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You searched for +publisher:"Texas A&M University" +contributor:("Reinhart, Gregory D"). Showing records 1 – 30 of 50 total matches.

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Texas A&M University

1. Li, Lingling. Water-soluble bodipys: syntheses, derivatization and photophysical studies.

Degree: 2009, Texas A&M University

 A set of water-soluble 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) derivatives, has been prepared and their spectroscopic properties examined. These dyes can be used as either donor or acceptor… (more)

Subjects/Keywords: water-soluble; BODIPY

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APA (6th Edition):

Li, L. (2009). Water-soluble bodipys: syntheses, derivatization and photophysical studies. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2448

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

Chicago Manual of Style (16th Edition):

Li, Lingling. “Water-soluble bodipys: syntheses, derivatization and photophysical studies.” 2009. Thesis, Texas A&M University. Accessed October 20, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2448.

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

MLA Handbook (7th Edition):

Li, Lingling. “Water-soluble bodipys: syntheses, derivatization and photophysical studies.” 2009. Web. 20 Oct 2019.

Vancouver:

Li L. Water-soluble bodipys: syntheses, derivatization and photophysical studies. [Internet] [Thesis]. Texas A&M University; 2009. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2448.

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

Council of Science Editors:

Li L. Water-soluble bodipys: syntheses, derivatization and photophysical studies. [Thesis]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2448

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


Texas A&M University

2. Perez, Stephanie. Illuminating the Heterotropic Communication of the Pair-wise Interactions in Phosphofructokinase from Bacillus stearothermophilus.

Degree: 2012, Texas A&M University

 The number of allosteric sites and active sites in phosphofructokinase from Bacillus stearothermophilus create an intricate network of communication within the enzyme. With thermodynamic linkage… (more)

Subjects/Keywords: fluoresence; dynamics; phosphofructokinase; allostery

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APA (6th Edition):

Perez, S. (2012). Illuminating the Heterotropic Communication of the Pair-wise Interactions in Phosphofructokinase from Bacillus stearothermophilus. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/148105

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

Chicago Manual of Style (16th Edition):

Perez, Stephanie. “Illuminating the Heterotropic Communication of the Pair-wise Interactions in Phosphofructokinase from Bacillus stearothermophilus.” 2012. Thesis, Texas A&M University. Accessed October 20, 2019. http://hdl.handle.net/1969.1/148105.

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

MLA Handbook (7th Edition):

Perez, Stephanie. “Illuminating the Heterotropic Communication of the Pair-wise Interactions in Phosphofructokinase from Bacillus stearothermophilus.” 2012. Web. 20 Oct 2019.

Vancouver:

Perez S. Illuminating the Heterotropic Communication of the Pair-wise Interactions in Phosphofructokinase from Bacillus stearothermophilus. [Internet] [Thesis]. Texas A&M University; 2012. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1969.1/148105.

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

Council of Science Editors:

Perez S. Illuminating the Heterotropic Communication of the Pair-wise Interactions in Phosphofructokinase from Bacillus stearothermophilus. [Thesis]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/148105

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


Texas A&M University

3. Tindall, Amanda Jean. Expression, Purification, and Kinetic Characterization of Human Liver Phosphofructokinase.

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

 Phosphofructokinase (PFK) catalyzes the phosphorylation of fructose 6-phosphate (F6P) to fructose 1,6-bisphosphate (F16BP) in a MgATP dependent reaction. This reaction represents the first committed step… (more)

Subjects/Keywords: phosphofructokinase; glycolysis; allostery; human liver

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APA (6th Edition):

Tindall, A. J. (2016). Expression, Purification, and Kinetic Characterization of Human Liver Phosphofructokinase. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/156932

Chicago Manual of Style (16th Edition):

Tindall, Amanda Jean. “Expression, Purification, and Kinetic Characterization of Human Liver Phosphofructokinase.” 2016. Masters Thesis, Texas A&M University. Accessed October 20, 2019. http://hdl.handle.net/1969.1/156932.

MLA Handbook (7th Edition):

Tindall, Amanda Jean. “Expression, Purification, and Kinetic Characterization of Human Liver Phosphofructokinase.” 2016. Web. 20 Oct 2019.

Vancouver:

Tindall AJ. Expression, Purification, and Kinetic Characterization of Human Liver Phosphofructokinase. [Internet] [Masters thesis]. Texas A&M University; 2016. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1969.1/156932.

Council of Science Editors:

Tindall AJ. Expression, Purification, and Kinetic Characterization of Human Liver Phosphofructokinase. [Masters Thesis]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/156932


Texas A&M University

4. Pulukkody, Randara. Synthetic Analogues of Dinitrosyl Iron Complexes: Reactivity Studies and Improvements towards Therapeutic Applications.

Degree: 2015, Texas A&M University

 Dinitrosyl iron complexes (DNICs) are organometallic-like compounds formed endogenously as products of degradation of iron-sulfur clusters by NO or its interaction with the cellular chelatable… (more)

Subjects/Keywords: Dinitrosyl iron complexes; N-heterocyclic carbene; carbon monoxide

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APA (6th Edition):

Pulukkody, R. (2015). Synthetic Analogues of Dinitrosyl Iron Complexes: Reactivity Studies and Improvements towards Therapeutic Applications. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/155488

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

Chicago Manual of Style (16th Edition):

Pulukkody, Randara. “Synthetic Analogues of Dinitrosyl Iron Complexes: Reactivity Studies and Improvements towards Therapeutic Applications.” 2015. Thesis, Texas A&M University. Accessed October 20, 2019. http://hdl.handle.net/1969.1/155488.

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

MLA Handbook (7th Edition):

Pulukkody, Randara. “Synthetic Analogues of Dinitrosyl Iron Complexes: Reactivity Studies and Improvements towards Therapeutic Applications.” 2015. Web. 20 Oct 2019.

Vancouver:

Pulukkody R. Synthetic Analogues of Dinitrosyl Iron Complexes: Reactivity Studies and Improvements towards Therapeutic Applications. [Internet] [Thesis]. Texas A&M University; 2015. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1969.1/155488.

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

Council of Science Editors:

Pulukkody R. Synthetic Analogues of Dinitrosyl Iron Complexes: Reactivity Studies and Improvements towards Therapeutic Applications. [Thesis]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/155488

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


Texas A&M University

5. Diaz Vazquez, Arnaldo Joel. Solid-supported phospholipid bilayers: separation matrix for proteomics applications.

Degree: 2009, Texas A&M University

 This dissertation focuses on the development of biological platforms on which the function and characterization of transmembrane proteins can be performed simultaneously utilizing a biomembrane… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Diaz Vazquez, A. J. (2009). Solid-supported phospholipid bilayers: separation matrix for proteomics applications. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2652

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

Chicago Manual of Style (16th Edition):

Diaz Vazquez, Arnaldo Joel. “Solid-supported phospholipid bilayers: separation matrix for proteomics applications.” 2009. Thesis, Texas A&M University. Accessed October 20, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2652.

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

MLA Handbook (7th Edition):

Diaz Vazquez, Arnaldo Joel. “Solid-supported phospholipid bilayers: separation matrix for proteomics applications.” 2009. Web. 20 Oct 2019.

Vancouver:

Diaz Vazquez AJ. Solid-supported phospholipid bilayers: separation matrix for proteomics applications. [Internet] [Thesis]. Texas A&M University; 2009. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2652.

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

Council of Science Editors:

Diaz Vazquez AJ. Solid-supported phospholipid bilayers: separation matrix for proteomics applications. [Thesis]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2652

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


Texas A&M University

6. Knapp, Gwendowlyn Sue. Oligomerization of the lysr-type transcriptional regulators in Escherichia Coli.

Degree: 2009, Texas A&M University

 Protein-protein interactions regulate and drive biological processes and understanding the assembly of these interactions is important. The LysR-Type Transcriptional Regulators (LTTRs) are a large family… (more)

Subjects/Keywords: protein-protein interactions; LysR-Type Transcriptional Regulators

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APA (6th Edition):

Knapp, G. S. (2009). Oligomerization of the lysr-type transcriptional regulators in Escherichia Coli. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2655

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

Chicago Manual of Style (16th Edition):

Knapp, Gwendowlyn Sue. “Oligomerization of the lysr-type transcriptional regulators in Escherichia Coli.” 2009. Thesis, Texas A&M University. Accessed October 20, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2655.

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

MLA Handbook (7th Edition):

Knapp, Gwendowlyn Sue. “Oligomerization of the lysr-type transcriptional regulators in Escherichia Coli.” 2009. Web. 20 Oct 2019.

Vancouver:

Knapp GS. Oligomerization of the lysr-type transcriptional regulators in Escherichia Coli. [Internet] [Thesis]. Texas A&M University; 2009. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2655.

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

Council of Science Editors:

Knapp GS. Oligomerization of the lysr-type transcriptional regulators in Escherichia Coli. [Thesis]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2655

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


Texas A&M University

7. Fu, Hailong. UNDERSTANDING FORCES THAT CONTRIBUTE TO PROTEIN STABILITY: APPLICATION FOR INCREASING PROTEIN STABILITY.

Degree: 2010, Texas A&M University

 The aim of this study is to further our understanding of the forces that contribute to protein stability and to investigate how site-directed mutagenesis might… (more)

Subjects/Keywords: conformational stability; hydrophobic effect; thermostable; denatured state; heat capacity change; beta turn

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APA (6th Edition):

Fu, H. (2010). UNDERSTANDING FORCES THAT CONTRIBUTE TO PROTEIN STABILITY: APPLICATION FOR INCREASING PROTEIN STABILITY. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-444

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

Chicago Manual of Style (16th Edition):

Fu, Hailong. “UNDERSTANDING FORCES THAT CONTRIBUTE TO PROTEIN STABILITY: APPLICATION FOR INCREASING PROTEIN STABILITY.” 2010. Thesis, Texas A&M University. Accessed October 20, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-444.

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

MLA Handbook (7th Edition):

Fu, Hailong. “UNDERSTANDING FORCES THAT CONTRIBUTE TO PROTEIN STABILITY: APPLICATION FOR INCREASING PROTEIN STABILITY.” 2010. Web. 20 Oct 2019.

Vancouver:

Fu H. UNDERSTANDING FORCES THAT CONTRIBUTE TO PROTEIN STABILITY: APPLICATION FOR INCREASING PROTEIN STABILITY. [Internet] [Thesis]. Texas A&M University; 2010. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-444.

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

Council of Science Editors:

Fu H. UNDERSTANDING FORCES THAT CONTRIBUTE TO PROTEIN STABILITY: APPLICATION FOR INCREASING PROTEIN STABILITY. [Thesis]. Texas A&M University; 2010. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-444

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


Texas A&M University

8. Bigley, Andrew N. Investigations on the Mechanism of Allosteric Activtion of Rabbit Muscle Glycogen Phosphorylase b by AMP.

Degree: 2010, Texas A&M University

 Much work has been carried out on glycogen phosphorylase over the last seventy years. Interest has persisted due not only to the usefulness of phosphorylase… (more)

Subjects/Keywords: Allostery; Regulation; Glycogen Phosphorylase; AMP

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APA (6th Edition):

Bigley, A. N. (2010). Investigations on the Mechanism of Allosteric Activtion of Rabbit Muscle Glycogen Phosphorylase b by AMP. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-483

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

Chicago Manual of Style (16th Edition):

Bigley, Andrew N. “Investigations on the Mechanism of Allosteric Activtion of Rabbit Muscle Glycogen Phosphorylase b by AMP.” 2010. Thesis, Texas A&M University. Accessed October 20, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-483.

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

MLA Handbook (7th Edition):

Bigley, Andrew N. “Investigations on the Mechanism of Allosteric Activtion of Rabbit Muscle Glycogen Phosphorylase b by AMP.” 2010. Web. 20 Oct 2019.

Vancouver:

Bigley AN. Investigations on the Mechanism of Allosteric Activtion of Rabbit Muscle Glycogen Phosphorylase b by AMP. [Internet] [Thesis]. Texas A&M University; 2010. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-483.

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

Council of Science Editors:

Bigley AN. Investigations on the Mechanism of Allosteric Activtion of Rabbit Muscle Glycogen Phosphorylase b by AMP. [Thesis]. Texas A&M University; 2010. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-483

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


Texas A&M University

9. Jung, Hyunsook. SENSING AND SEPARATING BIOMOLECULES AT BIOINTERFACES.

Degree: 2010, Texas A&M University

 Ligand-receptor interactions are ubiquitous on cell membranes. Indeed, many important physiological functions primarily involve such interactions. These include cell signaling, pathogen binding, trafficking of lymphocytes,… (more)

Subjects/Keywords: supported lipid bilayer; ligand/receptor interactions

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APA (6th Edition):

Jung, H. (2010). SENSING AND SEPARATING BIOMOLECULES AT BIOINTERFACES. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-499

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

Chicago Manual of Style (16th Edition):

Jung, Hyunsook. “SENSING AND SEPARATING BIOMOLECULES AT BIOINTERFACES.” 2010. Thesis, Texas A&M University. Accessed October 20, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-499.

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

MLA Handbook (7th Edition):

Jung, Hyunsook. “SENSING AND SEPARATING BIOMOLECULES AT BIOINTERFACES.” 2010. Web. 20 Oct 2019.

Vancouver:

Jung H. SENSING AND SEPARATING BIOMOLECULES AT BIOINTERFACES. [Internet] [Thesis]. Texas A&M University; 2010. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-499.

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

Council of Science Editors:

Jung H. SENSING AND SEPARATING BIOMOLECULES AT BIOINTERFACES. [Thesis]. Texas A&M University; 2010. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-499

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


Texas A&M University

10. Nguyen, Tinh T. Mechanistic Insights into the Diverged Enzymes of the Amidohydrolase Superfamily.

Degree: 2011, Texas A&M University

 The amidohydrolase superfamily is a functionally diverse set of enzymes that catalyzes predominantly hydrolysis reactions involving sugars, nucleic acids, amino acids, and organophosphate esters. A… (more)

Subjects/Keywords: Amidohydrolase superfamily; uronate isomerase; renal dipeptidase

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APA (6th Edition):

Nguyen, T. T. (2011). Mechanistic Insights into the Diverged Enzymes of the Amidohydrolase Superfamily. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7237

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

Chicago Manual of Style (16th Edition):

Nguyen, Tinh T. “Mechanistic Insights into the Diverged Enzymes of the Amidohydrolase Superfamily.” 2011. Thesis, Texas A&M University. Accessed October 20, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7237.

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

MLA Handbook (7th Edition):

Nguyen, Tinh T. “Mechanistic Insights into the Diverged Enzymes of the Amidohydrolase Superfamily.” 2011. Web. 20 Oct 2019.

Vancouver:

Nguyen TT. Mechanistic Insights into the Diverged Enzymes of the Amidohydrolase Superfamily. [Internet] [Thesis]. Texas A&M University; 2011. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7237.

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

Council of Science Editors:

Nguyen TT. Mechanistic Insights into the Diverged Enzymes of the Amidohydrolase Superfamily. [Thesis]. Texas A&M University; 2011. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7237

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


Texas A&M University

11. Hall, Richard Stuart. Mechanistic Studies and Function Discovery of Mononuclear Amidohydrolase Enzymes.

Degree: 2011, Texas A&M University

 The amidohydrolase superfamily is a functionally diverse group of evolutionarily related proteins which utilize metal cofactors in the activation of a hydrolytic water molecule and… (more)

Subjects/Keywords: Amidohydrolase superfamily; enzyme mechanism and inhibition; evolution; function discovery; NagA; cytosine deaminase; guanine deaminase; 8-oxoguanine deaminase; isoxanthopterin deaminase

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APA (6th Edition):

Hall, R. S. (2011). Mechanistic Studies and Function Discovery of Mononuclear Amidohydrolase Enzymes. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7250

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

Chicago Manual of Style (16th Edition):

Hall, Richard Stuart. “Mechanistic Studies and Function Discovery of Mononuclear Amidohydrolase Enzymes.” 2011. Thesis, Texas A&M University. Accessed October 20, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7250.

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

MLA Handbook (7th Edition):

Hall, Richard Stuart. “Mechanistic Studies and Function Discovery of Mononuclear Amidohydrolase Enzymes.” 2011. Web. 20 Oct 2019.

Vancouver:

Hall RS. Mechanistic Studies and Function Discovery of Mononuclear Amidohydrolase Enzymes. [Internet] [Thesis]. Texas A&M University; 2011. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7250.

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

Council of Science Editors:

Hall RS. Mechanistic Studies and Function Discovery of Mononuclear Amidohydrolase Enzymes. [Thesis]. Texas A&M University; 2011. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7250

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


Texas A&M University

12. Ma, Zhen. Physicochemical Characterization of the Bacterial Cu(I) Sensor CsoR.

Degree: 2011, Texas A&M University

M. tuberculosis copper-sensitive operon repressor (Mtb CsoR) is the founding member of a new metalloregulatory protein family in prokaryotes that regulates the transcription of the… (more)

Subjects/Keywords: CsoR; Cu(I) sensor; allosteric regulation; native chemical ligation

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APA (6th Edition):

Ma, Z. (2011). Physicochemical Characterization of the Bacterial Cu(I) Sensor CsoR. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7351

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

Chicago Manual of Style (16th Edition):

Ma, Zhen. “Physicochemical Characterization of the Bacterial Cu(I) Sensor CsoR.” 2011. Thesis, Texas A&M University. Accessed October 20, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7351.

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

MLA Handbook (7th Edition):

Ma, Zhen. “Physicochemical Characterization of the Bacterial Cu(I) Sensor CsoR.” 2011. Web. 20 Oct 2019.

Vancouver:

Ma Z. Physicochemical Characterization of the Bacterial Cu(I) Sensor CsoR. [Internet] [Thesis]. Texas A&M University; 2011. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7351.

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

Council of Science Editors:

Ma Z. Physicochemical Characterization of the Bacterial Cu(I) Sensor CsoR. [Thesis]. Texas A&M University; 2011. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7351

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


Texas A&M University

13. Tsai, Ping-Chuan. Directed Evolution of Phosphotriesterase for Stereoselective Detoxification of Organophosphate Nerve Agents.

Degree: 2011, Texas A&M University

 The bacterial phosphotriesterase (PTE) from Pseudomonas diminuta possess very broad substrate specificity for organophosphorus compounds. It is capable of hydrolyzing several insecticides including paraoxon and… (more)

Subjects/Keywords: Phosphotriesterase (PTE)

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APA (6th Edition):

Tsai, P. (2011). Directed Evolution of Phosphotriesterase for Stereoselective Detoxification of Organophosphate Nerve Agents. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7428

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

Chicago Manual of Style (16th Edition):

Tsai, Ping-Chuan. “Directed Evolution of Phosphotriesterase for Stereoselective Detoxification of Organophosphate Nerve Agents.” 2011. Thesis, Texas A&M University. Accessed October 20, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7428.

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

MLA Handbook (7th Edition):

Tsai, Ping-Chuan. “Directed Evolution of Phosphotriesterase for Stereoselective Detoxification of Organophosphate Nerve Agents.” 2011. Web. 20 Oct 2019.

Vancouver:

Tsai P. Directed Evolution of Phosphotriesterase for Stereoselective Detoxification of Organophosphate Nerve Agents. [Internet] [Thesis]. Texas A&M University; 2011. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7428.

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

Council of Science Editors:

Tsai P. Directed Evolution of Phosphotriesterase for Stereoselective Detoxification of Organophosphate Nerve Agents. [Thesis]. Texas A&M University; 2011. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7428

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


Texas A&M University

14. Mosser, Rockann Elizabeth. A Structural and Kinetic Study into the Role of the Quaternary Shift in Bacillus stearothermophilus Phosphofructokinase.

Degree: 2011, Texas A&M University

 Bacillus stearothermophilus phosphofructokinase (BsPFK) is a homotetramer that is allosterically inhibited by phosphoenolpyruvate (PEP), which binds along one dimer-dimer interface. The substrate, fructose-6-phosphate (F6P), binds… (more)

Subjects/Keywords: Phosphofructokinase; PFK; Bacillus stearothermophilus; allostery; regulation; inhibition; NMR; x-ray crystallography; enzyme kinetics; energetics

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APA (6th Edition):

Mosser, R. E. (2011). A Structural and Kinetic Study into the Role of the Quaternary Shift in Bacillus stearothermophilus Phosphofructokinase. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8370

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

Chicago Manual of Style (16th Edition):

Mosser, Rockann Elizabeth. “A Structural and Kinetic Study into the Role of the Quaternary Shift in Bacillus stearothermophilus Phosphofructokinase.” 2011. Thesis, Texas A&M University. Accessed October 20, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8370.

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

MLA Handbook (7th Edition):

Mosser, Rockann Elizabeth. “A Structural and Kinetic Study into the Role of the Quaternary Shift in Bacillus stearothermophilus Phosphofructokinase.” 2011. Web. 20 Oct 2019.

Vancouver:

Mosser RE. A Structural and Kinetic Study into the Role of the Quaternary Shift in Bacillus stearothermophilus Phosphofructokinase. [Internet] [Thesis]. Texas A&M University; 2011. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8370.

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

Council of Science Editors:

Mosser RE. A Structural and Kinetic Study into the Role of the Quaternary Shift in Bacillus stearothermophilus Phosphofructokinase. [Thesis]. Texas A&M University; 2011. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8370

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


Texas A&M University

15. Panay Escobar, Aram Joel. Mechanistic and Structural Studies of Phenylalanine Hydroxylase from Chromobacterium violaceum.

Degree: 2011, Texas A&M University

 The phenylalanine hydroxylase from Chromobacterium violaceum (CvPheH) is a non-heme iron monooxygenase that catalyzes the hydroxylation of phenylalanine. This study presents the use of kinetic… (more)

Subjects/Keywords: Phenylalanine hydroxylase; Mechanistic studies; Isotope effects; NMR backbone assignment; ligand binding

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APA (6th Edition):

Panay Escobar, A. J. (2011). Mechanistic and Structural Studies of Phenylalanine Hydroxylase from Chromobacterium violaceum. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8584

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

Chicago Manual of Style (16th Edition):

Panay Escobar, Aram Joel. “Mechanistic and Structural Studies of Phenylalanine Hydroxylase from Chromobacterium violaceum.” 2011. Thesis, Texas A&M University. Accessed October 20, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8584.

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

MLA Handbook (7th Edition):

Panay Escobar, Aram Joel. “Mechanistic and Structural Studies of Phenylalanine Hydroxylase from Chromobacterium violaceum.” 2011. Web. 20 Oct 2019.

Vancouver:

Panay Escobar AJ. Mechanistic and Structural Studies of Phenylalanine Hydroxylase from Chromobacterium violaceum. [Internet] [Thesis]. Texas A&M University; 2011. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8584.

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

Council of Science Editors:

Panay Escobar AJ. Mechanistic and Structural Studies of Phenylalanine Hydroxylase from Chromobacterium violaceum. [Thesis]. Texas A&M University; 2011. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8584

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


Texas A&M University

16. Reed, Catrina Anne. Characterization of A2: The Lysis Protein of ssRNA Phage Qbeta.

Degree: 2012, Texas A&M University

 Lysis in cells infected with the ssRNA phage Qbeta is effected by the A2 protein. It was previously shown that a single copy of A2… (more)

Subjects/Keywords: Qbeta; ssRNA phage; MurA; A2; lysis protein

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APA (6th Edition):

Reed, C. A. (2012). Characterization of A2: The Lysis Protein of ssRNA Phage Qbeta. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11696

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

Chicago Manual of Style (16th Edition):

Reed, Catrina Anne. “Characterization of A2: The Lysis Protein of ssRNA Phage Qbeta.” 2012. Thesis, Texas A&M University. Accessed October 20, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11696.

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

MLA Handbook (7th Edition):

Reed, Catrina Anne. “Characterization of A2: The Lysis Protein of ssRNA Phage Qbeta.” 2012. Web. 20 Oct 2019.

Vancouver:

Reed CA. Characterization of A2: The Lysis Protein of ssRNA Phage Qbeta. [Internet] [Thesis]. Texas A&M University; 2012. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11696.

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

Council of Science Editors:

Reed CA. Characterization of A2: The Lysis Protein of ssRNA Phage Qbeta. [Thesis]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11696

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


Texas A&M University

17. Shubina-McGresham, Maria. Characterization of the Allosteric Properties of Thermus thermophilus Phosphofructokinase and the Sources of Strong Inhibitor Binding Affinity and Weak Inhibitory Response.

Degree: 2012, Texas A&M University

 Characterization of allosteric properties of phosphofructokinase from the extreme thermophile Thermus thermophilus (TtPFK) using thermodynamic linkage analysis revealed several peculiarities. Inhibition and activation of Fru-6-P… (more)

Subjects/Keywords: allostery; thermophile; Thermus thermophilus

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APA (6th Edition):

Shubina-McGresham, M. (2012). Characterization of the Allosteric Properties of Thermus thermophilus Phosphofructokinase and the Sources of Strong Inhibitor Binding Affinity and Weak Inhibitory Response. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11750

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

Chicago Manual of Style (16th Edition):

Shubina-McGresham, Maria. “Characterization of the Allosteric Properties of Thermus thermophilus Phosphofructokinase and the Sources of Strong Inhibitor Binding Affinity and Weak Inhibitory Response.” 2012. Thesis, Texas A&M University. Accessed October 20, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11750.

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

MLA Handbook (7th Edition):

Shubina-McGresham, Maria. “Characterization of the Allosteric Properties of Thermus thermophilus Phosphofructokinase and the Sources of Strong Inhibitor Binding Affinity and Weak Inhibitory Response.” 2012. Web. 20 Oct 2019.

Vancouver:

Shubina-McGresham M. Characterization of the Allosteric Properties of Thermus thermophilus Phosphofructokinase and the Sources of Strong Inhibitor Binding Affinity and Weak Inhibitory Response. [Internet] [Thesis]. Texas A&M University; 2012. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11750.

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

Council of Science Editors:

Shubina-McGresham M. Characterization of the Allosteric Properties of Thermus thermophilus Phosphofructokinase and the Sources of Strong Inhibitor Binding Affinity and Weak Inhibitory Response. [Thesis]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2012-08-11750

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


Texas A&M University

18. Wahlman, Judit. Fluorescent-detected retrotranslocation of an endoplasmic reticulum - associated degradation (ERAD) substrate in a mammalian in vitro system.

Degree: 2009, Texas A&M University

 Secretory proteins that are unable to assemble into native proteins in the endoplasmic reticulum (ER) are transported back into the cytosol for degradation. Many cytosolic… (more)

Subjects/Keywords: Fluorescence; endoplasmic reticulum

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APA (6th Edition):

Wahlman, J. (2009). Fluorescent-detected retrotranslocation of an endoplasmic reticulum - associated degradation (ERAD) substrate in a mammalian in vitro system. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2019

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

Chicago Manual of Style (16th Edition):

Wahlman, Judit. “Fluorescent-detected retrotranslocation of an endoplasmic reticulum - associated degradation (ERAD) substrate in a mammalian in vitro system.” 2009. Thesis, Texas A&M University. Accessed October 20, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2019.

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

MLA Handbook (7th Edition):

Wahlman, Judit. “Fluorescent-detected retrotranslocation of an endoplasmic reticulum - associated degradation (ERAD) substrate in a mammalian in vitro system.” 2009. Web. 20 Oct 2019.

Vancouver:

Wahlman J. Fluorescent-detected retrotranslocation of an endoplasmic reticulum - associated degradation (ERAD) substrate in a mammalian in vitro system. [Internet] [Thesis]. Texas A&M University; 2009. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2019.

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

Council of Science Editors:

Wahlman J. Fluorescent-detected retrotranslocation of an endoplasmic reticulum - associated degradation (ERAD) substrate in a mammalian in vitro system. [Thesis]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2019

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


Texas A&M University

19. Adase, Christopher A. 1981-. The C-Terminus of Transmembrane Helix 2 (TM2) of the Escherichia coli Tar Chemorecptor Determines Signal Output and Ligand Sensitivity.

Degree: 2012, Texas A&M University

 Methyl-accepting chemotaxis proteins MCPs can bind one or more receptor- specific ligands. In the case of the Tar MCP of Escherichia coli (TarEc), a primary… (more)

Subjects/Keywords: Transmembrane communication; Chemoreceptor; Signal transduction; Two component signaling; Chemotaxis

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APA (6th Edition):

Adase, C. A. 1. (2012). The C-Terminus of Transmembrane Helix 2 (TM2) of the Escherichia coli Tar Chemorecptor Determines Signal Output and Ligand Sensitivity. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/148210

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

Chicago Manual of Style (16th Edition):

Adase, Christopher A 1981-. “The C-Terminus of Transmembrane Helix 2 (TM2) of the Escherichia coli Tar Chemorecptor Determines Signal Output and Ligand Sensitivity.” 2012. Thesis, Texas A&M University. Accessed October 20, 2019. http://hdl.handle.net/1969.1/148210.

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

MLA Handbook (7th Edition):

Adase, Christopher A 1981-. “The C-Terminus of Transmembrane Helix 2 (TM2) of the Escherichia coli Tar Chemorecptor Determines Signal Output and Ligand Sensitivity.” 2012. Web. 20 Oct 2019.

Vancouver:

Adase CA1. The C-Terminus of Transmembrane Helix 2 (TM2) of the Escherichia coli Tar Chemorecptor Determines Signal Output and Ligand Sensitivity. [Internet] [Thesis]. Texas A&M University; 2012. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1969.1/148210.

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

Council of Science Editors:

Adase CA1. The C-Terminus of Transmembrane Helix 2 (TM2) of the Escherichia coli Tar Chemorecptor Determines Signal Output and Ligand Sensitivity. [Thesis]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/148210

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


Texas A&M University

20. Stewart, Mikaela D. Determining the Intrinsic Properties of the C1B Domain that Influence PKC Ligand Specificity and Sensitivity to Reactive Oxygen Species.

Degree: 2013, Texas A&M University

 Each member of the protein kinase C (PKC) family activates cell signaling pathways with different and sometimes opposing cell functions, such as cell division, migration,… (more)

Subjects/Keywords: protien kinase C; zinc finger; C1 domain; protein dynamics; nuclear magnetic resonance

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APA (6th Edition):

Stewart, M. D. (2013). Determining the Intrinsic Properties of the C1B Domain that Influence PKC Ligand Specificity and Sensitivity to Reactive Oxygen Species. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/151059

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

Chicago Manual of Style (16th Edition):

Stewart, Mikaela D. “Determining the Intrinsic Properties of the C1B Domain that Influence PKC Ligand Specificity and Sensitivity to Reactive Oxygen Species.” 2013. Thesis, Texas A&M University. Accessed October 20, 2019. http://hdl.handle.net/1969.1/151059.

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

MLA Handbook (7th Edition):

Stewart, Mikaela D. “Determining the Intrinsic Properties of the C1B Domain that Influence PKC Ligand Specificity and Sensitivity to Reactive Oxygen Species.” 2013. Web. 20 Oct 2019.

Vancouver:

Stewart MD. Determining the Intrinsic Properties of the C1B Domain that Influence PKC Ligand Specificity and Sensitivity to Reactive Oxygen Species. [Internet] [Thesis]. Texas A&M University; 2013. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1969.1/151059.

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

Council of Science Editors:

Stewart MD. Determining the Intrinsic Properties of the C1B Domain that Influence PKC Ligand Specificity and Sensitivity to Reactive Oxygen Species. [Thesis]. Texas A&M University; 2013. Available from: http://hdl.handle.net/1969.1/151059

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


Texas A&M University

21. Park, Jinkyu. Exploring Iron Metabolism and Regulation in Saccharomyces cerevisiae Using an Integrative Biophysical and Bioanalytical Approach.

Degree: 2013, Texas A&M University

 Fe metabolism in budding yeast Saccharomyces cerevisiae was studied using an integrative systems-level approach involving M?ssbauer, EPR, UV-Vis spectroscopy and LC-ICP-MS, combined with conventional biochemical… (more)

Subjects/Keywords: Saccharomyces cerevisiae; iron; M?ssbauer; growth mode; nutrient; mtm1

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APA (6th Edition):

Park, J. (2013). Exploring Iron Metabolism and Regulation in Saccharomyces cerevisiae Using an Integrative Biophysical and Bioanalytical Approach. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/151831

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

Chicago Manual of Style (16th Edition):

Park, Jinkyu. “Exploring Iron Metabolism and Regulation in Saccharomyces cerevisiae Using an Integrative Biophysical and Bioanalytical Approach.” 2013. Thesis, Texas A&M University. Accessed October 20, 2019. http://hdl.handle.net/1969.1/151831.

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

MLA Handbook (7th Edition):

Park, Jinkyu. “Exploring Iron Metabolism and Regulation in Saccharomyces cerevisiae Using an Integrative Biophysical and Bioanalytical Approach.” 2013. Web. 20 Oct 2019.

Vancouver:

Park J. Exploring Iron Metabolism and Regulation in Saccharomyces cerevisiae Using an Integrative Biophysical and Bioanalytical Approach. [Internet] [Thesis]. Texas A&M University; 2013. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1969.1/151831.

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

Council of Science Editors:

Park J. Exploring Iron Metabolism and Regulation in Saccharomyces cerevisiae Using an Integrative Biophysical and Bioanalytical Approach. [Thesis]. Texas A&M University; 2013. Available from: http://hdl.handle.net/1969.1/151831

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


Texas A&M University

22. Cong, Xiao. Interactions of Cu2+ with Phosphatidylserine and Their Biological Implications.

Degree: 2015, Texas A&M University

 Phosphatidylserine (PS) lipids in cell membranes play significant roles in cell apoptosis, blood clotting and neurodegenerative disorders such as Alzheimer?s disease (AD). A novel fluorescence… (more)

Subjects/Keywords: Lipid membrane; Transition metal ions; Ligand-receptor Interaction; Fluorescence; Alzheimer's Disease; Lipid oxidation damage

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APA (6th Edition):

Cong, X. (2015). Interactions of Cu2+ with Phosphatidylserine and Their Biological Implications. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/155048

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

Chicago Manual of Style (16th Edition):

Cong, Xiao. “Interactions of Cu2+ with Phosphatidylserine and Their Biological Implications.” 2015. Thesis, Texas A&M University. Accessed October 20, 2019. http://hdl.handle.net/1969.1/155048.

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

MLA Handbook (7th Edition):

Cong, Xiao. “Interactions of Cu2+ with Phosphatidylserine and Their Biological Implications.” 2015. Web. 20 Oct 2019.

Vancouver:

Cong X. Interactions of Cu2+ with Phosphatidylserine and Their Biological Implications. [Internet] [Thesis]. Texas A&M University; 2015. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1969.1/155048.

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

Council of Science Editors:

Cong X. Interactions of Cu2+ with Phosphatidylserine and Their Biological Implications. [Thesis]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/155048

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


Texas A&M University

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

Degree: 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. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/155385

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

Chicago Manual of Style (16th Edition):

Lai, Rung Yi. “The Mechanistic Investigation of the Bacterial Thiamin Thiazole Synthase and the Eukaryotic Thiamin Pyrimidine Synthase.” 2015. Thesis, Texas A&M University. Accessed October 20, 2019. http://hdl.handle.net/1969.1/155385.

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

MLA Handbook (7th Edition):

Lai, Rung Yi. “The Mechanistic Investigation of the Bacterial Thiamin Thiazole Synthase and the Eukaryotic Thiamin Pyrimidine Synthase.” 2015. Web. 20 Oct 2019.

Vancouver:

Lai RY. The Mechanistic Investigation of the Bacterial Thiamin Thiazole Synthase and the Eukaryotic Thiamin Pyrimidine Synthase. [Internet] [Thesis]. Texas A&M University; 2015. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1969.1/155385.

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

Council of Science Editors:

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

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


Texas A&M University

24. Mori, Shogo. Biosynthesis and Cellular Actions of Bioactive Natural Products.

Degree: 2015, Texas A&M University

 The utilization of natural products as therapeutic agents has been an invaluable resource throughout medicinal history. Through the combined application of combinatorial biosynthesis, the modification… (more)

Subjects/Keywords: natural product; polyketide; polyketide synthase; nonribosomal peptide synthetase; thioesterase; macrolactone; streptomyces; cyanobacteria

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APA (6th Edition):

Mori, S. (2015). Biosynthesis and Cellular Actions of Bioactive Natural Products. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/156485

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

Chicago Manual of Style (16th Edition):

Mori, Shogo. “Biosynthesis and Cellular Actions of Bioactive Natural Products.” 2015. Thesis, Texas A&M University. Accessed October 20, 2019. http://hdl.handle.net/1969.1/156485.

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

MLA Handbook (7th Edition):

Mori, Shogo. “Biosynthesis and Cellular Actions of Bioactive Natural Products.” 2015. Web. 20 Oct 2019.

Vancouver:

Mori S. Biosynthesis and Cellular Actions of Bioactive Natural Products. [Internet] [Thesis]. Texas A&M University; 2015. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1969.1/156485.

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

Council of Science Editors:

Mori S. Biosynthesis and Cellular Actions of Bioactive Natural Products. [Thesis]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/156485

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


Texas A&M University

25. Koenig, Robert Eli. Perturbations to the Allosteric Regulation of Carbamoyl Phosphate Synthetase upon Removal of Interfacial Restraints.

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

 Carbamoyl phosphate synthetase (CPS) from E. coli is an ?? heterodimeric allosterically regulated enzyme serving as a gatekeeper for entry into both the de novo… (more)

Subjects/Keywords: Allostery; Allosteric Coupling; Coupling Free Energy; Entropy-Enthaply Compensation

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APA (6th Edition):

Koenig, R. E. (2017). Perturbations to the Allosteric Regulation of Carbamoyl Phosphate Synthetase upon Removal of Interfacial Restraints. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/169667

Chicago Manual of Style (16th Edition):

Koenig, Robert Eli. “Perturbations to the Allosteric Regulation of Carbamoyl Phosphate Synthetase upon Removal of Interfacial Restraints.” 2017. Doctoral Dissertation, Texas A&M University. Accessed October 20, 2019. http://hdl.handle.net/1969.1/169667.

MLA Handbook (7th Edition):

Koenig, Robert Eli. “Perturbations to the Allosteric Regulation of Carbamoyl Phosphate Synthetase upon Removal of Interfacial Restraints.” 2017. Web. 20 Oct 2019.

Vancouver:

Koenig RE. Perturbations to the Allosteric Regulation of Carbamoyl Phosphate Synthetase upon Removal of Interfacial Restraints. [Internet] [Doctoral dissertation]. Texas A&M University; 2017. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1969.1/169667.

Council of Science Editors:

Koenig RE. Perturbations to the Allosteric Regulation of Carbamoyl Phosphate Synthetase upon Removal of Interfacial Restraints. [Doctoral Dissertation]. Texas A&M University; 2017. Available from: http://hdl.handle.net/1969.1/169667


Texas A&M University

26. Chandler, Aglaia. The role of RpoT;3 in chloroplast development and gene expression.

Degree: 2009, Texas A&M University

 The real-time PCR assay method was used to quantify the RNA abundance of twenty-eight plastid genes in a range of tissues and developmental stages of… (more)

Subjects/Keywords: chloroplast; NEP

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APA (6th Edition):

Chandler, A. (2009). The role of RpoT;3 in chloroplast development and gene expression. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-1701

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

Chicago Manual of Style (16th Edition):

Chandler, Aglaia. “The role of RpoT;3 in chloroplast development and gene expression.” 2009. Thesis, Texas A&M University. Accessed October 20, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-1701.

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

MLA Handbook (7th Edition):

Chandler, Aglaia. “The role of RpoT;3 in chloroplast development and gene expression.” 2009. Web. 20 Oct 2019.

Vancouver:

Chandler A. The role of RpoT;3 in chloroplast development and gene expression. [Internet] [Thesis]. Texas A&M University; 2009. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1701.

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

Council of Science Editors:

Chandler A. The role of RpoT;3 in chloroplast development and gene expression. [Thesis]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1701

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

27. Wang, Shanzhi. Identification of Structural Changes Associated with Regulation of Tyrosine Hydroxylase.

Degree: 2011, Texas A&M University

 Tyrosine hydroxylase (TyrH) is the first and rate-limiting enzyme of catecholamine synthetic pathway, and its regulation is critical for controlling catecholamine synthesis. The well recognized… (more)

Subjects/Keywords: tyrosine hydroxylase; enzyme; catecholamine; inhibition; activation; regulation; conformational change

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APA (6th Edition):

Wang, S. (2011). Identification of Structural Changes Associated with Regulation of Tyrosine Hydroxylase. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8208

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

Chicago Manual of Style (16th Edition):

Wang, Shanzhi. “Identification of Structural Changes Associated with Regulation of Tyrosine Hydroxylase.” 2011. Thesis, Texas A&M University. Accessed October 20, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8208.

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

MLA Handbook (7th Edition):

Wang, Shanzhi. “Identification of Structural Changes Associated with Regulation of Tyrosine Hydroxylase.” 2011. Web. 20 Oct 2019.

Vancouver:

Wang S. Identification of Structural Changes Associated with Regulation of Tyrosine Hydroxylase. [Internet] [Thesis]. Texas A&M University; 2011. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8208.

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

Council of Science Editors:

Wang S. Identification of Structural Changes Associated with Regulation of Tyrosine Hydroxylase. [Thesis]. Texas A&M University; 2011. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8208

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

28. Foulke-Abel, Jennifer. Natural Product Biosynthesis: Friend or Foe? From Anti-tumor Agent to Disease Causation.

Degree: 2012, Texas A&M University

 Biosynthetic natural products are invaluable resources that have been gleaned from the environment for generations, and they play an essential role in drug development. Natural… (more)

Subjects/Keywords: azinomycin B; beta-lactoglobulin; next-generation genome sequencing; natural product; bacterial resistance mechanism; biosynthesis

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APA (6th Edition):

Foulke-Abel, J. (2012). Natural Product Biosynthesis: Friend or Foe? From Anti-tumor Agent to Disease Causation. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2010-12-8705

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

Chicago Manual of Style (16th Edition):

Foulke-Abel, Jennifer. “Natural Product Biosynthesis: Friend or Foe? From Anti-tumor Agent to Disease Causation.” 2012. Thesis, Texas A&M University. Accessed October 20, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2010-12-8705.

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

MLA Handbook (7th Edition):

Foulke-Abel, Jennifer. “Natural Product Biosynthesis: Friend or Foe? From Anti-tumor Agent to Disease Causation.” 2012. Web. 20 Oct 2019.

Vancouver:

Foulke-Abel J. Natural Product Biosynthesis: Friend or Foe? From Anti-tumor Agent to Disease Causation. [Internet] [Thesis]. Texas A&M University; 2012. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-12-8705.

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

Council of Science Editors:

Foulke-Abel J. Natural Product Biosynthesis: Friend or Foe? From Anti-tumor Agent to Disease Causation. [Thesis]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-12-8705

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

29. Lund, Liliya. Biophysical and Mechanistic Characterization of Carbamoyl Phosphate Synthetase from Escherichia coli.

Degree: 2012, Texas A&M University

 Carbamoyl phosphate synthetase (CPS) from E. coli catalyzes the formation of carbamoyl phosphate, an intermediate in the biosynthesis of pyrimidine nucleotides and arginine, from glutamine,… (more)

Subjects/Keywords: Carbamoyl phosphate synthetase; intramolecular tunnels; ammonia transport; carbamate transport; formyl phosphate formation

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APA (6th Edition):

Lund, L. (2012). Biophysical and Mechanistic Characterization of Carbamoyl Phosphate Synthetase from Escherichia coli. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2010-12-8792

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

Chicago Manual of Style (16th Edition):

Lund, Liliya. “Biophysical and Mechanistic Characterization of Carbamoyl Phosphate Synthetase from Escherichia coli.” 2012. Thesis, Texas A&M University. Accessed October 20, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2010-12-8792.

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

MLA Handbook (7th Edition):

Lund, Liliya. “Biophysical and Mechanistic Characterization of Carbamoyl Phosphate Synthetase from Escherichia coli.” 2012. Web. 20 Oct 2019.

Vancouver:

Lund L. Biophysical and Mechanistic Characterization of Carbamoyl Phosphate Synthetase from Escherichia coli. [Internet] [Thesis]. Texas A&M University; 2012. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-12-8792.

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

Council of Science Editors:

Lund L. Biophysical and Mechanistic Characterization of Carbamoyl Phosphate Synthetase from Escherichia coli. [Thesis]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-12-8792

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

30. Cummings, Jennifer Ann. D-Aminoacylases and Dipeptidases within the Amidohydrolase Superfamily: Relationship Between Enzyme Structure and Substrate Specificity.

Degree: 2012, Texas A&M University

 Approximately one third of the genes for the completely sequenced bacterial genomes have an unknown, uncertain, or incorrect functional annotation. Approximately 11,000 putative proteins identified… (more)

Subjects/Keywords: Jennifer Cummings; Amidohydrolase Superfamily; TIM-barrel; alpha-beta barrel; D-aminoacylase; Dipeptidase; dipeptides; enzymology; phosphinate; phosphonate; D-amino acid; Clusters of Orthologous Groups; Cc2746; Gox2272; Bb3285; Rsp_0802; Lmo2462; Bh2271; Sco4986

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

APA (6th Edition):

Cummings, J. A. (2012). D-Aminoacylases and Dipeptidases within the Amidohydrolase Superfamily: Relationship Between Enzyme Structure and Substrate Specificity. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2010-12-9021

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

Chicago Manual of Style (16th Edition):

Cummings, Jennifer Ann. “D-Aminoacylases and Dipeptidases within the Amidohydrolase Superfamily: Relationship Between Enzyme Structure and Substrate Specificity.” 2012. Thesis, Texas A&M University. Accessed October 20, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2010-12-9021.

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

MLA Handbook (7th Edition):

Cummings, Jennifer Ann. “D-Aminoacylases and Dipeptidases within the Amidohydrolase Superfamily: Relationship Between Enzyme Structure and Substrate Specificity.” 2012. Web. 20 Oct 2019.

Vancouver:

Cummings JA. D-Aminoacylases and Dipeptidases within the Amidohydrolase Superfamily: Relationship Between Enzyme Structure and Substrate Specificity. [Internet] [Thesis]. Texas A&M University; 2012. [cited 2019 Oct 20]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-12-9021.

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

Council of Science Editors:

Cummings JA. D-Aminoacylases and Dipeptidases within the Amidohydrolase Superfamily: Relationship Between Enzyme Structure and Substrate Specificity. [Thesis]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-12-9021

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

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