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You searched for subject:(Src kinase). Showing records 1 – 30 of 75 total matches.

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Brandeis University

1. Gelles-Watnick, Sara. Progress towards mechanistic studies of Src tyrosine kinase using ligated protein constructs.

Degree: 2017, Brandeis University

 Tyrosine kinase c-Src is a ubiquitously expressed proto-oncogene implicated in many cancers. The Kern Lab hopes to use NMR to study the regulatory and catalytic… (more)

Subjects/Keywords: src tyrosine kinase; kinase; protein nmr; Sortase; c-Src

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APA (6th Edition):

Gelles-Watnick, S. (2017). Progress towards mechanistic studies of Src tyrosine kinase using ligated protein constructs. (Thesis). Brandeis University. Retrieved from http://hdl.handle.net/10192/33910

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):

Gelles-Watnick, Sara. “Progress towards mechanistic studies of Src tyrosine kinase using ligated protein constructs.” 2017. Thesis, Brandeis University. Accessed October 18, 2019. http://hdl.handle.net/10192/33910.

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

MLA Handbook (7th Edition):

Gelles-Watnick, Sara. “Progress towards mechanistic studies of Src tyrosine kinase using ligated protein constructs.” 2017. Web. 18 Oct 2019.

Vancouver:

Gelles-Watnick S. Progress towards mechanistic studies of Src tyrosine kinase using ligated protein constructs. [Internet] [Thesis]. Brandeis University; 2017. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10192/33910.

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

Council of Science Editors:

Gelles-Watnick S. Progress towards mechanistic studies of Src tyrosine kinase using ligated protein constructs. [Thesis]. Brandeis University; 2017. Available from: http://hdl.handle.net/10192/33910

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

2. Kratimenos, Panagiotis. Η έκφραση της Focal Adhesion Kinase, Src kinase και Paxillin σε κυτταρολογικό υλικό ασθενών με νευρoβλάστωμα.

Degree: 2015, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

 Background: Neuroblastoma (NB) is the most common extracranial tumor in children, arising from the neural crest of the sympathetic ganglia and accounts for 7-10% of… (more)

Subjects/Keywords: Νευροβλάστωμα; Παχιλλίνη; Neuroblastoma; Src kinase; FAK; Paxillin

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APA (6th Edition):

Kratimenos, P. (2015). Η έκφραση της Focal Adhesion Kinase, Src kinase και Paxillin σε κυτταρολογικό υλικό ασθενών με νευρoβλάστωμα. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/43066

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):

Kratimenos, Panagiotis. “Η έκφραση της Focal Adhesion Kinase, Src kinase και Paxillin σε κυτταρολογικό υλικό ασθενών με νευρoβλάστωμα.” 2015. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed October 18, 2019. http://hdl.handle.net/10442/hedi/43066.

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

MLA Handbook (7th Edition):

Kratimenos, Panagiotis. “Η έκφραση της Focal Adhesion Kinase, Src kinase και Paxillin σε κυτταρολογικό υλικό ασθενών με νευρoβλάστωμα.” 2015. Web. 18 Oct 2019.

Vancouver:

Kratimenos P. Η έκφραση της Focal Adhesion Kinase, Src kinase και Paxillin σε κυτταρολογικό υλικό ασθενών με νευρoβλάστωμα. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2015. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10442/hedi/43066.

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

Council of Science Editors:

Kratimenos P. Η έκφραση της Focal Adhesion Kinase, Src kinase και Paxillin σε κυτταρολογικό υλικό ασθενών με νευρoβλάστωμα. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2015. Available from: http://hdl.handle.net/10442/hedi/43066

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


University of Alberta

3. Marasinghe Arachchige, Bodhi Nirosha. Structural aspects of the interaction of the cytoplasmic domain of Mucin-1 (MUC1) with the SH3 domain of Src Kinase.

Degree: MS, Medical Sciences-Laboratory Medicine and Pathology, 2011, University of Alberta

 Abstract Breast cancer is the second most frequent cause of cancer deaths in Canadian women with death resulting from the spread of cancer cells or… (more)

Subjects/Keywords: Src Kinase; MUC1; NMR; SH3 domain

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APA (6th Edition):

Marasinghe Arachchige, B. N. (2011). Structural aspects of the interaction of the cytoplasmic domain of Mucin-1 (MUC1) with the SH3 domain of Src Kinase. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/wp988k67k

Chicago Manual of Style (16th Edition):

Marasinghe Arachchige, Bodhi Nirosha. “Structural aspects of the interaction of the cytoplasmic domain of Mucin-1 (MUC1) with the SH3 domain of Src Kinase.” 2011. Masters Thesis, University of Alberta. Accessed October 18, 2019. https://era.library.ualberta.ca/files/wp988k67k.

MLA Handbook (7th Edition):

Marasinghe Arachchige, Bodhi Nirosha. “Structural aspects of the interaction of the cytoplasmic domain of Mucin-1 (MUC1) with the SH3 domain of Src Kinase.” 2011. Web. 18 Oct 2019.

Vancouver:

Marasinghe Arachchige BN. Structural aspects of the interaction of the cytoplasmic domain of Mucin-1 (MUC1) with the SH3 domain of Src Kinase. [Internet] [Masters thesis]. University of Alberta; 2011. [cited 2019 Oct 18]. Available from: https://era.library.ualberta.ca/files/wp988k67k.

Council of Science Editors:

Marasinghe Arachchige BN. Structural aspects of the interaction of the cytoplasmic domain of Mucin-1 (MUC1) with the SH3 domain of Src Kinase. [Masters Thesis]. University of Alberta; 2011. Available from: https://era.library.ualberta.ca/files/wp988k67k


University of Illinois – Chicago

4. Klomp, Jennifer. Dissecting the Role of c-Src in the Regulation of Adherens Junctions using Engineered Kinases.

Degree: 2017, University of Illinois – Chicago

 Using an inducible kinase system, Rapamycin Regulated kinase (RapR-kinase), we directly activated the Src family tyrosine kinases c-Src (Src) and Lyn in human pulmonary arterial… (more)

Subjects/Keywords: Kinase; Src; VE cadherin; Lyn; Rac1; PI3K

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APA (6th Edition):

Klomp, J. (2017). Dissecting the Role of c-Src in the Regulation of Adherens Junctions using Engineered Kinases. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/22221

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):

Klomp, Jennifer. “Dissecting the Role of c-Src in the Regulation of Adherens Junctions using Engineered Kinases.” 2017. Thesis, University of Illinois – Chicago. Accessed October 18, 2019. http://hdl.handle.net/10027/22221.

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

MLA Handbook (7th Edition):

Klomp, Jennifer. “Dissecting the Role of c-Src in the Regulation of Adherens Junctions using Engineered Kinases.” 2017. Web. 18 Oct 2019.

Vancouver:

Klomp J. Dissecting the Role of c-Src in the Regulation of Adherens Junctions using Engineered Kinases. [Internet] [Thesis]. University of Illinois – Chicago; 2017. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10027/22221.

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

Council of Science Editors:

Klomp J. Dissecting the Role of c-Src in the Regulation of Adherens Junctions using Engineered Kinases. [Thesis]. University of Illinois – Chicago; 2017. Available from: http://hdl.handle.net/10027/22221

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


University of Vermont

5. 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 (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 October 18, 2019. 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. 18 Oct 2019.

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 2019 Oct 18]. 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

6. Aponte, Emilie. Régulation de la signalisation de Src par son domaine N-terminal intrinsèquement désordonné : Regulation of Src signaling by its N-terminal intrinsically disordered domain.

Degree: Docteur es, Biologie Santé, 2018, Montpellier

La tyrosine kinase cytoplasmique Src est un régulateur essentiel de la croissance et de l’adhésion cellulaires induites par de nombreux stimuli extracellulaires, dont les facteurs… (more)

Subjects/Keywords: Src; Tyrosine kinase; Cancer colorectal; Oncogène; Signalisation; Src; Colorectal cancer; Tyrosine kinase; Oncogene; Signalisation; Sfk

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APA (6th Edition):

Aponte, E. (2018). Régulation de la signalisation de Src par son domaine N-terminal intrinsèquement désordonné : Regulation of Src signaling by its N-terminal intrinsically disordered domain. (Doctoral Dissertation). Montpellier. Retrieved from http://www.theses.fr/2018MONTT095

Chicago Manual of Style (16th Edition):

Aponte, Emilie. “Régulation de la signalisation de Src par son domaine N-terminal intrinsèquement désordonné : Regulation of Src signaling by its N-terminal intrinsically disordered domain.” 2018. Doctoral Dissertation, Montpellier. Accessed October 18, 2019. http://www.theses.fr/2018MONTT095.

MLA Handbook (7th Edition):

Aponte, Emilie. “Régulation de la signalisation de Src par son domaine N-terminal intrinsèquement désordonné : Regulation of Src signaling by its N-terminal intrinsically disordered domain.” 2018. Web. 18 Oct 2019.

Vancouver:

Aponte E. Régulation de la signalisation de Src par son domaine N-terminal intrinsèquement désordonné : Regulation of Src signaling by its N-terminal intrinsically disordered domain. [Internet] [Doctoral dissertation]. Montpellier; 2018. [cited 2019 Oct 18]. Available from: http://www.theses.fr/2018MONTT095.

Council of Science Editors:

Aponte E. Régulation de la signalisation de Src par son domaine N-terminal intrinsèquement désordonné : Regulation of Src signaling by its N-terminal intrinsically disordered domain. [Doctoral Dissertation]. Montpellier; 2018. Available from: http://www.theses.fr/2018MONTT095


University of Toronto

7. Durbin, Joshua N. Phosphoproteomic Analysis of Acute Myeloid Leukemia.

Degree: 2012, University of Toronto

Acute myeloid leukemia (AML) is a clonal hematopoietic stem cell malignancy, marked by suppressed production of normal terminally differentiated and progenitor hematopoietic cells, and increased… (more)

Subjects/Keywords: tyrosine kinase; acute myeloid leukemia; AML; kinase; cancer; phosphoproteomics; src family kinase; 0760; 0379; 0307

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APA (6th Edition):

Durbin, J. N. (2012). Phosphoproteomic Analysis of Acute Myeloid Leukemia. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/33402

Chicago Manual of Style (16th Edition):

Durbin, Joshua N. “Phosphoproteomic Analysis of Acute Myeloid Leukemia.” 2012. Masters Thesis, University of Toronto. Accessed October 18, 2019. http://hdl.handle.net/1807/33402.

MLA Handbook (7th Edition):

Durbin, Joshua N. “Phosphoproteomic Analysis of Acute Myeloid Leukemia.” 2012. Web. 18 Oct 2019.

Vancouver:

Durbin JN. Phosphoproteomic Analysis of Acute Myeloid Leukemia. [Internet] [Masters thesis]. University of Toronto; 2012. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1807/33402.

Council of Science Editors:

Durbin JN. Phosphoproteomic Analysis of Acute Myeloid Leukemia. [Masters Thesis]. University of Toronto; 2012. Available from: http://hdl.handle.net/1807/33402

8. Shi, Xiaoli. Etude de la spécificité des interactions protéine-protéine : application au complexe Alix-domaine SH3 des Src Kinases : Studies on protein-protein interaction : and its applications in ALIX/SFKs-SH3 complexes.

Degree: Docteur es, Biochimie structurale, 2011, Aix-Marseille 1

Les domaines SH3 (Src Homology domain) représentent l'un des modules protéiques le plus largement répandu dans la nature. Ils participent à des interactions intra- et… (more)

Subjects/Keywords: Interaction Protéine-Protéine; Vih; Nef; Src Kinase; Domaine SH3; Alix; Protein-Protein Interaction; Hiv; Nef; Src Kinase; SH3 domain; Alix

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APA (6th Edition):

Shi, X. (2011). Etude de la spécificité des interactions protéine-protéine : application au complexe Alix-domaine SH3 des Src Kinases : Studies on protein-protein interaction : and its applications in ALIX/SFKs-SH3 complexes. (Doctoral Dissertation). Aix-Marseille 1. Retrieved from http://www.theses.fr/2011AIX10024

Chicago Manual of Style (16th Edition):

Shi, Xiaoli. “Etude de la spécificité des interactions protéine-protéine : application au complexe Alix-domaine SH3 des Src Kinases : Studies on protein-protein interaction : and its applications in ALIX/SFKs-SH3 complexes.” 2011. Doctoral Dissertation, Aix-Marseille 1. Accessed October 18, 2019. http://www.theses.fr/2011AIX10024.

MLA Handbook (7th Edition):

Shi, Xiaoli. “Etude de la spécificité des interactions protéine-protéine : application au complexe Alix-domaine SH3 des Src Kinases : Studies on protein-protein interaction : and its applications in ALIX/SFKs-SH3 complexes.” 2011. Web. 18 Oct 2019.

Vancouver:

Shi X. Etude de la spécificité des interactions protéine-protéine : application au complexe Alix-domaine SH3 des Src Kinases : Studies on protein-protein interaction : and its applications in ALIX/SFKs-SH3 complexes. [Internet] [Doctoral dissertation]. Aix-Marseille 1; 2011. [cited 2019 Oct 18]. Available from: http://www.theses.fr/2011AIX10024.

Council of Science Editors:

Shi X. Etude de la spécificité des interactions protéine-protéine : application au complexe Alix-domaine SH3 des Src Kinases : Studies on protein-protein interaction : and its applications in ALIX/SFKs-SH3 complexes. [Doctoral Dissertation]. Aix-Marseille 1; 2011. Available from: http://www.theses.fr/2011AIX10024

9. Hébert Chatelain, Etienne. Impact des phosphorylations sur tyrosine sur le métabolisme mitochondrial : régulation et impacts fonctionnels des phosphorylations induites par la Src kinase : Tyrosine phosphorylation impact on mitochondrial metabolism : regulation and functionnal impacts of phosphorylation mediated by the Src kinase.

Degree: Docteur es, Sciences, technologie, santé. Biologie cellulaire et physiopathologie, 2011, Université de Bordeaux Segalen

La mitochondrie est une organelle très importante vu son implication dans plusieurs processus cellulaires. Elle produit notamment la majeure partie de l'énergie qui est consommée… (more)

Subjects/Keywords: Mitochondrie; Phosphorylation oxydative; Tyrosine; Phosphorylation; Src kinase; PTP1B; Mitochondria; Oxidative phosphorylation; Tyrosine; Phosphorylation; Src kinase; PTP1B

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APA (6th Edition):

Hébert Chatelain, E. (2011). Impact des phosphorylations sur tyrosine sur le métabolisme mitochondrial : régulation et impacts fonctionnels des phosphorylations induites par la Src kinase : Tyrosine phosphorylation impact on mitochondrial metabolism : regulation and functionnal impacts of phosphorylation mediated by the Src kinase. (Doctoral Dissertation). Université de Bordeaux Segalen. Retrieved from http://www.theses.fr/2011BOR21830

Chicago Manual of Style (16th Edition):

Hébert Chatelain, Etienne. “Impact des phosphorylations sur tyrosine sur le métabolisme mitochondrial : régulation et impacts fonctionnels des phosphorylations induites par la Src kinase : Tyrosine phosphorylation impact on mitochondrial metabolism : regulation and functionnal impacts of phosphorylation mediated by the Src kinase.” 2011. Doctoral Dissertation, Université de Bordeaux Segalen. Accessed October 18, 2019. http://www.theses.fr/2011BOR21830.

MLA Handbook (7th Edition):

Hébert Chatelain, Etienne. “Impact des phosphorylations sur tyrosine sur le métabolisme mitochondrial : régulation et impacts fonctionnels des phosphorylations induites par la Src kinase : Tyrosine phosphorylation impact on mitochondrial metabolism : regulation and functionnal impacts of phosphorylation mediated by the Src kinase.” 2011. Web. 18 Oct 2019.

Vancouver:

Hébert Chatelain E. Impact des phosphorylations sur tyrosine sur le métabolisme mitochondrial : régulation et impacts fonctionnels des phosphorylations induites par la Src kinase : Tyrosine phosphorylation impact on mitochondrial metabolism : regulation and functionnal impacts of phosphorylation mediated by the Src kinase. [Internet] [Doctoral dissertation]. Université de Bordeaux Segalen; 2011. [cited 2019 Oct 18]. Available from: http://www.theses.fr/2011BOR21830.

Council of Science Editors:

Hébert Chatelain E. Impact des phosphorylations sur tyrosine sur le métabolisme mitochondrial : régulation et impacts fonctionnels des phosphorylations induites par la Src kinase : Tyrosine phosphorylation impact on mitochondrial metabolism : regulation and functionnal impacts of phosphorylation mediated by the Src kinase. [Doctoral Dissertation]. Université de Bordeaux Segalen; 2011. Available from: http://www.theses.fr/2011BOR21830


University of Otago

10. Tan, Chew Ling. Sonic hedgehog acts via Smoothened to stimulate neurite growth in gonadotropin-releasing hormone neurons .

Degree: 2013, University of Otago

 Gonadotropin-releasing hormone (GnRH) neurons are the central regulators of reproduction in vertebrates. GnRH cell bodies reside in the basal forebrain, and most extend long neurites… (more)

Subjects/Keywords: GnRH; MBH; Shh; Smo; neurite growth; Src family kinase

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APA (6th Edition):

Tan, C. L. (2013). Sonic hedgehog acts via Smoothened to stimulate neurite growth in gonadotropin-releasing hormone neurons . (Doctoral Dissertation). University of Otago. Retrieved from http://hdl.handle.net/10523/4524

Chicago Manual of Style (16th Edition):

Tan, Chew Ling. “Sonic hedgehog acts via Smoothened to stimulate neurite growth in gonadotropin-releasing hormone neurons .” 2013. Doctoral Dissertation, University of Otago. Accessed October 18, 2019. http://hdl.handle.net/10523/4524.

MLA Handbook (7th Edition):

Tan, Chew Ling. “Sonic hedgehog acts via Smoothened to stimulate neurite growth in gonadotropin-releasing hormone neurons .” 2013. Web. 18 Oct 2019.

Vancouver:

Tan CL. Sonic hedgehog acts via Smoothened to stimulate neurite growth in gonadotropin-releasing hormone neurons . [Internet] [Doctoral dissertation]. University of Otago; 2013. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10523/4524.

Council of Science Editors:

Tan CL. Sonic hedgehog acts via Smoothened to stimulate neurite growth in gonadotropin-releasing hormone neurons . [Doctoral Dissertation]. University of Otago; 2013. Available from: http://hdl.handle.net/10523/4524


University of Saskatchewan

11. Paul, James 1986-. Synthetic lethal interactions of EPHB6 in breast cancer cells.

Degree: 2016, University of Saskatchewan

 Sequencing of tumor genomes has shown that many loss-of-function alterations exist in cancer cells. Some of these alterations are a product of the cancerous progression… (more)

Subjects/Keywords: breast cancer; genetic interaction; synthetic lethality; EPHB6; SRC kinase; KX2-391

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APA (6th Edition):

Paul, J. 1. (2016). Synthetic lethal interactions of EPHB6 in breast cancer cells. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/7663

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):

Paul, James 1986-. “Synthetic lethal interactions of EPHB6 in breast cancer cells.” 2016. Thesis, University of Saskatchewan. Accessed October 18, 2019. http://hdl.handle.net/10388/7663.

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

MLA Handbook (7th Edition):

Paul, James 1986-. “Synthetic lethal interactions of EPHB6 in breast cancer cells.” 2016. Web. 18 Oct 2019.

Vancouver:

Paul J1. Synthetic lethal interactions of EPHB6 in breast cancer cells. [Internet] [Thesis]. University of Saskatchewan; 2016. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10388/7663.

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

Council of Science Editors:

Paul J1. Synthetic lethal interactions of EPHB6 in breast cancer cells. [Thesis]. University of Saskatchewan; 2016. Available from: http://hdl.handle.net/10388/7663

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


Vanderbilt University

12. Prewitt, Allison Renee. Src Kinase Activation in Pulmonary Arterial Hypertension.

Degree: PhD, Cell and Developmental Biology, 2015, Vanderbilt University

 Heritable Pulmonary Arterial Hypertension (HPAH) is a rare, fatal disease of the pulmonary vasculature for which there is no cure. The majority of HPAH patients… (more)

Subjects/Keywords: BMPR2; Endothelial Dysfunction; Src kinase; Caveolae; Caveolin-1; Pulmonary Hypertension

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APA (6th Edition):

Prewitt, A. R. (2015). Src Kinase Activation in Pulmonary Arterial Hypertension. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-07062015-155323/ ;

Chicago Manual of Style (16th Edition):

Prewitt, Allison Renee. “Src Kinase Activation in Pulmonary Arterial Hypertension.” 2015. Doctoral Dissertation, Vanderbilt University. Accessed October 18, 2019. http://etd.library.vanderbilt.edu/available/etd-07062015-155323/ ;.

MLA Handbook (7th Edition):

Prewitt, Allison Renee. “Src Kinase Activation in Pulmonary Arterial Hypertension.” 2015. Web. 18 Oct 2019.

Vancouver:

Prewitt AR. Src Kinase Activation in Pulmonary Arterial Hypertension. [Internet] [Doctoral dissertation]. Vanderbilt University; 2015. [cited 2019 Oct 18]. Available from: http://etd.library.vanderbilt.edu/available/etd-07062015-155323/ ;.

Council of Science Editors:

Prewitt AR. Src Kinase Activation in Pulmonary Arterial Hypertension. [Doctoral Dissertation]. Vanderbilt University; 2015. Available from: http://etd.library.vanderbilt.edu/available/etd-07062015-155323/ ;


University of Michigan

13. Agius, Michael. Modulating the Global Conformations of c-Src Kinase.

Degree: PhD, Medicinal Chemistry, 2017, University of Michigan

 Protein Kinases are key regulators of important cellular processes and have been a validated therapeutic target for cancer over the past two decades. Kinase signaling… (more)

Subjects/Keywords: Kinase; c-Src; Conformation; Medicinal Chemistry; Chemical Biology; Biological Chemistry; Science

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APA (6th Edition):

Agius, M. (2017). Modulating the Global Conformations of c-Src Kinase. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/140873

Chicago Manual of Style (16th Edition):

Agius, Michael. “Modulating the Global Conformations of c-Src Kinase.” 2017. Doctoral Dissertation, University of Michigan. Accessed October 18, 2019. http://hdl.handle.net/2027.42/140873.

MLA Handbook (7th Edition):

Agius, Michael. “Modulating the Global Conformations of c-Src Kinase.” 2017. Web. 18 Oct 2019.

Vancouver:

Agius M. Modulating the Global Conformations of c-Src Kinase. [Internet] [Doctoral dissertation]. University of Michigan; 2017. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2027.42/140873.

Council of Science Editors:

Agius M. Modulating the Global Conformations of c-Src Kinase. [Doctoral Dissertation]. University of Michigan; 2017. Available from: http://hdl.handle.net/2027.42/140873


University of Vermont

14. 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 (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 October 18, 2019. 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. 18 Oct 2019.

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 2019 Oct 18]. 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 Toledo Health Science Campus

15. Banerjee, Moumita. A Model for Domain-Specific Regulation of Src kinase by alpha-1 subunit of Na/K-ATPase.

Degree: PhD, College of Medicine, 2013, University of Toledo Health Science Campus

 Our previous results indicate that alpha-1 (a1) subunit of Na/K-ATPase interacts with Src kinase via two separate domains. While the nucleotide binding domain of a1… (more)

Subjects/Keywords: Biomedical Research; Pharmacology; Cellular Biology; sodium potassium atpase; src kinase; ouabain; cell signaling

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APA (6th Edition):

Banerjee, M. (2013). A Model for Domain-Specific Regulation of Src kinase by alpha-1 subunit of Na/K-ATPase. (Doctoral Dissertation). University of Toledo Health Science Campus. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=mco1385040354

Chicago Manual of Style (16th Edition):

Banerjee, Moumita. “A Model for Domain-Specific Regulation of Src kinase by alpha-1 subunit of Na/K-ATPase.” 2013. Doctoral Dissertation, University of Toledo Health Science Campus. Accessed October 18, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=mco1385040354.

MLA Handbook (7th Edition):

Banerjee, Moumita. “A Model for Domain-Specific Regulation of Src kinase by alpha-1 subunit of Na/K-ATPase.” 2013. Web. 18 Oct 2019.

Vancouver:

Banerjee M. A Model for Domain-Specific Regulation of Src kinase by alpha-1 subunit of Na/K-ATPase. [Internet] [Doctoral dissertation]. University of Toledo Health Science Campus; 2013. [cited 2019 Oct 18]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1385040354.

Council of Science Editors:

Banerjee M. A Model for Domain-Specific Regulation of Src kinase by alpha-1 subunit of Na/K-ATPase. [Doctoral Dissertation]. University of Toledo Health Science Campus; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=mco1385040354


University of Alberta

16. Wu, Frederick W. HSV-1 VP11/12-mediated initiation of Src family kinase-PI3 kinase-Akt signalling.

Degree: MS, Department of Medical Microbiology and Immunology, 2013, University of Alberta

 Herpes simplex virus type 1 is a ubiquitous human virus that causes cold sores and, increasingly, genital herpes. Upon virion-cell fusion, tegument proteins diffuse into… (more)

Subjects/Keywords: SH2; herpes; Lck; src family kinase activation; HHV; peptide competition assay; VP11/12; HSV

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APA (6th Edition):

Wu, F. W. (2013). HSV-1 VP11/12-mediated initiation of Src family kinase-PI3 kinase-Akt signalling. (Masters Thesis). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/vx021f83m

Chicago Manual of Style (16th Edition):

Wu, Frederick W. “HSV-1 VP11/12-mediated initiation of Src family kinase-PI3 kinase-Akt signalling.” 2013. Masters Thesis, University of Alberta. Accessed October 18, 2019. https://era.library.ualberta.ca/files/vx021f83m.

MLA Handbook (7th Edition):

Wu, Frederick W. “HSV-1 VP11/12-mediated initiation of Src family kinase-PI3 kinase-Akt signalling.” 2013. Web. 18 Oct 2019.

Vancouver:

Wu FW. HSV-1 VP11/12-mediated initiation of Src family kinase-PI3 kinase-Akt signalling. [Internet] [Masters thesis]. University of Alberta; 2013. [cited 2019 Oct 18]. Available from: https://era.library.ualberta.ca/files/vx021f83m.

Council of Science Editors:

Wu FW. HSV-1 VP11/12-mediated initiation of Src family kinase-PI3 kinase-Akt signalling. [Masters Thesis]. University of Alberta; 2013. Available from: https://era.library.ualberta.ca/files/vx021f83m


University of Saskatchewan

17. Goel, Raghuveera Kumar 1988-. Phosphoproteomics Analyses to Identify the Candidate Substrates and Signaling Intermediates of the Non-Receptor Tyrosine Kinase, SRMS.

Degree: 2018, University of Saskatchewan

 SRMS (Src-related kinase lacking C-terminal regulatory tyrosine and N-terminal myristoylaton sites) is a non-receptor tyrosine kinase that belongs to the BRK family kinases (BFKs) and… (more)

Subjects/Keywords: SRMS; PTK70; substrates; BRK; FRK; Src; phosphoproteomics; mass spectrometry; PTK6, PTK5; non-receptor tyrosine kinase

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APA (6th Edition):

Goel, R. K. 1. (2018). Phosphoproteomics Analyses to Identify the Candidate Substrates and Signaling Intermediates of the Non-Receptor Tyrosine Kinase, SRMS. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/9600

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):

Goel, Raghuveera Kumar 1988-. “Phosphoproteomics Analyses to Identify the Candidate Substrates and Signaling Intermediates of the Non-Receptor Tyrosine Kinase, SRMS.” 2018. Thesis, University of Saskatchewan. Accessed October 18, 2019. http://hdl.handle.net/10388/9600.

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

MLA Handbook (7th Edition):

Goel, Raghuveera Kumar 1988-. “Phosphoproteomics Analyses to Identify the Candidate Substrates and Signaling Intermediates of the Non-Receptor Tyrosine Kinase, SRMS.” 2018. Web. 18 Oct 2019.

Vancouver:

Goel RK1. Phosphoproteomics Analyses to Identify the Candidate Substrates and Signaling Intermediates of the Non-Receptor Tyrosine Kinase, SRMS. [Internet] [Thesis]. University of Saskatchewan; 2018. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10388/9600.

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

Council of Science Editors:

Goel RK1. Phosphoproteomics Analyses to Identify the Candidate Substrates and Signaling Intermediates of the Non-Receptor Tyrosine Kinase, SRMS. [Thesis]. University of Saskatchewan; 2018. Available from: http://hdl.handle.net/10388/9600

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


University of Illinois – Chicago

18. Lee, Sun Kyong. Effects of Mutant Alpha-Synuclein In the Activation of Retrograde Fast Axonal Transport.

Degree: 2013, University of Illinois – Chicago

 Parkinson’s disease (PD) is a progressive movement disorder affecting motor functions regulated by nigrostriatal pathway. Pathologically, PD is characterized by selective loss of dopaminergic neurons… (more)

Subjects/Keywords: 1-Parkinson's disease; 2-Alpha-synuclein; 3-Retrograde fast axonal transport; 4-Src family kinase

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APA (6th Edition):

Lee, S. K. (2013). Effects of Mutant Alpha-Synuclein In the Activation of Retrograde Fast Axonal Transport. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/10289

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):

Lee, Sun Kyong. “Effects of Mutant Alpha-Synuclein In the Activation of Retrograde Fast Axonal Transport.” 2013. Thesis, University of Illinois – Chicago. Accessed October 18, 2019. http://hdl.handle.net/10027/10289.

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

MLA Handbook (7th Edition):

Lee, Sun Kyong. “Effects of Mutant Alpha-Synuclein In the Activation of Retrograde Fast Axonal Transport.” 2013. Web. 18 Oct 2019.

Vancouver:

Lee SK. Effects of Mutant Alpha-Synuclein In the Activation of Retrograde Fast Axonal Transport. [Internet] [Thesis]. University of Illinois – Chicago; 2013. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10027/10289.

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

Council of Science Editors:

Lee SK. Effects of Mutant Alpha-Synuclein In the Activation of Retrograde Fast Axonal Transport. [Thesis]. University of Illinois – Chicago; 2013. Available from: http://hdl.handle.net/10027/10289

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


University of Illinois – Chicago

19. Shen, Bo. The Role of Galpha13 in Integrin Signaling and Function.

Degree: 2016, University of Illinois – Chicago

 Integrins are known to transmit signaling in two directions: intracellular signaling stimulates conformational changes in the extracellular domain, leading to increased ligand affinity (inside-out signaling).… (more)

Subjects/Keywords: Integrin; Galpha13; Platelet; Glycoprotein IIb/IIIa; Thrombosis; Cell Migration; SRC kinase; RhoA

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APA (6th Edition):

Shen, B. (2016). The Role of Galpha13 in Integrin Signaling and Function. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/20799

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):

Shen, Bo. “The Role of Galpha13 in Integrin Signaling and Function.” 2016. Thesis, University of Illinois – Chicago. Accessed October 18, 2019. http://hdl.handle.net/10027/20799.

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

MLA Handbook (7th Edition):

Shen, Bo. “The Role of Galpha13 in Integrin Signaling and Function.” 2016. Web. 18 Oct 2019.

Vancouver:

Shen B. The Role of Galpha13 in Integrin Signaling and Function. [Internet] [Thesis]. University of Illinois – Chicago; 2016. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10027/20799.

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

Council of Science Editors:

Shen B. The Role of Galpha13 in Integrin Signaling and Function. [Thesis]. University of Illinois – Chicago; 2016. Available from: http://hdl.handle.net/10027/20799

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

20. Ghotbaddini, Maryam. Over-Expression of Aryl Hydrocarbon Receptor (AhR) Enhances Src Kinase Activity to Functionally Induce AR Signaling and Promote Prostate Cancer Progression.

Degree: PhD, Biological Science, 2018, Clark University Atlanta

  The aryl hydrocarbon receptor (AhR) has been reported to interact with multiple signaling pathways during prostate development including the androgen receptor. AhR was overexpressed… (more)

Subjects/Keywords: Prostate cancer; Aryl Hydrocarbon Receptor (AhR); Androgen Receptor (AR); Src kinase; CRPC; Biology

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APA (6th Edition):

Ghotbaddini, M. (2018). Over-Expression of Aryl Hydrocarbon Receptor (AhR) Enhances Src Kinase Activity to Functionally Induce AR Signaling and Promote Prostate Cancer Progression. (Doctoral Dissertation). Clark University Atlanta. Retrieved from http://digitalcommons.auctr.edu/cauetds/125

Chicago Manual of Style (16th Edition):

Ghotbaddini, Maryam. “Over-Expression of Aryl Hydrocarbon Receptor (AhR) Enhances Src Kinase Activity to Functionally Induce AR Signaling and Promote Prostate Cancer Progression.” 2018. Doctoral Dissertation, Clark University Atlanta. Accessed October 18, 2019. http://digitalcommons.auctr.edu/cauetds/125.

MLA Handbook (7th Edition):

Ghotbaddini, Maryam. “Over-Expression of Aryl Hydrocarbon Receptor (AhR) Enhances Src Kinase Activity to Functionally Induce AR Signaling and Promote Prostate Cancer Progression.” 2018. Web. 18 Oct 2019.

Vancouver:

Ghotbaddini M. Over-Expression of Aryl Hydrocarbon Receptor (AhR) Enhances Src Kinase Activity to Functionally Induce AR Signaling and Promote Prostate Cancer Progression. [Internet] [Doctoral dissertation]. Clark University Atlanta; 2018. [cited 2019 Oct 18]. Available from: http://digitalcommons.auctr.edu/cauetds/125.

Council of Science Editors:

Ghotbaddini M. Over-Expression of Aryl Hydrocarbon Receptor (AhR) Enhances Src Kinase Activity to Functionally Induce AR Signaling and Promote Prostate Cancer Progression. [Doctoral Dissertation]. Clark University Atlanta; 2018. Available from: http://digitalcommons.auctr.edu/cauetds/125


Utah State University

21. Bayles, Ammon Hanson. Mechanisms and Signal Transduction Pathways Involved in Bovine Oocyte Activation.

Degree: PhD, Animal, Dairy, and Veterinary Sciences, 2012, Utah State University

  In addition to contributing genes at fertilization, the sperm cell induces the oocyte to leave its arrested state and resume metabolism in the process… (more)

Subjects/Keywords: bovine; fertilization; Oocyte Activation; Phospholipase C; Signal Transduction; Src Family Kinase; Animal Sciences

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APA (6th Edition):

Bayles, A. H. (2012). Mechanisms and Signal Transduction Pathways Involved in Bovine Oocyte Activation. (Doctoral Dissertation). Utah State University. Retrieved from https://digitalcommons.usu.edu/etd/1380

Chicago Manual of Style (16th Edition):

Bayles, Ammon Hanson. “Mechanisms and Signal Transduction Pathways Involved in Bovine Oocyte Activation.” 2012. Doctoral Dissertation, Utah State University. Accessed October 18, 2019. https://digitalcommons.usu.edu/etd/1380.

MLA Handbook (7th Edition):

Bayles, Ammon Hanson. “Mechanisms and Signal Transduction Pathways Involved in Bovine Oocyte Activation.” 2012. Web. 18 Oct 2019.

Vancouver:

Bayles AH. Mechanisms and Signal Transduction Pathways Involved in Bovine Oocyte Activation. [Internet] [Doctoral dissertation]. Utah State University; 2012. [cited 2019 Oct 18]. Available from: https://digitalcommons.usu.edu/etd/1380.

Council of Science Editors:

Bayles AH. Mechanisms and Signal Transduction Pathways Involved in Bovine Oocyte Activation. [Doctoral Dissertation]. Utah State University; 2012. Available from: https://digitalcommons.usu.edu/etd/1380


The Ohio State University

22. Tan, Pauline H. Sequence Specificity of Src Homology-2 Domains.

Degree: PhD, Chemistry, 2012, The Ohio State University

Src-homology domains are small modular domains that recognize phosphotyrosine-containing proteins and couple activated protein kinases to intracellular signaling pathways. Since they often have overlapping functions,… (more)

Subjects/Keywords: Biochemistry; Chemistry; SH2 Domain; Binding Specificity; Src kinase; kinase; SHP2; SH2 mutant; protein-protein interaction; peptide library; protein binding

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APA (6th Edition):

Tan, P. H. (2012). Sequence Specificity of Src Homology-2 Domains. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1324406526

Chicago Manual of Style (16th Edition):

Tan, Pauline H. “Sequence Specificity of Src Homology-2 Domains.” 2012. Doctoral Dissertation, The Ohio State University. Accessed October 18, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1324406526.

MLA Handbook (7th Edition):

Tan, Pauline H. “Sequence Specificity of Src Homology-2 Domains.” 2012. Web. 18 Oct 2019.

Vancouver:

Tan PH. Sequence Specificity of Src Homology-2 Domains. [Internet] [Doctoral dissertation]. The Ohio State University; 2012. [cited 2019 Oct 18]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1324406526.

Council of Science Editors:

Tan PH. Sequence Specificity of Src Homology-2 Domains. [Doctoral Dissertation]. The Ohio State University; 2012. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1324406526


University of Manchester

23. Nguyen, Loan. The role of interleukin-1 receptors in brain cell signalling.

Degree: PhD, 2010, University of Manchester

 IL-1α and IL-1β are two IL-1 agonists which signals at the same receptor complex composed of IL-1R1/IL-1RAcP. However, IL-1α and IL-1β exert differential actions. A… (more)

Subjects/Keywords: 573.8; IL-1 receptors, IL-1RAcPb, IL-1alpha, IL-1beta, cytokines, inflammation, IL-6, MAP kinase, Src kinase

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APA (6th Edition):

Nguyen, L. (2010). The role of interleukin-1 receptors in brain cell signalling. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/the-role-of-interleukin1-receptors-in-brain-cell-signalling(78c927ce-a654-4eac-b2d7-2ca4ca8c0fd4).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.529239

Chicago Manual of Style (16th Edition):

Nguyen, Loan. “The role of interleukin-1 receptors in brain cell signalling.” 2010. Doctoral Dissertation, University of Manchester. Accessed October 18, 2019. https://www.research.manchester.ac.uk/portal/en/theses/the-role-of-interleukin1-receptors-in-brain-cell-signalling(78c927ce-a654-4eac-b2d7-2ca4ca8c0fd4).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.529239.

MLA Handbook (7th Edition):

Nguyen, Loan. “The role of interleukin-1 receptors in brain cell signalling.” 2010. Web. 18 Oct 2019.

Vancouver:

Nguyen L. The role of interleukin-1 receptors in brain cell signalling. [Internet] [Doctoral dissertation]. University of Manchester; 2010. [cited 2019 Oct 18]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/the-role-of-interleukin1-receptors-in-brain-cell-signalling(78c927ce-a654-4eac-b2d7-2ca4ca8c0fd4).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.529239.

Council of Science Editors:

Nguyen L. The role of interleukin-1 receptors in brain cell signalling. [Doctoral Dissertation]. University of Manchester; 2010. Available from: https://www.research.manchester.ac.uk/portal/en/theses/the-role-of-interleukin1-receptors-in-brain-cell-signalling(78c927ce-a654-4eac-b2d7-2ca4ca8c0fd4).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.529239


University of Washington

24. Register, Ames C. Characterization and Exploitation of Bidirectional Allosteric Coupling in Multi-Domain Tyrosine Kinases using Conformation-Selective ATP-Competitive Inhibitors.

Degree: PhD, 2017, University of Washington

 Protein kinases are a large family of enzymes that play integral roles in cell signaling networks and are thus critical for effecting appropriate cellular responses… (more)

Subjects/Keywords: Ableson tyrosine kinase; Allosteric regulation; cell signaling; Conformation-selective inhibition; Small molecule inhibition; Src-family kinase; Chemistry; Biochemistry; Organic chemistry; chemistry

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APA (6th Edition):

Register, A. C. (2017). Characterization and Exploitation of Bidirectional Allosteric Coupling in Multi-Domain Tyrosine Kinases using Conformation-Selective ATP-Competitive Inhibitors. (Doctoral Dissertation). University of Washington. Retrieved from http://hdl.handle.net/1773/38087

Chicago Manual of Style (16th Edition):

Register, Ames C. “Characterization and Exploitation of Bidirectional Allosteric Coupling in Multi-Domain Tyrosine Kinases using Conformation-Selective ATP-Competitive Inhibitors.” 2017. Doctoral Dissertation, University of Washington. Accessed October 18, 2019. http://hdl.handle.net/1773/38087.

MLA Handbook (7th Edition):

Register, Ames C. “Characterization and Exploitation of Bidirectional Allosteric Coupling in Multi-Domain Tyrosine Kinases using Conformation-Selective ATP-Competitive Inhibitors.” 2017. Web. 18 Oct 2019.

Vancouver:

Register AC. Characterization and Exploitation of Bidirectional Allosteric Coupling in Multi-Domain Tyrosine Kinases using Conformation-Selective ATP-Competitive Inhibitors. [Internet] [Doctoral dissertation]. University of Washington; 2017. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/1773/38087.

Council of Science Editors:

Register AC. Characterization and Exploitation of Bidirectional Allosteric Coupling in Multi-Domain Tyrosine Kinases using Conformation-Selective ATP-Competitive Inhibitors. [Doctoral Dissertation]. University of Washington; 2017. Available from: http://hdl.handle.net/1773/38087


University of Manchester

25. Nguyen, Loan. The role of interleukin-1 receptors in brain cell signalling.

Degree: 2010, University of Manchester

 IL-1α and IL-1β are two IL-1 agonists which signals at the same receptor complex composed of IL-1R1/IL-1RAcP. However, IL-1α and IL-1β exert differential actions. A… (more)

Subjects/Keywords: IL-1 receptors; IL-1RAcPb; IL-1alpha; IL-1beta; cytokines; inflammation; IL-6; MAP kinase; Src kinase

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APA (6th Edition):

Nguyen, L. (2010). The role of interleukin-1 receptors in brain cell signalling. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:90038

Chicago Manual of Style (16th Edition):

Nguyen, Loan. “The role of interleukin-1 receptors in brain cell signalling.” 2010. Doctoral Dissertation, University of Manchester. Accessed October 18, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:90038.

MLA Handbook (7th Edition):

Nguyen, Loan. “The role of interleukin-1 receptors in brain cell signalling.” 2010. Web. 18 Oct 2019.

Vancouver:

Nguyen L. The role of interleukin-1 receptors in brain cell signalling. [Internet] [Doctoral dissertation]. University of Manchester; 2010. [cited 2019 Oct 18]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:90038.

Council of Science Editors:

Nguyen L. The role of interleukin-1 receptors in brain cell signalling. [Doctoral Dissertation]. University of Manchester; 2010. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:90038

26. Kwarcinski, Frank. Developing Kinase Inhibitors as Chemical Tools and Potential Drugs.

Degree: PhD, Medicinal Chemistry, 2016, University of Michigan

Kinase inhibitors have experienced a dramatic evolution over the last two decades, as multi-targeted kinase chemical probes have gradually given way to highly specific, clinically… (more)

Subjects/Keywords: Kinase inhibitor; Src kinase; Biological Chemistry; Science

…comparison for wt, V313I, and V377I c-Src. 131 A.1 Kinase P-loop sequence alignment. 158 A.2… …PP2 binding to c-Src kinase. 291 D.2 Kinase P-loop sequence alignment. 291 D.3… …binding loop (P-loop) of c-Src kinase. A promiscuous kinase inhibitor scaffold served… …initial screen with c-Src kinase resulted xvii in two potent furanyl derivatives, compounds… …Src inhibitors. c-Src is a cytosolic protein tyrosine kinase that has been validated as a… 

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APA (6th Edition):

Kwarcinski, F. (2016). Developing Kinase Inhibitors as Chemical Tools and Potential Drugs. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/120774

Chicago Manual of Style (16th Edition):

Kwarcinski, Frank. “Developing Kinase Inhibitors as Chemical Tools and Potential Drugs.” 2016. Doctoral Dissertation, University of Michigan. Accessed October 18, 2019. http://hdl.handle.net/2027.42/120774.

MLA Handbook (7th Edition):

Kwarcinski, Frank. “Developing Kinase Inhibitors as Chemical Tools and Potential Drugs.” 2016. Web. 18 Oct 2019.

Vancouver:

Kwarcinski F. Developing Kinase Inhibitors as Chemical Tools and Potential Drugs. [Internet] [Doctoral dissertation]. University of Michigan; 2016. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/2027.42/120774.

Council of Science Editors:

Kwarcinski F. Developing Kinase Inhibitors as Chemical Tools and Potential Drugs. [Doctoral Dissertation]. University of Michigan; 2016. Available from: http://hdl.handle.net/2027.42/120774


University of Illinois – Chicago

27. Huang, Renhua. Generation of FN3 Monobodies That Selectively Bind to the Src Family of Protein Kinases.

Degree: 2013, University of Illinois – Chicago

 Protein kinases, known for phosphorylating their protein substrates to relay signaling events in cells, contain 518 members and encompass ~2% of human genes. One subgroup… (more)

Subjects/Keywords: Phage display; FN3 monobody; Kunkel mutagenesis; Src family kinases; SH3 domain; Fyn tyrosine kinase; Lyn tyrosine Kinase; Pak1 serine/threonine kinase; Biosensor; Kinase activation; Affinity maturation; Library construction; Specificity

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APA (6th Edition):

Huang, R. (2013). Generation of FN3 Monobodies That Selectively Bind to the Src Family of Protein Kinases. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/9802

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):

Huang, Renhua. “Generation of FN3 Monobodies That Selectively Bind to the Src Family of Protein Kinases.” 2013. Thesis, University of Illinois – Chicago. Accessed October 18, 2019. http://hdl.handle.net/10027/9802.

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

MLA Handbook (7th Edition):

Huang, Renhua. “Generation of FN3 Monobodies That Selectively Bind to the Src Family of Protein Kinases.” 2013. Web. 18 Oct 2019.

Vancouver:

Huang R. Generation of FN3 Monobodies That Selectively Bind to the Src Family of Protein Kinases. [Internet] [Thesis]. University of Illinois – Chicago; 2013. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10027/9802.

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

Council of Science Editors:

Huang R. Generation of FN3 Monobodies That Selectively Bind to the Src Family of Protein Kinases. [Thesis]. University of Illinois – Chicago; 2013. Available from: http://hdl.handle.net/10027/9802

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


University of Illinois – Chicago

28. Peng, Maoyu. The Role of Protein Tyrosine Kinase 6 in the Mammary Gland Epithelium and Breast Cancer.

Degree: 2014, University of Illinois – Chicago

 Breast cancer is the second leading cause of cancer-related death in women in US. A non-receptor tyrosine kinase named Protein Tyrosine Kinase 6 (PTK6) has… (more)

Subjects/Keywords: Protein tyrosine kinase 6 (PTK6); Breast tumor kinase (BRK); Src-related intestinal kinase (Sik); Transgnic mouse; Estrogen receptor BB2 (ERBB2); breast tumor

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APA (6th Edition):

Peng, M. (2014). The Role of Protein Tyrosine Kinase 6 in the Mammary Gland Epithelium and Breast Cancer. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/18890

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):

Peng, Maoyu. “The Role of Protein Tyrosine Kinase 6 in the Mammary Gland Epithelium and Breast Cancer.” 2014. Thesis, University of Illinois – Chicago. Accessed October 18, 2019. http://hdl.handle.net/10027/18890.

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

MLA Handbook (7th Edition):

Peng, Maoyu. “The Role of Protein Tyrosine Kinase 6 in the Mammary Gland Epithelium and Breast Cancer.” 2014. Web. 18 Oct 2019.

Vancouver:

Peng M. The Role of Protein Tyrosine Kinase 6 in the Mammary Gland Epithelium and Breast Cancer. [Internet] [Thesis]. University of Illinois – Chicago; 2014. [cited 2019 Oct 18]. Available from: http://hdl.handle.net/10027/18890.

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

Council of Science Editors:

Peng M. The Role of Protein Tyrosine Kinase 6 in the Mammary Gland Epithelium and Breast Cancer. [Thesis]. University of Illinois – Chicago; 2014. Available from: http://hdl.handle.net/10027/18890

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

29. Aira Diaz, Lazaro Emilio. Nouveaux rôles de la protéine kinase Lyn dans le développement du psoriasis et dans la mort cellulaire : New roles of the Lyn tyrosine kinase in psoriasis development and cell death.

Degree: Docteur es, Interactions moléculaires et cellulaires, 2018, Côte d'Azur

 La famille des kinases Src, dont Lyn fait partie, joue un rôle clé dans le contrôle de nombreux processus biologiques. Lyn a une fonction bien… (more)

Subjects/Keywords: Famille des Src protéines; Lyn; Famille de Bcl-2 protéines; Bim; Caspases pro-inflammatoires; Psoriasis; Src-family kinase; Lyn; Bcl-2 family; Bim; Inflammatory caspases; Psoriasis

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

APA (6th Edition):

Aira Diaz, L. E. (2018). Nouveaux rôles de la protéine kinase Lyn dans le développement du psoriasis et dans la mort cellulaire : New roles of the Lyn tyrosine kinase in psoriasis development and cell death. (Doctoral Dissertation). Côte d'Azur. Retrieved from http://www.theses.fr/2018AZUR4027

Chicago Manual of Style (16th Edition):

Aira Diaz, Lazaro Emilio. “Nouveaux rôles de la protéine kinase Lyn dans le développement du psoriasis et dans la mort cellulaire : New roles of the Lyn tyrosine kinase in psoriasis development and cell death.” 2018. Doctoral Dissertation, Côte d'Azur. Accessed October 18, 2019. http://www.theses.fr/2018AZUR4027.

MLA Handbook (7th Edition):

Aira Diaz, Lazaro Emilio. “Nouveaux rôles de la protéine kinase Lyn dans le développement du psoriasis et dans la mort cellulaire : New roles of the Lyn tyrosine kinase in psoriasis development and cell death.” 2018. Web. 18 Oct 2019.

Vancouver:

Aira Diaz LE. Nouveaux rôles de la protéine kinase Lyn dans le développement du psoriasis et dans la mort cellulaire : New roles of the Lyn tyrosine kinase in psoriasis development and cell death. [Internet] [Doctoral dissertation]. Côte d'Azur; 2018. [cited 2019 Oct 18]. Available from: http://www.theses.fr/2018AZUR4027.

Council of Science Editors:

Aira Diaz LE. Nouveaux rôles de la protéine kinase Lyn dans le développement du psoriasis et dans la mort cellulaire : New roles of the Lyn tyrosine kinase in psoriasis development and cell death. [Doctoral Dissertation]. Côte d'Azur; 2018. Available from: http://www.theses.fr/2018AZUR4027


Texas Medical Center

30. Jeong, Yun Seong. THE ROLE OF TRAF6 PHOSPHORYLATION IN Src/TRAF6-MEDIATED IKK, JNK, Akt ACTIVATION AND TUMORIGENESIS.

Degree: PhD, 2014, Texas Medical Center

  TRAF6 E3 ligase regulates numerous essential biological processes such as innate immune response, cell survival and osteoclast differentiation. Upon activation, it mediates activation of… (more)

Subjects/Keywords: TRAF6 E3 ligase; Src tyrosine kinase; Ubiquitination; IKK; JNK; Akt; Tumorigenesis; Biological Phenomena, Cell Phenomena, and Immunity; Biology

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

APA (6th Edition):

Jeong, Y. S. (2014). THE ROLE OF TRAF6 PHOSPHORYLATION IN Src/TRAF6-MEDIATED IKK, JNK, Akt ACTIVATION AND TUMORIGENESIS. (Doctoral Dissertation). Texas Medical Center. Retrieved from http://digitalcommons.library.tmc.edu/utgsbs_dissertations/494

Chicago Manual of Style (16th Edition):

Jeong, Yun Seong. “THE ROLE OF TRAF6 PHOSPHORYLATION IN Src/TRAF6-MEDIATED IKK, JNK, Akt ACTIVATION AND TUMORIGENESIS.” 2014. Doctoral Dissertation, Texas Medical Center. Accessed October 18, 2019. http://digitalcommons.library.tmc.edu/utgsbs_dissertations/494.

MLA Handbook (7th Edition):

Jeong, Yun Seong. “THE ROLE OF TRAF6 PHOSPHORYLATION IN Src/TRAF6-MEDIATED IKK, JNK, Akt ACTIVATION AND TUMORIGENESIS.” 2014. Web. 18 Oct 2019.

Vancouver:

Jeong YS. THE ROLE OF TRAF6 PHOSPHORYLATION IN Src/TRAF6-MEDIATED IKK, JNK, Akt ACTIVATION AND TUMORIGENESIS. [Internet] [Doctoral dissertation]. Texas Medical Center; 2014. [cited 2019 Oct 18]. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/494.

Council of Science Editors:

Jeong YS. THE ROLE OF TRAF6 PHOSPHORYLATION IN Src/TRAF6-MEDIATED IKK, JNK, Akt ACTIVATION AND TUMORIGENESIS. [Doctoral Dissertation]. Texas Medical Center; 2014. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/494

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