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You searched for subject:(RNA polymerase II). Showing records 1 – 30 of 128 total matches.

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Texas A&M University

1. Kaster, Benjamin Catlin. The Role of RNA Polymerase II Subunit Rpb9: In and Out of the Active Site.

Degree: PhD, Biochemistry, 2016, Texas A&M University

 Rpb9 is a conserved RNA polymerase II (pol II) subunit, the absence of which confers alterations to pol II enzymatic properties and transcription fidelity. It… (more)

Subjects/Keywords: RNA Polymerase II; Rpb9

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APA (6th Edition):

Kaster, B. C. (2016). The Role of RNA Polymerase II Subunit Rpb9: In and Out of the Active Site. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/156869

Chicago Manual of Style (16th Edition):

Kaster, Benjamin Catlin. “The Role of RNA Polymerase II Subunit Rpb9: In and Out of the Active Site.” 2016. Doctoral Dissertation, Texas A&M University. Accessed September 23, 2020. http://hdl.handle.net/1969.1/156869.

MLA Handbook (7th Edition):

Kaster, Benjamin Catlin. “The Role of RNA Polymerase II Subunit Rpb9: In and Out of the Active Site.” 2016. Web. 23 Sep 2020.

Vancouver:

Kaster BC. The Role of RNA Polymerase II Subunit Rpb9: In and Out of the Active Site. [Internet] [Doctoral dissertation]. Texas A&M University; 2016. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1969.1/156869.

Council of Science Editors:

Kaster BC. The Role of RNA Polymerase II Subunit Rpb9: In and Out of the Active Site. [Doctoral Dissertation]. Texas A&M University; 2016. Available from: http://hdl.handle.net/1969.1/156869


Duke University

2. Bartkowiak, Bartlomiej. Characterization of dCDK12, hCDK12, and hCDK13 in the Context of RNA Polymerase II CTD Phosphorylation and Transcription-Associated Events .

Degree: 2014, Duke University

  Eukaryotic RNA polymerase II (RNAPII) not only synthesizes mRNA, but also coordinates transcription-related processes through the post-translational modification of its unique C-terminal repeat domain… (more)

Subjects/Keywords: Biochemistry; RNA Polymerase II CTD

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APA (6th Edition):

Bartkowiak, B. (2014). Characterization of dCDK12, hCDK12, and hCDK13 in the Context of RNA Polymerase II CTD Phosphorylation and Transcription-Associated Events . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/9415

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):

Bartkowiak, Bartlomiej. “Characterization of dCDK12, hCDK12, and hCDK13 in the Context of RNA Polymerase II CTD Phosphorylation and Transcription-Associated Events .” 2014. Thesis, Duke University. Accessed September 23, 2020. http://hdl.handle.net/10161/9415.

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

MLA Handbook (7th Edition):

Bartkowiak, Bartlomiej. “Characterization of dCDK12, hCDK12, and hCDK13 in the Context of RNA Polymerase II CTD Phosphorylation and Transcription-Associated Events .” 2014. Web. 23 Sep 2020.

Vancouver:

Bartkowiak B. Characterization of dCDK12, hCDK12, and hCDK13 in the Context of RNA Polymerase II CTD Phosphorylation and Transcription-Associated Events . [Internet] [Thesis]. Duke University; 2014. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/10161/9415.

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

Council of Science Editors:

Bartkowiak B. Characterization of dCDK12, hCDK12, and hCDK13 in the Context of RNA Polymerase II CTD Phosphorylation and Transcription-Associated Events . [Thesis]. Duke University; 2014. Available from: http://hdl.handle.net/10161/9415

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


Texas A&M University

3. Qiu, Chenxi. FUNCTIONAL DISSECTION OF RNA POLYMERASE II ACTIVE SITE AND MECHANISM OF ACTION OF TRANSCRIPTION INHIBITOR THIOLUTIN.

Degree: PhD, Biochemistry, 2017, Texas A&M University

 mRNA synthesis by RNA polymerase II (Pol II) is an essential process in eukaryotes. In my dissertation, I have undertaken two parallel approaches to expand… (more)

Subjects/Keywords: RNA Polymerase II; Function; Trigger Loop; Thiolutin

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APA (6th Edition):

Qiu, C. (2017). FUNCTIONAL DISSECTION OF RNA POLYMERASE II ACTIVE SITE AND MECHANISM OF ACTION OF TRANSCRIPTION INHIBITOR THIOLUTIN. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/173208

Chicago Manual of Style (16th Edition):

Qiu, Chenxi. “FUNCTIONAL DISSECTION OF RNA POLYMERASE II ACTIVE SITE AND MECHANISM OF ACTION OF TRANSCRIPTION INHIBITOR THIOLUTIN.” 2017. Doctoral Dissertation, Texas A&M University. Accessed September 23, 2020. http://hdl.handle.net/1969.1/173208.

MLA Handbook (7th Edition):

Qiu, Chenxi. “FUNCTIONAL DISSECTION OF RNA POLYMERASE II ACTIVE SITE AND MECHANISM OF ACTION OF TRANSCRIPTION INHIBITOR THIOLUTIN.” 2017. Web. 23 Sep 2020.

Vancouver:

Qiu C. FUNCTIONAL DISSECTION OF RNA POLYMERASE II ACTIVE SITE AND MECHANISM OF ACTION OF TRANSCRIPTION INHIBITOR THIOLUTIN. [Internet] [Doctoral dissertation]. Texas A&M University; 2017. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1969.1/173208.

Council of Science Editors:

Qiu C. FUNCTIONAL DISSECTION OF RNA POLYMERASE II ACTIVE SITE AND MECHANISM OF ACTION OF TRANSCRIPTION INHIBITOR THIOLUTIN. [Doctoral Dissertation]. Texas A&M University; 2017. Available from: http://hdl.handle.net/1969.1/173208


Vanderbilt University

4. McCann, Tyler Scott. Elucidation of the Biological Function of the RPC Family Ubiquitin Ligase Asr1.

Degree: PhD, Cell and Developmental Biology, 2016, Vanderbilt University

 Proper regulation of gene transcription is an essential process for any cell. Failure to precisely control the procedure of transcription can lead to developmental defects,… (more)

Subjects/Keywords: ubiquitin; silencing; RNA polymerase II; transcription; chromatin

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APA (6th Edition):

McCann, T. S. (2016). Elucidation of the Biological Function of the RPC Family Ubiquitin Ligase Asr1. (Doctoral Dissertation). Vanderbilt University. Retrieved from http://hdl.handle.net/1803/10415

Chicago Manual of Style (16th Edition):

McCann, Tyler Scott. “Elucidation of the Biological Function of the RPC Family Ubiquitin Ligase Asr1.” 2016. Doctoral Dissertation, Vanderbilt University. Accessed September 23, 2020. http://hdl.handle.net/1803/10415.

MLA Handbook (7th Edition):

McCann, Tyler Scott. “Elucidation of the Biological Function of the RPC Family Ubiquitin Ligase Asr1.” 2016. Web. 23 Sep 2020.

Vancouver:

McCann TS. Elucidation of the Biological Function of the RPC Family Ubiquitin Ligase Asr1. [Internet] [Doctoral dissertation]. Vanderbilt University; 2016. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1803/10415.

Council of Science Editors:

McCann TS. Elucidation of the Biological Function of the RPC Family Ubiquitin Ligase Asr1. [Doctoral Dissertation]. Vanderbilt University; 2016. Available from: http://hdl.handle.net/1803/10415


University of California – Berkeley

5. Zamft, Bradley Michael. Single Molecule and Synthetic Biology Studies of Transcription.

Degree: Physics, 2011, University of California – Berkeley

 The horizons of biology are ever expanding, from the discernment of the detailed mechanisms of enzyme function, to the manipulation of the physiological processes of… (more)

Subjects/Keywords: Biophysics; Biology; Mitochondria; RNA Polymerase; RNA Polymerase II; Rpo41; Transcription; Transcriptional Pausing

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APA (6th Edition):

Zamft, B. M. (2011). Single Molecule and Synthetic Biology Studies of Transcription. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/00c6w2pc

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):

Zamft, Bradley Michael. “Single Molecule and Synthetic Biology Studies of Transcription.” 2011. Thesis, University of California – Berkeley. Accessed September 23, 2020. http://www.escholarship.org/uc/item/00c6w2pc.

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

MLA Handbook (7th Edition):

Zamft, Bradley Michael. “Single Molecule and Synthetic Biology Studies of Transcription.” 2011. Web. 23 Sep 2020.

Vancouver:

Zamft BM. Single Molecule and Synthetic Biology Studies of Transcription. [Internet] [Thesis]. University of California – Berkeley; 2011. [cited 2020 Sep 23]. Available from: http://www.escholarship.org/uc/item/00c6w2pc.

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

Council of Science Editors:

Zamft BM. Single Molecule and Synthetic Biology Studies of Transcription. [Thesis]. University of California – Berkeley; 2011. Available from: http://www.escholarship.org/uc/item/00c6w2pc

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

6. Yu, Changwei. Analysis of the composition and the function of oocyte-specific TBP2-containing transcription machinery during mouse oogenesis : Analyse de la composition et de la fonction de la machinerie basale de transcription associée à TBP2 et spécifique des ovocytes au cours de l’ovogenèse murine.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2018, Université de Strasbourg

La synthèse d’ARN au cours de la différenciation des ovocytes est essentielle à la fécondation et à l'initiation du développement précoce. La nature de la… (more)

Subjects/Keywords: TFIID; TBP2; RNA polymerase II; TFIIA; MaLR; Oocytes; TFIID; TBP2; RNA polymerase II; TFIIA; MaLR; Oocytes; 571.86

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APA (6th Edition):

Yu, C. (2018). Analysis of the composition and the function of oocyte-specific TBP2-containing transcription machinery during mouse oogenesis : Analyse de la composition et de la fonction de la machinerie basale de transcription associée à TBP2 et spécifique des ovocytes au cours de l’ovogenèse murine. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2018STRAJ127

Chicago Manual of Style (16th Edition):

Yu, Changwei. “Analysis of the composition and the function of oocyte-specific TBP2-containing transcription machinery during mouse oogenesis : Analyse de la composition et de la fonction de la machinerie basale de transcription associée à TBP2 et spécifique des ovocytes au cours de l’ovogenèse murine.” 2018. Doctoral Dissertation, Université de Strasbourg. Accessed September 23, 2020. http://www.theses.fr/2018STRAJ127.

MLA Handbook (7th Edition):

Yu, Changwei. “Analysis of the composition and the function of oocyte-specific TBP2-containing transcription machinery during mouse oogenesis : Analyse de la composition et de la fonction de la machinerie basale de transcription associée à TBP2 et spécifique des ovocytes au cours de l’ovogenèse murine.” 2018. Web. 23 Sep 2020.

Vancouver:

Yu C. Analysis of the composition and the function of oocyte-specific TBP2-containing transcription machinery during mouse oogenesis : Analyse de la composition et de la fonction de la machinerie basale de transcription associée à TBP2 et spécifique des ovocytes au cours de l’ovogenèse murine. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2018. [cited 2020 Sep 23]. Available from: http://www.theses.fr/2018STRAJ127.

Council of Science Editors:

Yu C. Analysis of the composition and the function of oocyte-specific TBP2-containing transcription machinery during mouse oogenesis : Analyse de la composition et de la fonction de la machinerie basale de transcription associée à TBP2 et spécifique des ovocytes au cours de l’ovogenèse murine. [Doctoral Dissertation]. Université de Strasbourg; 2018. Available from: http://www.theses.fr/2018STRAJ127


Ruhr Universität Bochum

7. Eilebrecht, Sebastian. Identifizierung einer neuen Funktion der 7SK RNA als Regulator der Genexpression.

Degree: 2008, Ruhr Universität Bochum

 In dieser Arbeit wurde die Interaktion einer sn RNA mit dem p20.1-Protein untersucht. Es wurde der direkte Nachweis erbracht, dass die Wechselwirkung in intakten Zellen… (more)

Subjects/Keywords: RNS-Polymerase II; Small nuclear RNA; RNS-Polymerase III; RNS-Bindungsproteine; Genexpression

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APA (6th Edition):

Eilebrecht, S. (2008). Identifizierung einer neuen Funktion der 7SK RNA als Regulator der Genexpression. (Thesis). Ruhr Universität Bochum. Retrieved from http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-28260

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):

Eilebrecht, Sebastian. “Identifizierung einer neuen Funktion der 7SK RNA als Regulator der Genexpression.” 2008. Thesis, Ruhr Universität Bochum. Accessed September 23, 2020. http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-28260.

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

MLA Handbook (7th Edition):

Eilebrecht, Sebastian. “Identifizierung einer neuen Funktion der 7SK RNA als Regulator der Genexpression.” 2008. Web. 23 Sep 2020.

Vancouver:

Eilebrecht S. Identifizierung einer neuen Funktion der 7SK RNA als Regulator der Genexpression. [Internet] [Thesis]. Ruhr Universität Bochum; 2008. [cited 2020 Sep 23]. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-28260.

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

Council of Science Editors:

Eilebrecht S. Identifizierung einer neuen Funktion der 7SK RNA als Regulator der Genexpression. [Thesis]. Ruhr Universität Bochum; 2008. Available from: http://nbn-resolving.de/urn/resolver.pl?urn=urn:nbn:de:hbz:294-28260

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


University of California – Berkeley

8. Kassube, Susanne Anke. Molecular mechanisms of transcription regulation by non-coding RNAs and the DNA helicase RECQL5.

Degree: Biophysics, 2013, University of California – Berkeley

 Transcription is the process of copying a fragment of DNA in the cell's nucleus into RNA. This copy is then used as a template to… (more)

Subjects/Keywords: Biophysics; DNA repair; electron microscopy; helicase; RECQL5; RNA polymerase II; transcription

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APA (6th Edition):

Kassube, S. A. (2013). Molecular mechanisms of transcription regulation by non-coding RNAs and the DNA helicase RECQL5. (Thesis). University of California – Berkeley. Retrieved from http://www.escholarship.org/uc/item/0hs6d20h

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):

Kassube, Susanne Anke. “Molecular mechanisms of transcription regulation by non-coding RNAs and the DNA helicase RECQL5.” 2013. Thesis, University of California – Berkeley. Accessed September 23, 2020. http://www.escholarship.org/uc/item/0hs6d20h.

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

MLA Handbook (7th Edition):

Kassube, Susanne Anke. “Molecular mechanisms of transcription regulation by non-coding RNAs and the DNA helicase RECQL5.” 2013. Web. 23 Sep 2020.

Vancouver:

Kassube SA. Molecular mechanisms of transcription regulation by non-coding RNAs and the DNA helicase RECQL5. [Internet] [Thesis]. University of California – Berkeley; 2013. [cited 2020 Sep 23]. Available from: http://www.escholarship.org/uc/item/0hs6d20h.

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

Council of Science Editors:

Kassube SA. Molecular mechanisms of transcription regulation by non-coding RNAs and the DNA helicase RECQL5. [Thesis]. University of California – Berkeley; 2013. Available from: http://www.escholarship.org/uc/item/0hs6d20h

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


University of California – San Diego

9. Shin, JI. The mechanism of recognition and processing of DNA damage and modifications by RNA polymerase II.

Degree: Biology, 2016, University of California – San Diego

RNA polymerase II (pol II) recognizes many obstacles during transcription elongation, including DNA damage lesions and modifications, via specific interactions and leads to distinct transcriptional… (more)

Subjects/Keywords: Biology; Biochemistry; DNA damage; DNA modifications; RNA polymerase II; transcription

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APA (6th Edition):

Shin, J. (2016). The mechanism of recognition and processing of DNA damage and modifications by RNA polymerase II. (Thesis). University of California – San Diego. Retrieved from http://www.escholarship.org/uc/item/9mn2j734

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):

Shin, JI. “The mechanism of recognition and processing of DNA damage and modifications by RNA polymerase II.” 2016. Thesis, University of California – San Diego. Accessed September 23, 2020. http://www.escholarship.org/uc/item/9mn2j734.

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

MLA Handbook (7th Edition):

Shin, JI. “The mechanism of recognition and processing of DNA damage and modifications by RNA polymerase II.” 2016. Web. 23 Sep 2020.

Vancouver:

Shin J. The mechanism of recognition and processing of DNA damage and modifications by RNA polymerase II. [Internet] [Thesis]. University of California – San Diego; 2016. [cited 2020 Sep 23]. Available from: http://www.escholarship.org/uc/item/9mn2j734.

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

Council of Science Editors:

Shin J. The mechanism of recognition and processing of DNA damage and modifications by RNA polymerase II. [Thesis]. University of California – San Diego; 2016. Available from: http://www.escholarship.org/uc/item/9mn2j734

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


University of California – Irvine

10. Ou, Mark. Searching for RNAP II on the Compact HSV-1 Genome.

Degree: Biological Sciences, 2014, University of California – Irvine

 Herpes Simplex Virus type-1 (HSV-1) is one of the eight human herpes viruses and it causes cold sores in infected individuals. HSV-1 infects epithelial cells,… (more)

Subjects/Keywords: Microbiology; cdk9; ChIP; Herpes Simplex Virus; RNA polymerase II; transcription

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APA (6th Edition):

Ou, M. (2014). Searching for RNAP II on the Compact HSV-1 Genome. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/4186x38f

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):

Ou, Mark. “Searching for RNAP II on the Compact HSV-1 Genome.” 2014. Thesis, University of California – Irvine. Accessed September 23, 2020. http://www.escholarship.org/uc/item/4186x38f.

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

MLA Handbook (7th Edition):

Ou, Mark. “Searching for RNAP II on the Compact HSV-1 Genome.” 2014. Web. 23 Sep 2020.

Vancouver:

Ou M. Searching for RNAP II on the Compact HSV-1 Genome. [Internet] [Thesis]. University of California – Irvine; 2014. [cited 2020 Sep 23]. Available from: http://www.escholarship.org/uc/item/4186x38f.

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

Council of Science Editors:

Ou M. Searching for RNAP II on the Compact HSV-1 Genome. [Thesis]. University of California – Irvine; 2014. Available from: http://www.escholarship.org/uc/item/4186x38f

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


UCLA

11. Alhadid, Yazan Khalaf. Single-molecule studies of different steps in human RNA polymerase II and bacterial RNA polymerase transcription.

Degree: Molec, Cell, & Integ Physiology, 2018, UCLA

 Transcription of genomic DNA of all organisms is carried out by members of the multi-subunit RNA polymerase family. Regulation of RNA polymerase localization and activity… (more)

Subjects/Keywords: Biochemistry; Biophysics; FRET; Pol II; RNA Polymerase; Single-molecule; Transcription

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APA (6th Edition):

Alhadid, Y. K. (2018). Single-molecule studies of different steps in human RNA polymerase II and bacterial RNA polymerase transcription. (Thesis). UCLA. Retrieved from http://www.escholarship.org/uc/item/1d858964

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):

Alhadid, Yazan Khalaf. “Single-molecule studies of different steps in human RNA polymerase II and bacterial RNA polymerase transcription.” 2018. Thesis, UCLA. Accessed September 23, 2020. http://www.escholarship.org/uc/item/1d858964.

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

MLA Handbook (7th Edition):

Alhadid, Yazan Khalaf. “Single-molecule studies of different steps in human RNA polymerase II and bacterial RNA polymerase transcription.” 2018. Web. 23 Sep 2020.

Vancouver:

Alhadid YK. Single-molecule studies of different steps in human RNA polymerase II and bacterial RNA polymerase transcription. [Internet] [Thesis]. UCLA; 2018. [cited 2020 Sep 23]. Available from: http://www.escholarship.org/uc/item/1d858964.

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

Council of Science Editors:

Alhadid YK. Single-molecule studies of different steps in human RNA polymerase II and bacterial RNA polymerase transcription. [Thesis]. UCLA; 2018. Available from: http://www.escholarship.org/uc/item/1d858964

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


Cornell University

12. Kwak, Hojoong. Dissection Of The Precise Mechanisms Of Rna Polymerase Ii Pausing And Elongation Using Nascent Transcript Analysis.

Degree: PhD, Molecular and Cell Biology, 2013, Cornell University

 Limiting RNA polymerase II (Pol II) at various stages of the transcription cycle is critical for gene regulation, which often occurs during the elongation stage… (more)

Subjects/Keywords: RNA polymerase II pausing; Nascent transcript analysis; PRO-seq

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APA (6th Edition):

Kwak, H. (2013). Dissection Of The Precise Mechanisms Of Rna Polymerase Ii Pausing And Elongation Using Nascent Transcript Analysis. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/34251

Chicago Manual of Style (16th Edition):

Kwak, Hojoong. “Dissection Of The Precise Mechanisms Of Rna Polymerase Ii Pausing And Elongation Using Nascent Transcript Analysis.” 2013. Doctoral Dissertation, Cornell University. Accessed September 23, 2020. http://hdl.handle.net/1813/34251.

MLA Handbook (7th Edition):

Kwak, Hojoong. “Dissection Of The Precise Mechanisms Of Rna Polymerase Ii Pausing And Elongation Using Nascent Transcript Analysis.” 2013. Web. 23 Sep 2020.

Vancouver:

Kwak H. Dissection Of The Precise Mechanisms Of Rna Polymerase Ii Pausing And Elongation Using Nascent Transcript Analysis. [Internet] [Doctoral dissertation]. Cornell University; 2013. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1813/34251.

Council of Science Editors:

Kwak H. Dissection Of The Precise Mechanisms Of Rna Polymerase Ii Pausing And Elongation Using Nascent Transcript Analysis. [Doctoral Dissertation]. Cornell University; 2013. Available from: http://hdl.handle.net/1813/34251


Cornell University

13. Fuda, Nicholas. Factors Controlling Promoter-Proximal Pausing By Rna Polymerase Ii.

Degree: PhD, Molecular and Cell Biology, 2012, Cornell University

 Most gene expression is regulated at the level of transcription, and the transition from initiation to productive elongation is a key point of regulation. This… (more)

Subjects/Keywords: promoter-proximal pausing; transcription regulation; RNA polymerase II

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APA (6th Edition):

Fuda, N. (2012). Factors Controlling Promoter-Proximal Pausing By Rna Polymerase Ii. (Doctoral Dissertation). Cornell University. Retrieved from http://hdl.handle.net/1813/31114

Chicago Manual of Style (16th Edition):

Fuda, Nicholas. “Factors Controlling Promoter-Proximal Pausing By Rna Polymerase Ii.” 2012. Doctoral Dissertation, Cornell University. Accessed September 23, 2020. http://hdl.handle.net/1813/31114.

MLA Handbook (7th Edition):

Fuda, Nicholas. “Factors Controlling Promoter-Proximal Pausing By Rna Polymerase Ii.” 2012. Web. 23 Sep 2020.

Vancouver:

Fuda N. Factors Controlling Promoter-Proximal Pausing By Rna Polymerase Ii. [Internet] [Doctoral dissertation]. Cornell University; 2012. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1813/31114.

Council of Science Editors:

Fuda N. Factors Controlling Promoter-Proximal Pausing By Rna Polymerase Ii. [Doctoral Dissertation]. Cornell University; 2012. Available from: http://hdl.handle.net/1813/31114


Penn State University

14. Fisher, Michael James. AN IN VITRO BIOCHEMICAL STUDY OF THE DROSOPHILA NEGATIVE ELONGATION FACTOR.

Degree: 2017, Penn State University

 The concentration of transcriptionally engaged RNA polymerase II (Pol II) at the 5’ ends of genes, a phenomenon called promoter-proximal pausing, is a common mode… (more)

Subjects/Keywords: Transcription; Pausing; NELF; Drosophila; RNA Polymerase II; Gene regulation

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APA (6th Edition):

Fisher, M. J. (2017). AN IN VITRO BIOCHEMICAL STUDY OF THE DROSOPHILA NEGATIVE ELONGATION FACTOR. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/14009mjf346

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):

Fisher, Michael James. “AN IN VITRO BIOCHEMICAL STUDY OF THE DROSOPHILA NEGATIVE ELONGATION FACTOR.” 2017. Thesis, Penn State University. Accessed September 23, 2020. https://submit-etda.libraries.psu.edu/catalog/14009mjf346.

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

MLA Handbook (7th Edition):

Fisher, Michael James. “AN IN VITRO BIOCHEMICAL STUDY OF THE DROSOPHILA NEGATIVE ELONGATION FACTOR.” 2017. Web. 23 Sep 2020.

Vancouver:

Fisher MJ. AN IN VITRO BIOCHEMICAL STUDY OF THE DROSOPHILA NEGATIVE ELONGATION FACTOR. [Internet] [Thesis]. Penn State University; 2017. [cited 2020 Sep 23]. Available from: https://submit-etda.libraries.psu.edu/catalog/14009mjf346.

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

Council of Science Editors:

Fisher MJ. AN IN VITRO BIOCHEMICAL STUDY OF THE DROSOPHILA NEGATIVE ELONGATION FACTOR. [Thesis]. Penn State University; 2017. Available from: https://submit-etda.libraries.psu.edu/catalog/14009mjf346

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


Penn State University

15. Crickard, John B. A BIOCHEMICAL CHARACTERIZATION OF TRANSCRIPTION ELONGATION FACTORS THAT FACILITATE THE PROCESSIVITY OF RNA POLYMERASE II.

Degree: 2016, Penn State University

 The processivity of RNA Polymerase II across the body of a gene is a complex and dynamic process that involves the contribution of many transcription… (more)

Subjects/Keywords: Transcription Elongation; Spt4/5; RNA Polymerase II; Chromatin; Nucleosome; FACT

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APA (6th Edition):

Crickard, J. B. (2016). A BIOCHEMICAL CHARACTERIZATION OF TRANSCRIPTION ELONGATION FACTORS THAT FACILITATE THE PROCESSIVITY OF RNA POLYMERASE II. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/3j333224f

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):

Crickard, John B. “A BIOCHEMICAL CHARACTERIZATION OF TRANSCRIPTION ELONGATION FACTORS THAT FACILITATE THE PROCESSIVITY OF RNA POLYMERASE II.” 2016. Thesis, Penn State University. Accessed September 23, 2020. https://submit-etda.libraries.psu.edu/catalog/3j333224f.

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

MLA Handbook (7th Edition):

Crickard, John B. “A BIOCHEMICAL CHARACTERIZATION OF TRANSCRIPTION ELONGATION FACTORS THAT FACILITATE THE PROCESSIVITY OF RNA POLYMERASE II.” 2016. Web. 23 Sep 2020.

Vancouver:

Crickard JB. A BIOCHEMICAL CHARACTERIZATION OF TRANSCRIPTION ELONGATION FACTORS THAT FACILITATE THE PROCESSIVITY OF RNA POLYMERASE II. [Internet] [Thesis]. Penn State University; 2016. [cited 2020 Sep 23]. Available from: https://submit-etda.libraries.psu.edu/catalog/3j333224f.

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

Council of Science Editors:

Crickard JB. A BIOCHEMICAL CHARACTERIZATION OF TRANSCRIPTION ELONGATION FACTORS THAT FACILITATE THE PROCESSIVITY OF RNA POLYMERASE II. [Thesis]. Penn State University; 2016. Available from: https://submit-etda.libraries.psu.edu/catalog/3j333224f

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


University of Texas Southwestern Medical Center

16. Wang, Yi. Regulatory Mechanisms for the Pol II Associated Histone Methyltransferase Set2.

Degree: 2014, University of Texas Southwestern Medical Center

 Nucleosomes are building blocks of the eukaryotic chromatin which package genomic DNA with histones. The modification patterns of histones constitute an important signaling pathway for… (more)

Subjects/Keywords: Chromatin; Histone-Lysine N-Methyltransferase; RNA Polymerase II; Transcription, Genetic

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APA (6th Edition):

Wang, Y. (2014). Regulatory Mechanisms for the Pol II Associated Histone Methyltransferase Set2. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/3943

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. “Regulatory Mechanisms for the Pol II Associated Histone Methyltransferase Set2.” 2014. Thesis, University of Texas Southwestern Medical Center. Accessed September 23, 2020. http://hdl.handle.net/2152.5/3943.

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. “Regulatory Mechanisms for the Pol II Associated Histone Methyltransferase Set2.” 2014. Web. 23 Sep 2020.

Vancouver:

Wang Y. Regulatory Mechanisms for the Pol II Associated Histone Methyltransferase Set2. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2014. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/2152.5/3943.

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. Regulatory Mechanisms for the Pol II Associated Histone Methyltransferase Set2. [Thesis]. University of Texas Southwestern Medical Center; 2014. Available from: http://hdl.handle.net/2152.5/3943

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

17. Samarakkody, Ann Sanoji. Molecular Mechanisms Regulating Rna Polymerase Ii Pausing During Gene Activation.

Degree: PhD, Biomedical Sciences, 2017, University of North Dakota

RNA Polymerase II (Pol II), the enzyme that transcribes all messenger RNAs (mRNAs) has another activity by pausing at gene promoters. The paused Pol… (more)

Subjects/Keywords: gene activation; heat shock response; pause duration; RNA Polymerase II pausing

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

APA (6th Edition):

Samarakkody, A. S. (2017). Molecular Mechanisms Regulating Rna Polymerase Ii Pausing During Gene Activation. (Doctoral Dissertation). University of North Dakota. Retrieved from https://commons.und.edu/theses/2142

Chicago Manual of Style (16th Edition):

Samarakkody, Ann Sanoji. “Molecular Mechanisms Regulating Rna Polymerase Ii Pausing During Gene Activation.” 2017. Doctoral Dissertation, University of North Dakota. Accessed September 23, 2020. https://commons.und.edu/theses/2142.

MLA Handbook (7th Edition):

Samarakkody, Ann Sanoji. “Molecular Mechanisms Regulating Rna Polymerase Ii Pausing During Gene Activation.” 2017. Web. 23 Sep 2020.

Vancouver:

Samarakkody AS. Molecular Mechanisms Regulating Rna Polymerase Ii Pausing During Gene Activation. [Internet] [Doctoral dissertation]. University of North Dakota; 2017. [cited 2020 Sep 23]. Available from: https://commons.und.edu/theses/2142.

Council of Science Editors:

Samarakkody AS. Molecular Mechanisms Regulating Rna Polymerase Ii Pausing During Gene Activation. [Doctoral Dissertation]. University of North Dakota; 2017. Available from: https://commons.und.edu/theses/2142


University of Texas Southwestern Medical Center

18. Tastemel, Melodi Damla. Regulation of Transcription Through RNA Polymerase II Promoter-Proximal Pausing.

Degree: 2018, University of Texas Southwestern Medical Center

Note: The general metadata  – e.g., title, author, abstract, subject headings, etc.  – is publicly available, but access to the submitted files is restricted to… (more)

Subjects/Keywords: Cell Differentiation; Mouse Embryonic Stem Cells; RNA Polymerase II; Transcription, Genetic

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APA (6th Edition):

Tastemel, M. D. (2018). Regulation of Transcription Through RNA Polymerase II Promoter-Proximal Pausing. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/8342

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):

Tastemel, Melodi Damla. “Regulation of Transcription Through RNA Polymerase II Promoter-Proximal Pausing.” 2018. Thesis, University of Texas Southwestern Medical Center. Accessed September 23, 2020. http://hdl.handle.net/2152.5/8342.

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

MLA Handbook (7th Edition):

Tastemel, Melodi Damla. “Regulation of Transcription Through RNA Polymerase II Promoter-Proximal Pausing.” 2018. Web. 23 Sep 2020.

Vancouver:

Tastemel MD. Regulation of Transcription Through RNA Polymerase II Promoter-Proximal Pausing. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2018. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/2152.5/8342.

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

Council of Science Editors:

Tastemel MD. Regulation of Transcription Through RNA Polymerase II Promoter-Proximal Pausing. [Thesis]. University of Texas Southwestern Medical Center; 2018. Available from: http://hdl.handle.net/2152.5/8342

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


University of Colorado

19. Gao, Yuefeng. Biochemical Characterization of the Human Mediator Complex.

Degree: MS, Chemistry & Biochemistry, 2010, University of Colorado

RNA polymerase II coordinates with a wide range of factors and catalyzes DNA transcription to synthesize mRNA. One critical step of transcription initiation is… (more)

Subjects/Keywords: Mediator complexes; DNA transcription; RNA polymerase II; Biochemistry; Genetics and Genomics

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

APA (6th Edition):

Gao, Y. (2010). Biochemical Characterization of the Human Mediator Complex. (Masters Thesis). University of Colorado. Retrieved from https://scholar.colorado.edu/chem_gradetds/16

Chicago Manual of Style (16th Edition):

Gao, Yuefeng. “Biochemical Characterization of the Human Mediator Complex.” 2010. Masters Thesis, University of Colorado. Accessed September 23, 2020. https://scholar.colorado.edu/chem_gradetds/16.

MLA Handbook (7th Edition):

Gao, Yuefeng. “Biochemical Characterization of the Human Mediator Complex.” 2010. Web. 23 Sep 2020.

Vancouver:

Gao Y. Biochemical Characterization of the Human Mediator Complex. [Internet] [Masters thesis]. University of Colorado; 2010. [cited 2020 Sep 23]. Available from: https://scholar.colorado.edu/chem_gradetds/16.

Council of Science Editors:

Gao Y. Biochemical Characterization of the Human Mediator Complex. [Masters Thesis]. University of Colorado; 2010. Available from: https://scholar.colorado.edu/chem_gradetds/16


University of Oxford

20. Skourti-Stathaki, Konstantina. Role of R-loops in pause-dependent transcriptional termination of RNA polymerase II.

Degree: PhD, 2012, University of Oxford

 Transcription termination of RNA polymerase II (Pol II) in mammals requires a functional poly(A) signal and either downstream pause sites or co-transcriptional cleavage (CoTC) sequences… (more)

Subjects/Keywords: 572.8; Biology (medical sciences); termination; R-loops; RNA polymerase II; pause

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APA (6th Edition):

Skourti-Stathaki, K. (2012). Role of R-loops in pause-dependent transcriptional termination of RNA polymerase II. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:977b94b3-529a-4639-9126-e2d3707c3bba ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.580974

Chicago Manual of Style (16th Edition):

Skourti-Stathaki, Konstantina. “Role of R-loops in pause-dependent transcriptional termination of RNA polymerase II.” 2012. Doctoral Dissertation, University of Oxford. Accessed September 23, 2020. http://ora.ox.ac.uk/objects/uuid:977b94b3-529a-4639-9126-e2d3707c3bba ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.580974.

MLA Handbook (7th Edition):

Skourti-Stathaki, Konstantina. “Role of R-loops in pause-dependent transcriptional termination of RNA polymerase II.” 2012. Web. 23 Sep 2020.

Vancouver:

Skourti-Stathaki K. Role of R-loops in pause-dependent transcriptional termination of RNA polymerase II. [Internet] [Doctoral dissertation]. University of Oxford; 2012. [cited 2020 Sep 23]. Available from: http://ora.ox.ac.uk/objects/uuid:977b94b3-529a-4639-9126-e2d3707c3bba ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.580974.

Council of Science Editors:

Skourti-Stathaki K. Role of R-loops in pause-dependent transcriptional termination of RNA polymerase II. [Doctoral Dissertation]. University of Oxford; 2012. Available from: http://ora.ox.ac.uk/objects/uuid:977b94b3-529a-4639-9126-e2d3707c3bba ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.580974


Purdue University

21. Zhang, Yueping. The Role of the Set1 RNA Polymerase II Interacting Motif (SRIM) in Set1 Recruitment and Histone H3K4 Methylation.

Degree: PhD, Biochemistry, 2016, Purdue University

 In eukaryotes, gene expression is regulated by epigenetic modifications. Among these modifications, histone H3 lysine 4 (H3K4) methylation has been associated with transcription activation. Set1… (more)

Subjects/Keywords: CTD; H3K4 methylation; N-ICE plasmid; Paf1; RNA polymerase II; Set1

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APA (6th Edition):

Zhang, Y. (2016). The Role of the Set1 RNA Polymerase II Interacting Motif (SRIM) in Set1 Recruitment and Histone H3K4 Methylation. (Doctoral Dissertation). Purdue University. Retrieved from https://docs.lib.purdue.edu/open_access_dissertations/1236

Chicago Manual of Style (16th Edition):

Zhang, Yueping. “The Role of the Set1 RNA Polymerase II Interacting Motif (SRIM) in Set1 Recruitment and Histone H3K4 Methylation.” 2016. Doctoral Dissertation, Purdue University. Accessed September 23, 2020. https://docs.lib.purdue.edu/open_access_dissertations/1236.

MLA Handbook (7th Edition):

Zhang, Yueping. “The Role of the Set1 RNA Polymerase II Interacting Motif (SRIM) in Set1 Recruitment and Histone H3K4 Methylation.” 2016. Web. 23 Sep 2020.

Vancouver:

Zhang Y. The Role of the Set1 RNA Polymerase II Interacting Motif (SRIM) in Set1 Recruitment and Histone H3K4 Methylation. [Internet] [Doctoral dissertation]. Purdue University; 2016. [cited 2020 Sep 23]. Available from: https://docs.lib.purdue.edu/open_access_dissertations/1236.

Council of Science Editors:

Zhang Y. The Role of the Set1 RNA Polymerase II Interacting Motif (SRIM) in Set1 Recruitment and Histone H3K4 Methylation. [Doctoral Dissertation]. Purdue University; 2016. Available from: https://docs.lib.purdue.edu/open_access_dissertations/1236


IUPUI

22. McCracken, Neil Andrew. The impact of the termination override mutation on the activity of SSU72.

Degree: 2016, IUPUI

Indiana University-Purdue University Indianapolis (IUPUI)

Ssu72, an RNA Pol II CTD phosphatase that is conserved across eukaryotes, has been reported to have a wide array… (more)

Subjects/Keywords: Ssu72; CTD; Transcription; L84F; L84A; RNA Polymerase II

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APA (6th Edition):

McCracken, N. A. (2016). The impact of the termination override mutation on the activity of SSU72. (Thesis). IUPUI. Retrieved from http://hdl.handle.net/1805/11873

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):

McCracken, Neil Andrew. “The impact of the termination override mutation on the activity of SSU72.” 2016. Thesis, IUPUI. Accessed September 23, 2020. http://hdl.handle.net/1805/11873.

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

MLA Handbook (7th Edition):

McCracken, Neil Andrew. “The impact of the termination override mutation on the activity of SSU72.” 2016. Web. 23 Sep 2020.

Vancouver:

McCracken NA. The impact of the termination override mutation on the activity of SSU72. [Internet] [Thesis]. IUPUI; 2016. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/1805/11873.

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

Council of Science Editors:

McCracken NA. The impact of the termination override mutation on the activity of SSU72. [Thesis]. IUPUI; 2016. Available from: http://hdl.handle.net/1805/11873

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


Duke University

23. MacKellar, April. Characterization of the Association of mRNA Export Factor Yra1 with the C-terminal Domain of RNA Polymerase II in vivo and in vitro .

Degree: 2011, Duke University

  The unique C-terminal domain (CTD) of RNA polymerase II (RNAPII), composed of tandem heptad repeats of the consensus sequence YSPTSPS, is subject to differential… (more)

Subjects/Keywords: Biochemistry; mRNA export; mRNA transcription; RNA polymerase II; yeast; Yra1

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APA (6th Edition):

MacKellar, A. (2011). Characterization of the Association of mRNA Export Factor Yra1 with the C-terminal Domain of RNA Polymerase II in vivo and in vitro . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/5704

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):

MacKellar, April. “Characterization of the Association of mRNA Export Factor Yra1 with the C-terminal Domain of RNA Polymerase II in vivo and in vitro .” 2011. Thesis, Duke University. Accessed September 23, 2020. http://hdl.handle.net/10161/5704.

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

MLA Handbook (7th Edition):

MacKellar, April. “Characterization of the Association of mRNA Export Factor Yra1 with the C-terminal Domain of RNA Polymerase II in vivo and in vitro .” 2011. Web. 23 Sep 2020.

Vancouver:

MacKellar A. Characterization of the Association of mRNA Export Factor Yra1 with the C-terminal Domain of RNA Polymerase II in vivo and in vitro . [Internet] [Thesis]. Duke University; 2011. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/10161/5704.

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

Council of Science Editors:

MacKellar A. Characterization of the Association of mRNA Export Factor Yra1 with the C-terminal Domain of RNA Polymerase II in vivo and in vitro . [Thesis]. Duke University; 2011. Available from: http://hdl.handle.net/10161/5704

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


Duquesne University

24. Adamik, Juraj. Molecular Insights into the Distinct Mechanisms Regulating the TLR4 Mediated Activation, Shut Down, and Endotoxin Tolerance of the IL1B and TNF Genes.

Degree: PhD, Biological Sciences, 2013, Duquesne University

 The first wave of the inducible gene network up-regulated by pathogen-stimulated mononuclear cells encodes a variety of effector proteins with pleitropic biological activities. This class… (more)

Subjects/Keywords: Chromatin; IL1B; Immediate early; RNA Polymerase II; TNF; Transcription

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APA (6th Edition):

Adamik, J. (2013). Molecular Insights into the Distinct Mechanisms Regulating the TLR4 Mediated Activation, Shut Down, and Endotoxin Tolerance of the IL1B and TNF Genes. (Doctoral Dissertation). Duquesne University. Retrieved from https://dsc.duq.edu/etd/283

Chicago Manual of Style (16th Edition):

Adamik, Juraj. “Molecular Insights into the Distinct Mechanisms Regulating the TLR4 Mediated Activation, Shut Down, and Endotoxin Tolerance of the IL1B and TNF Genes.” 2013. Doctoral Dissertation, Duquesne University. Accessed September 23, 2020. https://dsc.duq.edu/etd/283.

MLA Handbook (7th Edition):

Adamik, Juraj. “Molecular Insights into the Distinct Mechanisms Regulating the TLR4 Mediated Activation, Shut Down, and Endotoxin Tolerance of the IL1B and TNF Genes.” 2013. Web. 23 Sep 2020.

Vancouver:

Adamik J. Molecular Insights into the Distinct Mechanisms Regulating the TLR4 Mediated Activation, Shut Down, and Endotoxin Tolerance of the IL1B and TNF Genes. [Internet] [Doctoral dissertation]. Duquesne University; 2013. [cited 2020 Sep 23]. Available from: https://dsc.duq.edu/etd/283.

Council of Science Editors:

Adamik J. Molecular Insights into the Distinct Mechanisms Regulating the TLR4 Mediated Activation, Shut Down, and Endotoxin Tolerance of the IL1B and TNF Genes. [Doctoral Dissertation]. Duquesne University; 2013. Available from: https://dsc.duq.edu/etd/283


University of Georgia

25. Ekanayake, Dilrukshi Kumari. Epigenetic regulation of transcription and virulence in Trypanosoma cruzi by O-linked thymidine glucosylation of DNA.

Degree: 2014, University of Georgia

 In trypanosomes, unlike most eukaryotes, genes transcribed by RNA polymerase II (Pol II) are arranged in polycistronic transcription units (PTUs). Based on this organization, it… (more)

Subjects/Keywords: Trypanosomes; Base J; Gene expression; Chromatin; RNA polymerase II

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APA (6th Edition):

Ekanayake, D. K. (2014). Epigenetic regulation of transcription and virulence in Trypanosoma cruzi by O-linked thymidine glucosylation of DNA. (Thesis). University of Georgia. Retrieved from http://hdl.handle.net/10724/27441

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):

Ekanayake, Dilrukshi Kumari. “Epigenetic regulation of transcription and virulence in Trypanosoma cruzi by O-linked thymidine glucosylation of DNA.” 2014. Thesis, University of Georgia. Accessed September 23, 2020. http://hdl.handle.net/10724/27441.

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

MLA Handbook (7th Edition):

Ekanayake, Dilrukshi Kumari. “Epigenetic regulation of transcription and virulence in Trypanosoma cruzi by O-linked thymidine glucosylation of DNA.” 2014. Web. 23 Sep 2020.

Vancouver:

Ekanayake DK. Epigenetic regulation of transcription and virulence in Trypanosoma cruzi by O-linked thymidine glucosylation of DNA. [Internet] [Thesis]. University of Georgia; 2014. [cited 2020 Sep 23]. Available from: http://hdl.handle.net/10724/27441.

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

Council of Science Editors:

Ekanayake DK. Epigenetic regulation of transcription and virulence in Trypanosoma cruzi by O-linked thymidine glucosylation of DNA. [Thesis]. University of Georgia; 2014. Available from: http://hdl.handle.net/10724/27441

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


Indian Institute of Science

26. Deshpande, Swati. Study Of Rpb4, A Component Of RNA Polymerase II As A Coordinator Of Transcription Initiation And Elongation In S. Cerevisiae.

Degree: PhD, Faculty of Science, 2017, Indian Institute of Science

RNA polymerase II (Pol II) is the enzyme responsible for the synthesis of all mRNAs in eukaryotic cells. As the central component of the eukaryotic… (more)

Subjects/Keywords: Yeast Genetics; RNA Polymerase; Saccharomyces cerevisiae; RNA Transcription; Rpb4; RNA Polymerase II; Rpb1 Protein-C-Terminal Domain Phosphorylation; Genetic Transcription; Rpb1-CTD; RNA Pol II; Biochemical Genetics

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APA (6th Edition):

Deshpande, S. (2017). Study Of Rpb4, A Component Of RNA Polymerase II As A Coordinator Of Transcription Initiation And Elongation In S. Cerevisiae. (Doctoral Dissertation). Indian Institute of Science. Retrieved from http://etd.iisc.ac.in/handle/2005/2624

Chicago Manual of Style (16th Edition):

Deshpande, Swati. “Study Of Rpb4, A Component Of RNA Polymerase II As A Coordinator Of Transcription Initiation And Elongation In S. Cerevisiae.” 2017. Doctoral Dissertation, Indian Institute of Science. Accessed September 23, 2020. http://etd.iisc.ac.in/handle/2005/2624.

MLA Handbook (7th Edition):

Deshpande, Swati. “Study Of Rpb4, A Component Of RNA Polymerase II As A Coordinator Of Transcription Initiation And Elongation In S. Cerevisiae.” 2017. Web. 23 Sep 2020.

Vancouver:

Deshpande S. Study Of Rpb4, A Component Of RNA Polymerase II As A Coordinator Of Transcription Initiation And Elongation In S. Cerevisiae. [Internet] [Doctoral dissertation]. Indian Institute of Science; 2017. [cited 2020 Sep 23]. Available from: http://etd.iisc.ac.in/handle/2005/2624.

Council of Science Editors:

Deshpande S. Study Of Rpb4, A Component Of RNA Polymerase II As A Coordinator Of Transcription Initiation And Elongation In S. Cerevisiae. [Doctoral Dissertation]. Indian Institute of Science; 2017. Available from: http://etd.iisc.ac.in/handle/2005/2624

27. Vosnakis, Nikolaos. Investigating the role of human HAT (histone acetyltransferase) containing complexes, ATAC and SAGA, in living cells : Etude du rôle des complexes HAT (histone acetyltransferase) humains, ATAC et SAGA, dans les cellules vivantes.

Degree: Docteur es, Aspects moléculaires et cellulaires de la biologie, 2014, Université de Strasbourg

Les complexes acétyltransférases (HAT), SAGA et ATAC, sont des régulateurs de la transcription des gènes. Cependant, peu d’études ont été menées sur la dynamique de… (more)

Subjects/Keywords: Transcription; ARN polymerase II; ATAC; SAGA; Acetyltransferase; Chromatine; Transcription; RNA polymerase II; ATAC; SAGA; Acetyltransferase; Chromatin; Fluorescence microscopy; Quantitative proteomics; 572.8

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APA (6th Edition):

Vosnakis, N. (2014). Investigating the role of human HAT (histone acetyltransferase) containing complexes, ATAC and SAGA, in living cells : Etude du rôle des complexes HAT (histone acetyltransferase) humains, ATAC et SAGA, dans les cellules vivantes. (Doctoral Dissertation). Université de Strasbourg. Retrieved from http://www.theses.fr/2014STRAJ119

Chicago Manual of Style (16th Edition):

Vosnakis, Nikolaos. “Investigating the role of human HAT (histone acetyltransferase) containing complexes, ATAC and SAGA, in living cells : Etude du rôle des complexes HAT (histone acetyltransferase) humains, ATAC et SAGA, dans les cellules vivantes.” 2014. Doctoral Dissertation, Université de Strasbourg. Accessed September 23, 2020. http://www.theses.fr/2014STRAJ119.

MLA Handbook (7th Edition):

Vosnakis, Nikolaos. “Investigating the role of human HAT (histone acetyltransferase) containing complexes, ATAC and SAGA, in living cells : Etude du rôle des complexes HAT (histone acetyltransferase) humains, ATAC et SAGA, dans les cellules vivantes.” 2014. Web. 23 Sep 2020.

Vancouver:

Vosnakis N. Investigating the role of human HAT (histone acetyltransferase) containing complexes, ATAC and SAGA, in living cells : Etude du rôle des complexes HAT (histone acetyltransferase) humains, ATAC et SAGA, dans les cellules vivantes. [Internet] [Doctoral dissertation]. Université de Strasbourg; 2014. [cited 2020 Sep 23]. Available from: http://www.theses.fr/2014STRAJ119.

Council of Science Editors:

Vosnakis N. Investigating the role of human HAT (histone acetyltransferase) containing complexes, ATAC and SAGA, in living cells : Etude du rôle des complexes HAT (histone acetyltransferase) humains, ATAC et SAGA, dans les cellules vivantes. [Doctoral Dissertation]. Université de Strasbourg; 2014. Available from: http://www.theses.fr/2014STRAJ119

28. Quintin, Justine. Organisation de la chromatine et signalisation par les oestrogènes : Impact of the chromatine organization in transcriptional regulation mediated by estrogen receptor.

Degree: Docteur es, Biologie, 2013, Rennes 1; Université européenne de Bretagne

En réponse à son environnement composé de signaux endogènes et exogènes, une cellule doit pouvoir adapter son transcriptome, et cela à travers une modulation fine… (more)

Subjects/Keywords: Adn; Transcription; ARN polymerase II; Régulation; Oestrogènes; Chromatine; DNA; Estrogen; RNA polymerase II; Chromatin; Genetic transcription

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

APA (6th Edition):

Quintin, J. (2013). Organisation de la chromatine et signalisation par les oestrogènes : Impact of the chromatine organization in transcriptional regulation mediated by estrogen receptor. (Doctoral Dissertation). Rennes 1; Université européenne de Bretagne. Retrieved from http://www.theses.fr/2013REN1S074

Chicago Manual of Style (16th Edition):

Quintin, Justine. “Organisation de la chromatine et signalisation par les oestrogènes : Impact of the chromatine organization in transcriptional regulation mediated by estrogen receptor.” 2013. Doctoral Dissertation, Rennes 1; Université européenne de Bretagne. Accessed September 23, 2020. http://www.theses.fr/2013REN1S074.

MLA Handbook (7th Edition):

Quintin, Justine. “Organisation de la chromatine et signalisation par les oestrogènes : Impact of the chromatine organization in transcriptional regulation mediated by estrogen receptor.” 2013. Web. 23 Sep 2020.

Vancouver:

Quintin J. Organisation de la chromatine et signalisation par les oestrogènes : Impact of the chromatine organization in transcriptional regulation mediated by estrogen receptor. [Internet] [Doctoral dissertation]. Rennes 1; Université européenne de Bretagne; 2013. [cited 2020 Sep 23]. Available from: http://www.theses.fr/2013REN1S074.

Council of Science Editors:

Quintin J. Organisation de la chromatine et signalisation par les oestrogènes : Impact of the chromatine organization in transcriptional regulation mediated by estrogen receptor. [Doctoral Dissertation]. Rennes 1; Université européenne de Bretagne; 2013. Available from: http://www.theses.fr/2013REN1S074

29. Descostes, Nicolas. Analyse bioinformatique des modifications post-traductionnelles du domaine carboxyl-terminal de l'Arn polymérase II : Bioinformatic analysis of post-translational modifications of the carboxy-terminal domain of RNA polymerase II.

Degree: Docteur es, Biologie. Bioinformatique et génomique, 2014, Aix Marseille Université

Le processus transcriptionnel par l'ARN polymérase II (Pol II) chez les eucaryotes se déroule en trois étapes : L'initiation, l'élongation et la terminaison. De nombreux… (more)

Subjects/Keywords: ARN Polymerase II; Transcription; Ctd; Bioinformatique; Séquençage; Chip-Seq; Rna-Seq; Génomique; RNA polymerase II; Transcription; Ctd; Bioinformatics; Sequencing; Chip-Seq; Rna-Seq; Genomics; 570

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

APA (6th Edition):

Descostes, N. (2014). Analyse bioinformatique des modifications post-traductionnelles du domaine carboxyl-terminal de l'Arn polymérase II : Bioinformatic analysis of post-translational modifications of the carboxy-terminal domain of RNA polymerase II. (Doctoral Dissertation). Aix Marseille Université. Retrieved from http://www.theses.fr/2014AIXM4089

Chicago Manual of Style (16th Edition):

Descostes, Nicolas. “Analyse bioinformatique des modifications post-traductionnelles du domaine carboxyl-terminal de l'Arn polymérase II : Bioinformatic analysis of post-translational modifications of the carboxy-terminal domain of RNA polymerase II.” 2014. Doctoral Dissertation, Aix Marseille Université. Accessed September 23, 2020. http://www.theses.fr/2014AIXM4089.

MLA Handbook (7th Edition):

Descostes, Nicolas. “Analyse bioinformatique des modifications post-traductionnelles du domaine carboxyl-terminal de l'Arn polymérase II : Bioinformatic analysis of post-translational modifications of the carboxy-terminal domain of RNA polymerase II.” 2014. Web. 23 Sep 2020.

Vancouver:

Descostes N. Analyse bioinformatique des modifications post-traductionnelles du domaine carboxyl-terminal de l'Arn polymérase II : Bioinformatic analysis of post-translational modifications of the carboxy-terminal domain of RNA polymerase II. [Internet] [Doctoral dissertation]. Aix Marseille Université 2014. [cited 2020 Sep 23]. Available from: http://www.theses.fr/2014AIXM4089.

Council of Science Editors:

Descostes N. Analyse bioinformatique des modifications post-traductionnelles du domaine carboxyl-terminal de l'Arn polymérase II : Bioinformatic analysis of post-translational modifications of the carboxy-terminal domain of RNA polymerase II. [Doctoral Dissertation]. Aix Marseille Université 2014. Available from: http://www.theses.fr/2014AIXM4089


Penn State University

30. Portz, Bede. STRUCTURAL HETEROGENEITY IN THE RNA POLYMERASE II C-TERMINAL DOMAIN.

Degree: 2017, Penn State University

RNA polymerase II contains a repetitive and intrinsically disordered C-Terminal Domain (CTD) composed of heptad repeats of the consensus sequence YSPTSPS. The CTD can be… (more)

Subjects/Keywords: transcription; gene regulation; RNA Polymerase II; RNA Pol II; Pol II; Pol II CTD; CTD; C-terminal domain; small angle X-ray scattering; SAXS; intrinsically disordered protein; IDP

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

APA (6th Edition):

Portz, B. (2017). STRUCTURAL HETEROGENEITY IN THE RNA POLYMERASE II C-TERMINAL DOMAIN. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/14228bzp105

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):

Portz, Bede. “STRUCTURAL HETEROGENEITY IN THE RNA POLYMERASE II C-TERMINAL DOMAIN.” 2017. Thesis, Penn State University. Accessed September 23, 2020. https://submit-etda.libraries.psu.edu/catalog/14228bzp105.

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

MLA Handbook (7th Edition):

Portz, Bede. “STRUCTURAL HETEROGENEITY IN THE RNA POLYMERASE II C-TERMINAL DOMAIN.” 2017. Web. 23 Sep 2020.

Vancouver:

Portz B. STRUCTURAL HETEROGENEITY IN THE RNA POLYMERASE II C-TERMINAL DOMAIN. [Internet] [Thesis]. Penn State University; 2017. [cited 2020 Sep 23]. Available from: https://submit-etda.libraries.psu.edu/catalog/14228bzp105.

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

Council of Science Editors:

Portz B. STRUCTURAL HETEROGENEITY IN THE RNA POLYMERASE II C-TERMINAL DOMAIN. [Thesis]. Penn State University; 2017. Available from: https://submit-etda.libraries.psu.edu/catalog/14228bzp105

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

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