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You searched for subject:(p53). Showing records 1 – 30 of 964 total matches.

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University of Georgia

1. Sarkar, Suparna Ajoy. Involvement of p53 and selected proto-oncogenes in all-trans-retinoic acid-mediated murine embryonic development.

Degree: PhD, Toxicology, 2001, University of Georgia

 Tumor-suppressor p53 regulates cell cycle, differentiation and apoptosis. The effect of all-trans-retinoic acid (RA) on p53, other protooncogenes and downstream signaling molecules were investigated during… (more)

Subjects/Keywords: p53

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APA (6th Edition):

Sarkar, S. A. (2001). Involvement of p53 and selected proto-oncogenes in all-trans-retinoic acid-mediated murine embryonic development. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/sarkar_suparna_a_200112_phd

Chicago Manual of Style (16th Edition):

Sarkar, Suparna Ajoy. “Involvement of p53 and selected proto-oncogenes in all-trans-retinoic acid-mediated murine embryonic development.” 2001. Doctoral Dissertation, University of Georgia. Accessed April 20, 2019. http://purl.galileo.usg.edu/uga_etd/sarkar_suparna_a_200112_phd.

MLA Handbook (7th Edition):

Sarkar, Suparna Ajoy. “Involvement of p53 and selected proto-oncogenes in all-trans-retinoic acid-mediated murine embryonic development.” 2001. Web. 20 Apr 2019.

Vancouver:

Sarkar SA. Involvement of p53 and selected proto-oncogenes in all-trans-retinoic acid-mediated murine embryonic development. [Internet] [Doctoral dissertation]. University of Georgia; 2001. [cited 2019 Apr 20]. Available from: http://purl.galileo.usg.edu/uga_etd/sarkar_suparna_a_200112_phd.

Council of Science Editors:

Sarkar SA. Involvement of p53 and selected proto-oncogenes in all-trans-retinoic acid-mediated murine embryonic development. [Doctoral Dissertation]. University of Georgia; 2001. Available from: http://purl.galileo.usg.edu/uga_etd/sarkar_suparna_a_200112_phd


University of Texas Southwestern Medical Center

2. 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 April 20, 2019. 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. 20 Apr 2019.

Vancouver:

Wylie AD. P53 Genes Act to Restrain Mobile Elements. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2015. [cited 2019 Apr 20]. 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

3. 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 April 20, 2019. 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. 20 Apr 2019.

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 2019 Apr 20]. 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

4. Estermann, Fanny. Etude d'un nouveau mécanisme épigénétique d'inactivation de p53 par une protéine adénovirale et son implication dans la création d'un virus oncolytique : Heterochromatin silencing of p53 target genes by a small adenoviral protein and its implication in oncolytic virus development.

Degree: Docteur es, Cancérologie, génétique, hématologie, immunologie, 2010, Université Montpellier I

P53 empêche la réplication d'ADN cellulaire pathologique ainsi que viral en activant la transcription d'effecteurs en aval. L'augmentation d'expression de p53 et sa phosphorylation en… (more)

Subjects/Keywords: Adénovirus; Épigénétique; P53; Adenovirus; Epigenetic; P53

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APA (6th Edition):

Estermann, F. (2010). Etude d'un nouveau mécanisme épigénétique d'inactivation de p53 par une protéine adénovirale et son implication dans la création d'un virus oncolytique : Heterochromatin silencing of p53 target genes by a small adenoviral protein and its implication in oncolytic virus development. (Doctoral Dissertation). Université Montpellier I. Retrieved from http://www.theses.fr/2010MON13510

Chicago Manual of Style (16th Edition):

Estermann, Fanny. “Etude d'un nouveau mécanisme épigénétique d'inactivation de p53 par une protéine adénovirale et son implication dans la création d'un virus oncolytique : Heterochromatin silencing of p53 target genes by a small adenoviral protein and its implication in oncolytic virus development.” 2010. Doctoral Dissertation, Université Montpellier I. Accessed April 20, 2019. http://www.theses.fr/2010MON13510.

MLA Handbook (7th Edition):

Estermann, Fanny. “Etude d'un nouveau mécanisme épigénétique d'inactivation de p53 par une protéine adénovirale et son implication dans la création d'un virus oncolytique : Heterochromatin silencing of p53 target genes by a small adenoviral protein and its implication in oncolytic virus development.” 2010. Web. 20 Apr 2019.

Vancouver:

Estermann F. Etude d'un nouveau mécanisme épigénétique d'inactivation de p53 par une protéine adénovirale et son implication dans la création d'un virus oncolytique : Heterochromatin silencing of p53 target genes by a small adenoviral protein and its implication in oncolytic virus development. [Internet] [Doctoral dissertation]. Université Montpellier I; 2010. [cited 2019 Apr 20]. Available from: http://www.theses.fr/2010MON13510.

Council of Science Editors:

Estermann F. Etude d'un nouveau mécanisme épigénétique d'inactivation de p53 par une protéine adénovirale et son implication dans la création d'un virus oncolytique : Heterochromatin silencing of p53 target genes by a small adenoviral protein and its implication in oncolytic virus development. [Doctoral Dissertation]. Université Montpellier I; 2010. Available from: http://www.theses.fr/2010MON13510


Université Paris-Sud – Paris XI

5. Jemaâ, Mohamed. Chimiothérapie ciblant les cellules cancéreuses p53 déficientes : Chemotherapy Targeting p53 Deficient Tumor Cells.

Degree: Docteur es, Cancérologie : Biologie, Médecine, Santé, 2012, Université Paris-Sud – Paris XI

L’altération génétique et/ou fonctionnelle de p53 est très répondue dans les cancers humains et est répertoriée dans plus d’un cas sur deux. Les traitements et… (more)

Subjects/Keywords: P53; Vidéomicroscopie; MPS1; P53; Videomicroscopy; MPS1

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APA (6th Edition):

Jemaâ, M. (2012). Chimiothérapie ciblant les cellules cancéreuses p53 déficientes : Chemotherapy Targeting p53 Deficient Tumor Cells. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2012PA11T040

Chicago Manual of Style (16th Edition):

Jemaâ, Mohamed. “Chimiothérapie ciblant les cellules cancéreuses p53 déficientes : Chemotherapy Targeting p53 Deficient Tumor Cells.” 2012. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed April 20, 2019. http://www.theses.fr/2012PA11T040.

MLA Handbook (7th Edition):

Jemaâ, Mohamed. “Chimiothérapie ciblant les cellules cancéreuses p53 déficientes : Chemotherapy Targeting p53 Deficient Tumor Cells.” 2012. Web. 20 Apr 2019.

Vancouver:

Jemaâ M. Chimiothérapie ciblant les cellules cancéreuses p53 déficientes : Chemotherapy Targeting p53 Deficient Tumor Cells. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2012. [cited 2019 Apr 20]. Available from: http://www.theses.fr/2012PA11T040.

Council of Science Editors:

Jemaâ M. Chimiothérapie ciblant les cellules cancéreuses p53 déficientes : Chemotherapy Targeting p53 Deficient Tumor Cells. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2012. Available from: http://www.theses.fr/2012PA11T040

6. Gastou, Marc François Philippe. Rôle de la protéine HSP70 au cours de l'anémie de Blackfan-Diamond : Role of HSP70 protein in Blacfan-Diamond anemia.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2016, Sorbonne Paris Cité

 L’anémie de Blackfan-Diamond (ABD) est une érythroblastopénie congénitale rare, secondaire à un blocage de la maturation érythroïde entre les stades BFU-e et CFU-e. L’ABD est… (more)

Subjects/Keywords: Erythroblastopénie; HSP70; P53; Erythroblastopenia; HSP70; P53

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APA (6th Edition):

Gastou, M. F. P. (2016). Rôle de la protéine HSP70 au cours de l'anémie de Blackfan-Diamond : Role of HSP70 protein in Blacfan-Diamond anemia. (Doctoral Dissertation). Sorbonne Paris Cité. Retrieved from http://www.theses.fr/2016USPCC231

Chicago Manual of Style (16th Edition):

Gastou, Marc François Philippe. “Rôle de la protéine HSP70 au cours de l'anémie de Blackfan-Diamond : Role of HSP70 protein in Blacfan-Diamond anemia.” 2016. Doctoral Dissertation, Sorbonne Paris Cité. Accessed April 20, 2019. http://www.theses.fr/2016USPCC231.

MLA Handbook (7th Edition):

Gastou, Marc François Philippe. “Rôle de la protéine HSP70 au cours de l'anémie de Blackfan-Diamond : Role of HSP70 protein in Blacfan-Diamond anemia.” 2016. Web. 20 Apr 2019.

Vancouver:

Gastou MFP. Rôle de la protéine HSP70 au cours de l'anémie de Blackfan-Diamond : Role of HSP70 protein in Blacfan-Diamond anemia. [Internet] [Doctoral dissertation]. Sorbonne Paris Cité; 2016. [cited 2019 Apr 20]. Available from: http://www.theses.fr/2016USPCC231.

Council of Science Editors:

Gastou MFP. Rôle de la protéine HSP70 au cours de l'anémie de Blackfan-Diamond : Role of HSP70 protein in Blacfan-Diamond anemia. [Doctoral Dissertation]. Sorbonne Paris Cité; 2016. Available from: http://www.theses.fr/2016USPCC231


Vanderbilt University

7. Eby, Kathryn Grace. Identification and Characterization of p53 Target Genes.

Degree: PhD, Biochemistry, 2010, Vanderbilt University

 After 30 years of research, p53 is recognized as one of the most frequently mutated genes in human cancer (Baker et al, 1989; Nigro et… (more)

Subjects/Keywords: ISG20L1; p53; autophagy

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APA (6th Edition):

Eby, K. G. (2010). Identification and Characterization of p53 Target Genes. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu//available/etd-05242010-175410/ ;

Chicago Manual of Style (16th Edition):

Eby, Kathryn Grace. “Identification and Characterization of p53 Target Genes.” 2010. Doctoral Dissertation, Vanderbilt University. Accessed April 20, 2019. http://etd.library.vanderbilt.edu//available/etd-05242010-175410/ ;.

MLA Handbook (7th Edition):

Eby, Kathryn Grace. “Identification and Characterization of p53 Target Genes.” 2010. Web. 20 Apr 2019.

Vancouver:

Eby KG. Identification and Characterization of p53 Target Genes. [Internet] [Doctoral dissertation]. Vanderbilt University; 2010. [cited 2019 Apr 20]. Available from: http://etd.library.vanderbilt.edu//available/etd-05242010-175410/ ;.

Council of Science Editors:

Eby KG. Identification and Characterization of p53 Target Genes. [Doctoral Dissertation]. Vanderbilt University; 2010. Available from: http://etd.library.vanderbilt.edu//available/etd-05242010-175410/ ;

8. Gillardin, Pierre. Régulation épigénétique et protéique de p73 dans le Myélome Multiple : Epigenetic and post-translational régulation of p73 in Multiple Myeloma.

Degree: Docteur es, Biologie des organismes, 2017, Nantes

Les anomalies de TP53, que sont la délétion génique associée ou non à des mutations somatiques, demeurent un facteur de résistance au traitement dans le… (more)

Subjects/Keywords: Décitabine; P53; P73

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APA (6th Edition):

Gillardin, P. (2017). Régulation épigénétique et protéique de p73 dans le Myélome Multiple : Epigenetic and post-translational régulation of p73 in Multiple Myeloma. (Doctoral Dissertation). Nantes. Retrieved from http://www.theses.fr/2017NANT1037

Chicago Manual of Style (16th Edition):

Gillardin, Pierre. “Régulation épigénétique et protéique de p73 dans le Myélome Multiple : Epigenetic and post-translational régulation of p73 in Multiple Myeloma.” 2017. Doctoral Dissertation, Nantes. Accessed April 20, 2019. http://www.theses.fr/2017NANT1037.

MLA Handbook (7th Edition):

Gillardin, Pierre. “Régulation épigénétique et protéique de p73 dans le Myélome Multiple : Epigenetic and post-translational régulation of p73 in Multiple Myeloma.” 2017. Web. 20 Apr 2019.

Vancouver:

Gillardin P. Régulation épigénétique et protéique de p73 dans le Myélome Multiple : Epigenetic and post-translational régulation of p73 in Multiple Myeloma. [Internet] [Doctoral dissertation]. Nantes; 2017. [cited 2019 Apr 20]. Available from: http://www.theses.fr/2017NANT1037.

Council of Science Editors:

Gillardin P. Régulation épigénétique et protéique de p73 dans le Myélome Multiple : Epigenetic and post-translational régulation of p73 in Multiple Myeloma. [Doctoral Dissertation]. Nantes; 2017. Available from: http://www.theses.fr/2017NANT1037


University of New South Wales

9. Shaw, Alexander. Regulation of the p53 tumour suppressor by miR-380.

Degree: Biotechnology & Biomolecular Sciences, 2010, University of New South Wales

p53 is a critical tumour suppressor gene at the centre of the cell’s innate tumour suppressive network. p53 function is eliminated via mutation in the… (more)

Subjects/Keywords: Cancer; microRNA; p53

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APA (6th Edition):

Shaw, A. (2010). Regulation of the p53 tumour suppressor by miR-380. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/50303 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9184/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Shaw, Alexander. “Regulation of the p53 tumour suppressor by miR-380.” 2010. Doctoral Dissertation, University of New South Wales. Accessed April 20, 2019. http://handle.unsw.edu.au/1959.4/50303 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9184/SOURCE02?view=true.

MLA Handbook (7th Edition):

Shaw, Alexander. “Regulation of the p53 tumour suppressor by miR-380.” 2010. Web. 20 Apr 2019.

Vancouver:

Shaw A. Regulation of the p53 tumour suppressor by miR-380. [Internet] [Doctoral dissertation]. University of New South Wales; 2010. [cited 2019 Apr 20]. Available from: http://handle.unsw.edu.au/1959.4/50303 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9184/SOURCE02?view=true.

Council of Science Editors:

Shaw A. Regulation of the p53 tumour suppressor by miR-380. [Doctoral Dissertation]. University of New South Wales; 2010. Available from: http://handle.unsw.edu.au/1959.4/50303 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:9184/SOURCE02?view=true

10. Tomas, Fanny. Caractérisation fonctionnelle de la relation entre le suppresseur de tumeur p53 et son isoforme Delta133p53 dans les cellules humaines normales : Functional relationship between the tumor suppressor p53 and its isoform Delta133p53 in normal human cells.

Degree: Docteur es, Biologie Santé, 2018, Montpellier

La sénescence réplicative (SR) dans les fibroblastes humains primaires est causée par l’érosion des télomères et est contrôlée par p53. La régulation dynamique de l’activation… (more)

Subjects/Keywords: Isoformes p53; Sénescence; P53 suppresseur de tumeur; P53 isoforms; Senescence; Tumor supressor p53

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APA (6th Edition):

Tomas, F. (2018). Caractérisation fonctionnelle de la relation entre le suppresseur de tumeur p53 et son isoforme Delta133p53 dans les cellules humaines normales : Functional relationship between the tumor suppressor p53 and its isoform Delta133p53 in normal human cells. (Doctoral Dissertation). Montpellier. Retrieved from http://www.theses.fr/2018MONTT085

Chicago Manual of Style (16th Edition):

Tomas, Fanny. “Caractérisation fonctionnelle de la relation entre le suppresseur de tumeur p53 et son isoforme Delta133p53 dans les cellules humaines normales : Functional relationship between the tumor suppressor p53 and its isoform Delta133p53 in normal human cells.” 2018. Doctoral Dissertation, Montpellier. Accessed April 20, 2019. http://www.theses.fr/2018MONTT085.

MLA Handbook (7th Edition):

Tomas, Fanny. “Caractérisation fonctionnelle de la relation entre le suppresseur de tumeur p53 et son isoforme Delta133p53 dans les cellules humaines normales : Functional relationship between the tumor suppressor p53 and its isoform Delta133p53 in normal human cells.” 2018. Web. 20 Apr 2019.

Vancouver:

Tomas F. Caractérisation fonctionnelle de la relation entre le suppresseur de tumeur p53 et son isoforme Delta133p53 dans les cellules humaines normales : Functional relationship between the tumor suppressor p53 and its isoform Delta133p53 in normal human cells. [Internet] [Doctoral dissertation]. Montpellier; 2018. [cited 2019 Apr 20]. Available from: http://www.theses.fr/2018MONTT085.

Council of Science Editors:

Tomas F. Caractérisation fonctionnelle de la relation entre le suppresseur de tumeur p53 et son isoforme Delta133p53 dans les cellules humaines normales : Functional relationship between the tumor suppressor p53 and its isoform Delta133p53 in normal human cells. [Doctoral Dissertation]. Montpellier; 2018. Available from: http://www.theses.fr/2018MONTT085


University of Alberta

11. 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 April 20, 2019. 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. 20 Apr 2019.

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 2019 Apr 20]. 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


Texas A&M University

12. Sreenivasappa, Harini Bytaraya. Raster Image Correlation Spectroscopy [RICS] Analysis of HeLa cells.

Degree: 2011, Texas A&M University

 The objective of the project is to use the RICS analysis technique in complement with confocal microscopy to determine the diffusion coefficient of the selectively… (more)

Subjects/Keywords: HeLa cells; p53; RICS

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APA (6th Edition):

Sreenivasappa, H. B. (2011). Raster Image Correlation Spectroscopy [RICS] Analysis of HeLa cells. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7590

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):

Sreenivasappa, Harini Bytaraya. “Raster Image Correlation Spectroscopy [RICS] Analysis of HeLa cells.” 2011. Thesis, Texas A&M University. Accessed April 20, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7590.

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

MLA Handbook (7th Edition):

Sreenivasappa, Harini Bytaraya. “Raster Image Correlation Spectroscopy [RICS] Analysis of HeLa cells.” 2011. Web. 20 Apr 2019.

Vancouver:

Sreenivasappa HB. Raster Image Correlation Spectroscopy [RICS] Analysis of HeLa cells. [Internet] [Thesis]. Texas A&M University; 2011. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7590.

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

Council of Science Editors:

Sreenivasappa HB. Raster Image Correlation Spectroscopy [RICS] Analysis of HeLa cells. [Thesis]. Texas A&M University; 2011. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2009-12-7590

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


University of Edinburgh

13. Wawrzynów, Bartosz. Allosteric regulation of MDM2 protein.

Degree: 2010, University of Edinburgh

 The diverse functions of the MDM2 oncoprotein in growth control and tumourigenesis are managed through coordinated regulation of its discrete domains induced by both extrinsic… (more)

Subjects/Keywords: 616.994; MDM2; P53; allostery

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APA (6th Edition):

Wawrzynów, B. (2010). Allosteric regulation of MDM2 protein. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/4507

Chicago Manual of Style (16th Edition):

Wawrzynów, Bartosz. “Allosteric regulation of MDM2 protein.” 2010. Doctoral Dissertation, University of Edinburgh. Accessed April 20, 2019. http://hdl.handle.net/1842/4507.

MLA Handbook (7th Edition):

Wawrzynów, Bartosz. “Allosteric regulation of MDM2 protein.” 2010. Web. 20 Apr 2019.

Vancouver:

Wawrzynów B. Allosteric regulation of MDM2 protein. [Internet] [Doctoral dissertation]. University of Edinburgh; 2010. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1842/4507.

Council of Science Editors:

Wawrzynów B. Allosteric regulation of MDM2 protein. [Doctoral Dissertation]. University of Edinburgh; 2010. Available from: http://hdl.handle.net/1842/4507


Univerzitet u Beogradu

14. Janković, Radmila N., 1969-. Detekcija mutacija u p53 genu kod bolesnica sa primarnim operabilnim karcinomom dojke.

Degree: Biološki fakultet, 2014, Univerzitet u Beogradu

Molekularna biologija, onkologija, karcinom dojke / Molecular biology, oncology, breast cancer

Uvod: Zbog svoje uloge u očuvanju genomskog integriteta, produkt normalnog p53 gena se često… (more)

Subjects/Keywords: malignanant neoplasms; breast cancer; p53

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

APA (6th Edition):

Janković, Radmila N., 1. (2014). Detekcija mutacija u p53 genu kod bolesnica sa primarnim operabilnim karcinomom dojke. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:6813/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):

Janković, Radmila N., 1969-. “Detekcija mutacija u p53 genu kod bolesnica sa primarnim operabilnim karcinomom dojke.” 2014. Thesis, Univerzitet u Beogradu. Accessed April 20, 2019. https://fedorabg.bg.ac.rs/fedora/get/o:6813/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):

Janković, Radmila N., 1969-. “Detekcija mutacija u p53 genu kod bolesnica sa primarnim operabilnim karcinomom dojke.” 2014. Web. 20 Apr 2019.

Vancouver:

Janković, Radmila N. 1. Detekcija mutacija u p53 genu kod bolesnica sa primarnim operabilnim karcinomom dojke. [Internet] [Thesis]. Univerzitet u Beogradu; 2014. [cited 2019 Apr 20]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:6813/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:

Janković, Radmila N. 1. Detekcija mutacija u p53 genu kod bolesnica sa primarnim operabilnim karcinomom dojke. [Thesis]. Univerzitet u Beogradu; 2014. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:6813/bdef:Content/get

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


NSYSU

15. Chang, Tsung-ming. Prox1 suppresses growth and metastasis of hepatocellular carcinoma by downregulating Twist1.

Degree: PhD, Institute of Biomedical Sciences, 2013, NSYSU

 Prospero-related homeobox 1 (Prox1) was cloned as homeobox gene which homologous to the Drosophila prospero gene. As a transcription factor, Prox1 is important for liver… (more)

Subjects/Keywords: AKT2; p53; Prox1; Twist1

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APA (6th Edition):

Chang, T. (2013). Prox1 suppresses growth and metastasis of hepatocellular carcinoma by downregulating Twist1. (Doctoral Dissertation). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0110113-155844

Chicago Manual of Style (16th Edition):

Chang, Tsung-ming. “Prox1 suppresses growth and metastasis of hepatocellular carcinoma by downregulating Twist1.” 2013. Doctoral Dissertation, NSYSU. Accessed April 20, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0110113-155844.

MLA Handbook (7th Edition):

Chang, Tsung-ming. “Prox1 suppresses growth and metastasis of hepatocellular carcinoma by downregulating Twist1.” 2013. Web. 20 Apr 2019.

Vancouver:

Chang T. Prox1 suppresses growth and metastasis of hepatocellular carcinoma by downregulating Twist1. [Internet] [Doctoral dissertation]. NSYSU; 2013. [cited 2019 Apr 20]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0110113-155844.

Council of Science Editors:

Chang T. Prox1 suppresses growth and metastasis of hepatocellular carcinoma by downregulating Twist1. [Doctoral Dissertation]. NSYSU; 2013. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0110113-155844

16. Luiz Ivando Pires Ferreira Filho. AlteraÃÃes citogenÃmicas na medula Ãssea de trabalhadores rurais expostos a agrotÃxicos.

Degree: Master, 2013, Universidade Federal do Ceará

 Os pesticidas sÃo produtos quÃmicos de uso disseminado no controle das pragas nas lavouras agrÃcolas. Estes produtos sÃo classificados em herbicidas, inseticidas e fungicidas e… (more)

Subjects/Keywords: MEDICINA; AberraÃÃes CromossÃmicas; Genes p53

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APA (6th Edition):

Filho, L. I. P. F. (2013). AlteraÃÃes citogenÃmicas na medula Ãssea de trabalhadores rurais expostos a agrotÃxicos. (Masters Thesis). Universidade Federal do Ceará. Retrieved from http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=11240 ;

Chicago Manual of Style (16th Edition):

Filho, Luiz Ivando Pires Ferreira. “AlteraÃÃes citogenÃmicas na medula Ãssea de trabalhadores rurais expostos a agrotÃxicos.” 2013. Masters Thesis, Universidade Federal do Ceará. Accessed April 20, 2019. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=11240 ;.

MLA Handbook (7th Edition):

Filho, Luiz Ivando Pires Ferreira. “AlteraÃÃes citogenÃmicas na medula Ãssea de trabalhadores rurais expostos a agrotÃxicos.” 2013. Web. 20 Apr 2019.

Vancouver:

Filho LIPF. AlteraÃÃes citogenÃmicas na medula Ãssea de trabalhadores rurais expostos a agrotÃxicos. [Internet] [Masters thesis]. Universidade Federal do Ceará 2013. [cited 2019 Apr 20]. Available from: http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=11240 ;.

Council of Science Editors:

Filho LIPF. AlteraÃÃes citogenÃmicas na medula Ãssea de trabalhadores rurais expostos a agrotÃxicos. [Masters Thesis]. Universidade Federal do Ceará 2013. Available from: http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=11240 ;

17. Cezar Feitosa de Paula Machado, Marcos. Imunoexpressão das proteínas KI67 e p53 em pacientes com retocolite ulcerativa inespecífica tratados clinicamente e cirurgicamente .

Degree: 2008, Universidade Federal de Pernambuco

 Os métodos imunohistoquímicos associados aos sistemas computadorizados de análise de imagens tem sido de extrema importância, como ferramentas auxiliares, no estudo da expressão de proteínas… (more)

Subjects/Keywords: Retocolite Ulcerativa; Imunohistoquímica; p53; Ki67

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APA (6th Edition):

Cezar Feitosa de Paula Machado, M. (2008). Imunoexpressão das proteínas KI67 e p53 em pacientes com retocolite ulcerativa inespecífica tratados clinicamente e cirurgicamente . (Thesis). Universidade Federal de Pernambuco. Retrieved from http://repositorio.ufpe.br/handle/123456789/8810

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):

Cezar Feitosa de Paula Machado, Marcos. “Imunoexpressão das proteínas KI67 e p53 em pacientes com retocolite ulcerativa inespecífica tratados clinicamente e cirurgicamente .” 2008. Thesis, Universidade Federal de Pernambuco. Accessed April 20, 2019. http://repositorio.ufpe.br/handle/123456789/8810.

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

MLA Handbook (7th Edition):

Cezar Feitosa de Paula Machado, Marcos. “Imunoexpressão das proteínas KI67 e p53 em pacientes com retocolite ulcerativa inespecífica tratados clinicamente e cirurgicamente .” 2008. Web. 20 Apr 2019.

Vancouver:

Cezar Feitosa de Paula Machado M. Imunoexpressão das proteínas KI67 e p53 em pacientes com retocolite ulcerativa inespecífica tratados clinicamente e cirurgicamente . [Internet] [Thesis]. Universidade Federal de Pernambuco; 2008. [cited 2019 Apr 20]. Available from: http://repositorio.ufpe.br/handle/123456789/8810.

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

Council of Science Editors:

Cezar Feitosa de Paula Machado M. Imunoexpressão das proteínas KI67 e p53 em pacientes com retocolite ulcerativa inespecífica tratados clinicamente e cirurgicamente . [Thesis]. Universidade Federal de Pernambuco; 2008. Available from: http://repositorio.ufpe.br/handle/123456789/8810

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


Oregon State University

18. 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 April 20, 2019. 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. 20 Apr 2019.

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 2019 Apr 20]. 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


University of Sydney

19. Cole, Alexander John. The role of p53 and histone H2B monoubiquitination in high-grade serous ovarian carcinoma .

Degree: 2017, University of Sydney

 Ovarian cancer is the eleventh most frequently diagnosed cancer in women and the fifth most common cause of cancer-related deaths. Epithelial ovarian cancer accounts for… (more)

Subjects/Keywords: H2Bub1; Ovarian cancer; Epigenetics; p53

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APA (6th Edition):

Cole, A. J. (2017). The role of p53 and histone H2B monoubiquitination in high-grade serous ovarian carcinoma . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/17639

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):

Cole, Alexander John. “The role of p53 and histone H2B monoubiquitination in high-grade serous ovarian carcinoma .” 2017. Thesis, University of Sydney. Accessed April 20, 2019. http://hdl.handle.net/2123/17639.

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

MLA Handbook (7th Edition):

Cole, Alexander John. “The role of p53 and histone H2B monoubiquitination in high-grade serous ovarian carcinoma .” 2017. Web. 20 Apr 2019.

Vancouver:

Cole AJ. The role of p53 and histone H2B monoubiquitination in high-grade serous ovarian carcinoma . [Internet] [Thesis]. University of Sydney; 2017. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/2123/17639.

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

Council of Science Editors:

Cole AJ. The role of p53 and histone H2B monoubiquitination in high-grade serous ovarian carcinoma . [Thesis]. University of Sydney; 2017. Available from: http://hdl.handle.net/2123/17639

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


University of Sydney

20. Al Mazi, Juhura Gania. P53 responses to fludarabine in human B-lymphoid cancers .

Degree: 2013, University of Sydney

 The tumour suppressor protein p53, is a transcription factor responsible for regulating the cell cycle and/or apoptosis in proliferating cells subjected to a variety of… (more)

Subjects/Keywords: Fludarabine; B-lymphoma; P53; Phosphorylation

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APA (6th Edition):

Al Mazi, J. G. (2013). P53 responses to fludarabine in human B-lymphoid cancers . (Thesis). University of Sydney. Retrieved from http://hdl.handle.net/2123/10401

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):

Al Mazi, Juhura Gania. “P53 responses to fludarabine in human B-lymphoid cancers .” 2013. Thesis, University of Sydney. Accessed April 20, 2019. http://hdl.handle.net/2123/10401.

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

MLA Handbook (7th Edition):

Al Mazi, Juhura Gania. “P53 responses to fludarabine in human B-lymphoid cancers .” 2013. Web. 20 Apr 2019.

Vancouver:

Al Mazi JG. P53 responses to fludarabine in human B-lymphoid cancers . [Internet] [Thesis]. University of Sydney; 2013. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/2123/10401.

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

Council of Science Editors:

Al Mazi JG. P53 responses to fludarabine in human B-lymphoid cancers . [Thesis]. University of Sydney; 2013. Available from: http://hdl.handle.net/2123/10401

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


University of Manchester

21. Dickinson, Eleanor Rose. Characterising Disordered Proteins of the Cancer Genome using Biophysical Techniques.

Degree: 2017, University of Manchester

 Protein function and dysfunction, and their intimate ties to protein structure, has been a core focus of research for several decades. More recently, research into… (more)

Subjects/Keywords: IDP; Protein; p53; mass spectrometry

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APA (6th Edition):

Dickinson, E. R. (2017). Characterising Disordered Proteins of the Cancer Genome using Biophysical Techniques. (Doctoral Dissertation). University of Manchester. Retrieved from http://www.manchester.ac.uk/escholar/uk-ac-man-scw:307062

Chicago Manual of Style (16th Edition):

Dickinson, Eleanor Rose. “Characterising Disordered Proteins of the Cancer Genome using Biophysical Techniques.” 2017. Doctoral Dissertation, University of Manchester. Accessed April 20, 2019. http://www.manchester.ac.uk/escholar/uk-ac-man-scw:307062.

MLA Handbook (7th Edition):

Dickinson, Eleanor Rose. “Characterising Disordered Proteins of the Cancer Genome using Biophysical Techniques.” 2017. Web. 20 Apr 2019.

Vancouver:

Dickinson ER. Characterising Disordered Proteins of the Cancer Genome using Biophysical Techniques. [Internet] [Doctoral dissertation]. University of Manchester; 2017. [cited 2019 Apr 20]. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:307062.

Council of Science Editors:

Dickinson ER. Characterising Disordered Proteins of the Cancer Genome using Biophysical Techniques. [Doctoral Dissertation]. University of Manchester; 2017. Available from: http://www.manchester.ac.uk/escholar/uk-ac-man-scw:307062

22. Rey, Christophe. Etude de la fonction de HIPK1, sa régulation et son implication en oncologie : Study of HIPK1 function, regulation and oncological implication.

Degree: Docteur es, Sciences, technologie, santé. Biologie cellulaire et physiopathologie, 2010, Université de Bordeaux Segalen

HIPK1 (Homeodomain Interacting Protein Kinase 1) est une sérine/thréonine kinase de la superfamille des CMGC kinases. Les HIPKs, initialement identifiées comme des régulateurs des facteurs… (more)

Subjects/Keywords: Hipk1; P53; Prolifération cellulaire

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APA (6th Edition):

Rey, C. (2010). Etude de la fonction de HIPK1, sa régulation et son implication en oncologie : Study of HIPK1 function, regulation and oncological implication. (Doctoral Dissertation). Université de Bordeaux Segalen. Retrieved from http://www.theses.fr/2010BOR21756

Chicago Manual of Style (16th Edition):

Rey, Christophe. “Etude de la fonction de HIPK1, sa régulation et son implication en oncologie : Study of HIPK1 function, regulation and oncological implication.” 2010. Doctoral Dissertation, Université de Bordeaux Segalen. Accessed April 20, 2019. http://www.theses.fr/2010BOR21756.

MLA Handbook (7th Edition):

Rey, Christophe. “Etude de la fonction de HIPK1, sa régulation et son implication en oncologie : Study of HIPK1 function, regulation and oncological implication.” 2010. Web. 20 Apr 2019.

Vancouver:

Rey C. Etude de la fonction de HIPK1, sa régulation et son implication en oncologie : Study of HIPK1 function, regulation and oncological implication. [Internet] [Doctoral dissertation]. Université de Bordeaux Segalen; 2010. [cited 2019 Apr 20]. Available from: http://www.theses.fr/2010BOR21756.

Council of Science Editors:

Rey C. Etude de la fonction de HIPK1, sa régulation et son implication en oncologie : Study of HIPK1 function, regulation and oncological implication. [Doctoral Dissertation]. Université de Bordeaux Segalen; 2010. Available from: http://www.theses.fr/2010BOR21756


Université de Sherbrooke

23. Forget, Karolyn. Les agrégats de la protéine p53 comportent certaines propriétés des prions .

Degree: 2013, Université de Sherbrooke

 Les maladies à prion sont un cas unique de pathologie où l’agent infectieux, le prion, est une protéine. La protéine prion possède plusieurs caractéristiques qui… (more)

Subjects/Keywords: Agrégation protéique; P53; Prions

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APA (6th Edition):

Forget, K. (2013). Les agrégats de la protéine p53 comportent certaines propriétés des prions . (Masters Thesis). Université de Sherbrooke. Retrieved from http://hdl.handle.net/11143/6301

Chicago Manual of Style (16th Edition):

Forget, Karolyn. “Les agrégats de la protéine p53 comportent certaines propriétés des prions .” 2013. Masters Thesis, Université de Sherbrooke. Accessed April 20, 2019. http://hdl.handle.net/11143/6301.

MLA Handbook (7th Edition):

Forget, Karolyn. “Les agrégats de la protéine p53 comportent certaines propriétés des prions .” 2013. Web. 20 Apr 2019.

Vancouver:

Forget K. Les agrégats de la protéine p53 comportent certaines propriétés des prions . [Internet] [Masters thesis]. Université de Sherbrooke; 2013. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/11143/6301.

Council of Science Editors:

Forget K. Les agrégats de la protéine p53 comportent certaines propriétés des prions . [Masters Thesis]. Université de Sherbrooke; 2013. Available from: http://hdl.handle.net/11143/6301


Vanderbilt University

24. Liu, Dan. The roles of LZAP in vertebrate embryogenesis and head and neck carcinogenesis.

Degree: PhD, Cancer Biology, 2012, Vanderbilt University

 To improve our understanding of LZAPâs role in normal and cancer cell biology, the work in this thesis explored LZAP activities in development and carcinogenesis.… (more)

Subjects/Keywords: LZAP epiboly p53 radiation

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APA (6th Edition):

Liu, D. (2012). The roles of LZAP in vertebrate embryogenesis and head and neck carcinogenesis. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://etd.library.vanderbilt.edu/available/etd-11142012-065537/ ;

Chicago Manual of Style (16th Edition):

Liu, Dan. “The roles of LZAP in vertebrate embryogenesis and head and neck carcinogenesis.” 2012. Doctoral Dissertation, Vanderbilt University. Accessed April 20, 2019. http://etd.library.vanderbilt.edu/available/etd-11142012-065537/ ;.

MLA Handbook (7th Edition):

Liu, Dan. “The roles of LZAP in vertebrate embryogenesis and head and neck carcinogenesis.” 2012. Web. 20 Apr 2019.

Vancouver:

Liu D. The roles of LZAP in vertebrate embryogenesis and head and neck carcinogenesis. [Internet] [Doctoral dissertation]. Vanderbilt University; 2012. [cited 2019 Apr 20]. Available from: http://etd.library.vanderbilt.edu/available/etd-11142012-065537/ ;.

Council of Science Editors:

Liu D. The roles of LZAP in vertebrate embryogenesis and head and neck carcinogenesis. [Doctoral Dissertation]. Vanderbilt University; 2012. Available from: http://etd.library.vanderbilt.edu/available/etd-11142012-065537/ ;


Princeton University

25. DeHart, Caroline. Extensive Post-Translational Modification of Endogenous Human p53 .

Degree: PhD, 2013, Princeton University

 The p53 tumor suppressor protein is a central component of numerous cellular signaling pathways and frequently mutated in human cancers. p53 undergoes extensive post-translational modification… (more)

Subjects/Keywords: Adenovirus; Mass spectrometry; p53; PTM

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APA (6th Edition):

DeHart, C. (2013). Extensive Post-Translational Modification of Endogenous Human p53 . (Doctoral Dissertation). Princeton University. Retrieved from http://arks.princeton.edu/ark:/88435/dsp01bv73c053r

Chicago Manual of Style (16th Edition):

DeHart, Caroline. “Extensive Post-Translational Modification of Endogenous Human p53 .” 2013. Doctoral Dissertation, Princeton University. Accessed April 20, 2019. http://arks.princeton.edu/ark:/88435/dsp01bv73c053r.

MLA Handbook (7th Edition):

DeHart, Caroline. “Extensive Post-Translational Modification of Endogenous Human p53 .” 2013. Web. 20 Apr 2019.

Vancouver:

DeHart C. Extensive Post-Translational Modification of Endogenous Human p53 . [Internet] [Doctoral dissertation]. Princeton University; 2013. [cited 2019 Apr 20]. Available from: http://arks.princeton.edu/ark:/88435/dsp01bv73c053r.

Council of Science Editors:

DeHart C. Extensive Post-Translational Modification of Endogenous Human p53 . [Doctoral Dissertation]. Princeton University; 2013. Available from: http://arks.princeton.edu/ark:/88435/dsp01bv73c053r


University of Edinburgh

26. Huart, Anne-Sophie. Casein kinase 1 alpha-MDM2 complex : phosphorylation and ubiquitination signals converging on p53 pathway.

Degree: PhD, 2014, University of Edinburgh

 The tumour suppressor p53 is a key regulatory protein that prevents proliferation of damaged cells. Under unperturbed conditions, the ubiquitin ligase murine double minute 2… (more)

Subjects/Keywords: 572; CK1; MDM2; P53

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APA (6th Edition):

Huart, A. (2014). Casein kinase 1 alpha-MDM2 complex : phosphorylation and ubiquitination signals converging on p53 pathway. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/17282

Chicago Manual of Style (16th Edition):

Huart, Anne-Sophie. “Casein kinase 1 alpha-MDM2 complex : phosphorylation and ubiquitination signals converging on p53 pathway.” 2014. Doctoral Dissertation, University of Edinburgh. Accessed April 20, 2019. http://hdl.handle.net/1842/17282.

MLA Handbook (7th Edition):

Huart, Anne-Sophie. “Casein kinase 1 alpha-MDM2 complex : phosphorylation and ubiquitination signals converging on p53 pathway.” 2014. Web. 20 Apr 2019.

Vancouver:

Huart A. Casein kinase 1 alpha-MDM2 complex : phosphorylation and ubiquitination signals converging on p53 pathway. [Internet] [Doctoral dissertation]. University of Edinburgh; 2014. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/1842/17282.

Council of Science Editors:

Huart A. Casein kinase 1 alpha-MDM2 complex : phosphorylation and ubiquitination signals converging on p53 pathway. [Doctoral Dissertation]. University of Edinburgh; 2014. Available from: http://hdl.handle.net/1842/17282


Université Catholique de Louvain

27. Demoulin, Benjamin. Influence of MAGEA and effects of resveratrol on p53 biology.

Degree: 2015, Université Catholique de Louvain

MAGEA1 and -A2 impair the stabilization and activation of p53 in presence of a genotoxic stress. MAGEA (Melanoma AntiGEn-A) genes are silenced in the vast… (more)

Subjects/Keywords: Cancer; MAGEA; p53; Resveratrol

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APA (6th Edition):

Demoulin, B. (2015). Influence of MAGEA and effects of resveratrol on p53 biology. (Thesis). Université Catholique de Louvain. Retrieved from http://hdl.handle.net/2078.1/160850

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):

Demoulin, Benjamin. “Influence of MAGEA and effects of resveratrol on p53 biology.” 2015. Thesis, Université Catholique de Louvain. Accessed April 20, 2019. http://hdl.handle.net/2078.1/160850.

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

MLA Handbook (7th Edition):

Demoulin, Benjamin. “Influence of MAGEA and effects of resveratrol on p53 biology.” 2015. Web. 20 Apr 2019.

Vancouver:

Demoulin B. Influence of MAGEA and effects of resveratrol on p53 biology. [Internet] [Thesis]. Université Catholique de Louvain; 2015. [cited 2019 Apr 20]. Available from: http://hdl.handle.net/2078.1/160850.

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

Council of Science Editors:

Demoulin B. Influence of MAGEA and effects of resveratrol on p53 biology. [Thesis]. Université Catholique de Louvain; 2015. Available from: http://hdl.handle.net/2078.1/160850

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


University of New South Wales

28. Johal, Harpreet. The mouse mammary tumour virus - like virus in hormonally influenced human tissues.

Degree: Biotechnology & Biomolecular Sciences, 2009, University of New South Wales

 The identification of Mouse Mammary Tumour Virus (MMTV) as the causal factor for breast cancer in mice, initiated investigation into a viral cause for human… (more)

Subjects/Keywords: PgR; MMTV; ER-α;

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APA (6th Edition):

Johal, H. (2009). The mouse mammary tumour virus - like virus in hormonally influenced human tissues. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/44734 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:8033/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Johal, Harpreet. “The mouse mammary tumour virus - like virus in hormonally influenced human tissues.” 2009. Doctoral Dissertation, University of New South Wales. Accessed April 20, 2019. http://handle.unsw.edu.au/1959.4/44734 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:8033/SOURCE02?view=true.

MLA Handbook (7th Edition):

Johal, Harpreet. “The mouse mammary tumour virus - like virus in hormonally influenced human tissues.” 2009. Web. 20 Apr 2019.

Vancouver:

Johal H. The mouse mammary tumour virus - like virus in hormonally influenced human tissues. [Internet] [Doctoral dissertation]. University of New South Wales; 2009. [cited 2019 Apr 20]. Available from: http://handle.unsw.edu.au/1959.4/44734 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:8033/SOURCE02?view=true.

Council of Science Editors:

Johal H. The mouse mammary tumour virus - like virus in hormonally influenced human tissues. [Doctoral Dissertation]. University of New South Wales; 2009. Available from: http://handle.unsw.edu.au/1959.4/44734 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:8033/SOURCE02?view=true

29. Jones, Rhiannon N. Towards the design and synthesis of a p53 mutant Y220C rescue drug.

Degree: PhD, 2018, University of Sussex

 The DNA damage response is an important barrier to tumorigenesis. Impairment of p53 function is crucial to tumorigenesis by allowing evasion of p53 dependent responses.… (more)

Subjects/Keywords: 540; RC0268.44.P16 p53 antioncogene

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

APA (6th Edition):

Jones, R. N. (2018). Towards the design and synthesis of a p53 mutant Y220C rescue drug. (Doctoral Dissertation). University of Sussex. Retrieved from http://sro.sussex.ac.uk/id/eprint/74884/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.742125

Chicago Manual of Style (16th Edition):

Jones, Rhiannon N. “Towards the design and synthesis of a p53 mutant Y220C rescue drug.” 2018. Doctoral Dissertation, University of Sussex. Accessed April 20, 2019. http://sro.sussex.ac.uk/id/eprint/74884/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.742125.

MLA Handbook (7th Edition):

Jones, Rhiannon N. “Towards the design and synthesis of a p53 mutant Y220C rescue drug.” 2018. Web. 20 Apr 2019.

Vancouver:

Jones RN. Towards the design and synthesis of a p53 mutant Y220C rescue drug. [Internet] [Doctoral dissertation]. University of Sussex; 2018. [cited 2019 Apr 20]. Available from: http://sro.sussex.ac.uk/id/eprint/74884/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.742125.

Council of Science Editors:

Jones RN. Towards the design and synthesis of a p53 mutant Y220C rescue drug. [Doctoral Dissertation]. University of Sussex; 2018. Available from: http://sro.sussex.ac.uk/id/eprint/74884/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.742125

30. Chiang, Shih-Chieh. Investigating the role of Tyrosyl-DNA Phosphodiesterase 1 in nuclear and mitochondrial DNA repair.

Degree: PhD, 2017, University of Sussex

 Damages to the genetic materials arise throughout the lifespan of a cell, and elicit upregulation of DNA repair factors. Tyrosyl-DNA phosphodiesterase 1 (TDP1) is part… (more)

Subjects/Keywords: 572.8; QP0609.P53 Phosphodiesterase

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

APA (6th Edition):

Chiang, S. (2017). Investigating the role of Tyrosyl-DNA Phosphodiesterase 1 in nuclear and mitochondrial DNA repair. (Doctoral Dissertation). University of Sussex. Retrieved from http://sro.sussex.ac.uk/id/eprint/68554/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.714835

Chicago Manual of Style (16th Edition):

Chiang, Shih-Chieh. “Investigating the role of Tyrosyl-DNA Phosphodiesterase 1 in nuclear and mitochondrial DNA repair.” 2017. Doctoral Dissertation, University of Sussex. Accessed April 20, 2019. http://sro.sussex.ac.uk/id/eprint/68554/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.714835.

MLA Handbook (7th Edition):

Chiang, Shih-Chieh. “Investigating the role of Tyrosyl-DNA Phosphodiesterase 1 in nuclear and mitochondrial DNA repair.” 2017. Web. 20 Apr 2019.

Vancouver:

Chiang S. Investigating the role of Tyrosyl-DNA Phosphodiesterase 1 in nuclear and mitochondrial DNA repair. [Internet] [Doctoral dissertation]. University of Sussex; 2017. [cited 2019 Apr 20]. Available from: http://sro.sussex.ac.uk/id/eprint/68554/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.714835.

Council of Science Editors:

Chiang S. Investigating the role of Tyrosyl-DNA Phosphodiesterase 1 in nuclear and mitochondrial DNA repair. [Doctoral Dissertation]. University of Sussex; 2017. Available from: http://sro.sussex.ac.uk/id/eprint/68554/ ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.714835

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