Characterization Of The Regulation Of Formin Protein Bni1P In Saccharomyces Cerevisiae. [Doctoral Dissertation]. Cornell University; 2011. Available from: http://hdl.handle.net/1813/30737

6. Gustafson, Margaret Ann. The Arf-GEFs Gea1 and Gea2 integrate signals to coordinate vesicle trafficking at the Golgi complex.

Degree: PhD, Biochemistry, Molecular and Cell Biology, 2017, Cornell University

 At the Golgi complex, the biosynthetic sorting center of the cell, the Arf GTPases are responsible for coordinating vesicle formation. The Arf-GEFs activate Arf GTPases… (more)

Subjects/Keywords: Cellular biology; Molecular biology; Biochemistry; Arf; Arf-GEF; Gea1; Gea2; Golgi complex; membrane trafficking

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APA (6th Edition):

Gustafson, M. A. (2017). The Arf-GEFs Gea1 and Gea2 integrate signals to coordinate vesicle trafficking at the Golgi complex. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/56834

Chicago Manual of Style (16th Edition):

Gustafson, Margaret Ann. “The Arf-GEFs Gea1 and Gea2 integrate signals to coordinate vesicle trafficking at the Golgi complex.” 2017. Doctoral Dissertation, Cornell University. Accessed December 02, 2020. http://hdl.handle.net/1813/56834.

MLA Handbook (7th Edition):

Gustafson, Margaret Ann. “The Arf-GEFs Gea1 and Gea2 integrate signals to coordinate vesicle trafficking at the Golgi complex.” 2017. Web. 02 Dec 2020.

Vancouver:

Gustafson MA. The Arf-GEFs Gea1 and Gea2 integrate signals to coordinate vesicle trafficking at the Golgi complex. [Internet] [Doctoral dissertation]. Cornell University; 2017. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1813/56834.

Council of Science Editors:

Gustafson MA. The Arf-GEFs Gea1 and Gea2 integrate signals to coordinate vesicle trafficking at the Golgi complex. [Doctoral Dissertation]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/56834


Cornell University

7. Kalkofen, Danielle. A Role For Ceramide Kinase In Membrane Trafficking And Organelle Morphology In Mammalian Cells.

Degree: PhD, Molecular and Cell Biology, 2015, Cornell University

 The correct functioning of the cell, and hence a multicellular organism, is dependent on proteins and lipids reaching their proper destination at the correct time.… (more)

Subjects/Keywords: ceramide kinase; membrane trafficking; sphingolipids

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APA (6th Edition):

Kalkofen, D. (2015). A Role For Ceramide Kinase In Membrane Trafficking And Organelle Morphology In Mammalian Cells. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/39324

Chicago Manual of Style (16th Edition):

Kalkofen, Danielle. “A Role For Ceramide Kinase In Membrane Trafficking And Organelle Morphology In Mammalian Cells.” 2015. Doctoral Dissertation, Cornell University. Accessed December 02, 2020. http://hdl.handle.net/1813/39324.

MLA Handbook (7th Edition):

Kalkofen, Danielle. “A Role For Ceramide Kinase In Membrane Trafficking And Organelle Morphology In Mammalian Cells.” 2015. Web. 02 Dec 2020.

Vancouver:

Kalkofen D. A Role For Ceramide Kinase In Membrane Trafficking And Organelle Morphology In Mammalian Cells. [Internet] [Doctoral dissertation]. Cornell University; 2015. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1813/39324.

Council of Science Editors:

Kalkofen D. A Role For Ceramide Kinase In Membrane Trafficking And Organelle Morphology In Mammalian Cells. [Doctoral Dissertation]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/39324


Cornell University

8. Clarke, Benjamin. Characterization Of Human Lysophospholipid Acyltransferases In The Regulation Of Membrane Trafficking.

Degree: PhD, Molecular and Cell Biology, 2014, Cornell University

 Lysophospholipid acyltransferases (LPATs) catalyze the addition of an acyl chain to a lysophospholipid to form a phospholipid, dramatically altering lipid structure and behavior. These changes… (more)

Subjects/Keywords: LPACT3; retrograde transport; COPI vesicle

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APA (6th Edition):

Clarke, B. (2014). Characterization Of Human Lysophospholipid Acyltransferases In The Regulation Of Membrane Trafficking. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/37157

Chicago Manual of Style (16th Edition):

Clarke, Benjamin. “Characterization Of Human Lysophospholipid Acyltransferases In The Regulation Of Membrane Trafficking.” 2014. Doctoral Dissertation, Cornell University. Accessed December 02, 2020. http://hdl.handle.net/1813/37157.

MLA Handbook (7th Edition):

Clarke, Benjamin. “Characterization Of Human Lysophospholipid Acyltransferases In The Regulation Of Membrane Trafficking.” 2014. Web. 02 Dec 2020.

Vancouver:

Clarke B. Characterization Of Human Lysophospholipid Acyltransferases In The Regulation Of Membrane Trafficking. [Internet] [Doctoral dissertation]. Cornell University; 2014. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1813/37157.

Council of Science Editors:

Clarke B. Characterization Of Human Lysophospholipid Acyltransferases In The Regulation Of Membrane Trafficking. [Doctoral Dissertation]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/37157


Cornell University

9. Allen, Krystal. The Gnrh Receptor-Associated Membrane Raft Proteome In Mouse Gonadotrope Cells.

Degree: PhD, Veterinary Medicine, 2012, Cornell University

 Gonadotropin releasing hormone (GnRH) is the central hormone of reproduction in vertebrates. This hormone is secreted from the hypothalamus in response to environmental, steroid hormone… (more)

Subjects/Keywords: Gonadotropin Releasing Hormone Receptor; Proteomic; Membrane Raft

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APA (6th Edition):

Allen, K. (2012). The Gnrh Receptor-Associated Membrane Raft Proteome In Mouse Gonadotrope Cells. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/31077

Chicago Manual of Style (16th Edition):

Allen, Krystal. “The Gnrh Receptor-Associated Membrane Raft Proteome In Mouse Gonadotrope Cells.” 2012. Doctoral Dissertation, Cornell University. Accessed December 02, 2020. http://hdl.handle.net/1813/31077.

MLA Handbook (7th Edition):

Allen, Krystal. “The Gnrh Receptor-Associated Membrane Raft Proteome In Mouse Gonadotrope Cells.” 2012. Web. 02 Dec 2020.

Vancouver:

Allen K. The Gnrh Receptor-Associated Membrane Raft Proteome In Mouse Gonadotrope Cells. [Internet] [Doctoral dissertation]. Cornell University; 2012. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1813/31077.

Council of Science Editors:

Allen K. The Gnrh Receptor-Associated Membrane Raft Proteome In Mouse Gonadotrope Cells. [Doctoral Dissertation]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/31077


Cornell University

10. Brady, Owen. Investigating Mechanisms Of Ftld-Tdp Pathogenesis.

Degree: PhD, Molecular and Cell Biology, 2014, Cornell University

 Frontotemporal lobar degeneration (FTLD) is a devastating dementia disorder that causes profound changes in personality, behavior, and language abilities. Major breakthroughs in the past decade… (more)

Subjects/Keywords: Neurodegeneration; Lysosomes; TMEM106B

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APA (6th Edition):

Brady, O. (2014). Investigating Mechanisms Of Ftld-Tdp Pathogenesis. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/36146

Chicago Manual of Style (16th Edition):

Brady, Owen. “Investigating Mechanisms Of Ftld-Tdp Pathogenesis.” 2014. Doctoral Dissertation, Cornell University. Accessed December 02, 2020. http://hdl.handle.net/1813/36146.

MLA Handbook (7th Edition):

Brady, Owen. “Investigating Mechanisms Of Ftld-Tdp Pathogenesis.” 2014. Web. 02 Dec 2020.

Vancouver:

Brady O. Investigating Mechanisms Of Ftld-Tdp Pathogenesis. [Internet] [Doctoral dissertation]. Cornell University; 2014. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1813/36146.

Council of Science Editors:

Brady O. Investigating Mechanisms Of Ftld-Tdp Pathogenesis. [Doctoral Dissertation]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/36146


Cornell University

11. Nicklow, Erin Elizabeth. Regulation of Hsp70 chaperone cycle via reversible methionine oxidation of the nucleotide exchange factor Fes1.

Degree: PhD, Biochemistry, Molecular and Cell Biology, 2019, Cornell University

 Elevated levels of reactive oxygen species (ROS) are associated with the pathologies of many degenerative disorders (like aging, Alzheimer’s disease, atherosclerosis, and diabetes). Cells employ… (more)

Subjects/Keywords: 70 kilodalton heat shock protein (Hsp70); Fes1; methionine oxidation; methionine sulfoxide reductase; nucleotide exchange factor (NEF); reactive oxygen species (ROS); Cellular biology; Biochemistry

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APA (6th Edition):

Nicklow, E. E. (2019). Regulation of Hsp70 chaperone cycle via reversible methionine oxidation of the nucleotide exchange factor Fes1. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/67786

Chicago Manual of Style (16th Edition):

Nicklow, Erin Elizabeth. “Regulation of Hsp70 chaperone cycle via reversible methionine oxidation of the nucleotide exchange factor Fes1.” 2019. Doctoral Dissertation, Cornell University. Accessed December 02, 2020. http://hdl.handle.net/1813/67786.

MLA Handbook (7th Edition):

Nicklow, Erin Elizabeth. “Regulation of Hsp70 chaperone cycle via reversible methionine oxidation of the nucleotide exchange factor Fes1.” 2019. Web. 02 Dec 2020.

Vancouver:

Nicklow EE. Regulation of Hsp70 chaperone cycle via reversible methionine oxidation of the nucleotide exchange factor Fes1. [Internet] [Doctoral dissertation]. Cornell University; 2019. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1813/67786.

Council of Science Editors:

Nicklow EE. Regulation of Hsp70 chaperone cycle via reversible methionine oxidation of the nucleotide exchange factor Fes1. [Doctoral Dissertation]. Cornell University; 2019. Available from: http://hdl.handle.net/1813/67786


Cornell University

12. Wayt, Jessica. Actin Nucleators In Microvillar Assembly: Cordon Bleu As A Novel Microvillar Protein.

Degree: PhD, Molecular and Cell Biology, 2015, Cornell University

 Epithelial cells polarize through reorganization of the actin cytoskeleton which results in distinct apical and basolateral domains. At the apical domain are structures called microvilli,… (more)

Subjects/Keywords: Polarity; Actin Cytoskeleton; Microvilli

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APA (6th Edition):

Wayt, J. (2015). Actin Nucleators In Microvillar Assembly: Cordon Bleu As A Novel Microvillar Protein. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/39365

Chicago Manual of Style (16th Edition):

Wayt, Jessica. “Actin Nucleators In Microvillar Assembly: Cordon Bleu As A Novel Microvillar Protein.” 2015. Doctoral Dissertation, Cornell University. Accessed December 02, 2020. http://hdl.handle.net/1813/39365.

MLA Handbook (7th Edition):

Wayt, Jessica. “Actin Nucleators In Microvillar Assembly: Cordon Bleu As A Novel Microvillar Protein.” 2015. Web. 02 Dec 2020.

Vancouver:

Wayt J. Actin Nucleators In Microvillar Assembly: Cordon Bleu As A Novel Microvillar Protein. [Internet] [Doctoral dissertation]. Cornell University; 2015. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1813/39365.

Council of Science Editors:

Wayt J. Actin Nucleators In Microvillar Assembly: Cordon Bleu As A Novel Microvillar Protein. [Doctoral Dissertation]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/39365


Cornell University

13. Thorsen, Kevin. A ROLE FOR DIACYLGLYCEROL KINASE [gamma] IN TRAFFICKING OUT OF THE trans GOLGI NETWORK.

Degree: M.S., Biochemistry, Molecular and Cell Biology, Biochemistry, Molecular and Cell Biology, 2017, Cornell University

 The formation of cargo carriers in the secretory pathway occurs primarily through the action of coat proteins (i.e. COPI, COPII and clathrin coats). However, a… (more)

Subjects/Keywords: Cellular biology; Biochemistry; diacylglycerol kinase; Golgi; secretion; tubules; Molecular biology; membrane trafficking

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APA (6th Edition):

Thorsen, K. (2017). A ROLE FOR DIACYLGLYCEROL KINASE [gamma] IN TRAFFICKING OUT OF THE trans GOLGI NETWORK. (Masters Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/59018

Chicago Manual of Style (16th Edition):

Thorsen, Kevin. “A ROLE FOR DIACYLGLYCEROL KINASE [gamma] IN TRAFFICKING OUT OF THE trans GOLGI NETWORK.” 2017. Masters Thesis, Cornell University. Accessed December 02, 2020. http://hdl.handle.net/1813/59018.

MLA Handbook (7th Edition):

Thorsen, Kevin. “A ROLE FOR DIACYLGLYCEROL KINASE [gamma] IN TRAFFICKING OUT OF THE trans GOLGI NETWORK.” 2017. Web. 02 Dec 2020.

Vancouver:

Thorsen K. A ROLE FOR DIACYLGLYCEROL KINASE [gamma] IN TRAFFICKING OUT OF THE trans GOLGI NETWORK. [Internet] [Masters thesis]. Cornell University; 2017. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1813/59018.

Council of Science Editors:

Thorsen K. A ROLE FOR DIACYLGLYCEROL KINASE [gamma] IN TRAFFICKING OUT OF THE trans GOLGI NETWORK. [Masters Thesis]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/59018


Cornell University

14. Kim, Brian. Microfabricated Devices For Direct Measurements Of Quantal Transmitter Release From Living Cells.

Degree: PhD, Biophysics, 2013, Cornell University

 Neurotransmitters are released in packets or quanta from vesicles that fuse with the cell membrane. The machinery proteins called Soluble N-ethylmaleimide-sensitive factor Attachment Protein Receptor… (more)

Subjects/Keywords: Biosensor; Exocytosis; CMOS Integrated Circuit

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APA (6th Edition):

Kim, B. (2013). Microfabricated Devices For Direct Measurements Of Quantal Transmitter Release From Living Cells. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/33818

Chicago Manual of Style (16th Edition):

Kim, Brian. “Microfabricated Devices For Direct Measurements Of Quantal Transmitter Release From Living Cells.” 2013. Doctoral Dissertation, Cornell University. Accessed December 02, 2020. http://hdl.handle.net/1813/33818.

MLA Handbook (7th Edition):

Kim, Brian. “Microfabricated Devices For Direct Measurements Of Quantal Transmitter Release From Living Cells.” 2013. Web. 02 Dec 2020.

Vancouver:

Kim B. Microfabricated Devices For Direct Measurements Of Quantal Transmitter Release From Living Cells. [Internet] [Doctoral dissertation]. Cornell University; 2013. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1813/33818.

Council of Science Editors:

Kim B. Microfabricated Devices For Direct Measurements Of Quantal Transmitter Release From Living Cells. [Doctoral Dissertation]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/33818


Cornell University

15. Pagan, Mitchell. UNCOVERING THE LYSOSOMAL ROLE OF PROGRANULIN.

Degree: M.S., Biochemistry, Molecular and Cell Biology, Biochemistry, Molecular and Cell Biology, 2019, Cornell University

 Lysosomes are the degradative centers of the cell and their dysfunction can give rise to lysosomal storage disorders (LSDs). Frontotemporal lobar degeneration (FTLD) is a… (more)

Subjects/Keywords: Progranulin; Lysosome; Cellular biology; Biochemistry; Molecular biology; Frontotemporal lobar degeneration; Neurodegeneration

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APA (6th Edition):

Pagan, M. (2019). UNCOVERING THE LYSOSOMAL ROLE OF PROGRANULIN. (Masters Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/67268

Chicago Manual of Style (16th Edition):

Pagan, Mitchell. “UNCOVERING THE LYSOSOMAL ROLE OF PROGRANULIN.” 2019. Masters Thesis, Cornell University. Accessed December 02, 2020. http://hdl.handle.net/1813/67268.

MLA Handbook (7th Edition):

Pagan, Mitchell. “UNCOVERING THE LYSOSOMAL ROLE OF PROGRANULIN.” 2019. Web. 02 Dec 2020.

Vancouver:

Pagan M. UNCOVERING THE LYSOSOMAL ROLE OF PROGRANULIN. [Internet] [Masters thesis]. Cornell University; 2019. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1813/67268.

Council of Science Editors:

Pagan M. UNCOVERING THE LYSOSOMAL ROLE OF PROGRANULIN. [Masters Thesis]. Cornell University; 2019. Available from: http://hdl.handle.net/1813/67268


Cornell University

16. Chuang, Ya-Shan. A Bipartite Sorting Signal Ensures Specificity of Retromer Complex in Membrane Protein Recycling.

Degree: PhD, Biochemistry, Molecular and Cell Biology, 2019, Cornell University

 In the endosomal network, membrane proteins are either sorted into intraluminal vesicles for the lysosomal degradative pathway or exported from the endosome to the trans-Golgi… (more)

Subjects/Keywords: recycling; Rsp5; Cellular biology; Molecular biology; CPY; Ear1; retromer; Vps10

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APA (6th Edition):

Chuang, Y. (2019). A Bipartite Sorting Signal Ensures Specificity of Retromer Complex in Membrane Protein Recycling. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/67543

Chicago Manual of Style (16th Edition):

Chuang, Ya-Shan. “A Bipartite Sorting Signal Ensures Specificity of Retromer Complex in Membrane Protein Recycling.” 2019. Doctoral Dissertation, Cornell University. Accessed December 02, 2020. http://hdl.handle.net/1813/67543.

MLA Handbook (7th Edition):

Chuang, Ya-Shan. “A Bipartite Sorting Signal Ensures Specificity of Retromer Complex in Membrane Protein Recycling.” 2019. Web. 02 Dec 2020.

Vancouver:

Chuang Y. A Bipartite Sorting Signal Ensures Specificity of Retromer Complex in Membrane Protein Recycling. [Internet] [Doctoral dissertation]. Cornell University; 2019. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1813/67543.

Council of Science Editors:

Chuang Y. A Bipartite Sorting Signal Ensures Specificity of Retromer Complex in Membrane Protein Recycling. [Doctoral Dissertation]. Cornell University; 2019. Available from: http://hdl.handle.net/1813/67543


Cornell University

17. Manford, Andrew. Endoplasmic Reticulum-Plasma Membrane Junctions: Novel Sites For Phosphoinositide Regulation.

Degree: PhD, Biochemistry, 2014, Cornell University

 Endoplasmic reticulum-plasma membrane (ER-PM) contact sites are specialized stable regions of the ER that are tightly apposed to the PM. These conserved organelle junctions are… (more)

Subjects/Keywords: Phosphoinositide; Endoplasmic Reticulum; Plasma Membrane

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APA (6th Edition):

Manford, A. (2014). Endoplasmic Reticulum-Plasma Membrane Junctions: Novel Sites For Phosphoinositide Regulation. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/36042

Chicago Manual of Style (16th Edition):

Manford, Andrew. “Endoplasmic Reticulum-Plasma Membrane Junctions: Novel Sites For Phosphoinositide Regulation.” 2014. Doctoral Dissertation, Cornell University. Accessed December 02, 2020. http://hdl.handle.net/1813/36042.

MLA Handbook (7th Edition):

Manford, Andrew. “Endoplasmic Reticulum-Plasma Membrane Junctions: Novel Sites For Phosphoinositide Regulation.” 2014. Web. 02 Dec 2020.

Vancouver:

Manford A. Endoplasmic Reticulum-Plasma Membrane Junctions: Novel Sites For Phosphoinositide Regulation. [Internet] [Doctoral dissertation]. Cornell University; 2014. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1813/36042.

Council of Science Editors:

Manford A. Endoplasmic Reticulum-Plasma Membrane Junctions: Novel Sites For Phosphoinositide Regulation. [Doctoral Dissertation]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/36042


Cornell University

18. Pareja, Kristeen Alcaide. A ROLE FOR THE N-TERMINAL DOMAIN IN MODULATING THE ACTIVITIES OF THE NUCLEOTIDE EXCHANGE FACTOR SIL1.

Degree: PhD, Pharmacology, 2018, Cornell University

 Excessive cellular reactive oxygen species (ROS), or oxidative stress, can lead to cell damage and is implicated in diseases such as cancer, aging and neurodegenerative… (more)

Subjects/Keywords: Cellular biology; Pharmacology

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APA (6th Edition):

Pareja, K. A. (2018). A ROLE FOR THE N-TERMINAL DOMAIN IN MODULATING THE ACTIVITIES OF THE NUCLEOTIDE EXCHANGE FACTOR SIL1. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/59801

Chicago Manual of Style (16th Edition):

Pareja, Kristeen Alcaide. “A ROLE FOR THE N-TERMINAL DOMAIN IN MODULATING THE ACTIVITIES OF THE NUCLEOTIDE EXCHANGE FACTOR SIL1.” 2018. Doctoral Dissertation, Cornell University. Accessed December 02, 2020. http://hdl.handle.net/1813/59801.

MLA Handbook (7th Edition):

Pareja, Kristeen Alcaide. “A ROLE FOR THE N-TERMINAL DOMAIN IN MODULATING THE ACTIVITIES OF THE NUCLEOTIDE EXCHANGE FACTOR SIL1.” 2018. Web. 02 Dec 2020.

Vancouver:

Pareja KA. A ROLE FOR THE N-TERMINAL DOMAIN IN MODULATING THE ACTIVITIES OF THE NUCLEOTIDE EXCHANGE FACTOR SIL1. [Internet] [Doctoral dissertation]. Cornell University; 2018. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1813/59801.

Council of Science Editors:

Pareja KA. A ROLE FOR THE N-TERMINAL DOMAIN IN MODULATING THE ACTIVITIES OF THE NUCLEOTIDE EXCHANGE FACTOR SIL1. [Doctoral Dissertation]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59801


Cornell University

19. Goh, Shih Lin. Model Systems For Studies At The Plasma Membrane: Investigating Lipid Phase Behavior And Protein-Mediated Membrane Remodeling.

Degree: PhD, Biochemistry, 2013, Cornell University

 The plasma membrane is a multicomponent mixture of lipids and proteins. Functional domains ("lipid rafts") that arise from nonrandom mixing of membrane components are believed… (more)

Subjects/Keywords: model membranes; BAR domain; patterned phases

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APA (6th Edition):

Goh, S. L. (2013). Model Systems For Studies At The Plasma Membrane: Investigating Lipid Phase Behavior And Protein-Mediated Membrane Remodeling. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/34075

Chicago Manual of Style (16th Edition):

Goh, Shih Lin. “Model Systems For Studies At The Plasma Membrane: Investigating Lipid Phase Behavior And Protein-Mediated Membrane Remodeling.” 2013. Doctoral Dissertation, Cornell University. Accessed December 02, 2020. http://hdl.handle.net/1813/34075.

MLA Handbook (7th Edition):

Goh, Shih Lin. “Model Systems For Studies At The Plasma Membrane: Investigating Lipid Phase Behavior And Protein-Mediated Membrane Remodeling.” 2013. Web. 02 Dec 2020.

Vancouver:

Goh SL. Model Systems For Studies At The Plasma Membrane: Investigating Lipid Phase Behavior And Protein-Mediated Membrane Remodeling. [Internet] [Doctoral dissertation]. Cornell University; 2013. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1813/34075.

Council of Science Editors:

Goh SL. Model Systems For Studies At The Plasma Membrane: Investigating Lipid Phase Behavior And Protein-Mediated Membrane Remodeling. [Doctoral Dissertation]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/34075


Cornell University

20. Zhao, Zeping. Inflammation requires an anti-inflammatory/regenerating protein REG3[beta] to induce insulin resistance.

Degree: PhD, Animal Science, 2018, Cornell University

 Inflammation is a well-accepted cause of insulin resistance (IR), and anti-inflammatory treatments (AITs) are supposed to improve insulin sensitivity. Herein, we revealed that knockout of… (more)

Subjects/Keywords: anti-inflammation; Insulin resistance; REG3β; Inflammation; Genetics; Molecular biology; Nutrition

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APA (6th Edition):

Zhao, Z. (2018). Inflammation requires an anti-inflammatory/regenerating protein REG3[beta] to induce insulin resistance. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/59543

Chicago Manual of Style (16th Edition):

Zhao, Zeping. “Inflammation requires an anti-inflammatory/regenerating protein REG3[beta] to induce insulin resistance.” 2018. Doctoral Dissertation, Cornell University. Accessed December 02, 2020. http://hdl.handle.net/1813/59543.

MLA Handbook (7th Edition):

Zhao, Zeping. “Inflammation requires an anti-inflammatory/regenerating protein REG3[beta] to induce insulin resistance.” 2018. Web. 02 Dec 2020.

Vancouver:

Zhao Z. Inflammation requires an anti-inflammatory/regenerating protein REG3[beta] to induce insulin resistance. [Internet] [Doctoral dissertation]. Cornell University; 2018. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1813/59543.

Council of Science Editors:

Zhao Z. Inflammation requires an anti-inflammatory/regenerating protein REG3[beta] to induce insulin resistance. [Doctoral Dissertation]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59543


Cornell University

21. Cragun, David. Investigation Of The Molecular Role(S) Of Yop1 And Rtn1 Shaping The Peripheral Er.

Degree: PhD, Molecular and Cell Biology, 2011, Cornell University

 A defining feature of eukaryotic life is the presence of membrane-bound organelles. While the energetically most stable shape for a membrane is likely a sphere,… (more)

Subjects/Keywords: membrane; curvature; yop1

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APA (6th Edition):

Cragun, D. (2011). Investigation Of The Molecular Role(S) Of Yop1 And Rtn1 Shaping The Peripheral Er. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/33508

Chicago Manual of Style (16th Edition):

Cragun, David. “Investigation Of The Molecular Role(S) Of Yop1 And Rtn1 Shaping The Peripheral Er.” 2011. Doctoral Dissertation, Cornell University. Accessed December 02, 2020. http://hdl.handle.net/1813/33508.

MLA Handbook (7th Edition):

Cragun, David. “Investigation Of The Molecular Role(S) Of Yop1 And Rtn1 Shaping The Peripheral Er.” 2011. Web. 02 Dec 2020.

Vancouver:

Cragun D. Investigation Of The Molecular Role(S) Of Yop1 And Rtn1 Shaping The Peripheral Er. [Internet] [Doctoral dissertation]. Cornell University; 2011. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1813/33508.

Council of Science Editors:

Cragun D. Investigation Of The Molecular Role(S) Of Yop1 And Rtn1 Shaping The Peripheral Er. [Doctoral Dissertation]. Cornell University; 2011. Available from: http://hdl.handle.net/1813/33508


Cornell University

22. Harbison, Carole. Receptor Binding And Early Steps Of Cellular Infection By Parvoviruses.

Degree: PhD, Veterinary Medicine, 2011, Cornell University

 Parvoviruses are small, non-enveloped, single stranded DNA viruses. The specific attributes of the capsid and genome dictate how the virus interacts with the environment and… (more)

Subjects/Keywords: Virus Entry; Virus Evolution; Anti-viral Immunity

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APA (6th Edition):

Harbison, C. (2011). Receptor Binding And Early Steps Of Cellular Infection By Parvoviruses. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/29255

Chicago Manual of Style (16th Edition):

Harbison, Carole. “Receptor Binding And Early Steps Of Cellular Infection By Parvoviruses.” 2011. Doctoral Dissertation, Cornell University. Accessed December 02, 2020. http://hdl.handle.net/1813/29255.

MLA Handbook (7th Edition):

Harbison, Carole. “Receptor Binding And Early Steps Of Cellular Infection By Parvoviruses.” 2011. Web. 02 Dec 2020.

Vancouver:

Harbison C. Receptor Binding And Early Steps Of Cellular Infection By Parvoviruses. [Internet] [Doctoral dissertation]. Cornell University; 2011. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1813/29255.

Council of Science Editors:

Harbison C. Receptor Binding And Early Steps Of Cellular Infection By Parvoviruses. [Doctoral Dissertation]. Cornell University; 2011. Available from: http://hdl.handle.net/1813/29255


Cornell University

23. Byrnes, Laura. Molecular Basis For Nucleotide-Dependent Conformational Changes Of The Large Gtpase Atlastin.

Degree: PhD, Biophysics, 2013, Cornell University

 The membrane of the endoplasmic reticulum (ER) is the site of numerous complex activities essential to the survival of eukaryotic cells. In the membrane sheets… (more)

Subjects/Keywords: atlastin; dynamin; membrane fusion

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APA (6th Edition):

Byrnes, L. (2013). Molecular Basis For Nucleotide-Dependent Conformational Changes Of The Large Gtpase Atlastin. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/34301

Chicago Manual of Style (16th Edition):

Byrnes, Laura. “Molecular Basis For Nucleotide-Dependent Conformational Changes Of The Large Gtpase Atlastin.” 2013. Doctoral Dissertation, Cornell University. Accessed December 02, 2020. http://hdl.handle.net/1813/34301.

MLA Handbook (7th Edition):

Byrnes, Laura. “Molecular Basis For Nucleotide-Dependent Conformational Changes Of The Large Gtpase Atlastin.” 2013. Web. 02 Dec 2020.

Vancouver:

Byrnes L. Molecular Basis For Nucleotide-Dependent Conformational Changes Of The Large Gtpase Atlastin. [Internet] [Doctoral dissertation]. Cornell University; 2013. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1813/34301.

Council of Science Editors:

Byrnes L. Molecular Basis For Nucleotide-Dependent Conformational Changes Of The Large Gtpase Atlastin. [Doctoral Dissertation]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/34301


Cornell University

24. Bialecki, Michele. Characterization Of The Entry Mechanisms Of JunÍN Arenavirus.

Degree: PhD, Veterinary Medicine, 2013, Cornell University

 Junín Arenavirus causes Viral Hemorrhagic Fever with a 30% fatality rate in those infected. Yet the exact pathogenesis of disease is still unknown. To date,… (more)

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APA (6th Edition):

Bialecki, M. (2013). Characterization Of The Entry Mechanisms Of JunÍN Arenavirus. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/34308

Chicago Manual of Style (16th Edition):

Bialecki, Michele. “Characterization Of The Entry Mechanisms Of JunÍN Arenavirus.” 2013. Doctoral Dissertation, Cornell University. Accessed December 02, 2020. http://hdl.handle.net/1813/34308.

MLA Handbook (7th Edition):

Bialecki, Michele. “Characterization Of The Entry Mechanisms Of JunÍN Arenavirus.” 2013. Web. 02 Dec 2020.

Vancouver:

Bialecki M. Characterization Of The Entry Mechanisms Of JunÍN Arenavirus. [Internet] [Doctoral dissertation]. Cornell University; 2013. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1813/34308.

Council of Science Editors:

Bialecki M. Characterization Of The Entry Mechanisms Of JunÍN Arenavirus. [Doctoral Dissertation]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/34308


Cornell University

25. Sun, Shengyi. The Role Of Inflammation And Endoplasmic Reticulum Homeostasis In Health And Disease.

Degree: PhD, Molecular and Cell Biology, 2015, Cornell University

 A growing epidemic of obesity and inflammatory bowel disease is threatening the health of millions of people around the world. Recent studies have established that… (more)

Subjects/Keywords: Inflammation; Endoplasmic reticulum; Disease

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APA (6th Edition):

Sun, S. (2015). The Role Of Inflammation And Endoplasmic Reticulum Homeostasis In Health And Disease. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/39422

Chicago Manual of Style (16th Edition):

Sun, Shengyi. “The Role Of Inflammation And Endoplasmic Reticulum Homeostasis In Health And Disease.” 2015. Doctoral Dissertation, Cornell University. Accessed December 02, 2020. http://hdl.handle.net/1813/39422.

MLA Handbook (7th Edition):

Sun, Shengyi. “The Role Of Inflammation And Endoplasmic Reticulum Homeostasis In Health And Disease.” 2015. Web. 02 Dec 2020.

Vancouver:

Sun S. The Role Of Inflammation And Endoplasmic Reticulum Homeostasis In Health And Disease. [Internet] [Doctoral dissertation]. Cornell University; 2015. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1813/39422.

Council of Science Editors:

Sun S. The Role Of Inflammation And Endoplasmic Reticulum Homeostasis In Health And Disease. [Doctoral Dissertation]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/39422

26. Akturk, Anil. MODULATION OF UBIQUITINATION PATHWAY BY LEGIONELLA SidE EFFECTOR FAMILY.

Degree: PhD, Biochemistry, Molecular and Cell Biology, 2018, Cornell University

 Legionella pneumophila manipulates a wide array of host cellular processes during infection; one that appears to be highly altered is the ubiquitination pathway. The SidE… (more)

Subjects/Keywords: Deubiquitinase; Legionella pneumophila; Phosphodiesterase; SidE family; Ubiquitin; Ubiquitination; Biochemistry; Biophysics

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APA (6th Edition):

Akturk, A. (2018). MODULATION OF UBIQUITINATION PATHWAY BY LEGIONELLA SidE EFFECTOR FAMILY. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/59276

Chicago Manual of Style (16th Edition):

Akturk, Anil. “MODULATION OF UBIQUITINATION PATHWAY BY LEGIONELLA SidE EFFECTOR FAMILY.” 2018. Doctoral Dissertation, Cornell University. Accessed December 02, 2020. http://hdl.handle.net/1813/59276.

MLA Handbook (7th Edition):

Akturk, Anil. “MODULATION OF UBIQUITINATION PATHWAY BY LEGIONELLA SidE EFFECTOR FAMILY.” 2018. Web. 02 Dec 2020.

Vancouver:

Akturk A. MODULATION OF UBIQUITINATION PATHWAY BY LEGIONELLA SidE EFFECTOR FAMILY. [Internet] [Doctoral dissertation]. Cornell University; 2018. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1813/59276.

Council of Science Editors:

Akturk A. MODULATION OF UBIQUITINATION PATHWAY BY LEGIONELLA SidE EFFECTOR FAMILY. [Doctoral Dissertation]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59276


Cornell University

27. Cyphers, Soreen. Inhibition Of Influenza Virus And Human Parainfluenza I Virus Infection By The Protease Inhibitor Hai-2.

Degree: M.S., Molecular and Cell Biology, Molecular and Cell Biology, 2013, Cornell University

Subjects/Keywords: Influenza; Protease Inhibitor; HPIV-1

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APA (6th Edition):

Cyphers, S. (2013). Inhibition Of Influenza Virus And Human Parainfluenza I Virus Infection By The Protease Inhibitor Hai-2. (Masters Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/45366

Chicago Manual of Style (16th Edition):

Cyphers, Soreen. “Inhibition Of Influenza Virus And Human Parainfluenza I Virus Infection By The Protease Inhibitor Hai-2.” 2013. Masters Thesis, Cornell University. Accessed December 02, 2020. http://hdl.handle.net/1813/45366.

MLA Handbook (7th Edition):

Cyphers, Soreen. “Inhibition Of Influenza Virus And Human Parainfluenza I Virus Infection By The Protease Inhibitor Hai-2.” 2013. Web. 02 Dec 2020.

Vancouver:

Cyphers S. Inhibition Of Influenza Virus And Human Parainfluenza I Virus Infection By The Protease Inhibitor Hai-2. [Internet] [Masters thesis]. Cornell University; 2013. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1813/45366.

Council of Science Editors:

Cyphers S. Inhibition Of Influenza Virus And Human Parainfluenza I Virus Infection By The Protease Inhibitor Hai-2. [Masters Thesis]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/45366


Cornell University

28. Kreger, Bridget. Extracellular Vesicles And Their Role In Cancer Progression And Therapy Resistance.

Degree: PhD, Molecular and Cell Biology, 2016, Cornell University

Subjects/Keywords: cancer; extracellular vesicles; exosomes

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APA (6th Edition):

Kreger, B. (2016). Extracellular Vesicles And Their Role In Cancer Progression And Therapy Resistance. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/45139

Chicago Manual of Style (16th Edition):

Kreger, Bridget. “Extracellular Vesicles And Their Role In Cancer Progression And Therapy Resistance.” 2016. Doctoral Dissertation, Cornell University. Accessed December 02, 2020. http://hdl.handle.net/1813/45139.

MLA Handbook (7th Edition):

Kreger, Bridget. “Extracellular Vesicles And Their Role In Cancer Progression And Therapy Resistance.” 2016. Web. 02 Dec 2020.

Vancouver:

Kreger B. Extracellular Vesicles And Their Role In Cancer Progression And Therapy Resistance. [Internet] [Doctoral dissertation]. Cornell University; 2016. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1813/45139.

Council of Science Editors:

Kreger B. Extracellular Vesicles And Their Role In Cancer Progression And Therapy Resistance. [Doctoral Dissertation]. Cornell University; 2016. Available from: http://hdl.handle.net/1813/45139


Cornell University

29. Paczkowski, Jon. Molecular Architecture Of The Exomer Secretory Vesicle Cargo Adaptor Complex: The Structural Basis For Membrane Recruitment And Remodeling.

Degree: PhD, Molecular and Cell Biology, 2014, Cornell University

Subjects/Keywords: Membrane trafficking; Exomer secretory cargo adaptor; Membrane remodeling

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APA (6th Edition):

Paczkowski, J. (2014). Molecular Architecture Of The Exomer Secretory Vesicle Cargo Adaptor Complex: The Structural Basis For Membrane Recruitment And Remodeling. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/37073

Chicago Manual of Style (16th Edition):

Paczkowski, Jon. “Molecular Architecture Of The Exomer Secretory Vesicle Cargo Adaptor Complex: The Structural Basis For Membrane Recruitment And Remodeling.” 2014. Doctoral Dissertation, Cornell University. Accessed December 02, 2020. http://hdl.handle.net/1813/37073.

MLA Handbook (7th Edition):

Paczkowski, Jon. “Molecular Architecture Of The Exomer Secretory Vesicle Cargo Adaptor Complex: The Structural Basis For Membrane Recruitment And Remodeling.” 2014. Web. 02 Dec 2020.

Vancouver:

Paczkowski J. Molecular Architecture Of The Exomer Secretory Vesicle Cargo Adaptor Complex: The Structural Basis For Membrane Recruitment And Remodeling. [Internet] [Doctoral dissertation]. Cornell University; 2014. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1813/37073.

Council of Science Editors:

Paczkowski J. Molecular Architecture Of The Exomer Secretory Vesicle Cargo Adaptor Complex: The Structural Basis For Membrane Recruitment And Remodeling. [Doctoral Dissertation]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/37073


Cornell University

30. Frasheri, Dorina. Sex And Tissue Expression Patterns Of Members Of A Family Of Gene Duplicates In Drosophila.

Degree: M.S., Molecular and Cell Biology, Molecular and Cell Biology, 2013, Cornell University

Subjects/Keywords: Gene duplication; Drosophila; Sex- and tissue-expression patterns

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APA (6th Edition):

Frasheri, D. (2013). Sex And Tissue Expression Patterns Of Members Of A Family Of Gene Duplicates In Drosophila. (Masters Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/45161

Chicago Manual of Style (16th Edition):

Frasheri, Dorina. “Sex And Tissue Expression Patterns Of Members Of A Family Of Gene Duplicates In Drosophila.” 2013. Masters Thesis, Cornell University. Accessed December 02, 2020. http://hdl.handle.net/1813/45161.

MLA Handbook (7th Edition):

Frasheri, Dorina. “Sex And Tissue Expression Patterns Of Members Of A Family Of Gene Duplicates In Drosophila.” 2013. Web. 02 Dec 2020.

Vancouver:

Frasheri D. Sex And Tissue Expression Patterns Of Members Of A Family Of Gene Duplicates In Drosophila. [Internet] [Masters thesis]. Cornell University; 2013. [cited 2020 Dec 02]. Available from: http://hdl.handle.net/1813/45161.

Council of Science Editors:

Frasheri D. Sex And Tissue Expression Patterns Of Members Of A Family Of Gene Duplicates In Drosophila. [Masters Thesis]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/45161

.