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You searched for subject:(PP1). Showing records 1 – 25 of 25 total matches.

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University of Alberta

1. Obeidat, Marya Mr. A Study of the Protein Phosphatase 1 (PP1) Regulatory Subunit, TIMAP, in Human Glomerular Endothelial Cells.

Degree: PhD, Department of Medicine, 2015, University of Alberta

 TIMAP is a prenylated endothelial-predominant regulatory subunit for the serine/threonine (Ser,S/Thr,T) protein phosphatase 1 catalytic subunit (PP1c). TIMAP was first discovered in glomerular endothelial cells.… (more)

Subjects/Keywords: PP1; Endothelial; TIMAP

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

APA (6th Edition):

Obeidat, M. M. (2015). A Study of the Protein Phosphatase 1 (PP1) Regulatory Subunit, TIMAP, in Human Glomerular Endothelial Cells. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/n296x1771

Chicago Manual of Style (16th Edition):

Obeidat, Marya Mr. “A Study of the Protein Phosphatase 1 (PP1) Regulatory Subunit, TIMAP, in Human Glomerular Endothelial Cells.” 2015. Doctoral Dissertation, University of Alberta. Accessed November 28, 2020. https://era.library.ualberta.ca/files/n296x1771.

MLA Handbook (7th Edition):

Obeidat, Marya Mr. “A Study of the Protein Phosphatase 1 (PP1) Regulatory Subunit, TIMAP, in Human Glomerular Endothelial Cells.” 2015. Web. 28 Nov 2020.

Vancouver:

Obeidat MM. A Study of the Protein Phosphatase 1 (PP1) Regulatory Subunit, TIMAP, in Human Glomerular Endothelial Cells. [Internet] [Doctoral dissertation]. University of Alberta; 2015. [cited 2020 Nov 28]. Available from: https://era.library.ualberta.ca/files/n296x1771.

Council of Science Editors:

Obeidat MM. A Study of the Protein Phosphatase 1 (PP1) Regulatory Subunit, TIMAP, in Human Glomerular Endothelial Cells. [Doctoral Dissertation]. University of Alberta; 2015. Available from: https://era.library.ualberta.ca/files/n296x1771


University of Debrecen

2. Katona, Frida. A növényi foszfoprotein foszfatázok működésének vizsgálata .

Degree: DE – TEK – Természettudományi és Technológiai Kar – Biológiai és Ökológiai Intézet, 2012, University of Debrecen

 A protein foszfatáz 1 (PP1) fontos szerepet tölt be az állatok sejtciklusának szabályozásában, többek között a retinoblasztóma fehérjéket is defoszforilálja. Az Orvosi Vegytani Intézet és… (more)

Subjects/Keywords: foszfatázok; PP1; protein foszfatáz

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APA (6th Edition):

Katona, F. (2012). A növényi foszfoprotein foszfatázok működésének vizsgálata . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/128259

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):

Katona, Frida. “A növényi foszfoprotein foszfatázok működésének vizsgálata .” 2012. Thesis, University of Debrecen. Accessed November 28, 2020. http://hdl.handle.net/2437/128259.

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

MLA Handbook (7th Edition):

Katona, Frida. “A növényi foszfoprotein foszfatázok működésének vizsgálata .” 2012. Web. 28 Nov 2020.

Vancouver:

Katona F. A növényi foszfoprotein foszfatázok működésének vizsgálata . [Internet] [Thesis]. University of Debrecen; 2012. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/2437/128259.

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

Council of Science Editors:

Katona F. A növényi foszfoprotein foszfatázok működésének vizsgálata . [Thesis]. University of Debrecen; 2012. Available from: http://hdl.handle.net/2437/128259

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

3. Lenne, Astrid. Caractérisation moléculaire et fonctionnelle de deux nouveaux partenaires potentiels de la protéine phosphatase de type 1 (PP1) chez plasmodium falciparum : Molecular and functional characterization of two new potential partners of the protein phosphatase type-1 (PP1) in plasmodium falciparum.

Degree: Docteur es, Biochimie et biologie moléculaire, 2016, Université Lille II – Droit et Santé

 Plasmodium falciparum (Pf) est un parasite intracellulaire capable d’infecter l’Homme. Dans les 48h après l’invasion des érythrocytes, il passe par le stade d’une cellule géante… (more)

Subjects/Keywords: Partenaires de PP1; Protéines phosphatases 1; Plasmodium falciparum; Plasmodium; PP1; Interactome; RVxF motif

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APA (6th Edition):

Lenne, A. (2016). Caractérisation moléculaire et fonctionnelle de deux nouveaux partenaires potentiels de la protéine phosphatase de type 1 (PP1) chez plasmodium falciparum : Molecular and functional characterization of two new potential partners of the protein phosphatase type-1 (PP1) in plasmodium falciparum. (Doctoral Dissertation). Université Lille II – Droit et Santé. Retrieved from http://www.theses.fr/2016LIL2S016

Chicago Manual of Style (16th Edition):

Lenne, Astrid. “Caractérisation moléculaire et fonctionnelle de deux nouveaux partenaires potentiels de la protéine phosphatase de type 1 (PP1) chez plasmodium falciparum : Molecular and functional characterization of two new potential partners of the protein phosphatase type-1 (PP1) in plasmodium falciparum.” 2016. Doctoral Dissertation, Université Lille II – Droit et Santé. Accessed November 28, 2020. http://www.theses.fr/2016LIL2S016.

MLA Handbook (7th Edition):

Lenne, Astrid. “Caractérisation moléculaire et fonctionnelle de deux nouveaux partenaires potentiels de la protéine phosphatase de type 1 (PP1) chez plasmodium falciparum : Molecular and functional characterization of two new potential partners of the protein phosphatase type-1 (PP1) in plasmodium falciparum.” 2016. Web. 28 Nov 2020.

Vancouver:

Lenne A. Caractérisation moléculaire et fonctionnelle de deux nouveaux partenaires potentiels de la protéine phosphatase de type 1 (PP1) chez plasmodium falciparum : Molecular and functional characterization of two new potential partners of the protein phosphatase type-1 (PP1) in plasmodium falciparum. [Internet] [Doctoral dissertation]. Université Lille II – Droit et Santé 2016. [cited 2020 Nov 28]. Available from: http://www.theses.fr/2016LIL2S016.

Council of Science Editors:

Lenne A. Caractérisation moléculaire et fonctionnelle de deux nouveaux partenaires potentiels de la protéine phosphatase de type 1 (PP1) chez plasmodium falciparum : Molecular and functional characterization of two new potential partners of the protein phosphatase type-1 (PP1) in plasmodium falciparum. [Doctoral Dissertation]. Université Lille II – Droit et Santé 2016. Available from: http://www.theses.fr/2016LIL2S016

4. Hollin, Thomas. Analyse de l’interactome de la Ser/Thr protéine phosphatase de type 1 (PP1) chez plasmodium falciparum : caractérisation moléculaire et fonctionnelle de Gametocyte EXported Protein 15 : Analysis of the Ser/Thr protein phosphatase type 1 (PP1) interactome in plasmodium falciparum : molecular and functional characterization of the Gametocyte EXported Protein 15.

Degree: Docteur es, Biochimie et biologie moléculaire, 2017, Université Lille II – Droit et Santé

L’un des obstacles majeurs au développement de nouveaux antipaludiques est notre connaissance limitée de la biologie parasitaire et la rareté des cibles thérapeutiques potentielles identifiées.… (more)

Subjects/Keywords: Interactome; GEXP15; Motif RVxF; Plasmodium; PP1; Interactome; Plasmodium; PP1; GEXP15; RVxF motif

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

APA (6th Edition):

Hollin, T. (2017). Analyse de l’interactome de la Ser/Thr protéine phosphatase de type 1 (PP1) chez plasmodium falciparum : caractérisation moléculaire et fonctionnelle de Gametocyte EXported Protein 15 : Analysis of the Ser/Thr protein phosphatase type 1 (PP1) interactome in plasmodium falciparum : molecular and functional characterization of the Gametocyte EXported Protein 15. (Doctoral Dissertation). Université Lille II – Droit et Santé. Retrieved from http://www.theses.fr/2017LIL2S020

Chicago Manual of Style (16th Edition):

Hollin, Thomas. “Analyse de l’interactome de la Ser/Thr protéine phosphatase de type 1 (PP1) chez plasmodium falciparum : caractérisation moléculaire et fonctionnelle de Gametocyte EXported Protein 15 : Analysis of the Ser/Thr protein phosphatase type 1 (PP1) interactome in plasmodium falciparum : molecular and functional characterization of the Gametocyte EXported Protein 15.” 2017. Doctoral Dissertation, Université Lille II – Droit et Santé. Accessed November 28, 2020. http://www.theses.fr/2017LIL2S020.

MLA Handbook (7th Edition):

Hollin, Thomas. “Analyse de l’interactome de la Ser/Thr protéine phosphatase de type 1 (PP1) chez plasmodium falciparum : caractérisation moléculaire et fonctionnelle de Gametocyte EXported Protein 15 : Analysis of the Ser/Thr protein phosphatase type 1 (PP1) interactome in plasmodium falciparum : molecular and functional characterization of the Gametocyte EXported Protein 15.” 2017. Web. 28 Nov 2020.

Vancouver:

Hollin T. Analyse de l’interactome de la Ser/Thr protéine phosphatase de type 1 (PP1) chez plasmodium falciparum : caractérisation moléculaire et fonctionnelle de Gametocyte EXported Protein 15 : Analysis of the Ser/Thr protein phosphatase type 1 (PP1) interactome in plasmodium falciparum : molecular and functional characterization of the Gametocyte EXported Protein 15. [Internet] [Doctoral dissertation]. Université Lille II – Droit et Santé 2017. [cited 2020 Nov 28]. Available from: http://www.theses.fr/2017LIL2S020.

Council of Science Editors:

Hollin T. Analyse de l’interactome de la Ser/Thr protéine phosphatase de type 1 (PP1) chez plasmodium falciparum : caractérisation moléculaire et fonctionnelle de Gametocyte EXported Protein 15 : Analysis of the Ser/Thr protein phosphatase type 1 (PP1) interactome in plasmodium falciparum : molecular and functional characterization of the Gametocyte EXported Protein 15. [Doctoral Dissertation]. Université Lille II – Droit et Santé 2017. Available from: http://www.theses.fr/2017LIL2S020

5. Tellier, Géraldine. Etudes moléculaires et fonctionnelles de deux régulateurs de la protéine phosphatase de type 1 chez Plasmodium falciparum : I2 et eIF2ß : Molecular and functional studies of two regulators of the phosphatase protein type 1 in Plasmodium falciparum : I2 and eIF2ß.

Degree: Docteur es, Biochimie et biologie moléculaire, 2015, Université Lille II – Droit et Santé

 La malaria est la 1ère parasitose mondiale du fait de son taux de morbidité et de mortalité. Elle est responsable de 198 millions de cas… (more)

Subjects/Keywords: EIF2ß; Régulateurs de PP1; Inhibiteur 2; Plasmodium falciparum; Protéines phosphatases; Protein phosphatase; PP1; Inhibitor-2; Plasmodium

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APA (6th Edition):

Tellier, G. (2015). Etudes moléculaires et fonctionnelles de deux régulateurs de la protéine phosphatase de type 1 chez Plasmodium falciparum : I2 et eIF2ß : Molecular and functional studies of two regulators of the phosphatase protein type 1 in Plasmodium falciparum : I2 and eIF2ß. (Doctoral Dissertation). Université Lille II – Droit et Santé. Retrieved from http://www.theses.fr/2015LIL2S039

Chicago Manual of Style (16th Edition):

Tellier, Géraldine. “Etudes moléculaires et fonctionnelles de deux régulateurs de la protéine phosphatase de type 1 chez Plasmodium falciparum : I2 et eIF2ß : Molecular and functional studies of two regulators of the phosphatase protein type 1 in Plasmodium falciparum : I2 and eIF2ß.” 2015. Doctoral Dissertation, Université Lille II – Droit et Santé. Accessed November 28, 2020. http://www.theses.fr/2015LIL2S039.

MLA Handbook (7th Edition):

Tellier, Géraldine. “Etudes moléculaires et fonctionnelles de deux régulateurs de la protéine phosphatase de type 1 chez Plasmodium falciparum : I2 et eIF2ß : Molecular and functional studies of two regulators of the phosphatase protein type 1 in Plasmodium falciparum : I2 and eIF2ß.” 2015. Web. 28 Nov 2020.

Vancouver:

Tellier G. Etudes moléculaires et fonctionnelles de deux régulateurs de la protéine phosphatase de type 1 chez Plasmodium falciparum : I2 et eIF2ß : Molecular and functional studies of two regulators of the phosphatase protein type 1 in Plasmodium falciparum : I2 and eIF2ß. [Internet] [Doctoral dissertation]. Université Lille II – Droit et Santé 2015. [cited 2020 Nov 28]. Available from: http://www.theses.fr/2015LIL2S039.

Council of Science Editors:

Tellier G. Etudes moléculaires et fonctionnelles de deux régulateurs de la protéine phosphatase de type 1 chez Plasmodium falciparum : I2 et eIF2ß : Molecular and functional studies of two regulators of the phosphatase protein type 1 in Plasmodium falciparum : I2 and eIF2ß. [Doctoral Dissertation]. Université Lille II – Droit et Santé 2015. Available from: http://www.theses.fr/2015LIL2S039

6. Sundermann, Lena. Identification and characterization of new Greatwall kinase substrates : Identification et caractérisation de nouveaux substrats de la kinase Greatwall.

Degree: Docteur es, Biologie Santé, 2018, Montpellier

La Division mitotique est une phase essentielle du cycle cellulaire qui assure la répartition correcte du contenu génétique. La mitose implique une réorganisation cellulaire profonde… (more)

Subjects/Keywords: Greatwall; Substrats des kinases; Mitose; Pp1; Régulation des phosphatases; Greatwall; Kinase substrates; Mitosis; Pp1; Phosphatase regulation

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

APA (6th Edition):

Sundermann, L. (2018). Identification and characterization of new Greatwall kinase substrates : Identification et caractérisation de nouveaux substrats de la kinase Greatwall. (Doctoral Dissertation). Montpellier. Retrieved from http://www.theses.fr/2018MONTT016

Chicago Manual of Style (16th Edition):

Sundermann, Lena. “Identification and characterization of new Greatwall kinase substrates : Identification et caractérisation de nouveaux substrats de la kinase Greatwall.” 2018. Doctoral Dissertation, Montpellier. Accessed November 28, 2020. http://www.theses.fr/2018MONTT016.

MLA Handbook (7th Edition):

Sundermann, Lena. “Identification and characterization of new Greatwall kinase substrates : Identification et caractérisation de nouveaux substrats de la kinase Greatwall.” 2018. Web. 28 Nov 2020.

Vancouver:

Sundermann L. Identification and characterization of new Greatwall kinase substrates : Identification et caractérisation de nouveaux substrats de la kinase Greatwall. [Internet] [Doctoral dissertation]. Montpellier; 2018. [cited 2020 Nov 28]. Available from: http://www.theses.fr/2018MONTT016.

Council of Science Editors:

Sundermann L. Identification and characterization of new Greatwall kinase substrates : Identification et caractérisation de nouveaux substrats de la kinase Greatwall. [Doctoral Dissertation]. Montpellier; 2018. Available from: http://www.theses.fr/2018MONTT016


IUPUI

7. Beiraghi Salek, Asma. Mechanisms and consequences of regulating the spinophilin/NMDA receptor interaction.

Degree: 2016, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

Parkinson disease (PD) is the second most common neurodegenerative disease. It is characterized by loss of dopaminergic cells in the… (more)

Subjects/Keywords: Spinophilin; NMDA Receptor; Kinase; PP1; Phosphorylation; Parkinson disease

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APA (6th Edition):

Beiraghi Salek, A. (2016). Mechanisms and consequences of regulating the spinophilin/NMDA receptor interaction. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/10898

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):

Beiraghi Salek, Asma. “Mechanisms and consequences of regulating the spinophilin/NMDA receptor interaction.” 2016. Thesis, IUPUI. Accessed November 28, 2020. http://hdl.handle.net/1805/10898.

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

MLA Handbook (7th Edition):

Beiraghi Salek, Asma. “Mechanisms and consequences of regulating the spinophilin/NMDA receptor interaction.” 2016. Web. 28 Nov 2020.

Vancouver:

Beiraghi Salek A. Mechanisms and consequences of regulating the spinophilin/NMDA receptor interaction. [Internet] [Thesis]. IUPUI; 2016. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/1805/10898.

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

Council of Science Editors:

Beiraghi Salek A. Mechanisms and consequences of regulating the spinophilin/NMDA receptor interaction. [Thesis]. IUPUI; 2016. Available from: http://hdl.handle.net/1805/10898

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


Duke University

8. Mueller, Sarah Beth. Characterizing the Role of the Previously Undescribed Protein Caskin2 in Vascular Biology .

Degree: 2016, Duke University

  Maintenance of vascular homeostasis is an active process that is dependent on continuous signaling by the quiescent endothelial cells (ECs) that line mature vessels.… (more)

Subjects/Keywords: Molecular biology; Cellular biology; angiogenesis; Caskin1; Caskin2; endothelial cells; hypertension; PP1

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APA (6th Edition):

Mueller, S. B. (2016). Characterizing the Role of the Previously Undescribed Protein Caskin2 in Vascular Biology . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/12824

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):

Mueller, Sarah Beth. “Characterizing the Role of the Previously Undescribed Protein Caskin2 in Vascular Biology .” 2016. Thesis, Duke University. Accessed November 28, 2020. http://hdl.handle.net/10161/12824.

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

MLA Handbook (7th Edition):

Mueller, Sarah Beth. “Characterizing the Role of the Previously Undescribed Protein Caskin2 in Vascular Biology .” 2016. Web. 28 Nov 2020.

Vancouver:

Mueller SB. Characterizing the Role of the Previously Undescribed Protein Caskin2 in Vascular Biology . [Internet] [Thesis]. Duke University; 2016. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10161/12824.

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

Council of Science Editors:

Mueller SB. Characterizing the Role of the Previously Undescribed Protein Caskin2 in Vascular Biology . [Thesis]. Duke University; 2016. Available from: http://hdl.handle.net/10161/12824

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


Universitat de Valencia

9. Rubio Villena, Mª Carla. Regulación de la homeostasis del glucógeno: el papel de R6 y la enfermedad de Lafora .

Degree: 2016, Universitat de Valencia

 El glucógeno es la principal reserva de energía en nuestras células y es una molécula esencial para nuestro cerebro. Sin embargo, muchas cuestiones sobre el… (more)

Subjects/Keywords: Glucógeno; Enfermedad de Lafora; Metabolismo; R6; PP1; Epilepsia; Neurodegeneración

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APA (6th Edition):

Rubio Villena, M. C. (2016). Regulación de la homeostasis del glucógeno: el papel de R6 y la enfermedad de Lafora . (Doctoral Dissertation). Universitat de Valencia. Retrieved from http://hdl.handle.net/10550/56936

Chicago Manual of Style (16th Edition):

Rubio Villena, Mª Carla. “Regulación de la homeostasis del glucógeno: el papel de R6 y la enfermedad de Lafora .” 2016. Doctoral Dissertation, Universitat de Valencia. Accessed November 28, 2020. http://hdl.handle.net/10550/56936.

MLA Handbook (7th Edition):

Rubio Villena, Mª Carla. “Regulación de la homeostasis del glucógeno: el papel de R6 y la enfermedad de Lafora .” 2016. Web. 28 Nov 2020.

Vancouver:

Rubio Villena MC. Regulación de la homeostasis del glucógeno: el papel de R6 y la enfermedad de Lafora . [Internet] [Doctoral dissertation]. Universitat de Valencia; 2016. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10550/56936.

Council of Science Editors:

Rubio Villena MC. Regulación de la homeostasis del glucógeno: el papel de R6 y la enfermedad de Lafora . [Doctoral Dissertation]. Universitat de Valencia; 2016. Available from: http://hdl.handle.net/10550/56936


Kent State University

10. Gilker, Eva Adeline, Gilker. INTERACTIONS AND LOCALIZATION OF PROTEIN PHOSPHATASES, YWHA PROTEINS AND CELL CYCLE CONTROL PROTEINS IN MEIOSIS.

Degree: MS, College of Arts and Sciences / Department of Biological Sciences, 2018, Kent State University

 Oocytes, the female gametes, are produced during oogenesis and held at meiotic prophase I arrest in the ovary until reproductive maturity. In mammals, the oocyte… (more)

Subjects/Keywords: Biology; Cellular Biology; Oocyte maturation; Meiosis; YWHA; PP1; CDC25B; Oocyte

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APA (6th Edition):

Gilker, Eva Adeline, G. (2018). INTERACTIONS AND LOCALIZATION OF PROTEIN PHOSPHATASES, YWHA PROTEINS AND CELL CYCLE CONTROL PROTEINS IN MEIOSIS. (Masters Thesis). Kent State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=kent1532699317257539

Chicago Manual of Style (16th Edition):

Gilker, Eva Adeline, Gilker. “INTERACTIONS AND LOCALIZATION OF PROTEIN PHOSPHATASES, YWHA PROTEINS AND CELL CYCLE CONTROL PROTEINS IN MEIOSIS.” 2018. Masters Thesis, Kent State University. Accessed November 28, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=kent1532699317257539.

MLA Handbook (7th Edition):

Gilker, Eva Adeline, Gilker. “INTERACTIONS AND LOCALIZATION OF PROTEIN PHOSPHATASES, YWHA PROTEINS AND CELL CYCLE CONTROL PROTEINS IN MEIOSIS.” 2018. Web. 28 Nov 2020.

Vancouver:

Gilker, Eva Adeline G. INTERACTIONS AND LOCALIZATION OF PROTEIN PHOSPHATASES, YWHA PROTEINS AND CELL CYCLE CONTROL PROTEINS IN MEIOSIS. [Internet] [Masters thesis]. Kent State University; 2018. [cited 2020 Nov 28]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1532699317257539.

Council of Science Editors:

Gilker, Eva Adeline G. INTERACTIONS AND LOCALIZATION OF PROTEIN PHOSPHATASES, YWHA PROTEINS AND CELL CYCLE CONTROL PROTEINS IN MEIOSIS. [Masters Thesis]. Kent State University; 2018. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1532699317257539


Universiteit Utrecht

11. Mourik, T.R.M. van. Inhibiting the inhibitor: how the Spindle Assembly Checkpoint gets silenced.

Degree: 2011, Universiteit Utrecht

 To prevent chromosome mis-segregation, the Spindle Assembly Checkpoint causes a mitotic arrest in cells containing unattached kinetochores through inhibition of CDC20-dependent APC/C activation. The robustness… (more)

Subjects/Keywords: Spindle Assembly Checkpoint; CDC20; MCC; silencing; p31comet; PP1; dynein dependent stripping; MCC disassembly; kinetochore attachment

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APA (6th Edition):

Mourik, T. R. M. v. (2011). Inhibiting the inhibitor: how the Spindle Assembly Checkpoint gets silenced. (Masters Thesis). Universiteit Utrecht. Retrieved from http://dspace.library.uu.nl:8080/handle/1874/209025

Chicago Manual of Style (16th Edition):

Mourik, T R M van. “Inhibiting the inhibitor: how the Spindle Assembly Checkpoint gets silenced.” 2011. Masters Thesis, Universiteit Utrecht. Accessed November 28, 2020. http://dspace.library.uu.nl:8080/handle/1874/209025.

MLA Handbook (7th Edition):

Mourik, T R M van. “Inhibiting the inhibitor: how the Spindle Assembly Checkpoint gets silenced.” 2011. Web. 28 Nov 2020.

Vancouver:

Mourik TRMv. Inhibiting the inhibitor: how the Spindle Assembly Checkpoint gets silenced. [Internet] [Masters thesis]. Universiteit Utrecht; 2011. [cited 2020 Nov 28]. Available from: http://dspace.library.uu.nl:8080/handle/1874/209025.

Council of Science Editors:

Mourik TRMv. Inhibiting the inhibitor: how the Spindle Assembly Checkpoint gets silenced. [Masters Thesis]. Universiteit Utrecht; 2011. Available from: http://dspace.library.uu.nl:8080/handle/1874/209025


University of South Florida

12. Nelson, Nadine D. Ikaros Deficiency Leads To An Imbalance in Effector and Regulatory T Cell Homeostasis in Murine Pancreatic Cancer.

Degree: 2015, University of South Florida

 Pancreatic cancer is one of the deadliest cancers with a five-year survival rate of 6%. Pancreatic cancer is resistant to conventional chemotherapy and is usually… (more)

Subjects/Keywords: Transcription Factor; CK2; PP1; Ubiquitination; Apigenin; Cell Biology; Medical Molecular Biology; Medical Sciences

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APA (6th Edition):

Nelson, N. D. (2015). Ikaros Deficiency Leads To An Imbalance in Effector and Regulatory T Cell Homeostasis in Murine Pancreatic Cancer. (Thesis). University of South Florida. Retrieved from https://scholarcommons.usf.edu/etd/5810

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):

Nelson, Nadine D. “Ikaros Deficiency Leads To An Imbalance in Effector and Regulatory T Cell Homeostasis in Murine Pancreatic Cancer.” 2015. Thesis, University of South Florida. Accessed November 28, 2020. https://scholarcommons.usf.edu/etd/5810.

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

MLA Handbook (7th Edition):

Nelson, Nadine D. “Ikaros Deficiency Leads To An Imbalance in Effector and Regulatory T Cell Homeostasis in Murine Pancreatic Cancer.” 2015. Web. 28 Nov 2020.

Vancouver:

Nelson ND. Ikaros Deficiency Leads To An Imbalance in Effector and Regulatory T Cell Homeostasis in Murine Pancreatic Cancer. [Internet] [Thesis]. University of South Florida; 2015. [cited 2020 Nov 28]. Available from: https://scholarcommons.usf.edu/etd/5810.

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

Council of Science Editors:

Nelson ND. Ikaros Deficiency Leads To An Imbalance in Effector and Regulatory T Cell Homeostasis in Murine Pancreatic Cancer. [Thesis]. University of South Florida; 2015. Available from: https://scholarcommons.usf.edu/etd/5810

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


Indian Institute of Science

13. 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 November 28, 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. 28 Nov 2020.

Vancouver:

Saha K. Development of a Selective Cell-Permeable Protein Phosphatase 1 Inhibitor. [Internet] [Masters thesis]. Indian Institute of Science; 2018. [cited 2020 Nov 28]. 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


East Carolina University

14. DeVaul, Nicole. PPP1R42 is a positive regulator of PP1 in centrosome duplication and separation and cilia dynamics.

Degree: PhD, Anatomy and Cell Biology, 2014, East Carolina University

 The centrosome is a dynamic structure that undergoes structural and functional transitions, which are coordinated with the cell cycle. It functions as the microtubule organizing… (more)

Subjects/Keywords: Cellular biology; Aurora A; Centrosome; Cilia; Nek2; PP1; PPP1R42; Neoplasms; Phosphoprotein Phosphatases – physiology; Protein-Serine-Threonine Kinases – physiology; Centrosome – physiology

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APA (6th Edition):

DeVaul, N. (2014). PPP1R42 is a positive regulator of PP1 in centrosome duplication and separation and cilia dynamics. (Doctoral Dissertation). East Carolina University. Retrieved from http://hdl.handle.net/10342/4670

Chicago Manual of Style (16th Edition):

DeVaul, Nicole. “PPP1R42 is a positive regulator of PP1 in centrosome duplication and separation and cilia dynamics.” 2014. Doctoral Dissertation, East Carolina University. Accessed November 28, 2020. http://hdl.handle.net/10342/4670.

MLA Handbook (7th Edition):

DeVaul, Nicole. “PPP1R42 is a positive regulator of PP1 in centrosome duplication and separation and cilia dynamics.” 2014. Web. 28 Nov 2020.

Vancouver:

DeVaul N. PPP1R42 is a positive regulator of PP1 in centrosome duplication and separation and cilia dynamics. [Internet] [Doctoral dissertation]. East Carolina University; 2014. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10342/4670.

Council of Science Editors:

DeVaul N. PPP1R42 is a positive regulator of PP1 in centrosome duplication and separation and cilia dynamics. [Doctoral Dissertation]. East Carolina University; 2014. Available from: http://hdl.handle.net/10342/4670

15. Puri, Pawan. Role of the Protein 14-3-3 in Spermatogenesis and Sperm Motility.

Degree: PhD, College of Arts and Sciences / Department of Biological Sciences, 2009, Kent State University

 The 14-3-3 proteins are a highly conserved family of acidic proteins and interact with various cellular phosphoproteins. The ability to bind phosphorylated proteins implicates 14-3-3… (more)

Subjects/Keywords: Biology; Sperm; 14-3-3; PP1; Difopein

…most predominant isoform of PP1 present in testes and the only isoform of protein phosphatase… …protein phosphatase 1. Testis contain all isoforms of PP1 (PP1α, PP1β, PP1γ) expressed… …and is the only form of PP1 in spermatozoa. Immotile caput spermatozoa were found to have… …high PP1 activity as compared to caudal epididymal spermatozoa (Vijayaraghavan et al… …stimulated in caudal sperm by the specific and potent PP1 inhibitors, calyculin A and okadaic acid… 

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APA (6th Edition):

Puri, P. (2009). Role of the Protein 14-3-3 in Spermatogenesis and Sperm Motility. (Doctoral Dissertation). Kent State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=kent1247848954

Chicago Manual of Style (16th Edition):

Puri, Pawan. “Role of the Protein 14-3-3 in Spermatogenesis and Sperm Motility.” 2009. Doctoral Dissertation, Kent State University. Accessed November 28, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=kent1247848954.

MLA Handbook (7th Edition):

Puri, Pawan. “Role of the Protein 14-3-3 in Spermatogenesis and Sperm Motility.” 2009. Web. 28 Nov 2020.

Vancouver:

Puri P. Role of the Protein 14-3-3 in Spermatogenesis and Sperm Motility. [Internet] [Doctoral dissertation]. Kent State University; 2009. [cited 2020 Nov 28]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1247848954.

Council of Science Editors:

Puri P. Role of the Protein 14-3-3 in Spermatogenesis and Sperm Motility. [Doctoral Dissertation]. Kent State University; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1247848954


Kent State University

16. Bhattacharjee, Rahul. ROLE OF GSK3a IN SPERM FUNCTION AND MALE FERTILITY.

Degree: PhD, College of Arts and Sciences / Department of Biological Sciences, 2018, Kent State University

 Glycogen synthase kinase 3 (GSK3) is a highly conserved protein-serine kinase regulating key cellular functions. In mammals GSK3 is expressed as two isoforms, GSK3a and… (more)

Subjects/Keywords: Biochemistry; Biology; Cellular Biology; Molecular Biology; Kinase, GSK3,Spermatogenesis, Sperm, Phosphatase, PP1,Sperm motility, Reproduction, ATP, Hexokinase

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APA (6th Edition):

Bhattacharjee, R. (2018). ROLE OF GSK3a IN SPERM FUNCTION AND MALE FERTILITY. (Doctoral Dissertation). Kent State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=kent1532949151866613

Chicago Manual of Style (16th Edition):

Bhattacharjee, Rahul. “ROLE OF GSK3a IN SPERM FUNCTION AND MALE FERTILITY.” 2018. Doctoral Dissertation, Kent State University. Accessed November 28, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=kent1532949151866613.

MLA Handbook (7th Edition):

Bhattacharjee, Rahul. “ROLE OF GSK3a IN SPERM FUNCTION AND MALE FERTILITY.” 2018. Web. 28 Nov 2020.

Vancouver:

Bhattacharjee R. ROLE OF GSK3a IN SPERM FUNCTION AND MALE FERTILITY. [Internet] [Doctoral dissertation]. Kent State University; 2018. [cited 2020 Nov 28]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1532949151866613.

Council of Science Editors:

Bhattacharjee R. ROLE OF GSK3a IN SPERM FUNCTION AND MALE FERTILITY. [Doctoral Dissertation]. Kent State University; 2018. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1532949151866613


Kent State University

17. Cheng, Lina. Regulation of Protein Phosphatase 1, PP1γ2, in Testis/Spermatozoa by PPP1r11, PPP1r7 and PPP1r2.

Degree: PhD, College of Arts and Sciences / School of Biomedical Sciences, 2008, Kent State University

  In mouse testis, PP1γ1 is restricted mainly to somatic cells, while PP1γ2 is primarily located in secondary spermatocytes and germ cells, and the only… (more)

Subjects/Keywords: Biomedical Research; PP1&947; 2; PPP1R11; I3; PPP1R7; Sds22

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APA (6th Edition):

Cheng, L. (2008). Regulation of Protein Phosphatase 1, PP1γ2, in Testis/Spermatozoa by PPP1r11, PPP1r7 and PPP1r2. (Doctoral Dissertation). Kent State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=kent1208813693

Chicago Manual of Style (16th Edition):

Cheng, Lina. “Regulation of Protein Phosphatase 1, PP1γ2, in Testis/Spermatozoa by PPP1r11, PPP1r7 and PPP1r2.” 2008. Doctoral Dissertation, Kent State University. Accessed November 28, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=kent1208813693.

MLA Handbook (7th Edition):

Cheng, Lina. “Regulation of Protein Phosphatase 1, PP1γ2, in Testis/Spermatozoa by PPP1r11, PPP1r7 and PPP1r2.” 2008. Web. 28 Nov 2020.

Vancouver:

Cheng L. Regulation of Protein Phosphatase 1, PP1γ2, in Testis/Spermatozoa by PPP1r11, PPP1r7 and PPP1r2. [Internet] [Doctoral dissertation]. Kent State University; 2008. [cited 2020 Nov 28]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1208813693.

Council of Science Editors:

Cheng L. Regulation of Protein Phosphatase 1, PP1γ2, in Testis/Spermatozoa by PPP1r11, PPP1r7 and PPP1r2. [Doctoral Dissertation]. Kent State University; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1208813693

18. Gnangnon, Bénédicte. Caractérisation moléculaire et fonctionnelle de la pseudo-tyrosine kinase-like (pTKL) de plasmodium : Molecular and functional characterization of plasmodium pseudo-tyrosine kinase-like (pTKL).

Degree: Docteur es, Biochimie et biologie moléculaire, 2019, Université Lille II – Droit et Santé

 Le paludisme, première endémie parasitaire mondiale ayant engendré près d’un demi-million de morts en 2017 (d’après l’OMS), est due à une infection par un parasite… (more)

Subjects/Keywords: Pseudo-kinase; SERA5; PP1; Paludisme; Plasmodium; Export des protéines; Protein protein interaction; SErine Repeat Antigen 5; Pseudo-kinase; Malaria; Protein protein interaction

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APA (6th Edition):

Gnangnon, B. (2019). Caractérisation moléculaire et fonctionnelle de la pseudo-tyrosine kinase-like (pTKL) de plasmodium : Molecular and functional characterization of plasmodium pseudo-tyrosine kinase-like (pTKL). (Doctoral Dissertation). Université Lille II – Droit et Santé. Retrieved from http://www.theses.fr/2019LIL2S003

Chicago Manual of Style (16th Edition):

Gnangnon, Bénédicte. “Caractérisation moléculaire et fonctionnelle de la pseudo-tyrosine kinase-like (pTKL) de plasmodium : Molecular and functional characterization of plasmodium pseudo-tyrosine kinase-like (pTKL).” 2019. Doctoral Dissertation, Université Lille II – Droit et Santé. Accessed November 28, 2020. http://www.theses.fr/2019LIL2S003.

MLA Handbook (7th Edition):

Gnangnon, Bénédicte. “Caractérisation moléculaire et fonctionnelle de la pseudo-tyrosine kinase-like (pTKL) de plasmodium : Molecular and functional characterization of plasmodium pseudo-tyrosine kinase-like (pTKL).” 2019. Web. 28 Nov 2020.

Vancouver:

Gnangnon B. Caractérisation moléculaire et fonctionnelle de la pseudo-tyrosine kinase-like (pTKL) de plasmodium : Molecular and functional characterization of plasmodium pseudo-tyrosine kinase-like (pTKL). [Internet] [Doctoral dissertation]. Université Lille II – Droit et Santé 2019. [cited 2020 Nov 28]. Available from: http://www.theses.fr/2019LIL2S003.

Council of Science Editors:

Gnangnon B. Caractérisation moléculaire et fonctionnelle de la pseudo-tyrosine kinase-like (pTKL) de plasmodium : Molecular and functional characterization of plasmodium pseudo-tyrosine kinase-like (pTKL). [Doctoral Dissertation]. Université Lille II – Droit et Santé 2019. Available from: http://www.theses.fr/2019LIL2S003


Universidade de Lisboa

19. Gonçalves, Maria Inês Cardoso. O papel do DNA-PKcs na transcrição mediada pelo promotor LTR do HIV-1.

Degree: 2017, Universidade de Lisboa

Tese de mestrado em Biologia Molecular e Genética, apresentada à Universidade de Lisboa, através da Faculdade de Ciências, 2017

O DNA-PK (Cinase dependente de DNA)… (more)

Subjects/Keywords: Vírus da Imunodeficiência Humana tipo 1 (HIV-1); Cinase dependente de DNA (DNA-PK); Transativador do LTR do HIV-1 (Tat); Elementos cis; Proteína de especificidade 1 (Pp1); Teses de mestrado - 2017; Domínio/Área Científica::Ciências Naturais::Ciências Biológicas

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APA (6th Edition):

Gonçalves, M. I. C. (2017). O papel do DNA-PKcs na transcrição mediada pelo promotor LTR do HIV-1. (Thesis). Universidade de Lisboa. Retrieved from https://www.rcaap.pt/detail.jsp?id=oai:repositorio.ul.pt:10451/31528

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):

Gonçalves, Maria Inês Cardoso. “O papel do DNA-PKcs na transcrição mediada pelo promotor LTR do HIV-1.” 2017. Thesis, Universidade de Lisboa. Accessed November 28, 2020. https://www.rcaap.pt/detail.jsp?id=oai:repositorio.ul.pt:10451/31528.

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

MLA Handbook (7th Edition):

Gonçalves, Maria Inês Cardoso. “O papel do DNA-PKcs na transcrição mediada pelo promotor LTR do HIV-1.” 2017. Web. 28 Nov 2020.

Vancouver:

Gonçalves MIC. O papel do DNA-PKcs na transcrição mediada pelo promotor LTR do HIV-1. [Internet] [Thesis]. Universidade de Lisboa; 2017. [cited 2020 Nov 28]. Available from: https://www.rcaap.pt/detail.jsp?id=oai:repositorio.ul.pt:10451/31528.

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

Council of Science Editors:

Gonçalves MIC. O papel do DNA-PKcs na transcrição mediada pelo promotor LTR do HIV-1. [Thesis]. Universidade de Lisboa; 2017. Available from: https://www.rcaap.pt/detail.jsp?id=oai:repositorio.ul.pt:10451/31528

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


University of Southern California

20. Li, Xu. Post-translational modification crosstalk regulates KAP1 co-repressor functions in response to DNA damages.

Degree: PhD, Molecular Pharmacology & Toxicology, 2009, University of Southern California

 As a multifunctional protein, KRAB domain-associated protein 1 (KAP1) is reportedly subjected to multiple protein post-translational modifications, including phosphorylation and SUMOylation. However, gaps exist in… (more)

Subjects/Keywords: DNA damage responses; KAP1; PP1; RNF4; SUMOylation; phosphorylation; ubiquitination; post-translational modifications crosstalk; doxorubicin

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APA (6th Edition):

Li, X. (2009). Post-translational modification crosstalk regulates KAP1 co-repressor functions in response to DNA damages. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/279861/rec/5130

Chicago Manual of Style (16th Edition):

Li, Xu. “Post-translational modification crosstalk regulates KAP1 co-repressor functions in response to DNA damages.” 2009. Doctoral Dissertation, University of Southern California. Accessed November 28, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/279861/rec/5130.

MLA Handbook (7th Edition):

Li, Xu. “Post-translational modification crosstalk regulates KAP1 co-repressor functions in response to DNA damages.” 2009. Web. 28 Nov 2020.

Vancouver:

Li X. Post-translational modification crosstalk regulates KAP1 co-repressor functions in response to DNA damages. [Internet] [Doctoral dissertation]. University of Southern California; 2009. [cited 2020 Nov 28]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/279861/rec/5130.

Council of Science Editors:

Li X. Post-translational modification crosstalk regulates KAP1 co-repressor functions in response to DNA damages. [Doctoral Dissertation]. University of Southern California; 2009. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/279861/rec/5130

21. Ramdas, Shandilya. Role of PP1γ2 Binding Partners in Spermatogenesis and Sperm Function.

Degree: PhD, College of Arts and Sciences / Department of Biological Sciences, 2012, Kent State University

  PP1γ2 (PPP1CC2) is a serine/threonine phosphatase that is highly expressed in testis and the only isoform expressed in mature spermatozoa. It belongs to a… (more)

Subjects/Keywords: Biology; PP1&947; 2,I2,I3,sds22,Rsph1,testis,spermatogenesis,sperm,phosphatase

…different subfamilies of PPPs. Protein phosphates 1 (PP1), protein phosphatase 2 (… …Selected inhibitors Ref PPP PP1 (PPP1) 3 a, b, g1, g2 >50 Heterodimer and higher… …PPM FCP a ? Monomer ? PP1 is a highly conserved protein that is present in organisms… …humans and in present in multiple isoforms. There are four isoforms of PP1 encoded by Figure 1… …highly elongated catalytic cleft into which myosin light chain conserved genes. Like PP1, the… 

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APA (6th Edition):

Ramdas, S. (2012). Role of PP1γ2 Binding Partners in Spermatogenesis and Sperm Function. (Doctoral Dissertation). Kent State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=kent1352418328

Chicago Manual of Style (16th Edition):

Ramdas, Shandilya. “Role of PP1γ2 Binding Partners in Spermatogenesis and Sperm Function.” 2012. Doctoral Dissertation, Kent State University. Accessed November 28, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=kent1352418328.

MLA Handbook (7th Edition):

Ramdas, Shandilya. “Role of PP1γ2 Binding Partners in Spermatogenesis and Sperm Function.” 2012. Web. 28 Nov 2020.

Vancouver:

Ramdas S. Role of PP1γ2 Binding Partners in Spermatogenesis and Sperm Function. [Internet] [Doctoral dissertation]. Kent State University; 2012. [cited 2020 Nov 28]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1352418328.

Council of Science Editors:

Ramdas S. Role of PP1γ2 Binding Partners in Spermatogenesis and Sperm Function. [Doctoral Dissertation]. Kent State University; 2012. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1352418328


Virginia Commonwealth University

22. Mukerjee, Prabhat. Identification of the RNA Cis-Elements that Interact with SRp30a to Regulate the Alternative Splicing of Caspase 9 Pre-mRNA.

Degree: MS, Biochemistry, 2005, Virginia Commonwealth University

 Studies have shown that the alternative splicing of caspase 9 and the phospho-status of SR proteins, a conserved family of splicing factors, are regulated by… (more)

Subjects/Keywords: PP1; mutagenesis; chemotherapy; cancer; CAPPs; immunoblotting; PP2A; CAPK; capcase; splice; ceramide; apoptosis; ceramide; caspase 9; cathepsin D; Biochemistry, Biophysics, and Structural Biology; Life Sciences

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APA (6th Edition):

Mukerjee, P. (2005). Identification of the RNA Cis-Elements that Interact with SRp30a to Regulate the Alternative Splicing of Caspase 9 Pre-mRNA. (Thesis). Virginia Commonwealth University. Retrieved from https://doi.org/10.25772/ZMB5-1291 ; https://scholarscompass.vcu.edu/etd/1506

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):

Mukerjee, Prabhat. “Identification of the RNA Cis-Elements that Interact with SRp30a to Regulate the Alternative Splicing of Caspase 9 Pre-mRNA.” 2005. Thesis, Virginia Commonwealth University. Accessed November 28, 2020. https://doi.org/10.25772/ZMB5-1291 ; https://scholarscompass.vcu.edu/etd/1506.

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

MLA Handbook (7th Edition):

Mukerjee, Prabhat. “Identification of the RNA Cis-Elements that Interact with SRp30a to Regulate the Alternative Splicing of Caspase 9 Pre-mRNA.” 2005. Web. 28 Nov 2020.

Vancouver:

Mukerjee P. Identification of the RNA Cis-Elements that Interact with SRp30a to Regulate the Alternative Splicing of Caspase 9 Pre-mRNA. [Internet] [Thesis]. Virginia Commonwealth University; 2005. [cited 2020 Nov 28]. Available from: https://doi.org/10.25772/ZMB5-1291 ; https://scholarscompass.vcu.edu/etd/1506.

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

Council of Science Editors:

Mukerjee P. Identification of the RNA Cis-Elements that Interact with SRp30a to Regulate the Alternative Splicing of Caspase 9 Pre-mRNA. [Thesis]. Virginia Commonwealth University; 2005. Available from: https://doi.org/10.25772/ZMB5-1291 ; https://scholarscompass.vcu.edu/etd/1506

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


York University

23. Silverio, Amanda. The Role of Myosin Phosphorylation on Bivalent Oscillations in Mesostoma ehrenbergii Primary Spermatocytes.

Degree: MSc -MS, Biology, 2017, York University

 The main aspect of my thesis looks at the role of myosin phosphorylation and total myosin inhibition on bivalent oscillations during prometaphase in primary spermatocytes… (more)

Subjects/Keywords: Cellular biology; Myosin; Phosphorylation; MLCK; ROCK; PP1; ML-7; H-7; Y-27632; BDM; Okadaic acid; Calyculin A; Mesostoma ehrenbergii; Primary spermatocytes; Cell division; Meiosis; Prometaphase; Spindle; Bivalent oscillations; Distance segregation; Precocious cleavage furrow; Spindle myosin; Oscillation velocity; Oscillation amplitude; Oscillation period; Myosin inhibition; Myosin enhancement; Phosphorylation pathways

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APA (6th Edition):

Silverio, A. (2017). The Role of Myosin Phosphorylation on Bivalent Oscillations in Mesostoma ehrenbergii Primary Spermatocytes. (Masters Thesis). York University. Retrieved from http://hdl.handle.net/10315/33615

Chicago Manual of Style (16th Edition):

Silverio, Amanda. “The Role of Myosin Phosphorylation on Bivalent Oscillations in Mesostoma ehrenbergii Primary Spermatocytes.” 2017. Masters Thesis, York University. Accessed November 28, 2020. http://hdl.handle.net/10315/33615.

MLA Handbook (7th Edition):

Silverio, Amanda. “The Role of Myosin Phosphorylation on Bivalent Oscillations in Mesostoma ehrenbergii Primary Spermatocytes.” 2017. Web. 28 Nov 2020.

Vancouver:

Silverio A. The Role of Myosin Phosphorylation on Bivalent Oscillations in Mesostoma ehrenbergii Primary Spermatocytes. [Internet] [Masters thesis]. York University; 2017. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10315/33615.

Council of Science Editors:

Silverio A. The Role of Myosin Phosphorylation on Bivalent Oscillations in Mesostoma ehrenbergii Primary Spermatocytes. [Masters Thesis]. York University; 2017. Available from: http://hdl.handle.net/10315/33615

24. Dudiki, Tejasvi. SERINE/THREONINE PHOSPHATASES: ROLE IN SPERMATOGENESIS AND SPERM FUNCTION.

Degree: PhD, College of Arts and Sciences / School of Biomedical Sciences, 2014, Kent State University

 In mammals, sperm attain motility and the ability to fertilize eggs during their passage through the epididymis. Changes in motility characteristics, called hyperactivation, occur in… (more)

Subjects/Keywords: Biomedical Research; Serine and threonine phosphatase; PP2A; PP1; Epididymal spermatozoa; Methylation; Phosphorylation; Sperm motility; Spermatogenesis; Transgene; Sperm morphogenesis; Fertility

…5.13. PP1 in Rescue I testis and sperm …....114 Figure 5.14. Rescue I sperm… …DIC 115 Figure 5.15. Western blot analysis for PP1 levels in Rescue… …Figure 5.17. Western blot analysis for quantification of PP1in Rescue testis ….…118… …PP1 in testis ..…137 viii Figure 5.27. PP1γ levels in sperm… …80 Table 5.1. Levels of PP1 in testis …104 Table 5.2. Levels of PP1… 

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APA (6th Edition):

Dudiki, T. (2014). SERINE/THREONINE PHOSPHATASES: ROLE IN SPERMATOGENESIS AND SPERM FUNCTION. (Doctoral Dissertation). Kent State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=kent1416354965

Chicago Manual of Style (16th Edition):

Dudiki, Tejasvi. “SERINE/THREONINE PHOSPHATASES: ROLE IN SPERMATOGENESIS AND SPERM FUNCTION.” 2014. Doctoral Dissertation, Kent State University. Accessed November 28, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=kent1416354965.

MLA Handbook (7th Edition):

Dudiki, Tejasvi. “SERINE/THREONINE PHOSPHATASES: ROLE IN SPERMATOGENESIS AND SPERM FUNCTION.” 2014. Web. 28 Nov 2020.

Vancouver:

Dudiki T. SERINE/THREONINE PHOSPHATASES: ROLE IN SPERMATOGENESIS AND SPERM FUNCTION. [Internet] [Doctoral dissertation]. Kent State University; 2014. [cited 2020 Nov 28]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1416354965.

Council of Science Editors:

Dudiki T. SERINE/THREONINE PHOSPHATASES: ROLE IN SPERMATOGENESIS AND SPERM FUNCTION. [Doctoral Dissertation]. Kent State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1416354965

25. Pagiatakis, Christina. Signal-Dependent Transcriptional Regulation of Vascular Smooth Muscle Cell Differentiation.

Degree: PhD, Biology, 2015, York University

 Vascular smooth muscle cells (VSMCs) play a key role in development as they are the major source of extracellular matrix components of vessel walls. During… (more)

Subjects/Keywords: Biology; Molecular biology; Developmental biology; Vascular smooth muscle cells; Differentiation; Signalling; Calcium signalling; Myogenesis; MEF2; SRF; Myocardin; CPI-17; PP1; Smooth muscle α-actin; TGF-β; TAZ; RhoA/ROCK; Vascular disease; Vascular development; Cardiovascular disease

…of three subunits: the catalytic subunit (protein phosphatase 1, PP1), the… …17 FUNCTION AND REGULATION IN VSMC ROLE OF PP1 IN VSMC CONTRACTION Calcium sensitivity in… …myocardin-family of SRF co-activators (58). Protein phosphatase 1 (PP1) has… …The 38kDa catalytic subunit of PP1, along with its 16 non-catalytic subunits, is localized… …modulator proteins that regulate PP1 activity, including inhibitor-1, inhibitor-2, DARPP32 and… 

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

APA (6th Edition):

Pagiatakis, C. (2015). Signal-Dependent Transcriptional Regulation of Vascular Smooth Muscle Cell Differentiation. (Doctoral Dissertation). York University. Retrieved from http://hdl.handle.net/10315/30062

Chicago Manual of Style (16th Edition):

Pagiatakis, Christina. “Signal-Dependent Transcriptional Regulation of Vascular Smooth Muscle Cell Differentiation.” 2015. Doctoral Dissertation, York University. Accessed November 28, 2020. http://hdl.handle.net/10315/30062.

MLA Handbook (7th Edition):

Pagiatakis, Christina. “Signal-Dependent Transcriptional Regulation of Vascular Smooth Muscle Cell Differentiation.” 2015. Web. 28 Nov 2020.

Vancouver:

Pagiatakis C. Signal-Dependent Transcriptional Regulation of Vascular Smooth Muscle Cell Differentiation. [Internet] [Doctoral dissertation]. York University; 2015. [cited 2020 Nov 28]. Available from: http://hdl.handle.net/10315/30062.

Council of Science Editors:

Pagiatakis C. Signal-Dependent Transcriptional Regulation of Vascular Smooth Muscle Cell Differentiation. [Doctoral Dissertation]. York University; 2015. Available from: http://hdl.handle.net/10315/30062

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