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You searched for subject:(Antagonist). Showing records 1 – 30 of 293 total matches.

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1. Mårtensson, Linn. Sympathy for the Devil : Mottagares föredragna karaktärsdrag hos antagonister.

Degree: Informatics, 2016, University of Skövde

  De senaste åren har det blivit viktigare och viktigare att utveckla djupa och trovärdiga antagonister för olika narrativ. Men det är inte alltid självklart… (more)

Subjects/Keywords: Antagonist; Karaktärsskapande; Sympati

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

APA (6th Edition):

Mårtensson, L. (2016). Sympathy for the Devil : Mottagares föredragna karaktärsdrag hos antagonister. (Thesis). University of Skövde. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-12401

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):

Mårtensson, Linn. “Sympathy for the Devil : Mottagares föredragna karaktärsdrag hos antagonister.” 2016. Thesis, University of Skövde. Accessed March 06, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-12401.

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

MLA Handbook (7th Edition):

Mårtensson, Linn. “Sympathy for the Devil : Mottagares föredragna karaktärsdrag hos antagonister.” 2016. Web. 06 Mar 2021.

Vancouver:

Mårtensson L. Sympathy for the Devil : Mottagares föredragna karaktärsdrag hos antagonister. [Internet] [Thesis]. University of Skövde; 2016. [cited 2021 Mar 06]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-12401.

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

Council of Science Editors:

Mårtensson L. Sympathy for the Devil : Mottagares föredragna karaktärsdrag hos antagonister. [Thesis]. University of Skövde; 2016. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:his:diva-12401

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


Halmstad University

2. Carlsson, Sofia. Bonds Antagonister : En kvalitativ studie om hur hotbilder förändrats genom åren.

Degree: Social and Health Sciences (HOS), 2013, Halmstad University

  Titel: Bonds antagonister - En kvalitativ studie om hur hotbilder förändrats genom åren Handledare: Lennart Hast Examinator: Thomas Knoll Rapport: Kandidatuppsats Utbildning: Medie- och… (more)

Subjects/Keywords: James Bond; antagonist; hotbild; stereotyp

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APA (6th Edition):

Carlsson, S. (2013). Bonds Antagonister : En kvalitativ studie om hur hotbilder förändrats genom åren. (Thesis). Halmstad University. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:hh:diva-21288

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):

Carlsson, Sofia. “Bonds Antagonister : En kvalitativ studie om hur hotbilder förändrats genom åren.” 2013. Thesis, Halmstad University. Accessed March 06, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:hh:diva-21288.

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

MLA Handbook (7th Edition):

Carlsson, Sofia. “Bonds Antagonister : En kvalitativ studie om hur hotbilder förändrats genom åren.” 2013. Web. 06 Mar 2021.

Vancouver:

Carlsson S. Bonds Antagonister : En kvalitativ studie om hur hotbilder förändrats genom åren. [Internet] [Thesis]. Halmstad University; 2013. [cited 2021 Mar 06]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:hh:diva-21288.

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

Council of Science Editors:

Carlsson S. Bonds Antagonister : En kvalitativ studie om hur hotbilder förändrats genom åren. [Thesis]. Halmstad University; 2013. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:hh:diva-21288

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


UCLA

3. Curtin, Brice Harrison. Strategies to Synthesize Template-Constrained Macrocycles with Improved Pharmacological Properties – from Tryptophan Alkylations to cIAP-Selective Antagonists & Glycosylated Peptidomimetics.

Degree: Chemistry, 2017, UCLA

 Peptide-derived macrocycles are a potentially rich source of biologically active lead structures, which are capable of recapitulating a therapeutic protein-protein surface interaction. Their three-dimensional shape… (more)

Subjects/Keywords: Organic chemistry; IAP Antagonist; Macrocyclization; Peptidomimetics; Pyrroloindoline

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APA (6th Edition):

Curtin, B. H. (2017). Strategies to Synthesize Template-Constrained Macrocycles with Improved Pharmacological Properties – from Tryptophan Alkylations to cIAP-Selective Antagonists & Glycosylated Peptidomimetics. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/3jq5r85m

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):

Curtin, Brice Harrison. “Strategies to Synthesize Template-Constrained Macrocycles with Improved Pharmacological Properties – from Tryptophan Alkylations to cIAP-Selective Antagonists & Glycosylated Peptidomimetics.” 2017. Thesis, UCLA. Accessed March 06, 2021. http://www.escholarship.org/uc/item/3jq5r85m.

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

MLA Handbook (7th Edition):

Curtin, Brice Harrison. “Strategies to Synthesize Template-Constrained Macrocycles with Improved Pharmacological Properties – from Tryptophan Alkylations to cIAP-Selective Antagonists & Glycosylated Peptidomimetics.” 2017. Web. 06 Mar 2021.

Vancouver:

Curtin BH. Strategies to Synthesize Template-Constrained Macrocycles with Improved Pharmacological Properties – from Tryptophan Alkylations to cIAP-Selective Antagonists & Glycosylated Peptidomimetics. [Internet] [Thesis]. UCLA; 2017. [cited 2021 Mar 06]. Available from: http://www.escholarship.org/uc/item/3jq5r85m.

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

Council of Science Editors:

Curtin BH. Strategies to Synthesize Template-Constrained Macrocycles with Improved Pharmacological Properties – from Tryptophan Alkylations to cIAP-Selective Antagonists & Glycosylated Peptidomimetics. [Thesis]. UCLA; 2017. Available from: http://www.escholarship.org/uc/item/3jq5r85m

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

4. Chaya, M K. Molecular characterization of Pochonia Chlamydosporia, Zare and Bio-Management of disease complex in Okra (Abelmoselus esculentus L. Moench) Using Microbial Antagonist; -.

Degree: Biotechnology, 2013, Jawaharlal Nehru Technological University, Hyderabad

The nematophagous fungus Pochonia chlamydosporia Goddard is a potential bio-agent agent of root-knot nematode. Itis a wide spread bio-control fungus of Heterodera spp. strains of… (more)

Subjects/Keywords: Antagonist; Chlamydosporia; Esculentus; Molecular; Pochonia; Zare

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APA (6th Edition):

Chaya, M. K. (2013). Molecular characterization of Pochonia Chlamydosporia, Zare and Bio-Management of disease complex in Okra (Abelmoselus esculentus L. Moench) Using Microbial Antagonist; -. (Thesis). Jawaharlal Nehru Technological University, Hyderabad. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/19335

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):

Chaya, M K. “Molecular characterization of Pochonia Chlamydosporia, Zare and Bio-Management of disease complex in Okra (Abelmoselus esculentus L. Moench) Using Microbial Antagonist; -.” 2013. Thesis, Jawaharlal Nehru Technological University, Hyderabad. Accessed March 06, 2021. http://shodhganga.inflibnet.ac.in/handle/10603/19335.

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

MLA Handbook (7th Edition):

Chaya, M K. “Molecular characterization of Pochonia Chlamydosporia, Zare and Bio-Management of disease complex in Okra (Abelmoselus esculentus L. Moench) Using Microbial Antagonist; -.” 2013. Web. 06 Mar 2021.

Vancouver:

Chaya MK. Molecular characterization of Pochonia Chlamydosporia, Zare and Bio-Management of disease complex in Okra (Abelmoselus esculentus L. Moench) Using Microbial Antagonist; -. [Internet] [Thesis]. Jawaharlal Nehru Technological University, Hyderabad; 2013. [cited 2021 Mar 06]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/19335.

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

Council of Science Editors:

Chaya MK. Molecular characterization of Pochonia Chlamydosporia, Zare and Bio-Management of disease complex in Okra (Abelmoselus esculentus L. Moench) Using Microbial Antagonist; -. [Thesis]. Jawaharlal Nehru Technological University, Hyderabad; 2013. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/19335

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

5. 김, 혜란. Wnt Inhibitory Factor (WIF)-1 Promotes Melanogenesis in Normal Human Melanocytes.

Degree: 2011, Ajou University

Background: Wnt inhibitory factor-1 (WIF-1) acts as a suppressor of Wnt antagonists. There is no study available on melanogenesis effect of human melanocytes. Objectives: In… (more)

Subjects/Keywords: melanocyte; melanogenesis; WIF-1; pigmentation; Wnt antagonist

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APA (6th Edition):

김, . (2011). Wnt Inhibitory Factor (WIF)-1 Promotes Melanogenesis in Normal Human Melanocytes. (Thesis). Ajou University. Retrieved from http://repository.ajou.ac.kr/handle/201003/4418 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000011924

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):

김, 혜란. “Wnt Inhibitory Factor (WIF)-1 Promotes Melanogenesis in Normal Human Melanocytes.” 2011. Thesis, Ajou University. Accessed March 06, 2021. http://repository.ajou.ac.kr/handle/201003/4418 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000011924.

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

MLA Handbook (7th Edition):

김, 혜란. “Wnt Inhibitory Factor (WIF)-1 Promotes Melanogenesis in Normal Human Melanocytes.” 2011. Web. 06 Mar 2021.

Vancouver:

김 . Wnt Inhibitory Factor (WIF)-1 Promotes Melanogenesis in Normal Human Melanocytes. [Internet] [Thesis]. Ajou University; 2011. [cited 2021 Mar 06]. Available from: http://repository.ajou.ac.kr/handle/201003/4418 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000011924.

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

Council of Science Editors:

김 . Wnt Inhibitory Factor (WIF)-1 Promotes Melanogenesis in Normal Human Melanocytes. [Thesis]. Ajou University; 2011. Available from: http://repository.ajou.ac.kr/handle/201003/4418 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000011924

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

6. Kato, Takahiro. Long-term administration of fluvoxamine attenuates neuropathic pain and involvement of spinal serotonin receptors in diabetic model rats : 糖尿病モデルラットに対するフルボキサミンの長期投与は神経障害性疼痛を減弱させ、脊髄におけるセロトニン受容体の関与を変化させる.

Degree: 博士(医学), 2014, Hiroshima University / 広島大学

 Diabetic neuropathic pain management is difficult even with non-steroidal anti-inflammatory drugs and narcotic analgesics such as morphine. Fluvoxamine, a class of selective serotonin reuptake inhibitors… (more)

Subjects/Keywords: Fluvoxamine; Diabetes; Serotonin receptor antagonist; Hyperalgesia

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APA (6th Edition):

Kato, T. (2014). Long-term administration of fluvoxamine attenuates neuropathic pain and involvement of spinal serotonin receptors in diabetic model rats : 糖尿病モデルラットに対するフルボキサミンの長期投与は神経障害性疼痛を減弱させ、脊髄におけるセロトニン受容体の関与を変化させる. (Thesis). Hiroshima University / 広島大学. Retrieved from http://ir.lib.hiroshima-u.ac.jp/00036308

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):

Kato, Takahiro. “Long-term administration of fluvoxamine attenuates neuropathic pain and involvement of spinal serotonin receptors in diabetic model rats : 糖尿病モデルラットに対するフルボキサミンの長期投与は神経障害性疼痛を減弱させ、脊髄におけるセロトニン受容体の関与を変化させる.” 2014. Thesis, Hiroshima University / 広島大学. Accessed March 06, 2021. http://ir.lib.hiroshima-u.ac.jp/00036308.

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

MLA Handbook (7th Edition):

Kato, Takahiro. “Long-term administration of fluvoxamine attenuates neuropathic pain and involvement of spinal serotonin receptors in diabetic model rats : 糖尿病モデルラットに対するフルボキサミンの長期投与は神経障害性疼痛を減弱させ、脊髄におけるセロトニン受容体の関与を変化させる.” 2014. Web. 06 Mar 2021.

Vancouver:

Kato T. Long-term administration of fluvoxamine attenuates neuropathic pain and involvement of spinal serotonin receptors in diabetic model rats : 糖尿病モデルラットに対するフルボキサミンの長期投与は神経障害性疼痛を減弱させ、脊髄におけるセロトニン受容体の関与を変化させる. [Internet] [Thesis]. Hiroshima University / 広島大学; 2014. [cited 2021 Mar 06]. Available from: http://ir.lib.hiroshima-u.ac.jp/00036308.

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

Council of Science Editors:

Kato T. Long-term administration of fluvoxamine attenuates neuropathic pain and involvement of spinal serotonin receptors in diabetic model rats : 糖尿病モデルラットに対するフルボキサミンの長期投与は神経障害性疼痛を減弱させ、脊髄におけるセロトニン受容体の関与を変化させる. [Thesis]. Hiroshima University / 広島大学; 2014. Available from: http://ir.lib.hiroshima-u.ac.jp/00036308

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


Univerzitet u Beogradu

7. Savić Vujović, Katarina R., 1979-. Efekti opioida i antagonista NMDA receptora na telesnu temperaturu i akutni nociceptivni bol kod pacova.

Degree: Medicinski fakultet, 2015, Univerzitet u Beogradu

Farmakologija / Pharmacology

Uvod: Pored antinocicepcije, opioidi ispoljavaju značajne efekte i na telesnu temperaturu. Brojni dokazi podržavaju postojanje endogenog glutamatergičkog sistema koji moduliše telesnu temperaturu… (more)

Subjects/Keywords: NMDA antagonist; opioids; body temperature; acute pain

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APA (6th Edition):

Savić Vujović, Katarina R., 1. (2015). Efekti opioida i antagonista NMDA receptora na telesnu temperaturu i akutni nociceptivni bol kod pacova. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:9777/bdef:Content/get

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):

Savić Vujović, Katarina R., 1979-. “Efekti opioida i antagonista NMDA receptora na telesnu temperaturu i akutni nociceptivni bol kod pacova.” 2015. Thesis, Univerzitet u Beogradu. Accessed March 06, 2021. https://fedorabg.bg.ac.rs/fedora/get/o:9777/bdef:Content/get.

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

MLA Handbook (7th Edition):

Savić Vujović, Katarina R., 1979-. “Efekti opioida i antagonista NMDA receptora na telesnu temperaturu i akutni nociceptivni bol kod pacova.” 2015. Web. 06 Mar 2021.

Vancouver:

Savić Vujović, Katarina R. 1. Efekti opioida i antagonista NMDA receptora na telesnu temperaturu i akutni nociceptivni bol kod pacova. [Internet] [Thesis]. Univerzitet u Beogradu; 2015. [cited 2021 Mar 06]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:9777/bdef:Content/get.

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

Council of Science Editors:

Savić Vujović, Katarina R. 1. Efekti opioida i antagonista NMDA receptora na telesnu temperaturu i akutni nociceptivni bol kod pacova. [Thesis]. Univerzitet u Beogradu; 2015. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:9777/bdef:Content/get

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


University of Melbourne

8. Jani, Nitya Vipin. In vitro and in vivo assays of novel molecules with combined antioxidant and angiotensin AT1 receptor antagonism.

Degree: 2011, University of Melbourne

 This project determined the AT1 receptor antagonist potency and antioxidant capacity of novel antioxidant-containing angiotensin II receptor antagonists. The rationale behind combining these two pharmacophores… (more)

Subjects/Keywords: antioxidant; AT1 receptor antagonist; dual action drug

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APA (6th Edition):

Jani, N. V. (2011). In vitro and in vivo assays of novel molecules with combined antioxidant and angiotensin AT1 receptor antagonism. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/36348

Chicago Manual of Style (16th Edition):

Jani, Nitya Vipin. “In vitro and in vivo assays of novel molecules with combined antioxidant and angiotensin AT1 receptor antagonism.” 2011. Doctoral Dissertation, University of Melbourne. Accessed March 06, 2021. http://hdl.handle.net/11343/36348.

MLA Handbook (7th Edition):

Jani, Nitya Vipin. “In vitro and in vivo assays of novel molecules with combined antioxidant and angiotensin AT1 receptor antagonism.” 2011. Web. 06 Mar 2021.

Vancouver:

Jani NV. In vitro and in vivo assays of novel molecules with combined antioxidant and angiotensin AT1 receptor antagonism. [Internet] [Doctoral dissertation]. University of Melbourne; 2011. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/11343/36348.

Council of Science Editors:

Jani NV. In vitro and in vivo assays of novel molecules with combined antioxidant and angiotensin AT1 receptor antagonism. [Doctoral Dissertation]. University of Melbourne; 2011. Available from: http://hdl.handle.net/11343/36348

9. Roos, Amanda. Ultrasonic Vocalization Response to NMDA Receptor Antagonists in Rats .

Degree: 2014, California State University – San Marcos

 Affect (or mood) changes induced by drugs of abuse play a large part in the development of reward surrounding addictive behaviors. The appraisal of drug… (more)

Subjects/Keywords: NMDA receptor antagonist; rats; ultrasonic vocalization

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APA (6th Edition):

Roos, A. (2014). Ultrasonic Vocalization Response to NMDA Receptor Antagonists in Rats . (Thesis). California State University – San Marcos. Retrieved from http://hdl.handle.net/10211.3/130964

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):

Roos, Amanda. “Ultrasonic Vocalization Response to NMDA Receptor Antagonists in Rats .” 2014. Thesis, California State University – San Marcos. Accessed March 06, 2021. http://hdl.handle.net/10211.3/130964.

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

MLA Handbook (7th Edition):

Roos, Amanda. “Ultrasonic Vocalization Response to NMDA Receptor Antagonists in Rats .” 2014. Web. 06 Mar 2021.

Vancouver:

Roos A. Ultrasonic Vocalization Response to NMDA Receptor Antagonists in Rats . [Internet] [Thesis]. California State University – San Marcos; 2014. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/10211.3/130964.

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

Council of Science Editors:

Roos A. Ultrasonic Vocalization Response to NMDA Receptor Antagonists in Rats . [Thesis]. California State University – San Marcos; 2014. Available from: http://hdl.handle.net/10211.3/130964

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


University of Melbourne

10. ARUMUGAM, BASKAR. Strategies to inhibit myopia: pharmacological and optical approaches.

Degree: 2011, University of Melbourne

 Aims: Myopia is a significant public health issue affecting around 30% of the world’s population and is a major cause of blindness because of the… (more)

Subjects/Keywords: myopia; tree shrews; chicks; muscarinic antagonist; MT3; MT7; dopamine antagonist; spiperone; intermittent positive lenses; hyperopic defocus and myopic defocus

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APA (6th Edition):

ARUMUGAM, B. (2011). Strategies to inhibit myopia: pharmacological and optical approaches. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/36411

Chicago Manual of Style (16th Edition):

ARUMUGAM, BASKAR. “Strategies to inhibit myopia: pharmacological and optical approaches.” 2011. Doctoral Dissertation, University of Melbourne. Accessed March 06, 2021. http://hdl.handle.net/11343/36411.

MLA Handbook (7th Edition):

ARUMUGAM, BASKAR. “Strategies to inhibit myopia: pharmacological and optical approaches.” 2011. Web. 06 Mar 2021.

Vancouver:

ARUMUGAM B. Strategies to inhibit myopia: pharmacological and optical approaches. [Internet] [Doctoral dissertation]. University of Melbourne; 2011. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/11343/36411.

Council of Science Editors:

ARUMUGAM B. Strategies to inhibit myopia: pharmacological and optical approaches. [Doctoral Dissertation]. University of Melbourne; 2011. Available from: http://hdl.handle.net/11343/36411

11. Papakosta, Vasiliki- Maria. Διερεύνηση στοιχείων παθοφυσιολογίας/νευροψυχολογίας της ιδεοψυχαναγκαστικής διαταραχής μέσω του πειραματικού μοντέλου ενισχυόμενης εναλλαγής κατεύθυνσης.

Degree: 2017, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

 Introduction: Obsessive- compulsive disorder (OCD) pathophysiology remains unclear, despite the considerable research effort invested in this field. There have been made many attempts to develop… (more)

Subjects/Keywords: Ιδεοψυχαναγκαστική διαταραχή; Πειραματικά μοντέλα; Σεροτονίνη; Ανταγονιστές 5HT2A; Ανταγονιστές 5HT2C; Obsessive - compulsive disorder; Animal models; Serotonin receptors; mcPP; 5HT2A antagonist; 5HT2C antagonist

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APA (6th Edition):

Papakosta, V. M. (2017). Διερεύνηση στοιχείων παθοφυσιολογίας/νευροψυχολογίας της ιδεοψυχαναγκαστικής διαταραχής μέσω του πειραματικού μοντέλου ενισχυόμενης εναλλαγής κατεύθυνσης. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/41767

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):

Papakosta, Vasiliki- Maria. “Διερεύνηση στοιχείων παθοφυσιολογίας/νευροψυχολογίας της ιδεοψυχαναγκαστικής διαταραχής μέσω του πειραματικού μοντέλου ενισχυόμενης εναλλαγής κατεύθυνσης.” 2017. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed March 06, 2021. http://hdl.handle.net/10442/hedi/41767.

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

MLA Handbook (7th Edition):

Papakosta, Vasiliki- Maria. “Διερεύνηση στοιχείων παθοφυσιολογίας/νευροψυχολογίας της ιδεοψυχαναγκαστικής διαταραχής μέσω του πειραματικού μοντέλου ενισχυόμενης εναλλαγής κατεύθυνσης.” 2017. Web. 06 Mar 2021.

Vancouver:

Papakosta VM. Διερεύνηση στοιχείων παθοφυσιολογίας/νευροψυχολογίας της ιδεοψυχαναγκαστικής διαταραχής μέσω του πειραματικού μοντέλου ενισχυόμενης εναλλαγής κατεύθυνσης. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2017. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/10442/hedi/41767.

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

Council of Science Editors:

Papakosta VM. Διερεύνηση στοιχείων παθοφυσιολογίας/νευροψυχολογίας της ιδεοψυχαναγκαστικής διαταραχής μέσω του πειραματικού μοντέλου ενισχυόμενης εναλλαγής κατεύθυνσης. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2017. Available from: http://hdl.handle.net/10442/hedi/41767

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

12. Miyake, Hitoshi; Nakagawa, Ichiro; Takeshima, Yasuhiro; Nishimura, Fumihiko; Park, Young-Su; Nakamura, Mitsutoshi. Post-ischemic administration of vascular endothelial growth factor inhibitor in a rat model of cerebral venous infarction. : ラット脳静脈モデルにおける血管内皮増殖因子桔抗薬の虚血後投与.

Degree: 博士(医学), 2013, Nara Medical University / 奈良県立医科大学

Cerebral venous ischemia can result in severe brain edema. Inhibition of vascular endothelial growth factor (VEGF) activity by a neutralizing antibody can completely block the… (more)

Subjects/Keywords: cerebral venous infarction; vascular endothelial growth factor; antagonist; brain edema

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APA (6th Edition):

Miyake, Hitoshi; Nakagawa, Ichiro; Takeshima, Yasuhiro; Nishimura, Fumihiko; Park, Young-Su; Nakamura, M. (2013). Post-ischemic administration of vascular endothelial growth factor inhibitor in a rat model of cerebral venous infarction. : ラット脳静脈モデルにおける血管内皮増殖因子桔抗薬の虚血後投与. (Thesis). Nara Medical University / 奈良県立医科大学. Retrieved from http://hdl.handle.net/10564/2676

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):

Miyake, Hitoshi; Nakagawa, Ichiro; Takeshima, Yasuhiro; Nishimura, Fumihiko; Park, Young-Su; Nakamura, Mitsutoshi. “Post-ischemic administration of vascular endothelial growth factor inhibitor in a rat model of cerebral venous infarction. : ラット脳静脈モデルにおける血管内皮増殖因子桔抗薬の虚血後投与.” 2013. Thesis, Nara Medical University / 奈良県立医科大学. Accessed March 06, 2021. http://hdl.handle.net/10564/2676.

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

MLA Handbook (7th Edition):

Miyake, Hitoshi; Nakagawa, Ichiro; Takeshima, Yasuhiro; Nishimura, Fumihiko; Park, Young-Su; Nakamura, Mitsutoshi. “Post-ischemic administration of vascular endothelial growth factor inhibitor in a rat model of cerebral venous infarction. : ラット脳静脈モデルにおける血管内皮増殖因子桔抗薬の虚血後投与.” 2013. Web. 06 Mar 2021.

Vancouver:

Miyake, Hitoshi; Nakagawa, Ichiro; Takeshima, Yasuhiro; Nishimura, Fumihiko; Park, Young-Su; Nakamura M. Post-ischemic administration of vascular endothelial growth factor inhibitor in a rat model of cerebral venous infarction. : ラット脳静脈モデルにおける血管内皮増殖因子桔抗薬の虚血後投与. [Internet] [Thesis]. Nara Medical University / 奈良県立医科大学; 2013. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/10564/2676.

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

Council of Science Editors:

Miyake, Hitoshi; Nakagawa, Ichiro; Takeshima, Yasuhiro; Nishimura, Fumihiko; Park, Young-Su; Nakamura M. Post-ischemic administration of vascular endothelial growth factor inhibitor in a rat model of cerebral venous infarction. : ラット脳静脈モデルにおける血管内皮増殖因子桔抗薬の虚血後投与. [Thesis]. Nara Medical University / 奈良県立医科大学; 2013. Available from: http://hdl.handle.net/10564/2676

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

13. Sato, Yuichi. Combination of Urinary Sodium/Creatinine Ratio and Plasma Brain Natriuretic Peptide Level Predicts Successful Tolvaptan Therapy in Patients with Heart Failure and Volume Overload.

Degree: 博士(医学), 2017, Mie University / 三重大学

To evaluate short-term clinical and hemodynamic effects of tolvaptan therapy and to identify predictors of the therapeutic outcomes, we retrospectively recruited sixty consecutive hospitalized heart… (more)

Subjects/Keywords: vasopressin V2-receptor antagonist; loop diuretics; diuresis; heart failure

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APA (6th Edition):

Sato, Y. (2017). Combination of Urinary Sodium/Creatinine Ratio and Plasma Brain Natriuretic Peptide Level Predicts Successful Tolvaptan Therapy in Patients with Heart Failure and Volume Overload. (Thesis). Mie University / 三重大学. Retrieved from http://hdl.handle.net/10076/00016981

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):

Sato, Yuichi. “Combination of Urinary Sodium/Creatinine Ratio and Plasma Brain Natriuretic Peptide Level Predicts Successful Tolvaptan Therapy in Patients with Heart Failure and Volume Overload.” 2017. Thesis, Mie University / 三重大学. Accessed March 06, 2021. http://hdl.handle.net/10076/00016981.

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

MLA Handbook (7th Edition):

Sato, Yuichi. “Combination of Urinary Sodium/Creatinine Ratio and Plasma Brain Natriuretic Peptide Level Predicts Successful Tolvaptan Therapy in Patients with Heart Failure and Volume Overload.” 2017. Web. 06 Mar 2021.

Vancouver:

Sato Y. Combination of Urinary Sodium/Creatinine Ratio and Plasma Brain Natriuretic Peptide Level Predicts Successful Tolvaptan Therapy in Patients with Heart Failure and Volume Overload. [Internet] [Thesis]. Mie University / 三重大学; 2017. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/10076/00016981.

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

Council of Science Editors:

Sato Y. Combination of Urinary Sodium/Creatinine Ratio and Plasma Brain Natriuretic Peptide Level Predicts Successful Tolvaptan Therapy in Patients with Heart Failure and Volume Overload. [Thesis]. Mie University / 三重大学; 2017. Available from: http://hdl.handle.net/10076/00016981

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


University of Rochester

14. Sridharan, Rajashri. Relationship between Receptor Occupancy and Signaling Responses in Ste2p, a G Protein Coupled Receptor in Saccharomyces cerevisiae.

Degree: PhD, 2015, University of Rochester

 It has been generally assumed that signaling responses to an agonist are proportional to the number of receptors occupied on the cell surface. On studying… (more)

Subjects/Keywords: GPCR; Ste2p; Yeast; Agonist Occupancy; Antagonist; Dose Response Alignment; Schild Ratio

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APA (6th Edition):

Sridharan, R. (2015). Relationship between Receptor Occupancy and Signaling Responses in Ste2p, a G Protein Coupled Receptor in Saccharomyces cerevisiae. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/29354

Chicago Manual of Style (16th Edition):

Sridharan, Rajashri. “Relationship between Receptor Occupancy and Signaling Responses in Ste2p, a G Protein Coupled Receptor in Saccharomyces cerevisiae.” 2015. Doctoral Dissertation, University of Rochester. Accessed March 06, 2021. http://hdl.handle.net/1802/29354.

MLA Handbook (7th Edition):

Sridharan, Rajashri. “Relationship between Receptor Occupancy and Signaling Responses in Ste2p, a G Protein Coupled Receptor in Saccharomyces cerevisiae.” 2015. Web. 06 Mar 2021.

Vancouver:

Sridharan R. Relationship between Receptor Occupancy and Signaling Responses in Ste2p, a G Protein Coupled Receptor in Saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. University of Rochester; 2015. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/1802/29354.

Council of Science Editors:

Sridharan R. Relationship between Receptor Occupancy and Signaling Responses in Ste2p, a G Protein Coupled Receptor in Saccharomyces cerevisiae. [Doctoral Dissertation]. University of Rochester; 2015. Available from: http://hdl.handle.net/1802/29354


University of Manchester

15. Irshad, Abdur Rehman. Approaches towards a total synthesis of the phomactins.

Degree: 2011, University of Manchester

 Within this thesis are described synthetic approaches towards thephomactins which are novel platelet activating factor antagonists. The workwas carried out at the University of Manchester… (more)

Subjects/Keywords: Phomactins; natural product; diterpene; platelet-activating factor antagonist

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APA (6th Edition):

Irshad, A. R. (2011). Approaches towards a total synthesis of the phomactins. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:121244

Chicago Manual of Style (16th Edition):

Irshad, Abdur Rehman. “Approaches towards a total synthesis of the phomactins.” 2011. Doctoral Dissertation, University of Manchester. Accessed March 06, 2021. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:121244.

MLA Handbook (7th Edition):

Irshad, Abdur Rehman. “Approaches towards a total synthesis of the phomactins.” 2011. Web. 06 Mar 2021.

Vancouver:

Irshad AR. Approaches towards a total synthesis of the phomactins. [Internet] [Doctoral dissertation]. University of Manchester; 2011. [cited 2021 Mar 06]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:121244.

Council of Science Editors:

Irshad AR. Approaches towards a total synthesis of the phomactins. [Doctoral Dissertation]. University of Manchester; 2011. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:121244


Vanderbilt University

16. McCollum, Andrea Lindsey. Lead Optimization for Discovery of Potent and Selective Dopamine Receptor D4 Antagonist.

Degree: MS, Chemistry, 2015, Vanderbilt University

 Stimulant dependence is a prolonged relapsing condition that can be exhibited by reinstatement animal models. Dopamine D4 receptor antagonists are shown to interrupt drug seeking… (more)

Subjects/Keywords: Medicinal chemistry; Dopamine receptor; Dopamine receptor antagonist; cocaine dependence

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APA (6th Edition):

McCollum, A. L. (2015). Lead Optimization for Discovery of Potent and Selective Dopamine Receptor D4 Antagonist. (Thesis). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/14658

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):

McCollum, Andrea Lindsey. “Lead Optimization for Discovery of Potent and Selective Dopamine Receptor D4 Antagonist.” 2015. Thesis, Vanderbilt University. Accessed March 06, 2021. http://hdl.handle.net/1803/14658.

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

MLA Handbook (7th Edition):

McCollum, Andrea Lindsey. “Lead Optimization for Discovery of Potent and Selective Dopamine Receptor D4 Antagonist.” 2015. Web. 06 Mar 2021.

Vancouver:

McCollum AL. Lead Optimization for Discovery of Potent and Selective Dopamine Receptor D4 Antagonist. [Internet] [Thesis]. Vanderbilt University; 2015. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/1803/14658.

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

Council of Science Editors:

McCollum AL. Lead Optimization for Discovery of Potent and Selective Dopamine Receptor D4 Antagonist. [Thesis]. Vanderbilt University; 2015. Available from: http://hdl.handle.net/1803/14658

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


Universidade Federal de Viçosa

17. Thais Ribeiro Santiago. Selection of rhizobacteria for biological control of bacterial wilt of Eucalyptus.

Degree: 2010, Universidade Federal de Viçosa

Avaliou-se o potencial antagônico de 298 rizobactérias obtidas da rizosfera e rizoplano de tomateiro e de eucalipto contra Ralstonia solanacearum, agente causal da murcha bacteriana.… (more)

Subjects/Keywords: FITOPATOLOGIA; Antagonista; Bactéria; Rizobactéria; Eucalipto; Antagonist; Rhizobacteria; Bacteria; Eucalyptus

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APA (6th Edition):

Santiago, T. R. (2010). Selection of rhizobacteria for biological control of bacterial wilt of Eucalyptus. (Thesis). Universidade Federal de Viçosa. Retrieved from http://www.tede.ufv.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=4097

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):

Santiago, Thais Ribeiro. “Selection of rhizobacteria for biological control of bacterial wilt of Eucalyptus.” 2010. Thesis, Universidade Federal de Viçosa. Accessed March 06, 2021. http://www.tede.ufv.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=4097.

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

MLA Handbook (7th Edition):

Santiago, Thais Ribeiro. “Selection of rhizobacteria for biological control of bacterial wilt of Eucalyptus.” 2010. Web. 06 Mar 2021.

Vancouver:

Santiago TR. Selection of rhizobacteria for biological control of bacterial wilt of Eucalyptus. [Internet] [Thesis]. Universidade Federal de Viçosa; 2010. [cited 2021 Mar 06]. Available from: http://www.tede.ufv.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=4097.

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

Council of Science Editors:

Santiago TR. Selection of rhizobacteria for biological control of bacterial wilt of Eucalyptus. [Thesis]. Universidade Federal de Viçosa; 2010. Available from: http://www.tede.ufv.br/tedesimplificado/tde_busca/arquivo.php?codArquivo=4097

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


Addis Ababa University

18. ABAYNEH, TUNASHA BANATA. Evaluation of Biological Control Agents against Bacterial Wilt .

Degree: 2012, Addis Ababa University

 The present study was designed with the objective of isolating, screening, evaluating and characterizing antagonistic isolates against bacterial wilt of ensete from rhizosphere and phyllosphere… (more)

Subjects/Keywords: Ensete,Xanthomonas campestris pv. musacearum; Fungal and bacterial antagonist

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APA (6th Edition):

ABAYNEH, T. B. (2012). Evaluation of Biological Control Agents against Bacterial Wilt . (Thesis). Addis Ababa University. Retrieved from http://etd.aau.edu.et/dspace/handle/123456789/353

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):

ABAYNEH, TUNASHA BANATA. “Evaluation of Biological Control Agents against Bacterial Wilt .” 2012. Thesis, Addis Ababa University. Accessed March 06, 2021. http://etd.aau.edu.et/dspace/handle/123456789/353.

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

MLA Handbook (7th Edition):

ABAYNEH, TUNASHA BANATA. “Evaluation of Biological Control Agents against Bacterial Wilt .” 2012. Web. 06 Mar 2021.

Vancouver:

ABAYNEH TB. Evaluation of Biological Control Agents against Bacterial Wilt . [Internet] [Thesis]. Addis Ababa University; 2012. [cited 2021 Mar 06]. Available from: http://etd.aau.edu.et/dspace/handle/123456789/353.

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

Council of Science Editors:

ABAYNEH TB. Evaluation of Biological Control Agents against Bacterial Wilt . [Thesis]. Addis Ababa University; 2012. Available from: http://etd.aau.edu.et/dspace/handle/123456789/353

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


University of Toronto

19. Kalia, Aditi. Comparative Effects of a D2 and Mixed D1-D2 Dopamine Antagonist on Gambling Reinforcement in Pathological Gamblers and Healthy Controls.

Degree: 2011, University of Toronto

Pathological Gambling (PG) is an impulse control disorder with lifetime prevalence of 1-3%. Available treatments are limited by uncertain classification and complexity of implicated neurotransmitter… (more)

Subjects/Keywords: dopamine; pathological gambling; addiction; haloperidol; fluphenazine; dopamine antagonist; 0419

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APA (6th Edition):

Kalia, A. (2011). Comparative Effects of a D2 and Mixed D1-D2 Dopamine Antagonist on Gambling Reinforcement in Pathological Gamblers and Healthy Controls. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/31270

Chicago Manual of Style (16th Edition):

Kalia, Aditi. “Comparative Effects of a D2 and Mixed D1-D2 Dopamine Antagonist on Gambling Reinforcement in Pathological Gamblers and Healthy Controls.” 2011. Masters Thesis, University of Toronto. Accessed March 06, 2021. http://hdl.handle.net/1807/31270.

MLA Handbook (7th Edition):

Kalia, Aditi. “Comparative Effects of a D2 and Mixed D1-D2 Dopamine Antagonist on Gambling Reinforcement in Pathological Gamblers and Healthy Controls.” 2011. Web. 06 Mar 2021.

Vancouver:

Kalia A. Comparative Effects of a D2 and Mixed D1-D2 Dopamine Antagonist on Gambling Reinforcement in Pathological Gamblers and Healthy Controls. [Internet] [Masters thesis]. University of Toronto; 2011. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/1807/31270.

Council of Science Editors:

Kalia A. Comparative Effects of a D2 and Mixed D1-D2 Dopamine Antagonist on Gambling Reinforcement in Pathological Gamblers and Healthy Controls. [Masters Thesis]. University of Toronto; 2011. Available from: http://hdl.handle.net/1807/31270

20. M. Salvi. Preparation of bicyclic nitrogen intermediates as useful scaffolds for the synthesis of new biologically active compounds.

Degree: 2014, Università degli Studi di Milano

 The discovery of the orexin (also known as hypocretin) neuropeptide system determined a major advancement in the understanding of sleep and arousal states and its… (more)

Subjects/Keywords: norbornane scaffolds, orexin receptors antagonist; Settore CHIM/06 - Chimica Organica

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APA (6th Edition):

Salvi, M. (2014). Preparation of bicyclic nitrogen intermediates as useful scaffolds for the synthesis of new biologically active compounds. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/243983

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):

Salvi, M.. “Preparation of bicyclic nitrogen intermediates as useful scaffolds for the synthesis of new biologically active compounds.” 2014. Thesis, Università degli Studi di Milano. Accessed March 06, 2021. http://hdl.handle.net/2434/243983.

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

MLA Handbook (7th Edition):

Salvi, M.. “Preparation of bicyclic nitrogen intermediates as useful scaffolds for the synthesis of new biologically active compounds.” 2014. Web. 06 Mar 2021.

Vancouver:

Salvi M. Preparation of bicyclic nitrogen intermediates as useful scaffolds for the synthesis of new biologically active compounds. [Internet] [Thesis]. Università degli Studi di Milano; 2014. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/2434/243983.

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

Council of Science Editors:

Salvi M. Preparation of bicyclic nitrogen intermediates as useful scaffolds for the synthesis of new biologically active compounds. [Thesis]. Università degli Studi di Milano; 2014. Available from: http://hdl.handle.net/2434/243983

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


University of Adelaide

21. Lewis, Kate. The role of substance P in the progression and complications of secondary brain tumours.

Degree: 2012, University of Adelaide

 Secondary brain tumours occur when cancer cells enter the circulation from their primary site and colonise the brain, previously shown to occur across the blood-brain… (more)

Subjects/Keywords: brain metastases; substance P; Nk1 antagonist; dexamethasone; oedema; blood-brain barrier

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APA (6th Edition):

Lewis, K. (2012). The role of substance P in the progression and complications of secondary brain tumours. (Thesis). University of Adelaide. Retrieved from http://hdl.handle.net/2440/82257

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):

Lewis, Kate. “The role of substance P in the progression and complications of secondary brain tumours.” 2012. Thesis, University of Adelaide. Accessed March 06, 2021. http://hdl.handle.net/2440/82257.

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

MLA Handbook (7th Edition):

Lewis, Kate. “The role of substance P in the progression and complications of secondary brain tumours.” 2012. Web. 06 Mar 2021.

Vancouver:

Lewis K. The role of substance P in the progression and complications of secondary brain tumours. [Internet] [Thesis]. University of Adelaide; 2012. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/2440/82257.

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

Council of Science Editors:

Lewis K. The role of substance P in the progression and complications of secondary brain tumours. [Thesis]. University of Adelaide; 2012. Available from: http://hdl.handle.net/2440/82257

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


University of Toronto

22. Lopez, Ana Sofia. Exploring the Suitability of a Specifici Glucocorticoid Receptor Antagonist as a Tool in the Study of the Regulation of Rat Lung Alveolarization by Glucocorticoids.

Degree: 2010, University of Toronto

Background: Intracellular glucocorticoid receptors (GRs) mediate the regulation of lung development, including alveolarization, by glucocorticoids (GCs). One potential approach to determining the role of GC-GR… (more)

Subjects/Keywords: alveolarization; glucocorticoids; rat lung development; glucocorticoid receptor antagonist; 0719

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APA (6th Edition):

Lopez, A. S. (2010). Exploring the Suitability of a Specifici Glucocorticoid Receptor Antagonist as a Tool in the Study of the Regulation of Rat Lung Alveolarization by Glucocorticoids. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/25774

Chicago Manual of Style (16th Edition):

Lopez, Ana Sofia. “Exploring the Suitability of a Specifici Glucocorticoid Receptor Antagonist as a Tool in the Study of the Regulation of Rat Lung Alveolarization by Glucocorticoids.” 2010. Masters Thesis, University of Toronto. Accessed March 06, 2021. http://hdl.handle.net/1807/25774.

MLA Handbook (7th Edition):

Lopez, Ana Sofia. “Exploring the Suitability of a Specifici Glucocorticoid Receptor Antagonist as a Tool in the Study of the Regulation of Rat Lung Alveolarization by Glucocorticoids.” 2010. Web. 06 Mar 2021.

Vancouver:

Lopez AS. Exploring the Suitability of a Specifici Glucocorticoid Receptor Antagonist as a Tool in the Study of the Regulation of Rat Lung Alveolarization by Glucocorticoids. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/1807/25774.

Council of Science Editors:

Lopez AS. Exploring the Suitability of a Specifici Glucocorticoid Receptor Antagonist as a Tool in the Study of the Regulation of Rat Lung Alveolarization by Glucocorticoids. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/25774


University of Houston

23. -8238-9376. Linker Functionalization of a Bivalent Ligand for the Study of the 5-HT2AR/ 5-HT2CR Heterodimer.

Degree: MS, Chemistry, 2017, University of Houston

 G-protein-coupled receptors (GPCRs) are important pharmaceutical targets. In recent years, it has been found that GPCRs can function as homo- and hetero- dimers. The serotonin… (more)

Subjects/Keywords: Serotonin; Bivalent ligand; 5-HT2AR antagonist; 5-HT2CR agonist; Fluorophores

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APA (6th Edition):

-8238-9376. (2017). Linker Functionalization of a Bivalent Ligand for the Study of the 5-HT2AR/ 5-HT2CR Heterodimer. (Masters Thesis). University of Houston. Retrieved from http://hdl.handle.net/10657/4799

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Chicago Manual of Style (16th Edition):

-8238-9376. “Linker Functionalization of a Bivalent Ligand for the Study of the 5-HT2AR/ 5-HT2CR Heterodimer.” 2017. Masters Thesis, University of Houston. Accessed March 06, 2021. http://hdl.handle.net/10657/4799.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

-8238-9376. “Linker Functionalization of a Bivalent Ligand for the Study of the 5-HT2AR/ 5-HT2CR Heterodimer.” 2017. Web. 06 Mar 2021.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-8238-9376. Linker Functionalization of a Bivalent Ligand for the Study of the 5-HT2AR/ 5-HT2CR Heterodimer. [Internet] [Masters thesis]. University of Houston; 2017. [cited 2021 Mar 06]. Available from: http://hdl.handle.net/10657/4799.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

-8238-9376. Linker Functionalization of a Bivalent Ligand for the Study of the 5-HT2AR/ 5-HT2CR Heterodimer. [Masters Thesis]. University of Houston; 2017. Available from: http://hdl.handle.net/10657/4799

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete


Univerzitet u Beogradu

24. Srebro , Dragana P., 1986-. Farmakodinamska ispitivanja magnezijum-sulfata i dizocilpina u modelima somatskog i visceralnog bola kod pacova.

Degree: Medicinski fakultet, 2016, Univerzitet u Beogradu

Medicina - Farmakologija / Medicine - Pharmacology

Magnezijum je mineral koji u organizmu ima brojne uloge. On je kofaktor u više od 300 enzimskih reakcija, održava membranski potencijal, ima modulatorno dejstvo na jonske kanale, neurotransmisiju, i drugo...

Subjects/Keywords: magnesium sulfate; dizocilpine; NMDA antagonist; TRP channels; inflammatory pain; edema

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APA (6th Edition):

Srebro , Dragana P., 1. (2016). Farmakodinamska ispitivanja magnezijum-sulfata i dizocilpina u modelima somatskog i visceralnog bola kod pacova. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:11645/bdef:Content/get

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):

Srebro , Dragana P., 1986-. “Farmakodinamska ispitivanja magnezijum-sulfata i dizocilpina u modelima somatskog i visceralnog bola kod pacova.” 2016. Thesis, Univerzitet u Beogradu. Accessed March 06, 2021. https://fedorabg.bg.ac.rs/fedora/get/o:11645/bdef:Content/get.

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

MLA Handbook (7th Edition):

Srebro , Dragana P., 1986-. “Farmakodinamska ispitivanja magnezijum-sulfata i dizocilpina u modelima somatskog i visceralnog bola kod pacova.” 2016. Web. 06 Mar 2021.

Vancouver:

Srebro , Dragana P. 1. Farmakodinamska ispitivanja magnezijum-sulfata i dizocilpina u modelima somatskog i visceralnog bola kod pacova. [Internet] [Thesis]. Univerzitet u Beogradu; 2016. [cited 2021 Mar 06]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:11645/bdef:Content/get.

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

Council of Science Editors:

Srebro , Dragana P. 1. Farmakodinamska ispitivanja magnezijum-sulfata i dizocilpina u modelima somatskog i visceralnog bola kod pacova. [Thesis]. Univerzitet u Beogradu; 2016. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:11645/bdef:Content/get

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


University of Connecticut

25. Yang, Xiao. 1-norm Support Vector Machine on Single-trial EEG and ECG Data to Identify Neural Oscillatory Features in the Ketamine Model for Schizophrenia.

Degree: MS, Psychological Sciences, 2019, University of Connecticut

  Ketamine provides a useful model for studying the physiopathology of schizophrenia as it induces and exacerbates schizophrenic symptoms in healthy individuals and patients, respectively.… (more)

Subjects/Keywords: Ketamine; NMDA antagonist; GABA/glutamate; neural oscillations; schizophrenia

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APA (6th Edition):

Yang, X. (2019). 1-norm Support Vector Machine on Single-trial EEG and ECG Data to Identify Neural Oscillatory Features in the Ketamine Model for Schizophrenia. (Masters Thesis). University of Connecticut. Retrieved from https://opencommons.uconn.edu/gs_theses/1382

Chicago Manual of Style (16th Edition):

Yang, Xiao. “1-norm Support Vector Machine on Single-trial EEG and ECG Data to Identify Neural Oscillatory Features in the Ketamine Model for Schizophrenia.” 2019. Masters Thesis, University of Connecticut. Accessed March 06, 2021. https://opencommons.uconn.edu/gs_theses/1382.

MLA Handbook (7th Edition):

Yang, Xiao. “1-norm Support Vector Machine on Single-trial EEG and ECG Data to Identify Neural Oscillatory Features in the Ketamine Model for Schizophrenia.” 2019. Web. 06 Mar 2021.

Vancouver:

Yang X. 1-norm Support Vector Machine on Single-trial EEG and ECG Data to Identify Neural Oscillatory Features in the Ketamine Model for Schizophrenia. [Internet] [Masters thesis]. University of Connecticut; 2019. [cited 2021 Mar 06]. Available from: https://opencommons.uconn.edu/gs_theses/1382.

Council of Science Editors:

Yang X. 1-norm Support Vector Machine on Single-trial EEG and ECG Data to Identify Neural Oscillatory Features in the Ketamine Model for Schizophrenia. [Masters Thesis]. University of Connecticut; 2019. Available from: https://opencommons.uconn.edu/gs_theses/1382


University of Manchester

26. Irshad, Abdur Rehman. Approaches towards a total synthesis of the phomactins.

Degree: PhD, 2011, University of Manchester

 Within this thesis are described synthetic approaches towards the phomactins which are novel platelet activating factor antagonists. The synthesis of known alcohol 162 is described,… (more)

Subjects/Keywords: 547.71; Phomactins; natural product; diterpene; platelet-activating factor antagonist

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APA (6th Edition):

Irshad, A. R. (2011). Approaches towards a total synthesis of the phomactins. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/approaches-towards-a-total-synthesis-of-the-phomactins(49b617f3-dd49-4217-8828-be93af835554).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.538357

Chicago Manual of Style (16th Edition):

Irshad, Abdur Rehman. “Approaches towards a total synthesis of the phomactins.” 2011. Doctoral Dissertation, University of Manchester. Accessed March 06, 2021. https://www.research.manchester.ac.uk/portal/en/theses/approaches-towards-a-total-synthesis-of-the-phomactins(49b617f3-dd49-4217-8828-be93af835554).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.538357.

MLA Handbook (7th Edition):

Irshad, Abdur Rehman. “Approaches towards a total synthesis of the phomactins.” 2011. Web. 06 Mar 2021.

Vancouver:

Irshad AR. Approaches towards a total synthesis of the phomactins. [Internet] [Doctoral dissertation]. University of Manchester; 2011. [cited 2021 Mar 06]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/approaches-towards-a-total-synthesis-of-the-phomactins(49b617f3-dd49-4217-8828-be93af835554).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.538357.

Council of Science Editors:

Irshad AR. Approaches towards a total synthesis of the phomactins. [Doctoral Dissertation]. University of Manchester; 2011. Available from: https://www.research.manchester.ac.uk/portal/en/theses/approaches-towards-a-total-synthesis-of-the-phomactins(49b617f3-dd49-4217-8828-be93af835554).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.538357


University of Bath

27. Pillinger, Kathryn. New antagonists for the Kappa Opioid receptor.

Degree: PhD, 2009, University of Bath

 There has been much evidence in recent years to suggest that the kappa opioid receptor plays a significant role in mediating a number of behavioural… (more)

Subjects/Keywords: 615.7822; kappa; aminotetralin; antagonist; opioid

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APA (6th Edition):

Pillinger, K. (2009). New antagonists for the Kappa Opioid receptor. (Doctoral Dissertation). University of Bath. Retrieved from https://researchportal.bath.ac.uk/en/studentthesis/new-antagonists-for-the-kappa-opioid-receptor(322dc880-278b-4617-b9b5-db550f9cc3f1).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.501626

Chicago Manual of Style (16th Edition):

Pillinger, Kathryn. “New antagonists for the Kappa Opioid receptor.” 2009. Doctoral Dissertation, University of Bath. Accessed March 06, 2021. https://researchportal.bath.ac.uk/en/studentthesis/new-antagonists-for-the-kappa-opioid-receptor(322dc880-278b-4617-b9b5-db550f9cc3f1).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.501626.

MLA Handbook (7th Edition):

Pillinger, Kathryn. “New antagonists for the Kappa Opioid receptor.” 2009. Web. 06 Mar 2021.

Vancouver:

Pillinger K. New antagonists for the Kappa Opioid receptor. [Internet] [Doctoral dissertation]. University of Bath; 2009. [cited 2021 Mar 06]. Available from: https://researchportal.bath.ac.uk/en/studentthesis/new-antagonists-for-the-kappa-opioid-receptor(322dc880-278b-4617-b9b5-db550f9cc3f1).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.501626.

Council of Science Editors:

Pillinger K. New antagonists for the Kappa Opioid receptor. [Doctoral Dissertation]. University of Bath; 2009. Available from: https://researchportal.bath.ac.uk/en/studentthesis/new-antagonists-for-the-kappa-opioid-receptor(322dc880-278b-4617-b9b5-db550f9cc3f1).html ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.501626


Jönköping University

28. Johnsson, Amanda. Vad är vi rädda för? : En jämförande semiotisk innehållsanalys av antagonisten i två versioner av filmen “IT”.

Degree: Media and Communication Studies, 2018, Jönköping University

  Syftet med studien är att jämföra framställningen av skräck i originalversionen och nyinspelningen av skräckfilmen IT. Med en semiotisk innehållsanalys analyserar vi framställningen av… (more)

Subjects/Keywords: Semiotik; IT; Pennywise; skräck; innehållsanalys; Stephen King; antagonist; Communication Studies; Kommunikationsvetenskap

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APA (6th Edition):

Johnsson, A. (2018). Vad är vi rädda för? : En jämförande semiotisk innehållsanalys av antagonisten i två versioner av filmen “IT”. (Thesis). Jönköping University. Retrieved from http://urn.kb.se/resolve?urn=urn:nbn:se:hj:diva-38798

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):

Johnsson, Amanda. “Vad är vi rädda för? : En jämförande semiotisk innehållsanalys av antagonisten i två versioner av filmen “IT”.” 2018. Thesis, Jönköping University. Accessed March 06, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:hj:diva-38798.

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

MLA Handbook (7th Edition):

Johnsson, Amanda. “Vad är vi rädda för? : En jämförande semiotisk innehållsanalys av antagonisten i två versioner av filmen “IT”.” 2018. Web. 06 Mar 2021.

Vancouver:

Johnsson A. Vad är vi rädda för? : En jämförande semiotisk innehållsanalys av antagonisten i två versioner av filmen “IT”. [Internet] [Thesis]. Jönköping University; 2018. [cited 2021 Mar 06]. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:hj:diva-38798.

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

Council of Science Editors:

Johnsson A. Vad är vi rädda för? : En jämförande semiotisk innehållsanalys av antagonisten i två versioner av filmen “IT”. [Thesis]. Jönköping University; 2018. Available from: http://urn.kb.se/resolve?urn=urn:nbn:se:hj:diva-38798

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


Utah State University

29. Sandberg, John B. Acute Effects of Antagonist Stretching on Jump Height and Knee Extension Peak Torque.

Degree: MS, Health, Physical Education, and Recreation, 2012, Utah State University

  A great deal of research has shown decrements in force and power following static stretching. There has been little research investigating the acute effects… (more)

Subjects/Keywords: antagonist; stretching; jump height; knee extension; torque; Physiology

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APA (6th Edition):

Sandberg, J. B. (2012). Acute Effects of Antagonist Stretching on Jump Height and Knee Extension Peak Torque. (Masters Thesis). Utah State University. Retrieved from https://digitalcommons.usu.edu/etd/1156

Chicago Manual of Style (16th Edition):

Sandberg, John B. “Acute Effects of Antagonist Stretching on Jump Height and Knee Extension Peak Torque.” 2012. Masters Thesis, Utah State University. Accessed March 06, 2021. https://digitalcommons.usu.edu/etd/1156.

MLA Handbook (7th Edition):

Sandberg, John B. “Acute Effects of Antagonist Stretching on Jump Height and Knee Extension Peak Torque.” 2012. Web. 06 Mar 2021.

Vancouver:

Sandberg JB. Acute Effects of Antagonist Stretching on Jump Height and Knee Extension Peak Torque. [Internet] [Masters thesis]. Utah State University; 2012. [cited 2021 Mar 06]. Available from: https://digitalcommons.usu.edu/etd/1156.

Council of Science Editors:

Sandberg JB. Acute Effects of Antagonist Stretching on Jump Height and Knee Extension Peak Torque. [Masters Thesis]. Utah State University; 2012. Available from: https://digitalcommons.usu.edu/etd/1156

30. Vinnakota, Harsha. Pharmacokinetic Evaluation of a Novel Compound, Sn79, a Putative Sigma-2 Receptor Antagonist, By Intravenous and Oral Administration in Rats.

Degree: PhD, Pharmaceutical Sciences, 2011, University of Mississippi

 Considering the alarming rates at which substance drug abuse, especially cocaine, is increasing in today's society, there is a lot of impetus on the development… (more)

Subjects/Keywords: Antagonist; Cocaine; Pharmacokinetics; Sigma; Pharmacy and Pharmaceutical Sciences

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APA (6th Edition):

Vinnakota, H. (2011). Pharmacokinetic Evaluation of a Novel Compound, Sn79, a Putative Sigma-2 Receptor Antagonist, By Intravenous and Oral Administration in Rats. (Doctoral Dissertation). University of Mississippi. Retrieved from https://egrove.olemiss.edu/etd/294

Chicago Manual of Style (16th Edition):

Vinnakota, Harsha. “Pharmacokinetic Evaluation of a Novel Compound, Sn79, a Putative Sigma-2 Receptor Antagonist, By Intravenous and Oral Administration in Rats.” 2011. Doctoral Dissertation, University of Mississippi. Accessed March 06, 2021. https://egrove.olemiss.edu/etd/294.

MLA Handbook (7th Edition):

Vinnakota, Harsha. “Pharmacokinetic Evaluation of a Novel Compound, Sn79, a Putative Sigma-2 Receptor Antagonist, By Intravenous and Oral Administration in Rats.” 2011. Web. 06 Mar 2021.

Vancouver:

Vinnakota H. Pharmacokinetic Evaluation of a Novel Compound, Sn79, a Putative Sigma-2 Receptor Antagonist, By Intravenous and Oral Administration in Rats. [Internet] [Doctoral dissertation]. University of Mississippi; 2011. [cited 2021 Mar 06]. Available from: https://egrove.olemiss.edu/etd/294.

Council of Science Editors:

Vinnakota H. Pharmacokinetic Evaluation of a Novel Compound, Sn79, a Putative Sigma-2 Receptor Antagonist, By Intravenous and Oral Administration in Rats. [Doctoral Dissertation]. University of Mississippi; 2011. Available from: https://egrove.olemiss.edu/etd/294

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