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You searched for subject:(High throughput screening). Showing records 1 – 30 of 317 total matches.

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University of Cambridge

1. Chong, Zheng Shan. Extracellular Interaction Screening Using CRISPR Activation .

Degree: 2019, University of Cambridge

 Extracellular interactions between cell surface receptors are necessary for signaling and adhesion but identifying them remains technically challenging. We describe a cell-based genome-wide approach employing… (more)

Subjects/Keywords: CRISPR; protein-protein interactions; high-throughput screening

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APA (6th Edition):

Chong, Z. S. (2019). Extracellular Interaction Screening Using CRISPR Activation . (Thesis). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/291972

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):

Chong, Zheng Shan. “Extracellular Interaction Screening Using CRISPR Activation .” 2019. Thesis, University of Cambridge. Accessed October 18, 2019. https://www.repository.cam.ac.uk/handle/1810/291972.

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

MLA Handbook (7th Edition):

Chong, Zheng Shan. “Extracellular Interaction Screening Using CRISPR Activation .” 2019. Web. 18 Oct 2019.

Vancouver:

Chong ZS. Extracellular Interaction Screening Using CRISPR Activation . [Internet] [Thesis]. University of Cambridge; 2019. [cited 2019 Oct 18]. Available from: https://www.repository.cam.ac.uk/handle/1810/291972.

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

Council of Science Editors:

Chong ZS. Extracellular Interaction Screening Using CRISPR Activation . [Thesis]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/291972

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


McMaster University

2. Hansen, Drew M. Development of High Throughput Screening Approaches to Target TN1549 and F Plasmid Movement.

Degree: MSc, 2019, McMaster University

The antimicrobial resistance (AMR) crisis, where new antibiotic discovery is not keeping pace with the emergence of resistant pathogens, is driven by mobile genetic elements… (more)

Subjects/Keywords: high throughput screening; antimicrobial resistance; conjugation; mobile genetic elements; Tn1549; F plasmid

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APA (6th Edition):

Hansen, D. M. (2019). Development of High Throughput Screening Approaches to Target TN1549 and F Plasmid Movement. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/24805

Chicago Manual of Style (16th Edition):

Hansen, Drew M. “Development of High Throughput Screening Approaches to Target TN1549 and F Plasmid Movement.” 2019. Masters Thesis, McMaster University. Accessed October 18, 2019. http://hdl.handle.net/11375/24805.

MLA Handbook (7th Edition):

Hansen, Drew M. “Development of High Throughput Screening Approaches to Target TN1549 and F Plasmid Movement.” 2019. Web. 18 Oct 2019.

Vancouver:

Hansen DM. Development of High Throughput Screening Approaches to Target TN1549 and F Plasmid Movement. [Internet] [Masters thesis]. McMaster University; 2019. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/11375/24805.

Council of Science Editors:

Hansen DM. Development of High Throughput Screening Approaches to Target TN1549 and F Plasmid Movement. [Masters Thesis]. McMaster University; 2019. Available from: http://hdl.handle.net/11375/24805


University of Rochester

3. Trombetta, Ryan P. Sustained delivery of antimicrobials from 3D printed calcium phosphate scaffolds in single-stage management of osteomyelitis.

Degree: PhD, 2019, University of Rochester

 Implant-associated osteomyelitis is a bacterial bone infection that is the bane of existence for orthopedic surgeons due to its relapsing nature. The gold standard for… (more)

Subjects/Keywords: 1-stage revision; 3D printing; Drug delivery; High throughput screening; Osteomyelitis; Staphylococcus aureus

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APA (6th Edition):

Trombetta, R. P. (2019). Sustained delivery of antimicrobials from 3D printed calcium phosphate scaffolds in single-stage management of osteomyelitis. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/35290

Chicago Manual of Style (16th Edition):

Trombetta, Ryan P. “Sustained delivery of antimicrobials from 3D printed calcium phosphate scaffolds in single-stage management of osteomyelitis.” 2019. Doctoral Dissertation, University of Rochester. Accessed October 18, 2019. http://hdl.handle.net/1802/35290.

MLA Handbook (7th Edition):

Trombetta, Ryan P. “Sustained delivery of antimicrobials from 3D printed calcium phosphate scaffolds in single-stage management of osteomyelitis.” 2019. Web. 18 Oct 2019.

Vancouver:

Trombetta RP. Sustained delivery of antimicrobials from 3D printed calcium phosphate scaffolds in single-stage management of osteomyelitis. [Internet] [Doctoral dissertation]. University of Rochester; 2019. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1802/35290.

Council of Science Editors:

Trombetta RP. Sustained delivery of antimicrobials from 3D printed calcium phosphate scaffolds in single-stage management of osteomyelitis. [Doctoral Dissertation]. University of Rochester; 2019. Available from: http://hdl.handle.net/1802/35290


The Ohio State University

4. Martin, Alexander Charles. Initial Weldability of High Entropy Alloys for High Temperature Applications.

Degree: MS, Welding Engineering, 2019, The Ohio State University

High Entropy Alloys (HEA) are a new class of alloys that was introduced in the early 2000's. These alloys are composed of five or more… (more)

Subjects/Keywords: Engineering; Aerospace Materials; Metallurgy; Materials Science; Welding; high entropy alloys; HEA; weldability; GTAW; laser; alloy development; high throughput screening; AlCoCrCuFeNi; AlMoNbTaTiZr; AlCoCrFeNiTi; CALPHAD; cast pin tear testing

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APA (6th Edition):

Martin, A. C. (2019). Initial Weldability of High Entropy Alloys for High Temperature Applications. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1555496040477991

Chicago Manual of Style (16th Edition):

Martin, Alexander Charles. “Initial Weldability of High Entropy Alloys for High Temperature Applications.” 2019. Masters Thesis, The Ohio State University. Accessed October 18, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1555496040477991.

MLA Handbook (7th Edition):

Martin, Alexander Charles. “Initial Weldability of High Entropy Alloys for High Temperature Applications.” 2019. Web. 18 Oct 2019.

Vancouver:

Martin AC. Initial Weldability of High Entropy Alloys for High Temperature Applications. [Internet] [Masters thesis]. The Ohio State University; 2019. [cited 2019 Oct 18]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1555496040477991.

Council of Science Editors:

Martin AC. Initial Weldability of High Entropy Alloys for High Temperature Applications. [Masters Thesis]. The Ohio State University; 2019. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1555496040477991

5. Nandy, Argha. Development of drugs targeting the human tRNA ligase RtcB in breast cancer.

Degree: 2019, NUI Galway

The RNA ligase RtcB has been shown to regulate RNA function by direct exon ligation of spliced XBP1 messenger RNA cleaved by the endoplasmic reticulum… (more)

Subjects/Keywords: Human RtcB; tRNA ligase; Homology modeling; Human RtcB active site; Virtual high-throughput screening; Small-molecule screening; Cell-based assays; XBP1 mRNA splicing; RNA ligation; Triple-negative breast cancer; Biochemistry; Natural Sciences; Science

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APA (6th Edition):

Nandy, A. (2019). Development of drugs targeting the human tRNA ligase RtcB in breast cancer. (Thesis). NUI Galway. Retrieved from http://hdl.handle.net/10379/15324

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):

Nandy, Argha. “Development of drugs targeting the human tRNA ligase RtcB in breast cancer.” 2019. Thesis, NUI Galway. Accessed October 18, 2019. http://hdl.handle.net/10379/15324.

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

MLA Handbook (7th Edition):

Nandy, Argha. “Development of drugs targeting the human tRNA ligase RtcB in breast cancer.” 2019. Web. 18 Oct 2019.

Vancouver:

Nandy A. Development of drugs targeting the human tRNA ligase RtcB in breast cancer. [Internet] [Thesis]. NUI Galway; 2019. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10379/15324.

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

Council of Science Editors:

Nandy A. Development of drugs targeting the human tRNA ligase RtcB in breast cancer. [Thesis]. NUI Galway; 2019. Available from: http://hdl.handle.net/10379/15324

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


University of Ottawa

6. Ben Halima, Taoufik. Engaging Esters as Cross-Coupling Electrophiles .

Degree: 2019, University of Ottawa

 Cross-coupling reactions, where a transition metal catalyst facilitates the formation of a new carbon-carbon or carbon-heteroatom bond between two coupling partners, has become one of… (more)

Subjects/Keywords: Esters; Electrophiles; cross-coupling reactions; Suzuki-Miyaura coupling; Amide bond formation; High-throughput screening

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APA (6th Edition):

Ben Halima, T. (2019). Engaging Esters as Cross-Coupling Electrophiles . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/39493

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):

Ben Halima, Taoufik. “Engaging Esters as Cross-Coupling Electrophiles .” 2019. Thesis, University of Ottawa. Accessed October 18, 2019. http://hdl.handle.net/10393/39493.

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

MLA Handbook (7th Edition):

Ben Halima, Taoufik. “Engaging Esters as Cross-Coupling Electrophiles .” 2019. Web. 18 Oct 2019.

Vancouver:

Ben Halima T. Engaging Esters as Cross-Coupling Electrophiles . [Internet] [Thesis]. University of Ottawa; 2019. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10393/39493.

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

Council of Science Editors:

Ben Halima T. Engaging Esters as Cross-Coupling Electrophiles . [Thesis]. University of Ottawa; 2019. Available from: http://hdl.handle.net/10393/39493

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


Bowling Green State University

7. Pushina, Mariia. Sensing of Anions, Amines, Diols, and Saccharides by Supramolecular Fluorescent Sensors.

Degree: PhD, Photochemical Sciences, 2019, Bowling Green State University

 With first appearance of science and all the way to the present, analytical chemistry playscrucial role in our daily life that depends on chemical analysis.… (more)

Subjects/Keywords: Chemistry; supramolecular chemistry; fluorescense sensors; enantiomeric excess; indicator displacement assays; anions; diols; hydroxy acids; amines; amino alcohols; saccharides; high-throughput screening

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APA (6th Edition):

Pushina, M. (2019). Sensing of Anions, Amines, Diols, and Saccharides by Supramolecular Fluorescent Sensors. (Doctoral Dissertation). Bowling Green State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1558539245401457

Chicago Manual of Style (16th Edition):

Pushina, Mariia. “Sensing of Anions, Amines, Diols, and Saccharides by Supramolecular Fluorescent Sensors.” 2019. Doctoral Dissertation, Bowling Green State University. Accessed October 18, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1558539245401457.

MLA Handbook (7th Edition):

Pushina, Mariia. “Sensing of Anions, Amines, Diols, and Saccharides by Supramolecular Fluorescent Sensors.” 2019. Web. 18 Oct 2019.

Vancouver:

Pushina M. Sensing of Anions, Amines, Diols, and Saccharides by Supramolecular Fluorescent Sensors. [Internet] [Doctoral dissertation]. Bowling Green State University; 2019. [cited 2019 Oct 18]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1558539245401457.

Council of Science Editors:

Pushina M. Sensing of Anions, Amines, Diols, and Saccharides by Supramolecular Fluorescent Sensors. [Doctoral Dissertation]. Bowling Green State University; 2019. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=bgsu1558539245401457


University of Akron

8. Sidi, Zhao. Synthesis, Characterization and High-throughput Screening of Photoiniferter/RAFT Agent for Well-controlled Radical Polymerization of Block Copolymers.

Degree: MS, Polymer Science, 2019, University of Akron

 This work evaluates the use of benzyl dodecyl trithiocarbonate (BDTC) as both a reversible addition fragmentation chain transfer (RAFT) agent and photoiniferter in the polymerization… (more)

Subjects/Keywords: Polymer Chemistry; Polymers; Controlled Radical Polymerization; Reversible Addition Fragmentation Chain Transfer Polymerization; Photoiniferter; Block Copolymer; 3D Printing; Combinatorial High-throughput Screening

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APA (6th Edition):

Sidi, Z. (2019). Synthesis, Characterization and High-throughput Screening of Photoiniferter/RAFT Agent for Well-controlled Radical Polymerization of Block Copolymers. (Masters Thesis). University of Akron. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=akron1555435272696644

Chicago Manual of Style (16th Edition):

Sidi, Zhao. “Synthesis, Characterization and High-throughput Screening of Photoiniferter/RAFT Agent for Well-controlled Radical Polymerization of Block Copolymers.” 2019. Masters Thesis, University of Akron. Accessed October 18, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=akron1555435272696644.

MLA Handbook (7th Edition):

Sidi, Zhao. “Synthesis, Characterization and High-throughput Screening of Photoiniferter/RAFT Agent for Well-controlled Radical Polymerization of Block Copolymers.” 2019. Web. 18 Oct 2019.

Vancouver:

Sidi Z. Synthesis, Characterization and High-throughput Screening of Photoiniferter/RAFT Agent for Well-controlled Radical Polymerization of Block Copolymers. [Internet] [Masters thesis]. University of Akron; 2019. [cited 2019 Oct 18]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=akron1555435272696644.

Council of Science Editors:

Sidi Z. Synthesis, Characterization and High-throughput Screening of Photoiniferter/RAFT Agent for Well-controlled Radical Polymerization of Block Copolymers. [Masters Thesis]. University of Akron; 2019. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=akron1555435272696644


University of Queensland

9. Spicer, Timothy Patrick. Identification of Anti-malarial Drug Candidate Inhibitors using Ultra-high Throughput Screening Methods and Subsequent Mechanism of Action Studies Aimed at the Treatment and Prevention of Plasmodium falciparum.

Degree: Faculty of Medicine, 2019, University of Queensland

Subjects/Keywords: malaria; Plasmodium falciparum; aspartyl aminopeptidase; exopeptidase; gametocyte; High Throughput Screening; 0601 Biochemistry and Cell Biology; 0699 Other Biological Sciences

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APA (6th Edition):

Spicer, T. P. (2019). Identification of Anti-malarial Drug Candidate Inhibitors using Ultra-high Throughput Screening Methods and Subsequent Mechanism of Action Studies Aimed at the Treatment and Prevention of Plasmodium falciparum. (Thesis). University of Queensland. Retrieved from http://espace.library.uq.edu.au/view/UQ:26291

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):

Spicer, Timothy Patrick. “Identification of Anti-malarial Drug Candidate Inhibitors using Ultra-high Throughput Screening Methods and Subsequent Mechanism of Action Studies Aimed at the Treatment and Prevention of Plasmodium falciparum.” 2019. Thesis, University of Queensland. Accessed October 18, 2019. http://espace.library.uq.edu.au/view/UQ:26291.

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

MLA Handbook (7th Edition):

Spicer, Timothy Patrick. “Identification of Anti-malarial Drug Candidate Inhibitors using Ultra-high Throughput Screening Methods and Subsequent Mechanism of Action Studies Aimed at the Treatment and Prevention of Plasmodium falciparum.” 2019. Web. 18 Oct 2019.

Vancouver:

Spicer TP. Identification of Anti-malarial Drug Candidate Inhibitors using Ultra-high Throughput Screening Methods and Subsequent Mechanism of Action Studies Aimed at the Treatment and Prevention of Plasmodium falciparum. [Internet] [Thesis]. University of Queensland; 2019. [cited 2019 Oct 18]. Available from: http://espace.library.uq.edu.au/view/UQ:26291.

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

Council of Science Editors:

Spicer TP. Identification of Anti-malarial Drug Candidate Inhibitors using Ultra-high Throughput Screening Methods and Subsequent Mechanism of Action Studies Aimed at the Treatment and Prevention of Plasmodium falciparum. [Thesis]. University of Queensland; 2019. Available from: http://espace.library.uq.edu.au/view/UQ:26291

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


Cleveland State University

10. Joshi, Pranav. Three-Dimensional Human Neural Stem Cell Culture for High-Throughput Assessment of Developmental Neurotoxicity.

Degree: PhD, Washkewicz College of Engineering, 2019, Cleveland State University

 Only a few hundred of compounds, among tens of thousands of commercially available compounds, have been tested for developmental neurotoxicity (DNT) due to the limitations… (more)

Subjects/Keywords: Biomedical Engineering; Toxicology; Neurosciences; Developmental neurotoxicity, High-throughput screening, high content imaging, 3D cell culture, in vitro, assays, neural stem cell

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APA (6th Edition):

Joshi, P. (2019). Three-Dimensional Human Neural Stem Cell Culture for High-Throughput Assessment of Developmental Neurotoxicity. (Doctoral Dissertation). Cleveland State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=csu155965254496159

Chicago Manual of Style (16th Edition):

Joshi, Pranav. “Three-Dimensional Human Neural Stem Cell Culture for High-Throughput Assessment of Developmental Neurotoxicity.” 2019. Doctoral Dissertation, Cleveland State University. Accessed October 18, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=csu155965254496159.

MLA Handbook (7th Edition):

Joshi, Pranav. “Three-Dimensional Human Neural Stem Cell Culture for High-Throughput Assessment of Developmental Neurotoxicity.” 2019. Web. 18 Oct 2019.

Vancouver:

Joshi P. Three-Dimensional Human Neural Stem Cell Culture for High-Throughput Assessment of Developmental Neurotoxicity. [Internet] [Doctoral dissertation]. Cleveland State University; 2019. [cited 2019 Oct 18]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=csu155965254496159.

Council of Science Editors:

Joshi P. Three-Dimensional Human Neural Stem Cell Culture for High-Throughput Assessment of Developmental Neurotoxicity. [Doctoral Dissertation]. Cleveland State University; 2019. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=csu155965254496159


University of Western Ontario

11. Pinto, Nicole. Anaplastic Thyroid Cancer: Identification of Candidate Therapeutics and Mechanisms of Disease Progression.

Degree: 2019, University of Western Ontario

 Malignancies derived from follicular cells of the thyroid can be divided into well-differentiated thyroid cancer (WDTC), poorly differentiated thyroid cancer and anaplastic (undifferentiated) thyroid cancer… (more)

Subjects/Keywords: Anaplastic thyroid cancer; papillary thyroid cancer; targeted therapy; disease progression; high-throughput screening; small molecule inhibitors; Medicine and Health Sciences; Translational Medical Research

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APA (6th Edition):

Pinto, N. (2019). Anaplastic Thyroid Cancer: Identification of Candidate Therapeutics and Mechanisms of Disease Progression. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/6333

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):

Pinto, Nicole. “Anaplastic Thyroid Cancer: Identification of Candidate Therapeutics and Mechanisms of Disease Progression.” 2019. Thesis, University of Western Ontario. Accessed October 18, 2019. https://ir.lib.uwo.ca/etd/6333.

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

MLA Handbook (7th Edition):

Pinto, Nicole. “Anaplastic Thyroid Cancer: Identification of Candidate Therapeutics and Mechanisms of Disease Progression.” 2019. Web. 18 Oct 2019.

Vancouver:

Pinto N. Anaplastic Thyroid Cancer: Identification of Candidate Therapeutics and Mechanisms of Disease Progression. [Internet] [Thesis]. University of Western Ontario; 2019. [cited 2019 Oct 18]. Available from: https://ir.lib.uwo.ca/etd/6333.

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

Council of Science Editors:

Pinto N. Anaplastic Thyroid Cancer: Identification of Candidate Therapeutics and Mechanisms of Disease Progression. [Thesis]. University of Western Ontario; 2019. Available from: https://ir.lib.uwo.ca/etd/6333

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


University of Washington

12. Basanta, Benjamin. Beyond single-protein de novo design: A generative algorithm for the NTF2-like superfamily.

Degree: PhD, 2019, University of Washington

 Natural proteins evolved over billions of years to regulate cellular growth, ward off infection and capture and store solar energy. Proteins thus serve as the… (more)

Subjects/Keywords: Computational Biology; generative algorithm; generative design; High-throughput screening; Protein design; Biochemistry; Biological chemistry

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APA (6th Edition):

Basanta, B. (2019). Beyond single-protein de novo design: A generative algorithm for the NTF2-like superfamily. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/43640

Chicago Manual of Style (16th Edition):

Basanta, Benjamin. “Beyond single-protein de novo design: A generative algorithm for the NTF2-like superfamily.” 2019. Doctoral Dissertation, University of Washington. Accessed October 18, 2019. http://hdl.handle.net/1773/43640.

MLA Handbook (7th Edition):

Basanta, Benjamin. “Beyond single-protein de novo design: A generative algorithm for the NTF2-like superfamily.” 2019. Web. 18 Oct 2019.

Vancouver:

Basanta B. Beyond single-protein de novo design: A generative algorithm for the NTF2-like superfamily. [Internet] [Doctoral dissertation]. University of Washington; 2019. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1773/43640.

Council of Science Editors:

Basanta B. Beyond single-protein de novo design: A generative algorithm for the NTF2-like superfamily. [Doctoral Dissertation]. University of Washington; 2019. Available from: http://hdl.handle.net/1773/43640


Université de Montréal

13. Rousseau, Olivier. Accélération de l'exploration de l'espace chimique du cytochrome P450 BM3 par des méthodes de criblage à haut débit et bio-informatiques .

Degree: 2019, Université de Montréal

Subjects/Keywords: Analyse de composantes indépendantes du temps et de la structure; analyse statistique; automatisation; biocatalyse; cétone de framboise; criblage à haut débit; cytochrome P450 BM3; dynamique moléculaire; indigo; ingénierie de protéines; modélisation; mutagénèse; oxydation; séquençage nouvelle génération; Automation; Biocatalysis; High-throughput screening; Modeling; Molecular dynamics; Mutagenesis; Next-generation sequencing; Oxidation; Protein engineering; Raspberry ketone; Statistical analysis; Time-structure independent component analysis

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APA (6th Edition):

Rousseau, O. (2019). Accélération de l'exploration de l'espace chimique du cytochrome P450 BM3 par des méthodes de criblage à haut débit et bio-informatiques . (Thesis). Université de Montréal. Retrieved from http://hdl.handle.net/1866/21949

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):

Rousseau, Olivier. “Accélération de l'exploration de l'espace chimique du cytochrome P450 BM3 par des méthodes de criblage à haut débit et bio-informatiques .” 2019. Thesis, Université de Montréal. Accessed October 18, 2019. http://hdl.handle.net/1866/21949.

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

MLA Handbook (7th Edition):

Rousseau, Olivier. “Accélération de l'exploration de l'espace chimique du cytochrome P450 BM3 par des méthodes de criblage à haut débit et bio-informatiques .” 2019. Web. 18 Oct 2019.

Vancouver:

Rousseau O. Accélération de l'exploration de l'espace chimique du cytochrome P450 BM3 par des méthodes de criblage à haut débit et bio-informatiques . [Internet] [Thesis]. Université de Montréal; 2019. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1866/21949.

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

Council of Science Editors:

Rousseau O. Accélération de l'exploration de l'espace chimique du cytochrome P450 BM3 par des méthodes de criblage à haut débit et bio-informatiques . [Thesis]. Université de Montréal; 2019. Available from: http://hdl.handle.net/1866/21949

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


Univerzitet u Beogradu

14. Kovačević, Gordana N., 1987-. Proteinski inženjering i razvoj visoko efikasnih metoda za pretraživanje biblioteke gena glukoza-oksidaze iz Aspergillus niger u cilju povećanja enzimske aktivnosti i stabilnosti.

Degree: Hemijski fakultet, 2019, Univerzitet u Beogradu

Hemija - Biohemija / Chemistry - Biochemistry

Glukoza-oksidaza (GOx) je vaţan industrijski enzim koji se predominantno koristi kao biokatalizator u industriji hrane za proizvodnju glukonske… (more)

Subjects/Keywords: glucose oxidase; high-throughput screening; oxidative stability; yeast surface display; green fluorescent protein; Pichia pastoris

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APA (6th Edition):

Kovačević, Gordana N., 1. (2019). Proteinski inženjering i razvoj visoko efikasnih metoda za pretraživanje biblioteke gena glukoza-oksidaze iz Aspergillus niger u cilju povećanja enzimske aktivnosti i stabilnosti. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:19139/bdef:Content/get

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):

Kovačević, Gordana N., 1987-. “Proteinski inženjering i razvoj visoko efikasnih metoda za pretraživanje biblioteke gena glukoza-oksidaze iz Aspergillus niger u cilju povećanja enzimske aktivnosti i stabilnosti.” 2019. Thesis, Univerzitet u Beogradu. Accessed October 18, 2019. https://fedorabg.bg.ac.rs/fedora/get/o:19139/bdef:Content/get.

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

MLA Handbook (7th Edition):

Kovačević, Gordana N., 1987-. “Proteinski inženjering i razvoj visoko efikasnih metoda za pretraživanje biblioteke gena glukoza-oksidaze iz Aspergillus niger u cilju povećanja enzimske aktivnosti i stabilnosti.” 2019. Web. 18 Oct 2019.

Vancouver:

Kovačević, Gordana N. 1. Proteinski inženjering i razvoj visoko efikasnih metoda za pretraživanje biblioteke gena glukoza-oksidaze iz Aspergillus niger u cilju povećanja enzimske aktivnosti i stabilnosti. [Internet] [Thesis]. Univerzitet u Beogradu; 2019. [cited 2019 Oct 18]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:19139/bdef:Content/get.

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

Council of Science Editors:

Kovačević, Gordana N. 1. Proteinski inženjering i razvoj visoko efikasnih metoda za pretraživanje biblioteke gena glukoza-oksidaze iz Aspergillus niger u cilju povećanja enzimske aktivnosti i stabilnosti. [Thesis]. Univerzitet u Beogradu; 2019. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:19139/bdef:Content/get

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


University of California – San Diego

15. Limsakul, Praopim. Engineering Molecular Modules Through Directed Evolution for Applications in Single-Cell Imaging and Immunotherapy.

Degree: Bioengineering, 2019, University of California – San Diego

 Protein engineering through directed evolution has been extensively used to improve and modify the structure and function of proteins for wide range of applications. In… (more)

Subjects/Keywords: Bioengineering; CAR T cell therapy; Directed evolution; FACS-based FRET; FRET biosensors; High-throughput screening; MT1-MMP

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APA (6th Edition):

Limsakul, P. (2019). Engineering Molecular Modules Through Directed Evolution for Applications in Single-Cell Imaging and Immunotherapy. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/7x01b05n

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):

Limsakul, Praopim. “Engineering Molecular Modules Through Directed Evolution for Applications in Single-Cell Imaging and Immunotherapy.” 2019. Thesis, University of California – San Diego. Accessed October 18, 2019. http://www.escholarship.org/uc/item/7x01b05n.

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

MLA Handbook (7th Edition):

Limsakul, Praopim. “Engineering Molecular Modules Through Directed Evolution for Applications in Single-Cell Imaging and Immunotherapy.” 2019. Web. 18 Oct 2019.

Vancouver:

Limsakul P. Engineering Molecular Modules Through Directed Evolution for Applications in Single-Cell Imaging and Immunotherapy. [Internet] [Thesis]. University of California – San Diego; 2019. [cited 2019 Oct 18]. Available from: http://www.escholarship.org/uc/item/7x01b05n.

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

Council of Science Editors:

Limsakul P. Engineering Molecular Modules Through Directed Evolution for Applications in Single-Cell Imaging and Immunotherapy. [Thesis]. University of California – San Diego; 2019. Available from: http://www.escholarship.org/uc/item/7x01b05n

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


University of Adelaide

16. Tarzia, Andrew. [EMBARGOED] Computational Screening and Analysis of Functional Porous Materials.

Degree: 2019, University of Adelaide

 Functional porous materials are a class of materials that have found use in many industrial applications. In particular, extended framework materials, such as metal–organic frameworks… (more)

Subjects/Keywords: Porous materials; metal-organic frameworks; high-throughput screening; coarse grained molecular dynamics

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APA (6th Edition):

Tarzia, A. (2019). [EMBARGOED] Computational Screening and Analysis of Functional Porous Materials. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/120096

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):

Tarzia, Andrew. “[EMBARGOED] Computational Screening and Analysis of Functional Porous Materials.” 2019. Thesis, University of Adelaide. Accessed October 18, 2019. http://hdl.handle.net/2440/120096.

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

MLA Handbook (7th Edition):

Tarzia, Andrew. “[EMBARGOED] Computational Screening and Analysis of Functional Porous Materials.” 2019. Web. 18 Oct 2019.

Vancouver:

Tarzia A. [EMBARGOED] Computational Screening and Analysis of Functional Porous Materials. [Internet] [Thesis]. University of Adelaide; 2019. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2440/120096.

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

Council of Science Editors:

Tarzia A. [EMBARGOED] Computational Screening and Analysis of Functional Porous Materials. [Thesis]. University of Adelaide; 2019. Available from: http://hdl.handle.net/2440/120096

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


University of Arkansas

17. Hu, Zhijian. Targeting Sec61α by Ipomoeassin F Leads to Highly Cytotoxic Effect.

Degree: PhD, 2019, University of Arkansas

  Ipomoeassin F is a flagship congener of a resin glycoside family that inhibits growth of many tumor cell lines with only single-digital nanomolar IC50… (more)

Subjects/Keywords: anti-cancer; cytotoxicity; high throughput screening; ipomoeassin F; Sec61; target protein identification; Amino Acids, Peptides, and Proteins; Biochemistry; Cancer Biology; Cell Biology

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

APA (6th Edition):

Hu, Z. (2019). Targeting Sec61α by Ipomoeassin F Leads to Highly Cytotoxic Effect. (Doctoral Dissertation). University of Arkansas. Retrieved from https://scholarworks.uark.edu/etd/3231

Chicago Manual of Style (16th Edition):

Hu, Zhijian. “Targeting Sec61α by Ipomoeassin F Leads to Highly Cytotoxic Effect.” 2019. Doctoral Dissertation, University of Arkansas. Accessed October 18, 2019. https://scholarworks.uark.edu/etd/3231.

MLA Handbook (7th Edition):

Hu, Zhijian. “Targeting Sec61α by Ipomoeassin F Leads to Highly Cytotoxic Effect.” 2019. Web. 18 Oct 2019.

Vancouver:

Hu Z. Targeting Sec61α by Ipomoeassin F Leads to Highly Cytotoxic Effect. [Internet] [Doctoral dissertation]. University of Arkansas; 2019. [cited 2019 Oct 18]. Available from: https://scholarworks.uark.edu/etd/3231.

Council of Science Editors:

Hu Z. Targeting Sec61α by Ipomoeassin F Leads to Highly Cytotoxic Effect. [Doctoral Dissertation]. University of Arkansas; 2019. Available from: https://scholarworks.uark.edu/etd/3231


University of Cambridge

18. Chong, Zheng Shan. Extracellular interaction screening using CRISPR activation.

Degree: PhD, 2019, University of Cambridge

 Extracellular interactions between cell surface receptors are necessary for signaling and adhesion but identifying them remains technically challenging. We describe a cell-based genome-wide approach employing… (more)

Subjects/Keywords: CRISPR; protein-protein interactions; high-throughput screening

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APA (6th Edition):

Chong, Z. S. (2019). Extracellular interaction screening using CRISPR activation. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/291972 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774750

Chicago Manual of Style (16th Edition):

Chong, Zheng Shan. “Extracellular interaction screening using CRISPR activation.” 2019. Doctoral Dissertation, University of Cambridge. Accessed October 18, 2019. https://www.repository.cam.ac.uk/handle/1810/291972 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774750.

MLA Handbook (7th Edition):

Chong, Zheng Shan. “Extracellular interaction screening using CRISPR activation.” 2019. Web. 18 Oct 2019.

Vancouver:

Chong ZS. Extracellular interaction screening using CRISPR activation. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2019 Oct 18]. Available from: https://www.repository.cam.ac.uk/handle/1810/291972 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774750.

Council of Science Editors:

Chong ZS. Extracellular interaction screening using CRISPR activation. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/291972 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.774750


University of Michigan

19. Saleski, Tatyana. Harnessing the Power of Synthetic Microbial Consortia: New Approaches for Microbial Engineering in Biochemical Production.

Degree: PhD, Chemical Engineering, 2019, University of Michigan

 Microbial biosynthesis is a sustainable and high-specificity means of producing various bioproducts, including pharmaceuticals, specialty and commodity chemicals, and biofuels. Due to the complexity of… (more)

Subjects/Keywords: High-throughput strain screening; Cross-feeding; Microbial consortia; Biosensor; Cellulosic biofuels; Microbial engineering; Chemical Engineering; Engineering

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

APA (6th Edition):

Saleski, T. (2019). Harnessing the Power of Synthetic Microbial Consortia: New Approaches for Microbial Engineering in Biochemical Production. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/149851

Chicago Manual of Style (16th Edition):

Saleski, Tatyana. “Harnessing the Power of Synthetic Microbial Consortia: New Approaches for Microbial Engineering in Biochemical Production.” 2019. Doctoral Dissertation, University of Michigan. Accessed October 18, 2019. http://hdl.handle.net/2027.42/149851.

MLA Handbook (7th Edition):

Saleski, Tatyana. “Harnessing the Power of Synthetic Microbial Consortia: New Approaches for Microbial Engineering in Biochemical Production.” 2019. Web. 18 Oct 2019.

Vancouver:

Saleski T. Harnessing the Power of Synthetic Microbial Consortia: New Approaches for Microbial Engineering in Biochemical Production. [Internet] [Doctoral dissertation]. University of Michigan; 2019. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2027.42/149851.

Council of Science Editors:

Saleski T. Harnessing the Power of Synthetic Microbial Consortia: New Approaches for Microbial Engineering in Biochemical Production. [Doctoral Dissertation]. University of Michigan; 2019. Available from: http://hdl.handle.net/2027.42/149851


University of Michigan

20. Bradford, Shayna. Developing Novel Therapeutics for Chronic Kidney Disease.

Degree: PhD, Molecular & Cellular Pathology, 2019, University of Michigan

 Chronic Kidney Disease (CKD) is a major global health burden. In the United States alone, roughly 30 million Americans have CKD. Each year in the… (more)

Subjects/Keywords: Drug Discovery; HTS (High-Throughput Screening); Kidney Fibrosis; BMP (Bone Morphogenetic Protein); PKD (Polycystic Kidney Disease); Kidney Cancer; Pax2 (Paired-homeobox 2); Biological Chemistry; Genetics; Molecular, Cellular and Developmental Biology; Science (General); Science

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APA (6th Edition):

Bradford, S. (2019). Developing Novel Therapeutics for Chronic Kidney Disease. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/150009

Chicago Manual of Style (16th Edition):

Bradford, Shayna. “Developing Novel Therapeutics for Chronic Kidney Disease.” 2019. Doctoral Dissertation, University of Michigan. Accessed October 18, 2019. http://hdl.handle.net/2027.42/150009.

MLA Handbook (7th Edition):

Bradford, Shayna. “Developing Novel Therapeutics for Chronic Kidney Disease.” 2019. Web. 18 Oct 2019.

Vancouver:

Bradford S. Developing Novel Therapeutics for Chronic Kidney Disease. [Internet] [Doctoral dissertation]. University of Michigan; 2019. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2027.42/150009.

Council of Science Editors:

Bradford S. Developing Novel Therapeutics for Chronic Kidney Disease. [Doctoral Dissertation]. University of Michigan; 2019. Available from: http://hdl.handle.net/2027.42/150009


Freie Universität Berlin

21. Secker, Christopher. EGCG directly targets intracellular amyloid-β(1-42) aggregates and promotes their lysosomal degradation.

Degree: 2019, Freie Universität Berlin

 Einleitung: Zahlreiche Studien haben gezeigt, dass die Aggregation und Akkumulation von Amyloid-β(1-42) (Aβ42) eine zelluläre Dysfunktion und Zelltoxizität zur Folge haben. Neben der Entstehung von… (more)

Subjects/Keywords: Alzheimer’s disease; amyloid-beta; high-throughput screening; Epigallocatechin gallate (EGCG); lysosome; cathepsin; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit

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APA (6th Edition):

Secker, C. (2019). EGCG directly targets intracellular amyloid-β(1-42) aggregates and promotes their lysosomal degradation. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-1752

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):

Secker, Christopher. “EGCG directly targets intracellular amyloid-β(1-42) aggregates and promotes their lysosomal degradation.” 2019. Thesis, Freie Universität Berlin. Accessed October 18, 2019. http://dx.doi.org/10.17169/refubium-1752.

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

MLA Handbook (7th Edition):

Secker, Christopher. “EGCG directly targets intracellular amyloid-β(1-42) aggregates and promotes their lysosomal degradation.” 2019. Web. 18 Oct 2019.

Vancouver:

Secker C. EGCG directly targets intracellular amyloid-β(1-42) aggregates and promotes their lysosomal degradation. [Internet] [Thesis]. Freie Universität Berlin; 2019. [cited 2019 Oct 18]. Available from: http://dx.doi.org/10.17169/refubium-1752.

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

Council of Science Editors:

Secker C. EGCG directly targets intracellular amyloid-β(1-42) aggregates and promotes their lysosomal degradation. [Thesis]. Freie Universität Berlin; 2019. Available from: http://dx.doi.org/10.17169/refubium-1752

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

22. CHIA CHEE GENG. CHARACTERISATION OF TOLQRA COMPLEX AND ITS RECONSTITUTION INTO LIPOSOME.

Degree: 2018, National University of Singapore

Subjects/Keywords: TolQRA purification; High throughput detergent screening

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APA (6th Edition):

GENG, C. C. (2018). CHARACTERISATION OF TOLQRA COMPLEX AND ITS RECONSTITUTION INTO LIPOSOME. (Thesis). National University of Singapore. Retrieved from https://scholarbank.nus.edu.sg/handle/10635/155103

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):

GENG, CHIA CHEE. “CHARACTERISATION OF TOLQRA COMPLEX AND ITS RECONSTITUTION INTO LIPOSOME.” 2018. Thesis, National University of Singapore. Accessed October 18, 2019. https://scholarbank.nus.edu.sg/handle/10635/155103.

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

MLA Handbook (7th Edition):

GENG, CHIA CHEE. “CHARACTERISATION OF TOLQRA COMPLEX AND ITS RECONSTITUTION INTO LIPOSOME.” 2018. Web. 18 Oct 2019.

Vancouver:

GENG CC. CHARACTERISATION OF TOLQRA COMPLEX AND ITS RECONSTITUTION INTO LIPOSOME. [Internet] [Thesis]. National University of Singapore; 2018. [cited 2019 Oct 18]. Available from: https://scholarbank.nus.edu.sg/handle/10635/155103.

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

Council of Science Editors:

GENG CC. CHARACTERISATION OF TOLQRA COMPLEX AND ITS RECONSTITUTION INTO LIPOSOME. [Thesis]. National University of Singapore; 2018. Available from: https://scholarbank.nus.edu.sg/handle/10635/155103

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

23. Fourier, Anthony. Vers un marqueur biochimique des dégénérescences lobaires fronto-temporales : variations quantitatives et profils protéiques de la protéine TDP43 dans différentes matrices biologiques : Towards a biochemical marker of fronto temporal lobar degeneration : quantitative variations and qualitative patterns of TDP43 protein in different biological matrices.

Degree: Docteur es, Neurosciences cliniques, 2018, Lyon

Les dégénérescences lobaires frontotemporales (DLFT) représentent la deuxième étiologie neurodégénérative chez l’adulte de moins de 65 ans. Les DLFT sont constituées d’un ensemble hétérogène de… (more)

Subjects/Keywords: Dégénérescence lobaire frontotemporale; Protéinopathies; TDP43; C9ORF72; Profils protéiques; Criblage à haut débit; Biomarqueurs; Frontotemporal lobar degeneration; Proteinopathies; TDP43; C9ORF72; Protein patterns; High throughput screening; Biomarkers; 612.8

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APA (6th Edition):

Fourier, A. (2018). Vers un marqueur biochimique des dégénérescences lobaires fronto-temporales : variations quantitatives et profils protéiques de la protéine TDP43 dans différentes matrices biologiques : Towards a biochemical marker of fronto temporal lobar degeneration : quantitative variations and qualitative patterns of TDP43 protein in different biological matrices. (Doctoral Dissertation). Lyon. Retrieved from http://www.theses.fr/2018LYSE1269

Chicago Manual of Style (16th Edition):

Fourier, Anthony. “Vers un marqueur biochimique des dégénérescences lobaires fronto-temporales : variations quantitatives et profils protéiques de la protéine TDP43 dans différentes matrices biologiques : Towards a biochemical marker of fronto temporal lobar degeneration : quantitative variations and qualitative patterns of TDP43 protein in different biological matrices.” 2018. Doctoral Dissertation, Lyon. Accessed October 18, 2019. http://www.theses.fr/2018LYSE1269.

MLA Handbook (7th Edition):

Fourier, Anthony. “Vers un marqueur biochimique des dégénérescences lobaires fronto-temporales : variations quantitatives et profils protéiques de la protéine TDP43 dans différentes matrices biologiques : Towards a biochemical marker of fronto temporal lobar degeneration : quantitative variations and qualitative patterns of TDP43 protein in different biological matrices.” 2018. Web. 18 Oct 2019.

Vancouver:

Fourier A. Vers un marqueur biochimique des dégénérescences lobaires fronto-temporales : variations quantitatives et profils protéiques de la protéine TDP43 dans différentes matrices biologiques : Towards a biochemical marker of fronto temporal lobar degeneration : quantitative variations and qualitative patterns of TDP43 protein in different biological matrices. [Internet] [Doctoral dissertation]. Lyon; 2018. [cited 2019 Oct 18]. Available from: http://www.theses.fr/2018LYSE1269.

Council of Science Editors:

Fourier A. Vers un marqueur biochimique des dégénérescences lobaires fronto-temporales : variations quantitatives et profils protéiques de la protéine TDP43 dans différentes matrices biologiques : Towards a biochemical marker of fronto temporal lobar degeneration : quantitative variations and qualitative patterns of TDP43 protein in different biological matrices. [Doctoral Dissertation]. Lyon; 2018. Available from: http://www.theses.fr/2018LYSE1269

24. Nikolaev, Anton. Inhibition studies of metalloproteins by means of electrochemistry and spectroscopy : Etudes d'inhibition de métalloprotéines par électrochimie et spectroscopie.

Degree: Docteur es, Chimie, 2018, Université de Strasbourg

Les études d'interaction protéine-ligand aident à mieux comprendre la structure et la fonction des protéines. Dans la première partie de la thèse, la cyt bd… (more)

Subjects/Keywords: Cytochrome bd; Complexe IV; Quinol oxydase; MitoNEET; Résonance Raman; Spectroscopie IR; Criblage à haut débit; Biocapteur; Aurachin D; Quinazoline; Cytochrome bd; Complexe IV; Quinol oxydase; MitoNEET; Bioelectrochemistry; Resonance Raman; IR spectroscopy; High-throughput screening; Biosensor; Aurachin D; Quinazoline; 572.6

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APA (6th Edition):

Nikolaev, A. (2018). Inhibition studies of metalloproteins by means of electrochemistry and spectroscopy : Etudes d'inhibition de métalloprotéines par électrochimie et spectroscopie. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2018STRAF053

Chicago Manual of Style (16th Edition):

Nikolaev, Anton. “Inhibition studies of metalloproteins by means of electrochemistry and spectroscopy : Etudes d'inhibition de métalloprotéines par électrochimie et spectroscopie.” 2018. Doctoral Dissertation, Université de Strasbourg. Accessed October 18, 2019. http://www.theses.fr/2018STRAF053.

MLA Handbook (7th Edition):

Nikolaev, Anton. “Inhibition studies of metalloproteins by means of electrochemistry and spectroscopy : Etudes d'inhibition de métalloprotéines par électrochimie et spectroscopie.” 2018. Web. 18 Oct 2019.

Vancouver:

Nikolaev A. Inhibition studies of metalloproteins by means of electrochemistry and spectroscopy : Etudes d'inhibition de métalloprotéines par électrochimie et spectroscopie. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2018. [cited 2019 Oct 18]. Available from: http://www.theses.fr/2018STRAF053.

Council of Science Editors:

Nikolaev A. Inhibition studies of metalloproteins by means of electrochemistry and spectroscopy : Etudes d'inhibition de métalloprotéines par électrochimie et spectroscopie. [Doctoral Dissertation]. Université de Strasbourg; 2018. Available from: http://www.theses.fr/2018STRAF053


University of Minnesota

25. Simpkins, Scott. Analysis and interpretation of high-throughput chemical-genetic interaction screens.

Degree: PhD, Biomedical Informatics and Computational Biology, 2018, University of Minnesota

Screening chemical compounds against genome-wide mutant arrays identifies genetic perturbations that cause sensitivity or resistance to compounds of interest. The resulting chemical-genetic interaction profiles contain… (more)

Subjects/Keywords: chemical-genetic interactions; computational biology; drug discovery; genetic interactions; high-throughput screening; saccharomyces cerevisiae

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APA (6th Edition):

Simpkins, S. (2018). Analysis and interpretation of high-throughput chemical-genetic interaction screens. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/206377

Chicago Manual of Style (16th Edition):

Simpkins, Scott. “Analysis and interpretation of high-throughput chemical-genetic interaction screens.” 2018. Doctoral Dissertation, University of Minnesota. Accessed October 18, 2019. http://hdl.handle.net/11299/206377.

MLA Handbook (7th Edition):

Simpkins, Scott. “Analysis and interpretation of high-throughput chemical-genetic interaction screens.” 2018. Web. 18 Oct 2019.

Vancouver:

Simpkins S. Analysis and interpretation of high-throughput chemical-genetic interaction screens. [Internet] [Doctoral dissertation]. University of Minnesota; 2018. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/11299/206377.

Council of Science Editors:

Simpkins S. Analysis and interpretation of high-throughput chemical-genetic interaction screens. [Doctoral Dissertation]. University of Minnesota; 2018. Available from: http://hdl.handle.net/11299/206377


Univerzitet u Beogradu

26. Petrović-Bulatović, Katarina, 1970-. Razvoj visoko automatizovanih mikrotitarskih testova na Saccharomyces cerevisiae za detekciju jedinjenja sa antifungalnim i citostatskim dejstvom.

Degree: Biološki fakultet, 2018, Univerzitet u Beogradu

Biologija - Mikrobiologija / Biology - Microbiology

Kvasac Saccharomyces cerevisiae je široko upotrebljavan model za istraživanje potencijala malih molekula u modulaciji signalnih puteva relevantnih za… (more)

Subjects/Keywords: High-Throughput screening; Saccharomyces cerevisiae; alamarBlue®; optical density

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APA (6th Edition):

Petrović-Bulatović, Katarina, 1. (2018). Razvoj visoko automatizovanih mikrotitarskih testova na Saccharomyces cerevisiae za detekciju jedinjenja sa antifungalnim i citostatskim dejstvom. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:17753/bdef:Content/get

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):

Petrović-Bulatović, Katarina, 1970-. “Razvoj visoko automatizovanih mikrotitarskih testova na Saccharomyces cerevisiae za detekciju jedinjenja sa antifungalnim i citostatskim dejstvom.” 2018. Thesis, Univerzitet u Beogradu. Accessed October 18, 2019. https://fedorabg.bg.ac.rs/fedora/get/o:17753/bdef:Content/get.

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

MLA Handbook (7th Edition):

Petrović-Bulatović, Katarina, 1970-. “Razvoj visoko automatizovanih mikrotitarskih testova na Saccharomyces cerevisiae za detekciju jedinjenja sa antifungalnim i citostatskim dejstvom.” 2018. Web. 18 Oct 2019.

Vancouver:

Petrović-Bulatović, Katarina 1. Razvoj visoko automatizovanih mikrotitarskih testova na Saccharomyces cerevisiae za detekciju jedinjenja sa antifungalnim i citostatskim dejstvom. [Internet] [Thesis]. Univerzitet u Beogradu; 2018. [cited 2019 Oct 18]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:17753/bdef:Content/get.

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

Council of Science Editors:

Petrović-Bulatović, Katarina 1. Razvoj visoko automatizovanih mikrotitarskih testova na Saccharomyces cerevisiae za detekciju jedinjenja sa antifungalnim i citostatskim dejstvom. [Thesis]. Univerzitet u Beogradu; 2018. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:17753/bdef:Content/get

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


Vrije Universiteit Amsterdam

27. Straver, R. Bioinformatic Approaches to Detecting Copy Number Variation in Next Generation Sequencing Data for Clinical Diagnostics .

Degree: 2018, Vrije Universiteit Amsterdam

Subjects/Keywords: Bioinformatics; Diagnostics; Noninvasive; Prenatal; Testing; Screening; Diagnostics; NIPT; NIPS; NIPD; Cell free DNA; Fetal DNA; Fetal fraction; cfDNA; cffDNA; Chromosomal aberration; Aneuploidy; Trisomy; Monosomy; Copy number variation; CNV; FRA10B; Fragile sites; Nucleosome; Next generation sequencing; High throughput sequencing; Whole exome sequencing; Whole genome sequencing; Low coverage; WISECONDOR; WISExome; SANEFALCON; DEFRAG; Within-sample comparison; Liquid biopsy

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

APA (6th Edition):

Straver, R. (2018). Bioinformatic Approaches to Detecting Copy Number Variation in Next Generation Sequencing Data for Clinical Diagnostics . (Doctoral Dissertation). Vrije Universiteit Amsterdam. Retrieved from http://hdl.handle.net/1871/55674

Chicago Manual of Style (16th Edition):

Straver, R. “Bioinformatic Approaches to Detecting Copy Number Variation in Next Generation Sequencing Data for Clinical Diagnostics .” 2018. Doctoral Dissertation, Vrije Universiteit Amsterdam. Accessed October 18, 2019. http://hdl.handle.net/1871/55674.

MLA Handbook (7th Edition):

Straver, R. “Bioinformatic Approaches to Detecting Copy Number Variation in Next Generation Sequencing Data for Clinical Diagnostics .” 2018. Web. 18 Oct 2019.

Vancouver:

Straver R. Bioinformatic Approaches to Detecting Copy Number Variation in Next Generation Sequencing Data for Clinical Diagnostics . [Internet] [Doctoral dissertation]. Vrije Universiteit Amsterdam; 2018. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1871/55674.

Council of Science Editors:

Straver R. Bioinformatic Approaches to Detecting Copy Number Variation in Next Generation Sequencing Data for Clinical Diagnostics . [Doctoral Dissertation]. Vrije Universiteit Amsterdam; 2018. Available from: http://hdl.handle.net/1871/55674


University of Akron

28. Chen, Jonathan Jun Feng. Data Mining/Machine Learning Techniques for Drug Discovery: Computational and Experimental Pipeline Development.

Degree: PhD, Biology, 2018, University of Akron

 Medicine is a precious commodity that saves, prolongs, or increases the quality of life. However, medicinal active ingredient discovery is challenging and is one of… (more)

Subjects/Keywords: Bioinformatics; Biology; Biochemistry; Chemical Engineering; Computer Science; vHTS; virtual; high-throughput; screening; bioinformatics; biological; informatics; machine-learning; QSAR; quantitative structure-activity relationship; cheminformatics; chemical; chemoinformatics; data-mining; pipeline; PubChem; drug; discovery

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

APA (6th Edition):

Chen, J. J. F. (2018). Data Mining/Machine Learning Techniques for Drug Discovery: Computational and Experimental Pipeline Development. (Doctoral Dissertation). University of Akron. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=akron1524661027035591

Chicago Manual of Style (16th Edition):

Chen, Jonathan Jun Feng. “Data Mining/Machine Learning Techniques for Drug Discovery: Computational and Experimental Pipeline Development.” 2018. Doctoral Dissertation, University of Akron. Accessed October 18, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=akron1524661027035591.

MLA Handbook (7th Edition):

Chen, Jonathan Jun Feng. “Data Mining/Machine Learning Techniques for Drug Discovery: Computational and Experimental Pipeline Development.” 2018. Web. 18 Oct 2019.

Vancouver:

Chen JJF. Data Mining/Machine Learning Techniques for Drug Discovery: Computational and Experimental Pipeline Development. [Internet] [Doctoral dissertation]. University of Akron; 2018. [cited 2019 Oct 18]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=akron1524661027035591.

Council of Science Editors:

Chen JJF. Data Mining/Machine Learning Techniques for Drug Discovery: Computational and Experimental Pipeline Development. [Doctoral Dissertation]. University of Akron; 2018. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=akron1524661027035591


University of Houston

29. Wang, Zhiqing. Design and Application of Regulatory-Protein-Based Biosensors.

Degree: Chemical and Biomolecular Engineering, Department of, 2018, University of Houston

 Metabolic engineering for microbial overproduction of biochemicals benefits from continued advances in directed evolution techniques. Rational design of both proteins and metabolic pathways is often… (more)

Subjects/Keywords: Biosensor; regulatory protein; triacetic acid lactone; polyketide; high-throughput screening

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

APA (6th Edition):

Wang, Z. (2018). Design and Application of Regulatory-Protein-Based Biosensors. (Thesis). University of Houston. Retrieved from http://hdl.handle.net/10657/3512

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

Chicago Manual of Style (16th Edition):

Wang, Zhiqing. “Design and Application of Regulatory-Protein-Based Biosensors.” 2018. Thesis, University of Houston. Accessed October 18, 2019. http://hdl.handle.net/10657/3512.

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

MLA Handbook (7th Edition):

Wang, Zhiqing. “Design and Application of Regulatory-Protein-Based Biosensors.” 2018. Web. 18 Oct 2019.

Vancouver:

Wang Z. Design and Application of Regulatory-Protein-Based Biosensors. [Internet] [Thesis]. University of Houston; 2018. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10657/3512.

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

Council of Science Editors:

Wang Z. Design and Application of Regulatory-Protein-Based Biosensors. [Thesis]. University of Houston; 2018. Available from: http://hdl.handle.net/10657/3512

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


McMaster University

30. Buzon, Beverly Diana. Characterization and inhibition of interstrand crosslink repair nuclease SNM1A.

Degree: PhD, 2018, McMaster University

Interstrand cross-links (ICLs) are a type of DNA damage that prevents strand separation required for basic cellular processes. ICL-based anti-cancer therapies exploit the cytotoxic consequences… (more)

Subjects/Keywords: SNM1A; beta-CASP nuclease; small molecule inhibitors; translesion nuclease; chemoresistance; structure-specific endonuclease; interstrand crosslinking repair; high throughput screening

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

APA (6th Edition):

Buzon, B. D. (2018). Characterization and inhibition of interstrand crosslink repair nuclease SNM1A. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/22872

Chicago Manual of Style (16th Edition):

Buzon, Beverly Diana. “Characterization and inhibition of interstrand crosslink repair nuclease SNM1A.” 2018. Doctoral Dissertation, McMaster University. Accessed October 18, 2019. http://hdl.handle.net/11375/22872.

MLA Handbook (7th Edition):

Buzon, Beverly Diana. “Characterization and inhibition of interstrand crosslink repair nuclease SNM1A.” 2018. Web. 18 Oct 2019.

Vancouver:

Buzon BD. Characterization and inhibition of interstrand crosslink repair nuclease SNM1A. [Internet] [Doctoral dissertation]. McMaster University; 2018. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/11375/22872.

Council of Science Editors:

Buzon BD. Characterization and inhibition of interstrand crosslink repair nuclease SNM1A. [Doctoral Dissertation]. McMaster University; 2018. Available from: http://hdl.handle.net/11375/22872

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