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You searched for +publisher:"Dalhousie University" +contributor:("Eileen Denovan-Wright"). Showing records 1 – 19 of 19 total matches.

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Dalhousie University

1. MacDonald, Jennifer. The Estrous Cycle Modulates Contractile Function and Ca2+ Homeostasis In Isolated Mouse Ventricular Myocytes.

Degree: MS, Department of Pharmacology, 2012, Dalhousie University

 This study investigated the effect of the mouse estrous cycle on myocyte contractile function. Female mice displayed irregular estrous cycles unless induced to cycle though… (more)

Subjects/Keywords: estrous cycle; ventricular myocyte; calcium homeostasis; contractile function; sex hormones

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APA (6th Edition):

MacDonald, J. (2012). The Estrous Cycle Modulates Contractile Function and Ca2+ Homeostasis In Isolated Mouse Ventricular Myocytes. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/15262

Chicago Manual of Style (16th Edition):

MacDonald, Jennifer. “The Estrous Cycle Modulates Contractile Function and Ca2+ Homeostasis In Isolated Mouse Ventricular Myocytes.” 2012. Masters Thesis, Dalhousie University. Accessed March 03, 2021. http://hdl.handle.net/10222/15262.

MLA Handbook (7th Edition):

MacDonald, Jennifer. “The Estrous Cycle Modulates Contractile Function and Ca2+ Homeostasis In Isolated Mouse Ventricular Myocytes.” 2012. Web. 03 Mar 2021.

Vancouver:

MacDonald J. The Estrous Cycle Modulates Contractile Function and Ca2+ Homeostasis In Isolated Mouse Ventricular Myocytes. [Internet] [Masters thesis]. Dalhousie University; 2012. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/10222/15262.

Council of Science Editors:

MacDonald J. The Estrous Cycle Modulates Contractile Function and Ca2+ Homeostasis In Isolated Mouse Ventricular Myocytes. [Masters Thesis]. Dalhousie University; 2012. Available from: http://hdl.handle.net/10222/15262


Dalhousie University

2. Bagher, Amina M. Distribution, Dimerization and Function of Human Cannabinoid Receptor Type 1 Coding Region Splice Variants.

Degree: MS, Department of Pharmacology, 2012, Dalhousie University

MSc Thesis

The pharmacological functions of the type 1 human cannabinoid receptor (hCB1) are thought to be modulated through the isoform encoded by the fourth… (more)

Subjects/Keywords: Subject Not Available

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APA (6th Edition):

Bagher, A. M. (2012). Distribution, Dimerization and Function of Human Cannabinoid Receptor Type 1 Coding Region Splice Variants. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/15267

Chicago Manual of Style (16th Edition):

Bagher, Amina M. “Distribution, Dimerization and Function of Human Cannabinoid Receptor Type 1 Coding Region Splice Variants.” 2012. Masters Thesis, Dalhousie University. Accessed March 03, 2021. http://hdl.handle.net/10222/15267.

MLA Handbook (7th Edition):

Bagher, Amina M. “Distribution, Dimerization and Function of Human Cannabinoid Receptor Type 1 Coding Region Splice Variants.” 2012. Web. 03 Mar 2021.

Vancouver:

Bagher AM. Distribution, Dimerization and Function of Human Cannabinoid Receptor Type 1 Coding Region Splice Variants. [Internet] [Masters thesis]. Dalhousie University; 2012. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/10222/15267.

Council of Science Editors:

Bagher AM. Distribution, Dimerization and Function of Human Cannabinoid Receptor Type 1 Coding Region Splice Variants. [Masters Thesis]. Dalhousie University; 2012. Available from: http://hdl.handle.net/10222/15267


Dalhousie University

3. Clattenburg, Leanne Marie. Identification and characterization of NOS1APc interacting proteins.

Degree: MS, Department of Pharmacology, 2013, Dalhousie University

 The current study characterizes novel interacting proteins for the neuronal nitric oxide synthase 1 adaptor protein (NOS1AP) isoform NOS1APc. NOS1APc is a 100kDa isoform of… (more)

Subjects/Keywords: Subject Not Available

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APA (6th Edition):

Clattenburg, L. M. (2013). Identification and characterization of NOS1APc interacting proteins. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/36317

Chicago Manual of Style (16th Edition):

Clattenburg, Leanne Marie. “Identification and characterization of NOS1APc interacting proteins.” 2013. Masters Thesis, Dalhousie University. Accessed March 03, 2021. http://hdl.handle.net/10222/36317.

MLA Handbook (7th Edition):

Clattenburg, Leanne Marie. “Identification and characterization of NOS1APc interacting proteins.” 2013. Web. 03 Mar 2021.

Vancouver:

Clattenburg LM. Identification and characterization of NOS1APc interacting proteins. [Internet] [Masters thesis]. Dalhousie University; 2013. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/10222/36317.

Council of Science Editors:

Clattenburg LM. Identification and characterization of NOS1APc interacting proteins. [Masters Thesis]. Dalhousie University; 2013. Available from: http://hdl.handle.net/10222/36317


Dalhousie University

4. Laprairie, Robert. CANNABINOIDS REGULATE TYPE 1 CANNABINOID RECEPTOR EXPRESSION IN CELL CULTURE MODELS OF HUNTINGTON'S DISEASE.

Degree: MS, Department of Pharmacology with Neuroscience, 2012, Dalhousie University

 Type 1 cannabinoid receptor (CB1) levels decline in the striatum of animal models of Huntington’s disease (HD) and in the brains of human patients suffering… (more)

Subjects/Keywords: Cannabinoid; Huntington's disease; Pharmacology; Neuroscience

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APA (6th Edition):

Laprairie, R. (2012). CANNABINOIDS REGULATE TYPE 1 CANNABINOID RECEPTOR EXPRESSION IN CELL CULTURE MODELS OF HUNTINGTON'S DISEASE. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/15199

Chicago Manual of Style (16th Edition):

Laprairie, Robert. “CANNABINOIDS REGULATE TYPE 1 CANNABINOID RECEPTOR EXPRESSION IN CELL CULTURE MODELS OF HUNTINGTON'S DISEASE.” 2012. Masters Thesis, Dalhousie University. Accessed March 03, 2021. http://hdl.handle.net/10222/15199.

MLA Handbook (7th Edition):

Laprairie, Robert. “CANNABINOIDS REGULATE TYPE 1 CANNABINOID RECEPTOR EXPRESSION IN CELL CULTURE MODELS OF HUNTINGTON'S DISEASE.” 2012. Web. 03 Mar 2021.

Vancouver:

Laprairie R. CANNABINOIDS REGULATE TYPE 1 CANNABINOID RECEPTOR EXPRESSION IN CELL CULTURE MODELS OF HUNTINGTON'S DISEASE. [Internet] [Masters thesis]. Dalhousie University; 2012. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/10222/15199.

Council of Science Editors:

Laprairie R. CANNABINOIDS REGULATE TYPE 1 CANNABINOID RECEPTOR EXPRESSION IN CELL CULTURE MODELS OF HUNTINGTON'S DISEASE. [Masters Thesis]. Dalhousie University; 2012. Available from: http://hdl.handle.net/10222/15199


Dalhousie University

5. Hosier, Gregory. Overexpressing Fragments of CREB-Binding Protein (CBP) to Block Transcriptional Dysregulation and Toxicity in Huntington's Disease.

Degree: MS, Department of Pharmacology with Neuroscience, 2012, Dalhousie University

 Huntington’s disease (HD) is caused by expression of the huntingtin gene containing an expanded CAG repeat. N-terminal mutant huntingtin protein (N-mHtt) accumulates in the nucleus… (more)

Subjects/Keywords: Huntington's disease; CREB-binding protein; CBP; transcriptional dysregulation; neurodegeneration; histone acetyltransferase

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APA (6th Edition):

Hosier, G. (2012). Overexpressing Fragments of CREB-Binding Protein (CBP) to Block Transcriptional Dysregulation and Toxicity in Huntington's Disease. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/15247

Chicago Manual of Style (16th Edition):

Hosier, Gregory. “Overexpressing Fragments of CREB-Binding Protein (CBP) to Block Transcriptional Dysregulation and Toxicity in Huntington's Disease.” 2012. Masters Thesis, Dalhousie University. Accessed March 03, 2021. http://hdl.handle.net/10222/15247.

MLA Handbook (7th Edition):

Hosier, Gregory. “Overexpressing Fragments of CREB-Binding Protein (CBP) to Block Transcriptional Dysregulation and Toxicity in Huntington's Disease.” 2012. Web. 03 Mar 2021.

Vancouver:

Hosier G. Overexpressing Fragments of CREB-Binding Protein (CBP) to Block Transcriptional Dysregulation and Toxicity in Huntington's Disease. [Internet] [Masters thesis]. Dalhousie University; 2012. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/10222/15247.

Council of Science Editors:

Hosier G. Overexpressing Fragments of CREB-Binding Protein (CBP) to Block Transcriptional Dysregulation and Toxicity in Huntington's Disease. [Masters Thesis]. Dalhousie University; 2012. Available from: http://hdl.handle.net/10222/15247


Dalhousie University

6. Holland, Patrick. DRUGS, DIMERS, AND MUTATIONS: INVESTIGATING THE EFFECTS OF LIGANDS AND A ?2-ADRENERGIC POLYMORPHISM ON HOMO/HETERODIMERIZATION OF ?2-ADRENERGIC AND ANGIOTENSIN II TYPE 1 RECEPTORS.

Degree: MS, Department of Pharmacology, 2012, Dalhousie University

 GPCRs are known to form dimeric structures, and this affects their pharmacological properties. The ?2AR and AT1aR are GPCRs that are involved the regulation of… (more)

Subjects/Keywords: GPCRs; Signalling; Polymorphism; Dimerization; Receptor Pharmacology

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APA (6th Edition):

Holland, P. (2012). DRUGS, DIMERS, AND MUTATIONS: INVESTIGATING THE EFFECTS OF LIGANDS AND A ?2-ADRENERGIC POLYMORPHISM ON HOMO/HETERODIMERIZATION OF ?2-ADRENERGIC AND ANGIOTENSIN II TYPE 1 RECEPTORS. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/15245

Chicago Manual of Style (16th Edition):

Holland, Patrick. “DRUGS, DIMERS, AND MUTATIONS: INVESTIGATING THE EFFECTS OF LIGANDS AND A ?2-ADRENERGIC POLYMORPHISM ON HOMO/HETERODIMERIZATION OF ?2-ADRENERGIC AND ANGIOTENSIN II TYPE 1 RECEPTORS.” 2012. Masters Thesis, Dalhousie University. Accessed March 03, 2021. http://hdl.handle.net/10222/15245.

MLA Handbook (7th Edition):

Holland, Patrick. “DRUGS, DIMERS, AND MUTATIONS: INVESTIGATING THE EFFECTS OF LIGANDS AND A ?2-ADRENERGIC POLYMORPHISM ON HOMO/HETERODIMERIZATION OF ?2-ADRENERGIC AND ANGIOTENSIN II TYPE 1 RECEPTORS.” 2012. Web. 03 Mar 2021.

Vancouver:

Holland P. DRUGS, DIMERS, AND MUTATIONS: INVESTIGATING THE EFFECTS OF LIGANDS AND A ?2-ADRENERGIC POLYMORPHISM ON HOMO/HETERODIMERIZATION OF ?2-ADRENERGIC AND ANGIOTENSIN II TYPE 1 RECEPTORS. [Internet] [Masters thesis]. Dalhousie University; 2012. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/10222/15245.

Council of Science Editors:

Holland P. DRUGS, DIMERS, AND MUTATIONS: INVESTIGATING THE EFFECTS OF LIGANDS AND A ?2-ADRENERGIC POLYMORPHISM ON HOMO/HETERODIMERIZATION OF ?2-ADRENERGIC AND ANGIOTENSIN II TYPE 1 RECEPTORS. [Masters Thesis]. Dalhousie University; 2012. Available from: http://hdl.handle.net/10222/15245


Dalhousie University

7. Richier, Lindsay. THE NITRIC OXIDE SYNTHASE ADAPTOR PROTEIN (NOS1AP) ASSOCIATES WITH SCRIBBLE AND REGULATES DENDRITIC SPINE DEVELOPMENT.

Degree: MS, Department of Pharmacology, 2010, Dalhousie University

 In a targeted proteomic screen to identify polarity protein complexes, a number of Scribble (Scrib) -associating proteins were identified; of particular interest was the Nitric… (more)

Subjects/Keywords: NOS1AP; Polarity; Scribble; dendritic protrusion; RhoGTPases

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APA (6th Edition):

Richier, L. (2010). THE NITRIC OXIDE SYNTHASE ADAPTOR PROTEIN (NOS1AP) ASSOCIATES WITH SCRIBBLE AND REGULATES DENDRITIC SPINE DEVELOPMENT. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/12823

Chicago Manual of Style (16th Edition):

Richier, Lindsay. “THE NITRIC OXIDE SYNTHASE ADAPTOR PROTEIN (NOS1AP) ASSOCIATES WITH SCRIBBLE AND REGULATES DENDRITIC SPINE DEVELOPMENT.” 2010. Masters Thesis, Dalhousie University. Accessed March 03, 2021. http://hdl.handle.net/10222/12823.

MLA Handbook (7th Edition):

Richier, Lindsay. “THE NITRIC OXIDE SYNTHASE ADAPTOR PROTEIN (NOS1AP) ASSOCIATES WITH SCRIBBLE AND REGULATES DENDRITIC SPINE DEVELOPMENT.” 2010. Web. 03 Mar 2021.

Vancouver:

Richier L. THE NITRIC OXIDE SYNTHASE ADAPTOR PROTEIN (NOS1AP) ASSOCIATES WITH SCRIBBLE AND REGULATES DENDRITIC SPINE DEVELOPMENT. [Internet] [Masters thesis]. Dalhousie University; 2010. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/10222/12823.

Council of Science Editors:

Richier L. THE NITRIC OXIDE SYNTHASE ADAPTOR PROTEIN (NOS1AP) ASSOCIATES WITH SCRIBBLE AND REGULATES DENDRITIC SPINE DEVELOPMENT. [Masters Thesis]. Dalhousie University; 2010. Available from: http://hdl.handle.net/10222/12823


Dalhousie University

8. Hammad, Maha. CHARACTERIZATION OF THE ANGIOTENSIN TYPE 1 RECEPTOR AND THE BETA2 ADRENERGIC RECEPTOR PROPERTIES: THE INVOLVEMENT OF ARRESTIN2, RAB1 AND SOME MOLECULAR CHAPERONES IN THE ASSEMBLY AND TRAFFICKING OF GPCRS.

Degree: MS, Department of Pharmacology, 2010, Dalhousie University

 Current drugs used to treat Congestive Heart Failure target the renin-angiotensin and adrenergic systems. Studies showed increased mortality rates in patients treated with a combination… (more)

Subjects/Keywords: G Protein Coupled Receptors; Congestive Heart Failure; Adrenergic Receptors; Angiotensin Receptors; Rab GTPases; Molecular Chaperones; Bimolecular Fluorescence Complementation; GPCRs Oligomerization

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APA (6th Edition):

Hammad, M. (2010). CHARACTERIZATION OF THE ANGIOTENSIN TYPE 1 RECEPTOR AND THE BETA2 ADRENERGIC RECEPTOR PROPERTIES: THE INVOLVEMENT OF ARRESTIN2, RAB1 AND SOME MOLECULAR CHAPERONES IN THE ASSEMBLY AND TRAFFICKING OF GPCRS. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/13068

Chicago Manual of Style (16th Edition):

Hammad, Maha. “CHARACTERIZATION OF THE ANGIOTENSIN TYPE 1 RECEPTOR AND THE BETA2 ADRENERGIC RECEPTOR PROPERTIES: THE INVOLVEMENT OF ARRESTIN2, RAB1 AND SOME MOLECULAR CHAPERONES IN THE ASSEMBLY AND TRAFFICKING OF GPCRS.” 2010. Masters Thesis, Dalhousie University. Accessed March 03, 2021. http://hdl.handle.net/10222/13068.

MLA Handbook (7th Edition):

Hammad, Maha. “CHARACTERIZATION OF THE ANGIOTENSIN TYPE 1 RECEPTOR AND THE BETA2 ADRENERGIC RECEPTOR PROPERTIES: THE INVOLVEMENT OF ARRESTIN2, RAB1 AND SOME MOLECULAR CHAPERONES IN THE ASSEMBLY AND TRAFFICKING OF GPCRS.” 2010. Web. 03 Mar 2021.

Vancouver:

Hammad M. CHARACTERIZATION OF THE ANGIOTENSIN TYPE 1 RECEPTOR AND THE BETA2 ADRENERGIC RECEPTOR PROPERTIES: THE INVOLVEMENT OF ARRESTIN2, RAB1 AND SOME MOLECULAR CHAPERONES IN THE ASSEMBLY AND TRAFFICKING OF GPCRS. [Internet] [Masters thesis]. Dalhousie University; 2010. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/10222/13068.

Council of Science Editors:

Hammad M. CHARACTERIZATION OF THE ANGIOTENSIN TYPE 1 RECEPTOR AND THE BETA2 ADRENERGIC RECEPTOR PROPERTIES: THE INVOLVEMENT OF ARRESTIN2, RAB1 AND SOME MOLECULAR CHAPERONES IN THE ASSEMBLY AND TRAFFICKING OF GPCRS. [Masters Thesis]. Dalhousie University; 2010. Available from: http://hdl.handle.net/10222/13068


Dalhousie University

9. Slusar, Joanna. Examination of the Neuroprotective Effects of URB597 in Young and Aged Rat Retina.

Degree: MS, Department of Pharmacology with Neuroscience, 2010, Dalhousie University

 Anandamide (AEA), a well characterized endocannabinoid that has actions at multiple targets in the eye, may have potential as a novel therapeutic in the treatment… (more)

Subjects/Keywords: aging; endocannabinoids; retinal vasculature; optic nerve injury; neuroprotection; ischemia

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APA (6th Edition):

Slusar, J. (2010). Examination of the Neuroprotective Effects of URB597 in Young and Aged Rat Retina. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/13126

Chicago Manual of Style (16th Edition):

Slusar, Joanna. “Examination of the Neuroprotective Effects of URB597 in Young and Aged Rat Retina.” 2010. Masters Thesis, Dalhousie University. Accessed March 03, 2021. http://hdl.handle.net/10222/13126.

MLA Handbook (7th Edition):

Slusar, Joanna. “Examination of the Neuroprotective Effects of URB597 in Young and Aged Rat Retina.” 2010. Web. 03 Mar 2021.

Vancouver:

Slusar J. Examination of the Neuroprotective Effects of URB597 in Young and Aged Rat Retina. [Internet] [Masters thesis]. Dalhousie University; 2010. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/10222/13126.

Council of Science Editors:

Slusar J. Examination of the Neuroprotective Effects of URB597 in Young and Aged Rat Retina. [Masters Thesis]. Dalhousie University; 2010. Available from: http://hdl.handle.net/10222/13126


Dalhousie University

10. Roy, Jeremy. THE CONTRIBUTION OF K+ ION CHANNELS AND THE Ca2+-PERMEABLE TRPM8 CHANNEL TO BREAST CANCER CELL PROLIFERATION.

Degree: PhD, Department of Physiology & Biophysics, 2010, Dalhousie University

 Breast cancer is the most prevalent cancer type among Canadian women. Breast cancers originate from the malignant transformation of mammary epithelial cells, which causes them… (more)

Subjects/Keywords: Cancer; Ion channels; Breast Cancer; Potassium Channels; Calcium Channels; Cell Proliferation; TRPM8

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APA (6th Edition):

Roy, J. (2010). THE CONTRIBUTION OF K+ ION CHANNELS AND THE Ca2+-PERMEABLE TRPM8 CHANNEL TO BREAST CANCER CELL PROLIFERATION. (Doctoral Dissertation). Dalhousie University. Retrieved from http://hdl.handle.net/10222/13118

Chicago Manual of Style (16th Edition):

Roy, Jeremy. “THE CONTRIBUTION OF K+ ION CHANNELS AND THE Ca2+-PERMEABLE TRPM8 CHANNEL TO BREAST CANCER CELL PROLIFERATION.” 2010. Doctoral Dissertation, Dalhousie University. Accessed March 03, 2021. http://hdl.handle.net/10222/13118.

MLA Handbook (7th Edition):

Roy, Jeremy. “THE CONTRIBUTION OF K+ ION CHANNELS AND THE Ca2+-PERMEABLE TRPM8 CHANNEL TO BREAST CANCER CELL PROLIFERATION.” 2010. Web. 03 Mar 2021.

Vancouver:

Roy J. THE CONTRIBUTION OF K+ ION CHANNELS AND THE Ca2+-PERMEABLE TRPM8 CHANNEL TO BREAST CANCER CELL PROLIFERATION. [Internet] [Doctoral dissertation]. Dalhousie University; 2010. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/10222/13118.

Council of Science Editors:

Roy J. THE CONTRIBUTION OF K+ ION CHANNELS AND THE Ca2+-PERMEABLE TRPM8 CHANNEL TO BREAST CANCER CELL PROLIFERATION. [Doctoral Dissertation]. Dalhousie University; 2010. Available from: http://hdl.handle.net/10222/13118


Dalhousie University

11. O'Brien, Michael. CHARACTERIZATION OF A NOVEL ISOFORM OF NOS1AP: NOS1APc.

Degree: MS, Department of Pharmacology, 2012, Dalhousie University

 The current study characterizes a novel isoform of the Nitric Oxide Synthase 1 Adaptor Protein (NOS1AP), herein NOS1APc. NOS1APc was identified in a proteomic screen… (more)

Subjects/Keywords: NOS1AP; NOS1APc; Scribble; cerebellum; cell cycle

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APA (6th Edition):

O'Brien, M. (2012). CHARACTERIZATION OF A NOVEL ISOFORM OF NOS1AP: NOS1APc. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/15490

Chicago Manual of Style (16th Edition):

O'Brien, Michael. “CHARACTERIZATION OF A NOVEL ISOFORM OF NOS1AP: NOS1APc.” 2012. Masters Thesis, Dalhousie University. Accessed March 03, 2021. http://hdl.handle.net/10222/15490.

MLA Handbook (7th Edition):

O'Brien, Michael. “CHARACTERIZATION OF A NOVEL ISOFORM OF NOS1AP: NOS1APc.” 2012. Web. 03 Mar 2021.

Vancouver:

O'Brien M. CHARACTERIZATION OF A NOVEL ISOFORM OF NOS1AP: NOS1APc. [Internet] [Masters thesis]. Dalhousie University; 2012. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/10222/15490.

Council of Science Editors:

O'Brien M. CHARACTERIZATION OF A NOVEL ISOFORM OF NOS1AP: NOS1APc. [Masters Thesis]. Dalhousie University; 2012. Available from: http://hdl.handle.net/10222/15490


Dalhousie University

12. Charette, Nicholle Jeanine. INVOLVEMENT OF DIFFERENT RAB GTPASES IN THE TRAFFICKING OF CXCR4 AND CCR5 HOMO- AND HETERODIMERS BETWEEN THE ENDOPLASMIC RETICULUM AND PLASMA MEMBRANE IN HEK293 AND JURKAT CELLS.

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

 Little is known about the outward trafficking of receptor dimers from the endoplasmic reticulum to the plasma membrane, or the role that trafficking plays in… (more)

Subjects/Keywords: G protein coupled receptor; CXCR4; CCR5; Rab GTPase; Trafficking; Dimerization

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APA (6th Edition):

Charette, N. J. (2011). INVOLVEMENT OF DIFFERENT RAB GTPASES IN THE TRAFFICKING OF CXCR4 AND CCR5 HOMO- AND HETERODIMERS BETWEEN THE ENDOPLASMIC RETICULUM AND PLASMA MEMBRANE IN HEK293 AND JURKAT CELLS. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/14023

Chicago Manual of Style (16th Edition):

Charette, Nicholle Jeanine. “INVOLVEMENT OF DIFFERENT RAB GTPASES IN THE TRAFFICKING OF CXCR4 AND CCR5 HOMO- AND HETERODIMERS BETWEEN THE ENDOPLASMIC RETICULUM AND PLASMA MEMBRANE IN HEK293 AND JURKAT CELLS.” 2011. Masters Thesis, Dalhousie University. Accessed March 03, 2021. http://hdl.handle.net/10222/14023.

MLA Handbook (7th Edition):

Charette, Nicholle Jeanine. “INVOLVEMENT OF DIFFERENT RAB GTPASES IN THE TRAFFICKING OF CXCR4 AND CCR5 HOMO- AND HETERODIMERS BETWEEN THE ENDOPLASMIC RETICULUM AND PLASMA MEMBRANE IN HEK293 AND JURKAT CELLS.” 2011. Web. 03 Mar 2021.

Vancouver:

Charette NJ. INVOLVEMENT OF DIFFERENT RAB GTPASES IN THE TRAFFICKING OF CXCR4 AND CCR5 HOMO- AND HETERODIMERS BETWEEN THE ENDOPLASMIC RETICULUM AND PLASMA MEMBRANE IN HEK293 AND JURKAT CELLS. [Internet] [Masters thesis]. Dalhousie University; 2011. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/10222/14023.

Council of Science Editors:

Charette NJ. INVOLVEMENT OF DIFFERENT RAB GTPASES IN THE TRAFFICKING OF CXCR4 AND CCR5 HOMO- AND HETERODIMERS BETWEEN THE ENDOPLASMIC RETICULUM AND PLASMA MEMBRANE IN HEK293 AND JURKAT CELLS. [Masters Thesis]. Dalhousie University; 2011. Available from: http://hdl.handle.net/10222/14023


Dalhousie University

13. Jones, Quinton RD. THE EFFECT OF INSULIN ON STRESS-RESPONSE PATHWAYS IN A CELLULAR MODEL OF RAT CARDIOMYOCYTES.

Degree: MS, Department of Anatomy & Neurobiolgy with Neuroscience, 2011, Dalhousie University

Insulin was used on a model on H9c2 myotubes to determine the effect of oxygen-glucose deprivation and reoxygenation on the localization and phosphorylation of Hsp27… (more)

Subjects/Keywords: insulin h9c2 cardiomyocytes OGD anoxia ischemia hsp27 p38 mapk

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APA (6th Edition):

Jones, Q. R. (2011). THE EFFECT OF INSULIN ON STRESS-RESPONSE PATHWAYS IN A CELLULAR MODEL OF RAT CARDIOMYOCYTES. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/14058

Chicago Manual of Style (16th Edition):

Jones, Quinton RD. “THE EFFECT OF INSULIN ON STRESS-RESPONSE PATHWAYS IN A CELLULAR MODEL OF RAT CARDIOMYOCYTES.” 2011. Masters Thesis, Dalhousie University. Accessed March 03, 2021. http://hdl.handle.net/10222/14058.

MLA Handbook (7th Edition):

Jones, Quinton RD. “THE EFFECT OF INSULIN ON STRESS-RESPONSE PATHWAYS IN A CELLULAR MODEL OF RAT CARDIOMYOCYTES.” 2011. Web. 03 Mar 2021.

Vancouver:

Jones QR. THE EFFECT OF INSULIN ON STRESS-RESPONSE PATHWAYS IN A CELLULAR MODEL OF RAT CARDIOMYOCYTES. [Internet] [Masters thesis]. Dalhousie University; 2011. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/10222/14058.

Council of Science Editors:

Jones QR. THE EFFECT OF INSULIN ON STRESS-RESPONSE PATHWAYS IN A CELLULAR MODEL OF RAT CARDIOMYOCYTES. [Masters Thesis]. Dalhousie University; 2011. Available from: http://hdl.handle.net/10222/14058


Dalhousie University

14. Tweel, Kristin. Competing Influences Of The Tumor Microenvironment On CD26 And The Cancer Phenotype Of Colorectal Carcinoma Cells.

Degree: PhD, Department of Pharmacology, 2013, Dalhousie University

 In Canada, colorectal cancer is the second leading cause of cancer death for both men and women. There are many different factors that contribute to… (more)

Subjects/Keywords: Colorectal Cancer; Metastasis; CD26; Adenosine; MMP-13; CXCL12; Tumor Microenvironment

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APA (6th Edition):

Tweel, K. (2013). Competing Influences Of The Tumor Microenvironment On CD26 And The Cancer Phenotype Of Colorectal Carcinoma Cells. (Doctoral Dissertation). Dalhousie University. Retrieved from http://hdl.handle.net/10222/21904

Chicago Manual of Style (16th Edition):

Tweel, Kristin. “Competing Influences Of The Tumor Microenvironment On CD26 And The Cancer Phenotype Of Colorectal Carcinoma Cells.” 2013. Doctoral Dissertation, Dalhousie University. Accessed March 03, 2021. http://hdl.handle.net/10222/21904.

MLA Handbook (7th Edition):

Tweel, Kristin. “Competing Influences Of The Tumor Microenvironment On CD26 And The Cancer Phenotype Of Colorectal Carcinoma Cells.” 2013. Web. 03 Mar 2021.

Vancouver:

Tweel K. Competing Influences Of The Tumor Microenvironment On CD26 And The Cancer Phenotype Of Colorectal Carcinoma Cells. [Internet] [Doctoral dissertation]. Dalhousie University; 2013. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/10222/21904.

Council of Science Editors:

Tweel K. Competing Influences Of The Tumor Microenvironment On CD26 And The Cancer Phenotype Of Colorectal Carcinoma Cells. [Doctoral Dissertation]. Dalhousie University; 2013. Available from: http://hdl.handle.net/10222/21904


Dalhousie University

15. Liu, Jean. Further Studies in Adenosinergic and Monoaminergic Mechanisms of Analgesia by Amitriptyline.

Degree: MS, Department of Pharmacology with Neuroscience, 2012, Dalhousie University

 In this thesis, rodent models of chronic pain were used to explore analgesic mechanisms that may potentially be engaged in spinal and peripheral compartments by… (more)

Subjects/Keywords: amitriptyline; persistent post-surgical pain; adenosine A1 receptor; serotonin 5-HT7 receptor; formalin test; antinociception; spared nerve injury; preventive analgesia; antidepressants; pain

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APA (6th Edition):

Liu, J. (2012). Further Studies in Adenosinergic and Monoaminergic Mechanisms of Analgesia by Amitriptyline. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/15329

Chicago Manual of Style (16th Edition):

Liu, Jean. “Further Studies in Adenosinergic and Monoaminergic Mechanisms of Analgesia by Amitriptyline.” 2012. Masters Thesis, Dalhousie University. Accessed March 03, 2021. http://hdl.handle.net/10222/15329.

MLA Handbook (7th Edition):

Liu, Jean. “Further Studies in Adenosinergic and Monoaminergic Mechanisms of Analgesia by Amitriptyline.” 2012. Web. 03 Mar 2021.

Vancouver:

Liu J. Further Studies in Adenosinergic and Monoaminergic Mechanisms of Analgesia by Amitriptyline. [Internet] [Masters thesis]. Dalhousie University; 2012. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/10222/15329.

Council of Science Editors:

Liu J. Further Studies in Adenosinergic and Monoaminergic Mechanisms of Analgesia by Amitriptyline. [Masters Thesis]. Dalhousie University; 2012. Available from: http://hdl.handle.net/10222/15329

16. Dunlop, Kate Elizabeth. Neuroprotective Effects of a Novel Apple Peel Extract AF4 in a Mouse Model of Hypoxic-Ischemic Brain Injury.

Degree: MS, Department of Pharmacology, 2012, Dalhousie University

 The neuroprotective effects of AF4, a flavonoid-enriched extract derived from the peel of Northern Spy apples (containing quercetin-3-O-glucoside, quercetin-3-O-galactoside, quercetin-3-O-rhamnoside, quercetin-3-O-rutinoside, epicatechin, and cyanidin-3-O-galactoside) were… (more)

Subjects/Keywords: Flavonoids; Stroke; Cytoprotective; Anti-inflammatory; Anti-oxidative

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APA (6th Edition):

Dunlop, K. E. (2012). Neuroprotective Effects of a Novel Apple Peel Extract AF4 in a Mouse Model of Hypoxic-Ischemic Brain Injury. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/15722

Chicago Manual of Style (16th Edition):

Dunlop, Kate Elizabeth. “Neuroprotective Effects of a Novel Apple Peel Extract AF4 in a Mouse Model of Hypoxic-Ischemic Brain Injury.” 2012. Masters Thesis, Dalhousie University. Accessed March 03, 2021. http://hdl.handle.net/10222/15722.

MLA Handbook (7th Edition):

Dunlop, Kate Elizabeth. “Neuroprotective Effects of a Novel Apple Peel Extract AF4 in a Mouse Model of Hypoxic-Ischemic Brain Injury.” 2012. Web. 03 Mar 2021.

Vancouver:

Dunlop KE. Neuroprotective Effects of a Novel Apple Peel Extract AF4 in a Mouse Model of Hypoxic-Ischemic Brain Injury. [Internet] [Masters thesis]. Dalhousie University; 2012. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/10222/15722.

Council of Science Editors:

Dunlop KE. Neuroprotective Effects of a Novel Apple Peel Extract AF4 in a Mouse Model of Hypoxic-Ischemic Brain Injury. [Masters Thesis]. Dalhousie University; 2012. Available from: http://hdl.handle.net/10222/15722

17. Fares, Elias. The Impact of Aging and Ovariectomy on Cardiac Contractile Function in Isolated Ventricular Myocytes.

Degree: PhD, Department of Pharmacology, 2012, Dalhousie University

 Previous studies have shown that cardiac contractile function declines with age in ventricular myocytes from 24 month old males but not females. As estrogen modulates… (more)

Subjects/Keywords: Subject Not Available

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APA (6th Edition):

Fares, E. (2012). The Impact of Aging and Ovariectomy on Cardiac Contractile Function in Isolated Ventricular Myocytes. (Doctoral Dissertation). Dalhousie University. Retrieved from http://hdl.handle.net/10222/15388

Chicago Manual of Style (16th Edition):

Fares, Elias. “The Impact of Aging and Ovariectomy on Cardiac Contractile Function in Isolated Ventricular Myocytes.” 2012. Doctoral Dissertation, Dalhousie University. Accessed March 03, 2021. http://hdl.handle.net/10222/15388.

MLA Handbook (7th Edition):

Fares, Elias. “The Impact of Aging and Ovariectomy on Cardiac Contractile Function in Isolated Ventricular Myocytes.” 2012. Web. 03 Mar 2021.

Vancouver:

Fares E. The Impact of Aging and Ovariectomy on Cardiac Contractile Function in Isolated Ventricular Myocytes. [Internet] [Doctoral dissertation]. Dalhousie University; 2012. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/10222/15388.

Council of Science Editors:

Fares E. The Impact of Aging and Ovariectomy on Cardiac Contractile Function in Isolated Ventricular Myocytes. [Doctoral Dissertation]. Dalhousie University; 2012. Available from: http://hdl.handle.net/10222/15388

18. Hogel, Matthew. INVESTIGATING THE MECHANISM OF PROMOTER-SPECIFIC N-TERMINAL MUTANT HUNTINGTIN-MEDIATED TRANSCRIPTIONAL DYSREGULATION.

Degree: PhD, Department of Pharmacology with Neuroscience, 2012, Dalhousie University

 Huntington’s disease (HD) is a neurodegenerative disorder caused by the inheritance of one mutant copy of the huntingtin gene. Mutant huntingtin protein (mHtt) contains an… (more)

Subjects/Keywords: Huntington's; Transcription; Repression; Huntingtin; Polyglutamine; Transcriptional Dysregulation; in vitro transcription; N548; ST14A; Dual-luciferase assay; Chromatin Immunoprecipitation; Promoter Deletion; Linker Scanning Mutagenesis; Quantitative PCR; Promoter binding assay; TBP; RAP30

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

APA (6th Edition):

Hogel, M. (2012). INVESTIGATING THE MECHANISM OF PROMOTER-SPECIFIC N-TERMINAL MUTANT HUNTINGTIN-MEDIATED TRANSCRIPTIONAL DYSREGULATION. (Doctoral Dissertation). Dalhousie University. Retrieved from http://hdl.handle.net/10222/15723

Chicago Manual of Style (16th Edition):

Hogel, Matthew. “INVESTIGATING THE MECHANISM OF PROMOTER-SPECIFIC N-TERMINAL MUTANT HUNTINGTIN-MEDIATED TRANSCRIPTIONAL DYSREGULATION.” 2012. Doctoral Dissertation, Dalhousie University. Accessed March 03, 2021. http://hdl.handle.net/10222/15723.

MLA Handbook (7th Edition):

Hogel, Matthew. “INVESTIGATING THE MECHANISM OF PROMOTER-SPECIFIC N-TERMINAL MUTANT HUNTINGTIN-MEDIATED TRANSCRIPTIONAL DYSREGULATION.” 2012. Web. 03 Mar 2021.

Vancouver:

Hogel M. INVESTIGATING THE MECHANISM OF PROMOTER-SPECIFIC N-TERMINAL MUTANT HUNTINGTIN-MEDIATED TRANSCRIPTIONAL DYSREGULATION. [Internet] [Doctoral dissertation]. Dalhousie University; 2012. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/10222/15723.

Council of Science Editors:

Hogel M. INVESTIGATING THE MECHANISM OF PROMOTER-SPECIFIC N-TERMINAL MUTANT HUNTINGTIN-MEDIATED TRANSCRIPTIONAL DYSREGULATION. [Doctoral Dissertation]. Dalhousie University; 2012. Available from: http://hdl.handle.net/10222/15723

19. Thirumaran, Aruloli. THE FATTY ACID-BINDING PROTEIN (fabp) GENES OF SPOTTED GREEN PUFFERFISH (TETRAODON NIGROVIRIDIS) - COMPARATIVE STRUCTURAL GENOMICS AND TISSUE-SPECIFIC DISTRIBUTION OF THEIR TRANSCRIPTS.

Degree: MS, Department of Biology, 2013, Dalhousie University

 The fatty acid-binding protein (fabp) genes belong to the multigene family of intracellular lipid-binding proteins (iLBP). To date, 12 different FABPs have been identified in… (more)

Subjects/Keywords: Spotted green pufferfish; Tetraodon; Fatty acid-binding protein genes; structural genomics

…throughout this study. I would like to extend my heartfelt thanks to Dr. Eileen Denovan-Wright, for… …financial support from NSERC and Dalhousie University, without which none of this work would have… …conditions and experimental protocols were reviewed by the Animal Care Committee of Dalhousie… …University, in accordance with the recommendations of Canadian Council on Animal Care. 8 2.3… 

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APA (6th Edition):

Thirumaran, A. (2013). THE FATTY ACID-BINDING PROTEIN (fabp) GENES OF SPOTTED GREEN PUFFERFISH (TETRAODON NIGROVIRIDIS) - COMPARATIVE STRUCTURAL GENOMICS AND TISSUE-SPECIFIC DISTRIBUTION OF THEIR TRANSCRIPTS. (Masters Thesis). Dalhousie University. Retrieved from http://hdl.handle.net/10222/40663

Chicago Manual of Style (16th Edition):

Thirumaran, Aruloli. “THE FATTY ACID-BINDING PROTEIN (fabp) GENES OF SPOTTED GREEN PUFFERFISH (TETRAODON NIGROVIRIDIS) - COMPARATIVE STRUCTURAL GENOMICS AND TISSUE-SPECIFIC DISTRIBUTION OF THEIR TRANSCRIPTS.” 2013. Masters Thesis, Dalhousie University. Accessed March 03, 2021. http://hdl.handle.net/10222/40663.

MLA Handbook (7th Edition):

Thirumaran, Aruloli. “THE FATTY ACID-BINDING PROTEIN (fabp) GENES OF SPOTTED GREEN PUFFERFISH (TETRAODON NIGROVIRIDIS) - COMPARATIVE STRUCTURAL GENOMICS AND TISSUE-SPECIFIC DISTRIBUTION OF THEIR TRANSCRIPTS.” 2013. Web. 03 Mar 2021.

Vancouver:

Thirumaran A. THE FATTY ACID-BINDING PROTEIN (fabp) GENES OF SPOTTED GREEN PUFFERFISH (TETRAODON NIGROVIRIDIS) - COMPARATIVE STRUCTURAL GENOMICS AND TISSUE-SPECIFIC DISTRIBUTION OF THEIR TRANSCRIPTS. [Internet] [Masters thesis]. Dalhousie University; 2013. [cited 2021 Mar 03]. Available from: http://hdl.handle.net/10222/40663.

Council of Science Editors:

Thirumaran A. THE FATTY ACID-BINDING PROTEIN (fabp) GENES OF SPOTTED GREEN PUFFERFISH (TETRAODON NIGROVIRIDIS) - COMPARATIVE STRUCTURAL GENOMICS AND TISSUE-SPECIFIC DISTRIBUTION OF THEIR TRANSCRIPTS. [Masters Thesis]. Dalhousie University; 2013. Available from: http://hdl.handle.net/10222/40663

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