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You searched for subject:(Inhibitor). Showing records 1 – 30 of 1697 total matches.

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University of Debrecen

1. Kiss, Gabriella Mónika. Amiláz enzim inhibitorainak vizsgálata .

Degree: DE – TEK – Természettudományi és Technológiai Kar – Kémiai Intézet, 2010, University of Debrecen

 Az enzimek az élő szervezet számára nélkülözhetetlenek. Az anyagcsere-folyamatokat katalizáló fehérjék, az aktiválási energiát csökkentik, ezáltal biokatalizátoroknak tekinthetők. „Titkuk” igényeikben rejlik, vagyis az élet körülményei… (more)

Subjects/Keywords: Amiláz; inhibitor

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APA (6th Edition):

Kiss, G. M. (2010). Amiláz enzim inhibitorainak vizsgálata . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/95913

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):

Kiss, Gabriella Mónika. “Amiláz enzim inhibitorainak vizsgálata .” 2010. Thesis, University of Debrecen. Accessed October 30, 2020. http://hdl.handle.net/2437/95913.

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

MLA Handbook (7th Edition):

Kiss, Gabriella Mónika. “Amiláz enzim inhibitorainak vizsgálata .” 2010. Web. 30 Oct 2020.

Vancouver:

Kiss GM. Amiláz enzim inhibitorainak vizsgálata . [Internet] [Thesis]. University of Debrecen; 2010. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/2437/95913.

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

Council of Science Editors:

Kiss GM. Amiláz enzim inhibitorainak vizsgálata . [Thesis]. University of Debrecen; 2010. Available from: http://hdl.handle.net/2437/95913

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


University of Debrecen

2. Sótér, Zsanett. Gyümölcskivonatok alfa-amiláz gátló hatásának vizsgálata .

Degree: DE – TEK – Természettudományi és Technológiai Kar – Kémiai Intézet, 2013, University of Debrecen

Kétféle tradicionális magyar gyümölcs a meggy és az alma gátló hatásának vizsgálata HSA enzimen, GALG2-CNP szubsztráton. Advisors/Committee Members: Gyémánt, Gyöngyi (advisor).

Subjects/Keywords: alfa-amiláz; inhibitor

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APA (6th Edition):

Sótér, Z. (2013). Gyümölcskivonatok alfa-amiláz gátló hatásának vizsgálata . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/167564

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):

Sótér, Zsanett. “Gyümölcskivonatok alfa-amiláz gátló hatásának vizsgálata .” 2013. Thesis, University of Debrecen. Accessed October 30, 2020. http://hdl.handle.net/2437/167564.

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

MLA Handbook (7th Edition):

Sótér, Zsanett. “Gyümölcskivonatok alfa-amiláz gátló hatásának vizsgálata .” 2013. Web. 30 Oct 2020.

Vancouver:

Sótér Z. Gyümölcskivonatok alfa-amiláz gátló hatásának vizsgálata . [Internet] [Thesis]. University of Debrecen; 2013. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/2437/167564.

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

Council of Science Editors:

Sótér Z. Gyümölcskivonatok alfa-amiláz gátló hatásának vizsgálata . [Thesis]. University of Debrecen; 2013. Available from: http://hdl.handle.net/2437/167564

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


University of Melbourne

3. NEWBOLD, ANDREA. Mechanisms of action of histone deacetylase inhibitors.

Degree: 2011, University of Melbourne

 The opposing activities of histone acetyltransferases (HATs) and histone deacetylases (HDACs) play important roles in tightly regulating gene expression through regulated chromatin remodelling. It is… (more)

Subjects/Keywords: histone deacetylase inhibitor

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APA (6th Edition):

NEWBOLD, A. (2011). Mechanisms of action of histone deacetylase inhibitors. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/36731

Chicago Manual of Style (16th Edition):

NEWBOLD, ANDREA. “Mechanisms of action of histone deacetylase inhibitors.” 2011. Doctoral Dissertation, University of Melbourne. Accessed October 30, 2020. http://hdl.handle.net/11343/36731.

MLA Handbook (7th Edition):

NEWBOLD, ANDREA. “Mechanisms of action of histone deacetylase inhibitors.” 2011. Web. 30 Oct 2020.

Vancouver:

NEWBOLD A. Mechanisms of action of histone deacetylase inhibitors. [Internet] [Doctoral dissertation]. University of Melbourne; 2011. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/11343/36731.

Council of Science Editors:

NEWBOLD A. Mechanisms of action of histone deacetylase inhibitors. [Doctoral Dissertation]. University of Melbourne; 2011. Available from: http://hdl.handle.net/11343/36731


University of Melbourne

4. Ngoei, Kevin Ronald. Investigation of the structural and functional properties of the c-Jun N-terminal kinase (JNK).

Degree: 2013, University of Melbourne

 The c-Jun N-terminal kinases (JNKs) are members of the larger group of mitogen-activated protein kinases (MAPKs), and are activated in response to various stimuli such… (more)

Subjects/Keywords: kinase; protein; inhibitor

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APA (6th Edition):

Ngoei, K. R. (2013). Investigation of the structural and functional properties of the c-Jun N-terminal kinase (JNK). (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/39763

Chicago Manual of Style (16th Edition):

Ngoei, Kevin Ronald. “Investigation of the structural and functional properties of the c-Jun N-terminal kinase (JNK).” 2013. Doctoral Dissertation, University of Melbourne. Accessed October 30, 2020. http://hdl.handle.net/11343/39763.

MLA Handbook (7th Edition):

Ngoei, Kevin Ronald. “Investigation of the structural and functional properties of the c-Jun N-terminal kinase (JNK).” 2013. Web. 30 Oct 2020.

Vancouver:

Ngoei KR. Investigation of the structural and functional properties of the c-Jun N-terminal kinase (JNK). [Internet] [Doctoral dissertation]. University of Melbourne; 2013. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/11343/39763.

Council of Science Editors:

Ngoei KR. Investigation of the structural and functional properties of the c-Jun N-terminal kinase (JNK). [Doctoral Dissertation]. University of Melbourne; 2013. Available from: http://hdl.handle.net/11343/39763


University of Montana

5. Barney, Patrick Anthony. THE DESIGN AND SYNTHESIS OF SMALL MOLECULE DRUGS TO INHIBIT EPIGENETIC ALTERATIONS CAUSED BY DNA METHYLTRANSFERASE 1.

Degree: PhD, 2016, University of Montana

 The acquisition of genomic alterations is a defining feature of human cancers. Many cancer chemotherapies rely upon an apoptotic pathway to eradicate cells containing those… (more)

Subjects/Keywords: DNMT1; inhibitor; methylation

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APA (6th Edition):

Barney, P. A. (2016). THE DESIGN AND SYNTHESIS OF SMALL MOLECULE DRUGS TO INHIBIT EPIGENETIC ALTERATIONS CAUSED BY DNA METHYLTRANSFERASE 1. (Doctoral Dissertation). University of Montana. Retrieved from https://scholarworks.umt.edu/etd/10737

Chicago Manual of Style (16th Edition):

Barney, Patrick Anthony. “THE DESIGN AND SYNTHESIS OF SMALL MOLECULE DRUGS TO INHIBIT EPIGENETIC ALTERATIONS CAUSED BY DNA METHYLTRANSFERASE 1.” 2016. Doctoral Dissertation, University of Montana. Accessed October 30, 2020. https://scholarworks.umt.edu/etd/10737.

MLA Handbook (7th Edition):

Barney, Patrick Anthony. “THE DESIGN AND SYNTHESIS OF SMALL MOLECULE DRUGS TO INHIBIT EPIGENETIC ALTERATIONS CAUSED BY DNA METHYLTRANSFERASE 1.” 2016. Web. 30 Oct 2020.

Vancouver:

Barney PA. THE DESIGN AND SYNTHESIS OF SMALL MOLECULE DRUGS TO INHIBIT EPIGENETIC ALTERATIONS CAUSED BY DNA METHYLTRANSFERASE 1. [Internet] [Doctoral dissertation]. University of Montana; 2016. [cited 2020 Oct 30]. Available from: https://scholarworks.umt.edu/etd/10737.

Council of Science Editors:

Barney PA. THE DESIGN AND SYNTHESIS OF SMALL MOLECULE DRUGS TO INHIBIT EPIGENETIC ALTERATIONS CAUSED BY DNA METHYLTRANSFERASE 1. [Doctoral Dissertation]. University of Montana; 2016. Available from: https://scholarworks.umt.edu/etd/10737


University of Manitoba

6. Shi, Lan. A quantitative assessment of the anti-nutritional properties of Canadian pulses.

Degree: Food Science, 2015, University of Manitoba

 This study has assessed the effects of pulse type and processing (soaking and cooking) on antinutritional factors (α-amylase inhibitor, trypsin inhibitor, chymotrypsin inhibitor, lectins, phytic… (more)

Subjects/Keywords: Antinutritional factors; Trypsin inhibitor; Chymotrypsin inhibitor; α-Amylase inhibitor; Lectins; Phytic acid; Oxalates; Canadian pulses

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APA (6th Edition):

Shi, L. (2015). A quantitative assessment of the anti-nutritional properties of Canadian pulses. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/30983

Chicago Manual of Style (16th Edition):

Shi, Lan. “A quantitative assessment of the anti-nutritional properties of Canadian pulses.” 2015. Masters Thesis, University of Manitoba. Accessed October 30, 2020. http://hdl.handle.net/1993/30983.

MLA Handbook (7th Edition):

Shi, Lan. “A quantitative assessment of the anti-nutritional properties of Canadian pulses.” 2015. Web. 30 Oct 2020.

Vancouver:

Shi L. A quantitative assessment of the anti-nutritional properties of Canadian pulses. [Internet] [Masters thesis]. University of Manitoba; 2015. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/1993/30983.

Council of Science Editors:

Shi L. A quantitative assessment of the anti-nutritional properties of Canadian pulses. [Masters Thesis]. University of Manitoba; 2015. Available from: http://hdl.handle.net/1993/30983


University of Toronto

7. Falkenhagen, Alexander. A Novel Gene Therapy Approach Based on Secreted Antiviral Proteins for the Control of HIV Replication.

Degree: PhD, 2017, University of Toronto

 HIV entry into target cells requires the interaction of the HIV envelope glycoprotein (Env) with a primary receptor (CD4) and a co-receptor (most commonly CCR5… (more)

Subjects/Keywords: Bifunctional entry inhibitor; Fusion inhibitor; Gene therapy; HIV entry; Lentiviral vector; Secreted entry inhibitor; 0307

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APA (6th Edition):

Falkenhagen, A. (2017). A Novel Gene Therapy Approach Based on Secreted Antiviral Proteins for the Control of HIV Replication. (Doctoral Dissertation). University of Toronto. Retrieved from http://hdl.handle.net/1807/78957

Chicago Manual of Style (16th Edition):

Falkenhagen, Alexander. “A Novel Gene Therapy Approach Based on Secreted Antiviral Proteins for the Control of HIV Replication.” 2017. Doctoral Dissertation, University of Toronto. Accessed October 30, 2020. http://hdl.handle.net/1807/78957.

MLA Handbook (7th Edition):

Falkenhagen, Alexander. “A Novel Gene Therapy Approach Based on Secreted Antiviral Proteins for the Control of HIV Replication.” 2017. Web. 30 Oct 2020.

Vancouver:

Falkenhagen A. A Novel Gene Therapy Approach Based on Secreted Antiviral Proteins for the Control of HIV Replication. [Internet] [Doctoral dissertation]. University of Toronto; 2017. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/1807/78957.

Council of Science Editors:

Falkenhagen A. A Novel Gene Therapy Approach Based on Secreted Antiviral Proteins for the Control of HIV Replication. [Doctoral Dissertation]. University of Toronto; 2017. Available from: http://hdl.handle.net/1807/78957


Universiteit Utrecht

8. Wildt, B. van der. Synthesis and development of neuraminidase inhibitors.

Degree: 2012, Universiteit Utrecht

 The influenza virus is a serious threat to the world's population. A lot of research is focussed on inhibition of an essential viral enzyme: neuraminidase.… (more)

Subjects/Keywords: Neuraminase inhibitor; influenza; neuraminidase assay

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APA (6th Edition):

Wildt, B. v. d. (2012). Synthesis and development of neuraminidase inhibitors. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/256464

Chicago Manual of Style (16th Edition):

Wildt, B van der. “Synthesis and development of neuraminidase inhibitors.” 2012. Masters Thesis, Universiteit Utrecht. Accessed October 30, 2020. http://dspace.library.uu.nl:8080/handle/1874/256464.

MLA Handbook (7th Edition):

Wildt, B van der. “Synthesis and development of neuraminidase inhibitors.” 2012. Web. 30 Oct 2020.

Vancouver:

Wildt Bvd. Synthesis and development of neuraminidase inhibitors. [Internet] [Masters thesis]. Universiteit Utrecht; 2012. [cited 2020 Oct 30]. Available from: http://dspace.library.uu.nl:8080/handle/1874/256464.

Council of Science Editors:

Wildt Bvd. Synthesis and development of neuraminidase inhibitors. [Masters Thesis]. Universiteit Utrecht; 2012. Available from: http://dspace.library.uu.nl:8080/handle/1874/256464

9. Nakamura, Kasumi. Effects of hydroxy groups in the A-ring on the anti-proteasome activity of flavone : フラボンの抗プロテアソーム活性におけるA環のヒドロキシル基の効果.

Degree: 博士(医学), 2016, Hamamatsu University School of Medicine / 浜松医科大学

The ubiquitin–proteasome pathway plays an important role in regulating apoptosis and the cell cycle. Recently, proteasome inhibitors have been shown to have antitumor effects and… (more)

Subjects/Keywords: ubiquitin; flavonoid; proteasome; inhibitor

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APA (6th Edition):

Nakamura, K. (2016). Effects of hydroxy groups in the A-ring on the anti-proteasome activity of flavone : フラボンの抗プロテアソーム活性におけるA環のヒドロキシル基の効果. (Thesis). Hamamatsu University School of Medicine / 浜松医科大学. Retrieved from http://hdl.handle.net/10271/3143

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):

Nakamura, Kasumi. “Effects of hydroxy groups in the A-ring on the anti-proteasome activity of flavone : フラボンの抗プロテアソーム活性におけるA環のヒドロキシル基の効果.” 2016. Thesis, Hamamatsu University School of Medicine / 浜松医科大学. Accessed October 30, 2020. http://hdl.handle.net/10271/3143.

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

MLA Handbook (7th Edition):

Nakamura, Kasumi. “Effects of hydroxy groups in the A-ring on the anti-proteasome activity of flavone : フラボンの抗プロテアソーム活性におけるA環のヒドロキシル基の効果.” 2016. Web. 30 Oct 2020.

Vancouver:

Nakamura K. Effects of hydroxy groups in the A-ring on the anti-proteasome activity of flavone : フラボンの抗プロテアソーム活性におけるA環のヒドロキシル基の効果. [Internet] [Thesis]. Hamamatsu University School of Medicine / 浜松医科大学; 2016. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/10271/3143.

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

Council of Science Editors:

Nakamura K. Effects of hydroxy groups in the A-ring on the anti-proteasome activity of flavone : フラボンの抗プロテアソーム活性におけるA環のヒドロキシル基の効果. [Thesis]. Hamamatsu University School of Medicine / 浜松医科大学; 2016. Available from: http://hdl.handle.net/10271/3143

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


Texas A&M University

10. Goldsberry, Reece Keith. Electrochemical Evaluation of Self-Healing Epoxy Coated Rebar in Simulated Concrete Pore Solution.

Degree: MS, Materials Science and Engineering, 2019, Texas A&M University

 The use of epoxy-coated rebar (ECR) has become a major form of protection for reinforcing steel in concrete bridges in North America. ECR has been… (more)

Subjects/Keywords: Epoxy coated rebar; Corrosion inhibitor

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APA (6th Edition):

Goldsberry, R. K. (2019). Electrochemical Evaluation of Self-Healing Epoxy Coated Rebar in Simulated Concrete Pore Solution. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/184995

Chicago Manual of Style (16th Edition):

Goldsberry, Reece Keith. “Electrochemical Evaluation of Self-Healing Epoxy Coated Rebar in Simulated Concrete Pore Solution.” 2019. Masters Thesis, Texas A&M University. Accessed October 30, 2020. http://hdl.handle.net/1969.1/184995.

MLA Handbook (7th Edition):

Goldsberry, Reece Keith. “Electrochemical Evaluation of Self-Healing Epoxy Coated Rebar in Simulated Concrete Pore Solution.” 2019. Web. 30 Oct 2020.

Vancouver:

Goldsberry RK. Electrochemical Evaluation of Self-Healing Epoxy Coated Rebar in Simulated Concrete Pore Solution. [Internet] [Masters thesis]. Texas A&M University; 2019. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/1969.1/184995.

Council of Science Editors:

Goldsberry RK. Electrochemical Evaluation of Self-Healing Epoxy Coated Rebar in Simulated Concrete Pore Solution. [Masters Thesis]. Texas A&M University; 2019. Available from: http://hdl.handle.net/1969.1/184995


Texas A&M University

11. Chalaire, Katelyn Cox. The Biological and Molecular Analysis of a Tick-Encoded Serine Protease Inhibitor (S6) and its Role in the Feeding Cycle of the Lone Star Tick, Amblyomma americanum (L) (Acari: ixodidae).

Degree: MS, Entomology, 2011, Texas A&M University

 Serine protease inhibitors (serpins) are a large superfamily of proteins that regulate critical proteolytic pathways by inhibiting serine proteases. Tick-encoded serpins are thought to play… (more)

Subjects/Keywords: Amblyomma americanum; Serine Protease Inhibitor

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APA (6th Edition):

Chalaire, K. C. (2011). The Biological and Molecular Analysis of a Tick-Encoded Serine Protease Inhibitor (S6) and its Role in the Feeding Cycle of the Lone Star Tick, Amblyomma americanum (L) (Acari: ixodidae). (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8255

Chicago Manual of Style (16th Edition):

Chalaire, Katelyn Cox. “The Biological and Molecular Analysis of a Tick-Encoded Serine Protease Inhibitor (S6) and its Role in the Feeding Cycle of the Lone Star Tick, Amblyomma americanum (L) (Acari: ixodidae).” 2011. Masters Thesis, Texas A&M University. Accessed October 30, 2020. http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8255.

MLA Handbook (7th Edition):

Chalaire, Katelyn Cox. “The Biological and Molecular Analysis of a Tick-Encoded Serine Protease Inhibitor (S6) and its Role in the Feeding Cycle of the Lone Star Tick, Amblyomma americanum (L) (Acari: ixodidae).” 2011. Web. 30 Oct 2020.

Vancouver:

Chalaire KC. The Biological and Molecular Analysis of a Tick-Encoded Serine Protease Inhibitor (S6) and its Role in the Feeding Cycle of the Lone Star Tick, Amblyomma americanum (L) (Acari: ixodidae). [Internet] [Masters thesis]. Texas A&M University; 2011. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8255.

Council of Science Editors:

Chalaire KC. The Biological and Molecular Analysis of a Tick-Encoded Serine Protease Inhibitor (S6) and its Role in the Feeding Cycle of the Lone Star Tick, Amblyomma americanum (L) (Acari: ixodidae). [Masters Thesis]. Texas A&M University; 2011. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-08-8255


Texas A&M University

12. Goldsberry, Reece Keith. Electrochemical Evaluation of Self-Healing Epoxy Coated Rebar in Simulated Concrete Pore Solution.

Degree: MS, Materials Science and Engineering, 2019, Texas A&M University

 The use of epoxy-coated rebar (ECR) has become a major form of protection for reinforcing steel in concrete bridges in North America. ECR has been… (more)

Subjects/Keywords: Epoxy coated rebar; Corrosion inhibitor

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

APA (6th Edition):

Goldsberry, R. K. (2019). Electrochemical Evaluation of Self-Healing Epoxy Coated Rebar in Simulated Concrete Pore Solution. (Masters Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/184992

Chicago Manual of Style (16th Edition):

Goldsberry, Reece Keith. “Electrochemical Evaluation of Self-Healing Epoxy Coated Rebar in Simulated Concrete Pore Solution.” 2019. Masters Thesis, Texas A&M University. Accessed October 30, 2020. http://hdl.handle.net/1969.1/184992.

MLA Handbook (7th Edition):

Goldsberry, Reece Keith. “Electrochemical Evaluation of Self-Healing Epoxy Coated Rebar in Simulated Concrete Pore Solution.” 2019. Web. 30 Oct 2020.

Vancouver:

Goldsberry RK. Electrochemical Evaluation of Self-Healing Epoxy Coated Rebar in Simulated Concrete Pore Solution. [Internet] [Masters thesis]. Texas A&M University; 2019. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/1969.1/184992.

Council of Science Editors:

Goldsberry RK. Electrochemical Evaluation of Self-Healing Epoxy Coated Rebar in Simulated Concrete Pore Solution. [Masters Thesis]. Texas A&M University; 2019. Available from: http://hdl.handle.net/1969.1/184992


Texas Tech University

13. -4621-5627. Characterization, mutagenesis and mechanistic analysis of the sterol C24-methyltransferase: Implications for understanding active site requirements for sterol biosynthesis.

Degree: PhD, Chemistry, 2016, Texas Tech University

 Previous studies that have defined regions of the sterol C24-methyltransferase (SMT) primary structure involved with catalysis failed to show the full identity of essential amino… (more)

Subjects/Keywords: sterol; methyltransferase; mutagenesis; inhibitor

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APA (6th Edition):

-4621-5627. (2016). Characterization, mutagenesis and mechanistic analysis of the sterol C24-methyltransferase: Implications for understanding active site requirements for sterol biosynthesis. (Doctoral Dissertation). Texas Tech University. Retrieved from http://hdl.handle.net/2346/72372

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

Chicago Manual of Style (16th Edition):

-4621-5627. “Characterization, mutagenesis and mechanistic analysis of the sterol C24-methyltransferase: Implications for understanding active site requirements for sterol biosynthesis.” 2016. Doctoral Dissertation, Texas Tech University. Accessed October 30, 2020. http://hdl.handle.net/2346/72372.

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

MLA Handbook (7th Edition):

-4621-5627. “Characterization, mutagenesis and mechanistic analysis of the sterol C24-methyltransferase: Implications for understanding active site requirements for sterol biosynthesis.” 2016. Web. 30 Oct 2020.

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

Vancouver:

-4621-5627. Characterization, mutagenesis and mechanistic analysis of the sterol C24-methyltransferase: Implications for understanding active site requirements for sterol biosynthesis. [Internet] [Doctoral dissertation]. Texas Tech University; 2016. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/2346/72372.

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

Council of Science Editors:

-4621-5627. Characterization, mutagenesis and mechanistic analysis of the sterol C24-methyltransferase: Implications for understanding active site requirements for sterol biosynthesis. [Doctoral Dissertation]. Texas Tech University; 2016. Available from: http://hdl.handle.net/2346/72372

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


University of Adelaide

14. Chua, Krystle Chia Hsien. Defining peptide structure with metathesis.

Degree: 2013, University of Adelaide

 Understanding protein structure and function is central for the development of therapeutics for the treatment of diseases and also novel biocompatible materials. Herein describes studies… (more)

Subjects/Keywords: peptide; metathesis; inhibitor; assays; hydrogels

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APA (6th Edition):

Chua, K. C. H. (2013). Defining peptide structure with metathesis. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/92334

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):

Chua, Krystle Chia Hsien. “Defining peptide structure with metathesis.” 2013. Thesis, University of Adelaide. Accessed October 30, 2020. http://hdl.handle.net/2440/92334.

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

MLA Handbook (7th Edition):

Chua, Krystle Chia Hsien. “Defining peptide structure with metathesis.” 2013. Web. 30 Oct 2020.

Vancouver:

Chua KCH. Defining peptide structure with metathesis. [Internet] [Thesis]. University of Adelaide; 2013. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/2440/92334.

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

Council of Science Editors:

Chua KCH. Defining peptide structure with metathesis. [Thesis]. University of Adelaide; 2013. Available from: http://hdl.handle.net/2440/92334

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


Baylor University

15. Foster, Taylor Ann. Inhibition of β-lactamase I from Bacillus cereus by ssDNA.

Degree: MS, Biomedical Studies., 2011, Baylor University

 Inhibitors of β-lactamases are important to the treatment of infectious diseases when used in conjunction with a β-lactam antibiotic. Current inhibitors of β-lactamase such as… (more)

Subjects/Keywords: Beta-lactamase inhibitor.; SELEX.; ssDNA.

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

APA (6th Edition):

Foster, T. A. (2011). Inhibition of β-lactamase I from Bacillus cereus by ssDNA. (Masters Thesis). Baylor University. Retrieved from http://hdl.handle.net/2104/8211

Chicago Manual of Style (16th Edition):

Foster, Taylor Ann. “Inhibition of β-lactamase I from Bacillus cereus by ssDNA.” 2011. Masters Thesis, Baylor University. Accessed October 30, 2020. http://hdl.handle.net/2104/8211.

MLA Handbook (7th Edition):

Foster, Taylor Ann. “Inhibition of β-lactamase I from Bacillus cereus by ssDNA.” 2011. Web. 30 Oct 2020.

Vancouver:

Foster TA. Inhibition of β-lactamase I from Bacillus cereus by ssDNA. [Internet] [Masters thesis]. Baylor University; 2011. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/2104/8211.

Council of Science Editors:

Foster TA. Inhibition of β-lactamase I from Bacillus cereus by ssDNA. [Masters Thesis]. Baylor University; 2011. Available from: http://hdl.handle.net/2104/8211


University of Debrecen

16. Polyák, Mária. 3(5)-Aril-1,2,4-oxadiazol-5(3)-il heterociklust tartalmazó glükóz analóg glikogén foszforiláz inhibitor vegyületek előállítása .

Degree: DE – TEK – Természettudományi és Technológiai Kar – Kémiai Intézet, 2011, University of Debrecen

 A Debreceni Egyetem Szerves Kémia Tanszékén már régóta folynak kutatások a nem inzulin-függő cukorbetegség kezelésére használható glükóz analóg glikogén foszforiláz (GP) inhibitor molekulák előállítására, mely… (more)

Subjects/Keywords: GP inhibitor; szerves kémia

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

APA (6th Edition):

Polyák, M. (2011). 3(5)-Aril-1,2,4-oxadiazol-5(3)-il heterociklust tartalmazó glükóz analóg glikogén foszforiláz inhibitor vegyületek előállítása . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/108163

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):

Polyák, Mária. “3(5)-Aril-1,2,4-oxadiazol-5(3)-il heterociklust tartalmazó glükóz analóg glikogén foszforiláz inhibitor vegyületek előállítása .” 2011. Thesis, University of Debrecen. Accessed October 30, 2020. http://hdl.handle.net/2437/108163.

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

MLA Handbook (7th Edition):

Polyák, Mária. “3(5)-Aril-1,2,4-oxadiazol-5(3)-il heterociklust tartalmazó glükóz analóg glikogén foszforiláz inhibitor vegyületek előállítása .” 2011. Web. 30 Oct 2020.

Vancouver:

Polyák M. 3(5)-Aril-1,2,4-oxadiazol-5(3)-il heterociklust tartalmazó glükóz analóg glikogén foszforiláz inhibitor vegyületek előállítása . [Internet] [Thesis]. University of Debrecen; 2011. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/2437/108163.

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

Council of Science Editors:

Polyák M. 3(5)-Aril-1,2,4-oxadiazol-5(3)-il heterociklust tartalmazó glükóz analóg glikogén foszforiláz inhibitor vegyületek előállítása . [Thesis]. University of Debrecen; 2011. Available from: http://hdl.handle.net/2437/108163

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


University of Debrecen

17. Szilágyi, Bence. 1,3,4-Oxadiazol egységet tartalmazó N-glükopiranozil-amid típusú glikogén foszforiláz inhibitorok előállítása .

Degree: DE – TEK – Természettudományi és Technológiai Kar – Kémiai Intézet, 2011, University of Debrecen

 A Debreceni Egyetem Szerves Kémiai Tanszéken már régóta folynak kutatások a nem inzulinfüggő cukorbetegség kezelésére használható glükóz analóg glikogén foszforiláz inhibitor molekulák előállítására, mely munka… (more)

Subjects/Keywords: 1,3,4-oxadiazolok; glikogén foszforiláz inhibitor

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APA (6th Edition):

Szilágyi, B. (2011). 1,3,4-Oxadiazol egységet tartalmazó N-glükopiranozil-amid típusú glikogén foszforiláz inhibitorok előállítása . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/108180

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):

Szilágyi, Bence. “1,3,4-Oxadiazol egységet tartalmazó N-glükopiranozil-amid típusú glikogén foszforiláz inhibitorok előállítása .” 2011. Thesis, University of Debrecen. Accessed October 30, 2020. http://hdl.handle.net/2437/108180.

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

MLA Handbook (7th Edition):

Szilágyi, Bence. “1,3,4-Oxadiazol egységet tartalmazó N-glükopiranozil-amid típusú glikogén foszforiláz inhibitorok előállítása .” 2011. Web. 30 Oct 2020.

Vancouver:

Szilágyi B. 1,3,4-Oxadiazol egységet tartalmazó N-glükopiranozil-amid típusú glikogén foszforiláz inhibitorok előállítása . [Internet] [Thesis]. University of Debrecen; 2011. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/2437/108180.

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

Council of Science Editors:

Szilágyi B. 1,3,4-Oxadiazol egységet tartalmazó N-glükopiranozil-amid típusú glikogén foszforiláz inhibitorok előállítása . [Thesis]. University of Debrecen; 2011. Available from: http://hdl.handle.net/2437/108180

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


University of Debrecen

18. Sztankovics, Andrea. Természetes eredetű glikogén foszforiláz gátló hatású vegyület analogonjainak szintézise és kinetikai vizsgálata .

Degree: DE – TEK – Természettudományi és Technológiai Kar – Kémiai Intézet, 2011, University of Debrecen

 A cukorbetegségben szenvedő emberek számának növekedése napjainkban járványszerű méreteket ölt, és a WHO becslése szerint 2030-ra meghaladja a 300 millió főt. A betegség gyógyítására napjainkban… (more)

Subjects/Keywords: glikogén foszforiláz; inhibitor; analogon; szintézis

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APA (6th Edition):

Sztankovics, A. (2011). Természetes eredetű glikogén foszforiláz gátló hatású vegyület analogonjainak szintézise és kinetikai vizsgálata . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/119003

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):

Sztankovics, Andrea. “Természetes eredetű glikogén foszforiláz gátló hatású vegyület analogonjainak szintézise és kinetikai vizsgálata .” 2011. Thesis, University of Debrecen. Accessed October 30, 2020. http://hdl.handle.net/2437/119003.

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

MLA Handbook (7th Edition):

Sztankovics, Andrea. “Természetes eredetű glikogén foszforiláz gátló hatású vegyület analogonjainak szintézise és kinetikai vizsgálata .” 2011. Web. 30 Oct 2020.

Vancouver:

Sztankovics A. Természetes eredetű glikogén foszforiláz gátló hatású vegyület analogonjainak szintézise és kinetikai vizsgálata . [Internet] [Thesis]. University of Debrecen; 2011. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/2437/119003.

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

Council of Science Editors:

Sztankovics A. Természetes eredetű glikogén foszforiláz gátló hatású vegyület analogonjainak szintézise és kinetikai vizsgálata . [Thesis]. University of Debrecen; 2011. Available from: http://hdl.handle.net/2437/119003

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


University of Debrecen

19. Bereczki, Anita. Glikogén foszforiláz inhibitorok kinetikai vizsgálata és hatásuk tanulmányozása különböző humán sejtvonalakban .

Degree: DE – TEK – Természettudományi és Technológiai Kar – Biológiai és Ökológiai Intézet, 2013, University of Debrecen

 A glikogén foszforiláz a glikogén lebontását katalizálja a májban és az izomban. A glikogén foszforilázhoz specifikusan kapcsolódó inhibitor molekulák megakadályozzák az enzim aktiválódását, ezáltal a… (more)

Subjects/Keywords: glikogén foszforiláz inhibitor; sejtproliferáció

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APA (6th Edition):

Bereczki, A. (2013). Glikogén foszforiláz inhibitorok kinetikai vizsgálata és hatásuk tanulmányozása különböző humán sejtvonalakban . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/168157

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):

Bereczki, Anita. “Glikogén foszforiláz inhibitorok kinetikai vizsgálata és hatásuk tanulmányozása különböző humán sejtvonalakban .” 2013. Thesis, University of Debrecen. Accessed October 30, 2020. http://hdl.handle.net/2437/168157.

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

MLA Handbook (7th Edition):

Bereczki, Anita. “Glikogén foszforiláz inhibitorok kinetikai vizsgálata és hatásuk tanulmányozása különböző humán sejtvonalakban .” 2013. Web. 30 Oct 2020.

Vancouver:

Bereczki A. Glikogén foszforiláz inhibitorok kinetikai vizsgálata és hatásuk tanulmányozása különböző humán sejtvonalakban . [Internet] [Thesis]. University of Debrecen; 2013. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/2437/168157.

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

Council of Science Editors:

Bereczki A. Glikogén foszforiláz inhibitorok kinetikai vizsgálata és hatásuk tanulmányozása különböző humán sejtvonalakban . [Thesis]. University of Debrecen; 2013. Available from: http://hdl.handle.net/2437/168157

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


University of Debrecen

20. Szabó, Éva. Kísérletek donor-szubsztát analóg galaktoziltranszferáz inhibitorok szintézisére .

Degree: DE – Természettudományi és Technológiai Kar – Kémiai Intézet, University of Debrecen

 Vizsgálataink során célul tűztük ki háromféle donor szubsztrát-analóg galaktoziltranszferáz inhibitor, egy diszulfon, egy monoszulfon és egy szulfonamid típusú vegyület szintézisét. A szintetizálandó vegyületeimhez három építőegységet… (more)

Subjects/Keywords: galaktoziltranszferáz; inhibitor

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APA (6th Edition):

Szabó, . (n.d.). Kísérletek donor-szubsztát analóg galaktoziltranszferáz inhibitorok szintézisére . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/227253

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Szabó, Éva. “Kísérletek donor-szubsztát analóg galaktoziltranszferáz inhibitorok szintézisére .” Thesis, University of Debrecen. Accessed October 30, 2020. http://hdl.handle.net/2437/227253.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Szabó, Éva. “Kísérletek donor-szubsztát analóg galaktoziltranszferáz inhibitorok szintézisére .” Web. 30 Oct 2020.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Szabó . Kísérletek donor-szubsztát analóg galaktoziltranszferáz inhibitorok szintézisére . [Internet] [Thesis]. University of Debrecen; [cited 2020 Oct 30]. Available from: http://hdl.handle.net/2437/227253.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Szabó . Kísérletek donor-szubsztát analóg galaktoziltranszferáz inhibitorok szintézisére . [Thesis]. University of Debrecen; Available from: http://hdl.handle.net/2437/227253

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


University of Debrecen

21. Szabó, Erzsébet Katalin. N-[(C-2,3,4,6-Tetra-O-benzoil-B-D-glükopiranozil-metilidén)amino] karboximidamidok szintézise és átalakítási lehetőségeinek vizsgálata 1,2,4-triazol származékokká .

Degree: DE – TEK – Természettudományi és Technológiai Kar – Kémiai Intézet, 2010, University of Debrecen

Szakdolgozatom keretében a glikogén foszforiláz enzim új, glükózanalóg inhibitorainak szintézisét vizsgáltam, amelyek hozzájárulhatnak a II. típusú cukorbetegség egy új kezelési lehetőségének kifejlesztéséhez. Munkám során célul tűztük ki N-[(C-2,3,4,6-tetra-O-benzoil-B-D-glükopiranozil-metilidén)amino]karboximidamidok szintézisét, és azok átalakítási lehetőségeinek vizsgálatát 3-glükopiranozil-5-aril-1,2,4-triazolokká. Advisors/Committee Members: Vágvölgyiné Tóth, Marietta (advisor).

Subjects/Keywords: Glikogén foszforiláz inhibitor; glükopiranozil

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APA (6th Edition):

Szabó, E. K. (2010). N-[(C-2,3,4,6-Tetra-O-benzoil-B-D-glükopiranozil-metilidén)amino] karboximidamidok szintézise és átalakítási lehetőségeinek vizsgálata 1,2,4-triazol származékokká . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/96468

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):

Szabó, Erzsébet Katalin. “N-[(C-2,3,4,6-Tetra-O-benzoil-B-D-glükopiranozil-metilidén)amino] karboximidamidok szintézise és átalakítási lehetőségeinek vizsgálata 1,2,4-triazol származékokká .” 2010. Thesis, University of Debrecen. Accessed October 30, 2020. http://hdl.handle.net/2437/96468.

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

MLA Handbook (7th Edition):

Szabó, Erzsébet Katalin. “N-[(C-2,3,4,6-Tetra-O-benzoil-B-D-glükopiranozil-metilidén)amino] karboximidamidok szintézise és átalakítási lehetőségeinek vizsgálata 1,2,4-triazol származékokká .” 2010. Web. 30 Oct 2020.

Vancouver:

Szabó EK. N-[(C-2,3,4,6-Tetra-O-benzoil-B-D-glükopiranozil-metilidén)amino] karboximidamidok szintézise és átalakítási lehetőségeinek vizsgálata 1,2,4-triazol származékokká . [Internet] [Thesis]. University of Debrecen; 2010. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/2437/96468.

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

Council of Science Editors:

Szabó EK. N-[(C-2,3,4,6-Tetra-O-benzoil-B-D-glükopiranozil-metilidén)amino] karboximidamidok szintézise és átalakítási lehetőségeinek vizsgálata 1,2,4-triazol származékokká . [Thesis]. University of Debrecen; 2010. Available from: http://hdl.handle.net/2437/96468

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


University of Debrecen

22. Kocsis, Kristóf. A multifunkciós transzglutamináz 2 különböző típusú transzglutamináz aktivitásainak modulálása reverzibilis inhibitorral .

Degree: DE – Gyógyszerésztudományi Kar, University of Debrecen

 A humán transzglutamináz 2 (TG2) számos biológiai folyamatban szerepet játszó multifunkcionális fehérje. A legismertebb a Ca2+-függő transzglutamináz aktivitása, amely transzamidáz, dezamidáz, izopeptidáz típusú katalitikus reakciókat… (more)

Subjects/Keywords: transzglutamináz; inhibitor

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APA (6th Edition):

Kocsis, K. (n.d.). A multifunkciós transzglutamináz 2 különböző típusú transzglutamináz aktivitásainak modulálása reverzibilis inhibitorral . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/251634

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

Chicago Manual of Style (16th Edition):

Kocsis, Kristóf. “A multifunkciós transzglutamináz 2 különböző típusú transzglutamináz aktivitásainak modulálása reverzibilis inhibitorral .” Thesis, University of Debrecen. Accessed October 30, 2020. http://hdl.handle.net/2437/251634.

Note: this citation may be lacking information needed for this citation format:
No year of publication.
Not specified: Masters Thesis or Doctoral Dissertation

MLA Handbook (7th Edition):

Kocsis, Kristóf. “A multifunkciós transzglutamináz 2 különböző típusú transzglutamináz aktivitásainak modulálása reverzibilis inhibitorral .” Web. 30 Oct 2020.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Kocsis K. A multifunkciós transzglutamináz 2 különböző típusú transzglutamináz aktivitásainak modulálása reverzibilis inhibitorral . [Internet] [Thesis]. University of Debrecen; [cited 2020 Oct 30]. Available from: http://hdl.handle.net/2437/251634.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.

Council of Science Editors:

Kocsis K. A multifunkciós transzglutamináz 2 különböző típusú transzglutamináz aktivitásainak modulálása reverzibilis inhibitorral . [Thesis]. University of Debrecen; Available from: http://hdl.handle.net/2437/251634

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No year of publication.


Rice University

23. Zhang, Nan. Interaction of phosphonates onto the immobilized surface: application to scale control in oil and gas flow assurance.

Degree: PhD, Engineering, 2013, Rice University

 The flow assurance in oil and gas production faces several challenges related to scale formation and control. In order to assess scaling risk in pipes,… (more)

Subjects/Keywords: CaCO3; Phosphonates; Scale inhibitor; Alklinity

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APA (6th Edition):

Zhang, N. (2013). Interaction of phosphonates onto the immobilized surface: application to scale control in oil and gas flow assurance. (Doctoral Dissertation). Rice University. Retrieved from http://hdl.handle.net/1911/77600

Chicago Manual of Style (16th Edition):

Zhang, Nan. “Interaction of phosphonates onto the immobilized surface: application to scale control in oil and gas flow assurance.” 2013. Doctoral Dissertation, Rice University. Accessed October 30, 2020. http://hdl.handle.net/1911/77600.

MLA Handbook (7th Edition):

Zhang, Nan. “Interaction of phosphonates onto the immobilized surface: application to scale control in oil and gas flow assurance.” 2013. Web. 30 Oct 2020.

Vancouver:

Zhang N. Interaction of phosphonates onto the immobilized surface: application to scale control in oil and gas flow assurance. [Internet] [Doctoral dissertation]. Rice University; 2013. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/1911/77600.

Council of Science Editors:

Zhang N. Interaction of phosphonates onto the immobilized surface: application to scale control in oil and gas flow assurance. [Doctoral Dissertation]. Rice University; 2013. Available from: http://hdl.handle.net/1911/77600


University of Notre Dame

24. Michael William Handlogten. Design of a Heterobivalent Inhibitor of Allergy and More Physiologically Relevant Allergy Models</h1>.

Degree: Chemical Engineering, 2013, University of Notre Dame

  One of the challenges in current therapies used to treat allergies is the non-specific suppression of the immune system which puts patients at increased… (more)

Subjects/Keywords: Heterobivalent; Inhibitor; Multivalency; Allergy

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APA (6th Edition):

Handlogten, M. W. (2013). Design of a Heterobivalent Inhibitor of Allergy and More Physiologically Relevant Allergy Models</h1>. (Thesis). University of Notre Dame. Retrieved from https://curate.nd.edu/show/1r66j100r5h

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):

Handlogten, Michael William. “Design of a Heterobivalent Inhibitor of Allergy and More Physiologically Relevant Allergy Models</h1>.” 2013. Thesis, University of Notre Dame. Accessed October 30, 2020. https://curate.nd.edu/show/1r66j100r5h.

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

MLA Handbook (7th Edition):

Handlogten, Michael William. “Design of a Heterobivalent Inhibitor of Allergy and More Physiologically Relevant Allergy Models</h1>.” 2013. Web. 30 Oct 2020.

Vancouver:

Handlogten MW. Design of a Heterobivalent Inhibitor of Allergy and More Physiologically Relevant Allergy Models</h1>. [Internet] [Thesis]. University of Notre Dame; 2013. [cited 2020 Oct 30]. Available from: https://curate.nd.edu/show/1r66j100r5h.

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

Council of Science Editors:

Handlogten MW. Design of a Heterobivalent Inhibitor of Allergy and More Physiologically Relevant Allergy Models</h1>. [Thesis]. University of Notre Dame; 2013. Available from: https://curate.nd.edu/show/1r66j100r5h

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


University of Georgia

25. Loeffler, Tamara. The effect of trypsin inhibitors on the nutritional value of various soy products and broiler performance.

Degree: 2014, University of Georgia

 In the United States and most other countries in the world, soybeans and their co-products are a staple in livestock and human diets as a… (more)

Subjects/Keywords: Soybean; Trypsin inhibitor; Broiler

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

APA (6th Edition):

Loeffler, T. (2014). The effect of trypsin inhibitors on the nutritional value of various soy products and broiler performance. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/28036

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):

Loeffler, Tamara. “The effect of trypsin inhibitors on the nutritional value of various soy products and broiler performance.” 2014. Thesis, University of Georgia. Accessed October 30, 2020. http://hdl.handle.net/10724/28036.

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

MLA Handbook (7th Edition):

Loeffler, Tamara. “The effect of trypsin inhibitors on the nutritional value of various soy products and broiler performance.” 2014. Web. 30 Oct 2020.

Vancouver:

Loeffler T. The effect of trypsin inhibitors on the nutritional value of various soy products and broiler performance. [Internet] [Thesis]. University of Georgia; 2014. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/10724/28036.

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

Council of Science Editors:

Loeffler T. The effect of trypsin inhibitors on the nutritional value of various soy products and broiler performance. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/28036

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


University of Canterbury

26. Chen, Hongyuan. Development of macrocyclic β-strand calpain cysteine protease inhibitors.

Degree: PhD, Chemistry, 2011, University of Canterbury

 The work in this thesis reports studies directed to developing a calpain cysteine protease inhibitor that could be of value in slowing cataract development in… (more)

Subjects/Keywords: macrocycle; calpain; inhibitor; strand

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

APA (6th Edition):

Chen, H. (2011). Development of macrocyclic β-strand calpain cysteine protease inhibitors. (Doctoral Dissertation). University of Canterbury. Retrieved from http://dx.doi.org/10.26021/6242

Chicago Manual of Style (16th Edition):

Chen, Hongyuan. “Development of macrocyclic β-strand calpain cysteine protease inhibitors.” 2011. Doctoral Dissertation, University of Canterbury. Accessed October 30, 2020. http://dx.doi.org/10.26021/6242.

MLA Handbook (7th Edition):

Chen, Hongyuan. “Development of macrocyclic β-strand calpain cysteine protease inhibitors.” 2011. Web. 30 Oct 2020.

Vancouver:

Chen H. Development of macrocyclic β-strand calpain cysteine protease inhibitors. [Internet] [Doctoral dissertation]. University of Canterbury; 2011. [cited 2020 Oct 30]. Available from: http://dx.doi.org/10.26021/6242.

Council of Science Editors:

Chen H. Development of macrocyclic β-strand calpain cysteine protease inhibitors. [Doctoral Dissertation]. University of Canterbury; 2011. Available from: http://dx.doi.org/10.26021/6242


University of Manchester

27. Potter, Garrett Thomas. Chemical Synthesis of a Mimetic Heparanase Inhibitor.

Degree: 2015, University of Manchester

 Heparanase (Hpa1) is an enzyme overexpressed in nearly all cancers, typically at the tumour growth front. It cleaves proteoglycan heparan sulfate (HS) chains to release… (more)

Subjects/Keywords: heparanase; heparan sulfate; cancer; inhibitor

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APA (6th Edition):

Potter, G. T. (2015). Chemical Synthesis of a Mimetic Heparanase Inhibitor. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:280892

Chicago Manual of Style (16th Edition):

Potter, Garrett Thomas. “Chemical Synthesis of a Mimetic Heparanase Inhibitor.” 2015. Doctoral Dissertation, University of Manchester. Accessed October 30, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:280892.

MLA Handbook (7th Edition):

Potter, Garrett Thomas. “Chemical Synthesis of a Mimetic Heparanase Inhibitor.” 2015. Web. 30 Oct 2020.

Vancouver:

Potter GT. Chemical Synthesis of a Mimetic Heparanase Inhibitor. [Internet] [Doctoral dissertation]. University of Manchester; 2015. [cited 2020 Oct 30]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:280892.

Council of Science Editors:

Potter GT. Chemical Synthesis of a Mimetic Heparanase Inhibitor. [Doctoral Dissertation]. University of Manchester; 2015. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:280892


University of New South Wales

28. Shrestha, Sudichhya. The Effects of Cholesteryl Ester Transfer Protein Inhibition on High Density Lipoprotein Function.

Degree: Medical Sciences, 2018, University of New South Wales

 Cardiovascular disease affects about 1.4 million Australians and was responsible for more than 45000 deaths in 2011. Compelling evidence from human population studies has shown… (more)

Subjects/Keywords: Cardiovascular; CETP inhibitor; HDL function

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APA (6th Edition):

Shrestha, S. (2018). The Effects of Cholesteryl Ester Transfer Protein Inhibition on High Density Lipoprotein Function. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/59618 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:49119/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Shrestha, Sudichhya. “The Effects of Cholesteryl Ester Transfer Protein Inhibition on High Density Lipoprotein Function.” 2018. Doctoral Dissertation, University of New South Wales. Accessed October 30, 2020. http://handle.unsw.edu.au/1959.4/59618 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:49119/SOURCE02?view=true.

MLA Handbook (7th Edition):

Shrestha, Sudichhya. “The Effects of Cholesteryl Ester Transfer Protein Inhibition on High Density Lipoprotein Function.” 2018. Web. 30 Oct 2020.

Vancouver:

Shrestha S. The Effects of Cholesteryl Ester Transfer Protein Inhibition on High Density Lipoprotein Function. [Internet] [Doctoral dissertation]. University of New South Wales; 2018. [cited 2020 Oct 30]. Available from: http://handle.unsw.edu.au/1959.4/59618 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:49119/SOURCE02?view=true.

Council of Science Editors:

Shrestha S. The Effects of Cholesteryl Ester Transfer Protein Inhibition on High Density Lipoprotein Function. [Doctoral Dissertation]. University of New South Wales; 2018. Available from: http://handle.unsw.edu.au/1959.4/59618 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:49119/SOURCE02?view=true


Vanderbilt University

29. Mrozowski, Roman Michal. Targeting the Ser/Thr protein kinase RSK to reduce breast cancer metastasis.

Degree: PhD, Pathology, 2015, Vanderbilt University

 RSK is a family of four Ser/Thr protein kinases activated by ERK1/2 signaling. RSK is often misregulated in a variety of cancers, including breast and… (more)

Subjects/Keywords: kinase inhibitor; allosteric inhibitor; ribosomal S6 kinase; RSK; cancer metabolism; SL0101

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

APA (6th Edition):

Mrozowski, R. M. (2015). Targeting the Ser/Thr protein kinase RSK to reduce breast cancer metastasis. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/13000

Chicago Manual of Style (16th Edition):

Mrozowski, Roman Michal. “Targeting the Ser/Thr protein kinase RSK to reduce breast cancer metastasis.” 2015. Doctoral Dissertation, Vanderbilt University. Accessed October 30, 2020. http://hdl.handle.net/1803/13000.

MLA Handbook (7th Edition):

Mrozowski, Roman Michal. “Targeting the Ser/Thr protein kinase RSK to reduce breast cancer metastasis.” 2015. Web. 30 Oct 2020.

Vancouver:

Mrozowski RM. Targeting the Ser/Thr protein kinase RSK to reduce breast cancer metastasis. [Internet] [Doctoral dissertation]. Vanderbilt University; 2015. [cited 2020 Oct 30]. Available from: http://hdl.handle.net/1803/13000.

Council of Science Editors:

Mrozowski RM. Targeting the Ser/Thr protein kinase RSK to reduce breast cancer metastasis. [Doctoral Dissertation]. Vanderbilt University; 2015. Available from: http://hdl.handle.net/1803/13000

30. Hofer, Walter. Entwicklung von Inhibitoren für Lipoproteintransporterproteine, Hh-Coaktivatoren und einer γ-selektiven C-Ferrier-Umlagerung.

Degree: 2018, Technische Universität Dortmund

 Krebs zeichnet sich durch eine Fehlregulierung entscheidender Prozesse in der Zelle aus. Eine der prominentesten Vertreter, die zur Deregulierung als Onkogene für wichtige Zellfunktionen wie… (more)

Subjects/Keywords: UNC 119; PDEδ; Inhibitor; Hh-Coaktivator; Vinyloge Ferrier-Umlagerung; 570; Inhibitor

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

APA (6th Edition):

Hofer, W. (2018). Entwicklung von Inhibitoren für Lipoproteintransporterproteine, Hh-Coaktivatoren und einer γ-selektiven C-Ferrier-Umlagerung. (Doctoral Dissertation). Technische Universität Dortmund. Retrieved from http://dx.doi.org/10.17877/DE290R-18929

Chicago Manual of Style (16th Edition):

Hofer, Walter. “Entwicklung von Inhibitoren für Lipoproteintransporterproteine, Hh-Coaktivatoren und einer γ-selektiven C-Ferrier-Umlagerung.” 2018. Doctoral Dissertation, Technische Universität Dortmund. Accessed October 30, 2020. http://dx.doi.org/10.17877/DE290R-18929.

MLA Handbook (7th Edition):

Hofer, Walter. “Entwicklung von Inhibitoren für Lipoproteintransporterproteine, Hh-Coaktivatoren und einer γ-selektiven C-Ferrier-Umlagerung.” 2018. Web. 30 Oct 2020.

Vancouver:

Hofer W. Entwicklung von Inhibitoren für Lipoproteintransporterproteine, Hh-Coaktivatoren und einer γ-selektiven C-Ferrier-Umlagerung. [Internet] [Doctoral dissertation]. Technische Universität Dortmund; 2018. [cited 2020 Oct 30]. Available from: http://dx.doi.org/10.17877/DE290R-18929.

Council of Science Editors:

Hofer W. Entwicklung von Inhibitoren für Lipoproteintransporterproteine, Hh-Coaktivatoren und einer γ-selektiven C-Ferrier-Umlagerung. [Doctoral Dissertation]. Technische Universität Dortmund; 2018. Available from: http://dx.doi.org/10.17877/DE290R-18929

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