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You searched for +publisher:"University of Arizona" +contributor:("Porreca, Frank"). Showing records 1 – 30 of 46 total matches.

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University of Arizona

1. Gu, Pengfei. Sumatriptan-Induced Sensitization of the Trigeminal System to Cortical Spreading Depression (CSD) is Blocked by Topiramate .

Degree: 2012, University of Arizona

 The studies in this thesis research were conducted to investigate if sensitivity to induced cortical spread depression (CSD) or the consequence of a CSD event… (more)

Subjects/Keywords: Sumatriptan; Topiramate; Medical Pharmacology; Bright light stress; Cortical Spreading Depression

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APA (6th Edition):

Gu, P. (2012). Sumatriptan-Induced Sensitization of the Trigeminal System to Cortical Spreading Depression (CSD) is Blocked by Topiramate . (Masters Thesis). University of Arizona. Retrieved from http://hdl.handle.net/10150/243092

Chicago Manual of Style (16th Edition):

Gu, Pengfei. “Sumatriptan-Induced Sensitization of the Trigeminal System to Cortical Spreading Depression (CSD) is Blocked by Topiramate .” 2012. Masters Thesis, University of Arizona. Accessed October 27, 2020. http://hdl.handle.net/10150/243092.

MLA Handbook (7th Edition):

Gu, Pengfei. “Sumatriptan-Induced Sensitization of the Trigeminal System to Cortical Spreading Depression (CSD) is Blocked by Topiramate .” 2012. Web. 27 Oct 2020.

Vancouver:

Gu P. Sumatriptan-Induced Sensitization of the Trigeminal System to Cortical Spreading Depression (CSD) is Blocked by Topiramate . [Internet] [Masters thesis]. University of Arizona; 2012. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10150/243092.

Council of Science Editors:

Gu P. Sumatriptan-Induced Sensitization of the Trigeminal System to Cortical Spreading Depression (CSD) is Blocked by Topiramate . [Masters Thesis]. University of Arizona; 2012. Available from: http://hdl.handle.net/10150/243092


University of Arizona

2. Sukhtankar, Devki. Mechanisms Underlying Cancer-Induced Bone Pain .

Degree: 2011, University of Arizona

 Pain from bone metastases is multifaceted with clinical descriptors including ongoing pain, hypersensitivity to external stimuli and intermittent episodes of breakthrough pain characterized as a… (more)

Subjects/Keywords: Cancer; Interleukin; p38 MAPK; Pain; Cancer Biology; Bone; breakthrough pain

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APA (6th Edition):

Sukhtankar, D. (2011). Mechanisms Underlying Cancer-Induced Bone Pain . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/202718

Chicago Manual of Style (16th Edition):

Sukhtankar, Devki. “Mechanisms Underlying Cancer-Induced Bone Pain .” 2011. Doctoral Dissertation, University of Arizona. Accessed October 27, 2020. http://hdl.handle.net/10150/202718.

MLA Handbook (7th Edition):

Sukhtankar, Devki. “Mechanisms Underlying Cancer-Induced Bone Pain .” 2011. Web. 27 Oct 2020.

Vancouver:

Sukhtankar D. Mechanisms Underlying Cancer-Induced Bone Pain . [Internet] [Doctoral dissertation]. University of Arizona; 2011. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10150/202718.

Council of Science Editors:

Sukhtankar D. Mechanisms Underlying Cancer-Induced Bone Pain . [Doctoral Dissertation]. University of Arizona; 2011. Available from: http://hdl.handle.net/10150/202718


University of Arizona

3. Gee, Taylor Allison. The Dopaminergic Encoding of Pain and Pain Relief in the Mesolimbic Pathway .

Degree: 2020, University of Arizona

 Elucidating the chemical changes that underlie dysfunction of the central nervous system requires tools and techniques that enable rapid and accurate neurotransmitter quantification. The dopaminergic… (more)

Subjects/Keywords: Anesthesia; Dopamine; Opioids; Pain; Voltammetry

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APA (6th Edition):

Gee, T. A. (2020). The Dopaminergic Encoding of Pain and Pain Relief in the Mesolimbic Pathway . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/642164

Chicago Manual of Style (16th Edition):

Gee, Taylor Allison. “The Dopaminergic Encoding of Pain and Pain Relief in the Mesolimbic Pathway .” 2020. Doctoral Dissertation, University of Arizona. Accessed October 27, 2020. http://hdl.handle.net/10150/642164.

MLA Handbook (7th Edition):

Gee, Taylor Allison. “The Dopaminergic Encoding of Pain and Pain Relief in the Mesolimbic Pathway .” 2020. Web. 27 Oct 2020.

Vancouver:

Gee TA. The Dopaminergic Encoding of Pain and Pain Relief in the Mesolimbic Pathway . [Internet] [Doctoral dissertation]. University of Arizona; 2020. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10150/642164.

Council of Science Editors:

Gee TA. The Dopaminergic Encoding of Pain and Pain Relief in the Mesolimbic Pathway . [Doctoral Dissertation]. University of Arizona; 2020. Available from: http://hdl.handle.net/10150/642164


University of Arizona

4. 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 October 27, 2020. 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. 27 Oct 2020.

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 2020 Oct 27]. 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 Arizona

5. LaVigne, Justin Edward. Exploring Opioid and Cannabis Pharmacology: Biased Signaling of Endogenous Opioid Peptides and Cannabimimetic Properties of Cannabis Sativa Terpenes .

Degree: 2020, University of Arizona

 The United States has roughly 100 million people suffering from pain disorders, including chronic pain, which is becoming an ever increasing medical and economic burden.… (more)

Subjects/Keywords: Biased Signaling; Cannabinoid; Cannabis; Entourage Effect; Opioid; Terpenes

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APA (6th Edition):

LaVigne, J. E. (2020). Exploring Opioid and Cannabis Pharmacology: Biased Signaling of Endogenous Opioid Peptides and Cannabimimetic Properties of Cannabis Sativa Terpenes . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/641706

Chicago Manual of Style (16th Edition):

LaVigne, Justin Edward. “Exploring Opioid and Cannabis Pharmacology: Biased Signaling of Endogenous Opioid Peptides and Cannabimimetic Properties of Cannabis Sativa Terpenes .” 2020. Doctoral Dissertation, University of Arizona. Accessed October 27, 2020. http://hdl.handle.net/10150/641706.

MLA Handbook (7th Edition):

LaVigne, Justin Edward. “Exploring Opioid and Cannabis Pharmacology: Biased Signaling of Endogenous Opioid Peptides and Cannabimimetic Properties of Cannabis Sativa Terpenes .” 2020. Web. 27 Oct 2020.

Vancouver:

LaVigne JE. Exploring Opioid and Cannabis Pharmacology: Biased Signaling of Endogenous Opioid Peptides and Cannabimimetic Properties of Cannabis Sativa Terpenes . [Internet] [Doctoral dissertation]. University of Arizona; 2020. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10150/641706.

Council of Science Editors:

LaVigne JE. Exploring Opioid and Cannabis Pharmacology: Biased Signaling of Endogenous Opioid Peptides and Cannabimimetic Properties of Cannabis Sativa Terpenes . [Doctoral Dissertation]. University of Arizona; 2020. Available from: http://hdl.handle.net/10150/641706


University of Arizona

6. LI, YINGXUE. DESIGN, SYNTHESIS, AND CHARACTERIZATION OF HELICAL OPIOID GLYCOPEPTIDE AGONISTS: THE STUDY OF THE STRUCTURE-ACTIVITY RELATIONSHIP AND TRANSPORT OF GLYCOPEPTIDES RELATED TO BETA-ENDORPHIN AND DYNORPHIN .

Degree: 2011, University of Arizona

 Structure-activity relationships (SAR) of opioid peptide analogues related to endorphin or dynorphin have provided rational and powerful approaches toward the design of peptide therapeutics. A… (more)

Subjects/Keywords: Chemistry

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APA (6th Edition):

LI, Y. (2011). DESIGN, SYNTHESIS, AND CHARACTERIZATION OF HELICAL OPIOID GLYCOPEPTIDE AGONISTS: THE STUDY OF THE STRUCTURE-ACTIVITY RELATIONSHIP AND TRANSPORT OF GLYCOPEPTIDES RELATED TO BETA-ENDORPHIN AND DYNORPHIN . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/203033

Chicago Manual of Style (16th Edition):

LI, YINGXUE. “DESIGN, SYNTHESIS, AND CHARACTERIZATION OF HELICAL OPIOID GLYCOPEPTIDE AGONISTS: THE STUDY OF THE STRUCTURE-ACTIVITY RELATIONSHIP AND TRANSPORT OF GLYCOPEPTIDES RELATED TO BETA-ENDORPHIN AND DYNORPHIN .” 2011. Doctoral Dissertation, University of Arizona. Accessed October 27, 2020. http://hdl.handle.net/10150/203033.

MLA Handbook (7th Edition):

LI, YINGXUE. “DESIGN, SYNTHESIS, AND CHARACTERIZATION OF HELICAL OPIOID GLYCOPEPTIDE AGONISTS: THE STUDY OF THE STRUCTURE-ACTIVITY RELATIONSHIP AND TRANSPORT OF GLYCOPEPTIDES RELATED TO BETA-ENDORPHIN AND DYNORPHIN .” 2011. Web. 27 Oct 2020.

Vancouver:

LI Y. DESIGN, SYNTHESIS, AND CHARACTERIZATION OF HELICAL OPIOID GLYCOPEPTIDE AGONISTS: THE STUDY OF THE STRUCTURE-ACTIVITY RELATIONSHIP AND TRANSPORT OF GLYCOPEPTIDES RELATED TO BETA-ENDORPHIN AND DYNORPHIN . [Internet] [Doctoral dissertation]. University of Arizona; 2011. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10150/203033.

Council of Science Editors:

LI Y. DESIGN, SYNTHESIS, AND CHARACTERIZATION OF HELICAL OPIOID GLYCOPEPTIDE AGONISTS: THE STUDY OF THE STRUCTURE-ACTIVITY RELATIONSHIP AND TRANSPORT OF GLYCOPEPTIDES RELATED TO BETA-ENDORPHIN AND DYNORPHIN . [Doctoral Dissertation]. University of Arizona; 2011. Available from: http://hdl.handle.net/10150/203033


University of Arizona

7. Yan, Jin. UNDERSTANDING THE PATHOPHYSIOLOGY OF MIGRAINE: ACTIVATION AND SENSITIZATION OF DURAL AFFERENTS .

Degree: 2011, University of Arizona

 Migraine is one of the most common neurological disorders. The pathological conditions that initiate and sensitize afferent pain signaling are poorly understood. The goal of… (more)

Subjects/Keywords: Interleukin 6; Migraine; Nav1.7; Medical Pharmacology; acid sensing ion channels; dural afferents

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APA (6th Edition):

Yan, J. (2011). UNDERSTANDING THE PATHOPHYSIOLOGY OF MIGRAINE: ACTIVATION AND SENSITIZATION OF DURAL AFFERENTS . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/205415

Chicago Manual of Style (16th Edition):

Yan, Jin. “UNDERSTANDING THE PATHOPHYSIOLOGY OF MIGRAINE: ACTIVATION AND SENSITIZATION OF DURAL AFFERENTS .” 2011. Doctoral Dissertation, University of Arizona. Accessed October 27, 2020. http://hdl.handle.net/10150/205415.

MLA Handbook (7th Edition):

Yan, Jin. “UNDERSTANDING THE PATHOPHYSIOLOGY OF MIGRAINE: ACTIVATION AND SENSITIZATION OF DURAL AFFERENTS .” 2011. Web. 27 Oct 2020.

Vancouver:

Yan J. UNDERSTANDING THE PATHOPHYSIOLOGY OF MIGRAINE: ACTIVATION AND SENSITIZATION OF DURAL AFFERENTS . [Internet] [Doctoral dissertation]. University of Arizona; 2011. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10150/205415.

Council of Science Editors:

Yan J. UNDERSTANDING THE PATHOPHYSIOLOGY OF MIGRAINE: ACTIVATION AND SENSITIZATION OF DURAL AFFERENTS . [Doctoral Dissertation]. University of Arizona; 2011. Available from: http://hdl.handle.net/10150/205415


University of Arizona

8. Tillu, Dipti Vilas. AMPK as a Novel Target for Treatment of Neuropathic and Post-Surgical Pain .

Degree: 2014, University of Arizona

 Chronic pain is a major health problem affecting more than 1.5 billion people worldwide. Specifically, neuropathic pain and chronic post-surgical pain are debilitating clinical conditions… (more)

Subjects/Keywords: Chronic Pain; Metformin; Post-surgical Pain; Medical Pharmacology; AMP Kinase

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APA (6th Edition):

Tillu, D. V. (2014). AMPK as a Novel Target for Treatment of Neuropathic and Post-Surgical Pain . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/315856

Chicago Manual of Style (16th Edition):

Tillu, Dipti Vilas. “AMPK as a Novel Target for Treatment of Neuropathic and Post-Surgical Pain .” 2014. Doctoral Dissertation, University of Arizona. Accessed October 27, 2020. http://hdl.handle.net/10150/315856.

MLA Handbook (7th Edition):

Tillu, Dipti Vilas. “AMPK as a Novel Target for Treatment of Neuropathic and Post-Surgical Pain .” 2014. Web. 27 Oct 2020.

Vancouver:

Tillu DV. AMPK as a Novel Target for Treatment of Neuropathic and Post-Surgical Pain . [Internet] [Doctoral dissertation]. University of Arizona; 2014. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10150/315856.

Council of Science Editors:

Tillu DV. AMPK as a Novel Target for Treatment of Neuropathic and Post-Surgical Pain . [Doctoral Dissertation]. University of Arizona; 2014. Available from: http://hdl.handle.net/10150/315856


University of Arizona

9. 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 October 27, 2020. 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. 27 Oct 2020.

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 2020 Oct 27]. 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

10. Remeniuk, Bethany Lynne. Capturing Affective Dimensions of Cancer-Induced Bone Pain Preclinically .

Degree: 2015, University of Arizona

 Pain is the most feared symptom of cancer and can impact patients' lives more than the cancer itself. Despite improvements in cancer prevention and detection,… (more)

Subjects/Keywords: breast cancer bone metastasis; cancer bone pain; interleukin-6; ongoing pain; transient receptor potential vanilloid-1; Cancer Biology; breakthrough pain

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APA (6th Edition):

Remeniuk, B. L. (2015). Capturing Affective Dimensions of Cancer-Induced Bone Pain Preclinically . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/556862

Chicago Manual of Style (16th Edition):

Remeniuk, Bethany Lynne. “Capturing Affective Dimensions of Cancer-Induced Bone Pain Preclinically .” 2015. Doctoral Dissertation, University of Arizona. Accessed October 27, 2020. http://hdl.handle.net/10150/556862.

MLA Handbook (7th Edition):

Remeniuk, Bethany Lynne. “Capturing Affective Dimensions of Cancer-Induced Bone Pain Preclinically .” 2015. Web. 27 Oct 2020.

Vancouver:

Remeniuk BL. Capturing Affective Dimensions of Cancer-Induced Bone Pain Preclinically . [Internet] [Doctoral dissertation]. University of Arizona; 2015. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10150/556862.

Council of Science Editors:

Remeniuk BL. Capturing Affective Dimensions of Cancer-Induced Bone Pain Preclinically . [Doctoral Dissertation]. University of Arizona; 2015. Available from: http://hdl.handle.net/10150/556862

11. Okun, Alec. Mechanistic Evaluation of Affective Dimensions of Pain in Rats .

Degree: 2012, University of Arizona

 Pain is the primary reason why patients seek medical care and there is a great unmet need for the development of pain relieving medications. The… (more)

Subjects/Keywords: ongoing pain; pain; pain relief is rewarding; spontaneous pain; Medical Pharmacology; anterior cingulate cortex; measuring pain preclinically

…reviewed and approved by the Institutional Animal Care and Use Committee of the University of… …Arizona, and were in accord with the guidelines established by the National Institutes of Health… 

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APA (6th Edition):

Okun, A. (2012). Mechanistic Evaluation of Affective Dimensions of Pain in Rats . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/243095

Chicago Manual of Style (16th Edition):

Okun, Alec. “Mechanistic Evaluation of Affective Dimensions of Pain in Rats .” 2012. Doctoral Dissertation, University of Arizona. Accessed October 27, 2020. http://hdl.handle.net/10150/243095.

MLA Handbook (7th Edition):

Okun, Alec. “Mechanistic Evaluation of Affective Dimensions of Pain in Rats .” 2012. Web. 27 Oct 2020.

Vancouver:

Okun A. Mechanistic Evaluation of Affective Dimensions of Pain in Rats . [Internet] [Doctoral dissertation]. University of Arizona; 2012. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10150/243095.

Council of Science Editors:

Okun A. Mechanistic Evaluation of Affective Dimensions of Pain in Rats . [Doctoral Dissertation]. University of Arizona; 2012. Available from: http://hdl.handle.net/10150/243095

12. Gomtsian, Lusine. Evaluation of Cortical and Sub-Cortical Opioid-Sensitive Pain Neurocircuitry in Rodents .

Degree: 2018, University of Arizona

 Mu-opioid (MOR) and kappa-opioid receptors (KOR) are expressed throughout the pain pathways and in pain-related brain areas to provide endogenous pain control. MOR circuits in… (more)

Subjects/Keywords: Amygdala; Anterior Cingulate Cortex; Descending pain modulation; Opioids; Pain

…of the University of Arizona. Animals were monitored throughout the duration of the study… 

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APA (6th Edition):

Gomtsian, L. (2018). Evaluation of Cortical and Sub-Cortical Opioid-Sensitive Pain Neurocircuitry in Rodents . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/631908

Chicago Manual of Style (16th Edition):

Gomtsian, Lusine. “Evaluation of Cortical and Sub-Cortical Opioid-Sensitive Pain Neurocircuitry in Rodents .” 2018. Doctoral Dissertation, University of Arizona. Accessed October 27, 2020. http://hdl.handle.net/10150/631908.

MLA Handbook (7th Edition):

Gomtsian, Lusine. “Evaluation of Cortical and Sub-Cortical Opioid-Sensitive Pain Neurocircuitry in Rodents .” 2018. Web. 27 Oct 2020.

Vancouver:

Gomtsian L. Evaluation of Cortical and Sub-Cortical Opioid-Sensitive Pain Neurocircuitry in Rodents . [Internet] [Doctoral dissertation]. University of Arizona; 2018. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10150/631908.

Council of Science Editors:

Gomtsian L. Evaluation of Cortical and Sub-Cortical Opioid-Sensitive Pain Neurocircuitry in Rodents . [Doctoral Dissertation]. University of Arizona; 2018. Available from: http://hdl.handle.net/10150/631908


University of Arizona

13. Gardell, Luis. Dynorphin promotes opioid-induced abnormal pain and antinociceptive tolerance .

Degree: 2002, University of Arizona

 Consequences of injury to peripheral nerves and opioid tolerance share features including tactile and thermal hypersensitivity, decreased spinal opioid antinociception and upregulation of spinal dynorphin.… (more)

Subjects/Keywords: Health Sciences; Pharmacology.

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APA (6th Edition):

Gardell, L. (2002). Dynorphin promotes opioid-induced abnormal pain and antinociceptive tolerance . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/280121

Chicago Manual of Style (16th Edition):

Gardell, Luis. “Dynorphin promotes opioid-induced abnormal pain and antinociceptive tolerance .” 2002. Doctoral Dissertation, University of Arizona. Accessed October 27, 2020. http://hdl.handle.net/10150/280121.

MLA Handbook (7th Edition):

Gardell, Luis. “Dynorphin promotes opioid-induced abnormal pain and antinociceptive tolerance .” 2002. Web. 27 Oct 2020.

Vancouver:

Gardell L. Dynorphin promotes opioid-induced abnormal pain and antinociceptive tolerance . [Internet] [Doctoral dissertation]. University of Arizona; 2002. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10150/280121.

Council of Science Editors:

Gardell L. Dynorphin promotes opioid-induced abnormal pain and antinociceptive tolerance . [Doctoral Dissertation]. University of Arizona; 2002. Available from: http://hdl.handle.net/10150/280121


University of Arizona

14. Bilsky, Edward James, 1967-. Studies on opioid delta receptor mediated antinociception, opioid antinociceptive tolerance and physical dependence .

Degree: 1997, University of Arizona

 The central hypothesis of this dissertation is that agonists and antagonists acting at the delta opioid receptor will have therapeutic applications in treating acute and… (more)

Subjects/Keywords: Biology, Neuroscience.; Health Sciences, Pharmacology.; Biology, Animal Physiology.

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APA (6th Edition):

Bilsky, Edward James, 1. (1997). Studies on opioid delta receptor mediated antinociception, opioid antinociceptive tolerance and physical dependence . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/282311

Chicago Manual of Style (16th Edition):

Bilsky, Edward James, 1967-. “Studies on opioid delta receptor mediated antinociception, opioid antinociceptive tolerance and physical dependence .” 1997. Doctoral Dissertation, University of Arizona. Accessed October 27, 2020. http://hdl.handle.net/10150/282311.

MLA Handbook (7th Edition):

Bilsky, Edward James, 1967-. “Studies on opioid delta receptor mediated antinociception, opioid antinociceptive tolerance and physical dependence .” 1997. Web. 27 Oct 2020.

Vancouver:

Bilsky, Edward James 1. Studies on opioid delta receptor mediated antinociception, opioid antinociceptive tolerance and physical dependence . [Internet] [Doctoral dissertation]. University of Arizona; 1997. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10150/282311.

Council of Science Editors:

Bilsky, Edward James 1. Studies on opioid delta receptor mediated antinociception, opioid antinociceptive tolerance and physical dependence . [Doctoral Dissertation]. University of Arizona; 1997. Available from: http://hdl.handle.net/10150/282311


University of Arizona

15. Nichols, Michael Lorne, 1967-. Mechanisms of reduced opioid effectiveness in a rat model of neuropathic pain .

Degree: 1997, University of Arizona

 Peripheral nerve injury can result in long-lasting, abnormal pain states referred to as neuropathic pains. These pains can result in increased sensitivity to both noxious… (more)

Subjects/Keywords: Biology; Neuroscience.

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APA (6th Edition):

Nichols, Michael Lorne, 1. (1997). Mechanisms of reduced opioid effectiveness in a rat model of neuropathic pain . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/282342

Chicago Manual of Style (16th Edition):

Nichols, Michael Lorne, 1967-. “Mechanisms of reduced opioid effectiveness in a rat model of neuropathic pain .” 1997. Doctoral Dissertation, University of Arizona. Accessed October 27, 2020. http://hdl.handle.net/10150/282342.

MLA Handbook (7th Edition):

Nichols, Michael Lorne, 1967-. “Mechanisms of reduced opioid effectiveness in a rat model of neuropathic pain .” 1997. Web. 27 Oct 2020.

Vancouver:

Nichols, Michael Lorne 1. Mechanisms of reduced opioid effectiveness in a rat model of neuropathic pain . [Internet] [Doctoral dissertation]. University of Arizona; 1997. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10150/282342.

Council of Science Editors:

Nichols, Michael Lorne 1. Mechanisms of reduced opioid effectiveness in a rat model of neuropathic pain . [Doctoral Dissertation]. University of Arizona; 1997. Available from: http://hdl.handle.net/10150/282342


University of Arizona

16. Bian, Di. Peripheral and spinal mechanisms of neuropathic pain in the rat .

Degree: 2000, University of Arizona

 The Chung peripheral nerve injury model shows consistent allodynia and thermal hyperalgesia, which represent the most common clinical neuropathic pain symptoms. Also clinically relevant, in… (more)

Subjects/Keywords: Biology, Neuroscience.; Health Sciences, Pharmacology.; Health Sciences, Medicine and Surgery.

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APA (6th Edition):

Bian, D. (2000). Peripheral and spinal mechanisms of neuropathic pain in the rat . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/284087

Chicago Manual of Style (16th Edition):

Bian, Di. “Peripheral and spinal mechanisms of neuropathic pain in the rat .” 2000. Doctoral Dissertation, University of Arizona. Accessed October 27, 2020. http://hdl.handle.net/10150/284087.

MLA Handbook (7th Edition):

Bian, Di. “Peripheral and spinal mechanisms of neuropathic pain in the rat .” 2000. Web. 27 Oct 2020.

Vancouver:

Bian D. Peripheral and spinal mechanisms of neuropathic pain in the rat . [Internet] [Doctoral dissertation]. University of Arizona; 2000. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10150/284087.

Council of Science Editors:

Bian D. Peripheral and spinal mechanisms of neuropathic pain in the rat . [Doctoral Dissertation]. University of Arizona; 2000. Available from: http://hdl.handle.net/10150/284087


University of Arizona

17. Kovelowski, Carl Joseph. Supraspinal opioid delta receptor mediated antinociception: Supraspinal modulation of neuropathic pain .

Degree: 1999, University of Arizona

 The central objective of this dissertation focuses on the influence of supraspinal descending nociceptive inhibitory and facilitatory systems in the modulation of both nociceptive input… (more)

Subjects/Keywords: Biology, Neuroscience.; Health Sciences, Pharmacology.; Health Sciences, Medicine and Surgery.

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APA (6th Edition):

Kovelowski, C. J. (1999). Supraspinal opioid delta receptor mediated antinociception: Supraspinal modulation of neuropathic pain . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/284132

Chicago Manual of Style (16th Edition):

Kovelowski, Carl Joseph. “Supraspinal opioid delta receptor mediated antinociception: Supraspinal modulation of neuropathic pain .” 1999. Doctoral Dissertation, University of Arizona. Accessed October 27, 2020. http://hdl.handle.net/10150/284132.

MLA Handbook (7th Edition):

Kovelowski, Carl Joseph. “Supraspinal opioid delta receptor mediated antinociception: Supraspinal modulation of neuropathic pain .” 1999. Web. 27 Oct 2020.

Vancouver:

Kovelowski CJ. Supraspinal opioid delta receptor mediated antinociception: Supraspinal modulation of neuropathic pain . [Internet] [Doctoral dissertation]. University of Arizona; 1999. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10150/284132.

Council of Science Editors:

Kovelowski CJ. Supraspinal opioid delta receptor mediated antinociception: Supraspinal modulation of neuropathic pain . [Doctoral Dissertation]. University of Arizona; 1999. Available from: http://hdl.handle.net/10150/284132


University of Arizona

18. Jiang, Qi, 1957-. Site of clonidine action to inhibit gut propulsion in mice: Demonstration of a central component .

Degree: 1989, University of Arizona

 The role of supraspinal, spinal and peripheral alpha-2 adrenoceptors in the regulation of gastrointestinal motility in mice was investigated using anatomically site specific administration of… (more)

Subjects/Keywords: Clonidine.; Gastrointestinal system  – Motility.; Neurotransmitters.; Mice  – Physiology.

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APA (6th Edition):

Jiang, Qi, 1. (1989). Site of clonidine action to inhibit gut propulsion in mice: Demonstration of a central component . (Masters Thesis). University of Arizona. Retrieved from http://hdl.handle.net/10150/291819

Chicago Manual of Style (16th Edition):

Jiang, Qi, 1957-. “Site of clonidine action to inhibit gut propulsion in mice: Demonstration of a central component .” 1989. Masters Thesis, University of Arizona. Accessed October 27, 2020. http://hdl.handle.net/10150/291819.

MLA Handbook (7th Edition):

Jiang, Qi, 1957-. “Site of clonidine action to inhibit gut propulsion in mice: Demonstration of a central component .” 1989. Web. 27 Oct 2020.

Vancouver:

Jiang, Qi 1. Site of clonidine action to inhibit gut propulsion in mice: Demonstration of a central component . [Internet] [Masters thesis]. University of Arizona; 1989. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10150/291819.

Council of Science Editors:

Jiang, Qi 1. Site of clonidine action to inhibit gut propulsion in mice: Demonstration of a central component . [Masters Thesis]. University of Arizona; 1989. Available from: http://hdl.handle.net/10150/291819

19. Nation, Kelsey Marie. The Role of Kappa Opioid Receptor Signaling in Injury-Free Pain .

Degree: 2018, University of Arizona

 Kappa opioid receptor (KOR) signaling has been shown to be involved in the production of negative affective states. We hypothesized that KOR signaling in the… (more)

Subjects/Keywords: Amygdala; Conditioned pain modulation; Diffuse noxious inhibitory controls; Functional pain syndromes; kappa opioid receptor antagonist

…laboratory animals and approval from the IACUC at the University of Arizona. Rats were kept in a… 

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APA (6th Edition):

Nation, K. M. (2018). The Role of Kappa Opioid Receptor Signaling in Injury-Free Pain . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/628005

Chicago Manual of Style (16th Edition):

Nation, Kelsey Marie. “The Role of Kappa Opioid Receptor Signaling in Injury-Free Pain .” 2018. Doctoral Dissertation, University of Arizona. Accessed October 27, 2020. http://hdl.handle.net/10150/628005.

MLA Handbook (7th Edition):

Nation, Kelsey Marie. “The Role of Kappa Opioid Receptor Signaling in Injury-Free Pain .” 2018. Web. 27 Oct 2020.

Vancouver:

Nation KM. The Role of Kappa Opioid Receptor Signaling in Injury-Free Pain . [Internet] [Doctoral dissertation]. University of Arizona; 2018. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10150/628005.

Council of Science Editors:

Nation KM. The Role of Kappa Opioid Receptor Signaling in Injury-Free Pain . [Doctoral Dissertation]. University of Arizona; 2018. Available from: http://hdl.handle.net/10150/628005

20. Meske, Diana S. Neurochemical Studies of Reward from Pain Relief .

Degree: 2015, University of Arizona

 Chronic pain has been estimated to impact the economy of the United States by an annual cost of $635 billion per year and to affect… (more)

Subjects/Keywords: Medical Pharmacology

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APA (6th Edition):

Meske, D. S. (2015). Neurochemical Studies of Reward from Pain Relief . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/555887

Chicago Manual of Style (16th Edition):

Meske, Diana S. “Neurochemical Studies of Reward from Pain Relief .” 2015. Doctoral Dissertation, University of Arizona. Accessed October 27, 2020. http://hdl.handle.net/10150/555887.

MLA Handbook (7th Edition):

Meske, Diana S. “Neurochemical Studies of Reward from Pain Relief .” 2015. Web. 27 Oct 2020.

Vancouver:

Meske DS. Neurochemical Studies of Reward from Pain Relief . [Internet] [Doctoral dissertation]. University of Arizona; 2015. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10150/555887.

Council of Science Editors:

Meske DS. Neurochemical Studies of Reward from Pain Relief . [Doctoral Dissertation]. University of Arizona; 2015. Available from: http://hdl.handle.net/10150/555887

21. Kulkarni, Vinod V. Novel Bifunctional Ligands For Neuropathic Pain: Design and Synthesis of Overlapping Pharmacophores of Opioid and Melanocortin Ligands .

Degree: 2012, University of Arizona

 Biologically many disease states lead to changes in expressed proteins. Therefore, "system changes" that occur must be considered in any treatment for the disease. This… (more)

Subjects/Keywords: microwave; opioid; peptide cyclization; Chemistry; bifunctional ligands; melanocortin

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APA (6th Edition):

Kulkarni, V. V. (2012). Novel Bifunctional Ligands For Neuropathic Pain: Design and Synthesis of Overlapping Pharmacophores of Opioid and Melanocortin Ligands . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/228191

Chicago Manual of Style (16th Edition):

Kulkarni, Vinod V. “Novel Bifunctional Ligands For Neuropathic Pain: Design and Synthesis of Overlapping Pharmacophores of Opioid and Melanocortin Ligands .” 2012. Doctoral Dissertation, University of Arizona. Accessed October 27, 2020. http://hdl.handle.net/10150/228191.

MLA Handbook (7th Edition):

Kulkarni, Vinod V. “Novel Bifunctional Ligands For Neuropathic Pain: Design and Synthesis of Overlapping Pharmacophores of Opioid and Melanocortin Ligands .” 2012. Web. 27 Oct 2020.

Vancouver:

Kulkarni VV. Novel Bifunctional Ligands For Neuropathic Pain: Design and Synthesis of Overlapping Pharmacophores of Opioid and Melanocortin Ligands . [Internet] [Doctoral dissertation]. University of Arizona; 2012. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10150/228191.

Council of Science Editors:

Kulkarni VV. Novel Bifunctional Ligands For Neuropathic Pain: Design and Synthesis of Overlapping Pharmacophores of Opioid and Melanocortin Ligands . [Doctoral Dissertation]. University of Arizona; 2012. Available from: http://hdl.handle.net/10150/228191

22. Wei, Xiaomei. Investigating Meningeal Ion Channels As New Molecular Targets For Migraine .

Degree: 2014, University of Arizona

 This dissertation will present the four manuscripts I published or am ready to publish on the study of the pathophysiology of migraine headache. The first… (more)

Subjects/Keywords: Dural fibroblasts; Ion Channel; Migraine; NE; TRPV4; Medical Pharmacology; ASIC

…Care and Use Committee of the University of Arizona. 2.3.2. Surgery 2.3.2.1. Tracer… 

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APA (6th Edition):

Wei, X. (2014). Investigating Meningeal Ion Channels As New Molecular Targets For Migraine . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/565832

Chicago Manual of Style (16th Edition):

Wei, Xiaomei. “Investigating Meningeal Ion Channels As New Molecular Targets For Migraine .” 2014. Doctoral Dissertation, University of Arizona. Accessed October 27, 2020. http://hdl.handle.net/10150/565832.

MLA Handbook (7th Edition):

Wei, Xiaomei. “Investigating Meningeal Ion Channels As New Molecular Targets For Migraine .” 2014. Web. 27 Oct 2020.

Vancouver:

Wei X. Investigating Meningeal Ion Channels As New Molecular Targets For Migraine . [Internet] [Doctoral dissertation]. University of Arizona; 2014. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10150/565832.

Council of Science Editors:

Wei X. Investigating Meningeal Ion Channels As New Molecular Targets For Migraine . [Doctoral Dissertation]. University of Arizona; 2014. Available from: http://hdl.handle.net/10150/565832

23. Asiedu, Marina N. Spinal Sensitization Mechanisms Promoting Pain: Gabaergic Disinhibition and Pkmζ-Mediated Plasticity .

Degree: 2012, University of Arizona

 As a major public health problem affecting more that 76.5 million Americans, chronic pain is one main reason why people seek medical attention. It is… (more)

Subjects/Keywords: PKM zeta; Sensitization; Medical Pharmacology; Chronic pain; GABA

…Committee of the University of Arizona. Solutions and Drugs: Acetazolamide (ACT) and… 

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APA (6th Edition):

Asiedu, M. N. (2012). Spinal Sensitization Mechanisms Promoting Pain: Gabaergic Disinhibition and Pkmζ-Mediated Plasticity . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/232496

Chicago Manual of Style (16th Edition):

Asiedu, Marina N. “Spinal Sensitization Mechanisms Promoting Pain: Gabaergic Disinhibition and Pkmζ-Mediated Plasticity .” 2012. Doctoral Dissertation, University of Arizona. Accessed October 27, 2020. http://hdl.handle.net/10150/232496.

MLA Handbook (7th Edition):

Asiedu, Marina N. “Spinal Sensitization Mechanisms Promoting Pain: Gabaergic Disinhibition and Pkmζ-Mediated Plasticity .” 2012. Web. 27 Oct 2020.

Vancouver:

Asiedu MN. Spinal Sensitization Mechanisms Promoting Pain: Gabaergic Disinhibition and Pkmζ-Mediated Plasticity . [Internet] [Doctoral dissertation]. University of Arizona; 2012. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10150/232496.

Council of Science Editors:

Asiedu MN. Spinal Sensitization Mechanisms Promoting Pain: Gabaergic Disinhibition and Pkmζ-Mediated Plasticity . [Doctoral Dissertation]. University of Arizona; 2012. Available from: http://hdl.handle.net/10150/232496


University of Arizona

24. Li, Zhiwei. The use of brain slices for the study of enzymatic metabolism of Des-enkephalin-tau-endorphin (DEtauE) and its analogues .

Degree: 1989, University of Arizona

 The present study utilized a newly developed rat brain slice and incubation techniques to determine the effects of peptide structural modifications and brain peptidase regional… (more)

Subjects/Keywords: Endorphins - Metabolism; Neuropeptides - Metabolism; Pharmacology

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APA (6th Edition):

Li, Z. (1989). The use of brain slices for the study of enzymatic metabolism of Des-enkephalin-tau-endorphin (DEtauE) and its analogues . (Masters Thesis). University of Arizona. Retrieved from http://hdl.handle.net/10150/144671

Chicago Manual of Style (16th Edition):

Li, Zhiwei. “The use of brain slices for the study of enzymatic metabolism of Des-enkephalin-tau-endorphin (DEtauE) and its analogues .” 1989. Masters Thesis, University of Arizona. Accessed October 27, 2020. http://hdl.handle.net/10150/144671.

MLA Handbook (7th Edition):

Li, Zhiwei. “The use of brain slices for the study of enzymatic metabolism of Des-enkephalin-tau-endorphin (DEtauE) and its analogues .” 1989. Web. 27 Oct 2020.

Vancouver:

Li Z. The use of brain slices for the study of enzymatic metabolism of Des-enkephalin-tau-endorphin (DEtauE) and its analogues . [Internet] [Masters thesis]. University of Arizona; 1989. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10150/144671.

Council of Science Editors:

Li Z. The use of brain slices for the study of enzymatic metabolism of Des-enkephalin-tau-endorphin (DEtauE) and its analogues . [Masters Thesis]. University of Arizona; 1989. Available from: http://hdl.handle.net/10150/144671


University of Arizona

25. Clark, David Albert. The effect of protease inhibitors and gastrin releasing peptide receptor antagonists on human small cell lung cancer growth .

Degree: 1993, University of Arizona

 The effect of the protease inhibitors BBI and aprotinin on the in vitro clonal growth of two human small cell lung cancer (SCLC) cell lines… (more)

Subjects/Keywords: Dissertations, Academic.; Pharmacology.

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APA (6th Edition):

Clark, D. A. (1993). The effect of protease inhibitors and gastrin releasing peptide receptor antagonists on human small cell lung cancer growth . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/186391

Chicago Manual of Style (16th Edition):

Clark, David Albert. “The effect of protease inhibitors and gastrin releasing peptide receptor antagonists on human small cell lung cancer growth .” 1993. Doctoral Dissertation, University of Arizona. Accessed October 27, 2020. http://hdl.handle.net/10150/186391.

MLA Handbook (7th Edition):

Clark, David Albert. “The effect of protease inhibitors and gastrin releasing peptide receptor antagonists on human small cell lung cancer growth .” 1993. Web. 27 Oct 2020.

Vancouver:

Clark DA. The effect of protease inhibitors and gastrin releasing peptide receptor antagonists on human small cell lung cancer growth . [Internet] [Doctoral dissertation]. University of Arizona; 1993. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10150/186391.

Council of Science Editors:

Clark DA. The effect of protease inhibitors and gastrin releasing peptide receptor antagonists on human small cell lung cancer growth . [Doctoral Dissertation]. University of Arizona; 1993. Available from: http://hdl.handle.net/10150/186391


University of Arizona

26. Fang, Lei. The cloning, expression and partial characterization of a human delta opioid receptor .

Degree: 1994, University of Arizona

 A human delta (δ) opioid receptor (hDOR) was cloned from human brain cDNA libraries by filter replica hybridization screening methods. A single clone (44-11) from… (more)

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APA (6th Edition):

Fang, L. (1994). The cloning, expression and partial characterization of a human delta opioid receptor . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/186784

Chicago Manual of Style (16th Edition):

Fang, Lei. “The cloning, expression and partial characterization of a human delta opioid receptor .” 1994. Doctoral Dissertation, University of Arizona. Accessed October 27, 2020. http://hdl.handle.net/10150/186784.

MLA Handbook (7th Edition):

Fang, Lei. “The cloning, expression and partial characterization of a human delta opioid receptor .” 1994. Web. 27 Oct 2020.

Vancouver:

Fang L. The cloning, expression and partial characterization of a human delta opioid receptor . [Internet] [Doctoral dissertation]. University of Arizona; 1994. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10150/186784.

Council of Science Editors:

Fang L. The cloning, expression and partial characterization of a human delta opioid receptor . [Doctoral Dissertation]. University of Arizona; 1994. Available from: http://hdl.handle.net/10150/186784


University of Arizona

27. Oakes, Mary Geraldine. The ontogeny of peptidases involved in the post-transitional processing of cholecystokinin .

Degree: 1994, University of Arizona

 There are three levels at which biologically active peptides may be regulated: transcription, translation, and post-translational processing. The data presented in this study focused on… (more)

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APA (6th Edition):

Oakes, M. G. (1994). The ontogeny of peptidases involved in the post-transitional processing of cholecystokinin . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/186940

Chicago Manual of Style (16th Edition):

Oakes, Mary Geraldine. “The ontogeny of peptidases involved in the post-transitional processing of cholecystokinin .” 1994. Doctoral Dissertation, University of Arizona. Accessed October 27, 2020. http://hdl.handle.net/10150/186940.

MLA Handbook (7th Edition):

Oakes, Mary Geraldine. “The ontogeny of peptidases involved in the post-transitional processing of cholecystokinin .” 1994. Web. 27 Oct 2020.

Vancouver:

Oakes MG. The ontogeny of peptidases involved in the post-transitional processing of cholecystokinin . [Internet] [Doctoral dissertation]. University of Arizona; 1994. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10150/186940.

Council of Science Editors:

Oakes MG. The ontogeny of peptidases involved in the post-transitional processing of cholecystokinin . [Doctoral Dissertation]. University of Arizona; 1994. Available from: http://hdl.handle.net/10150/186940


University of Arizona

28. Bumanglag, Argyle V. INJURY-INDUCED HIPPOCAMPAL EPILEPTOGENESIS IN EXPERIMENTAL MODELS OF TEMPORAL LOBE EPILEPSY IN THE RAT .

Degree: 2010, University of Arizona

 The mechanism by which brain injuries cause temporal lobe epilepsy is unknown. Suspected epileptogenic insults include neuron loss and secondary processes triggered by injury. Difficulties… (more)

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APA (6th Edition):

Bumanglag, A. V. (2010). INJURY-INDUCED HIPPOCAMPAL EPILEPTOGENESIS IN EXPERIMENTAL MODELS OF TEMPORAL LOBE EPILEPSY IN THE RAT . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/146070

Chicago Manual of Style (16th Edition):

Bumanglag, Argyle V. “INJURY-INDUCED HIPPOCAMPAL EPILEPTOGENESIS IN EXPERIMENTAL MODELS OF TEMPORAL LOBE EPILEPSY IN THE RAT .” 2010. Doctoral Dissertation, University of Arizona. Accessed October 27, 2020. http://hdl.handle.net/10150/146070.

MLA Handbook (7th Edition):

Bumanglag, Argyle V. “INJURY-INDUCED HIPPOCAMPAL EPILEPTOGENESIS IN EXPERIMENTAL MODELS OF TEMPORAL LOBE EPILEPSY IN THE RAT .” 2010. Web. 27 Oct 2020.

Vancouver:

Bumanglag AV. INJURY-INDUCED HIPPOCAMPAL EPILEPTOGENESIS IN EXPERIMENTAL MODELS OF TEMPORAL LOBE EPILEPSY IN THE RAT . [Internet] [Doctoral dissertation]. University of Arizona; 2010. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10150/146070.

Council of Science Editors:

Bumanglag AV. INJURY-INDUCED HIPPOCAMPAL EPILEPTOGENESIS IN EXPERIMENTAL MODELS OF TEMPORAL LOBE EPILEPSY IN THE RAT . [Doctoral Dissertation]. University of Arizona; 2010. Available from: http://hdl.handle.net/10150/146070


University of Arizona

29. Largent- Milnes, Tally Marie. NEUROKININ 1 RECEPTORS AND THEIR ROLE IN OPIOID-INDUCED HYPERALGESIA, ANTINOCICEPTIVE TOLERANCE AND REWARD .

Degree: 2010, University of Arizona

 Pain is the most common and debilitating sign of a medical problem, with nearly 15 million patients suffering from chronic pain, including neuropathic pain. Widely… (more)

Subjects/Keywords: antinociceptive tolerance; neurokinin; neuropharmacology; opioid induced hyperalgesia; pain; reward

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APA (6th Edition):

Largent- Milnes, T. M. (2010). NEUROKININ 1 RECEPTORS AND THEIR ROLE IN OPIOID-INDUCED HYPERALGESIA, ANTINOCICEPTIVE TOLERANCE AND REWARD . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/193763

Chicago Manual of Style (16th Edition):

Largent- Milnes, Tally Marie. “NEUROKININ 1 RECEPTORS AND THEIR ROLE IN OPIOID-INDUCED HYPERALGESIA, ANTINOCICEPTIVE TOLERANCE AND REWARD .” 2010. Doctoral Dissertation, University of Arizona. Accessed October 27, 2020. http://hdl.handle.net/10150/193763.

MLA Handbook (7th Edition):

Largent- Milnes, Tally Marie. “NEUROKININ 1 RECEPTORS AND THEIR ROLE IN OPIOID-INDUCED HYPERALGESIA, ANTINOCICEPTIVE TOLERANCE AND REWARD .” 2010. Web. 27 Oct 2020.

Vancouver:

Largent- Milnes TM. NEUROKININ 1 RECEPTORS AND THEIR ROLE IN OPIOID-INDUCED HYPERALGESIA, ANTINOCICEPTIVE TOLERANCE AND REWARD . [Internet] [Doctoral dissertation]. University of Arizona; 2010. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10150/193763.

Council of Science Editors:

Largent- Milnes TM. NEUROKININ 1 RECEPTORS AND THEIR ROLE IN OPIOID-INDUCED HYPERALGESIA, ANTINOCICEPTIVE TOLERANCE AND REWARD . [Doctoral Dissertation]. University of Arizona; 2010. Available from: http://hdl.handle.net/10150/193763


University of Arizona

30. Marshall, Timothy McCoy. Neuropeptides in the RVM Promote Descending Facilitation and Abnormal Pain .

Degree: 2008, University of Arizona

 The neuropeptides dynorphin and cholecystokinin (CCK), and their associated pronociceptive effects were investigated in the RVM. Utilizing a nerve-injury model (SNL), RT-PCR analysis revealed increases… (more)

Subjects/Keywords: rostral ventromedial medulla; descending facilitation; cholecystokinin; dynorphin; bradykinin receptor; PGE2

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APA (6th Edition):

Marshall, T. M. (2008). Neuropeptides in the RVM Promote Descending Facilitation and Abnormal Pain . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/193963

Chicago Manual of Style (16th Edition):

Marshall, Timothy McCoy. “Neuropeptides in the RVM Promote Descending Facilitation and Abnormal Pain .” 2008. Doctoral Dissertation, University of Arizona. Accessed October 27, 2020. http://hdl.handle.net/10150/193963.

MLA Handbook (7th Edition):

Marshall, Timothy McCoy. “Neuropeptides in the RVM Promote Descending Facilitation and Abnormal Pain .” 2008. Web. 27 Oct 2020.

Vancouver:

Marshall TM. Neuropeptides in the RVM Promote Descending Facilitation and Abnormal Pain . [Internet] [Doctoral dissertation]. University of Arizona; 2008. [cited 2020 Oct 27]. Available from: http://hdl.handle.net/10150/193963.

Council of Science Editors:

Marshall TM. Neuropeptides in the RVM Promote Descending Facilitation and Abnormal Pain . [Doctoral Dissertation]. University of Arizona; 2008. Available from: http://hdl.handle.net/10150/193963

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