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You searched for subject:(p53 Protein). Showing records 1 – 30 of 175 total matches.

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University of Texas Southwestern Medical Center

1. Wylie, Annika Dawn. P53 Genes Act to Restrain Mobile Elements.

Degree: 2015, University of Texas Southwestern Medical Center

 Oncogenic stress provokes tumor suppression by p53 but the extent to which this regulatory axis is conserved remains unknown. Using a biosensor to visualize p53(more)

Subjects/Keywords: Genes, p53; Retroelements; Tumor Suppressor Protein p53

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APA (6th Edition):

Wylie, A. D. (2015). P53 Genes Act to Restrain Mobile Elements. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/4461

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):

Wylie, Annika Dawn. “P53 Genes Act to Restrain Mobile Elements.” 2015. Thesis, University of Texas Southwestern Medical Center. Accessed December 05, 2020. http://hdl.handle.net/2152.5/4461.

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

MLA Handbook (7th Edition):

Wylie, Annika Dawn. “P53 Genes Act to Restrain Mobile Elements.” 2015. Web. 05 Dec 2020.

Vancouver:

Wylie AD. P53 Genes Act to Restrain Mobile Elements. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/2152.5/4461.

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

Council of Science Editors:

Wylie AD. P53 Genes Act to Restrain Mobile Elements. [Thesis]. University of Texas Southwestern Medical Center; 2015. Available from: http://hdl.handle.net/2152.5/4461

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


Oregon State University

2. Stoner, Christopher S. Control of p53 tumor suppressor and peroxiredoxin activity through shifts in cellular redox balance.

Degree: PhD, Biochemistry and Biophysics, 2007, Oregon State University

 Aerobic organisms have evolved many sensory mechanisms that allow response to oxidants in the environment. One area of interest is the relationship between the activity… (more)

Subjects/Keywords: p53; p53 protein

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APA (6th Edition):

Stoner, C. S. (2007). Control of p53 tumor suppressor and peroxiredoxin activity through shifts in cellular redox balance. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/6120

Chicago Manual of Style (16th Edition):

Stoner, Christopher S. “Control of p53 tumor suppressor and peroxiredoxin activity through shifts in cellular redox balance.” 2007. Doctoral Dissertation, Oregon State University. Accessed December 05, 2020. http://hdl.handle.net/1957/6120.

MLA Handbook (7th Edition):

Stoner, Christopher S. “Control of p53 tumor suppressor and peroxiredoxin activity through shifts in cellular redox balance.” 2007. Web. 05 Dec 2020.

Vancouver:

Stoner CS. Control of p53 tumor suppressor and peroxiredoxin activity through shifts in cellular redox balance. [Internet] [Doctoral dissertation]. Oregon State University; 2007. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1957/6120.

Council of Science Editors:

Stoner CS. Control of p53 tumor suppressor and peroxiredoxin activity through shifts in cellular redox balance. [Doctoral Dissertation]. Oregon State University; 2007. Available from: http://hdl.handle.net/1957/6120


University of Alberta

3. 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 December 05, 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. 05 Dec 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 Dec 05]. 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


Oregon State University

4. Merwin, Jason R. Transactivational activity of the tumor suppressor protein p53 is dependent on thioredoxin reductase activity in mammalian cells.

Degree: PhD, Molecular and Cellular Biology, 2003, Oregon State University

 Reporter gene transactivation by human p53 is inhibited in budding yeast lacking the TRR1 gene encoding thioredoxin reductase. Thioredoxin reductase specifically catalyzes the NADPH-dependent reduction… (more)

Subjects/Keywords: p53 protein

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APA (6th Edition):

Merwin, J. R. (2003). Transactivational activity of the tumor suppressor protein p53 is dependent on thioredoxin reductase activity in mammalian cells. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/30498

Chicago Manual of Style (16th Edition):

Merwin, Jason R. “Transactivational activity of the tumor suppressor protein p53 is dependent on thioredoxin reductase activity in mammalian cells.” 2003. Doctoral Dissertation, Oregon State University. Accessed December 05, 2020. http://hdl.handle.net/1957/30498.

MLA Handbook (7th Edition):

Merwin, Jason R. “Transactivational activity of the tumor suppressor protein p53 is dependent on thioredoxin reductase activity in mammalian cells.” 2003. Web. 05 Dec 2020.

Vancouver:

Merwin JR. Transactivational activity of the tumor suppressor protein p53 is dependent on thioredoxin reductase activity in mammalian cells. [Internet] [Doctoral dissertation]. Oregon State University; 2003. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1957/30498.

Council of Science Editors:

Merwin JR. Transactivational activity of the tumor suppressor protein p53 is dependent on thioredoxin reductase activity in mammalian cells. [Doctoral Dissertation]. Oregon State University; 2003. Available from: http://hdl.handle.net/1957/30498


Rutgers University

5. Zhao, Yuhan, 1985-. The role of P53 signaling pathway in aging and cancer.

Degree: PhD, Pharmacology, Cellular and Molecular, 2018, Rutgers University

 Part I: p53 codon 72 SNP and aging p53 has dual functions on longevity. p53 plays a crucial role in tumor suppression to prevent early… (more)

Subjects/Keywords: Aging; Carcinogenesis; p53 protein

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APA (6th Edition):

Zhao, Yuhan, 1. (2018). The role of P53 signaling pathway in aging and cancer. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/59291/

Chicago Manual of Style (16th Edition):

Zhao, Yuhan, 1985-. “The role of P53 signaling pathway in aging and cancer.” 2018. Doctoral Dissertation, Rutgers University. Accessed December 05, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/59291/.

MLA Handbook (7th Edition):

Zhao, Yuhan, 1985-. “The role of P53 signaling pathway in aging and cancer.” 2018. Web. 05 Dec 2020.

Vancouver:

Zhao, Yuhan 1. The role of P53 signaling pathway in aging and cancer. [Internet] [Doctoral dissertation]. Rutgers University; 2018. [cited 2020 Dec 05]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/59291/.

Council of Science Editors:

Zhao, Yuhan 1. The role of P53 signaling pathway in aging and cancer. [Doctoral Dissertation]. Rutgers University; 2018. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/59291/


Brno University of Technology

6. Osadchuk, Olha. Optimalizace izolace mutantního proteinu p53 a jeho DNA vazebné vlastnosti: Optimization of p53 mutant protein isolation and its DNA binding properties.

Degree: 2020, Brno University of Technology

P53 protein is one of the most important molecules in the human body. It is responsible for several cellular processes such as DNA repair, cell… (more)

Subjects/Keywords: proteín p53; mutantní p53; gatway klonování; protein p53; mutant p53; gateway cloning

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APA (6th Edition):

Osadchuk, O. (2020). Optimalizace izolace mutantního proteinu p53 a jeho DNA vazebné vlastnosti: Optimization of p53 mutant protein isolation and its DNA binding properties. (Thesis). Brno University of Technology. Retrieved from http://hdl.handle.net/11012/190402

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):

Osadchuk, Olha. “Optimalizace izolace mutantního proteinu p53 a jeho DNA vazebné vlastnosti: Optimization of p53 mutant protein isolation and its DNA binding properties.” 2020. Thesis, Brno University of Technology. Accessed December 05, 2020. http://hdl.handle.net/11012/190402.

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

MLA Handbook (7th Edition):

Osadchuk, Olha. “Optimalizace izolace mutantního proteinu p53 a jeho DNA vazebné vlastnosti: Optimization of p53 mutant protein isolation and its DNA binding properties.” 2020. Web. 05 Dec 2020.

Vancouver:

Osadchuk O. Optimalizace izolace mutantního proteinu p53 a jeho DNA vazebné vlastnosti: Optimization of p53 mutant protein isolation and its DNA binding properties. [Internet] [Thesis]. Brno University of Technology; 2020. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/11012/190402.

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

Council of Science Editors:

Osadchuk O. Optimalizace izolace mutantního proteinu p53 a jeho DNA vazebné vlastnosti: Optimization of p53 mutant protein isolation and its DNA binding properties. [Thesis]. Brno University of Technology; 2020. Available from: http://hdl.handle.net/11012/190402

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


Brno University of Technology

7. Wikarská, Monika. Příprava a exprese izoforem proteinu p53 pomocí GATEWAY expresního systému: Preparation and expression of p53 protein isoforms using the GATEWAY expression system.

Degree: 2019, Brno University of Technology

 The TP53 gene can express protein p53 and 11 another isoform proteins N- and/or C-terminally truncated by using two promoters and alternative splicing. The p53(more)

Subjects/Keywords: proteín p53; izoformy p53; gateway klonovanie; protein p53; isoforms p53; gateway cloning

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APA (6th Edition):

Wikarská, M. (2019). Příprava a exprese izoforem proteinu p53 pomocí GATEWAY expresního systému: Preparation and expression of p53 protein isoforms using the GATEWAY expression system. (Thesis). Brno University of Technology. Retrieved from http://hdl.handle.net/11012/177453

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):

Wikarská, Monika. “Příprava a exprese izoforem proteinu p53 pomocí GATEWAY expresního systému: Preparation and expression of p53 protein isoforms using the GATEWAY expression system.” 2019. Thesis, Brno University of Technology. Accessed December 05, 2020. http://hdl.handle.net/11012/177453.

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

MLA Handbook (7th Edition):

Wikarská, Monika. “Příprava a exprese izoforem proteinu p53 pomocí GATEWAY expresního systému: Preparation and expression of p53 protein isoforms using the GATEWAY expression system.” 2019. Web. 05 Dec 2020.

Vancouver:

Wikarská M. Příprava a exprese izoforem proteinu p53 pomocí GATEWAY expresního systému: Preparation and expression of p53 protein isoforms using the GATEWAY expression system. [Internet] [Thesis]. Brno University of Technology; 2019. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/11012/177453.

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

Council of Science Editors:

Wikarská M. Příprava a exprese izoforem proteinu p53 pomocí GATEWAY expresního systému: Preparation and expression of p53 protein isoforms using the GATEWAY expression system. [Thesis]. Brno University of Technology; 2019. Available from: http://hdl.handle.net/11012/177453

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


Brno University of Technology

8. Osadchuk, Olha. Příprava konstruktů pro izolaci proteinů a jejich testování: Preparation of constructs for protein isolation and its testing.

Degree: 2018, Brno University of Technology

 This study is focused on describing of recombinant protein production. Protein p53 was chosen, as one of the most important tumor suppressor proteins, for studying… (more)

Subjects/Keywords: protein p53; Gateway klonování; purifikace proteinu; p53 protein; Gateway cloning systém; protein purification

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APA (6th Edition):

Osadchuk, O. (2018). Příprava konstruktů pro izolaci proteinů a jejich testování: Preparation of constructs for protein isolation and its testing. (Thesis). Brno University of Technology. Retrieved from http://hdl.handle.net/11012/82632

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):

Osadchuk, Olha. “Příprava konstruktů pro izolaci proteinů a jejich testování: Preparation of constructs for protein isolation and its testing.” 2018. Thesis, Brno University of Technology. Accessed December 05, 2020. http://hdl.handle.net/11012/82632.

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

MLA Handbook (7th Edition):

Osadchuk, Olha. “Příprava konstruktů pro izolaci proteinů a jejich testování: Preparation of constructs for protein isolation and its testing.” 2018. Web. 05 Dec 2020.

Vancouver:

Osadchuk O. Příprava konstruktů pro izolaci proteinů a jejich testování: Preparation of constructs for protein isolation and its testing. [Internet] [Thesis]. Brno University of Technology; 2018. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/11012/82632.

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

Council of Science Editors:

Osadchuk O. Příprava konstruktů pro izolaci proteinů a jejich testování: Preparation of constructs for protein isolation and its testing. [Thesis]. Brno University of Technology; 2018. Available from: http://hdl.handle.net/11012/82632

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


Texas State University – San Marcos

9. Schaub, Leasha J. Quantifying the Energetics of Binding Between p53 and DNA Using Electrophoretic Mobility Shift Assays.

Degree: MS, Biochemistry, 2012, Texas State University – San Marcos

 A new class of proteins has been termed “intrinsically disordered” or “ID” for short. The proteins within this class appear to lack tertiary stability, though… (more)

Subjects/Keywords: p53; Intrinsically disordered protein; Binding; p53 protein; DNA; DNA-protein interactions; DNA-binding proteins; Electrophoresis

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APA (6th Edition):

Schaub, L. J. (2012). Quantifying the Energetics of Binding Between p53 and DNA Using Electrophoretic Mobility Shift Assays. (Masters Thesis). Texas State University – San Marcos. Retrieved from https://digital.library.txstate.edu/handle/10877/4371

Chicago Manual of Style (16th Edition):

Schaub, Leasha J. “Quantifying the Energetics of Binding Between p53 and DNA Using Electrophoretic Mobility Shift Assays.” 2012. Masters Thesis, Texas State University – San Marcos. Accessed December 05, 2020. https://digital.library.txstate.edu/handle/10877/4371.

MLA Handbook (7th Edition):

Schaub, Leasha J. “Quantifying the Energetics of Binding Between p53 and DNA Using Electrophoretic Mobility Shift Assays.” 2012. Web. 05 Dec 2020.

Vancouver:

Schaub LJ. Quantifying the Energetics of Binding Between p53 and DNA Using Electrophoretic Mobility Shift Assays. [Internet] [Masters thesis]. Texas State University – San Marcos; 2012. [cited 2020 Dec 05]. Available from: https://digital.library.txstate.edu/handle/10877/4371.

Council of Science Editors:

Schaub LJ. Quantifying the Energetics of Binding Between p53 and DNA Using Electrophoretic Mobility Shift Assays. [Masters Thesis]. Texas State University – San Marcos; 2012. Available from: https://digital.library.txstate.edu/handle/10877/4371


Columbia University

10. Wu, Danyi. Unraveling the link between the Mdm2-p53 axis and aging.

Degree: 2017, Columbia University

 The transcription factor p53 is an important master regulator of the cellular response to stress. Mdm2 is an E3 ubiquitin ligase that is the primary… (more)

Subjects/Keywords: Biology; Molecular biology; Aging; p53 protein

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APA (6th Edition):

Wu, D. (2017). Unraveling the link between the Mdm2-p53 axis and aging. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D85Q57GW

Chicago Manual of Style (16th Edition):

Wu, Danyi. “Unraveling the link between the Mdm2-p53 axis and aging.” 2017. Doctoral Dissertation, Columbia University. Accessed December 05, 2020. https://doi.org/10.7916/D85Q57GW.

MLA Handbook (7th Edition):

Wu, Danyi. “Unraveling the link between the Mdm2-p53 axis and aging.” 2017. Web. 05 Dec 2020.

Vancouver:

Wu D. Unraveling the link between the Mdm2-p53 axis and aging. [Internet] [Doctoral dissertation]. Columbia University; 2017. [cited 2020 Dec 05]. Available from: https://doi.org/10.7916/D85Q57GW.

Council of Science Editors:

Wu D. Unraveling the link between the Mdm2-p53 axis and aging. [Doctoral Dissertation]. Columbia University; 2017. Available from: https://doi.org/10.7916/D85Q57GW


University of Texas – Austin

11. Chandrasekaran, Yamini. The role of p53 in death receptor-mediated apoptosis of testicular germ cells in response to mono-(2-ethylhexyl) phthalate treatment.

Degree: PhD, Pharmacy, 2005, University of Texas – Austin

 Mono-(2-ethylhexyl) phthalate (MEHP) is the toxic metabolite of the common plasticizer di-(2-ethylhexyl) phthalate (DEHP). Exposure to DEHP or MEHP typically leads to testicular atrophy in… (more)

Subjects/Keywords: p53 protein; Apoptosis

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APA (6th Edition):

Chandrasekaran, Y. (2005). The role of p53 in death receptor-mediated apoptosis of testicular germ cells in response to mono-(2-ethylhexyl) phthalate treatment. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/1840

Chicago Manual of Style (16th Edition):

Chandrasekaran, Yamini. “The role of p53 in death receptor-mediated apoptosis of testicular germ cells in response to mono-(2-ethylhexyl) phthalate treatment.” 2005. Doctoral Dissertation, University of Texas – Austin. Accessed December 05, 2020. http://hdl.handle.net/2152/1840.

MLA Handbook (7th Edition):

Chandrasekaran, Yamini. “The role of p53 in death receptor-mediated apoptosis of testicular germ cells in response to mono-(2-ethylhexyl) phthalate treatment.” 2005. Web. 05 Dec 2020.

Vancouver:

Chandrasekaran Y. The role of p53 in death receptor-mediated apoptosis of testicular germ cells in response to mono-(2-ethylhexyl) phthalate treatment. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2005. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/2152/1840.

Council of Science Editors:

Chandrasekaran Y. The role of p53 in death receptor-mediated apoptosis of testicular germ cells in response to mono-(2-ethylhexyl) phthalate treatment. [Doctoral Dissertation]. University of Texas – Austin; 2005. Available from: http://hdl.handle.net/2152/1840

12. Vaillant, Remi. The role of adenoviral capsid protein VI in cell cycle modulation : Le rôle de la protéine adénovirale de capside VI dans la modulation du cycle cellulaire.

Degree: Docteur es, Microbiologie-Immunologie, 2014, Bordeaux; Universität Hamburg

Les Adénovirus humains sont des virus non enveloppés se répliquant dans le noyau des cellules hôtes.Durant l’infection et après leur entrée par endocytose, les Adénovirus… (more)

Subjects/Keywords: Adenovirus; Protein VI; P53; Cycle cellulaire; Adenovirus; Protein VI; P53; Cell cycle

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APA (6th Edition):

Vaillant, R. (2014). The role of adenoviral capsid protein VI in cell cycle modulation : Le rôle de la protéine adénovirale de capside VI dans la modulation du cycle cellulaire. (Doctoral Dissertation). Bordeaux; Universität Hamburg. Retrieved from http://www.theses.fr/2014BORD0297

Chicago Manual of Style (16th Edition):

Vaillant, Remi. “The role of adenoviral capsid protein VI in cell cycle modulation : Le rôle de la protéine adénovirale de capside VI dans la modulation du cycle cellulaire.” 2014. Doctoral Dissertation, Bordeaux; Universität Hamburg. Accessed December 05, 2020. http://www.theses.fr/2014BORD0297.

MLA Handbook (7th Edition):

Vaillant, Remi. “The role of adenoviral capsid protein VI in cell cycle modulation : Le rôle de la protéine adénovirale de capside VI dans la modulation du cycle cellulaire.” 2014. Web. 05 Dec 2020.

Vancouver:

Vaillant R. The role of adenoviral capsid protein VI in cell cycle modulation : Le rôle de la protéine adénovirale de capside VI dans la modulation du cycle cellulaire. [Internet] [Doctoral dissertation]. Bordeaux; Universität Hamburg; 2014. [cited 2020 Dec 05]. Available from: http://www.theses.fr/2014BORD0297.

Council of Science Editors:

Vaillant R. The role of adenoviral capsid protein VI in cell cycle modulation : Le rôle de la protéine adénovirale de capside VI dans la modulation du cycle cellulaire. [Doctoral Dissertation]. Bordeaux; Universität Hamburg; 2014. Available from: http://www.theses.fr/2014BORD0297


Brno University of Technology

13. Vadovičová, Natália. Produkce a purifikace izoforem proteinu p53 v bakteriálním expresním systému: P53 protein isoforms production and purification in the bacterial expression system.

Degree: 2019, Brno University of Technology

 Apart from the p53 protein, the TP53 tumor-suppressor gene is expressed as another eleven protein isoforms with the use of alternative splicing, alternative promotors and… (more)

Subjects/Keywords: protein p53; izoformy; rakovina; gateway klonování; p53 protein; isoforms; cancer; gateway cloning system

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APA (6th Edition):

Vadovičová, N. (2019). Produkce a purifikace izoforem proteinu p53 v bakteriálním expresním systému: P53 protein isoforms production and purification in the bacterial expression system. (Thesis). Brno University of Technology. Retrieved from http://hdl.handle.net/11012/80642

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):

Vadovičová, Natália. “Produkce a purifikace izoforem proteinu p53 v bakteriálním expresním systému: P53 protein isoforms production and purification in the bacterial expression system.” 2019. Thesis, Brno University of Technology. Accessed December 05, 2020. http://hdl.handle.net/11012/80642.

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

MLA Handbook (7th Edition):

Vadovičová, Natália. “Produkce a purifikace izoforem proteinu p53 v bakteriálním expresním systému: P53 protein isoforms production and purification in the bacterial expression system.” 2019. Web. 05 Dec 2020.

Vancouver:

Vadovičová N. Produkce a purifikace izoforem proteinu p53 v bakteriálním expresním systému: P53 protein isoforms production and purification in the bacterial expression system. [Internet] [Thesis]. Brno University of Technology; 2019. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/11012/80642.

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

Council of Science Editors:

Vadovičová N. Produkce a purifikace izoforem proteinu p53 v bakteriálním expresním systému: P53 protein isoforms production and purification in the bacterial expression system. [Thesis]. Brno University of Technology; 2019. Available from: http://hdl.handle.net/11012/80642

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


Indian Institute of Science

14. Arandkar, Sharath Chandra. Characterization of the Cis and Trans Acting Factors that Influence p53 IRES Function.

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

p53 is a nodal tumor suppressor protein that acts as a major defense against cancers. Approximately 50% of human tumours have mutations in p53 gene.… (more)

Subjects/Keywords: Tumor Supressor Protein p53; Cancer Therapy; p53 Internal Ribosome Entry Sites (IRES) Function; p53 RNA; IRES RNA; Annexin A2 - p53 IRES Function; PSF-Polypyrimidine Tract Binding Protein-Associated Splicing Factor; p53 Gene Expression - Regulation; p53 Mediated Apoptosis; Cis Acting Factors - p53 IRES Function; p53 IRES Function; p53 Isoforms; p53 mRNA; p53 IRES RNA; Molecular Biology

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

APA (6th Edition):

Arandkar, S. C. (2018). Characterization of the Cis and Trans Acting Factors that Influence p53 IRES Function. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/3243

Chicago Manual of Style (16th Edition):

Arandkar, Sharath Chandra. “Characterization of the Cis and Trans Acting Factors that Influence p53 IRES Function.” 2018. Doctoral Dissertation, Indian Institute of Science. Accessed December 05, 2020. http://etd.iisc.ac.in/handle/2005/3243.

MLA Handbook (7th Edition):

Arandkar, Sharath Chandra. “Characterization of the Cis and Trans Acting Factors that Influence p53 IRES Function.” 2018. Web. 05 Dec 2020.

Vancouver:

Arandkar SC. Characterization of the Cis and Trans Acting Factors that Influence p53 IRES Function. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2018. [cited 2020 Dec 05]. Available from: http://etd.iisc.ac.in/handle/2005/3243.

Council of Science Editors:

Arandkar SC. Characterization of the Cis and Trans Acting Factors that Influence p53 IRES Function. [Doctoral Dissertation]. Indian Institute of Science; 2018. Available from: http://etd.iisc.ac.in/handle/2005/3243


Columbia University

15. Ou, Yang. Dissecting the role of p53-mediated metabolic regulation in tumor suppression.

Degree: 2016, Columbia University

 The p53 tumor suppressor protein has been well-characterized for its role in inducing growth arrest, senescence, and apoptosis upon various types of stresses. Recently, however,… (more)

Subjects/Keywords: p53 antioncogene; Tumor suppressor proteins; Antioncogenes; Metabolism – Regulation; p53 protein; Biology; Oncology; Cytology

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APA (6th Edition):

Ou, Y. (2016). Dissecting the role of p53-mediated metabolic regulation in tumor suppression. (Doctoral Dissertation). Columbia University. Retrieved from https://doi.org/10.7916/D8BZ66K5

Chicago Manual of Style (16th Edition):

Ou, Yang. “Dissecting the role of p53-mediated metabolic regulation in tumor suppression.” 2016. Doctoral Dissertation, Columbia University. Accessed December 05, 2020. https://doi.org/10.7916/D8BZ66K5.

MLA Handbook (7th Edition):

Ou, Yang. “Dissecting the role of p53-mediated metabolic regulation in tumor suppression.” 2016. Web. 05 Dec 2020.

Vancouver:

Ou Y. Dissecting the role of p53-mediated metabolic regulation in tumor suppression. [Internet] [Doctoral dissertation]. Columbia University; 2016. [cited 2020 Dec 05]. Available from: https://doi.org/10.7916/D8BZ66K5.

Council of Science Editors:

Ou Y. Dissecting the role of p53-mediated metabolic regulation in tumor suppression. [Doctoral Dissertation]. Columbia University; 2016. Available from: https://doi.org/10.7916/D8BZ66K5


University of Edinburgh

16. Saunders, Alexander William. New approaches to stapled peptides targeting the p53-MDM2 interaction.

Degree: PhD, 2016, University of Edinburgh

 Recent approaches to constraining peptide sequences into more structurally-defined α- helical secondary structures, so-called peptide stapling, are discussed. Stapled peptides are a class of therapeutics… (more)

Subjects/Keywords: 572; p53 protein; MDM2; peptides; peptide stapling; protein-protein interaction; stapled peptomer inhibitors

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APA (6th Edition):

Saunders, A. W. (2016). New approaches to stapled peptides targeting the p53-MDM2 interaction. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/25664

Chicago Manual of Style (16th Edition):

Saunders, Alexander William. “New approaches to stapled peptides targeting the p53-MDM2 interaction.” 2016. Doctoral Dissertation, University of Edinburgh. Accessed December 05, 2020. http://hdl.handle.net/1842/25664.

MLA Handbook (7th Edition):

Saunders, Alexander William. “New approaches to stapled peptides targeting the p53-MDM2 interaction.” 2016. Web. 05 Dec 2020.

Vancouver:

Saunders AW. New approaches to stapled peptides targeting the p53-MDM2 interaction. [Internet] [Doctoral dissertation]. University of Edinburgh; 2016. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1842/25664.

Council of Science Editors:

Saunders AW. New approaches to stapled peptides targeting the p53-MDM2 interaction. [Doctoral Dissertation]. University of Edinburgh; 2016. Available from: http://hdl.handle.net/1842/25664


Brno University of Technology

17. Hlávka, Ondřej. Vyhledávání vazebních míst transkripčních faktorů: Detection of Transcription Factor Binding Sites.

Degree: 2019, Brno University of Technology

 Nowadays, it is very important to study gene expression mechanism in molecular biology. Gene expression is also regulated by sequence specific transcription factors which binds… (more)

Subjects/Keywords: Transkripční faktor; protein p53; regulace genové exprese; vyhledávání TFBS; Transcription factor; protein p53; gene regulation; TFBS searching

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APA (6th Edition):

Hlávka, O. (2019). Vyhledávání vazebních míst transkripčních faktorů: Detection of Transcription Factor Binding Sites. (Thesis). Brno University of Technology. Retrieved from http://hdl.handle.net/11012/53518

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):

Hlávka, Ondřej. “Vyhledávání vazebních míst transkripčních faktorů: Detection of Transcription Factor Binding Sites.” 2019. Thesis, Brno University of Technology. Accessed December 05, 2020. http://hdl.handle.net/11012/53518.

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

MLA Handbook (7th Edition):

Hlávka, Ondřej. “Vyhledávání vazebních míst transkripčních faktorů: Detection of Transcription Factor Binding Sites.” 2019. Web. 05 Dec 2020.

Vancouver:

Hlávka O. Vyhledávání vazebních míst transkripčních faktorů: Detection of Transcription Factor Binding Sites. [Internet] [Thesis]. Brno University of Technology; 2019. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/11012/53518.

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

Council of Science Editors:

Hlávka O. Vyhledávání vazebních míst transkripčních faktorů: Detection of Transcription Factor Binding Sites. [Thesis]. Brno University of Technology; 2019. Available from: http://hdl.handle.net/11012/53518

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

18. Hafsi, Hind. N-terminal isoforms of the p53 tumour suppressor protein : effects on p53 transcriptional activity and expression in cutaneous melanoma : Isoformes du domaine N-terminal du suppresseur de tumeur p53 : sur l’activité transcriptionnelle de p53 et expression dans les mélanomes cutanés.

Degree: Docteur es, Oncologie et biologie moléculaire, 2012, Université Claude Bernard – Lyon I

La protéine suppresseur de tumeur p53 est soumise à de complexes régulations transcriptionnelles et posttraductionnelles. La découverte d’isoformes de p53 a introduit un degré de… (more)

Subjects/Keywords: Protéine suppresseur de tumeur p53; Isoformes; Régulation transcriptionnelle; Mélanomes; Inactivation de p53; P53 tumour suppressor protein; Isoforms; Transcriptional regulation; Melanoma; Inactivation of p53; 616.99

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APA (6th Edition):

Hafsi, H. (2012). N-terminal isoforms of the p53 tumour suppressor protein : effects on p53 transcriptional activity and expression in cutaneous melanoma : Isoformes du domaine N-terminal du suppresseur de tumeur p53 : sur l’activité transcriptionnelle de p53 et expression dans les mélanomes cutanés. (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2012LYO10302

Chicago Manual of Style (16th Edition):

Hafsi, Hind. “N-terminal isoforms of the p53 tumour suppressor protein : effects on p53 transcriptional activity and expression in cutaneous melanoma : Isoformes du domaine N-terminal du suppresseur de tumeur p53 : sur l’activité transcriptionnelle de p53 et expression dans les mélanomes cutanés.” 2012. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed December 05, 2020. http://www.theses.fr/2012LYO10302.

MLA Handbook (7th Edition):

Hafsi, Hind. “N-terminal isoforms of the p53 tumour suppressor protein : effects on p53 transcriptional activity and expression in cutaneous melanoma : Isoformes du domaine N-terminal du suppresseur de tumeur p53 : sur l’activité transcriptionnelle de p53 et expression dans les mélanomes cutanés.” 2012. Web. 05 Dec 2020.

Vancouver:

Hafsi H. N-terminal isoforms of the p53 tumour suppressor protein : effects on p53 transcriptional activity and expression in cutaneous melanoma : Isoformes du domaine N-terminal du suppresseur de tumeur p53 : sur l’activité transcriptionnelle de p53 et expression dans les mélanomes cutanés. [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2012. [cited 2020 Dec 05]. Available from: http://www.theses.fr/2012LYO10302.

Council of Science Editors:

Hafsi H. N-terminal isoforms of the p53 tumour suppressor protein : effects on p53 transcriptional activity and expression in cutaneous melanoma : Isoformes du domaine N-terminal du suppresseur de tumeur p53 : sur l’activité transcriptionnelle de p53 et expression dans les mélanomes cutanés. [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2012. Available from: http://www.theses.fr/2012LYO10302


University of California – Riverside

19. Sati, Sandeep. Investigating the Interaction of p53 with Proteins Involved in Nucleotide Excision Repair Pathway.

Degree: Environmental Toxicology, 2017, University of California – Riverside

 DNA is exposed to relentless challenges by a variety of chemical, enzymatic and environmental agents. Maintaining the integrity of the genome by immediate and precise… (more)

Subjects/Keywords: Biochemistry; DNA repair; ERCC1-XPF; NER; p53; Protein interaction; XPB

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APA (6th Edition):

Sati, S. (2017). Investigating the Interaction of p53 with Proteins Involved in Nucleotide Excision Repair Pathway. (Thesis). University of California – Riverside. Retrieved from http://www.escholarship.org/uc/item/3666w3pn

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):

Sati, Sandeep. “Investigating the Interaction of p53 with Proteins Involved in Nucleotide Excision Repair Pathway.” 2017. Thesis, University of California – Riverside. Accessed December 05, 2020. http://www.escholarship.org/uc/item/3666w3pn.

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

MLA Handbook (7th Edition):

Sati, Sandeep. “Investigating the Interaction of p53 with Proteins Involved in Nucleotide Excision Repair Pathway.” 2017. Web. 05 Dec 2020.

Vancouver:

Sati S. Investigating the Interaction of p53 with Proteins Involved in Nucleotide Excision Repair Pathway. [Internet] [Thesis]. University of California – Riverside; 2017. [cited 2020 Dec 05]. Available from: http://www.escholarship.org/uc/item/3666w3pn.

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

Council of Science Editors:

Sati S. Investigating the Interaction of p53 with Proteins Involved in Nucleotide Excision Repair Pathway. [Thesis]. University of California – Riverside; 2017. Available from: http://www.escholarship.org/uc/item/3666w3pn

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


University of California – San Diego

20. Offutt, Tavina. Studying Proteins Implicated in Cancer with a Computational Toolbox.

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

 Cancer formation is a complex, multi-step process that allows cells to grow abnormally and potentially invade and spread throughout the body. A single genetic or… (more)

Subjects/Keywords: Computational chemistry; cancer; molecular dynamics; p53; protein kinases; virtual screening

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APA (6th Edition):

Offutt, T. (2017). Studying Proteins Implicated in Cancer with a Computational Toolbox. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/4rw973hd

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):

Offutt, Tavina. “Studying Proteins Implicated in Cancer with a Computational Toolbox.” 2017. Thesis, University of California – San Diego. Accessed December 05, 2020. http://www.escholarship.org/uc/item/4rw973hd.

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

MLA Handbook (7th Edition):

Offutt, Tavina. “Studying Proteins Implicated in Cancer with a Computational Toolbox.” 2017. Web. 05 Dec 2020.

Vancouver:

Offutt T. Studying Proteins Implicated in Cancer with a Computational Toolbox. [Internet] [Thesis]. University of California – San Diego; 2017. [cited 2020 Dec 05]. Available from: http://www.escholarship.org/uc/item/4rw973hd.

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

Council of Science Editors:

Offutt T. Studying Proteins Implicated in Cancer with a Computational Toolbox. [Thesis]. University of California – San Diego; 2017. Available from: http://www.escholarship.org/uc/item/4rw973hd

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

21. Schaub, Leasha. QUANTIFYING THE ENERGETICS OF BINDING BETWEEN p53 AND DNA USING ELECTROPHORETIC MOBILITY SHIFT ASSAYS.

Degree: 2013

Subjects/Keywords: p53; intrinsically disordered protein; binding

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APA (6th Edition):

Schaub, L. (2013). QUANTIFYING THE ENERGETICS OF BINDING BETWEEN p53 AND DNA USING ELECTROPHORETIC MOBILITY SHIFT ASSAYS. (Thesis). [No school.] Retrieved from http://hdl.handle.net/2249.1/62699

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No school.

Chicago Manual of Style (16th Edition):

Schaub, Leasha. “QUANTIFYING THE ENERGETICS OF BINDING BETWEEN p53 AND DNA USING ELECTROPHORETIC MOBILITY SHIFT ASSAYS.” 2013. Thesis, [No school]. Accessed December 05, 2020. http://hdl.handle.net/2249.1/62699.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No school.

MLA Handbook (7th Edition):

Schaub, Leasha. “QUANTIFYING THE ENERGETICS OF BINDING BETWEEN p53 AND DNA USING ELECTROPHORETIC MOBILITY SHIFT ASSAYS.” 2013. Web. 05 Dec 2020.

Vancouver:

Schaub L. QUANTIFYING THE ENERGETICS OF BINDING BETWEEN p53 AND DNA USING ELECTROPHORETIC MOBILITY SHIFT ASSAYS. [Internet] [Thesis]. [No school]; 2013. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/2249.1/62699.

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No school.

Council of Science Editors:

Schaub L. QUANTIFYING THE ENERGETICS OF BINDING BETWEEN p53 AND DNA USING ELECTROPHORETIC MOBILITY SHIFT ASSAYS. [Thesis]. [No school]; 2013. Available from: http://hdl.handle.net/2249.1/62699

Note: this citation may be lacking information needed for this citation format:
Not specified: Masters Thesis or Doctoral Dissertation
No school.


Harvard University

22. Gaglia, Giorgio. Dynamics of p53 tetramers in live single cells.

Degree: PhD, Systems Biology, 2014, Harvard University

Protein homo-oligomerization is the process through which identical peptides bind together to form higher order complexes. Self-interactions in many cases are constitutive and stable, used… (more)

Subjects/Keywords: Systematic biology; DNA damage; mathematical modeling; p53; protein dynamics; tetramerization

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APA (6th Edition):

Gaglia, G. (2014). Dynamics of p53 tetramers in live single cells. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:12269874

Chicago Manual of Style (16th Edition):

Gaglia, Giorgio. “Dynamics of p53 tetramers in live single cells.” 2014. Doctoral Dissertation, Harvard University. Accessed December 05, 2020. http://nrs.harvard.edu/urn-3:HUL.InstRepos:12269874.

MLA Handbook (7th Edition):

Gaglia, Giorgio. “Dynamics of p53 tetramers in live single cells.” 2014. Web. 05 Dec 2020.

Vancouver:

Gaglia G. Dynamics of p53 tetramers in live single cells. [Internet] [Doctoral dissertation]. Harvard University; 2014. [cited 2020 Dec 05]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:12269874.

Council of Science Editors:

Gaglia G. Dynamics of p53 tetramers in live single cells. [Doctoral Dissertation]. Harvard University; 2014. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:12269874


Univerzitet u Beogradu

23. Kanjer, Ksenija S., 1963-. Terapijski odgovor karcinoma dojke na citotoksične lekove analizom markera apoptoze i proliferacije ćelija.

Degree: Medicinski fakultet, 2015, Univerzitet u Beogradu

Onkologija - Karcinom dojke / Oncology - Breast cancer

Terapijski odgovor karcinoma dojke na delovanje citotoksičnih lekova se znatno razlikuje i samo će deo pacijentkinja… (more)

Subjects/Keywords: Breast cancer; chemoresponsiveness; Ki-67; AI; p53 and bcl-2 protein

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APA (6th Edition):

Kanjer, Ksenija S., 1. (2015). Terapijski odgovor karcinoma dojke na citotoksične lekove analizom markera apoptoze i proliferacije ćelija. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:7783/bdef:Content/get

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):

Kanjer, Ksenija S., 1963-. “Terapijski odgovor karcinoma dojke na citotoksične lekove analizom markera apoptoze i proliferacije ćelija.” 2015. Thesis, Univerzitet u Beogradu. Accessed December 05, 2020. https://fedorabg.bg.ac.rs/fedora/get/o:7783/bdef:Content/get.

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

MLA Handbook (7th Edition):

Kanjer, Ksenija S., 1963-. “Terapijski odgovor karcinoma dojke na citotoksične lekove analizom markera apoptoze i proliferacije ćelija.” 2015. Web. 05 Dec 2020.

Vancouver:

Kanjer, Ksenija S. 1. Terapijski odgovor karcinoma dojke na citotoksične lekove analizom markera apoptoze i proliferacije ćelija. [Internet] [Thesis]. Univerzitet u Beogradu; 2015. [cited 2020 Dec 05]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:7783/bdef:Content/get.

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

Council of Science Editors:

Kanjer, Ksenija S. 1. Terapijski odgovor karcinoma dojke na citotoksične lekove analizom markera apoptoze i proliferacije ćelija. [Thesis]. Univerzitet u Beogradu; 2015. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:7783/bdef:Content/get

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


University of Edinburgh

24. Jurneczko, Ewa. Resolving intrinsically disordered proteins of the cancer genome with ion mobility mass spectrometry.

Degree: PhD, 2014, University of Edinburgh

 For proteins the link between their structure and their function is a central tenet of biology. A common approach to understanding protein function is to… (more)

Subjects/Keywords: 572.8; conformation; p53 protein; mass spectrometry; ion mobility; disordered

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APA (6th Edition):

Jurneczko, E. (2014). Resolving intrinsically disordered proteins of the cancer genome with ion mobility mass spectrometry. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/8844

Chicago Manual of Style (16th Edition):

Jurneczko, Ewa. “Resolving intrinsically disordered proteins of the cancer genome with ion mobility mass spectrometry.” 2014. Doctoral Dissertation, University of Edinburgh. Accessed December 05, 2020. http://hdl.handle.net/1842/8844.

MLA Handbook (7th Edition):

Jurneczko, Ewa. “Resolving intrinsically disordered proteins of the cancer genome with ion mobility mass spectrometry.” 2014. Web. 05 Dec 2020.

Vancouver:

Jurneczko E. Resolving intrinsically disordered proteins of the cancer genome with ion mobility mass spectrometry. [Internet] [Doctoral dissertation]. University of Edinburgh; 2014. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1842/8844.

Council of Science Editors:

Jurneczko E. Resolving intrinsically disordered proteins of the cancer genome with ion mobility mass spectrometry. [Doctoral Dissertation]. University of Edinburgh; 2014. Available from: http://hdl.handle.net/1842/8844


East Carolina University

25. Trumbo, Caitlin M. Electrochemical Detection of Benzo[a]Pyrene-Induced DNA Damage at TP53 Oligomers : Impact of 5'-Methyl Cytosine and Bioactivation on the Genotoxicity Process.

Degree: MS, Chemistry, 2014, East Carolina University

 DNA houses the blueprint that dictates how an organism will develop. However, DNA features numerous reactive sites that can be attacked by chemicals and radiation,… (more)

Subjects/Keywords: Chemistry; DNA damage; Mutation (Biology); Electrochemical sensors; p53 protein

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APA (6th Edition):

Trumbo, C. M. (2014). Electrochemical Detection of Benzo[a]Pyrene-Induced DNA Damage at TP53 Oligomers : Impact of 5'-Methyl Cytosine and Bioactivation on the Genotoxicity Process. (Masters Thesis). East Carolina University. Retrieved from http://hdl.handle.net/10342/4527

Chicago Manual of Style (16th Edition):

Trumbo, Caitlin M. “Electrochemical Detection of Benzo[a]Pyrene-Induced DNA Damage at TP53 Oligomers : Impact of 5'-Methyl Cytosine and Bioactivation on the Genotoxicity Process.” 2014. Masters Thesis, East Carolina University. Accessed December 05, 2020. http://hdl.handle.net/10342/4527.

MLA Handbook (7th Edition):

Trumbo, Caitlin M. “Electrochemical Detection of Benzo[a]Pyrene-Induced DNA Damage at TP53 Oligomers : Impact of 5'-Methyl Cytosine and Bioactivation on the Genotoxicity Process.” 2014. Web. 05 Dec 2020.

Vancouver:

Trumbo CM. Electrochemical Detection of Benzo[a]Pyrene-Induced DNA Damage at TP53 Oligomers : Impact of 5'-Methyl Cytosine and Bioactivation on the Genotoxicity Process. [Internet] [Masters thesis]. East Carolina University; 2014. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/10342/4527.

Council of Science Editors:

Trumbo CM. Electrochemical Detection of Benzo[a]Pyrene-Induced DNA Damage at TP53 Oligomers : Impact of 5'-Methyl Cytosine and Bioactivation on the Genotoxicity Process. [Masters Thesis]. East Carolina University; 2014. Available from: http://hdl.handle.net/10342/4527


University of Kansas

26. Khar, Karen Rene. A Step Closer to Precision Oncology: Computational, Biochemical, and Cell-Based Screening to Find Compounds that Stabilize p53.

Degree: PhD, Biochemistry & Molecular Biology, 2018, University of Kansas

 Personalized medicine in cancer aims to tailor a treatment plan that takes into account the unique features of a patient's malignancy. One therapeutic target that… (more)

Subjects/Keywords: Bioinformatics; Cancer; GPU; p53; Protein Ligand Docking; Rosetta; Virtual Screen

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APA (6th Edition):

Khar, K. R. (2018). A Step Closer to Precision Oncology: Computational, Biochemical, and Cell-Based Screening to Find Compounds that Stabilize p53. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/27887

Chicago Manual of Style (16th Edition):

Khar, Karen Rene. “A Step Closer to Precision Oncology: Computational, Biochemical, and Cell-Based Screening to Find Compounds that Stabilize p53.” 2018. Doctoral Dissertation, University of Kansas. Accessed December 05, 2020. http://hdl.handle.net/1808/27887.

MLA Handbook (7th Edition):

Khar, Karen Rene. “A Step Closer to Precision Oncology: Computational, Biochemical, and Cell-Based Screening to Find Compounds that Stabilize p53.” 2018. Web. 05 Dec 2020.

Vancouver:

Khar KR. A Step Closer to Precision Oncology: Computational, Biochemical, and Cell-Based Screening to Find Compounds that Stabilize p53. [Internet] [Doctoral dissertation]. University of Kansas; 2018. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/1808/27887.

Council of Science Editors:

Khar KR. A Step Closer to Precision Oncology: Computational, Biochemical, and Cell-Based Screening to Find Compounds that Stabilize p53. [Doctoral Dissertation]. University of Kansas; 2018. Available from: http://hdl.handle.net/1808/27887


Virginia Tech

27. Liu, Jingjing. Identification and Regulatory Role of E3 Ligases in the Time-Dependent Degradation of the Circadian Factor Period 2.

Degree: PhD, Biological Sciences, 2016, Virginia Tech

 Circadian rhythms are self-sustained, 24h, biological oscillatory processes that are present in organisms ranging from bacteria to human. Circadian rhythms, which can be synchronized by… (more)

Subjects/Keywords: Circadian rhythm; Period 2; ubiquitination; Mdm2; Protein stability; p53

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

APA (6th Edition):

Liu, J. (2016). Identification and Regulatory Role of E3 Ligases in the Time-Dependent Degradation of the Circadian Factor Period 2. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/81179

Chicago Manual of Style (16th Edition):

Liu, Jingjing. “Identification and Regulatory Role of E3 Ligases in the Time-Dependent Degradation of the Circadian Factor Period 2.” 2016. Doctoral Dissertation, Virginia Tech. Accessed December 05, 2020. http://hdl.handle.net/10919/81179.

MLA Handbook (7th Edition):

Liu, Jingjing. “Identification and Regulatory Role of E3 Ligases in the Time-Dependent Degradation of the Circadian Factor Period 2.” 2016. Web. 05 Dec 2020.

Vancouver:

Liu J. Identification and Regulatory Role of E3 Ligases in the Time-Dependent Degradation of the Circadian Factor Period 2. [Internet] [Doctoral dissertation]. Virginia Tech; 2016. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/10919/81179.

Council of Science Editors:

Liu J. Identification and Regulatory Role of E3 Ligases in the Time-Dependent Degradation of the Circadian Factor Period 2. [Doctoral Dissertation]. Virginia Tech; 2016. Available from: http://hdl.handle.net/10919/81179

28. Kogan, Samuel. Cellular zinc homeostasis: a regulator of the pharmacodynamics and innate resistance of zinc metallochaperones.

Degree: PhD, Pharmacology, Cellular and Molecular, 2018, Rutgers University

TP53 is the most commonly mutated gene in cancer; therefore, small molecule restoration of wild type structure and function to mutant p53 (hereafter referred to… (more)

Subjects/Keywords: Cancer – Treatment; p53 protein

…87 ix 1 INTRODUCTION TP53 gene/p53 protein The TP53 gene is the most frequently mutated… …et al., 2013). The p53 protein is one of the most well characterized tumor suppressors… …target gene, which labels p53 for proteasomal degradation. The p53 protein is primarily… …levels of the acetylated protein correlate with p53 activation and stabilization (Kruse… …dependent mediators of tumor suppression. The mutant p53 protein expressed in these mice was still… 

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

APA (6th Edition):

Kogan, S. (2018). Cellular zinc homeostasis: a regulator of the pharmacodynamics and innate resistance of zinc metallochaperones. (Doctoral Dissertation). Rutgers University. Retrieved from https://rucore.libraries.rutgers.edu/rutgers-lib/59140/

Chicago Manual of Style (16th Edition):

Kogan, Samuel. “Cellular zinc homeostasis: a regulator of the pharmacodynamics and innate resistance of zinc metallochaperones.” 2018. Doctoral Dissertation, Rutgers University. Accessed December 05, 2020. https://rucore.libraries.rutgers.edu/rutgers-lib/59140/.

MLA Handbook (7th Edition):

Kogan, Samuel. “Cellular zinc homeostasis: a regulator of the pharmacodynamics and innate resistance of zinc metallochaperones.” 2018. Web. 05 Dec 2020.

Vancouver:

Kogan S. Cellular zinc homeostasis: a regulator of the pharmacodynamics and innate resistance of zinc metallochaperones. [Internet] [Doctoral dissertation]. Rutgers University; 2018. [cited 2020 Dec 05]. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/59140/.

Council of Science Editors:

Kogan S. Cellular zinc homeostasis: a regulator of the pharmacodynamics and innate resistance of zinc metallochaperones. [Doctoral Dissertation]. Rutgers University; 2018. Available from: https://rucore.libraries.rutgers.edu/rutgers-lib/59140/


Temple University

29. Akula, Kavitha. Expanding the Spiroligomers Toolbox as Protein-Protein Interaction Inhibitors.

Degree: PhD, 2017, Temple University

Chemistry

This work presents the application of spiroligomers as inhibitors of protein-protein interactions. After the discovery of an acyl-transfer coupling reaction by Dr. Zachary Brown,… (more)

Subjects/Keywords: Chemistry; Biochemistry;

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

APA (6th Edition):

Akula, K. (2017). Expanding the Spiroligomers Toolbox as Protein-Protein Interaction Inhibitors. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,422281

Chicago Manual of Style (16th Edition):

Akula, Kavitha. “Expanding the Spiroligomers Toolbox as Protein-Protein Interaction Inhibitors.” 2017. Doctoral Dissertation, Temple University. Accessed December 05, 2020. http://digital.library.temple.edu/u?/p245801coll10,422281.

MLA Handbook (7th Edition):

Akula, Kavitha. “Expanding the Spiroligomers Toolbox as Protein-Protein Interaction Inhibitors.” 2017. Web. 05 Dec 2020.

Vancouver:

Akula K. Expanding the Spiroligomers Toolbox as Protein-Protein Interaction Inhibitors. [Internet] [Doctoral dissertation]. Temple University; 2017. [cited 2020 Dec 05]. Available from: http://digital.library.temple.edu/u?/p245801coll10,422281.

Council of Science Editors:

Akula K. Expanding the Spiroligomers Toolbox as Protein-Protein Interaction Inhibitors. [Doctoral Dissertation]. Temple University; 2017. Available from: http://digital.library.temple.edu/u?/p245801coll10,422281


Durban University of Technology

30. Cele, Nosipho Magnificat. Computational studies on the identification and analyses of p53 cancer associated mutations.

Degree: 2017, Durban University of Technology

Submitted in the fulfillment of the requirement for the Degree of Master's in Chemistry, Durban University of Technology, 2017.

P53 is a tumour suppressor protein(more)

Subjects/Keywords: p53 antioncogene; p53 protein; Tumor suppressor proteins; Cancer – Computer simulation; Mutation (Biology) – Computer simulation; Cancer – Genetic aspects; Cancer – Molecular aspects

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

APA (6th Edition):

Cele, N. M. (2017). Computational studies on the identification and analyses of p53 cancer associated mutations. (Thesis). Durban University of Technology. Retrieved from http://hdl.handle.net/10321/2617

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):

Cele, Nosipho Magnificat. “Computational studies on the identification and analyses of p53 cancer associated mutations.” 2017. Thesis, Durban University of Technology. Accessed December 05, 2020. http://hdl.handle.net/10321/2617.

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

MLA Handbook (7th Edition):

Cele, Nosipho Magnificat. “Computational studies on the identification and analyses of p53 cancer associated mutations.” 2017. Web. 05 Dec 2020.

Vancouver:

Cele NM. Computational studies on the identification and analyses of p53 cancer associated mutations. [Internet] [Thesis]. Durban University of Technology; 2017. [cited 2020 Dec 05]. Available from: http://hdl.handle.net/10321/2617.

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

Council of Science Editors:

Cele NM. Computational studies on the identification and analyses of p53 cancer associated mutations. [Thesis]. Durban University of Technology; 2017. Available from: http://hdl.handle.net/10321/2617

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

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