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You searched for subject:(Serotonin 2A receptor). Showing records 1 – 8 of 8 total matches.

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The Ohio State University

1. Schmid, Cullen L. Differential regulation of serotonin 2A receptor responsiveness by agonist-directed interactions with beta-arrestin2.

Degree: PhD, Neuroscience Graduate Studies Program, 2011, The Ohio State University

 The G protein-coupled, serotonin 2A (5-HT2A) receptor is a major drug target for the treatment of a number of mental health disorders, including schizophrenia, anxiety… (more)

Subjects/Keywords: Neurosciences; Pharmacology; G protein-coupled receptor; Serotonin 2A receptor; beta-arrestin2; hallucinogens; functional selectivity

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

APA (6th Edition):

Schmid, C. L. (2011). Differential regulation of serotonin 2A receptor responsiveness by agonist-directed interactions with beta-arrestin2. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1300287547

Chicago Manual of Style (16th Edition):

Schmid, Cullen L. “Differential regulation of serotonin 2A receptor responsiveness by agonist-directed interactions with beta-arrestin2.” 2011. Doctoral Dissertation, The Ohio State University. Accessed December 15, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1300287547.

MLA Handbook (7th Edition):

Schmid, Cullen L. “Differential regulation of serotonin 2A receptor responsiveness by agonist-directed interactions with beta-arrestin2.” 2011. Web. 15 Dec 2019.

Vancouver:

Schmid CL. Differential regulation of serotonin 2A receptor responsiveness by agonist-directed interactions with beta-arrestin2. [Internet] [Doctoral dissertation]. The Ohio State University; 2011. [cited 2019 Dec 15]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1300287547.

Council of Science Editors:

Schmid CL. Differential regulation of serotonin 2A receptor responsiveness by agonist-directed interactions with beta-arrestin2. [Doctoral Dissertation]. The Ohio State University; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1300287547


Universidade do Rio Grande do Sul

2. Jobim, Paulo Fernandes Costa. Possível influencia do polimorfismo T102C do gene 5HT²A no tempo de vida médio dos seres humanos.

Degree: 2008, Universidade do Rio Grande do Sul

Doenças e comportamentos de risco relacionados ao polimorfismo T102C do gene 5- HT2A, como esquizofrenia, suicídio, impulsividade, alcoolismo, tabagismo, entre outros, podem encurtar o tempo… (more)

Subjects/Keywords: Esperança de vida; Mean life span; Serotonin; Polimorfismo genético; Envelhecimento; Receptor 2A of serotonin; Serotonina; T102C polymorphism; Aging; 5-HT2A gene

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APA (6th Edition):

Jobim, P. F. C. (2008). Possível influencia do polimorfismo T102C do gene 5HT²A no tempo de vida médio dos seres humanos. (Thesis). Universidade do Rio Grande do Sul. Retrieved from http://hdl.handle.net/10183/12634

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):

Jobim, Paulo Fernandes Costa. “Possível influencia do polimorfismo T102C do gene 5HT²A no tempo de vida médio dos seres humanos.” 2008. Thesis, Universidade do Rio Grande do Sul. Accessed December 15, 2019. http://hdl.handle.net/10183/12634.

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

MLA Handbook (7th Edition):

Jobim, Paulo Fernandes Costa. “Possível influencia do polimorfismo T102C do gene 5HT²A no tempo de vida médio dos seres humanos.” 2008. Web. 15 Dec 2019.

Vancouver:

Jobim PFC. Possível influencia do polimorfismo T102C do gene 5HT²A no tempo de vida médio dos seres humanos. [Internet] [Thesis]. Universidade do Rio Grande do Sul; 2008. [cited 2019 Dec 15]. Available from: http://hdl.handle.net/10183/12634.

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

Council of Science Editors:

Jobim PFC. Possível influencia do polimorfismo T102C do gene 5HT²A no tempo de vida médio dos seres humanos. [Thesis]. Universidade do Rio Grande do Sul; 2008. Available from: http://hdl.handle.net/10183/12634

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


Virginia Commonwealth University

3. Huang, Miao. Decoding the signaling of the D2R-2AR heteromer: relevance to schizophrenia.

Degree: PhD, Chemistry, 2018, Virginia Commonwealth University

  Schizophrenia is a severe mental disorder affecting ~1% of world population. Two G protein coupled receptors (GPCRs): Gi-coupled dopamine D2 receptor (D2R), and Gq-coupled… (more)

Subjects/Keywords: GPCR; schizophrenia; dopamine D2 receptor; serotonin 2A receptor; heteromer; antipsychotic; Biochemistry, Biophysics, and Structural Biology; Neuroscience and Neurobiology; Pharmacology

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

APA (6th Edition):

Huang, M. (2018). Decoding the signaling of the D2R-2AR heteromer: relevance to schizophrenia. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/5696

Chicago Manual of Style (16th Edition):

Huang, Miao. “Decoding the signaling of the D2R-2AR heteromer: relevance to schizophrenia.” 2018. Doctoral Dissertation, Virginia Commonwealth University. Accessed December 15, 2019. https://scholarscompass.vcu.edu/etd/5696.

MLA Handbook (7th Edition):

Huang, Miao. “Decoding the signaling of the D2R-2AR heteromer: relevance to schizophrenia.” 2018. Web. 15 Dec 2019.

Vancouver:

Huang M. Decoding the signaling of the D2R-2AR heteromer: relevance to schizophrenia. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2018. [cited 2019 Dec 15]. Available from: https://scholarscompass.vcu.edu/etd/5696.

Council of Science Editors:

Huang M. Decoding the signaling of the D2R-2AR heteromer: relevance to schizophrenia. [Doctoral Dissertation]. Virginia Commonwealth University; 2018. Available from: https://scholarscompass.vcu.edu/etd/5696


University of Toronto

4. Costa, Laura Anne Da. Genetic Modifiers of Caffeine Consumption and Risk of Myocardial Infarction.

Degree: 2011, University of Toronto

The variability in caffeine consumption and inconsistencies among studies linking caffeine to heart disease may be explained by genetic variation. Caffeine antagonizes adenosine receptors with… (more)

Subjects/Keywords: Caffeine; Gene-Environment Interaction; Myocardial Infarction; Coffee; HTR2A; DRD2; Serotonin Receptor 2A; Dopamine D2 Receptor; Polymorphism; 0570; 0766; 0369

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APA (6th Edition):

Costa, L. A. D. (2011). Genetic Modifiers of Caffeine Consumption and Risk of Myocardial Infarction. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/29516

Chicago Manual of Style (16th Edition):

Costa, Laura Anne Da. “Genetic Modifiers of Caffeine Consumption and Risk of Myocardial Infarction.” 2011. Masters Thesis, University of Toronto. Accessed December 15, 2019. http://hdl.handle.net/1807/29516.

MLA Handbook (7th Edition):

Costa, Laura Anne Da. “Genetic Modifiers of Caffeine Consumption and Risk of Myocardial Infarction.” 2011. Web. 15 Dec 2019.

Vancouver:

Costa LAD. Genetic Modifiers of Caffeine Consumption and Risk of Myocardial Infarction. [Internet] [Masters thesis]. University of Toronto; 2011. [cited 2019 Dec 15]. Available from: http://hdl.handle.net/1807/29516.

Council of Science Editors:

Costa LAD. Genetic Modifiers of Caffeine Consumption and Risk of Myocardial Infarction. [Masters Thesis]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/29516


University of Kansas

5. Mi, Zhen. REGULATION OF DENDRITIC SPINES BY 5-HT2A RECEPTOR SIGNALING PATHWAYS.

Degree: PhD, Pharmacology & Toxicology, 2015, University of Kansas

 Dendritic spines are small membranous protrusions from the dendrites of neuron, which are thought to serve as basic units of synaptic transmission, learning and memory.… (more)

Subjects/Keywords: Neurosciences; Molecular biology; atypical antipsychotics; dendritic spines; JAK/STAT; serotonin 2A receptor; small G protein of the Rho family; transamidation

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

APA (6th Edition):

Mi, Z. (2015). REGULATION OF DENDRITIC SPINES BY 5-HT2A RECEPTOR SIGNALING PATHWAYS. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/21731

Chicago Manual of Style (16th Edition):

Mi, Zhen. “REGULATION OF DENDRITIC SPINES BY 5-HT2A RECEPTOR SIGNALING PATHWAYS.” 2015. Doctoral Dissertation, University of Kansas. Accessed December 15, 2019. http://hdl.handle.net/1808/21731.

MLA Handbook (7th Edition):

Mi, Zhen. “REGULATION OF DENDRITIC SPINES BY 5-HT2A RECEPTOR SIGNALING PATHWAYS.” 2015. Web. 15 Dec 2019.

Vancouver:

Mi Z. REGULATION OF DENDRITIC SPINES BY 5-HT2A RECEPTOR SIGNALING PATHWAYS. [Internet] [Doctoral dissertation]. University of Kansas; 2015. [cited 2019 Dec 15]. Available from: http://hdl.handle.net/1808/21731.

Council of Science Editors:

Mi Z. REGULATION OF DENDRITIC SPINES BY 5-HT2A RECEPTOR SIGNALING PATHWAYS. [Doctoral Dissertation]. University of Kansas; 2015. Available from: http://hdl.handle.net/1808/21731


Virginia Commonwealth University

6. Vohra, Hiba Z. Molecular Targets of Psychedelics and Their Role in Behavioral Models of Hallucinogenic Action.

Degree: MS, Physiology and Biophysics, 2019, Virginia Commonwealth University

  Psychedelics are a subset of hallucinogenic drugs that exert their characteristic effects through agonist activity at the serotonin receptor 2A (5-HT2A). In this study,… (more)

Subjects/Keywords: psychedelics; serotonin 2A receptor; head twitch response; prepulse inhibition; psychosis; gene knockout mice; Animal Experimentation and Research; Behavioral Neurobiology; Molecular and Cellular Neuroscience; Pharmacology; Physiology

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

APA (6th Edition):

Vohra, H. Z. (2019). Molecular Targets of Psychedelics and Their Role in Behavioral Models of Hallucinogenic Action. (Thesis). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/6012

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):

Vohra, Hiba Z. “Molecular Targets of Psychedelics and Their Role in Behavioral Models of Hallucinogenic Action.” 2019. Thesis, Virginia Commonwealth University. Accessed December 15, 2019. https://scholarscompass.vcu.edu/etd/6012.

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

MLA Handbook (7th Edition):

Vohra, Hiba Z. “Molecular Targets of Psychedelics and Their Role in Behavioral Models of Hallucinogenic Action.” 2019. Web. 15 Dec 2019.

Vancouver:

Vohra HZ. Molecular Targets of Psychedelics and Their Role in Behavioral Models of Hallucinogenic Action. [Internet] [Thesis]. Virginia Commonwealth University; 2019. [cited 2019 Dec 15]. Available from: https://scholarscompass.vcu.edu/etd/6012.

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

Council of Science Editors:

Vohra HZ. Molecular Targets of Psychedelics and Their Role in Behavioral Models of Hallucinogenic Action. [Thesis]. Virginia Commonwealth University; 2019. Available from: https://scholarscompass.vcu.edu/etd/6012

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

7. 石金, 朋人. ラット線条体におけるハロペリドール誘発性ドパミンD2受容体upregulationに対するセロトニン系薬物の影響.

Degree: 博士(医学), 医学, 1998, Hokkaido University

 We examined the modulatory effect of serotonergic activities on haloperidolinduced up-regulation of dopamine D2 receptors in rat striatum. Chronic treatment with haloperidol (0.1, 0.5mg/kg, i.p.,… (more)

Subjects/Keywords: Up-regulation; dopamine D2 receptor; atypical antipsychotic drug; serotonin(5-HT)2A receptor; striatum

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APA (6th Edition):

石金, . (1998). ラット線条体におけるハロペリドール誘発性ドパミンD2受容体upregulationに対するセロトニン系薬物の影響. (Doctoral Dissertation). Hokkaido University. Retrieved from http://hdl.handle.net/2115/51570

Chicago Manual of Style (16th Edition):

石金, 朋人. “ラット線条体におけるハロペリドール誘発性ドパミンD2受容体upregulationに対するセロトニン系薬物の影響.” 1998. Doctoral Dissertation, Hokkaido University. Accessed December 15, 2019. http://hdl.handle.net/2115/51570.

MLA Handbook (7th Edition):

石金, 朋人. “ラット線条体におけるハロペリドール誘発性ドパミンD2受容体upregulationに対するセロトニン系薬物の影響.” 1998. Web. 15 Dec 2019.

Vancouver:

石金 . ラット線条体におけるハロペリドール誘発性ドパミンD2受容体upregulationに対するセロトニン系薬物の影響. [Internet] [Doctoral dissertation]. Hokkaido University; 1998. [cited 2019 Dec 15]. Available from: http://hdl.handle.net/2115/51570.

Council of Science Editors:

石金 . ラット線条体におけるハロペリドール誘発性ドパミンD2受容体upregulationに対するセロトニン系薬物の影響. [Doctoral Dissertation]. Hokkaido University; 1998. Available from: http://hdl.handle.net/2115/51570


North-West University

8. Bodenstein, Johannes. Antagonism by selected classical irreversible competitive antagonists : an investigation into the proposed non-specific mechanisms involved / Johannes Bodenstein .

Degree: 2003, North-West University

 Many irreversible antagonists are known to bind irreversibly to pharmacological receptors. However, few studies suggest that these irreversible antagonists may also display irreversible non-specific antagonism… (more)

Subjects/Keywords: 5HT[2A]-serotonin receptor; 4-DAMP mustard; Alpha[2A]-adrenoceptor; Benextramine; G protein-coupled receptor; Irreversible antagonist; Muscarinic acetylcholine receptor; Non-syntopic binding site; Phenoxybenzamine; Specific receptor; 4-DAMP mosterd; 5HT[2A]-serotonienreseptor; Alpha[2A]-adrenoseptor; Benekstramien; Fenoksibensamien; G-proteïengekoppelde reseptor; Muskariniese asetielcholienreseptor; Non-sintopiese bindingsetel; Onomkeerbare antagonis

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APA (6th Edition):

Bodenstein, J. (2003). Antagonism by selected classical irreversible competitive antagonists : an investigation into the proposed non-specific mechanisms involved / Johannes Bodenstein . (Thesis). North-West University. Retrieved from http://hdl.handle.net/10394/92

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):

Bodenstein, Johannes. “Antagonism by selected classical irreversible competitive antagonists : an investigation into the proposed non-specific mechanisms involved / Johannes Bodenstein .” 2003. Thesis, North-West University. Accessed December 15, 2019. http://hdl.handle.net/10394/92.

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

MLA Handbook (7th Edition):

Bodenstein, Johannes. “Antagonism by selected classical irreversible competitive antagonists : an investigation into the proposed non-specific mechanisms involved / Johannes Bodenstein .” 2003. Web. 15 Dec 2019.

Vancouver:

Bodenstein J. Antagonism by selected classical irreversible competitive antagonists : an investigation into the proposed non-specific mechanisms involved / Johannes Bodenstein . [Internet] [Thesis]. North-West University; 2003. [cited 2019 Dec 15]. Available from: http://hdl.handle.net/10394/92.

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

Council of Science Editors:

Bodenstein J. Antagonism by selected classical irreversible competitive antagonists : an investigation into the proposed non-specific mechanisms involved / Johannes Bodenstein . [Thesis]. North-West University; 2003. Available from: http://hdl.handle.net/10394/92

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

.