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You searched for +publisher:"McMaster University" +contributor:("Junop, Murray"). Showing records 1 – 17 of 17 total matches.

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McMaster University

1. Andres, Sara N. Functional Structures: The Role of XRCC4 and XLF in Mammalian DNA Double-Strand Break Repair.

Degree: PhD, 2011, McMaster University

DNA double-strand breaks pose a serious threat to genomic integrity. Double-strand breaks can cause chromosomal rearrangement, leading to uncontrolled cell proliferation, or even cell… (more)

Subjects/Keywords: XRCC4; XLF; Non-homologous end-joining; DNA repair; X-ray crystallography; Biochemistry, Biophysics, and Structural Biology; Biochemistry, Biophysics, and Structural Biology

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APA (6th Edition):

Andres, S. N. (2011). Functional Structures: The Role of XRCC4 and XLF in Mammalian DNA Double-Strand Break Repair. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/11265

Chicago Manual of Style (16th Edition):

Andres, Sara N. “Functional Structures: The Role of XRCC4 and XLF in Mammalian DNA Double-Strand Break Repair.” 2011. Doctoral Dissertation, McMaster University. Accessed June 17, 2019. http://hdl.handle.net/11375/11265.

MLA Handbook (7th Edition):

Andres, Sara N. “Functional Structures: The Role of XRCC4 and XLF in Mammalian DNA Double-Strand Break Repair.” 2011. Web. 17 Jun 2019.

Vancouver:

Andres SN. Functional Structures: The Role of XRCC4 and XLF in Mammalian DNA Double-Strand Break Repair. [Internet] [Doctoral dissertation]. McMaster University; 2011. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/11375/11265.

Council of Science Editors:

Andres SN. Functional Structures: The Role of XRCC4 and XLF in Mammalian DNA Double-Strand Break Repair. [Doctoral Dissertation]. McMaster University; 2011. Available from: http://hdl.handle.net/11375/11265


McMaster University

2. Mok, Mac. Characterization of protein and DNA interactions of the human DNA repair protein XRCC1.

Degree: PhD, 2016, McMaster University

DNA single strand break repair and base excision repair are two repair pathways essential for life in humans. XRCC1 is required for repair in both… (more)

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APA (6th Edition):

Mok, M. (2016). Characterization of protein and DNA interactions of the human DNA repair protein XRCC1. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/20650

Chicago Manual of Style (16th Edition):

Mok, Mac. “Characterization of protein and DNA interactions of the human DNA repair protein XRCC1.” 2016. Doctoral Dissertation, McMaster University. Accessed June 17, 2019. http://hdl.handle.net/11375/20650.

MLA Handbook (7th Edition):

Mok, Mac. “Characterization of protein and DNA interactions of the human DNA repair protein XRCC1.” 2016. Web. 17 Jun 2019.

Vancouver:

Mok M. Characterization of protein and DNA interactions of the human DNA repair protein XRCC1. [Internet] [Doctoral dissertation]. McMaster University; 2016. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/11375/20650.

Council of Science Editors:

Mok M. Characterization of protein and DNA interactions of the human DNA repair protein XRCC1. [Doctoral Dissertation]. McMaster University; 2016. Available from: http://hdl.handle.net/11375/20650


McMaster University

3. Brown, Christopher, M. CHARACTERIZATION OF THE END BRIDGING COMPLEX OF NON-HOMOLOGOUS END JOINING REPAIR OF DNA DOUBLE STRAND BREAKS.

Degree: PhD, 2018, McMaster University

DNA double strand breaks represent the single most dangerous type of damage that can afflict the genome. Given the severity of such a lesion, higher… (more)

Subjects/Keywords: Structural biology; DNA repair

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APA (6th Edition):

Brown, Christopher, M. (2018). CHARACTERIZATION OF THE END BRIDGING COMPLEX OF NON-HOMOLOGOUS END JOINING REPAIR OF DNA DOUBLE STRAND BREAKS. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/22876

Chicago Manual of Style (16th Edition):

Brown, Christopher, M. “CHARACTERIZATION OF THE END BRIDGING COMPLEX OF NON-HOMOLOGOUS END JOINING REPAIR OF DNA DOUBLE STRAND BREAKS.” 2018. Doctoral Dissertation, McMaster University. Accessed June 17, 2019. http://hdl.handle.net/11375/22876.

MLA Handbook (7th Edition):

Brown, Christopher, M. “CHARACTERIZATION OF THE END BRIDGING COMPLEX OF NON-HOMOLOGOUS END JOINING REPAIR OF DNA DOUBLE STRAND BREAKS.” 2018. Web. 17 Jun 2019.

Vancouver:

Brown, Christopher M. CHARACTERIZATION OF THE END BRIDGING COMPLEX OF NON-HOMOLOGOUS END JOINING REPAIR OF DNA DOUBLE STRAND BREAKS. [Internet] [Doctoral dissertation]. McMaster University; 2018. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/11375/22876.

Council of Science Editors:

Brown, Christopher M. CHARACTERIZATION OF THE END BRIDGING COMPLEX OF NON-HOMOLOGOUS END JOINING REPAIR OF DNA DOUBLE STRAND BREAKS. [Doctoral Dissertation]. McMaster University; 2018. Available from: http://hdl.handle.net/11375/22876


McMaster University

4. Buzon, Beverly Diana. Characterization and inhibition of interstrand crosslink repair nuclease SNM1A.

Degree: PhD, 2018, McMaster University

Interstrand cross-links (ICLs) are a type of DNA damage that prevents strand separation required for basic cellular processes. ICL-based anti-cancer therapies exploit the cytotoxic consequences… (more)

Subjects/Keywords: SNM1A; beta-CASP nuclease; small molecule inhibitors; translesion nuclease; chemoresistance; structure-specific endonuclease; interstrand crosslinking repair; high throughput screening

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APA (6th Edition):

Buzon, B. D. (2018). Characterization and inhibition of interstrand crosslink repair nuclease SNM1A. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/22872

Chicago Manual of Style (16th Edition):

Buzon, Beverly Diana. “Characterization and inhibition of interstrand crosslink repair nuclease SNM1A.” 2018. Doctoral Dissertation, McMaster University. Accessed June 17, 2019. http://hdl.handle.net/11375/22872.

MLA Handbook (7th Edition):

Buzon, Beverly Diana. “Characterization and inhibition of interstrand crosslink repair nuclease SNM1A.” 2018. Web. 17 Jun 2019.

Vancouver:

Buzon BD. Characterization and inhibition of interstrand crosslink repair nuclease SNM1A. [Internet] [Doctoral dissertation]. McMaster University; 2018. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/11375/22872.

Council of Science Editors:

Buzon BD. Characterization and inhibition of interstrand crosslink repair nuclease SNM1A. [Doctoral Dissertation]. McMaster University; 2018. Available from: http://hdl.handle.net/11375/22872


McMaster University

5. Rana, Navpreet K. Pseudomonas aeruginosa Major Pseudopilin XcpT is Incorporated into The Type IV Pilus Under Native Conditions.

Degree: MSc, 2011, McMaster University

Retractable surface appendages Type IV pili (T4P) are one of the major virulence determinants in the opportunistic pathogen Pseudomonas aeruginosa (Pa), that is the… (more)

Subjects/Keywords: Pseudomonas aeruginosa; Type IV pili; Type II secretion; Pseudopilin; Bacterial Infections and Mycoses; Bacteriology; Biochemistry; Molecular Biology; Pathogenic Microbiology; Respiratory Tract Diseases; Bacterial Infections and Mycoses

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APA (6th Edition):

Rana, N. K. (2011). Pseudomonas aeruginosa Major Pseudopilin XcpT is Incorporated into The Type IV Pilus Under Native Conditions. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/11314

Chicago Manual of Style (16th Edition):

Rana, Navpreet K. “Pseudomonas aeruginosa Major Pseudopilin XcpT is Incorporated into The Type IV Pilus Under Native Conditions.” 2011. Masters Thesis, McMaster University. Accessed June 17, 2019. http://hdl.handle.net/11375/11314.

MLA Handbook (7th Edition):

Rana, Navpreet K. “Pseudomonas aeruginosa Major Pseudopilin XcpT is Incorporated into The Type IV Pilus Under Native Conditions.” 2011. Web. 17 Jun 2019.

Vancouver:

Rana NK. Pseudomonas aeruginosa Major Pseudopilin XcpT is Incorporated into The Type IV Pilus Under Native Conditions. [Internet] [Masters thesis]. McMaster University; 2011. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/11375/11314.

Council of Science Editors:

Rana NK. Pseudomonas aeruginosa Major Pseudopilin XcpT is Incorporated into The Type IV Pilus Under Native Conditions. [Masters Thesis]. McMaster University; 2011. Available from: http://hdl.handle.net/11375/11314


McMaster University

6. Li, Sidi. CLONING AND CHARACTERIZATION OF FULL LENGTH GCD AND INTERNAL TRUNCATIONS OF TGCD.

Degree: MSc, 2012, McMaster University

No Comment

The increase in antibiotic resistance has accelerated the search for novel antibacterial agents. As proteins with toxic properties appear to be… (more)

Subjects/Keywords: antimicrobial peptides; bacteria; Biochemistry; Biochemistry

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APA (6th Edition):

Li, S. (2012). CLONING AND CHARACTERIZATION OF FULL LENGTH GCD AND INTERNAL TRUNCATIONS OF TGCD. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/12336

Chicago Manual of Style (16th Edition):

Li, Sidi. “CLONING AND CHARACTERIZATION OF FULL LENGTH GCD AND INTERNAL TRUNCATIONS OF TGCD.” 2012. Masters Thesis, McMaster University. Accessed June 17, 2019. http://hdl.handle.net/11375/12336.

MLA Handbook (7th Edition):

Li, Sidi. “CLONING AND CHARACTERIZATION OF FULL LENGTH GCD AND INTERNAL TRUNCATIONS OF TGCD.” 2012. Web. 17 Jun 2019.

Vancouver:

Li S. CLONING AND CHARACTERIZATION OF FULL LENGTH GCD AND INTERNAL TRUNCATIONS OF TGCD. [Internet] [Masters thesis]. McMaster University; 2012. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/11375/12336.

Council of Science Editors:

Li S. CLONING AND CHARACTERIZATION OF FULL LENGTH GCD AND INTERNAL TRUNCATIONS OF TGCD. [Masters Thesis]. McMaster University; 2012. Available from: http://hdl.handle.net/11375/12336


McMaster University

7. Buzon, Beverlee D. Functional studies of the interstrand cross-link repair protein, SNM1A and its beta-CASP domain.

Degree: MSc, 2012, McMaster University

Interstrand cross-linking (ICL) damage to DNA is cytotoxic as it blocks replication and transcription. This cytotoxicity is exploited in anti-cancer therapies, but increased ICL… (more)

Subjects/Keywords: SNM1A; interstrand crosslink repair; beta-CASP; inclusion body protein refolding; nuclease; cisplatin; Biochemistry; Biochemistry

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APA (6th Edition):

Buzon, B. D. (2012). Functional studies of the interstrand cross-link repair protein, SNM1A and its beta-CASP domain. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/12675

Chicago Manual of Style (16th Edition):

Buzon, Beverlee D. “Functional studies of the interstrand cross-link repair protein, SNM1A and its beta-CASP domain.” 2012. Masters Thesis, McMaster University. Accessed June 17, 2019. http://hdl.handle.net/11375/12675.

MLA Handbook (7th Edition):

Buzon, Beverlee D. “Functional studies of the interstrand cross-link repair protein, SNM1A and its beta-CASP domain.” 2012. Web. 17 Jun 2019.

Vancouver:

Buzon BD. Functional studies of the interstrand cross-link repair protein, SNM1A and its beta-CASP domain. [Internet] [Masters thesis]. McMaster University; 2012. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/11375/12675.

Council of Science Editors:

Buzon BD. Functional studies of the interstrand cross-link repair protein, SNM1A and its beta-CASP domain. [Masters Thesis]. McMaster University; 2012. Available from: http://hdl.handle.net/11375/12675


McMaster University

8. Lee, KY Wilson. CHARACTERIZATION OF THE OLIGOMERIZATION OF THE HUMAN XRCC4 DNA REPAIR PROTEIN: IMPLICATIONS TO NON-HOMOLOGOUS END JOINING.

Degree: MSc, 2013, McMaster University

If not efficiently repaired, DNA double-stranded breaks can result in cell death. A major contributor to the repair of this DNA damage is the… (more)

Subjects/Keywords: XRCC4; XLF; NHEJ; DNA repair; Biochemistry; Biochemistry

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APA (6th Edition):

Lee, K. W. (2013). CHARACTERIZATION OF THE OLIGOMERIZATION OF THE HUMAN XRCC4 DNA REPAIR PROTEIN: IMPLICATIONS TO NON-HOMOLOGOUS END JOINING. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/13012

Chicago Manual of Style (16th Edition):

Lee, KY Wilson. “CHARACTERIZATION OF THE OLIGOMERIZATION OF THE HUMAN XRCC4 DNA REPAIR PROTEIN: IMPLICATIONS TO NON-HOMOLOGOUS END JOINING.” 2013. Masters Thesis, McMaster University. Accessed June 17, 2019. http://hdl.handle.net/11375/13012.

MLA Handbook (7th Edition):

Lee, KY Wilson. “CHARACTERIZATION OF THE OLIGOMERIZATION OF THE HUMAN XRCC4 DNA REPAIR PROTEIN: IMPLICATIONS TO NON-HOMOLOGOUS END JOINING.” 2013. Web. 17 Jun 2019.

Vancouver:

Lee KW. CHARACTERIZATION OF THE OLIGOMERIZATION OF THE HUMAN XRCC4 DNA REPAIR PROTEIN: IMPLICATIONS TO NON-HOMOLOGOUS END JOINING. [Internet] [Masters thesis]. McMaster University; 2013. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/11375/13012.

Council of Science Editors:

Lee KW. CHARACTERIZATION OF THE OLIGOMERIZATION OF THE HUMAN XRCC4 DNA REPAIR PROTEIN: IMPLICATIONS TO NON-HOMOLOGOUS END JOINING. [Masters Thesis]. McMaster University; 2013. Available from: http://hdl.handle.net/11375/13012


McMaster University

9. Khan, Refat Arin S. Structural and Functional Studies of hAPTX.

Degree: MSc, 2011, McMaster University

DNA integrity is continuously compromised by cellular metabolic activity and environmental factors resulting in many lesions per cell per day (Lindahl et al.,2009). If… (more)

Subjects/Keywords: APTX; DNA Repair; Crystallography; Protein Purification; Biochemical Assay; Radioactivity; Biochemistry; Structural Biology; Biochemistry

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APA (6th Edition):

Khan, R. A. S. (2011). Structural and Functional Studies of hAPTX. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/11747

Chicago Manual of Style (16th Edition):

Khan, Refat Arin S. “Structural and Functional Studies of hAPTX.” 2011. Masters Thesis, McMaster University. Accessed June 17, 2019. http://hdl.handle.net/11375/11747.

MLA Handbook (7th Edition):

Khan, Refat Arin S. “Structural and Functional Studies of hAPTX.” 2011. Web. 17 Jun 2019.

Vancouver:

Khan RAS. Structural and Functional Studies of hAPTX. [Internet] [Masters thesis]. McMaster University; 2011. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/11375/11747.

Council of Science Editors:

Khan RAS. Structural and Functional Studies of hAPTX. [Masters Thesis]. McMaster University; 2011. Available from: http://hdl.handle.net/11375/11747


McMaster University

10. Jeyanthan, Kajaparan. Biochemical analysis of telomeric repeat binding factor 1.

Degree: MSc, 2012, McMaster University

TRF1 is an essential shelterin protein that binds to double stranded telomeric DNA. TRF1 is best known for its role as a negative regulator… (more)

Subjects/Keywords: Telomere; TRF1; phosphorylation; Pin2; Biochemistry; Molecular Biology; Biochemistry

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APA (6th Edition):

Jeyanthan, K. (2012). Biochemical analysis of telomeric repeat binding factor 1. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/15247

Chicago Manual of Style (16th Edition):

Jeyanthan, Kajaparan. “Biochemical analysis of telomeric repeat binding factor 1.” 2012. Masters Thesis, McMaster University. Accessed June 17, 2019. http://hdl.handle.net/11375/15247.

MLA Handbook (7th Edition):

Jeyanthan, Kajaparan. “Biochemical analysis of telomeric repeat binding factor 1.” 2012. Web. 17 Jun 2019.

Vancouver:

Jeyanthan K. Biochemical analysis of telomeric repeat binding factor 1. [Internet] [Masters thesis]. McMaster University; 2012. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/11375/15247.

Council of Science Editors:

Jeyanthan K. Biochemical analysis of telomeric repeat binding factor 1. [Masters Thesis]. McMaster University; 2012. Available from: http://hdl.handle.net/11375/15247


McMaster University

11. Sugiman-Marangos, Seiji N. Structural Analysis of DdrB from Deinococcus radiodurans: Insight into the Mechanism of Protein Mediated Single-Stranded DNA Annealing.

Degree: PhD, 2013, McMaster University

Bacteria of the genus Deinococcus are perhaps the most resilient life forms ever discovered, demonstrating extreme resistance to ionizing radiation, ultraviolet radiation, desiccation, and… (more)

Subjects/Keywords: DdrB; Deinococcus radiodurans; single-stranded DNA annealing; structural biology; Structural Biology; Structural Biology

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APA (6th Edition):

Sugiman-Marangos, S. N. (2013). Structural Analysis of DdrB from Deinococcus radiodurans: Insight into the Mechanism of Protein Mediated Single-Stranded DNA Annealing. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/15263

Chicago Manual of Style (16th Edition):

Sugiman-Marangos, Seiji N. “Structural Analysis of DdrB from Deinococcus radiodurans: Insight into the Mechanism of Protein Mediated Single-Stranded DNA Annealing.” 2013. Doctoral Dissertation, McMaster University. Accessed June 17, 2019. http://hdl.handle.net/11375/15263.

MLA Handbook (7th Edition):

Sugiman-Marangos, Seiji N. “Structural Analysis of DdrB from Deinococcus radiodurans: Insight into the Mechanism of Protein Mediated Single-Stranded DNA Annealing.” 2013. Web. 17 Jun 2019.

Vancouver:

Sugiman-Marangos SN. Structural Analysis of DdrB from Deinococcus radiodurans: Insight into the Mechanism of Protein Mediated Single-Stranded DNA Annealing. [Internet] [Doctoral dissertation]. McMaster University; 2013. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/11375/15263.

Council of Science Editors:

Sugiman-Marangos SN. Structural Analysis of DdrB from Deinococcus radiodurans: Insight into the Mechanism of Protein Mediated Single-Stranded DNA Annealing. [Doctoral Dissertation]. McMaster University; 2013. Available from: http://hdl.handle.net/11375/15263


McMaster University

12. Czerwinski, Matthew. Characterization of a Pleiotropic Protein Promoting DNA Repair.

Degree: MSc, 2013, McMaster University

DNA double-strand breaks (DSBs) represent the most severe form of chromosomal damage. In higher organisms, one DSB represents a lethal event. Unlike any other… (more)

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APA (6th Edition):

Czerwinski, M. (2013). Characterization of a Pleiotropic Protein Promoting DNA Repair. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/15321

Chicago Manual of Style (16th Edition):

Czerwinski, Matthew. “Characterization of a Pleiotropic Protein Promoting DNA Repair.” 2013. Masters Thesis, McMaster University. Accessed June 17, 2019. http://hdl.handle.net/11375/15321.

MLA Handbook (7th Edition):

Czerwinski, Matthew. “Characterization of a Pleiotropic Protein Promoting DNA Repair.” 2013. Web. 17 Jun 2019.

Vancouver:

Czerwinski M. Characterization of a Pleiotropic Protein Promoting DNA Repair. [Internet] [Masters thesis]. McMaster University; 2013. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/11375/15321.

Council of Science Editors:

Czerwinski M. Characterization of a Pleiotropic Protein Promoting DNA Repair. [Masters Thesis]. McMaster University; 2013. Available from: http://hdl.handle.net/11375/15321


McMaster University

13. Huang, Simon Y. Structural and Functional Characterization of Human SNM1A.

Degree: MSc, 2013, McMaster University

DNA interstrand cross-links (ICLs) occur when various chemical agents bind to chromosomal DNA and form a covalent bond between adjacent strands, preventing unwinding of… (more)

Subjects/Keywords: DNA Repair; SNM1A; Interstrand Cross-link; Biochemistry; Biochemistry

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APA (6th Edition):

Huang, S. Y. (2013). Structural and Functional Characterization of Human SNM1A. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/15329

Chicago Manual of Style (16th Edition):

Huang, Simon Y. “Structural and Functional Characterization of Human SNM1A.” 2013. Masters Thesis, McMaster University. Accessed June 17, 2019. http://hdl.handle.net/11375/15329.

MLA Handbook (7th Edition):

Huang, Simon Y. “Structural and Functional Characterization of Human SNM1A.” 2013. Web. 17 Jun 2019.

Vancouver:

Huang SY. Structural and Functional Characterization of Human SNM1A. [Internet] [Masters thesis]. McMaster University; 2013. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/11375/15329.

Council of Science Editors:

Huang SY. Structural and Functional Characterization of Human SNM1A. [Masters Thesis]. McMaster University; 2013. Available from: http://hdl.handle.net/11375/15329


McMaster University

14. Tiefenbach, Tracy E. Functional analysis of Pso2 reveals a novel DNA hairpin endonuclease activity: Implications for interstrand crosslink repair.

Degree: PhD, 2011, McMaster University

DNA interstrand crosslinks provide a challenge for repair machinery given that both strands contain the lesion. Cells have evolved a sophisticated mechanism to overcome… (more)

Subjects/Keywords: DNA Repair; interstrand crosslinks; Pso2; DNA hairpin.; Biochemistry; Biochemistry

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APA (6th Edition):

Tiefenbach, T. E. (2011). Functional analysis of Pso2 reveals a novel DNA hairpin endonuclease activity: Implications for interstrand crosslink repair. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/11308

Chicago Manual of Style (16th Edition):

Tiefenbach, Tracy E. “Functional analysis of Pso2 reveals a novel DNA hairpin endonuclease activity: Implications for interstrand crosslink repair.” 2011. Doctoral Dissertation, McMaster University. Accessed June 17, 2019. http://hdl.handle.net/11375/11308.

MLA Handbook (7th Edition):

Tiefenbach, Tracy E. “Functional analysis of Pso2 reveals a novel DNA hairpin endonuclease activity: Implications for interstrand crosslink repair.” 2011. Web. 17 Jun 2019.

Vancouver:

Tiefenbach TE. Functional analysis of Pso2 reveals a novel DNA hairpin endonuclease activity: Implications for interstrand crosslink repair. [Internet] [Doctoral dissertation]. McMaster University; 2011. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/11375/11308.

Council of Science Editors:

Tiefenbach TE. Functional analysis of Pso2 reveals a novel DNA hairpin endonuclease activity: Implications for interstrand crosslink repair. [Doctoral Dissertation]. McMaster University; 2011. Available from: http://hdl.handle.net/11375/11308


McMaster University

15. Scott, Benjamin M. Applying Phage Display to Screen a Library of α1-Proteinase Inhibitor Mutants for Improved Thrombin Binding Activity.

Degree: MSc, 2013, McMaster University

  α1-proteinase inhibitor (α1-PI) is the most abundant serine protease inhibitor (serpin) in plasma. The α1-PI M358R mutant exhibits greatly increased rates of thrombin inhibition… (more)

Subjects/Keywords: protein engineering; thrombin; phage display; coagulation; serpin; thrombin inhibitor; Amino Acids, Peptides, and Proteins; Amino Acids, Peptides, and Proteins

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APA (6th Edition):

Scott, B. M. (2013). Applying Phage Display to Screen a Library of α1-Proteinase Inhibitor Mutants for Improved Thrombin Binding Activity. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/13367

Chicago Manual of Style (16th Edition):

Scott, Benjamin M. “Applying Phage Display to Screen a Library of α1-Proteinase Inhibitor Mutants for Improved Thrombin Binding Activity.” 2013. Masters Thesis, McMaster University. Accessed June 17, 2019. http://hdl.handle.net/11375/13367.

MLA Handbook (7th Edition):

Scott, Benjamin M. “Applying Phage Display to Screen a Library of α1-Proteinase Inhibitor Mutants for Improved Thrombin Binding Activity.” 2013. Web. 17 Jun 2019.

Vancouver:

Scott BM. Applying Phage Display to Screen a Library of α1-Proteinase Inhibitor Mutants for Improved Thrombin Binding Activity. [Internet] [Masters thesis]. McMaster University; 2013. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/11375/13367.

Council of Science Editors:

Scott BM. Applying Phage Display to Screen a Library of α1-Proteinase Inhibitor Mutants for Improved Thrombin Binding Activity. [Masters Thesis]. McMaster University; 2013. Available from: http://hdl.handle.net/11375/13367


McMaster University

16. McFadden, Meghan J. Application of Magnetic “Fishing” and Mass Spectrometry for Function-based Assays of Biomolecular Interactions.

Degree: PhD, 2013, McMaster University

The human interactome presents a goldmine of potentially powerful therapeutic targets, yet very few small molecule modulators of protein-protein interactions (PPI) have been identified.… (more)

Subjects/Keywords: Protein-Protein Interactions; Mass Spectrometry; Magnetic Beads; Modulator; High-Throughput Screening; Analytical Chemistry; Analytical Chemistry

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APA (6th Edition):

McFadden, M. J. (2013). Application of Magnetic “Fishing” and Mass Spectrometry for Function-based Assays of Biomolecular Interactions. (Doctoral Dissertation). McMaster University. Retrieved from http://hdl.handle.net/11375/13715

Chicago Manual of Style (16th Edition):

McFadden, Meghan J. “Application of Magnetic “Fishing” and Mass Spectrometry for Function-based Assays of Biomolecular Interactions.” 2013. Doctoral Dissertation, McMaster University. Accessed June 17, 2019. http://hdl.handle.net/11375/13715.

MLA Handbook (7th Edition):

McFadden, Meghan J. “Application of Magnetic “Fishing” and Mass Spectrometry for Function-based Assays of Biomolecular Interactions.” 2013. Web. 17 Jun 2019.

Vancouver:

McFadden MJ. Application of Magnetic “Fishing” and Mass Spectrometry for Function-based Assays of Biomolecular Interactions. [Internet] [Doctoral dissertation]. McMaster University; 2013. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/11375/13715.

Council of Science Editors:

McFadden MJ. Application of Magnetic “Fishing” and Mass Spectrometry for Function-based Assays of Biomolecular Interactions. [Doctoral Dissertation]. McMaster University; 2013. Available from: http://hdl.handle.net/11375/13715


McMaster University

17. Dowling, Michelle L. Functional Studies of the Interstrand Cross-link Repair Protein, Pso2.

Degree: MSc, 2013, McMaster University

  DNA interstrand cross-links (ICLs) constitute one of the most severe types of DNA damage. ICLs covalently tether both strands of duplex DNA, preventing unwinding… (more)

Subjects/Keywords: DNA repair; Interstrand cross-link (ICL); Pso2; Exonuclease; Endonuclease; Hairpin; Biochemistry; Biochemistry

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APA (6th Edition):

Dowling, M. L. (2013). Functional Studies of the Interstrand Cross-link Repair Protein, Pso2. (Masters Thesis). McMaster University. Retrieved from http://hdl.handle.net/11375/15259

Chicago Manual of Style (16th Edition):

Dowling, Michelle L. “Functional Studies of the Interstrand Cross-link Repair Protein, Pso2.” 2013. Masters Thesis, McMaster University. Accessed June 17, 2019. http://hdl.handle.net/11375/15259.

MLA Handbook (7th Edition):

Dowling, Michelle L. “Functional Studies of the Interstrand Cross-link Repair Protein, Pso2.” 2013. Web. 17 Jun 2019.

Vancouver:

Dowling ML. Functional Studies of the Interstrand Cross-link Repair Protein, Pso2. [Internet] [Masters thesis]. McMaster University; 2013. [cited 2019 Jun 17]. Available from: http://hdl.handle.net/11375/15259.

Council of Science Editors:

Dowling ML. Functional Studies of the Interstrand Cross-link Repair Protein, Pso2. [Masters Thesis]. McMaster University; 2013. Available from: http://hdl.handle.net/11375/15259

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