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You searched for subject:(Receptor Pharmacology). Showing records 1 – 30 of 252 total matches.

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University of Debrecen

1. Yousaf, Bilal. Angiotensin Receptor Blockers .

Degree: DE – Általános Orvostudományi Kar, 2014, University of Debrecen

 Hypertension, commonly found in billion of people in the world, is the leading cause of many diseases in these patients such as stoke, heart failure… (more)

Subjects/Keywords: Angiotensin; Receptor blockers; Pharmacology

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APA (6th Edition):

Yousaf, B. (2014). Angiotensin Receptor Blockers . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/194736

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):

Yousaf, Bilal. “Angiotensin Receptor Blockers .” 2014. Thesis, University of Debrecen. Accessed April 18, 2021. http://hdl.handle.net/2437/194736.

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

MLA Handbook (7th Edition):

Yousaf, Bilal. “Angiotensin Receptor Blockers .” 2014. Web. 18 Apr 2021.

Vancouver:

Yousaf B. Angiotensin Receptor Blockers . [Internet] [Thesis]. University of Debrecen; 2014. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/2437/194736.

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

Council of Science Editors:

Yousaf B. Angiotensin Receptor Blockers . [Thesis]. University of Debrecen; 2014. Available from: http://hdl.handle.net/2437/194736

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


Dalhousie University

2. Holland, Patrick. DRUGS, DIMERS, AND MUTATIONS: INVESTIGATING THE EFFECTS OF LIGANDS AND A ?2-ADRENERGIC POLYMORPHISM ON HOMO/HETERODIMERIZATION OF ?2-ADRENERGIC AND ANGIOTENSIN II TYPE 1 RECEPTORS.

Degree: MS, Department of Pharmacology, 2012, Dalhousie University

 GPCRs are known to form dimeric structures, and this affects their pharmacological properties. The ?2AR and AT1aR are GPCRs that are involved the regulation of… (more)

Subjects/Keywords: GPCRs; Signalling; Polymorphism; Dimerization; Receptor Pharmacology

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APA (6th Edition):

Holland, P. (2012). DRUGS, DIMERS, AND MUTATIONS: INVESTIGATING THE EFFECTS OF LIGANDS AND A ?2-ADRENERGIC POLYMORPHISM ON HOMO/HETERODIMERIZATION OF ?2-ADRENERGIC AND ANGIOTENSIN II TYPE 1 RECEPTORS. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/15245

Chicago Manual of Style (16th Edition):

Holland, Patrick. “DRUGS, DIMERS, AND MUTATIONS: INVESTIGATING THE EFFECTS OF LIGANDS AND A ?2-ADRENERGIC POLYMORPHISM ON HOMO/HETERODIMERIZATION OF ?2-ADRENERGIC AND ANGIOTENSIN II TYPE 1 RECEPTORS.” 2012. Masters Thesis, Dalhousie University. Accessed April 18, 2021. http://hdl.handle.net/10222/15245.

MLA Handbook (7th Edition):

Holland, Patrick. “DRUGS, DIMERS, AND MUTATIONS: INVESTIGATING THE EFFECTS OF LIGANDS AND A ?2-ADRENERGIC POLYMORPHISM ON HOMO/HETERODIMERIZATION OF ?2-ADRENERGIC AND ANGIOTENSIN II TYPE 1 RECEPTORS.” 2012. Web. 18 Apr 2021.

Vancouver:

Holland P. DRUGS, DIMERS, AND MUTATIONS: INVESTIGATING THE EFFECTS OF LIGANDS AND A ?2-ADRENERGIC POLYMORPHISM ON HOMO/HETERODIMERIZATION OF ?2-ADRENERGIC AND ANGIOTENSIN II TYPE 1 RECEPTORS. [Internet] [Masters thesis]. Dalhousie University; 2012. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/10222/15245.

Council of Science Editors:

Holland P. DRUGS, DIMERS, AND MUTATIONS: INVESTIGATING THE EFFECTS OF LIGANDS AND A ?2-ADRENERGIC POLYMORPHISM ON HOMO/HETERODIMERIZATION OF ?2-ADRENERGIC AND ANGIOTENSIN II TYPE 1 RECEPTORS. [Masters Thesis]. Dalhousie University; 2012. Available from: http://hdl.handle.net/10222/15245


University of Minnesota

3. Fagan, Dedra Hannah. Examination of molecular changes in acquired tamoxifen resistance and subsequent response to anti-IGF1R therapy.

Degree: PhD, 2012, University of Minnesota

 The type-I insulin like growth factor (IGF1R) contributes to the proliferation, survival, and metastasis of breast cancer cells. Disruption of IGF1R signaling alone or in… (more)

Subjects/Keywords: Endocrine resistance; IGF1R; Insulin receptor; Pharmacology

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APA (6th Edition):

Fagan, D. H. (2012). Examination of molecular changes in acquired tamoxifen resistance and subsequent response to anti-IGF1R therapy. (Doctoral Dissertation). University of Minnesota. Retrieved from http://purl.umn.edu/131512

Chicago Manual of Style (16th Edition):

Fagan, Dedra Hannah. “Examination of molecular changes in acquired tamoxifen resistance and subsequent response to anti-IGF1R therapy.” 2012. Doctoral Dissertation, University of Minnesota. Accessed April 18, 2021. http://purl.umn.edu/131512.

MLA Handbook (7th Edition):

Fagan, Dedra Hannah. “Examination of molecular changes in acquired tamoxifen resistance and subsequent response to anti-IGF1R therapy.” 2012. Web. 18 Apr 2021.

Vancouver:

Fagan DH. Examination of molecular changes in acquired tamoxifen resistance and subsequent response to anti-IGF1R therapy. [Internet] [Doctoral dissertation]. University of Minnesota; 2012. [cited 2021 Apr 18]. Available from: http://purl.umn.edu/131512.

Council of Science Editors:

Fagan DH. Examination of molecular changes in acquired tamoxifen resistance and subsequent response to anti-IGF1R therapy. [Doctoral Dissertation]. University of Minnesota; 2012. Available from: http://purl.umn.edu/131512


Boston University

4. Piche-Nicholas, Nicole Melissa. Changes in complementarity-determining regions significantly alter IgG binding to the neonatal Fc receptor.

Degree: 2014, Boston University

 A large body of data exists demonstrating the key role of FcRn in extending the half-life of therapeutic antibodies by rescuing them from lysosomal degradation.… (more)

Subjects/Keywords: Pharmacology; FcRn; IgG; Neonatal Fc receptor

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APA (6th Edition):

Piche-Nicholas, N. M. (2014). Changes in complementarity-determining regions significantly alter IgG binding to the neonatal Fc receptor. (Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/14377

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):

Piche-Nicholas, Nicole Melissa. “Changes in complementarity-determining regions significantly alter IgG binding to the neonatal Fc receptor.” 2014. Thesis, Boston University. Accessed April 18, 2021. http://hdl.handle.net/2144/14377.

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

MLA Handbook (7th Edition):

Piche-Nicholas, Nicole Melissa. “Changes in complementarity-determining regions significantly alter IgG binding to the neonatal Fc receptor.” 2014. Web. 18 Apr 2021.

Vancouver:

Piche-Nicholas NM. Changes in complementarity-determining regions significantly alter IgG binding to the neonatal Fc receptor. [Internet] [Thesis]. Boston University; 2014. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/2144/14377.

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

Council of Science Editors:

Piche-Nicholas NM. Changes in complementarity-determining regions significantly alter IgG binding to the neonatal Fc receptor. [Thesis]. Boston University; 2014. Available from: http://hdl.handle.net/2144/14377

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


University of Southern California

5. Wyatt, Letisha Renee. Regulation of ethanol intake by purinergic P2X4 receptors.

Degree: PhD, Molecular Pharmacology and Toxicology, 2013, University of Southern California

 P2X receptors (P2XRs) are a family of cation-permeable, ligand-gated ion channels gated by synaptically released extracellular adenosine-5'-triphosphate (ATP). Of the seven P2XR subtypes (P2X1-P2X7), P2X4… (more)

Subjects/Keywords: P2X receptor; alcohol; mice; behavior; neuroscience; pharmacology

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APA (6th Edition):

Wyatt, L. R. (2013). Regulation of ethanol intake by purinergic P2X4 receptors. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/248523/rec/5495

Chicago Manual of Style (16th Edition):

Wyatt, Letisha Renee. “Regulation of ethanol intake by purinergic P2X4 receptors.” 2013. Doctoral Dissertation, University of Southern California. Accessed April 18, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/248523/rec/5495.

MLA Handbook (7th Edition):

Wyatt, Letisha Renee. “Regulation of ethanol intake by purinergic P2X4 receptors.” 2013. Web. 18 Apr 2021.

Vancouver:

Wyatt LR. Regulation of ethanol intake by purinergic P2X4 receptors. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2021 Apr 18]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/248523/rec/5495.

Council of Science Editors:

Wyatt LR. Regulation of ethanol intake by purinergic P2X4 receptors. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/248523/rec/5495


University of Arizona

6. Hanlon, Katherine Emily. Cannabinoid Receptor 2: A Novel Multi-Targeted Approach in the Treatment of Breast Cancer and Related Skeletal Metastasis .

Degree: 2012, University of Arizona

 Breast cancer, which in advanced stages often leads to bone metastasis, is the most frequent malignant tumor and the second deadliest form of cancer among… (more)

Subjects/Keywords: Medical Pharmacology; Breast cancer; Cannabinoid receptor 2

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APA (6th Edition):

Hanlon, K. E. (2012). Cannabinoid Receptor 2: A Novel Multi-Targeted Approach in the Treatment of Breast Cancer and Related Skeletal Metastasis . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/241934

Chicago Manual of Style (16th Edition):

Hanlon, Katherine Emily. “Cannabinoid Receptor 2: A Novel Multi-Targeted Approach in the Treatment of Breast Cancer and Related Skeletal Metastasis .” 2012. Doctoral Dissertation, University of Arizona. Accessed April 18, 2021. http://hdl.handle.net/10150/241934.

MLA Handbook (7th Edition):

Hanlon, Katherine Emily. “Cannabinoid Receptor 2: A Novel Multi-Targeted Approach in the Treatment of Breast Cancer and Related Skeletal Metastasis .” 2012. Web. 18 Apr 2021.

Vancouver:

Hanlon KE. Cannabinoid Receptor 2: A Novel Multi-Targeted Approach in the Treatment of Breast Cancer and Related Skeletal Metastasis . [Internet] [Doctoral dissertation]. University of Arizona; 2012. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/10150/241934.

Council of Science Editors:

Hanlon KE. Cannabinoid Receptor 2: A Novel Multi-Targeted Approach in the Treatment of Breast Cancer and Related Skeletal Metastasis . [Doctoral Dissertation]. University of Arizona; 2012. Available from: http://hdl.handle.net/10150/241934


Temple University

7. Chiu, Yi-Ting. STUDIES ON NEURITE OUTGROWTH AND RECEPTOR PHOSPHORYLATION FOLLOWING KAPPA OPIOID RECEPTOR ACTIVATION.

Degree: PhD, 2016, Temple University

Pharmacology

Kappa opioid receptor (KOPR) is involved in many physiological functions and pharmacological responses such as analgesia, anti-pruritic effect, sedation, motor incoordination and aversion (Simonin… (more)

Subjects/Keywords: Pharmacology;

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APA (6th Edition):

Chiu, Y. (2016). STUDIES ON NEURITE OUTGROWTH AND RECEPTOR PHOSPHORYLATION FOLLOWING KAPPA OPIOID RECEPTOR ACTIVATION. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,384383

Chicago Manual of Style (16th Edition):

Chiu, Yi-Ting. “STUDIES ON NEURITE OUTGROWTH AND RECEPTOR PHOSPHORYLATION FOLLOWING KAPPA OPIOID RECEPTOR ACTIVATION.” 2016. Doctoral Dissertation, Temple University. Accessed April 18, 2021. http://digital.library.temple.edu/u?/p245801coll10,384383.

MLA Handbook (7th Edition):

Chiu, Yi-Ting. “STUDIES ON NEURITE OUTGROWTH AND RECEPTOR PHOSPHORYLATION FOLLOWING KAPPA OPIOID RECEPTOR ACTIVATION.” 2016. Web. 18 Apr 2021.

Vancouver:

Chiu Y. STUDIES ON NEURITE OUTGROWTH AND RECEPTOR PHOSPHORYLATION FOLLOWING KAPPA OPIOID RECEPTOR ACTIVATION. [Internet] [Doctoral dissertation]. Temple University; 2016. [cited 2021 Apr 18]. Available from: http://digital.library.temple.edu/u?/p245801coll10,384383.

Council of Science Editors:

Chiu Y. STUDIES ON NEURITE OUTGROWTH AND RECEPTOR PHOSPHORYLATION FOLLOWING KAPPA OPIOID RECEPTOR ACTIVATION. [Doctoral Dissertation]. Temple University; 2016. Available from: http://digital.library.temple.edu/u?/p245801coll10,384383

8. Xu, Chenshu. REGULATION OF DRUG METABOLISM AND INFLAMMATION BY PREGNANE X RECEPTOR.

Degree: PhD, Pharmacology & Toxicology, 2011, University of Kansas

 Liver-enriched nuclear receptor (NR) proteins regulate the expression and activity of several pivotal hepatic biochemical pathways including the uptake, metabolism and excretion of cholesterol, bile… (more)

Subjects/Keywords: Pharmacology; Toxicology; Carboxylesterase; Constitutive androstane receptor; Inflammation; Pregnane x receptor; Sumoylation

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APA (6th Edition):

Xu, C. (2011). REGULATION OF DRUG METABOLISM AND INFLAMMATION BY PREGNANE X RECEPTOR. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/9708

Chicago Manual of Style (16th Edition):

Xu, Chenshu. “REGULATION OF DRUG METABOLISM AND INFLAMMATION BY PREGNANE X RECEPTOR.” 2011. Doctoral Dissertation, University of Kansas. Accessed April 18, 2021. http://hdl.handle.net/1808/9708.

MLA Handbook (7th Edition):

Xu, Chenshu. “REGULATION OF DRUG METABOLISM AND INFLAMMATION BY PREGNANE X RECEPTOR.” 2011. Web. 18 Apr 2021.

Vancouver:

Xu C. REGULATION OF DRUG METABOLISM AND INFLAMMATION BY PREGNANE X RECEPTOR. [Internet] [Doctoral dissertation]. University of Kansas; 2011. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/1808/9708.

Council of Science Editors:

Xu C. REGULATION OF DRUG METABOLISM AND INFLAMMATION BY PREGNANE X RECEPTOR. [Doctoral Dissertation]. University of Kansas; 2011. Available from: http://hdl.handle.net/1808/9708

9. Dripps, Isaac. Investigating Mechanisms Regulating the In Vivo Actions of Delta Opioid Receptor Ligands.

Degree: PhD, Pharmacology, 2017, University of Michigan

 Chronic pain and depression are widespread and debilitating diseases that, for many people, cannot be adequately addressed with current treatment options. Delta opioid receptor (DOR)… (more)

Subjects/Keywords: Delta opioid receptor; Behavior; Pharmacology; Pharmacy and Pharmacology; Health Sciences

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APA (6th Edition):

Dripps, I. (2017). Investigating Mechanisms Regulating the In Vivo Actions of Delta Opioid Receptor Ligands. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/138549

Chicago Manual of Style (16th Edition):

Dripps, Isaac. “Investigating Mechanisms Regulating the In Vivo Actions of Delta Opioid Receptor Ligands.” 2017. Doctoral Dissertation, University of Michigan. Accessed April 18, 2021. http://hdl.handle.net/2027.42/138549.

MLA Handbook (7th Edition):

Dripps, Isaac. “Investigating Mechanisms Regulating the In Vivo Actions of Delta Opioid Receptor Ligands.” 2017. Web. 18 Apr 2021.

Vancouver:

Dripps I. Investigating Mechanisms Regulating the In Vivo Actions of Delta Opioid Receptor Ligands. [Internet] [Doctoral dissertation]. University of Michigan; 2017. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/2027.42/138549.

Council of Science Editors:

Dripps I. Investigating Mechanisms Regulating the In Vivo Actions of Delta Opioid Receptor Ligands. [Doctoral Dissertation]. University of Michigan; 2017. Available from: http://hdl.handle.net/2027.42/138549


University of Washington

10. Cohen, Josh. Novel KOR Antidepressant and Analgesic Strategies.

Degree: PhD, 2018, University of Washington

 The broad goal of this thesis has been to gain a better understanding of the mechanisms involved in depression and pain. These disorders are highly… (more)

Subjects/Keywords: depression; dynorphin; kappa opioid receptor; serotonin; stress; Pharmacology; Neurosciences; Biochemistry; Pharmacology

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APA (6th Edition):

Cohen, J. (2018). Novel KOR Antidepressant and Analgesic Strategies. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/43127

Chicago Manual of Style (16th Edition):

Cohen, Josh. “Novel KOR Antidepressant and Analgesic Strategies.” 2018. Doctoral Dissertation, University of Washington. Accessed April 18, 2021. http://hdl.handle.net/1773/43127.

MLA Handbook (7th Edition):

Cohen, Josh. “Novel KOR Antidepressant and Analgesic Strategies.” 2018. Web. 18 Apr 2021.

Vancouver:

Cohen J. Novel KOR Antidepressant and Analgesic Strategies. [Internet] [Doctoral dissertation]. University of Washington; 2018. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/1773/43127.

Council of Science Editors:

Cohen J. Novel KOR Antidepressant and Analgesic Strategies. [Doctoral Dissertation]. University of Washington; 2018. Available from: http://hdl.handle.net/1773/43127


Temple University

11. Inan, Saadet. Pharmacological and Neuroanatomical Analysis of GNTI-Induced Repetitive Behavior in Mice.

Degree: PhD, 2010, Temple University

Pharmacology

This thesis is comprised of two parts. In the first part, we investigated a) the pharmacology of GNTI, a selective kappa opioid receptor antagonist,… (more)

Subjects/Keywords: Health Sciences, Pharmacology; Neurobiology; GNTI; Itch; Kappa opioid receptor; Muscarinic receptor; Nalfurafine; Pain

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APA (6th Edition):

Inan, S. (2010). Pharmacological and Neuroanatomical Analysis of GNTI-Induced Repetitive Behavior in Mice. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,75332

Chicago Manual of Style (16th Edition):

Inan, Saadet. “Pharmacological and Neuroanatomical Analysis of GNTI-Induced Repetitive Behavior in Mice.” 2010. Doctoral Dissertation, Temple University. Accessed April 18, 2021. http://digital.library.temple.edu/u?/p245801coll10,75332.

MLA Handbook (7th Edition):

Inan, Saadet. “Pharmacological and Neuroanatomical Analysis of GNTI-Induced Repetitive Behavior in Mice.” 2010. Web. 18 Apr 2021.

Vancouver:

Inan S. Pharmacological and Neuroanatomical Analysis of GNTI-Induced Repetitive Behavior in Mice. [Internet] [Doctoral dissertation]. Temple University; 2010. [cited 2021 Apr 18]. Available from: http://digital.library.temple.edu/u?/p245801coll10,75332.

Council of Science Editors:

Inan S. Pharmacological and Neuroanatomical Analysis of GNTI-Induced Repetitive Behavior in Mice. [Doctoral Dissertation]. Temple University; 2010. Available from: http://digital.library.temple.edu/u?/p245801coll10,75332


Temple University

12. Marcu, Jahan Phillip. Novel Insights into CB1 Receptor Signaling and the Anabolic Role of Cannabinoid Receptors in Bone.

Degree: PhD, 2013, Temple University

Cell Biology

Activation of the CB1 receptor is modulated by aspartate residue D2.63176 in transmembrane helix (TMH) II. Interestingly, D2.63 does not affect the affinity… (more)

Subjects/Keywords: Molecular biology; Pharmacology; Biochemistry;

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APA (6th Edition):

Marcu, J. P. (2013). Novel Insights into CB1 Receptor Signaling and the Anabolic Role of Cannabinoid Receptors in Bone. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,233543

Chicago Manual of Style (16th Edition):

Marcu, Jahan Phillip. “Novel Insights into CB1 Receptor Signaling and the Anabolic Role of Cannabinoid Receptors in Bone.” 2013. Doctoral Dissertation, Temple University. Accessed April 18, 2021. http://digital.library.temple.edu/u?/p245801coll10,233543.

MLA Handbook (7th Edition):

Marcu, Jahan Phillip. “Novel Insights into CB1 Receptor Signaling and the Anabolic Role of Cannabinoid Receptors in Bone.” 2013. Web. 18 Apr 2021.

Vancouver:

Marcu JP. Novel Insights into CB1 Receptor Signaling and the Anabolic Role of Cannabinoid Receptors in Bone. [Internet] [Doctoral dissertation]. Temple University; 2013. [cited 2021 Apr 18]. Available from: http://digital.library.temple.edu/u?/p245801coll10,233543.

Council of Science Editors:

Marcu JP. Novel Insights into CB1 Receptor Signaling and the Anabolic Role of Cannabinoid Receptors in Bone. [Doctoral Dissertation]. Temple University; 2013. Available from: http://digital.library.temple.edu/u?/p245801coll10,233543


University of Cambridge

13. Read, Cai. The identification and pharmacological characterisation of novel apelin receptor agonists in vitro and in vivo.

Degree: PhD, 2019, University of Cambridge

 The apelin system is an evolving transmitter system consisting of the G protein coupled apelin receptor and two endogenous peptide ligands, apelin and elabela. It… (more)

Subjects/Keywords: 572; Ligand bias; Apelin Receptor; G protein coupled receptor; Cardiovascular pharmacology; Pulmonary arterial hypertension

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APA (6th Edition):

Read, C. (2019). The identification and pharmacological characterisation of novel apelin receptor agonists in vitro and in vivo. (Doctoral Dissertation). University of Cambridge. Retrieved from https://doi.org/10.17863/CAM.35320 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.763886

Chicago Manual of Style (16th Edition):

Read, Cai. “The identification and pharmacological characterisation of novel apelin receptor agonists in vitro and in vivo.” 2019. Doctoral Dissertation, University of Cambridge. Accessed April 18, 2021. https://doi.org/10.17863/CAM.35320 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.763886.

MLA Handbook (7th Edition):

Read, Cai. “The identification and pharmacological characterisation of novel apelin receptor agonists in vitro and in vivo.” 2019. Web. 18 Apr 2021.

Vancouver:

Read C. The identification and pharmacological characterisation of novel apelin receptor agonists in vitro and in vivo. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2021 Apr 18]. Available from: https://doi.org/10.17863/CAM.35320 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.763886.

Council of Science Editors:

Read C. The identification and pharmacological characterisation of novel apelin receptor agonists in vitro and in vivo. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://doi.org/10.17863/CAM.35320 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.763886


University of Washington

14. Janezic, Eric M Jennings. Elucidating the role of unique structural features of the α1D-adrenergic receptor: A tale of two tails.

Degree: PhD, 2020, University of Washington

 G protein-coupled receptors (GPCRs) are seven transmembrane domain proteins accounting for ~4% of the human genome, and the predicted target of ~30% FDA approved therapeutics.… (more)

Subjects/Keywords: adrenergic; G protein-coupled receptors; Glycosylation; GPCR; Receptor; Trafficking; Pharmacology; Biochemistry; Cellular biology; Pharmacology

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APA (6th Edition):

Janezic, E. M. J. (2020). Elucidating the role of unique structural features of the α1D-adrenergic receptor: A tale of two tails. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/46152

Chicago Manual of Style (16th Edition):

Janezic, Eric M Jennings. “Elucidating the role of unique structural features of the α1D-adrenergic receptor: A tale of two tails.” 2020. Doctoral Dissertation, University of Washington. Accessed April 18, 2021. http://hdl.handle.net/1773/46152.

MLA Handbook (7th Edition):

Janezic, Eric M Jennings. “Elucidating the role of unique structural features of the α1D-adrenergic receptor: A tale of two tails.” 2020. Web. 18 Apr 2021.

Vancouver:

Janezic EMJ. Elucidating the role of unique structural features of the α1D-adrenergic receptor: A tale of two tails. [Internet] [Doctoral dissertation]. University of Washington; 2020. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/1773/46152.

Council of Science Editors:

Janezic EMJ. Elucidating the role of unique structural features of the α1D-adrenergic receptor: A tale of two tails. [Doctoral Dissertation]. University of Washington; 2020. Available from: http://hdl.handle.net/1773/46152


University of Washington

15. Schattauer, Selena Schreiber. Molecular Regulation of Opioid Receptor Signaling.

Degree: PhD, 2013, University of Washington

 The varied behavioral effects of kappa opioid receptors (KOR) are mediated through different signaling cascades. KOR activation of G protein-dependent signaling results in analgesia, whereas… (more)

Subjects/Keywords: analgesia; aversion; kappa opioid receptor; MAPK; opioid; signaling; Pharmacology; Neurosciences; Cellular biology; Pharmacology

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APA (6th Edition):

Schattauer, S. S. (2013). Molecular Regulation of Opioid Receptor Signaling. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/22023

Chicago Manual of Style (16th Edition):

Schattauer, Selena Schreiber. “Molecular Regulation of Opioid Receptor Signaling.” 2013. Doctoral Dissertation, University of Washington. Accessed April 18, 2021. http://hdl.handle.net/1773/22023.

MLA Handbook (7th Edition):

Schattauer, Selena Schreiber. “Molecular Regulation of Opioid Receptor Signaling.” 2013. Web. 18 Apr 2021.

Vancouver:

Schattauer SS. Molecular Regulation of Opioid Receptor Signaling. [Internet] [Doctoral dissertation]. University of Washington; 2013. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/1773/22023.

Council of Science Editors:

Schattauer SS. Molecular Regulation of Opioid Receptor Signaling. [Doctoral Dissertation]. University of Washington; 2013. Available from: http://hdl.handle.net/1773/22023


UCLA

16. Cheng, Guo. Transforming a Macromolecular Therapeutic Factor into Small Molecules that Target its Transmembrane Receptors.

Degree: Molec, Cell, & Integ Physiology, 2015, UCLA

 Pigment Epithelium-Derived Factor (PEDF) is a natural factor with surprisingly diverse therapeutic functions. Since its identification more than 20 years ago, PEDF has been recognized… (more)

Subjects/Keywords: Biochemistry; Physiology; Pharmacology; Angiogenesis; PEDF; PLXDC1; PLXDC2; Receptor; Small molecule

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APA (6th Edition):

Cheng, G. (2015). Transforming a Macromolecular Therapeutic Factor into Small Molecules that Target its Transmembrane Receptors. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/35q241wh

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):

Cheng, Guo. “Transforming a Macromolecular Therapeutic Factor into Small Molecules that Target its Transmembrane Receptors.” 2015. Thesis, UCLA. Accessed April 18, 2021. http://www.escholarship.org/uc/item/35q241wh.

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

MLA Handbook (7th Edition):

Cheng, Guo. “Transforming a Macromolecular Therapeutic Factor into Small Molecules that Target its Transmembrane Receptors.” 2015. Web. 18 Apr 2021.

Vancouver:

Cheng G. Transforming a Macromolecular Therapeutic Factor into Small Molecules that Target its Transmembrane Receptors. [Internet] [Thesis]. UCLA; 2015. [cited 2021 Apr 18]. Available from: http://www.escholarship.org/uc/item/35q241wh.

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

Council of Science Editors:

Cheng G. Transforming a Macromolecular Therapeutic Factor into Small Molecules that Target its Transmembrane Receptors. [Thesis]. UCLA; 2015. Available from: http://www.escholarship.org/uc/item/35q241wh

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


University of California – San Diego

17. Busija, Anna. Caveolin-3 Overexpression Increases the Responsivity of Beta Adrenergic Receptors in Cardiac Myocytes.

Degree: Biomedical Sciences, 2017, University of California – San Diego

 Heart failure is a leading cause of human morbidity and mortality and has been linked to neurohormonal dysregulation of β-adrenergic receptor (βAR) expression and responsivity… (more)

Subjects/Keywords: Pharmacology; Physiology; Cellular biology; beta adrenergic receptor; cardiac; caveolae; caveolin

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APA (6th Edition):

Busija, A. (2017). Caveolin-3 Overexpression Increases the Responsivity of Beta Adrenergic Receptors in Cardiac Myocytes. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/4c21h6zb

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):

Busija, Anna. “Caveolin-3 Overexpression Increases the Responsivity of Beta Adrenergic Receptors in Cardiac Myocytes.” 2017. Thesis, University of California – San Diego. Accessed April 18, 2021. http://www.escholarship.org/uc/item/4c21h6zb.

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

MLA Handbook (7th Edition):

Busija, Anna. “Caveolin-3 Overexpression Increases the Responsivity of Beta Adrenergic Receptors in Cardiac Myocytes.” 2017. Web. 18 Apr 2021.

Vancouver:

Busija A. Caveolin-3 Overexpression Increases the Responsivity of Beta Adrenergic Receptors in Cardiac Myocytes. [Internet] [Thesis]. University of California – San Diego; 2017. [cited 2021 Apr 18]. Available from: http://www.escholarship.org/uc/item/4c21h6zb.

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

Council of Science Editors:

Busija A. Caveolin-3 Overexpression Increases the Responsivity of Beta Adrenergic Receptors in Cardiac Myocytes. [Thesis]. University of California – San Diego; 2017. Available from: http://www.escholarship.org/uc/item/4c21h6zb

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


Temple University

18. Huang, Xiaofang. Functional study of amylin and regulation of amylin receptor.

Degree: PhD, 2010, Temple University

Pharmacology

Amylin, a 37 amino acid peptide secreted from pancreatic beta cells upon stimulation by meal/glucose, belongs to the family of the calcitonin or calcitonin… (more)

Subjects/Keywords: Pharmacology; amylin; antinociceptive; calcitonin receptor; RAMP; spinal cord

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APA (6th Edition):

Huang, X. (2010). Functional study of amylin and regulation of amylin receptor. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,114036

Chicago Manual of Style (16th Edition):

Huang, Xiaofang. “Functional study of amylin and regulation of amylin receptor.” 2010. Doctoral Dissertation, Temple University. Accessed April 18, 2021. http://digital.library.temple.edu/u?/p245801coll10,114036.

MLA Handbook (7th Edition):

Huang, Xiaofang. “Functional study of amylin and regulation of amylin receptor.” 2010. Web. 18 Apr 2021.

Vancouver:

Huang X. Functional study of amylin and regulation of amylin receptor. [Internet] [Doctoral dissertation]. Temple University; 2010. [cited 2021 Apr 18]. Available from: http://digital.library.temple.edu/u?/p245801coll10,114036.

Council of Science Editors:

Huang X. Functional study of amylin and regulation of amylin receptor. [Doctoral Dissertation]. Temple University; 2010. Available from: http://digital.library.temple.edu/u?/p245801coll10,114036


Temple University

19. Reichenbach, Zachary Wilmer. Modulation of the Endogenous Cannabinoid System to Attenuate Inflammation in Central Nervous System Injury.

Degree: PhD, 2015, Temple University

Physiology

In non-pathological states the central nervous system maintains a degree of immunological privilege. When illness or injury occur, this privilege can be lost and… (more)

Subjects/Keywords: Neurosciences; Immunology; Pharmacology;

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APA (6th Edition):

Reichenbach, Z. W. (2015). Modulation of the Endogenous Cannabinoid System to Attenuate Inflammation in Central Nervous System Injury. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,253514

Chicago Manual of Style (16th Edition):

Reichenbach, Zachary Wilmer. “Modulation of the Endogenous Cannabinoid System to Attenuate Inflammation in Central Nervous System Injury.” 2015. Doctoral Dissertation, Temple University. Accessed April 18, 2021. http://digital.library.temple.edu/u?/p245801coll10,253514.

MLA Handbook (7th Edition):

Reichenbach, Zachary Wilmer. “Modulation of the Endogenous Cannabinoid System to Attenuate Inflammation in Central Nervous System Injury.” 2015. Web. 18 Apr 2021.

Vancouver:

Reichenbach ZW. Modulation of the Endogenous Cannabinoid System to Attenuate Inflammation in Central Nervous System Injury. [Internet] [Doctoral dissertation]. Temple University; 2015. [cited 2021 Apr 18]. Available from: http://digital.library.temple.edu/u?/p245801coll10,253514.

Council of Science Editors:

Reichenbach ZW. Modulation of the Endogenous Cannabinoid System to Attenuate Inflammation in Central Nervous System Injury. [Doctoral Dissertation]. Temple University; 2015. Available from: http://digital.library.temple.edu/u?/p245801coll10,253514


Temple University

20. Regan, Patrick M. Regulation and Functional Impact of Opioid Receptor Splicing in Response to Morphine.

Degree: PhD, 2015, Temple University

Biomedical Neuroscience

Multiple classes of pharmaceuticals, including acetaminophen, aspirin, and other nonsteroidal anti-inflammatory drugs (NSAIDs), are used to relieve mild to moderate pain; however, one… (more)

Subjects/Keywords: Neurosciences; Pharmacology; Virology;

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APA (6th Edition):

Regan, P. M. (2015). Regulation and Functional Impact of Opioid Receptor Splicing in Response to Morphine. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,344730

Chicago Manual of Style (16th Edition):

Regan, Patrick M. “Regulation and Functional Impact of Opioid Receptor Splicing in Response to Morphine.” 2015. Doctoral Dissertation, Temple University. Accessed April 18, 2021. http://digital.library.temple.edu/u?/p245801coll10,344730.

MLA Handbook (7th Edition):

Regan, Patrick M. “Regulation and Functional Impact of Opioid Receptor Splicing in Response to Morphine.” 2015. Web. 18 Apr 2021.

Vancouver:

Regan PM. Regulation and Functional Impact of Opioid Receptor Splicing in Response to Morphine. [Internet] [Doctoral dissertation]. Temple University; 2015. [cited 2021 Apr 18]. Available from: http://digital.library.temple.edu/u?/p245801coll10,344730.

Council of Science Editors:

Regan PM. Regulation and Functional Impact of Opioid Receptor Splicing in Response to Morphine. [Doctoral Dissertation]. Temple University; 2015. Available from: http://digital.library.temple.edu/u?/p245801coll10,344730


University of California – Irvine

21. Liu, Shiwei. Investigating Neuroinflammation and Opioid Receptor Signaling Mechanisms in Chronic Pain Pathology.

Degree: Pharmacology and Toxicology, 2018, University of California – Irvine

 Chronic pain represents a substantial burden to society and is difficult to manage for both physicians and patients due to lack of effective therapies. There… (more)

Subjects/Keywords: Pharmacology; Neurosciences; Medicine; Biology; Brain Injury; Inflammation; Opioid Receptor; Pain

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APA (6th Edition):

Liu, S. (2018). Investigating Neuroinflammation and Opioid Receptor Signaling Mechanisms in Chronic Pain Pathology. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/9wk750dt

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, Shiwei. “Investigating Neuroinflammation and Opioid Receptor Signaling Mechanisms in Chronic Pain Pathology.” 2018. Thesis, University of California – Irvine. Accessed April 18, 2021. http://www.escholarship.org/uc/item/9wk750dt.

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

MLA Handbook (7th Edition):

Liu, Shiwei. “Investigating Neuroinflammation and Opioid Receptor Signaling Mechanisms in Chronic Pain Pathology.” 2018. Web. 18 Apr 2021.

Vancouver:

Liu S. Investigating Neuroinflammation and Opioid Receptor Signaling Mechanisms in Chronic Pain Pathology. [Internet] [Thesis]. University of California – Irvine; 2018. [cited 2021 Apr 18]. Available from: http://www.escholarship.org/uc/item/9wk750dt.

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

Council of Science Editors:

Liu S. Investigating Neuroinflammation and Opioid Receptor Signaling Mechanisms in Chronic Pain Pathology. [Thesis]. University of California – Irvine; 2018. Available from: http://www.escholarship.org/uc/item/9wk750dt

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


Penn State University

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

Degree: 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. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/19919

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):

Jayasuriya, Gihan Muthumala. “The Allosteric Modulating Effects of Dronedarone on Muscarinic Receptor Subtypes at a Novel Allosteric Binding Site.” 2013. Thesis, Penn State University. Accessed April 18, 2021. https://submit-etda.libraries.psu.edu/catalog/19919.

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

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. 18 Apr 2021.

Vancouver:

Jayasuriya GM. The Allosteric Modulating Effects of Dronedarone on Muscarinic Receptor Subtypes at a Novel Allosteric Binding Site. [Internet] [Thesis]. Penn State University; 2013. [cited 2021 Apr 18]. Available from: https://submit-etda.libraries.psu.edu/catalog/19919.

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

Council of Science Editors:

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

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


Boston University

23. Smith, Conor C. Non-canonical cell signaling actions of pregnenolone sulfate, a neurosteroid that increases intracellular calcium, activates creb phosphorylation and stimulates trafficking of NMDA receptors to the surface of neurons.

Degree: PhD, Pharmacology & Experimental Therapeutics, 2014, Boston University

 Preclinical results support the use of N-methyl D-aspartate receptor (NMDAR) modulators for cognition enhancement therapeutics. Pregnenolone sulfate (PregS) is a neuroactive steroid derived from cholesterol… (more)

Subjects/Keywords: Pharmacology; CREB; NMDA receptor; Calcium; Pregnenolone sulfate; Steroid

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APA (6th Edition):

Smith, C. C. (2014). Non-canonical cell signaling actions of pregnenolone sulfate, a neurosteroid that increases intracellular calcium, activates creb phosphorylation and stimulates trafficking of NMDA receptors to the surface of neurons. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/15222

Chicago Manual of Style (16th Edition):

Smith, Conor C. “Non-canonical cell signaling actions of pregnenolone sulfate, a neurosteroid that increases intracellular calcium, activates creb phosphorylation and stimulates trafficking of NMDA receptors to the surface of neurons.” 2014. Doctoral Dissertation, Boston University. Accessed April 18, 2021. http://hdl.handle.net/2144/15222.

MLA Handbook (7th Edition):

Smith, Conor C. “Non-canonical cell signaling actions of pregnenolone sulfate, a neurosteroid that increases intracellular calcium, activates creb phosphorylation and stimulates trafficking of NMDA receptors to the surface of neurons.” 2014. Web. 18 Apr 2021.

Vancouver:

Smith CC. Non-canonical cell signaling actions of pregnenolone sulfate, a neurosteroid that increases intracellular calcium, activates creb phosphorylation and stimulates trafficking of NMDA receptors to the surface of neurons. [Internet] [Doctoral dissertation]. Boston University; 2014. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/2144/15222.

Council of Science Editors:

Smith CC. Non-canonical cell signaling actions of pregnenolone sulfate, a neurosteroid that increases intracellular calcium, activates creb phosphorylation and stimulates trafficking of NMDA receptors to the surface of neurons. [Doctoral Dissertation]. Boston University; 2014. Available from: http://hdl.handle.net/2144/15222


Wayne State University

24. Mitchell-Ryan, Shermaine Kimberly. The Therapeutic Targeting Of Folate Receptor Alpha Positive Tumors Via Folate Receptor Selective Novel 5- And 6- Substituted Pyrrolo [2,3-D]pyrimidine Antifolates".

Degree: PhD, Cancer Biology, 2015, Wayne State University

  Ovarian Cancer is the fifth leading cause of cancer-related death of women in the United States. Epithelial Ovarian Cancer (EOC) constitutes 85-90% of malignancies… (more)

Subjects/Keywords: folate receptor; ovarian cancer; Molecular Biology; Oncology; Pharmacology

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APA (6th Edition):

Mitchell-Ryan, S. K. (2015). The Therapeutic Targeting Of Folate Receptor Alpha Positive Tumors Via Folate Receptor Selective Novel 5- And 6- Substituted Pyrrolo [2,3-D]pyrimidine Antifolates". (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/1155

Chicago Manual of Style (16th Edition):

Mitchell-Ryan, Shermaine Kimberly. “The Therapeutic Targeting Of Folate Receptor Alpha Positive Tumors Via Folate Receptor Selective Novel 5- And 6- Substituted Pyrrolo [2,3-D]pyrimidine Antifolates".” 2015. Doctoral Dissertation, Wayne State University. Accessed April 18, 2021. https://digitalcommons.wayne.edu/oa_dissertations/1155.

MLA Handbook (7th Edition):

Mitchell-Ryan, Shermaine Kimberly. “The Therapeutic Targeting Of Folate Receptor Alpha Positive Tumors Via Folate Receptor Selective Novel 5- And 6- Substituted Pyrrolo [2,3-D]pyrimidine Antifolates".” 2015. Web. 18 Apr 2021.

Vancouver:

Mitchell-Ryan SK. The Therapeutic Targeting Of Folate Receptor Alpha Positive Tumors Via Folate Receptor Selective Novel 5- And 6- Substituted Pyrrolo [2,3-D]pyrimidine Antifolates". [Internet] [Doctoral dissertation]. Wayne State University; 2015. [cited 2021 Apr 18]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/1155.

Council of Science Editors:

Mitchell-Ryan SK. The Therapeutic Targeting Of Folate Receptor Alpha Positive Tumors Via Folate Receptor Selective Novel 5- And 6- Substituted Pyrrolo [2,3-D]pyrimidine Antifolates". [Doctoral Dissertation]. Wayne State University; 2015. Available from: https://digitalcommons.wayne.edu/oa_dissertations/1155

25. Basheer, Haneen Adel Daoud. Pharmacological characterization of chemokine receptor 7 (CCR7) as a potential therapeutic target in cancer.

Degree: PhD, 2017, University of Bradford

 The expression of CCR7 was evaluated in different cancer cell lines by using flow cytometry, western blot, Immunofluorescence and immunohistochemistry. We showed for the selected… (more)

Subjects/Keywords: 616.99; Cancer; Chemokine receptor 7; CCR7; Therapeutic target; Pharmacology

Page 1 Page 2

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APA (6th Edition):

Basheer, H. A. D. (2017). Pharmacological characterization of chemokine receptor 7 (CCR7) as a potential therapeutic target in cancer. (Doctoral Dissertation). University of Bradford. Retrieved from http://hdl.handle.net/10454/15100

Chicago Manual of Style (16th Edition):

Basheer, Haneen Adel Daoud. “Pharmacological characterization of chemokine receptor 7 (CCR7) as a potential therapeutic target in cancer.” 2017. Doctoral Dissertation, University of Bradford. Accessed April 18, 2021. http://hdl.handle.net/10454/15100.

MLA Handbook (7th Edition):

Basheer, Haneen Adel Daoud. “Pharmacological characterization of chemokine receptor 7 (CCR7) as a potential therapeutic target in cancer.” 2017. Web. 18 Apr 2021.

Vancouver:

Basheer HAD. Pharmacological characterization of chemokine receptor 7 (CCR7) as a potential therapeutic target in cancer. [Internet] [Doctoral dissertation]. University of Bradford; 2017. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/10454/15100.

Council of Science Editors:

Basheer HAD. Pharmacological characterization of chemokine receptor 7 (CCR7) as a potential therapeutic target in cancer. [Doctoral Dissertation]. University of Bradford; 2017. Available from: http://hdl.handle.net/10454/15100


University of Manchester

26. Zheng, Wenxuan. Properties of mammalian P2X₇ receptors.

Degree: PhD, 2012, University of Manchester

 To establish comprehensive pharmacology of P2X₇ receptors, membrane current recording, intracellular calcium transient recording and ethidium bromide uptake were carried out to examine several selective… (more)

Subjects/Keywords: 616.994; P2X7 receptor; pharmacology; cancer; amino acid substitution

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APA (6th Edition):

Zheng, W. (2012). Properties of mammalian P2X₇ receptors. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/properties-of-mammalian-p2x7-receptors(1ff23f4a-47eb-4d06-b54c-bd7488c9700c).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555526

Chicago Manual of Style (16th Edition):

Zheng, Wenxuan. “Properties of mammalian P2X₇ receptors.” 2012. Doctoral Dissertation, University of Manchester. Accessed April 18, 2021. https://www.research.manchester.ac.uk/portal/en/theses/properties-of-mammalian-p2x7-receptors(1ff23f4a-47eb-4d06-b54c-bd7488c9700c).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555526.

MLA Handbook (7th Edition):

Zheng, Wenxuan. “Properties of mammalian P2X₇ receptors.” 2012. Web. 18 Apr 2021.

Vancouver:

Zheng W. Properties of mammalian P2X₇ receptors. [Internet] [Doctoral dissertation]. University of Manchester; 2012. [cited 2021 Apr 18]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/properties-of-mammalian-p2x7-receptors(1ff23f4a-47eb-4d06-b54c-bd7488c9700c).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555526.

Council of Science Editors:

Zheng W. Properties of mammalian P2X₇ receptors. [Doctoral Dissertation]. University of Manchester; 2012. Available from: https://www.research.manchester.ac.uk/portal/en/theses/properties-of-mammalian-p2x7-receptors(1ff23f4a-47eb-4d06-b54c-bd7488c9700c).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.555526


University of Oxford

27. Christou, Ivy. Novel family of CB2R agonists regulates inflammatory responses.

Degree: PhD, 2012, University of Oxford

 Inflammation is a multifactorial response towards noxious stimuli, however appropriate regulation and resolution of inflammation is crucial for the prevention of chronic inflammatory diseases such… (more)

Subjects/Keywords: 616; Biology; Immunology; Pharmacology; Chemical biology; cannabinoid; receptor; macrophage; inflammation

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APA (6th Edition):

Christou, I. (2012). Novel family of CB2R agonists regulates inflammatory responses. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:fd7a7b39-7225-4cdf-b01d-2d5ccb9cd0da ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.692844

Chicago Manual of Style (16th Edition):

Christou, Ivy. “Novel family of CB2R agonists regulates inflammatory responses.” 2012. Doctoral Dissertation, University of Oxford. Accessed April 18, 2021. http://ora.ox.ac.uk/objects/uuid:fd7a7b39-7225-4cdf-b01d-2d5ccb9cd0da ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.692844.

MLA Handbook (7th Edition):

Christou, Ivy. “Novel family of CB2R agonists regulates inflammatory responses.” 2012. Web. 18 Apr 2021.

Vancouver:

Christou I. Novel family of CB2R agonists regulates inflammatory responses. [Internet] [Doctoral dissertation]. University of Oxford; 2012. [cited 2021 Apr 18]. Available from: http://ora.ox.ac.uk/objects/uuid:fd7a7b39-7225-4cdf-b01d-2d5ccb9cd0da ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.692844.

Council of Science Editors:

Christou I. Novel family of CB2R agonists regulates inflammatory responses. [Doctoral Dissertation]. University of Oxford; 2012. Available from: http://ora.ox.ac.uk/objects/uuid:fd7a7b39-7225-4cdf-b01d-2d5ccb9cd0da ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.692844


University of Gothenburg / Göteborgs Universitet

28. Bergendal, Anna, 1962-. Long-acting §2-adrenoceptor agonists : mechanisms of relaxant effects in the airways.

Degree: 1995, University of Gothenburg / Göteborgs Universitet

Subjects/Keywords: Adrenergic beta receptor agonists: pharmacology

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APA (6th Edition):

Bergendal, Anna, 1. (1995). Long-acting §2-adrenoceptor agonists : mechanisms of relaxant effects in the airways. (Thesis). University of Gothenburg / Göteborgs Universitet. Retrieved from http://hdl.handle.net/2077/13948

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):

Bergendal, Anna, 1962-. “Long-acting §2-adrenoceptor agonists : mechanisms of relaxant effects in the airways.” 1995. Thesis, University of Gothenburg / Göteborgs Universitet. Accessed April 18, 2021. http://hdl.handle.net/2077/13948.

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

MLA Handbook (7th Edition):

Bergendal, Anna, 1962-. “Long-acting §2-adrenoceptor agonists : mechanisms of relaxant effects in the airways.” 1995. Web. 18 Apr 2021.

Vancouver:

Bergendal, Anna 1. Long-acting §2-adrenoceptor agonists : mechanisms of relaxant effects in the airways. [Internet] [Thesis]. University of Gothenburg / Göteborgs Universitet; 1995. [cited 2021 Apr 18]. Available from: http://hdl.handle.net/2077/13948.

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

Council of Science Editors:

Bergendal, Anna 1. Long-acting §2-adrenoceptor agonists : mechanisms of relaxant effects in the airways. [Thesis]. University of Gothenburg / Göteborgs Universitet; 1995. Available from: http://hdl.handle.net/2077/13948

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


University of Iowa

29. Gupte, Raeesa Prashant. Phosphoregulation of somatodendritic voltage-gated potassium channels by pituitary adenylate cyclase-activating polypeptide.

Degree: PhD, Pharmacology, 2015, University of Iowa

  The endogenous neuropeptide pituitary adenylate cyclase-activating polypeptide (PACAP) exerts various neuromodulatory functions in mammalian brain. Enhancement of synaptic activity, mediation of chronic inflammatory and… (more)

Subjects/Keywords: G-protein coupled receptor; Hyperexcitability; Ion channels; Kinase; Neuroprotection; Phosphorylation; Pharmacology

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

APA (6th Edition):

Gupte, R. P. (2015). Phosphoregulation of somatodendritic voltage-gated potassium channels by pituitary adenylate cyclase-activating polypeptide. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/5766

Chicago Manual of Style (16th Edition):

Gupte, Raeesa Prashant. “Phosphoregulation of somatodendritic voltage-gated potassium channels by pituitary adenylate cyclase-activating polypeptide.” 2015. Doctoral Dissertation, University of Iowa. Accessed April 18, 2021. https://ir.uiowa.edu/etd/5766.

MLA Handbook (7th Edition):

Gupte, Raeesa Prashant. “Phosphoregulation of somatodendritic voltage-gated potassium channels by pituitary adenylate cyclase-activating polypeptide.” 2015. Web. 18 Apr 2021.

Vancouver:

Gupte RP. Phosphoregulation of somatodendritic voltage-gated potassium channels by pituitary adenylate cyclase-activating polypeptide. [Internet] [Doctoral dissertation]. University of Iowa; 2015. [cited 2021 Apr 18]. Available from: https://ir.uiowa.edu/etd/5766.

Council of Science Editors:

Gupte RP. Phosphoregulation of somatodendritic voltage-gated potassium channels by pituitary adenylate cyclase-activating polypeptide. [Doctoral Dissertation]. University of Iowa; 2015. Available from: https://ir.uiowa.edu/etd/5766


University of Pennsylvania

30. Greineder, Colin F. Augmenting the Protein C Pathway with Endothelial Targeted Biotherapeutics: Strategies to Promote Partnering of TM and EPCR.

Degree: 2014, University of Pennsylvania

 The design of targeted recombinant biotherapeutics is a rapidly growing area of translational biomedical research, with particular relevance to acute and life-threatening conditions, in which… (more)

Subjects/Keywords: Endothelial Protein C Receptor; Endothelium; Targeted Drug Delivery; Thrombomodulin; Biomedical; Pharmacology

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

APA (6th Edition):

Greineder, C. F. (2014). Augmenting the Protein C Pathway with Endothelial Targeted Biotherapeutics: Strategies to Promote Partnering of TM and EPCR. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/1296

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):

Greineder, Colin F. “Augmenting the Protein C Pathway with Endothelial Targeted Biotherapeutics: Strategies to Promote Partnering of TM and EPCR.” 2014. Thesis, University of Pennsylvania. Accessed April 18, 2021. https://repository.upenn.edu/edissertations/1296.

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

MLA Handbook (7th Edition):

Greineder, Colin F. “Augmenting the Protein C Pathway with Endothelial Targeted Biotherapeutics: Strategies to Promote Partnering of TM and EPCR.” 2014. Web. 18 Apr 2021.

Vancouver:

Greineder CF. Augmenting the Protein C Pathway with Endothelial Targeted Biotherapeutics: Strategies to Promote Partnering of TM and EPCR. [Internet] [Thesis]. University of Pennsylvania; 2014. [cited 2021 Apr 18]. Available from: https://repository.upenn.edu/edissertations/1296.

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

Council of Science Editors:

Greineder CF. Augmenting the Protein C Pathway with Endothelial Targeted Biotherapeutics: Strategies to Promote Partnering of TM and EPCR. [Thesis]. University of Pennsylvania; 2014. Available from: https://repository.upenn.edu/edissertations/1296

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

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