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You searched for +publisher:"MIT" +contributor:("John M. Essigmann"). Showing records 1 – 30 of 31 total matches.

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1. Delaney, James Cullen, 1970-. Influence of DNA sequence context on O⁶-methylguanine mutagenicity in Escherichia coli ; Influence of DNA sequence context on m⁶G mutagenicity in Escherichia coli .

Degree: PhD, Department of Chemistry, 1999, MIT

Subjects/Keywords: Chemistry.

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APA (6th Edition):

Delaney, James Cullen, 1. (1999). Influence of DNA sequence context on O⁶-methylguanine mutagenicity in Escherichia coli ; Influence of DNA sequence context on m⁶G mutagenicity in Escherichia coli . (Doctoral Dissertation). MIT. Retrieved from http://hdl.handle.net/1721.1/84755

Chicago Manual of Style (16th Edition):

Delaney, James Cullen, 1970-. “Influence of DNA sequence context on O⁶-methylguanine mutagenicity in Escherichia coli ; Influence of DNA sequence context on m⁶G mutagenicity in Escherichia coli .” 1999. Doctoral Dissertation, MIT. Accessed November 21, 2019. http://hdl.handle.net/1721.1/84755.

MLA Handbook (7th Edition):

Delaney, James Cullen, 1970-. “Influence of DNA sequence context on O⁶-methylguanine mutagenicity in Escherichia coli ; Influence of DNA sequence context on m⁶G mutagenicity in Escherichia coli .” 1999. Web. 21 Nov 2019.

Vancouver:

Delaney, James Cullen 1. Influence of DNA sequence context on O⁶-methylguanine mutagenicity in Escherichia coli ; Influence of DNA sequence context on m⁶G mutagenicity in Escherichia coli . [Internet] [Doctoral dissertation]. MIT; 1999. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/1721.1/84755.

Council of Science Editors:

Delaney, James Cullen 1. Influence of DNA sequence context on O⁶-methylguanine mutagenicity in Escherichia coli ; Influence of DNA sequence context on m⁶G mutagenicity in Escherichia coli . [Doctoral Dissertation]. MIT; 1999. Available from: http://hdl.handle.net/1721.1/84755

2. Śrīvāstava, Nidhi. Response of DNA repair and replication systems to exocyclic nucleic acid base damage ; Response of deoxyribonucleic acid repair and replication systems to exocyclic nucleic acid base damage .

Degree: PhD, Biological Engineering, 2012, MIT

 Genomes experience an often hostile environment that creates a vast array of damages that can give rise to myriad biological outcomes. Fortunately, cells are equipped… (more)

Subjects/Keywords: Biological Engineering.

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APA (6th Edition):

Śrīvāstava, N. (2012). Response of DNA repair and replication systems to exocyclic nucleic acid base damage ; Response of deoxyribonucleic acid repair and replication systems to exocyclic nucleic acid base damage . (Doctoral Dissertation). MIT. Retrieved from http://hdl.handle.net/1721.1/71468

Chicago Manual of Style (16th Edition):

Śrīvāstava, Nidhi. “Response of DNA repair and replication systems to exocyclic nucleic acid base damage ; Response of deoxyribonucleic acid repair and replication systems to exocyclic nucleic acid base damage .” 2012. Doctoral Dissertation, MIT. Accessed November 21, 2019. http://hdl.handle.net/1721.1/71468.

MLA Handbook (7th Edition):

Śrīvāstava, Nidhi. “Response of DNA repair and replication systems to exocyclic nucleic acid base damage ; Response of deoxyribonucleic acid repair and replication systems to exocyclic nucleic acid base damage .” 2012. Web. 21 Nov 2019.

Vancouver:

Śrīvāstava N. Response of DNA repair and replication systems to exocyclic nucleic acid base damage ; Response of deoxyribonucleic acid repair and replication systems to exocyclic nucleic acid base damage . [Internet] [Doctoral dissertation]. MIT; 2012. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/1721.1/71468.

Council of Science Editors:

Śrīvāstava N. Response of DNA repair and replication systems to exocyclic nucleic acid base damage ; Response of deoxyribonucleic acid repair and replication systems to exocyclic nucleic acid base damage . [Doctoral Dissertation]. MIT; 2012. Available from: http://hdl.handle.net/1721.1/71468


MIT

3. Chang, Shiou-chi, Ph. D. Massachusetts Institute of Technology. Next-generation sequencing as a tool for investigating the in vivo biological consequences of DNA lesions and its applications on the ethenoguanine, 8-oxoguanine and 1,3-butadiene-induced lesions .

Degree: Department of Biological Engineering, 2017, MIT

 DNA damaging agents produce a plethora of DNA lesions, which can lead to various outcomes. In order to understand the biological consequences of DNA lesions,… (more)

Subjects/Keywords: Biological Engineering.

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APA (6th Edition):

Chang, Shiou-chi, P. D. M. I. o. (2017). Next-generation sequencing as a tool for investigating the in vivo biological consequences of DNA lesions and its applications on the ethenoguanine, 8-oxoguanine and 1,3-butadiene-induced lesions . (Thesis). MIT. Retrieved from http://hdl.handle.net/1721.1/112497

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):

Chang, Shiou-chi, Ph D Massachusetts Institute of. “Next-generation sequencing as a tool for investigating the in vivo biological consequences of DNA lesions and its applications on the ethenoguanine, 8-oxoguanine and 1,3-butadiene-induced lesions .” 2017. Thesis, MIT. Accessed November 21, 2019. http://hdl.handle.net/1721.1/112497.

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

MLA Handbook (7th Edition):

Chang, Shiou-chi, Ph D Massachusetts Institute of. “Next-generation sequencing as a tool for investigating the in vivo biological consequences of DNA lesions and its applications on the ethenoguanine, 8-oxoguanine and 1,3-butadiene-induced lesions .” 2017. Web. 21 Nov 2019.

Vancouver:

Chang, Shiou-chi PDMIo. Next-generation sequencing as a tool for investigating the in vivo biological consequences of DNA lesions and its applications on the ethenoguanine, 8-oxoguanine and 1,3-butadiene-induced lesions . [Internet] [Thesis]. MIT; 2017. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/1721.1/112497.

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

Council of Science Editors:

Chang, Shiou-chi PDMIo. Next-generation sequencing as a tool for investigating the in vivo biological consequences of DNA lesions and its applications on the ethenoguanine, 8-oxoguanine and 1,3-butadiene-induced lesions . [Thesis]. MIT; 2017. Available from: http://hdl.handle.net/1721.1/112497

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


MIT

4. Silvestre, Katherine J. Spectroscopic analysis and synthesis of nucleoside analogs for lethal mutagenesis .

Degree: Department of Chemistry, 2014, MIT

 The high mutation rate of HIV makes treatment of HIV/AIDS difficult, as the virus can develop resistance to existing therapeutics. A novel antiviral nucleoside analog,… (more)

Subjects/Keywords: Chemistry.

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APA (6th Edition):

Silvestre, K. J. (2014). Spectroscopic analysis and synthesis of nucleoside analogs for lethal mutagenesis . (Thesis). MIT. Retrieved from http://hdl.handle.net/1721.1/100159

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):

Silvestre, Katherine J. “Spectroscopic analysis and synthesis of nucleoside analogs for lethal mutagenesis .” 2014. Thesis, MIT. Accessed November 21, 2019. http://hdl.handle.net/1721.1/100159.

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

MLA Handbook (7th Edition):

Silvestre, Katherine J. “Spectroscopic analysis and synthesis of nucleoside analogs for lethal mutagenesis .” 2014. Web. 21 Nov 2019.

Vancouver:

Silvestre KJ. Spectroscopic analysis and synthesis of nucleoside analogs for lethal mutagenesis . [Internet] [Thesis]. MIT; 2014. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/1721.1/100159.

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

Council of Science Editors:

Silvestre KJ. Spectroscopic analysis and synthesis of nucleoside analogs for lethal mutagenesis . [Thesis]. MIT; 2014. Available from: http://hdl.handle.net/1721.1/100159

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


MIT

5. Fedeleş, Bogdan I. The androgen receptor independent mechanism of toxicity of the novel anti-tumor agent 11[beta]-dichloro ; AR independent mechanism of toxicity of the novel anti-tumor agent 11[beta]-dichloro ; multifaceted toxicological puzzle : investigating the androgen receptor independent cellular responses to the novel anti-tumor agent 11[beta]-dichloro .

Degree: PhD, Biological Engineering, 2009, MIT

 Inspired by the toxicity mechanism of cisplatin in testicular cancer, a series of bi-functional genotoxicants has been designed that supplement their DNA damaging properties with… (more)

Subjects/Keywords: Biological Engineering.

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APA (6th Edition):

Fedeleş, B. I. (2009). The androgen receptor independent mechanism of toxicity of the novel anti-tumor agent 11[beta]-dichloro ; AR independent mechanism of toxicity of the novel anti-tumor agent 11[beta]-dichloro ; multifaceted toxicological puzzle : investigating the androgen receptor independent cellular responses to the novel anti-tumor agent 11[beta]-dichloro . (Doctoral Dissertation). MIT. Retrieved from http://hdl.handle.net/1721.1/61222

Chicago Manual of Style (16th Edition):

Fedeleş, Bogdan I. “The androgen receptor independent mechanism of toxicity of the novel anti-tumor agent 11[beta]-dichloro ; AR independent mechanism of toxicity of the novel anti-tumor agent 11[beta]-dichloro ; multifaceted toxicological puzzle : investigating the androgen receptor independent cellular responses to the novel anti-tumor agent 11[beta]-dichloro .” 2009. Doctoral Dissertation, MIT. Accessed November 21, 2019. http://hdl.handle.net/1721.1/61222.

MLA Handbook (7th Edition):

Fedeleş, Bogdan I. “The androgen receptor independent mechanism of toxicity of the novel anti-tumor agent 11[beta]-dichloro ; AR independent mechanism of toxicity of the novel anti-tumor agent 11[beta]-dichloro ; multifaceted toxicological puzzle : investigating the androgen receptor independent cellular responses to the novel anti-tumor agent 11[beta]-dichloro .” 2009. Web. 21 Nov 2019.

Vancouver:

Fedeleş BI. The androgen receptor independent mechanism of toxicity of the novel anti-tumor agent 11[beta]-dichloro ; AR independent mechanism of toxicity of the novel anti-tumor agent 11[beta]-dichloro ; multifaceted toxicological puzzle : investigating the androgen receptor independent cellular responses to the novel anti-tumor agent 11[beta]-dichloro . [Internet] [Doctoral dissertation]. MIT; 2009. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/1721.1/61222.

Council of Science Editors:

Fedeleş BI. The androgen receptor independent mechanism of toxicity of the novel anti-tumor agent 11[beta]-dichloro ; AR independent mechanism of toxicity of the novel anti-tumor agent 11[beta]-dichloro ; multifaceted toxicological puzzle : investigating the androgen receptor independent cellular responses to the novel anti-tumor agent 11[beta]-dichloro . [Doctoral Dissertation]. MIT; 2009. Available from: http://hdl.handle.net/1721.1/61222


MIT

6. Gopal, Sreeja. Mechanistic investigation of anticancer agents that damage DNA and interact with the estrogen receptor .

Degree: PhD, Biological Engineering, 2009, MIT

 One of the primary goals of cancer chemotherapy is the design of antitumor agents that achieve selective targeting of tumor cells while minimizing toxicity to… (more)

Subjects/Keywords: Biological Engineering.

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APA (6th Edition):

Gopal, S. (2009). Mechanistic investigation of anticancer agents that damage DNA and interact with the estrogen receptor . (Doctoral Dissertation). MIT. Retrieved from http://hdl.handle.net/1721.1/61223

Chicago Manual of Style (16th Edition):

Gopal, Sreeja. “Mechanistic investigation of anticancer agents that damage DNA and interact with the estrogen receptor .” 2009. Doctoral Dissertation, MIT. Accessed November 21, 2019. http://hdl.handle.net/1721.1/61223.

MLA Handbook (7th Edition):

Gopal, Sreeja. “Mechanistic investigation of anticancer agents that damage DNA and interact with the estrogen receptor .” 2009. Web. 21 Nov 2019.

Vancouver:

Gopal S. Mechanistic investigation of anticancer agents that damage DNA and interact with the estrogen receptor . [Internet] [Doctoral dissertation]. MIT; 2009. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/1721.1/61223.

Council of Science Editors:

Gopal S. Mechanistic investigation of anticancer agents that damage DNA and interact with the estrogen receptor . [Doctoral Dissertation]. MIT; 2009. Available from: http://hdl.handle.net/1721.1/61223


MIT

7. Morton, Charles Ingalls, IV. Metabolic and mechanistic exploration of a novel programmable genotoxicant against prostate cancer .

Degree: PhD, Biological Engineering, 2009, MIT

 Molecular design of novel pharmaceutical agents depends on a mechanistic paradigm. A library of compounds was designed to mimic some features of cisplatin that are… (more)

Subjects/Keywords: Biological Engineering.

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APA (6th Edition):

Morton, Charles Ingalls, I. (2009). Metabolic and mechanistic exploration of a novel programmable genotoxicant against prostate cancer . (Doctoral Dissertation). MIT. Retrieved from http://hdl.handle.net/1721.1/61229

Chicago Manual of Style (16th Edition):

Morton, Charles Ingalls, IV. “Metabolic and mechanistic exploration of a novel programmable genotoxicant against prostate cancer .” 2009. Doctoral Dissertation, MIT. Accessed November 21, 2019. http://hdl.handle.net/1721.1/61229.

MLA Handbook (7th Edition):

Morton, Charles Ingalls, IV. “Metabolic and mechanistic exploration of a novel programmable genotoxicant against prostate cancer .” 2009. Web. 21 Nov 2019.

Vancouver:

Morton, Charles Ingalls I. Metabolic and mechanistic exploration of a novel programmable genotoxicant against prostate cancer . [Internet] [Doctoral dissertation]. MIT; 2009. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/1721.1/61229.

Council of Science Editors:

Morton, Charles Ingalls I. Metabolic and mechanistic exploration of a novel programmable genotoxicant against prostate cancer . [Doctoral Dissertation]. MIT; 2009. Available from: http://hdl.handle.net/1721.1/61229


MIT

8. Kadaba, Neena Sujata, 1981-. Design and synthesis of inhibitors of dTDP-D-glucose 4,6-dehydrate (Rm1B), and enzyme required for dTDP-L-rhamnose production in M. tuberculosis .

Degree: Biological Engineering, 2003, MIT

 The purpose of this work is to probe the dTDP-L-rhamnose pathway in an effort to develop small molecule inhibitors that could act as therapeutics for… (more)

Subjects/Keywords: Biological Engineering.

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APA (6th Edition):

Kadaba, Neena Sujata, 1. (2003). Design and synthesis of inhibitors of dTDP-D-glucose 4,6-dehydrate (Rm1B), and enzyme required for dTDP-L-rhamnose production in M. tuberculosis . (Thesis). MIT. Retrieved from http://hdl.handle.net/1721.1/73350

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):

Kadaba, Neena Sujata, 1981-. “Design and synthesis of inhibitors of dTDP-D-glucose 4,6-dehydrate (Rm1B), and enzyme required for dTDP-L-rhamnose production in M. tuberculosis .” 2003. Thesis, MIT. Accessed November 21, 2019. http://hdl.handle.net/1721.1/73350.

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

MLA Handbook (7th Edition):

Kadaba, Neena Sujata, 1981-. “Design and synthesis of inhibitors of dTDP-D-glucose 4,6-dehydrate (Rm1B), and enzyme required for dTDP-L-rhamnose production in M. tuberculosis .” 2003. Web. 21 Nov 2019.

Vancouver:

Kadaba, Neena Sujata 1. Design and synthesis of inhibitors of dTDP-D-glucose 4,6-dehydrate (Rm1B), and enzyme required for dTDP-L-rhamnose production in M. tuberculosis . [Internet] [Thesis]. MIT; 2003. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/1721.1/73350.

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

Council of Science Editors:

Kadaba, Neena Sujata 1. Design and synthesis of inhibitors of dTDP-D-glucose 4,6-dehydrate (Rm1B), and enzyme required for dTDP-L-rhamnose production in M. tuberculosis . [Thesis]. MIT; 2003. Available from: http://hdl.handle.net/1721.1/73350

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


MIT

9. Chen, Zheng-Huan, 1964-. Studies of DNA lesion-protein interactions : toward the development of DNA repair-inhibiting chemotherapeutic agents .

Degree: PhD, 1996, MIT

Subjects/Keywords: Division of Toxicology

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APA (6th Edition):

Chen, Zheng-Huan, 1. (1996). Studies of DNA lesion-protein interactions : toward the development of DNA repair-inhibiting chemotherapeutic agents . (Doctoral Dissertation). MIT. Retrieved from http://hdl.handle.net/1721.1/41342

Chicago Manual of Style (16th Edition):

Chen, Zheng-Huan, 1964-. “Studies of DNA lesion-protein interactions : toward the development of DNA repair-inhibiting chemotherapeutic agents .” 1996. Doctoral Dissertation, MIT. Accessed November 21, 2019. http://hdl.handle.net/1721.1/41342.

MLA Handbook (7th Edition):

Chen, Zheng-Huan, 1964-. “Studies of DNA lesion-protein interactions : toward the development of DNA repair-inhibiting chemotherapeutic agents .” 1996. Web. 21 Nov 2019.

Vancouver:

Chen, Zheng-Huan 1. Studies of DNA lesion-protein interactions : toward the development of DNA repair-inhibiting chemotherapeutic agents . [Internet] [Doctoral dissertation]. MIT; 1996. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/1721.1/41342.

Council of Science Editors:

Chen, Zheng-Huan 1. Studies of DNA lesion-protein interactions : toward the development of DNA repair-inhibiting chemotherapeutic agents . [Doctoral Dissertation]. MIT; 1996. Available from: http://hdl.handle.net/1721.1/41342


MIT

10. Mello, Jill Ann, 1966-. Transcription and mismatch repair in the mechanism of action of the anticancer drug cisplatin .

Degree: PhD, Chemistry, 1997, MIT

 cis-Diamminedichloroplatinum(II) (cis-DDP or cisplatin) is a powerful cytotoxin and anticancer therapeutic, used most effectively in the treatment of testicular and ovarian cancers. By contrast, the… (more)

Subjects/Keywords: Chemistry.

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APA (6th Edition):

Mello, Jill Ann, 1. (1997). Transcription and mismatch repair in the mechanism of action of the anticancer drug cisplatin . (Doctoral Dissertation). MIT. Retrieved from http://hdl.handle.net/1721.1/42993

Chicago Manual of Style (16th Edition):

Mello, Jill Ann, 1966-. “Transcription and mismatch repair in the mechanism of action of the anticancer drug cisplatin .” 1997. Doctoral Dissertation, MIT. Accessed November 21, 2019. http://hdl.handle.net/1721.1/42993.

MLA Handbook (7th Edition):

Mello, Jill Ann, 1966-. “Transcription and mismatch repair in the mechanism of action of the anticancer drug cisplatin .” 1997. Web. 21 Nov 2019.

Vancouver:

Mello, Jill Ann 1. Transcription and mismatch repair in the mechanism of action of the anticancer drug cisplatin . [Internet] [Doctoral dissertation]. MIT; 1997. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/1721.1/42993.

Council of Science Editors:

Mello, Jill Ann 1. Transcription and mismatch repair in the mechanism of action of the anticancer drug cisplatin . [Doctoral Dissertation]. MIT; 1997. Available from: http://hdl.handle.net/1721.1/42993


MIT

11. Frick, Lauren Elizabeth. The versatile E. coli adaptive response protein AlkB mitigates toxicity and mutagenicity of etheno-, ethano-, and methyl-modified bases in vivo ; Versatile Escherichia coli adaptive response protein AlkB mitigates toxicity and mutagenicity of etheno-, ethano-, and methyl- modified bases in vivo .

Degree: PhD, Biological Engineering Division, 2007, MIT

 The Escherichia coli AlkB protein is an exceptionally versatile DNA repair enzyme. Its expression is induced upon exposure to alkylating agents as part of the… (more)

Subjects/Keywords: Biological Engineering Division.

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APA (6th Edition):

Frick, L. E. (2007). The versatile E. coli adaptive response protein AlkB mitigates toxicity and mutagenicity of etheno-, ethano-, and methyl-modified bases in vivo ; Versatile Escherichia coli adaptive response protein AlkB mitigates toxicity and mutagenicity of etheno-, ethano-, and methyl- modified bases in vivo . (Doctoral Dissertation). MIT. Retrieved from http://hdl.handle.net/1721.1/42382

Chicago Manual of Style (16th Edition):

Frick, Lauren Elizabeth. “The versatile E. coli adaptive response protein AlkB mitigates toxicity and mutagenicity of etheno-, ethano-, and methyl-modified bases in vivo ; Versatile Escherichia coli adaptive response protein AlkB mitigates toxicity and mutagenicity of etheno-, ethano-, and methyl- modified bases in vivo .” 2007. Doctoral Dissertation, MIT. Accessed November 21, 2019. http://hdl.handle.net/1721.1/42382.

MLA Handbook (7th Edition):

Frick, Lauren Elizabeth. “The versatile E. coli adaptive response protein AlkB mitigates toxicity and mutagenicity of etheno-, ethano-, and methyl-modified bases in vivo ; Versatile Escherichia coli adaptive response protein AlkB mitigates toxicity and mutagenicity of etheno-, ethano-, and methyl- modified bases in vivo .” 2007. Web. 21 Nov 2019.

Vancouver:

Frick LE. The versatile E. coli adaptive response protein AlkB mitigates toxicity and mutagenicity of etheno-, ethano-, and methyl-modified bases in vivo ; Versatile Escherichia coli adaptive response protein AlkB mitigates toxicity and mutagenicity of etheno-, ethano-, and methyl- modified bases in vivo . [Internet] [Doctoral dissertation]. MIT; 2007. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/1721.1/42382.

Council of Science Editors:

Frick LE. The versatile E. coli adaptive response protein AlkB mitigates toxicity and mutagenicity of etheno-, ethano-, and methyl-modified bases in vivo ; Versatile Escherichia coli adaptive response protein AlkB mitigates toxicity and mutagenicity of etheno-, ethano-, and methyl- modified bases in vivo . [Doctoral Dissertation]. MIT; 2007. Available from: http://hdl.handle.net/1721.1/42382


MIT

12. Trimmer, Elizabeth Eloise, 1966-. Specific binding of human SRY (Sex-Determining Region Y) to DNA adducts of the anticancer drug cisplatin .

Degree: PhD, 1997, MIT

Subjects/Keywords: Chemistry

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APA (6th Edition):

Trimmer, Elizabeth Eloise, 1. (1997). Specific binding of human SRY (Sex-Determining Region Y) to DNA adducts of the anticancer drug cisplatin . (Doctoral Dissertation). MIT. Retrieved from http://hdl.handle.net/1721.1/46076

Chicago Manual of Style (16th Edition):

Trimmer, Elizabeth Eloise, 1966-. “Specific binding of human SRY (Sex-Determining Region Y) to DNA adducts of the anticancer drug cisplatin .” 1997. Doctoral Dissertation, MIT. Accessed November 21, 2019. http://hdl.handle.net/1721.1/46076.

MLA Handbook (7th Edition):

Trimmer, Elizabeth Eloise, 1966-. “Specific binding of human SRY (Sex-Determining Region Y) to DNA adducts of the anticancer drug cisplatin .” 1997. Web. 21 Nov 2019.

Vancouver:

Trimmer, Elizabeth Eloise 1. Specific binding of human SRY (Sex-Determining Region Y) to DNA adducts of the anticancer drug cisplatin . [Internet] [Doctoral dissertation]. MIT; 1997. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/1721.1/46076.

Council of Science Editors:

Trimmer, Elizabeth Eloise 1. Specific binding of human SRY (Sex-Determining Region Y) to DNA adducts of the anticancer drug cisplatin . [Doctoral Dissertation]. MIT; 1997. Available from: http://hdl.handle.net/1721.1/46076


MIT

13. Wang, David, 1970-. Formation and repair of DNA lesions : studies of oxidized cytosines and aflatoxin B₁ adducts .

Degree: PhD, 1998, MIT

Subjects/Keywords: Chemistry

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APA (6th Edition):

Wang, David, 1. (1998). Formation and repair of DNA lesions : studies of oxidized cytosines and aflatoxin B₁ adducts . (Doctoral Dissertation). MIT. Retrieved from http://hdl.handle.net/1721.1/50342

Chicago Manual of Style (16th Edition):

Wang, David, 1970-. “Formation and repair of DNA lesions : studies of oxidized cytosines and aflatoxin B₁ adducts .” 1998. Doctoral Dissertation, MIT. Accessed November 21, 2019. http://hdl.handle.net/1721.1/50342.

MLA Handbook (7th Edition):

Wang, David, 1970-. “Formation and repair of DNA lesions : studies of oxidized cytosines and aflatoxin B₁ adducts .” 1998. Web. 21 Nov 2019.

Vancouver:

Wang, David 1. Formation and repair of DNA lesions : studies of oxidized cytosines and aflatoxin B₁ adducts . [Internet] [Doctoral dissertation]. MIT; 1998. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/1721.1/50342.

Council of Science Editors:

Wang, David 1. Formation and repair of DNA lesions : studies of oxidized cytosines and aflatoxin B₁ adducts . [Doctoral Dissertation]. MIT; 1998. Available from: http://hdl.handle.net/1721.1/50342


MIT

14. Kobertz, William Rudolf, 1968-. Total synthesis of a Furan-side psoralen-thymidine monoadduct and its biochemical applications .

Degree: PhD, 1998, MIT

Subjects/Keywords: Chemistry

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APA (6th Edition):

Kobertz, William Rudolf, 1. (1998). Total synthesis of a Furan-side psoralen-thymidine monoadduct and its biochemical applications . (Doctoral Dissertation). MIT. Retrieved from http://hdl.handle.net/1721.1/50343

Chicago Manual of Style (16th Edition):

Kobertz, William Rudolf, 1968-. “Total synthesis of a Furan-side psoralen-thymidine monoadduct and its biochemical applications .” 1998. Doctoral Dissertation, MIT. Accessed November 21, 2019. http://hdl.handle.net/1721.1/50343.

MLA Handbook (7th Edition):

Kobertz, William Rudolf, 1968-. “Total synthesis of a Furan-side psoralen-thymidine monoadduct and its biochemical applications .” 1998. Web. 21 Nov 2019.

Vancouver:

Kobertz, William Rudolf 1. Total synthesis of a Furan-side psoralen-thymidine monoadduct and its biochemical applications . [Internet] [Doctoral dissertation]. MIT; 1998. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/1721.1/50343.

Council of Science Editors:

Kobertz, William Rudolf 1. Total synthesis of a Furan-side psoralen-thymidine monoadduct and its biochemical applications . [Doctoral Dissertation]. MIT; 1998. Available from: http://hdl.handle.net/1721.1/50343


MIT

15. Kreutzer, Deborah A. Oxidative DNA damage : mutagenic properties of 5-hydorxycytosine, 5-hydroxyuracil and uracil glycol in Eschericia coli .

Degree: PhD, 1998, MIT

Subjects/Keywords: Division of Toxicology

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APA (6th Edition):

Kreutzer, D. A. (1998). Oxidative DNA damage : mutagenic properties of 5-hydorxycytosine, 5-hydroxyuracil and uracil glycol in Eschericia coli . (Doctoral Dissertation). MIT. Retrieved from http://hdl.handle.net/1721.1/50413

Chicago Manual of Style (16th Edition):

Kreutzer, Deborah A. “Oxidative DNA damage : mutagenic properties of 5-hydorxycytosine, 5-hydroxyuracil and uracil glycol in Eschericia coli .” 1998. Doctoral Dissertation, MIT. Accessed November 21, 2019. http://hdl.handle.net/1721.1/50413.

MLA Handbook (7th Edition):

Kreutzer, Deborah A. “Oxidative DNA damage : mutagenic properties of 5-hydorxycytosine, 5-hydroxyuracil and uracil glycol in Eschericia coli .” 1998. Web. 21 Nov 2019.

Vancouver:

Kreutzer DA. Oxidative DNA damage : mutagenic properties of 5-hydorxycytosine, 5-hydroxyuracil and uracil glycol in Eschericia coli . [Internet] [Doctoral dissertation]. MIT; 1998. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/1721.1/50413.

Council of Science Editors:

Kreutzer DA. Oxidative DNA damage : mutagenic properties of 5-hydorxycytosine, 5-hydroxyuracil and uracil glycol in Eschericia coli . [Doctoral Dissertation]. MIT; 1998. Available from: http://hdl.handle.net/1721.1/50413


MIT

16. Verghis, Susan Bina Malaikal, 1960-. Investigation of the mechanism of mutagenesis by the DNA adducts of the human bladder carcinogen, 4-aminobiphenyl .

Degree: PhD, 1992, MIT

Subjects/Keywords: Division of Toxicology

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APA (6th Edition):

Verghis, Susan Bina Malaikal, 1. (1992). Investigation of the mechanism of mutagenesis by the DNA adducts of the human bladder carcinogen, 4-aminobiphenyl . (Doctoral Dissertation). MIT. Retrieved from http://hdl.handle.net/1721.1/73326

Chicago Manual of Style (16th Edition):

Verghis, Susan Bina Malaikal, 1960-. “Investigation of the mechanism of mutagenesis by the DNA adducts of the human bladder carcinogen, 4-aminobiphenyl .” 1992. Doctoral Dissertation, MIT. Accessed November 21, 2019. http://hdl.handle.net/1721.1/73326.

MLA Handbook (7th Edition):

Verghis, Susan Bina Malaikal, 1960-. “Investigation of the mechanism of mutagenesis by the DNA adducts of the human bladder carcinogen, 4-aminobiphenyl .” 1992. Web. 21 Nov 2019.

Vancouver:

Verghis, Susan Bina Malaikal 1. Investigation of the mechanism of mutagenesis by the DNA adducts of the human bladder carcinogen, 4-aminobiphenyl . [Internet] [Doctoral dissertation]. MIT; 1992. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/1721.1/73326.

Council of Science Editors:

Verghis, Susan Bina Malaikal 1. Investigation of the mechanism of mutagenesis by the DNA adducts of the human bladder carcinogen, 4-aminobiphenyl . [Doctoral Dissertation]. MIT; 1992. Available from: http://hdl.handle.net/1721.1/73326


MIT

17. Kartalou, Maria, 1972-. The role of base excision repair proteins in the cellular responses to the anticancer drug cisplatin .

Degree: PhD, Division of Bioengineering and Environmental Health, 2000, MIT

Subjects/Keywords: Division of Bioengineering and Environmental Health.

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APA (6th Edition):

Kartalou, Maria, 1. (2000). The role of base excision repair proteins in the cellular responses to the anticancer drug cisplatin . (Doctoral Dissertation). MIT. Retrieved from http://hdl.handle.net/1721.1/73346

Chicago Manual of Style (16th Edition):

Kartalou, Maria, 1972-. “The role of base excision repair proteins in the cellular responses to the anticancer drug cisplatin .” 2000. Doctoral Dissertation, MIT. Accessed November 21, 2019. http://hdl.handle.net/1721.1/73346.

MLA Handbook (7th Edition):

Kartalou, Maria, 1972-. “The role of base excision repair proteins in the cellular responses to the anticancer drug cisplatin .” 2000. Web. 21 Nov 2019.

Vancouver:

Kartalou, Maria 1. The role of base excision repair proteins in the cellular responses to the anticancer drug cisplatin . [Internet] [Doctoral dissertation]. MIT; 2000. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/1721.1/73346.

Council of Science Editors:

Kartalou, Maria 1. The role of base excision repair proteins in the cellular responses to the anticancer drug cisplatin . [Doctoral Dissertation]. MIT; 2000. Available from: http://hdl.handle.net/1721.1/73346


MIT

18. Lee, Annie S. (Annie Sang), 1975-. Molecular mechanism of interactions between estrogen receptor and estrogen receptor selective genotoxins .

Degree: MS, Division of Bioengineering and Environmental Health, 2000, MIT

 Although one million new breast cancer cases arise each year worldwide, therapies to treat the disease are limited. Conventional treatments including the chemotherapeutic agent, Tamoxifen,… (more)

Subjects/Keywords: Division of Bioengineering and Environmental Health.

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APA (6th Edition):

Lee, Annie S. (Annie Sang), 1. (2000). Molecular mechanism of interactions between estrogen receptor and estrogen receptor selective genotoxins . (Masters Thesis). MIT. Retrieved from http://hdl.handle.net/1721.1/73348

Chicago Manual of Style (16th Edition):

Lee, Annie S. (Annie Sang), 1975-. “Molecular mechanism of interactions between estrogen receptor and estrogen receptor selective genotoxins .” 2000. Masters Thesis, MIT. Accessed November 21, 2019. http://hdl.handle.net/1721.1/73348.

MLA Handbook (7th Edition):

Lee, Annie S. (Annie Sang), 1975-. “Molecular mechanism of interactions between estrogen receptor and estrogen receptor selective genotoxins .” 2000. Web. 21 Nov 2019.

Vancouver:

Lee, Annie S. (Annie Sang) 1. Molecular mechanism of interactions between estrogen receptor and estrogen receptor selective genotoxins . [Internet] [Masters thesis]. MIT; 2000. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/1721.1/73348.

Council of Science Editors:

Lee, Annie S. (Annie Sang) 1. Molecular mechanism of interactions between estrogen receptor and estrogen receptor selective genotoxins . [Masters Thesis]. MIT; 2000. Available from: http://hdl.handle.net/1721.1/73348


MIT

19. Bailey, Elisabeth Ann, 1967-. Mutagenesis by the primary aflatoxin B₁ DNA adduct in Escherichia coli .

Degree: PhD, 1996, MIT

Subjects/Keywords: Chemistry

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APA (6th Edition):

Bailey, Elisabeth Ann, 1. (1996). Mutagenesis by the primary aflatoxin B₁ DNA adduct in Escherichia coli . (Doctoral Dissertation). MIT. Retrieved from http://hdl.handle.net/1721.1/40572

Chicago Manual of Style (16th Edition):

Bailey, Elisabeth Ann, 1967-. “Mutagenesis by the primary aflatoxin B₁ DNA adduct in Escherichia coli .” 1996. Doctoral Dissertation, MIT. Accessed November 21, 2019. http://hdl.handle.net/1721.1/40572.

MLA Handbook (7th Edition):

Bailey, Elisabeth Ann, 1967-. “Mutagenesis by the primary aflatoxin B₁ DNA adduct in Escherichia coli .” 1996. Web. 21 Nov 2019.

Vancouver:

Bailey, Elisabeth Ann 1. Mutagenesis by the primary aflatoxin B₁ DNA adduct in Escherichia coli . [Internet] [Doctoral dissertation]. MIT; 1996. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/1721.1/40572.

Council of Science Editors:

Bailey, Elisabeth Ann 1. Mutagenesis by the primary aflatoxin B₁ DNA adduct in Escherichia coli . [Doctoral Dissertation]. MIT; 1996. Available from: http://hdl.handle.net/1721.1/40572


MIT

20. Zdraveski, Zoran Z. (Zoran Zare), 1969-. The role of mismatch repair and recombination in cellular responses to the DNA damaging anticancer drug Cisplatin .

Degree: PhD, Chemistry, 2002, MIT

 Cisplatin (cis-diamminedichloroplatinum(ll)) is a successful DNA-damaging anticancer drug used in the treatment of testicular, ovarian and other tumors. In the past decade, several mutually non-exclusive… (more)

Subjects/Keywords: Chemistry.

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APA (6th Edition):

Zdraveski, Z. Z. (. Z. (2002). The role of mismatch repair and recombination in cellular responses to the DNA damaging anticancer drug Cisplatin . (Doctoral Dissertation). MIT. Retrieved from http://hdl.handle.net/1721.1/8363

Chicago Manual of Style (16th Edition):

Zdraveski, Zoran Z (Zoran Zare),. “The role of mismatch repair and recombination in cellular responses to the DNA damaging anticancer drug Cisplatin .” 2002. Doctoral Dissertation, MIT. Accessed November 21, 2019. http://hdl.handle.net/1721.1/8363.

MLA Handbook (7th Edition):

Zdraveski, Zoran Z (Zoran Zare),. “The role of mismatch repair and recombination in cellular responses to the DNA damaging anticancer drug Cisplatin .” 2002. Web. 21 Nov 2019.

Vancouver:

Zdraveski ZZ(Z. The role of mismatch repair and recombination in cellular responses to the DNA damaging anticancer drug Cisplatin . [Internet] [Doctoral dissertation]. MIT; 2002. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/1721.1/8363.

Council of Science Editors:

Zdraveski ZZ(Z. The role of mismatch repair and recombination in cellular responses to the DNA damaging anticancer drug Cisplatin . [Doctoral Dissertation]. MIT; 2002. Available from: http://hdl.handle.net/1721.1/8363


MIT

21. Froim, Doriana, 1973-. Cisplatin cytotoxicity associated with tetracycline resistance determinants in Escherichia coli .

Degree: PhD, Biological Engineering Division, 2005, MIT

 Tetracyclines, a broad-spectrum class of antibiotics, were discovered in the late 1940s, and became widely used because of their important advantages: they are inexpensive, safe,… (more)

Subjects/Keywords: Biological Engineering Division.

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APA (6th Edition):

Froim, Doriana, 1. (2005). Cisplatin cytotoxicity associated with tetracycline resistance determinants in Escherichia coli . (Doctoral Dissertation). MIT. Retrieved from http://hdl.handle.net/1721.1/35701

Chicago Manual of Style (16th Edition):

Froim, Doriana, 1973-. “Cisplatin cytotoxicity associated with tetracycline resistance determinants in Escherichia coli .” 2005. Doctoral Dissertation, MIT. Accessed November 21, 2019. http://hdl.handle.net/1721.1/35701.

MLA Handbook (7th Edition):

Froim, Doriana, 1973-. “Cisplatin cytotoxicity associated with tetracycline resistance determinants in Escherichia coli .” 2005. Web. 21 Nov 2019.

Vancouver:

Froim, Doriana 1. Cisplatin cytotoxicity associated with tetracycline resistance determinants in Escherichia coli . [Internet] [Doctoral dissertation]. MIT; 2005. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/1721.1/35701.

Council of Science Editors:

Froim, Doriana 1. Cisplatin cytotoxicity associated with tetracycline resistance determinants in Escherichia coli . [Doctoral Dissertation]. MIT; 2005. Available from: http://hdl.handle.net/1721.1/35701


MIT

22. Robbins, Jennifer L. The role of mismatch repair in mediating cellular sensitivity to cisplatin : the Escherichia coli methyl-directed repair paradigm .

Degree: PhD, Biological Engineering Division, 2006, MIT

 The anticancer drug cisplatin is in widespread use but its mechanism of action is only poorly understood. Moreover, human cancers acquire resistance to the drug,… (more)

Subjects/Keywords: Biological Engineering Division.

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APA (6th Edition):

Robbins, J. L. (2006). The role of mismatch repair in mediating cellular sensitivity to cisplatin : the Escherichia coli methyl-directed repair paradigm . (Doctoral Dissertation). MIT. Retrieved from http://hdl.handle.net/1721.1/34155

Chicago Manual of Style (16th Edition):

Robbins, Jennifer L. “The role of mismatch repair in mediating cellular sensitivity to cisplatin : the Escherichia coli methyl-directed repair paradigm .” 2006. Doctoral Dissertation, MIT. Accessed November 21, 2019. http://hdl.handle.net/1721.1/34155.

MLA Handbook (7th Edition):

Robbins, Jennifer L. “The role of mismatch repair in mediating cellular sensitivity to cisplatin : the Escherichia coli methyl-directed repair paradigm .” 2006. Web. 21 Nov 2019.

Vancouver:

Robbins JL. The role of mismatch repair in mediating cellular sensitivity to cisplatin : the Escherichia coli methyl-directed repair paradigm . [Internet] [Doctoral dissertation]. MIT; 2006. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/1721.1/34155.

Council of Science Editors:

Robbins JL. The role of mismatch repair in mediating cellular sensitivity to cisplatin : the Escherichia coli methyl-directed repair paradigm . [Doctoral Dissertation]. MIT; 2006. Available from: http://hdl.handle.net/1721.1/34155


MIT

23. Rye, Peter Thomas. Biochemical characterization of the E. coli Very Short Patch Repair pathway and its coordination with methyltransferase repair of 0⁶-methylguanine ; Biochemical characterization of the Escherichia coli VSPR pathway and its coordination with methyltransferase repair of 0⁶mG .

Degree: PhD, Chemistry, 2006, MIT

 The E. coli Very Short Patch Repair (VSPR) system corrects T:G mismatches that arise through Dcm-mediated methylation and subsequent deamination of the underlined cytosine residue… (more)

Subjects/Keywords: Chemistry.

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APA (6th Edition):

Rye, P. T. (2006). Biochemical characterization of the E. coli Very Short Patch Repair pathway and its coordination with methyltransferase repair of 0⁶-methylguanine ; Biochemical characterization of the Escherichia coli VSPR pathway and its coordination with methyltransferase repair of 0⁶mG . (Doctoral Dissertation). MIT. Retrieved from http://hdl.handle.net/1721.1/36263

Chicago Manual of Style (16th Edition):

Rye, Peter Thomas. “Biochemical characterization of the E. coli Very Short Patch Repair pathway and its coordination with methyltransferase repair of 0⁶-methylguanine ; Biochemical characterization of the Escherichia coli VSPR pathway and its coordination with methyltransferase repair of 0⁶mG .” 2006. Doctoral Dissertation, MIT. Accessed November 21, 2019. http://hdl.handle.net/1721.1/36263.

MLA Handbook (7th Edition):

Rye, Peter Thomas. “Biochemical characterization of the E. coli Very Short Patch Repair pathway and its coordination with methyltransferase repair of 0⁶-methylguanine ; Biochemical characterization of the Escherichia coli VSPR pathway and its coordination with methyltransferase repair of 0⁶mG .” 2006. Web. 21 Nov 2019.

Vancouver:

Rye PT. Biochemical characterization of the E. coli Very Short Patch Repair pathway and its coordination with methyltransferase repair of 0⁶-methylguanine ; Biochemical characterization of the Escherichia coli VSPR pathway and its coordination with methyltransferase repair of 0⁶mG . [Internet] [Doctoral dissertation]. MIT; 2006. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/1721.1/36263.

Council of Science Editors:

Rye PT. Biochemical characterization of the E. coli Very Short Patch Repair pathway and its coordination with methyltransferase repair of 0⁶-methylguanine ; Biochemical characterization of the Escherichia coli VSPR pathway and its coordination with methyltransferase repair of 0⁶mG . [Doctoral Dissertation]. MIT; 2006. Available from: http://hdl.handle.net/1721.1/36263


MIT

24. Neeley, William Louis. Genomic consequences of DNA oxidation by peroxynitrite ; Genomic consequences of deoxyribonucleic acid oxidation by peroxynitrite .

Degree: PhD, Chemistry, 2006, MIT

 The radicals nitric oxide and superoxide are produced endogenously by activated macrophages and neutrophils and combine in a diffusion-limited reaction to form peroxynitrite, a powerful… (more)

Subjects/Keywords: Chemistry.

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APA (6th Edition):

Neeley, W. L. (2006). Genomic consequences of DNA oxidation by peroxynitrite ; Genomic consequences of deoxyribonucleic acid oxidation by peroxynitrite . (Doctoral Dissertation). MIT. Retrieved from http://hdl.handle.net/1721.1/37359

Chicago Manual of Style (16th Edition):

Neeley, William Louis. “Genomic consequences of DNA oxidation by peroxynitrite ; Genomic consequences of deoxyribonucleic acid oxidation by peroxynitrite .” 2006. Doctoral Dissertation, MIT. Accessed November 21, 2019. http://hdl.handle.net/1721.1/37359.

MLA Handbook (7th Edition):

Neeley, William Louis. “Genomic consequences of DNA oxidation by peroxynitrite ; Genomic consequences of deoxyribonucleic acid oxidation by peroxynitrite .” 2006. Web. 21 Nov 2019.

Vancouver:

Neeley WL. Genomic consequences of DNA oxidation by peroxynitrite ; Genomic consequences of deoxyribonucleic acid oxidation by peroxynitrite . [Internet] [Doctoral dissertation]. MIT; 2006. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/1721.1/37359.

Council of Science Editors:

Neeley WL. Genomic consequences of DNA oxidation by peroxynitrite ; Genomic consequences of deoxyribonucleic acid oxidation by peroxynitrite . [Doctoral Dissertation]. MIT; 2006. Available from: http://hdl.handle.net/1721.1/37359


MIT

25. Hillier, Shawn M. (Shawn Matthew). Novel genotoxins that target estrogen receptor- and androgen receptor- positive cancers : identification of DNA adducts, pharmacokinetics, and mechanism .

Degree: PhD, Chemistry, 2005, MIT

 We have designed and synthesized novel molecules capable of selectively killing tumor cells that aberrantly express steroid hormone receptors. Many human breast cancers express high… (more)

Subjects/Keywords: Chemistry.

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APA (6th Edition):

Hillier, S. M. (. M. (2005). Novel genotoxins that target estrogen receptor- and androgen receptor- positive cancers : identification of DNA adducts, pharmacokinetics, and mechanism . (Doctoral Dissertation). MIT. Retrieved from http://hdl.handle.net/1721.1/32480

Chicago Manual of Style (16th Edition):

Hillier, Shawn M (Shawn Matthew). “Novel genotoxins that target estrogen receptor- and androgen receptor- positive cancers : identification of DNA adducts, pharmacokinetics, and mechanism .” 2005. Doctoral Dissertation, MIT. Accessed November 21, 2019. http://hdl.handle.net/1721.1/32480.

MLA Handbook (7th Edition):

Hillier, Shawn M (Shawn Matthew). “Novel genotoxins that target estrogen receptor- and androgen receptor- positive cancers : identification of DNA adducts, pharmacokinetics, and mechanism .” 2005. Web. 21 Nov 2019.

Vancouver:

Hillier SM(M. Novel genotoxins that target estrogen receptor- and androgen receptor- positive cancers : identification of DNA adducts, pharmacokinetics, and mechanism . [Internet] [Doctoral dissertation]. MIT; 2005. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/1721.1/32480.

Council of Science Editors:

Hillier SM(M. Novel genotoxins that target estrogen receptor- and androgen receptor- positive cancers : identification of DNA adducts, pharmacokinetics, and mechanism . [Doctoral Dissertation]. MIT; 2005. Available from: http://hdl.handle.net/1721.1/32480


MIT

26. Bradley, Lisa Jolene Naser, 1957-. Mutagenesis and genotoxicity of the major DNA adduct of Cis-diamminedichloroplatinum(II) .

Degree: PhD, 1991, MIT

Subjects/Keywords: Division of Toxicology

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APA (6th Edition):

Bradley, Lisa Jolene Naser, 1. (1991). Mutagenesis and genotoxicity of the major DNA adduct of Cis-diamminedichloroplatinum(II) . (Doctoral Dissertation). MIT. Retrieved from http://hdl.handle.net/1721.1/13956

Chicago Manual of Style (16th Edition):

Bradley, Lisa Jolene Naser, 1957-. “Mutagenesis and genotoxicity of the major DNA adduct of Cis-diamminedichloroplatinum(II) .” 1991. Doctoral Dissertation, MIT. Accessed November 21, 2019. http://hdl.handle.net/1721.1/13956.

MLA Handbook (7th Edition):

Bradley, Lisa Jolene Naser, 1957-. “Mutagenesis and genotoxicity of the major DNA adduct of Cis-diamminedichloroplatinum(II) .” 1991. Web. 21 Nov 2019.

Vancouver:

Bradley, Lisa Jolene Naser 1. Mutagenesis and genotoxicity of the major DNA adduct of Cis-diamminedichloroplatinum(II) . [Internet] [Doctoral dissertation]. MIT; 1991. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/1721.1/13956.

Council of Science Editors:

Bradley, Lisa Jolene Naser 1. Mutagenesis and genotoxicity of the major DNA adduct of Cis-diamminedichloroplatinum(II) . [Doctoral Dissertation]. MIT; 1991. Available from: http://hdl.handle.net/1721.1/13956


MIT

27. Barrera, Esequiel Eduardo. Synthesis and characterization of oligonucleotides containing deoxyxanthosine : a probe for the mutagentic and genotoxic activity of an oxidized DNA base .

Degree: MS, 1995, MIT

Subjects/Keywords: Division of Toxicology

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APA (6th Edition):

Barrera, E. E. (1995). Synthesis and characterization of oligonucleotides containing deoxyxanthosine : a probe for the mutagentic and genotoxic activity of an oxidized DNA base . (Masters Thesis). MIT. Retrieved from http://hdl.handle.net/1721.1/36650

Chicago Manual of Style (16th Edition):

Barrera, Esequiel Eduardo. “Synthesis and characterization of oligonucleotides containing deoxyxanthosine : a probe for the mutagentic and genotoxic activity of an oxidized DNA base .” 1995. Masters Thesis, MIT. Accessed November 21, 2019. http://hdl.handle.net/1721.1/36650.

MLA Handbook (7th Edition):

Barrera, Esequiel Eduardo. “Synthesis and characterization of oligonucleotides containing deoxyxanthosine : a probe for the mutagentic and genotoxic activity of an oxidized DNA base .” 1995. Web. 21 Nov 2019.

Vancouver:

Barrera EE. Synthesis and characterization of oligonucleotides containing deoxyxanthosine : a probe for the mutagentic and genotoxic activity of an oxidized DNA base . [Internet] [Masters thesis]. MIT; 1995. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/1721.1/36650.

Council of Science Editors:

Barrera EE. Synthesis and characterization of oligonucleotides containing deoxyxanthosine : a probe for the mutagentic and genotoxic activity of an oxidized DNA base . [Masters Thesis]. MIT; 1995. Available from: http://hdl.handle.net/1721.1/36650


MIT

28. Treiber, Daniel Kelly, 1965-. The role of damaged DNA recognition proteins in the genotoxicities of ultraviolet light and the anticancer drug cisplatin .

Degree: PhD, 1994, MIT

Subjects/Keywords: Division of Toxicology

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APA (6th Edition):

Treiber, Daniel Kelly, 1. (1994). The role of damaged DNA recognition proteins in the genotoxicities of ultraviolet light and the anticancer drug cisplatin . (Doctoral Dissertation). MIT. Retrieved from http://hdl.handle.net/1721.1/37508

Chicago Manual of Style (16th Edition):

Treiber, Daniel Kelly, 1965-. “The role of damaged DNA recognition proteins in the genotoxicities of ultraviolet light and the anticancer drug cisplatin .” 1994. Doctoral Dissertation, MIT. Accessed November 21, 2019. http://hdl.handle.net/1721.1/37508.

MLA Handbook (7th Edition):

Treiber, Daniel Kelly, 1965-. “The role of damaged DNA recognition proteins in the genotoxicities of ultraviolet light and the anticancer drug cisplatin .” 1994. Web. 21 Nov 2019.

Vancouver:

Treiber, Daniel Kelly 1. The role of damaged DNA recognition proteins in the genotoxicities of ultraviolet light and the anticancer drug cisplatin . [Internet] [Doctoral dissertation]. MIT; 1994. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/1721.1/37508.

Council of Science Editors:

Treiber, Daniel Kelly 1. The role of damaged DNA recognition proteins in the genotoxicities of ultraviolet light and the anticancer drug cisplatin . [Doctoral Dissertation]. MIT; 1994. Available from: http://hdl.handle.net/1721.1/37508


MIT

29. Altshuler, Kara Denise Best, 1965-. Alkylation damage in mammalian cells : an analysis of the mutagenic potential of O4-methylthymine adducts .

Degree: PhD, 1994, MIT

Subjects/Keywords: Division of Toxicology

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APA (6th Edition):

Altshuler, Kara Denise Best, 1. (1994). Alkylation damage in mammalian cells : an analysis of the mutagenic potential of O4-methylthymine adducts . (Doctoral Dissertation). MIT. Retrieved from http://hdl.handle.net/1721.1/38001

Chicago Manual of Style (16th Edition):

Altshuler, Kara Denise Best, 1965-. “Alkylation damage in mammalian cells : an analysis of the mutagenic potential of O4-methylthymine adducts .” 1994. Doctoral Dissertation, MIT. Accessed November 21, 2019. http://hdl.handle.net/1721.1/38001.

MLA Handbook (7th Edition):

Altshuler, Kara Denise Best, 1965-. “Alkylation damage in mammalian cells : an analysis of the mutagenic potential of O4-methylthymine adducts .” 1994. Web. 21 Nov 2019.

Vancouver:

Altshuler, Kara Denise Best 1. Alkylation damage in mammalian cells : an analysis of the mutagenic potential of O4-methylthymine adducts . [Internet] [Doctoral dissertation]. MIT; 1994. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/1721.1/38001.

Council of Science Editors:

Altshuler, Kara Denise Best 1. Alkylation damage in mammalian cells : an analysis of the mutagenic potential of O4-methylthymine adducts . [Doctoral Dissertation]. MIT; 1994. Available from: http://hdl.handle.net/1721.1/38001


MIT

30. Smela, Maryann E. (Maryann Elizabeth), 1974-. The toxicity and mutagenicity of the aflatoxin B₁ formamidopyrimidine DNA adduct .

Degree: PhD, Division of Bioengineering and Environmental Health, 2002, MIT

 Aflatoxin B1 (AFB1) is a fungal metabolite that contaminates the food supply in certain areas of the world. It is produced by Aspergillusflavus and related… (more)

Subjects/Keywords: Division of Bioengineering and Environmental Health.

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APA (6th Edition):

Smela, M. E. (. E. (2002). The toxicity and mutagenicity of the aflatoxin B₁ formamidopyrimidine DNA adduct . (Doctoral Dissertation). MIT. Retrieved from http://hdl.handle.net/1721.1/8392

Chicago Manual of Style (16th Edition):

Smela, Maryann E (Maryann Elizabeth),. “The toxicity and mutagenicity of the aflatoxin B₁ formamidopyrimidine DNA adduct .” 2002. Doctoral Dissertation, MIT. Accessed November 21, 2019. http://hdl.handle.net/1721.1/8392.

MLA Handbook (7th Edition):

Smela, Maryann E (Maryann Elizabeth),. “The toxicity and mutagenicity of the aflatoxin B₁ formamidopyrimidine DNA adduct .” 2002. Web. 21 Nov 2019.

Vancouver:

Smela ME(E. The toxicity and mutagenicity of the aflatoxin B₁ formamidopyrimidine DNA adduct . [Internet] [Doctoral dissertation]. MIT; 2002. [cited 2019 Nov 21]. Available from: http://hdl.handle.net/1721.1/8392.

Council of Science Editors:

Smela ME(E. The toxicity and mutagenicity of the aflatoxin B₁ formamidopyrimidine DNA adduct . [Doctoral Dissertation]. MIT; 2002. Available from: http://hdl.handle.net/1721.1/8392

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