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You searched for subject:(bromodomain). Showing records 1 – 30 of 50 total matches.

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University of Melbourne

1. Hogg, Simon John. BET bromodomain inhibition as combined apoptotic and immunomodulatory therapy for the treatment of MYC-driven lymphoma.

Degree: 2017, University of Melbourne

Bromodomain and Extra-Terminal (BET) proteins are a conserved family of ‘epigenetic readers’ that bind to acetylated lysine residues on histone and non-histone proteins to modulate… (more)

Subjects/Keywords: bromodomain; epigenetics; PD-L1; cancer

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APA (6th Edition):

Hogg, S. J. (2017). BET bromodomain inhibition as combined apoptotic and immunomodulatory therapy for the treatment of MYC-driven lymphoma. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/191790

Chicago Manual of Style (16th Edition):

Hogg, Simon John. “BET bromodomain inhibition as combined apoptotic and immunomodulatory therapy for the treatment of MYC-driven lymphoma.” 2017. Doctoral Dissertation, University of Melbourne. Accessed April 15, 2021. http://hdl.handle.net/11343/191790.

MLA Handbook (7th Edition):

Hogg, Simon John. “BET bromodomain inhibition as combined apoptotic and immunomodulatory therapy for the treatment of MYC-driven lymphoma.” 2017. Web. 15 Apr 2021.

Vancouver:

Hogg SJ. BET bromodomain inhibition as combined apoptotic and immunomodulatory therapy for the treatment of MYC-driven lymphoma. [Internet] [Doctoral dissertation]. University of Melbourne; 2017. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/11343/191790.

Council of Science Editors:

Hogg SJ. BET bromodomain inhibition as combined apoptotic and immunomodulatory therapy for the treatment of MYC-driven lymphoma. [Doctoral Dissertation]. University of Melbourne; 2017. Available from: http://hdl.handle.net/11343/191790


IUPUI

2. Hanquier, Jocelyne Nicole. Investigating the Function and Therapeutic Potential of the GCN5b Bromodomain in Toxoplasma Gondii.

Degree: 2020, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

The obligate intracellular protozoan parasite Toxoplasma gondii is a medically relevant pathogen that has infected a third of the world’s… (more)

Subjects/Keywords: L-Moses; Bromodomain Inhibitor; Bromodomain; GCN5; Lysine Acetyltransferase; Toxoplasma

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APA (6th Edition):

Hanquier, J. N. (2020). Investigating the Function and Therapeutic Potential of the GCN5b Bromodomain in Toxoplasma Gondii. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/23184

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):

Hanquier, Jocelyne Nicole. “Investigating the Function and Therapeutic Potential of the GCN5b Bromodomain in Toxoplasma Gondii.” 2020. Thesis, IUPUI. Accessed April 15, 2021. http://hdl.handle.net/1805/23184.

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

MLA Handbook (7th Edition):

Hanquier, Jocelyne Nicole. “Investigating the Function and Therapeutic Potential of the GCN5b Bromodomain in Toxoplasma Gondii.” 2020. Web. 15 Apr 2021.

Vancouver:

Hanquier JN. Investigating the Function and Therapeutic Potential of the GCN5b Bromodomain in Toxoplasma Gondii. [Internet] [Thesis]. IUPUI; 2020. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1805/23184.

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

Council of Science Editors:

Hanquier JN. Investigating the Function and Therapeutic Potential of the GCN5b Bromodomain in Toxoplasma Gondii. [Thesis]. IUPUI; 2020. Available from: http://hdl.handle.net/1805/23184

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


Texas A&M University

3. Misra, Anjali. The Bromodomain Proteins GTE9 and GTE11 Associate with BT2-based E3 Ligase Complex and Mediate Responses to Multiple Signals in Arabidopsis thaliana.

Degree: PhD, Molecular and Environmental Plant Sciences, 2012, Texas A&M University

 BT2 is an Arabidopsis thaliana protein with N-terminal BTB, central TAZ and a C-terminal calmodulin binding domain and associates with Cullin3 to form an E3… (more)

Subjects/Keywords: Bromodomain protein; Global transcription Factor group E; Arabidopsis GTE protein; Activation tagging, AtBT2, Bromodomain extraterminal class of protein; Arabidopsis BET protein

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APA (6th Edition):

Misra, A. (2012). The Bromodomain Proteins GTE9 and GTE11 Associate with BT2-based E3 Ligase Complex and Mediate Responses to Multiple Signals in Arabidopsis thaliana. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2011-12-10219

Chicago Manual of Style (16th Edition):

Misra, Anjali. “The Bromodomain Proteins GTE9 and GTE11 Associate with BT2-based E3 Ligase Complex and Mediate Responses to Multiple Signals in Arabidopsis thaliana.” 2012. Doctoral Dissertation, Texas A&M University. Accessed April 15, 2021. http://hdl.handle.net/1969.1/ETD-TAMU-2011-12-10219.

MLA Handbook (7th Edition):

Misra, Anjali. “The Bromodomain Proteins GTE9 and GTE11 Associate with BT2-based E3 Ligase Complex and Mediate Responses to Multiple Signals in Arabidopsis thaliana.” 2012. Web. 15 Apr 2021.

Vancouver:

Misra A. The Bromodomain Proteins GTE9 and GTE11 Associate with BT2-based E3 Ligase Complex and Mediate Responses to Multiple Signals in Arabidopsis thaliana. [Internet] [Doctoral dissertation]. Texas A&M University; 2012. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2011-12-10219.

Council of Science Editors:

Misra A. The Bromodomain Proteins GTE9 and GTE11 Associate with BT2-based E3 Ligase Complex and Mediate Responses to Multiple Signals in Arabidopsis thaliana. [Doctoral Dissertation]. Texas A&M University; 2012. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2011-12-10219

4. Champleboux, Morgane. Etude fonctionnelle et inhibition de la protéine Bdf1 chez Candida albicans : Functional role and inhibition of Bdf1 protein in Candida albicans.

Degree: Docteur es, Biologie cellulaire, 2016, Université Grenoble Alpes (ComUE)

Candida albicans représente la première cause d’infection fongique chez l’Homme. Chez les patients immunodéficients, ce pathogène est extrêmement virulent et le nombre de décès suite… (more)

Subjects/Keywords: Bdf1; Candida albicans; Bromodomain; Inhibiteurs; Molécules antifongiques; Bdf1; Candida albicans; Bromodomain; Inhibitors; Antifungal drugs; 570; 610

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APA (6th Edition):

Champleboux, M. (2016). Etude fonctionnelle et inhibition de la protéine Bdf1 chez Candida albicans : Functional role and inhibition of Bdf1 protein in Candida albicans. (Doctoral Dissertation). Université Grenoble Alpes (ComUE). Retrieved from http://www.theses.fr/2016GREAV037

Chicago Manual of Style (16th Edition):

Champleboux, Morgane. “Etude fonctionnelle et inhibition de la protéine Bdf1 chez Candida albicans : Functional role and inhibition of Bdf1 protein in Candida albicans.” 2016. Doctoral Dissertation, Université Grenoble Alpes (ComUE). Accessed April 15, 2021. http://www.theses.fr/2016GREAV037.

MLA Handbook (7th Edition):

Champleboux, Morgane. “Etude fonctionnelle et inhibition de la protéine Bdf1 chez Candida albicans : Functional role and inhibition of Bdf1 protein in Candida albicans.” 2016. Web. 15 Apr 2021.

Vancouver:

Champleboux M. Etude fonctionnelle et inhibition de la protéine Bdf1 chez Candida albicans : Functional role and inhibition of Bdf1 protein in Candida albicans. [Internet] [Doctoral dissertation]. Université Grenoble Alpes (ComUE); 2016. [cited 2021 Apr 15]. Available from: http://www.theses.fr/2016GREAV037.

Council of Science Editors:

Champleboux M. Etude fonctionnelle et inhibition de la protéine Bdf1 chez Candida albicans : Functional role and inhibition of Bdf1 protein in Candida albicans. [Doctoral Dissertation]. Université Grenoble Alpes (ComUE); 2016. Available from: http://www.theses.fr/2016GREAV037


University of California – Berkeley

5. Lombardi, Laura. Maintenance of Open Chromatin States by Histone H3 Eviction and H2A.Z.

Degree: Molecular & Cell Biology, 2011, University of California – Berkeley

 The size constraints of the nucleus necessitate condensation of eukaryotic DNA into chromatin. The fundamental subunit of chromatin is the nucleosome, ~147 bp of DNA… (more)

Subjects/Keywords: Molecular biology; Genetics; AAA-ATPase; bromodomain; gene induction; histone dosage; Yta7

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APA (6th Edition):

Lombardi, L. (2011). Maintenance of Open Chromatin States by Histone H3 Eviction and H2A.Z. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/9b25f7wf

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):

Lombardi, Laura. “Maintenance of Open Chromatin States by Histone H3 Eviction and H2A.Z.” 2011. Thesis, University of California – Berkeley. Accessed April 15, 2021. http://www.escholarship.org/uc/item/9b25f7wf.

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

MLA Handbook (7th Edition):

Lombardi, Laura. “Maintenance of Open Chromatin States by Histone H3 Eviction and H2A.Z.” 2011. Web. 15 Apr 2021.

Vancouver:

Lombardi L. Maintenance of Open Chromatin States by Histone H3 Eviction and H2A.Z. [Internet] [Thesis]. University of California – Berkeley; 2011. [cited 2021 Apr 15]. Available from: http://www.escholarship.org/uc/item/9b25f7wf.

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

Council of Science Editors:

Lombardi L. Maintenance of Open Chromatin States by Histone H3 Eviction and H2A.Z. [Thesis]. University of California – Berkeley; 2011. Available from: http://www.escholarship.org/uc/item/9b25f7wf

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


University of Rochester

6. Chatterjee, Nirmalya. Identification and characterization of proteins with novel functions in Nrf2 signaling.

Degree: PhD, 2016, University of Rochester

 Oxidative stress causes widespread damage to biomolecules, leads to different pathological conditions and contributes to aging. The Nrf2 transcription factor, a major mediator of oxidative… (more)

Subjects/Keywords: BET proteins; Bromodomain; Drosophila; Oxidative stress; Transcription factor Nrf2

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APA (6th Edition):

Chatterjee, N. (2016). Identification and characterization of proteins with novel functions in Nrf2 signaling. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/30407

Chicago Manual of Style (16th Edition):

Chatterjee, Nirmalya. “Identification and characterization of proteins with novel functions in Nrf2 signaling.” 2016. Doctoral Dissertation, University of Rochester. Accessed April 15, 2021. http://hdl.handle.net/1802/30407.

MLA Handbook (7th Edition):

Chatterjee, Nirmalya. “Identification and characterization of proteins with novel functions in Nrf2 signaling.” 2016. Web. 15 Apr 2021.

Vancouver:

Chatterjee N. Identification and characterization of proteins with novel functions in Nrf2 signaling. [Internet] [Doctoral dissertation]. University of Rochester; 2016. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1802/30407.

Council of Science Editors:

Chatterjee N. Identification and characterization of proteins with novel functions in Nrf2 signaling. [Doctoral Dissertation]. University of Rochester; 2016. Available from: http://hdl.handle.net/1802/30407


University of Michigan

7. Wang, Jingya. The Role of the MLL-HOXA9 Axis in Normal and Malignant Hematopoiesis.

Degree: PhD, Molecular & Cellular Pathology, 2013, University of Michigan

 The MLL-HOXA9 axis plays a critical role in the regulation of development and hematopoiesis. Chromosome translocations of MLL are closely associated with human leukemia and… (more)

Subjects/Keywords: MLL; ASB2; Ubiquitination; Bromodomain; PHD Finger; HOXA9; Pathology; Health Sciences

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APA (6th Edition):

Wang, J. (2013). The Role of the MLL-HOXA9 Axis in Normal and Malignant Hematopoiesis. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/100097

Chicago Manual of Style (16th Edition):

Wang, Jingya. “The Role of the MLL-HOXA9 Axis in Normal and Malignant Hematopoiesis.” 2013. Doctoral Dissertation, University of Michigan. Accessed April 15, 2021. http://hdl.handle.net/2027.42/100097.

MLA Handbook (7th Edition):

Wang, Jingya. “The Role of the MLL-HOXA9 Axis in Normal and Malignant Hematopoiesis.” 2013. Web. 15 Apr 2021.

Vancouver:

Wang J. The Role of the MLL-HOXA9 Axis in Normal and Malignant Hematopoiesis. [Internet] [Doctoral dissertation]. University of Michigan; 2013. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/2027.42/100097.

Council of Science Editors:

Wang J. The Role of the MLL-HOXA9 Axis in Normal and Malignant Hematopoiesis. [Doctoral Dissertation]. University of Michigan; 2013. Available from: http://hdl.handle.net/2027.42/100097


Harvard University

8. McKeown, Michael Robert. Chemical Probes and the Exploration of Bromodomains in Cancer Biology.

Degree: PhD, Chemical Biology, 2014, Harvard University

 The post-translational modification of histones and their interaction with transcription factors is essential to gene regulation. Furthermore, these targets would greatly benefit from probe molecules… (more)

Subjects/Keywords: Biochemistry; Cellular biology; Oncology; Bromodomain; Cancer; DLBCL; Inhibitor; Lymphoma; Oncology

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APA (6th Edition):

McKeown, M. R. (2014). Chemical Probes and the Exploration of Bromodomains in Cancer Biology. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:12269851

Chicago Manual of Style (16th Edition):

McKeown, Michael Robert. “Chemical Probes and the Exploration of Bromodomains in Cancer Biology.” 2014. Doctoral Dissertation, Harvard University. Accessed April 15, 2021. http://nrs.harvard.edu/urn-3:HUL.InstRepos:12269851.

MLA Handbook (7th Edition):

McKeown, Michael Robert. “Chemical Probes and the Exploration of Bromodomains in Cancer Biology.” 2014. Web. 15 Apr 2021.

Vancouver:

McKeown MR. Chemical Probes and the Exploration of Bromodomains in Cancer Biology. [Internet] [Doctoral dissertation]. Harvard University; 2014. [cited 2021 Apr 15]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:12269851.

Council of Science Editors:

McKeown MR. Chemical Probes and the Exploration of Bromodomains in Cancer Biology. [Doctoral Dissertation]. Harvard University; 2014. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:12269851


University of Miami

9. Rudman, Michelle Diane. Bromodomain and Extraterminal Domain-Containing Protein Inhibition Decreases Inflammation after Spinal Cord Injury.

Degree: PhD, Neuroscience (Medicine), 2017, University of Miami

  Spinal cord injury (SCI) is a devastating condition resulting in loss of function below the level of injury. Inflammation after SCI promotes cell death,… (more)

Subjects/Keywords: Bromodomain; Thermal Hyperalgesia; Spinal Cord Injury; JQ1; Cytokines; Leukocyte Infiltration

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APA (6th Edition):

Rudman, M. D. (2017). Bromodomain and Extraterminal Domain-Containing Protein Inhibition Decreases Inflammation after Spinal Cord Injury. (Doctoral Dissertation). University of Miami. Retrieved from https://scholarlyrepository.miami.edu/oa_dissertations/1956

Chicago Manual of Style (16th Edition):

Rudman, Michelle Diane. “Bromodomain and Extraterminal Domain-Containing Protein Inhibition Decreases Inflammation after Spinal Cord Injury.” 2017. Doctoral Dissertation, University of Miami. Accessed April 15, 2021. https://scholarlyrepository.miami.edu/oa_dissertations/1956.

MLA Handbook (7th Edition):

Rudman, Michelle Diane. “Bromodomain and Extraterminal Domain-Containing Protein Inhibition Decreases Inflammation after Spinal Cord Injury.” 2017. Web. 15 Apr 2021.

Vancouver:

Rudman MD. Bromodomain and Extraterminal Domain-Containing Protein Inhibition Decreases Inflammation after Spinal Cord Injury. [Internet] [Doctoral dissertation]. University of Miami; 2017. [cited 2021 Apr 15]. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/1956.

Council of Science Editors:

Rudman MD. Bromodomain and Extraterminal Domain-Containing Protein Inhibition Decreases Inflammation after Spinal Cord Injury. [Doctoral Dissertation]. University of Miami; 2017. Available from: https://scholarlyrepository.miami.edu/oa_dissertations/1956


Colorado State University

10. Luebben, Whitney R. Integrating p300 functions in HTLV-1 transcription initiation.

Degree: PhD, Biochemistry and Molecular Biology, 2014, Colorado State University

 The HTLV-1 provirus overcomes a repressive chromatin environment for efficient transcription of its genome. This is accomplished by the robust recruitment of the coactivator protein,… (more)

Subjects/Keywords: histone acetylation; transcription; p300; nucleosome; HTLV-1; bromodomain

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APA (6th Edition):

Luebben, W. R. (2014). Integrating p300 functions in HTLV-1 transcription initiation. (Doctoral Dissertation). Colorado State University. Retrieved from http://hdl.handle.net/10217/83762

Chicago Manual of Style (16th Edition):

Luebben, Whitney R. “Integrating p300 functions in HTLV-1 transcription initiation.” 2014. Doctoral Dissertation, Colorado State University. Accessed April 15, 2021. http://hdl.handle.net/10217/83762.

MLA Handbook (7th Edition):

Luebben, Whitney R. “Integrating p300 functions in HTLV-1 transcription initiation.” 2014. Web. 15 Apr 2021.

Vancouver:

Luebben WR. Integrating p300 functions in HTLV-1 transcription initiation. [Internet] [Doctoral dissertation]. Colorado State University; 2014. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10217/83762.

Council of Science Editors:

Luebben WR. Integrating p300 functions in HTLV-1 transcription initiation. [Doctoral Dissertation]. Colorado State University; 2014. Available from: http://hdl.handle.net/10217/83762


University of Oxford

11. Clark, Peter George Keith. Discovery of epigenetic probes against the bromodomain family of proteins.

Degree: PhD, 2015, University of Oxford

 Chemical probes are necessary for elucidating the biochemical roles of proteins. Bromodomains are protein-interaction modules found in a family of proteins implicated in the epigenetic… (more)

Subjects/Keywords: 572; Chemistry, Organic; Chemistry, Medicinal; Chemical Probe; Bromodomain; Enantioselective Organocatalysis; Epigenetics

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APA (6th Edition):

Clark, P. G. K. (2015). Discovery of epigenetic probes against the bromodomain family of proteins. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:a589d1f3-c8f6-4219-a10b-79099eafe1c8 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.712078

Chicago Manual of Style (16th Edition):

Clark, Peter George Keith. “Discovery of epigenetic probes against the bromodomain family of proteins.” 2015. Doctoral Dissertation, University of Oxford. Accessed April 15, 2021. http://ora.ox.ac.uk/objects/uuid:a589d1f3-c8f6-4219-a10b-79099eafe1c8 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.712078.

MLA Handbook (7th Edition):

Clark, Peter George Keith. “Discovery of epigenetic probes against the bromodomain family of proteins.” 2015. Web. 15 Apr 2021.

Vancouver:

Clark PGK. Discovery of epigenetic probes against the bromodomain family of proteins. [Internet] [Doctoral dissertation]. University of Oxford; 2015. [cited 2021 Apr 15]. Available from: http://ora.ox.ac.uk/objects/uuid:a589d1f3-c8f6-4219-a10b-79099eafe1c8 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.712078.

Council of Science Editors:

Clark PGK. Discovery of epigenetic probes against the bromodomain family of proteins. [Doctoral Dissertation]. University of Oxford; 2015. Available from: http://ora.ox.ac.uk/objects/uuid:a589d1f3-c8f6-4219-a10b-79099eafe1c8 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.712078


University of Melbourne

12. JOSLING, GABRIELLE. Identifying important regulators of transcription in Plasmodium falciparum.

Degree: 2014, University of Melbourne

 In the malaria parasite Plasmodium falciparum, many key pathogenic processes are regulated through epigenetic mechanisms. One of the best studied of these mechanisms is the… (more)

Subjects/Keywords: malaria; Plasmodium falciparum; epigenetic; histone modification; gene regulation; bromodomain

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APA (6th Edition):

JOSLING, G. (2014). Identifying important regulators of transcription in Plasmodium falciparum. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/42078

Chicago Manual of Style (16th Edition):

JOSLING, GABRIELLE. “Identifying important regulators of transcription in Plasmodium falciparum.” 2014. Doctoral Dissertation, University of Melbourne. Accessed April 15, 2021. http://hdl.handle.net/11343/42078.

MLA Handbook (7th Edition):

JOSLING, GABRIELLE. “Identifying important regulators of transcription in Plasmodium falciparum.” 2014. Web. 15 Apr 2021.

Vancouver:

JOSLING G. Identifying important regulators of transcription in Plasmodium falciparum. [Internet] [Doctoral dissertation]. University of Melbourne; 2014. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/11343/42078.

Council of Science Editors:

JOSLING G. Identifying important regulators of transcription in Plasmodium falciparum. [Doctoral Dissertation]. University of Melbourne; 2014. Available from: http://hdl.handle.net/11343/42078


University of Southern California

13. Tolani, Bhairavi (Vivi). Molecular strategies towards inhibition of KSHV-associated malignancies.

Degree: PhD, Molecular Biology, 2014, University of Southern California

 Primary Effusion Lymphoma (PEL) is an aggressive form of non-Hodgkin’s B cell lymphoma associated with infection by Kaposi’s sarcoma associated herpesvirus (KSHV). To perpetuate viral… (more)

Subjects/Keywords: Myc; PEL; BET; Bromodomain; KSHV; NEMO; K13; IKK

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APA (6th Edition):

Tolani, B. (. (2014). Molecular strategies towards inhibition of KSHV-associated malignancies. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/128105/rec/4206

Chicago Manual of Style (16th Edition):

Tolani, Bhairavi (Vivi). “Molecular strategies towards inhibition of KSHV-associated malignancies.” 2014. Doctoral Dissertation, University of Southern California. Accessed April 15, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/128105/rec/4206.

MLA Handbook (7th Edition):

Tolani, Bhairavi (Vivi). “Molecular strategies towards inhibition of KSHV-associated malignancies.” 2014. Web. 15 Apr 2021.

Vancouver:

Tolani B(. Molecular strategies towards inhibition of KSHV-associated malignancies. [Internet] [Doctoral dissertation]. University of Southern California; 2014. [cited 2021 Apr 15]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/128105/rec/4206.

Council of Science Editors:

Tolani B(. Molecular strategies towards inhibition of KSHV-associated malignancies. [Doctoral Dissertation]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/128105/rec/4206


University of Texas – Austin

14. Gong, Fade. Role of bromodomain containing proteins in the DNA damage response.

Degree: PhD, Cell and Molecular Biology, 2016, University of Texas – Austin

 Chromatin-based DNA damage response (DDR) mechanisms are fundamental for preventing genome and epigenome instability, which are hallmarks of cancer. How chromatin promotes genome-epigenome integrity in… (more)

Subjects/Keywords: DNA damage response; DNA repair; Chromatin; Acetylation; Bromodomain

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APA (6th Edition):

Gong, F. (2016). Role of bromodomain containing proteins in the DNA damage response. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/68576

Chicago Manual of Style (16th Edition):

Gong, Fade. “Role of bromodomain containing proteins in the DNA damage response.” 2016. Doctoral Dissertation, University of Texas – Austin. Accessed April 15, 2021. http://hdl.handle.net/2152/68576.

MLA Handbook (7th Edition):

Gong, Fade. “Role of bromodomain containing proteins in the DNA damage response.” 2016. Web. 15 Apr 2021.

Vancouver:

Gong F. Role of bromodomain containing proteins in the DNA damage response. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2016. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/2152/68576.

Council of Science Editors:

Gong F. Role of bromodomain containing proteins in the DNA damage response. [Doctoral Dissertation]. University of Texas – Austin; 2016. Available from: http://hdl.handle.net/2152/68576


University of Minnesota

15. Jiang, Jiewei. Part 1: Design and Synthesis of BRDT Selective Inhibitors as Male Contraceptive Agents Part 2: Focused Library Synthesis for TGR5 (Takeda G Protein-Coupled Receptor 5) Antagonist.

Degree: PhD, Medicinal Chemistry, 2020, University of Minnesota

 Unintended pregnancies can have significant adverse socioeconomic effects and health risks for women. One approach to reducing unintended pregnancies is the use of effective contraceptive… (more)

Subjects/Keywords: Bromodomain; Male contraception; Polycystic liver disease; Structure-activity relationship; TGR5

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APA (6th Edition):

Jiang, J. (2020). Part 1: Design and Synthesis of BRDT Selective Inhibitors as Male Contraceptive Agents Part 2: Focused Library Synthesis for TGR5 (Takeda G Protein-Coupled Receptor 5) Antagonist. (Doctoral Dissertation). University of Minnesota. Retrieved from http://hdl.handle.net/11299/218709

Chicago Manual of Style (16th Edition):

Jiang, Jiewei. “Part 1: Design and Synthesis of BRDT Selective Inhibitors as Male Contraceptive Agents Part 2: Focused Library Synthesis for TGR5 (Takeda G Protein-Coupled Receptor 5) Antagonist.” 2020. Doctoral Dissertation, University of Minnesota. Accessed April 15, 2021. http://hdl.handle.net/11299/218709.

MLA Handbook (7th Edition):

Jiang, Jiewei. “Part 1: Design and Synthesis of BRDT Selective Inhibitors as Male Contraceptive Agents Part 2: Focused Library Synthesis for TGR5 (Takeda G Protein-Coupled Receptor 5) Antagonist.” 2020. Web. 15 Apr 2021.

Vancouver:

Jiang J. Part 1: Design and Synthesis of BRDT Selective Inhibitors as Male Contraceptive Agents Part 2: Focused Library Synthesis for TGR5 (Takeda G Protein-Coupled Receptor 5) Antagonist. [Internet] [Doctoral dissertation]. University of Minnesota; 2020. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/11299/218709.

Council of Science Editors:

Jiang J. Part 1: Design and Synthesis of BRDT Selective Inhibitors as Male Contraceptive Agents Part 2: Focused Library Synthesis for TGR5 (Takeda G Protein-Coupled Receptor 5) Antagonist. [Doctoral Dissertation]. University of Minnesota; 2020. Available from: http://hdl.handle.net/11299/218709

16. Silva, Gabriel Dalio Bernardes. Planejamento, síntese e avaliação farmacológica de inibidores de bromodomínio-3 indutores de hemoglobina fetal.

Degree: 2018, Universidade Estadual Paulista (UNESP)

Submitted by Gabriel Dalio Bernardes da Silva ([email protected]) on 2018-06-12T15:44:12Z No. of bitstreams: 1 20180612093911dissertacao_qualificacao_gabriel_dalio_bernardes_da_silva_versaodefesa_v7corrigida.pdf: 5205153 bytes, checksum: 319a6ecb19a6cb45143cf48f67831acd (MD5)

Approved for entry into archive… (more)

Subjects/Keywords: Anemia falciforme; Hemoglobina fetal; Bromodomínio; Sickle cell anemia; Fetal hemoglobin; Bromodomain

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APA (6th Edition):

Silva, G. D. B. (2018). Planejamento, síntese e avaliação farmacológica de inibidores de bromodomínio-3 indutores de hemoglobina fetal. (Masters Thesis). Universidade Estadual Paulista (UNESP). Retrieved from http://hdl.handle.net/11449/154243

Chicago Manual of Style (16th Edition):

Silva, Gabriel Dalio Bernardes. “Planejamento, síntese e avaliação farmacológica de inibidores de bromodomínio-3 indutores de hemoglobina fetal.” 2018. Masters Thesis, Universidade Estadual Paulista (UNESP). Accessed April 15, 2021. http://hdl.handle.net/11449/154243.

MLA Handbook (7th Edition):

Silva, Gabriel Dalio Bernardes. “Planejamento, síntese e avaliação farmacológica de inibidores de bromodomínio-3 indutores de hemoglobina fetal.” 2018. Web. 15 Apr 2021.

Vancouver:

Silva GDB. Planejamento, síntese e avaliação farmacológica de inibidores de bromodomínio-3 indutores de hemoglobina fetal. [Internet] [Masters thesis]. Universidade Estadual Paulista (UNESP); 2018. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/11449/154243.

Council of Science Editors:

Silva GDB. Planejamento, síntese e avaliação farmacológica de inibidores de bromodomínio-3 indutores de hemoglobina fetal. [Masters Thesis]. Universidade Estadual Paulista (UNESP); 2018. Available from: http://hdl.handle.net/11449/154243

17. Abeywickrama Samarakoon, Natali. Small hepatitis Delta antigen mimics a histone H3 epitope to facilitate the remodeling of the Hepatitis D virus (HDV) viral ribonucleoprotein : La petite protéine du virus de l’hépatite Delta (HDV) imite un épitope de l’histone H3 pour faciliter le remodelage de la ribonucléoprotéine virale pour la réplication de l’ARN viral.

Degree: Docteur es, Virologie et biologie cellulaire, 2016, Lyon

 Le virus de l'hépatite Delta (HDV) est un agent infectieux transmissible satellite du virus de l'hépatite B (HBV), induisant des maladies du foie plus sévères… (more)

Subjects/Keywords: Virus de l’hépatite Delta; Remodellage de la chromatine; Imitation d'histone; Protéine à bromodomain; Hepatitis Delta virus; Chromatin remodeling; Histone mimicry; Bromodomain protein; 571.6

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APA (6th Edition):

Abeywickrama Samarakoon, N. (2016). Small hepatitis Delta antigen mimics a histone H3 epitope to facilitate the remodeling of the Hepatitis D virus (HDV) viral ribonucleoprotein : La petite protéine du virus de l’hépatite Delta (HDV) imite un épitope de l’histone H3 pour faciliter le remodelage de la ribonucléoprotéine virale pour la réplication de l’ARN viral. (Doctoral Dissertation). Lyon. Retrieved from http://www.theses.fr/2016LYSE1193

Chicago Manual of Style (16th Edition):

Abeywickrama Samarakoon, Natali. “Small hepatitis Delta antigen mimics a histone H3 epitope to facilitate the remodeling of the Hepatitis D virus (HDV) viral ribonucleoprotein : La petite protéine du virus de l’hépatite Delta (HDV) imite un épitope de l’histone H3 pour faciliter le remodelage de la ribonucléoprotéine virale pour la réplication de l’ARN viral.” 2016. Doctoral Dissertation, Lyon. Accessed April 15, 2021. http://www.theses.fr/2016LYSE1193.

MLA Handbook (7th Edition):

Abeywickrama Samarakoon, Natali. “Small hepatitis Delta antigen mimics a histone H3 epitope to facilitate the remodeling of the Hepatitis D virus (HDV) viral ribonucleoprotein : La petite protéine du virus de l’hépatite Delta (HDV) imite un épitope de l’histone H3 pour faciliter le remodelage de la ribonucléoprotéine virale pour la réplication de l’ARN viral.” 2016. Web. 15 Apr 2021.

Vancouver:

Abeywickrama Samarakoon N. Small hepatitis Delta antigen mimics a histone H3 epitope to facilitate the remodeling of the Hepatitis D virus (HDV) viral ribonucleoprotein : La petite protéine du virus de l’hépatite Delta (HDV) imite un épitope de l’histone H3 pour faciliter le remodelage de la ribonucléoprotéine virale pour la réplication de l’ARN viral. [Internet] [Doctoral dissertation]. Lyon; 2016. [cited 2021 Apr 15]. Available from: http://www.theses.fr/2016LYSE1193.

Council of Science Editors:

Abeywickrama Samarakoon N. Small hepatitis Delta antigen mimics a histone H3 epitope to facilitate the remodeling of the Hepatitis D virus (HDV) viral ribonucleoprotein : La petite protéine du virus de l’hépatite Delta (HDV) imite un épitope de l’histone H3 pour faciliter le remodelage de la ribonucléoprotéine virale pour la réplication de l’ARN viral. [Doctoral Dissertation]. Lyon; 2016. Available from: http://www.theses.fr/2016LYSE1193


Penn State University

18. Chandy, Mark. HISTONE MODIFICATIONS INFLUENCE CHROMATIN MODIFYING AND CHROMATIN REMODELING COMPLEXES .

Degree: 2008, Penn State University

 Chromatin condenses DNA and packages it into the nucleus. The fundamental unit of chromatin is the nucleosome, which compacts and forms higher order structures. Chromatin… (more)

Subjects/Keywords: SAGA; SWI/SNF; chromatin remodeling; bromodomain

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

APA (6th Edition):

Chandy, M. (2008). HISTONE MODIFICATIONS INFLUENCE CHROMATIN MODIFYING AND CHROMATIN REMODELING COMPLEXES . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/6926

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):

Chandy, Mark. “HISTONE MODIFICATIONS INFLUENCE CHROMATIN MODIFYING AND CHROMATIN REMODELING COMPLEXES .” 2008. Thesis, Penn State University. Accessed April 15, 2021. https://submit-etda.libraries.psu.edu/catalog/6926.

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

MLA Handbook (7th Edition):

Chandy, Mark. “HISTONE MODIFICATIONS INFLUENCE CHROMATIN MODIFYING AND CHROMATIN REMODELING COMPLEXES .” 2008. Web. 15 Apr 2021.

Vancouver:

Chandy M. HISTONE MODIFICATIONS INFLUENCE CHROMATIN MODIFYING AND CHROMATIN REMODELING COMPLEXES . [Internet] [Thesis]. Penn State University; 2008. [cited 2021 Apr 15]. Available from: https://submit-etda.libraries.psu.edu/catalog/6926.

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

Council of Science Editors:

Chandy M. HISTONE MODIFICATIONS INFLUENCE CHROMATIN MODIFYING AND CHROMATIN REMODELING COMPLEXES . [Thesis]. Penn State University; 2008. Available from: https://submit-etda.libraries.psu.edu/catalog/6926

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


University of Newcastle

19. Nguyen, Thi Hiep. Modeling of respiratory syncytial virus-induced exacerbation of allergic airways disease.

Degree: PhD, 2017, University of Newcastle

Research Doctorate - Doctor of Philosophy (PhD)

Asthma is a chronic inflammatory disorder of the airways characterised by clinical symptoms such as wheeze, shortness of… (more)

Subjects/Keywords: asthma exacerbation; respiratory syncytial virus; steroid resistance; bromodomain and extra terminal protein

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APA (6th Edition):

Nguyen, T. H. (2017). Modeling of respiratory syncytial virus-induced exacerbation of allergic airways disease. (Doctoral Dissertation). University of Newcastle. Retrieved from http://hdl.handle.net/1959.13/1337694

Chicago Manual of Style (16th Edition):

Nguyen, Thi Hiep. “Modeling of respiratory syncytial virus-induced exacerbation of allergic airways disease.” 2017. Doctoral Dissertation, University of Newcastle. Accessed April 15, 2021. http://hdl.handle.net/1959.13/1337694.

MLA Handbook (7th Edition):

Nguyen, Thi Hiep. “Modeling of respiratory syncytial virus-induced exacerbation of allergic airways disease.” 2017. Web. 15 Apr 2021.

Vancouver:

Nguyen TH. Modeling of respiratory syncytial virus-induced exacerbation of allergic airways disease. [Internet] [Doctoral dissertation]. University of Newcastle; 2017. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1959.13/1337694.

Council of Science Editors:

Nguyen TH. Modeling of respiratory syncytial virus-induced exacerbation of allergic airways disease. [Doctoral Dissertation]. University of Newcastle; 2017. Available from: http://hdl.handle.net/1959.13/1337694


Texas Medical Center

20. Villar-Prados, Alejandro. IDENTIFYING MOLECULAR TARGETS AND VALIDATING NOVEL THERAPIES FOR OVARIAN CANCER.

Degree: PhD, 2018, Texas Medical Center

  Re-purposing of targeted therapies for additional tumor types is a promising avenue for expanding treatment options for cancer patients, however accurately predicting what re-purposed… (more)

Subjects/Keywords: ovarian cancer; targeted therapies; BRD4; Notch3; Bromodomain and extraterminal domain inhibitors; Medicine and Health Sciences

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APA (6th Edition):

Villar-Prados, A. (2018). IDENTIFYING MOLECULAR TARGETS AND VALIDATING NOVEL THERAPIES FOR OVARIAN CANCER. (Doctoral Dissertation). Texas Medical Center. Retrieved from https://digitalcommons.library.tmc.edu/utgsbs_dissertations/840

Chicago Manual of Style (16th Edition):

Villar-Prados, Alejandro. “IDENTIFYING MOLECULAR TARGETS AND VALIDATING NOVEL THERAPIES FOR OVARIAN CANCER.” 2018. Doctoral Dissertation, Texas Medical Center. Accessed April 15, 2021. https://digitalcommons.library.tmc.edu/utgsbs_dissertations/840.

MLA Handbook (7th Edition):

Villar-Prados, Alejandro. “IDENTIFYING MOLECULAR TARGETS AND VALIDATING NOVEL THERAPIES FOR OVARIAN CANCER.” 2018. Web. 15 Apr 2021.

Vancouver:

Villar-Prados A. IDENTIFYING MOLECULAR TARGETS AND VALIDATING NOVEL THERAPIES FOR OVARIAN CANCER. [Internet] [Doctoral dissertation]. Texas Medical Center; 2018. [cited 2021 Apr 15]. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/840.

Council of Science Editors:

Villar-Prados A. IDENTIFYING MOLECULAR TARGETS AND VALIDATING NOVEL THERAPIES FOR OVARIAN CANCER. [Doctoral Dissertation]. Texas Medical Center; 2018. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/840


Universitat Pompeu Fabra

21. Abner, Erik, 1986-. Identification of HIV-1 reactivating quinoline compounds as bromodomain inhibitors.

Degree: Departament de Ciències Experimentals i de la Salut, 2016, Universitat Pompeu Fabra

 Upon HIV-1 infection, a reservoir of HIV latently infected resting T cells prevents the eradication of the virus from patients. To achieve eradication, the existing… (more)

Subjects/Keywords: Keywords: HIV; Transcription; Latency; Quinoline; Bromodomain; Palabras clave: VIH; Bromodominio; Latencia; Quinolin; Transcripción; 578

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APA (6th Edition):

Abner, Erik, 1. (2016). Identification of HIV-1 reactivating quinoline compounds as bromodomain inhibitors. (Thesis). Universitat Pompeu Fabra. Retrieved from http://hdl.handle.net/10803/565528

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):

Abner, Erik, 1986-. “Identification of HIV-1 reactivating quinoline compounds as bromodomain inhibitors.” 2016. Thesis, Universitat Pompeu Fabra. Accessed April 15, 2021. http://hdl.handle.net/10803/565528.

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

MLA Handbook (7th Edition):

Abner, Erik, 1986-. “Identification of HIV-1 reactivating quinoline compounds as bromodomain inhibitors.” 2016. Web. 15 Apr 2021.

Vancouver:

Abner, Erik 1. Identification of HIV-1 reactivating quinoline compounds as bromodomain inhibitors. [Internet] [Thesis]. Universitat Pompeu Fabra; 2016. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/10803/565528.

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

Council of Science Editors:

Abner, Erik 1. Identification of HIV-1 reactivating quinoline compounds as bromodomain inhibitors. [Thesis]. Universitat Pompeu Fabra; 2016. Available from: http://hdl.handle.net/10803/565528

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


Université Paris-Sud – Paris XI

22. Penglong, Tipparat. Molecular Basis of Erythroid Cell Proliferation and Differentiation : Les bases moléculaires de la prolifération et de la différentiation érythroide.

Degree: Docteur es, Ascpects moléculaires et cellulaires de la biologie, 2015, Université Paris-Sud – Paris XI

 Pour assurer la production de milliards de globules rouges, l’érythropoièse doit parfaitement contrôler les processus de prolifération et de différenciation. Ces deux processus sont régulés… (more)

Subjects/Keywords: Erythropoïèse; GATA-1; PRB; C-MYC; Bromodomaine; Erythropoiesis; GATA-1; PRB; C-MYC; Bromodomain

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APA (6th Edition):

Penglong, T. (2015). Molecular Basis of Erythroid Cell Proliferation and Differentiation : Les bases moléculaires de la prolifération et de la différentiation érythroide. (Doctoral Dissertation). Université Paris-Sud – Paris XI. Retrieved from http://www.theses.fr/2015PA11T022

Chicago Manual of Style (16th Edition):

Penglong, Tipparat. “Molecular Basis of Erythroid Cell Proliferation and Differentiation : Les bases moléculaires de la prolifération et de la différentiation érythroide.” 2015. Doctoral Dissertation, Université Paris-Sud – Paris XI. Accessed April 15, 2021. http://www.theses.fr/2015PA11T022.

MLA Handbook (7th Edition):

Penglong, Tipparat. “Molecular Basis of Erythroid Cell Proliferation and Differentiation : Les bases moléculaires de la prolifération et de la différentiation érythroide.” 2015. Web. 15 Apr 2021.

Vancouver:

Penglong T. Molecular Basis of Erythroid Cell Proliferation and Differentiation : Les bases moléculaires de la prolifération et de la différentiation érythroide. [Internet] [Doctoral dissertation]. Université Paris-Sud – Paris XI; 2015. [cited 2021 Apr 15]. Available from: http://www.theses.fr/2015PA11T022.

Council of Science Editors:

Penglong T. Molecular Basis of Erythroid Cell Proliferation and Differentiation : Les bases moléculaires de la prolifération et de la différentiation érythroide. [Doctoral Dissertation]. Université Paris-Sud – Paris XI; 2015. Available from: http://www.theses.fr/2015PA11T022


University of California – San Francisco

23. Bagley, Joshua Adam. The Molecular Regulation of Dendritic Arbor Shape During Development and Disease.

Degree: Neuroscience, 2015, University of California – San Francisco

 The brain is composed of a network of neural cells which have elaborate cellular structures, especially their dendritic arbors. The correct function of neural networks… (more)

Subjects/Keywords: Neurosciences; Cellular biology; Genetics; aging; BET protein; bromodomain; dendrite morphology; epigenetics; polyQ

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APA (6th Edition):

Bagley, J. A. (2015). The Molecular Regulation of Dendritic Arbor Shape During Development and Disease. (Thesis). University of California – San Francisco. Retrieved from http://www.escholarship.org/uc/item/5w4182d0

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):

Bagley, Joshua Adam. “The Molecular Regulation of Dendritic Arbor Shape During Development and Disease.” 2015. Thesis, University of California – San Francisco. Accessed April 15, 2021. http://www.escholarship.org/uc/item/5w4182d0.

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

MLA Handbook (7th Edition):

Bagley, Joshua Adam. “The Molecular Regulation of Dendritic Arbor Shape During Development and Disease.” 2015. Web. 15 Apr 2021.

Vancouver:

Bagley JA. The Molecular Regulation of Dendritic Arbor Shape During Development and Disease. [Internet] [Thesis]. University of California – San Francisco; 2015. [cited 2021 Apr 15]. Available from: http://www.escholarship.org/uc/item/5w4182d0.

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

Council of Science Editors:

Bagley JA. The Molecular Regulation of Dendritic Arbor Shape During Development and Disease. [Thesis]. University of California – San Francisco; 2015. Available from: http://www.escholarship.org/uc/item/5w4182d0

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


Université de Grenoble

24. Gaucher, Jonathan. Rôle de la protéine à double bromodomaine BRDT dans le remodelage de la chromatine au cours de la spermatogenèse : Chromatin reorganization during spermatogenesis : double bromodomain protein BRDT multiple task.

Degree: Docteur es, Biologie du développement oncogenèse, 2011, Université de Grenoble

BRDT et la réorganisation de la chromatine au cours de la spermatogénèsePendant la spermiogenèse, phase haploïde de la gamétogenèse mâle, le génome mâle subit une… (more)

Subjects/Keywords: Brdt; Bromodomaine; Chromatine; Acétylation; Méiose; Spermiogénèse; Spermiogenesis; Meiosis; Acetylation; Brdt; Chromatin; Bromodomain; 570

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APA (6th Edition):

Gaucher, J. (2011). Rôle de la protéine à double bromodomaine BRDT dans le remodelage de la chromatine au cours de la spermatogenèse : Chromatin reorganization during spermatogenesis : double bromodomain protein BRDT multiple task. (Doctoral Dissertation). Université de Grenoble. Retrieved from http://www.theses.fr/2011GRENV088

Chicago Manual of Style (16th Edition):

Gaucher, Jonathan. “Rôle de la protéine à double bromodomaine BRDT dans le remodelage de la chromatine au cours de la spermatogenèse : Chromatin reorganization during spermatogenesis : double bromodomain protein BRDT multiple task.” 2011. Doctoral Dissertation, Université de Grenoble. Accessed April 15, 2021. http://www.theses.fr/2011GRENV088.

MLA Handbook (7th Edition):

Gaucher, Jonathan. “Rôle de la protéine à double bromodomaine BRDT dans le remodelage de la chromatine au cours de la spermatogenèse : Chromatin reorganization during spermatogenesis : double bromodomain protein BRDT multiple task.” 2011. Web. 15 Apr 2021.

Vancouver:

Gaucher J. Rôle de la protéine à double bromodomaine BRDT dans le remodelage de la chromatine au cours de la spermatogenèse : Chromatin reorganization during spermatogenesis : double bromodomain protein BRDT multiple task. [Internet] [Doctoral dissertation]. Université de Grenoble; 2011. [cited 2021 Apr 15]. Available from: http://www.theses.fr/2011GRENV088.

Council of Science Editors:

Gaucher J. Rôle de la protéine à double bromodomaine BRDT dans le remodelage de la chromatine au cours de la spermatogenèse : Chromatin reorganization during spermatogenesis : double bromodomain protein BRDT multiple task. [Doctoral Dissertation]. Université de Grenoble; 2011. Available from: http://www.theses.fr/2011GRENV088


University of Edinburgh

25. Bruton, Peter Christopher. Epigenetic regulation of heterochromatin structure and tumour progression.

Degree: PhD, 2018, University of Edinburgh

 Since the discovery of DNA packaging into chromatin, and McClintock's (1951) work on position-effect variegation providing evidence of non-mendelian inheritance, the principal of a genome… (more)

Subjects/Keywords: 572.8; brd4; bromodomain; EMT; epithelial mesenchymal transition; drug resistance; H3K9me3; H3K9 methylation; jq1

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APA (6th Edition):

Bruton, P. C. (2018). Epigenetic regulation of heterochromatin structure and tumour progression. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/33232

Chicago Manual of Style (16th Edition):

Bruton, Peter Christopher. “Epigenetic regulation of heterochromatin structure and tumour progression.” 2018. Doctoral Dissertation, University of Edinburgh. Accessed April 15, 2021. http://hdl.handle.net/1842/33232.

MLA Handbook (7th Edition):

Bruton, Peter Christopher. “Epigenetic regulation of heterochromatin structure and tumour progression.” 2018. Web. 15 Apr 2021.

Vancouver:

Bruton PC. Epigenetic regulation of heterochromatin structure and tumour progression. [Internet] [Doctoral dissertation]. University of Edinburgh; 2018. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1842/33232.

Council of Science Editors:

Bruton PC. Epigenetic regulation of heterochromatin structure and tumour progression. [Doctoral Dissertation]. University of Edinburgh; 2018. Available from: http://hdl.handle.net/1842/33232

26. Wei, Kaiyao. Développement d'une nouvelle stratégie antifongique ciblant un domaine de lecture épigénétique : Developing a novel antifungal strategy by targeting an epigenetic reader domain.

Degree: Docteur es, Virologie microbiologie immunologie, 2020, Université Grenoble Alpes

Candida glabrata est une levure pathogène associée à une mortalité élevée chez les patients immunodéprimés. Une croissance importante des souches résistantes aux médicaments antifongiques au… (more)

Subjects/Keywords: Infectiologie; Antifongique; Candida glabrata; Bdf1; Bromodomaine; Infectiology; Antifungal; Candida glabrata; Bdf1; Bromodomain; 570

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APA (6th Edition):

Wei, K. (2020). Développement d'une nouvelle stratégie antifongique ciblant un domaine de lecture épigénétique : Developing a novel antifungal strategy by targeting an epigenetic reader domain. (Doctoral Dissertation). Université Grenoble Alpes. Retrieved from http://www.theses.fr/2020GRALV013

Chicago Manual of Style (16th Edition):

Wei, Kaiyao. “Développement d'une nouvelle stratégie antifongique ciblant un domaine de lecture épigénétique : Developing a novel antifungal strategy by targeting an epigenetic reader domain.” 2020. Doctoral Dissertation, Université Grenoble Alpes. Accessed April 15, 2021. http://www.theses.fr/2020GRALV013.

MLA Handbook (7th Edition):

Wei, Kaiyao. “Développement d'une nouvelle stratégie antifongique ciblant un domaine de lecture épigénétique : Developing a novel antifungal strategy by targeting an epigenetic reader domain.” 2020. Web. 15 Apr 2021.

Vancouver:

Wei K. Développement d'une nouvelle stratégie antifongique ciblant un domaine de lecture épigénétique : Developing a novel antifungal strategy by targeting an epigenetic reader domain. [Internet] [Doctoral dissertation]. Université Grenoble Alpes; 2020. [cited 2021 Apr 15]. Available from: http://www.theses.fr/2020GRALV013.

Council of Science Editors:

Wei K. Développement d'une nouvelle stratégie antifongique ciblant un domaine de lecture épigénétique : Developing a novel antifungal strategy by targeting an epigenetic reader domain. [Doctoral Dissertation]. Université Grenoble Alpes; 2020. Available from: http://www.theses.fr/2020GRALV013


Texas A&M University

27. Carvin, Christopher Dumas. Transcriptional regulation and chromatin remodeling mechanisms at PHO5.

Degree: PhD, Biochemistry, 2005, Texas A&M University

 Regulation of gene expression is vital for proper growth and prevention of disease states. In eukaryotes this regulation occurs in the context of chromatin which… (more)

Subjects/Keywords: chromatin; Set1; bromodomain; PHO5; targeted DNA methylation

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APA (6th Edition):

Carvin, C. D. (2005). Transcriptional regulation and chromatin remodeling mechanisms at PHO5. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/2193

Chicago Manual of Style (16th Edition):

Carvin, Christopher Dumas. “Transcriptional regulation and chromatin remodeling mechanisms at PHO5.” 2005. Doctoral Dissertation, Texas A&M University. Accessed April 15, 2021. http://hdl.handle.net/1969.1/2193.

MLA Handbook (7th Edition):

Carvin, Christopher Dumas. “Transcriptional regulation and chromatin remodeling mechanisms at PHO5.” 2005. Web. 15 Apr 2021.

Vancouver:

Carvin CD. Transcriptional regulation and chromatin remodeling mechanisms at PHO5. [Internet] [Doctoral dissertation]. Texas A&M University; 2005. [cited 2021 Apr 15]. Available from: http://hdl.handle.net/1969.1/2193.

Council of Science Editors:

Carvin CD. Transcriptional regulation and chromatin remodeling mechanisms at PHO5. [Doctoral Dissertation]. Texas A&M University; 2005. Available from: http://hdl.handle.net/1969.1/2193


Penn State University

28. Sermwittayawong, Decha. MECHANISMS OF THE SAGA COACTIVATOR COMPLEX IN REGULATION OF GENE TRANSCRIPTION .

Degree: 2008, Penn State University

 The SAGA coactivator complex functions in response to an activator protein to activate gene transcription. This thesis describes my investigations into two major functions of… (more)

Subjects/Keywords: Gcn5; competition; Spt3; TBP; Spt8; SAGA; bromodomain

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APA (6th Edition):

Sermwittayawong, D. (2008). MECHANISMS OF THE SAGA COACTIVATOR COMPLEX IN REGULATION OF GENE TRANSCRIPTION . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/7141

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):

Sermwittayawong, Decha. “MECHANISMS OF THE SAGA COACTIVATOR COMPLEX IN REGULATION OF GENE TRANSCRIPTION .” 2008. Thesis, Penn State University. Accessed April 15, 2021. https://submit-etda.libraries.psu.edu/catalog/7141.

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

MLA Handbook (7th Edition):

Sermwittayawong, Decha. “MECHANISMS OF THE SAGA COACTIVATOR COMPLEX IN REGULATION OF GENE TRANSCRIPTION .” 2008. Web. 15 Apr 2021.

Vancouver:

Sermwittayawong D. MECHANISMS OF THE SAGA COACTIVATOR COMPLEX IN REGULATION OF GENE TRANSCRIPTION . [Internet] [Thesis]. Penn State University; 2008. [cited 2021 Apr 15]. Available from: https://submit-etda.libraries.psu.edu/catalog/7141.

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

Council of Science Editors:

Sermwittayawong D. MECHANISMS OF THE SAGA COACTIVATOR COMPLEX IN REGULATION OF GENE TRANSCRIPTION . [Thesis]. Penn State University; 2008. Available from: https://submit-etda.libraries.psu.edu/catalog/7141

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


University of Oxford

29. Hewings, David Stephen. Developing inhibitors of bromodomain-histone interactions.

Degree: PhD, 2014, University of Oxford

 Lysine acetylation is a widespread protein post-translational modification that influences diverse cellular processes. An association between acetylation of histone N-terminal tails and transcriptional activation has… (more)

Subjects/Keywords: 547; Physical Sciences; Chemistry & allied sciences; Chemical biology; Organic chemistry; Organic synthesis; bromodomain; acetyl-lysine; post-translational modification; isoxazole; histone; cancer

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

APA (6th Edition):

Hewings, D. S. (2014). Developing inhibitors of bromodomain-histone interactions. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:7ee6647c-4ac7-41ba-9f15-dfd49de9f6c2 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.604505

Chicago Manual of Style (16th Edition):

Hewings, David Stephen. “Developing inhibitors of bromodomain-histone interactions.” 2014. Doctoral Dissertation, University of Oxford. Accessed April 15, 2021. http://ora.ox.ac.uk/objects/uuid:7ee6647c-4ac7-41ba-9f15-dfd49de9f6c2 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.604505.

MLA Handbook (7th Edition):

Hewings, David Stephen. “Developing inhibitors of bromodomain-histone interactions.” 2014. Web. 15 Apr 2021.

Vancouver:

Hewings DS. Developing inhibitors of bromodomain-histone interactions. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2021 Apr 15]. Available from: http://ora.ox.ac.uk/objects/uuid:7ee6647c-4ac7-41ba-9f15-dfd49de9f6c2 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.604505.

Council of Science Editors:

Hewings DS. Developing inhibitors of bromodomain-histone interactions. [Doctoral Dissertation]. University of Oxford; 2014. Available from: http://ora.ox.ac.uk/objects/uuid:7ee6647c-4ac7-41ba-9f15-dfd49de9f6c2 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.604505


University of Oxford

30. Rooney, Timothy Patrick Christopher. Development of small molecule inhibitors of the bromodomain-histone interaction.

Degree: PhD, 2014, University of Oxford

 Bromodomains bind to acetylated lysine residues 1 to mediate a wide range of biological processes, including the assembly of transcriptional machinery at modified histones. This… (more)

Subjects/Keywords: 547; Physical Sciences; Chemistry & allied sciences; Organic chemistry; Chemical biology; Synthetic organic chemistry; Bromodomain; Epigenetics; Ligand Discovery

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

APA (6th Edition):

Rooney, T. P. C. (2014). Development of small molecule inhibitors of the bromodomain-histone interaction. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:dfe22076-befc-4881-8433-b563a9329478 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.666992

Chicago Manual of Style (16th Edition):

Rooney, Timothy Patrick Christopher. “Development of small molecule inhibitors of the bromodomain-histone interaction.” 2014. Doctoral Dissertation, University of Oxford. Accessed April 15, 2021. http://ora.ox.ac.uk/objects/uuid:dfe22076-befc-4881-8433-b563a9329478 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.666992.

MLA Handbook (7th Edition):

Rooney, Timothy Patrick Christopher. “Development of small molecule inhibitors of the bromodomain-histone interaction.” 2014. Web. 15 Apr 2021.

Vancouver:

Rooney TPC. Development of small molecule inhibitors of the bromodomain-histone interaction. [Internet] [Doctoral dissertation]. University of Oxford; 2014. [cited 2021 Apr 15]. Available from: http://ora.ox.ac.uk/objects/uuid:dfe22076-befc-4881-8433-b563a9329478 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.666992.

Council of Science Editors:

Rooney TPC. Development of small molecule inhibitors of the bromodomain-histone interaction. [Doctoral Dissertation]. University of Oxford; 2014. Available from: http://ora.ox.ac.uk/objects/uuid:dfe22076-befc-4881-8433-b563a9329478 ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.666992

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