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You searched for subject:(helicases). Showing records 1 – 30 of 62 total matches.

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Rutgers University

1. Chen, Chi-Fu, 1975-. The Bloom's syndrome DNA helicase complex: identification and characterization of activities conserved in the orthologous complex from saccharomyces cerevisiae.

Degree: PhD, Biochemistry, 2010, Rutgers University

Bloom's Syndrome (BS) is a rare human disease characterized by genome instability and cancer predispostion. The gene mutated in BS, BLM, encodes a member of… (more)

Subjects/Keywords: Genomics; DNA helicases

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APA (6th Edition):

Chen, Chi-Fu, 1. (2010). The Bloom's syndrome DNA helicase complex: identification and characterization of activities conserved in the orthologous complex from saccharomyces cerevisiae. (Doctoral Dissertation). Rutgers University. Retrieved from http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000053567

Chicago Manual of Style (16th Edition):

Chen, Chi-Fu, 1975-. “The Bloom's syndrome DNA helicase complex: identification and characterization of activities conserved in the orthologous complex from saccharomyces cerevisiae.” 2010. Doctoral Dissertation, Rutgers University. Accessed January 20, 2020. http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000053567.

MLA Handbook (7th Edition):

Chen, Chi-Fu, 1975-. “The Bloom's syndrome DNA helicase complex: identification and characterization of activities conserved in the orthologous complex from saccharomyces cerevisiae.” 2010. Web. 20 Jan 2020.

Vancouver:

Chen, Chi-Fu 1. The Bloom's syndrome DNA helicase complex: identification and characterization of activities conserved in the orthologous complex from saccharomyces cerevisiae. [Internet] [Doctoral dissertation]. Rutgers University; 2010. [cited 2020 Jan 20]. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000053567.

Council of Science Editors:

Chen, Chi-Fu 1. The Bloom's syndrome DNA helicase complex: identification and characterization of activities conserved in the orthologous complex from saccharomyces cerevisiae. [Doctoral Dissertation]. Rutgers University; 2010. Available from: http://hdl.rutgers.edu/1782.1/rucore10001600001.ETD.000053567


University of Texas Southwestern Medical Center

2. Owen, David Matthew. Hepatitis C Virus Entry into Hepatocytes and Engagement of Innate Immune Defenses.

Degree: 2011, University of Texas Southwestern Medical Center

 Hepatitis C virus (HCV) infection is a major cause of liver disease and a global health problem with inadequate treatment options. An improved understanding of… (more)

Subjects/Keywords: RNA Helicases; Immunity, Innate; Hepacivirus

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APA (6th Edition):

Owen, D. M. (2011). Hepatitis C Virus Entry into Hepatocytes and Engagement of Innate Immune Defenses. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/874

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):

Owen, David Matthew. “Hepatitis C Virus Entry into Hepatocytes and Engagement of Innate Immune Defenses.” 2011. Thesis, University of Texas Southwestern Medical Center. Accessed January 20, 2020. http://hdl.handle.net/2152.5/874.

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

MLA Handbook (7th Edition):

Owen, David Matthew. “Hepatitis C Virus Entry into Hepatocytes and Engagement of Innate Immune Defenses.” 2011. Web. 20 Jan 2020.

Vancouver:

Owen DM. Hepatitis C Virus Entry into Hepatocytes and Engagement of Innate Immune Defenses. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2011. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2152.5/874.

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

Council of Science Editors:

Owen DM. Hepatitis C Virus Entry into Hepatocytes and Engagement of Innate Immune Defenses. [Thesis]. University of Texas Southwestern Medical Center; 2011. Available from: http://hdl.handle.net/2152.5/874

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


University of Texas Southwestern Medical Center

3. Jiang, Xiaomo. Mechanism of Ubiquitin Induced Activation of RIG-I Like Receptors in Antiviral Innate Immunity.

Degree: 2012, University of Texas Southwestern Medical Center

 The innate immune response is the first line of defense against viral infections. Innate immune recognition is mediated by a set of host pattern recognition… (more)

Subjects/Keywords: Polyubiquitin; DEAD-box RNA Helicases; Encephalomyocarditis virus

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APA (6th Edition):

Jiang, X. (2012). Mechanism of Ubiquitin Induced Activation of RIG-I Like Receptors in Antiviral Innate Immunity. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/1026

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):

Jiang, Xiaomo. “Mechanism of Ubiquitin Induced Activation of RIG-I Like Receptors in Antiviral Innate Immunity.” 2012. Thesis, University of Texas Southwestern Medical Center. Accessed January 20, 2020. http://hdl.handle.net/2152.5/1026.

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

MLA Handbook (7th Edition):

Jiang, Xiaomo. “Mechanism of Ubiquitin Induced Activation of RIG-I Like Receptors in Antiviral Innate Immunity.” 2012. Web. 20 Jan 2020.

Vancouver:

Jiang X. Mechanism of Ubiquitin Induced Activation of RIG-I Like Receptors in Antiviral Innate Immunity. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2012. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2152.5/1026.

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

Council of Science Editors:

Jiang X. Mechanism of Ubiquitin Induced Activation of RIG-I Like Receptors in Antiviral Innate Immunity. [Thesis]. University of Texas Southwestern Medical Center; 2012. Available from: http://hdl.handle.net/2152.5/1026

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


Indian Institute of Science

4. Sharma, Ruchika. Functional Characterization And Regulation Of UvrD Helicases From Haemophilus Influenzae And Helicobacter Pylori, And Recj Exonuclease Fron Haemophilus Influenzae.

Degree: 2011, Indian Institute of Science

 DNA repair processes are crucial for mutation avoidance and the maintenance of genetic integrity in all organisms. Organisms rely on repair processes to combat genotoxic… (more)

Subjects/Keywords: Helicobacter pylori; Hameophilus influenzae; Recj Exonuclease; UvrD helicases DNA; MutL; MutS; HiUvrD; HpUvrD; UvrD Helicases; HiRecJ; Haemophilus influenzae RecJ; Biochemical Genetics

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APA (6th Edition):

Sharma, R. (2011). Functional Characterization And Regulation Of UvrD Helicases From Haemophilus Influenzae And Helicobacter Pylori, And Recj Exonuclease Fron Haemophilus Influenzae. (Thesis). Indian Institute of Science. Retrieved from http://hdl.handle.net/2005/1960

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):

Sharma, Ruchika. “Functional Characterization And Regulation Of UvrD Helicases From Haemophilus Influenzae And Helicobacter Pylori, And Recj Exonuclease Fron Haemophilus Influenzae.” 2011. Thesis, Indian Institute of Science. Accessed January 20, 2020. http://hdl.handle.net/2005/1960.

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

MLA Handbook (7th Edition):

Sharma, Ruchika. “Functional Characterization And Regulation Of UvrD Helicases From Haemophilus Influenzae And Helicobacter Pylori, And Recj Exonuclease Fron Haemophilus Influenzae.” 2011. Web. 20 Jan 2020.

Vancouver:

Sharma R. Functional Characterization And Regulation Of UvrD Helicases From Haemophilus Influenzae And Helicobacter Pylori, And Recj Exonuclease Fron Haemophilus Influenzae. [Internet] [Thesis]. Indian Institute of Science; 2011. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2005/1960.

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

Council of Science Editors:

Sharma R. Functional Characterization And Regulation Of UvrD Helicases From Haemophilus Influenzae And Helicobacter Pylori, And Recj Exonuclease Fron Haemophilus Influenzae. [Thesis]. Indian Institute of Science; 2011. Available from: http://hdl.handle.net/2005/1960

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


Indian Institute of Science

5. Sharma, Ruchika. Functional Characterization And Regulation Of UvrD Helicases From Haemophilus Influenzae And Helicobacter Pylori, And Recj Exonuclease Fron Haemophilus Influenzae.

Degree: 2011, Indian Institute of Science

 DNA repair processes are crucial for mutation avoidance and the maintenance of genetic integrity in all organisms. Organisms rely on repair processes to combat genotoxic… (more)

Subjects/Keywords: Helicobacter pylori; Hameophilus influenzae; Recj Exonuclease; UvrD helicases DNA; MutL; MutS; HiUvrD; HpUvrD; UvrD Helicases; HiRecJ; Haemophilus influenzae RecJ; Biochemical Genetics

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APA (6th Edition):

Sharma, R. (2011). Functional Characterization And Regulation Of UvrD Helicases From Haemophilus Influenzae And Helicobacter Pylori, And Recj Exonuclease Fron Haemophilus Influenzae. (Thesis). Indian Institute of Science. Retrieved from http://etd.iisc.ernet.in/handle/2005/1960 ; http://etd.ncsi.iisc.ernet.in/abstracts/2539/G25029-Abs.pdf

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):

Sharma, Ruchika. “Functional Characterization And Regulation Of UvrD Helicases From Haemophilus Influenzae And Helicobacter Pylori, And Recj Exonuclease Fron Haemophilus Influenzae.” 2011. Thesis, Indian Institute of Science. Accessed January 20, 2020. http://etd.iisc.ernet.in/handle/2005/1960 ; http://etd.ncsi.iisc.ernet.in/abstracts/2539/G25029-Abs.pdf.

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

MLA Handbook (7th Edition):

Sharma, Ruchika. “Functional Characterization And Regulation Of UvrD Helicases From Haemophilus Influenzae And Helicobacter Pylori, And Recj Exonuclease Fron Haemophilus Influenzae.” 2011. Web. 20 Jan 2020.

Vancouver:

Sharma R. Functional Characterization And Regulation Of UvrD Helicases From Haemophilus Influenzae And Helicobacter Pylori, And Recj Exonuclease Fron Haemophilus Influenzae. [Internet] [Thesis]. Indian Institute of Science; 2011. [cited 2020 Jan 20]. Available from: http://etd.iisc.ernet.in/handle/2005/1960 ; http://etd.ncsi.iisc.ernet.in/abstracts/2539/G25029-Abs.pdf.

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

Council of Science Editors:

Sharma R. Functional Characterization And Regulation Of UvrD Helicases From Haemophilus Influenzae And Helicobacter Pylori, And Recj Exonuclease Fron Haemophilus Influenzae. [Thesis]. Indian Institute of Science; 2011. Available from: http://etd.iisc.ernet.in/handle/2005/1960 ; http://etd.ncsi.iisc.ernet.in/abstracts/2539/G25029-Abs.pdf

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

6. Gueddouda, Nassima Meriem. Dénaturation et stabilisation des G-quadruplexes : interaction avec des hélicases et criblage de nouveaux ligands : G-quadruplex denaturation and stabilization : interaction with helicases and screening of G4 ligands.

Degree: Docteur es, Biochimie, 2016, Bordeaux

Les quadruplexes de guanines (G4) sont des structures polymorphiques adoptées in vitro par les séquences d’ADN et d’ARN riches en guanines. L’utilisation d’anticorps et de… (more)

Subjects/Keywords: G-quadruplexes; Hélicases; Ligands G4; G-quadruplexes; Helicases; G4 Ligands

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APA (6th Edition):

Gueddouda, N. M. (2016). Dénaturation et stabilisation des G-quadruplexes : interaction avec des hélicases et criblage de nouveaux ligands : G-quadruplex denaturation and stabilization : interaction with helicases and screening of G4 ligands. (Doctoral Dissertation). Bordeaux. Retrieved from http://www.theses.fr/2016BORD0215

Chicago Manual of Style (16th Edition):

Gueddouda, Nassima Meriem. “Dénaturation et stabilisation des G-quadruplexes : interaction avec des hélicases et criblage de nouveaux ligands : G-quadruplex denaturation and stabilization : interaction with helicases and screening of G4 ligands.” 2016. Doctoral Dissertation, Bordeaux. Accessed January 20, 2020. http://www.theses.fr/2016BORD0215.

MLA Handbook (7th Edition):

Gueddouda, Nassima Meriem. “Dénaturation et stabilisation des G-quadruplexes : interaction avec des hélicases et criblage de nouveaux ligands : G-quadruplex denaturation and stabilization : interaction with helicases and screening of G4 ligands.” 2016. Web. 20 Jan 2020.

Vancouver:

Gueddouda NM. Dénaturation et stabilisation des G-quadruplexes : interaction avec des hélicases et criblage de nouveaux ligands : G-quadruplex denaturation and stabilization : interaction with helicases and screening of G4 ligands. [Internet] [Doctoral dissertation]. Bordeaux; 2016. [cited 2020 Jan 20]. Available from: http://www.theses.fr/2016BORD0215.

Council of Science Editors:

Gueddouda NM. Dénaturation et stabilisation des G-quadruplexes : interaction avec des hélicases et criblage de nouveaux ligands : G-quadruplex denaturation and stabilization : interaction with helicases and screening of G4 ligands. [Doctoral Dissertation]. Bordeaux; 2016. Available from: http://www.theses.fr/2016BORD0215


Leiden University

7. Vlieg, Elger. Helicase induced G-quadruplex unwrapping studied by single-molecule FRET.

Degree: 2017, Leiden University

 G-quadruplexes are non-canonical secondary DNA structures, that are formed by G-rich sequences. Evidence for their existence in vivo has been increasing, and it is suggested… (more)

Subjects/Keywords: Biophysics; G-quadruplexes; Nanyang Technological University; smFRET; Helicases

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APA (6th Edition):

Vlieg, E. (2017). Helicase induced G-quadruplex unwrapping studied by single-molecule FRET. (Masters Thesis). Leiden University. Retrieved from http://hdl.handle.net/1887/47027

Chicago Manual of Style (16th Edition):

Vlieg, Elger. “Helicase induced G-quadruplex unwrapping studied by single-molecule FRET.” 2017. Masters Thesis, Leiden University. Accessed January 20, 2020. http://hdl.handle.net/1887/47027.

MLA Handbook (7th Edition):

Vlieg, Elger. “Helicase induced G-quadruplex unwrapping studied by single-molecule FRET.” 2017. Web. 20 Jan 2020.

Vancouver:

Vlieg E. Helicase induced G-quadruplex unwrapping studied by single-molecule FRET. [Internet] [Masters thesis]. Leiden University; 2017. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/1887/47027.

Council of Science Editors:

Vlieg E. Helicase induced G-quadruplex unwrapping studied by single-molecule FRET. [Masters Thesis]. Leiden University; 2017. Available from: http://hdl.handle.net/1887/47027


Case Western Reserve University

8. Liu, Fei. ATP Utilization by the DEAD-Box Protein DED1P.

Degree: PhD, Physics, 2010, Case Western Reserve University

 DEAD-box proteins, the largest family of RNA helicases, are involved in virtually all aspects of RNA metabolism. DEAD-box proteins catalyze ATP-driven unwinding of RNA duplexes… (more)

Subjects/Keywords: Biochemistry; Biophysics; ATP hydrolysis; RNA helicases; unwinding; DEAD box

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APA (6th Edition):

Liu, F. (2010). ATP Utilization by the DEAD-Box Protein DED1P. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1259924176

Chicago Manual of Style (16th Edition):

Liu, Fei. “ATP Utilization by the DEAD-Box Protein DED1P.” 2010. Doctoral Dissertation, Case Western Reserve University. Accessed January 20, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=case1259924176.

MLA Handbook (7th Edition):

Liu, Fei. “ATP Utilization by the DEAD-Box Protein DED1P.” 2010. Web. 20 Jan 2020.

Vancouver:

Liu F. ATP Utilization by the DEAD-Box Protein DED1P. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2010. [cited 2020 Jan 20]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1259924176.

Council of Science Editors:

Liu F. ATP Utilization by the DEAD-Box Protein DED1P. [Doctoral Dissertation]. Case Western Reserve University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1259924176


Case Western Reserve University

9. Yang, Quansheng. MECHANISM OF RNA REMODELING BY DEAD-BOX HELICASES.

Degree: PhD, Biochemistry, 2007, Case Western Reserve University

 DEAD-box proteins remodel RNA duplexes and displace proteins from RNA in an ATP-dependent fashion. To understand how DEAD-box proteins remodel duplex RNA, I studied the… (more)

Subjects/Keywords: Biology, Molecular; RNA helicases; DEAD-box proteins; Unwinding; Annealing; Structure conversion

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APA (6th Edition):

Yang, Q. (2007). MECHANISM OF RNA REMODELING BY DEAD-BOX HELICASES. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1173812791

Chicago Manual of Style (16th Edition):

Yang, Quansheng. “MECHANISM OF RNA REMODELING BY DEAD-BOX HELICASES.” 2007. Doctoral Dissertation, Case Western Reserve University. Accessed January 20, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=case1173812791.

MLA Handbook (7th Edition):

Yang, Quansheng. “MECHANISM OF RNA REMODELING BY DEAD-BOX HELICASES.” 2007. Web. 20 Jan 2020.

Vancouver:

Yang Q. MECHANISM OF RNA REMODELING BY DEAD-BOX HELICASES. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2007. [cited 2020 Jan 20]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1173812791.

Council of Science Editors:

Yang Q. MECHANISM OF RNA REMODELING BY DEAD-BOX HELICASES. [Doctoral Dissertation]. Case Western Reserve University; 2007. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1173812791


University of British Columbia

10. Youds, Jillian L. Roles of the DOG-1 and JRH-1 helicase-like proteins in DNA repair in Caenorhabditis elegans .

Degree: 2007, University of British Columbia

Helicases perform vital roles in the cell by unwinding D N A to make it accessible for the essential processes of replication, transcription and repair.… (more)

Subjects/Keywords: Helicases; C. elegans; DOG-1

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APA (6th Edition):

Youds, J. L. (2007). Roles of the DOG-1 and JRH-1 helicase-like proteins in DNA repair in Caenorhabditis elegans . (Thesis). University of British Columbia. Retrieved from http://hdl.handle.net/2429/2832

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):

Youds, Jillian L. “Roles of the DOG-1 and JRH-1 helicase-like proteins in DNA repair in Caenorhabditis elegans .” 2007. Thesis, University of British Columbia. Accessed January 20, 2020. http://hdl.handle.net/2429/2832.

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

MLA Handbook (7th Edition):

Youds, Jillian L. “Roles of the DOG-1 and JRH-1 helicase-like proteins in DNA repair in Caenorhabditis elegans .” 2007. Web. 20 Jan 2020.

Vancouver:

Youds JL. Roles of the DOG-1 and JRH-1 helicase-like proteins in DNA repair in Caenorhabditis elegans . [Internet] [Thesis]. University of British Columbia; 2007. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2429/2832.

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

Council of Science Editors:

Youds JL. Roles of the DOG-1 and JRH-1 helicase-like proteins in DNA repair in Caenorhabditis elegans . [Thesis]. University of British Columbia; 2007. Available from: http://hdl.handle.net/2429/2832

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


Wayne State University

11. Kumar, Amit. Differential Activation Of Dead Box Rna Helicases Rhlb And Rhle By Hfq/srnas And Their Target Mrnas.

Degree: MS, Chemistry, 2017, Wayne State University

  Number of small RNA (sRNA) gene regulators have mounted in E. coli over the years whereas the number of validated protein partners has not… (more)

Subjects/Keywords: DEAD-box; Helicases; Hfq; mRNA; sRNA; Biochemistry; Chemistry

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APA (6th Edition):

Kumar, A. (2017). Differential Activation Of Dead Box Rna Helicases Rhlb And Rhle By Hfq/srnas And Their Target Mrnas. (Masters Thesis). Wayne State University. Retrieved from https://digitalcommons.wayne.edu/oa_theses/574

Chicago Manual of Style (16th Edition):

Kumar, Amit. “Differential Activation Of Dead Box Rna Helicases Rhlb And Rhle By Hfq/srnas And Their Target Mrnas.” 2017. Masters Thesis, Wayne State University. Accessed January 20, 2020. https://digitalcommons.wayne.edu/oa_theses/574.

MLA Handbook (7th Edition):

Kumar, Amit. “Differential Activation Of Dead Box Rna Helicases Rhlb And Rhle By Hfq/srnas And Their Target Mrnas.” 2017. Web. 20 Jan 2020.

Vancouver:

Kumar A. Differential Activation Of Dead Box Rna Helicases Rhlb And Rhle By Hfq/srnas And Their Target Mrnas. [Internet] [Masters thesis]. Wayne State University; 2017. [cited 2020 Jan 20]. Available from: https://digitalcommons.wayne.edu/oa_theses/574.

Council of Science Editors:

Kumar A. Differential Activation Of Dead Box Rna Helicases Rhlb And Rhle By Hfq/srnas And Their Target Mrnas. [Masters Thesis]. Wayne State University; 2017. Available from: https://digitalcommons.wayne.edu/oa_theses/574


University of Edinburgh

12. Thelakkad Chathoth, Keerthi. An investigation of splicing-dependent transcriptional checkpoints.

Degree: PhD, 2013, University of Edinburgh

 Pre-mRNA splicing and other RNA processing events occur co-transcriptionally. High resolution kinetic studies performed in our lab showed splicing-dependent RNA Pol II (RNA polymerase II)… (more)

Subjects/Keywords: 572.8; mRNA splicing; splicing helicases; stalled spliceosome; splicing

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APA (6th Edition):

Thelakkad Chathoth, K. (2013). An investigation of splicing-dependent transcriptional checkpoints. (Doctoral Dissertation). University of Edinburgh. Retrieved from http://hdl.handle.net/1842/17547

Chicago Manual of Style (16th Edition):

Thelakkad Chathoth, Keerthi. “An investigation of splicing-dependent transcriptional checkpoints.” 2013. Doctoral Dissertation, University of Edinburgh. Accessed January 20, 2020. http://hdl.handle.net/1842/17547.

MLA Handbook (7th Edition):

Thelakkad Chathoth, Keerthi. “An investigation of splicing-dependent transcriptional checkpoints.” 2013. Web. 20 Jan 2020.

Vancouver:

Thelakkad Chathoth K. An investigation of splicing-dependent transcriptional checkpoints. [Internet] [Doctoral dissertation]. University of Edinburgh; 2013. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/1842/17547.

Council of Science Editors:

Thelakkad Chathoth K. An investigation of splicing-dependent transcriptional checkpoints. [Doctoral Dissertation]. University of Edinburgh; 2013. Available from: http://hdl.handle.net/1842/17547


University of South Florida

13. Kennedy, Jessica Ashley. Structure-Function Analysis of the DNA Damage Repair Complex STR in Saccharomyces cerevisiae.

Degree: 2015, University of South Florida

 The RecQ family of helicases has been termed the “Caretakers of the Genome,” and rightfully so. These proteins are highly conserved from bacteria to humans… (more)

Subjects/Keywords: DNA Repair; Helicases; IDPs; Protein Disorder; Sgs1; Biology

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APA (6th Edition):

Kennedy, J. A. (2015). Structure-Function Analysis of the DNA Damage Repair Complex STR in Saccharomyces cerevisiae. (Thesis). University of South Florida. Retrieved from https://scholarcommons.usf.edu/etd/5713

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):

Kennedy, Jessica Ashley. “Structure-Function Analysis of the DNA Damage Repair Complex STR in Saccharomyces cerevisiae.” 2015. Thesis, University of South Florida. Accessed January 20, 2020. https://scholarcommons.usf.edu/etd/5713.

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

MLA Handbook (7th Edition):

Kennedy, Jessica Ashley. “Structure-Function Analysis of the DNA Damage Repair Complex STR in Saccharomyces cerevisiae.” 2015. Web. 20 Jan 2020.

Vancouver:

Kennedy JA. Structure-Function Analysis of the DNA Damage Repair Complex STR in Saccharomyces cerevisiae. [Internet] [Thesis]. University of South Florida; 2015. [cited 2020 Jan 20]. Available from: https://scholarcommons.usf.edu/etd/5713.

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

Council of Science Editors:

Kennedy JA. Structure-Function Analysis of the DNA Damage Repair Complex STR in Saccharomyces cerevisiae. [Thesis]. University of South Florida; 2015. Available from: https://scholarcommons.usf.edu/etd/5713

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


University of Texas Southwestern Medical Center

14. Foy, Eileen. Control of the Interferon Regulatory Factor - 3 Antiviral Pathway by The Hepatitis C Virus Ns3/4a Protease.

Degree: 2007, University of Texas Southwestern Medical Center

 Hepatitis C Virus (HCV) is a major human pathogen that affects 200 million people worldwide. A majority of people exposed to HCV become chronically infected.… (more)

Subjects/Keywords: RNA Helicases; Signal Transduction; Hepacivirus

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APA (6th Edition):

Foy, E. (2007). Control of the Interferon Regulatory Factor - 3 Antiviral Pathway by The Hepatitis C Virus Ns3/4a Protease. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/281

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):

Foy, Eileen. “Control of the Interferon Regulatory Factor - 3 Antiviral Pathway by The Hepatitis C Virus Ns3/4a Protease.” 2007. Thesis, University of Texas Southwestern Medical Center. Accessed January 20, 2020. http://hdl.handle.net/2152.5/281.

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

MLA Handbook (7th Edition):

Foy, Eileen. “Control of the Interferon Regulatory Factor - 3 Antiviral Pathway by The Hepatitis C Virus Ns3/4a Protease.” 2007. Web. 20 Jan 2020.

Vancouver:

Foy E. Control of the Interferon Regulatory Factor - 3 Antiviral Pathway by The Hepatitis C Virus Ns3/4a Protease. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2007. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2152.5/281.

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

Council of Science Editors:

Foy E. Control of the Interferon Regulatory Factor - 3 Antiviral Pathway by The Hepatitis C Virus Ns3/4a Protease. [Thesis]. University of Texas Southwestern Medical Center; 2007. Available from: http://hdl.handle.net/2152.5/281

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


University of Illinois – Urbana-Champaign

15. Whitley, Kevin D. Single-molecule studies of mechanical and helicase-catalyzed disruption of nucleic acid duplexes.

Degree: PhD, Biophysics & Computnl Biology, 2017, University of Illinois – Urbana-Champaign

 Nucleic acids (e.g. DNA, RNA) are subjected to numerous twisting, bending, and stretching forces within cells, and enzymes process them in a variety of ways.… (more)

Subjects/Keywords: Nucleic acids; Optical tweezers; Single-molecule; Fluorescence; Helicases

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APA (6th Edition):

Whitley, K. D. (2017). Single-molecule studies of mechanical and helicase-catalyzed disruption of nucleic acid duplexes. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/97690

Chicago Manual of Style (16th Edition):

Whitley, Kevin D. “Single-molecule studies of mechanical and helicase-catalyzed disruption of nucleic acid duplexes.” 2017. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed January 20, 2020. http://hdl.handle.net/2142/97690.

MLA Handbook (7th Edition):

Whitley, Kevin D. “Single-molecule studies of mechanical and helicase-catalyzed disruption of nucleic acid duplexes.” 2017. Web. 20 Jan 2020.

Vancouver:

Whitley KD. Single-molecule studies of mechanical and helicase-catalyzed disruption of nucleic acid duplexes. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2017. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2142/97690.

Council of Science Editors:

Whitley KD. Single-molecule studies of mechanical and helicase-catalyzed disruption of nucleic acid duplexes. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2017. Available from: http://hdl.handle.net/2142/97690

16. Willis, Nicholas Adrian. Checkpoint Regulation of Replication Forks in Response to DNA Damage: A Dissertation.

Degree: Interdisciplinary Graduate Program, Biochemistry and Molecular Pharmacology, 2009, U of Massachusetts : Med

  Faithful duplication and segregation of undamaged DNA is critical to the survival of all organisms and prevention of oncogenesis in multicellular organisms. To ensure… (more)

Subjects/Keywords: DNA Damage; DNA Helicases; DNA-Binding Proteins; Endonucleases; S Phase; Schizosaccharomyces; Schizosaccharomyces pombe Proteins; RecQ Helicases; Amino Acids, Peptides, and Proteins; Enzymes and Coenzymes; Fungi; Genetic Phenomena

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APA (6th Edition):

Willis, N. A. (2009). Checkpoint Regulation of Replication Forks in Response to DNA Damage: A Dissertation. (Doctoral Dissertation). U of Massachusetts : Med. Retrieved from https://escholarship.umassmed.edu/gsbs_diss/427

Chicago Manual of Style (16th Edition):

Willis, Nicholas Adrian. “Checkpoint Regulation of Replication Forks in Response to DNA Damage: A Dissertation.” 2009. Doctoral Dissertation, U of Massachusetts : Med. Accessed January 20, 2020. https://escholarship.umassmed.edu/gsbs_diss/427.

MLA Handbook (7th Edition):

Willis, Nicholas Adrian. “Checkpoint Regulation of Replication Forks in Response to DNA Damage: A Dissertation.” 2009. Web. 20 Jan 2020.

Vancouver:

Willis NA. Checkpoint Regulation of Replication Forks in Response to DNA Damage: A Dissertation. [Internet] [Doctoral dissertation]. U of Massachusetts : Med; 2009. [cited 2020 Jan 20]. Available from: https://escholarship.umassmed.edu/gsbs_diss/427.

Council of Science Editors:

Willis NA. Checkpoint Regulation of Replication Forks in Response to DNA Damage: A Dissertation. [Doctoral Dissertation]. U of Massachusetts : Med; 2009. Available from: https://escholarship.umassmed.edu/gsbs_diss/427

17. Auzon-Cape, Maxime. Étude des voies de régulation de la méthylation de l’ADN et du relâchement du silencing après choc thermique chez Arabidopsis thaliana : Study of DNA methylation regulation pathways and release of silencing after heat shock in Arabidopsis thaliana.

Degree: Docteur es, Physiologie et Génétique Moléculaire, 2017, Clermont Auvergne

Chez Arabidopsis thaliana, le silencing transcriptionnel est associé notamment aux modifications post-traductionnelles des queues des histones et à la méthylation des cytosines en contexte CG,… (more)

Subjects/Keywords: Arabidopsis thaliana; Silencing; Stress thermique; Relâchement du silencing; ROS1; RH35; RNA DEAD box helicases; Arabidopsis thaliana; Silencing; Heat stress; Release of silencing; ROS1; RH35; RNA DEAD box helicases

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APA (6th Edition):

Auzon-Cape, M. (2017). Étude des voies de régulation de la méthylation de l’ADN et du relâchement du silencing après choc thermique chez Arabidopsis thaliana : Study of DNA methylation regulation pathways and release of silencing after heat shock in Arabidopsis thaliana. (Doctoral Dissertation). Clermont Auvergne. Retrieved from http://www.theses.fr/2017CLFAC108

Chicago Manual of Style (16th Edition):

Auzon-Cape, Maxime. “Étude des voies de régulation de la méthylation de l’ADN et du relâchement du silencing après choc thermique chez Arabidopsis thaliana : Study of DNA methylation regulation pathways and release of silencing after heat shock in Arabidopsis thaliana.” 2017. Doctoral Dissertation, Clermont Auvergne. Accessed January 20, 2020. http://www.theses.fr/2017CLFAC108.

MLA Handbook (7th Edition):

Auzon-Cape, Maxime. “Étude des voies de régulation de la méthylation de l’ADN et du relâchement du silencing après choc thermique chez Arabidopsis thaliana : Study of DNA methylation regulation pathways and release of silencing after heat shock in Arabidopsis thaliana.” 2017. Web. 20 Jan 2020.

Vancouver:

Auzon-Cape M. Étude des voies de régulation de la méthylation de l’ADN et du relâchement du silencing après choc thermique chez Arabidopsis thaliana : Study of DNA methylation regulation pathways and release of silencing after heat shock in Arabidopsis thaliana. [Internet] [Doctoral dissertation]. Clermont Auvergne; 2017. [cited 2020 Jan 20]. Available from: http://www.theses.fr/2017CLFAC108.

Council of Science Editors:

Auzon-Cape M. Étude des voies de régulation de la méthylation de l’ADN et du relâchement du silencing après choc thermique chez Arabidopsis thaliana : Study of DNA methylation regulation pathways and release of silencing after heat shock in Arabidopsis thaliana. [Doctoral Dissertation]. Clermont Auvergne; 2017. Available from: http://www.theses.fr/2017CLFAC108


University of Southern California

18. Ding, Lin. Essential and non-essential helicases maintain genome stability in Schizosaccharomyces pombe.

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

 A healthy cell needs to accurately duplicate its genome and pass one copy to each of its daughter cells. The DNA double helix is accessed… (more)

Subjects/Keywords: replication fork; helicases; MCM; S. pombe; ubiquitin ligase; fork regression; fork recovery; homologous recombination

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APA (6th Edition):

Ding, L. (2014). Essential and non-essential helicases maintain genome stability in Schizosaccharomyces pombe. (Doctoral Dissertation). University of Southern California. Retrieved from http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/360582/rec/2492

Chicago Manual of Style (16th Edition):

Ding, Lin. “Essential and non-essential helicases maintain genome stability in Schizosaccharomyces pombe.” 2014. Doctoral Dissertation, University of Southern California. Accessed January 20, 2020. http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/360582/rec/2492.

MLA Handbook (7th Edition):

Ding, Lin. “Essential and non-essential helicases maintain genome stability in Schizosaccharomyces pombe.” 2014. Web. 20 Jan 2020.

Vancouver:

Ding L. Essential and non-essential helicases maintain genome stability in Schizosaccharomyces pombe. [Internet] [Doctoral dissertation]. University of Southern California; 2014. [cited 2020 Jan 20]. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/360582/rec/2492.

Council of Science Editors:

Ding L. Essential and non-essential helicases maintain genome stability in Schizosaccharomyces pombe. [Doctoral Dissertation]. University of Southern California; 2014. Available from: http://digitallibrary.usc.edu/cdm/compoundobject/collection/p15799coll3/id/360582/rec/2492

19. L. DARDAEI ALGHALANDIS. UNRAVELING MOLECULAR MECHANISMS UNDERLYING MEIS1ONCOGENIC ACTIVITY; POSSIBLE COMPETITION WITH PREP1.

Degree: 2013, Università degli Studi di Milano

 Meis1 and Prep1 homeodomain-containing transcription factors are essential for the normal embryonic development of several tissues and organs. Although they both can recruit Pbx at… (more)

Subjects/Keywords: Meis1; Prep1; RNA helicases; Oncogene; tumor suppressor; tumorigenesis; Settore BIO/11 - Biologia Molecolare

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APA (6th Edition):

ALGHALANDIS, L. D. (2013). UNRAVELING MOLECULAR MECHANISMS UNDERLYING MEIS1ONCOGENIC ACTIVITY; POSSIBLE COMPETITION WITH PREP1. (Thesis). Università degli Studi di Milano. Retrieved from http://hdl.handle.net/2434/219063

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):

ALGHALANDIS, L. DARDAEI. “UNRAVELING MOLECULAR MECHANISMS UNDERLYING MEIS1ONCOGENIC ACTIVITY; POSSIBLE COMPETITION WITH PREP1.” 2013. Thesis, Università degli Studi di Milano. Accessed January 20, 2020. http://hdl.handle.net/2434/219063.

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

MLA Handbook (7th Edition):

ALGHALANDIS, L. DARDAEI. “UNRAVELING MOLECULAR MECHANISMS UNDERLYING MEIS1ONCOGENIC ACTIVITY; POSSIBLE COMPETITION WITH PREP1.” 2013. Web. 20 Jan 2020.

Vancouver:

ALGHALANDIS LD. UNRAVELING MOLECULAR MECHANISMS UNDERLYING MEIS1ONCOGENIC ACTIVITY; POSSIBLE COMPETITION WITH PREP1. [Internet] [Thesis]. Università degli Studi di Milano; 2013. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2434/219063.

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

Council of Science Editors:

ALGHALANDIS LD. UNRAVELING MOLECULAR MECHANISMS UNDERLYING MEIS1ONCOGENIC ACTIVITY; POSSIBLE COMPETITION WITH PREP1. [Thesis]. Università degli Studi di Milano; 2013. Available from: http://hdl.handle.net/2434/219063

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


Washington University in St. Louis

20. Wu, Colin. Transient-State Kinetic Studies of The Mechanisms of Dna Unwinding And Translocation of The E. Coli Recbc And Recbcd Helicases.

Degree: PhD, Biology and Biomedical Sciences: Biochemistry, 2010, Washington University in St. Louis

 This thesis presents mechanistic studies of the E. coli RecBC and RecBCD helicases using transient-state kinetic approaches to understand the relationship between DNA unwinding and… (more)

Subjects/Keywords: Biology, Molecular; Biophysics, General; Chemistry, Biochemistry; Allostery, Fluorescence, Helicases, Kinetics, Motors, Unwinding

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APA (6th Edition):

Wu, C. (2010). Transient-State Kinetic Studies of The Mechanisms of Dna Unwinding And Translocation of The E. Coli Recbc And Recbcd Helicases. (Doctoral Dissertation). Washington University in St. Louis. Retrieved from https://openscholarship.wustl.edu/etd/382

Chicago Manual of Style (16th Edition):

Wu, Colin. “Transient-State Kinetic Studies of The Mechanisms of Dna Unwinding And Translocation of The E. Coli Recbc And Recbcd Helicases.” 2010. Doctoral Dissertation, Washington University in St. Louis. Accessed January 20, 2020. https://openscholarship.wustl.edu/etd/382.

MLA Handbook (7th Edition):

Wu, Colin. “Transient-State Kinetic Studies of The Mechanisms of Dna Unwinding And Translocation of The E. Coli Recbc And Recbcd Helicases.” 2010. Web. 20 Jan 2020.

Vancouver:

Wu C. Transient-State Kinetic Studies of The Mechanisms of Dna Unwinding And Translocation of The E. Coli Recbc And Recbcd Helicases. [Internet] [Doctoral dissertation]. Washington University in St. Louis; 2010. [cited 2020 Jan 20]. Available from: https://openscholarship.wustl.edu/etd/382.

Council of Science Editors:

Wu C. Transient-State Kinetic Studies of The Mechanisms of Dna Unwinding And Translocation of The E. Coli Recbc And Recbcd Helicases. [Doctoral Dissertation]. Washington University in St. Louis; 2010. Available from: https://openscholarship.wustl.edu/etd/382

21. Bercy, Mathilde. Les structures secondaires dans l'ARN : une étude par mesure de forces sur molécules uniques : RNA secondary structures : a single molecules force measurements study.

Degree: Docteur es, Physique, 2015, Université Pierre et Marie Curie – Paris VI

L'ARN s'est longtemps vu attribuer un simple role de transmission entre l'ADN, garant de l'information genetique, et les proteines, assurant les fonctions et donc la… (more)

Subjects/Keywords: Molécule unique; Pièges optiques; Arn; Hairpins; Helicases; Surétirement; Single molecule; Optical tweezers; RNA; 530

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APA (6th Edition):

Bercy, M. (2015). Les structures secondaires dans l'ARN : une étude par mesure de forces sur molécules uniques : RNA secondary structures : a single molecules force measurements study. (Doctoral Dissertation). Université Pierre et Marie Curie – Paris VI. Retrieved from http://www.theses.fr/2015PA066718

Chicago Manual of Style (16th Edition):

Bercy, Mathilde. “Les structures secondaires dans l'ARN : une étude par mesure de forces sur molécules uniques : RNA secondary structures : a single molecules force measurements study.” 2015. Doctoral Dissertation, Université Pierre et Marie Curie – Paris VI. Accessed January 20, 2020. http://www.theses.fr/2015PA066718.

MLA Handbook (7th Edition):

Bercy, Mathilde. “Les structures secondaires dans l'ARN : une étude par mesure de forces sur molécules uniques : RNA secondary structures : a single molecules force measurements study.” 2015. Web. 20 Jan 2020.

Vancouver:

Bercy M. Les structures secondaires dans l'ARN : une étude par mesure de forces sur molécules uniques : RNA secondary structures : a single molecules force measurements study. [Internet] [Doctoral dissertation]. Université Pierre et Marie Curie – Paris VI; 2015. [cited 2020 Jan 20]. Available from: http://www.theses.fr/2015PA066718.

Council of Science Editors:

Bercy M. Les structures secondaires dans l'ARN : une étude par mesure de forces sur molécules uniques : RNA secondary structures : a single molecules force measurements study. [Doctoral Dissertation]. Université Pierre et Marie Curie – Paris VI; 2015. Available from: http://www.theses.fr/2015PA066718


University of South Florida

22. Syed, Salahuddin. Nonreplicative DNA Helicases Involved in Maintaining Genome Stability.

Degree: 2016, University of South Florida

 Double-strand breaks and stalled forks arise when the replication machinery encounters damage from exogenous sources like DNA damaging agents or ionizing radiation, and require specific… (more)

Subjects/Keywords: RecQ Helicases; DNA repair; Sgs1; RECQL5; Rrm3; Cell Biology; Genetics; Molecular Biology

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APA (6th Edition):

Syed, S. (2016). Nonreplicative DNA Helicases Involved in Maintaining Genome Stability. (Thesis). University of South Florida. Retrieved from https://scholarcommons.usf.edu/etd/6408

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):

Syed, Salahuddin. “Nonreplicative DNA Helicases Involved in Maintaining Genome Stability.” 2016. Thesis, University of South Florida. Accessed January 20, 2020. https://scholarcommons.usf.edu/etd/6408.

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

MLA Handbook (7th Edition):

Syed, Salahuddin. “Nonreplicative DNA Helicases Involved in Maintaining Genome Stability.” 2016. Web. 20 Jan 2020.

Vancouver:

Syed S. Nonreplicative DNA Helicases Involved in Maintaining Genome Stability. [Internet] [Thesis]. University of South Florida; 2016. [cited 2020 Jan 20]. Available from: https://scholarcommons.usf.edu/etd/6408.

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

Council of Science Editors:

Syed S. Nonreplicative DNA Helicases Involved in Maintaining Genome Stability. [Thesis]. University of South Florida; 2016. Available from: https://scholarcommons.usf.edu/etd/6408

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

23. Campos-Doerfler, Lillian. The Role of Sgs1 and Exo1 in the Maintenance of Genome Stability.

Degree: 2017, University of South Florida

 Genome instability is a hallmark of human cancers. Patients with Bloom’s syndrome, a rare chromosome breakage syndrome caused by inactivation of the RecQ helicase BLM,… (more)

Subjects/Keywords: Genome Instability; DNA repair; RecQ Helicases; Sgs1; Exo1; Cell Biology; Molecular Biology

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APA (6th Edition):

Campos-Doerfler, L. (2017). The Role of Sgs1 and Exo1 in the Maintenance of Genome Stability. (Thesis). University of South Florida. Retrieved from https://scholarcommons.usf.edu/etd/7006

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):

Campos-Doerfler, Lillian. “The Role of Sgs1 and Exo1 in the Maintenance of Genome Stability.” 2017. Thesis, University of South Florida. Accessed January 20, 2020. https://scholarcommons.usf.edu/etd/7006.

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

MLA Handbook (7th Edition):

Campos-Doerfler, Lillian. “The Role of Sgs1 and Exo1 in the Maintenance of Genome Stability.” 2017. Web. 20 Jan 2020.

Vancouver:

Campos-Doerfler L. The Role of Sgs1 and Exo1 in the Maintenance of Genome Stability. [Internet] [Thesis]. University of South Florida; 2017. [cited 2020 Jan 20]. Available from: https://scholarcommons.usf.edu/etd/7006.

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

Council of Science Editors:

Campos-Doerfler L. The Role of Sgs1 and Exo1 in the Maintenance of Genome Stability. [Thesis]. University of South Florida; 2017. Available from: https://scholarcommons.usf.edu/etd/7006

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


Case Western Reserve University

24. Gao, Zhaofeng. Molecular Mechanism of the Ded1p-eIF4F Complex.

Degree: PhD, Biochemistry, 2016, Case Western Reserve University

 The eukaryotic translation initiation factor 4F (eIF4F) consists of the large scaffolding and RNA binding protein eIF4G, the cap-binding protein eIF4E, and the DEAD-box RNA… (more)

Subjects/Keywords: Biochemistry; DEAD-box RNA helicases, translation initiation, Ded1p, eIF4A, eIF4G, eIF4E, eIF4F

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APA (6th Edition):

Gao, Z. (2016). Molecular Mechanism of the Ded1p-eIF4F Complex. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1467824941

Chicago Manual of Style (16th Edition):

Gao, Zhaofeng. “Molecular Mechanism of the Ded1p-eIF4F Complex.” 2016. Doctoral Dissertation, Case Western Reserve University. Accessed January 20, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=case1467824941.

MLA Handbook (7th Edition):

Gao, Zhaofeng. “Molecular Mechanism of the Ded1p-eIF4F Complex.” 2016. Web. 20 Jan 2020.

Vancouver:

Gao Z. Molecular Mechanism of the Ded1p-eIF4F Complex. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2016. [cited 2020 Jan 20]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1467824941.

Council of Science Editors:

Gao Z. Molecular Mechanism of the Ded1p-eIF4F Complex. [Doctoral Dissertation]. Case Western Reserve University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1467824941


University of Texas Southwestern Medical Center

25. Tagal, Vural. SMARCA4/BRG1-Inactivating Mutations as Potential Predictive Markers for Aurora Kinase A-Targeted Therapy in NSCLCs.

Degree: 2014, University of Texas Southwestern Medical Center

 SMARCA4 encodes a catalytic subunit of the SWI/SNF chromatin remodeling complex, BRG1. Frequent occurrence of SMARCA4/BRG1-inactivating mutations and their mutually exclusive nature from EGFR and… (more)

Subjects/Keywords: Aurora Kinase A; Carcinoma, Non-Small-Cell Lung; DNA Helicases; Nuclear Proteins; Transcription Factors

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APA (6th Edition):

Tagal, V. (2014). SMARCA4/BRG1-Inactivating Mutations as Potential Predictive Markers for Aurora Kinase A-Targeted Therapy in NSCLCs. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/3570

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):

Tagal, Vural. “SMARCA4/BRG1-Inactivating Mutations as Potential Predictive Markers for Aurora Kinase A-Targeted Therapy in NSCLCs.” 2014. Thesis, University of Texas Southwestern Medical Center. Accessed January 20, 2020. http://hdl.handle.net/2152.5/3570.

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

MLA Handbook (7th Edition):

Tagal, Vural. “SMARCA4/BRG1-Inactivating Mutations as Potential Predictive Markers for Aurora Kinase A-Targeted Therapy in NSCLCs.” 2014. Web. 20 Jan 2020.

Vancouver:

Tagal V. SMARCA4/BRG1-Inactivating Mutations as Potential Predictive Markers for Aurora Kinase A-Targeted Therapy in NSCLCs. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2014. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/2152.5/3570.

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

Council of Science Editors:

Tagal V. SMARCA4/BRG1-Inactivating Mutations as Potential Predictive Markers for Aurora Kinase A-Targeted Therapy in NSCLCs. [Thesis]. University of Texas Southwestern Medical Center; 2014. Available from: http://hdl.handle.net/2152.5/3570

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


Michigan State University

26. Ziebarth, Tawn Denise. Modular architecture and dynamic oligomeric structure of the human mitochondrial replicative DNA helicase.

Degree: MS, Department of Biochemistry and Molecular Biology, 2006, Michigan State University

Subjects/Keywords: Mitochondrial DNA; DNA helicases; Nucleotide sequence

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APA (6th Edition):

Ziebarth, T. D. (2006). Modular architecture and dynamic oligomeric structure of the human mitochondrial replicative DNA helicase. (Masters Thesis). Michigan State University. Retrieved from http://etd.lib.msu.edu/islandora/object/etd:38217

Chicago Manual of Style (16th Edition):

Ziebarth, Tawn Denise. “Modular architecture and dynamic oligomeric structure of the human mitochondrial replicative DNA helicase.” 2006. Masters Thesis, Michigan State University. Accessed January 20, 2020. http://etd.lib.msu.edu/islandora/object/etd:38217.

MLA Handbook (7th Edition):

Ziebarth, Tawn Denise. “Modular architecture and dynamic oligomeric structure of the human mitochondrial replicative DNA helicase.” 2006. Web. 20 Jan 2020.

Vancouver:

Ziebarth TD. Modular architecture and dynamic oligomeric structure of the human mitochondrial replicative DNA helicase. [Internet] [Masters thesis]. Michigan State University; 2006. [cited 2020 Jan 20]. Available from: http://etd.lib.msu.edu/islandora/object/etd:38217.

Council of Science Editors:

Ziebarth TD. Modular architecture and dynamic oligomeric structure of the human mitochondrial replicative DNA helicase. [Masters Thesis]. Michigan State University; 2006. Available from: http://etd.lib.msu.edu/islandora/object/etd:38217

27. Ναθαναηλίδου, Πατρούλα. Μελέτη του ορθολόγου της ελικάσης RecQ4, Hrq1, στον σχιζοσακχαρομύκητα.

Degree: 2014, University of Patras

Η διατήρηση της γονιδιωματικής ακεραιότητας είναι απαραίτητη για την επιβίωση των κυττάρων και κατ’ επέκταση των οργανισμών. Δύο είναι οι κύριοι παράγοντες που συμβάλλουν στην… (more)

Subjects/Keywords: Ελικάσες; Επιδιόρθωση του DNA; Αντιγραφή του DNA; Σχιζοσακχαρομύκητας; 612.015; Helicases; Hrq1; RecQ; DNA repair; DNA replication; S. pombe

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APA (6th Edition):

Ναθαναηλίδου, . (2014). Μελέτη του ορθολόγου της ελικάσης RecQ4, Hrq1, στον σχιζοσακχαρομύκητα. (Masters Thesis). University of Patras. Retrieved from http://hdl.handle.net/10889/8394

Chicago Manual of Style (16th Edition):

Ναθαναηλίδου, Πατρούλα. “Μελέτη του ορθολόγου της ελικάσης RecQ4, Hrq1, στον σχιζοσακχαρομύκητα.” 2014. Masters Thesis, University of Patras. Accessed January 20, 2020. http://hdl.handle.net/10889/8394.

MLA Handbook (7th Edition):

Ναθαναηλίδου, Πατρούλα. “Μελέτη του ορθολόγου της ελικάσης RecQ4, Hrq1, στον σχιζοσακχαρομύκητα.” 2014. Web. 20 Jan 2020.

Vancouver:

Ναθαναηλίδου . Μελέτη του ορθολόγου της ελικάσης RecQ4, Hrq1, στον σχιζοσακχαρομύκητα. [Internet] [Masters thesis]. University of Patras; 2014. [cited 2020 Jan 20]. Available from: http://hdl.handle.net/10889/8394.

Council of Science Editors:

Ναθαναηλίδου . Μελέτη του ορθολόγου της ελικάσης RecQ4, Hrq1, στον σχιζοσακχαρομύκητα. [Masters Thesis]. University of Patras; 2014. Available from: http://hdl.handle.net/10889/8394


University of Hong Kong

28. 沈家滔.; Shum, Ka-to. A comparative study of G-quadruplex aptamers against multiple protein targets.

Degree: PhD, 2010, University of Hong Kong

published_or_final_version

Biochemistry

Doctoral

Doctor of Philosophy

Advisors/Committee Members: Huang, J, Tanner, JA.

Subjects/Keywords: Protein kinases.; Oligonucleotides.; DNA helicases.; Polyphosphates.; Glycoproteins.

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APA (6th Edition):

沈家滔.; Shum, K. (2010). A comparative study of G-quadruplex aptamers against multiple protein targets. (Doctoral Dissertation). University of Hong Kong. Retrieved from Shum, K. [沈家滔]. (2010). A comparative study of G-quadruplex aptamers against multiple protein targets. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4581623 ; http://dx.doi.org/10.5353/th_b4581623 ; http://hdl.handle.net/10722/133291

Chicago Manual of Style (16th Edition):

沈家滔.; Shum, Ka-to. “A comparative study of G-quadruplex aptamers against multiple protein targets.” 2010. Doctoral Dissertation, University of Hong Kong. Accessed January 20, 2020. Shum, K. [沈家滔]. (2010). A comparative study of G-quadruplex aptamers against multiple protein targets. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4581623 ; http://dx.doi.org/10.5353/th_b4581623 ; http://hdl.handle.net/10722/133291.

MLA Handbook (7th Edition):

沈家滔.; Shum, Ka-to. “A comparative study of G-quadruplex aptamers against multiple protein targets.” 2010. Web. 20 Jan 2020.

Vancouver:

沈家滔.; Shum K. A comparative study of G-quadruplex aptamers against multiple protein targets. [Internet] [Doctoral dissertation]. University of Hong Kong; 2010. [cited 2020 Jan 20]. Available from: Shum, K. [沈家滔]. (2010). A comparative study of G-quadruplex aptamers against multiple protein targets. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4581623 ; http://dx.doi.org/10.5353/th_b4581623 ; http://hdl.handle.net/10722/133291.

Council of Science Editors:

沈家滔.; Shum K. A comparative study of G-quadruplex aptamers against multiple protein targets. [Doctoral Dissertation]. University of Hong Kong; 2010. Available from: Shum, K. [沈家滔]. (2010). A comparative study of G-quadruplex aptamers against multiple protein targets. (Thesis). University of Hong Kong, Pokfulam, Hong Kong SAR. Retrieved from http://dx.doi.org/10.5353/th_b4581623 ; http://dx.doi.org/10.5353/th_b4581623 ; http://hdl.handle.net/10722/133291


Kent State University

29. Budhathoki, Jagat B. Interactions of RecQ-Family Helicases with G-quadruplex Structures at the Single Molecule Level.

Degree: PhD, College of Arts and Sciences / Department of Physics, 2016, Kent State University

 Human RecQ helicases are members of superfamily 2 helicases and consist of five proteins: RECQ1, Bloom (BLM), Werner (WRN), RECQ4, and RECQ5. RecQ helicases take… (more)

Subjects/Keywords: Biophysics; Biomechanics; RecQ helicases, BLM, WRN, RECQ5, G-quadruplex, smFRET, three-color FRET, GQ unfolding, ssDNA reeling, ATP

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APA (6th Edition):

Budhathoki, J. B. (2016). Interactions of RecQ-Family Helicases with G-quadruplex Structures at the Single Molecule Level. (Doctoral Dissertation). Kent State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=kent1467765011

Chicago Manual of Style (16th Edition):

Budhathoki, Jagat B. “Interactions of RecQ-Family Helicases with G-quadruplex Structures at the Single Molecule Level.” 2016. Doctoral Dissertation, Kent State University. Accessed January 20, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=kent1467765011.

MLA Handbook (7th Edition):

Budhathoki, Jagat B. “Interactions of RecQ-Family Helicases with G-quadruplex Structures at the Single Molecule Level.” 2016. Web. 20 Jan 2020.

Vancouver:

Budhathoki JB. Interactions of RecQ-Family Helicases with G-quadruplex Structures at the Single Molecule Level. [Internet] [Doctoral dissertation]. Kent State University; 2016. [cited 2020 Jan 20]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1467765011.

Council of Science Editors:

Budhathoki JB. Interactions of RecQ-Family Helicases with G-quadruplex Structures at the Single Molecule Level. [Doctoral Dissertation]. Kent State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=kent1467765011

30. Polay Espinoza, Micaela. Fonctions moléculaires des hélicases ARN DDX5 et DDX17 dans la biologie du muscle dans un contexte sain et pathologique : Molecular functions of RNA helicases DDX5 and DDX17 in muscle biology in healthy and pathological context.

Degree: Docteur es, Biologie, 2014, Université Claude Bernard – Lyon I

Les ARN hélicases DDX5 et DDX17 sont des protéines « multi-tâches », elles sont impliquées dans de nombreuses étapes de la régulation du métabolisme des… (more)

Subjects/Keywords: Épissage alternatif; Hélicases ARN; Myogénèse; Différenciation myogénique; DM1; Alternative splicing; RNA helicases; Myogenesis; Myogenic differentiation; DM1; 572.8

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APA (6th Edition):

Polay Espinoza, M. (2014). Fonctions moléculaires des hélicases ARN DDX5 et DDX17 dans la biologie du muscle dans un contexte sain et pathologique : Molecular functions of RNA helicases DDX5 and DDX17 in muscle biology in healthy and pathological context. (Doctoral Dissertation). Université Claude Bernard – Lyon I. Retrieved from http://www.theses.fr/2014LYO10041

Chicago Manual of Style (16th Edition):

Polay Espinoza, Micaela. “Fonctions moléculaires des hélicases ARN DDX5 et DDX17 dans la biologie du muscle dans un contexte sain et pathologique : Molecular functions of RNA helicases DDX5 and DDX17 in muscle biology in healthy and pathological context.” 2014. Doctoral Dissertation, Université Claude Bernard – Lyon I. Accessed January 20, 2020. http://www.theses.fr/2014LYO10041.

MLA Handbook (7th Edition):

Polay Espinoza, Micaela. “Fonctions moléculaires des hélicases ARN DDX5 et DDX17 dans la biologie du muscle dans un contexte sain et pathologique : Molecular functions of RNA helicases DDX5 and DDX17 in muscle biology in healthy and pathological context.” 2014. Web. 20 Jan 2020.

Vancouver:

Polay Espinoza M. Fonctions moléculaires des hélicases ARN DDX5 et DDX17 dans la biologie du muscle dans un contexte sain et pathologique : Molecular functions of RNA helicases DDX5 and DDX17 in muscle biology in healthy and pathological context. [Internet] [Doctoral dissertation]. Université Claude Bernard – Lyon I; 2014. [cited 2020 Jan 20]. Available from: http://www.theses.fr/2014LYO10041.

Council of Science Editors:

Polay Espinoza M. Fonctions moléculaires des hélicases ARN DDX5 et DDX17 dans la biologie du muscle dans un contexte sain et pathologique : Molecular functions of RNA helicases DDX5 and DDX17 in muscle biology in healthy and pathological context. [Doctoral Dissertation]. Université Claude Bernard – Lyon I; 2014. Available from: http://www.theses.fr/2014LYO10041

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