Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for +publisher:"Texas A&M University" +contributor:("Sacchettini, James"). Showing records 1 – 30 of 57 total matches.

[1] [2]

Search Limiters

Last 2 Years | English Only

▼ Search Limiters


Texas A&M University

1. LaiHing, Steven 1983-. Using High Throughput Screening to Acquire Promising Drug Candidates Against Mycobacterium tuberculosis.

Degree: 2011, Texas A&M University

 Mycobacterium tuberculosis currently affects 1/3 of the world's population. Over the past 20 years tuberculosis has become more resistant to all front line drugs used… (more)

Subjects/Keywords: HTS; TB; MTB; Drug Development and Design; High Throughput Screening; Tuberculosis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

LaiHing, S. 1. (2011). Using High Throughput Screening to Acquire Promising Drug Candidates Against Mycobacterium tuberculosis. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/153195

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):

LaiHing, Steven 1983-. “Using High Throughput Screening to Acquire Promising Drug Candidates Against Mycobacterium tuberculosis.” 2011. Thesis, Texas A&M University. Accessed February 21, 2020. http://hdl.handle.net/1969.1/153195.

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

MLA Handbook (7th Edition):

LaiHing, Steven 1983-. “Using High Throughput Screening to Acquire Promising Drug Candidates Against Mycobacterium tuberculosis.” 2011. Web. 21 Feb 2020.

Vancouver:

LaiHing S1. Using High Throughput Screening to Acquire Promising Drug Candidates Against Mycobacterium tuberculosis. [Internet] [Thesis]. Texas A&M University; 2011. [cited 2020 Feb 21]. Available from: http://hdl.handle.net/1969.1/153195.

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

Council of Science Editors:

LaiHing S1. Using High Throughput Screening to Acquire Promising Drug Candidates Against Mycobacterium tuberculosis. [Thesis]. Texas A&M University; 2011. Available from: http://hdl.handle.net/1969.1/153195

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


Texas A&M University

2. Tian, Xinxin. Probing the Details of the Allosteric Inhibition in Phosphofructokinase from Thermus thermophilus.

Degree: 2016, Texas A&M University

 The enzyme phosphofructokinase (PFK,) catalyzes the phosphorylation of fructose-6-phosphate in the glycolysis pathway. Phosphoenolpyruvate (PEP) allosterically inhibits the binding of the substrate fructose-6-phosphate (Fru-6-P) in… (more)

Subjects/Keywords: Phosphofructokinase from Thermus thermophilus; Allosteric Inhibition; Coupling Free Energy; Fluorescence

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Tian, X. (2016). Probing the Details of the Allosteric Inhibition in Phosphofructokinase from Thermus thermophilus. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/158944

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):

Tian, Xinxin. “Probing the Details of the Allosteric Inhibition in Phosphofructokinase from Thermus thermophilus.” 2016. Thesis, Texas A&M University. Accessed February 21, 2020. http://hdl.handle.net/1969.1/158944.

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

MLA Handbook (7th Edition):

Tian, Xinxin. “Probing the Details of the Allosteric Inhibition in Phosphofructokinase from Thermus thermophilus.” 2016. Web. 21 Feb 2020.

Vancouver:

Tian X. Probing the Details of the Allosteric Inhibition in Phosphofructokinase from Thermus thermophilus. [Internet] [Thesis]. Texas A&M University; 2016. [cited 2020 Feb 21]. Available from: http://hdl.handle.net/1969.1/158944.

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

Council of Science Editors:

Tian X. Probing the Details of the Allosteric Inhibition in Phosphofructokinase from Thermus thermophilus. [Thesis]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/158944

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


Texas A&M University

3. Wu, Fei. Comparative activation of estrogen receptor alpha (er alpha) by endocrine disruptors.

Degree: 2009, Texas A&M University

 Estrogen receptor ? (ER?) is a ligand activated transcription factor. Many widely used synthetic compounds and natural chemicals can activate ER?. The compounds investigated in… (more)

Subjects/Keywords: estrogen receptor; endocrine disruptors; breast cancer

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Wu, F. (2009). Comparative activation of estrogen receptor alpha (er alpha) by endocrine disruptors. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2433

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):

Wu, Fei. “Comparative activation of estrogen receptor alpha (er alpha) by endocrine disruptors.” 2009. Thesis, Texas A&M University. Accessed February 21, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2433.

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

MLA Handbook (7th Edition):

Wu, Fei. “Comparative activation of estrogen receptor alpha (er alpha) by endocrine disruptors.” 2009. Web. 21 Feb 2020.

Vancouver:

Wu F. Comparative activation of estrogen receptor alpha (er alpha) by endocrine disruptors. [Internet] [Thesis]. Texas A&M University; 2009. [cited 2020 Feb 21]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2433.

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

Council of Science Editors:

Wu F. Comparative activation of estrogen receptor alpha (er alpha) by endocrine disruptors. [Thesis]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2433

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


Texas A&M University

4. Qu, Xiaotao. A Molecular Mechanics Knowledge Base Applied to Template Based Structure Prediction.

Degree: 2011, Texas A&M University

 Predicting protein structure using its primary sequence has always been a challenging topic in biochemistry. Although it seems as simple as finding the minimal energy… (more)

Subjects/Keywords: structure prediction; molecular dynamics; casp; protein packing; beta hairpin

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Qu, X. (2011). A Molecular Mechanics Knowledge Base Applied to Template Based Structure Prediction. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7234

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):

Qu, Xiaotao. “A Molecular Mechanics Knowledge Base Applied to Template Based Structure Prediction.” 2011. Thesis, Texas A&M University. Accessed February 21, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7234.

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

MLA Handbook (7th Edition):

Qu, Xiaotao. “A Molecular Mechanics Knowledge Base Applied to Template Based Structure Prediction.” 2011. Web. 21 Feb 2020.

Vancouver:

Qu X. A Molecular Mechanics Knowledge Base Applied to Template Based Structure Prediction. [Internet] [Thesis]. Texas A&M University; 2011. [cited 2020 Feb 21]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7234.

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

Council of Science Editors:

Qu X. A Molecular Mechanics Knowledge Base Applied to Template Based Structure Prediction. [Thesis]. Texas A&M University; 2011. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7234

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


Texas A&M University

5. Zhu, Wan Wen. Structural and Functional Studies of Mycothiol Biosynthesis Precursor Enzyme in Mycobacterium tuberculosis.

Degree: 2012, Texas A&M University

 MshA is a glycosyltransferase that synthesizes the precursor of mycothiol, a low-molecular-weight thiol found exclusively in Actinomycetes, including the virulent pathogen Mycobacterium tuberculosis (Mtb). The… (more)

Subjects/Keywords: MshA; glycosyltransferase; mycothiol; Mycobacterium tuberculosis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Zhu, W. W. (2012). Structural and Functional Studies of Mycothiol Biosynthesis Precursor Enzyme in Mycobacterium tuberculosis. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2011-08-9929

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):

Zhu, Wan Wen. “Structural and Functional Studies of Mycothiol Biosynthesis Precursor Enzyme in Mycobacterium tuberculosis.” 2012. Thesis, Texas A&M University. Accessed February 21, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2011-08-9929.

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

MLA Handbook (7th Edition):

Zhu, Wan Wen. “Structural and Functional Studies of Mycothiol Biosynthesis Precursor Enzyme in Mycobacterium tuberculosis.” 2012. Web. 21 Feb 2020.

Vancouver:

Zhu WW. Structural and Functional Studies of Mycothiol Biosynthesis Precursor Enzyme in Mycobacterium tuberculosis. [Internet] [Thesis]. Texas A&M University; 2012. [cited 2020 Feb 21]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2011-08-9929.

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

Council of Science Editors:

Zhu WW. Structural and Functional Studies of Mycothiol Biosynthesis Precursor Enzyme in Mycobacterium tuberculosis. [Thesis]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2011-08-9929

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


Texas A&M University

6. Kuznetsov, Vladimir 1973-. Structural Studies of Phage Lysis Proteins and Their Targets.

Degree: 2011, Texas A&M University

 Bacteriophages (phages) are viruses that infect bacteria. The phages that are described by this dissertation encompass 2 classes, double-stranded DNA phages and single-stranded RNA phages.… (more)

Subjects/Keywords: phage T4; antiholin; holin

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Kuznetsov, V. 1. (2011). Structural Studies of Phage Lysis Proteins and Their Targets. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/150953

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):

Kuznetsov, Vladimir 1973-. “Structural Studies of Phage Lysis Proteins and Their Targets.” 2011. Thesis, Texas A&M University. Accessed February 21, 2020. http://hdl.handle.net/1969.1/150953.

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

MLA Handbook (7th Edition):

Kuznetsov, Vladimir 1973-. “Structural Studies of Phage Lysis Proteins and Their Targets.” 2011. Web. 21 Feb 2020.

Vancouver:

Kuznetsov V1. Structural Studies of Phage Lysis Proteins and Their Targets. [Internet] [Thesis]. Texas A&M University; 2011. [cited 2020 Feb 21]. Available from: http://hdl.handle.net/1969.1/150953.

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

Council of Science Editors:

Kuznetsov V1. Structural Studies of Phage Lysis Proteins and Their Targets. [Thesis]. Texas A&M University; 2011. Available from: http://hdl.handle.net/1969.1/150953

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


Texas A&M University

7. Liu, Zhen. Understanding and Targeting Lipid Metabolism of Mycobacterium tuberculosis.

Degree: 2013, Texas A&M University

 Mycobacterium tuberculosis (M. tuberculosis) contains a wide array of genes responsible for the synthesis and secretion of a variety of bioactive lipids. The genes represent… (more)

Subjects/Keywords: Structural biology; Enzymology; Drug discovery; Lipid metabolism

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Liu, Z. (2013). Understanding and Targeting Lipid Metabolism of Mycobacterium tuberculosis. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/151650

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):

Liu, Zhen. “Understanding and Targeting Lipid Metabolism of Mycobacterium tuberculosis.” 2013. Thesis, Texas A&M University. Accessed February 21, 2020. http://hdl.handle.net/1969.1/151650.

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

MLA Handbook (7th Edition):

Liu, Zhen. “Understanding and Targeting Lipid Metabolism of Mycobacterium tuberculosis.” 2013. Web. 21 Feb 2020.

Vancouver:

Liu Z. Understanding and Targeting Lipid Metabolism of Mycobacterium tuberculosis. [Internet] [Thesis]. Texas A&M University; 2013. [cited 2020 Feb 21]. Available from: http://hdl.handle.net/1969.1/151650.

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

Council of Science Editors:

Liu Z. Understanding and Targeting Lipid Metabolism of Mycobacterium tuberculosis. [Thesis]. Texas A&M University; 2013. Available from: http://hdl.handle.net/1969.1/151650

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


Texas A&M University

8. Lalgondar, Mallikarjun. Structural Studies and Evaluation of Inhibitors of Mycobacterium tuberculosis H37Rv Shikimate Dehydrogenase (MtSDH).

Degree: 2014, Texas A&M University

 Shikimate dehydrogenase (SDH) is a reversible enzyme catalyzing the reduction of 3-dehydroshikimate (3DHS) to shikimate (SKM) utilizing NADPH cofactor in the shikimate pathway, a central… (more)

Subjects/Keywords: Mycobacterium tuberculosis; Shikimate dehydrogenase; Crystal structure; Inhibitors

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lalgondar, M. (2014). Structural Studies and Evaluation of Inhibitors of Mycobacterium tuberculosis H37Rv Shikimate Dehydrogenase (MtSDH). (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/152582

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):

Lalgondar, Mallikarjun. “Structural Studies and Evaluation of Inhibitors of Mycobacterium tuberculosis H37Rv Shikimate Dehydrogenase (MtSDH).” 2014. Thesis, Texas A&M University. Accessed February 21, 2020. http://hdl.handle.net/1969.1/152582.

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

MLA Handbook (7th Edition):

Lalgondar, Mallikarjun. “Structural Studies and Evaluation of Inhibitors of Mycobacterium tuberculosis H37Rv Shikimate Dehydrogenase (MtSDH).” 2014. Web. 21 Feb 2020.

Vancouver:

Lalgondar M. Structural Studies and Evaluation of Inhibitors of Mycobacterium tuberculosis H37Rv Shikimate Dehydrogenase (MtSDH). [Internet] [Thesis]. Texas A&M University; 2014. [cited 2020 Feb 21]. Available from: http://hdl.handle.net/1969.1/152582.

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

Council of Science Editors:

Lalgondar M. Structural Studies and Evaluation of Inhibitors of Mycobacterium tuberculosis H37Rv Shikimate Dehydrogenase (MtSDH). [Thesis]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/152582

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


Texas A&M University

9. Joseph, Sonia. The Biochemical Investigation and Isolation of Small Molecule Inhibitors for Two Essential Proteins of Mycobacterium tuberculosis H37Rv: IspD and Wag31.

Degree: 2014, Texas A&M University

 Tuberculosis is one of the leading causes of death due to infectious disease. The causative agent, Mycobacterium tuberculosis, is a facultative intracellular parasite with a… (more)

Subjects/Keywords: IspD; Wag31; Isoprenoid biosynthesis; DivIVa protein family; screening; Tuberculosis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Joseph, S. (2014). The Biochemical Investigation and Isolation of Small Molecule Inhibitors for Two Essential Proteins of Mycobacterium tuberculosis H37Rv: IspD and Wag31. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/153274

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):

Joseph, Sonia. “The Biochemical Investigation and Isolation of Small Molecule Inhibitors for Two Essential Proteins of Mycobacterium tuberculosis H37Rv: IspD and Wag31.” 2014. Thesis, Texas A&M University. Accessed February 21, 2020. http://hdl.handle.net/1969.1/153274.

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

MLA Handbook (7th Edition):

Joseph, Sonia. “The Biochemical Investigation and Isolation of Small Molecule Inhibitors for Two Essential Proteins of Mycobacterium tuberculosis H37Rv: IspD and Wag31.” 2014. Web. 21 Feb 2020.

Vancouver:

Joseph S. The Biochemical Investigation and Isolation of Small Molecule Inhibitors for Two Essential Proteins of Mycobacterium tuberculosis H37Rv: IspD and Wag31. [Internet] [Thesis]. Texas A&M University; 2014. [cited 2020 Feb 21]. Available from: http://hdl.handle.net/1969.1/153274.

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

Council of Science Editors:

Joseph S. The Biochemical Investigation and Isolation of Small Molecule Inhibitors for Two Essential Proteins of Mycobacterium tuberculosis H37Rv: IspD and Wag31. [Thesis]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/153274

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


Texas A&M University

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

Degree: 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

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

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

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):

Fox, Nicholas G. “A Biophysical Approach to Investigate the Human Fe-S Cluster Assembly Pathway.” 2014. Thesis, Texas A&M University. Accessed February 21, 2020. http://hdl.handle.net/1969.1/153303.

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

MLA Handbook (7th Edition):

Fox, Nicholas G. “A Biophysical Approach to Investigate the Human Fe-S Cluster Assembly Pathway.” 2014. Web. 21 Feb 2020.

Vancouver:

Fox NG. A Biophysical Approach to Investigate the Human Fe-S Cluster Assembly Pathway. [Internet] [Thesis]. Texas A&M University; 2014. [cited 2020 Feb 21]. Available from: http://hdl.handle.net/1969.1/153303.

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

Council of Science Editors:

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

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


Texas A&M University

11. Li, Zhanyong. Synthesis, Characterization and Investigation of Metal-Metal Bonded Dirhodium Complexes.

Degree: 2014, Texas A&M University

 This dissertation focuses on the design and tailoring of dirhodium complexes and the investigation of their structural, spectroscopic and theoretical properties. The variation of the… (more)

Subjects/Keywords: dirhodium; photodynamic therapy; photocatalysis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Li, Z. (2014). Synthesis, Characterization and Investigation of Metal-Metal Bonded Dirhodium Complexes. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/153325

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, Zhanyong. “Synthesis, Characterization and Investigation of Metal-Metal Bonded Dirhodium Complexes.” 2014. Thesis, Texas A&M University. Accessed February 21, 2020. http://hdl.handle.net/1969.1/153325.

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

MLA Handbook (7th Edition):

Li, Zhanyong. “Synthesis, Characterization and Investigation of Metal-Metal Bonded Dirhodium Complexes.” 2014. Web. 21 Feb 2020.

Vancouver:

Li Z. Synthesis, Characterization and Investigation of Metal-Metal Bonded Dirhodium Complexes. [Internet] [Thesis]. Texas A&M University; 2014. [cited 2020 Feb 21]. Available from: http://hdl.handle.net/1969.1/153325.

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

Council of Science Editors:

Li Z. Synthesis, Characterization and Investigation of Metal-Metal Bonded Dirhodium Complexes. [Thesis]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/153325

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


Texas A&M University

12. Ragavan, Mukundan. Dissolution Dynamic Nuclear Polarization of Polypeptides.

Degree: 2014, Texas A&M University

 Nuclear Magnetic Resonance (NMR) spectroscopy provides remarkable site resolution, but often requires signal averaging because of low sensitivity. Dissolution dynamic nuclear polarization (DNP), which offers… (more)

Subjects/Keywords: dnp; protein; nmr

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ragavan, M. (2014). Dissolution Dynamic Nuclear Polarization of Polypeptides. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/153352

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):

Ragavan, Mukundan. “Dissolution Dynamic Nuclear Polarization of Polypeptides.” 2014. Thesis, Texas A&M University. Accessed February 21, 2020. http://hdl.handle.net/1969.1/153352.

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

MLA Handbook (7th Edition):

Ragavan, Mukundan. “Dissolution Dynamic Nuclear Polarization of Polypeptides.” 2014. Web. 21 Feb 2020.

Vancouver:

Ragavan M. Dissolution Dynamic Nuclear Polarization of Polypeptides. [Internet] [Thesis]. Texas A&M University; 2014. [cited 2020 Feb 21]. Available from: http://hdl.handle.net/1969.1/153352.

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

Council of Science Editors:

Ragavan M. Dissolution Dynamic Nuclear Polarization of Polypeptides. [Thesis]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/153352

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


Texas A&M University

13. Vargas Bautista, Carol M. Complex Organization and Dynamic Regulation of the pks Gene Cluster in Bacillus subtilis.

Degree: 2014, Texas A&M University

 The pks genes are the largest antibiotic- encoding gene cluster in Bacillus subtilis and encode the Pks enzymatic complex that produces bacillaene. Bacillaene plays important… (more)

Subjects/Keywords: Bacillaene; Regulation

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Vargas Bautista, C. M. (2014). Complex Organization and Dynamic Regulation of the pks Gene Cluster in Bacillus subtilis. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/153831

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):

Vargas Bautista, Carol M. “Complex Organization and Dynamic Regulation of the pks Gene Cluster in Bacillus subtilis.” 2014. Thesis, Texas A&M University. Accessed February 21, 2020. http://hdl.handle.net/1969.1/153831.

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

MLA Handbook (7th Edition):

Vargas Bautista, Carol M. “Complex Organization and Dynamic Regulation of the pks Gene Cluster in Bacillus subtilis.” 2014. Web. 21 Feb 2020.

Vancouver:

Vargas Bautista CM. Complex Organization and Dynamic Regulation of the pks Gene Cluster in Bacillus subtilis. [Internet] [Thesis]. Texas A&M University; 2014. [cited 2020 Feb 21]. Available from: http://hdl.handle.net/1969.1/153831.

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

Council of Science Editors:

Vargas Bautista CM. Complex Organization and Dynamic Regulation of the pks Gene Cluster in Bacillus subtilis. [Thesis]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/153831

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


Texas A&M University

14. Sekar, Giridhar. NMR Studies of Membrane Associating Peptides and Implications in Autotransporter Function.

Degree: 2014, Texas A&M University

 Membrane associating peptides such as antimicrobial peptides and viral fusion peptides are involved in a diverse set of physiological processes. Their functions often require a… (more)

Subjects/Keywords: Membrane Associating Peptide; NMR Spectroscopy; CD Spectroscopy; Autotransporters; Thermal Denaturation

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Sekar, G. (2014). NMR Studies of Membrane Associating Peptides and Implications in Autotransporter Function. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/153902

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):

Sekar, Giridhar. “NMR Studies of Membrane Associating Peptides and Implications in Autotransporter Function.” 2014. Thesis, Texas A&M University. Accessed February 21, 2020. http://hdl.handle.net/1969.1/153902.

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

MLA Handbook (7th Edition):

Sekar, Giridhar. “NMR Studies of Membrane Associating Peptides and Implications in Autotransporter Function.” 2014. Web. 21 Feb 2020.

Vancouver:

Sekar G. NMR Studies of Membrane Associating Peptides and Implications in Autotransporter Function. [Internet] [Thesis]. Texas A&M University; 2014. [cited 2020 Feb 21]. Available from: http://hdl.handle.net/1969.1/153902.

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

Council of Science Editors:

Sekar G. NMR Studies of Membrane Associating Peptides and Implications in Autotransporter Function. [Thesis]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/153902

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


Texas A&M University

15. Harshbarger, Wayne. X-Ray Crystal Structure of Human 20s Proteasome in Complex with Carfilzomib.

Degree: 2015, Texas A&M University

 20S proteasomes are large, multicatalytic N- terminal threonine proteases which are tasked with maintaining intracellular homeostasis by the breaking down of mis-folded, oxidized, or tagged… (more)

Subjects/Keywords: 20S Proteasome; carfilzomib; multiple myeloma; cellular regulation

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Harshbarger, W. (2015). X-Ray Crystal Structure of Human 20s Proteasome in Complex with Carfilzomib. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/155004

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):

Harshbarger, Wayne. “X-Ray Crystal Structure of Human 20s Proteasome in Complex with Carfilzomib.” 2015. Thesis, Texas A&M University. Accessed February 21, 2020. http://hdl.handle.net/1969.1/155004.

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

MLA Handbook (7th Edition):

Harshbarger, Wayne. “X-Ray Crystal Structure of Human 20s Proteasome in Complex with Carfilzomib.” 2015. Web. 21 Feb 2020.

Vancouver:

Harshbarger W. X-Ray Crystal Structure of Human 20s Proteasome in Complex with Carfilzomib. [Internet] [Thesis]. Texas A&M University; 2015. [cited 2020 Feb 21]. Available from: http://hdl.handle.net/1969.1/155004.

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

Council of Science Editors:

Harshbarger W. X-Ray Crystal Structure of Human 20s Proteasome in Complex with Carfilzomib. [Thesis]. Texas A&M University; 2015. Available from: http://hdl.handle.net/1969.1/155004

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


Texas A&M University

16. Hughes, Ryan C. Identification of Whole Cell Active Molecules of Mycobacterium Tuberculosis, Elucidation of Molecular Mechanisms Responsible for Resistance, and Characterization of Rv0272: A potential Therapeutic Target.

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

 Current therapies for treatment of mycobacterial infections are adequate when diagnosis and pathology is well defined. Yet more evidence is beginning to accumulate for the… (more)

Subjects/Keywords: Tuberculosis; Drug Discovery; Crystallography; Serine Hydrolase

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Hughes, R. C. (2016). Identification of Whole Cell Active Molecules of Mycobacterium Tuberculosis, Elucidation of Molecular Mechanisms Responsible for Resistance, and Characterization of Rv0272: A potential Therapeutic Target. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/159056

Chicago Manual of Style (16th Edition):

Hughes, Ryan C. “Identification of Whole Cell Active Molecules of Mycobacterium Tuberculosis, Elucidation of Molecular Mechanisms Responsible for Resistance, and Characterization of Rv0272: A potential Therapeutic Target.” 2016. Doctoral Dissertation, Texas A&M University. Accessed February 21, 2020. http://hdl.handle.net/1969.1/159056.

MLA Handbook (7th Edition):

Hughes, Ryan C. “Identification of Whole Cell Active Molecules of Mycobacterium Tuberculosis, Elucidation of Molecular Mechanisms Responsible for Resistance, and Characterization of Rv0272: A potential Therapeutic Target.” 2016. Web. 21 Feb 2020.

Vancouver:

Hughes RC. Identification of Whole Cell Active Molecules of Mycobacterium Tuberculosis, Elucidation of Molecular Mechanisms Responsible for Resistance, and Characterization of Rv0272: A potential Therapeutic Target. [Internet] [Doctoral dissertation]. Texas A&M University; 2016. [cited 2020 Feb 21]. Available from: http://hdl.handle.net/1969.1/159056.

Council of Science Editors:

Hughes RC. Identification of Whole Cell Active Molecules of Mycobacterium Tuberculosis, Elucidation of Molecular Mechanisms Responsible for Resistance, and Characterization of Rv0272: A potential Therapeutic Target. [Doctoral Dissertation]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/159056


Texas A&M University

17. Najjar, Kristina. Identifying and Characterizing Molecular Parameters that Modulate the Endosomal Escape of Cationic Cell- Penetrating Peptides: A Structure Activity Approach.

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

 For over 20 years, cell-penetrating peptides (CPPs) have been used as delivery vectors transporting macromolecules (cargos) into live cells for cell biology manipulations and therapeutic… (more)

Subjects/Keywords: Cell-penetrating peptides; Cell culture; Endocytic pathway

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Najjar, K. (2017). Identifying and Characterizing Molecular Parameters that Modulate the Endosomal Escape of Cationic Cell- Penetrating Peptides: A Structure Activity Approach. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/165896

Chicago Manual of Style (16th Edition):

Najjar, Kristina. “Identifying and Characterizing Molecular Parameters that Modulate the Endosomal Escape of Cationic Cell- Penetrating Peptides: A Structure Activity Approach.” 2017. Doctoral Dissertation, Texas A&M University. Accessed February 21, 2020. http://hdl.handle.net/1969.1/165896.

MLA Handbook (7th Edition):

Najjar, Kristina. “Identifying and Characterizing Molecular Parameters that Modulate the Endosomal Escape of Cationic Cell- Penetrating Peptides: A Structure Activity Approach.” 2017. Web. 21 Feb 2020.

Vancouver:

Najjar K. Identifying and Characterizing Molecular Parameters that Modulate the Endosomal Escape of Cationic Cell- Penetrating Peptides: A Structure Activity Approach. [Internet] [Doctoral dissertation]. Texas A&M University; 2017. [cited 2020 Feb 21]. Available from: http://hdl.handle.net/1969.1/165896.

Council of Science Editors:

Najjar K. Identifying and Characterizing Molecular Parameters that Modulate the Endosomal Escape of Cationic Cell- Penetrating Peptides: A Structure Activity Approach. [Doctoral Dissertation]. Texas A&M University; 2017. Available from: http://hdl.handle.net/1969.1/165896


Texas A&M University

18. Shepherd, Tonya Fujina. RV3295 (LuxR1) Is a Transcriptional Regulator Important for Virulence in the Mycobacterium Tuberculosis and Mycobacterium Marinum In Vitro and In Vivo Models.

Degree: 2016, Texas A&M University

 Mycobacterium tuberculosis (Mtb) is the infectious agent that causes tuberculosis (Tb). In 2014, 1.5 million people succumbed to tuberculosis while an additional nine million became… (more)

Subjects/Keywords: LuxR; mycobacteria; regulator; virulence

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Shepherd, T. F. (2016). RV3295 (LuxR1) Is a Transcriptional Regulator Important for Virulence in the Mycobacterium Tuberculosis and Mycobacterium Marinum In Vitro and In Vivo Models. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/158086

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):

Shepherd, Tonya Fujina. “RV3295 (LuxR1) Is a Transcriptional Regulator Important for Virulence in the Mycobacterium Tuberculosis and Mycobacterium Marinum In Vitro and In Vivo Models.” 2016. Thesis, Texas A&M University. Accessed February 21, 2020. http://hdl.handle.net/1969.1/158086.

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

MLA Handbook (7th Edition):

Shepherd, Tonya Fujina. “RV3295 (LuxR1) Is a Transcriptional Regulator Important for Virulence in the Mycobacterium Tuberculosis and Mycobacterium Marinum In Vitro and In Vivo Models.” 2016. Web. 21 Feb 2020.

Vancouver:

Shepherd TF. RV3295 (LuxR1) Is a Transcriptional Regulator Important for Virulence in the Mycobacterium Tuberculosis and Mycobacterium Marinum In Vitro and In Vivo Models. [Internet] [Thesis]. Texas A&M University; 2016. [cited 2020 Feb 21]. Available from: http://hdl.handle.net/1969.1/158086.

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

Council of Science Editors:

Shepherd TF. RV3295 (LuxR1) Is a Transcriptional Regulator Important for Virulence in the Mycobacterium Tuberculosis and Mycobacterium Marinum In Vitro and In Vivo Models. [Thesis]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/158086

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


Texas A&M University

19. De Jesus Aneiro, Michael A. Statistical Analysis of Transposon Sequencing Data to Determine Essential Genes.

Degree: 2016, Texas A&M University

 Transposon Sequencing (TnSeq) has become a popular biological tool for assessing the phenotypes of large libraries of bacterial mutants at the same time. This allows… (more)

Subjects/Keywords: TnSeq; transposon mutagenesis; Bayesian Statistics; MCMC; Modeling; Classification

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

De Jesus Aneiro, M. A. (2016). Statistical Analysis of Transposon Sequencing Data to Determine Essential Genes. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/159011

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):

De Jesus Aneiro, Michael A. “Statistical Analysis of Transposon Sequencing Data to Determine Essential Genes.” 2016. Thesis, Texas A&M University. Accessed February 21, 2020. http://hdl.handle.net/1969.1/159011.

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

MLA Handbook (7th Edition):

De Jesus Aneiro, Michael A. “Statistical Analysis of Transposon Sequencing Data to Determine Essential Genes.” 2016. Web. 21 Feb 2020.

Vancouver:

De Jesus Aneiro MA. Statistical Analysis of Transposon Sequencing Data to Determine Essential Genes. [Internet] [Thesis]. Texas A&M University; 2016. [cited 2020 Feb 21]. Available from: http://hdl.handle.net/1969.1/159011.

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

Council of Science Editors:

De Jesus Aneiro MA. Statistical Analysis of Transposon Sequencing Data to Determine Essential Genes. [Thesis]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/159011

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


Texas A&M University

20. Van, Khoi Ngoc. I. Application of Chiral ?,?-Unsaturated Acylammonium Salts for Efficient Catalytic Transformations II. Studies toward the Total Synthesis of Rameswaralide.

Degree: 2017, Texas A&M University

 The developments of novel catalytic transformations are just as important as the discoveries of new reactions. In the most common way, catalysts provide more efficient… (more)

Subjects/Keywords: organocatalysis; ?,?-unsaturated acylammonium salts; multicomponent; MCR; tertiary amine; ?-lactone; rameswaralide

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Van, K. N. (2017). I. Application of Chiral ?,?-Unsaturated Acylammonium Salts for Efficient Catalytic Transformations II. Studies toward the Total Synthesis of Rameswaralide. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/161472

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):

Van, Khoi Ngoc. “I. Application of Chiral ?,?-Unsaturated Acylammonium Salts for Efficient Catalytic Transformations II. Studies toward the Total Synthesis of Rameswaralide.” 2017. Thesis, Texas A&M University. Accessed February 21, 2020. http://hdl.handle.net/1969.1/161472.

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

MLA Handbook (7th Edition):

Van, Khoi Ngoc. “I. Application of Chiral ?,?-Unsaturated Acylammonium Salts for Efficient Catalytic Transformations II. Studies toward the Total Synthesis of Rameswaralide.” 2017. Web. 21 Feb 2020.

Vancouver:

Van KN. I. Application of Chiral ?,?-Unsaturated Acylammonium Salts for Efficient Catalytic Transformations II. Studies toward the Total Synthesis of Rameswaralide. [Internet] [Thesis]. Texas A&M University; 2017. [cited 2020 Feb 21]. Available from: http://hdl.handle.net/1969.1/161472.

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

Council of Science Editors:

Van KN. I. Application of Chiral ?,?-Unsaturated Acylammonium Salts for Efficient Catalytic Transformations II. Studies toward the Total Synthesis of Rameswaralide. [Thesis]. Texas A&M University; 2017. Available from: http://hdl.handle.net/1969.1/161472

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


Texas A&M University

21. Dey, Sanghamitra. Structural insights into the enzymes of the serine and biotin biosynthetic pathways in mycobacterium tuberculosis.

Degree: 2009, Texas A&M University

 Mycobacterium tuberculosis (Mtb) utilizes different metabolic pathways for its survival during infection. Enzymes of these pathways are often targets for antibiotic development. Genetic studies indicate… (more)

Subjects/Keywords: serine biosynthesis; biotin biosynthesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Dey, S. (2009). Structural insights into the enzymes of the serine and biotin biosynthetic pathways in mycobacterium tuberculosis. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2882

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):

Dey, Sanghamitra. “Structural insights into the enzymes of the serine and biotin biosynthetic pathways in mycobacterium tuberculosis.” 2009. Thesis, Texas A&M University. Accessed February 21, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2882.

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

MLA Handbook (7th Edition):

Dey, Sanghamitra. “Structural insights into the enzymes of the serine and biotin biosynthetic pathways in mycobacterium tuberculosis.” 2009. Web. 21 Feb 2020.

Vancouver:

Dey S. Structural insights into the enzymes of the serine and biotin biosynthetic pathways in mycobacterium tuberculosis. [Internet] [Thesis]. Texas A&M University; 2009. [cited 2020 Feb 21]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2882.

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

Council of Science Editors:

Dey S. Structural insights into the enzymes of the serine and biotin biosynthetic pathways in mycobacterium tuberculosis. [Thesis]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2882

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


Texas A&M University

22. Ramesh, Arati. Structural studies of the Ro ribonucleoprotein and the metalloregulator CsoR.

Degree: 2009, Texas A&M University

 Ro ribonucleoproteins are antigenic protein-RNA particles that are the major targets of the immune reaction in autoimmune disorders like systemic lupus erythematosus. The Ro protein… (more)

Subjects/Keywords: protein-RNA interactions; transcriptional regulators

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Ramesh, A. (2009). Structural studies of the Ro ribonucleoprotein and the metalloregulator CsoR. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-1426

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):

Ramesh, Arati. “Structural studies of the Ro ribonucleoprotein and the metalloregulator CsoR.” 2009. Thesis, Texas A&M University. Accessed February 21, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-1426.

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

MLA Handbook (7th Edition):

Ramesh, Arati. “Structural studies of the Ro ribonucleoprotein and the metalloregulator CsoR.” 2009. Web. 21 Feb 2020.

Vancouver:

Ramesh A. Structural studies of the Ro ribonucleoprotein and the metalloregulator CsoR. [Internet] [Thesis]. Texas A&M University; 2009. [cited 2020 Feb 21]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1426.

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

Council of Science Editors:

Ramesh A. Structural studies of the Ro ribonucleoprotein and the metalloregulator CsoR. [Thesis]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1426

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


Texas A&M University

23. Wang, Feng. Structure-based drug mechanism study and inhibitor design targeting tuberculosis.

Degree: 2009, Texas A&M University

 The increase of multi-drug resistant and extensively drug resistant tuberculosis (TB) cases makes it urgent to develop a new generation of TB drugs to counter… (more)

Subjects/Keywords: Drug; tuberculosis; Structure

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Wang, F. (2009). Structure-based drug mechanism study and inhibitor design targeting tuberculosis. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-1439

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, Feng. “Structure-based drug mechanism study and inhibitor design targeting tuberculosis.” 2009. Thesis, Texas A&M University. Accessed February 21, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-1439.

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

MLA Handbook (7th Edition):

Wang, Feng. “Structure-based drug mechanism study and inhibitor design targeting tuberculosis.” 2009. Web. 21 Feb 2020.

Vancouver:

Wang F. Structure-based drug mechanism study and inhibitor design targeting tuberculosis. [Internet] [Thesis]. Texas A&M University; 2009. [cited 2020 Feb 21]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1439.

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

Council of Science Editors:

Wang F. Structure-based drug mechanism study and inhibitor design targeting tuberculosis. [Thesis]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1439

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


Texas A&M University

24. Yang, Dong. Structural studies of terpenoid biosynthesis and bacterial cell division.

Degree: 2009, Texas A&M University

 The objective of this work is to investigate the structures of two nucleotide binding proteins: mevalonate kinase (MVK) and FtsZ. MVK is the key enzyme… (more)

Subjects/Keywords: MVK; mevalonate; terpenoid; GHMP; FtsZ; protofilament; cytokinesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Yang, D. (2009). Structural studies of terpenoid biosynthesis and bacterial cell division. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-1737

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):

Yang, Dong. “Structural studies of terpenoid biosynthesis and bacterial cell division.” 2009. Thesis, Texas A&M University. Accessed February 21, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-1737.

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

MLA Handbook (7th Edition):

Yang, Dong. “Structural studies of terpenoid biosynthesis and bacterial cell division.” 2009. Web. 21 Feb 2020.

Vancouver:

Yang D. Structural studies of terpenoid biosynthesis and bacterial cell division. [Internet] [Thesis]. Texas A&M University; 2009. [cited 2020 Feb 21]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1737.

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

Council of Science Editors:

Yang D. Structural studies of terpenoid biosynthesis and bacterial cell division. [Thesis]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1737

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


Texas A&M University

25. Gopal, Kreshna. Efficient case-based reasoning through feature weighting, and its application in protein crystallography.

Degree: 2009, Texas A&M University

 Data preprocessing is critical for machine learning, data mining, and pattern recognition. In particular, selecting relevant and non-redundant features in highdimensional data is important to… (more)

Subjects/Keywords: Case-Based Reasoning; Nearest Neighbor Learning; Feature Selection; Feature Weighting; Protein Crystallography

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Gopal, K. (2009). Efficient case-based reasoning through feature weighting, and its application in protein crystallography. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-1906

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):

Gopal, Kreshna. “Efficient case-based reasoning through feature weighting, and its application in protein crystallography.” 2009. Thesis, Texas A&M University. Accessed February 21, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-1906.

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

MLA Handbook (7th Edition):

Gopal, Kreshna. “Efficient case-based reasoning through feature weighting, and its application in protein crystallography.” 2009. Web. 21 Feb 2020.

Vancouver:

Gopal K. Efficient case-based reasoning through feature weighting, and its application in protein crystallography. [Internet] [Thesis]. Texas A&M University; 2009. [cited 2020 Feb 21]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1906.

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

Council of Science Editors:

Gopal K. Efficient case-based reasoning through feature weighting, and its application in protein crystallography. [Thesis]. Texas A&M University; 2009. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-1906

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


Texas A&M University

26. Pai Karkala, Reetal. Fragment Based Protein Active Site Analysis Using Markov Random Field Combinations of Stereochemical Feature-Based Classifications.

Degree: 2010, Texas A&M University

 Recent improvements in structural genomics efforts have greatly increased the number of hypothetical proteins in the Protein Data Bank. Several computational methodologies have been developed… (more)

Subjects/Keywords: Active site analysis; Feature-based; Machine Learning; Markov Random Field

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Pai Karkala, R. (2010). Fragment Based Protein Active Site Analysis Using Markov Random Field Combinations of Stereochemical Feature-Based Classifications. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-550

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):

Pai Karkala, Reetal. “Fragment Based Protein Active Site Analysis Using Markov Random Field Combinations of Stereochemical Feature-Based Classifications.” 2010. Thesis, Texas A&M University. Accessed February 21, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-550.

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

MLA Handbook (7th Edition):

Pai Karkala, Reetal. “Fragment Based Protein Active Site Analysis Using Markov Random Field Combinations of Stereochemical Feature-Based Classifications.” 2010. Web. 21 Feb 2020.

Vancouver:

Pai Karkala R. Fragment Based Protein Active Site Analysis Using Markov Random Field Combinations of Stereochemical Feature-Based Classifications. [Internet] [Thesis]. Texas A&M University; 2010. [cited 2020 Feb 21]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-550.

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

Council of Science Editors:

Pai Karkala R. Fragment Based Protein Active Site Analysis Using Markov Random Field Combinations of Stereochemical Feature-Based Classifications. [Thesis]. Texas A&M University; 2010. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-05-550

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


Texas A&M University

27. Xue, Haoran. Toward the Total Synthesis of Norzoanthamine: The Development of a Transannular Michael Reaction Cascade.

Degree: 2013, Texas A&M University

 Norzoanthamine is a complex heptacyclic marine alkaloid isolated from colonial zoanthids. It potently inhibits loss of bone weight and strength in a postmenopausal osteoporosis mouse… (more)

Subjects/Keywords: Norzoanthamine; Transannular; Michael reaction; reaction cascade

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Xue, H. (2013). Toward the Total Synthesis of Norzoanthamine: The Development of a Transannular Michael Reaction Cascade. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/149334

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):

Xue, Haoran. “Toward the Total Synthesis of Norzoanthamine: The Development of a Transannular Michael Reaction Cascade.” 2013. Thesis, Texas A&M University. Accessed February 21, 2020. http://hdl.handle.net/1969.1/149334.

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

MLA Handbook (7th Edition):

Xue, Haoran. “Toward the Total Synthesis of Norzoanthamine: The Development of a Transannular Michael Reaction Cascade.” 2013. Web. 21 Feb 2020.

Vancouver:

Xue H. Toward the Total Synthesis of Norzoanthamine: The Development of a Transannular Michael Reaction Cascade. [Internet] [Thesis]. Texas A&M University; 2013. [cited 2020 Feb 21]. Available from: http://hdl.handle.net/1969.1/149334.

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

Council of Science Editors:

Xue H. Toward the Total Synthesis of Norzoanthamine: The Development of a Transannular Michael Reaction Cascade. [Thesis]. Texas A&M University; 2013. Available from: http://hdl.handle.net/1969.1/149334

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


Texas A&M University

28. Thorstad, Melissa. Functional Characterization and Surface Mapping of Frataxin (FXN) Interactions with the Fe-S Cluster Assembly Complex.

Degree: 2013, Texas A&M University

 In 1996, scientists discovered a connection between the gene for the human protein frataxin (FXN) and the neurodegenerative disease Friedreich?s ataxia (FRDA). Decreased FXN levels… (more)

Subjects/Keywords: Frataxin; iron sulfur cluster, iron sulfur cluster assembly; Friedreich's ataxia; FRDA; alanine scanning; lysine acetylation; allosteric regulation; oligomerization

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Thorstad, M. (2013). Functional Characterization and Surface Mapping of Frataxin (FXN) Interactions with the Fe-S Cluster Assembly Complex. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/151028

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):

Thorstad, Melissa. “Functional Characterization and Surface Mapping of Frataxin (FXN) Interactions with the Fe-S Cluster Assembly Complex.” 2013. Thesis, Texas A&M University. Accessed February 21, 2020. http://hdl.handle.net/1969.1/151028.

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

MLA Handbook (7th Edition):

Thorstad, Melissa. “Functional Characterization and Surface Mapping of Frataxin (FXN) Interactions with the Fe-S Cluster Assembly Complex.” 2013. Web. 21 Feb 2020.

Vancouver:

Thorstad M. Functional Characterization and Surface Mapping of Frataxin (FXN) Interactions with the Fe-S Cluster Assembly Complex. [Internet] [Thesis]. Texas A&M University; 2013. [cited 2020 Feb 21]. Available from: http://hdl.handle.net/1969.1/151028.

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

Council of Science Editors:

Thorstad M. Functional Characterization and Surface Mapping of Frataxin (FXN) Interactions with the Fe-S Cluster Assembly Complex. [Thesis]. Texas A&M University; 2013. Available from: http://hdl.handle.net/1969.1/151028

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


Texas A&M University

29. Tsai, Han-Chun. Structural Study of Lipid-binding Proteins.

Degree: 2013, Texas A&M University

 Tuberculosis and malaria are among the most deadly infectious diseases in the world. The prevalence in regions without well-established public health causes economical and financial… (more)

Subjects/Keywords: Mycobacterium tuberculosis; protein structure; lipoprotein; PfENR; mycobacteriophage; tail fiber protein

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Tsai, H. (2013). Structural Study of Lipid-binding Proteins. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/151067

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, Han-Chun. “Structural Study of Lipid-binding Proteins.” 2013. Thesis, Texas A&M University. Accessed February 21, 2020. http://hdl.handle.net/1969.1/151067.

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

MLA Handbook (7th Edition):

Tsai, Han-Chun. “Structural Study of Lipid-binding Proteins.” 2013. Web. 21 Feb 2020.

Vancouver:

Tsai H. Structural Study of Lipid-binding Proteins. [Internet] [Thesis]. Texas A&M University; 2013. [cited 2020 Feb 21]. Available from: http://hdl.handle.net/1969.1/151067.

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

Council of Science Editors:

Tsai H. Structural Study of Lipid-binding Proteins. [Thesis]. Texas A&M University; 2013. Available from: http://hdl.handle.net/1969.1/151067

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


Texas A&M University

30. Mire, Joseph Andrew. Application of Structure Activity Relationships of the Mycobacterium Tuberculosis Beta-Lactamase (BlaC) and the New Delhi Metallo-Beta-Lactamase (NDM-1) to Combating Beta-Lactamase Mediated Drug Resistance.

Degree: 2013, Texas A&M University

 ?-lactamase enzymes catalyze the irreversible hydrolysis of the four-membered cyclic amide ring characteristic of ?-lactam antibiotics rendering them inactive and useless against pathogenic bacteria. Understanding… (more)

Subjects/Keywords: beta-lactam; beta-lactamase

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Mire, J. A. (2013). Application of Structure Activity Relationships of the Mycobacterium Tuberculosis Beta-Lactamase (BlaC) and the New Delhi Metallo-Beta-Lactamase (NDM-1) to Combating Beta-Lactamase Mediated Drug Resistance. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/151238

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):

Mire, Joseph Andrew. “Application of Structure Activity Relationships of the Mycobacterium Tuberculosis Beta-Lactamase (BlaC) and the New Delhi Metallo-Beta-Lactamase (NDM-1) to Combating Beta-Lactamase Mediated Drug Resistance.” 2013. Thesis, Texas A&M University. Accessed February 21, 2020. http://hdl.handle.net/1969.1/151238.

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

MLA Handbook (7th Edition):

Mire, Joseph Andrew. “Application of Structure Activity Relationships of the Mycobacterium Tuberculosis Beta-Lactamase (BlaC) and the New Delhi Metallo-Beta-Lactamase (NDM-1) to Combating Beta-Lactamase Mediated Drug Resistance.” 2013. Web. 21 Feb 2020.

Vancouver:

Mire JA. Application of Structure Activity Relationships of the Mycobacterium Tuberculosis Beta-Lactamase (BlaC) and the New Delhi Metallo-Beta-Lactamase (NDM-1) to Combating Beta-Lactamase Mediated Drug Resistance. [Internet] [Thesis]. Texas A&M University; 2013. [cited 2020 Feb 21]. Available from: http://hdl.handle.net/1969.1/151238.

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

Council of Science Editors:

Mire JA. Application of Structure Activity Relationships of the Mycobacterium Tuberculosis Beta-Lactamase (BlaC) and the New Delhi Metallo-Beta-Lactamase (NDM-1) to Combating Beta-Lactamase Mediated Drug Resistance. [Thesis]. Texas A&M University; 2013. Available from: http://hdl.handle.net/1969.1/151238

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

[1] [2]

.