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You searched for subject:(DNA polymerase). Showing records 1 – 30 of 470 total matches.

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1. Sahashi, Ritsuko. Cell biological and genetical studies on DNA replication enzyme and protein modification enzyme in Drosophila : ショウジョウバエ DNA 複製酵素及びタンパク質修飾酵素の細胞生物学・遺伝学的解析.

Degree: 博士(学術), 2014, Kyoto Institute of Technology / 京都工芸繊維大学

DNAポリメラーゼα,δ,そしてε(polα, polδ,polε)はゲノムのDNA合成を行う酵素である。polαがRNAプライマーとそれに引き続く20〜30塩基のDNAを合成し、その後、polαと置き換わったpolδ,polεが、それぞれ、ラギング鎖、リーディング鎖の合成を行うことがわかっている。先行研究によりpolαと相互作用する因子の1つとして、ヒストンH4の20番目のリジン残基(H4-K20)をモノメチル化する酵素であるPr-Set7が同定された。第1章において、私はDNA複製とヒストンH4-K20メチル化との関係及び、polαとPr-Set7の相互作用について注目をした。翅原基特異的にショウジョウバエpolαの触媒サブユニットであるpolα180kDaサブユニット(dpolαp180)をノックダウンすると成虫翅の萎縮(atrophied wing表現型)が見られdpolαp180とdPr-Set7のダブルノックダウン系統では、atrophied wing表現型の増強が見られた。また、dpolαp180ノックダウン系統の翅原基でのDNA合成をモニターするためBrdU incorporation assayを行なった結果、BrdU ポジティブな細胞数に減少がみられ、dpolαp180とdPr-Set7のダブルノックダウン系統では、BrdU ポジティブな細胞数は、さらに減少した。これらのことより、個体レベルでも両者の機能的関連が示唆され、dPr-Set7がdpolαとの相互作用を介してDNA複製の制御に関与することが示唆された。また、dpolαp180をノックダウンした翅原基における抗H4-K20モノメチル化抗体を用いた免疫染色法の結果、H4-K20モノメチル化のシグナルが減少するこを明らかにした。このことより、Pr-Set7のメチル化活性制御にdpolαが重要な働きを担っている可能性が示された。 2章では、ショウジョウバエpolεの58 kDサブユニット(dpolεp58)の機能解析を行った。polεはヘテロ4量体タンパク質であることが報告されているが、ショウジョウバエでは、現在のところ、触媒サブユニットである255 kD (dpolεp255)サブユニットと、2番目サブユニットのdpolεp58サブユニットが同定されている。dpolεp58変異系統は、蛹で致死となり、3齢幼虫の成虫原基や唾腺が野生型と比較して小型化していた。これらのことからdpolεp58が組織の成長、細胞増殖および生存に必須であると示唆された。dpolεp58変異系統3齢幼虫の複眼原基では、形態形成溝の後極側におけるBrdUの取り込みが減少し、通常は増殖が停止し、分化している後極側の細胞でM期のシグナルが増加していた。S期の遅延が引き起こされたため、後極側の細胞におけるM期のシグナルが増加したと考えられる。これらの結果より、dpolεp58がS期の進行に関与している事が明らかとなった。また、唾腺の核が野生型と比較して小型化している事が観察され、dpolεp58のendoreplicationへの関与も示唆された。さらに、変異系統を用いて他の複製関連因子の抗体でウエスタン免疫ブロットを行った結果、複製開始因子であるdOrc2レベルの顕著な減少が見られた。このことからdpolεp58とdOrc2が細胞内で相互作用する可能性が示めされ、これらのことよりpolεが複製開始に関与することが示唆された。 第3章では、ショウジョウバエの発生において、私は、ショウジョウバエトランスグルタミナーゼ B(dTG-B)の働きを理解することを目的にdTG-B過剰発現系統を用いてその表現型の解析を行った。トランスグルタミナーゼ(TG)は、タンパク質間の架橋反応を触媒するタンパク質間翻訳後酵素で、様々な生物学的プロセスに関わっている。ショウジョウバエトランスグルタミナーゼの遺伝子は1種類で、A型とB型の2種類の転写産物が作られる。dTG-B過剰発現系統では、rough eye表現型と翅脈の過形成が観察された。これらの表現型は、先行研究により報告されているトランスグルタミナーゼA(dTG-A)の過剰発現系統において観察された表現型と同様であり、これらの結果からdTG-Aだけでなく、dTG-Bも複眼の形成と翅脈の形成において、その制御に関わっていることが示唆された。

Subjects/Keywords: DNA replication; DNA polymerase; Transglutaminase

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APA (6th Edition):

Sahashi, R. (2014). Cell biological and genetical studies on DNA replication enzyme and protein modification enzyme in Drosophila : ショウジョウバエ DNA 複製酵素及びタンパク質修飾酵素の細胞生物学・遺伝学的解析. (Thesis). Kyoto Institute of Technology / 京都工芸繊維大学. Retrieved from http://hdl.handle.net/10212/2155

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):

Sahashi, Ritsuko. “Cell biological and genetical studies on DNA replication enzyme and protein modification enzyme in Drosophila : ショウジョウバエ DNA 複製酵素及びタンパク質修飾酵素の細胞生物学・遺伝学的解析.” 2014. Thesis, Kyoto Institute of Technology / 京都工芸繊維大学. Accessed September 28, 2020. http://hdl.handle.net/10212/2155.

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

MLA Handbook (7th Edition):

Sahashi, Ritsuko. “Cell biological and genetical studies on DNA replication enzyme and protein modification enzyme in Drosophila : ショウジョウバエ DNA 複製酵素及びタンパク質修飾酵素の細胞生物学・遺伝学的解析.” 2014. Web. 28 Sep 2020.

Vancouver:

Sahashi R. Cell biological and genetical studies on DNA replication enzyme and protein modification enzyme in Drosophila : ショウジョウバエ DNA 複製酵素及びタンパク質修飾酵素の細胞生物学・遺伝学的解析. [Internet] [Thesis]. Kyoto Institute of Technology / 京都工芸繊維大学; 2014. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/10212/2155.

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

Council of Science Editors:

Sahashi R. Cell biological and genetical studies on DNA replication enzyme and protein modification enzyme in Drosophila : ショウジョウバエ DNA 複製酵素及びタンパク質修飾酵素の細胞生物学・遺伝学的解析. [Thesis]. Kyoto Institute of Technology / 京都工芸繊維大学; 2014. Available from: http://hdl.handle.net/10212/2155

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

2. Jatsenko, Tatjana. Role of translesion DNA polymerases in mutagenesis and DNA damage tolerance in Pseudomonads .

Degree: 2018, Tartu University

 Kahjustused DNA-s, mis tekivad kas rakkude normaalse elutegevuse käigus või erinevate keskonnategurite mõjul (näiteks UV-kiirgus, DNA-d kahjustavad kemikaalid), pärsivad genoomi replikatsiooni, takistades replikatiivse DNA polümeraasi… (more)

Subjects/Keywords: mutations; DNA damage; DNA polymerase; DNA repair

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APA (6th Edition):

Jatsenko, T. (2018). Role of translesion DNA polymerases in mutagenesis and DNA damage tolerance in Pseudomonads . (Thesis). Tartu University. Retrieved from http://hdl.handle.net/10062/61278

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):

Jatsenko, Tatjana. “Role of translesion DNA polymerases in mutagenesis and DNA damage tolerance in Pseudomonads .” 2018. Thesis, Tartu University. Accessed September 28, 2020. http://hdl.handle.net/10062/61278.

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

MLA Handbook (7th Edition):

Jatsenko, Tatjana. “Role of translesion DNA polymerases in mutagenesis and DNA damage tolerance in Pseudomonads .” 2018. Web. 28 Sep 2020.

Vancouver:

Jatsenko T. Role of translesion DNA polymerases in mutagenesis and DNA damage tolerance in Pseudomonads . [Internet] [Thesis]. Tartu University; 2018. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/10062/61278.

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

Council of Science Editors:

Jatsenko T. Role of translesion DNA polymerases in mutagenesis and DNA damage tolerance in Pseudomonads . [Thesis]. Tartu University; 2018. Available from: http://hdl.handle.net/10062/61278

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


University of Texas – Austin

3. -8850-5086. Structural analysis of hypoxanthine mutagenicity using DNA polymerase β and η: Structural analysis of hypoxanthine mutagenicity using DNA polymerase [beta] and [eta].

Degree: MA, Cell and Molecular Biology, 2019, University of Texas – Austin

 Cellular life is precarious. Dangers abound for a cell’s DNA, from both external and internal factors, and maintaining genomic integrity is crucial for cell survival.… (more)

Subjects/Keywords: DNA polymerase beta; DNA polymerase eta; Hypoxanthine; DNA repair; Mutation

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APA (6th Edition):

-8850-5086. (2019). Structural analysis of hypoxanthine mutagenicity using DNA polymerase β and η: Structural analysis of hypoxanthine mutagenicity using DNA polymerase [beta] and [eta]. (Masters Thesis). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/72726

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Chicago Manual of Style (16th Edition):

-8850-5086. “Structural analysis of hypoxanthine mutagenicity using DNA polymerase β and η: Structural analysis of hypoxanthine mutagenicity using DNA polymerase [beta] and [eta].” 2019. Masters Thesis, University of Texas – Austin. Accessed September 28, 2020. http://hdl.handle.net/2152/72726.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

MLA Handbook (7th Edition):

-8850-5086. “Structural analysis of hypoxanthine mutagenicity using DNA polymerase β and η: Structural analysis of hypoxanthine mutagenicity using DNA polymerase [beta] and [eta].” 2019. Web. 28 Sep 2020.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Vancouver:

-8850-5086. Structural analysis of hypoxanthine mutagenicity using DNA polymerase β and η: Structural analysis of hypoxanthine mutagenicity using DNA polymerase [beta] and [eta]. [Internet] [Masters thesis]. University of Texas – Austin; 2019. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/2152/72726.

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

Council of Science Editors:

-8850-5086. Structural analysis of hypoxanthine mutagenicity using DNA polymerase β and η: Structural analysis of hypoxanthine mutagenicity using DNA polymerase [beta] and [eta]. [Masters Thesis]. University of Texas – Austin; 2019. Available from: http://hdl.handle.net/2152/72726

Note: this citation may be lacking information needed for this citation format:
Author name may be incomplete

4. 山本, 崇史. 大腸菌DNA polymerase I の細胞内機能におけるβ-clampの役割 : Roles of β-clamp in cellular function of DNA polymerase I of Escherichia coli; ダイチョウキン DNA polymerase I ノ サイボウナイ キノウ ニ オケル β-clamp ノ ヤクワリ.

Degree: 博士(バイオサイエンス), 2016, Nara Institute of Science and Technology / 奈良先端科学技術大学院大学

Subjects/Keywords: DNA polymerase

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APA (6th Edition):

山本, . (2016). 大腸菌DNA polymerase I の細胞内機能におけるβ-clampの役割 : Roles of β-clamp in cellular function of DNA polymerase I of Escherichia coli; ダイチョウキン DNA polymerase I ノ サイボウナイ キノウ ニ オケル β-clamp ノ ヤクワリ. (Thesis). Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Retrieved from http://hdl.handle.net/10061/10991

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):

山本, 崇史. “大腸菌DNA polymerase I の細胞内機能におけるβ-clampの役割 : Roles of β-clamp in cellular function of DNA polymerase I of Escherichia coli; ダイチョウキン DNA polymerase I ノ サイボウナイ キノウ ニ オケル β-clamp ノ ヤクワリ.” 2016. Thesis, Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Accessed September 28, 2020. http://hdl.handle.net/10061/10991.

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

MLA Handbook (7th Edition):

山本, 崇史. “大腸菌DNA polymerase I の細胞内機能におけるβ-clampの役割 : Roles of β-clamp in cellular function of DNA polymerase I of Escherichia coli; ダイチョウキン DNA polymerase I ノ サイボウナイ キノウ ニ オケル β-clamp ノ ヤクワリ.” 2016. Web. 28 Sep 2020.

Vancouver:

山本 . 大腸菌DNA polymerase I の細胞内機能におけるβ-clampの役割 : Roles of β-clamp in cellular function of DNA polymerase I of Escherichia coli; ダイチョウキン DNA polymerase I ノ サイボウナイ キノウ ニ オケル β-clamp ノ ヤクワリ. [Internet] [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; 2016. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/10061/10991.

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

Council of Science Editors:

山本 . 大腸菌DNA polymerase I の細胞内機能におけるβ-clampの役割 : Roles of β-clamp in cellular function of DNA polymerase I of Escherichia coli; ダイチョウキン DNA polymerase I ノ サイボウナイ キノウ ニ オケル β-clamp ノ ヤクワリ. [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; 2016. Available from: http://hdl.handle.net/10061/10991

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


University of Pretoria

5. Nemakonde, Avhashoni Agnes. Efficacy of different DNA polymerase enzymes in PCR amplification of forensic bovine DNA.

Degree: Animal and Wildlife Sciences, 2012, University of Pretoria

DNA profiling of exhibits that originate from forensic stock theft cases is routinely used as a tool to link suspects to the crime or scene.… (more)

Subjects/Keywords: Dna polymerase enzymes; Forensic bovine dna; UCTD

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APA (6th Edition):

Nemakonde, A. (2012). Efficacy of different DNA polymerase enzymes in PCR amplification of forensic bovine DNA. (Masters Thesis). University of Pretoria. Retrieved from http://hdl.handle.net/2263/27077

Chicago Manual of Style (16th Edition):

Nemakonde, Avhashoni. “Efficacy of different DNA polymerase enzymes in PCR amplification of forensic bovine DNA.” 2012. Masters Thesis, University of Pretoria. Accessed September 28, 2020. http://hdl.handle.net/2263/27077.

MLA Handbook (7th Edition):

Nemakonde, Avhashoni. “Efficacy of different DNA polymerase enzymes in PCR amplification of forensic bovine DNA.” 2012. Web. 28 Sep 2020.

Vancouver:

Nemakonde A. Efficacy of different DNA polymerase enzymes in PCR amplification of forensic bovine DNA. [Internet] [Masters thesis]. University of Pretoria; 2012. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/2263/27077.

Council of Science Editors:

Nemakonde A. Efficacy of different DNA polymerase enzymes in PCR amplification of forensic bovine DNA. [Masters Thesis]. University of Pretoria; 2012. Available from: http://hdl.handle.net/2263/27077


University of Pretoria

6. [No author]. Efficacy of different DNA polymerase enzymes in PCR amplification of forensic bovine DNA .

Degree: 2012, University of Pretoria

DNA profiling of exhibits that originate from forensic stock theft cases is routinely used as a tool to link suspects to the crime or scene.… (more)

Subjects/Keywords: Dna polymerase enzymes; Forensic bovine dna; UCTD

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APA (6th Edition):

author], [. (2012). Efficacy of different DNA polymerase enzymes in PCR amplification of forensic bovine DNA . (Masters Thesis). University of Pretoria. Retrieved from http://upetd.up.ac.za/thesis/available/etd-08062012-144315/

Chicago Manual of Style (16th Edition):

author], [No. “Efficacy of different DNA polymerase enzymes in PCR amplification of forensic bovine DNA .” 2012. Masters Thesis, University of Pretoria. Accessed September 28, 2020. http://upetd.up.ac.za/thesis/available/etd-08062012-144315/.

MLA Handbook (7th Edition):

author], [No. “Efficacy of different DNA polymerase enzymes in PCR amplification of forensic bovine DNA .” 2012. Web. 28 Sep 2020.

Vancouver:

author] [. Efficacy of different DNA polymerase enzymes in PCR amplification of forensic bovine DNA . [Internet] [Masters thesis]. University of Pretoria; 2012. [cited 2020 Sep 28]. Available from: http://upetd.up.ac.za/thesis/available/etd-08062012-144315/.

Council of Science Editors:

author] [. Efficacy of different DNA polymerase enzymes in PCR amplification of forensic bovine DNA . [Masters Thesis]. University of Pretoria; 2012. Available from: http://upetd.up.ac.za/thesis/available/etd-08062012-144315/


University of Texas – Austin

7. Ziehr, Jessica Lea. Kinetics and specificity of human mitochondrial DNA polymerase gamma and HIV-1 reverse transcriptase.

Degree: PhD, Cell and Molecular Biology, 2014, University of Texas – Austin

 The human mitochondrial DNA (mtDNA) genome must be faithfully maintained by the mitochondrial DNA replication machinery. Deficiencies in mtDNA maintenance result in the accumulation of… (more)

Subjects/Keywords: DNA polymerase; Pre-steady state kinetics; HIV reverse transcriptase; Polymerase gamma

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

APA (6th Edition):

Ziehr, J. L. (2014). Kinetics and specificity of human mitochondrial DNA polymerase gamma and HIV-1 reverse transcriptase. (Doctoral Dissertation). University of Texas – Austin. Retrieved from http://hdl.handle.net/2152/31296

Chicago Manual of Style (16th Edition):

Ziehr, Jessica Lea. “Kinetics and specificity of human mitochondrial DNA polymerase gamma and HIV-1 reverse transcriptase.” 2014. Doctoral Dissertation, University of Texas – Austin. Accessed September 28, 2020. http://hdl.handle.net/2152/31296.

MLA Handbook (7th Edition):

Ziehr, Jessica Lea. “Kinetics and specificity of human mitochondrial DNA polymerase gamma and HIV-1 reverse transcriptase.” 2014. Web. 28 Sep 2020.

Vancouver:

Ziehr JL. Kinetics and specificity of human mitochondrial DNA polymerase gamma and HIV-1 reverse transcriptase. [Internet] [Doctoral dissertation]. University of Texas – Austin; 2014. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/2152/31296.

Council of Science Editors:

Ziehr JL. Kinetics and specificity of human mitochondrial DNA polymerase gamma and HIV-1 reverse transcriptase. [Doctoral Dissertation]. University of Texas – Austin; 2014. Available from: http://hdl.handle.net/2152/31296


University of Alberta

8. Gammon, Donald Brad. Vaccinia virus DNA polymerase and ribonucleotide reductase: their role in replication, recombination and drug resistance.

Degree: PhD, Department of Medical Microbiology and Immunology, 2009, University of Alberta

 Despite the eradication of smallpox, poxviruses continue to cause human disease around the world. At the core of poxvirus replication is the efficient and accurate… (more)

Subjects/Keywords: recombination; DNA polymerase; vaccinia virus; ribonucleotide reductase

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APA (6th Edition):

Gammon, D. B. (2009). Vaccinia virus DNA polymerase and ribonucleotide reductase: their role in replication, recombination and drug resistance. (Doctoral Dissertation). University of Alberta. Retrieved from https://era.library.ualberta.ca/files/1g05fd17k

Chicago Manual of Style (16th Edition):

Gammon, Donald Brad. “Vaccinia virus DNA polymerase and ribonucleotide reductase: their role in replication, recombination and drug resistance.” 2009. Doctoral Dissertation, University of Alberta. Accessed September 28, 2020. https://era.library.ualberta.ca/files/1g05fd17k.

MLA Handbook (7th Edition):

Gammon, Donald Brad. “Vaccinia virus DNA polymerase and ribonucleotide reductase: their role in replication, recombination and drug resistance.” 2009. Web. 28 Sep 2020.

Vancouver:

Gammon DB. Vaccinia virus DNA polymerase and ribonucleotide reductase: their role in replication, recombination and drug resistance. [Internet] [Doctoral dissertation]. University of Alberta; 2009. [cited 2020 Sep 28]. Available from: https://era.library.ualberta.ca/files/1g05fd17k.

Council of Science Editors:

Gammon DB. Vaccinia virus DNA polymerase and ribonucleotide reductase: their role in replication, recombination and drug resistance. [Doctoral Dissertation]. University of Alberta; 2009. Available from: https://era.library.ualberta.ca/files/1g05fd17k

9. Nayak, Shreenath. Cloning sequence analysis and characterization of DNA polymerase from Geobacillus sp. WBI.

Degree: Botany, 2014, Visva Bharti University

A thermostable DNA polymerase gene (DNA pol) was isolated from the genomic DNA of Geobacillus sp.WBI by polymerase chain reaction (PCR). PCR amplification with the… (more)

Subjects/Keywords: Geobacillus; Sequence analysis; Thermostable DNA polymerase

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APA (6th Edition):

Nayak, S. (2014). Cloning sequence analysis and characterization of DNA polymerase from Geobacillus sp. WBI. (Thesis). Visva Bharti University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/19542

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):

Nayak, Shreenath. “Cloning sequence analysis and characterization of DNA polymerase from Geobacillus sp. WBI.” 2014. Thesis, Visva Bharti University. Accessed September 28, 2020. http://shodhganga.inflibnet.ac.in/handle/10603/19542.

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

MLA Handbook (7th Edition):

Nayak, Shreenath. “Cloning sequence analysis and characterization of DNA polymerase from Geobacillus sp. WBI.” 2014. Web. 28 Sep 2020.

Vancouver:

Nayak S. Cloning sequence analysis and characterization of DNA polymerase from Geobacillus sp. WBI. [Internet] [Thesis]. Visva Bharti University; 2014. [cited 2020 Sep 28]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/19542.

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

Council of Science Editors:

Nayak S. Cloning sequence analysis and characterization of DNA polymerase from Geobacillus sp. WBI. [Thesis]. Visva Bharti University; 2014. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/19542

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


Penn State University

10. Almishwat, Mohammad Ali. Time-resolved X-ray crystallography of DNA polymerases: A platform for studies in structural and mechanistic enzymology.

Degree: 2013, Penn State University

DNA-dependent DNA polymerase is the enzyme responsible for carrying out DNA replication. DNA polymerase regulates the faithful transmission of an organism’s genetic material, and performs… (more)

Subjects/Keywords: DNA polymerase; X-ray crystallography; Time-reolved

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APA (6th Edition):

Almishwat, M. A. (2013). Time-resolved X-ray crystallography of DNA polymerases: A platform for studies in structural and mechanistic enzymology. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/19024

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):

Almishwat, Mohammad Ali. “Time-resolved X-ray crystallography of DNA polymerases: A platform for studies in structural and mechanistic enzymology.” 2013. Thesis, Penn State University. Accessed September 28, 2020. https://submit-etda.libraries.psu.edu/catalog/19024.

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

MLA Handbook (7th Edition):

Almishwat, Mohammad Ali. “Time-resolved X-ray crystallography of DNA polymerases: A platform for studies in structural and mechanistic enzymology.” 2013. Web. 28 Sep 2020.

Vancouver:

Almishwat MA. Time-resolved X-ray crystallography of DNA polymerases: A platform for studies in structural and mechanistic enzymology. [Internet] [Thesis]. Penn State University; 2013. [cited 2020 Sep 28]. Available from: https://submit-etda.libraries.psu.edu/catalog/19024.

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

Council of Science Editors:

Almishwat MA. Time-resolved X-ray crystallography of DNA polymerases: A platform for studies in structural and mechanistic enzymology. [Thesis]. Penn State University; 2013. Available from: https://submit-etda.libraries.psu.edu/catalog/19024

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


Penn State University

11. Barnes, Ryan Patrick. The Roles and Regulation of Specialized DNA Polymerases in Mitigating Replication Stress and Replicating Common Fragile Sites.

Degree: 2017, Penn State University

 Replicative DNA polymerases serve as the essential enzymes that duplicate our genome with high fidelity and efficiency. This function is compromised however, when repetitive DNA(more)

Subjects/Keywords: DNA polymerase; replication stress; genome stability

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APA (6th Edition):

Barnes, R. P. (2017). The Roles and Regulation of Specialized DNA Polymerases in Mitigating Replication Stress and Replicating Common Fragile Sites. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/14528rpb180

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):

Barnes, Ryan Patrick. “The Roles and Regulation of Specialized DNA Polymerases in Mitigating Replication Stress and Replicating Common Fragile Sites.” 2017. Thesis, Penn State University. Accessed September 28, 2020. https://submit-etda.libraries.psu.edu/catalog/14528rpb180.

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

MLA Handbook (7th Edition):

Barnes, Ryan Patrick. “The Roles and Regulation of Specialized DNA Polymerases in Mitigating Replication Stress and Replicating Common Fragile Sites.” 2017. Web. 28 Sep 2020.

Vancouver:

Barnes RP. The Roles and Regulation of Specialized DNA Polymerases in Mitigating Replication Stress and Replicating Common Fragile Sites. [Internet] [Thesis]. Penn State University; 2017. [cited 2020 Sep 28]. Available from: https://submit-etda.libraries.psu.edu/catalog/14528rpb180.

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

Council of Science Editors:

Barnes RP. The Roles and Regulation of Specialized DNA Polymerases in Mitigating Replication Stress and Replicating Common Fragile Sites. [Thesis]. Penn State University; 2017. Available from: https://submit-etda.libraries.psu.edu/catalog/14528rpb180

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


The Ohio State University

12. Brown, Jessica Ann. Kinetic Mechanisms of DNA Polymerases.

Degree: PhD, Biochemistry Program, Ohio State, 2010, The Ohio State University

  High-fidelity DNA polymerases accurately replicate an organism’s genomic DNA while low-fidelity DNA polymerases are specialized to function in DNA repair and DNA lesion bypass,… (more)

Subjects/Keywords: Biochemistry; DNA polymerase; transient state kinetics

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APA (6th Edition):

Brown, J. A. (2010). Kinetic Mechanisms of DNA Polymerases. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1290014566

Chicago Manual of Style (16th Edition):

Brown, Jessica Ann. “Kinetic Mechanisms of DNA Polymerases.” 2010. Doctoral Dissertation, The Ohio State University. Accessed September 28, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1290014566.

MLA Handbook (7th Edition):

Brown, Jessica Ann. “Kinetic Mechanisms of DNA Polymerases.” 2010. Web. 28 Sep 2020.

Vancouver:

Brown JA. Kinetic Mechanisms of DNA Polymerases. [Internet] [Doctoral dissertation]. The Ohio State University; 2010. [cited 2020 Sep 28]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1290014566.

Council of Science Editors:

Brown JA. Kinetic Mechanisms of DNA Polymerases. [Doctoral Dissertation]. The Ohio State University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1290014566

13. Thanh, Le Thi. Biochemical analysis revealing the molecular actions of Escherichia coli DNA polymerase III and IV at the replication fork : 大腸菌損傷乗り越え型DNAポリメラーゼⅣによる複製フォークでの複製型DNAポリメラーゼⅢとの交換機構の生化学的解析; ダイチョウキン ソンショウ ノリコエガタ DNA ポリメラーゼ Ⅳ ニ ヨル フクセイ フォーク デノ フクセイガタ DNA ポリメラーゼ Ⅲ トノ コウカン キコウ ノ セイカガクテキ カイセキ.

Degree: 博士(バイオサイエンス), 2017, Nara Institute of Science and Technology / 奈良先端科学技術大学院大学

Subjects/Keywords: DNA polymerase switching

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APA (6th Edition):

Thanh, L. T. (2017). Biochemical analysis revealing the molecular actions of Escherichia coli DNA polymerase III and IV at the replication fork : 大腸菌損傷乗り越え型DNAポリメラーゼⅣによる複製フォークでの複製型DNAポリメラーゼⅢとの交換機構の生化学的解析; ダイチョウキン ソンショウ ノリコエガタ DNA ポリメラーゼ Ⅳ ニ ヨル フクセイ フォーク デノ フクセイガタ DNA ポリメラーゼ Ⅲ トノ コウカン キコウ ノ セイカガクテキ カイセキ. (Thesis). Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Retrieved from http://hdl.handle.net/10061/11737

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):

Thanh, Le Thi. “Biochemical analysis revealing the molecular actions of Escherichia coli DNA polymerase III and IV at the replication fork : 大腸菌損傷乗り越え型DNAポリメラーゼⅣによる複製フォークでの複製型DNAポリメラーゼⅢとの交換機構の生化学的解析; ダイチョウキン ソンショウ ノリコエガタ DNA ポリメラーゼ Ⅳ ニ ヨル フクセイ フォーク デノ フクセイガタ DNA ポリメラーゼ Ⅲ トノ コウカン キコウ ノ セイカガクテキ カイセキ.” 2017. Thesis, Nara Institute of Science and Technology / 奈良先端科学技術大学院大学. Accessed September 28, 2020. http://hdl.handle.net/10061/11737.

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

MLA Handbook (7th Edition):

Thanh, Le Thi. “Biochemical analysis revealing the molecular actions of Escherichia coli DNA polymerase III and IV at the replication fork : 大腸菌損傷乗り越え型DNAポリメラーゼⅣによる複製フォークでの複製型DNAポリメラーゼⅢとの交換機構の生化学的解析; ダイチョウキン ソンショウ ノリコエガタ DNA ポリメラーゼ Ⅳ ニ ヨル フクセイ フォーク デノ フクセイガタ DNA ポリメラーゼ Ⅲ トノ コウカン キコウ ノ セイカガクテキ カイセキ.” 2017. Web. 28 Sep 2020.

Vancouver:

Thanh LT. Biochemical analysis revealing the molecular actions of Escherichia coli DNA polymerase III and IV at the replication fork : 大腸菌損傷乗り越え型DNAポリメラーゼⅣによる複製フォークでの複製型DNAポリメラーゼⅢとの交換機構の生化学的解析; ダイチョウキン ソンショウ ノリコエガタ DNA ポリメラーゼ Ⅳ ニ ヨル フクセイ フォーク デノ フクセイガタ DNA ポリメラーゼ Ⅲ トノ コウカン キコウ ノ セイカガクテキ カイセキ. [Internet] [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; 2017. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/10061/11737.

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

Council of Science Editors:

Thanh LT. Biochemical analysis revealing the molecular actions of Escherichia coli DNA polymerase III and IV at the replication fork : 大腸菌損傷乗り越え型DNAポリメラーゼⅣによる複製フォークでの複製型DNAポリメラーゼⅢとの交換機構の生化学的解析; ダイチョウキン ソンショウ ノリコエガタ DNA ポリメラーゼ Ⅳ ニ ヨル フクセイ フォーク デノ フクセイガタ DNA ポリメラーゼ Ⅲ トノ コウカン キコウ ノ セイカガクテキ カイセキ. [Thesis]. Nara Institute of Science and Technology / 奈良先端科学技術大学院大学; 2017. Available from: http://hdl.handle.net/10061/11737

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


Northeastern University

14. Ippoliti, Paul Joseph. DNA damage specificity of Escherichia coli DNA polymerase DinB.

Degree: MS, Department of Chemistry and Chemical Biology, 2012, Northeastern University

 Exogenous and endogenous DNA damaging agents such as UV light cause lesions in DNA, which halt the progress of DNA replication. Microbes such as E.… (more)

Subjects/Keywords: DinB; DNA; Escherichia coli; Polymerase; UmuC; Biochemistry

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APA (6th Edition):

Ippoliti, P. J. (2012). DNA damage specificity of Escherichia coli DNA polymerase DinB. (Masters Thesis). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20002749

Chicago Manual of Style (16th Edition):

Ippoliti, Paul Joseph. “DNA damage specificity of Escherichia coli DNA polymerase DinB.” 2012. Masters Thesis, Northeastern University. Accessed September 28, 2020. http://hdl.handle.net/2047/d20002749.

MLA Handbook (7th Edition):

Ippoliti, Paul Joseph. “DNA damage specificity of Escherichia coli DNA polymerase DinB.” 2012. Web. 28 Sep 2020.

Vancouver:

Ippoliti PJ. DNA damage specificity of Escherichia coli DNA polymerase DinB. [Internet] [Masters thesis]. Northeastern University; 2012. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/2047/d20002749.

Council of Science Editors:

Ippoliti PJ. DNA damage specificity of Escherichia coli DNA polymerase DinB. [Masters Thesis]. Northeastern University; 2012. Available from: http://hdl.handle.net/2047/d20002749


University of Oregon

15. Mostales, Joshua Calixterio. Investigating the Physiological Effects of Mutations in the Proposed Backtrack Site of Yeast RNA Polymerase II.

Degree: 2019, University of Oregon

 Transcription, the first step of gene expression, is a process fundamental to all known forms of life. In eukaryotic cells, the enzyme RNA polymerase II… (more)

Subjects/Keywords: Biochemistry; RNA Polymerase; Transcription; DNA; Mutations; Backtracking

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APA (6th Edition):

Mostales, J. C. (2019). Investigating the Physiological Effects of Mutations in the Proposed Backtrack Site of Yeast RNA Polymerase II. (Thesis). University of Oregon. Retrieved from https://scholarsbank.uoregon.edu/xmlui/handle/1794/25046

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):

Mostales, Joshua Calixterio. “Investigating the Physiological Effects of Mutations in the Proposed Backtrack Site of Yeast RNA Polymerase II.” 2019. Thesis, University of Oregon. Accessed September 28, 2020. https://scholarsbank.uoregon.edu/xmlui/handle/1794/25046.

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

MLA Handbook (7th Edition):

Mostales, Joshua Calixterio. “Investigating the Physiological Effects of Mutations in the Proposed Backtrack Site of Yeast RNA Polymerase II.” 2019. Web. 28 Sep 2020.

Vancouver:

Mostales JC. Investigating the Physiological Effects of Mutations in the Proposed Backtrack Site of Yeast RNA Polymerase II. [Internet] [Thesis]. University of Oregon; 2019. [cited 2020 Sep 28]. Available from: https://scholarsbank.uoregon.edu/xmlui/handle/1794/25046.

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

Council of Science Editors:

Mostales JC. Investigating the Physiological Effects of Mutations in the Proposed Backtrack Site of Yeast RNA Polymerase II. [Thesis]. University of Oregon; 2019. Available from: https://scholarsbank.uoregon.edu/xmlui/handle/1794/25046

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

16. Trujillo, Joshua T. The Origin and Evolution of Plant-Specific RNA Polymerases and Genes Involved in RNA-Directed DNA Methylation .

Degree: 2019, University of Arizona

 Gene evolution is one of the most significant contributors to the extensive number and diversity of organisms that have arisen on planet Earth. Gene duplication… (more)

Subjects/Keywords: RNA-directed DNA Methylation; RNA polymerase

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APA (6th Edition):

Trujillo, J. T. (2019). The Origin and Evolution of Plant-Specific RNA Polymerases and Genes Involved in RNA-Directed DNA Methylation . (Doctoral Dissertation). University of Arizona. Retrieved from http://hdl.handle.net/10150/632985

Chicago Manual of Style (16th Edition):

Trujillo, Joshua T. “The Origin and Evolution of Plant-Specific RNA Polymerases and Genes Involved in RNA-Directed DNA Methylation .” 2019. Doctoral Dissertation, University of Arizona. Accessed September 28, 2020. http://hdl.handle.net/10150/632985.

MLA Handbook (7th Edition):

Trujillo, Joshua T. “The Origin and Evolution of Plant-Specific RNA Polymerases and Genes Involved in RNA-Directed DNA Methylation .” 2019. Web. 28 Sep 2020.

Vancouver:

Trujillo JT. The Origin and Evolution of Plant-Specific RNA Polymerases and Genes Involved in RNA-Directed DNA Methylation . [Internet] [Doctoral dissertation]. University of Arizona; 2019. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/10150/632985.

Council of Science Editors:

Trujillo JT. The Origin and Evolution of Plant-Specific RNA Polymerases and Genes Involved in RNA-Directed DNA Methylation . [Doctoral Dissertation]. University of Arizona; 2019. Available from: http://hdl.handle.net/10150/632985


Brigham Young University

17. Brammer, Jeffrey M. Organellar DNA Polymerases Gamma I and II in Arabidopsis thaliana.

Degree: MS, 2010, Brigham Young University

  Plants have two organelles outside the nucleus which carry their own DNA, mitochondria and chloroplasts. These organelles are descendants of bacteria that were engulfed… (more)

Subjects/Keywords: DNA polymerase; Arabidopsis; Arabidopsis thaliana; gamma polymerase; mitochondrion; mitochondria; chloroplast; plastid; DNA replication; Microbiology

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APA (6th Edition):

Brammer, J. M. (2010). Organellar DNA Polymerases Gamma I and II in Arabidopsis thaliana. (Masters Thesis). Brigham Young University. Retrieved from https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=3533&context=etd

Chicago Manual of Style (16th Edition):

Brammer, Jeffrey M. “Organellar DNA Polymerases Gamma I and II in Arabidopsis thaliana.” 2010. Masters Thesis, Brigham Young University. Accessed September 28, 2020. https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=3533&context=etd.

MLA Handbook (7th Edition):

Brammer, Jeffrey M. “Organellar DNA Polymerases Gamma I and II in Arabidopsis thaliana.” 2010. Web. 28 Sep 2020.

Vancouver:

Brammer JM. Organellar DNA Polymerases Gamma I and II in Arabidopsis thaliana. [Internet] [Masters thesis]. Brigham Young University; 2010. [cited 2020 Sep 28]. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=3533&context=etd.

Council of Science Editors:

Brammer JM. Organellar DNA Polymerases Gamma I and II in Arabidopsis thaliana. [Masters Thesis]. Brigham Young University; 2010. Available from: https://scholarsarchive.byu.edu/cgi/viewcontent.cgi?article=3533&context=etd


University of Southern California

18. Corzett, Christopher Hale. Physiological roles and evolutionary implications of alternative DNA polymerases in Escherichia coli.

Degree: PhD, Molecular Biology, 2012, University of Southern California

 Escherichia coli DNA polymerases II, IV and V serve dual roles within cells by facilitating efficient replication past potentially lethal DNA damage while simultaneously introducing… (more)

Subjects/Keywords: alternative DNA polymerase; error-prone DNA polymerase; microbial evolution; SOS response; stationary phase; translesion synthesis

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APA (6th Edition):

Corzett, C. H. (2012). Physiological roles and evolutionary implications of alternative DNA polymerases in Escherichia coli. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/110357/rec/5048

Chicago Manual of Style (16th Edition):

Corzett, Christopher Hale. “Physiological roles and evolutionary implications of alternative DNA polymerases in Escherichia coli.” 2012. Doctoral Dissertation, University of Southern California. Accessed September 28, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/110357/rec/5048.

MLA Handbook (7th Edition):

Corzett, Christopher Hale. “Physiological roles and evolutionary implications of alternative DNA polymerases in Escherichia coli.” 2012. Web. 28 Sep 2020.

Vancouver:

Corzett CH. Physiological roles and evolutionary implications of alternative DNA polymerases in Escherichia coli. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2020 Sep 28]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/110357/rec/5048.

Council of Science Editors:

Corzett CH. Physiological roles and evolutionary implications of alternative DNA polymerases in Escherichia coli. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/110357/rec/5048


Wayne State University

19. Arrabi, Amanda Lynn. Effect Of Folate Deficiency And Aging On Mtor Signaling Network In The Liver Of Dna Polymerase B Haploinsufficient Mice.

Degree: MS, Nutrition and Food Science, 2013, Wayne State University

  EFFECT OF FOLATE DEFICIENCY AND AGING ON mTOR SIGNALING NETWORK IN THE LIVER OF DNA POLYMERASE B HAPLOINSUFFICIENT MICE by AMANDA ARRABI August 2013… (more)

Subjects/Keywords: Apoptosis; Beta polymerase; Cancer; DNA POLYMERASE B; DNA POLYMERASE B HAPLOINSUFFICIENT MICE; Folate Deficiency; Molecular Biology; Nutrition

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APA (6th Edition):

Arrabi, A. L. (2013). Effect Of Folate Deficiency And Aging On Mtor Signaling Network In The Liver Of Dna Polymerase B Haploinsufficient Mice. (Masters Thesis). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_theses/258

Chicago Manual of Style (16th Edition):

Arrabi, Amanda Lynn. “Effect Of Folate Deficiency And Aging On Mtor Signaling Network In The Liver Of Dna Polymerase B Haploinsufficient Mice.” 2013. Masters Thesis, Wayne State University. Accessed September 28, 2020. https://digitalcommons.wayne.edu/oa_theses/258.

MLA Handbook (7th Edition):

Arrabi, Amanda Lynn. “Effect Of Folate Deficiency And Aging On Mtor Signaling Network In The Liver Of Dna Polymerase B Haploinsufficient Mice.” 2013. Web. 28 Sep 2020.

Vancouver:

Arrabi AL. Effect Of Folate Deficiency And Aging On Mtor Signaling Network In The Liver Of Dna Polymerase B Haploinsufficient Mice. [Internet] [Masters thesis]. Wayne State University; 2013. [cited 2020 Sep 28]. Available from: https://digitalcommons.wayne.edu/oa_theses/258.

Council of Science Editors:

Arrabi AL. Effect Of Folate Deficiency And Aging On Mtor Signaling Network In The Liver Of Dna Polymerase B Haploinsufficient Mice. [Masters Thesis]. Wayne State University; 2013. Available from: https://digitalcommons.wayne.edu/oa_theses/258


Loma Linda University

20. Williams, Adides. The Impact of Nucleoside Sugar Modification on Biochemical DNA Transactions.

Degree: PhD, Basic Sciences, 2012, Loma Linda University

 Discrimination by DNA polymerases controls the fidelity of DNA replication, and reduced fidelity results in mutations essential in the etiology of cancer. Polymerase discrimination operates… (more)

Subjects/Keywords: Medical Biochemistry; DNA  – Synthesis; DNA  – Biosynthesis; Glycoproteins; DNA Polymerases;

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APA (6th Edition):

Williams, A. (2012). The Impact of Nucleoside Sugar Modification on Biochemical DNA Transactions. (Doctoral Dissertation). Loma Linda University. Retrieved from https://scholarsrepository.llu.edu/etd/104

Chicago Manual of Style (16th Edition):

Williams, Adides. “The Impact of Nucleoside Sugar Modification on Biochemical DNA Transactions.” 2012. Doctoral Dissertation, Loma Linda University. Accessed September 28, 2020. https://scholarsrepository.llu.edu/etd/104.

MLA Handbook (7th Edition):

Williams, Adides. “The Impact of Nucleoside Sugar Modification on Biochemical DNA Transactions.” 2012. Web. 28 Sep 2020.

Vancouver:

Williams A. The Impact of Nucleoside Sugar Modification on Biochemical DNA Transactions. [Internet] [Doctoral dissertation]. Loma Linda University; 2012. [cited 2020 Sep 28]. Available from: https://scholarsrepository.llu.edu/etd/104.

Council of Science Editors:

Williams A. The Impact of Nucleoside Sugar Modification on Biochemical DNA Transactions. [Doctoral Dissertation]. Loma Linda University; 2012. Available from: https://scholarsrepository.llu.edu/etd/104


University of California – Santa Cruz

21. Dahl, Joseph Michael. Single Molecule Studies of DNA Polymerase Fidelity.

Degree: Chemistry, 2016, University of California – Santa Cruz

 Replicative DNA polymerases (DNAPs) are molecular motors responsible for high fidelity replication of the genome prior to each cellular division. These enzymes require two divalent… (more)

Subjects/Keywords: Biochemistry; Biophysics; DNA Polymerase; DNA Replication Fidelity; Nanopore; Single Molecule

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APA (6th Edition):

Dahl, J. M. (2016). Single Molecule Studies of DNA Polymerase Fidelity. (Thesis). University of California – Santa Cruz. Retrieved from http://www.escholarship.org/uc/item/8c15v9br

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):

Dahl, Joseph Michael. “Single Molecule Studies of DNA Polymerase Fidelity.” 2016. Thesis, University of California – Santa Cruz. Accessed September 28, 2020. http://www.escholarship.org/uc/item/8c15v9br.

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

MLA Handbook (7th Edition):

Dahl, Joseph Michael. “Single Molecule Studies of DNA Polymerase Fidelity.” 2016. Web. 28 Sep 2020.

Vancouver:

Dahl JM. Single Molecule Studies of DNA Polymerase Fidelity. [Internet] [Thesis]. University of California – Santa Cruz; 2016. [cited 2020 Sep 28]. Available from: http://www.escholarship.org/uc/item/8c15v9br.

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

Council of Science Editors:

Dahl JM. Single Molecule Studies of DNA Polymerase Fidelity. [Thesis]. University of California – Santa Cruz; 2016. Available from: http://www.escholarship.org/uc/item/8c15v9br

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


University of California – San Diego

22. 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 28, 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. 28 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 28]. 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


Boston University

23. Chen, Emily. Preliminary investigation of thermostable DNA polymerases to reduce PCR amplification artifacts.

Degree: MS, Biomedical Forensic Sciences, 2020, Boston University

 Forensic genotyping uses a multiplex short tandem repeat (STR) assay to amplify deoxyribonucleic acid (DNA) samples. One of the artifacts mostly commonly encountered in forensic… (more)

Subjects/Keywords: Genetics; Artifacts; DNA polymerase; Forensic DNA; PCR; Slipped strand mispairing; Stutter

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APA (6th Edition):

Chen, E. (2020). Preliminary investigation of thermostable DNA polymerases to reduce PCR amplification artifacts. (Masters Thesis). Boston University. Retrieved from http://hdl.handle.net/2144/41190

Chicago Manual of Style (16th Edition):

Chen, Emily. “Preliminary investigation of thermostable DNA polymerases to reduce PCR amplification artifacts.” 2020. Masters Thesis, Boston University. Accessed September 28, 2020. http://hdl.handle.net/2144/41190.

MLA Handbook (7th Edition):

Chen, Emily. “Preliminary investigation of thermostable DNA polymerases to reduce PCR amplification artifacts.” 2020. Web. 28 Sep 2020.

Vancouver:

Chen E. Preliminary investigation of thermostable DNA polymerases to reduce PCR amplification artifacts. [Internet] [Masters thesis]. Boston University; 2020. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/2144/41190.

Council of Science Editors:

Chen E. Preliminary investigation of thermostable DNA polymerases to reduce PCR amplification artifacts. [Masters Thesis]. Boston University; 2020. Available from: http://hdl.handle.net/2144/41190


University of Wollongong

24. Horan, Nicholas. Investigations into the Architecture and Function of the Bacterial Replisome.

Degree: PhD, 2016, University of Wollongong

  The accurate and efficient replication of Escherichia coli DNA is catalysed by a 17‐subunit assembly of proteins termed the DNA polymerase III holoenzyme (Pol… (more)

Subjects/Keywords: protein structure; DNA replication; Escherichia coli; DNA polymerase III

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APA (6th Edition):

Horan, N. (2016). Investigations into the Architecture and Function of the Bacterial Replisome. (Doctoral Dissertation). University of Wollongong. Retrieved from 060106 Cellular Interactions (incl. Adhesion, Matrix, Cell Wall), 060107 Enzymes, 060112 Structural Biology (incl. Macromolecular Modelling) ; https://ro.uow.edu.au/theses/4937

Chicago Manual of Style (16th Edition):

Horan, Nicholas. “Investigations into the Architecture and Function of the Bacterial Replisome.” 2016. Doctoral Dissertation, University of Wollongong. Accessed September 28, 2020. 060106 Cellular Interactions (incl. Adhesion, Matrix, Cell Wall), 060107 Enzymes, 060112 Structural Biology (incl. Macromolecular Modelling) ; https://ro.uow.edu.au/theses/4937.

MLA Handbook (7th Edition):

Horan, Nicholas. “Investigations into the Architecture and Function of the Bacterial Replisome.” 2016. Web. 28 Sep 2020.

Vancouver:

Horan N. Investigations into the Architecture and Function of the Bacterial Replisome. [Internet] [Doctoral dissertation]. University of Wollongong; 2016. [cited 2020 Sep 28]. Available from: 060106 Cellular Interactions (incl. Adhesion, Matrix, Cell Wall), 060107 Enzymes, 060112 Structural Biology (incl. Macromolecular Modelling) ; https://ro.uow.edu.au/theses/4937.

Council of Science Editors:

Horan N. Investigations into the Architecture and Function of the Bacterial Replisome. [Doctoral Dissertation]. University of Wollongong; 2016. Available from: 060106 Cellular Interactions (incl. Adhesion, Matrix, Cell Wall), 060107 Enzymes, 060112 Structural Biology (incl. Macromolecular Modelling) ; https://ro.uow.edu.au/theses/4937


Wayne State University

25. Unnikrishnan, Archana. Base excision repair, folate deficiency and cancer.

Degree: PhD, Nutrition and Food Science, 2011, Wayne State University

  Folate, an essential water soluble vitamin has been implicated in the etiology of many types of cancer especially colorectal cancer. Folate deficiency has been… (more)

Subjects/Keywords: AP endonuclease, DNA polymerase Beta, DNA repair, Folate; Nutrition

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APA (6th Edition):

Unnikrishnan, A. (2011). Base excision repair, folate deficiency and cancer. (Doctoral Dissertation). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_dissertations/399

Chicago Manual of Style (16th Edition):

Unnikrishnan, Archana. “Base excision repair, folate deficiency and cancer.” 2011. Doctoral Dissertation, Wayne State University. Accessed September 28, 2020. https://digitalcommons.wayne.edu/oa_dissertations/399.

MLA Handbook (7th Edition):

Unnikrishnan, Archana. “Base excision repair, folate deficiency and cancer.” 2011. Web. 28 Sep 2020.

Vancouver:

Unnikrishnan A. Base excision repair, folate deficiency and cancer. [Internet] [Doctoral dissertation]. Wayne State University; 2011. [cited 2020 Sep 28]. Available from: https://digitalcommons.wayne.edu/oa_dissertations/399.

Council of Science Editors:

Unnikrishnan A. Base excision repair, folate deficiency and cancer. [Doctoral Dissertation]. Wayne State University; 2011. Available from: https://digitalcommons.wayne.edu/oa_dissertations/399


University of Vermont

26. Odell, Ian. Modulation of Base Excision Repair by Nucleosomes.

Degree: PhD, Microbiology and Molecular Genetics, 2010, University of Vermont

DNA in eukaryotes is packaged into nucleosomes, which present steric impediments to many of the factors and enzymes that act on DNA, including DNA repair… (more)

Subjects/Keywords: DNA Repair; Chromatin; Nucleosome; Polymerase Beta; hNTH1; DNA Ligase; APE

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APA (6th Edition):

Odell, I. (2010). Modulation of Base Excision Repair by Nucleosomes. (Doctoral Dissertation). University of Vermont. Retrieved from https://scholarworks.uvm.edu/graddis/170

Chicago Manual of Style (16th Edition):

Odell, Ian. “Modulation of Base Excision Repair by Nucleosomes.” 2010. Doctoral Dissertation, University of Vermont. Accessed September 28, 2020. https://scholarworks.uvm.edu/graddis/170.

MLA Handbook (7th Edition):

Odell, Ian. “Modulation of Base Excision Repair by Nucleosomes.” 2010. Web. 28 Sep 2020.

Vancouver:

Odell I. Modulation of Base Excision Repair by Nucleosomes. [Internet] [Doctoral dissertation]. University of Vermont; 2010. [cited 2020 Sep 28]. Available from: https://scholarworks.uvm.edu/graddis/170.

Council of Science Editors:

Odell I. Modulation of Base Excision Repair by Nucleosomes. [Doctoral Dissertation]. University of Vermont; 2010. Available from: https://scholarworks.uvm.edu/graddis/170


University of Oxford

27. Nicolay, N. H. The role of DNA polymerase eta in determining cellular responses to chemo-radiation treatment.

Degree: PhD, 2013, University of Oxford

DNA polymerase η (pol η), a crucial component of the cellular translesion synthesis pathway, allows cells to bypass and thereby temporarily tolerate DNA damage. Inherited… (more)

Subjects/Keywords: 616.99; DNA damage signalling; DNA polymerase; radiation; oxaliplatin

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APA (6th Edition):

Nicolay, N. H. (2013). The role of DNA polymerase eta in determining cellular responses to chemo-radiation treatment. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:73cef89c-319d-4a14-a3a6-93e8b8dd186a ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581330

Chicago Manual of Style (16th Edition):

Nicolay, N H. “The role of DNA polymerase eta in determining cellular responses to chemo-radiation treatment.” 2013. Doctoral Dissertation, University of Oxford. Accessed September 28, 2020. http://ora.ox.ac.uk/objects/uuid:73cef89c-319d-4a14-a3a6-93e8b8dd186a ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581330.

MLA Handbook (7th Edition):

Nicolay, N H. “The role of DNA polymerase eta in determining cellular responses to chemo-radiation treatment.” 2013. Web. 28 Sep 2020.

Vancouver:

Nicolay NH. The role of DNA polymerase eta in determining cellular responses to chemo-radiation treatment. [Internet] [Doctoral dissertation]. University of Oxford; 2013. [cited 2020 Sep 28]. Available from: http://ora.ox.ac.uk/objects/uuid:73cef89c-319d-4a14-a3a6-93e8b8dd186a ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581330.

Council of Science Editors:

Nicolay NH. The role of DNA polymerase eta in determining cellular responses to chemo-radiation treatment. [Doctoral Dissertation]. University of Oxford; 2013. Available from: http://ora.ox.ac.uk/objects/uuid:73cef89c-319d-4a14-a3a6-93e8b8dd186a ; https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581330


Northeastern University

28. Norton, Matthew. Discovery of a DNA damage response in Acinetobacter baumannii and analysis of translesion synthesis DNA polymerases of both A. baumannii and Escherichia coli.

Degree: PhD, Department of Biology, 2013, Northeastern University

 Acinetobacter baumannii is a dangerous opportunistic pathogen that has quickly emerged as a source of nosocomial infections for immunocompromised patients. It is able to survive… (more)

Subjects/Keywords: DNA damage; DNA polymerase; pathogen; translesion synthesis; Biology; Molecular Biology

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APA (6th Edition):

Norton, M. (2013). Discovery of a DNA damage response in Acinetobacter baumannii and analysis of translesion synthesis DNA polymerases of both A. baumannii and Escherichia coli. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20003375

Chicago Manual of Style (16th Edition):

Norton, Matthew. “Discovery of a DNA damage response in Acinetobacter baumannii and analysis of translesion synthesis DNA polymerases of both A. baumannii and Escherichia coli.” 2013. Doctoral Dissertation, Northeastern University. Accessed September 28, 2020. http://hdl.handle.net/2047/d20003375.

MLA Handbook (7th Edition):

Norton, Matthew. “Discovery of a DNA damage response in Acinetobacter baumannii and analysis of translesion synthesis DNA polymerases of both A. baumannii and Escherichia coli.” 2013. Web. 28 Sep 2020.

Vancouver:

Norton M. Discovery of a DNA damage response in Acinetobacter baumannii and analysis of translesion synthesis DNA polymerases of both A. baumannii and Escherichia coli. [Internet] [Doctoral dissertation]. Northeastern University; 2013. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/2047/d20003375.

Council of Science Editors:

Norton M. Discovery of a DNA damage response in Acinetobacter baumannii and analysis of translesion synthesis DNA polymerases of both A. baumannii and Escherichia coli. [Doctoral Dissertation]. Northeastern University; 2013. Available from: http://hdl.handle.net/2047/d20003375


University of Melbourne

29. Cameron, Donald Peter John. Investigating acquired resistance to Pol I transcription inhibitors for the treatment of haematologic malignancies.

Degree: 2018, University of Melbourne

 Previous work from our group and others has demonstrated that CX-5461 (Senhwa Biosciences), a first-in-class small molecule inhibitor of RNA Polymerase I transcription of the… (more)

Subjects/Keywords: topoisomerase; ribosomal DNA; RNA Polymerase I; cancer; drug resistance; DNA damage

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APA (6th Edition):

Cameron, D. P. J. (2018). Investigating acquired resistance to Pol I transcription inhibitors for the treatment of haematologic malignancies. (Doctoral Dissertation). University of Melbourne. Retrieved from http://hdl.handle.net/11343/216032

Chicago Manual of Style (16th Edition):

Cameron, Donald Peter John. “Investigating acquired resistance to Pol I transcription inhibitors for the treatment of haematologic malignancies.” 2018. Doctoral Dissertation, University of Melbourne. Accessed September 28, 2020. http://hdl.handle.net/11343/216032.

MLA Handbook (7th Edition):

Cameron, Donald Peter John. “Investigating acquired resistance to Pol I transcription inhibitors for the treatment of haematologic malignancies.” 2018. Web. 28 Sep 2020.

Vancouver:

Cameron DPJ. Investigating acquired resistance to Pol I transcription inhibitors for the treatment of haematologic malignancies. [Internet] [Doctoral dissertation]. University of Melbourne; 2018. [cited 2020 Sep 28]. Available from: http://hdl.handle.net/11343/216032.

Council of Science Editors:

Cameron DPJ. Investigating acquired resistance to Pol I transcription inhibitors for the treatment of haematologic malignancies. [Doctoral Dissertation]. University of Melbourne; 2018. Available from: http://hdl.handle.net/11343/216032


University of Southern California

30. Zhou, Bo. Structural and biochemical studies of large T antigen: the SV40 replicative helicase.

Degree: PhD, Molecular Biology, 2012, University of Southern California

 Simian Virus 40 (SV40) replication has long been regarded as a useful model system in circumventing the complexity of studying the eukaryotic DNA replication process.… (more)

Subjects/Keywords: large T antigen; helicase; DNA polymerase; Primase; DNA replication; crystallography

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APA (6th Edition):

Zhou, B. (2012). Structural and biochemical studies of large T antigen: the SV40 replicative helicase. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/13912/rec/6115

Chicago Manual of Style (16th Edition):

Zhou, Bo. “Structural and biochemical studies of large T antigen: the SV40 replicative helicase.” 2012. Doctoral Dissertation, University of Southern California. Accessed September 28, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/13912/rec/6115.

MLA Handbook (7th Edition):

Zhou, Bo. “Structural and biochemical studies of large T antigen: the SV40 replicative helicase.” 2012. Web. 28 Sep 2020.

Vancouver:

Zhou B. Structural and biochemical studies of large T antigen: the SV40 replicative helicase. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2020 Sep 28]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/13912/rec/6115.

Council of Science Editors:

Zhou B. Structural and biochemical studies of large T antigen: the SV40 replicative helicase. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/13912/rec/6115

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