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You searched for subject:(polymerase). Showing records 1 – 30 of 1609 total matches.

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University of Southern California

1. Oertell, Keriann Michelle. DNA polymerase mechanism and fidelity: using β,γ-bridging oxygen substituted dNTPs to study the mechanism of DNA polymerase β.

Degree: PhD, Chemistry, 2013, University of Southern California

 A β,γ-bridging oxygen substituted dNTP toolkit comprising a variety of steric and electrostatic properties has been synthesized and used to investigate DNA polymerase β. Surprisingly,… (more)

Subjects/Keywords: kinetics; fidelity; polymerase

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APA (6th Edition):

Oertell, K. M. (2013). DNA polymerase mechanism and fidelity: using β,γ-bridging oxygen substituted dNTPs to study the mechanism of DNA polymerase β. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/298584/rec/2071

Chicago Manual of Style (16th Edition):

Oertell, Keriann Michelle. “DNA polymerase mechanism and fidelity: using β,γ-bridging oxygen substituted dNTPs to study the mechanism of DNA polymerase β.” 2013. Doctoral Dissertation, University of Southern California. Accessed June 15, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/298584/rec/2071.

MLA Handbook (7th Edition):

Oertell, Keriann Michelle. “DNA polymerase mechanism and fidelity: using β,γ-bridging oxygen substituted dNTPs to study the mechanism of DNA polymerase β.” 2013. Web. 15 Jun 2019.

Vancouver:

Oertell KM. DNA polymerase mechanism and fidelity: using β,γ-bridging oxygen substituted dNTPs to study the mechanism of DNA polymerase β. [Internet] [Doctoral dissertation]. University of Southern California; 2013. [cited 2019 Jun 15]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/298584/rec/2071.

Council of Science Editors:

Oertell KM. DNA polymerase mechanism and fidelity: using β,γ-bridging oxygen substituted dNTPs to study the mechanism of DNA polymerase β. [Doctoral Dissertation]. University of Southern California; 2013. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/298584/rec/2071

2. 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 June 15, 2019. 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. 15 Jun 2019.

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 2019 Jun 15]. 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


Texas A&M University

3. 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 June 15, 2019. 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. 15 Jun 2019.

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 2019 Jun 15]. 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


Texas A&M University

4. Reddy Chinnaswamy, Sreedhar. De Novo Initiated RNA Synthesis by the Hepatitis C Virus RNA-dependent RNA Polymerase.

Degree: 2011, Texas A&M University

 Hepatitis C Virus (HCV) is a positive-strand RNA virus that has infected more than 3% of the world population. Chronic infections by the virus lead… (more)

Subjects/Keywords: HCV; RdRp; Polymerase; Conformation; Oligomerization

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APA (6th Edition):

Reddy Chinnaswamy, S. (2011). De Novo Initiated RNA Synthesis by the Hepatitis C Virus RNA-dependent RNA Polymerase. (Thesis). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/ETD-TAMU-2010-05-7816

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):

Reddy Chinnaswamy, Sreedhar. “De Novo Initiated RNA Synthesis by the Hepatitis C Virus RNA-dependent RNA Polymerase.” 2011. Thesis, Texas A&M University. Accessed June 15, 2019. http://hdl.handle.net/1969.1/ETD-TAMU-2010-05-7816.

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

MLA Handbook (7th Edition):

Reddy Chinnaswamy, Sreedhar. “De Novo Initiated RNA Synthesis by the Hepatitis C Virus RNA-dependent RNA Polymerase.” 2011. Web. 15 Jun 2019.

Vancouver:

Reddy Chinnaswamy S. De Novo Initiated RNA Synthesis by the Hepatitis C Virus RNA-dependent RNA Polymerase. [Internet] [Thesis]. Texas A&M University; 2011. [cited 2019 Jun 15]. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-05-7816.

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

Council of Science Editors:

Reddy Chinnaswamy S. De Novo Initiated RNA Synthesis by the Hepatitis C Virus RNA-dependent RNA Polymerase. [Thesis]. Texas A&M University; 2011. Available from: http://hdl.handle.net/1969.1/ETD-TAMU-2010-05-7816

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


Texas A&M University

5. Malik, Indranil. In Vivo Consequences of Altered Pol II Catalysis.

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

 Gene transcription by RNA polymerase II (Pol II) is an essential process. Using Saccharomyces cerevisiae as a model system, our lab has previously identified and… (more)

Subjects/Keywords: Transcription; RNA polymerase; Gene regulation

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APA (6th Edition):

Malik, I. (2017). In Vivo Consequences of Altered Pol II Catalysis. (Doctoral Dissertation). Texas A&M University. Retrieved from http://hdl.handle.net/1969.1/165890

Chicago Manual of Style (16th Edition):

Malik, Indranil. “In Vivo Consequences of Altered Pol II Catalysis.” 2017. Doctoral Dissertation, Texas A&M University. Accessed June 15, 2019. http://hdl.handle.net/1969.1/165890.

MLA Handbook (7th Edition):

Malik, Indranil. “In Vivo Consequences of Altered Pol II Catalysis.” 2017. Web. 15 Jun 2019.

Vancouver:

Malik I. In Vivo Consequences of Altered Pol II Catalysis. [Internet] [Doctoral dissertation]. Texas A&M University; 2017. [cited 2019 Jun 15]. Available from: http://hdl.handle.net/1969.1/165890.

Council of Science Editors:

Malik I. In Vivo Consequences of Altered Pol II Catalysis. [Doctoral Dissertation]. Texas A&M University; 2017. Available from: http://hdl.handle.net/1969.1/165890


University of Hong Kong

6. 尹章權; Wan, Cheung-kuen. Evaluation of real time PCR for quantitative detection of enterococci in coastal water.

Degree: Master of Medical Sciences, 2016, University of Hong Kong

 Introduction: In the past, various methods have been used for the quantification of faecal indicators in water samples. Currently, membrane filtration is widely used for… (more)

Subjects/Keywords: Enterococcus; Polymerase chain reaction

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APA (6th Edition):

尹章權; Wan, C. (2016). Evaluation of real time PCR for quantitative detection of enterococci in coastal water. (Masters Thesis). University of Hong Kong. Retrieved from http://hdl.handle.net/10722/227898

Chicago Manual of Style (16th Edition):

尹章權; Wan, Cheung-kuen. “Evaluation of real time PCR for quantitative detection of enterococci in coastal water.” 2016. Masters Thesis, University of Hong Kong. Accessed June 15, 2019. http://hdl.handle.net/10722/227898.

MLA Handbook (7th Edition):

尹章權; Wan, Cheung-kuen. “Evaluation of real time PCR for quantitative detection of enterococci in coastal water.” 2016. Web. 15 Jun 2019.

Vancouver:

尹章權; Wan C. Evaluation of real time PCR for quantitative detection of enterococci in coastal water. [Internet] [Masters thesis]. University of Hong Kong; 2016. [cited 2019 Jun 15]. Available from: http://hdl.handle.net/10722/227898.

Council of Science Editors:

尹章權; Wan C. Evaluation of real time PCR for quantitative detection of enterococci in coastal water. [Masters Thesis]. University of Hong Kong; 2016. Available from: http://hdl.handle.net/10722/227898


University of Louisville

7. Stallons, Lindsey Jay, 1983-. DNA polymerase iota promotes G2/M checkpoint activation and genetic stability after UV-induced DNA damage.

Degree: PhD, 2011, University of Louisville

 Unrepaired DNA damage poses a serious threat to the genetic stability of a replicating cell. One mechanism of tolerating this damage is translesion DNA synthesis… (more)

Subjects/Keywords: Mutagenesis; Cell cycle; Polymerase iota

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APA (6th Edition):

Stallons, Lindsey Jay, 1. (2011). DNA polymerase iota promotes G2/M checkpoint activation and genetic stability after UV-induced DNA damage. (Doctoral Dissertation). University of Louisville. Retrieved from 10.18297/etd/1369 ; https://ir.library.louisville.edu/etd/1369

Chicago Manual of Style (16th Edition):

Stallons, Lindsey Jay, 1983-. “DNA polymerase iota promotes G2/M checkpoint activation and genetic stability after UV-induced DNA damage.” 2011. Doctoral Dissertation, University of Louisville. Accessed June 15, 2019. 10.18297/etd/1369 ; https://ir.library.louisville.edu/etd/1369.

MLA Handbook (7th Edition):

Stallons, Lindsey Jay, 1983-. “DNA polymerase iota promotes G2/M checkpoint activation and genetic stability after UV-induced DNA damage.” 2011. Web. 15 Jun 2019.

Vancouver:

Stallons, Lindsey Jay 1. DNA polymerase iota promotes G2/M checkpoint activation and genetic stability after UV-induced DNA damage. [Internet] [Doctoral dissertation]. University of Louisville; 2011. [cited 2019 Jun 15]. Available from: 10.18297/etd/1369 ; https://ir.library.louisville.edu/etd/1369.

Council of Science Editors:

Stallons, Lindsey Jay 1. DNA polymerase iota promotes G2/M checkpoint activation and genetic stability after UV-induced DNA damage. [Doctoral Dissertation]. University of Louisville; 2011. Available from: 10.18297/etd/1369 ; https://ir.library.louisville.edu/etd/1369


Penn State University

8. Polizzi, Joanna Michelle. THE INCORPORATION OF GEMCITABINE AND CYTARABINE INTO DNA BY DNA.

Degree: MS, Biochemistry and Molecular Biology, 2009, Penn State University

 2'-Deoxy-2',2'-difluorocytidine (gemcitabine, dFdC) and 1-beta-D-arabinofuranosylcytosine (cytarabine, araC) are nucleoside analogues used in the treatment of a variety of malignancies. The active drug metabolites of both… (more)

Subjects/Keywords: polymerase beta; gemcitabine; ligase

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APA (6th Edition):

Polizzi, J. M. (2009). THE INCORPORATION OF GEMCITABINE AND CYTARABINE INTO DNA BY DNA. (Masters Thesis). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/9462

Chicago Manual of Style (16th Edition):

Polizzi, Joanna Michelle. “THE INCORPORATION OF GEMCITABINE AND CYTARABINE INTO DNA BY DNA.” 2009. Masters Thesis, Penn State University. Accessed June 15, 2019. https://etda.libraries.psu.edu/catalog/9462.

MLA Handbook (7th Edition):

Polizzi, Joanna Michelle. “THE INCORPORATION OF GEMCITABINE AND CYTARABINE INTO DNA BY DNA.” 2009. Web. 15 Jun 2019.

Vancouver:

Polizzi JM. THE INCORPORATION OF GEMCITABINE AND CYTARABINE INTO DNA BY DNA. [Internet] [Masters thesis]. Penn State University; 2009. [cited 2019 Jun 15]. Available from: https://etda.libraries.psu.edu/catalog/9462.

Council of Science Editors:

Polizzi JM. THE INCORPORATION OF GEMCITABINE AND CYTARABINE INTO DNA BY DNA. [Masters Thesis]. Penn State University; 2009. Available from: https://etda.libraries.psu.edu/catalog/9462


Penn State University

9. Missra, Anamika. BIOCHEMICAL ANALYSIS OF INTERACTIONS OF DSIF AND NELF WITH THE DROSOPHILA RNA POLYMERASE II TRANSCRIPTION ELONGATION COMPLEX.

Degree: PhD, Biochemistry, Microbiology, and Molecular Biology, 2010, Penn State University

 NELF (Negative Elongation Factor) and DSIF (DRB sensitivity inducing factor) are involved in pausing RNA Polymerase II (Pol II) in the promoter proximal region of… (more)

Subjects/Keywords: gene regulation; transcription; polymerase

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APA (6th Edition):

Missra, A. (2010). BIOCHEMICAL ANALYSIS OF INTERACTIONS OF DSIF AND NELF WITH THE DROSOPHILA RNA POLYMERASE II TRANSCRIPTION ELONGATION COMPLEX. (Doctoral Dissertation). Penn State University. Retrieved from https://etda.libraries.psu.edu/catalog/10560

Chicago Manual of Style (16th Edition):

Missra, Anamika. “BIOCHEMICAL ANALYSIS OF INTERACTIONS OF DSIF AND NELF WITH THE DROSOPHILA RNA POLYMERASE II TRANSCRIPTION ELONGATION COMPLEX.” 2010. Doctoral Dissertation, Penn State University. Accessed June 15, 2019. https://etda.libraries.psu.edu/catalog/10560.

MLA Handbook (7th Edition):

Missra, Anamika. “BIOCHEMICAL ANALYSIS OF INTERACTIONS OF DSIF AND NELF WITH THE DROSOPHILA RNA POLYMERASE II TRANSCRIPTION ELONGATION COMPLEX.” 2010. Web. 15 Jun 2019.

Vancouver:

Missra A. BIOCHEMICAL ANALYSIS OF INTERACTIONS OF DSIF AND NELF WITH THE DROSOPHILA RNA POLYMERASE II TRANSCRIPTION ELONGATION COMPLEX. [Internet] [Doctoral dissertation]. Penn State University; 2010. [cited 2019 Jun 15]. Available from: https://etda.libraries.psu.edu/catalog/10560.

Council of Science Editors:

Missra A. BIOCHEMICAL ANALYSIS OF INTERACTIONS OF DSIF AND NELF WITH THE DROSOPHILA RNA POLYMERASE II TRANSCRIPTION ELONGATION COMPLEX. [Doctoral Dissertation]. Penn State University; 2010. Available from: https://etda.libraries.psu.edu/catalog/10560


Louisiana State University

10. Duhon, Lauren E. In vitro and in vivo evaluation of a Brucella putative hemagglutinin.

Degree: PhD, Veterinary Pathology and Pathobiology, 2009, Louisiana State University

 Brucellosis, a zoonotic disease caused by Brucella spp., presents both health and economic difficulties for livestock, wildlife, and humans. While brucellosis is nearly eradicated in… (more)

Subjects/Keywords: Polymerase Chain Reaction; Hemagglutinin; Brucella

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APA (6th Edition):

Duhon, L. E. (2009). In vitro and in vivo evaluation of a Brucella putative hemagglutinin. (Doctoral Dissertation). Louisiana State University. Retrieved from etd-01272010-205801 ; https://digitalcommons.lsu.edu/gradschool_dissertations/2610

Chicago Manual of Style (16th Edition):

Duhon, Lauren E. “In vitro and in vivo evaluation of a Brucella putative hemagglutinin.” 2009. Doctoral Dissertation, Louisiana State University. Accessed June 15, 2019. etd-01272010-205801 ; https://digitalcommons.lsu.edu/gradschool_dissertations/2610.

MLA Handbook (7th Edition):

Duhon, Lauren E. “In vitro and in vivo evaluation of a Brucella putative hemagglutinin.” 2009. Web. 15 Jun 2019.

Vancouver:

Duhon LE. In vitro and in vivo evaluation of a Brucella putative hemagglutinin. [Internet] [Doctoral dissertation]. Louisiana State University; 2009. [cited 2019 Jun 15]. Available from: etd-01272010-205801 ; https://digitalcommons.lsu.edu/gradschool_dissertations/2610.

Council of Science Editors:

Duhon LE. In vitro and in vivo evaluation of a Brucella putative hemagglutinin. [Doctoral Dissertation]. Louisiana State University; 2009. Available from: etd-01272010-205801 ; https://digitalcommons.lsu.edu/gradschool_dissertations/2610


University of Southern California

11. Chamberlain, Brian Thomas. Deoxynucleotide analog probes and model compounds for studying DNA polymerase structure and mechanism: synthesis and evaluation of alkyl-, azido-, and halomethylene bisphosphonate-substituted triphosphates.

Degree: PhD, Chemistry, 2012, University of Southern California

 A variety of triphosphate analogs that replace a natural phosphate anhydride P-O-P linkage with a phosphonate P-CXY-P moiety have been synthesized for the characterization of… (more)

Subjects/Keywords: bisphosphonates; organoazides; nucleotides; polymerase

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APA (6th Edition):

Chamberlain, B. T. (2012). Deoxynucleotide analog probes and model compounds for studying DNA polymerase structure and mechanism: synthesis and evaluation of alkyl-, azido-, and halomethylene bisphosphonate-substituted triphosphates. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/44705/rec/1837

Chicago Manual of Style (16th Edition):

Chamberlain, Brian Thomas. “Deoxynucleotide analog probes and model compounds for studying DNA polymerase structure and mechanism: synthesis and evaluation of alkyl-, azido-, and halomethylene bisphosphonate-substituted triphosphates.” 2012. Doctoral Dissertation, University of Southern California. Accessed June 15, 2019. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/44705/rec/1837.

MLA Handbook (7th Edition):

Chamberlain, Brian Thomas. “Deoxynucleotide analog probes and model compounds for studying DNA polymerase structure and mechanism: synthesis and evaluation of alkyl-, azido-, and halomethylene bisphosphonate-substituted triphosphates.” 2012. Web. 15 Jun 2019.

Vancouver:

Chamberlain BT. Deoxynucleotide analog probes and model compounds for studying DNA polymerase structure and mechanism: synthesis and evaluation of alkyl-, azido-, and halomethylene bisphosphonate-substituted triphosphates. [Internet] [Doctoral dissertation]. University of Southern California; 2012. [cited 2019 Jun 15]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/44705/rec/1837.

Council of Science Editors:

Chamberlain BT. Deoxynucleotide analog probes and model compounds for studying DNA polymerase structure and mechanism: synthesis and evaluation of alkyl-, azido-, and halomethylene bisphosphonate-substituted triphosphates. [Doctoral Dissertation]. University of Southern California; 2012. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/44705/rec/1837

12. 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 June 15, 2019. 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. 15 Jun 2019.

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 2019 Jun 15]. 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


Duke University

13. 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 June 15, 2019. 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. 15 Jun 2019.

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 2019 Jun 15]. 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


University of Waikato

14. Anderson, Michael Andrew. Detection of Toxoplasma Gondii in Fresh New Zealand Farmed Meat by the Polymerase Chain Reaction .

Degree: 2015, University of Waikato

 Toxoplasma gondii is an obligate intracellular parasite that is estimated to infect one third of the world’s human population. Upon infection this parasite causes the… (more)

Subjects/Keywords: Toxoplasma; Polymerase Chain Reaction

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

APA (6th Edition):

Anderson, M. A. (2015). Detection of Toxoplasma Gondii in Fresh New Zealand Farmed Meat by the Polymerase Chain Reaction . (Masters Thesis). University of Waikato. Retrieved from http://hdl.handle.net/10289/10118

Chicago Manual of Style (16th Edition):

Anderson, Michael Andrew. “Detection of Toxoplasma Gondii in Fresh New Zealand Farmed Meat by the Polymerase Chain Reaction .” 2015. Masters Thesis, University of Waikato. Accessed June 15, 2019. http://hdl.handle.net/10289/10118.

MLA Handbook (7th Edition):

Anderson, Michael Andrew. “Detection of Toxoplasma Gondii in Fresh New Zealand Farmed Meat by the Polymerase Chain Reaction .” 2015. Web. 15 Jun 2019.

Vancouver:

Anderson MA. Detection of Toxoplasma Gondii in Fresh New Zealand Farmed Meat by the Polymerase Chain Reaction . [Internet] [Masters thesis]. University of Waikato; 2015. [cited 2019 Jun 15]. Available from: http://hdl.handle.net/10289/10118.

Council of Science Editors:

Anderson MA. Detection of Toxoplasma Gondii in Fresh New Zealand Farmed Meat by the Polymerase Chain Reaction . [Masters Thesis]. University of Waikato; 2015. Available from: http://hdl.handle.net/10289/10118


University of Rochester

15. Aggarwal, Shilpa. Biochemical Analysis of Enzyme Fidelity and Temperature-dependent Activity of Influenza A Virus RNA Polymerase Complex.

Degree: PhD, 2013, University of Rochester

 Influenza A viruses (IAV) are the cause of highly infectious respiratory illness that causes seasonal epidemics, which are sometimes life threatening. Wild aquatic birds are… (more)

Subjects/Keywords: Influenza; Polymerase; Fidelity; 627

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APA (6th Edition):

Aggarwal, S. (2013). Biochemical Analysis of Enzyme Fidelity and Temperature-dependent Activity of Influenza A Virus RNA Polymerase Complex. (Doctoral Dissertation). University of Rochester. Retrieved from http://hdl.handle.net/1802/27272

Chicago Manual of Style (16th Edition):

Aggarwal, Shilpa. “Biochemical Analysis of Enzyme Fidelity and Temperature-dependent Activity of Influenza A Virus RNA Polymerase Complex.” 2013. Doctoral Dissertation, University of Rochester. Accessed June 15, 2019. http://hdl.handle.net/1802/27272.

MLA Handbook (7th Edition):

Aggarwal, Shilpa. “Biochemical Analysis of Enzyme Fidelity and Temperature-dependent Activity of Influenza A Virus RNA Polymerase Complex.” 2013. Web. 15 Jun 2019.

Vancouver:

Aggarwal S. Biochemical Analysis of Enzyme Fidelity and Temperature-dependent Activity of Influenza A Virus RNA Polymerase Complex. [Internet] [Doctoral dissertation]. University of Rochester; 2013. [cited 2019 Jun 15]. Available from: http://hdl.handle.net/1802/27272.

Council of Science Editors:

Aggarwal S. Biochemical Analysis of Enzyme Fidelity and Temperature-dependent Activity of Influenza A Virus RNA Polymerase Complex. [Doctoral Dissertation]. University of Rochester; 2013. Available from: http://hdl.handle.net/1802/27272


University of Manitoba

16. Imperial, Robin John Lester. Identification of critical residues in the carboxyl-terminal extension of the mitochondrial DNA polymerase in Saccharomyces cerevisiae.

Degree: Microbiology, 2011, University of Manitoba

 Mip1p is the highly processive monomeric mitochondrial DNA polymerase in Saccharomyces cerevisiae. Despite differences in enzyme structure, substrate topology, and possible nucleoid interactions, Mip1p continues… (more)

Subjects/Keywords: mtDNA; polymerase; polg; cte

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APA (6th Edition):

Imperial, R. J. L. (2011). Identification of critical residues in the carboxyl-terminal extension of the mitochondrial DNA polymerase in Saccharomyces cerevisiae. (Masters Thesis). University of Manitoba. Retrieved from http://hdl.handle.net/1993/4798

Chicago Manual of Style (16th Edition):

Imperial, Robin John Lester. “Identification of critical residues in the carboxyl-terminal extension of the mitochondrial DNA polymerase in Saccharomyces cerevisiae.” 2011. Masters Thesis, University of Manitoba. Accessed June 15, 2019. http://hdl.handle.net/1993/4798.

MLA Handbook (7th Edition):

Imperial, Robin John Lester. “Identification of critical residues in the carboxyl-terminal extension of the mitochondrial DNA polymerase in Saccharomyces cerevisiae.” 2011. Web. 15 Jun 2019.

Vancouver:

Imperial RJL. Identification of critical residues in the carboxyl-terminal extension of the mitochondrial DNA polymerase in Saccharomyces cerevisiae. [Internet] [Masters thesis]. University of Manitoba; 2011. [cited 2019 Jun 15]. Available from: http://hdl.handle.net/1993/4798.

Council of Science Editors:

Imperial RJL. Identification of critical residues in the carboxyl-terminal extension of the mitochondrial DNA polymerase in Saccharomyces cerevisiae. [Masters Thesis]. University of Manitoba; 2011. Available from: http://hdl.handle.net/1993/4798


University of New South Wales

17. Wong, Karen Ka Yin. The influenza polymerase: the relationship between evolution and replication fidelity.

Degree: Medical Sciences, 2011, University of New South Wales

 Influenza viruses continue to pose health concerns for the human population. Central to the high mutation rate of the segmented influenza viruses is the low… (more)

Subjects/Keywords: Fidelity; Influenza; Polymerase; Replication

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APA (6th Edition):

Wong, K. K. Y. (2011). The influenza polymerase: the relationship between evolution and replication fidelity. (Doctoral Dissertation). University of New South Wales. Retrieved from http://handle.unsw.edu.au/1959.4/51568 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10233/SOURCE02?view=true

Chicago Manual of Style (16th Edition):

Wong, Karen Ka Yin. “The influenza polymerase: the relationship between evolution and replication fidelity.” 2011. Doctoral Dissertation, University of New South Wales. Accessed June 15, 2019. http://handle.unsw.edu.au/1959.4/51568 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10233/SOURCE02?view=true.

MLA Handbook (7th Edition):

Wong, Karen Ka Yin. “The influenza polymerase: the relationship between evolution and replication fidelity.” 2011. Web. 15 Jun 2019.

Vancouver:

Wong KKY. The influenza polymerase: the relationship between evolution and replication fidelity. [Internet] [Doctoral dissertation]. University of New South Wales; 2011. [cited 2019 Jun 15]. Available from: http://handle.unsw.edu.au/1959.4/51568 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10233/SOURCE02?view=true.

Council of Science Editors:

Wong KKY. The influenza polymerase: the relationship between evolution and replication fidelity. [Doctoral Dissertation]. University of New South Wales; 2011. Available from: http://handle.unsw.edu.au/1959.4/51568 ; https://unsworks.unsw.edu.au/fapi/datastream/unsworks:10233/SOURCE02?view=true


University of Texas – Austin

18. -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: Cellular 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]. (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
Not specified: Masters Thesis or Doctoral Dissertation

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. Thesis, University of Texas – Austin. Accessed June 15, 2019. http://hdl.handle.net/2152/72726.

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

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. 15 Jun 2019.

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] [Thesis]. University of Texas – Austin; 2019. [cited 2019 Jun 15]. 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
Not specified: Masters Thesis or Doctoral Dissertation

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]. [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
Not specified: Masters Thesis or Doctoral Dissertation


University of Texas – Austin

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

Degree: Cellular 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 (6th Edition):

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

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):

Ziehr, Jessica Lea. “Kinetics and specificity of human mitochondrial DNA polymerase gamma and HIV-1 reverse transcriptase.” 2014. Thesis, University of Texas – Austin. Accessed June 15, 2019. http://hdl.handle.net/2152/31296.

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

MLA Handbook (7th Edition):

Ziehr, Jessica Lea. “Kinetics and specificity of human mitochondrial DNA polymerase gamma and HIV-1 reverse transcriptase.” 2014. Web. 15 Jun 2019.

Vancouver:

Ziehr JL. Kinetics and specificity of human mitochondrial DNA polymerase gamma and HIV-1 reverse transcriptase. [Internet] [Thesis]. University of Texas – Austin; 2014. [cited 2019 Jun 15]. Available from: http://hdl.handle.net/2152/31296.

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

Council of Science Editors:

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

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


Indian Institute of Science

20. Mondal, Sudip. Development And Optimization Of A Microchip PCR System Using Fluorescence Detection.

Degree: 2007, Indian Institute of Science

 Microfabricated thermal cyclers for nucleic acid amplification by using polymerase chain reaction (PCR) have been demonstrated by several groups over the last decade, with improved… (more)

Subjects/Keywords: Polymerase Chain Reaction (PCR); Fluorescence; Microchip; Microchip Polymerase Chain Reaction; Real-time Polymerase Chain Reaction; Induction Heater; Microchip PCR; Biophysics

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APA (6th Edition):

Mondal, S. (2007). Development And Optimization Of A Microchip PCR System Using Fluorescence Detection. (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/1073

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):

Mondal, Sudip. “Development And Optimization Of A Microchip PCR System Using Fluorescence Detection.” 2007. Thesis, Indian Institute of Science. Accessed June 15, 2019. http://hdl.handle.net/2005/1073.

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

MLA Handbook (7th Edition):

Mondal, Sudip. “Development And Optimization Of A Microchip PCR System Using Fluorescence Detection.” 2007. Web. 15 Jun 2019.

Vancouver:

Mondal S. Development And Optimization Of A Microchip PCR System Using Fluorescence Detection. [Internet] [Thesis]. Indian Institute of Science; 2007. [cited 2019 Jun 15]. Available from: http://hdl.handle.net/2005/1073.

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

Council of Science Editors:

Mondal S. Development And Optimization Of A Microchip PCR System Using Fluorescence Detection. [Thesis]. Indian Institute of Science; 2007. Available from: http://hdl.handle.net/2005/1073

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


Wayne State University

21. 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 June 15, 2019. 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. 15 Jun 2019.

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 2019 Jun 15]. 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


University of Georgia

22. Henderson, Terri Lynn. Statistical modeling and analysis of the polymerase chain reaction.

Degree: MS, Statistics, 2002, University of Georgia

Polymerase chain reaction (PCR) is a popular method of detecting the presence of a target gene. A mathematical model is developed based upon the principals… (more)

Subjects/Keywords: Polymerase Chain Reaction

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APA (6th Edition):

Henderson, T. L. (2002). Statistical modeling and analysis of the polymerase chain reaction. (Masters Thesis). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/henderson_terri_l_200205_ms

Chicago Manual of Style (16th Edition):

Henderson, Terri Lynn. “Statistical modeling and analysis of the polymerase chain reaction.” 2002. Masters Thesis, University of Georgia. Accessed June 15, 2019. http://purl.galileo.usg.edu/uga_etd/henderson_terri_l_200205_ms.

MLA Handbook (7th Edition):

Henderson, Terri Lynn. “Statistical modeling and analysis of the polymerase chain reaction.” 2002. Web. 15 Jun 2019.

Vancouver:

Henderson TL. Statistical modeling and analysis of the polymerase chain reaction. [Internet] [Masters thesis]. University of Georgia; 2002. [cited 2019 Jun 15]. Available from: http://purl.galileo.usg.edu/uga_etd/henderson_terri_l_200205_ms.

Council of Science Editors:

Henderson TL. Statistical modeling and analysis of the polymerase chain reaction. [Masters Thesis]. University of Georgia; 2002. Available from: http://purl.galileo.usg.edu/uga_etd/henderson_terri_l_200205_ms


University of Oxford

23. Mogni, Maria Elena. Investigations into an archaeal RNA polymerase : structure to function analysis.

Degree: PhD, 2012, University of Oxford

 The archaeal RNA polymerase (RNAP) is similar to the eukaryotic RNAP-II in terms of subunit composition and overall protein structure. Despite its similarity, a new… (more)

Subjects/Keywords: 572.88; Biochemistry; archaea; RNA polymerase; Rpo13

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APA (6th Edition):

Mogni, M. E. (2012). Investigations into an archaeal RNA polymerase : structure to function analysis. (Doctoral Dissertation). University of Oxford. Retrieved from http://ora.ox.ac.uk/objects/uuid:7354996b-5e16-4141-8360-46ab4704c13e ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581130

Chicago Manual of Style (16th Edition):

Mogni, Maria Elena. “Investigations into an archaeal RNA polymerase : structure to function analysis.” 2012. Doctoral Dissertation, University of Oxford. Accessed June 15, 2019. http://ora.ox.ac.uk/objects/uuid:7354996b-5e16-4141-8360-46ab4704c13e ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581130.

MLA Handbook (7th Edition):

Mogni, Maria Elena. “Investigations into an archaeal RNA polymerase : structure to function analysis.” 2012. Web. 15 Jun 2019.

Vancouver:

Mogni ME. Investigations into an archaeal RNA polymerase : structure to function analysis. [Internet] [Doctoral dissertation]. University of Oxford; 2012. [cited 2019 Jun 15]. Available from: http://ora.ox.ac.uk/objects/uuid:7354996b-5e16-4141-8360-46ab4704c13e ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581130.

Council of Science Editors:

Mogni ME. Investigations into an archaeal RNA polymerase : structure to function analysis. [Doctoral Dissertation]. University of Oxford; 2012. Available from: http://ora.ox.ac.uk/objects/uuid:7354996b-5e16-4141-8360-46ab4704c13e ; http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.581130


University of Alberta

24. 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 June 15, 2019. 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. 15 Jun 2019.

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 2019 Jun 15]. 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


University of Pretoria

25. 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 June 15, 2019. 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. 15 Jun 2019.

Vancouver:

Nemakonde A. Efficacy of different DNA polymerase enzymes in PCR amplification of forensic bovine DNA. [Internet] [Masters thesis]. University of Pretoria; 2012. [cited 2019 Jun 15]. 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


Jawaharlal Nehru University

26. Sitaraman, Sujatha. Structure-function relationship in escherichia coli RNA polymerase subunits : a case study with a-subunit; -.

Degree: Biology, 1999, Jawaharlal Nehru University

Specific protein-protein and protein-DNA interactions govern the regulation of all cellular newlineprocesses which constitute a living cell. The basis of all essential biological functions is… (more)

Subjects/Keywords: Molecular Biology; Cellular Biology; polymerase; RNA

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APA (6th Edition):

Sitaraman, S. (1999). Structure-function relationship in escherichia coli RNA polymerase subunits : a case study with a-subunit; -. (Thesis). Jawaharlal Nehru University. Retrieved from http://shodhganga.inflibnet.ac.in/handle/10603/15162

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):

Sitaraman, Sujatha. “Structure-function relationship in escherichia coli RNA polymerase subunits : a case study with a-subunit; -.” 1999. Thesis, Jawaharlal Nehru University. Accessed June 15, 2019. http://shodhganga.inflibnet.ac.in/handle/10603/15162.

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

MLA Handbook (7th Edition):

Sitaraman, Sujatha. “Structure-function relationship in escherichia coli RNA polymerase subunits : a case study with a-subunit; -.” 1999. Web. 15 Jun 2019.

Vancouver:

Sitaraman S. Structure-function relationship in escherichia coli RNA polymerase subunits : a case study with a-subunit; -. [Internet] [Thesis]. Jawaharlal Nehru University; 1999. [cited 2019 Jun 15]. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/15162.

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

Council of Science Editors:

Sitaraman S. Structure-function relationship in escherichia coli RNA polymerase subunits : a case study with a-subunit; -. [Thesis]. Jawaharlal Nehru University; 1999. Available from: http://shodhganga.inflibnet.ac.in/handle/10603/15162

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

27. 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 June 15, 2019. 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. 15 Jun 2019.

Vancouver:

Nayak S. Cloning sequence analysis and characterization of DNA polymerase from Geobacillus sp. WBI. [Internet] [Thesis]. Visva Bharti University; 2014. [cited 2019 Jun 15]. 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


Univerzitet u Beogradu

28. Strelić, Nataša J., 1964-. Značaj molekularne detekcije bakterija u proceni efikasnosti terapije Rajterovog sindroma.

Degree: Biološki fakultet, 2016, Univerzitet u Beogradu

Biologija - Molekularna biologija / Biology - Molecular biology

Nalaz bakterija u sinoviji i sinovijskoj tečnosti inflamiranog zgloba je pobudilo nadu da bi antibiotska terapija mogla biti terapija izbora kod bolesnika sa Rajterovim sindromom...

Advisors/Committee Members: Magić, Zvonko.

Subjects/Keywords: Reiter's syndrome; therapy; polymerase chain reaction

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APA (6th Edition):

Strelić, Nataša J., 1. (2016). Značaj molekularne detekcije bakterija u proceni efikasnosti terapije Rajterovog sindroma. (Thesis). Univerzitet u Beogradu. Retrieved from https://fedorabg.bg.ac.rs/fedora/get/o:10683/bdef:Content/get

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):

Strelić, Nataša J., 1964-. “Značaj molekularne detekcije bakterija u proceni efikasnosti terapije Rajterovog sindroma.” 2016. Thesis, Univerzitet u Beogradu. Accessed June 15, 2019. https://fedorabg.bg.ac.rs/fedora/get/o:10683/bdef:Content/get.

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

MLA Handbook (7th Edition):

Strelić, Nataša J., 1964-. “Značaj molekularne detekcije bakterija u proceni efikasnosti terapije Rajterovog sindroma.” 2016. Web. 15 Jun 2019.

Vancouver:

Strelić, Nataša J. 1. Značaj molekularne detekcije bakterija u proceni efikasnosti terapije Rajterovog sindroma. [Internet] [Thesis]. Univerzitet u Beogradu; 2016. [cited 2019 Jun 15]. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:10683/bdef:Content/get.

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

Council of Science Editors:

Strelić, Nataša J. 1. Značaj molekularne detekcije bakterija u proceni efikasnosti terapije Rajterovog sindroma. [Thesis]. Univerzitet u Beogradu; 2016. Available from: https://fedorabg.bg.ac.rs/fedora/get/o:10683/bdef:Content/get

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


The Ohio State University

29. 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 June 15, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1290014566.

MLA Handbook (7th Edition):

Brown, Jessica Ann. “Kinetic Mechanisms of DNA Polymerases.” 2010. Web. 15 Jun 2019.

Vancouver:

Brown JA. Kinetic Mechanisms of DNA Polymerases. [Internet] [Doctoral dissertation]. The Ohio State University; 2010. [cited 2019 Jun 15]. 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


NSYSU

30. Weng, Chun-chih. Expression of the Vibrio phage ΦA318 RNA polymerase.

Degree: Master, Marine Biotechnology and Resources, 2014, NSYSU

 ããIn aquaculture Vibrio is a major microbial pathogen, Highest death rate may be 100%. ΦA318 is a newly discovered Vibrio phage in our lab, which… (more)

Subjects/Keywords: Vibrio Bacteriophage; phage Promoters; RNA polymerase

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APA (6th Edition):

Weng, C. (2014). Expression of the Vibrio phage ΦA318 RNA polymerase. (Thesis). NSYSU. Retrieved from http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0520114-164408

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):

Weng, Chun-chih. “Expression of the Vibrio phage ΦA318 RNA polymerase.” 2014. Thesis, NSYSU. Accessed June 15, 2019. http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0520114-164408.

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

MLA Handbook (7th Edition):

Weng, Chun-chih. “Expression of the Vibrio phage ΦA318 RNA polymerase.” 2014. Web. 15 Jun 2019.

Vancouver:

Weng C. Expression of the Vibrio phage ΦA318 RNA polymerase. [Internet] [Thesis]. NSYSU; 2014. [cited 2019 Jun 15]. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0520114-164408.

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

Council of Science Editors:

Weng C. Expression of the Vibrio phage ΦA318 RNA polymerase. [Thesis]. NSYSU; 2014. Available from: http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0520114-164408

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

[1] [2] [3] [4] [5] … [54]

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