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You searched for subject:(small molecular inhibitors). Showing records 1 – 9 of 9 total matches.

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NSYSU

1. Kao, Yu-Chen. Study the effects of Dibromotyrosine Derivative in TGF-β responsiveness.

Degree: Master, Biological Sciences, 2017, NSYSU

 The Transforming growth factor β1 (TGF-β1) is belong to transforming growth factor superfamily. Many tumor lesions process are related to TGF-β1, such as: cell proliferation,… (more)

Subjects/Keywords: TGF-β; bromotyrosine derivative; small molecular inhibitors; epithelial-to-mesenchymal transition

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APA (6th Edition):

Kao, Y. (2017). Study the effects of Dibromotyrosine Derivative in TGF-β responsiveness. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0718117-194840

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):

Kao, Yu-Chen. “Study the effects of Dibromotyrosine Derivative in TGF-β responsiveness.” 2017. Thesis, NSYSU. Accessed April 16, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0718117-194840.

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

MLA Handbook (7th Edition):

Kao, Yu-Chen. “Study the effects of Dibromotyrosine Derivative in TGF-β responsiveness.” 2017. Web. 16 Apr 2021.

Vancouver:

Kao Y. Study the effects of Dibromotyrosine Derivative in TGF-β responsiveness. [Internet] [Thesis]. NSYSU; 2017. [cited 2021 Apr 16]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0718117-194840.

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

Council of Science Editors:

Kao Y. Study the effects of Dibromotyrosine Derivative in TGF-β responsiveness. [Thesis]. NSYSU; 2017. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0718117-194840

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


University of Newcastle

2. Mashkani, Baratali. Small molecule inhibitors for type III receptor tyrosine kinases.

Degree: PhD, 2010, University of Newcastle

Research Doctorate - Doctor of Philosophy (PhD)

Colony stimulating Factor-1 Receptor (CSF-1R, FMS) and FMS-like Tyrosine Kinase-3 (FLT3) are members of the type III receptor… (more)

Subjects/Keywords: receptor tyrosine kinase; small molecule inhibitors; molecular docking; homology modelling

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APA (6th Edition):

Mashkani, B. (2010). Small molecule inhibitors for type III receptor tyrosine kinases. (Doctoral Dissertation). University of Newcastle. Retrieved from http://hdl.handle.net/1959.13/805670

Chicago Manual of Style (16th Edition):

Mashkani, Baratali. “Small molecule inhibitors for type III receptor tyrosine kinases.” 2010. Doctoral Dissertation, University of Newcastle. Accessed April 16, 2021. http://hdl.handle.net/1959.13/805670.

MLA Handbook (7th Edition):

Mashkani, Baratali. “Small molecule inhibitors for type III receptor tyrosine kinases.” 2010. Web. 16 Apr 2021.

Vancouver:

Mashkani B. Small molecule inhibitors for type III receptor tyrosine kinases. [Internet] [Doctoral dissertation]. University of Newcastle; 2010. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/1959.13/805670.

Council of Science Editors:

Mashkani B. Small molecule inhibitors for type III receptor tyrosine kinases. [Doctoral Dissertation]. University of Newcastle; 2010. Available from: http://hdl.handle.net/1959.13/805670


NSYSU

3. Chung, Chih-ling. Study the effects of myosin V inhibitor, pentabromopseudilin , in TGF-β-induced responsiveness.

Degree: Master, Biological Sciences, 2018, NSYSU

 Transforming Growth Factor-β (TGF-β) is a multifunctional cytokine that involved in many biological processes. TGF-β signaling transduction initiates when binding to Type II TGF-β receptor… (more)

Subjects/Keywords: Myosin Va; lipid raft; small molecular inhibitors; Pentabromopseudilin; TGF-β

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APA (6th Edition):

Chung, C. (2018). Study the effects of myosin V inhibitor, pentabromopseudilin , in TGF-β-induced responsiveness. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0626118-141345

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):

Chung, Chih-ling. “Study the effects of myosin V inhibitor, pentabromopseudilin , in TGF-β-induced responsiveness.” 2018. Thesis, NSYSU. Accessed April 16, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0626118-141345.

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

MLA Handbook (7th Edition):

Chung, Chih-ling. “Study the effects of myosin V inhibitor, pentabromopseudilin , in TGF-β-induced responsiveness.” 2018. Web. 16 Apr 2021.

Vancouver:

Chung C. Study the effects of myosin V inhibitor, pentabromopseudilin , in TGF-β-induced responsiveness. [Internet] [Thesis]. NSYSU; 2018. [cited 2021 Apr 16]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0626118-141345.

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

Council of Science Editors:

Chung C. Study the effects of myosin V inhibitor, pentabromopseudilin , in TGF-β-induced responsiveness. [Thesis]. NSYSU; 2018. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0626118-141345

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


University of Arizona

4. Moses, Sylvestor Andrea. Targeting Pleckstrin Homology Domains for the Inhibition of Cancer Growth and Metastasis .

Degree: 2013, University of Arizona

 Pleckstrin homology (PH) domains are structurally conserved domains, which generally bind to phosphatidylinositol phosphate (PtdInsP) lipids. They are present in a variety of proteins, including… (more)

Subjects/Keywords: Drug Discovery; Metastasis; Pleckstrin Homology Domains; Small Molecule Inhibitors; Tiam1; Molecular & Cellular Biology; Akt

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APA (6th Edition):

Moses, S. A. (2013). Targeting Pleckstrin Homology Domains for the Inhibition of Cancer Growth and Metastasis . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/293751

Chicago Manual of Style (16th Edition):

Moses, Sylvestor Andrea. “Targeting Pleckstrin Homology Domains for the Inhibition of Cancer Growth and Metastasis .” 2013. Doctoral Dissertation, University of Arizona. Accessed April 16, 2021. http://hdl.handle.net/10150/293751.

MLA Handbook (7th Edition):

Moses, Sylvestor Andrea. “Targeting Pleckstrin Homology Domains for the Inhibition of Cancer Growth and Metastasis .” 2013. Web. 16 Apr 2021.

Vancouver:

Moses SA. Targeting Pleckstrin Homology Domains for the Inhibition of Cancer Growth and Metastasis . [Internet] [Doctoral dissertation]. University of Arizona; 2013. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/10150/293751.

Council of Science Editors:

Moses SA. Targeting Pleckstrin Homology Domains for the Inhibition of Cancer Growth and Metastasis . [Doctoral Dissertation]. University of Arizona; 2013. Available from: http://hdl.handle.net/10150/293751


Georgia State University

5. Ferguson, Jalisa H. Synthesis, Development, and Exploration of Two Small Molecule Scaffolds Toward Discovery of Novel and Potent Inhibitors of the Hypoxia-Inducible Factor-1 Pathway.

Degree: PhD, Chemistry, 2017, Georgia State University

  The hypoxia inducible factor 1 (HIF-1) is an important transcription factor for cell survival in low oxygen concentrations. A variety of methods have been… (more)

Subjects/Keywords: Hypoxia inducible factor; anti-cancer therapeutics; molecular modeling; small molecule inhibitors; medicinal chemistry

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APA (6th Edition):

Ferguson, J. H. (2017). Synthesis, Development, and Exploration of Two Small Molecule Scaffolds Toward Discovery of Novel and Potent Inhibitors of the Hypoxia-Inducible Factor-1 Pathway. (Doctoral Dissertation). Georgia State University. Retrieved from https://scholarworks.gsu.edu/chemistry_diss/135

Chicago Manual of Style (16th Edition):

Ferguson, Jalisa H. “Synthesis, Development, and Exploration of Two Small Molecule Scaffolds Toward Discovery of Novel and Potent Inhibitors of the Hypoxia-Inducible Factor-1 Pathway.” 2017. Doctoral Dissertation, Georgia State University. Accessed April 16, 2021. https://scholarworks.gsu.edu/chemistry_diss/135.

MLA Handbook (7th Edition):

Ferguson, Jalisa H. “Synthesis, Development, and Exploration of Two Small Molecule Scaffolds Toward Discovery of Novel and Potent Inhibitors of the Hypoxia-Inducible Factor-1 Pathway.” 2017. Web. 16 Apr 2021.

Vancouver:

Ferguson JH. Synthesis, Development, and Exploration of Two Small Molecule Scaffolds Toward Discovery of Novel and Potent Inhibitors of the Hypoxia-Inducible Factor-1 Pathway. [Internet] [Doctoral dissertation]. Georgia State University; 2017. [cited 2021 Apr 16]. Available from: https://scholarworks.gsu.edu/chemistry_diss/135.

Council of Science Editors:

Ferguson JH. Synthesis, Development, and Exploration of Two Small Molecule Scaffolds Toward Discovery of Novel and Potent Inhibitors of the Hypoxia-Inducible Factor-1 Pathway. [Doctoral Dissertation]. Georgia State University; 2017. Available from: https://scholarworks.gsu.edu/chemistry_diss/135


University of California – San Francisco

6. Gable, Jonathan Edward. Developing protein-protein interaction inhibitors of the herpesvirus protease family.

Degree: Biophysics, 2015, University of California – San Francisco

 The herpesviruses are an exceptionally interesting pathogen and the cause of lifelong infection for more than 90% of the human population. They are also a… (more)

Subjects/Keywords: Biophysics; Biochemistry; Molecular biology; allostery; herpesvirus; high-throughput screening; protease; protein-protein interaction; small molecule inhibitors

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APA (6th Edition):

Gable, J. E. (2015). Developing protein-protein interaction inhibitors of the herpesvirus protease family. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/564079wq

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):

Gable, Jonathan Edward. “Developing protein-protein interaction inhibitors of the herpesvirus protease family.” 2015. Thesis, University of California – San Francisco. Accessed April 16, 2021. http://www.escholarship.org/uc/item/564079wq.

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

MLA Handbook (7th Edition):

Gable, Jonathan Edward. “Developing protein-protein interaction inhibitors of the herpesvirus protease family.” 2015. Web. 16 Apr 2021.

Vancouver:

Gable JE. Developing protein-protein interaction inhibitors of the herpesvirus protease family. [Internet] [Thesis]. University of California – San Francisco; 2015. [cited 2021 Apr 16]. Available from: http://www.escholarship.org/uc/item/564079wq.

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

Council of Science Editors:

Gable JE. Developing protein-protein interaction inhibitors of the herpesvirus protease family. [Thesis]. University of California – San Francisco; 2015. Available from: http://www.escholarship.org/uc/item/564079wq

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


The Ohio State University

7. Deblais, Loic. Understanding of Salmonella-phytopathogen-environment-plant interactions and development of novel antimicrobial to reduce the Salmonella burden in fresh tomato production.

Degree: PhD, Plant Pathology, 2018, The Ohio State University

 Salmonellosis cases caused by Salmonella enterica through pre-harvest contamination of fresh produce represent a risk to human health worldwide; however, little is known about the… (more)

Subjects/Keywords: Plant Pathology; Public Health; Molecular Biology; Environmental Health; Bioinformatics; Biology; Agriculture; Salmonella enterica; tomato production; fresh produce; whole genome sequencing; microbiota; small molecules; growth inhibitors; plant pathogenic bacteria; relative humidity; temperature; grafting; chicken; supernatant; antimicrobials; Typhimurium; rfbV

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APA (6th Edition):

Deblais, L. (2018). Understanding of Salmonella-phytopathogen-environment-plant interactions and development of novel antimicrobial to reduce the Salmonella burden in fresh tomato production. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1534437638478448

Chicago Manual of Style (16th Edition):

Deblais, Loic. “Understanding of Salmonella-phytopathogen-environment-plant interactions and development of novel antimicrobial to reduce the Salmonella burden in fresh tomato production.” 2018. Doctoral Dissertation, The Ohio State University. Accessed April 16, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=osu1534437638478448.

MLA Handbook (7th Edition):

Deblais, Loic. “Understanding of Salmonella-phytopathogen-environment-plant interactions and development of novel antimicrobial to reduce the Salmonella burden in fresh tomato production.” 2018. Web. 16 Apr 2021.

Vancouver:

Deblais L. Understanding of Salmonella-phytopathogen-environment-plant interactions and development of novel antimicrobial to reduce the Salmonella burden in fresh tomato production. [Internet] [Doctoral dissertation]. The Ohio State University; 2018. [cited 2021 Apr 16]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1534437638478448.

Council of Science Editors:

Deblais L. Understanding of Salmonella-phytopathogen-environment-plant interactions and development of novel antimicrobial to reduce the Salmonella burden in fresh tomato production. [Doctoral Dissertation]. The Ohio State University; 2018. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1534437638478448

8. Clemente-Vicario, Francisco. Biologic Activity of Selected Chemotherapeutic Agents and Small Molecule Inhibitors in Canine Lung Cancer Cell Lines.

Degree: MS, Comparative and Veterinary Medicine, 2015, The Ohio State University

 The prognosis for canine advanced lung cancer remains poor and new treatments are needed. Heat shock protein 90 (HSP90) is an ATPase-dependent molecular chaperone ubiquitously… (more)

Subjects/Keywords: Veterinary Services; Oncology; Molecular Biology; Canine, Lung cancer, HSP90, STA-1474, Ganetespib, Torceranib phosphate, Chemotherapy, Small Molecule Inhibitors

…Lung Cancer Cell Lines after Treatment with Small Molecule Inhibitors… …activity of currently used chemotherapeutic agents and the small molecule inhibitors, toceranib… …lower ICs50 compared to the CLAC line. 17 Of the three different small molecule inhibitors… …A) or small molecules inhibitors (B) and proliferation was evaluated after… …after Treatment with Small Molecule Inhibitors. 25 BACA and CLAC cells were seeded in… 

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APA (6th Edition):

Clemente-Vicario, F. (2015). Biologic Activity of Selected Chemotherapeutic Agents and Small Molecule Inhibitors in Canine Lung Cancer Cell Lines. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1429616111

Chicago Manual of Style (16th Edition):

Clemente-Vicario, Francisco. “Biologic Activity of Selected Chemotherapeutic Agents and Small Molecule Inhibitors in Canine Lung Cancer Cell Lines.” 2015. Masters Thesis, The Ohio State University. Accessed April 16, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=osu1429616111.

MLA Handbook (7th Edition):

Clemente-Vicario, Francisco. “Biologic Activity of Selected Chemotherapeutic Agents and Small Molecule Inhibitors in Canine Lung Cancer Cell Lines.” 2015. Web. 16 Apr 2021.

Vancouver:

Clemente-Vicario F. Biologic Activity of Selected Chemotherapeutic Agents and Small Molecule Inhibitors in Canine Lung Cancer Cell Lines. [Internet] [Masters thesis]. The Ohio State University; 2015. [cited 2021 Apr 16]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1429616111.

Council of Science Editors:

Clemente-Vicario F. Biologic Activity of Selected Chemotherapeutic Agents and Small Molecule Inhibitors in Canine Lung Cancer Cell Lines. [Masters Thesis]. The Ohio State University; 2015. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1429616111


Erasmus University Rotterdam

9. Polak, Roel. Molecular Drivers of Pediatric Acute Lymphoblastic Leukemia : Toward targeted therapy for children with ALL.

Degree: 2017, Erasmus University Rotterdam

textabstractThis thesis aims to identify leukemia-specific processes that can be used to target leukemic cells or the leukemic microenvironment.

Subjects/Keywords: Pediatric; Acute lymphoblastic leukemia; ALL; B-ALL; BCP-ALL; Targeted therapy; Selective targeting; Molecular drivers of leukemia; Pathobiology; Intrinsic characteristic(s); Extrinsic signal(s); PI3K; PKB / Akt; ETV6-RUNX1; TEL-AML1; Autophagy; Vps34; Autophagy inhibitors; Drug resistance; Chemotherapy resistance; L-Asparaginase resistance; Prednisolone resistance; LARG; ARHGEF 12; Migration; Leukemic niche; Bone marrow microenvironment; Leukemic microenvironment; Small molecule inhibition; CXCL12; CXCR4; Crosstalk; Tunneling nanotube(s); Mesenchymal stromal cell(s); IP10 / CXCL10; IL8 / CXCL8; MCP-1 / CCL2; CCR4; CXCR1; CXCR2; Ligands; Leukemic niche disruption

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APA (6th Edition):

Polak, R. (2017). Molecular Drivers of Pediatric Acute Lymphoblastic Leukemia : Toward targeted therapy for children with ALL. (Doctoral Dissertation). Erasmus University Rotterdam. Retrieved from http://hdl.handle.net/1765/102893

Chicago Manual of Style (16th Edition):

Polak, Roel. “Molecular Drivers of Pediatric Acute Lymphoblastic Leukemia : Toward targeted therapy for children with ALL.” 2017. Doctoral Dissertation, Erasmus University Rotterdam. Accessed April 16, 2021. http://hdl.handle.net/1765/102893.

MLA Handbook (7th Edition):

Polak, Roel. “Molecular Drivers of Pediatric Acute Lymphoblastic Leukemia : Toward targeted therapy for children with ALL.” 2017. Web. 16 Apr 2021.

Vancouver:

Polak R. Molecular Drivers of Pediatric Acute Lymphoblastic Leukemia : Toward targeted therapy for children with ALL. [Internet] [Doctoral dissertation]. Erasmus University Rotterdam; 2017. [cited 2021 Apr 16]. Available from: http://hdl.handle.net/1765/102893.

Council of Science Editors:

Polak R. Molecular Drivers of Pediatric Acute Lymphoblastic Leukemia : Toward targeted therapy for children with ALL. [Doctoral Dissertation]. Erasmus University Rotterdam; 2017. Available from: http://hdl.handle.net/1765/102893

.