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You searched for subject:(Opioid receptor). Showing records 1 – 30 of 172 total matches.

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Penn State University

1. Morse, Megan. Ligand-directed Functional Selectivity at the Opioid Receptor Family: An Epic Approach to Understanding Opioid Receptor Signaling.

Degree: 2012, Penn State University

Opioid receptors are G-protein coupled receptors (GPCRs) that are activated by opioid ligands. These ligands offer powerful medical benefits due to their analgesic properties, but… (more)

Subjects/Keywords: GPCR; Opioid; Receptor SIgnaling; DMR

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

APA (6th Edition):

Morse, M. (2012). Ligand-directed Functional Selectivity at the Opioid Receptor Family: An Epic Approach to Understanding Opioid Receptor Signaling. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/12691

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):

Morse, Megan. “Ligand-directed Functional Selectivity at the Opioid Receptor Family: An Epic Approach to Understanding Opioid Receptor Signaling.” 2012. Thesis, Penn State University. Accessed March 08, 2021. https://submit-etda.libraries.psu.edu/catalog/12691.

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

MLA Handbook (7th Edition):

Morse, Megan. “Ligand-directed Functional Selectivity at the Opioid Receptor Family: An Epic Approach to Understanding Opioid Receptor Signaling.” 2012. Web. 08 Mar 2021.

Vancouver:

Morse M. Ligand-directed Functional Selectivity at the Opioid Receptor Family: An Epic Approach to Understanding Opioid Receptor Signaling. [Internet] [Thesis]. Penn State University; 2012. [cited 2021 Mar 08]. Available from: https://submit-etda.libraries.psu.edu/catalog/12691.

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

Council of Science Editors:

Morse M. Ligand-directed Functional Selectivity at the Opioid Receptor Family: An Epic Approach to Understanding Opioid Receptor Signaling. [Thesis]. Penn State University; 2012. Available from: https://submit-etda.libraries.psu.edu/catalog/12691

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


University of Toronto

2. Kanawaty, Ashlin. The Role of EphB2 Receptors in the Development of Morphine Tolerance.

Degree: 2012, University of Toronto

Recently we have begun to investigate a novel role of EphB receptors in opiate-dependant analgesia. EphB2-β-galactosidase knockins demonstrate that EphB2 is persistently expressed within a… (more)

Subjects/Keywords: Eph receptor; Morphine; Mu opioid receptor; 0317

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APA (6th Edition):

Kanawaty, A. (2012). The Role of EphB2 Receptors in the Development of Morphine Tolerance. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/42889

Chicago Manual of Style (16th Edition):

Kanawaty, Ashlin. “The Role of EphB2 Receptors in the Development of Morphine Tolerance.” 2012. Masters Thesis, University of Toronto. Accessed March 08, 2021. http://hdl.handle.net/1807/42889.

MLA Handbook (7th Edition):

Kanawaty, Ashlin. “The Role of EphB2 Receptors in the Development of Morphine Tolerance.” 2012. Web. 08 Mar 2021.

Vancouver:

Kanawaty A. The Role of EphB2 Receptors in the Development of Morphine Tolerance. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2021 Mar 08]. Available from: http://hdl.handle.net/1807/42889.

Council of Science Editors:

Kanawaty A. The Role of EphB2 Receptors in the Development of Morphine Tolerance. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/42889

3. Atigari, Diana. Investigating the anti-cocaine, anti-nociceptive properties and side effects of MP1104, a novel mixed opioid receptor agonist.

Degree: 2019, Victoria University of Wellington

 Rationale: Drug addiction is a chronic, relapsing disease with great socioeconomic and morbidity costs. There are limited treatments, with no Food and Drug Administration approved… (more)

Subjects/Keywords: Mixed opioid receptor agonist; Drug self-administration; Kappa opioid receptor agonist

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APA (6th Edition):

Atigari, D. (2019). Investigating the anti-cocaine, anti-nociceptive properties and side effects of MP1104, a novel mixed opioid receptor agonist. (Doctoral Dissertation). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/8187

Chicago Manual of Style (16th Edition):

Atigari, Diana. “Investigating the anti-cocaine, anti-nociceptive properties and side effects of MP1104, a novel mixed opioid receptor agonist.” 2019. Doctoral Dissertation, Victoria University of Wellington. Accessed March 08, 2021. http://hdl.handle.net/10063/8187.

MLA Handbook (7th Edition):

Atigari, Diana. “Investigating the anti-cocaine, anti-nociceptive properties and side effects of MP1104, a novel mixed opioid receptor agonist.” 2019. Web. 08 Mar 2021.

Vancouver:

Atigari D. Investigating the anti-cocaine, anti-nociceptive properties and side effects of MP1104, a novel mixed opioid receptor agonist. [Internet] [Doctoral dissertation]. Victoria University of Wellington; 2019. [cited 2021 Mar 08]. Available from: http://hdl.handle.net/10063/8187.

Council of Science Editors:

Atigari D. Investigating the anti-cocaine, anti-nociceptive properties and side effects of MP1104, a novel mixed opioid receptor agonist. [Doctoral Dissertation]. Victoria University of Wellington; 2019. Available from: http://hdl.handle.net/10063/8187


University of Arizona

4. Olson, Keith Mathew. Atypical Opioid Interactions – Development of Selective Mu-Delta Heterodimer Antagonists, Clinical Opioids at Non-Mu Pain Targets and Endogenous Biased Signaling .

Degree: 2017, University of Arizona

 Most clinical opioids produce analgesia through the Mu Opioid Receptor (MOR) providing the only effective treatment for chronic pain patients. These studies explore three pre-clinical… (more)

Subjects/Keywords: Bivalent; Delta Opioid Receptor; Functional Selectivity; MDOR Heterodimer; Mu Opioid Receptor; Opioid Signaling

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APA (6th Edition):

Olson, K. M. (2017). Atypical Opioid Interactions – Development of Selective Mu-Delta Heterodimer Antagonists, Clinical Opioids at Non-Mu Pain Targets and Endogenous Biased Signaling . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/626669

Chicago Manual of Style (16th Edition):

Olson, Keith Mathew. “Atypical Opioid Interactions – Development of Selective Mu-Delta Heterodimer Antagonists, Clinical Opioids at Non-Mu Pain Targets and Endogenous Biased Signaling .” 2017. Doctoral Dissertation, University of Arizona. Accessed March 08, 2021. http://hdl.handle.net/10150/626669.

MLA Handbook (7th Edition):

Olson, Keith Mathew. “Atypical Opioid Interactions – Development of Selective Mu-Delta Heterodimer Antagonists, Clinical Opioids at Non-Mu Pain Targets and Endogenous Biased Signaling .” 2017. Web. 08 Mar 2021.

Vancouver:

Olson KM. Atypical Opioid Interactions – Development of Selective Mu-Delta Heterodimer Antagonists, Clinical Opioids at Non-Mu Pain Targets and Endogenous Biased Signaling . [Internet] [Doctoral dissertation]. University of Arizona; 2017. [cited 2021 Mar 08]. Available from: http://hdl.handle.net/10150/626669.

Council of Science Editors:

Olson KM. Atypical Opioid Interactions – Development of Selective Mu-Delta Heterodimer Antagonists, Clinical Opioids at Non-Mu Pain Targets and Endogenous Biased Signaling . [Doctoral Dissertation]. University of Arizona; 2017. Available from: http://hdl.handle.net/10150/626669


Penn State University

5. Justice-bitner, Stephanie Lynn. An Investigation of Mu-Opioid Receptor Interacting Proteins Within the Mu-Opioid Receptor Signaling Complex.

Degree: 2012, Penn State University

 Opioids are powerful analgesic drugs that lead to the development of tolerance, physical dependence, and addiction with prolonged use or abuse. Chronic exposure appears to… (more)

Subjects/Keywords: mu-opioid receptor; ubiquitin; G-protein; kappa-opioid receptor; delta-opioid receptor; yeast two-hybrid; SIAH1; SIAH2

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APA (6th Edition):

Justice-bitner, S. L. (2012). An Investigation of Mu-Opioid Receptor Interacting Proteins Within the Mu-Opioid Receptor Signaling Complex. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/15878

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):

Justice-bitner, Stephanie Lynn. “An Investigation of Mu-Opioid Receptor Interacting Proteins Within the Mu-Opioid Receptor Signaling Complex.” 2012. Thesis, Penn State University. Accessed March 08, 2021. https://submit-etda.libraries.psu.edu/catalog/15878.

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

MLA Handbook (7th Edition):

Justice-bitner, Stephanie Lynn. “An Investigation of Mu-Opioid Receptor Interacting Proteins Within the Mu-Opioid Receptor Signaling Complex.” 2012. Web. 08 Mar 2021.

Vancouver:

Justice-bitner SL. An Investigation of Mu-Opioid Receptor Interacting Proteins Within the Mu-Opioid Receptor Signaling Complex. [Internet] [Thesis]. Penn State University; 2012. [cited 2021 Mar 08]. Available from: https://submit-etda.libraries.psu.edu/catalog/15878.

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

Council of Science Editors:

Justice-bitner SL. An Investigation of Mu-Opioid Receptor Interacting Proteins Within the Mu-Opioid Receptor Signaling Complex. [Thesis]. Penn State University; 2012. Available from: https://submit-etda.libraries.psu.edu/catalog/15878

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


Temple University

6. Happel, Christine. Molecular Basis for Mu-Opioid Regulation of Chemokine Gene Expression.

Degree: PhD, 2009, Temple University

Molecular Biology and Genetics

Opioid receptor modulation of pro-inflammatory cytokine production is vital for host defense and the inflammatory response. Previous results have shown the… (more)

Subjects/Keywords: Biology, Microbiology; Chemokines; NF-kappaB; Opioid; Opioid receptor; PKC

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APA (6th Edition):

Happel, C. (2009). Molecular Basis for Mu-Opioid Regulation of Chemokine Gene Expression. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,28438

Chicago Manual of Style (16th Edition):

Happel, Christine. “Molecular Basis for Mu-Opioid Regulation of Chemokine Gene Expression.” 2009. Doctoral Dissertation, Temple University. Accessed March 08, 2021. http://digital.library.temple.edu/u?/p245801coll10,28438.

MLA Handbook (7th Edition):

Happel, Christine. “Molecular Basis for Mu-Opioid Regulation of Chemokine Gene Expression.” 2009. Web. 08 Mar 2021.

Vancouver:

Happel C. Molecular Basis for Mu-Opioid Regulation of Chemokine Gene Expression. [Internet] [Doctoral dissertation]. Temple University; 2009. [cited 2021 Mar 08]. Available from: http://digital.library.temple.edu/u?/p245801coll10,28438.

Council of Science Editors:

Happel C. Molecular Basis for Mu-Opioid Regulation of Chemokine Gene Expression. [Doctoral Dissertation]. Temple University; 2009. Available from: http://digital.library.temple.edu/u?/p245801coll10,28438

7. Daccache, Georges. Hyperalgésie induite par les opioïdes : intérêt du monitorage du tonus parasympathique chez l'homme et étude des mécanismes moléculaires de désensibilisation et de tolérance in vitro et chez la souris : Opioid induced hyperalgesia : interest of parasympathetic tone monitoring in humans and study of molecular mechanisms of desensitization and tolerance in vitro and in mice.

Degree: Docteur es, Recherche clinique, innovation technologique, sante publique, 2018, Normandie

L’utilisation des opioïdes est à l’origine de phénomènes de tolérance et d’hyperalgésie induite (HIO) aussi bien chez l’animal qu’en utilisation clinique. Ces phénomènes surviennent avec… (more)

Subjects/Keywords: Tolérance; Désensibilisation; Opioid Induced Hyperalgesia; Desensitization; Internalization,; Mu-opioid receptor

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APA (6th Edition):

Daccache, G. (2018). Hyperalgésie induite par les opioïdes : intérêt du monitorage du tonus parasympathique chez l'homme et étude des mécanismes moléculaires de désensibilisation et de tolérance in vitro et chez la souris : Opioid induced hyperalgesia : interest of parasympathetic tone monitoring in humans and study of molecular mechanisms of desensitization and tolerance in vitro and in mice. (Doctoral Dissertation). Normandie. Retrieved from http://www.theses.fr/2018NORMC410

Chicago Manual of Style (16th Edition):

Daccache, Georges. “Hyperalgésie induite par les opioïdes : intérêt du monitorage du tonus parasympathique chez l'homme et étude des mécanismes moléculaires de désensibilisation et de tolérance in vitro et chez la souris : Opioid induced hyperalgesia : interest of parasympathetic tone monitoring in humans and study of molecular mechanisms of desensitization and tolerance in vitro and in mice.” 2018. Doctoral Dissertation, Normandie. Accessed March 08, 2021. http://www.theses.fr/2018NORMC410.

MLA Handbook (7th Edition):

Daccache, Georges. “Hyperalgésie induite par les opioïdes : intérêt du monitorage du tonus parasympathique chez l'homme et étude des mécanismes moléculaires de désensibilisation et de tolérance in vitro et chez la souris : Opioid induced hyperalgesia : interest of parasympathetic tone monitoring in humans and study of molecular mechanisms of desensitization and tolerance in vitro and in mice.” 2018. Web. 08 Mar 2021.

Vancouver:

Daccache G. Hyperalgésie induite par les opioïdes : intérêt du monitorage du tonus parasympathique chez l'homme et étude des mécanismes moléculaires de désensibilisation et de tolérance in vitro et chez la souris : Opioid induced hyperalgesia : interest of parasympathetic tone monitoring in humans and study of molecular mechanisms of desensitization and tolerance in vitro and in mice. [Internet] [Doctoral dissertation]. Normandie; 2018. [cited 2021 Mar 08]. Available from: http://www.theses.fr/2018NORMC410.

Council of Science Editors:

Daccache G. Hyperalgésie induite par les opioïdes : intérêt du monitorage du tonus parasympathique chez l'homme et étude des mécanismes moléculaires de désensibilisation et de tolérance in vitro et chez la souris : Opioid induced hyperalgesia : interest of parasympathetic tone monitoring in humans and study of molecular mechanisms of desensitization and tolerance in vitro and in mice. [Doctoral Dissertation]. Normandie; 2018. Available from: http://www.theses.fr/2018NORMC410


Freie Universität Berlin

8. Seitz, Viola. Sensitization and inhibition of pain.

Degree: 2020, Freie Universität Berlin

 Currently available pain medications are limited by adverse side effects leading to enormous individual and socioeconomic costs. Therefore, the investigation of pathological receptor conformations and… (more)

Subjects/Keywords: Pain; Capsaicin; Opioid; Opioid receptor; TRPV1; ddc:610

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APA (6th Edition):

Seitz, V. (2020). Sensitization and inhibition of pain. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-26902

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):

Seitz, Viola. “Sensitization and inhibition of pain.” 2020. Thesis, Freie Universität Berlin. Accessed March 08, 2021. http://dx.doi.org/10.17169/refubium-26902.

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

MLA Handbook (7th Edition):

Seitz, Viola. “Sensitization and inhibition of pain.” 2020. Web. 08 Mar 2021.

Vancouver:

Seitz V. Sensitization and inhibition of pain. [Internet] [Thesis]. Freie Universität Berlin; 2020. [cited 2021 Mar 08]. Available from: http://dx.doi.org/10.17169/refubium-26902.

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

Council of Science Editors:

Seitz V. Sensitization and inhibition of pain. [Thesis]. Freie Universität Berlin; 2020. Available from: http://dx.doi.org/10.17169/refubium-26902

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


Penn State University

9. Marsan, Lynnsay A. Implications of the Mu-opioid receptor single nucleotide polymorphism on the regulation of the HPA axis.

Degree: 2014, Penn State University

 The activation of the hypothalamic-pituitary-adrenal (HPA) axis is modulated, in part, by the μ-opioid receptor. A relatively common single nucleotide polymorphism (SNP) (A118G) has been… (more)

Subjects/Keywords: neuroendocrinology; HPA axis; mu-opioid receptor; stress

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APA (6th Edition):

Marsan, L. A. (2014). Implications of the Mu-opioid receptor single nucleotide polymorphism on the regulation of the HPA axis. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/23605

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):

Marsan, Lynnsay A. “Implications of the Mu-opioid receptor single nucleotide polymorphism on the regulation of the HPA axis.” 2014. Thesis, Penn State University. Accessed March 08, 2021. https://submit-etda.libraries.psu.edu/catalog/23605.

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

MLA Handbook (7th Edition):

Marsan, Lynnsay A. “Implications of the Mu-opioid receptor single nucleotide polymorphism on the regulation of the HPA axis.” 2014. Web. 08 Mar 2021.

Vancouver:

Marsan LA. Implications of the Mu-opioid receptor single nucleotide polymorphism on the regulation of the HPA axis. [Internet] [Thesis]. Penn State University; 2014. [cited 2021 Mar 08]. Available from: https://submit-etda.libraries.psu.edu/catalog/23605.

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

Council of Science Editors:

Marsan LA. Implications of the Mu-opioid receptor single nucleotide polymorphism on the regulation of the HPA axis. [Thesis]. Penn State University; 2014. Available from: https://submit-etda.libraries.psu.edu/catalog/23605

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


Victoria University of Wellington

10. Simonson, Bridget. Investigating the Effects of Novel Kappa Opioid Receptor Agonists on the Dopamine Transporter.

Degree: 2011, Victoria University of Wellington

 Classic kappa opioid receptor (KOPr) agonists have shown anti-addictive properties in rat models of addiction (Heidbreder et al. 1998; Schenk et al. 1999; Sun et… (more)

Subjects/Keywords: Drug addiction; Kappa opioid receptor; Dopamine transporter

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APA (6th Edition):

Simonson, B. (2011). Investigating the Effects of Novel Kappa Opioid Receptor Agonists on the Dopamine Transporter. (Doctoral Dissertation). Victoria University of Wellington. Retrieved from http://hdl.handle.net/10063/1676

Chicago Manual of Style (16th Edition):

Simonson, Bridget. “Investigating the Effects of Novel Kappa Opioid Receptor Agonists on the Dopamine Transporter.” 2011. Doctoral Dissertation, Victoria University of Wellington. Accessed March 08, 2021. http://hdl.handle.net/10063/1676.

MLA Handbook (7th Edition):

Simonson, Bridget. “Investigating the Effects of Novel Kappa Opioid Receptor Agonists on the Dopamine Transporter.” 2011. Web. 08 Mar 2021.

Vancouver:

Simonson B. Investigating the Effects of Novel Kappa Opioid Receptor Agonists on the Dopamine Transporter. [Internet] [Doctoral dissertation]. Victoria University of Wellington; 2011. [cited 2021 Mar 08]. Available from: http://hdl.handle.net/10063/1676.

Council of Science Editors:

Simonson B. Investigating the Effects of Novel Kappa Opioid Receptor Agonists on the Dopamine Transporter. [Doctoral Dissertation]. Victoria University of Wellington; 2011. Available from: http://hdl.handle.net/10063/1676


West Virginia University

11. Kaski, Shane W. Genetic and Pharmacologic Studies Towards Prevention of opioid use disorder.

Degree: PhD, Physiology, Pharmacology & Neuroscience, 2019, West Virginia University

  Endogenous opioids mediate both analgesic and affective responses to stress. While the mu opioid receptor (MOR) produces the reinforcing euphoric effects responsible for the… (more)

Subjects/Keywords: kappa opioid receptor; addiction; biased agonist

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APA (6th Edition):

Kaski, S. W. (2019). Genetic and Pharmacologic Studies Towards Prevention of opioid use disorder. (Doctoral Dissertation). West Virginia University. Retrieved from https://doi.org/10.33915/etd.4124 ; https://researchrepository.wvu.edu/etd/4124

Chicago Manual of Style (16th Edition):

Kaski, Shane W. “Genetic and Pharmacologic Studies Towards Prevention of opioid use disorder.” 2019. Doctoral Dissertation, West Virginia University. Accessed March 08, 2021. https://doi.org/10.33915/etd.4124 ; https://researchrepository.wvu.edu/etd/4124.

MLA Handbook (7th Edition):

Kaski, Shane W. “Genetic and Pharmacologic Studies Towards Prevention of opioid use disorder.” 2019. Web. 08 Mar 2021.

Vancouver:

Kaski SW. Genetic and Pharmacologic Studies Towards Prevention of opioid use disorder. [Internet] [Doctoral dissertation]. West Virginia University; 2019. [cited 2021 Mar 08]. Available from: https://doi.org/10.33915/etd.4124 ; https://researchrepository.wvu.edu/etd/4124.

Council of Science Editors:

Kaski SW. Genetic and Pharmacologic Studies Towards Prevention of opioid use disorder. [Doctoral Dissertation]. West Virginia University; 2019. Available from: https://doi.org/10.33915/etd.4124 ; https://researchrepository.wvu.edu/etd/4124


University of Arizona

12. Chen, Yanxia. The Role of Prolactin/Prolactin Receptor System in Nociceptor Sensitization and Pain in Females .

Degree: 2019, University of Arizona

 Women have higher pain sensitivity and are over-represented as pain patients. However, the underlying biological mechanisms for sexual dimorphism in pain remain unclear. A puzzling… (more)

Subjects/Keywords: Opioid; Pain; Prolactin/Prolactin receptor; Sexual dimorphism

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APA (6th Edition):

Chen, Y. (2019). The Role of Prolactin/Prolactin Receptor System in Nociceptor Sensitization and Pain in Females . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/636517

Chicago Manual of Style (16th Edition):

Chen, Yanxia. “The Role of Prolactin/Prolactin Receptor System in Nociceptor Sensitization and Pain in Females .” 2019. Doctoral Dissertation, University of Arizona. Accessed March 08, 2021. http://hdl.handle.net/10150/636517.

MLA Handbook (7th Edition):

Chen, Yanxia. “The Role of Prolactin/Prolactin Receptor System in Nociceptor Sensitization and Pain in Females .” 2019. Web. 08 Mar 2021.

Vancouver:

Chen Y. The Role of Prolactin/Prolactin Receptor System in Nociceptor Sensitization and Pain in Females . [Internet] [Doctoral dissertation]. University of Arizona; 2019. [cited 2021 Mar 08]. Available from: http://hdl.handle.net/10150/636517.

Council of Science Editors:

Chen Y. The Role of Prolactin/Prolactin Receptor System in Nociceptor Sensitization and Pain in Females . [Doctoral Dissertation]. University of Arizona; 2019. Available from: http://hdl.handle.net/10150/636517


University of Bath

13. Ma, Qianhan. Sex differences in the effects of kappa opioid receptor agonists and acute stress on the mouse brain.

Degree: PhD, 2020, University of Bath

 Stress is a risk factor for the development of psychiatric disorders (e.g. depression, anxiety) and drug addiction. Stress induces the release of endogenous neuropeptide, dynorphin,… (more)

Subjects/Keywords: Stress; Kappa opioid receptor; Sex differences

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APA (6th Edition):

Ma, Q. (2020). Sex differences in the effects of kappa opioid receptor agonists and acute stress on the mouse brain. (Doctoral Dissertation). University of Bath. Retrieved from https://researchportal.bath.ac.uk/en/studentthesis/sex-differences-in-the-effects-of-kappa-opioid-receptors-agonists-and-acute-stress-on-the-mouse-brain(1a963e86-5e5b-44c1-a0c5-908af630f1ea).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.801372

Chicago Manual of Style (16th Edition):

Ma, Qianhan. “Sex differences in the effects of kappa opioid receptor agonists and acute stress on the mouse brain.” 2020. Doctoral Dissertation, University of Bath. Accessed March 08, 2021. https://researchportal.bath.ac.uk/en/studentthesis/sex-differences-in-the-effects-of-kappa-opioid-receptors-agonists-and-acute-stress-on-the-mouse-brain(1a963e86-5e5b-44c1-a0c5-908af630f1ea).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.801372.

MLA Handbook (7th Edition):

Ma, Qianhan. “Sex differences in the effects of kappa opioid receptor agonists and acute stress on the mouse brain.” 2020. Web. 08 Mar 2021.

Vancouver:

Ma Q. Sex differences in the effects of kappa opioid receptor agonists and acute stress on the mouse brain. [Internet] [Doctoral dissertation]. University of Bath; 2020. [cited 2021 Mar 08]. Available from: https://researchportal.bath.ac.uk/en/studentthesis/sex-differences-in-the-effects-of-kappa-opioid-receptors-agonists-and-acute-stress-on-the-mouse-brain(1a963e86-5e5b-44c1-a0c5-908af630f1ea).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.801372.

Council of Science Editors:

Ma Q. Sex differences in the effects of kappa opioid receptor agonists and acute stress on the mouse brain. [Doctoral Dissertation]. University of Bath; 2020. Available from: https://researchportal.bath.ac.uk/en/studentthesis/sex-differences-in-the-effects-of-kappa-opioid-receptors-agonists-and-acute-stress-on-the-mouse-brain(1a963e86-5e5b-44c1-a0c5-908af630f1ea).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.801372


University of Michigan

14. Henry, Sean. Structural Evolution of a Bifunctional Mu-Opioid Receptor (MOR)/Delta-Opioid Receptor (DOR) Peptidomimetic as Nonaddictive Opioid Analgesics.

Degree: PhD, Medicinal Chemistry, 2019, University of Michigan

 Opioids have been used since antiquity for their ability to treat chronic and severe pain. However, their potent analgesic activity comes with severe side effects,… (more)

Subjects/Keywords: Nonaddictive Opioids; Peptidomimetics; Mu-opioid Receptor Agonist; Delta-opioid Receptor Antagonist; Metabolic Stability; Chemistry; Science

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

APA (6th Edition):

Henry, S. (2019). Structural Evolution of a Bifunctional Mu-Opioid Receptor (MOR)/Delta-Opioid Receptor (DOR) Peptidomimetic as Nonaddictive Opioid Analgesics. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/153441

Chicago Manual of Style (16th Edition):

Henry, Sean. “Structural Evolution of a Bifunctional Mu-Opioid Receptor (MOR)/Delta-Opioid Receptor (DOR) Peptidomimetic as Nonaddictive Opioid Analgesics.” 2019. Doctoral Dissertation, University of Michigan. Accessed March 08, 2021. http://hdl.handle.net/2027.42/153441.

MLA Handbook (7th Edition):

Henry, Sean. “Structural Evolution of a Bifunctional Mu-Opioid Receptor (MOR)/Delta-Opioid Receptor (DOR) Peptidomimetic as Nonaddictive Opioid Analgesics.” 2019. Web. 08 Mar 2021.

Vancouver:

Henry S. Structural Evolution of a Bifunctional Mu-Opioid Receptor (MOR)/Delta-Opioid Receptor (DOR) Peptidomimetic as Nonaddictive Opioid Analgesics. [Internet] [Doctoral dissertation]. University of Michigan; 2019. [cited 2021 Mar 08]. Available from: http://hdl.handle.net/2027.42/153441.

Council of Science Editors:

Henry S. Structural Evolution of a Bifunctional Mu-Opioid Receptor (MOR)/Delta-Opioid Receptor (DOR) Peptidomimetic as Nonaddictive Opioid Analgesics. [Doctoral Dissertation]. University of Michigan; 2019. Available from: http://hdl.handle.net/2027.42/153441


University of Bristol

15. Alghazwani, Yahia S. A. Characterisation of compounds as potential inhibitors of G protein-coupled receptor kinases.

Degree: PhD, 2021, University of Bristol

 G-protein coupled receptor kinases (GRKs) are key regulators of GPCR signalling, and the search continues for potent and selective GRK inhibitors, for example, for the… (more)

Subjects/Keywords: Mu opioid receptor; Delta opioid receptor; Arrestins; GRKs; GRK2; GRK inhibitors; compound101

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

APA (6th Edition):

Alghazwani, Y. S. A. (2021). Characterisation of compounds as potential inhibitors of G protein-coupled receptor kinases. (Doctoral Dissertation). University of Bristol. Retrieved from http://hdl.handle.net/1983/f4624519-6f45-4ccd-aac0-d9f069ab65c9

Chicago Manual of Style (16th Edition):

Alghazwani, Yahia S A. “Characterisation of compounds as potential inhibitors of G protein-coupled receptor kinases.” 2021. Doctoral Dissertation, University of Bristol. Accessed March 08, 2021. http://hdl.handle.net/1983/f4624519-6f45-4ccd-aac0-d9f069ab65c9.

MLA Handbook (7th Edition):

Alghazwani, Yahia S A. “Characterisation of compounds as potential inhibitors of G protein-coupled receptor kinases.” 2021. Web. 08 Mar 2021.

Vancouver:

Alghazwani YSA. Characterisation of compounds as potential inhibitors of G protein-coupled receptor kinases. [Internet] [Doctoral dissertation]. University of Bristol; 2021. [cited 2021 Mar 08]. Available from: http://hdl.handle.net/1983/f4624519-6f45-4ccd-aac0-d9f069ab65c9.

Council of Science Editors:

Alghazwani YSA. Characterisation of compounds as potential inhibitors of G protein-coupled receptor kinases. [Doctoral Dissertation]. University of Bristol; 2021. Available from: http://hdl.handle.net/1983/f4624519-6f45-4ccd-aac0-d9f069ab65c9


Universitat Pompeu Fabra

16. Martínez Navarro, Miriam, 1990-. Affective disorders and neuropathic pain as mutually influential factors : contribution of the opioid system.

Degree: Departament de Ciències Experimentals i de la Salut, 2019, Universitat Pompeu Fabra

 The high inter-individual variability in the neuropathic pain manifestations may lead to differential response of patients to treatments, and suggest the suitability of more personalized… (more)

Subjects/Keywords: Neuropathic pain; Anxiety; Depression; Mu opioid receptor; Delta opioid receptor; Dolor neuropático; Ansiedad; Depresión; Receptor opioide mu; Receptor opioide delta; 616.8

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APA (6th Edition):

Martínez Navarro, Miriam, 1. (2019). Affective disorders and neuropathic pain as mutually influential factors : contribution of the opioid system. (Thesis). Universitat Pompeu Fabra. Retrieved from http://hdl.handle.net/10803/665963

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):

Martínez Navarro, Miriam, 1990-. “Affective disorders and neuropathic pain as mutually influential factors : contribution of the opioid system.” 2019. Thesis, Universitat Pompeu Fabra. Accessed March 08, 2021. http://hdl.handle.net/10803/665963.

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

MLA Handbook (7th Edition):

Martínez Navarro, Miriam, 1990-. “Affective disorders and neuropathic pain as mutually influential factors : contribution of the opioid system.” 2019. Web. 08 Mar 2021.

Vancouver:

Martínez Navarro, Miriam 1. Affective disorders and neuropathic pain as mutually influential factors : contribution of the opioid system. [Internet] [Thesis]. Universitat Pompeu Fabra; 2019. [cited 2021 Mar 08]. Available from: http://hdl.handle.net/10803/665963.

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

Council of Science Editors:

Martínez Navarro, Miriam 1. Affective disorders and neuropathic pain as mutually influential factors : contribution of the opioid system. [Thesis]. Universitat Pompeu Fabra; 2019. Available from: http://hdl.handle.net/10803/665963

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


Temple University

17. 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 March 08, 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. 08 Mar 2021.

Vancouver:

Chiu Y. STUDIES ON NEURITE OUTGROWTH AND RECEPTOR PHOSPHORYLATION FOLLOWING KAPPA OPIOID RECEPTOR ACTIVATION. [Internet] [Doctoral dissertation]. Temple University; 2016. [cited 2021 Mar 08]. 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


University of Illinois – Chicago

18. Moye, Laura S. The Delta Opioid Receptor: A Therapeutic Target For Headache Disorders.

Degree: 2019, University of Illinois – Chicago

 Headache disorders are incredibly common, and those with a migraine-like phenotype are one of the most disabling neurological disorders. Despite the very high prevalence of… (more)

Subjects/Keywords: migraine; headache; delta opioid receptor; CGRP; CGRP receptor

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

APA (6th Edition):

Moye, L. S. (2019). The Delta Opioid Receptor: A Therapeutic Target For Headache Disorders. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/23658

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):

Moye, Laura S. “The Delta Opioid Receptor: A Therapeutic Target For Headache Disorders.” 2019. Thesis, University of Illinois – Chicago. Accessed March 08, 2021. http://hdl.handle.net/10027/23658.

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

MLA Handbook (7th Edition):

Moye, Laura S. “The Delta Opioid Receptor: A Therapeutic Target For Headache Disorders.” 2019. Web. 08 Mar 2021.

Vancouver:

Moye LS. The Delta Opioid Receptor: A Therapeutic Target For Headache Disorders. [Internet] [Thesis]. University of Illinois – Chicago; 2019. [cited 2021 Mar 08]. Available from: http://hdl.handle.net/10027/23658.

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

Council of Science Editors:

Moye LS. The Delta Opioid Receptor: A Therapeutic Target For Headache Disorders. [Thesis]. University of Illinois – Chicago; 2019. Available from: http://hdl.handle.net/10027/23658

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


University of Sydney

19. Heath, Emily May Ling. δ-opioid receptor trafficking in the striatum .

Degree: 2015, University of Sydney

 While primarily studied for its role in analgesia and reward processing, the δ-opioid receptor (DOPr) has also been shown to play an important role in… (more)

Subjects/Keywords: delta-opioid receptor; receptor trafficking; substance P; dopamine; striatum; learning

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APA (6th Edition):

Heath, E. M. L. (2015). δ-opioid receptor trafficking in the striatum . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/15425

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):

Heath, Emily May Ling. “δ-opioid receptor trafficking in the striatum .” 2015. Thesis, University of Sydney. Accessed March 08, 2021. http://hdl.handle.net/2123/15425.

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

MLA Handbook (7th Edition):

Heath, Emily May Ling. “δ-opioid receptor trafficking in the striatum .” 2015. Web. 08 Mar 2021.

Vancouver:

Heath EML. δ-opioid receptor trafficking in the striatum . [Internet] [Thesis]. University of Sydney; 2015. [cited 2021 Mar 08]. Available from: http://hdl.handle.net/2123/15425.

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

Council of Science Editors:

Heath EML. δ-opioid receptor trafficking in the striatum . [Thesis]. University of Sydney; 2015. Available from: http://hdl.handle.net/2123/15425

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


University of Washington

20. 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 March 08, 2021. http://hdl.handle.net/1773/22023.

MLA Handbook (7th Edition):

Schattauer, Selena Schreiber. “Molecular Regulation of Opioid Receptor Signaling.” 2013. Web. 08 Mar 2021.

Vancouver:

Schattauer SS. Molecular Regulation of Opioid Receptor Signaling. [Internet] [Doctoral dissertation]. University of Washington; 2013. [cited 2021 Mar 08]. 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


University of Kansas

21. Caspers, Michael J. Investigations Of Salvinorin A: Synthetic Isolation, Quantification, And In Vivo Characteristics.

Degree: MS, Medicinal Chemistry, 2013, University of Kansas

 While many ligands are known to interact with the opioid receptor system, most can be traced back to the common morphine scaffold. In several cases… (more)

Subjects/Keywords: Chemistry; LC-MS/MS; Natural Product; Opioid; Opioid Receptor; Salvinorin A; Solid Support Reagent

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

APA (6th Edition):

Caspers, M. J. (2013). Investigations Of Salvinorin A: Synthetic Isolation, Quantification, And In Vivo Characteristics. (Masters Thesis). University of Kansas. Retrieved from http://hdl.handle.net/1808/21624

Chicago Manual of Style (16th Edition):

Caspers, Michael J. “Investigations Of Salvinorin A: Synthetic Isolation, Quantification, And In Vivo Characteristics.” 2013. Masters Thesis, University of Kansas. Accessed March 08, 2021. http://hdl.handle.net/1808/21624.

MLA Handbook (7th Edition):

Caspers, Michael J. “Investigations Of Salvinorin A: Synthetic Isolation, Quantification, And In Vivo Characteristics.” 2013. Web. 08 Mar 2021.

Vancouver:

Caspers MJ. Investigations Of Salvinorin A: Synthetic Isolation, Quantification, And In Vivo Characteristics. [Internet] [Masters thesis]. University of Kansas; 2013. [cited 2021 Mar 08]. Available from: http://hdl.handle.net/1808/21624.

Council of Science Editors:

Caspers MJ. Investigations Of Salvinorin A: Synthetic Isolation, Quantification, And In Vivo Characteristics. [Masters Thesis]. University of Kansas; 2013. Available from: http://hdl.handle.net/1808/21624

22. Lutz, Pierre-Eric. La comorbidité entre dépendance aux opiacés et dépression : mécanismes sérotoninergiques dans un modèle murin : Comorbidity between opiate addiction and depression : serotonergic mechanisms in a mouse model.

Degree: Docteur es, Neurosciences, 2012, Université de Strasbourg

L’addiction ou dépendance aux substances psychoactives est une affection chronique, fréquente et grave, émaillée de rechutes et de périodes d’abstinence. Les études épidémiologiques montrent que… (more)

Subjects/Keywords: Récepteur opioïde mu; Récepteur opioïde delta; Récepteur opioïde kappa; Addiction; Dépression; Émotions; Abstinence; Mu opioid receptor; Delta opioid receptor; Kappa opioid receptor; Addiction; Depression; Emotions; Abstinence; 572.8; 616.86

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

APA (6th Edition):

Lutz, P. (2012). La comorbidité entre dépendance aux opiacés et dépression : mécanismes sérotoninergiques dans un modèle murin : Comorbidity between opiate addiction and depression : serotonergic mechanisms in a mouse model. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2012STRAJ022

Chicago Manual of Style (16th Edition):

Lutz, Pierre-Eric. “La comorbidité entre dépendance aux opiacés et dépression : mécanismes sérotoninergiques dans un modèle murin : Comorbidity between opiate addiction and depression : serotonergic mechanisms in a mouse model.” 2012. Doctoral Dissertation, Université de Strasbourg. Accessed March 08, 2021. http://www.theses.fr/2012STRAJ022.

MLA Handbook (7th Edition):

Lutz, Pierre-Eric. “La comorbidité entre dépendance aux opiacés et dépression : mécanismes sérotoninergiques dans un modèle murin : Comorbidity between opiate addiction and depression : serotonergic mechanisms in a mouse model.” 2012. Web. 08 Mar 2021.

Vancouver:

Lutz P. La comorbidité entre dépendance aux opiacés et dépression : mécanismes sérotoninergiques dans un modèle murin : Comorbidity between opiate addiction and depression : serotonergic mechanisms in a mouse model. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2012. [cited 2021 Mar 08]. Available from: http://www.theses.fr/2012STRAJ022.

Council of Science Editors:

Lutz P. La comorbidité entre dépendance aux opiacés et dépression : mécanismes sérotoninergiques dans un modèle murin : Comorbidity between opiate addiction and depression : serotonergic mechanisms in a mouse model. [Doctoral Dissertation]. Université de Strasbourg; 2012. Available from: http://www.theses.fr/2012STRAJ022


Freie Universität Berlin

23. Jagla, Christina. eine randomisierte, doppel-blinde, Placebo-kontrollierte Studie.

Degree: 2015, Freie Universität Berlin

 Experimentelle Studien zeigen, dass ein beachtlicher Anteil von Opioidanalgesie durch periphere Opioidrezeptoren hervorgerufen werden kann. Diese Studie untersuchte den Beitrag dieser Rezeptoren an der klinischen… (more)

Subjects/Keywords: analgesia; morphine; opioids; opioid receptor; peripheral opioid receptor; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit

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APA (6th Edition):

Jagla, C. (2015). eine randomisierte, doppel-blinde, Placebo-kontrollierte Studie. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-5520

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):

Jagla, Christina. “eine randomisierte, doppel-blinde, Placebo-kontrollierte Studie.” 2015. Thesis, Freie Universität Berlin. Accessed March 08, 2021. http://dx.doi.org/10.17169/refubium-5520.

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

MLA Handbook (7th Edition):

Jagla, Christina. “eine randomisierte, doppel-blinde, Placebo-kontrollierte Studie.” 2015. Web. 08 Mar 2021.

Vancouver:

Jagla C. eine randomisierte, doppel-blinde, Placebo-kontrollierte Studie. [Internet] [Thesis]. Freie Universität Berlin; 2015. [cited 2021 Mar 08]. Available from: http://dx.doi.org/10.17169/refubium-5520.

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

Council of Science Editors:

Jagla C. eine randomisierte, doppel-blinde, Placebo-kontrollierte Studie. [Thesis]. Freie Universität Berlin; 2015. Available from: http://dx.doi.org/10.17169/refubium-5520

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

24. Rudén, Ludvig. Neurobiology of opioid addiction.

Degree: Bioscience, 2018, University of Skövde

  Since the use of opioids started to emerge for analgesic reasons in the 19th century with the synthetization of morphine, opioids have been studied… (more)

Subjects/Keywords: Opioids; reinforcement; mu opioid receptor; addiction; allostasis; cAMP; Opioider; belöning; mu opioid receptor; beroende; allostas; cAMP; Neurosciences; Neurovetenskaper

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APA (6th Edition):

Rudén, L. (2018). Neurobiology of opioid addiction. (Thesis). University of Skövde. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-15735

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):

Rudén, Ludvig. “Neurobiology of opioid addiction.” 2018. Thesis, University of Skövde. Accessed March 08, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-15735.

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

MLA Handbook (7th Edition):

Rudén, Ludvig. “Neurobiology of opioid addiction.” 2018. Web. 08 Mar 2021.

Vancouver:

Rudén L. Neurobiology of opioid addiction. [Internet] [Thesis]. University of Skövde; 2018. [cited 2021 Mar 08]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-15735.

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

Council of Science Editors:

Rudén L. Neurobiology of opioid addiction. [Thesis]. University of Skövde; 2018. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-15735

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


University of Rochester

25. Khimich, Maxim. Stage-specific inhibition of IL-7R expression by the kappa opioid receptor in double negative thymocytes.

Degree: PhD, 2009, University of Rochester

 Opioids are known to affect both immune cell functions and development. Administration of morphine as well as knockout of the kappa-, but not mu-opioid receptor(more)

Subjects/Keywords: Opioid receptor; Thymocytes; Interleukin 7 receptor

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

APA (6th Edition):

Khimich, M. (2009). Stage-specific inhibition of IL-7R expression by the kappa opioid receptor in double negative thymocytes. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/8483

Chicago Manual of Style (16th Edition):

Khimich, Maxim. “Stage-specific inhibition of IL-7R expression by the kappa opioid receptor in double negative thymocytes.” 2009. Doctoral Dissertation, University of Rochester. Accessed March 08, 2021. http://hdl.handle.net/1802/8483.

MLA Handbook (7th Edition):

Khimich, Maxim. “Stage-specific inhibition of IL-7R expression by the kappa opioid receptor in double negative thymocytes.” 2009. Web. 08 Mar 2021.

Vancouver:

Khimich M. Stage-specific inhibition of IL-7R expression by the kappa opioid receptor in double negative thymocytes. [Internet] [Doctoral dissertation]. University of Rochester; 2009. [cited 2021 Mar 08]. Available from: http://hdl.handle.net/1802/8483.

Council of Science Editors:

Khimich M. Stage-specific inhibition of IL-7R expression by the kappa opioid receptor in double negative thymocytes. [Doctoral Dissertation]. University of Rochester; 2009. Available from: http://hdl.handle.net/1802/8483


Temple University

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

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 March 08, 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. 08 Mar 2021.

Vancouver:

Inan S. Pharmacological and Neuroanatomical Analysis of GNTI-Induced Repetitive Behavior in Mice. [Internet] [Doctoral dissertation]. Temple University; 2010. [cited 2021 Mar 08]. 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


University of California – San Francisco

27. Viet, Chi Tonglien. Epigenetic Silencing is a Novel Mechanism Controlling Cancer-Induced Pain.

Degree: Nursing, 2011, University of California – San Francisco

 Cancer pain creates a poor quality of life for cancer patients. Chroniccancer pain is a major public health problem in which little progress has been… (more)

Subjects/Keywords: Oncology; cancer pain; demethylating drug; endothelin B receptor; methylation; mu-opioid receptor; oral cancer

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

APA (6th Edition):

Viet, C. T. (2011). Epigenetic Silencing is a Novel Mechanism Controlling Cancer-Induced Pain. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/0w61j9tp

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):

Viet, Chi Tonglien. “Epigenetic Silencing is a Novel Mechanism Controlling Cancer-Induced Pain.” 2011. Thesis, University of California – San Francisco. Accessed March 08, 2021. http://www.escholarship.org/uc/item/0w61j9tp.

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

MLA Handbook (7th Edition):

Viet, Chi Tonglien. “Epigenetic Silencing is a Novel Mechanism Controlling Cancer-Induced Pain.” 2011. Web. 08 Mar 2021.

Vancouver:

Viet CT. Epigenetic Silencing is a Novel Mechanism Controlling Cancer-Induced Pain. [Internet] [Thesis]. University of California – San Francisco; 2011. [cited 2021 Mar 08]. Available from: http://www.escholarship.org/uc/item/0w61j9tp.

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

Council of Science Editors:

Viet CT. Epigenetic Silencing is a Novel Mechanism Controlling Cancer-Induced Pain. [Thesis]. University of California – San Francisco; 2011. Available from: http://www.escholarship.org/uc/item/0w61j9tp

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


NSYSU

28. Chen, Yu-Shan. The Angiogenic Effects of β-endorphin in Endothelial Cells.

Degree: Master, Biological Sciences, 2011, NSYSU

 Angiogenesis is a fundamental process in reproduction and wound healing. Angiogenesis is also indispensable for solid tumor growth and metastasis, and also associated with angiogenic… (more)

Subjects/Keywords: angiogenesis; morphine; opioid receptor; endothelial cells; β-EP

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

APA (6th Edition):

Chen, Y. (2011). The Angiogenic Effects of β-endorphin in Endothelial Cells. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0828111-002130

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):

Chen, Yu-Shan. “The Angiogenic Effects of β-endorphin in Endothelial Cells.” 2011. Thesis, NSYSU. Accessed March 08, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0828111-002130.

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

MLA Handbook (7th Edition):

Chen, Yu-Shan. “The Angiogenic Effects of β-endorphin in Endothelial Cells.” 2011. Web. 08 Mar 2021.

Vancouver:

Chen Y. The Angiogenic Effects of β-endorphin in Endothelial Cells. [Internet] [Thesis]. NSYSU; 2011. [cited 2021 Mar 08]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0828111-002130.

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

Council of Science Editors:

Chen Y. The Angiogenic Effects of β-endorphin in Endothelial Cells. [Thesis]. NSYSU; 2011. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0828111-002130

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

29. Driscoll, Joseph. Effects of Corticotrophin Releasing Factor on Ventral Tegmental Area Neurons.

Degree: Neuroscience, 2017, University of California – Berkeley

 A major hypothesis in the pathology of addiction is that maladaptive behaviors result from a disruption in the homeostatic balance between stress and reward circuitry.… (more)

Subjects/Keywords: Neurosciences; addiction; CRF; kappa opioid receptor; ventral tegmental area

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

APA (6th Edition):

Driscoll, J. (2017). Effects of Corticotrophin Releasing Factor on Ventral Tegmental Area Neurons. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/3703d19q

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):

Driscoll, Joseph. “Effects of Corticotrophin Releasing Factor on Ventral Tegmental Area Neurons.” 2017. Thesis, University of California – Berkeley. Accessed March 08, 2021. http://www.escholarship.org/uc/item/3703d19q.

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

MLA Handbook (7th Edition):

Driscoll, Joseph. “Effects of Corticotrophin Releasing Factor on Ventral Tegmental Area Neurons.” 2017. Web. 08 Mar 2021.

Vancouver:

Driscoll J. Effects of Corticotrophin Releasing Factor on Ventral Tegmental Area Neurons. [Internet] [Thesis]. University of California – Berkeley; 2017. [cited 2021 Mar 08]. Available from: http://www.escholarship.org/uc/item/3703d19q.

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

Council of Science Editors:

Driscoll J. Effects of Corticotrophin Releasing Factor on Ventral Tegmental Area Neurons. [Thesis]. University of California – Berkeley; 2017. Available from: http://www.escholarship.org/uc/item/3703d19q

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


Temple University

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

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 March 08, 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. 08 Mar 2021.

Vancouver:

Regan PM. Regulation and Functional Impact of Opioid Receptor Splicing in Response to Morphine. [Internet] [Doctoral dissertation]. Temple University; 2015. [cited 2021 Mar 08]. 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

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