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You searched for subject:(Phosphatase). Showing records 1 – 30 of 674 total matches.

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University of Oregon

1. Yang, Ye. Investigation into the Regulation and Function of Alkaline Phosphatase (ALP) in Host-Microbe Interactions.

Degree: PhD, Department of Biology, 2013, University of Oregon

 This dissertation describes our investigation into the regulation and function of the innate immune modulator alkaline phosphatase (ALP). Animal intestine harbors a vast and complex… (more)

Subjects/Keywords: alkaline phosphatase

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APA (6th Edition):

Yang, Y. (2013). Investigation into the Regulation and Function of Alkaline Phosphatase (ALP) in Host-Microbe Interactions. (Doctoral Dissertation). University of Oregon. Retrieved from http://hdl.handle.net/1794/13235

Chicago Manual of Style (16th Edition):

Yang, Ye. “Investigation into the Regulation and Function of Alkaline Phosphatase (ALP) in Host-Microbe Interactions.” 2013. Doctoral Dissertation, University of Oregon. Accessed October 22, 2020. http://hdl.handle.net/1794/13235.

MLA Handbook (7th Edition):

Yang, Ye. “Investigation into the Regulation and Function of Alkaline Phosphatase (ALP) in Host-Microbe Interactions.” 2013. Web. 22 Oct 2020.

Vancouver:

Yang Y. Investigation into the Regulation and Function of Alkaline Phosphatase (ALP) in Host-Microbe Interactions. [Internet] [Doctoral dissertation]. University of Oregon; 2013. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/1794/13235.

Council of Science Editors:

Yang Y. Investigation into the Regulation and Function of Alkaline Phosphatase (ALP) in Host-Microbe Interactions. [Doctoral Dissertation]. University of Oregon; 2013. Available from: http://hdl.handle.net/1794/13235

2. Kint, Nicolas. Rôle du facteur sigma alternatif, SigmaB, dans la réponse aux stress chez l’entéropathogène Clostridium difficile au cours de son cycle infectieux : Role of the alternative sigma factor, SigmaB, in the stress response in the enteropathogen Clostridium difficile during its infectious cycle.

Degree: Docteur es, Sciences de la vie et de la santé. Microbiologie, 2017, Sorbonne Paris Cité

 Clostridium difficile est un bacille à gram-positif anaérobie strict et sporulant. Cet entéropathogène est responsable de diarrhées post-antibiotiques et de colites pseudomembraneuses. Après germination des… (more)

Subjects/Keywords: SigmaB; NO; Phosphatase; SigmaB; Colonisation; NO; Phosphatase

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APA (6th Edition):

Kint, N. (2017). Rôle du facteur sigma alternatif, SigmaB, dans la réponse aux stress chez l’entéropathogène Clostridium difficile au cours de son cycle infectieux : Role of the alternative sigma factor, SigmaB, in the stress response in the enteropathogen Clostridium difficile during its infectious cycle. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2017USPCC120

Chicago Manual of Style (16th Edition):

Kint, Nicolas. “Rôle du facteur sigma alternatif, SigmaB, dans la réponse aux stress chez l’entéropathogène Clostridium difficile au cours de son cycle infectieux : Role of the alternative sigma factor, SigmaB, in the stress response in the enteropathogen Clostridium difficile during its infectious cycle.” 2017. Doctoral Dissertation, Sorbonne Paris Cité. Accessed October 22, 2020. http://www.theses.fr/2017USPCC120.

MLA Handbook (7th Edition):

Kint, Nicolas. “Rôle du facteur sigma alternatif, SigmaB, dans la réponse aux stress chez l’entéropathogène Clostridium difficile au cours de son cycle infectieux : Role of the alternative sigma factor, SigmaB, in the stress response in the enteropathogen Clostridium difficile during its infectious cycle.” 2017. Web. 22 Oct 2020.

Vancouver:

Kint N. Rôle du facteur sigma alternatif, SigmaB, dans la réponse aux stress chez l’entéropathogène Clostridium difficile au cours de son cycle infectieux : Role of the alternative sigma factor, SigmaB, in the stress response in the enteropathogen Clostridium difficile during its infectious cycle. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2017. [cited 2020 Oct 22]. Available from: http://www.theses.fr/2017USPCC120.

Council of Science Editors:

Kint N. Rôle du facteur sigma alternatif, SigmaB, dans la réponse aux stress chez l’entéropathogène Clostridium difficile au cours de son cycle infectieux : Role of the alternative sigma factor, SigmaB, in the stress response in the enteropathogen Clostridium difficile during its infectious cycle. [Doctoral Dissertation]. Sorbonne Paris Cité; 2017. Available from: http://www.theses.fr/2017USPCC120

3. Ragusa, Michael J. The Regulation of Protein Phosphatase 1 by Targeting Proteins.

Degree: PhD, Molecular Biology, Cell Biology, and Biochemistry, 2011, Brown University

 Protein phosphatase-1 (PP1) is a major serine/threonine phosphatase that dephorphorylates numerous substrates, thereby regulating many cellular events. PP1 contains little substrate specificity on its own,… (more)

Subjects/Keywords: protein phosphatase 1

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APA (6th Edition):

Ragusa, M. J. (2011). The Regulation of Protein Phosphatase 1 by Targeting Proteins. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:11183/

Chicago Manual of Style (16th Edition):

Ragusa, Michael J. “The Regulation of Protein Phosphatase 1 by Targeting Proteins.” 2011. Doctoral Dissertation, Brown University. Accessed October 22, 2020. https://repository.library.brown.edu/studio/item/bdr:11183/.

MLA Handbook (7th Edition):

Ragusa, Michael J. “The Regulation of Protein Phosphatase 1 by Targeting Proteins.” 2011. Web. 22 Oct 2020.

Vancouver:

Ragusa MJ. The Regulation of Protein Phosphatase 1 by Targeting Proteins. [Internet] [Doctoral dissertation]. Brown University; 2011. [cited 2020 Oct 22]. Available from: https://repository.library.brown.edu/studio/item/bdr:11183/.

Council of Science Editors:

Ragusa MJ. The Regulation of Protein Phosphatase 1 by Targeting Proteins. [Doctoral Dissertation]. Brown University; 2011. Available from: https://repository.library.brown.edu/studio/item/bdr:11183/

4. Vandomme, Audrey. Caractérisation fonctionnelle du PhosphoTyrosyl Phosphatase Activator chez Plasmodium falciparum : rôle dans la régulation de PP2A et de PP1 : Functional characterization of PTPA in Plasmodium falciparum : role in PP2A and PP1 regulation.

Degree: Docteur es, Parasitologie et mycologie, 2014, Université Lille II – Droit et Santé

 Le paludisme est la première endémie parasitaire mondiale causée par le protozoaire Plasmodium. Cette parasitose est responsable de 219 millions de cas et 660 000… (more)

Subjects/Keywords: PhosphoTyrosyl phosphatase activator; Paludisme; Protein phosphatase type 1; Protein phosphatase type 2A; Paludism

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APA (6th Edition):

Vandomme, A. (2014). Caractérisation fonctionnelle du PhosphoTyrosyl Phosphatase Activator chez Plasmodium falciparum : rôle dans la régulation de PP2A et de PP1 : Functional characterization of PTPA in Plasmodium falciparum : role in PP2A and PP1 regulation. (Doctoral Dissertation). Université Lille II – Droit et Santé. Retrieved from http://www.theses.fr/2014LIL2S010

Chicago Manual of Style (16th Edition):

Vandomme, Audrey. “Caractérisation fonctionnelle du PhosphoTyrosyl Phosphatase Activator chez Plasmodium falciparum : rôle dans la régulation de PP2A et de PP1 : Functional characterization of PTPA in Plasmodium falciparum : role in PP2A and PP1 regulation.” 2014. Doctoral Dissertation, Université Lille II – Droit et Santé. Accessed October 22, 2020. http://www.theses.fr/2014LIL2S010.

MLA Handbook (7th Edition):

Vandomme, Audrey. “Caractérisation fonctionnelle du PhosphoTyrosyl Phosphatase Activator chez Plasmodium falciparum : rôle dans la régulation de PP2A et de PP1 : Functional characterization of PTPA in Plasmodium falciparum : role in PP2A and PP1 regulation.” 2014. Web. 22 Oct 2020.

Vancouver:

Vandomme A. Caractérisation fonctionnelle du PhosphoTyrosyl Phosphatase Activator chez Plasmodium falciparum : rôle dans la régulation de PP2A et de PP1 : Functional characterization of PTPA in Plasmodium falciparum : role in PP2A and PP1 regulation. [Internet] [Doctoral dissertation]. Université Lille II – Droit et Santé 2014. [cited 2020 Oct 22]. Available from: http://www.theses.fr/2014LIL2S010.

Council of Science Editors:

Vandomme A. Caractérisation fonctionnelle du PhosphoTyrosyl Phosphatase Activator chez Plasmodium falciparum : rôle dans la régulation de PP2A et de PP1 : Functional characterization of PTPA in Plasmodium falciparum : role in PP2A and PP1 regulation. [Doctoral Dissertation]. Université Lille II – Droit et Santé 2014. Available from: http://www.theses.fr/2014LIL2S010


University of Otago

5. Shaaly, Aishath. Characterisation of Bacitracin Stress Response and Undecaprenyl pyrophosphate phosphatase in Enterococcus faecalis .

Degree: 2013, University of Otago

 Bacitracin is a mixture of closely related polypeptide antibiotics and is widely used as a topical antibiotic in humans and extensively for prophylaxis and therapy… (more)

Subjects/Keywords: Bacitracin Stress; Undecaprenyl pyrophosphate phosphatase

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APA (6th Edition):

Shaaly, A. (2013). Characterisation of Bacitracin Stress Response and Undecaprenyl pyrophosphate phosphatase in Enterococcus faecalis . (Doctoral Dissertation). University of Otago. Retrieved from http://hdl.handle.net/10523/4213

Chicago Manual of Style (16th Edition):

Shaaly, Aishath. “Characterisation of Bacitracin Stress Response and Undecaprenyl pyrophosphate phosphatase in Enterococcus faecalis .” 2013. Doctoral Dissertation, University of Otago. Accessed October 22, 2020. http://hdl.handle.net/10523/4213.

MLA Handbook (7th Edition):

Shaaly, Aishath. “Characterisation of Bacitracin Stress Response and Undecaprenyl pyrophosphate phosphatase in Enterococcus faecalis .” 2013. Web. 22 Oct 2020.

Vancouver:

Shaaly A. Characterisation of Bacitracin Stress Response and Undecaprenyl pyrophosphate phosphatase in Enterococcus faecalis . [Internet] [Doctoral dissertation]. University of Otago; 2013. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/10523/4213.

Council of Science Editors:

Shaaly A. Characterisation of Bacitracin Stress Response and Undecaprenyl pyrophosphate phosphatase in Enterococcus faecalis . [Doctoral Dissertation]. University of Otago; 2013. Available from: http://hdl.handle.net/10523/4213


Rochester Institute of Technology

6. Moreno, Isreal. Discovery, Cloning, Expression, Purification, and Characterization of Phosphoglycolate Phosphatase from Staphylococcus aureus.

Degree: MS, School of Chemistry and Materials Science (COS), 2016, Rochester Institute of Technology

  Staphylococcus aureus is a major cause of hospital-acquired infections. The multi-drug resistant nature of certain S. aureus strains makes the discovery of new drug… (more)

Subjects/Keywords: PGPase; Phosphoglycolate phosphatase; S. aureus

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APA (6th Edition):

Moreno, I. (2016). Discovery, Cloning, Expression, Purification, and Characterization of Phosphoglycolate Phosphatase from Staphylococcus aureus. (Masters Thesis). Rochester Institute of Technology. Retrieved from https://scholarworks.rit.edu/theses/9168

Chicago Manual of Style (16th Edition):

Moreno, Isreal. “Discovery, Cloning, Expression, Purification, and Characterization of Phosphoglycolate Phosphatase from Staphylococcus aureus.” 2016. Masters Thesis, Rochester Institute of Technology. Accessed October 22, 2020. https://scholarworks.rit.edu/theses/9168.

MLA Handbook (7th Edition):

Moreno, Isreal. “Discovery, Cloning, Expression, Purification, and Characterization of Phosphoglycolate Phosphatase from Staphylococcus aureus.” 2016. Web. 22 Oct 2020.

Vancouver:

Moreno I. Discovery, Cloning, Expression, Purification, and Characterization of Phosphoglycolate Phosphatase from Staphylococcus aureus. [Internet] [Masters thesis]. Rochester Institute of Technology; 2016. [cited 2020 Oct 22]. Available from: https://scholarworks.rit.edu/theses/9168.

Council of Science Editors:

Moreno I. Discovery, Cloning, Expression, Purification, and Characterization of Phosphoglycolate Phosphatase from Staphylococcus aureus. [Masters Thesis]. Rochester Institute of Technology; 2016. Available from: https://scholarworks.rit.edu/theses/9168


University of Alberta

7. Arnold, Tamara D. Molecular Mechanisms Underlying the Regulation of Protein Phosphatase-1c by the Apoptotic Stimulating Proteins of p53.

Degree: PhD, Department of Biochemistry, 2013, University of Alberta

 Protein phosphatase-1c (PP-1c) is a ubiquitous serine/threonine protein phosphatase regulated in part by association with a large number of different regulatory subunits. Apoptotic Stimulating Proteins… (more)

Subjects/Keywords: ASPP; p53; Protein Phosphatase-1

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APA (6th Edition):

Arnold, T. D. (2013). Molecular Mechanisms Underlying the Regulation of Protein Phosphatase-1c by the Apoptotic Stimulating Proteins of p53. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/r494vk345

Chicago Manual of Style (16th Edition):

Arnold, Tamara D. “Molecular Mechanisms Underlying the Regulation of Protein Phosphatase-1c by the Apoptotic Stimulating Proteins of p53.” 2013. Doctoral Dissertation, University of Alberta. Accessed October 22, 2020. https://era.library.ualberta.ca/files/r494vk345.

MLA Handbook (7th Edition):

Arnold, Tamara D. “Molecular Mechanisms Underlying the Regulation of Protein Phosphatase-1c by the Apoptotic Stimulating Proteins of p53.” 2013. Web. 22 Oct 2020.

Vancouver:

Arnold TD. Molecular Mechanisms Underlying the Regulation of Protein Phosphatase-1c by the Apoptotic Stimulating Proteins of p53. [Internet] [Doctoral dissertation]. University of Alberta; 2013. [cited 2020 Oct 22]. Available from: https://era.library.ualberta.ca/files/r494vk345.

Council of Science Editors:

Arnold TD. Molecular Mechanisms Underlying the Regulation of Protein Phosphatase-1c by the Apoptotic Stimulating Proteins of p53. [Doctoral Dissertation]. University of Alberta; 2013. Available from: https://era.library.ualberta.ca/files/r494vk345


University of Manchester

8. Currin, Andrew. A study of protein phosphatases from the genomes of trypanosomatid parasites.

Degree: 2013, University of Manchester

Trypanosomiases and leishmaniases are amongst the world’s most neglected infectious diseases. Trypanosoma brucei, Trypanosoma cruzi and Leishmania major are the primary human pathogens of the… (more)

Subjects/Keywords: Phosphatase; trypanosoma; leishmania; trypanosomatid

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APA (6th Edition):

Currin, A. (2013). A study of protein phosphatases from the genomes of trypanosomatid parasites. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:201557

Chicago Manual of Style (16th Edition):

Currin, Andrew. “A study of protein phosphatases from the genomes of trypanosomatid parasites.” 2013. Doctoral Dissertation, University of Manchester. Accessed October 22, 2020. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:201557.

MLA Handbook (7th Edition):

Currin, Andrew. “A study of protein phosphatases from the genomes of trypanosomatid parasites.” 2013. Web. 22 Oct 2020.

Vancouver:

Currin A. A study of protein phosphatases from the genomes of trypanosomatid parasites. [Internet] [Doctoral dissertation]. University of Manchester; 2013. [cited 2020 Oct 22]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:201557.

Council of Science Editors:

Currin A. A study of protein phosphatases from the genomes of trypanosomatid parasites. [Doctoral Dissertation]. University of Manchester; 2013. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:201557


Texas A&M University

9. Cao, Jin. Regulation of Gluconeogenesis by a Novel Protein Phosphatase.

Degree: PhD, Medical Sciences, 2014, Texas A&M University

 Gluconeogenesis is a biochemical process through which the organs or cells can synthesize glucose from non-carbohydrate carbon substrates and is important for blood glucose homeostasis.… (more)

Subjects/Keywords: SMP5; phosphatase; FoxO1/3a; gluconeogenesis

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APA (6th Edition):

Cao, J. (2014). Regulation of Gluconeogenesis by a Novel Protein Phosphatase. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/152650

Chicago Manual of Style (16th Edition):

Cao, Jin. “Regulation of Gluconeogenesis by a Novel Protein Phosphatase.” 2014. Doctoral Dissertation, Texas A&M University. Accessed October 22, 2020. http://hdl.handle.net/1969.1/152650.

MLA Handbook (7th Edition):

Cao, Jin. “Regulation of Gluconeogenesis by a Novel Protein Phosphatase.” 2014. Web. 22 Oct 2020.

Vancouver:

Cao J. Regulation of Gluconeogenesis by a Novel Protein Phosphatase. [Internet] [Doctoral dissertation]. Texas A&M University; 2014. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/1969.1/152650.

Council of Science Editors:

Cao J. Regulation of Gluconeogenesis by a Novel Protein Phosphatase. [Doctoral Dissertation]. Texas A&M University; 2014. Available from: http://hdl.handle.net/1969.1/152650

10. Critton, David Atwater. Molecular Basis for Phosphate Signaling by Prokaryotic and Eukaryotic Phosphatases.

Degree: PhD, Molecular Biology, Cell Biology, and Biochemistry, 2011, Brown University

 Protein tyrosine phosphatases (PTPs) regulate numerous critical biological processes, and PTPs themselves are tightly regulated. The overall structure of the PTP catalytic domain is well-conserved,… (more)

Subjects/Keywords: Protein tyrosine phosphatase (PTP)

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APA (6th Edition):

Critton, D. A. (2011). Molecular Basis for Phosphate Signaling by Prokaryotic and Eukaryotic Phosphatases. (Doctoral Dissertation). Brown University. Retrieved from https://repository.library.brown.edu/studio/item/bdr:11175/

Chicago Manual of Style (16th Edition):

Critton, David Atwater. “Molecular Basis for Phosphate Signaling by Prokaryotic and Eukaryotic Phosphatases.” 2011. Doctoral Dissertation, Brown University. Accessed October 22, 2020. https://repository.library.brown.edu/studio/item/bdr:11175/.

MLA Handbook (7th Edition):

Critton, David Atwater. “Molecular Basis for Phosphate Signaling by Prokaryotic and Eukaryotic Phosphatases.” 2011. Web. 22 Oct 2020.

Vancouver:

Critton DA. Molecular Basis for Phosphate Signaling by Prokaryotic and Eukaryotic Phosphatases. [Internet] [Doctoral dissertation]. Brown University; 2011. [cited 2020 Oct 22]. Available from: https://repository.library.brown.edu/studio/item/bdr:11175/.

Council of Science Editors:

Critton DA. Molecular Basis for Phosphate Signaling by Prokaryotic and Eukaryotic Phosphatases. [Doctoral Dissertation]. Brown University; 2011. Available from: https://repository.library.brown.edu/studio/item/bdr:11175/


Indian Institute of Science

11. Saha, Kaushik. Development of a Selective Cell-Permeable Protein Phosphatase 1 Inhibitor.

Degree: MS, Faculty of Science, 2018, Indian Institute of Science

 Selective ‘super-specific’ inhibitors of Protein Phosphatase 1 (PP1) are not available. Several natural product toxins possessing marginal selectivity between PP1 and the closely related Protein… (more)

Subjects/Keywords: Protein Phosphatase; Protein Phosphatase 1 (PP1); Protein Kinases; Protein Phosphatase 1 Inhibitor; Protein Phosphatase 2A (PP2A); Molecular Biology

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APA (6th Edition):

Saha, K. (2018). Development of a Selective Cell-Permeable Protein Phosphatase 1 Inhibitor. (Masters Thesis). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/3810

Chicago Manual of Style (16th Edition):

Saha, Kaushik. “Development of a Selective Cell-Permeable Protein Phosphatase 1 Inhibitor.” 2018. Masters Thesis, Indian Institute of Science. Accessed October 22, 2020. http://etd.iisc.ac.in/handle/2005/3810.

MLA Handbook (7th Edition):

Saha, Kaushik. “Development of a Selective Cell-Permeable Protein Phosphatase 1 Inhibitor.” 2018. Web. 22 Oct 2020.

Vancouver:

Saha K. Development of a Selective Cell-Permeable Protein Phosphatase 1 Inhibitor. [Internet] [Masters thesis]. Indian Institute of Science; 2018. [cited 2020 Oct 22]. Available from: http://etd.iisc.ac.in/handle/2005/3810.

Council of Science Editors:

Saha K. Development of a Selective Cell-Permeable Protein Phosphatase 1 Inhibitor. [Masters Thesis]. Indian Institute of Science; 2018. Available from: http://etd.iisc.ac.in/handle/2005/3810


Université Laval

12. Forest, Marie-Pier. Rôle de la PTPase Shp1 dans les adipocytes.

Degree: 2017, Université Laval

L’obésité, liée à la résistance à l’insuline, au diabète de type 2 et aux maladies cardiovasculaires, est un problème de santé majeur de notre société.… (more)

Subjects/Keywords: Protéine-tyrosine phosphatase; Adipocytes

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APA (6th Edition):

Forest, M. (2017). Rôle de la PTPase Shp1 dans les adipocytes. (Thesis). Université Laval. Retrieved from http://hdl.handle.net/20.500.11794/27945

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):

Forest, Marie-Pier. “Rôle de la PTPase Shp1 dans les adipocytes.” 2017. Thesis, Université Laval. Accessed October 22, 2020. http://hdl.handle.net/20.500.11794/27945.

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

MLA Handbook (7th Edition):

Forest, Marie-Pier. “Rôle de la PTPase Shp1 dans les adipocytes.” 2017. Web. 22 Oct 2020.

Vancouver:

Forest M. Rôle de la PTPase Shp1 dans les adipocytes. [Internet] [Thesis]. Université Laval; 2017. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/20.500.11794/27945.

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

Council of Science Editors:

Forest M. Rôle de la PTPase Shp1 dans les adipocytes. [Thesis]. Université Laval; 2017. Available from: http://hdl.handle.net/20.500.11794/27945

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


University of Toronto

13. D'Ambrosio, Lisa. Investigating the Higher-order Protein Interactions Surrounding the STRIPAK Complex.

Degree: 2010, University of Toronto

Reversible protein phosphorylation is an essential regulatory mechanism used by eukaryotes to coordinate the biochemical processes of the cell. The PP2A phosphatase functions to dephosphorylate… (more)

Subjects/Keywords: phosphatase; mass spectrometry; 0307

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APA (6th Edition):

D'Ambrosio, L. (2010). Investigating the Higher-order Protein Interactions Surrounding the STRIPAK Complex. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/24554

Chicago Manual of Style (16th Edition):

D'Ambrosio, Lisa. “Investigating the Higher-order Protein Interactions Surrounding the STRIPAK Complex.” 2010. Masters Thesis, University of Toronto. Accessed October 22, 2020. http://hdl.handle.net/1807/24554.

MLA Handbook (7th Edition):

D'Ambrosio, Lisa. “Investigating the Higher-order Protein Interactions Surrounding the STRIPAK Complex.” 2010. Web. 22 Oct 2020.

Vancouver:

D'Ambrosio L. Investigating the Higher-order Protein Interactions Surrounding the STRIPAK Complex. [Internet] [Masters thesis]. University of Toronto; 2010. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/1807/24554.

Council of Science Editors:

D'Ambrosio L. Investigating the Higher-order Protein Interactions Surrounding the STRIPAK Complex. [Masters Thesis]. University of Toronto; 2010. Available from: http://hdl.handle.net/1807/24554


University of Manchester

14. Currin, Andrew. A study of protein phosphatases from the genomes of trypanosomatid parasites.

Degree: PhD, 2013, University of Manchester

 Trypanosomiases and leishmaniases are amongst the world’s most neglected infectious diseases. Trypanosoma brucei, Trypanosoma cruzi and Leishmania major are the primary human pathogens of the… (more)

Subjects/Keywords: 616.9; Phosphatase; trypanosoma; leishmania; trypanosomatid

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APA (6th Edition):

Currin, A. (2013). A study of protein phosphatases from the genomes of trypanosomatid parasites. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/a-study-of-protein-phosphatases-from-the-genomes-of-trypanosomatid-parasites(6afd7092-b7e6-4816-903b-647d77942e95).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.617952

Chicago Manual of Style (16th Edition):

Currin, Andrew. “A study of protein phosphatases from the genomes of trypanosomatid parasites.” 2013. Doctoral Dissertation, University of Manchester. Accessed October 22, 2020. https://www.research.manchester.ac.uk/portal/en/theses/a-study-of-protein-phosphatases-from-the-genomes-of-trypanosomatid-parasites(6afd7092-b7e6-4816-903b-647d77942e95).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.617952.

MLA Handbook (7th Edition):

Currin, Andrew. “A study of protein phosphatases from the genomes of trypanosomatid parasites.” 2013. Web. 22 Oct 2020.

Vancouver:

Currin A. A study of protein phosphatases from the genomes of trypanosomatid parasites. [Internet] [Doctoral dissertation]. University of Manchester; 2013. [cited 2020 Oct 22]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/a-study-of-protein-phosphatases-from-the-genomes-of-trypanosomatid-parasites(6afd7092-b7e6-4816-903b-647d77942e95).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.617952.

Council of Science Editors:

Currin A. A study of protein phosphatases from the genomes of trypanosomatid parasites. [Doctoral Dissertation]. University of Manchester; 2013. Available from: https://www.research.manchester.ac.uk/portal/en/theses/a-study-of-protein-phosphatases-from-the-genomes-of-trypanosomatid-parasites(6afd7092-b7e6-4816-903b-647d77942e95).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.617952


University of Missouri – Columbia

15. Lewis, Sarah M. On the kinetics and mechanisms associated with covalent inactivation of protein tyrosine phosphatase 1b (ptp1b) by dietary phytochemicals and affinity labeling molecules.

Degree: 2015, University of Missouri – Columbia

 [ACCESS RESTRICTED TO THE UNIVERSITY OF MISSOURI AT REQUEST OF AUTHOR.] Phytochemical are compounds that occur naturally in plants. These compounds are what give many… (more)

Subjects/Keywords: Protein-tyrosine phosphatase; Phytochemicals; Brassica

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APA (6th Edition):

Lewis, S. M. (2015). On the kinetics and mechanisms associated with covalent inactivation of protein tyrosine phosphatase 1b (ptp1b) by dietary phytochemicals and affinity labeling molecules. (Thesis). University of Missouri – Columbia. Retrieved from http://hdl.handle.net/10355/47072

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

Chicago Manual of Style (16th Edition):

Lewis, Sarah M. “On the kinetics and mechanisms associated with covalent inactivation of protein tyrosine phosphatase 1b (ptp1b) by dietary phytochemicals and affinity labeling molecules.” 2015. Thesis, University of Missouri – Columbia. Accessed October 22, 2020. http://hdl.handle.net/10355/47072.

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

MLA Handbook (7th Edition):

Lewis, Sarah M. “On the kinetics and mechanisms associated with covalent inactivation of protein tyrosine phosphatase 1b (ptp1b) by dietary phytochemicals and affinity labeling molecules.” 2015. Web. 22 Oct 2020.

Vancouver:

Lewis SM. On the kinetics and mechanisms associated with covalent inactivation of protein tyrosine phosphatase 1b (ptp1b) by dietary phytochemicals and affinity labeling molecules. [Internet] [Thesis]. University of Missouri – Columbia; 2015. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/10355/47072.

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

Council of Science Editors:

Lewis SM. On the kinetics and mechanisms associated with covalent inactivation of protein tyrosine phosphatase 1b (ptp1b) by dietary phytochemicals and affinity labeling molecules. [Thesis]. University of Missouri – Columbia; 2015. Available from: http://hdl.handle.net/10355/47072

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


University of Missouri – Columbia

16. Punthasee, Puminan. The development of exo-affinity labeling agents, inactivators of protein tyrosine phosphatase 1B.

Degree: 2016, University of Missouri – Columbia

 The phosphorylation of a tyrosine substrate is one of the most crucial reactions that regulate numerous biological processes. The phosphorylation is controlled by protein tyrosine… (more)

Subjects/Keywords: Phosphorylation; Protein-tyrosine phosphatase

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APA (6th Edition):

Punthasee, P. (2016). The development of exo-affinity labeling agents, inactivators of protein tyrosine phosphatase 1B. (Thesis). University of Missouri – Columbia. Retrieved from https://doi.org/10.32469/10355/56831

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):

Punthasee, Puminan. “The development of exo-affinity labeling agents, inactivators of protein tyrosine phosphatase 1B.” 2016. Thesis, University of Missouri – Columbia. Accessed October 22, 2020. https://doi.org/10.32469/10355/56831.

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

MLA Handbook (7th Edition):

Punthasee, Puminan. “The development of exo-affinity labeling agents, inactivators of protein tyrosine phosphatase 1B.” 2016. Web. 22 Oct 2020.

Vancouver:

Punthasee P. The development of exo-affinity labeling agents, inactivators of protein tyrosine phosphatase 1B. [Internet] [Thesis]. University of Missouri – Columbia; 2016. [cited 2020 Oct 22]. Available from: https://doi.org/10.32469/10355/56831.

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

Council of Science Editors:

Punthasee P. The development of exo-affinity labeling agents, inactivators of protein tyrosine phosphatase 1B. [Thesis]. University of Missouri – Columbia; 2016. Available from: https://doi.org/10.32469/10355/56831

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


Rutgers University

17. Park, Yeonhee, 1983-. Lack of phosphatidate phosphatase causes reduced chronological life span through increased energy expenditure and oxidative stress.

Degree: PhD, Food Science, 2015, Rutgers University

In Saccharomyces cerevisiae, Pah1 phosphatidate phosphatase, which catalyzes the dephosphorylation of phosphatidic acid (PA) to yield diacylglycerol (DAG), plays a major role in the synthesis… (more)

Subjects/Keywords: Lipids – Metabolism; Phosphatidate phosphatase

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APA (6th Edition):

Park, Yeonhee, 1. (2015). Lack of phosphatidate phosphatase causes reduced chronological life span through increased energy expenditure and oxidative stress. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/47493/

Chicago Manual of Style (16th Edition):

Park, Yeonhee, 1983-. “Lack of phosphatidate phosphatase causes reduced chronological life span through increased energy expenditure and oxidative stress.” 2015. Doctoral Dissertation, Rutgers University. Accessed October 22, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/47493/.

MLA Handbook (7th Edition):

Park, Yeonhee, 1983-. “Lack of phosphatidate phosphatase causes reduced chronological life span through increased energy expenditure and oxidative stress.” 2015. Web. 22 Oct 2020.

Vancouver:

Park, Yeonhee 1. Lack of phosphatidate phosphatase causes reduced chronological life span through increased energy expenditure and oxidative stress. [Internet] [Doctoral dissertation]. Rutgers University; 2015. [cited 2020 Oct 22]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/47493/.

Council of Science Editors:

Park, Yeonhee 1. Lack of phosphatidate phosphatase causes reduced chronological life span through increased energy expenditure and oxidative stress. [Doctoral Dissertation]. Rutgers University; 2015. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/47493/


Ruhr Universität Bochum

18. Ackermann, Nadine. Biochemische und funktionelle Untersuchung der Multidomänenproteine PTPN13 und OCRL1.

Degree: 2013, Ruhr Universität Bochum

 In dieser Arbeit konnte zunächst die Interaktion zwischen der Proteintyrosinphosphatase PTPN13, dem am Recycling des TNF-Rezeptors beteiligten Protein SDCCAG3 sowie dem ArfGAP-Domäne-enthaltenden Protein GIT-1 biochemisch… (more)

Subjects/Keywords: Phosphoinositide; Zellteilung; Endocytose; Inositolpolyphosphat-Phosphatase / Inositolphophat 5-Phosphatase; Katalytische Aktivität

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APA (6th Edition):

Ackermann, N. (2013). Biochemische und funktionelle Untersuchung der Multidomänenproteine PTPN13 und OCRL1. (Thesis). Ruhr Universität Bochum. Retrieved from http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-38988

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):

Ackermann, Nadine. “Biochemische und funktionelle Untersuchung der Multidomänenproteine PTPN13 und OCRL1.” 2013. Thesis, Ruhr Universität Bochum. Accessed October 22, 2020. http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-38988.

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

MLA Handbook (7th Edition):

Ackermann, Nadine. “Biochemische und funktionelle Untersuchung der Multidomänenproteine PTPN13 und OCRL1.” 2013. Web. 22 Oct 2020.

Vancouver:

Ackermann N. Biochemische und funktionelle Untersuchung der Multidomänenproteine PTPN13 und OCRL1. [Internet] [Thesis]. Ruhr Universität Bochum; 2013. [cited 2020 Oct 22]. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-38988.

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

Council of Science Editors:

Ackermann N. Biochemische und funktionelle Untersuchung der Multidomänenproteine PTPN13 und OCRL1. [Thesis]. Ruhr Universität Bochum; 2013. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-38988

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

19. Ma, Sheng. Caractérisation du rôle des protéines phosphatases impliquées dans la déphosphorylation de la protéine kinase Greatwall lors de la sortie de mitose : Characterization of phosphatases involved in mitosis exit and its regulation mechanisms.

Degree: Docteur es, Biologie Santé, 2015, Montpellier

Chez la drolosophile, des mutants de Greatwall présentent des défauts de condensation des chromosomes lors de la mitose. Plus tard, la même équipe a montré… (more)

Subjects/Keywords: Biologie cellulaire; Mitose; Phosphatase; Kinase; Cell biology; Mitosis; Phosphatase; Kinase

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APA (6th Edition):

Ma, S. (2015). Caractérisation du rôle des protéines phosphatases impliquées dans la déphosphorylation de la protéine kinase Greatwall lors de la sortie de mitose : Characterization of phosphatases involved in mitosis exit and its regulation mechanisms. (Doctoral Dissertation). Montpellier. Retrieved from http://www.theses.fr/2015MONTS007

Chicago Manual of Style (16th Edition):

Ma, Sheng. “Caractérisation du rôle des protéines phosphatases impliquées dans la déphosphorylation de la protéine kinase Greatwall lors de la sortie de mitose : Characterization of phosphatases involved in mitosis exit and its regulation mechanisms.” 2015. Doctoral Dissertation, Montpellier. Accessed October 22, 2020. http://www.theses.fr/2015MONTS007.

MLA Handbook (7th Edition):

Ma, Sheng. “Caractérisation du rôle des protéines phosphatases impliquées dans la déphosphorylation de la protéine kinase Greatwall lors de la sortie de mitose : Characterization of phosphatases involved in mitosis exit and its regulation mechanisms.” 2015. Web. 22 Oct 2020.

Vancouver:

Ma S. Caractérisation du rôle des protéines phosphatases impliquées dans la déphosphorylation de la protéine kinase Greatwall lors de la sortie de mitose : Characterization of phosphatases involved in mitosis exit and its regulation mechanisms. [Internet] [Doctoral dissertation]. Montpellier; 2015. [cited 2020 Oct 22]. Available from: http://www.theses.fr/2015MONTS007.

Council of Science Editors:

Ma S. Caractérisation du rôle des protéines phosphatases impliquées dans la déphosphorylation de la protéine kinase Greatwall lors de la sortie de mitose : Characterization of phosphatases involved in mitosis exit and its regulation mechanisms. [Doctoral Dissertation]. Montpellier; 2015. Available from: http://www.theses.fr/2015MONTS007


California State University – Northridge

20. Deakers, Timothy William. Ultrastructural localization of enzymes in Polytomella agilis.

Degree: MS, Department of Biology, 1974, California State University – Northridge

 The combination of histochemical methods and electron microscopy provides useful technique for the ultrastructural localization of enzyme activities. Cells from log and stationary phase cultures… (more)

Subjects/Keywords: Glucose-6-phosphatase; Acid phosphatase

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APA (6th Edition):

Deakers, T. W. (1974). Ultrastructural localization of enzymes in Polytomella agilis. (Masters Thesis). California State University – Northridge. Retrieved from http://hdl.handle.net/10211.2/4692

Chicago Manual of Style (16th Edition):

Deakers, Timothy William. “Ultrastructural localization of enzymes in Polytomella agilis.” 1974. Masters Thesis, California State University – Northridge. Accessed October 22, 2020. http://hdl.handle.net/10211.2/4692.

MLA Handbook (7th Edition):

Deakers, Timothy William. “Ultrastructural localization of enzymes in Polytomella agilis.” 1974. Web. 22 Oct 2020.

Vancouver:

Deakers TW. Ultrastructural localization of enzymes in Polytomella agilis. [Internet] [Masters thesis]. California State University – Northridge; 1974. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/10211.2/4692.

Council of Science Editors:

Deakers TW. Ultrastructural localization of enzymes in Polytomella agilis. [Masters Thesis]. California State University – Northridge; 1974. Available from: http://hdl.handle.net/10211.2/4692


University of British Columbia

21. O'Day , Danton H. Alkaline phosphatase and embryogenesis in two urodele amphibian species.

Degree: MS- MSc, Zoology, 1969, University of British Columbia

 The development of alkaline phosphatase (AP) has been studied in two species of Urodele amphibian, Ambystoma qracile and Taricha torosa. The enzyme is present in… (more)

Subjects/Keywords: Phosphatase; Alkaline Phosphatase; Embryology  – Amphibians

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APA (6th Edition):

O'Day , D. H. (1969). Alkaline phosphatase and embryogenesis in two urodele amphibian species. (Masters Thesis). University of British Columbia. Retrieved from http://hdl.handle.net/2429/35139

Chicago Manual of Style (16th Edition):

O'Day , Danton H. “Alkaline phosphatase and embryogenesis in two urodele amphibian species.” 1969. Masters Thesis, University of British Columbia. Accessed October 22, 2020. http://hdl.handle.net/2429/35139.

MLA Handbook (7th Edition):

O'Day , Danton H. “Alkaline phosphatase and embryogenesis in two urodele amphibian species.” 1969. Web. 22 Oct 2020.

Vancouver:

O'Day DH. Alkaline phosphatase and embryogenesis in two urodele amphibian species. [Internet] [Masters thesis]. University of British Columbia; 1969. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/2429/35139.

Council of Science Editors:

O'Day DH. Alkaline phosphatase and embryogenesis in two urodele amphibian species. [Masters Thesis]. University of British Columbia; 1969. Available from: http://hdl.handle.net/2429/35139


University of Pretoria

22. Du Plessis, Erika Margarete. Development and evaluation of a reporter system for prokaryotic cells based on a secreted acid phosphatase from Staphylococcus aureus strain 154 .

Degree: 2010, University of Pretoria

 Reporter gene technology has facilitated greatly the analysis of gene expression and the study of individual promoters and their regulation. Although various reporter gene systems… (more)

Subjects/Keywords: Acid phosphatase; Staphylococcus aureus; Prokaryotic cells; UCTD

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APA (6th Edition):

Du Plessis, E. M. (2010). Development and evaluation of a reporter system for prokaryotic cells based on a secreted acid phosphatase from Staphylococcus aureus strain 154 . (Doctoral Dissertation). University of Pretoria. Retrieved from http://upetd.up.ac.za/thesis/available/etd-11182008-090253/

Chicago Manual of Style (16th Edition):

Du Plessis, Erika Margarete. “Development and evaluation of a reporter system for prokaryotic cells based on a secreted acid phosphatase from Staphylococcus aureus strain 154 .” 2010. Doctoral Dissertation, University of Pretoria. Accessed October 22, 2020. http://upetd.up.ac.za/thesis/available/etd-11182008-090253/.

MLA Handbook (7th Edition):

Du Plessis, Erika Margarete. “Development and evaluation of a reporter system for prokaryotic cells based on a secreted acid phosphatase from Staphylococcus aureus strain 154 .” 2010. Web. 22 Oct 2020.

Vancouver:

Du Plessis EM. Development and evaluation of a reporter system for prokaryotic cells based on a secreted acid phosphatase from Staphylococcus aureus strain 154 . [Internet] [Doctoral dissertation]. University of Pretoria; 2010. [cited 2020 Oct 22]. Available from: http://upetd.up.ac.za/thesis/available/etd-11182008-090253/.

Council of Science Editors:

Du Plessis EM. Development and evaluation of a reporter system for prokaryotic cells based on a secreted acid phosphatase from Staphylococcus aureus strain 154 . [Doctoral Dissertation]. University of Pretoria; 2010. Available from: http://upetd.up.ac.za/thesis/available/etd-11182008-090253/


Oregon State University

23. Saulez, Montague N. The determination of alkaline phosphatase activity and analysis with a portable clinical analyzer of serum and peritoneal fluid from horses suffering colic.

Degree: MS, Veterinary Science, 2003, Oregon State University

 Alkaline phosphatase (ALP) is an enzyme present in intestinal mucosa, bile, bone and renal tubule cells. Bile acids have been shown to decrease ALP activity… (more)

Subjects/Keywords: Alkaline phosphatase  – Analysis

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APA (6th Edition):

Saulez, M. N. (2003). The determination of alkaline phosphatase activity and analysis with a portable clinical analyzer of serum and peritoneal fluid from horses suffering colic. (Masters Thesis). Oregon State University. Retrieved from http://hdl.handle.net/1957/30812

Chicago Manual of Style (16th Edition):

Saulez, Montague N. “The determination of alkaline phosphatase activity and analysis with a portable clinical analyzer of serum and peritoneal fluid from horses suffering colic.” 2003. Masters Thesis, Oregon State University. Accessed October 22, 2020. http://hdl.handle.net/1957/30812.

MLA Handbook (7th Edition):

Saulez, Montague N. “The determination of alkaline phosphatase activity and analysis with a portable clinical analyzer of serum and peritoneal fluid from horses suffering colic.” 2003. Web. 22 Oct 2020.

Vancouver:

Saulez MN. The determination of alkaline phosphatase activity and analysis with a portable clinical analyzer of serum and peritoneal fluid from horses suffering colic. [Internet] [Masters thesis]. Oregon State University; 2003. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/1957/30812.

Council of Science Editors:

Saulez MN. The determination of alkaline phosphatase activity and analysis with a portable clinical analyzer of serum and peritoneal fluid from horses suffering colic. [Masters Thesis]. Oregon State University; 2003. Available from: http://hdl.handle.net/1957/30812


Vanderbilt University

24. Watkins, Guy Richard. Regulation of PP2Ac stability – discovery of a novel α4 monoubiquitination-dependent mechanism that is altered in Alzheimer’s disease.

Degree: PhD, Pharmacology, 2012, Vanderbilt University

 Studies described in this thesis identify a novel mechanism for α4’s regulation of PP2Ac stability. α4 binds the PP2A catalytic subunit (PP2Ac) and the microtubule-associated… (more)

Subjects/Keywords: Opitz syndrome; phosphatase; ubiquitin; PP2A; Alzheimers disease

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APA (6th Edition):

Watkins, G. R. (2012). Regulation of PP2Ac stability – discovery of a novel α4 monoubiquitination-dependent mechanism that is altered in Alzheimer’s disease. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/13840

Chicago Manual of Style (16th Edition):

Watkins, Guy Richard. “Regulation of PP2Ac stability – discovery of a novel α4 monoubiquitination-dependent mechanism that is altered in Alzheimer’s disease.” 2012. Doctoral Dissertation, Vanderbilt University. Accessed October 22, 2020. http://hdl.handle.net/1803/13840.

MLA Handbook (7th Edition):

Watkins, Guy Richard. “Regulation of PP2Ac stability – discovery of a novel α4 monoubiquitination-dependent mechanism that is altered in Alzheimer’s disease.” 2012. Web. 22 Oct 2020.

Vancouver:

Watkins GR. Regulation of PP2Ac stability – discovery of a novel α4 monoubiquitination-dependent mechanism that is altered in Alzheimer’s disease. [Internet] [Doctoral dissertation]. Vanderbilt University; 2012. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/1803/13840.

Council of Science Editors:

Watkins GR. Regulation of PP2Ac stability – discovery of a novel α4 monoubiquitination-dependent mechanism that is altered in Alzheimer’s disease. [Doctoral Dissertation]. Vanderbilt University; 2012. Available from: http://hdl.handle.net/1803/13840


McMaster University

25. Cabrera, Pablo. CALF INTESTINAL ALKALINE PHOSPHATASE APTAMER BASED BIOSENSORS.

Degree: MASc, 2014, McMaster University

In recent years, there has been an increasing demand for newer, more accurate, technologies that can detect and identify biomolecules or biological entities related to… (more)

Subjects/Keywords: aptamer; selex; Calf intestinal phosphatase; biosensor

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APA (6th Edition):

Cabrera, P. (2014). CALF INTESTINAL ALKALINE PHOSPHATASE APTAMER BASED BIOSENSORS. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/16431

Chicago Manual of Style (16th Edition):

Cabrera, Pablo. “CALF INTESTINAL ALKALINE PHOSPHATASE APTAMER BASED BIOSENSORS.” 2014. Masters Thesis, McMaster University. Accessed October 22, 2020. http://hdl.handle.net/11375/16431.

MLA Handbook (7th Edition):

Cabrera, Pablo. “CALF INTESTINAL ALKALINE PHOSPHATASE APTAMER BASED BIOSENSORS.” 2014. Web. 22 Oct 2020.

Vancouver:

Cabrera P. CALF INTESTINAL ALKALINE PHOSPHATASE APTAMER BASED BIOSENSORS. [Internet] [Masters thesis]. McMaster University; 2014. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/11375/16431.

Council of Science Editors:

Cabrera P. CALF INTESTINAL ALKALINE PHOSPHATASE APTAMER BASED BIOSENSORS. [Masters Thesis]. McMaster University; 2014. Available from: http://hdl.handle.net/11375/16431


University of Newcastle

26. Watt, Lauren Frances. The role of Protein Phosphatase 2A as a tumour suppressor in breast cancer.

Degree: PhD, 2012, University of Newcastle

Research Doctorate - Doctor of Philosophy (PhD)

Breast cancer is a worldwide health issue, and while many advances have been made in recent years, continued… (more)

Subjects/Keywords: PP2A; breast; cancer; MCF10A; tumour; suppressor; phosphatase

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APA (6th Edition):

Watt, L. F. (2012). The role of Protein Phosphatase 2A as a tumour suppressor in breast cancer. (Doctoral Dissertation). University of Newcastle. Retrieved from http://hdl.handle.net/1959.13/935337

Chicago Manual of Style (16th Edition):

Watt, Lauren Frances. “The role of Protein Phosphatase 2A as a tumour suppressor in breast cancer.” 2012. Doctoral Dissertation, University of Newcastle. Accessed October 22, 2020. http://hdl.handle.net/1959.13/935337.

MLA Handbook (7th Edition):

Watt, Lauren Frances. “The role of Protein Phosphatase 2A as a tumour suppressor in breast cancer.” 2012. Web. 22 Oct 2020.

Vancouver:

Watt LF. The role of Protein Phosphatase 2A as a tumour suppressor in breast cancer. [Internet] [Doctoral dissertation]. University of Newcastle; 2012. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/1959.13/935337.

Council of Science Editors:

Watt LF. The role of Protein Phosphatase 2A as a tumour suppressor in breast cancer. [Doctoral Dissertation]. University of Newcastle; 2012. Available from: http://hdl.handle.net/1959.13/935337


University of Pretoria

27. Du Plessis, Erika Margarete. Development and evaluation of a reporter system for prokaryotic cells based on a secreted acid phosphatase from Staphylococcus aureus strain 154.

Degree: Microbiology and Plant Pathology, 2010, University of Pretoria

 Reporter gene technology has facilitated greatly the analysis of gene expression and the study of individual promoters and their regulation. Although various reporter gene systems… (more)

Subjects/Keywords: Acid phosphatase; Staphylococcus aureus; Prokaryotic cells; UCTD

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APA (6th Edition):

Du Plessis, E. M. (2010). Development and evaluation of a reporter system for prokaryotic cells based on a secreted acid phosphatase from Staphylococcus aureus strain 154. (Doctoral Dissertation). University of Pretoria. Retrieved from http://hdl.handle.net/2263/29540

Chicago Manual of Style (16th Edition):

Du Plessis, Erika Margarete. “Development and evaluation of a reporter system for prokaryotic cells based on a secreted acid phosphatase from Staphylococcus aureus strain 154.” 2010. Doctoral Dissertation, University of Pretoria. Accessed October 22, 2020. http://hdl.handle.net/2263/29540.

MLA Handbook (7th Edition):

Du Plessis, Erika Margarete. “Development and evaluation of a reporter system for prokaryotic cells based on a secreted acid phosphatase from Staphylococcus aureus strain 154.” 2010. Web. 22 Oct 2020.

Vancouver:

Du Plessis EM. Development and evaluation of a reporter system for prokaryotic cells based on a secreted acid phosphatase from Staphylococcus aureus strain 154. [Internet] [Doctoral dissertation]. University of Pretoria; 2010. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/2263/29540.

Council of Science Editors:

Du Plessis EM. Development and evaluation of a reporter system for prokaryotic cells based on a secreted acid phosphatase from Staphylococcus aureus strain 154. [Doctoral Dissertation]. University of Pretoria; 2010. Available from: http://hdl.handle.net/2263/29540


University of Ottawa

28. Mehta, Virja. A Comprehensive Analysis of PP1c Leads to the Identification and Characterization of a Novel Family of Regulators for the Mypt1/PP1β Phosphatase .

Degree: 2017, University of Ottawa

 Reversible protein phosphorylation, the best studied post-translational modification, regulates most cellular processes, including signaling, migration, cell cycle progression, DNA damage repair, stress response and modulaton… (more)

Subjects/Keywords: Mass Spectrometry; Proteomics; Phosphatase; Phosphorylation; Mypt1; Specc1L

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APA (6th Edition):

Mehta, V. (2017). A Comprehensive Analysis of PP1c Leads to the Identification and Characterization of a Novel Family of Regulators for the Mypt1/PP1β Phosphatase . (Thesis). University of Ottawa. Retrieved from http://hdl.handle.net/10393/36465

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):

Mehta, Virja. “A Comprehensive Analysis of PP1c Leads to the Identification and Characterization of a Novel Family of Regulators for the Mypt1/PP1β Phosphatase .” 2017. Thesis, University of Ottawa. Accessed October 22, 2020. http://hdl.handle.net/10393/36465.

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

MLA Handbook (7th Edition):

Mehta, Virja. “A Comprehensive Analysis of PP1c Leads to the Identification and Characterization of a Novel Family of Regulators for the Mypt1/PP1β Phosphatase .” 2017. Web. 22 Oct 2020.

Vancouver:

Mehta V. A Comprehensive Analysis of PP1c Leads to the Identification and Characterization of a Novel Family of Regulators for the Mypt1/PP1β Phosphatase . [Internet] [Thesis]. University of Ottawa; 2017. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/10393/36465.

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

Council of Science Editors:

Mehta V. A Comprehensive Analysis of PP1c Leads to the Identification and Characterization of a Novel Family of Regulators for the Mypt1/PP1β Phosphatase . [Thesis]. University of Ottawa; 2017. Available from: http://hdl.handle.net/10393/36465

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


Université Laval

29. Lavallée-Bourget, Marie-Hélène. Rôle de la phosphorylation sur tyrosine dans la régulation de l'activité de PPARγ.

Degree: 2016, Université Laval

Tableau d'honneur de la Faculté des études supérieures et postdoctorales, 2016-2017.

L’obésité et ses complications telles le diabète et la stéatose hépatique non alcoolique sont… (more)

Subjects/Keywords: Phosphorylation; Protéine-tyrosine phosphatase; PPAR gamma

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

APA (6th Edition):

Lavallée-Bourget, M. (2016). Rôle de la phosphorylation sur tyrosine dans la régulation de l'activité de PPARγ. (Thesis). Université Laval. Retrieved from http://hdl.handle.net/20.500.11794/33285

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):

Lavallée-Bourget, Marie-Hélène. “Rôle de la phosphorylation sur tyrosine dans la régulation de l'activité de PPARγ.” 2016. Thesis, Université Laval. Accessed October 22, 2020. http://hdl.handle.net/20.500.11794/33285.

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

MLA Handbook (7th Edition):

Lavallée-Bourget, Marie-Hélène. “Rôle de la phosphorylation sur tyrosine dans la régulation de l'activité de PPARγ.” 2016. Web. 22 Oct 2020.

Vancouver:

Lavallée-Bourget M. Rôle de la phosphorylation sur tyrosine dans la régulation de l'activité de PPARγ. [Internet] [Thesis]. Université Laval; 2016. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/20.500.11794/33285.

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

Council of Science Editors:

Lavallée-Bourget M. Rôle de la phosphorylation sur tyrosine dans la régulation de l'activité de PPARγ. [Thesis]. Université Laval; 2016. Available from: http://hdl.handle.net/20.500.11794/33285

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


University of Texas Southwestern Medical Center

30. Adeyo, Oludotun. Elucidating the Role of Yeast Lipin (PAH1) in Lipid Droplet Biogenesis.

Degree: 2012, University of Texas Southwestern Medical Center

 Lipid droplets are unique organelles important for a host of cellular functions including the storage of neutral lipids, but factors that regulate the biogenesis and… (more)

Subjects/Keywords: Lipids; Phosphatidate Phosphatase; Saccharomyces cerevisiae Proteins

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

APA (6th Edition):

Adeyo, O. (2012). Elucidating the Role of Yeast Lipin (PAH1) in Lipid Droplet Biogenesis. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/1012

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):

Adeyo, Oludotun. “Elucidating the Role of Yeast Lipin (PAH1) in Lipid Droplet Biogenesis.” 2012. Thesis, University of Texas Southwestern Medical Center. Accessed October 22, 2020. http://hdl.handle.net/2152.5/1012.

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

MLA Handbook (7th Edition):

Adeyo, Oludotun. “Elucidating the Role of Yeast Lipin (PAH1) in Lipid Droplet Biogenesis.” 2012. Web. 22 Oct 2020.

Vancouver:

Adeyo O. Elucidating the Role of Yeast Lipin (PAH1) in Lipid Droplet Biogenesis. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2012. [cited 2020 Oct 22]. Available from: http://hdl.handle.net/2152.5/1012.

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

Council of Science Editors:

Adeyo O. Elucidating the Role of Yeast Lipin (PAH1) in Lipid Droplet Biogenesis. [Thesis]. University of Texas Southwestern Medical Center; 2012. Available from: http://hdl.handle.net/2152.5/1012

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

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