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You searched for subject:(PIP2). Showing records 1 – 30 of 35 total matches.

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University of Rochester

1. Wojtovich, Andrew Phillip. A Mechanistic Link Between Complex II and the mitoKATP Channel in Ischemic Preconditioning.

Degree: PhD, 2010, University of Rochester

 The preservation of mitochondrial function is a major protective strategy against damage induced by cardiac ischemia reperfusion (IR) injury. An endogenous cardioprotective mechanism is ischemic… (more)

Subjects/Keywords: Mitochondria; Ischemia; Reperfusion; PIP2; Fluoxetine; Malonate

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

APA (6th Edition):

Wojtovich, A. P. (2010). A Mechanistic Link Between Complex II and the mitoKATP Channel in Ischemic Preconditioning. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/11840

Chicago Manual of Style (16th Edition):

Wojtovich, Andrew Phillip. “A Mechanistic Link Between Complex II and the mitoKATP Channel in Ischemic Preconditioning.” 2010. Doctoral Dissertation, University of Rochester. Accessed November 14, 2019. http://hdl.handle.net/1802/11840.

MLA Handbook (7th Edition):

Wojtovich, Andrew Phillip. “A Mechanistic Link Between Complex II and the mitoKATP Channel in Ischemic Preconditioning.” 2010. Web. 14 Nov 2019.

Vancouver:

Wojtovich AP. A Mechanistic Link Between Complex II and the mitoKATP Channel in Ischemic Preconditioning. [Internet] [Doctoral dissertation]. University of Rochester; 2010. [cited 2019 Nov 14]. Available from: http://hdl.handle.net/1802/11840.

Council of Science Editors:

Wojtovich AP. A Mechanistic Link Between Complex II and the mitoKATP Channel in Ischemic Preconditioning. [Doctoral Dissertation]. University of Rochester; 2010. Available from: http://hdl.handle.net/1802/11840

2. Chouaki-Benmansour, Nassima. Analyse du rôle des PIP2 dans l'initiation de la signalisation TCR et l'activation lymphocytaire : Regulation of the T cell receptor membrane dynamics and triggering mechanism by phosphatidylinositol 4,5-bisphosphate.

Degree: Docteur es, Immunologie, 2014, Aix Marseille Université

L'activation des lymphocytes T est un événement fondamental de la réponse immunitaire adaptative. Elle est déclenchée par la transduction du signal médiée par le complexe… (more)

Subjects/Keywords: Tcr; Cd3; Pip2; Cellule T; Activation; Tcr; Cd3; Pip2; T Cell; Activation; 571

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APA (6th Edition):

Chouaki-Benmansour, N. (2014). Analyse du rôle des PIP2 dans l'initiation de la signalisation TCR et l'activation lymphocytaire : Regulation of the T cell receptor membrane dynamics and triggering mechanism by phosphatidylinositol 4,5-bisphosphate. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2014AIXM4052

Chicago Manual of Style (16th Edition):

Chouaki-Benmansour, Nassima. “Analyse du rôle des PIP2 dans l'initiation de la signalisation TCR et l'activation lymphocytaire : Regulation of the T cell receptor membrane dynamics and triggering mechanism by phosphatidylinositol 4,5-bisphosphate.” 2014. Doctoral Dissertation, Aix Marseille Université. Accessed November 14, 2019. http://www.theses.fr/2014AIXM4052.

MLA Handbook (7th Edition):

Chouaki-Benmansour, Nassima. “Analyse du rôle des PIP2 dans l'initiation de la signalisation TCR et l'activation lymphocytaire : Regulation of the T cell receptor membrane dynamics and triggering mechanism by phosphatidylinositol 4,5-bisphosphate.” 2014. Web. 14 Nov 2019.

Vancouver:

Chouaki-Benmansour N. Analyse du rôle des PIP2 dans l'initiation de la signalisation TCR et l'activation lymphocytaire : Regulation of the T cell receptor membrane dynamics and triggering mechanism by phosphatidylinositol 4,5-bisphosphate. [Internet] [Doctoral dissertation]. Aix Marseille Université 2014. [cited 2019 Nov 14]. Available from: http://www.theses.fr/2014AIXM4052.

Council of Science Editors:

Chouaki-Benmansour N. Analyse du rôle des PIP2 dans l'initiation de la signalisation TCR et l'activation lymphocytaire : Regulation of the T cell receptor membrane dynamics and triggering mechanism by phosphatidylinositol 4,5-bisphosphate. [Doctoral Dissertation]. Aix Marseille Université 2014. Available from: http://www.theses.fr/2014AIXM4052


The Ohio State University

3. Huang, Yongcheng. Structural functional analysis of disabled-1 in regulation of reelin signaling.

Degree: PhD, Pharmacy, 2007, The Ohio State University

 Reelin is a critical protein required for proper lamination of the brain. Dab1 relays Reelin signaling through its interaction with the Reelin receptors VLDLR and… (more)

Subjects/Keywords: Reelin; Dab1; VLDLR; ApoER2; tyrosine; serine; phosphorylation; degradation; PIP2; PKC

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APA (6th Edition):

Huang, Y. (2007). Structural functional analysis of disabled-1 in regulation of reelin signaling. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1193754102

Chicago Manual of Style (16th Edition):

Huang, Yongcheng. “Structural functional analysis of disabled-1 in regulation of reelin signaling.” 2007. Doctoral Dissertation, The Ohio State University. Accessed November 14, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1193754102.

MLA Handbook (7th Edition):

Huang, Yongcheng. “Structural functional analysis of disabled-1 in regulation of reelin signaling.” 2007. Web. 14 Nov 2019.

Vancouver:

Huang Y. Structural functional analysis of disabled-1 in regulation of reelin signaling. [Internet] [Doctoral dissertation]. The Ohio State University; 2007. [cited 2019 Nov 14]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1193754102.

Council of Science Editors:

Huang Y. Structural functional analysis of disabled-1 in regulation of reelin signaling. [Doctoral Dissertation]. The Ohio State University; 2007. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1193754102


Cleveland State University

4. Bakhautdin, Esen. Structural Studies of Talin-mediated Integrin Activation.

Degree: PhD, College of Science, 2009, Cleveland State University

  Activation of heterodimeric (alpha/beta) integrin transmembrane receptors by the cytoskeletal protein talin is essential for many important cell adhesive responses including cell-extracellular matrix contact,… (more)

Subjects/Keywords: Biochemistry; Biology; Biophysics; talin; integrin; integrin activation; PIP2

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APA (6th Edition):

Bakhautdin, E. (2009). Structural Studies of Talin-mediated Integrin Activation. (Doctoral Dissertation). Cleveland State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=csu1268240445

Chicago Manual of Style (16th Edition):

Bakhautdin, Esen. “Structural Studies of Talin-mediated Integrin Activation.” 2009. Doctoral Dissertation, Cleveland State University. Accessed November 14, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=csu1268240445.

MLA Handbook (7th Edition):

Bakhautdin, Esen. “Structural Studies of Talin-mediated Integrin Activation.” 2009. Web. 14 Nov 2019.

Vancouver:

Bakhautdin E. Structural Studies of Talin-mediated Integrin Activation. [Internet] [Doctoral dissertation]. Cleveland State University; 2009. [cited 2019 Nov 14]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=csu1268240445.

Council of Science Editors:

Bakhautdin E. Structural Studies of Talin-mediated Integrin Activation. [Doctoral Dissertation]. Cleveland State University; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=csu1268240445


Penn State University

5. Li, Xiaofan. Evolution origins and Pip2 modulation of voltage-gated K+ channels.

Degree: PhD, Molecular, Cellular and Integrative Biosciences, 2015, Penn State University

 Voltage-gated K+ channels are important regulators of neuronal excitability. Bilaterians have eight functionally distinct Voltage-gated K+ channel subfamilies: Shaker, Shab, Shaw, Shal, KCNQ, Eag, Erg… (more)

Subjects/Keywords: potassium channel; ion channel; evolution; phosphoinositide; PIP2; excitability; ctenophore; nematostella

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APA (6th Edition):

Li, X. (2015). Evolution origins and Pip2 modulation of voltage-gated K+ channels. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/26772

Chicago Manual of Style (16th Edition):

Li, Xiaofan. “Evolution origins and Pip2 modulation of voltage-gated K+ channels.” 2015. Doctoral Dissertation, Penn State University. Accessed November 14, 2019. https://etda.libraries.psu.edu/catalog/26772.

MLA Handbook (7th Edition):

Li, Xiaofan. “Evolution origins and Pip2 modulation of voltage-gated K+ channels.” 2015. Web. 14 Nov 2019.

Vancouver:

Li X. Evolution origins and Pip2 modulation of voltage-gated K+ channels. [Internet] [Doctoral dissertation]. Penn State University; 2015. [cited 2019 Nov 14]. Available from: https://etda.libraries.psu.edu/catalog/26772.

Council of Science Editors:

Li X. Evolution origins and Pip2 modulation of voltage-gated K+ channels. [Doctoral Dissertation]. Penn State University; 2015. Available from: https://etda.libraries.psu.edu/catalog/26772


University of California – San Diego

6. Vasquez, Alexis Marie. Phospholipase A2 enzymes: A multidisciplinary approach to studying the mechanisms of activation and inhibition.

Degree: Chemistry, 2017, University of California – San Diego

 Phospholipase A2 is a superfamily of enzymes that play a major role in cellular homeostasis and disease development. This class of enzymes acts on a… (more)

Subjects/Keywords: Biochemistry; activation; ATP; computational; inhibitor; phospholipase A2; PIP2

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APA (6th Edition):

Vasquez, A. M. (2017). Phospholipase A2 enzymes: A multidisciplinary approach to studying the mechanisms of activation and inhibition. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/39k3n6gz

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):

Vasquez, Alexis Marie. “Phospholipase A2 enzymes: A multidisciplinary approach to studying the mechanisms of activation and inhibition.” 2017. Thesis, University of California – San Diego. Accessed November 14, 2019. http://www.escholarship.org/uc/item/39k3n6gz.

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

MLA Handbook (7th Edition):

Vasquez, Alexis Marie. “Phospholipase A2 enzymes: A multidisciplinary approach to studying the mechanisms of activation and inhibition.” 2017. Web. 14 Nov 2019.

Vancouver:

Vasquez AM. Phospholipase A2 enzymes: A multidisciplinary approach to studying the mechanisms of activation and inhibition. [Internet] [Thesis]. University of California – San Diego; 2017. [cited 2019 Nov 14]. Available from: http://www.escholarship.org/uc/item/39k3n6gz.

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

Council of Science Editors:

Vasquez AM. Phospholipase A2 enzymes: A multidisciplinary approach to studying the mechanisms of activation and inhibition. [Thesis]. University of California – San Diego; 2017. Available from: http://www.escholarship.org/uc/item/39k3n6gz

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


University of Southern California

7. Zhang, Zheng. Gating mechanisms of transient receptor potential ion channels TRPM5 and TRPM4 in native and heterologous cells.

Degree: PhD, Neuroscience, 2007, University of Southern California

 There are 28 mammalian members of the Transient Receptor Potential (TRP) family of ion channels. Two closely related members TRPM4 and TRPM5 have been shown… (more)

Subjects/Keywords: TRP channel; taste; PIP2

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APA (6th Edition):

Zhang, Z. (2007). Gating mechanisms of transient receptor potential ion channels TRPM5 and TRPM4 in native and heterologous cells. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/557092/rec/2963

Chicago Manual of Style (16th Edition):

Zhang, Zheng. “Gating mechanisms of transient receptor potential ion channels TRPM5 and TRPM4 in native and heterologous cells.” 2007. Doctoral Dissertation, University of Southern California. Accessed November 14, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/557092/rec/2963.

MLA Handbook (7th Edition):

Zhang, Zheng. “Gating mechanisms of transient receptor potential ion channels TRPM5 and TRPM4 in native and heterologous cells.” 2007. Web. 14 Nov 2019.

Vancouver:

Zhang Z. Gating mechanisms of transient receptor potential ion channels TRPM5 and TRPM4 in native and heterologous cells. [Internet] [Doctoral dissertation]. University of Southern California; 2007. [cited 2019 Nov 14]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/557092/rec/2963.

Council of Science Editors:

Zhang Z. Gating mechanisms of transient receptor potential ion channels TRPM5 and TRPM4 in native and heterologous cells. [Doctoral Dissertation]. University of Southern California; 2007. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/557092/rec/2963


University of Illinois – Chicago

8. Mihaylov, Miroslav N. X-ray Investigations of Mixed Charge Amphiphilic Systems.

Degree: 2016, University of Illinois – Chicago

 The liquid vapor interface is of a fundamental importance for a wide range of applications from physics, chemistry and biology to material science and nanotechnology.… (more)

Subjects/Keywords: X-ray Reflectivity; Langmuir Films; Catanionic Systems; Surface Science; PIP2

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APA (6th Edition):

Mihaylov, M. N. (2016). X-ray Investigations of Mixed Charge Amphiphilic Systems. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/20197

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):

Mihaylov, Miroslav N. “X-ray Investigations of Mixed Charge Amphiphilic Systems.” 2016. Thesis, University of Illinois – Chicago. Accessed November 14, 2019. http://hdl.handle.net/10027/20197.

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

MLA Handbook (7th Edition):

Mihaylov, Miroslav N. “X-ray Investigations of Mixed Charge Amphiphilic Systems.” 2016. Web. 14 Nov 2019.

Vancouver:

Mihaylov MN. X-ray Investigations of Mixed Charge Amphiphilic Systems. [Internet] [Thesis]. University of Illinois – Chicago; 2016. [cited 2019 Nov 14]. Available from: http://hdl.handle.net/10027/20197.

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

Council of Science Editors:

Mihaylov MN. X-ray Investigations of Mixed Charge Amphiphilic Systems. [Thesis]. University of Illinois – Chicago; 2016. Available from: http://hdl.handle.net/10027/20197

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

9. TRAN, HOANG MAI. A study on PIP5Kalpha degradation by Nedd4-1-mediated ubiquitination.

Degree: 2016, Ajou University

Nedd4-1에 의해 매개되는 유비퀴틴화에 의한 PIP5Kalpha 분해에 관한 연구 포스파티딜이노시톨 4,5-비스포스페이트(PIP2)는 세포표면에서 일어나는 베시클수송, 액틴세포골격 역동성, 세포신호전달 등 다양한 세포막 현상들을 조절하는 중요한 지질매개인자이며 따라서… (more)

Subjects/Keywords: PIP5Kα

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APA (6th Edition):

TRAN, H. M. (2016). A study on PIP5Kalpha degradation by Nedd4-1-mediated ubiquitination. (Thesis). Ajou University. Retrieved from http://repository.ajou.ac.kr/handle/201003/13018 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000021983

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):

TRAN, HOANG MAI. “A study on PIP5Kalpha degradation by Nedd4-1-mediated ubiquitination.” 2016. Thesis, Ajou University. Accessed November 14, 2019. http://repository.ajou.ac.kr/handle/201003/13018 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000021983.

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

MLA Handbook (7th Edition):

TRAN, HOANG MAI. “A study on PIP5Kalpha degradation by Nedd4-1-mediated ubiquitination.” 2016. Web. 14 Nov 2019.

Vancouver:

TRAN HM. A study on PIP5Kalpha degradation by Nedd4-1-mediated ubiquitination. [Internet] [Thesis]. Ajou University; 2016. [cited 2019 Nov 14]. Available from: http://repository.ajou.ac.kr/handle/201003/13018 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000021983.

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

Council of Science Editors:

TRAN HM. A study on PIP5Kalpha degradation by Nedd4-1-mediated ubiquitination. [Thesis]. Ajou University; 2016. Available from: http://repository.ajou.ac.kr/handle/201003/13018 ; http://dcoll.ajou.ac.kr:9080/dcollection/jsp/common/DcLoOrgPer.jsp?sItemId=000000021983

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


Vanderbilt University

10. Jowhar, Dawit Kamil. Characterizing the mechanisms that regulate cell polarity during eukaryotic chemotaxis.

Degree: PhD, Biological Sciences, 2013, Vanderbilt University

 Cells that are migrating in a chemical gradient display a polarized distribution of signaling and cytoskeletal components. We have investigated the mechanism of polarity establishment… (more)

Subjects/Keywords: Dictyostelium; cell polarity; Ras; PTEN. microtubules; microfluidics; actin; PIP2

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APA (6th Edition):

Jowhar, D. K. (2013). Characterizing the mechanisms that regulate cell polarity during eukaryotic chemotaxis. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-07182013-092411/ ;

Chicago Manual of Style (16th Edition):

Jowhar, Dawit Kamil. “Characterizing the mechanisms that regulate cell polarity during eukaryotic chemotaxis.” 2013. Doctoral Dissertation, Vanderbilt University. Accessed November 14, 2019. http://etd.library.vanderbilt.edu/available/etd-07182013-092411/ ;.

MLA Handbook (7th Edition):

Jowhar, Dawit Kamil. “Characterizing the mechanisms that regulate cell polarity during eukaryotic chemotaxis.” 2013. Web. 14 Nov 2019.

Vancouver:

Jowhar DK. Characterizing the mechanisms that regulate cell polarity during eukaryotic chemotaxis. [Internet] [Doctoral dissertation]. Vanderbilt University; 2013. [cited 2019 Nov 14]. Available from: http://etd.library.vanderbilt.edu/available/etd-07182013-092411/ ;.

Council of Science Editors:

Jowhar DK. Characterizing the mechanisms that regulate cell polarity during eukaryotic chemotaxis. [Doctoral Dissertation]. Vanderbilt University; 2013. Available from: http://etd.library.vanderbilt.edu/available/etd-07182013-092411/ ;


Virginia Commonwealth University

11. Adney, Scott. Protein Kinase C Dependent Inhibition of Kir3.2 (GIRK2) Channel Activity and Its Molecular Determinants.

Degree: PhD, Physiology, 2013, Virginia Commonwealth University

 Inwardly rectifying potassium (Kir) channels are critically important for regulating resting membrane potential in excitable cells, a job underscored by the severe pathophysiology associated with… (more)

Subjects/Keywords: PKC; GIRK; PIP2; Kir3; potassium channel; Life Sciences; Physiology

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APA (6th Edition):

Adney, S. (2013). Protein Kinase C Dependent Inhibition of Kir3.2 (GIRK2) Channel Activity and Its Molecular Determinants. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/3214

Chicago Manual of Style (16th Edition):

Adney, Scott. “Protein Kinase C Dependent Inhibition of Kir3.2 (GIRK2) Channel Activity and Its Molecular Determinants.” 2013. Doctoral Dissertation, Virginia Commonwealth University. Accessed November 14, 2019. https://scholarscompass.vcu.edu/etd/3214.

MLA Handbook (7th Edition):

Adney, Scott. “Protein Kinase C Dependent Inhibition of Kir3.2 (GIRK2) Channel Activity and Its Molecular Determinants.” 2013. Web. 14 Nov 2019.

Vancouver:

Adney S. Protein Kinase C Dependent Inhibition of Kir3.2 (GIRK2) Channel Activity and Its Molecular Determinants. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2013. [cited 2019 Nov 14]. Available from: https://scholarscompass.vcu.edu/etd/3214.

Council of Science Editors:

Adney S. Protein Kinase C Dependent Inhibition of Kir3.2 (GIRK2) Channel Activity and Its Molecular Determinants. [Doctoral Dissertation]. Virginia Commonwealth University; 2013. Available from: https://scholarscompass.vcu.edu/etd/3214


University of Pennsylvania

12. Wang, Yu-Hsiu. Divalent Cation- and Cholesterol-Induced Perturbation in Pip2 Lateral Organization in Model Membranes - Cluster formation, Phase Partitioning, and PiP2-Protein interactions.

Degree: 2013, University of Pennsylvania

 The physiological importance of polyphosphoinositides (PPI), and especially phosphatidylinositol 4,5-bisphosphate (PIP2), has been documented in numerous reports. As large number of proteins bind PIP2 but… (more)

Subjects/Keywords: actin; Ca; cholesterol; cluster; gelsolin; PIP2; Biochemistry; Biophysics

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APA (6th Edition):

Wang, Y. (2013). Divalent Cation- and Cholesterol-Induced Perturbation in Pip2 Lateral Organization in Model Membranes - Cluster formation, Phase Partitioning, and PiP2-Protein interactions. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/939

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, Yu-Hsiu. “Divalent Cation- and Cholesterol-Induced Perturbation in Pip2 Lateral Organization in Model Membranes - Cluster formation, Phase Partitioning, and PiP2-Protein interactions.” 2013. Thesis, University of Pennsylvania. Accessed November 14, 2019. https://repository.upenn.edu/edissertations/939.

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

MLA Handbook (7th Edition):

Wang, Yu-Hsiu. “Divalent Cation- and Cholesterol-Induced Perturbation in Pip2 Lateral Organization in Model Membranes - Cluster formation, Phase Partitioning, and PiP2-Protein interactions.” 2013. Web. 14 Nov 2019.

Vancouver:

Wang Y. Divalent Cation- and Cholesterol-Induced Perturbation in Pip2 Lateral Organization in Model Membranes - Cluster formation, Phase Partitioning, and PiP2-Protein interactions. [Internet] [Thesis]. University of Pennsylvania; 2013. [cited 2019 Nov 14]. Available from: https://repository.upenn.edu/edissertations/939.

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. Divalent Cation- and Cholesterol-Induced Perturbation in Pip2 Lateral Organization in Model Membranes - Cluster formation, Phase Partitioning, and PiP2-Protein interactions. [Thesis]. University of Pennsylvania; 2013. Available from: https://repository.upenn.edu/edissertations/939

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

13. Rodriguez Peña, Marcelo Javier. Función de la proteína MARCKS en la exocitosis acrosomal de espermatozoides humanos.

Degree: Farmacia y Bioquímica, 2014, Universidad de Buenos Aires

Acrosomal exocytosis is an absolute requirement for physiological fertilization. In this thesis, we report that MARCKS is expressed in human spermatozoa. \nCalcium- and phorbol ester-triggered… (more)

Subjects/Keywords: MARCKS; Pip2; Exotosis Acrosomal; Espermatozoides; Ciencia de la vida

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APA (6th Edition):

Rodriguez Peña, M. J. (2014). Función de la proteína MARCKS en la exocitosis acrosomal de espermatozoides humanos. (Thesis). Universidad de Buenos Aires. Retrieved from http://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=posgrauba&cl=CL1&d=HWA_1340 ; http://repositoriouba.sisbi.uba.ar/gsdl/collect/posgrauba/index/assoc/HWA_1340.dir/1340.PDF

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):

Rodriguez Peña, Marcelo Javier. “Función de la proteína MARCKS en la exocitosis acrosomal de espermatozoides humanos.” 2014. Thesis, Universidad de Buenos Aires. Accessed November 14, 2019. http://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=posgrauba&cl=CL1&d=HWA_1340 ; http://repositoriouba.sisbi.uba.ar/gsdl/collect/posgrauba/index/assoc/HWA_1340.dir/1340.PDF.

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

MLA Handbook (7th Edition):

Rodriguez Peña, Marcelo Javier. “Función de la proteína MARCKS en la exocitosis acrosomal de espermatozoides humanos.” 2014. Web. 14 Nov 2019.

Vancouver:

Rodriguez Peña MJ. Función de la proteína MARCKS en la exocitosis acrosomal de espermatozoides humanos. [Internet] [Thesis]. Universidad de Buenos Aires; 2014. [cited 2019 Nov 14]. Available from: http://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=posgrauba&cl=CL1&d=HWA_1340 ; http://repositoriouba.sisbi.uba.ar/gsdl/collect/posgrauba/index/assoc/HWA_1340.dir/1340.PDF.

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

Council of Science Editors:

Rodriguez Peña MJ. Función de la proteína MARCKS en la exocitosis acrosomal de espermatozoides humanos. [Thesis]. Universidad de Buenos Aires; 2014. Available from: http://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=posgrauba&cl=CL1&d=HWA_1340 ; http://repositoriouba.sisbi.uba.ar/gsdl/collect/posgrauba/index/assoc/HWA_1340.dir/1340.PDF

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

14. Kasimova, Marina. Modulation de canaux potassiques sensibles au voltage par le phosphatidylinositol-4,5-bisphosphate : Modulation of voltage-gated potassium channels by phosphatidylinositol-4,5-bisphosphate.

Degree: Docteur es, Chimie, 2014, Université de Lorraine; Moskovskij gosudarstvennyj universitet imeni M. V. Lomonosova

Les canaux potassiques (Kv) dépendants du voltage sont des protéines transmembranaires qui permettent le flux passif d’ions potassium à travers une membrane plasmique lorsque celle-ci… (more)

Subjects/Keywords: Canaux potassiques sensibles au voltage; Domaine sensible à la tension; Kv1.2; Kv7.1; Pip2; Couplage; Voltage-Gated potassium channels; Voltage sensor domain; Kv1.2; Kv7.1; Pip2; Coupling; 571.643 74

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

APA (6th Edition):

Kasimova, M. (2014). Modulation de canaux potassiques sensibles au voltage par le phosphatidylinositol-4,5-bisphosphate : Modulation of voltage-gated potassium channels by phosphatidylinositol-4,5-bisphosphate. (Doctoral Dissertation). Université de Lorraine; Moskovskij gosudarstvennyj universitet imeni M. V. Lomonosova. Retrieved from http://www.theses.fr/2014LORR0204

Chicago Manual of Style (16th Edition):

Kasimova, Marina. “Modulation de canaux potassiques sensibles au voltage par le phosphatidylinositol-4,5-bisphosphate : Modulation of voltage-gated potassium channels by phosphatidylinositol-4,5-bisphosphate.” 2014. Doctoral Dissertation, Université de Lorraine; Moskovskij gosudarstvennyj universitet imeni M. V. Lomonosova. Accessed November 14, 2019. http://www.theses.fr/2014LORR0204.

MLA Handbook (7th Edition):

Kasimova, Marina. “Modulation de canaux potassiques sensibles au voltage par le phosphatidylinositol-4,5-bisphosphate : Modulation of voltage-gated potassium channels by phosphatidylinositol-4,5-bisphosphate.” 2014. Web. 14 Nov 2019.

Vancouver:

Kasimova M. Modulation de canaux potassiques sensibles au voltage par le phosphatidylinositol-4,5-bisphosphate : Modulation of voltage-gated potassium channels by phosphatidylinositol-4,5-bisphosphate. [Internet] [Doctoral dissertation]. Université de Lorraine; Moskovskij gosudarstvennyj universitet imeni M. V. Lomonosova; 2014. [cited 2019 Nov 14]. Available from: http://www.theses.fr/2014LORR0204.

Council of Science Editors:

Kasimova M. Modulation de canaux potassiques sensibles au voltage par le phosphatidylinositol-4,5-bisphosphate : Modulation of voltage-gated potassium channels by phosphatidylinositol-4,5-bisphosphate. [Doctoral Dissertation]. Université de Lorraine; Moskovskij gosudarstvennyj universitet imeni M. V. Lomonosova; 2014. Available from: http://www.theses.fr/2014LORR0204


University of Southern California

15. Daniels, Richard Luke. Functional regulation of the neuronal cold sensor TRPM8.

Degree: PhD, Neuroscience, 2009, University of Southern California

 The ability to detect cold temperatures is critical for survival. Cold-sensing neurons play important roles in thermosensation, pain sensation (nociception), thermoregulation, cooling-induced analgesia, and smooth… (more)

Subjects/Keywords: molecular biology; neuroscience; sensory biology; somatosensation; temperature; TRPM8; ion channels; physiology; PLC; PIP2; cold; cool

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

APA (6th Edition):

Daniels, R. L. (2009). Functional regulation of the neuronal cold sensor TRPM8. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/253414/rec/2942

Chicago Manual of Style (16th Edition):

Daniels, Richard Luke. “Functional regulation of the neuronal cold sensor TRPM8.” 2009. Doctoral Dissertation, University of Southern California. Accessed November 14, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/253414/rec/2942.

MLA Handbook (7th Edition):

Daniels, Richard Luke. “Functional regulation of the neuronal cold sensor TRPM8.” 2009. Web. 14 Nov 2019.

Vancouver:

Daniels RL. Functional regulation of the neuronal cold sensor TRPM8. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2019 Nov 14]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/253414/rec/2942.

Council of Science Editors:

Daniels RL. Functional regulation of the neuronal cold sensor TRPM8. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/253414/rec/2942


University of Saskatchewan

16. Bansal, Vimal 1977-. Characterization of a novel osmotically-evoked phospholipase C pathway and Slack and Slick-mediated Na+-activated K+ currents in rat supraoptic neurons.

Degree: 2016, University of Saskatchewan

 The magnocellular neurosecretory cells (MNCs) of the hypothalamus are important players in systemic osmoregulation that strives to stabilize water and salt levels inside the mammalian… (more)

Subjects/Keywords: Phospholipase C; MNCs; supraoptic; TRPV1; Calcium; Slack; Slick; Sodium activated potassium channel; KNa; PIP2

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APA (6th Edition):

Bansal, V. 1. (2016). Characterization of a novel osmotically-evoked phospholipase C pathway and Slack and Slick-mediated Na+-activated K+ currents in rat supraoptic neurons. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/7417

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):

Bansal, Vimal 1977-. “Characterization of a novel osmotically-evoked phospholipase C pathway and Slack and Slick-mediated Na+-activated K+ currents in rat supraoptic neurons.” 2016. Thesis, University of Saskatchewan. Accessed November 14, 2019. http://hdl.handle.net/10388/7417.

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

MLA Handbook (7th Edition):

Bansal, Vimal 1977-. “Characterization of a novel osmotically-evoked phospholipase C pathway and Slack and Slick-mediated Na+-activated K+ currents in rat supraoptic neurons.” 2016. Web. 14 Nov 2019.

Vancouver:

Bansal V1. Characterization of a novel osmotically-evoked phospholipase C pathway and Slack and Slick-mediated Na+-activated K+ currents in rat supraoptic neurons. [Internet] [Thesis]. University of Saskatchewan; 2016. [cited 2019 Nov 14]. Available from: http://hdl.handle.net/10388/7417.

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

Council of Science Editors:

Bansal V1. Characterization of a novel osmotically-evoked phospholipase C pathway and Slack and Slick-mediated Na+-activated K+ currents in rat supraoptic neurons. [Thesis]. University of Saskatchewan; 2016. Available from: http://hdl.handle.net/10388/7417

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


Universitat Pompeu Fabra

17. Mrkonjić, Sanela, 1983-. TRPV4 channel regulation and involvement in cell motility.

Degree: Departament de Ciències Experimentals i de la Salut, 2014, Universitat Pompeu Fabra

 El canal TRPV4 es un canal catiónico capaz de generar señales intracelulares de Ca2+ en diversos tejidos. La participación del canal TRPV4 en procesos de… (more)

Subjects/Keywords: Calcium; TRPV4; Hypotonicity; PIP2; Cell migration; Foal adhesions; Calci; Hipotonicitat; Migració cel·lular; Adhesions focals; 576

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APA (6th Edition):

Mrkonjić, Sanela, 1. (2014). TRPV4 channel regulation and involvement in cell motility. (Thesis). Universitat Pompeu Fabra. Retrieved from http://hdl.handle.net/10803/300754

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):

Mrkonjić, Sanela, 1983-. “TRPV4 channel regulation and involvement in cell motility.” 2014. Thesis, Universitat Pompeu Fabra. Accessed November 14, 2019. http://hdl.handle.net/10803/300754.

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

MLA Handbook (7th Edition):

Mrkonjić, Sanela, 1983-. “TRPV4 channel regulation and involvement in cell motility.” 2014. Web. 14 Nov 2019.

Vancouver:

Mrkonjić, Sanela 1. TRPV4 channel regulation and involvement in cell motility. [Internet] [Thesis]. Universitat Pompeu Fabra; 2014. [cited 2019 Nov 14]. Available from: http://hdl.handle.net/10803/300754.

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

Council of Science Editors:

Mrkonjić, Sanela 1. TRPV4 channel regulation and involvement in cell motility. [Thesis]. Universitat Pompeu Fabra; 2014. Available from: http://hdl.handle.net/10803/300754

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


Virginia Commonwealth University

18. Ha, Junghoon. Ion Channel Modulation by Photocaged Dioctanoyl PIP2.

Degree: MS, Physiology, 2009, Virginia Commonwealth University

 Phosphatidylinositol bisphosphate (PIP2) directly regulates electrophysiological activity in a diverse family of ion channels whether the effect is stimulatory or inhibitory. Much has been unveiled… (more)

Subjects/Keywords: PIP2; Ion Channel; Life Sciences; Physiology

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APA (6th Edition):

Ha, J. (2009). Ion Channel Modulation by Photocaged Dioctanoyl PIP2. (Thesis). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/1930

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):

Ha, Junghoon. “Ion Channel Modulation by Photocaged Dioctanoyl PIP2.” 2009. Thesis, Virginia Commonwealth University. Accessed November 14, 2019. https://scholarscompass.vcu.edu/etd/1930.

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

MLA Handbook (7th Edition):

Ha, Junghoon. “Ion Channel Modulation by Photocaged Dioctanoyl PIP2.” 2009. Web. 14 Nov 2019.

Vancouver:

Ha J. Ion Channel Modulation by Photocaged Dioctanoyl PIP2. [Internet] [Thesis]. Virginia Commonwealth University; 2009. [cited 2019 Nov 14]. Available from: https://scholarscompass.vcu.edu/etd/1930.

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

Council of Science Editors:

Ha J. Ion Channel Modulation by Photocaged Dioctanoyl PIP2. [Thesis]. Virginia Commonwealth University; 2009. Available from: https://scholarscompass.vcu.edu/etd/1930

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


University of Pennsylvania

19. Slochower, David. Multiscale Simulations of Phosphatidylinositol Bisphosphate: Understanding Its Biological Role Through Physical Chemistry.

Degree: 2014, University of Pennsylvania

 Proper functionality of biological membranes depends on the regulation of lipid composition and localization. Spatial localization of molecules within the lipid bilayer depends on both… (more)

Subjects/Keywords: Bilayers; Divalent Cations; Membranes; Molecular Dynamics; Phosphatidylinositol bisphosphate; PIP2; Biochemistry; Biophysics; Physical Chemistry

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APA (6th Edition):

Slochower, D. (2014). Multiscale Simulations of Phosphatidylinositol Bisphosphate: Understanding Its Biological Role Through Physical Chemistry. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/1445

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):

Slochower, David. “Multiscale Simulations of Phosphatidylinositol Bisphosphate: Understanding Its Biological Role Through Physical Chemistry.” 2014. Thesis, University of Pennsylvania. Accessed November 14, 2019. https://repository.upenn.edu/edissertations/1445.

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

MLA Handbook (7th Edition):

Slochower, David. “Multiscale Simulations of Phosphatidylinositol Bisphosphate: Understanding Its Biological Role Through Physical Chemistry.” 2014. Web. 14 Nov 2019.

Vancouver:

Slochower D. Multiscale Simulations of Phosphatidylinositol Bisphosphate: Understanding Its Biological Role Through Physical Chemistry. [Internet] [Thesis]. University of Pennsylvania; 2014. [cited 2019 Nov 14]. Available from: https://repository.upenn.edu/edissertations/1445.

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

Council of Science Editors:

Slochower D. Multiscale Simulations of Phosphatidylinositol Bisphosphate: Understanding Its Biological Role Through Physical Chemistry. [Thesis]. University of Pennsylvania; 2014. Available from: https://repository.upenn.edu/edissertations/1445

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

20. Jozefkowicz, Cintia. Estudio de acuaporinas vegetales pertenecientes a la familia PIP : análisis de las relaciones estructura-función de homo-tetrámeros y tetrámeros mixtos PIP1-PIP2.

Degree: Farmacia y Bioquímica, 2016, Universidad de Buenos Aires

In the present Thesis we evaluated the capacity of plant aquaporins belonging to the PIP subfamily to assembly as hetero-tetramers. With this aim, we investigated… (more)

Subjects/Keywords: PIP; PIP1; PIP2; Acuaporina; Membrana plasmáticas; Homotetrámeros; Tetrámeros; Ciencia de la vida

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APA (6th Edition):

Jozefkowicz, C. (2016). Estudio de acuaporinas vegetales pertenecientes a la familia PIP : análisis de las relaciones estructura-función de homo-tetrámeros y tetrámeros mixtos PIP1-PIP2. (Thesis). Universidad de Buenos Aires. Retrieved from http://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=posgrauba&cl=CL1&d=HWA_1175 ; http://repositoriouba.sisbi.uba.ar/gsdl/collect/posgrauba/index/assoc/HWA_1175.dir/1175.PDF

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):

Jozefkowicz, Cintia. “Estudio de acuaporinas vegetales pertenecientes a la familia PIP : análisis de las relaciones estructura-función de homo-tetrámeros y tetrámeros mixtos PIP1-PIP2.” 2016. Thesis, Universidad de Buenos Aires. Accessed November 14, 2019. http://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=posgrauba&cl=CL1&d=HWA_1175 ; http://repositoriouba.sisbi.uba.ar/gsdl/collect/posgrauba/index/assoc/HWA_1175.dir/1175.PDF.

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

MLA Handbook (7th Edition):

Jozefkowicz, Cintia. “Estudio de acuaporinas vegetales pertenecientes a la familia PIP : análisis de las relaciones estructura-función de homo-tetrámeros y tetrámeros mixtos PIP1-PIP2.” 2016. Web. 14 Nov 2019.

Vancouver:

Jozefkowicz C. Estudio de acuaporinas vegetales pertenecientes a la familia PIP : análisis de las relaciones estructura-función de homo-tetrámeros y tetrámeros mixtos PIP1-PIP2. [Internet] [Thesis]. Universidad de Buenos Aires; 2016. [cited 2019 Nov 14]. Available from: http://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=posgrauba&cl=CL1&d=HWA_1175 ; http://repositoriouba.sisbi.uba.ar/gsdl/collect/posgrauba/index/assoc/HWA_1175.dir/1175.PDF.

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

Council of Science Editors:

Jozefkowicz C. Estudio de acuaporinas vegetales pertenecientes a la familia PIP : análisis de las relaciones estructura-función de homo-tetrámeros y tetrámeros mixtos PIP1-PIP2. [Thesis]. Universidad de Buenos Aires; 2016. Available from: http://repositoriouba.sisbi.uba.ar/gsdl/cgi-bin/library.cgi?a=d&c=posgrauba&cl=CL1&d=HWA_1175 ; http://repositoriouba.sisbi.uba.ar/gsdl/collect/posgrauba/index/assoc/HWA_1175.dir/1175.PDF

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

21. Ντουχανιάρη, Αλεξάνδρα. Ρόλος και μηχανισμοί διακυτταρικών συνδέσεων στη λειτουργία του ενδοθηλιακού φραγμού.

Degree: 2010, University of Ioannina; Πανεπιστήμιο Ιωαννίνων

This work focuses on the study of the properties of transmembrane and juxtamembrane domain of ve-cadherin (ve-c) in a special lipid microenvironment and on its… (more)

Subjects/Keywords: Ενδοθήλιο; Αγγειακή ενδοθηλιακή καδερίνη; Φωσφολιπίδια; Λιπιδιακές μικροπεριοχές; Κυτταροσκελετός ακτίνης; Θρομβίνη; Endothelium; Cadherin; PIP2; Rho-gtpases; CDc42; IQGAP; Mikrotubules; Actin

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APA (6th Edition):

Ντουχανιάρη, . . (2010). Ρόλος και μηχανισμοί διακυτταρικών συνδέσεων στη λειτουργία του ενδοθηλιακού φραγμού. (Thesis). University of Ioannina; Πανεπιστήμιο Ιωαννίνων. Retrieved from http://hdl.handle.net/10442/hedi/23270

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):

Ντουχανιάρη, Αλεξάνδρα. “Ρόλος και μηχανισμοί διακυτταρικών συνδέσεων στη λειτουργία του ενδοθηλιακού φραγμού.” 2010. Thesis, University of Ioannina; Πανεπιστήμιο Ιωαννίνων. Accessed November 14, 2019. http://hdl.handle.net/10442/hedi/23270.

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

MLA Handbook (7th Edition):

Ντουχανιάρη, Αλεξάνδρα. “Ρόλος και μηχανισμοί διακυτταρικών συνδέσεων στη λειτουργία του ενδοθηλιακού φραγμού.” 2010. Web. 14 Nov 2019.

Vancouver:

Ντουχανιάρη . Ρόλος και μηχανισμοί διακυτταρικών συνδέσεων στη λειτουργία του ενδοθηλιακού φραγμού. [Internet] [Thesis]. University of Ioannina; Πανεπιστήμιο Ιωαννίνων; 2010. [cited 2019 Nov 14]. Available from: http://hdl.handle.net/10442/hedi/23270.

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

Council of Science Editors:

Ντουχανιάρη . Ρόλος και μηχανισμοί διακυτταρικών συνδέσεων στη λειτουργία του ενδοθηλιακού φραγμού. [Thesis]. University of Ioannina; Πανεπιστήμιο Ιωαννίνων; 2010. Available from: http://hdl.handle.net/10442/hedi/23270

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


Seton Hall University

22. Raymond, Kelly A. Structural Analysis of Transient Receptor Potential Vanilloid Type 1 (TRPV1) Channel Protein and Proline Mimics using Computational Techniques.

Degree: PhD, Chemistry and Biochemistry, 2016, Seton Hall University

  Chapter I The Transient Receptor Potential (TRP) family of ion channels encompasses more than 30 members, which are expressed in many different tissues and… (more)

Subjects/Keywords: Molecular Dynamics; Transmembrane proteins; TRPV1; PIP2; proline mimic; peptide synthesis; Biochemistry, Biophysics, and Structural Biology; Physical Chemistry

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APA (6th Edition):

Raymond, K. A. (2016). Structural Analysis of Transient Receptor Potential Vanilloid Type 1 (TRPV1) Channel Protein and Proline Mimics using Computational Techniques. (Doctoral Dissertation). Seton Hall University. Retrieved from http://scholarship.shu.edu/dissertations/2184

Chicago Manual of Style (16th Edition):

Raymond, Kelly A. “Structural Analysis of Transient Receptor Potential Vanilloid Type 1 (TRPV1) Channel Protein and Proline Mimics using Computational Techniques.” 2016. Doctoral Dissertation, Seton Hall University. Accessed November 14, 2019. http://scholarship.shu.edu/dissertations/2184.

MLA Handbook (7th Edition):

Raymond, Kelly A. “Structural Analysis of Transient Receptor Potential Vanilloid Type 1 (TRPV1) Channel Protein and Proline Mimics using Computational Techniques.” 2016. Web. 14 Nov 2019.

Vancouver:

Raymond KA. Structural Analysis of Transient Receptor Potential Vanilloid Type 1 (TRPV1) Channel Protein and Proline Mimics using Computational Techniques. [Internet] [Doctoral dissertation]. Seton Hall University; 2016. [cited 2019 Nov 14]. Available from: http://scholarship.shu.edu/dissertations/2184.

Council of Science Editors:

Raymond KA. Structural Analysis of Transient Receptor Potential Vanilloid Type 1 (TRPV1) Channel Protein and Proline Mimics using Computational Techniques. [Doctoral Dissertation]. Seton Hall University; 2016. Available from: http://scholarship.shu.edu/dissertations/2184

23. CHENG LEI. STRUCTURAL STUDIES ON CAPG: A CA2+-DEPENDENT ACTIN CAPPING PROTEIN.

Degree: 2016, National University of Singapore

Subjects/Keywords: CapG; Actin capping. Calcium binding; Solution Structure; PIP2

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APA (6th Edition):

LEI, C. (2016). STRUCTURAL STUDIES ON CAPG: A CA2+-DEPENDENT ACTIN CAPPING PROTEIN. (Thesis). National University of Singapore. Retrieved from http://scholarbank.nus.edu.sg/handle/10635/136185

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):

LEI, CHENG. “STRUCTURAL STUDIES ON CAPG: A CA2+-DEPENDENT ACTIN CAPPING PROTEIN.” 2016. Thesis, National University of Singapore. Accessed November 14, 2019. http://scholarbank.nus.edu.sg/handle/10635/136185.

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

MLA Handbook (7th Edition):

LEI, CHENG. “STRUCTURAL STUDIES ON CAPG: A CA2+-DEPENDENT ACTIN CAPPING PROTEIN.” 2016. Web. 14 Nov 2019.

Vancouver:

LEI C. STRUCTURAL STUDIES ON CAPG: A CA2+-DEPENDENT ACTIN CAPPING PROTEIN. [Internet] [Thesis]. National University of Singapore; 2016. [cited 2019 Nov 14]. Available from: http://scholarbank.nus.edu.sg/handle/10635/136185.

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

Council of Science Editors:

LEI C. STRUCTURAL STUDIES ON CAPG: A CA2+-DEPENDENT ACTIN CAPPING PROTEIN. [Thesis]. National University of Singapore; 2016. Available from: http://scholarbank.nus.edu.sg/handle/10635/136185

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

24. Lubart, Quentin. Les protéines ERM , Interactions entre la membrane cellulaire et le cytosquelette : une approche biomimétique. : Interactions between ERM proteins, cell membrane and cytoskeleton : a biomimetic approach.

Degree: Docteur es, Matériaux, Mécanique, Génie civil, Electrochimie, 2016, Grenoble Alpes

Les protéines ERMs (Ezrine, radixine et moésine) jouent un rôle central in cellulo, dans de nombreux processus cellulaires tels que les infections, la migration et… (more)

Subjects/Keywords: Ezrine-Radixine-Moésine; Phosphoinositides et PIP2; Cytosquelette; Membrane lipidique biomimétique; Protéine virale Gag; Interactions protéine-Lipide; Ezrin-Radixin-Moesin; Phosphoinositides and PIP2; Cytosqueleton; Biomimetic lipidic membranes; Viral Gag protein; Interaction protein-Lipid; 570

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APA (6th Edition):

Lubart, Q. (2016). Les protéines ERM , Interactions entre la membrane cellulaire et le cytosquelette : une approche biomimétique. : Interactions between ERM proteins, cell membrane and cytoskeleton : a biomimetic approach. (Doctoral Dissertation). Grenoble Alpes. Retrieved from http://www.theses.fr/2016GREAI108

Chicago Manual of Style (16th Edition):

Lubart, Quentin. “Les protéines ERM , Interactions entre la membrane cellulaire et le cytosquelette : une approche biomimétique. : Interactions between ERM proteins, cell membrane and cytoskeleton : a biomimetic approach.” 2016. Doctoral Dissertation, Grenoble Alpes. Accessed November 14, 2019. http://www.theses.fr/2016GREAI108.

MLA Handbook (7th Edition):

Lubart, Quentin. “Les protéines ERM , Interactions entre la membrane cellulaire et le cytosquelette : une approche biomimétique. : Interactions between ERM proteins, cell membrane and cytoskeleton : a biomimetic approach.” 2016. Web. 14 Nov 2019.

Vancouver:

Lubart Q. Les protéines ERM , Interactions entre la membrane cellulaire et le cytosquelette : une approche biomimétique. : Interactions between ERM proteins, cell membrane and cytoskeleton : a biomimetic approach. [Internet] [Doctoral dissertation]. Grenoble Alpes; 2016. [cited 2019 Nov 14]. Available from: http://www.theses.fr/2016GREAI108.

Council of Science Editors:

Lubart Q. Les protéines ERM , Interactions entre la membrane cellulaire et le cytosquelette : une approche biomimétique. : Interactions between ERM proteins, cell membrane and cytoskeleton : a biomimetic approach. [Doctoral Dissertation]. Grenoble Alpes; 2016. Available from: http://www.theses.fr/2016GREAI108


Virginia Commonwealth University

25. Ha, Junghoon. Hydrogen Sulfide Regulation of Kir Channels.

Degree: PhD, Physiology and Biophysics, 2017, Virginia Commonwealth University

  Inwardly rectifying potassium (Kir) channels establish and regulate the resting membrane potential of excitable cells in the heart, brain and other peripheral tissues. Phosphatidylinositol-… (more)

Subjects/Keywords: Hydrogen sulfide; potassium channels; PIP2; phosphoinositide; stroke; ischemia; phosphatidylinositol 4; 5-bisphosphate (PIP2); Inwardly rectifying K+ (Kir) Channels; GIRK channels; KATP channels; Gasotransmitters; Cellular and Molecular Physiology; Medicine and Health Sciences; Molecular and Cellular Neuroscience

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APA (6th Edition):

Ha, J. (2017). Hydrogen Sulfide Regulation of Kir Channels. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/5204

Chicago Manual of Style (16th Edition):

Ha, Junghoon. “Hydrogen Sulfide Regulation of Kir Channels.” 2017. Doctoral Dissertation, Virginia Commonwealth University. Accessed November 14, 2019. https://scholarscompass.vcu.edu/etd/5204.

MLA Handbook (7th Edition):

Ha, Junghoon. “Hydrogen Sulfide Regulation of Kir Channels.” 2017. Web. 14 Nov 2019.

Vancouver:

Ha J. Hydrogen Sulfide Regulation of Kir Channels. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2017. [cited 2019 Nov 14]. Available from: https://scholarscompass.vcu.edu/etd/5204.

Council of Science Editors:

Ha J. Hydrogen Sulfide Regulation of Kir Channels. [Doctoral Dissertation]. Virginia Commonwealth University; 2017. Available from: https://scholarscompass.vcu.edu/etd/5204

26. Rheenen, Jacobus Emiel van. PIP2 as local second messenger: a critical re-evaluation.

Degree: 2006, Leiden University, and Div. for Cell Biology, Netherlands Cancer Institute, Amsterdam

 Phosphatidylinositol 4,5-biphosphate (PIP2) has been proposed to act as a second messenger in the regulation of many cell processes. If so, then PIP2 should fulfill… (more)

Subjects/Keywords: PIP2; Rafts; Micro-domains; GFP-PH; FRET; PIP2; Rafts; Micro-domains; GFP-PH; FRET

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APA (6th Edition):

Rheenen, J. E. v. (2006). PIP2 as local second messenger: a critical re-evaluation. (Doctoral Dissertation). Leiden University, and Div. for Cell Biology, Netherlands Cancer Institute, Amsterdam. Retrieved from http://hdl.handle.net/1887/4337

Chicago Manual of Style (16th Edition):

Rheenen, Jacobus Emiel van. “PIP2 as local second messenger: a critical re-evaluation.” 2006. Doctoral Dissertation, Leiden University, and Div. for Cell Biology, Netherlands Cancer Institute, Amsterdam. Accessed November 14, 2019. http://hdl.handle.net/1887/4337.

MLA Handbook (7th Edition):

Rheenen, Jacobus Emiel van. “PIP2 as local second messenger: a critical re-evaluation.” 2006. Web. 14 Nov 2019.

Vancouver:

Rheenen JEv. PIP2 as local second messenger: a critical re-evaluation. [Internet] [Doctoral dissertation]. Leiden University, and Div. for Cell Biology, Netherlands Cancer Institute, Amsterdam; 2006. [cited 2019 Nov 14]. Available from: http://hdl.handle.net/1887/4337.

Council of Science Editors:

Rheenen JEv. PIP2 as local second messenger: a critical re-evaluation. [Doctoral Dissertation]. Leiden University, and Div. for Cell Biology, Netherlands Cancer Institute, Amsterdam; 2006. Available from: http://hdl.handle.net/1887/4337

27. Zeijl, Leonie van. Close the Gap: a study on the regulation of Connexin43 gap junctional communication.

Degree: 2009, Cellular Biochemistry, Netherlands Cancer Institute

 Gap junctions are groups of transmembrane channels that connect the cytoplasms of adjacent cells to mediate the diffusion of small molecules, such as ions, metabolites,… (more)

Subjects/Keywords: Connexin43; Gap junctional communication; GPCR signalling; Nedd4; PIP2; Ubiquitination; Connexin43; Gap junctional communication; GPCR signalling; Nedd4; PIP2; Ubiquitination

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APA (6th Edition):

Zeijl, L. v. (2009). Close the Gap: a study on the regulation of Connexin43 gap junctional communication. (Doctoral Dissertation). Cellular Biochemistry, Netherlands Cancer Institute. Retrieved from http://hdl.handle.net/1887/13799

Chicago Manual of Style (16th Edition):

Zeijl, Leonie van. “Close the Gap: a study on the regulation of Connexin43 gap junctional communication.” 2009. Doctoral Dissertation, Cellular Biochemistry, Netherlands Cancer Institute. Accessed November 14, 2019. http://hdl.handle.net/1887/13799.

MLA Handbook (7th Edition):

Zeijl, Leonie van. “Close the Gap: a study on the regulation of Connexin43 gap junctional communication.” 2009. Web. 14 Nov 2019.

Vancouver:

Zeijl Lv. Close the Gap: a study on the regulation of Connexin43 gap junctional communication. [Internet] [Doctoral dissertation]. Cellular Biochemistry, Netherlands Cancer Institute; 2009. [cited 2019 Nov 14]. Available from: http://hdl.handle.net/1887/13799.

Council of Science Editors:

Zeijl Lv. Close the Gap: a study on the regulation of Connexin43 gap junctional communication. [Doctoral Dissertation]. Cellular Biochemistry, Netherlands Cancer Institute; 2009. Available from: http://hdl.handle.net/1887/13799


Texas Medical Center

28. Thakur, Dhananjay P. GATING MECHANISMS OF THE CANONICAL TRP CHANNEL ISOFORM TRPC4.

Degree: PhD, 2015, Texas Medical Center

  Non-selective cation channels formed by Transient Receptor Potential Canonical (TRPC) proteins play important roles in regulatory and pathophysiological processes. These channels are known to… (more)

Subjects/Keywords: TRP Channels; G proteins; TRPC4; Phospholipase C; calcium; protons; calmodulin; PIP2; Biophysics; Cellular and Molecular Physiology; Integrative Biology; Medicine and Health Sciences

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APA (6th Edition):

Thakur, D. P. (2015). GATING MECHANISMS OF THE CANONICAL TRP CHANNEL ISOFORM TRPC4. (Doctoral Dissertation). Texas Medical Center. Retrieved from http://digitalcommons.library.tmc.edu/utgsbs_dissertations/621

Chicago Manual of Style (16th Edition):

Thakur, Dhananjay P. “GATING MECHANISMS OF THE CANONICAL TRP CHANNEL ISOFORM TRPC4.” 2015. Doctoral Dissertation, Texas Medical Center. Accessed November 14, 2019. http://digitalcommons.library.tmc.edu/utgsbs_dissertations/621.

MLA Handbook (7th Edition):

Thakur, Dhananjay P. “GATING MECHANISMS OF THE CANONICAL TRP CHANNEL ISOFORM TRPC4.” 2015. Web. 14 Nov 2019.

Vancouver:

Thakur DP. GATING MECHANISMS OF THE CANONICAL TRP CHANNEL ISOFORM TRPC4. [Internet] [Doctoral dissertation]. Texas Medical Center; 2015. [cited 2019 Nov 14]. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/621.

Council of Science Editors:

Thakur DP. GATING MECHANISMS OF THE CANONICAL TRP CHANNEL ISOFORM TRPC4. [Doctoral Dissertation]. Texas Medical Center; 2015. Available from: http://digitalcommons.library.tmc.edu/utgsbs_dissertations/621

29. Ganesan, Ramya. IDENTIFICATION OF THE SITES OF ACTION OF INHIBITORS OF MAMMALIAN PHOSPHOLIPASE D2 (PLD2) AND THE ROLE OF INTERACTING PROTEIN PARTNERS.

Degree: MS, Microbiology and Immunology, 2014, Wright State University

 Phospholipase D (PLD) is a key enzyme for the remodeling of phospholipids in the cell membrane. PLD has been implicated in many physiological functions such… (more)

Subjects/Keywords: Biochemistry; PLD2, inhibitors, FIPI and NBOD, Grb, Ras, PIP2

…60 Figure 21: Allosteric regulator (PIP2) of PLD: Enzyme kinetics . ....61… …phosphatidyl inositol 4,5 bis phosphate (PIP2) for its activation. PLD2 gene is on… …cytosol. PLD2 requires only PIP2 and minimally PKC for its activity. PLD2 is constitutively… …PIP2 were purchased from Avanti Polar Lipids. Matrigel inserts were purchased from BD (… …the following reagents to 50 µl of lysates: 3.5 mM PC8 phospholipid, 0.9 mM PIP2… 

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

APA (6th Edition):

Ganesan, R. (2014). IDENTIFICATION OF THE SITES OF ACTION OF INHIBITORS OF MAMMALIAN PHOSPHOLIPASE D2 (PLD2) AND THE ROLE OF INTERACTING PROTEIN PARTNERS. (Masters Thesis). Wright State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=wright1421201049

Chicago Manual of Style (16th Edition):

Ganesan, Ramya. “IDENTIFICATION OF THE SITES OF ACTION OF INHIBITORS OF MAMMALIAN PHOSPHOLIPASE D2 (PLD2) AND THE ROLE OF INTERACTING PROTEIN PARTNERS.” 2014. Masters Thesis, Wright State University. Accessed November 14, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=wright1421201049.

MLA Handbook (7th Edition):

Ganesan, Ramya. “IDENTIFICATION OF THE SITES OF ACTION OF INHIBITORS OF MAMMALIAN PHOSPHOLIPASE D2 (PLD2) AND THE ROLE OF INTERACTING PROTEIN PARTNERS.” 2014. Web. 14 Nov 2019.

Vancouver:

Ganesan R. IDENTIFICATION OF THE SITES OF ACTION OF INHIBITORS OF MAMMALIAN PHOSPHOLIPASE D2 (PLD2) AND THE ROLE OF INTERACTING PROTEIN PARTNERS. [Internet] [Masters thesis]. Wright State University; 2014. [cited 2019 Nov 14]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1421201049.

Council of Science Editors:

Ganesan R. IDENTIFICATION OF THE SITES OF ACTION OF INHIBITORS OF MAMMALIAN PHOSPHOLIPASE D2 (PLD2) AND THE ROLE OF INTERACTING PROTEIN PARTNERS. [Masters Thesis]. Wright State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=wright1421201049


Virginia Tech

30. Ercetin, Mustafa Edib. Molecular Characterization and Loss-of-Function Analysis of an Arabidopsis thaliana Gene Encoding a Phospholipid-Specific Inositol Polyphosphate 5-Phosphatase.

Degree: PhD, Biochemistry, 2005, Virginia Tech

 The phosphatidylinositol signaling pathway utilizes inositol-containing second messengers to mediate signaling events. The enzymes that metabolize phosphoinositides can in some cases serve to terminate the… (more)

Subjects/Keywords: PIP2; Arabidopsis thaliana; inositol polyphosphate 5-phosphatase; IP3; phosphatidylinositol signaling

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APA (6th Edition):

Ercetin, M. E. (2005). Molecular Characterization and Loss-of-Function Analysis of an Arabidopsis thaliana Gene Encoding a Phospholipid-Specific Inositol Polyphosphate 5-Phosphatase. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/27884

Chicago Manual of Style (16th Edition):

Ercetin, Mustafa Edib. “Molecular Characterization and Loss-of-Function Analysis of an Arabidopsis thaliana Gene Encoding a Phospholipid-Specific Inositol Polyphosphate 5-Phosphatase.” 2005. Doctoral Dissertation, Virginia Tech. Accessed November 14, 2019. http://hdl.handle.net/10919/27884.

MLA Handbook (7th Edition):

Ercetin, Mustafa Edib. “Molecular Characterization and Loss-of-Function Analysis of an Arabidopsis thaliana Gene Encoding a Phospholipid-Specific Inositol Polyphosphate 5-Phosphatase.” 2005. Web. 14 Nov 2019.

Vancouver:

Ercetin ME. Molecular Characterization and Loss-of-Function Analysis of an Arabidopsis thaliana Gene Encoding a Phospholipid-Specific Inositol Polyphosphate 5-Phosphatase. [Internet] [Doctoral dissertation]. Virginia Tech; 2005. [cited 2019 Nov 14]. Available from: http://hdl.handle.net/10919/27884.

Council of Science Editors:

Ercetin ME. Molecular Characterization and Loss-of-Function Analysis of an Arabidopsis thaliana Gene Encoding a Phospholipid-Specific Inositol Polyphosphate 5-Phosphatase. [Doctoral Dissertation]. Virginia Tech; 2005. Available from: http://hdl.handle.net/10919/27884

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