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You searched for subject:(Hexokinase HK Drug target). Showing records 1 – 30 of 12270 total matches.

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Texas A&M University

1. Eltahan, Rana Abbas Khedr. Exploring the Glycolytic Enzymes, Glucose-6-phosphate isomerase (CpGPI) and Hexokinase (CpHK) as Potential Drug Targets in Cryptosporidium parvum.

Degree: PhD, Biomedical Sciences, 2018, Texas A&M University

 Cryptosporidium parvum is a water-borne and food-borne apicomplexan pathogen. It is one of the top four diarrheal-causing pathogens in children under the age of five… (more)

Subjects/Keywords: : Apicomplexan; Cryptosporidium parvum; Glucose-6-phosphate isomerase (GPI); Ebselen; Hexokinase (HK): Drug target

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APA (6th Edition):

Eltahan, R. A. K. (2018). Exploring the Glycolytic Enzymes, Glucose-6-phosphate isomerase (CpGPI) and Hexokinase (CpHK) as Potential Drug Targets in Cryptosporidium parvum. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/173649

Chicago Manual of Style (16th Edition):

Eltahan, Rana Abbas Khedr. “Exploring the Glycolytic Enzymes, Glucose-6-phosphate isomerase (CpGPI) and Hexokinase (CpHK) as Potential Drug Targets in Cryptosporidium parvum.” 2018. Doctoral Dissertation, Texas A&M University. Accessed August 22, 2019. http://hdl.handle.net/1969.1/173649.

MLA Handbook (7th Edition):

Eltahan, Rana Abbas Khedr. “Exploring the Glycolytic Enzymes, Glucose-6-phosphate isomerase (CpGPI) and Hexokinase (CpHK) as Potential Drug Targets in Cryptosporidium parvum.” 2018. Web. 22 Aug 2019.

Vancouver:

Eltahan RAK. Exploring the Glycolytic Enzymes, Glucose-6-phosphate isomerase (CpGPI) and Hexokinase (CpHK) as Potential Drug Targets in Cryptosporidium parvum. [Internet] [Doctoral dissertation]. Texas A&M University; 2018. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/1969.1/173649.

Council of Science Editors:

Eltahan RAK. Exploring the Glycolytic Enzymes, Glucose-6-phosphate isomerase (CpGPI) and Hexokinase (CpHK) as Potential Drug Targets in Cryptosporidium parvum. [Doctoral Dissertation]. Texas A&M University; 2018. Available from: http://hdl.handle.net/1969.1/173649


Universiteit Utrecht

2. Batenburg, A.A. van. Rap1 as a potential drug target in tissue colonization of invasive leukemia tumor cells.

Degree: 2013, Universiteit Utrecht

 The actin skeleton is involved in many morphological cell processes, like cell shape, cell and extracellular matrix adhesion and migration. For this, the actin skeleton… (more)

Subjects/Keywords: Rap1; GTPase; Leukemia; drug target

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APA (6th Edition):

Batenburg, A. A. v. (2013). Rap1 as a potential drug target in tissue colonization of invasive leukemia tumor cells. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/280398

Chicago Manual of Style (16th Edition):

Batenburg, A A van. “Rap1 as a potential drug target in tissue colonization of invasive leukemia tumor cells.” 2013. Masters Thesis, Universiteit Utrecht. Accessed August 22, 2019. http://dspace.library.uu.nl:8080/handle/1874/280398.

MLA Handbook (7th Edition):

Batenburg, A A van. “Rap1 as a potential drug target in tissue colonization of invasive leukemia tumor cells.” 2013. Web. 22 Aug 2019.

Vancouver:

Batenburg AAv. Rap1 as a potential drug target in tissue colonization of invasive leukemia tumor cells. [Internet] [Masters thesis]. Universiteit Utrecht; 2013. [cited 2019 Aug 22]. Available from: http://dspace.library.uu.nl:8080/handle/1874/280398.

Council of Science Editors:

Batenburg AAv. Rap1 as a potential drug target in tissue colonization of invasive leukemia tumor cells. [Masters Thesis]. Universiteit Utrecht; 2013. Available from: http://dspace.library.uu.nl:8080/handle/1874/280398


University of Texas – Austin

3. -3365-2702. Computational discovery of genetic targets and interactions : applications to lung cancer.

Degree: Computational Science, Engineering, and Mathematics, 2016, University of Texas – Austin

 We present new modes of computational drug discovery in each of the three key themes of target identification, mechanism, and therapy regimen design. In identifying… (more)

Subjects/Keywords: Drug target; Data mining

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APA (6th Edition):

-3365-2702. (2016). Computational discovery of genetic targets and interactions : applications to lung cancer. (Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/40285

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

Chicago Manual of Style (16th Edition):

-3365-2702. “Computational discovery of genetic targets and interactions : applications to lung cancer.” 2016. Thesis, University of Texas – Austin. Accessed August 22, 2019. http://hdl.handle.net/2152/40285.

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

MLA Handbook (7th Edition):

-3365-2702. “Computational discovery of genetic targets and interactions : applications to lung cancer.” 2016. Web. 22 Aug 2019.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-3365-2702. Computational discovery of genetic targets and interactions : applications to lung cancer. [Internet] [Thesis]. University of Texas – Austin; 2016. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2152/40285.

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

Council of Science Editors:

-3365-2702. Computational discovery of genetic targets and interactions : applications to lung cancer. [Thesis]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/40285

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


Penn State University

4. Draper, Jeremiah Michael. Identification of Human DHHC20 as a Transforming Palmitoyl Acyltransferase.

Degree: PhD, Pharmacology, 2008, Penn State University

 Many important signaling proteins require the post-translational addition of fatty acid chains for their proper subcellular localization and function. One such modification is the addition… (more)

Subjects/Keywords: localization; transformation; Palmitoyl acyltransferase; drug target

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APA (6th Edition):

Draper, J. M. (2008). Identification of Human DHHC20 as a Transforming Palmitoyl Acyltransferase. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/8983

Chicago Manual of Style (16th Edition):

Draper, Jeremiah Michael. “Identification of Human DHHC20 as a Transforming Palmitoyl Acyltransferase.” 2008. Doctoral Dissertation, Penn State University. Accessed August 22, 2019. https://etda.libraries.psu.edu/catalog/8983.

MLA Handbook (7th Edition):

Draper, Jeremiah Michael. “Identification of Human DHHC20 as a Transforming Palmitoyl Acyltransferase.” 2008. Web. 22 Aug 2019.

Vancouver:

Draper JM. Identification of Human DHHC20 as a Transforming Palmitoyl Acyltransferase. [Internet] [Doctoral dissertation]. Penn State University; 2008. [cited 2019 Aug 22]. Available from: https://etda.libraries.psu.edu/catalog/8983.

Council of Science Editors:

Draper JM. Identification of Human DHHC20 as a Transforming Palmitoyl Acyltransferase. [Doctoral Dissertation]. Penn State University; 2008. Available from: https://etda.libraries.psu.edu/catalog/8983


North Carolina State University

5. Barb, Adam Wesley. Phosphomannose isomerase in Nicotiana tabacum L. NT1 and Apium graveolens var. dulce L. cell suspension cultures.

Degree: MS, Horticultural Science, 2002, North Carolina State University

 Phosphomannose isomerase (PMI) [E.C. 5.3.1.8] is a key enzyme required for Man metabolism in plants, and PMI activity is important in both mannitol metabolizing and… (more)

Subjects/Keywords: purification; fructokinase; fk; hexokinase; hk; mannose-6-phosphate isomerase; phosphomannose isomerase; pmi; tobacco; celery; apium graveolens; nicotiana tabacum; mutant

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APA (6th Edition):

Barb, A. W. (2002). Phosphomannose isomerase in Nicotiana tabacum L. NT1 and Apium graveolens var. dulce L. cell suspension cultures. (Thesis). North Carolina State University. Retrieved from http://www.lib.ncsu.edu/resolver/1840.16/2545

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):

Barb, Adam Wesley. “Phosphomannose isomerase in Nicotiana tabacum L. NT1 and Apium graveolens var. dulce L. cell suspension cultures.” 2002. Thesis, North Carolina State University. Accessed August 22, 2019. http://www.lib.ncsu.edu/resolver/1840.16/2545.

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

MLA Handbook (7th Edition):

Barb, Adam Wesley. “Phosphomannose isomerase in Nicotiana tabacum L. NT1 and Apium graveolens var. dulce L. cell suspension cultures.” 2002. Web. 22 Aug 2019.

Vancouver:

Barb AW. Phosphomannose isomerase in Nicotiana tabacum L. NT1 and Apium graveolens var. dulce L. cell suspension cultures. [Internet] [Thesis]. North Carolina State University; 2002. [cited 2019 Aug 22]. Available from: http://www.lib.ncsu.edu/resolver/1840.16/2545.

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

Council of Science Editors:

Barb AW. Phosphomannose isomerase in Nicotiana tabacum L. NT1 and Apium graveolens var. dulce L. cell suspension cultures. [Thesis]. North Carolina State University; 2002. Available from: http://www.lib.ncsu.edu/resolver/1840.16/2545

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


Virginia Commonwealth University

6. Wang, Chen. High-throughput prediction and analysis of drug-protein interactions in the druggable human proteome.

Degree: PhD, Computer Science, 2018, Virginia Commonwealth University

  Drugs exert their (therapeutic) effects via molecular-level interactions with proteins and other biomolecules. Computational prediction of drug-protein interactions plays a significant role in the… (more)

Subjects/Keywords: drug-protein interactions; computational prediction; drug target database; drug repurposing; drug side-effects; Bioinformatics

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APA (6th Edition):

Wang, C. (2018). High-throughput prediction and analysis of drug-protein interactions in the druggable human proteome. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/5509

Chicago Manual of Style (16th Edition):

Wang, Chen. “High-throughput prediction and analysis of drug-protein interactions in the druggable human proteome.” 2018. Doctoral Dissertation, Virginia Commonwealth University. Accessed August 22, 2019. https://scholarscompass.vcu.edu/etd/5509.

MLA Handbook (7th Edition):

Wang, Chen. “High-throughput prediction and analysis of drug-protein interactions in the druggable human proteome.” 2018. Web. 22 Aug 2019.

Vancouver:

Wang C. High-throughput prediction and analysis of drug-protein interactions in the druggable human proteome. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2018. [cited 2019 Aug 22]. Available from: https://scholarscompass.vcu.edu/etd/5509.

Council of Science Editors:

Wang C. High-throughput prediction and analysis of drug-protein interactions in the druggable human proteome. [Doctoral Dissertation]. Virginia Commonwealth University; 2018. Available from: https://scholarscompass.vcu.edu/etd/5509


University of California – San Diego

7. Goldgof, Gregory Mark. Drug Target Discovery Using Designer Drug Sensitive Yeast.

Degree: Biomedical Sciences, 2017, University of California – San Diego

 Determining the protein target(s) and mechanism(s) of drug candidates found in phenotypic screens is critical to subsequent structure-activity-based development and optimization, but existing methods for… (more)

Subjects/Keywords: Medicine; Biology; Genetics; Chemogenomics; Drug Discovery; Drug Target; Malaria; Yeast

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APA (6th Edition):

Goldgof, G. M. (2017). Drug Target Discovery Using Designer Drug Sensitive Yeast. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/42b8231t

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):

Goldgof, Gregory Mark. “Drug Target Discovery Using Designer Drug Sensitive Yeast.” 2017. Thesis, University of California – San Diego. Accessed August 22, 2019. http://www.escholarship.org/uc/item/42b8231t.

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

MLA Handbook (7th Edition):

Goldgof, Gregory Mark. “Drug Target Discovery Using Designer Drug Sensitive Yeast.” 2017. Web. 22 Aug 2019.

Vancouver:

Goldgof GM. Drug Target Discovery Using Designer Drug Sensitive Yeast. [Internet] [Thesis]. University of California – San Diego; 2017. [cited 2019 Aug 22]. Available from: http://www.escholarship.org/uc/item/42b8231t.

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

Council of Science Editors:

Goldgof GM. Drug Target Discovery Using Designer Drug Sensitive Yeast. [Thesis]. University of California – San Diego; 2017. Available from: http://www.escholarship.org/uc/item/42b8231t

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


University of California – San Francisco

8. Yera, Emmanuel Ramon. Rationalizing Drug Pharmacology based on Computational Methods.

Degree: Biological and Medical Informatics, 2013, University of California – San Francisco

 Large-scale experimental determination of the protein targets of small molecules is both time-consuming and costly. Computational methods can be used to predict interactions between small… (more)

Subjects/Keywords: Bioinformatics; drug discovery; drug effects; molecular similarity; natural language processing; target prediction

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APA (6th Edition):

Yera, E. R. (2013). Rationalizing Drug Pharmacology based on Computational Methods. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/3mf2z296

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):

Yera, Emmanuel Ramon. “Rationalizing Drug Pharmacology based on Computational Methods.” 2013. Thesis, University of California – San Francisco. Accessed August 22, 2019. http://www.escholarship.org/uc/item/3mf2z296.

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

MLA Handbook (7th Edition):

Yera, Emmanuel Ramon. “Rationalizing Drug Pharmacology based on Computational Methods.” 2013. Web. 22 Aug 2019.

Vancouver:

Yera ER. Rationalizing Drug Pharmacology based on Computational Methods. [Internet] [Thesis]. University of California – San Francisco; 2013. [cited 2019 Aug 22]. Available from: http://www.escholarship.org/uc/item/3mf2z296.

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

Council of Science Editors:

Yera ER. Rationalizing Drug Pharmacology based on Computational Methods. [Thesis]. University of California – San Francisco; 2013. Available from: http://www.escholarship.org/uc/item/3mf2z296

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

9. Harris, Michael Timothy. A SURVEY OF PROTOZOAN PARASITE HEXOKINASES: CHARACTERIZATION STUDIES AND POTENTIAL FOR THERAPEUTIC INTERVENTIONS.

Degree: PhD, Genetics, 2015, Clemson University

  Protozoan parasites find a glucose rich environment when inhabiting the human host. As a consequence of this glucose rich environment, many parasites have evolved… (more)

Subjects/Keywords: Drug development; Glycolysis; Hexokinase; Leishmania; Plasmodium; Trypansoma brucei

…al.1998; Helfert et al. 2001). The two ATP consuming enzymes hexokinase (HK)… …make it a heretofore -underappreciated drug target. A recent high throughput screening (… …potential drug target. Plasmodium The Parasite and the Disease Protozoan parasites in the genus… …disease stage each drug is effective against. Suramin or pentamidine are used against the… …by Bayer (Steverding 2010). The diamidine drug pentamidine was developed in the… 

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APA (6th Edition):

Harris, M. T. (2015). A SURVEY OF PROTOZOAN PARASITE HEXOKINASES: CHARACTERIZATION STUDIES AND POTENTIAL FOR THERAPEUTIC INTERVENTIONS. (Doctoral Dissertation). Clemson University. Retrieved from https://tigerprints.clemson.edu/all_dissertations/1496

Chicago Manual of Style (16th Edition):

Harris, Michael Timothy. “A SURVEY OF PROTOZOAN PARASITE HEXOKINASES: CHARACTERIZATION STUDIES AND POTENTIAL FOR THERAPEUTIC INTERVENTIONS.” 2015. Doctoral Dissertation, Clemson University. Accessed August 22, 2019. https://tigerprints.clemson.edu/all_dissertations/1496.

MLA Handbook (7th Edition):

Harris, Michael Timothy. “A SURVEY OF PROTOZOAN PARASITE HEXOKINASES: CHARACTERIZATION STUDIES AND POTENTIAL FOR THERAPEUTIC INTERVENTIONS.” 2015. Web. 22 Aug 2019.

Vancouver:

Harris MT. A SURVEY OF PROTOZOAN PARASITE HEXOKINASES: CHARACTERIZATION STUDIES AND POTENTIAL FOR THERAPEUTIC INTERVENTIONS. [Internet] [Doctoral dissertation]. Clemson University; 2015. [cited 2019 Aug 22]. Available from: https://tigerprints.clemson.edu/all_dissertations/1496.

Council of Science Editors:

Harris MT. A SURVEY OF PROTOZOAN PARASITE HEXOKINASES: CHARACTERIZATION STUDIES AND POTENTIAL FOR THERAPEUTIC INTERVENTIONS. [Doctoral Dissertation]. Clemson University; 2015. Available from: https://tigerprints.clemson.edu/all_dissertations/1496


University of Kansas

10. Bailey, Kyle. Improving the Yeast Three-Hybrid System for High-Throughput Target Discovery.

Degree: MS, Medicinal Chemistry, 2011, University of Kansas

 High-throughput screening and rational design can be used to create bioactive compounds with high affinity for selected therapeutic targets. However, a significant challenge in preclinical… (more)

Subjects/Keywords: Molecular biology; Pharmacology; Drug; Gfp; Target; Three-hybrid; Yeast

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APA (6th Edition):

Bailey, K. (2011). Improving the Yeast Three-Hybrid System for High-Throughput Target Discovery. (Masters Thesis). University of Kansas. Retrieved from http://hdl.handle.net/1808/8040

Chicago Manual of Style (16th Edition):

Bailey, Kyle. “Improving the Yeast Three-Hybrid System for High-Throughput Target Discovery.” 2011. Masters Thesis, University of Kansas. Accessed August 22, 2019. http://hdl.handle.net/1808/8040.

MLA Handbook (7th Edition):

Bailey, Kyle. “Improving the Yeast Three-Hybrid System for High-Throughput Target Discovery.” 2011. Web. 22 Aug 2019.

Vancouver:

Bailey K. Improving the Yeast Three-Hybrid System for High-Throughput Target Discovery. [Internet] [Masters thesis]. University of Kansas; 2011. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/1808/8040.

Council of Science Editors:

Bailey K. Improving the Yeast Three-Hybrid System for High-Throughput Target Discovery. [Masters Thesis]. University of Kansas; 2011. Available from: http://hdl.handle.net/1808/8040


University of St. Andrews

11. Menzies, Stefanie Kate. Investigating the trypanocidal activity of simplified natural product-like analogs and the characterization of a novel trypanosomatid-specific secondary alternative oxidase .

Degree: 2017, University of St. Andrews

 This thesis aimed to identify the trypanocidal mode of action of non-natural chamuvarinin analogs, and to assess the previously uncharacterized secondary alternative oxidase (AOX2) as… (more)

Subjects/Keywords: Trypanosome; Drug discovery; Target identification; Mitochondria; Alternative oxidase; Leishmania

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APA (6th Edition):

Menzies, S. K. (2017). Investigating the trypanocidal activity of simplified natural product-like analogs and the characterization of a novel trypanosomatid-specific secondary alternative oxidase . (Thesis). University of St. Andrews. Retrieved from http://hdl.handle.net/10023/12041

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):

Menzies, Stefanie Kate. “Investigating the trypanocidal activity of simplified natural product-like analogs and the characterization of a novel trypanosomatid-specific secondary alternative oxidase .” 2017. Thesis, University of St. Andrews. Accessed August 22, 2019. http://hdl.handle.net/10023/12041.

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

MLA Handbook (7th Edition):

Menzies, Stefanie Kate. “Investigating the trypanocidal activity of simplified natural product-like analogs and the characterization of a novel trypanosomatid-specific secondary alternative oxidase .” 2017. Web. 22 Aug 2019.

Vancouver:

Menzies SK. Investigating the trypanocidal activity of simplified natural product-like analogs and the characterization of a novel trypanosomatid-specific secondary alternative oxidase . [Internet] [Thesis]. University of St. Andrews; 2017. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/10023/12041.

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

Council of Science Editors:

Menzies SK. Investigating the trypanocidal activity of simplified natural product-like analogs and the characterization of a novel trypanosomatid-specific secondary alternative oxidase . [Thesis]. University of St. Andrews; 2017. Available from: http://hdl.handle.net/10023/12041

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


Case Western Reserve University

12. Yang, Sen. Disease, Drug, and Target Association Predictions by Integrating Multiple Heterogeneous Sources.

Degree: MSs (Engineering), EECS - Computer and Information Sciences, 2012, Case Western Reserve University

 Computational methods for new drug development can greatly reduce time and costs compared with experimental methods. A core problem in computational drug discovery is to… (more)

Subjects/Keywords: Bioinformatics; Computer Science; disease; drug; target; association predictions; multiple heterogeneous information

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APA (6th Edition):

Yang, S. (2012). Disease, Drug, and Target Association Predictions by Integrating Multiple Heterogeneous Sources. (Masters Thesis). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1342194249

Chicago Manual of Style (16th Edition):

Yang, Sen. “Disease, Drug, and Target Association Predictions by Integrating Multiple Heterogeneous Sources.” 2012. Masters Thesis, Case Western Reserve University. Accessed August 22, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1342194249.

MLA Handbook (7th Edition):

Yang, Sen. “Disease, Drug, and Target Association Predictions by Integrating Multiple Heterogeneous Sources.” 2012. Web. 22 Aug 2019.

Vancouver:

Yang S. Disease, Drug, and Target Association Predictions by Integrating Multiple Heterogeneous Sources. [Internet] [Masters thesis]. Case Western Reserve University; 2012. [cited 2019 Aug 22]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1342194249.

Council of Science Editors:

Yang S. Disease, Drug, and Target Association Predictions by Integrating Multiple Heterogeneous Sources. [Masters Thesis]. Case Western Reserve University; 2012. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1342194249


University of Manchester

13. Swami, Shalini. Structure and biochemistry of the orphan cytochrome P450s CYP126A1 and CYP143A1 from the human pathogen Mycobacterium tuberculosis.

Degree: PhD, 2015, University of Manchester

 Mycobacterium tuberculosis (Mtb) causes tuberculosis (TB) and poses a global threat to human health. A third of the world’s population is infected with Mtb. Multi-drug(more)

Subjects/Keywords: 612; Cytochrome P450; Mycobacterium tuberculosis: drug target enzymes

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APA (6th Edition):

Swami, S. (2015). Structure and biochemistry of the orphan cytochrome P450s CYP126A1 and CYP143A1 from the human pathogen Mycobacterium tuberculosis. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/structure-and-biochemistry-of-the-orphan-cytochrome-p450s-cyp126a1-and-cyp143a1-from-the-human-pathogen-mycobacterium-tuberculosis(a8dc4eea-678c-419a-a3b3-206253c400b7).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.634939

Chicago Manual of Style (16th Edition):

Swami, Shalini. “Structure and biochemistry of the orphan cytochrome P450s CYP126A1 and CYP143A1 from the human pathogen Mycobacterium tuberculosis.” 2015. Doctoral Dissertation, University of Manchester. Accessed August 22, 2019. https://www.research.manchester.ac.uk/portal/en/theses/structure-and-biochemistry-of-the-orphan-cytochrome-p450s-cyp126a1-and-cyp143a1-from-the-human-pathogen-mycobacterium-tuberculosis(a8dc4eea-678c-419a-a3b3-206253c400b7).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.634939.

MLA Handbook (7th Edition):

Swami, Shalini. “Structure and biochemistry of the orphan cytochrome P450s CYP126A1 and CYP143A1 from the human pathogen Mycobacterium tuberculosis.” 2015. Web. 22 Aug 2019.

Vancouver:

Swami S. Structure and biochemistry of the orphan cytochrome P450s CYP126A1 and CYP143A1 from the human pathogen Mycobacterium tuberculosis. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2019 Aug 22]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/structure-and-biochemistry-of-the-orphan-cytochrome-p450s-cyp126a1-and-cyp143a1-from-the-human-pathogen-mycobacterium-tuberculosis(a8dc4eea-678c-419a-a3b3-206253c400b7).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.634939.

Council of Science Editors:

Swami S. Structure and biochemistry of the orphan cytochrome P450s CYP126A1 and CYP143A1 from the human pathogen Mycobacterium tuberculosis. [Doctoral Dissertation]. University of Manchester; 2015. Available from: https://www.research.manchester.ac.uk/portal/en/theses/structure-and-biochemistry-of-the-orphan-cytochrome-p450s-cyp126a1-and-cyp143a1-from-the-human-pathogen-mycobacterium-tuberculosis(a8dc4eea-678c-419a-a3b3-206253c400b7).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.634939


UCLA

14. Lo, Yu-Chen. Chemical Dissection of the Cell Cycle for Anticancer Drug Discovery and Target Identification.

Degree: Bioengineering, 2016, UCLA

 The cell cycle is governed by highly regulated mechanisms that mandate organism’s proliferation and survival. On the other hand, malignant human diseases like cancer often… (more)

Subjects/Keywords: Biomedical engineering; Chemistry; Biochemistry; cell cycle; drug discovery; microtubule; target identification

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

APA (6th Edition):

Lo, Y. (2016). Chemical Dissection of the Cell Cycle for Anticancer Drug Discovery and Target Identification. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/57z058n7

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):

Lo, Yu-Chen. “Chemical Dissection of the Cell Cycle for Anticancer Drug Discovery and Target Identification.” 2016. Thesis, UCLA. Accessed August 22, 2019. http://www.escholarship.org/uc/item/57z058n7.

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

MLA Handbook (7th Edition):

Lo, Yu-Chen. “Chemical Dissection of the Cell Cycle for Anticancer Drug Discovery and Target Identification.” 2016. Web. 22 Aug 2019.

Vancouver:

Lo Y. Chemical Dissection of the Cell Cycle for Anticancer Drug Discovery and Target Identification. [Internet] [Thesis]. UCLA; 2016. [cited 2019 Aug 22]. Available from: http://www.escholarship.org/uc/item/57z058n7.

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

Council of Science Editors:

Lo Y. Chemical Dissection of the Cell Cycle for Anticancer Drug Discovery and Target Identification. [Thesis]. UCLA; 2016. Available from: http://www.escholarship.org/uc/item/57z058n7

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


University of California – Santa Cruz

15. Woehrmann, Marcos H. Predicting the Mode of Action of Bioactive Compounds via High Throughput Screening and Computational Algorithms.

Degree: Biomolecular Engineering and Bioinformatics, 2015, University of California – Santa Cruz

 To develop more effective therapies to treat human diseases, a better method of finding the biological targets and modes of action of new compounds is… (more)

Subjects/Keywords: Bioinformatics; Bioinformatics; Cytological Profiling; Drug Target Prediction; High-throughput Screening; HTS

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APA (6th Edition):

Woehrmann, M. H. (2015). Predicting the Mode of Action of Bioactive Compounds via High Throughput Screening and Computational Algorithms. (Thesis). University of California – Santa Cruz. Retrieved from http://www.escholarship.org/uc/item/9976p4ch

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):

Woehrmann, Marcos H. “Predicting the Mode of Action of Bioactive Compounds via High Throughput Screening and Computational Algorithms.” 2015. Thesis, University of California – Santa Cruz. Accessed August 22, 2019. http://www.escholarship.org/uc/item/9976p4ch.

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

MLA Handbook (7th Edition):

Woehrmann, Marcos H. “Predicting the Mode of Action of Bioactive Compounds via High Throughput Screening and Computational Algorithms.” 2015. Web. 22 Aug 2019.

Vancouver:

Woehrmann MH. Predicting the Mode of Action of Bioactive Compounds via High Throughput Screening and Computational Algorithms. [Internet] [Thesis]. University of California – Santa Cruz; 2015. [cited 2019 Aug 22]. Available from: http://www.escholarship.org/uc/item/9976p4ch.

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

Council of Science Editors:

Woehrmann MH. Predicting the Mode of Action of Bioactive Compounds via High Throughput Screening and Computational Algorithms. [Thesis]. University of California – Santa Cruz; 2015. Available from: http://www.escholarship.org/uc/item/9976p4ch

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


University of Tennessee – Knoxville

16. Cassilly, Chelsi Danielle. The Biochemical Characterization of the Phosphatidylserine Synthase from <i>Candida albicans</i> as a Drug Target.

Degree: 2017, University of Tennessee – Knoxville

 Treatments for Candida albicans systemic infections are limited to three classes of antifungals, some of which have harmful side effects or increasing instances of antifungal… (more)

Subjects/Keywords: Candida albicans; Phospholipid; Phosphatidylserine; Drug Target; Fungus; Biochemistry

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APA (6th Edition):

Cassilly, C. D. (2017). The Biochemical Characterization of the Phosphatidylserine Synthase from <i>Candida albicans</i> as a Drug Target. (Doctoral Dissertation). University of Tennessee – Knoxville. Retrieved from https://trace.tennessee.edu/utk_graddiss/4846

Chicago Manual of Style (16th Edition):

Cassilly, Chelsi Danielle. “The Biochemical Characterization of the Phosphatidylserine Synthase from <i>Candida albicans</i> as a Drug Target.” 2017. Doctoral Dissertation, University of Tennessee – Knoxville. Accessed August 22, 2019. https://trace.tennessee.edu/utk_graddiss/4846.

MLA Handbook (7th Edition):

Cassilly, Chelsi Danielle. “The Biochemical Characterization of the Phosphatidylserine Synthase from <i>Candida albicans</i> as a Drug Target.” 2017. Web. 22 Aug 2019.

Vancouver:

Cassilly CD. The Biochemical Characterization of the Phosphatidylserine Synthase from <i>Candida albicans</i> as a Drug Target. [Internet] [Doctoral dissertation]. University of Tennessee – Knoxville; 2017. [cited 2019 Aug 22]. Available from: https://trace.tennessee.edu/utk_graddiss/4846.

Council of Science Editors:

Cassilly CD. The Biochemical Characterization of the Phosphatidylserine Synthase from <i>Candida albicans</i> as a Drug Target. [Doctoral Dissertation]. University of Tennessee – Knoxville; 2017. Available from: https://trace.tennessee.edu/utk_graddiss/4846


Indiana University

17. Seal, Abhik. RANDOM WALK APPLIED TO HETEROGENOUS DRUG-TARGET NETWORKS FOR PREDICTING BIOLOGICAL OUTCOMES .

Degree: 2016, Indiana University

 Prediction of unknown drug target interactions from bioassay data is critical not only for the understanding of various interactions but also crucial for the development… (more)

Subjects/Keywords: Random walk; drug target; link prediction; disease; metabolic pathway; R; Shiny

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APA (6th Edition):

Seal, A. (2016). RANDOM WALK APPLIED TO HETEROGENOUS DRUG-TARGET NETWORKS FOR PREDICTING BIOLOGICAL OUTCOMES . (Thesis). Indiana University. Retrieved from http://hdl.handle.net/2022/20765

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):

Seal, Abhik. “RANDOM WALK APPLIED TO HETEROGENOUS DRUG-TARGET NETWORKS FOR PREDICTING BIOLOGICAL OUTCOMES .” 2016. Thesis, Indiana University. Accessed August 22, 2019. http://hdl.handle.net/2022/20765.

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

MLA Handbook (7th Edition):

Seal, Abhik. “RANDOM WALK APPLIED TO HETEROGENOUS DRUG-TARGET NETWORKS FOR PREDICTING BIOLOGICAL OUTCOMES .” 2016. Web. 22 Aug 2019.

Vancouver:

Seal A. RANDOM WALK APPLIED TO HETEROGENOUS DRUG-TARGET NETWORKS FOR PREDICTING BIOLOGICAL OUTCOMES . [Internet] [Thesis]. Indiana University; 2016. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/2022/20765.

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

Council of Science Editors:

Seal A. RANDOM WALK APPLIED TO HETEROGENOUS DRUG-TARGET NETWORKS FOR PREDICTING BIOLOGICAL OUTCOMES . [Thesis]. Indiana University; 2016. Available from: http://hdl.handle.net/2022/20765

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


Purdue University

18. Mohammad, Haroon. ANTIMICROBIAL CHARACTERIZATION AND THERAPEUTIC APPLICATIONS OF NOVEL SYNTHETIC THIAZOLE COMPOUNDS AGAINST MULTIDRUG-RESISTANT STAPHYLOCOCCI AND ENTEROCOCCI.

Degree: PhD, Comparative Pathobiology, 2016, Purdue University

 For more than a century, antibiotics have been valuable allies in combating an array of bacterial infections. However, each year nearly 23,000 people in the… (more)

Subjects/Keywords: antibiotic; drug-resistance; MRSA; target identification; undecaprenyl diphosphate phosphatase; VRE

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APA (6th Edition):

Mohammad, H. (2016). ANTIMICROBIAL CHARACTERIZATION AND THERAPEUTIC APPLICATIONS OF NOVEL SYNTHETIC THIAZOLE COMPOUNDS AGAINST MULTIDRUG-RESISTANT STAPHYLOCOCCI AND ENTEROCOCCI. (Doctoral Dissertation). Purdue University. Retrieved from https://docs.lib.purdue.edu/open_access_dissertations/1466

Chicago Manual of Style (16th Edition):

Mohammad, Haroon. “ANTIMICROBIAL CHARACTERIZATION AND THERAPEUTIC APPLICATIONS OF NOVEL SYNTHETIC THIAZOLE COMPOUNDS AGAINST MULTIDRUG-RESISTANT STAPHYLOCOCCI AND ENTEROCOCCI.” 2016. Doctoral Dissertation, Purdue University. Accessed August 22, 2019. https://docs.lib.purdue.edu/open_access_dissertations/1466.

MLA Handbook (7th Edition):

Mohammad, Haroon. “ANTIMICROBIAL CHARACTERIZATION AND THERAPEUTIC APPLICATIONS OF NOVEL SYNTHETIC THIAZOLE COMPOUNDS AGAINST MULTIDRUG-RESISTANT STAPHYLOCOCCI AND ENTEROCOCCI.” 2016. Web. 22 Aug 2019.

Vancouver:

Mohammad H. ANTIMICROBIAL CHARACTERIZATION AND THERAPEUTIC APPLICATIONS OF NOVEL SYNTHETIC THIAZOLE COMPOUNDS AGAINST MULTIDRUG-RESISTANT STAPHYLOCOCCI AND ENTEROCOCCI. [Internet] [Doctoral dissertation]. Purdue University; 2016. [cited 2019 Aug 22]. Available from: https://docs.lib.purdue.edu/open_access_dissertations/1466.

Council of Science Editors:

Mohammad H. ANTIMICROBIAL CHARACTERIZATION AND THERAPEUTIC APPLICATIONS OF NOVEL SYNTHETIC THIAZOLE COMPOUNDS AGAINST MULTIDRUG-RESISTANT STAPHYLOCOCCI AND ENTEROCOCCI. [Doctoral Dissertation]. Purdue University; 2016. Available from: https://docs.lib.purdue.edu/open_access_dissertations/1466


MIT

19. Cheung, Hoi Kwan (Hoi Kwan Dennis). Covert resistance : an Embodiment of the "One Country. Two Systems" Principle in Hong Kong .

Degree: M. Arch., Department of Architecture, 2013, MIT

 Architecture is always political. Always. Society shapes the built environment and architecture impacts the social systems. Yet how far can architects push in changing society?… (more)

Subjects/Keywords: a-cc-hk; Architecture.

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APA (6th Edition):

Cheung, H. K. (. K. D. (2013). Covert resistance : an Embodiment of the "One Country. Two Systems" Principle in Hong Kong . (Masters Thesis). MIT. Retrieved from http://hdl.handle.net/1721.1/79172

Chicago Manual of Style (16th Edition):

Cheung, Hoi Kwan (Hoi Kwan Dennis). “Covert resistance : an Embodiment of the "One Country. Two Systems" Principle in Hong Kong .” 2013. Masters Thesis, MIT. Accessed August 22, 2019. http://hdl.handle.net/1721.1/79172.

MLA Handbook (7th Edition):

Cheung, Hoi Kwan (Hoi Kwan Dennis). “Covert resistance : an Embodiment of the "One Country. Two Systems" Principle in Hong Kong .” 2013. Web. 22 Aug 2019.

Vancouver:

Cheung HK(KD. Covert resistance : an Embodiment of the "One Country. Two Systems" Principle in Hong Kong . [Internet] [Masters thesis]. MIT; 2013. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/1721.1/79172.

Council of Science Editors:

Cheung HK(KD. Covert resistance : an Embodiment of the "One Country. Two Systems" Principle in Hong Kong . [Masters Thesis]. MIT; 2013. Available from: http://hdl.handle.net/1721.1/79172


MIT

20. Wang, Yan-Ping, M. Arch. Massachusetts Institute of Technology. C.A.S.H. - communal affordable singles housing : a platform for proactive affordability in Hong Kong ; Communal affordable singles housing ; Platform for proactive affordability in Hong Kong .

Degree: M. Arch., Department of Architecture, 2013, MIT

 In Hong Kong, young singles are left out of the affordable housing equation. They require much more space per person in comparison to those living… (more)

Subjects/Keywords: a-cc-hk; Architecture.

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APA (6th Edition):

Wang, Yan-Ping, M. A. M. I. o. (2013). C.A.S.H. - communal affordable singles housing : a platform for proactive affordability in Hong Kong ; Communal affordable singles housing ; Platform for proactive affordability in Hong Kong . (Masters Thesis). MIT. Retrieved from http://hdl.handle.net/1721.1/79181

Chicago Manual of Style (16th Edition):

Wang, Yan-Ping, M Arch Massachusetts Institute of. “C.A.S.H. - communal affordable singles housing : a platform for proactive affordability in Hong Kong ; Communal affordable singles housing ; Platform for proactive affordability in Hong Kong .” 2013. Masters Thesis, MIT. Accessed August 22, 2019. http://hdl.handle.net/1721.1/79181.

MLA Handbook (7th Edition):

Wang, Yan-Ping, M Arch Massachusetts Institute of. “C.A.S.H. - communal affordable singles housing : a platform for proactive affordability in Hong Kong ; Communal affordable singles housing ; Platform for proactive affordability in Hong Kong .” 2013. Web. 22 Aug 2019.

Vancouver:

Wang, Yan-Ping MAMIo. C.A.S.H. - communal affordable singles housing : a platform for proactive affordability in Hong Kong ; Communal affordable singles housing ; Platform for proactive affordability in Hong Kong . [Internet] [Masters thesis]. MIT; 2013. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/1721.1/79181.

Council of Science Editors:

Wang, Yan-Ping MAMIo. C.A.S.H. - communal affordable singles housing : a platform for proactive affordability in Hong Kong ; Communal affordable singles housing ; Platform for proactive affordability in Hong Kong . [Masters Thesis]. MIT; 2013. Available from: http://hdl.handle.net/1721.1/79181


MIT

21. Beagen, Barry. Public figures : town hall for the new interior ; Public figures : new town hall for the interior .

Degree: Department of Architecture, 2015, MIT

 The thesis examines the formal figuration of public space for a new agonistic public sphere within the contemporary condition of the late capitalist city where… (more)

Subjects/Keywords: a-cc-hk; Architecture.

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APA (6th Edition):

Beagen, B. (2015). Public figures : town hall for the new interior ; Public figures : new town hall for the interior . (Thesis). MIT. Retrieved from http://hdl.handle.net/1721.1/99259

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):

Beagen, Barry. “Public figures : town hall for the new interior ; Public figures : new town hall for the interior .” 2015. Thesis, MIT. Accessed August 22, 2019. http://hdl.handle.net/1721.1/99259.

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

MLA Handbook (7th Edition):

Beagen, Barry. “Public figures : town hall for the new interior ; Public figures : new town hall for the interior .” 2015. Web. 22 Aug 2019.

Vancouver:

Beagen B. Public figures : town hall for the new interior ; Public figures : new town hall for the interior . [Internet] [Thesis]. MIT; 2015. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/1721.1/99259.

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

Council of Science Editors:

Beagen B. Public figures : town hall for the new interior ; Public figures : new town hall for the interior . [Thesis]. MIT; 2015. Available from: http://hdl.handle.net/1721.1/99259

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


MIT

22. Ting, Sze Ngai. Park and chill : redesign parking garage in Hong Kong ; Redesign parking garage in Hong Kong .

Degree: M. Arch., Architecture, 2011, MIT

 What are the aesthetics of urban infrastructure? Urban infrastructure has remained isolated to human activities. We all share memory and experience with urban infrastructure, e.g.… (more)

Subjects/Keywords: a-cc-hk; Architecture.

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APA (6th Edition):

Ting, S. N. (2011). Park and chill : redesign parking garage in Hong Kong ; Redesign parking garage in Hong Kong . (Masters Thesis). MIT. Retrieved from http://hdl.handle.net/1721.1/63055

Chicago Manual of Style (16th Edition):

Ting, Sze Ngai. “Park and chill : redesign parking garage in Hong Kong ; Redesign parking garage in Hong Kong .” 2011. Masters Thesis, MIT. Accessed August 22, 2019. http://hdl.handle.net/1721.1/63055.

MLA Handbook (7th Edition):

Ting, Sze Ngai. “Park and chill : redesign parking garage in Hong Kong ; Redesign parking garage in Hong Kong .” 2011. Web. 22 Aug 2019.

Vancouver:

Ting SN. Park and chill : redesign parking garage in Hong Kong ; Redesign parking garage in Hong Kong . [Internet] [Masters thesis]. MIT; 2011. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/1721.1/63055.

Council of Science Editors:

Ting SN. Park and chill : redesign parking garage in Hong Kong ; Redesign parking garage in Hong Kong . [Masters Thesis]. MIT; 2011. Available from: http://hdl.handle.net/1721.1/63055


Clemson University

23. Joice, April. An Investigation of <i>Trypanosoma brucei</i> Hexokinases: Localization, Oligomerization, and Inhibition.

Degree: PhD, Biochemistry and Molecular Biology, 2012, Clemson University

 Trypanosoma brucei is the causative agent of African sleeping sickness in humans and nagana in livestock. The parasite inhabits multiple environmental niches including the bloodstream… (more)

Subjects/Keywords: flagella; hexokinase; peroxisome; trypanosome; Biochemistry

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APA (6th Edition):

Joice, A. (2012). An Investigation of <i>Trypanosoma brucei</i> Hexokinases: Localization, Oligomerization, and Inhibition. (Doctoral Dissertation). Clemson University. Retrieved from https://tigerprints.clemson.edu/all_dissertations/916

Chicago Manual of Style (16th Edition):

Joice, April. “An Investigation of <i>Trypanosoma brucei</i> Hexokinases: Localization, Oligomerization, and Inhibition.” 2012. Doctoral Dissertation, Clemson University. Accessed August 22, 2019. https://tigerprints.clemson.edu/all_dissertations/916.

MLA Handbook (7th Edition):

Joice, April. “An Investigation of <i>Trypanosoma brucei</i> Hexokinases: Localization, Oligomerization, and Inhibition.” 2012. Web. 22 Aug 2019.

Vancouver:

Joice A. An Investigation of <i>Trypanosoma brucei</i> Hexokinases: Localization, Oligomerization, and Inhibition. [Internet] [Doctoral dissertation]. Clemson University; 2012. [cited 2019 Aug 22]. Available from: https://tigerprints.clemson.edu/all_dissertations/916.

Council of Science Editors:

Joice A. An Investigation of <i>Trypanosoma brucei</i> Hexokinases: Localization, Oligomerization, and Inhibition. [Doctoral Dissertation]. Clemson University; 2012. Available from: https://tigerprints.clemson.edu/all_dissertations/916


University of Central Florida

24. Chehtane, Mounir. The Cytokine, Interleukin-7, Transcriptionally Regulates The Gene Expression Of The Hexokinase Ii To Mediate Glucose Utilization.

Degree: 2010, University of Central Florida

 The cytokine, interleukin-7 (IL-7), has essential growth activities that maintain the homeostatic balance of the immune system. Little is known of the mechanism by which… (more)

Subjects/Keywords: IL-7; Hexokinase II; Glucose

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APA (6th Edition):

Chehtane, M. (2010). The Cytokine, Interleukin-7, Transcriptionally Regulates The Gene Expression Of The Hexokinase Ii To Mediate Glucose Utilization. (Doctoral Dissertation). University of Central Florida. Retrieved from https://stars.library.ucf.edu/etd/4329

Chicago Manual of Style (16th Edition):

Chehtane, Mounir. “The Cytokine, Interleukin-7, Transcriptionally Regulates The Gene Expression Of The Hexokinase Ii To Mediate Glucose Utilization.” 2010. Doctoral Dissertation, University of Central Florida. Accessed August 22, 2019. https://stars.library.ucf.edu/etd/4329.

MLA Handbook (7th Edition):

Chehtane, Mounir. “The Cytokine, Interleukin-7, Transcriptionally Regulates The Gene Expression Of The Hexokinase Ii To Mediate Glucose Utilization.” 2010. Web. 22 Aug 2019.

Vancouver:

Chehtane M. The Cytokine, Interleukin-7, Transcriptionally Regulates The Gene Expression Of The Hexokinase Ii To Mediate Glucose Utilization. [Internet] [Doctoral dissertation]. University of Central Florida; 2010. [cited 2019 Aug 22]. Available from: https://stars.library.ucf.edu/etd/4329.

Council of Science Editors:

Chehtane M. The Cytokine, Interleukin-7, Transcriptionally Regulates The Gene Expression Of The Hexokinase Ii To Mediate Glucose Utilization. [Doctoral Dissertation]. University of Central Florida; 2010. Available from: https://stars.library.ucf.edu/etd/4329


Jawaharlal Nehru University

25. Desai, Dhwani K. Computational methods applied to drug target identification and inhibitor design; -.

Degree: Information Technology, 2008, Jawaharlal Nehru University

None

Bibliography p.137-151, Appendices p.135-136

Advisors/Committee Members: Lynn, Andrew.

Subjects/Keywords: Information Technology; drug target; inhibitor design

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APA (6th Edition):

Desai, D. K. (2008). Computational methods applied to drug target identification and inhibitor design; -. (Thesis). Jawaharlal Nehru University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/14632

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):

Desai, Dhwani K. “Computational methods applied to drug target identification and inhibitor design; -.” 2008. Thesis, Jawaharlal Nehru University. Accessed August 22, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/14632.

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

MLA Handbook (7th Edition):

Desai, Dhwani K. “Computational methods applied to drug target identification and inhibitor design; -.” 2008. Web. 22 Aug 2019.

Vancouver:

Desai DK. Computational methods applied to drug target identification and inhibitor design; -. [Internet] [Thesis]. Jawaharlal Nehru University; 2008. [cited 2019 Aug 22]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/14632.

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

Council of Science Editors:

Desai DK. Computational methods applied to drug target identification and inhibitor design; -. [Thesis]. Jawaharlal Nehru University; 2008. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/14632

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


Uppsala University

26. Congreve, Samantha; Elias, Reham Faris; Tidestav, Gabriel. Antibody drug conjugates (ADC) : Current status and mapping of ADC:s in clinical programs.

Degree: Engineering Sciences, 2018, Uppsala University

  A literature study was performed on a new type of cancer medicine: antibody drug conjugates, or ADCs. These consist of a monoclonal antibody, chemically… (more)

Subjects/Keywords: ADC; antibody; drug; conjugate; biopharmaceuticals; structure; linker; payload; target; conjugation; market; Chemical Engineering; Kemiteknik

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APA (6th Edition):

Congreve, Samantha; Elias, Reham Faris; Tidestav, G. (2018). Antibody drug conjugates (ADC) : Current status and mapping of ADC:s in clinical programs. (Thesis). Uppsala University. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-352917

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):

Congreve, Samantha; Elias, Reham Faris; Tidestav, Gabriel. “Antibody drug conjugates (ADC) : Current status and mapping of ADC:s in clinical programs.” 2018. Thesis, Uppsala University. Accessed August 22, 2019. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-352917.

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

MLA Handbook (7th Edition):

Congreve, Samantha; Elias, Reham Faris; Tidestav, Gabriel. “Antibody drug conjugates (ADC) : Current status and mapping of ADC:s in clinical programs.” 2018. Web. 22 Aug 2019.

Vancouver:

Congreve, Samantha; Elias, Reham Faris; Tidestav G. Antibody drug conjugates (ADC) : Current status and mapping of ADC:s in clinical programs. [Internet] [Thesis]. Uppsala University; 2018. [cited 2019 Aug 22]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-352917.

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

Council of Science Editors:

Congreve, Samantha; Elias, Reham Faris; Tidestav G. Antibody drug conjugates (ADC) : Current status and mapping of ADC:s in clinical programs. [Thesis]. Uppsala University; 2018. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-352917

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


UCLA

27. Lomenick, Brett Eugene. Small Molecule Target Identification using Drug Affinity Responsive Target Stability (DARTS).

Degree: Molec & Med Pharmacology, 2013, UCLA

 Small molecule target identification is a monumental task. Knowledge of the binding interactions between small molecule compounds and cellular macromolecules such as proteins is crucial… (more)

Subjects/Keywords: Pharmacology; Molecular biology; Biochemistry; compound; DARTS; drug; ligand; small molecule; target identification

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

APA (6th Edition):

Lomenick, B. E. (2013). Small Molecule Target Identification using Drug Affinity Responsive Target Stability (DARTS). (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/2fk1b99n

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):

Lomenick, Brett Eugene. “Small Molecule Target Identification using Drug Affinity Responsive Target Stability (DARTS).” 2013. Thesis, UCLA. Accessed August 22, 2019. http://www.escholarship.org/uc/item/2fk1b99n.

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

MLA Handbook (7th Edition):

Lomenick, Brett Eugene. “Small Molecule Target Identification using Drug Affinity Responsive Target Stability (DARTS).” 2013. Web. 22 Aug 2019.

Vancouver:

Lomenick BE. Small Molecule Target Identification using Drug Affinity Responsive Target Stability (DARTS). [Internet] [Thesis]. UCLA; 2013. [cited 2019 Aug 22]. Available from: http://www.escholarship.org/uc/item/2fk1b99n.

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

Council of Science Editors:

Lomenick BE. Small Molecule Target Identification using Drug Affinity Responsive Target Stability (DARTS). [Thesis]. UCLA; 2013. Available from: http://www.escholarship.org/uc/item/2fk1b99n

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


Virginia Tech

28. Xu, Guoyan. Pin1 Inhibitors: Towards Understanding the Enzymatic Mechanism.

Degree: PhD, Chemistry, 2010, Virginia Tech

 An important role of Pin1 is to catalyze the cis-trans isomerization of pSer/Thr-Pro bonds; as such, it plays an important role in many cellular events… (more)

Subjects/Keywords: PPIase assay; inhibition; Pin1; anti-cancer drug target; transition-state analogues; ketoamides; ketones; reduced amides

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

APA (6th Edition):

Xu, G. (2010). Pin1 Inhibitors: Towards Understanding the Enzymatic Mechanism. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/37823

Chicago Manual of Style (16th Edition):

Xu, Guoyan. “Pin1 Inhibitors: Towards Understanding the Enzymatic Mechanism.” 2010. Doctoral Dissertation, Virginia Tech. Accessed August 22, 2019. http://hdl.handle.net/10919/37823.

MLA Handbook (7th Edition):

Xu, Guoyan. “Pin1 Inhibitors: Towards Understanding the Enzymatic Mechanism.” 2010. Web. 22 Aug 2019.

Vancouver:

Xu G. Pin1 Inhibitors: Towards Understanding the Enzymatic Mechanism. [Internet] [Doctoral dissertation]. Virginia Tech; 2010. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/10919/37823.

Council of Science Editors:

Xu G. Pin1 Inhibitors: Towards Understanding the Enzymatic Mechanism. [Doctoral Dissertation]. Virginia Tech; 2010. Available from: http://hdl.handle.net/10919/37823


IUPUI

29. Pandey, Ragini. A Novel Network Biology Approach To Drug Target Selections.

Degree: 2010, IUPUI

Subjects/Keywords: Network Biology Approach; Drug Target Selections

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

APA (6th Edition):

Pandey, R. (2010). A Novel Network Biology Approach To Drug Target Selections. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/2148

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):

Pandey, Ragini. “A Novel Network Biology Approach To Drug Target Selections.” 2010. Thesis, IUPUI. Accessed August 22, 2019. http://hdl.handle.net/1805/2148.

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

MLA Handbook (7th Edition):

Pandey, Ragini. “A Novel Network Biology Approach To Drug Target Selections.” 2010. Web. 22 Aug 2019.

Vancouver:

Pandey R. A Novel Network Biology Approach To Drug Target Selections. [Internet] [Thesis]. IUPUI; 2010. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/1805/2148.

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

Council of Science Editors:

Pandey R. A Novel Network Biology Approach To Drug Target Selections. [Thesis]. IUPUI; 2010. Available from: http://hdl.handle.net/1805/2148

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


Brno University of Technology

30. Überall, Martin. Solubilizace v sonografických systémech .

Degree: 2016, Brno University of Technology

 V diplomové práci byly pomocí metody UV-VIS spektrofotometrie studovány solubilizační schopnosti fosfolipidů, z nichž je tvořen komerční přípravek SonoVue® využívájící se v ultrasonografii, a poté… (more)

Subjects/Keywords: Ultrasonografie; solubilizace; mikrobubliny; cílená distribuce léčiv; SonoVue®; Ultrasonography; solubilization; microbubbles; target drug delivery; SonoVue®

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

APA (6th Edition):

Überall, M. (2016). Solubilizace v sonografických systémech . (Thesis). Brno University of Technology. Retrieved from http://hdl.handle.net/11012/58386

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):

Überall, Martin. “Solubilizace v sonografických systémech .” 2016. Thesis, Brno University of Technology. Accessed August 22, 2019. http://hdl.handle.net/11012/58386.

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

MLA Handbook (7th Edition):

Überall, Martin. “Solubilizace v sonografických systémech .” 2016. Web. 22 Aug 2019.

Vancouver:

Überall M. Solubilizace v sonografických systémech . [Internet] [Thesis]. Brno University of Technology; 2016. [cited 2019 Aug 22]. Available from: http://hdl.handle.net/11012/58386.

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

Council of Science Editors:

Überall M. Solubilizace v sonografických systémech . [Thesis]. Brno University of Technology; 2016. Available from: http://hdl.handle.net/11012/58386

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

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