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You searched for +publisher:"Texas A&M University" +contributor:("Liu, Wenshe"). Showing records 1 – 26 of 26 total matches.

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Texas A&M University

1. Deonarine-Chihak, Sasha Mala. A Tetrazine-Terminal Alkene System for Profiling Protein Fatty Acylation Modifications.

Degree: MS, Chemistry, 2016, Texas A&M University

 Protein fatty acylation is included in the class of modifications where attachment via an acyl linkage is employed including myristoylation and palmitoylation. This work focuses… (more)

Subjects/Keywords: Tetrazine; Fatty Acid Modification; inverse electron demand; Diels Alder cycloaddition

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APA (6th Edition):

Deonarine-Chihak, S. M. (2016). A Tetrazine-Terminal Alkene System for Profiling Protein Fatty Acylation Modifications. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/158940

Chicago Manual of Style (16th Edition):

Deonarine-Chihak, Sasha Mala. “A Tetrazine-Terminal Alkene System for Profiling Protein Fatty Acylation Modifications.” 2016. Masters Thesis, Texas A&M University. Accessed May 11, 2021. http://hdl.handle.net/1969.1/158940.

MLA Handbook (7th Edition):

Deonarine-Chihak, Sasha Mala. “A Tetrazine-Terminal Alkene System for Profiling Protein Fatty Acylation Modifications.” 2016. Web. 11 May 2021.

Vancouver:

Deonarine-Chihak SM. A Tetrazine-Terminal Alkene System for Profiling Protein Fatty Acylation Modifications. [Internet] [Masters thesis]. Texas A&M University; 2016. [cited 2021 May 11]. Available from: http://hdl.handle.net/1969.1/158940.

Council of Science Editors:

Deonarine-Chihak SM. A Tetrazine-Terminal Alkene System for Profiling Protein Fatty Acylation Modifications. [Masters Thesis]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/158940


Texas A&M University

2. Sharma, Vangmayee. The Engineering and Optimization of Pyrrolysyl-Synthetase as a Tool for Noncanonical Amino Acid Incorporation.

Degree: PhD, Chemistry, 2017, Texas A&M University

 Since the discovery of pyrrolysine as the 22nd amino acid, the field of chemical biology has expanded tremendously with important developments made in genetic noncanonical… (more)

Subjects/Keywords: Noncanonical Amino Acid; Pyrrolysyl-synthetase; Histidine mimetics

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APA (6th Edition):

Sharma, V. (2017). The Engineering and Optimization of Pyrrolysyl-Synthetase as a Tool for Noncanonical Amino Acid Incorporation. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/165910

Chicago Manual of Style (16th Edition):

Sharma, Vangmayee. “The Engineering and Optimization of Pyrrolysyl-Synthetase as a Tool for Noncanonical Amino Acid Incorporation.” 2017. Doctoral Dissertation, Texas A&M University. Accessed May 11, 2021. http://hdl.handle.net/1969.1/165910.

MLA Handbook (7th Edition):

Sharma, Vangmayee. “The Engineering and Optimization of Pyrrolysyl-Synthetase as a Tool for Noncanonical Amino Acid Incorporation.” 2017. Web. 11 May 2021.

Vancouver:

Sharma V. The Engineering and Optimization of Pyrrolysyl-Synthetase as a Tool for Noncanonical Amino Acid Incorporation. [Internet] [Doctoral dissertation]. Texas A&M University; 2017. [cited 2021 May 11]. Available from: http://hdl.handle.net/1969.1/165910.

Council of Science Editors:

Sharma V. The Engineering and Optimization of Pyrrolysyl-Synthetase as a Tool for Noncanonical Amino Acid Incorporation. [Doctoral Dissertation]. Texas A&M University; 2017. Available from: http://hdl.handle.net/1969.1/165910


Texas A&M University

3. Odoi, Keturah Amarkie. Protein Engineering: Amending Proteins with Chemical Functionalities.

Degree: PhD, Chemistry, 2016, Texas A&M University

 Directly incorporating noncanonical amino acids (NCAAs) into proteins in living cells is an indispensible technique for investigating structures and functions of proteins. This co-translational insertion… (more)

Subjects/Keywords: Posttranslational modifications; Noncanonical amino acids; Pyrrolysine

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APA (6th Edition):

Odoi, K. A. (2016). Protein Engineering: Amending Proteins with Chemical Functionalities. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/174261

Chicago Manual of Style (16th Edition):

Odoi, Keturah Amarkie. “Protein Engineering: Amending Proteins with Chemical Functionalities.” 2016. Doctoral Dissertation, Texas A&M University. Accessed May 11, 2021. http://hdl.handle.net/1969.1/174261.

MLA Handbook (7th Edition):

Odoi, Keturah Amarkie. “Protein Engineering: Amending Proteins with Chemical Functionalities.” 2016. Web. 11 May 2021.

Vancouver:

Odoi KA. Protein Engineering: Amending Proteins with Chemical Functionalities. [Internet] [Doctoral dissertation]. Texas A&M University; 2016. [cited 2021 May 11]. Available from: http://hdl.handle.net/1969.1/174261.

Council of Science Editors:

Odoi KA. Protein Engineering: Amending Proteins with Chemical Functionalities. [Doctoral Dissertation]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/174261


Texas A&M University

4. Wang, Xiaoshan. The Nitrilimine-Alkene Cycloaddition Mechanism and Phage-displayed Cyclic Peptide Libraries for Drug Discovery.

Degree: PhD, Chemistry, 2018, Texas A&M University

 This study is composed of two parts. In the first part, we discussed nitrilimine-alkene cycloaddition for protein labeling. The mechanism of this nitrilimine-alkene cycloaddition was… (more)

Subjects/Keywords: nitrilimine-alkene cycloaddition; cyclic peptide; HDAC8 inhibitor

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APA (6th Edition):

Wang, X. (2018). The Nitrilimine-Alkene Cycloaddition Mechanism and Phage-displayed Cyclic Peptide Libraries for Drug Discovery. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/173491

Chicago Manual of Style (16th Edition):

Wang, Xiaoshan. “The Nitrilimine-Alkene Cycloaddition Mechanism and Phage-displayed Cyclic Peptide Libraries for Drug Discovery.” 2018. Doctoral Dissertation, Texas A&M University. Accessed May 11, 2021. http://hdl.handle.net/1969.1/173491.

MLA Handbook (7th Edition):

Wang, Xiaoshan. “The Nitrilimine-Alkene Cycloaddition Mechanism and Phage-displayed Cyclic Peptide Libraries for Drug Discovery.” 2018. Web. 11 May 2021.

Vancouver:

Wang X. The Nitrilimine-Alkene Cycloaddition Mechanism and Phage-displayed Cyclic Peptide Libraries for Drug Discovery. [Internet] [Doctoral dissertation]. Texas A&M University; 2018. [cited 2021 May 11]. Available from: http://hdl.handle.net/1969.1/173491.

Council of Science Editors:

Wang X. The Nitrilimine-Alkene Cycloaddition Mechanism and Phage-displayed Cyclic Peptide Libraries for Drug Discovery. [Doctoral Dissertation]. Texas A&M University; 2018. Available from: http://hdl.handle.net/1969.1/173491


Texas A&M University

5. Fox, Nicholas G. A Biophysical Approach to Investigate the Human Fe-S Cluster Assembly Pathway.

Degree: PhD, Chemistry, 2014, Texas A&M University

 Iron sulfur (Fe-S) clusters are essential cofactors that function in electron transport, catalyzing substrate turnover, environmental sensing, and initiating radical chemistry. Elaborate multi-component systems have… (more)

Subjects/Keywords: Fe-S

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APA (6th Edition):

Fox, N. G. (2014). A Biophysical Approach to Investigate the Human Fe-S Cluster Assembly Pathway. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/153303

Chicago Manual of Style (16th Edition):

Fox, Nicholas G. “A Biophysical Approach to Investigate the Human Fe-S Cluster Assembly Pathway.” 2014. Doctoral Dissertation, Texas A&M University. Accessed May 11, 2021. http://hdl.handle.net/1969.1/153303.

MLA Handbook (7th Edition):

Fox, Nicholas G. “A Biophysical Approach to Investigate the Human Fe-S Cluster Assembly Pathway.” 2014. Web. 11 May 2021.

Vancouver:

Fox NG. A Biophysical Approach to Investigate the Human Fe-S Cluster Assembly Pathway. [Internet] [Doctoral dissertation]. Texas A&M University; 2014. [cited 2021 May 11]. Available from: http://hdl.handle.net/1969.1/153303.

Council of Science Editors:

Fox NG. A Biophysical Approach to Investigate the Human Fe-S Cluster Assembly Pathway. [Doctoral Dissertation]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/153303


Texas A&M University

6. Erazo, Alfredo. Cytosolic Delivery of Proteins, Peptides and Cell-Impermeable Small Molecules Into Live Cells Utilizing Virus-Inspired Multivalent Cell-Penetrating Peptides: Principles and Mechanisms.

Degree: PhD, Biochemistry, 2014, Texas A&M University

 Cell-penetrating peptides (CPPs) facilitate the delivery of cell-impermeable macrmolecules across the plasma membrane of live cells. CPPs act as biological Trojan horses by hijacking and… (more)

Subjects/Keywords: protein delivery; cell-penetrating peptides

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APA (6th Edition):

Erazo, A. (2014). Cytosolic Delivery of Proteins, Peptides and Cell-Impermeable Small Molecules Into Live Cells Utilizing Virus-Inspired Multivalent Cell-Penetrating Peptides: Principles and Mechanisms. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/154025

Chicago Manual of Style (16th Edition):

Erazo, Alfredo. “Cytosolic Delivery of Proteins, Peptides and Cell-Impermeable Small Molecules Into Live Cells Utilizing Virus-Inspired Multivalent Cell-Penetrating Peptides: Principles and Mechanisms.” 2014. Doctoral Dissertation, Texas A&M University. Accessed May 11, 2021. http://hdl.handle.net/1969.1/154025.

MLA Handbook (7th Edition):

Erazo, Alfredo. “Cytosolic Delivery of Proteins, Peptides and Cell-Impermeable Small Molecules Into Live Cells Utilizing Virus-Inspired Multivalent Cell-Penetrating Peptides: Principles and Mechanisms.” 2014. Web. 11 May 2021.

Vancouver:

Erazo A. Cytosolic Delivery of Proteins, Peptides and Cell-Impermeable Small Molecules Into Live Cells Utilizing Virus-Inspired Multivalent Cell-Penetrating Peptides: Principles and Mechanisms. [Internet] [Doctoral dissertation]. Texas A&M University; 2014. [cited 2021 May 11]. Available from: http://hdl.handle.net/1969.1/154025.

Council of Science Editors:

Erazo A. Cytosolic Delivery of Proteins, Peptides and Cell-Impermeable Small Molecules Into Live Cells Utilizing Virus-Inspired Multivalent Cell-Penetrating Peptides: Principles and Mechanisms. [Doctoral Dissertation]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/154025


Texas A&M University

7. Lee, Youngbok. Application of Dissolution Dynamic Nuclear Polarization to the Characterization of Reactions Involving Large Molecules.

Degree: PhD, Chemistry, 2013, Texas A&M University

 Nuclear magnetic resonance (NMR) spectroscopy is one of the most important analytical tools for organic and biological chemistry. It provides not only detailed information on… (more)

Subjects/Keywords: NMR; DNP

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APA (6th Edition):

Lee, Y. (2013). Application of Dissolution Dynamic Nuclear Polarization to the Characterization of Reactions Involving Large Molecules. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/149344

Chicago Manual of Style (16th Edition):

Lee, Youngbok. “Application of Dissolution Dynamic Nuclear Polarization to the Characterization of Reactions Involving Large Molecules.” 2013. Doctoral Dissertation, Texas A&M University. Accessed May 11, 2021. http://hdl.handle.net/1969.1/149344.

MLA Handbook (7th Edition):

Lee, Youngbok. “Application of Dissolution Dynamic Nuclear Polarization to the Characterization of Reactions Involving Large Molecules.” 2013. Web. 11 May 2021.

Vancouver:

Lee Y. Application of Dissolution Dynamic Nuclear Polarization to the Characterization of Reactions Involving Large Molecules. [Internet] [Doctoral dissertation]. Texas A&M University; 2013. [cited 2021 May 11]. Available from: http://hdl.handle.net/1969.1/149344.

Council of Science Editors:

Lee Y. Application of Dissolution Dynamic Nuclear Polarization to the Characterization of Reactions Involving Large Molecules. [Doctoral Dissertation]. Texas A&M University; 2013. Available from: http://hdl.handle.net/1969.1/149344


Texas A&M University

8. Tuvilla, Mavreen Rose. Enzymatic Digestion in Aqueous-Organic Solvents: A Mass Spectrometry-Based Approach in Monitoring Protein Conformation Changes.

Degree: MS, Chemistry, 2013, Texas A&M University

 The three dimensional structure of a protein is important for its function. When misfolded, a protein may be rendered inactive or adapt a conformation that… (more)

Subjects/Keywords: Mass Spectrometry; Protein Conformation

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APA (6th Edition):

Tuvilla, M. R. (2013). Enzymatic Digestion in Aqueous-Organic Solvents: A Mass Spectrometry-Based Approach in Monitoring Protein Conformation Changes. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/149503

Chicago Manual of Style (16th Edition):

Tuvilla, Mavreen Rose. “Enzymatic Digestion in Aqueous-Organic Solvents: A Mass Spectrometry-Based Approach in Monitoring Protein Conformation Changes.” 2013. Masters Thesis, Texas A&M University. Accessed May 11, 2021. http://hdl.handle.net/1969.1/149503.

MLA Handbook (7th Edition):

Tuvilla, Mavreen Rose. “Enzymatic Digestion in Aqueous-Organic Solvents: A Mass Spectrometry-Based Approach in Monitoring Protein Conformation Changes.” 2013. Web. 11 May 2021.

Vancouver:

Tuvilla MR. Enzymatic Digestion in Aqueous-Organic Solvents: A Mass Spectrometry-Based Approach in Monitoring Protein Conformation Changes. [Internet] [Masters thesis]. Texas A&M University; 2013. [cited 2021 May 11]. Available from: http://hdl.handle.net/1969.1/149503.

Council of Science Editors:

Tuvilla MR. Enzymatic Digestion in Aqueous-Organic Solvents: A Mass Spectrometry-Based Approach in Monitoring Protein Conformation Changes. [Masters Thesis]. Texas A&M University; 2013. Available from: http://hdl.handle.net/1969.1/149503


Texas A&M University

9. Odoi, Keturah. Orthogonality and Codon Preference of the Pyrrolysyl-tRNA Synthetase-tRNAPyl pair in Escherichia coli for the Genetic Code Expansion.

Degree: MS, Chemistry, 2012, Texas A&M University

 Systematic studies of basal nonsense suppression, orthogonality of tRNAPyl variants, and cross recognition between codons and tRNA anticodons are reported. E. coli displays detectable basal… (more)

Subjects/Keywords: Pyl, pyrrolysine; PylRS, pyrrolysyl-tRNA synthetase; NAA, noncanonical amino acid; BocK, Ntert-butyloxycarbonyl)-L-lysine; aaRS, aminoacyl-tRNA synthetase; MjTyrRS, Methanococcus jannaschii tyrosyl-tRNA synthetase; T4 PNK, T4 polynucleotide kinase; AzF, para-azido-L-phenylalanine; ESI-MS, electrospray ionization mass spectrometry; PCR, polymerase chain reaction; sfGFP, superfolder green fluorescent protein; sfGFP134TAG, the sfGFP gene with an amber mutation at N134 and a 6×His tag at its C-terminus; sfGFP134TGA,the sfGFP gene with an opal mutation at N134 and a 6×His tag at its C-terminus; sfGFP134TAA,the sfGFP gene with an ochre mutation at N134 and a 6×His tag at its C-terminus; sfGFP134AGGA,the sfGFP gene with an quadruple AGGA mutation at N134 and a 6×His tag at its C-terminus; sfGFP2TAG134TAA, the sfGFP gene with an amber mutation at S2, an ochre mutation at N134, and a 6×His tag at its C-terminus; sfGFP2TGA, the sfGFP gene with an opal mutation at S2 and a 6×His tag at its C-terminus; IPTG, isopropyl -D-thiogalactopyranoside; RF, release factor; TrpRS, tryptophanyl-tRNA synthetase; ArgRS, arginyl-tRNA synthetase; Trp, tryptophan; Lys, lysine; Glu, glutamate; Gln, glutamine; Phe, phenylalanine; Arg, arginine.

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APA (6th Edition):

Odoi, K. (2012). Orthogonality and Codon Preference of the Pyrrolysyl-tRNA Synthetase-tRNAPyl pair in Escherichia coli for the Genetic Code Expansion. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-11037

Chicago Manual of Style (16th Edition):

Odoi, Keturah. “Orthogonality and Codon Preference of the Pyrrolysyl-tRNA Synthetase-tRNAPyl pair in Escherichia coli for the Genetic Code Expansion.” 2012. Masters Thesis, Texas A&M University. Accessed May 11, 2021. http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-11037.

MLA Handbook (7th Edition):

Odoi, Keturah. “Orthogonality and Codon Preference of the Pyrrolysyl-tRNA Synthetase-tRNAPyl pair in Escherichia coli for the Genetic Code Expansion.” 2012. Web. 11 May 2021.

Vancouver:

Odoi K. Orthogonality and Codon Preference of the Pyrrolysyl-tRNA Synthetase-tRNAPyl pair in Escherichia coli for the Genetic Code Expansion. [Internet] [Masters thesis]. Texas A&M University; 2012. [cited 2021 May 11]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-11037.

Council of Science Editors:

Odoi K. Orthogonality and Codon Preference of the Pyrrolysyl-tRNA Synthetase-tRNAPyl pair in Escherichia coli for the Genetic Code Expansion. [Masters Thesis]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-11037


Texas A&M University

10. Wang, Zhipeng. The Chemical Synthetic Investigation of Proteins with Sitespecific Lysine Post-Translational Modifications.

Degree: PhD, Chemistry, 2018, Texas A&M University

 In the recent decade, an increasing amount of protein post-translational modifications (PTMs) have been discovered, which are important epigenetic markers widespread on nucleic and cytoplasmic… (more)

Subjects/Keywords: Protein chemical biology; Post-translational modification; Lysine; noncanonical amino acids

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APA (6th Edition):

Wang, Z. (2018). The Chemical Synthetic Investigation of Proteins with Sitespecific Lysine Post-Translational Modifications. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/173444

Chicago Manual of Style (16th Edition):

Wang, Zhipeng. “The Chemical Synthetic Investigation of Proteins with Sitespecific Lysine Post-Translational Modifications.” 2018. Doctoral Dissertation, Texas A&M University. Accessed May 11, 2021. http://hdl.handle.net/1969.1/173444.

MLA Handbook (7th Edition):

Wang, Zhipeng. “The Chemical Synthetic Investigation of Proteins with Sitespecific Lysine Post-Translational Modifications.” 2018. Web. 11 May 2021.

Vancouver:

Wang Z. The Chemical Synthetic Investigation of Proteins with Sitespecific Lysine Post-Translational Modifications. [Internet] [Doctoral dissertation]. Texas A&M University; 2018. [cited 2021 May 11]. Available from: http://hdl.handle.net/1969.1/173444.

Council of Science Editors:

Wang Z. The Chemical Synthetic Investigation of Proteins with Sitespecific Lysine Post-Translational Modifications. [Doctoral Dissertation]. Texas A&M University; 2018. Available from: http://hdl.handle.net/1969.1/173444


Texas A&M University

11. Collins, Sean Christopher. Mechanistic Investigation into the Sommelet-Hauser Rearrangement of an Allyl Ammonium Ylide Through Determination of 13C KIEs.

Degree: MS, Chemistry, 2011, Texas A&M University

 The [2,3]-sigmatropic rearrangement is a pericyclic reaction of great synthetic utility to organic chemists. Within the scope of this reaction exist some cases in which… (more)

Subjects/Keywords: Kinetic Isotope Effects; KIEs; Mechanistic; Physical Organic; [2,3]-Sigmatropic Rearrangement; Sommelet-Hauser; Ammonium Ylide; Dynamic Effects; DFT; Theoretical Calculations

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APA (6th Edition):

Collins, S. C. (2011). Mechanistic Investigation into the Sommelet-Hauser Rearrangement of an Allyl Ammonium Ylide Through Determination of 13C KIEs. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8231

Chicago Manual of Style (16th Edition):

Collins, Sean Christopher. “Mechanistic Investigation into the Sommelet-Hauser Rearrangement of an Allyl Ammonium Ylide Through Determination of 13C KIEs.” 2011. Masters Thesis, Texas A&M University. Accessed May 11, 2021. http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8231.

MLA Handbook (7th Edition):

Collins, Sean Christopher. “Mechanistic Investigation into the Sommelet-Hauser Rearrangement of an Allyl Ammonium Ylide Through Determination of 13C KIEs.” 2011. Web. 11 May 2021.

Vancouver:

Collins SC. Mechanistic Investigation into the Sommelet-Hauser Rearrangement of an Allyl Ammonium Ylide Through Determination of 13C KIEs. [Internet] [Masters thesis]. Texas A&M University; 2011. [cited 2021 May 11]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8231.

Council of Science Editors:

Collins SC. Mechanistic Investigation into the Sommelet-Hauser Rearrangement of an Allyl Ammonium Ylide Through Determination of 13C KIEs. [Masters Thesis]. Texas A&M University; 2011. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8231


Texas A&M University

12. Liu, Yiquan. Development of Chemical Strategies for Specifically Probing and Identifying Sulfur Carrier Proteins and Vitamin B6-Dependent Enzymes in Bacteria.

Degree: PhD, Chemistry, 2015, Texas A&M University

 Activity based protein profiling (ABPP) is a functional proteomic technology that uses chemical probes to detect mechanistically related classes of enzymes. Chemically probing a certain… (more)

Subjects/Keywords: Activity based protein profiling; chemical probe; sulfur carrier protein; PLP-dependent enzymes

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APA (6th Edition):

Liu, Y. (2015). Development of Chemical Strategies for Specifically Probing and Identifying Sulfur Carrier Proteins and Vitamin B6-Dependent Enzymes in Bacteria. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/156431

Chicago Manual of Style (16th Edition):

Liu, Yiquan. “Development of Chemical Strategies for Specifically Probing and Identifying Sulfur Carrier Proteins and Vitamin B6-Dependent Enzymes in Bacteria.” 2015. Doctoral Dissertation, Texas A&M University. Accessed May 11, 2021. http://hdl.handle.net/1969.1/156431.

MLA Handbook (7th Edition):

Liu, Yiquan. “Development of Chemical Strategies for Specifically Probing and Identifying Sulfur Carrier Proteins and Vitamin B6-Dependent Enzymes in Bacteria.” 2015. Web. 11 May 2021.

Vancouver:

Liu Y. Development of Chemical Strategies for Specifically Probing and Identifying Sulfur Carrier Proteins and Vitamin B6-Dependent Enzymes in Bacteria. [Internet] [Doctoral dissertation]. Texas A&M University; 2015. [cited 2021 May 11]. Available from: http://hdl.handle.net/1969.1/156431.

Council of Science Editors:

Liu Y. Development of Chemical Strategies for Specifically Probing and Identifying Sulfur Carrier Proteins and Vitamin B6-Dependent Enzymes in Bacteria. [Doctoral Dissertation]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/156431


Texas A&M University

13. Tuley, Alfred. Expanding the Genetic Code to Probe Biological Systems.

Degree: PhD, Chemistry, 2015, Texas A&M University

 The chemical modification of proteins has been a longstanding interest in the scientific community. In addition to the natural modifications necessary for life to function,… (more)

Subjects/Keywords: Genetic Code Expansion; Pyrrolysine; Phenylalanine; Non-Canonical Amino Acids; Aldehyde; Click Chemistry; Phage Display

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APA (6th Edition):

Tuley, A. (2015). Expanding the Genetic Code to Probe Biological Systems. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/187469

Chicago Manual of Style (16th Edition):

Tuley, Alfred. “Expanding the Genetic Code to Probe Biological Systems.” 2015. Doctoral Dissertation, Texas A&M University. Accessed May 11, 2021. http://hdl.handle.net/1969.1/187469.

MLA Handbook (7th Edition):

Tuley, Alfred. “Expanding the Genetic Code to Probe Biological Systems.” 2015. Web. 11 May 2021.

Vancouver:

Tuley A. Expanding the Genetic Code to Probe Biological Systems. [Internet] [Doctoral dissertation]. Texas A&M University; 2015. [cited 2021 May 11]. Available from: http://hdl.handle.net/1969.1/187469.

Council of Science Editors:

Tuley A. Expanding the Genetic Code to Probe Biological Systems. [Doctoral Dissertation]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/187469


Texas A&M University

14. Wang, Yane-Shih 1977-. Expanding Genetic Code for Protein Lysine and Phenylalanine Modifications.

Degree: PhD, Chemistry, 2012, Texas A&M University

 The naturally occurring pyrrolysine (Pyl) incorporation machinery was discovered in methanogenic archaea and some bacteria. In these organisms, Pyl is cotranslationally inserted into proteins and… (more)

Subjects/Keywords: Protein labeling; Protein folding; Histones; Protein post-translational modifications; Amber codon suppression; Pyrrolysyl-tRNA synthetase

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APA (6th Edition):

Wang, Y. 1. (2012). Expanding Genetic Code for Protein Lysine and Phenylalanine Modifications. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/153198

Chicago Manual of Style (16th Edition):

Wang, Yane-Shih 1977-. “Expanding Genetic Code for Protein Lysine and Phenylalanine Modifications.” 2012. Doctoral Dissertation, Texas A&M University. Accessed May 11, 2021. http://hdl.handle.net/1969.1/153198.

MLA Handbook (7th Edition):

Wang, Yane-Shih 1977-. “Expanding Genetic Code for Protein Lysine and Phenylalanine Modifications.” 2012. Web. 11 May 2021.

Vancouver:

Wang Y1. Expanding Genetic Code for Protein Lysine and Phenylalanine Modifications. [Internet] [Doctoral dissertation]. Texas A&M University; 2012. [cited 2021 May 11]. Available from: http://hdl.handle.net/1969.1/153198.

Council of Science Editors:

Wang Y1. Expanding Genetic Code for Protein Lysine and Phenylalanine Modifications. [Doctoral Dissertation]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/153198


Texas A&M University

15. Wu, Bo. Synthesis of Proteins with Homogenous Chemical and Posttranslational Modifications.

Degree: PhD, Chemistry, 2014, Texas A&M University

 Genetic encoding non-canonical amino acids (NCAAs) is a facile approach to synthesize proteins with homogenous modifications. In my graduate study, I demonstrated the application of… (more)

Subjects/Keywords: Genetic incorporation; non-canonical amino acids; epigenetic

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APA (6th Edition):

Wu, B. (2014). Synthesis of Proteins with Homogenous Chemical and Posttranslational Modifications. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/153253

Chicago Manual of Style (16th Edition):

Wu, Bo. “Synthesis of Proteins with Homogenous Chemical and Posttranslational Modifications.” 2014. Doctoral Dissertation, Texas A&M University. Accessed May 11, 2021. http://hdl.handle.net/1969.1/153253.

MLA Handbook (7th Edition):

Wu, Bo. “Synthesis of Proteins with Homogenous Chemical and Posttranslational Modifications.” 2014. Web. 11 May 2021.

Vancouver:

Wu B. Synthesis of Proteins with Homogenous Chemical and Posttranslational Modifications. [Internet] [Doctoral dissertation]. Texas A&M University; 2014. [cited 2021 May 11]. Available from: http://hdl.handle.net/1969.1/153253.

Council of Science Editors:

Wu B. Synthesis of Proteins with Homogenous Chemical and Posttranslational Modifications. [Doctoral Dissertation]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/153253


Texas A&M University

16. Vladimirova, Anna V. Enzymes in COG2159 of the Amidohydrolase Superfamily: Structure and Mechanism of 5-Carboxyvanillate Decarboxylase (LIGW).

Degree: PhD, Chemistry, 2015, Texas A&M University

 COG2159 of the Amidohydrolase Superfamily (AHS) is composed of a wide range of enzymes, which catalyze hydration, hydrolysis, and decarboxylation reactions. 5-Carboxyvanillate decarboxylase (LigW) belongs… (more)

Subjects/Keywords: Enzymes; COG2159; Amidohydrolase Superfamily; 5-Carboxyvanillate Decarboxylase (LigW); Lignin

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APA (6th Edition):

Vladimirova, A. V. (2015). Enzymes in COG2159 of the Amidohydrolase Superfamily: Structure and Mechanism of 5-Carboxyvanillate Decarboxylase (LIGW). (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/155024

Chicago Manual of Style (16th Edition):

Vladimirova, Anna V. “Enzymes in COG2159 of the Amidohydrolase Superfamily: Structure and Mechanism of 5-Carboxyvanillate Decarboxylase (LIGW).” 2015. Doctoral Dissertation, Texas A&M University. Accessed May 11, 2021. http://hdl.handle.net/1969.1/155024.

MLA Handbook (7th Edition):

Vladimirova, Anna V. “Enzymes in COG2159 of the Amidohydrolase Superfamily: Structure and Mechanism of 5-Carboxyvanillate Decarboxylase (LIGW).” 2015. Web. 11 May 2021.

Vancouver:

Vladimirova AV. Enzymes in COG2159 of the Amidohydrolase Superfamily: Structure and Mechanism of 5-Carboxyvanillate Decarboxylase (LIGW). [Internet] [Doctoral dissertation]. Texas A&M University; 2015. [cited 2021 May 11]. Available from: http://hdl.handle.net/1969.1/155024.

Council of Science Editors:

Vladimirova AV. Enzymes in COG2159 of the Amidohydrolase Superfamily: Structure and Mechanism of 5-Carboxyvanillate Decarboxylase (LIGW). [Doctoral Dissertation]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/155024


Texas A&M University

17. Huang, Ying. Genetic Incorporation of Noncanonical Amino Acids into Proteins for Protein Function Investigation.

Degree: PhD, Chemistry, 2012, Texas A&M University

 With the objective to functionalize proteins for the understanding of their biological roles and developing protein-based biosensors, I have been developing methods to synthesize proteins… (more)

Subjects/Keywords: Noncanonical Amino Acids; PylRS

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APA (6th Edition):

Huang, Y. (2012). Genetic Incorporation of Noncanonical Amino Acids into Proteins for Protein Function Investigation. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-10730

Chicago Manual of Style (16th Edition):

Huang, Ying. “Genetic Incorporation of Noncanonical Amino Acids into Proteins for Protein Function Investigation.” 2012. Doctoral Dissertation, Texas A&M University. Accessed May 11, 2021. http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-10730.

MLA Handbook (7th Edition):

Huang, Ying. “Genetic Incorporation of Noncanonical Amino Acids into Proteins for Protein Function Investigation.” 2012. Web. 11 May 2021.

Vancouver:

Huang Y. Genetic Incorporation of Noncanonical Amino Acids into Proteins for Protein Function Investigation. [Internet] [Doctoral dissertation]. Texas A&M University; 2012. [cited 2021 May 11]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-10730.

Council of Science Editors:

Huang Y. Genetic Incorporation of Noncanonical Amino Acids into Proteins for Protein Function Investigation. [Doctoral Dissertation]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2012-05-10730


Texas A&M University

18. Agbo, Hillary. Functional Characterization of Azinomycin Biosynthetic Enzymes.

Degree: PhD, Chemistry, 2012, Texas A&M University

 Azinomycins A and B are antitumor compounds isolated from soil bacteria, Streptomyces sahachiroi. The azinomycin structure contains an unusual aziridine [1,2a] pyrrolidine ring and an… (more)

Subjects/Keywords: Azinomycin; lysW

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APA (6th Edition):

Agbo, H. (2012). Functional Characterization of Azinomycin Biosynthetic Enzymes. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11701

Chicago Manual of Style (16th Edition):

Agbo, Hillary. “Functional Characterization of Azinomycin Biosynthetic Enzymes.” 2012. Doctoral Dissertation, Texas A&M University. Accessed May 11, 2021. http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11701.

MLA Handbook (7th Edition):

Agbo, Hillary. “Functional Characterization of Azinomycin Biosynthetic Enzymes.” 2012. Web. 11 May 2021.

Vancouver:

Agbo H. Functional Characterization of Azinomycin Biosynthetic Enzymes. [Internet] [Doctoral dissertation]. Texas A&M University; 2012. [cited 2021 May 11]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11701.

Council of Science Editors:

Agbo H. Functional Characterization of Azinomycin Biosynthetic Enzymes. [Doctoral Dissertation]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11701


Texas A&M University

19. Aguirre-Flores, Jessica Dafhne. Structure Property Relationships for Dirhodium Antitumor Active Compounds: Reactions with Biomolecules and In Cellulo Studies.

Degree: PhD, Chemistry, 2011, Texas A&M University

 The molecular characteristics that affect the activity of various dirhodium complexes are reported. The importance of the axial position in the action of dirhodium compounds… (more)

Subjects/Keywords: Dirhodium complexes; anticancer compounds; metal-metal bonded complexes; HeLa cells; COLO-316 cells; comet assay

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APA (6th Edition):

Aguirre-Flores, J. D. (2011). Structure Property Relationships for Dirhodium Antitumor Active Compounds: Reactions with Biomolecules and In Cellulo Studies. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7614

Chicago Manual of Style (16th Edition):

Aguirre-Flores, Jessica Dafhne. “Structure Property Relationships for Dirhodium Antitumor Active Compounds: Reactions with Biomolecules and In Cellulo Studies.” 2011. Doctoral Dissertation, Texas A&M University. Accessed May 11, 2021. http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7614.

MLA Handbook (7th Edition):

Aguirre-Flores, Jessica Dafhne. “Structure Property Relationships for Dirhodium Antitumor Active Compounds: Reactions with Biomolecules and In Cellulo Studies.” 2011. Web. 11 May 2021.

Vancouver:

Aguirre-Flores JD. Structure Property Relationships for Dirhodium Antitumor Active Compounds: Reactions with Biomolecules and In Cellulo Studies. [Internet] [Doctoral dissertation]. Texas A&M University; 2011. [cited 2021 May 11]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7614.

Council of Science Editors:

Aguirre-Flores JD. Structure Property Relationships for Dirhodium Antitumor Active Compounds: Reactions with Biomolecules and In Cellulo Studies. [Doctoral Dissertation]. Texas A&M University; 2011. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7614


Texas A&M University

20. Lai, Rung Yi. The Mechanistic Investigation of the Bacterial Thiamin Thiazole Synthase and the Eukaryotic Thiamin Pyrimidine Synthase.

Degree: PhD, Chemistry, 2015, Texas A&M University

 Thiamin pyrophosphate is an essential cofactor in all living systems. Its biosynthesis involves two separate pathways to synthesize pyrimidine and thiazole, followed by a coupling… (more)

Subjects/Keywords: Thiamin; Eukaryotic Pyrimidine Synthase; Bacterial Thiazole Synthase

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APA (6th Edition):

Lai, R. Y. (2015). The Mechanistic Investigation of the Bacterial Thiamin Thiazole Synthase and the Eukaryotic Thiamin Pyrimidine Synthase. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/155385

Chicago Manual of Style (16th Edition):

Lai, Rung Yi. “The Mechanistic Investigation of the Bacterial Thiamin Thiazole Synthase and the Eukaryotic Thiamin Pyrimidine Synthase.” 2015. Doctoral Dissertation, Texas A&M University. Accessed May 11, 2021. http://hdl.handle.net/1969.1/155385.

MLA Handbook (7th Edition):

Lai, Rung Yi. “The Mechanistic Investigation of the Bacterial Thiamin Thiazole Synthase and the Eukaryotic Thiamin Pyrimidine Synthase.” 2015. Web. 11 May 2021.

Vancouver:

Lai RY. The Mechanistic Investigation of the Bacterial Thiamin Thiazole Synthase and the Eukaryotic Thiamin Pyrimidine Synthase. [Internet] [Doctoral dissertation]. Texas A&M University; 2015. [cited 2021 May 11]. Available from: http://hdl.handle.net/1969.1/155385.

Council of Science Editors:

Lai RY. The Mechanistic Investigation of the Bacterial Thiamin Thiazole Synthase and the Eukaryotic Thiamin Pyrimidine Synthase. [Doctoral Dissertation]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/155385


Texas A&M University

21. Lee, Yan-Jiun. Expanding the Genetic Code for Synthesis of Proteins with Native Biological Modifications and Novel Chemical, Biophysical Probes.

Degree: PhD, Chemistry, 2015, Texas A&M University

 Engineering of protein with new modifications essentially expands the protein functions which provide powerful tools for investigating significant biological questions. New modifications also offer scientists… (more)

Subjects/Keywords: Genetic code expansion; bioorthogonal reaction; bioconjugation; noncanonical amino acid

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APA (6th Edition):

Lee, Y. (2015). Expanding the Genetic Code for Synthesis of Proteins with Native Biological Modifications and Novel Chemical, Biophysical Probes. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/156402

Chicago Manual of Style (16th Edition):

Lee, Yan-Jiun. “Expanding the Genetic Code for Synthesis of Proteins with Native Biological Modifications and Novel Chemical, Biophysical Probes.” 2015. Doctoral Dissertation, Texas A&M University. Accessed May 11, 2021. http://hdl.handle.net/1969.1/156402.

MLA Handbook (7th Edition):

Lee, Yan-Jiun. “Expanding the Genetic Code for Synthesis of Proteins with Native Biological Modifications and Novel Chemical, Biophysical Probes.” 2015. Web. 11 May 2021.

Vancouver:

Lee Y. Expanding the Genetic Code for Synthesis of Proteins with Native Biological Modifications and Novel Chemical, Biophysical Probes. [Internet] [Doctoral dissertation]. Texas A&M University; 2015. [cited 2021 May 11]. Available from: http://hdl.handle.net/1969.1/156402.

Council of Science Editors:

Lee Y. Expanding the Genetic Code for Synthesis of Proteins with Native Biological Modifications and Novel Chemical, Biophysical Probes. [Doctoral Dissertation]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/156402


Texas A&M University

22. Hsu, Willie Weili. The Investigation of Sirtuin Activities on Short-Chained Mono-Acylated Histone H3 Tetramers and Nucleosomes.

Degree: PhD, Chemistry, 2017, Texas A&M University

 Lysine acylation serves as an epigenetic marker for myriad cellular processes, such as signaling, differentiation, DNA repair, angiogenesis, and the like. Sirtuin 1 (SIRT1) and… (more)

Subjects/Keywords: Histone; nucleosome; noncanonical amino acids; sirtuins; deacylation

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APA (6th Edition):

Hsu, W. W. (2017). The Investigation of Sirtuin Activities on Short-Chained Mono-Acylated Histone H3 Tetramers and Nucleosomes. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/165858

Chicago Manual of Style (16th Edition):

Hsu, Willie Weili. “The Investigation of Sirtuin Activities on Short-Chained Mono-Acylated Histone H3 Tetramers and Nucleosomes.” 2017. Doctoral Dissertation, Texas A&M University. Accessed May 11, 2021. http://hdl.handle.net/1969.1/165858.

MLA Handbook (7th Edition):

Hsu, Willie Weili. “The Investigation of Sirtuin Activities on Short-Chained Mono-Acylated Histone H3 Tetramers and Nucleosomes.” 2017. Web. 11 May 2021.

Vancouver:

Hsu WW. The Investigation of Sirtuin Activities on Short-Chained Mono-Acylated Histone H3 Tetramers and Nucleosomes. [Internet] [Doctoral dissertation]. Texas A&M University; 2017. [cited 2021 May 11]. Available from: http://hdl.handle.net/1969.1/165858.

Council of Science Editors:

Hsu WW. The Investigation of Sirtuin Activities on Short-Chained Mono-Acylated Histone H3 Tetramers and Nucleosomes. [Doctoral Dissertation]. Texas A&M University; 2017. Available from: http://hdl.handle.net/1969.1/165858


Texas A&M University

23. Kamkaew, Anyanee. TrkC Targeted Probes for Cancer Diagnosis and Therapeutics.

Degree: PhD, Chemistry, 2015, Texas A&M University

 This dissertation features a small molecule, non-peptidic, ligand designed to bind a cell surface receptor called tropomyosin receptor kinase C (TrkC). TrkC is overexpressed on… (more)

Subjects/Keywords: TrkC; Theranosis; targeting

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APA (6th Edition):

Kamkaew, A. (2015). TrkC Targeted Probes for Cancer Diagnosis and Therapeutics. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/187448

Chicago Manual of Style (16th Edition):

Kamkaew, Anyanee. “TrkC Targeted Probes for Cancer Diagnosis and Therapeutics.” 2015. Doctoral Dissertation, Texas A&M University. Accessed May 11, 2021. http://hdl.handle.net/1969.1/187448.

MLA Handbook (7th Edition):

Kamkaew, Anyanee. “TrkC Targeted Probes for Cancer Diagnosis and Therapeutics.” 2015. Web. 11 May 2021.

Vancouver:

Kamkaew A. TrkC Targeted Probes for Cancer Diagnosis and Therapeutics. [Internet] [Doctoral dissertation]. Texas A&M University; 2015. [cited 2021 May 11]. Available from: http://hdl.handle.net/1969.1/187448.

Council of Science Editors:

Kamkaew A. TrkC Targeted Probes for Cancer Diagnosis and Therapeutics. [Doctoral Dissertation]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/187448


Texas A&M University

24. Wang, Wei. SIRT6 and SIRT7 Target Identification Using Acyl-Nucleosomes.

Degree: PhD, Chemistry, 2018, Texas A&M University

 For eukaryotes, DNA is maintained in the form of chromatin, which is comprised of millions of repeated nucleosomes. Each nucleosome is assembled by wrapping 147… (more)

Subjects/Keywords: SIRT6; SIRT7; click chemistry; unnatural amino acid incorporation; site-specificity; nucleosome

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APA (6th Edition):

Wang, W. (2018). SIRT6 and SIRT7 Target Identification Using Acyl-Nucleosomes. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/174597

Chicago Manual of Style (16th Edition):

Wang, Wei. “SIRT6 and SIRT7 Target Identification Using Acyl-Nucleosomes.” 2018. Doctoral Dissertation, Texas A&M University. Accessed May 11, 2021. http://hdl.handle.net/1969.1/174597.

MLA Handbook (7th Edition):

Wang, Wei. “SIRT6 and SIRT7 Target Identification Using Acyl-Nucleosomes.” 2018. Web. 11 May 2021.

Vancouver:

Wang W. SIRT6 and SIRT7 Target Identification Using Acyl-Nucleosomes. [Internet] [Doctoral dissertation]. Texas A&M University; 2018. [cited 2021 May 11]. Available from: http://hdl.handle.net/1969.1/174597.

Council of Science Editors:

Wang W. SIRT6 and SIRT7 Target Identification Using Acyl-Nucleosomes. [Doctoral Dissertation]. Texas A&M University; 2018. Available from: http://hdl.handle.net/1969.1/174597


Texas A&M University

25. Wang, Xiaoyan. Design and Development of Novel Chemical Biology Tools for Investigating Deubiquitinating Enzymes.

Degree: PhD, Chemistry, 2016, Texas A&M University

 Ubiquitination, also known as ubiquitylation, is a major type of post-translational modification (PTM), which is closely associated with numerous cellular processes, such as protein degradation,… (more)

Subjects/Keywords: deubiquitinases; ubiquitination; ubiquitin functionalization; drug discovery; polyubiquitin chains; deubiquitinase substrates

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APA (6th Edition):

Wang, X. (2016). Design and Development of Novel Chemical Biology Tools for Investigating Deubiquitinating Enzymes. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/191967

Chicago Manual of Style (16th Edition):

Wang, Xiaoyan. “Design and Development of Novel Chemical Biology Tools for Investigating Deubiquitinating Enzymes.” 2016. Doctoral Dissertation, Texas A&M University. Accessed May 11, 2021. http://hdl.handle.net/1969.1/191967.

MLA Handbook (7th Edition):

Wang, Xiaoyan. “Design and Development of Novel Chemical Biology Tools for Investigating Deubiquitinating Enzymes.” 2016. Web. 11 May 2021.

Vancouver:

Wang X. Design and Development of Novel Chemical Biology Tools for Investigating Deubiquitinating Enzymes. [Internet] [Doctoral dissertation]. Texas A&M University; 2016. [cited 2021 May 11]. Available from: http://hdl.handle.net/1969.1/191967.

Council of Science Editors:

Wang X. Design and Development of Novel Chemical Biology Tools for Investigating Deubiquitinating Enzymes. [Doctoral Dissertation]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/191967

26. Lane, Sarah Margaret. Synthesis, Characterization, and Toxicity Studies of Dirhodium and Diiridium Metal-Metal Bonded Compounds.

Degree: MS, Chemistry, 2012, Texas A&M University

 The anticancer properties of dirhodium tetraacetate were discovered in the 1970's, and subsequently motivated the research of several dirhodium paddlewheel derivatives. The promising results of… (more)

Subjects/Keywords: Dirhodium; Diiridium; Cytotoxicity; Anticancer Drugs; Photodynamic Therapy

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APA (6th Edition):

Lane, S. M. (2012). Synthesis, Characterization, and Toxicity Studies of Dirhodium and Diiridium Metal-Metal Bonded Compounds. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11877

Chicago Manual of Style (16th Edition):

Lane, Sarah Margaret. “Synthesis, Characterization, and Toxicity Studies of Dirhodium and Diiridium Metal-Metal Bonded Compounds.” 2012. Masters Thesis, Texas A&M University. Accessed May 11, 2021. http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11877.

MLA Handbook (7th Edition):

Lane, Sarah Margaret. “Synthesis, Characterization, and Toxicity Studies of Dirhodium and Diiridium Metal-Metal Bonded Compounds.” 2012. Web. 11 May 2021.

Vancouver:

Lane SM. Synthesis, Characterization, and Toxicity Studies of Dirhodium and Diiridium Metal-Metal Bonded Compounds. [Internet] [Masters thesis]. Texas A&M University; 2012. [cited 2021 May 11]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11877.

Council of Science Editors:

Lane SM. Synthesis, Characterization, and Toxicity Studies of Dirhodium and Diiridium Metal-Metal Bonded Compounds. [Masters Thesis]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11877

.