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You searched for subject:(nucleolin). Showing records 1 – 30 of 33 total matches.

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NSYSU

1. Wu, Cian-rong. The relationship between C-reactive protein and hepatoma-derived growth factor in hepatoma carcinoma cell lines.

Degree: Master, Biological Sciences, 2014, NSYSU

 Hepatocellular carcinoma (HCC) is one of the most common malignancy and known as country disease in Taiwan. Hepatoma-derived growth factor (HDGF), a mitogen for various… (more)

Subjects/Keywords: HDGF; Liver cancer; nucleolin; CRP; CD64

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

APA (6th Edition):

Wu, C. (2014). The relationship between C-reactive protein and hepatoma-derived growth factor in hepatoma carcinoma cell lines. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0726114-095757

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):

Wu, Cian-rong. “The relationship between C-reactive protein and hepatoma-derived growth factor in hepatoma carcinoma cell lines.” 2014. Thesis, NSYSU. Accessed January 24, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0726114-095757.

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

MLA Handbook (7th Edition):

Wu, Cian-rong. “The relationship between C-reactive protein and hepatoma-derived growth factor in hepatoma carcinoma cell lines.” 2014. Web. 24 Jan 2021.

Vancouver:

Wu C. The relationship between C-reactive protein and hepatoma-derived growth factor in hepatoma carcinoma cell lines. [Internet] [Thesis]. NSYSU; 2014. [cited 2021 Jan 24]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0726114-095757.

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

Council of Science Editors:

Wu C. The relationship between C-reactive protein and hepatoma-derived growth factor in hepatoma carcinoma cell lines. [Thesis]. NSYSU; 2014. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0726114-095757

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


NSYSU

2. Han, Ai-jie. The mechanism of Hepatoma-derived growth factor (HDGF)-induced ROS production in HCC cells.

Degree: Master, Institute of Biomedical Sciences, 2016, NSYSU

 Hepatoma-derived growth factor (HDGF) is a mitogen of 240 residues involved in hepatocarcinogenesis. HDGF consists of a highly conserved PWWP domain in the N-terminal 100… (more)

Subjects/Keywords: Hepatoma; HDGF; Reactive Oxygen Species; mitochondria; nucleolin

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APA (6th Edition):

Han, A. (2016). The mechanism of Hepatoma-derived growth factor (HDGF)-induced ROS production in HCC cells. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0014116-035446

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):

Han, Ai-jie. “The mechanism of Hepatoma-derived growth factor (HDGF)-induced ROS production in HCC cells.” 2016. Thesis, NSYSU. Accessed January 24, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0014116-035446.

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

MLA Handbook (7th Edition):

Han, Ai-jie. “The mechanism of Hepatoma-derived growth factor (HDGF)-induced ROS production in HCC cells.” 2016. Web. 24 Jan 2021.

Vancouver:

Han A. The mechanism of Hepatoma-derived growth factor (HDGF)-induced ROS production in HCC cells. [Internet] [Thesis]. NSYSU; 2016. [cited 2021 Jan 24]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0014116-035446.

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

Council of Science Editors:

Han A. The mechanism of Hepatoma-derived growth factor (HDGF)-induced ROS production in HCC cells. [Thesis]. NSYSU; 2016. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0014116-035446

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


University of Toronto

3. Zhu, Daniel Zheng Yuan. Respiratory Syncytial Virus Fusion Protein Interaction with its Cellular Receptor, Nucleolin.

Degree: 2018, University of Toronto

Respiratory Syncytial virus (RSV) fusion protein (F) interacts with nucleolin during viral fusion. RNA binding domains 1 and 2 (RBDs) of nucleolin, when expressed as… (more)

Subjects/Keywords: fusion; nucleolin; respiratory; RSV; syncytial; 0720

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APA (6th Edition):

Zhu, D. Z. Y. (2018). Respiratory Syncytial Virus Fusion Protein Interaction with its Cellular Receptor, Nucleolin. (Masters Thesis). University of Toronto. Retrieved from http://hdl.handle.net/1807/82922

Chicago Manual of Style (16th Edition):

Zhu, Daniel Zheng Yuan. “Respiratory Syncytial Virus Fusion Protein Interaction with its Cellular Receptor, Nucleolin.” 2018. Masters Thesis, University of Toronto. Accessed January 24, 2021. http://hdl.handle.net/1807/82922.

MLA Handbook (7th Edition):

Zhu, Daniel Zheng Yuan. “Respiratory Syncytial Virus Fusion Protein Interaction with its Cellular Receptor, Nucleolin.” 2018. Web. 24 Jan 2021.

Vancouver:

Zhu DZY. Respiratory Syncytial Virus Fusion Protein Interaction with its Cellular Receptor, Nucleolin. [Internet] [Masters thesis]. University of Toronto; 2018. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/1807/82922.

Council of Science Editors:

Zhu DZY. Respiratory Syncytial Virus Fusion Protein Interaction with its Cellular Receptor, Nucleolin. [Masters Thesis]. University of Toronto; 2018. Available from: http://hdl.handle.net/1807/82922


University of California – Riverside

4. Gongol, Brendan. AMPK Mediates Endothelial Function Through the Phosphorylation of Nucleolin and PARP-1.

Degree: Biochemistry and Molecular Biology, 2013, University of California – Riverside

 Endothelial cells play an active role in maintaining vascular health. Their response to different flow patterns and circulating molecules initiate signaling cascades that determine endothelial… (more)

Subjects/Keywords: Biochemistry; AMPK; Bcl-6; endothelial; Inflammation; Nucleolin; PARP-1

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APA (6th Edition):

Gongol, B. (2013). AMPK Mediates Endothelial Function Through the Phosphorylation of Nucleolin and PARP-1. (Thesis). University of California – Riverside. Retrieved from http://www.escholarship.org/uc/item/0rf1k8ct

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):

Gongol, Brendan. “AMPK Mediates Endothelial Function Through the Phosphorylation of Nucleolin and PARP-1.” 2013. Thesis, University of California – Riverside. Accessed January 24, 2021. http://www.escholarship.org/uc/item/0rf1k8ct.

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

MLA Handbook (7th Edition):

Gongol, Brendan. “AMPK Mediates Endothelial Function Through the Phosphorylation of Nucleolin and PARP-1.” 2013. Web. 24 Jan 2021.

Vancouver:

Gongol B. AMPK Mediates Endothelial Function Through the Phosphorylation of Nucleolin and PARP-1. [Internet] [Thesis]. University of California – Riverside; 2013. [cited 2021 Jan 24]. Available from: http://www.escholarship.org/uc/item/0rf1k8ct.

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

Council of Science Editors:

Gongol B. AMPK Mediates Endothelial Function Through the Phosphorylation of Nucleolin and PARP-1. [Thesis]. University of California – Riverside; 2013. Available from: http://www.escholarship.org/uc/item/0rf1k8ct

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


UCLA

5. Monte, Emma Marie. Control of Cardiac Gene Expression by Chromatin Architectural Proteins: Mechanisms at the Level of Chromatin Fiber, Transcriptome Remodeling and Cellular Phenotype.

Degree: Molec, Cell, & Integ Physiology, 2015, UCLA

 When faced with chronic stress, the heart enters a compensatory hypertrophic stage; without intervention it eventually succumbs to decompensation marked by a dilated left ventricular… (more)

Subjects/Keywords: Molecular biology; Chromatin; CTCF; Heart Failure; HMGB2; Nucleolin

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APA (6th Edition):

Monte, E. M. (2015). Control of Cardiac Gene Expression by Chromatin Architectural Proteins: Mechanisms at the Level of Chromatin Fiber, Transcriptome Remodeling and Cellular Phenotype. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/1qd782bx

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):

Monte, Emma Marie. “Control of Cardiac Gene Expression by Chromatin Architectural Proteins: Mechanisms at the Level of Chromatin Fiber, Transcriptome Remodeling and Cellular Phenotype.” 2015. Thesis, UCLA. Accessed January 24, 2021. http://www.escholarship.org/uc/item/1qd782bx.

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

MLA Handbook (7th Edition):

Monte, Emma Marie. “Control of Cardiac Gene Expression by Chromatin Architectural Proteins: Mechanisms at the Level of Chromatin Fiber, Transcriptome Remodeling and Cellular Phenotype.” 2015. Web. 24 Jan 2021.

Vancouver:

Monte EM. Control of Cardiac Gene Expression by Chromatin Architectural Proteins: Mechanisms at the Level of Chromatin Fiber, Transcriptome Remodeling and Cellular Phenotype. [Internet] [Thesis]. UCLA; 2015. [cited 2021 Jan 24]. Available from: http://www.escholarship.org/uc/item/1qd782bx.

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

Council of Science Editors:

Monte EM. Control of Cardiac Gene Expression by Chromatin Architectural Proteins: Mechanisms at the Level of Chromatin Fiber, Transcriptome Remodeling and Cellular Phenotype. [Thesis]. UCLA; 2015. Available from: http://www.escholarship.org/uc/item/1qd782bx

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


University of Saskatchewan

6. Zhao, Xin 1984-. THE ROLE OF BOVINE ADENOVIRUS-3 PROTEIN V (pV) IN VIRUS REPLICATION.

Degree: 2016, University of Saskatchewan

 Bovine adenovirus type 3 (BAdV-3), which is a non-enveloped icosahedral particle with a double-stranded DNA genome of 34,446 base pair, has been developed as a… (more)

Subjects/Keywords: Adenovirus; pV; nuclear localization signal; nucleolar localization signal; nucleolin

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APA (6th Edition):

Zhao, X. 1. (2016). THE ROLE OF BOVINE ADENOVIRUS-3 PROTEIN V (pV) IN VIRUS REPLICATION. (Thesis). University of Saskatchewan. Retrieved from http://hdl.handle.net/10388/7327

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):

Zhao, Xin 1984-. “THE ROLE OF BOVINE ADENOVIRUS-3 PROTEIN V (pV) IN VIRUS REPLICATION.” 2016. Thesis, University of Saskatchewan. Accessed January 24, 2021. http://hdl.handle.net/10388/7327.

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

MLA Handbook (7th Edition):

Zhao, Xin 1984-. “THE ROLE OF BOVINE ADENOVIRUS-3 PROTEIN V (pV) IN VIRUS REPLICATION.” 2016. Web. 24 Jan 2021.

Vancouver:

Zhao X1. THE ROLE OF BOVINE ADENOVIRUS-3 PROTEIN V (pV) IN VIRUS REPLICATION. [Internet] [Thesis]. University of Saskatchewan; 2016. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/10388/7327.

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

Council of Science Editors:

Zhao X1. THE ROLE OF BOVINE ADENOVIRUS-3 PROTEIN V (pV) IN VIRUS REPLICATION. [Thesis]. University of Saskatchewan; 2016. Available from: http://hdl.handle.net/10388/7327

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

7. Dhez, Anne-Chloé. Thérapie ciblée des glioblastomes via l'internalisation d'une toxine grâce à des biopolymères dirigés à la surface des cellules cancéreuses : Glioblastoma targeted therapy approaches based on toxin internalization via cell surface directed biopolymers.

Degree: Docteur es, Biologie cellulaire et moléculaire, 2017, Université Paris-Est

 Les thérapies ciblées utilisent des agents thérapeutiques qui interfèrent specifiquement avec les molécules nécessaires pour la croissance et la progression tumorale. Les chimiothérapies classiques sont… (more)

Subjects/Keywords: Nucléoline; Glioblastome; Nucant; Saporine; Nucleolin; Glioblastoma; Nucant; Saporin; 616.994

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APA (6th Edition):

Dhez, A. (2017). Thérapie ciblée des glioblastomes via l'internalisation d'une toxine grâce à des biopolymères dirigés à la surface des cellules cancéreuses : Glioblastoma targeted therapy approaches based on toxin internalization via cell surface directed biopolymers. (Doctoral Dissertation). Université Paris-Est. Retrieved from http://www.theses.fr/2017PESC0026

Chicago Manual of Style (16th Edition):

Dhez, Anne-Chloé. “Thérapie ciblée des glioblastomes via l'internalisation d'une toxine grâce à des biopolymères dirigés à la surface des cellules cancéreuses : Glioblastoma targeted therapy approaches based on toxin internalization via cell surface directed biopolymers.” 2017. Doctoral Dissertation, Université Paris-Est. Accessed January 24, 2021. http://www.theses.fr/2017PESC0026.

MLA Handbook (7th Edition):

Dhez, Anne-Chloé. “Thérapie ciblée des glioblastomes via l'internalisation d'une toxine grâce à des biopolymères dirigés à la surface des cellules cancéreuses : Glioblastoma targeted therapy approaches based on toxin internalization via cell surface directed biopolymers.” 2017. Web. 24 Jan 2021.

Vancouver:

Dhez A. Thérapie ciblée des glioblastomes via l'internalisation d'une toxine grâce à des biopolymères dirigés à la surface des cellules cancéreuses : Glioblastoma targeted therapy approaches based on toxin internalization via cell surface directed biopolymers. [Internet] [Doctoral dissertation]. Université Paris-Est; 2017. [cited 2021 Jan 24]. Available from: http://www.theses.fr/2017PESC0026.

Council of Science Editors:

Dhez A. Thérapie ciblée des glioblastomes via l'internalisation d'une toxine grâce à des biopolymères dirigés à la surface des cellules cancéreuses : Glioblastoma targeted therapy approaches based on toxin internalization via cell surface directed biopolymers. [Doctoral Dissertation]. Université Paris-Est; 2017. Available from: http://www.theses.fr/2017PESC0026


Duke University

8. Kotula, Jonathan W. Achieving Cell-Specific Delivery of Multiple Oligonucleotide Therapeutics with Aptamer Chimeras .

Degree: 2012, Duke University

  Current standard cancer treatments such as chemotherapeutics, and radiation therapy are nearly as likely to kill the patient as cure the cancer. Therapies that… (more)

Subjects/Keywords: Molecular biology; Cellular biology; Biochemistry; Aptamer; Cancer; Delivery; Nucleolin; Therapeutic

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APA (6th Edition):

Kotula, J. W. (2012). Achieving Cell-Specific Delivery of Multiple Oligonucleotide Therapeutics with Aptamer Chimeras . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/6108

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):

Kotula, Jonathan W. “Achieving Cell-Specific Delivery of Multiple Oligonucleotide Therapeutics with Aptamer Chimeras .” 2012. Thesis, Duke University. Accessed January 24, 2021. http://hdl.handle.net/10161/6108.

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

MLA Handbook (7th Edition):

Kotula, Jonathan W. “Achieving Cell-Specific Delivery of Multiple Oligonucleotide Therapeutics with Aptamer Chimeras .” 2012. Web. 24 Jan 2021.

Vancouver:

Kotula JW. Achieving Cell-Specific Delivery of Multiple Oligonucleotide Therapeutics with Aptamer Chimeras . [Internet] [Thesis]. Duke University; 2012. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/10161/6108.

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

Council of Science Editors:

Kotula JW. Achieving Cell-Specific Delivery of Multiple Oligonucleotide Therapeutics with Aptamer Chimeras . [Thesis]. Duke University; 2012. Available from: http://hdl.handle.net/10161/6108

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


Louisiana State University

9. Pellar, Gregory James. The post-translational methylation of arginine in the glycine arginine rich region of CHO nucleoin.

Degree: PhD, 2002, Louisiana State University

Nucleolin is a nucleolar protein important for ribosome biogenesis. Nucleolin contains a conserved glycine arginine rich (GAR) domain near its carboxy terminus. GAR domains are… (more)

Subjects/Keywords: nucleolin; GAR domains; arginine methylation

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APA (6th Edition):

Pellar, G. J. (2002). The post-translational methylation of arginine in the glycine arginine rich region of CHO nucleoin. (Doctoral Dissertation). Louisiana State University. Retrieved from etd-0415102-111547 ; https://digitalcommons.lsu.edu/gradschool_dissertations/206

Chicago Manual of Style (16th Edition):

Pellar, Gregory James. “The post-translational methylation of arginine in the glycine arginine rich region of CHO nucleoin.” 2002. Doctoral Dissertation, Louisiana State University. Accessed January 24, 2021. etd-0415102-111547 ; https://digitalcommons.lsu.edu/gradschool_dissertations/206.

MLA Handbook (7th Edition):

Pellar, Gregory James. “The post-translational methylation of arginine in the glycine arginine rich region of CHO nucleoin.” 2002. Web. 24 Jan 2021.

Vancouver:

Pellar GJ. The post-translational methylation of arginine in the glycine arginine rich region of CHO nucleoin. [Internet] [Doctoral dissertation]. Louisiana State University; 2002. [cited 2021 Jan 24]. Available from: etd-0415102-111547 ; https://digitalcommons.lsu.edu/gradschool_dissertations/206.

Council of Science Editors:

Pellar GJ. The post-translational methylation of arginine in the glycine arginine rich region of CHO nucleoin. [Doctoral Dissertation]. Louisiana State University; 2002. Available from: etd-0415102-111547 ; https://digitalcommons.lsu.edu/gradschool_dissertations/206

10. Durut, Nathalie. Etudes fonctionnelles des protéines nucléaires dupliquées chez Arabidopsis thaliana : Functional study of duplicated nucleolin genes in A. thaliana.

Degree: Docteur es, Physiologie et biologie des organismes - populations - interactions, 2014, Perpignan

Chez les eucaryotes, les gènes d’ARNr 45S sont présents en un grand nombre de copies organisées dans des régions chromosomiques appelées NOR pour « Nucleolus… (more)

Subjects/Keywords: Nucléoline; A. thaliana; Chromatine; ADNr; Stress; Nucleolin; Chromatin; RDNA; 581.3

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APA (6th Edition):

Durut, N. (2014). Etudes fonctionnelles des protéines nucléaires dupliquées chez Arabidopsis thaliana : Functional study of duplicated nucleolin genes in A. thaliana. (Doctoral Dissertation). Perpignan. Retrieved from http://www.theses.fr/2014PERP1208

Chicago Manual of Style (16th Edition):

Durut, Nathalie. “Etudes fonctionnelles des protéines nucléaires dupliquées chez Arabidopsis thaliana : Functional study of duplicated nucleolin genes in A. thaliana.” 2014. Doctoral Dissertation, Perpignan. Accessed January 24, 2021. http://www.theses.fr/2014PERP1208.

MLA Handbook (7th Edition):

Durut, Nathalie. “Etudes fonctionnelles des protéines nucléaires dupliquées chez Arabidopsis thaliana : Functional study of duplicated nucleolin genes in A. thaliana.” 2014. Web. 24 Jan 2021.

Vancouver:

Durut N. Etudes fonctionnelles des protéines nucléaires dupliquées chez Arabidopsis thaliana : Functional study of duplicated nucleolin genes in A. thaliana. [Internet] [Doctoral dissertation]. Perpignan; 2014. [cited 2021 Jan 24]. Available from: http://www.theses.fr/2014PERP1208.

Council of Science Editors:

Durut N. Etudes fonctionnelles des protéines nucléaires dupliquées chez Arabidopsis thaliana : Functional study of duplicated nucleolin genes in A. thaliana. [Doctoral Dissertation]. Perpignan; 2014. Available from: http://www.theses.fr/2014PERP1208


University of Georgia

11. Stephens, Christopher Brad. Analysis of protein-protein interactions with cTHY28.

Degree: 2016, University of Georgia

 cTHY28 is a nuclear localized phosphoprotein that was previously isloated from chicken lymphocytes during a screening procedure for apoptotic genes; however, the function of this… (more)

Subjects/Keywords: cTHY28; nucleolin; DNA topoisomerase I; Protein-Protein Interactions; Co-Immunoprecipitation

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

APA (6th Edition):

Stephens, C. B. (2016). Analysis of protein-protein interactions with cTHY28. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/35464"

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):

Stephens, Christopher Brad. “Analysis of protein-protein interactions with cTHY28.” 2016. Thesis, University of Georgia. Accessed January 24, 2021. http://hdl.handle.net/10724/35464".

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

MLA Handbook (7th Edition):

Stephens, Christopher Brad. “Analysis of protein-protein interactions with cTHY28.” 2016. Web. 24 Jan 2021.

Vancouver:

Stephens CB. Analysis of protein-protein interactions with cTHY28. [Internet] [Thesis]. University of Georgia; 2016. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/10724/35464".

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

Council of Science Editors:

Stephens CB. Analysis of protein-protein interactions with cTHY28. [Thesis]. University of Georgia; 2016. Available from: http://hdl.handle.net/10724/35464"

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


University of Georgia

12. Stephens, Christoher B. Identification of putative interacting proteins with cTHY28.

Degree: 2014, University of Georgia

 cTHY28 is a highly conserved, nuclear protein that was identified in a screen of cellular proteins that mediate apoptosis in avian lymphocytes. To determine the… (more)

Subjects/Keywords: cTHY28; Nucleolin; DNA Topoisomerase I; Co-Immunoprecipitation; Protein-Protein Interactions

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APA (6th Edition):

Stephens, C. B. (2014). Identification of putative interacting proteins with cTHY28. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/27827

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):

Stephens, Christoher B. “Identification of putative interacting proteins with cTHY28.” 2014. Thesis, University of Georgia. Accessed January 24, 2021. http://hdl.handle.net/10724/27827.

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

MLA Handbook (7th Edition):

Stephens, Christoher B. “Identification of putative interacting proteins with cTHY28.” 2014. Web. 24 Jan 2021.

Vancouver:

Stephens CB. Identification of putative interacting proteins with cTHY28. [Internet] [Thesis]. University of Georgia; 2014. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/10724/27827.

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

Council of Science Editors:

Stephens CB. Identification of putative interacting proteins with cTHY28. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/27827

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


Texas Medical Center

13. Pickering, Brian. The regulation of microRNA biogenesis by ribosome-interacting proteins.

Degree: PhD, 2014, Texas Medical Center

  MicroRNA (miRNA) are small, non-coding RNAs that affect gene expression through degradation of complementary mRNA targets or inhibition of translation. As they affect approximately… (more)

Subjects/Keywords: Nucleolin; RRBP1; p180; ES130; breast cancer; CLaPP; Cancer Biology; Medicine and Health Sciences; Molecular Biology

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APA (6th Edition):

Pickering, B. (2014). The regulation of microRNA biogenesis by ribosome-interacting proteins. (Doctoral Dissertation). Texas Medical Center. Retrieved from https://digitalcommons.library.tmc.edu/utgsbs_dissertations/460

Chicago Manual of Style (16th Edition):

Pickering, Brian. “The regulation of microRNA biogenesis by ribosome-interacting proteins.” 2014. Doctoral Dissertation, Texas Medical Center. Accessed January 24, 2021. https://digitalcommons.library.tmc.edu/utgsbs_dissertations/460.

MLA Handbook (7th Edition):

Pickering, Brian. “The regulation of microRNA biogenesis by ribosome-interacting proteins.” 2014. Web. 24 Jan 2021.

Vancouver:

Pickering B. The regulation of microRNA biogenesis by ribosome-interacting proteins. [Internet] [Doctoral dissertation]. Texas Medical Center; 2014. [cited 2021 Jan 24]. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/460.

Council of Science Editors:

Pickering B. The regulation of microRNA biogenesis by ribosome-interacting proteins. [Doctoral Dissertation]. Texas Medical Center; 2014. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/460

14. Μπίρμπας, Χαράλαμπος. Μελέτη της αντι-αγγειογενετικής δράσης των συνθετικών πεπτιδίων HB-19 και N6L.

Degree: 2012, University of Patras

H νουκλεολίνη είναι μια πρωτεΐνη μοριακού βάρους 110 kDa και απαντάται στον πυρήνα, το κυτταρόπλασμα αλλά και στην επιφάνεια των κυττάρων, ενώ υπερεκφράζεται σε καρκινικά… (more)

Subjects/Keywords: Αγγειογένεση; Καρκίνος; Πεπτίδια; Νουκλεολίνη; 572.69; Angiogenesis; Cancer; Nucleolin; Peptides; HB-19; N6L

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APA (6th Edition):

Μπίρμπας, . (2012). Μελέτη της αντι-αγγειογενετικής δράσης των συνθετικών πεπτιδίων HB-19 και N6L. (Doctoral Dissertation). University of Patras. Retrieved from http://hdl.handle.net/10889/5914

Chicago Manual of Style (16th Edition):

Μπίρμπας, Χαράλαμπος. “Μελέτη της αντι-αγγειογενετικής δράσης των συνθετικών πεπτιδίων HB-19 και N6L.” 2012. Doctoral Dissertation, University of Patras. Accessed January 24, 2021. http://hdl.handle.net/10889/5914.

MLA Handbook (7th Edition):

Μπίρμπας, Χαράλαμπος. “Μελέτη της αντι-αγγειογενετικής δράσης των συνθετικών πεπτιδίων HB-19 και N6L.” 2012. Web. 24 Jan 2021.

Vancouver:

Μπίρμπας . Μελέτη της αντι-αγγειογενετικής δράσης των συνθετικών πεπτιδίων HB-19 και N6L. [Internet] [Doctoral dissertation]. University of Patras; 2012. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/10889/5914.

Council of Science Editors:

Μπίρμπας . Μελέτη της αντι-αγγειογενετικής δράσης των συνθετικών πεπτιδίων HB-19 και N6L. [Doctoral Dissertation]. University of Patras; 2012. Available from: http://hdl.handle.net/10889/5914

15. Gaume, Xavier. Localisation et fonctions de la nucléoline au centrosome : Localisation and functions of nucleolin at the centrosome.

Degree: Docteur es, Sciences de la Vie, 2014, Lyon, École normale supérieure

La nucléoline est une des protéines les plus abondantes des nucléoles. Ses fonctions ne sont cependant pas restreintes à la biogénèse des ribosomes. En absence… (more)

Subjects/Keywords: Nucléoline; Centrosome; Microtubules; Centriole mature; Ancrage; Nucléation; Nucleolin; Centrosome; Microtubules; Mature centriole; Anchoring; Nucleation

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APA (6th Edition):

Gaume, X. (2014). Localisation et fonctions de la nucléoline au centrosome : Localisation and functions of nucleolin at the centrosome. (Doctoral Dissertation). Lyon, École normale supérieure. Retrieved from http://www.theses.fr/2014ENSL0890

Chicago Manual of Style (16th Edition):

Gaume, Xavier. “Localisation et fonctions de la nucléoline au centrosome : Localisation and functions of nucleolin at the centrosome.” 2014. Doctoral Dissertation, Lyon, École normale supérieure. Accessed January 24, 2021. http://www.theses.fr/2014ENSL0890.

MLA Handbook (7th Edition):

Gaume, Xavier. “Localisation et fonctions de la nucléoline au centrosome : Localisation and functions of nucleolin at the centrosome.” 2014. Web. 24 Jan 2021.

Vancouver:

Gaume X. Localisation et fonctions de la nucléoline au centrosome : Localisation and functions of nucleolin at the centrosome. [Internet] [Doctoral dissertation]. Lyon, École normale supérieure; 2014. [cited 2021 Jan 24]. Available from: http://www.theses.fr/2014ENSL0890.

Council of Science Editors:

Gaume X. Localisation et fonctions de la nucléoline au centrosome : Localisation and functions of nucleolin at the centrosome. [Doctoral Dissertation]. Lyon, École normale supérieure; 2014. Available from: http://www.theses.fr/2014ENSL0890


Boston University

16. Shivakumar, Adarsha. Antigens and cancer pathways targeted by de-N-acetyl polysialic acid monoclonal antibodies.

Degree: MS, Medical Sciences, 2017, Boston University

 Polysialic acid (PSA) is a developmentally regulated glycan made of repeating sialic acid monomers with α2-8 linkages. PSA has very limited expression in adults, and… (more)

Subjects/Keywords: Immunology; Cancer; Cell motility; De-N-acetyl polysialic acid; Nucleolin; Polysialic acid; Polysialyltransferase

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APA (6th Edition):

Shivakumar, A. (2017). Antigens and cancer pathways targeted by de-N-acetyl polysialic acid monoclonal antibodies. (Masters Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/23840

Chicago Manual of Style (16th Edition):

Shivakumar, Adarsha. “Antigens and cancer pathways targeted by de-N-acetyl polysialic acid monoclonal antibodies.” 2017. Masters Thesis, Boston University. Accessed January 24, 2021. http://hdl.handle.net/2144/23840.

MLA Handbook (7th Edition):

Shivakumar, Adarsha. “Antigens and cancer pathways targeted by de-N-acetyl polysialic acid monoclonal antibodies.” 2017. Web. 24 Jan 2021.

Vancouver:

Shivakumar A. Antigens and cancer pathways targeted by de-N-acetyl polysialic acid monoclonal antibodies. [Internet] [Masters thesis]. Boston University; 2017. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/2144/23840.

Council of Science Editors:

Shivakumar A. Antigens and cancer pathways targeted by de-N-acetyl polysialic acid monoclonal antibodies. [Masters Thesis]. Boston University; 2017. Available from: http://hdl.handle.net/2144/23840


University of Louisville

17. Girvan, Allicia C., 1978-. Mechanistic studies of guanine-rich oligonucleotides.

Degree: PhD, 2006, University of Louisville

 Guanine-rich oligonucleotides (GROs) are being developed as a novel anticancer agents. GROs exhibit potent antiproliferative properties against several malignant cell lines and in established in… (more)

Subjects/Keywords: Guanine-rich; Oligonucleotides; Nucleolin; NF-kappaB

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APA (6th Edition):

Girvan, Allicia C., 1. (2006). Mechanistic studies of guanine-rich oligonucleotides. (Doctoral Dissertation). University of Louisville. Retrieved from 10.18297/etd/501 ; https://ir.library.louisville.edu/etd/501

Chicago Manual of Style (16th Edition):

Girvan, Allicia C., 1978-. “Mechanistic studies of guanine-rich oligonucleotides.” 2006. Doctoral Dissertation, University of Louisville. Accessed January 24, 2021. 10.18297/etd/501 ; https://ir.library.louisville.edu/etd/501.

MLA Handbook (7th Edition):

Girvan, Allicia C., 1978-. “Mechanistic studies of guanine-rich oligonucleotides.” 2006. Web. 24 Jan 2021.

Vancouver:

Girvan, Allicia C. 1. Mechanistic studies of guanine-rich oligonucleotides. [Internet] [Doctoral dissertation]. University of Louisville; 2006. [cited 2021 Jan 24]. Available from: 10.18297/etd/501 ; https://ir.library.louisville.edu/etd/501.

Council of Science Editors:

Girvan, Allicia C. 1. Mechanistic studies of guanine-rich oligonucleotides. [Doctoral Dissertation]. University of Louisville; 2006. Available from: 10.18297/etd/501 ; https://ir.library.louisville.edu/etd/501


NSYSU

18. Lin, Tzu-Wen. Investigation of hepatoma-derived growth factor (HDGF) membrane binding protein and biological functions in HDGF S103A mutation.

Degree: Master, Institute of Biomedical Sciences, 2018, NSYSU

 Hepatoma-derived growth factor (HDGF) is a nuclear targeted growth factor identified from human hepatocellular carcinoma (HCC) cell line, Huh7. Based on clinical studies, HDGF overexpression… (more)

Subjects/Keywords: Annexin A2 (ANXA2); GRP78; Nucleophosmin (B23); Nucleolin (NCL); Hepatoma-derived growth factor (HDGF); Hepatocellular carcinoma (HCC)

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APA (6th Edition):

Lin, T. (2018). Investigation of hepatoma-derived growth factor (HDGF) membrane binding protein and biological functions in HDGF S103A mutation. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0708118-093546

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):

Lin, Tzu-Wen. “Investigation of hepatoma-derived growth factor (HDGF) membrane binding protein and biological functions in HDGF S103A mutation.” 2018. Thesis, NSYSU. Accessed January 24, 2021. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0708118-093546.

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

MLA Handbook (7th Edition):

Lin, Tzu-Wen. “Investigation of hepatoma-derived growth factor (HDGF) membrane binding protein and biological functions in HDGF S103A mutation.” 2018. Web. 24 Jan 2021.

Vancouver:

Lin T. Investigation of hepatoma-derived growth factor (HDGF) membrane binding protein and biological functions in HDGF S103A mutation. [Internet] [Thesis]. NSYSU; 2018. [cited 2021 Jan 24]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0708118-093546.

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

Council of Science Editors:

Lin T. Investigation of hepatoma-derived growth factor (HDGF) membrane binding protein and biological functions in HDGF S103A mutation. [Thesis]. NSYSU; 2018. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0708118-093546

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

19. Kabirian Dehkordi, Samaneh. Biological Activities of Nucleolin Aptamer AS1411 Grafted to Gold Nanospheres : From Synthesis to Mechanistic Studies : Activités biologiques de l'aptamère nucléoline AS1411 associé à nanosphères d'or : de la synthèse aux études mécanistiques.

Degree: Docteur es, Biologie, 2019, Lyon; Université de technologie d'Isfahan (Isfahan, Iran)

Un oligonucléotide riche en G, AS1411, interagi avec la nucléoline et inhibe la prolifération des cellules cancéreuses et la croissance tumorale. Cette action antiproliférative est… (more)

Subjects/Keywords: AS1411; Nanosphères d'or; Nucléoline; Structure nucléolaire; ARN ribosomaux; AS1411; Gold nanospheres; Nucleolin; Cell cycle; Nucleolar structure; Ribosomal RNA; 570

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APA (6th Edition):

Kabirian Dehkordi, S. (2019). Biological Activities of Nucleolin Aptamer AS1411 Grafted to Gold Nanospheres : From Synthesis to Mechanistic Studies : Activités biologiques de l'aptamère nucléoline AS1411 associé à nanosphères d'or : de la synthèse aux études mécanistiques. (Doctoral Dissertation). Lyon; Université de technologie d'Isfahan (Isfahan, Iran). Retrieved from http://www.theses.fr/2019LYSE1216

Chicago Manual of Style (16th Edition):

Kabirian Dehkordi, Samaneh. “Biological Activities of Nucleolin Aptamer AS1411 Grafted to Gold Nanospheres : From Synthesis to Mechanistic Studies : Activités biologiques de l'aptamère nucléoline AS1411 associé à nanosphères d'or : de la synthèse aux études mécanistiques.” 2019. Doctoral Dissertation, Lyon; Université de technologie d'Isfahan (Isfahan, Iran). Accessed January 24, 2021. http://www.theses.fr/2019LYSE1216.

MLA Handbook (7th Edition):

Kabirian Dehkordi, Samaneh. “Biological Activities of Nucleolin Aptamer AS1411 Grafted to Gold Nanospheres : From Synthesis to Mechanistic Studies : Activités biologiques de l'aptamère nucléoline AS1411 associé à nanosphères d'or : de la synthèse aux études mécanistiques.” 2019. Web. 24 Jan 2021.

Vancouver:

Kabirian Dehkordi S. Biological Activities of Nucleolin Aptamer AS1411 Grafted to Gold Nanospheres : From Synthesis to Mechanistic Studies : Activités biologiques de l'aptamère nucléoline AS1411 associé à nanosphères d'or : de la synthèse aux études mécanistiques. [Internet] [Doctoral dissertation]. Lyon; Université de technologie d'Isfahan (Isfahan, Iran); 2019. [cited 2021 Jan 24]. Available from: http://www.theses.fr/2019LYSE1216.

Council of Science Editors:

Kabirian Dehkordi S. Biological Activities of Nucleolin Aptamer AS1411 Grafted to Gold Nanospheres : From Synthesis to Mechanistic Studies : Activités biologiques de l'aptamère nucléoline AS1411 associé à nanosphères d'or : de la synthèse aux études mécanistiques. [Doctoral Dissertation]. Lyon; Université de technologie d'Isfahan (Isfahan, Iran); 2019. Available from: http://www.theses.fr/2019LYSE1216

20. Κουτσιούμπα, Μαρίνα. Ταυτοποίηση πρωτεϊνών που αλληλεπιδρούν με τον αυξητικό παράγοντα πλειοτροπίνη και διερεύνηση του λειτουργικού τους ρόλου.

Degree: 2013, University of Patras

 Η πλειοτροπίνη (PTN) αποτελεί έναν αυξητικό παράγοντα με ποικίλες δράσεις και σημαντικό ρόλο στην ανάπτυξη όγκων και την αγγειογένεση. Διάφοροι υποδοχείς αλληλεπιδρούν με την ΡΤΝ… (more)

Subjects/Keywords: Πλειοτροπίνη; Νουκλεολίνη; Ιντεγκρίνη ανβ3; Κυτταρική μετανάστευση; Αγγειογένεση; Γλοιοβλαστώματα; 571.67; Pleiotrophin; Nucleolin; Integrin ανβ3; Cell migration; Angiogenesis; Glioblastomas; RPTPβ/ζ

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APA (6th Edition):

Κουτσιούμπα, . (2013). Ταυτοποίηση πρωτεϊνών που αλληλεπιδρούν με τον αυξητικό παράγοντα πλειοτροπίνη και διερεύνηση του λειτουργικού τους ρόλου. (Doctoral Dissertation). University of Patras. Retrieved from http://hdl.handle.net/10889/7823

Chicago Manual of Style (16th Edition):

Κουτσιούμπα, Μαρίνα. “Ταυτοποίηση πρωτεϊνών που αλληλεπιδρούν με τον αυξητικό παράγοντα πλειοτροπίνη και διερεύνηση του λειτουργικού τους ρόλου.” 2013. Doctoral Dissertation, University of Patras. Accessed January 24, 2021. http://hdl.handle.net/10889/7823.

MLA Handbook (7th Edition):

Κουτσιούμπα, Μαρίνα. “Ταυτοποίηση πρωτεϊνών που αλληλεπιδρούν με τον αυξητικό παράγοντα πλειοτροπίνη και διερεύνηση του λειτουργικού τους ρόλου.” 2013. Web. 24 Jan 2021.

Vancouver:

Κουτσιούμπα . Ταυτοποίηση πρωτεϊνών που αλληλεπιδρούν με τον αυξητικό παράγοντα πλειοτροπίνη και διερεύνηση του λειτουργικού τους ρόλου. [Internet] [Doctoral dissertation]. University of Patras; 2013. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/10889/7823.

Council of Science Editors:

Κουτσιούμπα . Ταυτοποίηση πρωτεϊνών που αλληλεπιδρούν με τον αυξητικό παράγοντα πλειοτροπίνη και διερεύνηση του λειτουργικού τους ρόλου. [Doctoral Dissertation]. University of Patras; 2013. Available from: http://hdl.handle.net/10889/7823


University of Arizona

21. Gonzalez, Veronica. Defining the Role of Nucleolin on the Transcriptional Regulation of c-MYC through Modulation of the c-MYC NHE III1 Element.

Degree: 2010, University of Arizona

 The activated product of the c-MYC proto-oncogene is one of the strongest known activators of carcinogenesis. It has been estimated that as many as one-seventh… (more)

Subjects/Keywords: c-MYC; C23; G-quadruplex; Nucleolin; Oncogene; Transcription

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APA (6th Edition):

Gonzalez, V. (2010). Defining the Role of Nucleolin on the Transcriptional Regulation of c-MYC through Modulation of the c-MYC NHE III1 Element. (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/195898

Chicago Manual of Style (16th Edition):

Gonzalez, Veronica. “Defining the Role of Nucleolin on the Transcriptional Regulation of c-MYC through Modulation of the c-MYC NHE III1 Element. ” 2010. Doctoral Dissertation, University of Arizona. Accessed January 24, 2021. http://hdl.handle.net/10150/195898.

MLA Handbook (7th Edition):

Gonzalez, Veronica. “Defining the Role of Nucleolin on the Transcriptional Regulation of c-MYC through Modulation of the c-MYC NHE III1 Element. ” 2010. Web. 24 Jan 2021.

Vancouver:

Gonzalez V. Defining the Role of Nucleolin on the Transcriptional Regulation of c-MYC through Modulation of the c-MYC NHE III1 Element. [Internet] [Doctoral dissertation]. University of Arizona; 2010. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/10150/195898.

Council of Science Editors:

Gonzalez V. Defining the Role of Nucleolin on the Transcriptional Regulation of c-MYC through Modulation of the c-MYC NHE III1 Element. [Doctoral Dissertation]. University of Arizona; 2010. Available from: http://hdl.handle.net/10150/195898

22. 河村, 香寿美. ゲノムストレスに対する細胞応答機構の解明 .

Degree: 2019, Kyoto University

Subjects/Keywords: genome instability; stress response; MRE11; nucleolin; DNA repair

Page 1 Page 2 Page 3 Page 4 Page 5

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APA (6th Edition):

河村, . (2019). ゲノムストレスに対する細胞応答機構の解明 . (Thesis). Kyoto University. Retrieved from http://hdl.handle.net/2433/242751

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):

河村, 香寿美. “ゲノムストレスに対する細胞応答機構の解明 .” 2019. Thesis, Kyoto University. Accessed January 24, 2021. http://hdl.handle.net/2433/242751.

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

MLA Handbook (7th Edition):

河村, 香寿美. “ゲノムストレスに対する細胞応答機構の解明 .” 2019. Web. 24 Jan 2021.

Vancouver:

河村 . ゲノムストレスに対する細胞応答機構の解明 . [Internet] [Thesis]. Kyoto University; 2019. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/2433/242751.

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

Council of Science Editors:

河村 . ゲノムストレスに対する細胞応答機構の解明 . [Thesis]. Kyoto University; 2019. Available from: http://hdl.handle.net/2433/242751

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


Universidade do Minho

23. Dias, Ana Isabel Oliveira da Silva. Effect of simulated microgravity on the cell cycle in cultured cells of Arabidopsis thaliana .

Degree: 2018, Universidade do Minho

 Life as we know it on planet Earth always evolved in the presence of the constant gravitational force, both in magnitude and direction. This physical… (more)

Subjects/Keywords: Simulated microgravity; Arabidopsis thaliana; Cell growth; Cell proliferation; Cultured cells; Nucleolin; Fibrillarin; Microgravidade simulada; Arabidopsis thaliana; Crescimento celular; Proliferação celular; Culturas celulares; Nucleolina; Fibrilarina

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APA (6th Edition):

Dias, A. I. O. d. S. (2018). Effect of simulated microgravity on the cell cycle in cultured cells of Arabidopsis thaliana . (Masters Thesis). Universidade do Minho. Retrieved from http://hdl.handle.net/1822/55508

Chicago Manual of Style (16th Edition):

Dias, Ana Isabel Oliveira da Silva. “Effect of simulated microgravity on the cell cycle in cultured cells of Arabidopsis thaliana .” 2018. Masters Thesis, Universidade do Minho. Accessed January 24, 2021. http://hdl.handle.net/1822/55508.

MLA Handbook (7th Edition):

Dias, Ana Isabel Oliveira da Silva. “Effect of simulated microgravity on the cell cycle in cultured cells of Arabidopsis thaliana .” 2018. Web. 24 Jan 2021.

Vancouver:

Dias AIOdS. Effect of simulated microgravity on the cell cycle in cultured cells of Arabidopsis thaliana . [Internet] [Masters thesis]. Universidade do Minho; 2018. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/1822/55508.

Council of Science Editors:

Dias AIOdS. Effect of simulated microgravity on the cell cycle in cultured cells of Arabidopsis thaliana . [Masters Thesis]. Universidade do Minho; 2018. Available from: http://hdl.handle.net/1822/55508

24. Das, Sadhan Chandra. Molecular mechanism of nucleolin-mediated Pol I transcription and characterization of nucleolin acetylation : Rôle de la nucléoline dans le mécanisme moléculaire de la regulation de la transcription par la polymérase I et caractérisation de son acétylation.

Degree: Docteur es, Sciences de la vie, 2012, Lyon, École normale supérieure

Nous montrons dans cette étude que dans les cellules déplétées pour la nucléoline, une plus faible accumulation de pré-ARNr est associée à une augmentation de… (more)

Subjects/Keywords: Nucléoline; ARN Polymérase I; Transcription de l’ADNr; Modifications post-traductionnelles; Acétylation; SC35; Facteurs d’épissage; Nucleolin; RNA polymerase I; RDNA transcription; Post-translational modification; Acetylation; SC35; Splicing factor

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APA (6th Edition):

Das, S. C. (2012). Molecular mechanism of nucleolin-mediated Pol I transcription and characterization of nucleolin acetylation : Rôle de la nucléoline dans le mécanisme moléculaire de la regulation de la transcription par la polymérase I et caractérisation de son acétylation. (Doctoral Dissertation). Lyon, École normale supérieure. Retrieved from http://www.theses.fr/2012ENSL0767

Chicago Manual of Style (16th Edition):

Das, Sadhan Chandra. “Molecular mechanism of nucleolin-mediated Pol I transcription and characterization of nucleolin acetylation : Rôle de la nucléoline dans le mécanisme moléculaire de la regulation de la transcription par la polymérase I et caractérisation de son acétylation.” 2012. Doctoral Dissertation, Lyon, École normale supérieure. Accessed January 24, 2021. http://www.theses.fr/2012ENSL0767.

MLA Handbook (7th Edition):

Das, Sadhan Chandra. “Molecular mechanism of nucleolin-mediated Pol I transcription and characterization of nucleolin acetylation : Rôle de la nucléoline dans le mécanisme moléculaire de la regulation de la transcription par la polymérase I et caractérisation de son acétylation.” 2012. Web. 24 Jan 2021.

Vancouver:

Das SC. Molecular mechanism of nucleolin-mediated Pol I transcription and characterization of nucleolin acetylation : Rôle de la nucléoline dans le mécanisme moléculaire de la regulation de la transcription par la polymérase I et caractérisation de son acétylation. [Internet] [Doctoral dissertation]. Lyon, École normale supérieure; 2012. [cited 2021 Jan 24]. Available from: http://www.theses.fr/2012ENSL0767.

Council of Science Editors:

Das SC. Molecular mechanism of nucleolin-mediated Pol I transcription and characterization of nucleolin acetylation : Rôle de la nucléoline dans le mécanisme moléculaire de la regulation de la transcription par la polymérase I et caractérisation de son acétylation. [Doctoral Dissertation]. Lyon, École normale supérieure; 2012. Available from: http://www.theses.fr/2012ENSL0767

25. Elahouel, Rania. Le Fibroblast Growth Factor 2 ( FGF-2 ) et la neuropiline-1 (NRP-1) : nouveaux partenaires moléculaires de Heparin Affin Regulatory Peptide ( HARP) : The Fibroblast Growth Factor 2 (FGF-2) and the neuropiline-1 (NRP-1) : new molecular partners of Heparin Affin Regulatory Peptide (HARP).

Degree: Docteur es, Pharmacologie et Biothérapies, 2012, Université Paris-Est

HARP (Heparin Affin regulatory peptide) est un facteur de croissance qui constitue avec la midkine une sous-famille des Heparin Binding Growth Factors (HBGFs). HARP est… (more)

Subjects/Keywords: Facteurs de croissance; Invasion tumorale; Migration des cellules; Harp; Nrp-1; Fgf-2; Molecular partners of nucleolin; Pharmacological agents; Harp; Neuropilin1; Interaction; Signal transduction

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APA (6th Edition):

Elahouel, R. (2012). Le Fibroblast Growth Factor 2 ( FGF-2 ) et la neuropiline-1 (NRP-1) : nouveaux partenaires moléculaires de Heparin Affin Regulatory Peptide ( HARP) : The Fibroblast Growth Factor 2 (FGF-2) and the neuropiline-1 (NRP-1) : new molecular partners of Heparin Affin Regulatory Peptide (HARP). (Doctoral Dissertation). Université Paris-Est. Retrieved from http://www.theses.fr/2012PEST0066

Chicago Manual of Style (16th Edition):

Elahouel, Rania. “Le Fibroblast Growth Factor 2 ( FGF-2 ) et la neuropiline-1 (NRP-1) : nouveaux partenaires moléculaires de Heparin Affin Regulatory Peptide ( HARP) : The Fibroblast Growth Factor 2 (FGF-2) and the neuropiline-1 (NRP-1) : new molecular partners of Heparin Affin Regulatory Peptide (HARP).” 2012. Doctoral Dissertation, Université Paris-Est. Accessed January 24, 2021. http://www.theses.fr/2012PEST0066.

MLA Handbook (7th Edition):

Elahouel, Rania. “Le Fibroblast Growth Factor 2 ( FGF-2 ) et la neuropiline-1 (NRP-1) : nouveaux partenaires moléculaires de Heparin Affin Regulatory Peptide ( HARP) : The Fibroblast Growth Factor 2 (FGF-2) and the neuropiline-1 (NRP-1) : new molecular partners of Heparin Affin Regulatory Peptide (HARP).” 2012. Web. 24 Jan 2021.

Vancouver:

Elahouel R. Le Fibroblast Growth Factor 2 ( FGF-2 ) et la neuropiline-1 (NRP-1) : nouveaux partenaires moléculaires de Heparin Affin Regulatory Peptide ( HARP) : The Fibroblast Growth Factor 2 (FGF-2) and the neuropiline-1 (NRP-1) : new molecular partners of Heparin Affin Regulatory Peptide (HARP). [Internet] [Doctoral dissertation]. Université Paris-Est; 2012. [cited 2021 Jan 24]. Available from: http://www.theses.fr/2012PEST0066.

Council of Science Editors:

Elahouel R. Le Fibroblast Growth Factor 2 ( FGF-2 ) et la neuropiline-1 (NRP-1) : nouveaux partenaires moléculaires de Heparin Affin Regulatory Peptide ( HARP) : The Fibroblast Growth Factor 2 (FGF-2) and the neuropiline-1 (NRP-1) : new molecular partners of Heparin Affin Regulatory Peptide (HARP). [Doctoral Dissertation]. Université Paris-Est; 2012. Available from: http://www.theses.fr/2012PEST0066

26. Cong, Rong. Functional analysis of nucleolin-chromatin interaction in vivo : L'analyse fonctionnelle de l'interaction nucléoline-chromatine in vivo.

Degree: Docteur es, Sciences de la vie, 2011, Lyon, École normale supérieure; East China normal university (Shanghai)

La nucléoline, une des protéines non-ribosomique les plus abondantes du nucléole, semble être impliquée dans de nombreux aspects du métabolisme de l'ADN en plus de… (more)

Subjects/Keywords: Nucléoline; ARN polymérase I; Transcription de l'ADNr; Modifications d’histone; Variants d'histone macroH2A; Nucleolin; RNA polymerase I; RDNA transcription; Histone modification; Histone variant macroH2A1; Epigenetics; Nucleolus

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APA (6th Edition):

Cong, R. (2011). Functional analysis of nucleolin-chromatin interaction in vivo : L'analyse fonctionnelle de l'interaction nucléoline-chromatine in vivo. (Doctoral Dissertation). Lyon, École normale supérieure; East China normal university (Shanghai). Retrieved from http://www.theses.fr/2011ENSL0636

Chicago Manual of Style (16th Edition):

Cong, Rong. “Functional analysis of nucleolin-chromatin interaction in vivo : L'analyse fonctionnelle de l'interaction nucléoline-chromatine in vivo.” 2011. Doctoral Dissertation, Lyon, École normale supérieure; East China normal university (Shanghai). Accessed January 24, 2021. http://www.theses.fr/2011ENSL0636.

MLA Handbook (7th Edition):

Cong, Rong. “Functional analysis of nucleolin-chromatin interaction in vivo : L'analyse fonctionnelle de l'interaction nucléoline-chromatine in vivo.” 2011. Web. 24 Jan 2021.

Vancouver:

Cong R. Functional analysis of nucleolin-chromatin interaction in vivo : L'analyse fonctionnelle de l'interaction nucléoline-chromatine in vivo. [Internet] [Doctoral dissertation]. Lyon, École normale supérieure; East China normal university (Shanghai); 2011. [cited 2021 Jan 24]. Available from: http://www.theses.fr/2011ENSL0636.

Council of Science Editors:

Cong R. Functional analysis of nucleolin-chromatin interaction in vivo : L'analyse fonctionnelle de l'interaction nucléoline-chromatine in vivo. [Doctoral Dissertation]. Lyon, École normale supérieure; East China normal university (Shanghai); 2011. Available from: http://www.theses.fr/2011ENSL0636


University of Kentucky

27. Jiang, Yi. IDENTIFICATION AND CHARACTERIZATION OF HOST FACTORS INVOLVED IN TOMBUSVIRUS REPLICATION.

Degree: 2009, University of Kentucky

 Positive strand RNA viruses are intracellular parasites, and their genome replication and infection involves complex virus-host interactions. Therefore, identification of host factors and dissection of… (more)

Subjects/Keywords: TBSV replication|host factors|Nsr1p/nucleolin|RNA binding|RNA recruitment; Plant Pathology

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APA (6th Edition):

Jiang, Y. (2009). IDENTIFICATION AND CHARACTERIZATION OF HOST FACTORS INVOLVED IN TOMBUSVIRUS REPLICATION. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/gradschool_diss/745

Chicago Manual of Style (16th Edition):

Jiang, Yi. “IDENTIFICATION AND CHARACTERIZATION OF HOST FACTORS INVOLVED IN TOMBUSVIRUS REPLICATION.” 2009. Doctoral Dissertation, University of Kentucky. Accessed January 24, 2021. https://uknowledge.uky.edu/gradschool_diss/745.

MLA Handbook (7th Edition):

Jiang, Yi. “IDENTIFICATION AND CHARACTERIZATION OF HOST FACTORS INVOLVED IN TOMBUSVIRUS REPLICATION.” 2009. Web. 24 Jan 2021.

Vancouver:

Jiang Y. IDENTIFICATION AND CHARACTERIZATION OF HOST FACTORS INVOLVED IN TOMBUSVIRUS REPLICATION. [Internet] [Doctoral dissertation]. University of Kentucky; 2009. [cited 2021 Jan 24]. Available from: https://uknowledge.uky.edu/gradschool_diss/745.

Council of Science Editors:

Jiang Y. IDENTIFICATION AND CHARACTERIZATION OF HOST FACTORS INVOLVED IN TOMBUSVIRUS REPLICATION. [Doctoral Dissertation]. University of Kentucky; 2009. Available from: https://uknowledge.uky.edu/gradschool_diss/745

28. Destouches, Damien. Ciblage de la nucléoline de surface par les pseudopeptides NucAnts dans l’inhibition de la croissance tumorale et de l’angiogenèse associée : Targeting cell surface-expressed nucleolin by NucAnts pseudopeptides in tumor growth and associated angiogenesis inhibition.

Degree: Docteur es, Sciences de la vie et de la santé. Aspects cellulaires et moléculaires de la biologie, 2009, Université Paris-Est

La recherche contre le cancer est aujourd’hui tournée vers les thérapies ciblées. Dans ce contexte, la nucléoline et la nucléophosmine sont fortement impliquées dans la… (more)

Subjects/Keywords: Thérapie anti-cancéreuse ciblée; Croissance tumorale; Néo-angiogenèse tumorale; Métastases; Pseudopeptide; HB-19; NucAnt; Nucléoline; Nucléophosmine; TIMP-3; Targeting anti-cancer therapy; Tumor growth; Tumor angiogenesis; Metastasis; Pseudopeptide; HB-19; NucAnt; Nucleolin; Nucleophosmin; TIMP-3

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

APA (6th Edition):

Destouches, D. (2009). Ciblage de la nucléoline de surface par les pseudopeptides NucAnts dans l’inhibition de la croissance tumorale et de l’angiogenèse associée : Targeting cell surface-expressed nucleolin by NucAnts pseudopeptides in tumor growth and associated angiogenesis inhibition. (Doctoral Dissertation). Université Paris-Est. Retrieved from http://www.theses.fr/2009PEST0045

Chicago Manual of Style (16th Edition):

Destouches, Damien. “Ciblage de la nucléoline de surface par les pseudopeptides NucAnts dans l’inhibition de la croissance tumorale et de l’angiogenèse associée : Targeting cell surface-expressed nucleolin by NucAnts pseudopeptides in tumor growth and associated angiogenesis inhibition.” 2009. Doctoral Dissertation, Université Paris-Est. Accessed January 24, 2021. http://www.theses.fr/2009PEST0045.

MLA Handbook (7th Edition):

Destouches, Damien. “Ciblage de la nucléoline de surface par les pseudopeptides NucAnts dans l’inhibition de la croissance tumorale et de l’angiogenèse associée : Targeting cell surface-expressed nucleolin by NucAnts pseudopeptides in tumor growth and associated angiogenesis inhibition.” 2009. Web. 24 Jan 2021.

Vancouver:

Destouches D. Ciblage de la nucléoline de surface par les pseudopeptides NucAnts dans l’inhibition de la croissance tumorale et de l’angiogenèse associée : Targeting cell surface-expressed nucleolin by NucAnts pseudopeptides in tumor growth and associated angiogenesis inhibition. [Internet] [Doctoral dissertation]. Université Paris-Est; 2009. [cited 2021 Jan 24]. Available from: http://www.theses.fr/2009PEST0045.

Council of Science Editors:

Destouches D. Ciblage de la nucléoline de surface par les pseudopeptides NucAnts dans l’inhibition de la croissance tumorale et de l’angiogenèse associée : Targeting cell surface-expressed nucleolin by NucAnts pseudopeptides in tumor growth and associated angiogenesis inhibition. [Doctoral Dissertation]. Université Paris-Est; 2009. Available from: http://www.theses.fr/2009PEST0045

29. Nguyen Van Long, Flora. Altérations de composition des ribosomes dans les cancers du sein : analyses de cohortes humaines et modèles cellulaires : Alterations of ribosomes composition in breast cancers : analyses of human cohorts and cellular models.

Degree: Docteur es, Oncologie, 2019, Lyon

Les ribosomes sont responsables de la traduction des ARNm en protéines. Des modifications de la composition des ribosomes altèrent son activité de traduction et favorisent… (more)

Subjects/Keywords: Ribosome; Méthylation 2’-O-ribose des ARNr; Biogénèse des ribosomes; Traduction; Fibrillarine; Nucléoline; Biomarqueurs pronostiques; Cancer du sein; Ribosome; RRNA 2’-O-ribose methylation; Ribosome biogenesis; Translation; Fibrillarin; Nucleolin; Prognostic biomarkers; Breast cancer; 570

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

APA (6th Edition):

Nguyen Van Long, F. (2019). Altérations de composition des ribosomes dans les cancers du sein : analyses de cohortes humaines et modèles cellulaires : Alterations of ribosomes composition in breast cancers : analyses of human cohorts and cellular models. (Doctoral Dissertation). Lyon. Retrieved from http://www.theses.fr/2019LYSE1095

Chicago Manual of Style (16th Edition):

Nguyen Van Long, Flora. “Altérations de composition des ribosomes dans les cancers du sein : analyses de cohortes humaines et modèles cellulaires : Alterations of ribosomes composition in breast cancers : analyses of human cohorts and cellular models.” 2019. Doctoral Dissertation, Lyon. Accessed January 24, 2021. http://www.theses.fr/2019LYSE1095.

MLA Handbook (7th Edition):

Nguyen Van Long, Flora. “Altérations de composition des ribosomes dans les cancers du sein : analyses de cohortes humaines et modèles cellulaires : Alterations of ribosomes composition in breast cancers : analyses of human cohorts and cellular models.” 2019. Web. 24 Jan 2021.

Vancouver:

Nguyen Van Long F. Altérations de composition des ribosomes dans les cancers du sein : analyses de cohortes humaines et modèles cellulaires : Alterations of ribosomes composition in breast cancers : analyses of human cohorts and cellular models. [Internet] [Doctoral dissertation]. Lyon; 2019. [cited 2021 Jan 24]. Available from: http://www.theses.fr/2019LYSE1095.

Council of Science Editors:

Nguyen Van Long F. Altérations de composition des ribosomes dans les cancers du sein : analyses de cohortes humaines et modèles cellulaires : Alterations of ribosomes composition in breast cancers : analyses of human cohorts and cellular models. [Doctoral Dissertation]. Lyon; 2019. Available from: http://www.theses.fr/2019LYSE1095

30. Poimenidi, Evangelia. Regulation of PTN expression by hypoxia and hypoxia-induced factors and possible functional significance.

Degree: 2016, University of Patras; Πανεπιστήμιο Πατρών

 Angiogenesis is a major aspect of tumor biology. Expanding tumors soon become hypoxic and demand new blood supply in order to support their rapid growth… (more)

Subjects/Keywords: Αγγειογένεση; Πλειοτροπίνη; Υποξία; Επαγόμενος από την υποξία παράγοντας; Αγγειακός ενδοθηλιακός αυξητικός παράγοντας (VEGF); Υποδοχέας αυξητικού ενδοθηλιακού παράγοντα ( VEGFR-2); Υποδοχέας RPTPβ/ζ; Integrin αν β3; Νουκλεολίνη; Angiogenesis; Pleiotrophin (HARP); Hypoxia; Hypoxia inducible factor ( HIF); Vascular endothelial growth factor (VEGF); VEGFR-2; RPTPβ/ζ; Integrin avb3; Nucleolin

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

APA (6th Edition):

Poimenidi, E. (2016). Regulation of PTN expression by hypoxia and hypoxia-induced factors and possible functional significance. (Thesis). University of Patras; Πανεπιστήμιο Πατρών. Retrieved from http://hdl.handle.net/10442/hedi/37508

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):

Poimenidi, Evangelia. “Regulation of PTN expression by hypoxia and hypoxia-induced factors and possible functional significance.” 2016. Thesis, University of Patras; Πανεπιστήμιο Πατρών. Accessed January 24, 2021. http://hdl.handle.net/10442/hedi/37508.

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

MLA Handbook (7th Edition):

Poimenidi, Evangelia. “Regulation of PTN expression by hypoxia and hypoxia-induced factors and possible functional significance.” 2016. Web. 24 Jan 2021.

Vancouver:

Poimenidi E. Regulation of PTN expression by hypoxia and hypoxia-induced factors and possible functional significance. [Internet] [Thesis]. University of Patras; Πανεπιστήμιο Πατρών; 2016. [cited 2021 Jan 24]. Available from: http://hdl.handle.net/10442/hedi/37508.

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

Council of Science Editors:

Poimenidi E. Regulation of PTN expression by hypoxia and hypoxia-induced factors and possible functional significance. [Thesis]. University of Patras; Πανεπιστήμιο Πατρών; 2016. Available from: http://hdl.handle.net/10442/hedi/37508

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

[1] [2]

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