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You searched for +publisher:"Cornell University" +contributor:("Crane, Brian"). Showing records 1 – 30 of 42 total matches.

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Cornell University

1. Payne, Thomas. Crystallographic And Spectroscopic Studies On The Complex Of Cytochrome C Peroxidase And Cytochrome C.

Degree: PhD, Biophysics, 2014, Cornell University

 Electron transfer (ET) is a ubiquitous process that underlies the physics of biology. Photosynthesis, respiration, and metabolism all require careful movement of electrons across long… (more)

Subjects/Keywords: protein electron transfer; cytochrome c peroxidase; crystallography

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APA (6th Edition):

Payne, T. (2014). Crystallographic And Spectroscopic Studies On The Complex Of Cytochrome C Peroxidase And Cytochrome C. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/36185

Chicago Manual of Style (16th Edition):

Payne, Thomas. “Crystallographic And Spectroscopic Studies On The Complex Of Cytochrome C Peroxidase And Cytochrome C.” 2014. Doctoral Dissertation, Cornell University. Accessed November 25, 2020. http://hdl.handle.net/1813/36185.

MLA Handbook (7th Edition):

Payne, Thomas. “Crystallographic And Spectroscopic Studies On The Complex Of Cytochrome C Peroxidase And Cytochrome C.” 2014. Web. 25 Nov 2020.

Vancouver:

Payne T. Crystallographic And Spectroscopic Studies On The Complex Of Cytochrome C Peroxidase And Cytochrome C. [Internet] [Doctoral dissertation]. Cornell University; 2014. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1813/36185.

Council of Science Editors:

Payne T. Crystallographic And Spectroscopic Studies On The Complex Of Cytochrome C Peroxidase And Cytochrome C. [Doctoral Dissertation]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/36185


Cornell University

2. Haegele, Joseph Andrew. THE DEVELOPMENT AND APPLICATION OF TARGETABLE REACTIVE ELECTROPHILES AND OXIDANTS ("T-REX") TOWARD THE DISCOVERY OF NOVEL REDOX SENSOR PROTEINS.

Degree: PhD, Chemistry and Chemical Biology, 2017, Cornell University

 Redox signaling has developed into a burgeoning field underpinning cellular signaling pathways important for health; the dysfunction of these pathways contributes to various diseases including… (more)

Subjects/Keywords: Chemistry

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APA (6th Edition):

Haegele, J. A. (2017). THE DEVELOPMENT AND APPLICATION OF TARGETABLE REACTIVE ELECTROPHILES AND OXIDANTS ("T-REX") TOWARD THE DISCOVERY OF NOVEL REDOX SENSOR PROTEINS. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/56750

Chicago Manual of Style (16th Edition):

Haegele, Joseph Andrew. “THE DEVELOPMENT AND APPLICATION OF TARGETABLE REACTIVE ELECTROPHILES AND OXIDANTS ("T-REX") TOWARD THE DISCOVERY OF NOVEL REDOX SENSOR PROTEINS.” 2017. Doctoral Dissertation, Cornell University. Accessed November 25, 2020. http://hdl.handle.net/1813/56750.

MLA Handbook (7th Edition):

Haegele, Joseph Andrew. “THE DEVELOPMENT AND APPLICATION OF TARGETABLE REACTIVE ELECTROPHILES AND OXIDANTS ("T-REX") TOWARD THE DISCOVERY OF NOVEL REDOX SENSOR PROTEINS.” 2017. Web. 25 Nov 2020.

Vancouver:

Haegele JA. THE DEVELOPMENT AND APPLICATION OF TARGETABLE REACTIVE ELECTROPHILES AND OXIDANTS ("T-REX") TOWARD THE DISCOVERY OF NOVEL REDOX SENSOR PROTEINS. [Internet] [Doctoral dissertation]. Cornell University; 2017. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1813/56750.

Council of Science Editors:

Haegele JA. THE DEVELOPMENT AND APPLICATION OF TARGETABLE REACTIVE ELECTROPHILES AND OXIDANTS ("T-REX") TOWARD THE DISCOVERY OF NOVEL REDOX SENSOR PROTEINS. [Doctoral Dissertation]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/56750


Cornell University

3. Forseth, Ry. Exploring Microbial Small-Molecule Chemistry Using 2D Nmr- And Lc/Esi-Ms-Based Comparative Metabolomics.

Degree: PhD, Chemistry and Chemical Biology, 2013, Cornell University

 Microbial biology is integrated with a seemingly endless number of pathways involving small organic molecules. The coordinated regulation of biosynthesis, export, and detection of metabolites… (more)

Subjects/Keywords: comparative metabolomics; non-ribosomal peptide synthetases; secondary metabolism

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APA (6th Edition):

Forseth, R. (2013). Exploring Microbial Small-Molecule Chemistry Using 2D Nmr- And Lc/Esi-Ms-Based Comparative Metabolomics. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/33926

Chicago Manual of Style (16th Edition):

Forseth, Ry. “Exploring Microbial Small-Molecule Chemistry Using 2D Nmr- And Lc/Esi-Ms-Based Comparative Metabolomics.” 2013. Doctoral Dissertation, Cornell University. Accessed November 25, 2020. http://hdl.handle.net/1813/33926.

MLA Handbook (7th Edition):

Forseth, Ry. “Exploring Microbial Small-Molecule Chemistry Using 2D Nmr- And Lc/Esi-Ms-Based Comparative Metabolomics.” 2013. Web. 25 Nov 2020.

Vancouver:

Forseth R. Exploring Microbial Small-Molecule Chemistry Using 2D Nmr- And Lc/Esi-Ms-Based Comparative Metabolomics. [Internet] [Doctoral dissertation]. Cornell University; 2013. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1813/33926.

Council of Science Editors:

Forseth R. Exploring Microbial Small-Molecule Chemistry Using 2D Nmr- And Lc/Esi-Ms-Based Comparative Metabolomics. [Doctoral Dissertation]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/33926


Cornell University

4. Keller, Aaron. Dynamic Multi-Body Protein Interactions Suggest Versatile Pathways For Copper Trafficking.

Degree: PhD, Chemistry and Chemical Biology, 2012, Cornell University

 As part of intracellular copper trafficking pathways, the human copper chaperone Hah1 delivers Cu+ to the Wilson's Disease Protein (WDP) via weak and dynamic protein-protein… (more)

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APA (6th Edition):

Keller, A. (2012). Dynamic Multi-Body Protein Interactions Suggest Versatile Pathways For Copper Trafficking. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/31396

Chicago Manual of Style (16th Edition):

Keller, Aaron. “Dynamic Multi-Body Protein Interactions Suggest Versatile Pathways For Copper Trafficking.” 2012. Doctoral Dissertation, Cornell University. Accessed November 25, 2020. http://hdl.handle.net/1813/31396.

MLA Handbook (7th Edition):

Keller, Aaron. “Dynamic Multi-Body Protein Interactions Suggest Versatile Pathways For Copper Trafficking.” 2012. Web. 25 Nov 2020.

Vancouver:

Keller A. Dynamic Multi-Body Protein Interactions Suggest Versatile Pathways For Copper Trafficking. [Internet] [Doctoral dissertation]. Cornell University; 2012. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1813/31396.

Council of Science Editors:

Keller A. Dynamic Multi-Body Protein Interactions Suggest Versatile Pathways For Copper Trafficking. [Doctoral Dissertation]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/31396


Cornell University

5. Baccile, Joshua Andrew. Uncovering hidden microbial metabolism using 2D NMR- and LC-MS-based comparative metabolomics.

Degree: PhD, Chemistry and Chemical Biology, 2017, Cornell University

 Recent advances in genomic sequencing technology have facilitated relatively inexpensive, high-fidelity sequencing of microbial genomes. Increased genome sequencing capacity has been accompanied by developments in… (more)

Subjects/Keywords: 2D NMR; aspergillus; biosynthesis; lc-ms; metabolomics; nrps; Chemistry

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APA (6th Edition):

Baccile, J. A. (2017). Uncovering hidden microbial metabolism using 2D NMR- and LC-MS-based comparative metabolomics. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/47790

Chicago Manual of Style (16th Edition):

Baccile, Joshua Andrew. “Uncovering hidden microbial metabolism using 2D NMR- and LC-MS-based comparative metabolomics.” 2017. Doctoral Dissertation, Cornell University. Accessed November 25, 2020. http://hdl.handle.net/1813/47790.

MLA Handbook (7th Edition):

Baccile, Joshua Andrew. “Uncovering hidden microbial metabolism using 2D NMR- and LC-MS-based comparative metabolomics.” 2017. Web. 25 Nov 2020.

Vancouver:

Baccile JA. Uncovering hidden microbial metabolism using 2D NMR- and LC-MS-based comparative metabolomics. [Internet] [Doctoral dissertation]. Cornell University; 2017. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1813/47790.

Council of Science Editors:

Baccile JA. Uncovering hidden microbial metabolism using 2D NMR- and LC-MS-based comparative metabolomics. [Doctoral Dissertation]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/47790


Cornell University

6. Luo, Xi. A Legionella Effector Sidc – A New Family Of E3 Ubiquitin Ligase With A Specific Pi(4)P Binding Domain.

Degree: PhD, Biophysics, 2015, Cornell University

 The opportunistic intracellular pathogen Legionella pneumophila is the causative agent of Legionnaires' disease. L. pneumophila delivers nearly 300 effector proteins into host cells for the… (more)

Subjects/Keywords: SidC; E3 Ubiquitin Ligase; PI(4)P

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APA (6th Edition):

Luo, X. (2015). A Legionella Effector Sidc – A New Family Of E3 Ubiquitin Ligase With A Specific Pi(4)P Binding Domain. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/41045

Chicago Manual of Style (16th Edition):

Luo, Xi. “A Legionella Effector Sidc – A New Family Of E3 Ubiquitin Ligase With A Specific Pi(4)P Binding Domain.” 2015. Doctoral Dissertation, Cornell University. Accessed November 25, 2020. http://hdl.handle.net/1813/41045.

MLA Handbook (7th Edition):

Luo, Xi. “A Legionella Effector Sidc – A New Family Of E3 Ubiquitin Ligase With A Specific Pi(4)P Binding Domain.” 2015. Web. 25 Nov 2020.

Vancouver:

Luo X. A Legionella Effector Sidc – A New Family Of E3 Ubiquitin Ligase With A Specific Pi(4)P Binding Domain. [Internet] [Doctoral dissertation]. Cornell University; 2015. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1813/41045.

Council of Science Editors:

Luo X. A Legionella Effector Sidc – A New Family Of E3 Ubiquitin Ligase With A Specific Pi(4)P Binding Domain. [Doctoral Dissertation]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/41045


Cornell University

7. Picciano, Angela L. THE BIOCHEMISTRY AND STRUCTURE OF A NOVEL NITRIC OXIDE SYNTHASE FROM CYANOBACTERIA.

Degree: PhD, Chemistry and Chemical Biology, 2019, Cornell University

 Nitric oxide synthases (NOS) are monooxygenase enzymes that catalyze the oxidation of L-arginine to L-citrulline and nitric oxide (NO). They are composed of a catalytic… (more)

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APA (6th Edition):

Picciano, A. L. (2019). THE BIOCHEMISTRY AND STRUCTURE OF A NOVEL NITRIC OXIDE SYNTHASE FROM CYANOBACTERIA. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/70046

Chicago Manual of Style (16th Edition):

Picciano, Angela L. “THE BIOCHEMISTRY AND STRUCTURE OF A NOVEL NITRIC OXIDE SYNTHASE FROM CYANOBACTERIA.” 2019. Doctoral Dissertation, Cornell University. Accessed November 25, 2020. http://hdl.handle.net/1813/70046.

MLA Handbook (7th Edition):

Picciano, Angela L. “THE BIOCHEMISTRY AND STRUCTURE OF A NOVEL NITRIC OXIDE SYNTHASE FROM CYANOBACTERIA.” 2019. Web. 25 Nov 2020.

Vancouver:

Picciano AL. THE BIOCHEMISTRY AND STRUCTURE OF A NOVEL NITRIC OXIDE SYNTHASE FROM CYANOBACTERIA. [Internet] [Doctoral dissertation]. Cornell University; 2019. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1813/70046.

Council of Science Editors:

Picciano AL. THE BIOCHEMISTRY AND STRUCTURE OF A NOVEL NITRIC OXIDE SYNTHASE FROM CYANOBACTERIA. [Doctoral Dissertation]. Cornell University; 2019. Available from: http://hdl.handle.net/1813/70046


Cornell University

8. Huang, Siyu. X-Ray Crystallographyic And Biochemical Studies Of Pseudouridine Monophosphate Glycosidase And Thiamin Pyrimidine Sytnthase.

Degree: PhD, Chemistry and Chemical Biology, 2013, Cornell University

 Enzymes are macromolecular machines in the cells that catalyze the chemistry of life. Structural and biochemical studies of enzymes and its ligands shed lights on… (more)

Subjects/Keywords: X-ray crystallography; Pseudouridine monophosphate glycosidase; Thiamin Pyrimidine Synthase

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APA (6th Edition):

Huang, S. (2013). X-Ray Crystallographyic And Biochemical Studies Of Pseudouridine Monophosphate Glycosidase And Thiamin Pyrimidine Sytnthase. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/33934

Chicago Manual of Style (16th Edition):

Huang, Siyu. “X-Ray Crystallographyic And Biochemical Studies Of Pseudouridine Monophosphate Glycosidase And Thiamin Pyrimidine Sytnthase.” 2013. Doctoral Dissertation, Cornell University. Accessed November 25, 2020. http://hdl.handle.net/1813/33934.

MLA Handbook (7th Edition):

Huang, Siyu. “X-Ray Crystallographyic And Biochemical Studies Of Pseudouridine Monophosphate Glycosidase And Thiamin Pyrimidine Sytnthase.” 2013. Web. 25 Nov 2020.

Vancouver:

Huang S. X-Ray Crystallographyic And Biochemical Studies Of Pseudouridine Monophosphate Glycosidase And Thiamin Pyrimidine Sytnthase. [Internet] [Doctoral dissertation]. Cornell University; 2013. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1813/33934.

Council of Science Editors:

Huang S. X-Ray Crystallographyic And Biochemical Studies Of Pseudouridine Monophosphate Glycosidase And Thiamin Pyrimidine Sytnthase. [Doctoral Dissertation]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/33934


Cornell University

9. Chen, Yi-fan. Phase Behavior Of Cardiolipin.

Degree: PhD, Biophysics, 2012, Cornell University

 Cardiolipin is a phospholipid with negatively charged headgroups. This lipid is structurally unique in its quadruple-chained configuration and functionally unique in its nearly exclusive involvement… (more)

Subjects/Keywords: lyotropic liquid crystal; lipid polymorphism; cardiolipin

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APA (6th Edition):

Chen, Y. (2012). Phase Behavior Of Cardiolipin. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/29517

Chicago Manual of Style (16th Edition):

Chen, Yi-fan. “Phase Behavior Of Cardiolipin.” 2012. Doctoral Dissertation, Cornell University. Accessed November 25, 2020. http://hdl.handle.net/1813/29517.

MLA Handbook (7th Edition):

Chen, Yi-fan. “Phase Behavior Of Cardiolipin.” 2012. Web. 25 Nov 2020.

Vancouver:

Chen Y. Phase Behavior Of Cardiolipin. [Internet] [Doctoral dissertation]. Cornell University; 2012. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1813/29517.

Council of Science Editors:

Chen Y. Phase Behavior Of Cardiolipin. [Doctoral Dissertation]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/29517


Cornell University

10. Lee, Wonsik. Carbon And Lipid Metabolism In Mycobacterium Tuberculosis.

Degree: PhD, Microbiology, 2014, Cornell University

 Mycobacterium tuberculosis is an air borne, facultative intracellular bacterial pathogen that resides in the phagosome of host cells. Virulence of M. tuberculosis is related to… (more)

Subjects/Keywords: Mycobacterium tuberculosis; carbon metabolism; lipid droplet

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APA (6th Edition):

Lee, W. (2014). Carbon And Lipid Metabolism In Mycobacterium Tuberculosis. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/36192

Chicago Manual of Style (16th Edition):

Lee, Wonsik. “Carbon And Lipid Metabolism In Mycobacterium Tuberculosis.” 2014. Doctoral Dissertation, Cornell University. Accessed November 25, 2020. http://hdl.handle.net/1813/36192.

MLA Handbook (7th Edition):

Lee, Wonsik. “Carbon And Lipid Metabolism In Mycobacterium Tuberculosis.” 2014. Web. 25 Nov 2020.

Vancouver:

Lee W. Carbon And Lipid Metabolism In Mycobacterium Tuberculosis. [Internet] [Doctoral dissertation]. Cornell University; 2014. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1813/36192.

Council of Science Editors:

Lee W. Carbon And Lipid Metabolism In Mycobacterium Tuberculosis. [Doctoral Dissertation]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/36192


Cornell University

11. Gudibanda, Pooja Ramakrishna. A FRAMEWORK OF STEROID METABOLISM AND NUCLEAR RECEPTOR INTERACTIONS IN NEMATODES.

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

 The primary mechanism for organisms to react to their rapidly changing environments is by alteration of gene expression profiles. An organism is capable of doing… (more)

Subjects/Keywords: Mass spectrometry; Nematodes; Nuclear receptor; Steroid; Biochemistry; Metabolism; Chemistry

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APA (6th Edition):

Gudibanda, P. R. (2019). A FRAMEWORK OF STEROID METABOLISM AND NUCLEAR RECEPTOR INTERACTIONS IN NEMATODES. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/67302

Chicago Manual of Style (16th Edition):

Gudibanda, Pooja Ramakrishna. “A FRAMEWORK OF STEROID METABOLISM AND NUCLEAR RECEPTOR INTERACTIONS IN NEMATODES.” 2019. Doctoral Dissertation, Cornell University. Accessed November 25, 2020. http://hdl.handle.net/1813/67302.

MLA Handbook (7th Edition):

Gudibanda, Pooja Ramakrishna. “A FRAMEWORK OF STEROID METABOLISM AND NUCLEAR RECEPTOR INTERACTIONS IN NEMATODES.” 2019. Web. 25 Nov 2020.

Vancouver:

Gudibanda PR. A FRAMEWORK OF STEROID METABOLISM AND NUCLEAR RECEPTOR INTERACTIONS IN NEMATODES. [Internet] [Doctoral dissertation]. Cornell University; 2019. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1813/67302.

Council of Science Editors:

Gudibanda PR. A FRAMEWORK OF STEROID METABOLISM AND NUCLEAR RECEPTOR INTERACTIONS IN NEMATODES. [Doctoral Dissertation]. Cornell University; 2019. Available from: http://hdl.handle.net/1813/67302


Cornell University

12. Sukomon, Nattakan. Signal Transduction Mechanisms of HAMP and PAS Domains in Bacterial Chemotaxis.

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

 Bacteria utilize two-component systems to respond and adapt to changes in their environments. Central to the systems are modular receptors that comprise various functional domains… (more)

Subjects/Keywords: Microbiology; Biochemistry; Chemotaxis; HAMP domain; PAS domain; Pulse-ESR spectroscopy; Signal transduction; Transmembrane receptors

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APA (6th Edition):

Sukomon, N. (2017). Signal Transduction Mechanisms of HAMP and PAS Domains in Bacterial Chemotaxis. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/47800

Chicago Manual of Style (16th Edition):

Sukomon, Nattakan. “Signal Transduction Mechanisms of HAMP and PAS Domains in Bacterial Chemotaxis.” 2017. Doctoral Dissertation, Cornell University. Accessed November 25, 2020. http://hdl.handle.net/1813/47800.

MLA Handbook (7th Edition):

Sukomon, Nattakan. “Signal Transduction Mechanisms of HAMP and PAS Domains in Bacterial Chemotaxis.” 2017. Web. 25 Nov 2020.

Vancouver:

Sukomon N. Signal Transduction Mechanisms of HAMP and PAS Domains in Bacterial Chemotaxis. [Internet] [Doctoral dissertation]. Cornell University; 2017. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1813/47800.

Council of Science Editors:

Sukomon N. Signal Transduction Mechanisms of HAMP and PAS Domains in Bacterial Chemotaxis. [Doctoral Dissertation]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/47800


Cornell University

13. Tokuda, Joshua. STRUCTURAL STUDIES OF NUCLEOSOMES WITH SMALL ANGLE X-RAY SCATTERING AND CONTRAST VARIATION.

Degree: PhD, Biophysics, 2017, Cornell University

 Nucleosomes are the fundamental units of DNA packaging and play central roles in regulating genetic activity in eukaryotic cells. High-resolution crystal structures deliver detailed snapshots… (more)

Subjects/Keywords: contrast variation; nucleosomes; SAXS; small angle x-ray scattering; time resolved; Biophysics

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APA (6th Edition):

Tokuda, J. (2017). STRUCTURAL STUDIES OF NUCLEOSOMES WITH SMALL ANGLE X-RAY SCATTERING AND CONTRAST VARIATION. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/56776

Chicago Manual of Style (16th Edition):

Tokuda, Joshua. “STRUCTURAL STUDIES OF NUCLEOSOMES WITH SMALL ANGLE X-RAY SCATTERING AND CONTRAST VARIATION.” 2017. Doctoral Dissertation, Cornell University. Accessed November 25, 2020. http://hdl.handle.net/1813/56776.

MLA Handbook (7th Edition):

Tokuda, Joshua. “STRUCTURAL STUDIES OF NUCLEOSOMES WITH SMALL ANGLE X-RAY SCATTERING AND CONTRAST VARIATION.” 2017. Web. 25 Nov 2020.

Vancouver:

Tokuda J. STRUCTURAL STUDIES OF NUCLEOSOMES WITH SMALL ANGLE X-RAY SCATTERING AND CONTRAST VARIATION. [Internet] [Doctoral dissertation]. Cornell University; 2017. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1813/56776.

Council of Science Editors:

Tokuda J. STRUCTURAL STUDIES OF NUCLEOSOMES WITH SMALL ANGLE X-RAY SCATTERING AND CONTRAST VARIATION. [Doctoral Dissertation]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/56776


Cornell University

14. Li, Bo. Tissue Transglutaminase And Its Role In Human Cancer Progression.

Degree: PhD, Chemistry and Chemical Biology, 2011, Cornell University

 Tissue transglutaminase (tTG) is a protein-crosslinking enzyme whose expression is up-regulated in several human cancers. Here I show that tTG is a key participant in… (more)

Subjects/Keywords: Tissue transglutaminase; Extracellular Matrix; Microvesicles

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APA (6th Edition):

Li, B. (2011). Tissue Transglutaminase And Its Role In Human Cancer Progression. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/30615

Chicago Manual of Style (16th Edition):

Li, Bo. “Tissue Transglutaminase And Its Role In Human Cancer Progression.” 2011. Doctoral Dissertation, Cornell University. Accessed November 25, 2020. http://hdl.handle.net/1813/30615.

MLA Handbook (7th Edition):

Li, Bo. “Tissue Transglutaminase And Its Role In Human Cancer Progression.” 2011. Web. 25 Nov 2020.

Vancouver:

Li B. Tissue Transglutaminase And Its Role In Human Cancer Progression. [Internet] [Doctoral dissertation]. Cornell University; 2011. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1813/30615.

Council of Science Editors:

Li B. Tissue Transglutaminase And Its Role In Human Cancer Progression. [Doctoral Dissertation]. Cornell University; 2011. Available from: http://hdl.handle.net/1813/30615


Cornell University

15. Smith, Meghan Anne. Structural, Spectroscopic, and Mechanistic Insights into the Three Phases of Nitrification Metallobiochemistry.

Degree: PhD, Chemistry and Chemical Biology, 2018, Cornell University

 Biological ammonia (NH3) oxidation, referred to as nitrification, is a critical part of the biogeochemical nitrogen cycle. Nitrification is mediated by both bacteria and archaea… (more)

Subjects/Keywords: Inorganic chemistry; Biochemistry; Nitrification; ammonia monooxygenase; cytochrome P460; hydroxylamine; metalloenzyme; nitrosocyanin

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APA (6th Edition):

Smith, M. A. (2018). Structural, Spectroscopic, and Mechanistic Insights into the Three Phases of Nitrification Metallobiochemistry. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/59777

Chicago Manual of Style (16th Edition):

Smith, Meghan Anne. “Structural, Spectroscopic, and Mechanistic Insights into the Three Phases of Nitrification Metallobiochemistry.” 2018. Doctoral Dissertation, Cornell University. Accessed November 25, 2020. http://hdl.handle.net/1813/59777.

MLA Handbook (7th Edition):

Smith, Meghan Anne. “Structural, Spectroscopic, and Mechanistic Insights into the Three Phases of Nitrification Metallobiochemistry.” 2018. Web. 25 Nov 2020.

Vancouver:

Smith MA. Structural, Spectroscopic, and Mechanistic Insights into the Three Phases of Nitrification Metallobiochemistry. [Internet] [Doctoral dissertation]. Cornell University; 2018. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1813/59777.

Council of Science Editors:

Smith MA. Structural, Spectroscopic, and Mechanistic Insights into the Three Phases of Nitrification Metallobiochemistry. [Doctoral Dissertation]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59777


Cornell University

16. Gadi, Deepti. Interplay Of Protein Kinase C, The Marcks Protein, And Phosphoinositides In Regulating Mast Cell Signaling.

Degree: PhD, Chemistry and Chemical Biology, 2012, Cornell University

 Stimulation of immunoglobulin E (IgE)-sensitized mast cells by multivalent antigen triggers a cascade of intracellular signaling events that results in granule exocytosis as a principal… (more)

Subjects/Keywords: Granule exocytosis; marcks; Phosphoinositides

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APA (6th Edition):

Gadi, D. (2012). Interplay Of Protein Kinase C, The Marcks Protein, And Phosphoinositides In Regulating Mast Cell Signaling. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/29275

Chicago Manual of Style (16th Edition):

Gadi, Deepti. “Interplay Of Protein Kinase C, The Marcks Protein, And Phosphoinositides In Regulating Mast Cell Signaling.” 2012. Doctoral Dissertation, Cornell University. Accessed November 25, 2020. http://hdl.handle.net/1813/29275.

MLA Handbook (7th Edition):

Gadi, Deepti. “Interplay Of Protein Kinase C, The Marcks Protein, And Phosphoinositides In Regulating Mast Cell Signaling.” 2012. Web. 25 Nov 2020.

Vancouver:

Gadi D. Interplay Of Protein Kinase C, The Marcks Protein, And Phosphoinositides In Regulating Mast Cell Signaling. [Internet] [Doctoral dissertation]. Cornell University; 2012. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1813/29275.

Council of Science Editors:

Gadi D. Interplay Of Protein Kinase C, The Marcks Protein, And Phosphoinositides In Regulating Mast Cell Signaling. [Doctoral Dissertation]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/29275


Cornell University

17. Greenswag, Anna. Structure And Enzymology Of The Chemotaxis Histidine Kinase, Chea.

Degree: PhD, Chemistry and Chemical Biology, 2015, Cornell University

 Bacterial chemotaxis enables changes in motility via response to the surrounding chemical environment and is noted for its high signal gain, range, and sensitivity. The… (more)

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APA (6th Edition):

Greenswag, A. (2015). Structure And Enzymology Of The Chemotaxis Histidine Kinase, Chea. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/39301

Chicago Manual of Style (16th Edition):

Greenswag, Anna. “Structure And Enzymology Of The Chemotaxis Histidine Kinase, Chea.” 2015. Doctoral Dissertation, Cornell University. Accessed November 25, 2020. http://hdl.handle.net/1813/39301.

MLA Handbook (7th Edition):

Greenswag, Anna. “Structure And Enzymology Of The Chemotaxis Histidine Kinase, Chea.” 2015. Web. 25 Nov 2020.

Vancouver:

Greenswag A. Structure And Enzymology Of The Chemotaxis Histidine Kinase, Chea. [Internet] [Doctoral dissertation]. Cornell University; 2015. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1813/39301.

Council of Science Editors:

Greenswag A. Structure And Enzymology Of The Chemotaxis Histidine Kinase, Chea. [Doctoral Dissertation]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/39301


Cornell University

18. Yoo, Sungsoo. A Novel Role For The Adaptor Protein And Arf Gtpase-Activating Protein Cat-1/Git-1 In Cellular Transformation.

Degree: PhD, Chemistry and Chemical Biology, 2012, Cornell University

 Cat-1/Git-1 is a multi-functional protein that acts as a GAP (GTPase-activating protein) for Arf GTPases, as well as serves as a scaffold for a number… (more)

Subjects/Keywords: Cat-1; Git1; transformation; paxillin; Arf GTPase

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APA (6th Edition):

Yoo, S. (2012). A Novel Role For The Adaptor Protein And Arf Gtpase-Activating Protein Cat-1/Git-1 In Cellular Transformation. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/31160

Chicago Manual of Style (16th Edition):

Yoo, Sungsoo. “A Novel Role For The Adaptor Protein And Arf Gtpase-Activating Protein Cat-1/Git-1 In Cellular Transformation.” 2012. Doctoral Dissertation, Cornell University. Accessed November 25, 2020. http://hdl.handle.net/1813/31160.

MLA Handbook (7th Edition):

Yoo, Sungsoo. “A Novel Role For The Adaptor Protein And Arf Gtpase-Activating Protein Cat-1/Git-1 In Cellular Transformation.” 2012. Web. 25 Nov 2020.

Vancouver:

Yoo S. A Novel Role For The Adaptor Protein And Arf Gtpase-Activating Protein Cat-1/Git-1 In Cellular Transformation. [Internet] [Doctoral dissertation]. Cornell University; 2012. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1813/31160.

Council of Science Editors:

Yoo S. A Novel Role For The Adaptor Protein And Arf Gtpase-Activating Protein Cat-1/Git-1 In Cellular Transformation. [Doctoral Dissertation]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/31160


Cornell University

19. Midthun, Kari. Associations Of Stim1 During Store-Operated Calcium Entry And Development Of A Novel Method For Multi-Biomolecule Patterning.

Degree: PhD, Chemistry and Chemical Biology, 2013, Cornell University

 To understand immune responses, such as asthma and allergies, we must first understand the inter- and intramolecular regulation of the signaling pathways responsible for these… (more)

Subjects/Keywords: STIM1; store-operated calcium entry; imprint lithography; multi-biomolecule patterning

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APA (6th Edition):

Midthun, K. (2013). Associations Of Stim1 During Store-Operated Calcium Entry And Development Of A Novel Method For Multi-Biomolecule Patterning. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/33889

Chicago Manual of Style (16th Edition):

Midthun, Kari. “Associations Of Stim1 During Store-Operated Calcium Entry And Development Of A Novel Method For Multi-Biomolecule Patterning.” 2013. Doctoral Dissertation, Cornell University. Accessed November 25, 2020. http://hdl.handle.net/1813/33889.

MLA Handbook (7th Edition):

Midthun, Kari. “Associations Of Stim1 During Store-Operated Calcium Entry And Development Of A Novel Method For Multi-Biomolecule Patterning.” 2013. Web. 25 Nov 2020.

Vancouver:

Midthun K. Associations Of Stim1 During Store-Operated Calcium Entry And Development Of A Novel Method For Multi-Biomolecule Patterning. [Internet] [Doctoral dissertation]. Cornell University; 2013. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1813/33889.

Council of Science Editors:

Midthun K. Associations Of Stim1 During Store-Operated Calcium Entry And Development Of A Novel Method For Multi-Biomolecule Patterning. [Doctoral Dissertation]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/33889

20. Gao, Yang. STRUCTURAL BASIS OF VERTEBRATE VISION, A G PROTEIN-COUPLED RECEPTOR SIGNALING CASCADE.

Degree: PhD, Chemistry and Chemical Biology, 2018, Cornell University

 The visual photo-transduction cascade is a prototypical G protein-coupled receptor (GPCR) signaling system, in which light-activated rhodopsin, the GPCR, catalyzes the exchange of GDP for… (more)

Subjects/Keywords: Transducin; Visual phototransduction; Biophysics; Biochemistry; Chemistry; Cryo-EM; GPCR-G protein complex; G protein-coupled receptor; Rhodopsin

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APA (6th Edition):

Gao, Y. (2018). STRUCTURAL BASIS OF VERTEBRATE VISION, A G PROTEIN-COUPLED RECEPTOR SIGNALING CASCADE. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/59736

Chicago Manual of Style (16th Edition):

Gao, Yang. “STRUCTURAL BASIS OF VERTEBRATE VISION, A G PROTEIN-COUPLED RECEPTOR SIGNALING CASCADE.” 2018. Doctoral Dissertation, Cornell University. Accessed November 25, 2020. http://hdl.handle.net/1813/59736.

MLA Handbook (7th Edition):

Gao, Yang. “STRUCTURAL BASIS OF VERTEBRATE VISION, A G PROTEIN-COUPLED RECEPTOR SIGNALING CASCADE.” 2018. Web. 25 Nov 2020.

Vancouver:

Gao Y. STRUCTURAL BASIS OF VERTEBRATE VISION, A G PROTEIN-COUPLED RECEPTOR SIGNALING CASCADE. [Internet] [Doctoral dissertation]. Cornell University; 2018. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1813/59736.

Council of Science Editors:

Gao Y. STRUCTURAL BASIS OF VERTEBRATE VISION, A G PROTEIN-COUPLED RECEPTOR SIGNALING CASCADE. [Doctoral Dissertation]. Cornell University; 2018. Available from: http://hdl.handle.net/1813/59736


Cornell University

21. Walroth, Richard Connor. Evaluating the Information Content of X-ray Spectroscopy: Structure, Covalency, and Oxidation States.

Degree: PhD, Chemistry and Chemical Biology, 2017, Cornell University

 X-ray spectroscopic methods were employed to study the electronic structure of transition metal complexes, toward rationalizing their reactivity or lack thereof. Information about the metal… (more)

Subjects/Keywords: Chemistry; Physical chemistry; Inorganic chemistry; Catalysis; Electronic structure; RIXS; XAS; XES; X-ray spectroscopy

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APA (6th Edition):

Walroth, R. C. (2017). Evaluating the Information Content of X-ray Spectroscopy: Structure, Covalency, and Oxidation States. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/56780

Chicago Manual of Style (16th Edition):

Walroth, Richard Connor. “Evaluating the Information Content of X-ray Spectroscopy: Structure, Covalency, and Oxidation States.” 2017. Doctoral Dissertation, Cornell University. Accessed November 25, 2020. http://hdl.handle.net/1813/56780.

MLA Handbook (7th Edition):

Walroth, Richard Connor. “Evaluating the Information Content of X-ray Spectroscopy: Structure, Covalency, and Oxidation States.” 2017. Web. 25 Nov 2020.

Vancouver:

Walroth RC. Evaluating the Information Content of X-ray Spectroscopy: Structure, Covalency, and Oxidation States. [Internet] [Doctoral dissertation]. Cornell University; 2017. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1813/56780.

Council of Science Editors:

Walroth RC. Evaluating the Information Content of X-ray Spectroscopy: Structure, Covalency, and Oxidation States. [Doctoral Dissertation]. Cornell University; 2017. Available from: http://hdl.handle.net/1813/56780


Cornell University

22. Gee, Kenneth. Characterization Of Transcriptional Activators In The Fungal Circadian Clock.

Degree: PhD, Chemistry and Chemical Biology, 2014, Cornell University

 Circadian clocks are a common biological feature that allows organisms to anticipate changes in their environments by synchronizing their biological activity to the Earth's day… (more)

Subjects/Keywords: White Collar; PAS

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APA (6th Edition):

Gee, K. (2014). Characterization Of Transcriptional Activators In The Fungal Circadian Clock. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/36105

Chicago Manual of Style (16th Edition):

Gee, Kenneth. “Characterization Of Transcriptional Activators In The Fungal Circadian Clock.” 2014. Doctoral Dissertation, Cornell University. Accessed November 25, 2020. http://hdl.handle.net/1813/36105.

MLA Handbook (7th Edition):

Gee, Kenneth. “Characterization Of Transcriptional Activators In The Fungal Circadian Clock.” 2014. Web. 25 Nov 2020.

Vancouver:

Gee K. Characterization Of Transcriptional Activators In The Fungal Circadian Clock. [Internet] [Doctoral dissertation]. Cornell University; 2014. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1813/36105.

Council of Science Editors:

Gee K. Characterization Of Transcriptional Activators In The Fungal Circadian Clock. [Doctoral Dissertation]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/36105


Cornell University

23. Li, Xiaoxiao. Architecture Of The Transmembrane Signaling Arrays That Regulate Bacterial Chemotaxis.

Degree: PhD, Chemistry and Chemical Biology, 2012, Cornell University

 Bacterial chemotaxis is the behavior of bacteria to swim towards favorable chemical locations, while away from unfavorable ones. The ternary complex, which is comprised of… (more)

Subjects/Keywords: bacterial chemotaxis; ternary complex; sensory; receptor; array

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APA (6th Edition):

Li, X. (2012). Architecture Of The Transmembrane Signaling Arrays That Regulate Bacterial Chemotaxis. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/31178

Chicago Manual of Style (16th Edition):

Li, Xiaoxiao. “Architecture Of The Transmembrane Signaling Arrays That Regulate Bacterial Chemotaxis.” 2012. Doctoral Dissertation, Cornell University. Accessed November 25, 2020. http://hdl.handle.net/1813/31178.

MLA Handbook (7th Edition):

Li, Xiaoxiao. “Architecture Of The Transmembrane Signaling Arrays That Regulate Bacterial Chemotaxis.” 2012. Web. 25 Nov 2020.

Vancouver:

Li X. Architecture Of The Transmembrane Signaling Arrays That Regulate Bacterial Chemotaxis. [Internet] [Doctoral dissertation]. Cornell University; 2012. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1813/31178.

Council of Science Editors:

Li X. Architecture Of The Transmembrane Signaling Arrays That Regulate Bacterial Chemotaxis. [Doctoral Dissertation]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/31178


Cornell University

24. Tse, Long Ping Victor. Sequence And Structure Of Influenza Hemagglutinin Cleavage Site Modulate Viral Pathogenesis.

Degree: PhD, Microbiology, 2014, Cornell University

 Viruses are obligatory intracellular pathogens requiring host machinery for survival and reproduction. Differing from living organisms, which can grow where nutrients are available, viruses absolutely… (more)

Subjects/Keywords: Influenza HA activation; Proteases; Pathogenesis

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APA (6th Edition):

Tse, L. P. V. (2014). Sequence And Structure Of Influenza Hemagglutinin Cleavage Site Modulate Viral Pathogenesis. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/36116

Chicago Manual of Style (16th Edition):

Tse, Long Ping Victor. “Sequence And Structure Of Influenza Hemagglutinin Cleavage Site Modulate Viral Pathogenesis.” 2014. Doctoral Dissertation, Cornell University. Accessed November 25, 2020. http://hdl.handle.net/1813/36116.

MLA Handbook (7th Edition):

Tse, Long Ping Victor. “Sequence And Structure Of Influenza Hemagglutinin Cleavage Site Modulate Viral Pathogenesis.” 2014. Web. 25 Nov 2020.

Vancouver:

Tse LPV. Sequence And Structure Of Influenza Hemagglutinin Cleavage Site Modulate Viral Pathogenesis. [Internet] [Doctoral dissertation]. Cornell University; 2014. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1813/36116.

Council of Science Editors:

Tse LPV. Sequence And Structure Of Influenza Hemagglutinin Cleavage Site Modulate Viral Pathogenesis. [Doctoral Dissertation]. Cornell University; 2014. Available from: http://hdl.handle.net/1813/36116


Cornell University

25. De, Soumya. Investigating The Role Of Pin1 And Phosphorylated Aicd In Alzheimerx19S Disease Using Nuclear Magnetic Resonance Spectroscopy, Isothermal Titration Calorimetry And Rational Design Of Small Molecules.

Degree: PhD, Biophysics, 2011, Cornell University

 Alzheimer‟s disease (AD) is a progressive neurodegenerative disorder caused by the degeneration of synapse and neuronal cell death in brain. The hallmarks of AD are… (more)

Subjects/Keywords: Alzheimers disease; nmr; itc; lineshape analysis; Pin1; kinetics; isomer specific interaction

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APA (6th Edition):

De, S. (2011). Investigating The Role Of Pin1 And Phosphorylated Aicd In Alzheimerx19S Disease Using Nuclear Magnetic Resonance Spectroscopy, Isothermal Titration Calorimetry And Rational Design Of Small Molecules. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/33610

Chicago Manual of Style (16th Edition):

De, Soumya. “Investigating The Role Of Pin1 And Phosphorylated Aicd In Alzheimerx19S Disease Using Nuclear Magnetic Resonance Spectroscopy, Isothermal Titration Calorimetry And Rational Design Of Small Molecules.” 2011. Doctoral Dissertation, Cornell University. Accessed November 25, 2020. http://hdl.handle.net/1813/33610.

MLA Handbook (7th Edition):

De, Soumya. “Investigating The Role Of Pin1 And Phosphorylated Aicd In Alzheimerx19S Disease Using Nuclear Magnetic Resonance Spectroscopy, Isothermal Titration Calorimetry And Rational Design Of Small Molecules.” 2011. Web. 25 Nov 2020.

Vancouver:

De S. Investigating The Role Of Pin1 And Phosphorylated Aicd In Alzheimerx19S Disease Using Nuclear Magnetic Resonance Spectroscopy, Isothermal Titration Calorimetry And Rational Design Of Small Molecules. [Internet] [Doctoral dissertation]. Cornell University; 2011. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1813/33610.

Council of Science Editors:

De S. Investigating The Role Of Pin1 And Phosphorylated Aicd In Alzheimerx19S Disease Using Nuclear Magnetic Resonance Spectroscopy, Isothermal Titration Calorimetry And Rational Design Of Small Molecules. [Doctoral Dissertation]. Cornell University; 2011. Available from: http://hdl.handle.net/1813/33610


Cornell University

26. Wang, Chenyue. Mechanism Of Retinal Cyclic Gmp Phosphodiesterase Activation By The Alpha Subunit Of Transducin.

Degree: PhD, Chemistry and Chemical Biology, 2015, Cornell University

 The heterotrimeric G protein, transducin, and its cognate effector, cyclic GMP (cGMP) phosphodiesterase (PDE) 6 in the vertebrate rod photoreceptors play a pivotal role in… (more)

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APA (6th Edition):

Wang, C. (2015). Mechanism Of Retinal Cyclic Gmp Phosphodiesterase Activation By The Alpha Subunit Of Transducin. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/39316

Chicago Manual of Style (16th Edition):

Wang, Chenyue. “Mechanism Of Retinal Cyclic Gmp Phosphodiesterase Activation By The Alpha Subunit Of Transducin.” 2015. Doctoral Dissertation, Cornell University. Accessed November 25, 2020. http://hdl.handle.net/1813/39316.

MLA Handbook (7th Edition):

Wang, Chenyue. “Mechanism Of Retinal Cyclic Gmp Phosphodiesterase Activation By The Alpha Subunit Of Transducin.” 2015. Web. 25 Nov 2020.

Vancouver:

Wang C. Mechanism Of Retinal Cyclic Gmp Phosphodiesterase Activation By The Alpha Subunit Of Transducin. [Internet] [Doctoral dissertation]. Cornell University; 2015. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1813/39316.

Council of Science Editors:

Wang C. Mechanism Of Retinal Cyclic Gmp Phosphodiesterase Activation By The Alpha Subunit Of Transducin. [Doctoral Dissertation]. Cornell University; 2015. Available from: http://hdl.handle.net/1813/39316


Cornell University

27. Smaldone, Gregory. A Biochemical And Genetic Investigation Of Redox-Active Transition Metal Ion Homeostasis.

Degree: PhD, Biochemistry, 2012, Cornell University

 Iron and copper are essential trace nutrients required for cell growth and proliferation. In excess, these metals pose a serious threat to the cell, either… (more)

Subjects/Keywords: iron; copper; Fur; CsoR; FsrA; sparing response; regulation

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APA (6th Edition):

Smaldone, G. (2012). A Biochemical And Genetic Investigation Of Redox-Active Transition Metal Ion Homeostasis. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/29311

Chicago Manual of Style (16th Edition):

Smaldone, Gregory. “A Biochemical And Genetic Investigation Of Redox-Active Transition Metal Ion Homeostasis.” 2012. Doctoral Dissertation, Cornell University. Accessed November 25, 2020. http://hdl.handle.net/1813/29311.

MLA Handbook (7th Edition):

Smaldone, Gregory. “A Biochemical And Genetic Investigation Of Redox-Active Transition Metal Ion Homeostasis.” 2012. Web. 25 Nov 2020.

Vancouver:

Smaldone G. A Biochemical And Genetic Investigation Of Redox-Active Transition Metal Ion Homeostasis. [Internet] [Doctoral dissertation]. Cornell University; 2012. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1813/29311.

Council of Science Editors:

Smaldone G. A Biochemical And Genetic Investigation Of Redox-Active Transition Metal Ion Homeostasis. [Doctoral Dissertation]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/29311


Cornell University

28. Bratkowski, Matthew. Biochemical Studies Of The Eukaryotic Rna Exosome.

Degree: PhD, Biophysics, 2012, Cornell University

 The RNA exosome is a multi-subunit protein complex involved in RNA maturation, surveillance, and turnover of cellular RNA. It is composed of a nine subunit… (more)

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APA (6th Edition):

Bratkowski, M. (2012). Biochemical Studies Of The Eukaryotic Rna Exosome. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/31093

Chicago Manual of Style (16th Edition):

Bratkowski, Matthew. “Biochemical Studies Of The Eukaryotic Rna Exosome.” 2012. Doctoral Dissertation, Cornell University. Accessed November 25, 2020. http://hdl.handle.net/1813/31093.

MLA Handbook (7th Edition):

Bratkowski, Matthew. “Biochemical Studies Of The Eukaryotic Rna Exosome.” 2012. Web. 25 Nov 2020.

Vancouver:

Bratkowski M. Biochemical Studies Of The Eukaryotic Rna Exosome. [Internet] [Doctoral dissertation]. Cornell University; 2012. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1813/31093.

Council of Science Editors:

Bratkowski M. Biochemical Studies Of The Eukaryotic Rna Exosome. [Doctoral Dissertation]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/31093


Cornell University

29. Kariya, Maro J. IDENTIFICATION OF SMALL MOLECULES THAT REGULATE NEMATODE – ENVIRONMENT INTERACTIONS.

Degree: PhD, Chemistry and Chemical Biology, 2019, Cornell University

 One of the central channels of nematode-environment interactions is through small molecules (non-polymeric chemical entities with a molecular mass <1000 Daltons). Nematodes release an abundance… (more)

Subjects/Keywords: Antibiotic; Avoidance; Cyclic; Predator; Sulfate; Sulfolipid

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APA (6th Edition):

Kariya, M. J. (2019). IDENTIFICATION OF SMALL MOLECULES THAT REGULATE NEMATODE – ENVIRONMENT INTERACTIONS. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/69994

Chicago Manual of Style (16th Edition):

Kariya, Maro J. “IDENTIFICATION OF SMALL MOLECULES THAT REGULATE NEMATODE – ENVIRONMENT INTERACTIONS.” 2019. Doctoral Dissertation, Cornell University. Accessed November 25, 2020. http://hdl.handle.net/1813/69994.

MLA Handbook (7th Edition):

Kariya, Maro J. “IDENTIFICATION OF SMALL MOLECULES THAT REGULATE NEMATODE – ENVIRONMENT INTERACTIONS.” 2019. Web. 25 Nov 2020.

Vancouver:

Kariya MJ. IDENTIFICATION OF SMALL MOLECULES THAT REGULATE NEMATODE – ENVIRONMENT INTERACTIONS. [Internet] [Doctoral dissertation]. Cornell University; 2019. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1813/69994.

Council of Science Editors:

Kariya MJ. IDENTIFICATION OF SMALL MOLECULES THAT REGULATE NEMATODE – ENVIRONMENT INTERACTIONS. [Doctoral Dissertation]. Cornell University; 2019. Available from: http://hdl.handle.net/1813/69994


Cornell University

30. Krasteva, Petya. Identification And Structure-Function Analyses Of Bacterial C-Di-Gmp Receptors.

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

 In recent years a novel, nucleotide-based small molecule, c-di-GMP, has emerged in the spotlight of scientific investigation as a second messenger unique to the bacterial… (more)

Subjects/Keywords: Bacteria; biofilm; persistence; second messenger; c-di-GMP; receptors; structure; mechanism

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APA (6th Edition):

Krasteva, P. (2011). Identification And Structure-Function Analyses Of Bacterial C-Di-Gmp Receptors. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/33598

Chicago Manual of Style (16th Edition):

Krasteva, Petya. “Identification And Structure-Function Analyses Of Bacterial C-Di-Gmp Receptors.” 2011. Doctoral Dissertation, Cornell University. Accessed November 25, 2020. http://hdl.handle.net/1813/33598.

MLA Handbook (7th Edition):

Krasteva, Petya. “Identification And Structure-Function Analyses Of Bacterial C-Di-Gmp Receptors.” 2011. Web. 25 Nov 2020.

Vancouver:

Krasteva P. Identification And Structure-Function Analyses Of Bacterial C-Di-Gmp Receptors. [Internet] [Doctoral dissertation]. Cornell University; 2011. [cited 2020 Nov 25]. Available from: http://hdl.handle.net/1813/33598.

Council of Science Editors:

Krasteva P. Identification And Structure-Function Analyses Of Bacterial C-Di-Gmp Receptors. [Doctoral Dissertation]. Cornell University; 2011. Available from: http://hdl.handle.net/1813/33598

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