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You searched for subject:( allosteric). Showing records 1 – 30 of 214 total matches.

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Texas A&M University

1. Mayorov, Shanna Quinn. Molecular Basis for Allosteric Control of Escherichia Coli Glycerol Kinase by Fructose 1,6-Bisphosphate and IIAglc.

Degree: 2012, Texas A&M University

 There has been progress towards elucidating the mechanism of Escherichia coli glycerol kinase (EcGK) control by its allosteric effectors fructose-1,6-bisphosphate (FBP) and IIAglc (a member… (more)

Subjects/Keywords: Glycerol Kinase; allosteric control; fructose

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APA (6th Edition):

Mayorov, S. Q. (2012). Molecular Basis for Allosteric Control of Escherichia Coli Glycerol Kinase by Fructose 1,6-Bisphosphate and IIAglc. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2011-12-10285

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):

Mayorov, Shanna Quinn. “Molecular Basis for Allosteric Control of Escherichia Coli Glycerol Kinase by Fructose 1,6-Bisphosphate and IIAglc.” 2012. Thesis, Texas A&M University. Accessed December 09, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2011-12-10285.

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

MLA Handbook (7th Edition):

Mayorov, Shanna Quinn. “Molecular Basis for Allosteric Control of Escherichia Coli Glycerol Kinase by Fructose 1,6-Bisphosphate and IIAglc.” 2012. Web. 09 Dec 2019.

Vancouver:

Mayorov SQ. Molecular Basis for Allosteric Control of Escherichia Coli Glycerol Kinase by Fructose 1,6-Bisphosphate and IIAglc. [Internet] [Thesis]. Texas A&M University; 2012. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2011-12-10285.

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

Council of Science Editors:

Mayorov SQ. Molecular Basis for Allosteric Control of Escherichia Coli Glycerol Kinase by Fructose 1,6-Bisphosphate and IIAglc. [Thesis]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2011-12-10285

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


University of Aberdeen

2. Abdelrahman, Mostafa Hamed. Design, synthesis and SAR of novel allosteric modulators of the Cannabinoid CBI receptor.

Degree: 2010, University of Aberdeen

 We report on the design, synthesis, and structure activity relationship studies of novel Org 27569 analogues as potential allosteric modulators of the CB1 receptors. We… (more)

Subjects/Keywords: 615; Cannabinoids : Allosteric regulation

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APA (6th Edition):

Abdelrahman, M. H. (2010). Design, synthesis and SAR of novel allosteric modulators of the Cannabinoid CBI receptor. (Doctoral Dissertation). University of Aberdeen. Retrieved from http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=159203 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.540507

Chicago Manual of Style (16th Edition):

Abdelrahman, Mostafa Hamed. “Design, synthesis and SAR of novel allosteric modulators of the Cannabinoid CBI receptor.” 2010. Doctoral Dissertation, University of Aberdeen. Accessed December 09, 2019. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=159203 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.540507.

MLA Handbook (7th Edition):

Abdelrahman, Mostafa Hamed. “Design, synthesis and SAR of novel allosteric modulators of the Cannabinoid CBI receptor.” 2010. Web. 09 Dec 2019.

Vancouver:

Abdelrahman MH. Design, synthesis and SAR of novel allosteric modulators of the Cannabinoid CBI receptor. [Internet] [Doctoral dissertation]. University of Aberdeen; 2010. [cited 2019 Dec 09]. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=159203 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.540507.

Council of Science Editors:

Abdelrahman MH. Design, synthesis and SAR of novel allosteric modulators of the Cannabinoid CBI receptor. [Doctoral Dissertation]. University of Aberdeen; 2010. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?pid=159203 ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.540507


University of North Carolina – Greensboro

3. Barber, Teresa S. The study of allosteric modulator sites at the cannabinoid CB1 receptor.

Degree: 2011, University of North Carolina – Greensboro

 Org 27569, Org 27759 and Org 29647 are the first discovered allosteric modulators of the cannabinoid CB1 receptor. These ligands are thought to bind to… (more)

Subjects/Keywords: Cannabinoids – Receptors; Allosteric regulation

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APA (6th Edition):

Barber, T. S. (2011). The study of allosteric modulator sites at the cannabinoid CB1 receptor. (Masters Thesis). University of North Carolina – Greensboro. Retrieved from http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=8081

Chicago Manual of Style (16th Edition):

Barber, Teresa S. “The study of allosteric modulator sites at the cannabinoid CB1 receptor.” 2011. Masters Thesis, University of North Carolina – Greensboro. Accessed December 09, 2019. http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=8081.

MLA Handbook (7th Edition):

Barber, Teresa S. “The study of allosteric modulator sites at the cannabinoid CB1 receptor.” 2011. Web. 09 Dec 2019.

Vancouver:

Barber TS. The study of allosteric modulator sites at the cannabinoid CB1 receptor. [Internet] [Masters thesis]. University of North Carolina – Greensboro; 2011. [cited 2019 Dec 09]. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=8081.

Council of Science Editors:

Barber TS. The study of allosteric modulator sites at the cannabinoid CB1 receptor. [Masters Thesis]. University of North Carolina – Greensboro; 2011. Available from: http://libres.uncg.edu/ir/listing.aspx?styp=ti&id=8081


Vanderbilt University

4. Wenthur, Cody James. Development and Characterization of Novel Allosteric Modulators Acting on Metabotropic Glutamate Receptors 2 and 3.

Degree: PhD, Pharmacology, 2015, Vanderbilt University

 The essential roles of glutamatergic signaling in both normal and impaired cognitive functioning have caused metabotropic glutamate (mGlu) receptors to become targets of interest for… (more)

Subjects/Keywords: allosteric; mglu2; mglu3; glutamate; metabotropic

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APA (6th Edition):

Wenthur, C. J. (2015). Development and Characterization of Novel Allosteric Modulators Acting on Metabotropic Glutamate Receptors 2 and 3. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-07102015-131401/ ;

Chicago Manual of Style (16th Edition):

Wenthur, Cody James. “Development and Characterization of Novel Allosteric Modulators Acting on Metabotropic Glutamate Receptors 2 and 3.” 2015. Doctoral Dissertation, Vanderbilt University. Accessed December 09, 2019. http://etd.library.vanderbilt.edu/available/etd-07102015-131401/ ;.

MLA Handbook (7th Edition):

Wenthur, Cody James. “Development and Characterization of Novel Allosteric Modulators Acting on Metabotropic Glutamate Receptors 2 and 3.” 2015. Web. 09 Dec 2019.

Vancouver:

Wenthur CJ. Development and Characterization of Novel Allosteric Modulators Acting on Metabotropic Glutamate Receptors 2 and 3. [Internet] [Doctoral dissertation]. Vanderbilt University; 2015. [cited 2019 Dec 09]. Available from: http://etd.library.vanderbilt.edu/available/etd-07102015-131401/ ;.

Council of Science Editors:

Wenthur CJ. Development and Characterization of Novel Allosteric Modulators Acting on Metabotropic Glutamate Receptors 2 and 3. [Doctoral Dissertation]. Vanderbilt University; 2015. Available from: http://etd.library.vanderbilt.edu/available/etd-07102015-131401/ ;


University of New South Wales

5. Campbell, Adrian. Identification of novel sites of interaction for α1 adrenoceptors.

Degree: Medical Sciences, 2015, University of New South Wales

 α1 adrenoceptors are three of the nine receptors that bind and respond to the hormones adrenaline and noradrenaline. α1 adrenoceptors mediate a number of physiological… (more)

Subjects/Keywords: Allosteric modulator; GPCR; Adrenoceptor

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APA (6th Edition):

Campbell, A. (2015). Identification of novel sites of interaction for α1 adrenoceptors. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/56285 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:40477/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Campbell, Adrian. “Identification of novel sites of interaction for α1 adrenoceptors.” 2015. Doctoral Dissertation, University of New South Wales. Accessed December 09, 2019. http://handle.unsw.edu.au/1959.4/56285 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:40477/SOURCE02?view=true.

MLA Handbook (7th Edition):

Campbell, Adrian. “Identification of novel sites of interaction for α1 adrenoceptors.” 2015. Web. 09 Dec 2019.

Vancouver:

Campbell A. Identification of novel sites of interaction for α1 adrenoceptors. [Internet] [Doctoral dissertation]. University of New South Wales; 2015. [cited 2019 Dec 09]. Available from: http://handle.unsw.edu.au/1959.4/56285 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:40477/SOURCE02?view=true.

Council of Science Editors:

Campbell A. Identification of novel sites of interaction for α1 adrenoceptors. [Doctoral Dissertation]. University of New South Wales; 2015. Available from: http://handle.unsw.edu.au/1959.4/56285 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:40477/SOURCE02?view=true


Penn State University

6. Jayasuriya, Gihan Muthumala. The Allosteric Modulating Effects of Dronedarone on Muscarinic Receptor Subtypes at a Novel Allosteric Binding Site.

Degree: MS, Cell and Molecular Biology, 2013, Penn State University

 This thesis analyzes the allosteric modulating properties of the antiarrhythmic agent dronedarone across muscarinic receptor subtypes. The allosteric effects of dronedarone were examined because of… (more)

Subjects/Keywords: allosteric; muscarinic receptors; receptor pharmacology; orthosteric; amiodarone; dronedarone; allosteric modulators

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APA (6th Edition):

Jayasuriya, G. M. (2013). The Allosteric Modulating Effects of Dronedarone on Muscarinic Receptor Subtypes at a Novel Allosteric Binding Site. (Masters Thesis). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/19919

Chicago Manual of Style (16th Edition):

Jayasuriya, Gihan Muthumala. “The Allosteric Modulating Effects of Dronedarone on Muscarinic Receptor Subtypes at a Novel Allosteric Binding Site.” 2013. Masters Thesis, Penn State University. Accessed December 09, 2019. https://etda.libraries.psu.edu/catalog/19919.

MLA Handbook (7th Edition):

Jayasuriya, Gihan Muthumala. “The Allosteric Modulating Effects of Dronedarone on Muscarinic Receptor Subtypes at a Novel Allosteric Binding Site.” 2013. Web. 09 Dec 2019.

Vancouver:

Jayasuriya GM. The Allosteric Modulating Effects of Dronedarone on Muscarinic Receptor Subtypes at a Novel Allosteric Binding Site. [Internet] [Masters thesis]. Penn State University; 2013. [cited 2019 Dec 09]. Available from: https://etda.libraries.psu.edu/catalog/19919.

Council of Science Editors:

Jayasuriya GM. The Allosteric Modulating Effects of Dronedarone on Muscarinic Receptor Subtypes at a Novel Allosteric Binding Site. [Masters Thesis]. Penn State University; 2013. Available from: https://etda.libraries.psu.edu/catalog/19919


University of California – Santa Cruz

7. Hoobler, Eric Kerstan. Structural and Therapeutic Investigations of Human Lipoxygenase.

Degree: Chemistry, 2013, University of California – Santa Cruz

 The research in this dissertation describes the investigations of potential therapeutics as well as structural and allosteric properties of human lipoxygenases. Lipoxygenases (LOX) are a… (more)

Subjects/Keywords: Biochemistry; allosteric; enzyme; inhibitor; lipoxygenase; pseudoperoxidase; reductive

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APA (6th Edition):

Hoobler, E. K. (2013). Structural and Therapeutic Investigations of Human Lipoxygenase. (Thesis). University of California – Santa Cruz. Retrieved from http://www.escholarship.org/uc/item/34p7m3mg

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):

Hoobler, Eric Kerstan. “Structural and Therapeutic Investigations of Human Lipoxygenase.” 2013. Thesis, University of California – Santa Cruz. Accessed December 09, 2019. http://www.escholarship.org/uc/item/34p7m3mg.

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

MLA Handbook (7th Edition):

Hoobler, Eric Kerstan. “Structural and Therapeutic Investigations of Human Lipoxygenase.” 2013. Web. 09 Dec 2019.

Vancouver:

Hoobler EK. Structural and Therapeutic Investigations of Human Lipoxygenase. [Internet] [Thesis]. University of California – Santa Cruz; 2013. [cited 2019 Dec 09]. Available from: http://www.escholarship.org/uc/item/34p7m3mg.

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

Council of Science Editors:

Hoobler EK. Structural and Therapeutic Investigations of Human Lipoxygenase. [Thesis]. University of California – Santa Cruz; 2013. Available from: http://www.escholarship.org/uc/item/34p7m3mg

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


University of Saskatchewan

8. Kgosisejo, Oarabile. X-RAY CRYSTALLOGRAPHY OF RECOMBINANT LACTOCCOCUS LACTIS PROLIDASE.

Degree: 2015, University of Saskatchewan

 Prolidase has potential applications in cheese debittering, organophosphate detoxification and as an enzyme replacement therapy in prolidase-deficient patients. Recombinant Lactococcus lactis prolidases and their catalytic… (more)

Subjects/Keywords: intersubunit interaction; loop structure; allosteric behaviour; metalloprotease

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APA (6th Edition):

Kgosisejo, O. (2015). X-RAY CRYSTALLOGRAPHY OF RECOMBINANT LACTOCCOCUS LACTIS PROLIDASE. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/ETD-2015-10-2385

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):

Kgosisejo, Oarabile. “X-RAY CRYSTALLOGRAPHY OF RECOMBINANT LACTOCCOCUS LACTIS PROLIDASE.” 2015. Thesis, University of Saskatchewan. Accessed December 09, 2019. http://hdl.handle.net/10388/ETD-2015-10-2385.

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

MLA Handbook (7th Edition):

Kgosisejo, Oarabile. “X-RAY CRYSTALLOGRAPHY OF RECOMBINANT LACTOCCOCUS LACTIS PROLIDASE.” 2015. Web. 09 Dec 2019.

Vancouver:

Kgosisejo O. X-RAY CRYSTALLOGRAPHY OF RECOMBINANT LACTOCCOCUS LACTIS PROLIDASE. [Internet] [Thesis]. University of Saskatchewan; 2015. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/10388/ETD-2015-10-2385.

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

Council of Science Editors:

Kgosisejo O. X-RAY CRYSTALLOGRAPHY OF RECOMBINANT LACTOCCOCUS LACTIS PROLIDASE. [Thesis]. University of Saskatchewan; 2015. Available from: http://hdl.handle.net/10388/ETD-2015-10-2385

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


University of Saskatchewan

9. Hu, Keke. The contributions of S1 site residues to substrate specificity and allosteric behaviour of Lactococcus lactis prolidase.

Degree: 2009, University of Saskatchewan

 Three residues, Phe190, Leu193 and Val302, which have been proposed to define the S1 site of prolidase of Lactococcus lactis NRRL B-1821 (L. lactis prolidase),… (more)

Subjects/Keywords: Allosteric Behaviour; Hydrophobicity; Prolidase; Structure-Function Relationships

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APA (6th Edition):

Hu, K. (2009). The contributions of S1 site residues to substrate specificity and allosteric behaviour of Lactococcus lactis prolidase. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/etd-11132009-111736

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):

Hu, Keke. “The contributions of S1 site residues to substrate specificity and allosteric behaviour of Lactococcus lactis prolidase.” 2009. Thesis, University of Saskatchewan. Accessed December 09, 2019. http://hdl.handle.net/10388/etd-11132009-111736.

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

MLA Handbook (7th Edition):

Hu, Keke. “The contributions of S1 site residues to substrate specificity and allosteric behaviour of Lactococcus lactis prolidase.” 2009. Web. 09 Dec 2019.

Vancouver:

Hu K. The contributions of S1 site residues to substrate specificity and allosteric behaviour of Lactococcus lactis prolidase. [Internet] [Thesis]. University of Saskatchewan; 2009. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/10388/etd-11132009-111736.

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

Council of Science Editors:

Hu K. The contributions of S1 site residues to substrate specificity and allosteric behaviour of Lactococcus lactis prolidase. [Thesis]. University of Saskatchewan; 2009. Available from: http://hdl.handle.net/10388/etd-11132009-111736

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


University of Sydney

10. Alice, Brown. Allosteric Coupling in the Dimeric Calcium Sensing Receptor .

Degree: 2017, University of Sydney

 The Calcium Sensing Receptor (CaSR) is a Class C GPCR that supports systemic calcium homeostasis by sensing and responding to small fluctuations in serum calcium… (more)

Subjects/Keywords: Calcium-sensing receptor; GPCR; allosteric coupling

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APA (6th Edition):

Alice, B. (2017). Allosteric Coupling in the Dimeric Calcium Sensing Receptor . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/17738

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):

Alice, Brown. “Allosteric Coupling in the Dimeric Calcium Sensing Receptor .” 2017. Thesis, University of Sydney. Accessed December 09, 2019. http://hdl.handle.net/2123/17738.

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

MLA Handbook (7th Edition):

Alice, Brown. “Allosteric Coupling in the Dimeric Calcium Sensing Receptor .” 2017. Web. 09 Dec 2019.

Vancouver:

Alice B. Allosteric Coupling in the Dimeric Calcium Sensing Receptor . [Internet] [Thesis]. University of Sydney; 2017. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/2123/17738.

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

Council of Science Editors:

Alice B. Allosteric Coupling in the Dimeric Calcium Sensing Receptor . [Thesis]. University of Sydney; 2017. Available from: http://hdl.handle.net/2123/17738

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


University of Illinois – Chicago

11. Dyer, Norman J. A Molecular Basis for Liquid State Information Processors.

Degree: 2012, University of Illinois – Chicago

 Information processing by excitable neuronal membranes at the molecular level is modeled, intended to serve the study of neuron behaviors resulting from arbitrary patterns of… (more)

Subjects/Keywords: Allosteric modulation; neural networks; binding kinetics; biocomputation

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APA (6th Edition):

Dyer, N. J. (2012). A Molecular Basis for Liquid State Information Processors. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/8649

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):

Dyer, Norman J. “A Molecular Basis for Liquid State Information Processors.” 2012. Thesis, University of Illinois – Chicago. Accessed December 09, 2019. http://hdl.handle.net/10027/8649.

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

MLA Handbook (7th Edition):

Dyer, Norman J. “A Molecular Basis for Liquid State Information Processors.” 2012. Web. 09 Dec 2019.

Vancouver:

Dyer NJ. A Molecular Basis for Liquid State Information Processors. [Internet] [Thesis]. University of Illinois – Chicago; 2012. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/10027/8649.

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

Council of Science Editors:

Dyer NJ. A Molecular Basis for Liquid State Information Processors. [Thesis]. University of Illinois – Chicago; 2012. Available from: http://hdl.handle.net/10027/8649

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


University of Ottawa

12. Blgacim, Nuria. Molecular Control of the δ-opioid Receptor Signaling and Functional Selectivity by Sodium .

Degree: 2018, University of Ottawa

 Accumulating evidence suggests a prominent role of the arrestin-dependent signaling pathway in triggering most of the deleterious side effects observed using δ-OR targeting drugs. Numerous… (more)

Subjects/Keywords: Delta opioid receptor; Sodium cavity; Allosteric modulators

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APA (6th Edition):

Blgacim, N. (2018). Molecular Control of the δ-opioid Receptor Signaling and Functional Selectivity by Sodium . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/37806

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):

Blgacim, Nuria. “Molecular Control of the δ-opioid Receptor Signaling and Functional Selectivity by Sodium .” 2018. Thesis, University of Ottawa. Accessed December 09, 2019. http://hdl.handle.net/10393/37806.

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

MLA Handbook (7th Edition):

Blgacim, Nuria. “Molecular Control of the δ-opioid Receptor Signaling and Functional Selectivity by Sodium .” 2018. Web. 09 Dec 2019.

Vancouver:

Blgacim N. Molecular Control of the δ-opioid Receptor Signaling and Functional Selectivity by Sodium . [Internet] [Thesis]. University of Ottawa; 2018. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/10393/37806.

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

Council of Science Editors:

Blgacim N. Molecular Control of the δ-opioid Receptor Signaling and Functional Selectivity by Sodium . [Thesis]. University of Ottawa; 2018. Available from: http://hdl.handle.net/10393/37806

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


University of Aberdeen

13. Abdelrahman, Mostafa Hamed. Design, synthesis and SAR of novel allosteric modulators of the Cannabinoid CBI receptor.

Degree: Dept. of Chemistry., 2010, University of Aberdeen

Subjects/Keywords: Cannabinoids; Allosteric regulation.

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APA (6th Edition):

Abdelrahman, M. H. (2010). Design, synthesis and SAR of novel allosteric modulators of the Cannabinoid CBI receptor. (Doctoral Dissertation). University of Aberdeen. Retrieved from http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=159203 ; http://digitool2.abdn.ac.uk:1801/webclient/DeliveryManager?pid=159203&custom_att_2=simple_viewer

Chicago Manual of Style (16th Edition):

Abdelrahman, Mostafa Hamed. “Design, synthesis and SAR of novel allosteric modulators of the Cannabinoid CBI receptor.” 2010. Doctoral Dissertation, University of Aberdeen. Accessed December 09, 2019. http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=159203 ; http://digitool2.abdn.ac.uk:1801/webclient/DeliveryManager?pid=159203&custom_att_2=simple_viewer.

MLA Handbook (7th Edition):

Abdelrahman, Mostafa Hamed. “Design, synthesis and SAR of novel allosteric modulators of the Cannabinoid CBI receptor.” 2010. Web. 09 Dec 2019.

Vancouver:

Abdelrahman MH. Design, synthesis and SAR of novel allosteric modulators of the Cannabinoid CBI receptor. [Internet] [Doctoral dissertation]. University of Aberdeen; 2010. [cited 2019 Dec 09]. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=159203 ; http://digitool2.abdn.ac.uk:1801/webclient/DeliveryManager?pid=159203&custom_att_2=simple_viewer.

Council of Science Editors:

Abdelrahman MH. Design, synthesis and SAR of novel allosteric modulators of the Cannabinoid CBI receptor. [Doctoral Dissertation]. University of Aberdeen; 2010. Available from: http://digitool.abdn.ac.uk:80/webclient/DeliveryManager?application=DIGITOOL-3&owner=resourcediscovery&custom_att_2=simple_viewer&pid=159203 ; http://digitool2.abdn.ac.uk:1801/webclient/DeliveryManager?pid=159203&custom_att_2=simple_viewer


University of Cambridge

14. Mitchell, Sophie Lousie. A fragment-based drug discovery approach for the development of selective inhibitors of protein kinase CK2.

Degree: PhD, 2018, University of Cambridge

 Over the last twenty years, fragment-based drug discovery (FBDD) has emerged as a highly successful way to provide lead compounds for subsequent optimisation into drug… (more)

Subjects/Keywords: CK2; fragment; allosteric; inhibitor; FBDD; SBDD; kinase

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APA (6th Edition):

Mitchell, S. L. (2018). A fragment-based drug discovery approach for the development of selective inhibitors of protein kinase CK2. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/278650 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.753402

Chicago Manual of Style (16th Edition):

Mitchell, Sophie Lousie. “A fragment-based drug discovery approach for the development of selective inhibitors of protein kinase CK2.” 2018. Doctoral Dissertation, University of Cambridge. Accessed December 09, 2019. https://www.repository.cam.ac.uk/handle/1810/278650 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.753402.

MLA Handbook (7th Edition):

Mitchell, Sophie Lousie. “A fragment-based drug discovery approach for the development of selective inhibitors of protein kinase CK2.” 2018. Web. 09 Dec 2019.

Vancouver:

Mitchell SL. A fragment-based drug discovery approach for the development of selective inhibitors of protein kinase CK2. [Internet] [Doctoral dissertation]. University of Cambridge; 2018. [cited 2019 Dec 09]. Available from: https://www.repository.cam.ac.uk/handle/1810/278650 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.753402.

Council of Science Editors:

Mitchell SL. A fragment-based drug discovery approach for the development of selective inhibitors of protein kinase CK2. [Doctoral Dissertation]. University of Cambridge; 2018. Available from: https://www.repository.cam.ac.uk/handle/1810/278650 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.753402


Columbia University

15. Xu, Yunyao. Studies of Allostery in the Potassium Channel Kcsa by Solid-state NMR.

Degree: 2018, Columbia University

 In this thesis, I focus on studies of the mechanism of inactivation in KcsA. Allosteric coupling between the pH gate and the selectivity filter in… (more)

Subjects/Keywords: Biophysics; Chemistry; Potassium channels; Allosteric regulation

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APA (6th Edition):

Xu, Y. (2018). Studies of Allostery in the Potassium Channel Kcsa by Solid-state NMR. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8BV908R

Chicago Manual of Style (16th Edition):

Xu, Yunyao. “Studies of Allostery in the Potassium Channel Kcsa by Solid-state NMR.” 2018. Doctoral Dissertation, Columbia University. Accessed December 09, 2019. https://doi.org/10.7916/D8BV908R.

MLA Handbook (7th Edition):

Xu, Yunyao. “Studies of Allostery in the Potassium Channel Kcsa by Solid-state NMR.” 2018. Web. 09 Dec 2019.

Vancouver:

Xu Y. Studies of Allostery in the Potassium Channel Kcsa by Solid-state NMR. [Internet] [Doctoral dissertation]. Columbia University; 2018. [cited 2019 Dec 09]. Available from: https://doi.org/10.7916/D8BV908R.

Council of Science Editors:

Xu Y. Studies of Allostery in the Potassium Channel Kcsa by Solid-state NMR. [Doctoral Dissertation]. Columbia University; 2018. Available from: https://doi.org/10.7916/D8BV908R


Vanderbilt University

16. Shirey-Rice, Jana Kristin. M1 and M4 Muscarinic Acetylcholine Receptor Regulation of Neurotransmission and Cell Excitability in Rodent Hippocampus and Prefrontal Cortex.

Degree: PhD, Pharmacology, 2010, Vanderbilt University

 Muscarinic acetylcholine receptors (mAChRs), specifically M1 and M4 subtypes, provide viable targets for the treatment of multiple central nervous system disorders. However, highly selective activators… (more)

Subjects/Keywords: Muscarinic; allosteric; GPCR; Alzheimer's disease; schizophrenia

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APA (6th Edition):

Shirey-Rice, J. K. (2010). M1 and M4 Muscarinic Acetylcholine Receptor Regulation of Neurotransmission and Cell Excitability in Rodent Hippocampus and Prefrontal Cortex. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-03312010-095129/ ;

Chicago Manual of Style (16th Edition):

Shirey-Rice, Jana Kristin. “M1 and M4 Muscarinic Acetylcholine Receptor Regulation of Neurotransmission and Cell Excitability in Rodent Hippocampus and Prefrontal Cortex.” 2010. Doctoral Dissertation, Vanderbilt University. Accessed December 09, 2019. http://etd.library.vanderbilt.edu/available/etd-03312010-095129/ ;.

MLA Handbook (7th Edition):

Shirey-Rice, Jana Kristin. “M1 and M4 Muscarinic Acetylcholine Receptor Regulation of Neurotransmission and Cell Excitability in Rodent Hippocampus and Prefrontal Cortex.” 2010. Web. 09 Dec 2019.

Vancouver:

Shirey-Rice JK. M1 and M4 Muscarinic Acetylcholine Receptor Regulation of Neurotransmission and Cell Excitability in Rodent Hippocampus and Prefrontal Cortex. [Internet] [Doctoral dissertation]. Vanderbilt University; 2010. [cited 2019 Dec 09]. Available from: http://etd.library.vanderbilt.edu/available/etd-03312010-095129/ ;.

Council of Science Editors:

Shirey-Rice JK. M1 and M4 Muscarinic Acetylcholine Receptor Regulation of Neurotransmission and Cell Excitability in Rodent Hippocampus and Prefrontal Cortex. [Doctoral Dissertation]. Vanderbilt University; 2010. Available from: http://etd.library.vanderbilt.edu/available/etd-03312010-095129/ ;


Vanderbilt University

17. Yin, Shen. Allosteric modulation of metabotropic glutamate receptors.

Degree: PhD, Pharmacology, 2013, Vanderbilt University

 Metabotropic glutamate receptors (mGlus) are a group of Family C Seven Transmembrane Spanning Receptors that play important roles in modulating signaling transduction, particularly within the… (more)

Subjects/Keywords: heterodimerization; functional selectivity; pharmacology; allosteric modulators; mGlu

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APA (6th Edition):

Yin, S. (2013). Allosteric modulation of metabotropic glutamate receptors. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu//available/etd-11262013-230503/ ;

Chicago Manual of Style (16th Edition):

Yin, Shen. “Allosteric modulation of metabotropic glutamate receptors.” 2013. Doctoral Dissertation, Vanderbilt University. Accessed December 09, 2019. http://etd.library.vanderbilt.edu//available/etd-11262013-230503/ ;.

MLA Handbook (7th Edition):

Yin, Shen. “Allosteric modulation of metabotropic glutamate receptors.” 2013. Web. 09 Dec 2019.

Vancouver:

Yin S. Allosteric modulation of metabotropic glutamate receptors. [Internet] [Doctoral dissertation]. Vanderbilt University; 2013. [cited 2019 Dec 09]. Available from: http://etd.library.vanderbilt.edu//available/etd-11262013-230503/ ;.

Council of Science Editors:

Yin S. Allosteric modulation of metabotropic glutamate receptors. [Doctoral Dissertation]. Vanderbilt University; 2013. Available from: http://etd.library.vanderbilt.edu//available/etd-11262013-230503/ ;


Brandeis University

18. Zheng, Yuejiao. Using ancestral proteins to unravel the molecular mechanism and druggability of Aurora A kinase.

Degree: 2016, Brandeis University

 Overexpression of Aurora A, a Ser/Thr kinase, underlies many human cancers. Aurora A’s activity is regulated by phosphorylation on the activation segment and/or binding of… (more)

Subjects/Keywords: Aurora A; TPX2; Kinase; Allosteric Activation

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

APA (6th Edition):

Zheng, Y. (2016). Using ancestral proteins to unravel the molecular mechanism and druggability of Aurora A kinase. (Thesis). Brandeis University. Retrieved from http://hdl.handle.net/10192/32319

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

Chicago Manual of Style (16th Edition):

Zheng, Yuejiao. “Using ancestral proteins to unravel the molecular mechanism and druggability of Aurora A kinase.” 2016. Thesis, Brandeis University. Accessed December 09, 2019. http://hdl.handle.net/10192/32319.

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

MLA Handbook (7th Edition):

Zheng, Yuejiao. “Using ancestral proteins to unravel the molecular mechanism and druggability of Aurora A kinase.” 2016. Web. 09 Dec 2019.

Vancouver:

Zheng Y. Using ancestral proteins to unravel the molecular mechanism and druggability of Aurora A kinase. [Internet] [Thesis]. Brandeis University; 2016. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/10192/32319.

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

Council of Science Editors:

Zheng Y. Using ancestral proteins to unravel the molecular mechanism and druggability of Aurora A kinase. [Thesis]. Brandeis University; 2016. Available from: http://hdl.handle.net/10192/32319

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


University of Wollongong

19. Jin, Tiantian. Investigation of lupane triterpene as a novel PTP1B allosteric inhibitor for the improvement of neurite outgrowth and synaptogenesis.

Degree: PhD, 2016, University of Wollongong

  An impaired synaptogenesis is known to be a common neuropathology in a number of severe mental disorders including schizophrenia, Parkinson disease, bipolar and dementia.… (more)

Subjects/Keywords: PTP1B; lupane triterpenes; allosteric inhibition; neurite outgrowth

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APA (6th Edition):

Jin, T. (2016). Investigation of lupane triterpene as a novel PTP1B allosteric inhibitor for the improvement of neurite outgrowth and synaptogenesis. (Doctoral Dissertation). University of Wollongong. Retrieved from 0601 BIOCHEMISTRY AND CELL BIOLOGY, 1109 NEUROSCIENCES, 060105 Cell Neurochemistry, 110903 Central Nervous System ; https://ro.uow.edu.au/theses/4931

Chicago Manual of Style (16th Edition):

Jin, Tiantian. “Investigation of lupane triterpene as a novel PTP1B allosteric inhibitor for the improvement of neurite outgrowth and synaptogenesis.” 2016. Doctoral Dissertation, University of Wollongong. Accessed December 09, 2019. 0601 BIOCHEMISTRY AND CELL BIOLOGY, 1109 NEUROSCIENCES, 060105 Cell Neurochemistry, 110903 Central Nervous System ; https://ro.uow.edu.au/theses/4931.

MLA Handbook (7th Edition):

Jin, Tiantian. “Investigation of lupane triterpene as a novel PTP1B allosteric inhibitor for the improvement of neurite outgrowth and synaptogenesis.” 2016. Web. 09 Dec 2019.

Vancouver:

Jin T. Investigation of lupane triterpene as a novel PTP1B allosteric inhibitor for the improvement of neurite outgrowth and synaptogenesis. [Internet] [Doctoral dissertation]. University of Wollongong; 2016. [cited 2019 Dec 09]. Available from: 0601 BIOCHEMISTRY AND CELL BIOLOGY, 1109 NEUROSCIENCES, 060105 Cell Neurochemistry, 110903 Central Nervous System ; https://ro.uow.edu.au/theses/4931.

Council of Science Editors:

Jin T. Investigation of lupane triterpene as a novel PTP1B allosteric inhibitor for the improvement of neurite outgrowth and synaptogenesis. [Doctoral Dissertation]. University of Wollongong; 2016. Available from: 0601 BIOCHEMISTRY AND CELL BIOLOGY, 1109 NEUROSCIENCES, 060105 Cell Neurochemistry, 110903 Central Nervous System ; https://ro.uow.edu.au/theses/4931


Boston College

20. Zheng, Yunan. Study of Allosteric Regulation of Escherichia coli Aspartate Transcarbamoylase.

Degree: MS, Chemistry, 2013, Boston College

 For nearly 60 years the ATP activation and the CTP inhibition of Escherichia coli aspartate transcarbamoylase (ATCase) has been the textbook example of allosteric regulation.… (more)

Subjects/Keywords: Allosteric Regulation; Aspartate Transcarbamylase; X-ray Crystallography

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APA (6th Edition):

Zheng, Y. (2013). Study of Allosteric Regulation of Escherichia coli Aspartate Transcarbamoylase. (Masters Thesis). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:101681

Chicago Manual of Style (16th Edition):

Zheng, Yunan. “Study of Allosteric Regulation of Escherichia coli Aspartate Transcarbamoylase.” 2013. Masters Thesis, Boston College. Accessed December 09, 2019. http://dlib.bc.edu/islandora/object/bc-ir:101681.

MLA Handbook (7th Edition):

Zheng, Yunan. “Study of Allosteric Regulation of Escherichia coli Aspartate Transcarbamoylase.” 2013. Web. 09 Dec 2019.

Vancouver:

Zheng Y. Study of Allosteric Regulation of Escherichia coli Aspartate Transcarbamoylase. [Internet] [Masters thesis]. Boston College; 2013. [cited 2019 Dec 09]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101681.

Council of Science Editors:

Zheng Y. Study of Allosteric Regulation of Escherichia coli Aspartate Transcarbamoylase. [Masters Thesis]. Boston College; 2013. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101681


Boston College

21. West, Jay M. Probing the Mechanism of the Allosteric Transition of Aspartate Transcarbamoylase via Fluorescence, Physical Entrapment, and Small-Angle X-Ray Scattering.

Degree: PhD, Chemistry, 2009, Boston College

 The regulatory mechanism of allostery is exhibited by certain proteins such as Escherichia coli aspartate transcarbamoylase (ATCase), and is defined as the change in shape… (more)

Subjects/Keywords: allosteric enzyme; aspartate transcarbamoylase; protein structure-function

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APA (6th Edition):

West, J. M. (2009). Probing the Mechanism of the Allosteric Transition of Aspartate Transcarbamoylase via Fluorescence, Physical Entrapment, and Small-Angle X-Ray Scattering. (Doctoral Dissertation). Boston College. Retrieved from http://dlib.bc.edu/islandora/object/bc-ir:101518

Chicago Manual of Style (16th Edition):

West, Jay M. “Probing the Mechanism of the Allosteric Transition of Aspartate Transcarbamoylase via Fluorescence, Physical Entrapment, and Small-Angle X-Ray Scattering.” 2009. Doctoral Dissertation, Boston College. Accessed December 09, 2019. http://dlib.bc.edu/islandora/object/bc-ir:101518.

MLA Handbook (7th Edition):

West, Jay M. “Probing the Mechanism of the Allosteric Transition of Aspartate Transcarbamoylase via Fluorescence, Physical Entrapment, and Small-Angle X-Ray Scattering.” 2009. Web. 09 Dec 2019.

Vancouver:

West JM. Probing the Mechanism of the Allosteric Transition of Aspartate Transcarbamoylase via Fluorescence, Physical Entrapment, and Small-Angle X-Ray Scattering. [Internet] [Doctoral dissertation]. Boston College; 2009. [cited 2019 Dec 09]. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101518.

Council of Science Editors:

West JM. Probing the Mechanism of the Allosteric Transition of Aspartate Transcarbamoylase via Fluorescence, Physical Entrapment, and Small-Angle X-Ray Scattering. [Doctoral Dissertation]. Boston College; 2009. Available from: http://dlib.bc.edu/islandora/object/bc-ir:101518


Northeastern University

22. Kulkarni, Abhijit Raghunath. Novel allosteric modulators of α7 nicotinic acetylcholine receptor and development of efficient methodologies enabling synthesis of tetrahydroquinolines and unsymmetrical ureas.

Degree: PhD, School of Pharmacy, 2016, Northeastern University

 This thesis work encompasses the design, synthesis, and profiling of novel ligands (modulators) binding to an important molecular target, α7 nicotinic acetylcholine receptor (nAChR), which… (more)

Subjects/Keywords: allosteric; alpha7; cannabinoid; methodology; modulators; nicotinic

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APA (6th Edition):

Kulkarni, A. R. (2016). Novel allosteric modulators of α7 nicotinic acetylcholine receptor and development of efficient methodologies enabling synthesis of tetrahydroquinolines and unsymmetrical ureas. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/D20237784

Chicago Manual of Style (16th Edition):

Kulkarni, Abhijit Raghunath. “Novel allosteric modulators of α7 nicotinic acetylcholine receptor and development of efficient methodologies enabling synthesis of tetrahydroquinolines and unsymmetrical ureas.” 2016. Doctoral Dissertation, Northeastern University. Accessed December 09, 2019. http://hdl.handle.net/2047/D20237784.

MLA Handbook (7th Edition):

Kulkarni, Abhijit Raghunath. “Novel allosteric modulators of α7 nicotinic acetylcholine receptor and development of efficient methodologies enabling synthesis of tetrahydroquinolines and unsymmetrical ureas.” 2016. Web. 09 Dec 2019.

Vancouver:

Kulkarni AR. Novel allosteric modulators of α7 nicotinic acetylcholine receptor and development of efficient methodologies enabling synthesis of tetrahydroquinolines and unsymmetrical ureas. [Internet] [Doctoral dissertation]. Northeastern University; 2016. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/2047/D20237784.

Council of Science Editors:

Kulkarni AR. Novel allosteric modulators of α7 nicotinic acetylcholine receptor and development of efficient methodologies enabling synthesis of tetrahydroquinolines and unsymmetrical ureas. [Doctoral Dissertation]. Northeastern University; 2016. Available from: http://hdl.handle.net/2047/D20237784


Drexel University

23. Liu, Xiaonan. Pharmacological Study of KM822 Analogs: A Novel Class of Dopamine Transporter Inhibitors.

Degree: 2018, Drexel University

The dopamine transporter (DAT) is a membrane protein that is responsible for the reuptake of dopamine back into the presynaptic neurons. DAT has been investigated… (more)

Subjects/Keywords: Pharmacology; Physiology; Neurotransmitters; Allosteric regulation; Dopamine

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APA (6th Edition):

Liu, X. (2018). Pharmacological Study of KM822 Analogs: A Novel Class of Dopamine Transporter Inhibitors. (Thesis). Drexel University. Retrieved from https://idea.library.drexel.edu/islandora/object/idea%3A8125

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):

Liu, Xiaonan. “Pharmacological Study of KM822 Analogs: A Novel Class of Dopamine Transporter Inhibitors.” 2018. Thesis, Drexel University. Accessed December 09, 2019. https://idea.library.drexel.edu/islandora/object/idea%3A8125.

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

MLA Handbook (7th Edition):

Liu, Xiaonan. “Pharmacological Study of KM822 Analogs: A Novel Class of Dopamine Transporter Inhibitors.” 2018. Web. 09 Dec 2019.

Vancouver:

Liu X. Pharmacological Study of KM822 Analogs: A Novel Class of Dopamine Transporter Inhibitors. [Internet] [Thesis]. Drexel University; 2018. [cited 2019 Dec 09]. Available from: https://idea.library.drexel.edu/islandora/object/idea%3A8125.

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

Council of Science Editors:

Liu X. Pharmacological Study of KM822 Analogs: A Novel Class of Dopamine Transporter Inhibitors. [Thesis]. Drexel University; 2018. Available from: https://idea.library.drexel.edu/islandora/object/idea%3A8125

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


Princeton University

24. Song, Yonghyun. DYNAMIC CONTROL OF DNA PRECURSOR SYNTHESIS IN EARLY EMBRYOS .

Degree: PhD, 2017, Princeton University

 Animal embryogenesis starts with multiple rounds of nuclear divisions. During and shortly after these divisions, the zygotic genome is activated, the body plan of the… (more)

Subjects/Keywords: allosteric regulation; dNTP metabolism; ribonucleotide reductase

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APA (6th Edition):

Song, Y. (2017). DYNAMIC CONTROL OF DNA PRECURSOR SYNTHESIS IN EARLY EMBRYOS . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp014x51hm675

Chicago Manual of Style (16th Edition):

Song, Yonghyun. “DYNAMIC CONTROL OF DNA PRECURSOR SYNTHESIS IN EARLY EMBRYOS .” 2017. Doctoral Dissertation, Princeton University. Accessed December 09, 2019. http://arks.princeton.edu/ark:/88435/dsp014x51hm675.

MLA Handbook (7th Edition):

Song, Yonghyun. “DYNAMIC CONTROL OF DNA PRECURSOR SYNTHESIS IN EARLY EMBRYOS .” 2017. Web. 09 Dec 2019.

Vancouver:

Song Y. DYNAMIC CONTROL OF DNA PRECURSOR SYNTHESIS IN EARLY EMBRYOS . [Internet] [Doctoral dissertation]. Princeton University; 2017. [cited 2019 Dec 09]. Available from: http://arks.princeton.edu/ark:/88435/dsp014x51hm675.

Council of Science Editors:

Song Y. DYNAMIC CONTROL OF DNA PRECURSOR SYNTHESIS IN EARLY EMBRYOS . [Doctoral Dissertation]. Princeton University; 2017. Available from: http://arks.princeton.edu/ark:/88435/dsp014x51hm675


Michigan State University

25. Howart, Michael. Analysis of water ligands within the allosteric forms of phenylalanine hydroxylase.

Degree: 2013, Michigan State University

Thesis Ph. D. Michigan State University. Chemistry 2013.

     Phenylalanine Hydroxylase (PheH) is a liver enzyme that catalyzes the conversion of L- phenylalnine to L-tyrosine using… (more)

Subjects/Keywords: Allosteric enzymes – Analysis; Ligands (Biochemistry) – Analysis; Chemistry

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APA (6th Edition):

Howart, M. (2013). Analysis of water ligands within the allosteric forms of phenylalanine hydroxylase. (Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:2240

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):

Howart, Michael. “Analysis of water ligands within the allosteric forms of phenylalanine hydroxylase.” 2013. Thesis, Michigan State University. Accessed December 09, 2019. http://etd.lib.msu.edu/islandora/object/etd:2240.

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

MLA Handbook (7th Edition):

Howart, Michael. “Analysis of water ligands within the allosteric forms of phenylalanine hydroxylase.” 2013. Web. 09 Dec 2019.

Vancouver:

Howart M. Analysis of water ligands within the allosteric forms of phenylalanine hydroxylase. [Internet] [Thesis]. Michigan State University; 2013. [cited 2019 Dec 09]. Available from: http://etd.lib.msu.edu/islandora/object/etd:2240.

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

Council of Science Editors:

Howart M. Analysis of water ligands within the allosteric forms of phenylalanine hydroxylase. [Thesis]. Michigan State University; 2013. Available from: http://etd.lib.msu.edu/islandora/object/etd:2240

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


University of Canterbury

26. Huisman, Frances Helen Adam. Studies into the allosteric regulation of α-isopropylmalate synthase.

Degree: Chemistry Department, 2012, University of Canterbury

 α-Isopropylmalate synthase (α-IPMS) catalyses the first committed step in leucine biosynthesis in bacteria, including Neisseria meningitidis and Mycobacterium tuberculosis. It catalyses the condensation of α-ketoisovalerate… (more)

Subjects/Keywords: α-Isopropylmalate synthase; α-IPMS; LeuA; allosteric regulation; allosteric inhibition; regulatory domain; leucine; enzyme

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APA (6th Edition):

Huisman, F. H. A. (2012). Studies into the allosteric regulation of α-isopropylmalate synthase. (Thesis). University of Canterbury. Retrieved from http://hdl.handle.net/10092/7599

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):

Huisman, Frances Helen Adam. “Studies into the allosteric regulation of α-isopropylmalate synthase.” 2012. Thesis, University of Canterbury. Accessed December 09, 2019. http://hdl.handle.net/10092/7599.

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

MLA Handbook (7th Edition):

Huisman, Frances Helen Adam. “Studies into the allosteric regulation of α-isopropylmalate synthase.” 2012. Web. 09 Dec 2019.

Vancouver:

Huisman FHA. Studies into the allosteric regulation of α-isopropylmalate synthase. [Internet] [Thesis]. University of Canterbury; 2012. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/10092/7599.

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

Council of Science Editors:

Huisman FHA. Studies into the allosteric regulation of α-isopropylmalate synthase. [Thesis]. University of Canterbury; 2012. Available from: http://hdl.handle.net/10092/7599

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


ETH Zürich

27. Buffing, Marieke Francisca. In Vivo and in Vitro Identifcation of Allosteric Enzyme Regulation by Metabolites.

Degree: 2018, ETH Zürich

 Microorganisms can thrive in a plethora of environmental niches. Not only are their environments diverse, they are also ever-changing. Since proliferation depends on a microorganism’s… (more)

Subjects/Keywords: mass spectrometry; BACILLUS (MICROBIOLOGY); Escherichia coli (E. coli); ALLOSTERIC ENZYMES + ALLOSTERIC PROTEINS; metabolomics; transcriptional regulation

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

APA (6th Edition):

Buffing, M. F. (2018). In Vivo and in Vitro Identifcation of Allosteric Enzyme Regulation by Metabolites. (Doctoral Dissertation). ETH Zürich. Retrieved from http://hdl.handle.net/20.500.11850/355004

Chicago Manual of Style (16th Edition):

Buffing, Marieke Francisca. “In Vivo and in Vitro Identifcation of Allosteric Enzyme Regulation by Metabolites.” 2018. Doctoral Dissertation, ETH Zürich. Accessed December 09, 2019. http://hdl.handle.net/20.500.11850/355004.

MLA Handbook (7th Edition):

Buffing, Marieke Francisca. “In Vivo and in Vitro Identifcation of Allosteric Enzyme Regulation by Metabolites.” 2018. Web. 09 Dec 2019.

Vancouver:

Buffing MF. In Vivo and in Vitro Identifcation of Allosteric Enzyme Regulation by Metabolites. [Internet] [Doctoral dissertation]. ETH Zürich; 2018. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/20.500.11850/355004.

Council of Science Editors:

Buffing MF. In Vivo and in Vitro Identifcation of Allosteric Enzyme Regulation by Metabolites. [Doctoral Dissertation]. ETH Zürich; 2018. Available from: http://hdl.handle.net/20.500.11850/355004


Northeastern University

28. Ranade, Ameya V. Design and synthesis of positive allosteric modulators of CB1 cannabinoid receptor.

Degree: MS, School of Pharmacy, 2014, Northeastern University

 The endocannabinoid system which consists of CB1 and CB2 receptors that belong to type A GPCRs, endogenous cannabinoids (endocannabinoids) and enzyme machinery involved in their… (more)

Subjects/Keywords: allosteric; CB1; endocannabinoid; Cannabinoids; Receptors; Therapeutic use; Allosteric regulation; Carbazole; Synthesis; Ligands (Biochemistry); Arrestins

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

APA (6th Edition):

Ranade, A. V. (2014). Design and synthesis of positive allosteric modulators of CB1 cannabinoid receptor. (Masters Thesis). Northeastern University. Retrieved from http://hdl.handle.net/2047/D20198049

Chicago Manual of Style (16th Edition):

Ranade, Ameya V. “Design and synthesis of positive allosteric modulators of CB1 cannabinoid receptor.” 2014. Masters Thesis, Northeastern University. Accessed December 09, 2019. http://hdl.handle.net/2047/D20198049.

MLA Handbook (7th Edition):

Ranade, Ameya V. “Design and synthesis of positive allosteric modulators of CB1 cannabinoid receptor.” 2014. Web. 09 Dec 2019.

Vancouver:

Ranade AV. Design and synthesis of positive allosteric modulators of CB1 cannabinoid receptor. [Internet] [Masters thesis]. Northeastern University; 2014. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/2047/D20198049.

Council of Science Editors:

Ranade AV. Design and synthesis of positive allosteric modulators of CB1 cannabinoid receptor. [Masters Thesis]. Northeastern University; 2014. Available from: http://hdl.handle.net/2047/D20198049


Virginia Commonwealth University

29. Alwassil, Osama. Small Molecules as Negative Allosteric Modulators of Alpha7 nAChRs.

Degree: MS, Pharmaceutical Sciences, 2012, Virginia Commonwealth University

 Alpha7 Neuronal nicotinic acetylcholine receptors (nAChRs) are involved in essential physiological functions and play a role in disorders such as Alzheimer’s disease. MD-354 (3-chlorophenylguanidine; 21),… (more)

Subjects/Keywords: Small Molecules; Negative Allosteric Modulators; NAM; nAChRs; Allosteric Modulators; Alpha7; Medicine and Health Sciences; Pharmacy and Pharmaceutical Sciences

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

APA (6th Edition):

Alwassil, O. (2012). Small Molecules as Negative Allosteric Modulators of Alpha7 nAChRs. (Thesis). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/2829

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):

Alwassil, Osama. “Small Molecules as Negative Allosteric Modulators of Alpha7 nAChRs.” 2012. Thesis, Virginia Commonwealth University. Accessed December 09, 2019. https://scholarscompass.vcu.edu/etd/2829.

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

MLA Handbook (7th Edition):

Alwassil, Osama. “Small Molecules as Negative Allosteric Modulators of Alpha7 nAChRs.” 2012. Web. 09 Dec 2019.

Vancouver:

Alwassil O. Small Molecules as Negative Allosteric Modulators of Alpha7 nAChRs. [Internet] [Thesis]. Virginia Commonwealth University; 2012. [cited 2019 Dec 09]. Available from: https://scholarscompass.vcu.edu/etd/2829.

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

Council of Science Editors:

Alwassil O. Small Molecules as Negative Allosteric Modulators of Alpha7 nAChRs. [Thesis]. Virginia Commonwealth University; 2012. Available from: https://scholarscompass.vcu.edu/etd/2829

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


Northeastern University

30. Johnson, Christian William. Allosteric communication in the activity of Ras GTPases.

Degree: PhD, Department of Chemistry and Chemical Biology, 2016, Northeastern University

 H-, N-, K-Ras are closely related (95% conserved) membrane associated hub proteins that act in a variety of signal transduction pathways, including cellular proliferation and… (more)

Subjects/Keywords: cancer; GTPases; protein allostery; protein crystallography; Ras; Allosteric proteins; Ras proteins; Structure; Guanosine triphosphatase; Allosteric regulation; Crystallography; Enzyme kinetics

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

APA (6th Edition):

Johnson, C. W. (2016). Allosteric communication in the activity of Ras GTPases. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/D20199679

Chicago Manual of Style (16th Edition):

Johnson, Christian William. “Allosteric communication in the activity of Ras GTPases.” 2016. Doctoral Dissertation, Northeastern University. Accessed December 09, 2019. http://hdl.handle.net/2047/D20199679.

MLA Handbook (7th Edition):

Johnson, Christian William. “Allosteric communication in the activity of Ras GTPases.” 2016. Web. 09 Dec 2019.

Vancouver:

Johnson CW. Allosteric communication in the activity of Ras GTPases. [Internet] [Doctoral dissertation]. Northeastern University; 2016. [cited 2019 Dec 09]. Available from: http://hdl.handle.net/2047/D20199679.

Council of Science Editors:

Johnson CW. Allosteric communication in the activity of Ras GTPases. [Doctoral Dissertation]. Northeastern University; 2016. Available from: http://hdl.handle.net/2047/D20199679

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