Advanced search options

Advanced Search Options 🞨

Browse by author name (“Author name starts with…”).

Find ETDs with:

in
/  
in
/  
in
/  
in

Written in Published in Earliest date Latest date

Sorted by

Results per page:

Sorted by: relevance · author · university · dateNew search

You searched for subject:(HDAC). Showing records 1 – 30 of 187 total matches.

[1] [2] [3] [4] [5] [6] [7]

Search Limiters

Last 2 Years | English Only

Degrees

Levels

Languages

Country

▼ Search Limiters

1. Damaskos, Christos. Δράση των αναστολέων της αστυλίωσης ιστονών στον καρκίνο του παγκρέατος.

Degree: 2015, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ)

Introduction: Acetylation and deacetylation of histones are important mechanisms of epigenetic transcriptional regulation, which are regulated by histone acetyltransferases (HAT) and histone deacetylases (HDAC), respectively.… (more)

Subjects/Keywords: HDAC; HDAC

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Damaskos, C. (2015). Δράση των αναστολέων της αστυλίωσης ιστονών στον καρκίνο του παγκρέατος. (Thesis). National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Retrieved from http://hdl.handle.net/10442/hedi/35992

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):

Damaskos, Christos. “Δράση των αναστολέων της αστυλίωσης ιστονών στον καρκίνο του παγκρέατος.” 2015. Thesis, National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ). Accessed January 16, 2021. http://hdl.handle.net/10442/hedi/35992.

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

MLA Handbook (7th Edition):

Damaskos, Christos. “Δράση των αναστολέων της αστυλίωσης ιστονών στον καρκίνο του παγκρέατος.” 2015. Web. 16 Jan 2021.

Vancouver:

Damaskos C. Δράση των αναστολέων της αστυλίωσης ιστονών στον καρκίνο του παγκρέατος. [Internet] [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2015. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/10442/hedi/35992.

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

Council of Science Editors:

Damaskos C. Δράση των αναστολέων της αστυλίωσης ιστονών στον καρκίνο του παγκρέατος. [Thesis]. National and Kapodistrian University of Athens; Εθνικό και Καποδιστριακό Πανεπιστήμιο Αθηνών (ΕΚΠΑ); 2015. Available from: http://hdl.handle.net/10442/hedi/35992

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


University of Debrecen

2. Farahnoosh, Hanna. Pharmacology of histone deacetylase inhibitors .

Degree: DE – Általános Orvostudományi Kar, University of Debrecen

 Currently three HDAC inhibitors have been approved by the FDA where the use of vorinostat and romidepsin against refractory cutaneous and peripheral T cell lymphoma… (more)

Subjects/Keywords: HDAC

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Farahnoosh, H. (n.d.). Pharmacology of histone deacetylase inhibitors . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/242876

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

Chicago Manual of Style (16th Edition):

Farahnoosh, Hanna. “Pharmacology of histone deacetylase inhibitors .” Thesis, University of Debrecen. Accessed January 16, 2021. http://hdl.handle.net/2437/242876.

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

MLA Handbook (7th Edition):

Farahnoosh, Hanna. “Pharmacology of histone deacetylase inhibitors .” Web. 16 Jan 2021.

Note: this citation may be lacking information needed for this citation format:
No year of publication.

Vancouver:

Farahnoosh H. Pharmacology of histone deacetylase inhibitors . [Internet] [Thesis]. University of Debrecen; [cited 2021 Jan 16]. Available from: http://hdl.handle.net/2437/242876.

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

Council of Science Editors:

Farahnoosh H. Pharmacology of histone deacetylase inhibitors . [Thesis]. University of Debrecen; Available from: http://hdl.handle.net/2437/242876

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


University of Minnesota

3. Lelich, Rosemary. Analyzing Loss of HDAC4 Expression: Effect on Osteoclastogenesis.

Degree: MS, Dentistry, 2016, University of Minnesota

 Histone deacetylases (HDACs) are intracellular enzymes that directly affect chromatin structure and transcription factor activity. HDACs have become an important focus in research due to… (more)

Subjects/Keywords: HDAC; Osteoclastogenesis

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lelich, R. (2016). Analyzing Loss of HDAC4 Expression: Effect on Osteoclastogenesis. (Masters Thesis). University of Minnesota. Retrieved from http://hdl.handle.net/11299/183294

Chicago Manual of Style (16th Edition):

Lelich, Rosemary. “Analyzing Loss of HDAC4 Expression: Effect on Osteoclastogenesis.” 2016. Masters Thesis, University of Minnesota. Accessed January 16, 2021. http://hdl.handle.net/11299/183294.

MLA Handbook (7th Edition):

Lelich, Rosemary. “Analyzing Loss of HDAC4 Expression: Effect on Osteoclastogenesis.” 2016. Web. 16 Jan 2021.

Vancouver:

Lelich R. Analyzing Loss of HDAC4 Expression: Effect on Osteoclastogenesis. [Internet] [Masters thesis]. University of Minnesota; 2016. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/11299/183294.

Council of Science Editors:

Lelich R. Analyzing Loss of HDAC4 Expression: Effect on Osteoclastogenesis. [Masters Thesis]. University of Minnesota; 2016. Available from: http://hdl.handle.net/11299/183294


Harvard University

4. Kuzmickas, Ryan. Therapeutic Targeting of Chromatin Modifiers in Advanced Prostate Cancer.

Degree: PhD, 2019, Harvard University

Prostate cancer is the second-most common cancer in North American men. Although early intervention can successfully treat prostate cancer, there are limited option for advanced… (more)

Subjects/Keywords: EZH2; ATF3; HDAC

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Kuzmickas, R. (2019). Therapeutic Targeting of Chromatin Modifiers in Advanced Prostate Cancer. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:42029548

Chicago Manual of Style (16th Edition):

Kuzmickas, Ryan. “Therapeutic Targeting of Chromatin Modifiers in Advanced Prostate Cancer.” 2019. Doctoral Dissertation, Harvard University. Accessed January 16, 2021. http://nrs.harvard.edu/urn-3:HUL.InstRepos:42029548.

MLA Handbook (7th Edition):

Kuzmickas, Ryan. “Therapeutic Targeting of Chromatin Modifiers in Advanced Prostate Cancer.” 2019. Web. 16 Jan 2021.

Vancouver:

Kuzmickas R. Therapeutic Targeting of Chromatin Modifiers in Advanced Prostate Cancer. [Internet] [Doctoral dissertation]. Harvard University; 2019. [cited 2021 Jan 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42029548.

Council of Science Editors:

Kuzmickas R. Therapeutic Targeting of Chromatin Modifiers in Advanced Prostate Cancer. [Doctoral Dissertation]. Harvard University; 2019. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42029548


Harvard University

5. Strebl, Martin Georg. Impacting Neuroscience With Chemistry: HDAC Neuroimaging Enabled by [18F]-Fluorination Methodology.

Degree: PhD, 2017, Harvard University

In this dissertation, innovative radiochemical methodology was leveraged to systematically advance radiotracer development. A novel organometallic radiofluorination was established, as well as two fluorinated radiotracers,… (more)

Subjects/Keywords: HDAC; Fluorine; PET; Neuroimaging

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Strebl, M. G. (2017). Impacting Neuroscience With Chemistry: HDAC Neuroimaging Enabled by [18F]-Fluorination Methodology. (Doctoral Dissertation). Harvard University. Retrieved from http://nrs.harvard.edu/urn-3:HUL.InstRepos:42061502

Chicago Manual of Style (16th Edition):

Strebl, Martin Georg. “Impacting Neuroscience With Chemistry: HDAC Neuroimaging Enabled by [18F]-Fluorination Methodology.” 2017. Doctoral Dissertation, Harvard University. Accessed January 16, 2021. http://nrs.harvard.edu/urn-3:HUL.InstRepos:42061502.

MLA Handbook (7th Edition):

Strebl, Martin Georg. “Impacting Neuroscience With Chemistry: HDAC Neuroimaging Enabled by [18F]-Fluorination Methodology.” 2017. Web. 16 Jan 2021.

Vancouver:

Strebl MG. Impacting Neuroscience With Chemistry: HDAC Neuroimaging Enabled by [18F]-Fluorination Methodology. [Internet] [Doctoral dissertation]. Harvard University; 2017. [cited 2021 Jan 16]. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42061502.

Council of Science Editors:

Strebl MG. Impacting Neuroscience With Chemistry: HDAC Neuroimaging Enabled by [18F]-Fluorination Methodology. [Doctoral Dissertation]. Harvard University; 2017. Available from: http://nrs.harvard.edu/urn-3:HUL.InstRepos:42061502


Oregon State University

6. Nian, Hui. Dietary organosulfur and organoselenium compounds as HDAC inhibitors.

Degree: PhD, Biochemistry and Biophysics, 2010, Oregon State University

 Histone deacetylase (HDAC) inhibitors have the potential to de-repress epigenetically silenced genes in cancer cells, leading to cell cycle arrest and apoptosis. Dietary HDAC inhibitors… (more)

Subjects/Keywords: HDAC; Histone deacetylase  – Inhibitors

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Nian, H. (2010). Dietary organosulfur and organoselenium compounds as HDAC inhibitors. (Doctoral Dissertation). Oregon State University. Retrieved from http://hdl.handle.net/1957/15093

Chicago Manual of Style (16th Edition):

Nian, Hui. “Dietary organosulfur and organoselenium compounds as HDAC inhibitors.” 2010. Doctoral Dissertation, Oregon State University. Accessed January 16, 2021. http://hdl.handle.net/1957/15093.

MLA Handbook (7th Edition):

Nian, Hui. “Dietary organosulfur and organoselenium compounds as HDAC inhibitors.” 2010. Web. 16 Jan 2021.

Vancouver:

Nian H. Dietary organosulfur and organoselenium compounds as HDAC inhibitors. [Internet] [Doctoral dissertation]. Oregon State University; 2010. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1957/15093.

Council of Science Editors:

Nian H. Dietary organosulfur and organoselenium compounds as HDAC inhibitors. [Doctoral Dissertation]. Oregon State University; 2010. Available from: http://hdl.handle.net/1957/15093

7. Linares, Aurélien. Histone désacétylases, signalisation œstrogénique et cancer du sein : établissement d’outils bioluminescents pour la détection d’inhibiteurs sélectifs de HDAC : expression et rôle de HDAC9 dans les lignées cellulaires de cancer du sein : Histone deacetylases, estrogen signaling and breast cancer : bioluminescent cell lines as screening tools for selective HDAC inhibitors : expression and role of HDAC9 in breast cancer cell lines.

Degree: Docteur es, Biologie Santé, 2011, Université Montpellier I

Le récepteur des oestrogènes (RE) peut moduler l’expression de gènes impliqués dans les processus de prolifération et d’apoptose cellulaires. Cette régulation est possible par le… (more)

Subjects/Keywords: Hdac; Cancer du sein; Récepteurs des oestrogènes; Inhibiteurs de HDAC; Hdac; Breast cancer; Estrogen receptor; HDAC inhibitor

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Linares, A. (2011). Histone désacétylases, signalisation œstrogénique et cancer du sein : établissement d’outils bioluminescents pour la détection d’inhibiteurs sélectifs de HDAC : expression et rôle de HDAC9 dans les lignées cellulaires de cancer du sein : Histone deacetylases, estrogen signaling and breast cancer : bioluminescent cell lines as screening tools for selective HDAC inhibitors : expression and role of HDAC9 in breast cancer cell lines. (Doctoral Dissertation). Université Montpellier I. Retrieved from http://www.theses.fr/2011MON13504

Chicago Manual of Style (16th Edition):

Linares, Aurélien. “Histone désacétylases, signalisation œstrogénique et cancer du sein : établissement d’outils bioluminescents pour la détection d’inhibiteurs sélectifs de HDAC : expression et rôle de HDAC9 dans les lignées cellulaires de cancer du sein : Histone deacetylases, estrogen signaling and breast cancer : bioluminescent cell lines as screening tools for selective HDAC inhibitors : expression and role of HDAC9 in breast cancer cell lines.” 2011. Doctoral Dissertation, Université Montpellier I. Accessed January 16, 2021. http://www.theses.fr/2011MON13504.

MLA Handbook (7th Edition):

Linares, Aurélien. “Histone désacétylases, signalisation œstrogénique et cancer du sein : établissement d’outils bioluminescents pour la détection d’inhibiteurs sélectifs de HDAC : expression et rôle de HDAC9 dans les lignées cellulaires de cancer du sein : Histone deacetylases, estrogen signaling and breast cancer : bioluminescent cell lines as screening tools for selective HDAC inhibitors : expression and role of HDAC9 in breast cancer cell lines.” 2011. Web. 16 Jan 2021.

Vancouver:

Linares A. Histone désacétylases, signalisation œstrogénique et cancer du sein : établissement d’outils bioluminescents pour la détection d’inhibiteurs sélectifs de HDAC : expression et rôle de HDAC9 dans les lignées cellulaires de cancer du sein : Histone deacetylases, estrogen signaling and breast cancer : bioluminescent cell lines as screening tools for selective HDAC inhibitors : expression and role of HDAC9 in breast cancer cell lines. [Internet] [Doctoral dissertation]. Université Montpellier I; 2011. [cited 2021 Jan 16]. Available from: http://www.theses.fr/2011MON13504.

Council of Science Editors:

Linares A. Histone désacétylases, signalisation œstrogénique et cancer du sein : établissement d’outils bioluminescents pour la détection d’inhibiteurs sélectifs de HDAC : expression et rôle de HDAC9 dans les lignées cellulaires de cancer du sein : Histone deacetylases, estrogen signaling and breast cancer : bioluminescent cell lines as screening tools for selective HDAC inhibitors : expression and role of HDAC9 in breast cancer cell lines. [Doctoral Dissertation]. Université Montpellier I; 2011. Available from: http://www.theses.fr/2011MON13504


University of Debrecen

8. Tisza, Ákos. A HDAC hatása a pozíció effektus variegációra Drosophila melanogaster -ben .

Degree: DE – TEK – Természettudományi és Technológiai Kar – Biológiai és Ökológiai Intézet, 2010, University of Debrecen

Subjects/Keywords: HDAC; PEV

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Tisza, . (2010). A HDAC hatása a pozíció effektus variegációra Drosophila melanogaster -ben . (Thesis). University of Debrecen. Retrieved from http://hdl.handle.net/2437/96118

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):

Tisza, Ákos. “A HDAC hatása a pozíció effektus variegációra Drosophila melanogaster -ben .” 2010. Thesis, University of Debrecen. Accessed January 16, 2021. http://hdl.handle.net/2437/96118.

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

MLA Handbook (7th Edition):

Tisza, Ákos. “A HDAC hatása a pozíció effektus variegációra Drosophila melanogaster -ben .” 2010. Web. 16 Jan 2021.

Vancouver:

Tisza . A HDAC hatása a pozíció effektus variegációra Drosophila melanogaster -ben . [Internet] [Thesis]. University of Debrecen; 2010. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/2437/96118.

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

Council of Science Editors:

Tisza . A HDAC hatása a pozíció effektus variegációra Drosophila melanogaster -ben . [Thesis]. University of Debrecen; 2010. Available from: http://hdl.handle.net/2437/96118

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


University of Melbourne

9. Bishton, Mark. Deciphering the molecular and biological processes that mediate histone deacetylase inhibitor-induced thrombocytopenia.

Degree: 2012, University of Melbourne

 Somatic mutations in a variety of genes involved in cell cycle, signalling, differentiation, proliferation and apoptotic pathways can lead to the initiation and progression of… (more)

Subjects/Keywords: HDAC inhibitors; platelets; Rho-GTPases

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Bishton, M. (2012). Deciphering the molecular and biological processes that mediate histone deacetylase inhibitor-induced thrombocytopenia. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/37587

Chicago Manual of Style (16th Edition):

Bishton, Mark. “Deciphering the molecular and biological processes that mediate histone deacetylase inhibitor-induced thrombocytopenia.” 2012. Doctoral Dissertation, University of Melbourne. Accessed January 16, 2021. http://hdl.handle.net/11343/37587.

MLA Handbook (7th Edition):

Bishton, Mark. “Deciphering the molecular and biological processes that mediate histone deacetylase inhibitor-induced thrombocytopenia.” 2012. Web. 16 Jan 2021.

Vancouver:

Bishton M. Deciphering the molecular and biological processes that mediate histone deacetylase inhibitor-induced thrombocytopenia. [Internet] [Doctoral dissertation]. University of Melbourne; 2012. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/11343/37587.

Council of Science Editors:

Bishton M. Deciphering the molecular and biological processes that mediate histone deacetylase inhibitor-induced thrombocytopenia. [Doctoral Dissertation]. University of Melbourne; 2012. Available from: http://hdl.handle.net/11343/37587

10. Zagni, Chiara. Progettazione e sintesi di nuovi inibitori delle istone deacetilasi.

Degree: 2011, Università degli Studi di Catania

Il controllo epigenetico dell'espressione genica e' operato da modifiche post-translazionali della cromatina, quali acetilazione e deacetilazione. Due enzimi sono respinsabili di questo processo: le HAT… (more)

Subjects/Keywords: HDAC, HDI, SAHA; Istone deacetilasi

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Zagni, C. (2011). Progettazione e sintesi di nuovi inibitori delle istone deacetilasi. (Thesis). Università degli Studi di Catania. Retrieved from http://hdl.handle.net/10761/253

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):

Zagni, Chiara. “Progettazione e sintesi di nuovi inibitori delle istone deacetilasi.” 2011. Thesis, Università degli Studi di Catania. Accessed January 16, 2021. http://hdl.handle.net/10761/253.

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

MLA Handbook (7th Edition):

Zagni, Chiara. “Progettazione e sintesi di nuovi inibitori delle istone deacetilasi.” 2011. Web. 16 Jan 2021.

Vancouver:

Zagni C. Progettazione e sintesi di nuovi inibitori delle istone deacetilasi. [Internet] [Thesis]. Università degli Studi di Catania; 2011. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/10761/253.

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

Council of Science Editors:

Zagni C. Progettazione e sintesi di nuovi inibitori delle istone deacetilasi. [Thesis]. Università degli Studi di Catania; 2011. Available from: http://hdl.handle.net/10761/253

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


University of Edinburgh

11. Huang, Rui. Roles of HDACs in chromatin remodelling and response to chemotherapy in cancer.

Degree: PhD, 2014, University of Edinburgh

 Background: The higher-order structure of chromatin changes in response to extracellular and environmental signals. We observed nuclear morphological changes in biopsied cancer tissue after chemotherapy.… (more)

Subjects/Keywords: 616.99; HDAC; chromatin remodeling; chemotherapy

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Huang, R. (2014). Roles of HDACs in chromatin remodelling and response to chemotherapy in cancer. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/9626

Chicago Manual of Style (16th Edition):

Huang, Rui. “Roles of HDACs in chromatin remodelling and response to chemotherapy in cancer.” 2014. Doctoral Dissertation, University of Edinburgh. Accessed January 16, 2021. http://hdl.handle.net/1842/9626.

MLA Handbook (7th Edition):

Huang, Rui. “Roles of HDACs in chromatin remodelling and response to chemotherapy in cancer.” 2014. Web. 16 Jan 2021.

Vancouver:

Huang R. Roles of HDACs in chromatin remodelling and response to chemotherapy in cancer. [Internet] [Doctoral dissertation]. University of Edinburgh; 2014. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1842/9626.

Council of Science Editors:

Huang R. Roles of HDACs in chromatin remodelling and response to chemotherapy in cancer. [Doctoral Dissertation]. University of Edinburgh; 2014. Available from: http://hdl.handle.net/1842/9626

12. Sena, Elena. The Transcription Factor Barhl2 Inhibits Wnt Canonical Signaling during Xenopus Embryogenesis : Le facteur de transcription Barhl2 inhibe la signalisation Wnt canonique au cours de l'embryogenese du Xenope.

Degree: Docteur es, Sciences de la vie et de la santé, 2018, Université Paris-Saclay (ComUE)

Le développement embryonnaire est un processus hautement contrôlé où différentes voies de signalisation se coordonnent pour la construction d'un organisme. L'une des principales voies de… (more)

Subjects/Keywords: Barhl2; Hdac; Wnt; Groucho; Spemann; Barhl2; Hdac; Wnt; Groucho; Spemann organizer

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Sena, E. (2018). The Transcription Factor Barhl2 Inhibits Wnt Canonical Signaling during Xenopus Embryogenesis : Le facteur de transcription Barhl2 inhibe la signalisation Wnt canonique au cours de l'embryogenese du Xenope. (Doctoral Dissertation). Université Paris-Saclay (ComUE). Retrieved from http://www.theses.fr/2018SACLS090

Chicago Manual of Style (16th Edition):

Sena, Elena. “The Transcription Factor Barhl2 Inhibits Wnt Canonical Signaling during Xenopus Embryogenesis : Le facteur de transcription Barhl2 inhibe la signalisation Wnt canonique au cours de l'embryogenese du Xenope.” 2018. Doctoral Dissertation, Université Paris-Saclay (ComUE). Accessed January 16, 2021. http://www.theses.fr/2018SACLS090.

MLA Handbook (7th Edition):

Sena, Elena. “The Transcription Factor Barhl2 Inhibits Wnt Canonical Signaling during Xenopus Embryogenesis : Le facteur de transcription Barhl2 inhibe la signalisation Wnt canonique au cours de l'embryogenese du Xenope.” 2018. Web. 16 Jan 2021.

Vancouver:

Sena E. The Transcription Factor Barhl2 Inhibits Wnt Canonical Signaling during Xenopus Embryogenesis : Le facteur de transcription Barhl2 inhibe la signalisation Wnt canonique au cours de l'embryogenese du Xenope. [Internet] [Doctoral dissertation]. Université Paris-Saclay (ComUE); 2018. [cited 2021 Jan 16]. Available from: http://www.theses.fr/2018SACLS090.

Council of Science Editors:

Sena E. The Transcription Factor Barhl2 Inhibits Wnt Canonical Signaling during Xenopus Embryogenesis : Le facteur de transcription Barhl2 inhibe la signalisation Wnt canonique au cours de l'embryogenese du Xenope. [Doctoral Dissertation]. Université Paris-Saclay (ComUE); 2018. Available from: http://www.theses.fr/2018SACLS090


University of Illinois – Chicago

13. Madriaga, Antonett P. Evaluation of Photoreactive and Phenothiazine-based HDAC Inhibitors.

Degree: 2014, University of Illinois – Chicago

 Increased histone deacetylase (HDAC) activity and decreased acetylation status have been implicated in a wide array of neurodegenerative diseases, including Alzheimer’s, Parkinson’s, and Huntington’s disease.… (more)

Subjects/Keywords: histone deacetylase; HDAC; HDAC inhibitor; photoaffinity probes; neuroprotection; oxidative stress

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Madriaga, A. P. (2014). Evaluation of Photoreactive and Phenothiazine-based HDAC Inhibitors. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/11303

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):

Madriaga, Antonett P. “Evaluation of Photoreactive and Phenothiazine-based HDAC Inhibitors.” 2014. Thesis, University of Illinois – Chicago. Accessed January 16, 2021. http://hdl.handle.net/10027/11303.

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

MLA Handbook (7th Edition):

Madriaga, Antonett P. “Evaluation of Photoreactive and Phenothiazine-based HDAC Inhibitors.” 2014. Web. 16 Jan 2021.

Vancouver:

Madriaga AP. Evaluation of Photoreactive and Phenothiazine-based HDAC Inhibitors. [Internet] [Thesis]. University of Illinois – Chicago; 2014. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/10027/11303.

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

Council of Science Editors:

Madriaga AP. Evaluation of Photoreactive and Phenothiazine-based HDAC Inhibitors. [Thesis]. University of Illinois – Chicago; 2014. Available from: http://hdl.handle.net/10027/11303

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


Georgia Tech

14. Sodji, Quaovi Hemeka. Improving histone deacetylase inhibition therapy through isoform selectivity and targeted delivery.

Degree: PhD, Chemistry and Biochemistry, 2014, Georgia Tech

 Histone deacetylase (HDAC) inhibition has recently emerged as a novel therapy for cancer treatment. However, currently approved histone deacetylase inhibitors (HDACi) are pan-inhibitors thus inhibiting… (more)

Subjects/Keywords: Histone deacetylase (HDAC); HDAC inhibitors; Isoform selectivity; Targeted delivery

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Sodji, Q. H. (2014). Improving histone deacetylase inhibition therapy through isoform selectivity and targeted delivery. (Doctoral Dissertation). Georgia Tech. Retrieved from http://hdl.handle.net/1853/53445

Chicago Manual of Style (16th Edition):

Sodji, Quaovi Hemeka. “Improving histone deacetylase inhibition therapy through isoform selectivity and targeted delivery.” 2014. Doctoral Dissertation, Georgia Tech. Accessed January 16, 2021. http://hdl.handle.net/1853/53445.

MLA Handbook (7th Edition):

Sodji, Quaovi Hemeka. “Improving histone deacetylase inhibition therapy through isoform selectivity and targeted delivery.” 2014. Web. 16 Jan 2021.

Vancouver:

Sodji QH. Improving histone deacetylase inhibition therapy through isoform selectivity and targeted delivery. [Internet] [Doctoral dissertation]. Georgia Tech; 2014. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1853/53445.

Council of Science Editors:

Sodji QH. Improving histone deacetylase inhibition therapy through isoform selectivity and targeted delivery. [Doctoral Dissertation]. Georgia Tech; 2014. Available from: http://hdl.handle.net/1853/53445


University of Rochester

15. Wang, Weiye. A Novel Role of HDAC5 in Flow-Induced Gene Expression.

Degree: PhD, 2011, University of Rochester

 Fluid shear stress, a frictional force generated by the blood flow upon the vascular endothelial cells, is a major determinant of vascular remodeling, arterial tone… (more)

Subjects/Keywords: Fluid Shear Stress; HDAC; eNOS; KLF2

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Wang, W. (2011). A Novel Role of HDAC5 in Flow-Induced Gene Expression. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/14601

Chicago Manual of Style (16th Edition):

Wang, Weiye. “A Novel Role of HDAC5 in Flow-Induced Gene Expression.” 2011. Doctoral Dissertation, University of Rochester. Accessed January 16, 2021. http://hdl.handle.net/1802/14601.

MLA Handbook (7th Edition):

Wang, Weiye. “A Novel Role of HDAC5 in Flow-Induced Gene Expression.” 2011. Web. 16 Jan 2021.

Vancouver:

Wang W. A Novel Role of HDAC5 in Flow-Induced Gene Expression. [Internet] [Doctoral dissertation]. University of Rochester; 2011. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1802/14601.

Council of Science Editors:

Wang W. A Novel Role of HDAC5 in Flow-Induced Gene Expression. [Doctoral Dissertation]. University of Rochester; 2011. Available from: http://hdl.handle.net/1802/14601


University of Wisconsin – Milwaukee

16. Skurski, Joseph. Histone Deacetylase Inhibition Induces Apoptosis and Cell Cycle Dysregulation in Human and Murine Cancer Cell Lines.

Degree: MS, Biological Sciences, 2017, University of Wisconsin – Milwaukee

  Carcinogenesis is a complex multistep process that requires tumor cells to grow rapidly while overcoming growth inhibitory signals and sustained challenges from the host… (more)

Subjects/Keywords: Cancer; HDAC; Tumor Cells; Cell Biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Skurski, J. (2017). Histone Deacetylase Inhibition Induces Apoptosis and Cell Cycle Dysregulation in Human and Murine Cancer Cell Lines. (Thesis). University of Wisconsin – Milwaukee. Retrieved from https://dc.uwm.edu/etd/1702

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):

Skurski, Joseph. “Histone Deacetylase Inhibition Induces Apoptosis and Cell Cycle Dysregulation in Human and Murine Cancer Cell Lines.” 2017. Thesis, University of Wisconsin – Milwaukee. Accessed January 16, 2021. https://dc.uwm.edu/etd/1702.

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

MLA Handbook (7th Edition):

Skurski, Joseph. “Histone Deacetylase Inhibition Induces Apoptosis and Cell Cycle Dysregulation in Human and Murine Cancer Cell Lines.” 2017. Web. 16 Jan 2021.

Vancouver:

Skurski J. Histone Deacetylase Inhibition Induces Apoptosis and Cell Cycle Dysregulation in Human and Murine Cancer Cell Lines. [Internet] [Thesis]. University of Wisconsin – Milwaukee; 2017. [cited 2021 Jan 16]. Available from: https://dc.uwm.edu/etd/1702.

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

Council of Science Editors:

Skurski J. Histone Deacetylase Inhibition Induces Apoptosis and Cell Cycle Dysregulation in Human and Murine Cancer Cell Lines. [Thesis]. University of Wisconsin – Milwaukee; 2017. Available from: https://dc.uwm.edu/etd/1702

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


Boston University

17. Dharampuriya, Priyanka. Role of epigenetics in hematopoietic stem cell development.

Degree: MS, Medical Sciences, 2017, Boston University

 In 2106, there were 171,550 new cases of blood cancers and over one million people in the United States living with one of these disorders.… (more)

Subjects/Keywords: Medicine; HDAC; Epigenetics; Hematopoiesis; Histone acetyltransferase

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Dharampuriya, P. (2017). Role of epigenetics in hematopoietic stem cell development. (Masters Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/23717

Chicago Manual of Style (16th Edition):

Dharampuriya, Priyanka. “Role of epigenetics in hematopoietic stem cell development.” 2017. Masters Thesis, Boston University. Accessed January 16, 2021. http://hdl.handle.net/2144/23717.

MLA Handbook (7th Edition):

Dharampuriya, Priyanka. “Role of epigenetics in hematopoietic stem cell development.” 2017. Web. 16 Jan 2021.

Vancouver:

Dharampuriya P. Role of epigenetics in hematopoietic stem cell development. [Internet] [Masters thesis]. Boston University; 2017. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/2144/23717.

Council of Science Editors:

Dharampuriya P. Role of epigenetics in hematopoietic stem cell development. [Masters Thesis]. Boston University; 2017. Available from: http://hdl.handle.net/2144/23717


University of Manchester

18. Yeh, Hsin-Hsien. Utility and validation of the histone deacetylase (HDAC) substrate, [18F]FAHA, as a positron emission tomography (PET) imaging biomarker in non-human primates and HD transgenic mice for evaluation of neurodegenerative diseases and HDAC inhibitor treatment.

Degree: PhD, 2013, University of Manchester

 Histone deacetylase (HDAC) inhibitors (HDACIs) have long been studied and shown promises in the treatment of various neurodegenerative disorders including Huntington’s disease (HD). Based on… (more)

Subjects/Keywords: 616.851; [18F]FAHA; HDAC; PET; Neurodegenerative Diseases

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Yeh, H. (2013). Utility and validation of the histone deacetylase (HDAC) substrate, [18F]FAHA, as a positron emission tomography (PET) imaging biomarker in non-human primates and HD transgenic mice for evaluation of neurodegenerative diseases and HDAC inhibitor treatment. (Doctoral Dissertation). University of Manchester. Retrieved from https://www.research.manchester.ac.uk/portal/en/theses/utility-and-validation-of-the-histone-deacetylase-hdac-substrate-18ffaha-as-a-positron-emission-tomography-pet-imaging-biomarker-in-nonhuman-primates-and-hd-transgenic-mice-for-evaluation-of-neurodegenerative-diseases-and-hdac-inhibitor-treatment(69cbe9a1-aa64-45d6-947f-9368eabb071c).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.574280

Chicago Manual of Style (16th Edition):

Yeh, Hsin-Hsien. “Utility and validation of the histone deacetylase (HDAC) substrate, [18F]FAHA, as a positron emission tomography (PET) imaging biomarker in non-human primates and HD transgenic mice for evaluation of neurodegenerative diseases and HDAC inhibitor treatment.” 2013. Doctoral Dissertation, University of Manchester. Accessed January 16, 2021. https://www.research.manchester.ac.uk/portal/en/theses/utility-and-validation-of-the-histone-deacetylase-hdac-substrate-18ffaha-as-a-positron-emission-tomography-pet-imaging-biomarker-in-nonhuman-primates-and-hd-transgenic-mice-for-evaluation-of-neurodegenerative-diseases-and-hdac-inhibitor-treatment(69cbe9a1-aa64-45d6-947f-9368eabb071c).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.574280.

MLA Handbook (7th Edition):

Yeh, Hsin-Hsien. “Utility and validation of the histone deacetylase (HDAC) substrate, [18F]FAHA, as a positron emission tomography (PET) imaging biomarker in non-human primates and HD transgenic mice for evaluation of neurodegenerative diseases and HDAC inhibitor treatment.” 2013. Web. 16 Jan 2021.

Vancouver:

Yeh H. Utility and validation of the histone deacetylase (HDAC) substrate, [18F]FAHA, as a positron emission tomography (PET) imaging biomarker in non-human primates and HD transgenic mice for evaluation of neurodegenerative diseases and HDAC inhibitor treatment. [Internet] [Doctoral dissertation]. University of Manchester; 2013. [cited 2021 Jan 16]. Available from: https://www.research.manchester.ac.uk/portal/en/theses/utility-and-validation-of-the-histone-deacetylase-hdac-substrate-18ffaha-as-a-positron-emission-tomography-pet-imaging-biomarker-in-nonhuman-primates-and-hd-transgenic-mice-for-evaluation-of-neurodegenerative-diseases-and-hdac-inhibitor-treatment(69cbe9a1-aa64-45d6-947f-9368eabb071c).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.574280.

Council of Science Editors:

Yeh H. Utility and validation of the histone deacetylase (HDAC) substrate, [18F]FAHA, as a positron emission tomography (PET) imaging biomarker in non-human primates and HD transgenic mice for evaluation of neurodegenerative diseases and HDAC inhibitor treatment. [Doctoral Dissertation]. University of Manchester; 2013. Available from: https://www.research.manchester.ac.uk/portal/en/theses/utility-and-validation-of-the-histone-deacetylase-hdac-substrate-18ffaha-as-a-positron-emission-tomography-pet-imaging-biomarker-in-nonhuman-primates-and-hd-transgenic-mice-for-evaluation-of-neurodegenerative-diseases-and-hdac-inhibitor-treatment(69cbe9a1-aa64-45d6-947f-9368eabb071c).html ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.574280


University of Manitoba

19. Lillico, Ryan. Overcoming off-target changes in gene expression by targeting epigenetic enzyme inhibitors to oncogenes using LNA-drug bioconjugates.

Degree: Pharmacy, 2019, University of Manitoba

 Inhibition of epigenetic drug targets is growing into a powerful tool to regulate gene expression for the treatment of many diseases. This has become the… (more)

Subjects/Keywords: Epigenetics; Mixed Lineage Leukemia; HDAC; DOT1L; LSD1

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lillico, R. (2019). Overcoming off-target changes in gene expression by targeting epigenetic enzyme inhibitors to oncogenes using LNA-drug bioconjugates. (Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/33761

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):

Lillico, Ryan. “Overcoming off-target changes in gene expression by targeting epigenetic enzyme inhibitors to oncogenes using LNA-drug bioconjugates.” 2019. Thesis, University of Manitoba. Accessed January 16, 2021. http://hdl.handle.net/1993/33761.

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

MLA Handbook (7th Edition):

Lillico, Ryan. “Overcoming off-target changes in gene expression by targeting epigenetic enzyme inhibitors to oncogenes using LNA-drug bioconjugates.” 2019. Web. 16 Jan 2021.

Vancouver:

Lillico R. Overcoming off-target changes in gene expression by targeting epigenetic enzyme inhibitors to oncogenes using LNA-drug bioconjugates. [Internet] [Thesis]. University of Manitoba; 2019. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/1993/33761.

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

Council of Science Editors:

Lillico R. Overcoming off-target changes in gene expression by targeting epigenetic enzyme inhibitors to oncogenes using LNA-drug bioconjugates. [Thesis]. University of Manitoba; 2019. Available from: http://hdl.handle.net/1993/33761

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


Duke University

20. Kim, Bumki. Design, Synthesis, and Biological Characterization of Largazole Analogues .

Degree: 2016, Duke University

  Histone deacetylases (HDACs) have been shown to play key roles in tumorigenesis, and have been validated as effective enzyme target for cancer treatment. Largazole,… (more)

Subjects/Keywords: Chemistry; analogues; cancer; HDAC; largazole; natural product

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Kim, B. (2016). Design, Synthesis, and Biological Characterization of Largazole Analogues . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/12114

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):

Kim, Bumki. “Design, Synthesis, and Biological Characterization of Largazole Analogues .” 2016. Thesis, Duke University. Accessed January 16, 2021. http://hdl.handle.net/10161/12114.

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

MLA Handbook (7th Edition):

Kim, Bumki. “Design, Synthesis, and Biological Characterization of Largazole Analogues .” 2016. Web. 16 Jan 2021.

Vancouver:

Kim B. Design, Synthesis, and Biological Characterization of Largazole Analogues . [Internet] [Thesis]. Duke University; 2016. [cited 2021 Jan 16]. Available from: http://hdl.handle.net/10161/12114.

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

Council of Science Editors:

Kim B. Design, Synthesis, and Biological Characterization of Largazole Analogues . [Thesis]. Duke University; 2016. Available from: http://hdl.handle.net/10161/12114

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


University of Toledo

21. Al-Hamashi, Ayad Abed Ali Chiad A. Design, Synthesis, and Biological Evaluation of Novel Histone Deacetylase Inhibitors as Anti-Cancer Agents.

Degree: PhD, Medicinal Chemistry, 2018, University of Toledo

 Despite major advances in cancer treatment strategies in recent years, significant limitations still remain. Selectively targeting cancer cells without affecting normal cells is a challenging… (more)

Subjects/Keywords: Pharmacy Sciences; HDAC, Inhibitors, epigenetic, histone

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Al-Hamashi, A. A. A. C. A. (2018). Design, Synthesis, and Biological Evaluation of Novel Histone Deacetylase Inhibitors as Anti-Cancer Agents. (Doctoral Dissertation). University of Toledo. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=toledo1525945712448479

Chicago Manual of Style (16th Edition):

Al-Hamashi, Ayad Abed Ali Chiad A. “Design, Synthesis, and Biological Evaluation of Novel Histone Deacetylase Inhibitors as Anti-Cancer Agents.” 2018. Doctoral Dissertation, University of Toledo. Accessed January 16, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1525945712448479.

MLA Handbook (7th Edition):

Al-Hamashi, Ayad Abed Ali Chiad A. “Design, Synthesis, and Biological Evaluation of Novel Histone Deacetylase Inhibitors as Anti-Cancer Agents.” 2018. Web. 16 Jan 2021.

Vancouver:

Al-Hamashi AAACA. Design, Synthesis, and Biological Evaluation of Novel Histone Deacetylase Inhibitors as Anti-Cancer Agents. [Internet] [Doctoral dissertation]. University of Toledo; 2018. [cited 2021 Jan 16]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1525945712448479.

Council of Science Editors:

Al-Hamashi AAACA. Design, Synthesis, and Biological Evaluation of Novel Histone Deacetylase Inhibitors as Anti-Cancer Agents. [Doctoral Dissertation]. University of Toledo; 2018. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1525945712448479


University of Toledo

22. Sindi, Shaimaa Hesham. Guanidine- Based HDAC-Inhibitors as Anti-Cancer Agents.

Degree: MS, Medicinal Chemistry, 2019, University of Toledo

 It is evident that epigenetics plays an important role in gene regulation. Consequently, any disruption in epigenetic memory will manifest into gene expression and lead… (more)

Subjects/Keywords: Pharmaceuticals; Chemistry; Pharmacy Sciences; Cancer; HDAC; guanidine

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Sindi, S. H. (2019). Guanidine- Based HDAC-Inhibitors as Anti-Cancer Agents. (Masters Thesis). University of Toledo. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=toledo1564676186975875

Chicago Manual of Style (16th Edition):

Sindi, Shaimaa Hesham. “Guanidine- Based HDAC-Inhibitors as Anti-Cancer Agents.” 2019. Masters Thesis, University of Toledo. Accessed January 16, 2021. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1564676186975875.

MLA Handbook (7th Edition):

Sindi, Shaimaa Hesham. “Guanidine- Based HDAC-Inhibitors as Anti-Cancer Agents.” 2019. Web. 16 Jan 2021.

Vancouver:

Sindi SH. Guanidine- Based HDAC-Inhibitors as Anti-Cancer Agents. [Internet] [Masters thesis]. University of Toledo; 2019. [cited 2021 Jan 16]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1564676186975875.

Council of Science Editors:

Sindi SH. Guanidine- Based HDAC-Inhibitors as Anti-Cancer Agents. [Masters Thesis]. University of Toledo; 2019. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1564676186975875


University of Pennsylvania

23. Wang, Yi. Class I Histone Deacetylases in Lung Development and Regeneration.

Degree: 2015, University of Pennsylvania

 The generation and development of the mammalian lung requires an elegantly regulated molecular program to control cell number, lineage specification, as well as morphogenetic remodeling.… (more)

Subjects/Keywords: Development; HDAC; Lung; Regeneration; Developmental Biology

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Wang, Y. (2015). Class I Histone Deacetylases in Lung Development and Regeneration. (Thesis). University of Pennsylvania. Retrieved from https://repository.upenn.edu/edissertations/2083

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):

Wang, Yi. “Class I Histone Deacetylases in Lung Development and Regeneration.” 2015. Thesis, University of Pennsylvania. Accessed January 16, 2021. https://repository.upenn.edu/edissertations/2083.

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

MLA Handbook (7th Edition):

Wang, Yi. “Class I Histone Deacetylases in Lung Development and Regeneration.” 2015. Web. 16 Jan 2021.

Vancouver:

Wang Y. Class I Histone Deacetylases in Lung Development and Regeneration. [Internet] [Thesis]. University of Pennsylvania; 2015. [cited 2021 Jan 16]. Available from: https://repository.upenn.edu/edissertations/2083.

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

Council of Science Editors:

Wang Y. Class I Histone Deacetylases in Lung Development and Regeneration. [Thesis]. University of Pennsylvania; 2015. Available from: https://repository.upenn.edu/edissertations/2083

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

24. Leteve, Mathieu. EPIADDICT - Synthèses de nouveaux inhibiteurs des histones désacétylases et leur intérêt dans un modèle préclinique d’addiction à l’alcool. : EPIADDICT - Synthesis of the new interest histone deacetylase inhibitors in a preclinical model of addiction to alcohol.

Degree: Docteur es, Chimie organique, minérale, industrielle, 2016, Reims

Le déséquilibre HAT/HDAC aurait une influence sur le développement de certains cancers ainsi que dans l’addiction à l’alcool ou à la cocaïne. En inhibant les… (more)

Subjects/Keywords: Inhibiteur; Hdac; Addiction; Alcool; Cyclodepsipeptide; Sulfonylhydrazide; Inhibitor; Hdac; Addiction; Alcohol; Cyclodepsipeptide; Sulfonylhydrazide

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Leteve, M. (2016). EPIADDICT - Synthèses de nouveaux inhibiteurs des histones désacétylases et leur intérêt dans un modèle préclinique d’addiction à l’alcool. : EPIADDICT - Synthesis of the new interest histone deacetylase inhibitors in a preclinical model of addiction to alcohol. (Doctoral Dissertation). Reims. Retrieved from http://www.theses.fr/2016REIMS026

Chicago Manual of Style (16th Edition):

Leteve, Mathieu. “EPIADDICT - Synthèses de nouveaux inhibiteurs des histones désacétylases et leur intérêt dans un modèle préclinique d’addiction à l’alcool. : EPIADDICT - Synthesis of the new interest histone deacetylase inhibitors in a preclinical model of addiction to alcohol.” 2016. Doctoral Dissertation, Reims. Accessed January 16, 2021. http://www.theses.fr/2016REIMS026.

MLA Handbook (7th Edition):

Leteve, Mathieu. “EPIADDICT - Synthèses de nouveaux inhibiteurs des histones désacétylases et leur intérêt dans un modèle préclinique d’addiction à l’alcool. : EPIADDICT - Synthesis of the new interest histone deacetylase inhibitors in a preclinical model of addiction to alcohol.” 2016. Web. 16 Jan 2021.

Vancouver:

Leteve M. EPIADDICT - Synthèses de nouveaux inhibiteurs des histones désacétylases et leur intérêt dans un modèle préclinique d’addiction à l’alcool. : EPIADDICT - Synthesis of the new interest histone deacetylase inhibitors in a preclinical model of addiction to alcohol. [Internet] [Doctoral dissertation]. Reims; 2016. [cited 2021 Jan 16]. Available from: http://www.theses.fr/2016REIMS026.

Council of Science Editors:

Leteve M. EPIADDICT - Synthèses de nouveaux inhibiteurs des histones désacétylases et leur intérêt dans un modèle préclinique d’addiction à l’alcool. : EPIADDICT - Synthesis of the new interest histone deacetylase inhibitors in a preclinical model of addiction to alcohol. [Doctoral Dissertation]. Reims; 2016. Available from: http://www.theses.fr/2016REIMS026


Texas Medical Center

25. Lopez, Gonzalo. Targeting Histone deacetylases (HDAC) for the treatment of soft tissue sarcoma.

Degree: PhD, 2013, Texas Medical Center

  Targeting Histone deacetylases (HDAC) for the treatment of genetically complex soft tissue sarcoma Histone deactylase inhibitors (HDACi) are a new class of anticancer therapeutics;… (more)

Subjects/Keywords: HDAC; HDAC inhibition; MPNST; soft tissue sarcoma; HDAC8; autophagy; Cancer Biology; Medicine and Health Sciences

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Lopez, G. (2013). Targeting Histone deacetylases (HDAC) for the treatment of soft tissue sarcoma. (Doctoral Dissertation). Texas Medical Center. Retrieved from https://digitalcommons.library.tmc.edu/utgsbs_dissertations/351

Chicago Manual of Style (16th Edition):

Lopez, Gonzalo. “Targeting Histone deacetylases (HDAC) for the treatment of soft tissue sarcoma.” 2013. Doctoral Dissertation, Texas Medical Center. Accessed January 16, 2021. https://digitalcommons.library.tmc.edu/utgsbs_dissertations/351.

MLA Handbook (7th Edition):

Lopez, Gonzalo. “Targeting Histone deacetylases (HDAC) for the treatment of soft tissue sarcoma.” 2013. Web. 16 Jan 2021.

Vancouver:

Lopez G. Targeting Histone deacetylases (HDAC) for the treatment of soft tissue sarcoma. [Internet] [Doctoral dissertation]. Texas Medical Center; 2013. [cited 2021 Jan 16]. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/351.

Council of Science Editors:

Lopez G. Targeting Histone deacetylases (HDAC) for the treatment of soft tissue sarcoma. [Doctoral Dissertation]. Texas Medical Center; 2013. Available from: https://digitalcommons.library.tmc.edu/utgsbs_dissertations/351

26. Traore, Mohamed Dit Mady. Synthèse et études de modélisation moléculaire dans l'optimisation de la sélectivité de nouveaux agents antiparasitaires inspirés de produits naturels : Synthesis and molecular modelisation in selectivity optimisation of novel antiparasitic agents inspired from natural products.

Degree: Docteur es, Chimie biologie, 2016, Université Grenoble Alpes (ComUE)

Les aculéatines et FR235222 sont deux familles de molécules d’origine naturelle qui agissent de façons très efficaces sur les parasites intracellulaires de la famille des… (more)

Subjects/Keywords: Epigénétique; Sélectivité; Antiparasitaire; Aculéatines; Fr235222; Hdac; Epigenetic; Selectivity; Antiparasitic; Aculeatines; Fr235222; Hdac; 540

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Traore, M. D. M. (2016). Synthèse et études de modélisation moléculaire dans l'optimisation de la sélectivité de nouveaux agents antiparasitaires inspirés de produits naturels : Synthesis and molecular modelisation in selectivity optimisation of novel antiparasitic agents inspired from natural products. (Doctoral Dissertation). Université Grenoble Alpes (ComUE). Retrieved from http://www.theses.fr/2016GREAV027

Chicago Manual of Style (16th Edition):

Traore, Mohamed Dit Mady. “Synthèse et études de modélisation moléculaire dans l'optimisation de la sélectivité de nouveaux agents antiparasitaires inspirés de produits naturels : Synthesis and molecular modelisation in selectivity optimisation of novel antiparasitic agents inspired from natural products.” 2016. Doctoral Dissertation, Université Grenoble Alpes (ComUE). Accessed January 16, 2021. http://www.theses.fr/2016GREAV027.

MLA Handbook (7th Edition):

Traore, Mohamed Dit Mady. “Synthèse et études de modélisation moléculaire dans l'optimisation de la sélectivité de nouveaux agents antiparasitaires inspirés de produits naturels : Synthesis and molecular modelisation in selectivity optimisation of novel antiparasitic agents inspired from natural products.” 2016. Web. 16 Jan 2021.

Vancouver:

Traore MDM. Synthèse et études de modélisation moléculaire dans l'optimisation de la sélectivité de nouveaux agents antiparasitaires inspirés de produits naturels : Synthesis and molecular modelisation in selectivity optimisation of novel antiparasitic agents inspired from natural products. [Internet] [Doctoral dissertation]. Université Grenoble Alpes (ComUE); 2016. [cited 2021 Jan 16]. Available from: http://www.theses.fr/2016GREAV027.

Council of Science Editors:

Traore MDM. Synthèse et études de modélisation moléculaire dans l'optimisation de la sélectivité de nouveaux agents antiparasitaires inspirés de produits naturels : Synthesis and molecular modelisation in selectivity optimisation of novel antiparasitic agents inspired from natural products. [Doctoral Dissertation]. Université Grenoble Alpes (ComUE); 2016. Available from: http://www.theses.fr/2016GREAV027


University of Southern California

27. Jayathilaka, Nimanthi. Inhibition of the interaction between class IIA histone deacetylases and myocyte enhancer factor 2 by small molecules.

Degree: PhD, Genetic, Molecular and Cellular Biology, 2012, University of Southern California

 Enzymes that modify epigenetic status provide attractive targets for therapy in various diseases including cardiac hypertrophy, cancer, neurodegenerative diseases, and immune dysfunction. The therapeutic development… (more)

Subjects/Keywords: histone deacetylases (HDAC); HDAC inhibitors; myocyte enhancer factor 2 (MEF2); transcription regulation

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Jayathilaka, N. (2012). Inhibition of the interaction between class IIA histone deacetylases and myocyte enhancer factor 2 by small molecules. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/649665/rec/3502

Chicago Manual of Style (16th Edition):

Jayathilaka, Nimanthi. “Inhibition of the interaction between class IIA histone deacetylases and myocyte enhancer factor 2 by small molecules.” 2012. Doctoral Dissertation, University of Southern California. Accessed January 16, 2021. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/649665/rec/3502.

MLA Handbook (7th Edition):

Jayathilaka, Nimanthi. “Inhibition of the interaction between class IIA histone deacetylases and myocyte enhancer factor 2 by small molecules.” 2012. Web. 16 Jan 2021.

Vancouver:

Jayathilaka N. Inhibition of the interaction between class IIA histone deacetylases and myocyte enhancer factor 2 by small molecules. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2021 Jan 16]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/649665/rec/3502.

Council of Science Editors:

Jayathilaka N. Inhibition of the interaction between class IIA histone deacetylases and myocyte enhancer factor 2 by small molecules. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll127/id/649665/rec/3502


Georgia State University

28. Rajan, Anubama. Histone acetylation modulates uncoupling protein1 expression in brown adipocytes.

Degree: MS, Biology, 2014, Georgia State University

  Uncoupling protein 1 (UCP1) is a classical feature of brown adipocytes and understanding its regulatory mechanism will help in the development of a pharmacological… (more)

Subjects/Keywords: Uncoupling protein 1; Brown fat; Epigenetics; Histone deacetylase (HDAC); HDAC inhibitors; Obesity

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Rajan, A. (2014). Histone acetylation modulates uncoupling protein1 expression in brown adipocytes. (Thesis). Georgia State University. Retrieved from https://scholarworks.gsu.edu/biology_theses/56

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):

Rajan, Anubama. “Histone acetylation modulates uncoupling protein1 expression in brown adipocytes.” 2014. Thesis, Georgia State University. Accessed January 16, 2021. https://scholarworks.gsu.edu/biology_theses/56.

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

MLA Handbook (7th Edition):

Rajan, Anubama. “Histone acetylation modulates uncoupling protein1 expression in brown adipocytes.” 2014. Web. 16 Jan 2021.

Vancouver:

Rajan A. Histone acetylation modulates uncoupling protein1 expression in brown adipocytes. [Internet] [Thesis]. Georgia State University; 2014. [cited 2021 Jan 16]. Available from: https://scholarworks.gsu.edu/biology_theses/56.

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

Council of Science Editors:

Rajan A. Histone acetylation modulates uncoupling protein1 expression in brown adipocytes. [Thesis]. Georgia State University; 2014. Available from: https://scholarworks.gsu.edu/biology_theses/56

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

29. Spaety, Marie-Élodie. Implication des régulations épigénétiques dans la réponse aux chimiothérapies dans les cancers gastriques : perspectives thérapeutiques : Implication of epigenetic modifications in response to chemotherapies in gastric cancer : therapeutic perspectives.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2016, Université de Strasbourg

Le cancer gastrique (CG) est traité par résection chirurgicale combinée à une chimiothérapie à base de composés de platine. La résistance croissante aux chimiothérapies renforce… (more)

Subjects/Keywords: Cancer gastrique; Platine; Ruthenium; Épigénétique; HDAC; MiRNA; P53 family; Gastric cancer; Platinum; Ruthenium; Epigenetic; HDAC; MiRNA; P53 family; 572.8; 616.99; 615.7

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Spaety, M. (2016). Implication des régulations épigénétiques dans la réponse aux chimiothérapies dans les cancers gastriques : perspectives thérapeutiques : Implication of epigenetic modifications in response to chemotherapies in gastric cancer : therapeutic perspectives. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2016STRAJ043

Chicago Manual of Style (16th Edition):

Spaety, Marie-Élodie. “Implication des régulations épigénétiques dans la réponse aux chimiothérapies dans les cancers gastriques : perspectives thérapeutiques : Implication of epigenetic modifications in response to chemotherapies in gastric cancer : therapeutic perspectives.” 2016. Doctoral Dissertation, Université de Strasbourg. Accessed January 16, 2021. http://www.theses.fr/2016STRAJ043.

MLA Handbook (7th Edition):

Spaety, Marie-Élodie. “Implication des régulations épigénétiques dans la réponse aux chimiothérapies dans les cancers gastriques : perspectives thérapeutiques : Implication of epigenetic modifications in response to chemotherapies in gastric cancer : therapeutic perspectives.” 2016. Web. 16 Jan 2021.

Vancouver:

Spaety M. Implication des régulations épigénétiques dans la réponse aux chimiothérapies dans les cancers gastriques : perspectives thérapeutiques : Implication of epigenetic modifications in response to chemotherapies in gastric cancer : therapeutic perspectives. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2016. [cited 2021 Jan 16]. Available from: http://www.theses.fr/2016STRAJ043.

Council of Science Editors:

Spaety M. Implication des régulations épigénétiques dans la réponse aux chimiothérapies dans les cancers gastriques : perspectives thérapeutiques : Implication of epigenetic modifications in response to chemotherapies in gastric cancer : therapeutic perspectives. [Doctoral Dissertation]. Université de Strasbourg; 2016. Available from: http://www.theses.fr/2016STRAJ043


Wayne State University

30. Negmeldin, Ahmed. Design, Synthesis And Biological Evaluation Of Histone Deacetylase (hdac) Inhibitors: Saha (vorinostat) Analogs And Biaryl Indolyl Benzamide Inhibitors Display Isoform Selectivity.

Degree: PhD, Chemistry, 2017, Wayne State University

HDAC proteins have emerged as interesting targets for anti-cancer drugs due to their involvement in cancers, as well as several other diseases. Several HDAC(more)

Subjects/Keywords: HDAC6 HDAC8 selective inhibitor; HDAC inhibitor; HDAC isoform selectivity; Histone Deacetylase; SAHA; Vorinostat; Biochemistry; Chemistry; Organic Chemistry

Record DetailsSimilar RecordsGoogle PlusoneFacebookTwitterCiteULikeMendeleyreddit

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

APA (6th Edition):

Negmeldin, A. (2017). Design, Synthesis And Biological Evaluation Of Histone Deacetylase (hdac) Inhibitors: Saha (vorinostat) Analogs And Biaryl Indolyl Benzamide Inhibitors Display Isoform Selectivity. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/1853

Chicago Manual of Style (16th Edition):

Negmeldin, Ahmed. “Design, Synthesis And Biological Evaluation Of Histone Deacetylase (hdac) Inhibitors: Saha (vorinostat) Analogs And Biaryl Indolyl Benzamide Inhibitors Display Isoform Selectivity.” 2017. Doctoral Dissertation, Wayne State University. Accessed January 16, 2021. https://digitalcommons.wayne.edu/oa_dissertations/1853.

MLA Handbook (7th Edition):

Negmeldin, Ahmed. “Design, Synthesis And Biological Evaluation Of Histone Deacetylase (hdac) Inhibitors: Saha (vorinostat) Analogs And Biaryl Indolyl Benzamide Inhibitors Display Isoform Selectivity.” 2017. Web. 16 Jan 2021.

Vancouver:

Negmeldin A. Design, Synthesis And Biological Evaluation Of Histone Deacetylase (hdac) Inhibitors: Saha (vorinostat) Analogs And Biaryl Indolyl Benzamide Inhibitors Display Isoform Selectivity. [Internet] [Doctoral dissertation]. Wayne State University; 2017. [cited 2021 Jan 16]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/1853.

Council of Science Editors:

Negmeldin A. Design, Synthesis And Biological Evaluation Of Histone Deacetylase (hdac) Inhibitors: Saha (vorinostat) Analogs And Biaryl Indolyl Benzamide Inhibitors Display Isoform Selectivity. [Doctoral Dissertation]. Wayne State University; 2017. Available from: https://digitalcommons.wayne.edu/oa_dissertations/1853

[1] [2] [3] [4] [5] [6] [7]

.