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You searched for subject:( homology modeling ). Showing records 1 – 30 of 29784 total matches.

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University of Vermont

1. Stanton, Suzanne Louise. Homology Modeling and Molecular Docking of Antagonists to Class B G-Protein Coupled Receptor Pituitary Adenylate Cyclase Type 1 (PAC1R).

Degree: MS, Chemistry, 2016, University of Vermont

  Recent studies have identified the Class B g-protein coupled receptor (GPCR) pituitary adenylate cyclase activating polypeptide type 1 (PAC1R) as a key component in… (more)

Subjects/Keywords: Computational; Homology; Modeling; Chemistry

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APA (6th Edition):

Stanton, S. L. (2016). Homology Modeling and Molecular Docking of Antagonists to Class B G-Protein Coupled Receptor Pituitary Adenylate Cyclase Type 1 (PAC1R). (Thesis). University of Vermont. Retrieved from https://scholarworks.uvm.edu/graddis/624

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):

Stanton, Suzanne Louise. “Homology Modeling and Molecular Docking of Antagonists to Class B G-Protein Coupled Receptor Pituitary Adenylate Cyclase Type 1 (PAC1R).” 2016. Thesis, University of Vermont. Accessed April 18, 2021. https://scholarworks.uvm.edu/graddis/624.

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

MLA Handbook (7th Edition):

Stanton, Suzanne Louise. “Homology Modeling and Molecular Docking of Antagonists to Class B G-Protein Coupled Receptor Pituitary Adenylate Cyclase Type 1 (PAC1R).” 2016. Web. 18 Apr 2021.

Vancouver:

Stanton SL. Homology Modeling and Molecular Docking of Antagonists to Class B G-Protein Coupled Receptor Pituitary Adenylate Cyclase Type 1 (PAC1R). [Internet] [Thesis]. University of Vermont; 2016. [cited 2021 Apr 18]. Available from: https://scholarworks.uvm.edu/graddis/624.

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

Council of Science Editors:

Stanton SL. Homology Modeling and Molecular Docking of Antagonists to Class B G-Protein Coupled Receptor Pituitary Adenylate Cyclase Type 1 (PAC1R). [Thesis]. University of Vermont; 2016. Available from: https://scholarworks.uvm.edu/graddis/624

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


Johannes Gutenberg Universität Mainz

2. Meesters, Christian. Die Verbindung von Kleinwinkelstreuung und in silico-Methodik zur Aufklärung von Konformationswechseln großer Proteinkomplexe.

Degree: 2008, Johannes Gutenberg Universität Mainz

 In dieser Dissertation wurden die Methoden Homologiemodellierung und Molekulardynamik genutzt, um die Struktur und das Verhalten von Proteinen in Lösung zu beschreiben. Mit Hilfe der… (more)

Subjects/Keywords: SAXS, Homologiemodellierung; SAXS, homology modeling; Life sciences

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APA (6th Edition):

Meesters, C. (2008). Die Verbindung von Kleinwinkelstreuung und in silico-Methodik zur Aufklärung von Konformationswechseln großer Proteinkomplexe. (Doctoral Dissertation). Johannes Gutenberg Universität Mainz. Retrieved from http://ubm.opus.hbz-nrw.de/volltexte/2008/1833/

Chicago Manual of Style (16th Edition):

Meesters, Christian. “Die Verbindung von Kleinwinkelstreuung und in silico-Methodik zur Aufklärung von Konformationswechseln großer Proteinkomplexe.” 2008. Doctoral Dissertation, Johannes Gutenberg Universität Mainz. Accessed April 18, 2021. http://ubm.opus.hbz-nrw.de/volltexte/2008/1833/.

MLA Handbook (7th Edition):

Meesters, Christian. “Die Verbindung von Kleinwinkelstreuung und in silico-Methodik zur Aufklärung von Konformationswechseln großer Proteinkomplexe.” 2008. Web. 18 Apr 2021.

Vancouver:

Meesters C. Die Verbindung von Kleinwinkelstreuung und in silico-Methodik zur Aufklärung von Konformationswechseln großer Proteinkomplexe. [Internet] [Doctoral dissertation]. Johannes Gutenberg Universität Mainz; 2008. [cited 2021 Apr 18]. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2008/1833/.

Council of Science Editors:

Meesters C. Die Verbindung von Kleinwinkelstreuung und in silico-Methodik zur Aufklärung von Konformationswechseln großer Proteinkomplexe. [Doctoral Dissertation]. Johannes Gutenberg Universität Mainz; 2008. Available from: http://ubm.opus.hbz-nrw.de/volltexte/2008/1833/


Vanderbilt University

3. Kaufmann, Kristian Wallace. Computational prediction of protein small molecule interfaces using ROSETTA.

Degree: PhD, Chemistry, 2011, Vanderbilt University

 Protein small molecule docking has focused on the modeling of small molecule flexibility and scoring of small molecules binding to fixed protein structures due to… (more)

Subjects/Keywords: homology modeling; virtual screening; drug design

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APA (6th Edition):

Kaufmann, K. W. (2011). Computational prediction of protein small molecule interfaces using ROSETTA. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14473

Chicago Manual of Style (16th Edition):

Kaufmann, Kristian Wallace. “Computational prediction of protein small molecule interfaces using ROSETTA.” 2011. Doctoral Dissertation, Vanderbilt University. Accessed April 18, 2021. http://hdl.handle.net/1803/14473.

MLA Handbook (7th Edition):

Kaufmann, Kristian Wallace. “Computational prediction of protein small molecule interfaces using ROSETTA.” 2011. Web. 18 Apr 2021.

Vancouver:

Kaufmann KW. Computational prediction of protein small molecule interfaces using ROSETTA. [Internet] [Doctoral dissertation]. Vanderbilt University; 2011. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/1803/14473.

Council of Science Editors:

Kaufmann KW. Computational prediction of protein small molecule interfaces using ROSETTA. [Doctoral Dissertation]. Vanderbilt University; 2011. Available from: http://hdl.handle.net/1803/14473

4. Haynes, Alexina. STRUCTURAL AND CATALYTIC FEATURES AFFECTING INACTIVATION OF TYPICAL 2-CYS HUMAN PEROXIREDOXINS 2 AND 3.

Degree: 2013, Wake Forest University

 Reactive oxygen species are key mediators of intracellular signaling and significantly influence the progression of several pathophysiologies. Oxidative stress damages macromolecules (lipids, nucleic acids and… (more)

Subjects/Keywords: Homology modeling

…crystallography, homology modeling and mass spectrometry. Previous studies conducted in cells indicate… …crystallography in addition to homology modeling to elucidate the molecular basis of hyperoxidation… …as a decamer. Homology modeling was used to generate models of Prx2 and Prx3 in the reduced… …ring catenane, a species first observed in bovine Prx3 that has an 89% homology with human… 

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APA (6th Edition):

Haynes, A. (2013). STRUCTURAL AND CATALYTIC FEATURES AFFECTING INACTIVATION OF TYPICAL 2-CYS HUMAN PEROXIREDOXINS 2 AND 3. (Thesis). Wake Forest University. Retrieved from http://hdl.handle.net/10339/38543

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):

Haynes, Alexina. “STRUCTURAL AND CATALYTIC FEATURES AFFECTING INACTIVATION OF TYPICAL 2-CYS HUMAN PEROXIREDOXINS 2 AND 3.” 2013. Thesis, Wake Forest University. Accessed April 18, 2021. http://hdl.handle.net/10339/38543.

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

MLA Handbook (7th Edition):

Haynes, Alexina. “STRUCTURAL AND CATALYTIC FEATURES AFFECTING INACTIVATION OF TYPICAL 2-CYS HUMAN PEROXIREDOXINS 2 AND 3.” 2013. Web. 18 Apr 2021.

Vancouver:

Haynes A. STRUCTURAL AND CATALYTIC FEATURES AFFECTING INACTIVATION OF TYPICAL 2-CYS HUMAN PEROXIREDOXINS 2 AND 3. [Internet] [Thesis]. Wake Forest University; 2013. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/10339/38543.

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

Council of Science Editors:

Haynes A. STRUCTURAL AND CATALYTIC FEATURES AFFECTING INACTIVATION OF TYPICAL 2-CYS HUMAN PEROXIREDOXINS 2 AND 3. [Thesis]. Wake Forest University; 2013. Available from: http://hdl.handle.net/10339/38543

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


University of Tennessee – Knoxville

5. Wuppalapati, Sai Keerthana. Subfunctionalization of Ethylene Receptors and Homology Modeling of Cytosolic Domains in <i>Arabidopsis thaliana</i>.

Degree: MS, Biochemistry and Cellular and Molecular Biology, 2015, University of Tennessee – Knoxville

  Ethylene is a gaseous phytohormone that initiates and modulates several mechanisms related to growth and development in plants through a family of five disulphide-linked… (more)

Subjects/Keywords: Ethylene; Homology Modeling; Receptors; Subfunctionalization; Silver ions; Homology modeling; Biochemistry, Biophysics, and Structural Biology

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APA (6th Edition):

Wuppalapati, S. K. (2015). Subfunctionalization of Ethylene Receptors and Homology Modeling of Cytosolic Domains in <i>Arabidopsis thaliana</i>. (Thesis). University of Tennessee – Knoxville. Retrieved from https://trace.tennessee.edu/utk_gradthes/3557

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):

Wuppalapati, Sai Keerthana. “Subfunctionalization of Ethylene Receptors and Homology Modeling of Cytosolic Domains in <i>Arabidopsis thaliana</i>.” 2015. Thesis, University of Tennessee – Knoxville. Accessed April 18, 2021. https://trace.tennessee.edu/utk_gradthes/3557.

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

MLA Handbook (7th Edition):

Wuppalapati, Sai Keerthana. “Subfunctionalization of Ethylene Receptors and Homology Modeling of Cytosolic Domains in <i>Arabidopsis thaliana</i>.” 2015. Web. 18 Apr 2021.

Vancouver:

Wuppalapati SK. Subfunctionalization of Ethylene Receptors and Homology Modeling of Cytosolic Domains in <i>Arabidopsis thaliana</i>. [Internet] [Thesis]. University of Tennessee – Knoxville; 2015. [cited 2021 Apr 18]. Available from: https://trace.tennessee.edu/utk_gradthes/3557.

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

Council of Science Editors:

Wuppalapati SK. Subfunctionalization of Ethylene Receptors and Homology Modeling of Cytosolic Domains in <i>Arabidopsis thaliana</i>. [Thesis]. University of Tennessee – Knoxville; 2015. Available from: https://trace.tennessee.edu/utk_gradthes/3557

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


Duquesne University

6. Raghavan, Sudhir. Synthesis and Molecular Modeling Studies of Bicyclic Inhibitors of Dihydrofolate Reductase, Receptor Tyrosine Kinases and Tubulin.

Degree: PhD, Medicinal Chemistry, 2013, Duquesne University

 The results from this work are reported into two sections listed below: Synthesis: Following structural classes of compounds have been designed, synthesized and studied as… (more)

Subjects/Keywords: Cancer; Docking; Homology modeling; Molecular modeling; Opportunistic infections

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APA (6th Edition):

Raghavan, S. (2013). Synthesis and Molecular Modeling Studies of Bicyclic Inhibitors of Dihydrofolate Reductase, Receptor Tyrosine Kinases and Tubulin. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/1080

Chicago Manual of Style (16th Edition):

Raghavan, Sudhir. “Synthesis and Molecular Modeling Studies of Bicyclic Inhibitors of Dihydrofolate Reductase, Receptor Tyrosine Kinases and Tubulin.” 2013. Doctoral Dissertation, Duquesne University. Accessed April 18, 2021. https://dsc.duq.edu/etd/1080.

MLA Handbook (7th Edition):

Raghavan, Sudhir. “Synthesis and Molecular Modeling Studies of Bicyclic Inhibitors of Dihydrofolate Reductase, Receptor Tyrosine Kinases and Tubulin.” 2013. Web. 18 Apr 2021.

Vancouver:

Raghavan S. Synthesis and Molecular Modeling Studies of Bicyclic Inhibitors of Dihydrofolate Reductase, Receptor Tyrosine Kinases and Tubulin. [Internet] [Doctoral dissertation]. Duquesne University; 2013. [cited 2021 Apr 18]. Available from: https://dsc.duq.edu/etd/1080.

Council of Science Editors:

Raghavan S. Synthesis and Molecular Modeling Studies of Bicyclic Inhibitors of Dihydrofolate Reductase, Receptor Tyrosine Kinases and Tubulin. [Doctoral Dissertation]. Duquesne University; 2013. Available from: https://dsc.duq.edu/etd/1080


University of Alberta

7. Hosamani, Ishwar V. Homology modeling of Suv39h1 and discovery of its small molecule inhibitors by virtual screening and their in vitro validation.

Degree: MS, Department of Oncology, 2013, University of Alberta

 Epigenetic modifications are carried out by specific enzymes and are reversible making them a viable and attractive target to design inhibitors to reset the epigenetic… (more)

Subjects/Keywords: virtual screening; Homology modeling; histones; SUV39h1; methyltransferases; epigenetics

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APA (6th Edition):

Hosamani, I. V. (2013). Homology modeling of Suv39h1 and discovery of its small molecule inhibitors by virtual screening and their in vitro validation. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/qj72p821p

Chicago Manual of Style (16th Edition):

Hosamani, Ishwar V. “Homology modeling of Suv39h1 and discovery of its small molecule inhibitors by virtual screening and their in vitro validation.” 2013. Masters Thesis, University of Alberta. Accessed April 18, 2021. https://era.library.ualberta.ca/files/qj72p821p.

MLA Handbook (7th Edition):

Hosamani, Ishwar V. “Homology modeling of Suv39h1 and discovery of its small molecule inhibitors by virtual screening and their in vitro validation.” 2013. Web. 18 Apr 2021.

Vancouver:

Hosamani IV. Homology modeling of Suv39h1 and discovery of its small molecule inhibitors by virtual screening and their in vitro validation. [Internet] [Masters thesis]. University of Alberta; 2013. [cited 2021 Apr 18]. Available from: https://era.library.ualberta.ca/files/qj72p821p.

Council of Science Editors:

Hosamani IV. Homology modeling of Suv39h1 and discovery of its small molecule inhibitors by virtual screening and their in vitro validation. [Masters Thesis]. University of Alberta; 2013. Available from: https://era.library.ualberta.ca/files/qj72p821p


Virginia Commonwealth University

8. Liu, Hebing. Three Dimensional Homology Modeling of Organic Cation Transporter 3 to Identify Structural Elements Mediating Transporter-substrate Interactions.

Degree: PhD, Pharmaceutical Sciences, 2017, Virginia Commonwealth University

  Organic cation transporters (OCTs) play a pivotal role in the absorption, tissue distribution, and excretion of a diverse array of substances, and currently the… (more)

Subjects/Keywords: OCT3; homology modeling; ligand interaction; affinity; Medicinal Chemistry and Pharmaceutics

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APA (6th Edition):

Liu, H. (2017). Three Dimensional Homology Modeling of Organic Cation Transporter 3 to Identify Structural Elements Mediating Transporter-substrate Interactions. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://doi.org/10.25772/27KT-3875 ; https://scholarscompass.vcu.edu/etd/4769

Chicago Manual of Style (16th Edition):

Liu, Hebing. “Three Dimensional Homology Modeling of Organic Cation Transporter 3 to Identify Structural Elements Mediating Transporter-substrate Interactions.” 2017. Doctoral Dissertation, Virginia Commonwealth University. Accessed April 18, 2021. https://doi.org/10.25772/27KT-3875 ; https://scholarscompass.vcu.edu/etd/4769.

MLA Handbook (7th Edition):

Liu, Hebing. “Three Dimensional Homology Modeling of Organic Cation Transporter 3 to Identify Structural Elements Mediating Transporter-substrate Interactions.” 2017. Web. 18 Apr 2021.

Vancouver:

Liu H. Three Dimensional Homology Modeling of Organic Cation Transporter 3 to Identify Structural Elements Mediating Transporter-substrate Interactions. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2017. [cited 2021 Apr 18]. Available from: https://doi.org/10.25772/27KT-3875 ; https://scholarscompass.vcu.edu/etd/4769.

Council of Science Editors:

Liu H. Three Dimensional Homology Modeling of Organic Cation Transporter 3 to Identify Structural Elements Mediating Transporter-substrate Interactions. [Doctoral Dissertation]. Virginia Commonwealth University; 2017. Available from: https://doi.org/10.25772/27KT-3875 ; https://scholarscompass.vcu.edu/etd/4769


University of California – San Francisco

9. Karpiak, Joel David. Shooting in the dark: Strategies for discovering magic bullets and magic shotguns for orphan GPCRs.

Degree: Chemistry and Chemical Biology, 2015, University of California – San Francisco

 It is now widely accepted that drugs achieve efficacy via interactions with multiple targets simultaneously, a serendipitous biological symphony that is typically only deconvoluted retrospectively.… (more)

Subjects/Keywords: Chemistry; Docking; GPCR; Homology Modeling; orphan; polypharmacology; structure-based design

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APA (6th Edition):

Karpiak, J. D. (2015). Shooting in the dark: Strategies for discovering magic bullets and magic shotguns for orphan GPCRs. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/0dd0c4z2

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):

Karpiak, Joel David. “Shooting in the dark: Strategies for discovering magic bullets and magic shotguns for orphan GPCRs.” 2015. Thesis, University of California – San Francisco. Accessed April 18, 2021. http://www.escholarship.org/uc/item/0dd0c4z2.

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

MLA Handbook (7th Edition):

Karpiak, Joel David. “Shooting in the dark: Strategies for discovering magic bullets and magic shotguns for orphan GPCRs.” 2015. Web. 18 Apr 2021.

Vancouver:

Karpiak JD. Shooting in the dark: Strategies for discovering magic bullets and magic shotguns for orphan GPCRs. [Internet] [Thesis]. University of California – San Francisco; 2015. [cited 2021 Apr 18]. Available from: http://www.escholarship.org/uc/item/0dd0c4z2.

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

Council of Science Editors:

Karpiak JD. Shooting in the dark: Strategies for discovering magic bullets and magic shotguns for orphan GPCRs. [Thesis]. University of California – San Francisco; 2015. Available from: http://www.escholarship.org/uc/item/0dd0c4z2

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


University of Illinois – Chicago

10. Bandela, Mounica. Role of Lysocardiolipin AcylTransferase in Lung Epithelial Cell Apoptosis.

Degree: 2018, University of Illinois – Chicago

 Chronic Obstructive Pulmonary Disorder (COPD), primarily caused by cigarette smoke (CS), is a leading cause of mortality in the US, and it is preventable by… (more)

Subjects/Keywords: Cigarette smoke extract; Apoptosis; ROS; Homology modeling; Modeller9.19; Lysocardiolipin acyltransferase.

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APA (6th Edition):

Bandela, M. (2018). Role of Lysocardiolipin AcylTransferase in Lung Epithelial Cell Apoptosis. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/22948

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):

Bandela, Mounica. “Role of Lysocardiolipin AcylTransferase in Lung Epithelial Cell Apoptosis.” 2018. Thesis, University of Illinois – Chicago. Accessed April 18, 2021. http://hdl.handle.net/10027/22948.

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

MLA Handbook (7th Edition):

Bandela, Mounica. “Role of Lysocardiolipin AcylTransferase in Lung Epithelial Cell Apoptosis.” 2018. Web. 18 Apr 2021.

Vancouver:

Bandela M. Role of Lysocardiolipin AcylTransferase in Lung Epithelial Cell Apoptosis. [Internet] [Thesis]. University of Illinois – Chicago; 2018. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/10027/22948.

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

Council of Science Editors:

Bandela M. Role of Lysocardiolipin AcylTransferase in Lung Epithelial Cell Apoptosis. [Thesis]. University of Illinois – Chicago; 2018. Available from: http://hdl.handle.net/10027/22948

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


East Tennessee State University

11. Kandel, Sangam, Mr. Structural and Functional Analysis of Grapefruit Flavonol-Specific-3-O-GT Mutant P145T.

Degree: MS, Biology, 2016, East Tennessee State University

  This research is focused on the study of the effect of mutating proline 145 to threonine on the substrate and regiospecificity of flavonol specific… (more)

Subjects/Keywords: Glucosyltrasnferase; Citrus paradisi; Mutation; Flavonoids; Glucosides; Homology modeling; Biology

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APA (6th Edition):

Kandel, Sangam, M. (2016). Structural and Functional Analysis of Grapefruit Flavonol-Specific-3-O-GT Mutant P145T. (Thesis). East Tennessee State University. Retrieved from https://dc.etsu.edu/etd/3150

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):

Kandel, Sangam, Mr. “Structural and Functional Analysis of Grapefruit Flavonol-Specific-3-O-GT Mutant P145T.” 2016. Thesis, East Tennessee State University. Accessed April 18, 2021. https://dc.etsu.edu/etd/3150.

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

MLA Handbook (7th Edition):

Kandel, Sangam, Mr. “Structural and Functional Analysis of Grapefruit Flavonol-Specific-3-O-GT Mutant P145T.” 2016. Web. 18 Apr 2021.

Vancouver:

Kandel, Sangam M. Structural and Functional Analysis of Grapefruit Flavonol-Specific-3-O-GT Mutant P145T. [Internet] [Thesis]. East Tennessee State University; 2016. [cited 2021 Apr 18]. Available from: https://dc.etsu.edu/etd/3150.

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

Council of Science Editors:

Kandel, Sangam M. Structural and Functional Analysis of Grapefruit Flavonol-Specific-3-O-GT Mutant P145T. [Thesis]. East Tennessee State University; 2016. Available from: https://dc.etsu.edu/etd/3150

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


Virginia Tech

12. Arnold, Matthew Scott. Characterization of the thermostable nature of the alpha and beta tubulin proteins in Cyanidium caldarium and Cyanidioschyzon merolae.

Degree: MS, Biology, 2004, Virginia Tech

 Microtubules are critically important cytoskeletal elements. Together with microtubule associated proteins (MAPs), they form the latticework on which eukaryotic life exists. Simply put, microtubules are… (more)

Subjects/Keywords: Tubulin; Homology Modeling; Microtubule

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APA (6th Edition):

Arnold, M. S. (2004). Characterization of the thermostable nature of the alpha and beta tubulin proteins in Cyanidium caldarium and Cyanidioschyzon merolae. (Masters Thesis). Virginia Tech. Retrieved from http://hdl.handle.net/10919/9745

Chicago Manual of Style (16th Edition):

Arnold, Matthew Scott. “Characterization of the thermostable nature of the alpha and beta tubulin proteins in Cyanidium caldarium and Cyanidioschyzon merolae.” 2004. Masters Thesis, Virginia Tech. Accessed April 18, 2021. http://hdl.handle.net/10919/9745.

MLA Handbook (7th Edition):

Arnold, Matthew Scott. “Characterization of the thermostable nature of the alpha and beta tubulin proteins in Cyanidium caldarium and Cyanidioschyzon merolae.” 2004. Web. 18 Apr 2021.

Vancouver:

Arnold MS. Characterization of the thermostable nature of the alpha and beta tubulin proteins in Cyanidium caldarium and Cyanidioschyzon merolae. [Internet] [Masters thesis]. Virginia Tech; 2004. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/10919/9745.

Council of Science Editors:

Arnold MS. Characterization of the thermostable nature of the alpha and beta tubulin proteins in Cyanidium caldarium and Cyanidioschyzon merolae. [Masters Thesis]. Virginia Tech; 2004. Available from: http://hdl.handle.net/10919/9745

13. LIMA, Sheyla Carla Barbosa da Silva. Isolamento e caracterização in silico de ciclotídeos em milho (Zea mays) e centeio (Secale cereale).

Degree: 2015, Federal University of Pernambuco

FACEPE

Ciclotídeos são uma classe de peptídeos antimicrobianos (AMPs - do inglês Antimicrobial peptide) cíclicos de plantas, compostos de, aproximadamente, 30 resíduos de aminoácidos, sendo… (more)

Subjects/Keywords: Bioinformática; Modelagem por homologia; AMPs; Poaceae; bioinformatics; homology modeling; AMPs; Poaceae

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APA (6th Edition):

LIMA, S. C. B. d. S. (2015). Isolamento e caracterização in silico de ciclotídeos em milho (Zea mays) e centeio (Secale cereale). (Masters Thesis). Federal University of Pernambuco. Retrieved from https://repositorio.ufpe.br/handle/123456789/16744

Chicago Manual of Style (16th Edition):

LIMA, Sheyla Carla Barbosa da Silva. “Isolamento e caracterização in silico de ciclotídeos em milho (Zea mays) e centeio (Secale cereale).” 2015. Masters Thesis, Federal University of Pernambuco. Accessed April 18, 2021. https://repositorio.ufpe.br/handle/123456789/16744.

MLA Handbook (7th Edition):

LIMA, Sheyla Carla Barbosa da Silva. “Isolamento e caracterização in silico de ciclotídeos em milho (Zea mays) e centeio (Secale cereale).” 2015. Web. 18 Apr 2021.

Vancouver:

LIMA SCBdS. Isolamento e caracterização in silico de ciclotídeos em milho (Zea mays) e centeio (Secale cereale). [Internet] [Masters thesis]. Federal University of Pernambuco; 2015. [cited 2021 Apr 18]. Available from: https://repositorio.ufpe.br/handle/123456789/16744.

Council of Science Editors:

LIMA SCBdS. Isolamento e caracterização in silico de ciclotídeos em milho (Zea mays) e centeio (Secale cereale). [Masters Thesis]. Federal University of Pernambuco; 2015. Available from: https://repositorio.ufpe.br/handle/123456789/16744

14. Χαϊντίνης, Βασίλειος. Μοριακή μοντελοποίηση και διαμορφωτική ανάλυση της δομής της πρωτείνης MuSK.

Degree: 2012, University of Patras

Η πρωτείνη MuSK (Muscle Specific Kinase) αποτελεί μέρος ενός συμπλόκου υποδοχέων της αγκρίνης (agrin) οι οποίοι διεγείρουν την φωσφορυλίωση της τυροσίνης και οδηγούν στην ομαδοποίηση… (more)

Subjects/Keywords: Πρωτείνη MuSK; Μοντελοποίηση; Μοριακή δυναμική; Ομολογία; 572.6; MuSK (Muscle Specific Kinase); Modeling; Molecular dynamics; Homology

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APA (6th Edition):

Χαϊντίνης, . (2012). Μοριακή μοντελοποίηση και διαμορφωτική ανάλυση της δομής της πρωτείνης MuSK. (Masters Thesis). University of Patras. Retrieved from http://hdl.handle.net/10889/5690

Chicago Manual of Style (16th Edition):

Χαϊντίνης, Βασίλειος. “Μοριακή μοντελοποίηση και διαμορφωτική ανάλυση της δομής της πρωτείνης MuSK.” 2012. Masters Thesis, University of Patras. Accessed April 18, 2021. http://hdl.handle.net/10889/5690.

MLA Handbook (7th Edition):

Χαϊντίνης, Βασίλειος. “Μοριακή μοντελοποίηση και διαμορφωτική ανάλυση της δομής της πρωτείνης MuSK.” 2012. Web. 18 Apr 2021.

Vancouver:

Χαϊντίνης . Μοριακή μοντελοποίηση και διαμορφωτική ανάλυση της δομής της πρωτείνης MuSK. [Internet] [Masters thesis]. University of Patras; 2012. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/10889/5690.

Council of Science Editors:

Χαϊντίνης . Μοριακή μοντελοποίηση και διαμορφωτική ανάλυση της δομής της πρωτείνης MuSK. [Masters Thesis]. University of Patras; 2012. Available from: http://hdl.handle.net/10889/5690


McMaster University

15. Khadka, Bijendra. Structural and Functional Aspects of Evolutionarily Conserved Signature Indels in Protein Sequences.

Degree: PhD, 2019, McMaster University

Analysis of genome sequences is enabling identification of numerous novel characteristics that provide valuable means for genetic and biochemical studies. Of these characteristics, Conserved Signature… (more)

Subjects/Keywords: Genomics; Molecular Signatures; Phylogenetic analysis; Protein evolution; Homology modeling; Protein-protein docking; Molecular dynamics simulations

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APA (6th Edition):

Khadka, B. (2019). Structural and Functional Aspects of Evolutionarily Conserved Signature Indels in Protein Sequences. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/25115

Chicago Manual of Style (16th Edition):

Khadka, Bijendra. “Structural and Functional Aspects of Evolutionarily Conserved Signature Indels in Protein Sequences.” 2019. Doctoral Dissertation, McMaster University. Accessed April 18, 2021. http://hdl.handle.net/11375/25115.

MLA Handbook (7th Edition):

Khadka, Bijendra. “Structural and Functional Aspects of Evolutionarily Conserved Signature Indels in Protein Sequences.” 2019. Web. 18 Apr 2021.

Vancouver:

Khadka B. Structural and Functional Aspects of Evolutionarily Conserved Signature Indels in Protein Sequences. [Internet] [Doctoral dissertation]. McMaster University; 2019. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/11375/25115.

Council of Science Editors:

Khadka B. Structural and Functional Aspects of Evolutionarily Conserved Signature Indels in Protein Sequences. [Doctoral Dissertation]. McMaster University; 2019. Available from: http://hdl.handle.net/11375/25115


University of KwaZulu-Natal

16. Munsamy, Geraldene. Size does not matter: a molecular insight into the biological activity of chemical fragments utilizing computational approaches.

Degree: 2016, University of KwaZulu-Natal

 Insight into the functional and physiological state of a drug target is of essential importance in the drug discovery process, with the lack of emerging… (more)

Subjects/Keywords: Chemical fragments.; Drug target.; Drug discovery process.; Homology modeling.; 3D protein structures.

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

APA (6th Edition):

Munsamy, G. (2016). Size does not matter: a molecular insight into the biological activity of chemical fragments utilizing computational approaches. (Thesis). University of KwaZulu-Natal. Retrieved from https://researchspace.ukzn.ac.za/handle/10413/18135

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):

Munsamy, Geraldene. “Size does not matter: a molecular insight into the biological activity of chemical fragments utilizing computational approaches.” 2016. Thesis, University of KwaZulu-Natal. Accessed April 18, 2021. https://researchspace.ukzn.ac.za/handle/10413/18135.

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

MLA Handbook (7th Edition):

Munsamy, Geraldene. “Size does not matter: a molecular insight into the biological activity of chemical fragments utilizing computational approaches.” 2016. Web. 18 Apr 2021.

Vancouver:

Munsamy G. Size does not matter: a molecular insight into the biological activity of chemical fragments utilizing computational approaches. [Internet] [Thesis]. University of KwaZulu-Natal; 2016. [cited 2021 Apr 18]. Available from: https://researchspace.ukzn.ac.za/handle/10413/18135.

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

Council of Science Editors:

Munsamy G. Size does not matter: a molecular insight into the biological activity of chemical fragments utilizing computational approaches. [Thesis]. University of KwaZulu-Natal; 2016. Available from: https://researchspace.ukzn.ac.za/handle/10413/18135

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


University of Vienna

17. Jurik, Andreas. Flexible docking studies of a series of ligands in a homology model of the human serotonin transporter.

Degree: 2010, University of Vienna

Bei der vorliegenden Arbeit wurden flexible Docking Studien an einem Homologiemodell des humanen Serotonintransporters durchgeführt. Der Schwerpunkt lag dabei darin, sowohl Liganden als auch Rezeptor… (more)

Subjects/Keywords: 44.42 Pharmazeutische Chemie; Homologiemodell / SERT / Induced Fit Docking; homology modeling / SERT / Induced Fit Docking

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

APA (6th Edition):

Jurik, A. (2010). Flexible docking studies of a series of ligands in a homology model of the human serotonin transporter. (Thesis). University of Vienna. Retrieved from http://othes.univie.ac.at/9669/

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):

Jurik, Andreas. “Flexible docking studies of a series of ligands in a homology model of the human serotonin transporter.” 2010. Thesis, University of Vienna. Accessed April 18, 2021. http://othes.univie.ac.at/9669/.

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

MLA Handbook (7th Edition):

Jurik, Andreas. “Flexible docking studies of a series of ligands in a homology model of the human serotonin transporter.” 2010. Web. 18 Apr 2021.

Vancouver:

Jurik A. Flexible docking studies of a series of ligands in a homology model of the human serotonin transporter. [Internet] [Thesis]. University of Vienna; 2010. [cited 2021 Apr 18]. Available from: http://othes.univie.ac.at/9669/.

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

Council of Science Editors:

Jurik A. Flexible docking studies of a series of ligands in a homology model of the human serotonin transporter. [Thesis]. University of Vienna; 2010. Available from: http://othes.univie.ac.at/9669/

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


University of Manchester

18. Ivanov, Stefan. Specificity determinants within families of protein - protein interactions.

Degree: 2018, University of Manchester

 Protein - protein interactions govern every aspect of the cellular life cycle. Despite the pivotal role of interprotein association, many of its aspects remain poorly… (more)

Subjects/Keywords: protein - protein interactions; free energy calculations; MM-PBSA; thermodynamic integration; bioinformatics; homology modeling

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

APA (6th Edition):

Ivanov, S. (2018). Specificity determinants within families of protein - protein interactions. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:312942

Chicago Manual of Style (16th Edition):

Ivanov, Stefan. “Specificity determinants within families of protein - protein interactions.” 2018. Doctoral Dissertation, University of Manchester. Accessed April 18, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:312942.

MLA Handbook (7th Edition):

Ivanov, Stefan. “Specificity determinants within families of protein - protein interactions.” 2018. Web. 18 Apr 2021.

Vancouver:

Ivanov S. Specificity determinants within families of protein - protein interactions. [Internet] [Doctoral dissertation]. University of Manchester; 2018. [cited 2021 Apr 18]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:312942.

Council of Science Editors:

Ivanov S. Specificity determinants within families of protein - protein interactions. [Doctoral Dissertation]. University of Manchester; 2018. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:312942


Brigham Young University

19. Menlove, Kit J. Model Detection Based upon Amino Acid Properties.

Degree: MS, 2010, Brigham Young University

 Similarity searches are an essential component to most bioinformatic applications. They form the bases of structural motif identification, gene identification, and insights into functional associations.… (more)

Subjects/Keywords: similarity searching; fold recognition; homology modeling; sequence profiles; BLAST; sequence alignment; protein evolution; threading; Biology

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

APA (6th Edition):

Menlove, K. J. (2010). Model Detection Based upon Amino Acid Properties. (Masters Thesis). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=3252&context=etd

Chicago Manual of Style (16th Edition):

Menlove, Kit J. “Model Detection Based upon Amino Acid Properties.” 2010. Masters Thesis, Brigham Young University. Accessed April 18, 2021. https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=3252&context=etd.

MLA Handbook (7th Edition):

Menlove, Kit J. “Model Detection Based upon Amino Acid Properties.” 2010. Web. 18 Apr 2021.

Vancouver:

Menlove KJ. Model Detection Based upon Amino Acid Properties. [Internet] [Masters thesis]. Brigham Young University; 2010. [cited 2021 Apr 18]. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=3252&context=etd.

Council of Science Editors:

Menlove KJ. Model Detection Based upon Amino Acid Properties. [Masters Thesis]. Brigham Young University; 2010. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=3252&context=etd


University of Manchester

20. Ivanov, Stefan. Specificity determinants within families of protein-protein interactions.

Degree: PhD, 2018, University of Manchester

 Protein-protein interactions govern every aspect of the cellular life cycle. Despite the pivotal role of interprotein association, many of its aspects remain poorly understood. This… (more)

Subjects/Keywords: 540; homology modeling; bioinformatics; thermodynamic integration; free energy calculations; MM-PBSA; protein - protein interactions

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

APA (6th Edition):

Ivanov, S. (2018). Specificity determinants within families of protein-protein interactions. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/specificity-determinants-within-families-of-protein – protein-interactions(66a4ae9b-fb6b-49c1-bcce-0397f231cb97).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.771353

Chicago Manual of Style (16th Edition):

Ivanov, Stefan. “Specificity determinants within families of protein-protein interactions.” 2018. Doctoral Dissertation, University of Manchester. Accessed April 18, 2021. https://www.research.manchester.ac.uk/portal/en/theses/specificity-determinants-within-families-of-protein – protein-interactions(66a4ae9b-fb6b-49c1-bcce-0397f231cb97).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.771353.

MLA Handbook (7th Edition):

Ivanov, Stefan. “Specificity determinants within families of protein-protein interactions.” 2018. Web. 18 Apr 2021.

Vancouver:

Ivanov S. Specificity determinants within families of protein-protein interactions. [Internet] [Doctoral dissertation]. University of Manchester; 2018. [cited 2021 Apr 18]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/specificity-determinants-within-families-of-protein – protein-interactions(66a4ae9b-fb6b-49c1-bcce-0397f231cb97).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.771353.

Council of Science Editors:

Ivanov S. Specificity determinants within families of protein-protein interactions. [Doctoral Dissertation]. University of Manchester; 2018. Available from: https://www.research.manchester.ac.uk/portal/en/theses/specificity-determinants-within-families-of-protein – protein-interactions(66a4ae9b-fb6b-49c1-bcce-0397f231cb97).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.771353


Iowa State University

21. Zheng, Fudan. Structure-based drug discovery of Asu-ACR-16 agonists and allosteric modulators.

Degree: 2016, Iowa State University

 Ascariasis is a neglected tropical disease that is caused by the nematode parasite Ascaris. Ascaris infections have high morbidity, cause debilitating conditions and affect at… (more)

Subjects/Keywords: Analytical Chemistry; anthelmintics; Ascaris suum; electrophysiology; homology modeling; nAChR; pharmacology; Analytical Chemistry

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

APA (6th Edition):

Zheng, F. (2016). Structure-based drug discovery of Asu-ACR-16 agonists and allosteric modulators. (Thesis). Iowa State University. Retrieved from https://lib.dr.iastate.edu/etd/15201

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):

Zheng, Fudan. “Structure-based drug discovery of Asu-ACR-16 agonists and allosteric modulators.” 2016. Thesis, Iowa State University. Accessed April 18, 2021. https://lib.dr.iastate.edu/etd/15201.

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

MLA Handbook (7th Edition):

Zheng, Fudan. “Structure-based drug discovery of Asu-ACR-16 agonists and allosteric modulators.” 2016. Web. 18 Apr 2021.

Vancouver:

Zheng F. Structure-based drug discovery of Asu-ACR-16 agonists and allosteric modulators. [Internet] [Thesis]. Iowa State University; 2016. [cited 2021 Apr 18]. Available from: https://lib.dr.iastate.edu/etd/15201.

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

Council of Science Editors:

Zheng F. Structure-based drug discovery of Asu-ACR-16 agonists and allosteric modulators. [Thesis]. Iowa State University; 2016. Available from: https://lib.dr.iastate.edu/etd/15201

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


University of Notre Dame

22. Kevin William Kastner. Molecular Dynamics and Virtual Screening of the Octopamine Receptor: A GPCR Computational Biochemical Analysis</h1>.

Degree: Computer Science and Engineering, 2016, University of Notre Dame

  Octopamine receptors (OARs) perform key operations in the biological pathways of invertebrates only, making this class of G-Protein Coupled Receptors (GPCRs) a potentially good… (more)

Subjects/Keywords: Accelerated Molecular Dynamics; Homology Modeling; GPCR; Octopamine Receptor; Molecular Dynamics; Virtual Screening

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APA (6th Edition):

Kastner, K. W. (2016). Molecular Dynamics and Virtual Screening of the Octopamine Receptor: A GPCR Computational Biochemical Analysis</h1>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/mc87pn91r8k

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):

Kastner, Kevin William. “Molecular Dynamics and Virtual Screening of the Octopamine Receptor: A GPCR Computational Biochemical Analysis</h1>.” 2016. Thesis, University of Notre Dame. Accessed April 18, 2021. https://curate.nd.edu/show/mc87pn91r8k.

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

MLA Handbook (7th Edition):

Kastner, Kevin William. “Molecular Dynamics and Virtual Screening of the Octopamine Receptor: A GPCR Computational Biochemical Analysis</h1>.” 2016. Web. 18 Apr 2021.

Vancouver:

Kastner KW. Molecular Dynamics and Virtual Screening of the Octopamine Receptor: A GPCR Computational Biochemical Analysis</h1>. [Internet] [Thesis]. University of Notre Dame; 2016. [cited 2021 Apr 18]. Available from: https://curate.nd.edu/show/mc87pn91r8k.

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

Council of Science Editors:

Kastner KW. Molecular Dynamics and Virtual Screening of the Octopamine Receptor: A GPCR Computational Biochemical Analysis</h1>. [Thesis]. University of Notre Dame; 2016. Available from: https://curate.nd.edu/show/mc87pn91r8k

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


University of South Florida

23. Ramamoorthy, Divya. Design of Novel Inhibitors for Infectious Diseases using Structure-based Drug Design: Virtual Screening, Homology Modeling and Molecular Dynamics.

Degree: 2012, University of South Florida

 The main aim of the study in this thesis was to use structure-based protocols to design new drugs for enzymes, DXS and DXR in the… (more)

Subjects/Keywords: FabH; Homology Modeling; Malaria; Molecular Dynamics; Virtual Screening; Bioinformatics; Chemistry; Other Chemistry

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APA (6th Edition):

Ramamoorthy, D. (2012). Design of Novel Inhibitors for Infectious Diseases using Structure-based Drug Design: Virtual Screening, Homology Modeling and Molecular Dynamics. (Thesis). University of South Florida. Retrieved from https://scholarcommons.usf.edu/etd/4393

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):

Ramamoorthy, Divya. “Design of Novel Inhibitors for Infectious Diseases using Structure-based Drug Design: Virtual Screening, Homology Modeling and Molecular Dynamics.” 2012. Thesis, University of South Florida. Accessed April 18, 2021. https://scholarcommons.usf.edu/etd/4393.

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

MLA Handbook (7th Edition):

Ramamoorthy, Divya. “Design of Novel Inhibitors for Infectious Diseases using Structure-based Drug Design: Virtual Screening, Homology Modeling and Molecular Dynamics.” 2012. Web. 18 Apr 2021.

Vancouver:

Ramamoorthy D. Design of Novel Inhibitors for Infectious Diseases using Structure-based Drug Design: Virtual Screening, Homology Modeling and Molecular Dynamics. [Internet] [Thesis]. University of South Florida; 2012. [cited 2021 Apr 18]. Available from: https://scholarcommons.usf.edu/etd/4393.

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

Council of Science Editors:

Ramamoorthy D. Design of Novel Inhibitors for Infectious Diseases using Structure-based Drug Design: Virtual Screening, Homology Modeling and Molecular Dynamics. [Thesis]. University of South Florida; 2012. Available from: https://scholarcommons.usf.edu/etd/4393

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


University of South Florida

24. Mhashilkar, Amruta. Molecular and Phenotypic Studies Validating the Role of the Ecdysone Receptor in the Human Parasite <i>Brugia malayi</i>.

Degree: 2015, University of South Florida

 Filariasis and onchocerciasis are debilitating diseases affecting 120 million people globally. The massive socio-economic impact of these diseases energized the international community to declare a… (more)

Subjects/Keywords: Lymphatic filariasis; RNA-seq; transcriptomics; proteomics; homology modeling; drug discovery; Molecular Biology; Public Health

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APA (6th Edition):

Mhashilkar, A. (2015). Molecular and Phenotypic Studies Validating the Role of the Ecdysone Receptor in the Human Parasite <i>Brugia malayi</i>. (Thesis). University of South Florida. Retrieved from https://scholarcommons.usf.edu/etd/5994

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):

Mhashilkar, Amruta. “Molecular and Phenotypic Studies Validating the Role of the Ecdysone Receptor in the Human Parasite <i>Brugia malayi</i>.” 2015. Thesis, University of South Florida. Accessed April 18, 2021. https://scholarcommons.usf.edu/etd/5994.

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

MLA Handbook (7th Edition):

Mhashilkar, Amruta. “Molecular and Phenotypic Studies Validating the Role of the Ecdysone Receptor in the Human Parasite <i>Brugia malayi</i>.” 2015. Web. 18 Apr 2021.

Vancouver:

Mhashilkar A. Molecular and Phenotypic Studies Validating the Role of the Ecdysone Receptor in the Human Parasite <i>Brugia malayi</i>. [Internet] [Thesis]. University of South Florida; 2015. [cited 2021 Apr 18]. Available from: https://scholarcommons.usf.edu/etd/5994.

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

Council of Science Editors:

Mhashilkar A. Molecular and Phenotypic Studies Validating the Role of the Ecdysone Receptor in the Human Parasite <i>Brugia malayi</i>. [Thesis]. University of South Florida; 2015. Available from: https://scholarcommons.usf.edu/etd/5994

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


Duquesne University

25. Samuel, Andre Duane. The Search for Novel Antibiotic Compounds Through Molecular Modeling and Structure-Function Analysis of CspE in E. coli K12.

Degree: PhD, Biological Sciences, 2014, Duquesne University

 Escherichia coli K12 has the capacity to express nine Csp (Cold shock-related protein) gene products (CspA-I). These proteins share between 29 and 83 percent identity… (more)

Subjects/Keywords: Antibiotic; Cold Shock Protein; DNA binding protein; Drug Discovery; E. Coli; Homology Modeling

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

APA (6th Edition):

Samuel, A. D. (2014). The Search for Novel Antibiotic Compounds Through Molecular Modeling and Structure-Function Analysis of CspE in E. coli K12. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/1143

Chicago Manual of Style (16th Edition):

Samuel, Andre Duane. “The Search for Novel Antibiotic Compounds Through Molecular Modeling and Structure-Function Analysis of CspE in E. coli K12.” 2014. Doctoral Dissertation, Duquesne University. Accessed April 18, 2021. https://dsc.duq.edu/etd/1143.

MLA Handbook (7th Edition):

Samuel, Andre Duane. “The Search for Novel Antibiotic Compounds Through Molecular Modeling and Structure-Function Analysis of CspE in E. coli K12.” 2014. Web. 18 Apr 2021.

Vancouver:

Samuel AD. The Search for Novel Antibiotic Compounds Through Molecular Modeling and Structure-Function Analysis of CspE in E. coli K12. [Internet] [Doctoral dissertation]. Duquesne University; 2014. [cited 2021 Apr 18]. Available from: https://dsc.duq.edu/etd/1143.

Council of Science Editors:

Samuel AD. The Search for Novel Antibiotic Compounds Through Molecular Modeling and Structure-Function Analysis of CspE in E. coli K12. [Doctoral Dissertation]. Duquesne University; 2014. Available from: https://dsc.duq.edu/etd/1143


California State University – Sacramento

26. Nguyen, Thuy Dung. CRISPR/Cas9-mediated Homology Directed Repair disease modeling and lentiviral gene therapy for CDKL5 deficiency disorder.

Degree: MA, Biological Sciences (Stem Cell, 2019, California State University – Sacramento

 CDKL5 deficiency disorder (CDD) is a rare X-linked epileptic encephalopathy caused by de novo mutations in the cyclin-dependent kinase-like 5 (CDKL5) gene located on the… (more)

Subjects/Keywords: CDKL5 deficiency disorder; CRISPR/cas9; Homology directed repair; Disease modeling; Lentivirus; Seizures

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APA (6th Edition):

Nguyen, T. D. (2019). CRISPR/Cas9-mediated Homology Directed Repair disease modeling and lentiviral gene therapy for CDKL5 deficiency disorder. (Masters Thesis). California State University – Sacramento. Retrieved from http://hdl.handle.net/10211.3/210208

Chicago Manual of Style (16th Edition):

Nguyen, Thuy Dung. “CRISPR/Cas9-mediated Homology Directed Repair disease modeling and lentiviral gene therapy for CDKL5 deficiency disorder.” 2019. Masters Thesis, California State University – Sacramento. Accessed April 18, 2021. http://hdl.handle.net/10211.3/210208.

MLA Handbook (7th Edition):

Nguyen, Thuy Dung. “CRISPR/Cas9-mediated Homology Directed Repair disease modeling and lentiviral gene therapy for CDKL5 deficiency disorder.” 2019. Web. 18 Apr 2021.

Vancouver:

Nguyen TD. CRISPR/Cas9-mediated Homology Directed Repair disease modeling and lentiviral gene therapy for CDKL5 deficiency disorder. [Internet] [Masters thesis]. California State University – Sacramento; 2019. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/10211.3/210208.

Council of Science Editors:

Nguyen TD. CRISPR/Cas9-mediated Homology Directed Repair disease modeling and lentiviral gene therapy for CDKL5 deficiency disorder. [Masters Thesis]. California State University – Sacramento; 2019. Available from: http://hdl.handle.net/10211.3/210208


University of Georgia

27. Ji, Fei. Bioinformatics tools & analysis of protein structure and function.

Degree: 2016, University of Georgia

 This dissertation mainly focuses on protein structure and functional studies from the viewpoint of Bioinformatics. My dissertation consists of three bioinformatics projects, which all utilized… (more)

Subjects/Keywords: Bioinformatics; Machine Learning; Protein Structure; Threading; Homology Modeling; Nuclear Magnetic Resonance; Hydrogenase

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

APA (6th Edition):

Ji, F. (2016). Bioinformatics tools & analysis of protein structure and function. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/35338"

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):

Ji, Fei. “Bioinformatics tools & analysis of protein structure and function.” 2016. Thesis, University of Georgia. Accessed April 18, 2021. http://hdl.handle.net/10724/35338".

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

MLA Handbook (7th Edition):

Ji, Fei. “Bioinformatics tools & analysis of protein structure and function.” 2016. Web. 18 Apr 2021.

Vancouver:

Ji F. Bioinformatics tools & analysis of protein structure and function. [Internet] [Thesis]. University of Georgia; 2016. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/10724/35338".

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

Council of Science Editors:

Ji F. Bioinformatics tools & analysis of protein structure and function. [Thesis]. University of Georgia; 2016. Available from: http://hdl.handle.net/10724/35338"

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

28. Demos, Wendy. Causal Varian discovery in Familial Congenital Heart Disease - An Integrative -Omic Approach.

Degree: 2012, Marquette University

 Hypoplastic left heart syndrome (HLHS) is a congenital heart defect that leads to neonatal death or compromised quality of life for those affected and their… (more)

Subjects/Keywords: bioinformatics; congenital heart defect; homology modeling; Hypoplastic left heart syndrome; pathway analysis; Bioinformatics

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

APA (6th Edition):

Demos, W. (2012). Causal Varian discovery in Familial Congenital Heart Disease - An Integrative -Omic Approach. (Thesis). Marquette University. Retrieved from https://epublications.marquette.edu/theses_open/140

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):

Demos, Wendy. “Causal Varian discovery in Familial Congenital Heart Disease - An Integrative -Omic Approach.” 2012. Thesis, Marquette University. Accessed April 18, 2021. https://epublications.marquette.edu/theses_open/140.

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

MLA Handbook (7th Edition):

Demos, Wendy. “Causal Varian discovery in Familial Congenital Heart Disease - An Integrative -Omic Approach.” 2012. Web. 18 Apr 2021.

Vancouver:

Demos W. Causal Varian discovery in Familial Congenital Heart Disease - An Integrative -Omic Approach. [Internet] [Thesis]. Marquette University; 2012. [cited 2021 Apr 18]. Available from: https://epublications.marquette.edu/theses_open/140.

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

Council of Science Editors:

Demos W. Causal Varian discovery in Familial Congenital Heart Disease - An Integrative -Omic Approach. [Thesis]. Marquette University; 2012. Available from: https://epublications.marquette.edu/theses_open/140

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

29. Érico Torrieri. Análise Estrutural de Mutações na Enzima GALNS associadas à Mucopolissacaridose IVA utilizando a Técnica de Modelagem Comparativa.

Degree: 2015, University of São Paulo

As Mucopolissacaridoses (MPS) são um grupo de doenças de armazenamento lisossômico causadas por deficiência de enzimas que catalisam a degradação gradual das glicosaminoglicanas (GAGs). GAGs… (more)

Subjects/Keywords: GALNS; Modelagem por homologia; MPS IVA; Mutações missense; GALNS; Homology modeling; Missense mutations; MPS IVA

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

APA (6th Edition):

Torrieri, . (2015). Análise Estrutural de Mutações na Enzima GALNS associadas à Mucopolissacaridose IVA utilizando a Técnica de Modelagem Comparativa. (Masters Thesis). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/17/17135/tde-28072015-113748/

Chicago Manual of Style (16th Edition):

Torrieri, Érico. “Análise Estrutural de Mutações na Enzima GALNS associadas à Mucopolissacaridose IVA utilizando a Técnica de Modelagem Comparativa.” 2015. Masters Thesis, University of São Paulo. Accessed April 18, 2021. http://www.teses.usp.br/teses/disponiveis/17/17135/tde-28072015-113748/.

MLA Handbook (7th Edition):

Torrieri, Érico. “Análise Estrutural de Mutações na Enzima GALNS associadas à Mucopolissacaridose IVA utilizando a Técnica de Modelagem Comparativa.” 2015. Web. 18 Apr 2021.

Vancouver:

Torrieri . Análise Estrutural de Mutações na Enzima GALNS associadas à Mucopolissacaridose IVA utilizando a Técnica de Modelagem Comparativa. [Internet] [Masters thesis]. University of São Paulo; 2015. [cited 2021 Apr 18]. Available from: http://www.teses.usp.br/teses/disponiveis/17/17135/tde-28072015-113748/.

Council of Science Editors:

Torrieri . Análise Estrutural de Mutações na Enzima GALNS associadas à Mucopolissacaridose IVA utilizando a Técnica de Modelagem Comparativa. [Masters Thesis]. University of São Paulo; 2015. Available from: http://www.teses.usp.br/teses/disponiveis/17/17135/tde-28072015-113748/

30. Ludovico Migliolo. Construção de modelos de interação in silico e in vitro do inibidor do tipo Kunitz de Adenanthera pavonina L. para as enzimas cisteínicas e serínicas.

Degree: 2008, Universidade Federal do Rio Grande do Norte

Os inibidores de proteinases serínicas (IPs) estão extensamente distribuídos na natureza e inibem a atividade enzimática in vitro e in vivo. Estes IPs em sementes… (more)

Subjects/Keywords: Adenanthera pavonina; Inibidor bifuncional; Modelagem comparativa; Estudos de interação; BIOQUIMICA; Adenanthera pavonina; Bifunctional inhibitor; Homology modeling; Docking study

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

APA (6th Edition):

Migliolo, L. (2008). Construção de modelos de interação in silico e in vitro do inibidor do tipo Kunitz de Adenanthera pavonina L. para as enzimas cisteínicas e serínicas. (Thesis). Universidade Federal do Rio Grande do Norte. Retrieved from http://bdtd.bczm.ufrn.br/tedesimplificado//tde_busca/arquivo.php?codArquivo=1883

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):

Migliolo, Ludovico. “Construção de modelos de interação in silico e in vitro do inibidor do tipo Kunitz de Adenanthera pavonina L. para as enzimas cisteínicas e serínicas.” 2008. Thesis, Universidade Federal do Rio Grande do Norte. Accessed April 18, 2021. http://bdtd.bczm.ufrn.br/tedesimplificado//tde_busca/arquivo.php?codArquivo=1883.

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

MLA Handbook (7th Edition):

Migliolo, Ludovico. “Construção de modelos de interação in silico e in vitro do inibidor do tipo Kunitz de Adenanthera pavonina L. para as enzimas cisteínicas e serínicas.” 2008. Web. 18 Apr 2021.

Vancouver:

Migliolo L. Construção de modelos de interação in silico e in vitro do inibidor do tipo Kunitz de Adenanthera pavonina L. para as enzimas cisteínicas e serínicas. [Internet] [Thesis]. Universidade Federal do Rio Grande do Norte; 2008. [cited 2021 Apr 18]. Available from: http://bdtd.bczm.ufrn.br/tedesimplificado//tde_busca/arquivo.php?codArquivo=1883.

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

Council of Science Editors:

Migliolo L. Construção de modelos de interação in silico e in vitro do inibidor do tipo Kunitz de Adenanthera pavonina L. para as enzimas cisteínicas e serínicas. [Thesis]. Universidade Federal do Rio Grande do Norte; 2008. Available from: http://bdtd.bczm.ufrn.br/tedesimplificado//tde_busca/arquivo.php?codArquivo=1883

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

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