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Level: masters

You searched for subject:(TRPV1). Showing records 1 – 12 of 12 total matches.

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McMaster University

1. Balenko, Matthew. CAPSAZEPINE ATTENUATES CANCER-INDUCED BONE PAIN BY INHIBITING GLUTAMATE RELEASE.

Degree: MSc, 2014, McMaster University

Breast cancer has the highest incidence rate in women, accounting for more than 22% of all cancers and possessing a strong disposition to metastasize to… (more)

Subjects/Keywords: Glutamate; Cancer; Pain; TRPV1; Capsazepine; in vivo

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APA (6th Edition):

Balenko, M. (2014). CAPSAZEPINE ATTENUATES CANCER-INDUCED BONE PAIN BY INHIBITING GLUTAMATE RELEASE. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/15970

Chicago Manual of Style (16th Edition):

Balenko, Matthew. “CAPSAZEPINE ATTENUATES CANCER-INDUCED BONE PAIN BY INHIBITING GLUTAMATE RELEASE.” 2014. Masters Thesis, McMaster University. Accessed July 21, 2019. http://hdl.handle.net/11375/15970.

MLA Handbook (7th Edition):

Balenko, Matthew. “CAPSAZEPINE ATTENUATES CANCER-INDUCED BONE PAIN BY INHIBITING GLUTAMATE RELEASE.” 2014. Web. 21 Jul 2019.

Vancouver:

Balenko M. CAPSAZEPINE ATTENUATES CANCER-INDUCED BONE PAIN BY INHIBITING GLUTAMATE RELEASE. [Internet] [Masters thesis]. McMaster University; 2014. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/11375/15970.

Council of Science Editors:

Balenko M. CAPSAZEPINE ATTENUATES CANCER-INDUCED BONE PAIN BY INHIBITING GLUTAMATE RELEASE. [Masters Thesis]. McMaster University; 2014. Available from: http://hdl.handle.net/11375/15970


Duquesne University

2. Zeyzus Johns, Bree. TRPV1 mRNA is Differentially Expressed in Different Vertebral Levels of Rat Dorsal Root Ganglia Following Sciatic Nerve Injury.

Degree: MS, Biological Sciences, 2009, Duquesne University

 Transient Receptor Potential Vanilloid 1 plays an important role in the pain pathway. TRPV1 is expressed in primary afferent nociceptors and acts as a transducer… (more)

Subjects/Keywords: TRPV1; DRG; mRNA; CCI; pain; nociception

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APA (6th Edition):

Zeyzus Johns, B. (2009). TRPV1 mRNA is Differentially Expressed in Different Vertebral Levels of Rat Dorsal Root Ganglia Following Sciatic Nerve Injury. (Masters Thesis). Duquesne University. Retrieved from https://dsc.duq.edu/etd/1407

Chicago Manual of Style (16th Edition):

Zeyzus Johns, Bree. “TRPV1 mRNA is Differentially Expressed in Different Vertebral Levels of Rat Dorsal Root Ganglia Following Sciatic Nerve Injury.” 2009. Masters Thesis, Duquesne University. Accessed July 21, 2019. https://dsc.duq.edu/etd/1407.

MLA Handbook (7th Edition):

Zeyzus Johns, Bree. “TRPV1 mRNA is Differentially Expressed in Different Vertebral Levels of Rat Dorsal Root Ganglia Following Sciatic Nerve Injury.” 2009. Web. 21 Jul 2019.

Vancouver:

Zeyzus Johns B. TRPV1 mRNA is Differentially Expressed in Different Vertebral Levels of Rat Dorsal Root Ganglia Following Sciatic Nerve Injury. [Internet] [Masters thesis]. Duquesne University; 2009. [cited 2019 Jul 21]. Available from: https://dsc.duq.edu/etd/1407.

Council of Science Editors:

Zeyzus Johns B. TRPV1 mRNA is Differentially Expressed in Different Vertebral Levels of Rat Dorsal Root Ganglia Following Sciatic Nerve Injury. [Masters Thesis]. Duquesne University; 2009. Available from: https://dsc.duq.edu/etd/1407


Duquesne University

3. Andersen, Karl A. Exploration of TRPV1 Splice Variant Expression in Rat Dorsal Root Ganglia Following Sciatic Nerve Injury.

Degree: MS, Biological Sciences, 2010, Duquesne University

 Transient Receptor Potential Vanilloid 1 (TRPV1) is ligand-gated ion channel that plays an important role in the pain signaling pathway. It is predominantly expressed by… (more)

Subjects/Keywords: CCI; DRG; QPCR; Rat; Splice Variant; TRPV1

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APA (6th Edition):

Andersen, K. A. (2010). Exploration of TRPV1 Splice Variant Expression in Rat Dorsal Root Ganglia Following Sciatic Nerve Injury. (Masters Thesis). Duquesne University. Retrieved from https://dsc.duq.edu/etd/263

Chicago Manual of Style (16th Edition):

Andersen, Karl A. “Exploration of TRPV1 Splice Variant Expression in Rat Dorsal Root Ganglia Following Sciatic Nerve Injury.” 2010. Masters Thesis, Duquesne University. Accessed July 21, 2019. https://dsc.duq.edu/etd/263.

MLA Handbook (7th Edition):

Andersen, Karl A. “Exploration of TRPV1 Splice Variant Expression in Rat Dorsal Root Ganglia Following Sciatic Nerve Injury.” 2010. Web. 21 Jul 2019.

Vancouver:

Andersen KA. Exploration of TRPV1 Splice Variant Expression in Rat Dorsal Root Ganglia Following Sciatic Nerve Injury. [Internet] [Masters thesis]. Duquesne University; 2010. [cited 2019 Jul 21]. Available from: https://dsc.duq.edu/etd/263.

Council of Science Editors:

Andersen KA. Exploration of TRPV1 Splice Variant Expression in Rat Dorsal Root Ganglia Following Sciatic Nerve Injury. [Masters Thesis]. Duquesne University; 2010. Available from: https://dsc.duq.edu/etd/263

4. MarÃlia Leite Dias. Atividade antinociceptiva da riparina IV: participaÃÃo dos receptores TRPV1, TRPM8, receptores glutamatÃrgicos e do Ãxido nÃtrico.

Degree: Master, 2012, Universidade Federal do Ceará

A Riparina IV, uma alcamida sintetizada de Aniba riparia, foi testada em modelos animais padronizados de dor, bem como os possÃveis mecanismos de aÃÃo envolvidos.… (more)

Subjects/Keywords: FARMACOLOGIA; Riparina IV; Nociceptividade; TRPV1; TRPM8; Glutamate; Ãxido NÃtrico; Riparin IV; Nociception; TRPV1; TRPM8; Glutamate; Nitric oxide

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APA (6th Edition):

Dias, M. L. (2012). Atividade antinociceptiva da riparina IV: participaÃÃo dos receptores TRPV1, TRPM8, receptores glutamatÃrgicos e do Ãxido nÃtrico. (Masters Thesis). Universidade Federal do Ceará. Retrieved from http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=8632 ;

Chicago Manual of Style (16th Edition):

Dias, MarÃlia Leite. “Atividade antinociceptiva da riparina IV: participaÃÃo dos receptores TRPV1, TRPM8, receptores glutamatÃrgicos e do Ãxido nÃtrico.” 2012. Masters Thesis, Universidade Federal do Ceará. Accessed July 21, 2019. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=8632 ;.

MLA Handbook (7th Edition):

Dias, MarÃlia Leite. “Atividade antinociceptiva da riparina IV: participaÃÃo dos receptores TRPV1, TRPM8, receptores glutamatÃrgicos e do Ãxido nÃtrico.” 2012. Web. 21 Jul 2019.

Vancouver:

Dias ML. Atividade antinociceptiva da riparina IV: participaÃÃo dos receptores TRPV1, TRPM8, receptores glutamatÃrgicos e do Ãxido nÃtrico. [Internet] [Masters thesis]. Universidade Federal do Ceará 2012. [cited 2019 Jul 21]. Available from: http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=8632 ;.

Council of Science Editors:

Dias ML. Atividade antinociceptiva da riparina IV: participaÃÃo dos receptores TRPV1, TRPM8, receptores glutamatÃrgicos e do Ãxido nÃtrico. [Masters Thesis]. Universidade Federal do Ceará 2012. Available from: http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=8632 ;


Brigham Young University

5. Jensen, Tyron DeRay. Calcineurin is Required for TRPV1-induced LTD of CA1 Stratum Radiatum Interneurons.

Degree: MS, 2011, Brigham Young University

 Learning and memory in the brain are thought to be dependent on synaptic plasticity. In response to sensory input, synapses can be strengthened or weakened,… (more)

Subjects/Keywords: calcineurin; Long-term depression; TRPV1; Cell and Developmental Biology; Physiology

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APA (6th Edition):

Jensen, T. D. (2011). Calcineurin is Required for TRPV1-induced LTD of CA1 Stratum Radiatum Interneurons. (Masters Thesis). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=4056&context=etd

Chicago Manual of Style (16th Edition):

Jensen, Tyron DeRay. “Calcineurin is Required for TRPV1-induced LTD of CA1 Stratum Radiatum Interneurons.” 2011. Masters Thesis, Brigham Young University. Accessed July 21, 2019. https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=4056&context=etd.

MLA Handbook (7th Edition):

Jensen, Tyron DeRay. “Calcineurin is Required for TRPV1-induced LTD of CA1 Stratum Radiatum Interneurons.” 2011. Web. 21 Jul 2019.

Vancouver:

Jensen TD. Calcineurin is Required for TRPV1-induced LTD of CA1 Stratum Radiatum Interneurons. [Internet] [Masters thesis]. Brigham Young University; 2011. [cited 2019 Jul 21]. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=4056&context=etd.

Council of Science Editors:

Jensen TD. Calcineurin is Required for TRPV1-induced LTD of CA1 Stratum Radiatum Interneurons. [Masters Thesis]. Brigham Young University; 2011. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=4056&context=etd

6. Soutar, David. Piperine Modulates B cell Activation and Function.

Degree: MS, Department of Pathology, 2011, Dalhousie University

 Piperine, the major alkaloid derived from black pepper corns, has played an important role in traditional medicine worldwide. Current research has demonstrated piperine to have… (more)

Subjects/Keywords: B cell; lymphocyte; piperine; phytochemical; alkaloid; TRPV1

TRPV1… …80 3.1.6 INHIBITORY EFFECTS OF PIPERINE ON B CELL ACTIVATION ARE INDEPENDENT OF TRPV1… …T-dependent and T-independent activated TRPV1-/- B lymphocyte proliferation is inhibited… …TCR Td TH Ti TLR TNF Tpl2 TRAF TRPV1 wt μL μm μM Vav vs. [3H]-TdR Milligram… 

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APA (6th Edition):

Soutar, D. (2011). Piperine Modulates B cell Activation and Function. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/14329

Chicago Manual of Style (16th Edition):

Soutar, David. “Piperine Modulates B cell Activation and Function.” 2011. Masters Thesis, Dalhousie University. Accessed July 21, 2019. http://hdl.handle.net/10222/14329.

MLA Handbook (7th Edition):

Soutar, David. “Piperine Modulates B cell Activation and Function.” 2011. Web. 21 Jul 2019.

Vancouver:

Soutar D. Piperine Modulates B cell Activation and Function. [Internet] [Masters thesis]. Dalhousie University; 2011. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/10222/14329.

Council of Science Editors:

Soutar D. Piperine Modulates B cell Activation and Function. [Masters Thesis]. Dalhousie University; 2011. Available from: http://hdl.handle.net/10222/14329


University of Otago

7. Jamieson, Bradley. Bidirectional Control of Synaptic Transmission by Endocannabinoids from Corticotropin-Releasing Hormone Neurons .

Degree: University of Otago

 The stress response is a physiological process which allows an organism to rapidly change its function in order to cope with a changing environment and… (more)

Subjects/Keywords: Corticotropin-Releasing Hormone; Endocannabinoid; CB1R; TRPV1; Oxytocin

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APA (6th Edition):

Jamieson, B. (n.d.). Bidirectional Control of Synaptic Transmission by Endocannabinoids from Corticotropin-Releasing Hormone Neurons . (Masters Thesis). University of Otago. Retrieved from http://hdl.handle.net/10523/7324

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

Chicago Manual of Style (16th Edition):

Jamieson, Bradley. “Bidirectional Control of Synaptic Transmission by Endocannabinoids from Corticotropin-Releasing Hormone Neurons .” Masters Thesis, University of Otago. Accessed July 21, 2019. http://hdl.handle.net/10523/7324.

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

MLA Handbook (7th Edition):

Jamieson, Bradley. “Bidirectional Control of Synaptic Transmission by Endocannabinoids from Corticotropin-Releasing Hormone Neurons .” Web. 21 Jul 2019.

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

Vancouver:

Jamieson B. Bidirectional Control of Synaptic Transmission by Endocannabinoids from Corticotropin-Releasing Hormone Neurons . [Internet] [Masters thesis]. University of Otago; [cited 2019 Jul 21]. Available from: http://hdl.handle.net/10523/7324.

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

Council of Science Editors:

Jamieson B. Bidirectional Control of Synaptic Transmission by Endocannabinoids from Corticotropin-Releasing Hormone Neurons . [Masters Thesis]. University of Otago; Available from: http://hdl.handle.net/10523/7324

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


University of Stirling

8. Kortzon, Evelina C. Capsaicin protects against atrophy in human skeletal muscle cells.

Degree: M. Phil., 2014, University of Stirling

 Skeletal muscle atrophy occurs in many pathological conditions, e.g. AIDS, cancer, sepsis and starvation, and with increased age. There is currently no effective treatment to… (more)

Subjects/Keywords: Skeletal muscle; Capsaicin; Atrophy; TRPV1; Dexamethasone; TNF-alpha; Tumor Necrosis Factor alpha; Cell culture; Capsaicin; Musculoskeletal system; Muscular atrophy

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APA (6th Edition):

Kortzon, E. C. (2014). Capsaicin protects against atrophy in human skeletal muscle cells. (Masters Thesis). University of Stirling. Retrieved from http://hdl.handle.net/1893/22316

Chicago Manual of Style (16th Edition):

Kortzon, Evelina C. “Capsaicin protects against atrophy in human skeletal muscle cells.” 2014. Masters Thesis, University of Stirling. Accessed July 21, 2019. http://hdl.handle.net/1893/22316.

MLA Handbook (7th Edition):

Kortzon, Evelina C. “Capsaicin protects against atrophy in human skeletal muscle cells.” 2014. Web. 21 Jul 2019.

Vancouver:

Kortzon EC. Capsaicin protects against atrophy in human skeletal muscle cells. [Internet] [Masters thesis]. University of Stirling; 2014. [cited 2019 Jul 21]. Available from: http://hdl.handle.net/1893/22316.

Council of Science Editors:

Kortzon EC. Capsaicin protects against atrophy in human skeletal muscle cells. [Masters Thesis]. University of Stirling; 2014. Available from: http://hdl.handle.net/1893/22316

9. Roberto CÃsar Pereira Lima JÃnior. Antinociceptive effect of the mixture of pentacyclic triterpenes alpha- and beta- amyrin in models of visceral nociception in mice.

Degree: Master, 2005, Universidade Federal do Ceará

 Protium heptaphyllum March (Burseraceae), a medicinal plant commonly found in the Amazon and in the Northeast regions of Brazil, releases an oil-resin rich in pentacyclic… (more)

Subjects/Keywords: FARMACOLOGIA; Dor visceral; Receptor opiÃide; Receptor TRPV1; visceral pain; triterpenes; opioid-receptor; TRPV1 receptor; Burseraceae; Dor; Triterpenos

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APA (6th Edition):

JÃnior, R. C. P. L. (2005). Antinociceptive effect of the mixture of pentacyclic triterpenes alpha- and beta- amyrin in models of visceral nociception in mice. (Masters Thesis). Universidade Federal do Ceará. Retrieved from http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=4 ;

Chicago Manual of Style (16th Edition):

JÃnior, Roberto CÃsar Pereira Lima. “Antinociceptive effect of the mixture of pentacyclic triterpenes alpha- and beta- amyrin in models of visceral nociception in mice.” 2005. Masters Thesis, Universidade Federal do Ceará. Accessed July 21, 2019. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=4 ;.

MLA Handbook (7th Edition):

JÃnior, Roberto CÃsar Pereira Lima. “Antinociceptive effect of the mixture of pentacyclic triterpenes alpha- and beta- amyrin in models of visceral nociception in mice.” 2005. Web. 21 Jul 2019.

Vancouver:

JÃnior RCPL. Antinociceptive effect of the mixture of pentacyclic triterpenes alpha- and beta- amyrin in models of visceral nociception in mice. [Internet] [Masters thesis]. Universidade Federal do Ceará 2005. [cited 2019 Jul 21]. Available from: http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=4 ;.

Council of Science Editors:

JÃnior RCPL. Antinociceptive effect of the mixture of pentacyclic triterpenes alpha- and beta- amyrin in models of visceral nociception in mice. [Masters Thesis]. Universidade Federal do Ceará 2005. Available from: http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=4 ;

10. Juliana Lemos Maia. Estudo da atividade antinociceptiva e possÃveis mecanismos de aÃÃo do Ãcido oleanÃlico em modelos de nocicepÃÃo induzida por capsaicina e Ãleo de mostarda em camundongos.

Degree: Master, 2006, Universidade Federal do Ceará

O Ãcido oleanÃlico à um triterpeno pentacÃclico largamente encontrado em vÃrias plantas medicinais. Essa substÃncia demonstrou ter uma variedade de atividades farmacolÃgicas, dentre as quais… (more)

Subjects/Keywords: FARMACOLOGIA; Ãcido oleanÃlico; triterpenos; atividade antinociceptiva; receptor opiÃide; TRPV1; Ãxido NÃtrico; oleanolic acid; triterpenes; antinociceptive activity; opioid-receptor; TRPV1 receptor; oxide nitric

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APA (6th Edition):

Maia, J. L. (2006). Estudo da atividade antinociceptiva e possÃveis mecanismos de aÃÃo do Ãcido oleanÃlico em modelos de nocicepÃÃo induzida por capsaicina e Ãleo de mostarda em camundongos. (Masters Thesis). Universidade Federal do Ceará. Retrieved from http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=4511 ;

Chicago Manual of Style (16th Edition):

Maia, Juliana Lemos. “Estudo da atividade antinociceptiva e possÃveis mecanismos de aÃÃo do Ãcido oleanÃlico em modelos de nocicepÃÃo induzida por capsaicina e Ãleo de mostarda em camundongos.” 2006. Masters Thesis, Universidade Federal do Ceará. Accessed July 21, 2019. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=4511 ;.

MLA Handbook (7th Edition):

Maia, Juliana Lemos. “Estudo da atividade antinociceptiva e possÃveis mecanismos de aÃÃo do Ãcido oleanÃlico em modelos de nocicepÃÃo induzida por capsaicina e Ãleo de mostarda em camundongos.” 2006. Web. 21 Jul 2019.

Vancouver:

Maia JL. Estudo da atividade antinociceptiva e possÃveis mecanismos de aÃÃo do Ãcido oleanÃlico em modelos de nocicepÃÃo induzida por capsaicina e Ãleo de mostarda em camundongos. [Internet] [Masters thesis]. Universidade Federal do Ceará 2006. [cited 2019 Jul 21]. Available from: http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=4511 ;.

Council of Science Editors:

Maia JL. Estudo da atividade antinociceptiva e possÃveis mecanismos de aÃÃo do Ãcido oleanÃlico em modelos de nocicepÃÃo induzida por capsaicina e Ãleo de mostarda em camundongos. [Masters Thesis]. Universidade Federal do Ceará 2006. Available from: http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=4511 ;

11. Kmetz, John George, II. Differential Regulation of TRPV1 Channels in the Murine Coronary Vasculature by H2O2.

Degree: MS, College of Arts and Sciences / School of Biomedical Sciences, 2014, Kent State University

 A critical amount of reactive oxygen species (ROS) contributes to coronary blood flow (CBF) regulation; however, oxidative stress (OS) impairs CBF regulation and is elevated… (more)

Subjects/Keywords: Biomedical Research; TRPV1, 4-HNE, Reactive Oxygen Species, H2O2, Cardiovascular disease, Diabetic cardiomyopathy, Oxidative Stress, Microvascular Disease

…potential TRPP .. …. Transient Receptor Potential Polycystin TRPV1… …type 1 (TRPV1) channels have recently been shown to be modulated by H2O2 (… …independent, some TRP channels, particularly those that are temperature sensitive (i.e.: TRPV1… …stress, and hypoosmolarity. To date, the best characterized of the TRPV family is TRPV1 (… …its first member, TRPV1, and is a polymodal channel activated by the vanilloid compound… 

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APA (6th Edition):

Kmetz, John George, I. (2014). Differential Regulation of TRPV1 Channels in the Murine Coronary Vasculature by H2O2. (Masters Thesis). Kent State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=kent1398336723

Chicago Manual of Style (16th Edition):

Kmetz, John George, II. “Differential Regulation of TRPV1 Channels in the Murine Coronary Vasculature by H2O2.” 2014. Masters Thesis, Kent State University. Accessed July 21, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=kent1398336723.

MLA Handbook (7th Edition):

Kmetz, John George, II. “Differential Regulation of TRPV1 Channels in the Murine Coronary Vasculature by H2O2.” 2014. Web. 21 Jul 2019.

Vancouver:

Kmetz, John George I. Differential Regulation of TRPV1 Channels in the Murine Coronary Vasculature by H2O2. [Internet] [Masters thesis]. Kent State University; 2014. [cited 2019 Jul 21]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1398336723.

Council of Science Editors:

Kmetz, John George I. Differential Regulation of TRPV1 Channels in the Murine Coronary Vasculature by H2O2. [Masters Thesis]. Kent State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1398336723


University of Florida

12. Wexel, Melanie M. Central Targeting of Trigeminal Primary Afferent Nerve Terminals via Intracisternal Injection of RTX and Its Effect on Pain Behavior.

Degree: MS, Dental Sciences - Dentistry, 2008, University of Florida

 The TRPV1 selective neurotoxin resiniferatoxin (RTX) was evaluated for use in treating orofacial pain. RTX (250 ng) or vehicle was administered intracisternally in rats to… (more)

Subjects/Keywords: Brain stem; Facial pain; Health care outcome assessment; Inflammation; Neurons; Pain; Rats; Receptors; Trigeminal ganglion; TRPV cation channels; pain, rtx, trigeminal, trpv1

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APA (6th Edition):

Wexel, M. M. (2008). Central Targeting of Trigeminal Primary Afferent Nerve Terminals via Intracisternal Injection of RTX and Its Effect on Pain Behavior. (Masters Thesis). University of Florida. Retrieved from http://ufdc.ufl.edu/UFE0022187

Chicago Manual of Style (16th Edition):

Wexel, Melanie M. “Central Targeting of Trigeminal Primary Afferent Nerve Terminals via Intracisternal Injection of RTX and Its Effect on Pain Behavior.” 2008. Masters Thesis, University of Florida. Accessed July 21, 2019. http://ufdc.ufl.edu/UFE0022187.

MLA Handbook (7th Edition):

Wexel, Melanie M. “Central Targeting of Trigeminal Primary Afferent Nerve Terminals via Intracisternal Injection of RTX and Its Effect on Pain Behavior.” 2008. Web. 21 Jul 2019.

Vancouver:

Wexel MM. Central Targeting of Trigeminal Primary Afferent Nerve Terminals via Intracisternal Injection of RTX and Its Effect on Pain Behavior. [Internet] [Masters thesis]. University of Florida; 2008. [cited 2019 Jul 21]. Available from: http://ufdc.ufl.edu/UFE0022187.

Council of Science Editors:

Wexel MM. Central Targeting of Trigeminal Primary Afferent Nerve Terminals via Intracisternal Injection of RTX and Its Effect on Pain Behavior. [Masters Thesis]. University of Florida; 2008. Available from: http://ufdc.ufl.edu/UFE0022187

.