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You searched for subject:(protein kinase A). Showing records 1 – 30 of 120 total matches.

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University of Vermont

1. Todero, Jenna E. Establishing an Ovarian Cancer cell culture model system in order to study the molecular interaction between Src Family Kinases and Protein Kinase A.

Degree: Biology, 2016, University of Vermont

  Abstract: Protein kinase A (PKA) is a cyclic-AMP (cAMP) dependent kinase and is known to regulate many processes, specifically proliferation and migration. PKA activity… (more)

Subjects/Keywords: Protein Kinase A; PKA; src; phosphorylation

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

APA (6th Edition):

Todero, J. E. (2016). Establishing an Ovarian Cancer cell culture model system in order to study the molecular interaction between Src Family Kinases and Protein Kinase A. (Thesis). University of Vermont. Retrieved from https://scholarworks.uvm.edu/hcoltheses/210

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):

Todero, Jenna E. “Establishing an Ovarian Cancer cell culture model system in order to study the molecular interaction between Src Family Kinases and Protein Kinase A.” 2016. Thesis, University of Vermont. Accessed November 26, 2020. https://scholarworks.uvm.edu/hcoltheses/210.

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

MLA Handbook (7th Edition):

Todero, Jenna E. “Establishing an Ovarian Cancer cell culture model system in order to study the molecular interaction between Src Family Kinases and Protein Kinase A.” 2016. Web. 26 Nov 2020.

Vancouver:

Todero JE. Establishing an Ovarian Cancer cell culture model system in order to study the molecular interaction between Src Family Kinases and Protein Kinase A. [Internet] [Thesis]. University of Vermont; 2016. [cited 2020 Nov 26]. Available from: https://scholarworks.uvm.edu/hcoltheses/210.

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

Council of Science Editors:

Todero JE. Establishing an Ovarian Cancer cell culture model system in order to study the molecular interaction between Src Family Kinases and Protein Kinase A. [Thesis]. University of Vermont; 2016. Available from: https://scholarworks.uvm.edu/hcoltheses/210

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


University of Toronto

2. Hakem Zadeh, Farigol. Investigating the interaction of AKAPs with PLN to mediate phosphorylation processes.

Degree: 2018, University of Toronto

A common characteristic of cardiomyopathy is dysregulated Ca2+-cycling. During Ca2+-cycling, Sarco(endo)plasmic reticulum Ca2+-ATPase (SERCA) reuptakes Ca2+ into the sarcoplasmic reticulum (SR). SERCA is inhibited by… (more)

Subjects/Keywords: A-kinase associated protein (AKAP); cardiomyocyte; cardiomyopathy; heart; phospholamban (PLN); protein kinase A (PKA); 0719

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APA (6th Edition):

Hakem Zadeh, F. (2018). Investigating the interaction of AKAPs with PLN to mediate phosphorylation processes. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/94119

Chicago Manual of Style (16th Edition):

Hakem Zadeh, Farigol. “Investigating the interaction of AKAPs with PLN to mediate phosphorylation processes.” 2018. Masters Thesis, University of Toronto. Accessed November 26, 2020. http://hdl.handle.net/1807/94119.

MLA Handbook (7th Edition):

Hakem Zadeh, Farigol. “Investigating the interaction of AKAPs with PLN to mediate phosphorylation processes.” 2018. Web. 26 Nov 2020.

Vancouver:

Hakem Zadeh F. Investigating the interaction of AKAPs with PLN to mediate phosphorylation processes. [Internet] [Masters thesis]. University of Toronto; 2018. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1807/94119.

Council of Science Editors:

Hakem Zadeh F. Investigating the interaction of AKAPs with PLN to mediate phosphorylation processes. [Masters Thesis]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/94119


University of Western Ontario

3. King, Cason R. Functional and Structural Mimicry of A-Kinase Anchoring Proteins by Human Adenovirus E1A.

Degree: 2018, University of Western Ontario

 As an obligate intracellular parasite, human adenovirus (HAdV) must utilize host factors for survival and replication. Early during infection, its multifunctional E1A protein interacts with… (more)

Subjects/Keywords: Human adenovirus; E1A; Protein kinase A; A-kinase anchoring protein; Viral mimicry; Protein-protein interaction; Molecular Biology; Virology; Viruses

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APA (6th Edition):

King, C. R. (2018). Functional and Structural Mimicry of A-Kinase Anchoring Proteins by Human Adenovirus E1A. (Thesis). University of Western Ontario. Retrieved from https://ir.lib.uwo.ca/etd/5286

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):

King, Cason R. “Functional and Structural Mimicry of A-Kinase Anchoring Proteins by Human Adenovirus E1A.” 2018. Thesis, University of Western Ontario. Accessed November 26, 2020. https://ir.lib.uwo.ca/etd/5286.

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

MLA Handbook (7th Edition):

King, Cason R. “Functional and Structural Mimicry of A-Kinase Anchoring Proteins by Human Adenovirus E1A.” 2018. Web. 26 Nov 2020.

Vancouver:

King CR. Functional and Structural Mimicry of A-Kinase Anchoring Proteins by Human Adenovirus E1A. [Internet] [Thesis]. University of Western Ontario; 2018. [cited 2020 Nov 26]. Available from: https://ir.lib.uwo.ca/etd/5286.

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

Council of Science Editors:

King CR. Functional and Structural Mimicry of A-Kinase Anchoring Proteins by Human Adenovirus E1A. [Thesis]. University of Western Ontario; 2018. Available from: https://ir.lib.uwo.ca/etd/5286

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


University of Vermont

4. Linden, Anne K. PACAP-induced ERK phosphorylation in VPAC1 and VPAC2-expressing HEK cells is mediated by receptor endocytosis and PKC signaling.

Degree: Neuroscience, 2017, University of Vermont

  Pituitary adenylate-cyclase activating polypeptide (PACAP) is highly conserved signaling molecule in eukaryotes known to regulate a myriad of metabolic processes within the brain as… (more)

Subjects/Keywords: PACAP; VPAC receptors; Extracellular signal-dependent kinase (ERK); Receptor endocytosis; Protein Kinase A (PKA); Protein Kinase C (PKC)

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APA (6th Edition):

Linden, A. K. (2017). PACAP-induced ERK phosphorylation in VPAC1 and VPAC2-expressing HEK cells is mediated by receptor endocytosis and PKC signaling. (Thesis). University of Vermont. Retrieved from https://scholarworks.uvm.edu/castheses/45

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):

Linden, Anne K. “PACAP-induced ERK phosphorylation in VPAC1 and VPAC2-expressing HEK cells is mediated by receptor endocytosis and PKC signaling.” 2017. Thesis, University of Vermont. Accessed November 26, 2020. https://scholarworks.uvm.edu/castheses/45.

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

MLA Handbook (7th Edition):

Linden, Anne K. “PACAP-induced ERK phosphorylation in VPAC1 and VPAC2-expressing HEK cells is mediated by receptor endocytosis and PKC signaling.” 2017. Web. 26 Nov 2020.

Vancouver:

Linden AK. PACAP-induced ERK phosphorylation in VPAC1 and VPAC2-expressing HEK cells is mediated by receptor endocytosis and PKC signaling. [Internet] [Thesis]. University of Vermont; 2017. [cited 2020 Nov 26]. Available from: https://scholarworks.uvm.edu/castheses/45.

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

Council of Science Editors:

Linden AK. PACAP-induced ERK phosphorylation in VPAC1 and VPAC2-expressing HEK cells is mediated by receptor endocytosis and PKC signaling. [Thesis]. University of Vermont; 2017. Available from: https://scholarworks.uvm.edu/castheses/45

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


University of Washington

5. Whiting, Jennifer Lee. The AKAP220 signaling complex regulates renal aquaporin-2 localization.

Degree: PhD, 2015, University of Washington

 A kinase anchoring proteins (AKAPs) localize signaling molecules such as kinases and phosphatases in close proximity to their substrates to control the scope and duration… (more)

Subjects/Keywords: A kinase anchoring protein; aquaporin-2; diabetes insipidus; protein kinase A; signaling scaffold; signal transduction; Molecular biology; Cellular biology; Biochemistry; pharmacology

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APA (6th Edition):

Whiting, J. L. (2015). The AKAP220 signaling complex regulates renal aquaporin-2 localization. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/34119

Chicago Manual of Style (16th Edition):

Whiting, Jennifer Lee. “The AKAP220 signaling complex regulates renal aquaporin-2 localization.” 2015. Doctoral Dissertation, University of Washington. Accessed November 26, 2020. http://hdl.handle.net/1773/34119.

MLA Handbook (7th Edition):

Whiting, Jennifer Lee. “The AKAP220 signaling complex regulates renal aquaporin-2 localization.” 2015. Web. 26 Nov 2020.

Vancouver:

Whiting JL. The AKAP220 signaling complex regulates renal aquaporin-2 localization. [Internet] [Doctoral dissertation]. University of Washington; 2015. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1773/34119.

Council of Science Editors:

Whiting JL. The AKAP220 signaling complex regulates renal aquaporin-2 localization. [Doctoral Dissertation]. University of Washington; 2015. Available from: http://hdl.handle.net/1773/34119


University of Georgia

6. Wang, Yuxiao. Isoform-selective disruption of AKAP-mediated PKA localization using hydrocarbon stapled peptides.

Degree: 2015, University of Georgia

 A-kinase Anchoring Proteins (AKAPs) are key orchestrators that spatiotemporally regulate protein kinase A (PKA) activity by scaffolding pertinent intracellular proteins to form signaling complexes. Although… (more)

Subjects/Keywords: protein kinase A; A-kinase anchoring protein; all-hydrocarbon staple; peptide; fluorescence polarization; ring-closing metathesis

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APA (6th Edition):

Wang, Y. (2015). Isoform-selective disruption of AKAP-mediated PKA localization using hydrocarbon stapled peptides. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/31335

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):

Wang, Yuxiao. “Isoform-selective disruption of AKAP-mediated PKA localization using hydrocarbon stapled peptides.” 2015. Thesis, University of Georgia. Accessed November 26, 2020. http://hdl.handle.net/10724/31335.

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

MLA Handbook (7th Edition):

Wang, Yuxiao. “Isoform-selective disruption of AKAP-mediated PKA localization using hydrocarbon stapled peptides.” 2015. Web. 26 Nov 2020.

Vancouver:

Wang Y. Isoform-selective disruption of AKAP-mediated PKA localization using hydrocarbon stapled peptides. [Internet] [Thesis]. University of Georgia; 2015. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/10724/31335.

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

Council of Science Editors:

Wang Y. Isoform-selective disruption of AKAP-mediated PKA localization using hydrocarbon stapled peptides. [Thesis]. University of Georgia; 2015. Available from: http://hdl.handle.net/10724/31335

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


Purdue University

7. Li, Yang. Protein Kinase A Regulates Hyphal Growth by Relieving the Interaction of MoSfl1 with the Cyc8-Tup1 Co-repressor in Magnaporthe oryzae.

Degree: PhD, Botany and Plant Pathology, 2016, Purdue University

 The cAMP-dependent protein kinase A (PKA) signal transduction pathway plays an important role in morphogenesis and virulence in plant pathogenic fungi. In the rice blast… (more)

Subjects/Keywords: Cyc8-Tup1 co-repressor; Hyphal growth; MoSfl1; Protein Kinase A; protein-protein interaction; Repressor

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APA (6th Edition):

Li, Y. (2016). Protein Kinase A Regulates Hyphal Growth by Relieving the Interaction of MoSfl1 with the Cyc8-Tup1 Co-repressor in Magnaporthe oryzae. (Doctoral Dissertation). Purdue University. Retrieved from https://docs.lib.purdue.edu/open_access_dissertations/1256

Chicago Manual of Style (16th Edition):

Li, Yang. “Protein Kinase A Regulates Hyphal Growth by Relieving the Interaction of MoSfl1 with the Cyc8-Tup1 Co-repressor in Magnaporthe oryzae.” 2016. Doctoral Dissertation, Purdue University. Accessed November 26, 2020. https://docs.lib.purdue.edu/open_access_dissertations/1256.

MLA Handbook (7th Edition):

Li, Yang. “Protein Kinase A Regulates Hyphal Growth by Relieving the Interaction of MoSfl1 with the Cyc8-Tup1 Co-repressor in Magnaporthe oryzae.” 2016. Web. 26 Nov 2020.

Vancouver:

Li Y. Protein Kinase A Regulates Hyphal Growth by Relieving the Interaction of MoSfl1 with the Cyc8-Tup1 Co-repressor in Magnaporthe oryzae. [Internet] [Doctoral dissertation]. Purdue University; 2016. [cited 2020 Nov 26]. Available from: https://docs.lib.purdue.edu/open_access_dissertations/1256.

Council of Science Editors:

Li Y. Protein Kinase A Regulates Hyphal Growth by Relieving the Interaction of MoSfl1 with the Cyc8-Tup1 Co-repressor in Magnaporthe oryzae. [Doctoral Dissertation]. Purdue University; 2016. Available from: https://docs.lib.purdue.edu/open_access_dissertations/1256


University of Alberta

8. Hurd, Caitlin L. MODELING INCOMPLETE CERVICAL SPINAL CORD INJURY IN RATS TO EXPLORE MECHANISMS OF REHABILITATIVE TRAINING.

Degree: MS, Centre for Neuroscience, 2013, University of Alberta

 Although limited functional recovery is observed following spinal cord injury (SCI), the most successful approach to promote recovery to date has been rehabilitative training. However,… (more)

Subjects/Keywords: Rehabilitation; Protein Kinase A; Animal models; Spinal cord injury

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APA (6th Edition):

Hurd, C. L. (2013). MODELING INCOMPLETE CERVICAL SPINAL CORD INJURY IN RATS TO EXPLORE MECHANISMS OF REHABILITATIVE TRAINING. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/m326m2702

Chicago Manual of Style (16th Edition):

Hurd, Caitlin L. “MODELING INCOMPLETE CERVICAL SPINAL CORD INJURY IN RATS TO EXPLORE MECHANISMS OF REHABILITATIVE TRAINING.” 2013. Masters Thesis, University of Alberta. Accessed November 26, 2020. https://era.library.ualberta.ca/files/m326m2702.

MLA Handbook (7th Edition):

Hurd, Caitlin L. “MODELING INCOMPLETE CERVICAL SPINAL CORD INJURY IN RATS TO EXPLORE MECHANISMS OF REHABILITATIVE TRAINING.” 2013. Web. 26 Nov 2020.

Vancouver:

Hurd CL. MODELING INCOMPLETE CERVICAL SPINAL CORD INJURY IN RATS TO EXPLORE MECHANISMS OF REHABILITATIVE TRAINING. [Internet] [Masters thesis]. University of Alberta; 2013. [cited 2020 Nov 26]. Available from: https://era.library.ualberta.ca/files/m326m2702.

Council of Science Editors:

Hurd CL. MODELING INCOMPLETE CERVICAL SPINAL CORD INJURY IN RATS TO EXPLORE MECHANISMS OF REHABILITATIVE TRAINING. [Masters Thesis]. University of Alberta; 2013. Available from: https://era.library.ualberta.ca/files/m326m2702


University of Alberta

9. Ceholski, Delaine K. Molecular insights into the disease-causing mechanisms of human phospholamban mutations.

Degree: PhD, Department of Biochemistry, 2012, University of Alberta

 The movement of calcium across sarcoplasmic reticulum (SR) membranes is essential in the contraction-relaxation cycle of muscle. An influx of calcium into the muscle cell… (more)

Subjects/Keywords: phosphorylation by protein kinase A; hereditary mutations in phospholamban; SERCA dysregulation

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APA (6th Edition):

Ceholski, D. K. (2012). Molecular insights into the disease-causing mechanisms of human phospholamban mutations. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/fn1070088

Chicago Manual of Style (16th Edition):

Ceholski, Delaine K. “Molecular insights into the disease-causing mechanisms of human phospholamban mutations.” 2012. Doctoral Dissertation, University of Alberta. Accessed November 26, 2020. https://era.library.ualberta.ca/files/fn1070088.

MLA Handbook (7th Edition):

Ceholski, Delaine K. “Molecular insights into the disease-causing mechanisms of human phospholamban mutations.” 2012. Web. 26 Nov 2020.

Vancouver:

Ceholski DK. Molecular insights into the disease-causing mechanisms of human phospholamban mutations. [Internet] [Doctoral dissertation]. University of Alberta; 2012. [cited 2020 Nov 26]. Available from: https://era.library.ualberta.ca/files/fn1070088.

Council of Science Editors:

Ceholski DK. Molecular insights into the disease-causing mechanisms of human phospholamban mutations. [Doctoral Dissertation]. University of Alberta; 2012. Available from: https://era.library.ualberta.ca/files/fn1070088


University of Saskatchewan

10. Han, Jiayi. Regulation of acyl-CoA:diacylglycerol acyltransferase-1 by protein phosphorylation.

Degree: 2011, University of Saskatchewan

 Triacylglycerols are the predominant molecules of energy storage in eukaryotes. Triacylglycerol synthesis is catalyzed by acyl-CoA:diacylglycerol acyltransferase (DGAT) enzymes, DGAT1 and DGAT2. Although the use… (more)

Subjects/Keywords: phosphorylation; protein kinase A; mass spectrometry; triacylglycerols; acyl-CoA: diacylglycerol acyltransferase

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APA (6th Edition):

Han, J. (2011). Regulation of acyl-CoA:diacylglycerol acyltransferase-1 by protein phosphorylation. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/etd-06152011-123626

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):

Han, Jiayi. “Regulation of acyl-CoA:diacylglycerol acyltransferase-1 by protein phosphorylation.” 2011. Thesis, University of Saskatchewan. Accessed November 26, 2020. http://hdl.handle.net/10388/etd-06152011-123626.

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

MLA Handbook (7th Edition):

Han, Jiayi. “Regulation of acyl-CoA:diacylglycerol acyltransferase-1 by protein phosphorylation.” 2011. Web. 26 Nov 2020.

Vancouver:

Han J. Regulation of acyl-CoA:diacylglycerol acyltransferase-1 by protein phosphorylation. [Internet] [Thesis]. University of Saskatchewan; 2011. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/10388/etd-06152011-123626.

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

Council of Science Editors:

Han J. Regulation of acyl-CoA:diacylglycerol acyltransferase-1 by protein phosphorylation. [Thesis]. University of Saskatchewan; 2011. Available from: http://hdl.handle.net/10388/etd-06152011-123626

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


Universidade Nova

11. Estrada, Marta Maria Vieira Matutino Falcão. The role of gliptins on adipogenesis.

Degree: 2011, Universidade Nova

Dissertação elaborada com vista à obtenção do Grau de Mestre em Biotecnologia

This work was performed at the Neuroendocrinology and Neurogenesis Group at the Center… (more)

Subjects/Keywords: Dipeptidyl-peptidase IV; Gliptin; Neuropeptide Y; Adipocyte; Protein kinase A

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APA (6th Edition):

Estrada, M. M. V. M. F. (2011). The role of gliptins on adipogenesis. (Thesis). Universidade Nova. Retrieved from http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/10732

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):

Estrada, Marta Maria Vieira Matutino Falcão. “The role of gliptins on adipogenesis.” 2011. Thesis, Universidade Nova. Accessed November 26, 2020. http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/10732.

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

MLA Handbook (7th Edition):

Estrada, Marta Maria Vieira Matutino Falcão. “The role of gliptins on adipogenesis.” 2011. Web. 26 Nov 2020.

Vancouver:

Estrada MMVMF. The role of gliptins on adipogenesis. [Internet] [Thesis]. Universidade Nova; 2011. [cited 2020 Nov 26]. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/10732.

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

Council of Science Editors:

Estrada MMVMF. The role of gliptins on adipogenesis. [Thesis]. Universidade Nova; 2011. Available from: http://www.rcaap.pt/detail.jsp?id=oai:run.unl.pt:10362/10732

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


Universitat de Valencia

12. Baliño Remiro, Pablo. Role of intracellular calcium on ethanol-induced activation of protein kinase A: molecular model and behavioral consequences .

Degree: 2014, Universitat de Valencia

 Ethanol can be considered a weak drug when compared to most other drugs of abuse. The molecule of ethanol has no asymmetric carbon. Being so,… (more)

Subjects/Keywords: mice; calcium; protein kinase A; ethanol mechanism of action

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APA (6th Edition):

Baliño Remiro, P. (2014). Role of intracellular calcium on ethanol-induced activation of protein kinase A: molecular model and behavioral consequences . (Doctoral Dissertation). Universitat de Valencia. Retrieved from http://hdl.handle.net/10550/32973

Chicago Manual of Style (16th Edition):

Baliño Remiro, Pablo. “Role of intracellular calcium on ethanol-induced activation of protein kinase A: molecular model and behavioral consequences .” 2014. Doctoral Dissertation, Universitat de Valencia. Accessed November 26, 2020. http://hdl.handle.net/10550/32973.

MLA Handbook (7th Edition):

Baliño Remiro, Pablo. “Role of intracellular calcium on ethanol-induced activation of protein kinase A: molecular model and behavioral consequences .” 2014. Web. 26 Nov 2020.

Vancouver:

Baliño Remiro P. Role of intracellular calcium on ethanol-induced activation of protein kinase A: molecular model and behavioral consequences . [Internet] [Doctoral dissertation]. Universitat de Valencia; 2014. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/10550/32973.

Council of Science Editors:

Baliño Remiro P. Role of intracellular calcium on ethanol-induced activation of protein kinase A: molecular model and behavioral consequences . [Doctoral Dissertation]. Universitat de Valencia; 2014. Available from: http://hdl.handle.net/10550/32973

13. Rodier, Julie-Anne. Identification d'une forme phosphorylée de BDNF : un nouveau mécanisme de régulation de la plasticité synaptique et de la mémoire ? : Identification of a phosphorylated form of BDNF : a new mechanism for the regulation of synaptic plasticity and memory?.

Degree: Docteur es, Neurosciences neurobiologie, 2018, Université Grenoble Alpes (ComUE)

 Le facteur neurotrophique dérivé du cerveau (BDNF, Brain-Derived Neurotrophic Factor) est une protéine qui joue un rôle essentiel dans la survie et la différenciation des… (more)

Subjects/Keywords: Bdnf; Clivage; Phosphorylation; Protéine Kinase A; Ectokinases; Plasticité synaptique; Bdnf; Cleavage; Phosphorylation; Protein Kinase A; Ectokinases; Synaptic Plasticity; 570

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APA (6th Edition):

Rodier, J. (2018). Identification d'une forme phosphorylée de BDNF : un nouveau mécanisme de régulation de la plasticité synaptique et de la mémoire ? : Identification of a phosphorylated form of BDNF : a new mechanism for the regulation of synaptic plasticity and memory?. (Doctoral Dissertation). Université Grenoble Alpes (ComUE). Retrieved from http://www.theses.fr/2018GREAV015

Chicago Manual of Style (16th Edition):

Rodier, Julie-Anne. “Identification d'une forme phosphorylée de BDNF : un nouveau mécanisme de régulation de la plasticité synaptique et de la mémoire ? : Identification of a phosphorylated form of BDNF : a new mechanism for the regulation of synaptic plasticity and memory?.” 2018. Doctoral Dissertation, Université Grenoble Alpes (ComUE). Accessed November 26, 2020. http://www.theses.fr/2018GREAV015.

MLA Handbook (7th Edition):

Rodier, Julie-Anne. “Identification d'une forme phosphorylée de BDNF : un nouveau mécanisme de régulation de la plasticité synaptique et de la mémoire ? : Identification of a phosphorylated form of BDNF : a new mechanism for the regulation of synaptic plasticity and memory?.” 2018. Web. 26 Nov 2020.

Vancouver:

Rodier J. Identification d'une forme phosphorylée de BDNF : un nouveau mécanisme de régulation de la plasticité synaptique et de la mémoire ? : Identification of a phosphorylated form of BDNF : a new mechanism for the regulation of synaptic plasticity and memory?. [Internet] [Doctoral dissertation]. Université Grenoble Alpes (ComUE); 2018. [cited 2020 Nov 26]. Available from: http://www.theses.fr/2018GREAV015.

Council of Science Editors:

Rodier J. Identification d'une forme phosphorylée de BDNF : un nouveau mécanisme de régulation de la plasticité synaptique et de la mémoire ? : Identification of a phosphorylated form of BDNF : a new mechanism for the regulation of synaptic plasticity and memory?. [Doctoral Dissertation]. Université Grenoble Alpes (ComUE); 2018. Available from: http://www.theses.fr/2018GREAV015


Freie Universität Berlin

14. Skroblin, Philipp. GSKIP – ein neues A-Kinase-Ankerprotein, das PKA- und GSK3β-Signalwege integriert.

Degree: 2011, Freie Universität Berlin

 A-Kinase-Ankerproteine (AKAP) binden die cAMP-abhängige Proteinkinase A (PKA) durch direkte Proteininteraktion in spezifischen zellulären Kompartimenten. Dadurch wird die Phosphorylierung nahe gelegener Substrate ermöglicht. Außerdem interagieren… (more)

Subjects/Keywords: A-kinase anchoring protein (AKAP); cAMP-dependent protein kinase (PKA); glycogen synthase kinase 3β interaction protein (GSKIP); 500 Naturwissenschaften und Mathematik::570 Biowissenschaften; Biologie::572 Biochemie

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

APA (6th Edition):

Skroblin, P. (2011). GSKIP – ein neues A-Kinase-Ankerprotein, das PKA- und GSK3β-Signalwege integriert. (Thesis). Freie Universität Berlin. Retrieved from https://refubium.fu-berlin.de/handle/fub188/12794

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):

Skroblin, Philipp. “GSKIP – ein neues A-Kinase-Ankerprotein, das PKA- und GSK3β-Signalwege integriert.” 2011. Thesis, Freie Universität Berlin. Accessed November 26, 2020. https://refubium.fu-berlin.de/handle/fub188/12794.

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

MLA Handbook (7th Edition):

Skroblin, Philipp. “GSKIP – ein neues A-Kinase-Ankerprotein, das PKA- und GSK3β-Signalwege integriert.” 2011. Web. 26 Nov 2020.

Vancouver:

Skroblin P. GSKIP – ein neues A-Kinase-Ankerprotein, das PKA- und GSK3β-Signalwege integriert. [Internet] [Thesis]. Freie Universität Berlin; 2011. [cited 2020 Nov 26]. Available from: https://refubium.fu-berlin.de/handle/fub188/12794.

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

Council of Science Editors:

Skroblin P. GSKIP – ein neues A-Kinase-Ankerprotein, das PKA- und GSK3β-Signalwege integriert. [Thesis]. Freie Universität Berlin; 2011. Available from: https://refubium.fu-berlin.de/handle/fub188/12794

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


Tartu University

15. Kisseljova, Ksenija. Synthesis of aza-β3-amino acid containing peptides and kinetic study of their phosphorylation by protein kinase A .

Degree: 2012, Tartu University

 Paljud bioloogiliselt aktiivsed ained kuuluvad peptiidide klassi. Peptiidide kasutamist ravimitena segab aga nende kiire lagunemine elusorganismis seal leiduvate proteaaside toimel. Stabiilsuse suurendamiseks on võimalik keemiliselt… (more)

Subjects/Keywords: aminohapped; peptiidid; süntees; fosforüülimine; proteiinikinaas A; amino acids; peptides; synthesis; phosphorylation; protein kinase A

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APA (6th Edition):

Kisseljova, K. (2012). Synthesis of aza-β3-amino acid containing peptides and kinetic study of their phosphorylation by protein kinase A . (Thesis). Tartu University. Retrieved from http://hdl.handle.net/10062/25569

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):

Kisseljova, Ksenija. “Synthesis of aza-β3-amino acid containing peptides and kinetic study of their phosphorylation by protein kinase A .” 2012. Thesis, Tartu University. Accessed November 26, 2020. http://hdl.handle.net/10062/25569.

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

MLA Handbook (7th Edition):

Kisseljova, Ksenija. “Synthesis of aza-β3-amino acid containing peptides and kinetic study of their phosphorylation by protein kinase A .” 2012. Web. 26 Nov 2020.

Vancouver:

Kisseljova K. Synthesis of aza-β3-amino acid containing peptides and kinetic study of their phosphorylation by protein kinase A . [Internet] [Thesis]. Tartu University; 2012. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/10062/25569.

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

Council of Science Editors:

Kisseljova K. Synthesis of aza-β3-amino acid containing peptides and kinetic study of their phosphorylation by protein kinase A . [Thesis]. Tartu University; 2012. Available from: http://hdl.handle.net/10062/25569

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


University of Dundee

16. Ismail, Noor. Hormone-induced expression of the epithelial sodium channel in human airway cells.

Degree: PhD, 2013, University of Dundee

 Respiratory distress syndrome and pulmonary oedema often result in poor health and in the worst case scenario, death. Several studies have proposed that the eventual… (more)

Subjects/Keywords: 616.2; Epithelial Na+ Channel; SGK1; H441 cell line; Protein Kinase A; NEDD4-2; Ubiquitin; Glucocorticoid; PI3 kinase; TORC2

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APA (6th Edition):

Ismail, N. (2013). Hormone-induced expression of the epithelial sodium channel in human airway cells. (Doctoral Dissertation). University of Dundee. Retrieved from https://discovery.dundee.ac.uk/en/studentTheses/b0adffc7-eac8-49c4-b0ed-35cea636a3a9 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.578903

Chicago Manual of Style (16th Edition):

Ismail, Noor. “Hormone-induced expression of the epithelial sodium channel in human airway cells.” 2013. Doctoral Dissertation, University of Dundee. Accessed November 26, 2020. https://discovery.dundee.ac.uk/en/studentTheses/b0adffc7-eac8-49c4-b0ed-35cea636a3a9 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.578903.

MLA Handbook (7th Edition):

Ismail, Noor. “Hormone-induced expression of the epithelial sodium channel in human airway cells.” 2013. Web. 26 Nov 2020.

Vancouver:

Ismail N. Hormone-induced expression of the epithelial sodium channel in human airway cells. [Internet] [Doctoral dissertation]. University of Dundee; 2013. [cited 2020 Nov 26]. Available from: https://discovery.dundee.ac.uk/en/studentTheses/b0adffc7-eac8-49c4-b0ed-35cea636a3a9 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.578903.

Council of Science Editors:

Ismail N. Hormone-induced expression of the epithelial sodium channel in human airway cells. [Doctoral Dissertation]. University of Dundee; 2013. Available from: https://discovery.dundee.ac.uk/en/studentTheses/b0adffc7-eac8-49c4-b0ed-35cea636a3a9 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.578903


University of Georgia

17. Egan, John Duick. The role of calcineurin and protein phosphatase 2A in morphology, mating, pathogenicity and cell viability in ustilago maydis.

Degree: 2014, University of Georgia

 Ustilago maydis is a dimorphic basidiomycete and the causal agent of corn smut disease. It serves as a genetic model for understanding dimorphism, pathogenicity, and… (more)

Subjects/Keywords: USTILAGO MAYDIS; CALCINEURIN; CN; PROTEIN PHOSPHATASE 2B; PP2B; PROTEIN PHOSPHATASE 2A; PP2A; PROTEIN KINASE A; PKA; CAMP; MAP KINASE,; MAPK; SIGNAL TRANSDUCTION; BASIDOMYCETE; FUNGAL GENETICS

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APA (6th Edition):

Egan, J. D. (2014). The role of calcineurin and protein phosphatase 2A in morphology, mating, pathogenicity and cell viability in ustilago maydis. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/29161

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):

Egan, John Duick. “The role of calcineurin and protein phosphatase 2A in morphology, mating, pathogenicity and cell viability in ustilago maydis.” 2014. Thesis, University of Georgia. Accessed November 26, 2020. http://hdl.handle.net/10724/29161.

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

MLA Handbook (7th Edition):

Egan, John Duick. “The role of calcineurin and protein phosphatase 2A in morphology, mating, pathogenicity and cell viability in ustilago maydis.” 2014. Web. 26 Nov 2020.

Vancouver:

Egan JD. The role of calcineurin and protein phosphatase 2A in morphology, mating, pathogenicity and cell viability in ustilago maydis. [Internet] [Thesis]. University of Georgia; 2014. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/10724/29161.

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

Council of Science Editors:

Egan JD. The role of calcineurin and protein phosphatase 2A in morphology, mating, pathogenicity and cell viability in ustilago maydis. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/29161

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


University of California – San Francisco

18. Stewart-Ornstein, Jacob. Dimensionality and the Stress/Growth Axis of Gene Expression in S. cerevisiae.

Degree: Biochemistry and Molecular Biology, 2012, University of California – San Francisco

 To thrive in different circumstances cells tightly regulate and tune gene expression to optimize their protein complement to the environment. Understanding and manipulating this regulation… (more)

Subjects/Keywords: Biochemistry; Cell-to-Cell Variation; Gene Expression Noise; Msn2; Optogenetics; Protein Kinase A; Stress Response

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APA (6th Edition):

Stewart-Ornstein, J. (2012). Dimensionality and the Stress/Growth Axis of Gene Expression in S. cerevisiae. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/3gc9w4q1

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):

Stewart-Ornstein, Jacob. “Dimensionality and the Stress/Growth Axis of Gene Expression in S. cerevisiae.” 2012. Thesis, University of California – San Francisco. Accessed November 26, 2020. http://www.escholarship.org/uc/item/3gc9w4q1.

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

MLA Handbook (7th Edition):

Stewart-Ornstein, Jacob. “Dimensionality and the Stress/Growth Axis of Gene Expression in S. cerevisiae.” 2012. Web. 26 Nov 2020.

Vancouver:

Stewart-Ornstein J. Dimensionality and the Stress/Growth Axis of Gene Expression in S. cerevisiae. [Internet] [Thesis]. University of California – San Francisco; 2012. [cited 2020 Nov 26]. Available from: http://www.escholarship.org/uc/item/3gc9w4q1.

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

Council of Science Editors:

Stewart-Ornstein J. Dimensionality and the Stress/Growth Axis of Gene Expression in S. cerevisiae. [Thesis]. University of California – San Francisco; 2012. Available from: http://www.escholarship.org/uc/item/3gc9w4q1

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

19. Mantzouranis, Luciana. Análise do transcriptoma regulado pela YakA e do papel de KeaA no desenvolvimento de Dictyostelium discoideum.

Degree: PhD, Bioquímica, 2009, University of São Paulo

A YakA é uma proteína quinase necessária para a regulação da resposta a diversos estresses em Dictyostelium e é uma efetora chave da transição do… (more)

Subjects/Keywords: Desenvolvimento; Development; Kelch proteins; Protein kinase; Proteínas Kelch; Proteínas quinases; Resposta a estresses; Stress response

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APA (6th Edition):

Mantzouranis, L. (2009). Análise do transcriptoma regulado pela YakA e do papel de KeaA no desenvolvimento de Dictyostelium discoideum. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/46/46131/tde-10122009-093106/ ;

Chicago Manual of Style (16th Edition):

Mantzouranis, Luciana. “Análise do transcriptoma regulado pela YakA e do papel de KeaA no desenvolvimento de Dictyostelium discoideum.” 2009. Doctoral Dissertation, University of São Paulo. Accessed November 26, 2020. http://www.teses.usp.br/teses/disponiveis/46/46131/tde-10122009-093106/ ;.

MLA Handbook (7th Edition):

Mantzouranis, Luciana. “Análise do transcriptoma regulado pela YakA e do papel de KeaA no desenvolvimento de Dictyostelium discoideum.” 2009. Web. 26 Nov 2020.

Vancouver:

Mantzouranis L. Análise do transcriptoma regulado pela YakA e do papel de KeaA no desenvolvimento de Dictyostelium discoideum. [Internet] [Doctoral dissertation]. University of São Paulo; 2009. [cited 2020 Nov 26]. Available from: http://www.teses.usp.br/teses/disponiveis/46/46131/tde-10122009-093106/ ;.

Council of Science Editors:

Mantzouranis L. Análise do transcriptoma regulado pela YakA e do papel de KeaA no desenvolvimento de Dictyostelium discoideum. [Doctoral Dissertation]. University of São Paulo; 2009. Available from: http://www.teses.usp.br/teses/disponiveis/46/46131/tde-10122009-093106/ ;


University of Vermont

20. McKenzie, Andrew J. Mechanoregulation of leading edge PKA activity during ovarian cancer cell migration.

Degree: PhD, Pharmacology, 2014, University of Vermont

  Ovarian cancer is the deadliest of all the gynecologic cancers and is known for its clinically occult and asymptomatic dissemination. Most ovarian malignancies are… (more)

Subjects/Keywords: cancer; Cell migration; Cell signaling; Mechanobiology; metastasis; protein kinase A; Medical Cell Biology; Pharmacology

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

APA (6th Edition):

McKenzie, A. J. (2014). Mechanoregulation of leading edge PKA activity during ovarian cancer cell migration. (Doctoral Dissertation). University of Vermont. Retrieved from https://scholarworks.uvm.edu/graddis/273

Chicago Manual of Style (16th Edition):

McKenzie, Andrew J. “Mechanoregulation of leading edge PKA activity during ovarian cancer cell migration.” 2014. Doctoral Dissertation, University of Vermont. Accessed November 26, 2020. https://scholarworks.uvm.edu/graddis/273.

MLA Handbook (7th Edition):

McKenzie, Andrew J. “Mechanoregulation of leading edge PKA activity during ovarian cancer cell migration.” 2014. Web. 26 Nov 2020.

Vancouver:

McKenzie AJ. Mechanoregulation of leading edge PKA activity during ovarian cancer cell migration. [Internet] [Doctoral dissertation]. University of Vermont; 2014. [cited 2020 Nov 26]. Available from: https://scholarworks.uvm.edu/graddis/273.

Council of Science Editors:

McKenzie AJ. Mechanoregulation of leading edge PKA activity during ovarian cancer cell migration. [Doctoral Dissertation]. University of Vermont; 2014. Available from: https://scholarworks.uvm.edu/graddis/273


University of Vermont

21. Weir, Marion. Novel Mechanisms Governing Autoregulation of the Src Family Kinase Fyn and its Crosstalk with Protein Kinase A.

Degree: PhD, Biology, 2016, University of Vermont

  ABSTRACT Phosphorylation is a post-translational modification important for regulating protein activity and protein binding capacity. It is used in many different signaling pathways within… (more)

Subjects/Keywords: Autoregulation; Crosstalk; Phosphorylation; Protein Kinase A; Regulation; Src Family Kinases; Biochemistry; Biology

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

APA (6th Edition):

Weir, M. (2016). Novel Mechanisms Governing Autoregulation of the Src Family Kinase Fyn and its Crosstalk with Protein Kinase A. (Doctoral Dissertation). University of Vermont. Retrieved from https://scholarworks.uvm.edu/graddis/592

Chicago Manual of Style (16th Edition):

Weir, Marion. “Novel Mechanisms Governing Autoregulation of the Src Family Kinase Fyn and its Crosstalk with Protein Kinase A.” 2016. Doctoral Dissertation, University of Vermont. Accessed November 26, 2020. https://scholarworks.uvm.edu/graddis/592.

MLA Handbook (7th Edition):

Weir, Marion. “Novel Mechanisms Governing Autoregulation of the Src Family Kinase Fyn and its Crosstalk with Protein Kinase A.” 2016. Web. 26 Nov 2020.

Vancouver:

Weir M. Novel Mechanisms Governing Autoregulation of the Src Family Kinase Fyn and its Crosstalk with Protein Kinase A. [Internet] [Doctoral dissertation]. University of Vermont; 2016. [cited 2020 Nov 26]. Available from: https://scholarworks.uvm.edu/graddis/592.

Council of Science Editors:

Weir M. Novel Mechanisms Governing Autoregulation of the Src Family Kinase Fyn and its Crosstalk with Protein Kinase A. [Doctoral Dissertation]. University of Vermont; 2016. Available from: https://scholarworks.uvm.edu/graddis/592


University of Washington

22. Deem, Jennifer Dezet. Presynaptic Anchoring of PKA by AKAP7 is Required for Pattern Separation by Dentate Gyrus.

Degree: PhD, 2016, University of Washington

 The intracellular signaling molecule, 3',5'-cyclic adenosine monophosphate (cAMP), is produced by a cell in response to a physiological signal. A derivative of adenosine triphosphate (ATP),… (more)

Subjects/Keywords: AKAP; AKAP7; Mossy Fiber LTP; Protein Kinase A; Neurosciences; Molecular biology; Biochemistry; pharmacology

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APA (6th Edition):

Deem, J. D. (2016). Presynaptic Anchoring of PKA by AKAP7 is Required for Pattern Separation by Dentate Gyrus. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/36805

Chicago Manual of Style (16th Edition):

Deem, Jennifer Dezet. “Presynaptic Anchoring of PKA by AKAP7 is Required for Pattern Separation by Dentate Gyrus.” 2016. Doctoral Dissertation, University of Washington. Accessed November 26, 2020. http://hdl.handle.net/1773/36805.

MLA Handbook (7th Edition):

Deem, Jennifer Dezet. “Presynaptic Anchoring of PKA by AKAP7 is Required for Pattern Separation by Dentate Gyrus.” 2016. Web. 26 Nov 2020.

Vancouver:

Deem JD. Presynaptic Anchoring of PKA by AKAP7 is Required for Pattern Separation by Dentate Gyrus. [Internet] [Doctoral dissertation]. University of Washington; 2016. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1773/36805.

Council of Science Editors:

Deem JD. Presynaptic Anchoring of PKA by AKAP7 is Required for Pattern Separation by Dentate Gyrus. [Doctoral Dissertation]. University of Washington; 2016. Available from: http://hdl.handle.net/1773/36805


Australian National University

23. Tjhin, Erick Tanujaya. The pantothenate kinase of the human malaria parasite Plasmodium falciparum .

Degree: 2018, Australian National University

 The intraerythrocytic stage of the malaria parasite Plasmodium falciparum has an absolute requirement for vitamin B5 (also known as pantothenate) in order to survive. The… (more)

Subjects/Keywords: Plasmodium; antimalarial; Coenzyme A; pantothenate; drug-resistance; whole genome sequencing; kinase; enzyme kinetics; protein-protein interaction; mass spectrometry

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APA (6th Edition):

Tjhin, E. T. (2018). The pantothenate kinase of the human malaria parasite Plasmodium falciparum . (Thesis). Australian National University. Retrieved from http://hdl.handle.net/1885/163973

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):

Tjhin, Erick Tanujaya. “The pantothenate kinase of the human malaria parasite Plasmodium falciparum .” 2018. Thesis, Australian National University. Accessed November 26, 2020. http://hdl.handle.net/1885/163973.

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

MLA Handbook (7th Edition):

Tjhin, Erick Tanujaya. “The pantothenate kinase of the human malaria parasite Plasmodium falciparum .” 2018. Web. 26 Nov 2020.

Vancouver:

Tjhin ET. The pantothenate kinase of the human malaria parasite Plasmodium falciparum . [Internet] [Thesis]. Australian National University; 2018. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/1885/163973.

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

Council of Science Editors:

Tjhin ET. The pantothenate kinase of the human malaria parasite Plasmodium falciparum . [Thesis]. Australian National University; 2018. Available from: http://hdl.handle.net/1885/163973

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


University of California – San Francisco

24. Spindler, Matthew. Signaling Scaffolds in Cardiovascular Development and Disease.

Degree: Pharmaceutical Sciences and Pharmacogenomics, 2011, University of California – San Francisco

 Background: G-protein signaling pathways regulate many aspects of cardiovascular development and disease. A-kinase anchoring proteins (AKAPs) are scaffolding molecules that coordinate and integrate these signaling… (more)

Subjects/Keywords: Developmental Biology; Cellular Biology; Molecular Biology; AKAP13; A-kinase anchoring protein; cardiac hypertrophy; cardiovascular; gene-trap mutation; G-protein signaling

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APA (6th Edition):

Spindler, M. (2011). Signaling Scaffolds in Cardiovascular Development and Disease. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/9ns2x7cc

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):

Spindler, Matthew. “Signaling Scaffolds in Cardiovascular Development and Disease.” 2011. Thesis, University of California – San Francisco. Accessed November 26, 2020. http://www.escholarship.org/uc/item/9ns2x7cc.

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

MLA Handbook (7th Edition):

Spindler, Matthew. “Signaling Scaffolds in Cardiovascular Development and Disease.” 2011. Web. 26 Nov 2020.

Vancouver:

Spindler M. Signaling Scaffolds in Cardiovascular Development and Disease. [Internet] [Thesis]. University of California – San Francisco; 2011. [cited 2020 Nov 26]. Available from: http://www.escholarship.org/uc/item/9ns2x7cc.

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

Council of Science Editors:

Spindler M. Signaling Scaffolds in Cardiovascular Development and Disease. [Thesis]. University of California – San Francisco; 2011. Available from: http://www.escholarship.org/uc/item/9ns2x7cc

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


University of Connecticut

25. Plair, Akilah A. A-Kinase Anchoring Protein (AKAP7) Interaction with Adenylyl Cyclase (AC3) and Cell Division Cycle Protein (CDC25).

Degree: MS, Biomedical Science, 2016, University of Connecticut

  1.5 million women in the U.S. are infertile, but assisted reproduction success rates are low for many reasons, including our limited understanding of oocyte… (more)

Subjects/Keywords: A-kinase anchoring protein; AKAP7; Adenylyl cyclase; AC3; Cell division cycle protein; CDC25B; Meiotic arrest; Oocyte; PKA

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APA (6th Edition):

Plair, A. A. (2016). A-Kinase Anchoring Protein (AKAP7) Interaction with Adenylyl Cyclase (AC3) and Cell Division Cycle Protein (CDC25). (Masters Thesis). University of Connecticut. Retrieved from https://opencommons.uconn.edu/gs_theses/932

Chicago Manual of Style (16th Edition):

Plair, Akilah A. “A-Kinase Anchoring Protein (AKAP7) Interaction with Adenylyl Cyclase (AC3) and Cell Division Cycle Protein (CDC25).” 2016. Masters Thesis, University of Connecticut. Accessed November 26, 2020. https://opencommons.uconn.edu/gs_theses/932.

MLA Handbook (7th Edition):

Plair, Akilah A. “A-Kinase Anchoring Protein (AKAP7) Interaction with Adenylyl Cyclase (AC3) and Cell Division Cycle Protein (CDC25).” 2016. Web. 26 Nov 2020.

Vancouver:

Plair AA. A-Kinase Anchoring Protein (AKAP7) Interaction with Adenylyl Cyclase (AC3) and Cell Division Cycle Protein (CDC25). [Internet] [Masters thesis]. University of Connecticut; 2016. [cited 2020 Nov 26]. Available from: https://opencommons.uconn.edu/gs_theses/932.

Council of Science Editors:

Plair AA. A-Kinase Anchoring Protein (AKAP7) Interaction with Adenylyl Cyclase (AC3) and Cell Division Cycle Protein (CDC25). [Masters Thesis]. University of Connecticut; 2016. Available from: https://opencommons.uconn.edu/gs_theses/932


University of Minnesota

26. OGOKEH, STANISLAS. Cellular Retinoic Acid Binding Protein-I as a Drugable Target to Dampen Calcium-Calmodulin Dependent Protein Kinase II Activity.

Degree: MS, Pharmacology, 2016, University of Minnesota

 Heart failure is the leading cause of death in developed countries. Current therapeutic approaches target the autonomic nervous system’s β and α adrenergic receptors to… (more)

Subjects/Keywords: Calcium-Calmodulin Dependent Protein Kinase II; CaMKII; Cellular Retinoic Acid Binding Protein-I; CRABP; Retinoic Acid; Vitamin A

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APA (6th Edition):

OGOKEH, S. (2016). Cellular Retinoic Acid Binding Protein-I as a Drugable Target to Dampen Calcium-Calmodulin Dependent Protein Kinase II Activity. (Masters Thesis). University of Minnesota. Retrieved from http://hdl.handle.net/11299/182107

Chicago Manual of Style (16th Edition):

OGOKEH, STANISLAS. “Cellular Retinoic Acid Binding Protein-I as a Drugable Target to Dampen Calcium-Calmodulin Dependent Protein Kinase II Activity.” 2016. Masters Thesis, University of Minnesota. Accessed November 26, 2020. http://hdl.handle.net/11299/182107.

MLA Handbook (7th Edition):

OGOKEH, STANISLAS. “Cellular Retinoic Acid Binding Protein-I as a Drugable Target to Dampen Calcium-Calmodulin Dependent Protein Kinase II Activity.” 2016. Web. 26 Nov 2020.

Vancouver:

OGOKEH S. Cellular Retinoic Acid Binding Protein-I as a Drugable Target to Dampen Calcium-Calmodulin Dependent Protein Kinase II Activity. [Internet] [Masters thesis]. University of Minnesota; 2016. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/11299/182107.

Council of Science Editors:

OGOKEH S. Cellular Retinoic Acid Binding Protein-I as a Drugable Target to Dampen Calcium-Calmodulin Dependent Protein Kinase II Activity. [Masters Thesis]. University of Minnesota; 2016. Available from: http://hdl.handle.net/11299/182107


Kansas State University

27. Wise, Randi. The role of the secretory pathway and cell surface proteolysis in the regulation of the aggressiveness of breast cancer cells.

Degree: PhD, Biochemistry and Molecular Biophysics Interdepartmental Program, 2017, Kansas State University

 Cancer cells exploit key signaling pathways in order to survive, proliferate, and metastasize. Understanding the intricacies of the aberrant signaling in cancer may provide new… (more)

Subjects/Keywords: Protein disulfide isomerase; A disintegrin and metalloprotease; Breast cancer; Mitogen-activated protein kinase pathway; Cancer stem cells; Programmed death-ligand 1

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

APA (6th Edition):

Wise, R. (2017). The role of the secretory pathway and cell surface proteolysis in the regulation of the aggressiveness of breast cancer cells. (Doctoral Dissertation). Kansas State University. Retrieved from http://hdl.handle.net/2097/38199

Chicago Manual of Style (16th Edition):

Wise, Randi. “The role of the secretory pathway and cell surface proteolysis in the regulation of the aggressiveness of breast cancer cells.” 2017. Doctoral Dissertation, Kansas State University. Accessed November 26, 2020. http://hdl.handle.net/2097/38199.

MLA Handbook (7th Edition):

Wise, Randi. “The role of the secretory pathway and cell surface proteolysis in the regulation of the aggressiveness of breast cancer cells.” 2017. Web. 26 Nov 2020.

Vancouver:

Wise R. The role of the secretory pathway and cell surface proteolysis in the regulation of the aggressiveness of breast cancer cells. [Internet] [Doctoral dissertation]. Kansas State University; 2017. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/2097/38199.

Council of Science Editors:

Wise R. The role of the secretory pathway and cell surface proteolysis in the regulation of the aggressiveness of breast cancer cells. [Doctoral Dissertation]. Kansas State University; 2017. Available from: http://hdl.handle.net/2097/38199


Freie Universität Berlin

28. Gövercin, Mehmet. The role of the protein kinase inhibitor α in the modulation of the phospholamban-dependent Ca2+ - uptake into the sarcoplasmic reticulum.

Degree: 2012, Freie Universität Berlin

 The role of the protein kinase inhibitor α in the modulation of the phospholamban-dependent Ca2+-uptake into the sarcoplasmic reticulum Heart failure is the second most… (more)

Subjects/Keywords: protein kinase A; protein kinase inhibitor; phospholamban; SERCA2a; Ca2+; adenovector; AdV; gene therapy; chronic heart failure; 600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit

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

APA (6th Edition):

Gövercin, M. (2012). The role of the protein kinase inhibitor α in the modulation of the phospholamban-dependent Ca2+ - uptake into the sarcoplasmic reticulum. (Thesis). Freie Universität Berlin. Retrieved from http://dx.doi.org/10.17169/refubium-7044

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):

Gövercin, Mehmet. “The role of the protein kinase inhibitor α in the modulation of the phospholamban-dependent Ca2+ - uptake into the sarcoplasmic reticulum.” 2012. Thesis, Freie Universität Berlin. Accessed November 26, 2020. http://dx.doi.org/10.17169/refubium-7044.

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

MLA Handbook (7th Edition):

Gövercin, Mehmet. “The role of the protein kinase inhibitor α in the modulation of the phospholamban-dependent Ca2+ - uptake into the sarcoplasmic reticulum.” 2012. Web. 26 Nov 2020.

Vancouver:

Gövercin M. The role of the protein kinase inhibitor α in the modulation of the phospholamban-dependent Ca2+ - uptake into the sarcoplasmic reticulum. [Internet] [Thesis]. Freie Universität Berlin; 2012. [cited 2020 Nov 26]. Available from: http://dx.doi.org/10.17169/refubium-7044.

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

Council of Science Editors:

Gövercin M. The role of the protein kinase inhibitor α in the modulation of the phospholamban-dependent Ca2+ - uptake into the sarcoplasmic reticulum. [Thesis]. Freie Universität Berlin; 2012. Available from: http://dx.doi.org/10.17169/refubium-7044

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


University of Melbourne

29. Bhaskaracharya, Archana. Modulation of TRPV1 channel activity by phosphorylation.

Degree: 2014, University of Melbourne

 TRPV1 is a ligand-gated cation channel activated by heat, low pH, capsaicin and other vanilloid compounds. Several studies have identified putative phosphorylation sites of TRPV1… (more)

Subjects/Keywords: TRPV1; phosphorylation; ion channels; T704; S116; T144; T370; T406; S502; S774; S800; S820; protein kinase A; PKA; protein kinase C; PKC; CdK5; CaMKII; Flp In CHO cells

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

APA (6th Edition):

Bhaskaracharya, A. (2014). Modulation of TRPV1 channel activity by phosphorylation. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/43099

Chicago Manual of Style (16th Edition):

Bhaskaracharya, Archana. “Modulation of TRPV1 channel activity by phosphorylation.” 2014. Doctoral Dissertation, University of Melbourne. Accessed November 26, 2020. http://hdl.handle.net/11343/43099.

MLA Handbook (7th Edition):

Bhaskaracharya, Archana. “Modulation of TRPV1 channel activity by phosphorylation.” 2014. Web. 26 Nov 2020.

Vancouver:

Bhaskaracharya A. Modulation of TRPV1 channel activity by phosphorylation. [Internet] [Doctoral dissertation]. University of Melbourne; 2014. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/11343/43099.

Council of Science Editors:

Bhaskaracharya A. Modulation of TRPV1 channel activity by phosphorylation. [Doctoral Dissertation]. University of Melbourne; 2014. Available from: http://hdl.handle.net/11343/43099


University of Georgia

30. Flaherty, Briana. Novel approaches to targeted antimalarial development.

Degree: 2016, University of Georgia

 Malaria is an ancient disease that has likely plagued mankind for our entire existence. Today, malaria continues to be a leading cause of morbidity and… (more)

Subjects/Keywords: Plasmodium falciparum; malaria; placental malaria; antimalarial; cytoadherence; PfEMP1; CSA; VAR2CSA; peptide therapeutics; stapled peptides; protein kinase A; STAD-2; calcium dependent protein kinase-1; JDD

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

APA (6th Edition):

Flaherty, B. (2016). Novel approaches to targeted antimalarial development. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/35239

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):

Flaherty, Briana. “Novel approaches to targeted antimalarial development.” 2016. Thesis, University of Georgia. Accessed November 26, 2020. http://hdl.handle.net/10724/35239.

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

MLA Handbook (7th Edition):

Flaherty, Briana. “Novel approaches to targeted antimalarial development.” 2016. Web. 26 Nov 2020.

Vancouver:

Flaherty B. Novel approaches to targeted antimalarial development. [Internet] [Thesis]. University of Georgia; 2016. [cited 2020 Nov 26]. Available from: http://hdl.handle.net/10724/35239.

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

Council of Science Editors:

Flaherty B. Novel approaches to targeted antimalarial development. [Thesis]. University of Georgia; 2016. Available from: http://hdl.handle.net/10724/35239

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

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