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You searched for subject:(Biochemistry). Showing records 1 – 30 of 7169 total matches.

[1] [2] [3] [4] [5] … [239]

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University of Tennessee – Knoxville

1. Choi, Won-Gyu. Nodulin 26-like Intrinsic Protein NIP2;1 and NIP7;1: Characterization of Transport Functions and Roles in Developmental and Stress Responses in Arabidopsis.

Degree: 2009, University of Tennessee – Knoxville

 Nodulin-intrinsic proteins (NIPs) are plant-specific, water and solute transporters with homology to soybean nodulin 26. In this study, it is shown that Arabidopsis NIP2;1 (AtNIP2;1)… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Choi, W. (2009). Nodulin 26-like Intrinsic Protein NIP2;1 and NIP7;1: Characterization of Transport Functions and Roles in Developmental and Stress Responses in Arabidopsis. (Doctoral Dissertation). University of Tennessee – Knoxville. Retrieved from http://trace.tennessee.edu/utk_graddiss/26

Chicago Manual of Style (16th Edition):

Choi, Won-Gyu. “Nodulin 26-like Intrinsic Protein NIP2;1 and NIP7;1: Characterization of Transport Functions and Roles in Developmental and Stress Responses in Arabidopsis.” 2009. Doctoral Dissertation, University of Tennessee – Knoxville. Accessed July 16, 2018. http://trace.tennessee.edu/utk_graddiss/26.

MLA Handbook (7th Edition):

Choi, Won-Gyu. “Nodulin 26-like Intrinsic Protein NIP2;1 and NIP7;1: Characterization of Transport Functions and Roles in Developmental and Stress Responses in Arabidopsis.” 2009. Web. 16 Jul 2018.

Vancouver:

Choi W. Nodulin 26-like Intrinsic Protein NIP2;1 and NIP7;1: Characterization of Transport Functions and Roles in Developmental and Stress Responses in Arabidopsis. [Internet] [Doctoral dissertation]. University of Tennessee – Knoxville; 2009. [cited 2018 Jul 16]. Available from: http://trace.tennessee.edu/utk_graddiss/26.

Council of Science Editors:

Choi W. Nodulin 26-like Intrinsic Protein NIP2;1 and NIP7;1: Characterization of Transport Functions and Roles in Developmental and Stress Responses in Arabidopsis. [Doctoral Dissertation]. University of Tennessee – Knoxville; 2009. Available from: http://trace.tennessee.edu/utk_graddiss/26


Duke University

2. Liu, Junfei. MOLECULAR DISSECTION AND FUNCTIONAL DEFINITION OF ESTROGEN-RELATED RECEPTOR ALPHA SIGNALING PATHWAY .

Degree: 2013, Duke University

  The estrogen-related receptor alpha (ERRα) is an orphan nuclear receptor (NR) with no natural ligand identified. Recent studies report that ERRα expression and activity… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Liu, J. (2013). MOLECULAR DISSECTION AND FUNCTIONAL DEFINITION OF ESTROGEN-RELATED RECEPTOR ALPHA SIGNALING PATHWAY . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/8078

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):

Liu, Junfei. “MOLECULAR DISSECTION AND FUNCTIONAL DEFINITION OF ESTROGEN-RELATED RECEPTOR ALPHA SIGNALING PATHWAY .” 2013. Thesis, Duke University. Accessed July 16, 2018. http://hdl.handle.net/10161/8078.

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

MLA Handbook (7th Edition):

Liu, Junfei. “MOLECULAR DISSECTION AND FUNCTIONAL DEFINITION OF ESTROGEN-RELATED RECEPTOR ALPHA SIGNALING PATHWAY .” 2013. Web. 16 Jul 2018.

Vancouver:

Liu J. MOLECULAR DISSECTION AND FUNCTIONAL DEFINITION OF ESTROGEN-RELATED RECEPTOR ALPHA SIGNALING PATHWAY . [Internet] [Thesis]. Duke University; 2013. [cited 2018 Jul 16]. Available from: http://hdl.handle.net/10161/8078.

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

Council of Science Editors:

Liu J. MOLECULAR DISSECTION AND FUNCTIONAL DEFINITION OF ESTROGEN-RELATED RECEPTOR ALPHA SIGNALING PATHWAY . [Thesis]. Duke University; 2013. Available from: http://hdl.handle.net/10161/8078

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


Duke University

3. Almond, Joshua Richard. The Study of Fork Processing and DSB Repair in Bacteriophage T4: Roles of the MR Complex and Endonuclease VII .

Degree: 2013, Duke University

  Abstract During DNA replication, organisms often encounter different types of DNA damage or lesions that lead to the stalling or breakage of replication forks.… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Almond, J. R. (2013). The Study of Fork Processing and DSB Repair in Bacteriophage T4: Roles of the MR Complex and Endonuclease VII . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/8227

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):

Almond, Joshua Richard. “The Study of Fork Processing and DSB Repair in Bacteriophage T4: Roles of the MR Complex and Endonuclease VII .” 2013. Thesis, Duke University. Accessed July 16, 2018. http://hdl.handle.net/10161/8227.

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

MLA Handbook (7th Edition):

Almond, Joshua Richard. “The Study of Fork Processing and DSB Repair in Bacteriophage T4: Roles of the MR Complex and Endonuclease VII .” 2013. Web. 16 Jul 2018.

Vancouver:

Almond JR. The Study of Fork Processing and DSB Repair in Bacteriophage T4: Roles of the MR Complex and Endonuclease VII . [Internet] [Thesis]. Duke University; 2013. [cited 2018 Jul 16]. Available from: http://hdl.handle.net/10161/8227.

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

Council of Science Editors:

Almond JR. The Study of Fork Processing and DSB Repair in Bacteriophage T4: Roles of the MR Complex and Endonuclease VII . [Thesis]. Duke University; 2013. Available from: http://hdl.handle.net/10161/8227

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


Duke University

4. Yen, Tien-Jui. Structural Basis of RNA Recognition by Mycobacterium tuberculosis MazF Homologues .

Degree: 2016, Duke University

  The MazEF toxin-antitoxin (TA) system consists of the antitoxin MazE and the toxin MazF. MazF is a sequence-specific endoribonuclease that upon activation causes cellular… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Yen, T. (2016). Structural Basis of RNA Recognition by Mycobacterium tuberculosis MazF Homologues . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/12145

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):

Yen, Tien-Jui. “Structural Basis of RNA Recognition by Mycobacterium tuberculosis MazF Homologues .” 2016. Thesis, Duke University. Accessed July 16, 2018. http://hdl.handle.net/10161/12145.

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

MLA Handbook (7th Edition):

Yen, Tien-Jui. “Structural Basis of RNA Recognition by Mycobacterium tuberculosis MazF Homologues .” 2016. Web. 16 Jul 2018.

Vancouver:

Yen T. Structural Basis of RNA Recognition by Mycobacterium tuberculosis MazF Homologues . [Internet] [Thesis]. Duke University; 2016. [cited 2018 Jul 16]. Available from: http://hdl.handle.net/10161/12145.

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

Council of Science Editors:

Yen T. Structural Basis of RNA Recognition by Mycobacterium tuberculosis MazF Homologues . [Thesis]. Duke University; 2016. Available from: http://hdl.handle.net/10161/12145

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


Duke University

5. Hoertz, Amanda J. Studies of Ramoplanin Biosynthesis in Actinoplanes ATCC 33076 .

Degree: 2010, Duke University

  The natural progression from the introduction of an antibiotic into the market to the emergence of resistant strains demands the constant influx of new… (more)

Subjects/Keywords: Biochemistry;

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APA (6th Edition):

Hoertz, A. J. (2010). Studies of Ramoplanin Biosynthesis in Actinoplanes ATCC 33076 . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/3105

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):

Hoertz, Amanda J. “Studies of Ramoplanin Biosynthesis in Actinoplanes ATCC 33076 .” 2010. Thesis, Duke University. Accessed July 16, 2018. http://hdl.handle.net/10161/3105.

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

MLA Handbook (7th Edition):

Hoertz, Amanda J. “Studies of Ramoplanin Biosynthesis in Actinoplanes ATCC 33076 .” 2010. Web. 16 Jul 2018.

Vancouver:

Hoertz AJ. Studies of Ramoplanin Biosynthesis in Actinoplanes ATCC 33076 . [Internet] [Thesis]. Duke University; 2010. [cited 2018 Jul 16]. Available from: http://hdl.handle.net/10161/3105.

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

Council of Science Editors:

Hoertz AJ. Studies of Ramoplanin Biosynthesis in Actinoplanes ATCC 33076 . [Thesis]. Duke University; 2010. Available from: http://hdl.handle.net/10161/3105

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


Duke University

6. Shaw, Porsha. Structural and Biochemical Characterization of Trypanosoma brucei MRB1590, a kRNA Editing Accessory Protein .

Degree: 2015, Duke University

  The typical flow of genetic information involves DNA being transcribed into RNA, which is then translated into protein. However, in some organisms this pathway… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Shaw, P. (2015). Structural and Biochemical Characterization of Trypanosoma brucei MRB1590, a kRNA Editing Accessory Protein . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/11343

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):

Shaw, Porsha. “Structural and Biochemical Characterization of Trypanosoma brucei MRB1590, a kRNA Editing Accessory Protein .” 2015. Thesis, Duke University. Accessed July 16, 2018. http://hdl.handle.net/10161/11343.

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

MLA Handbook (7th Edition):

Shaw, Porsha. “Structural and Biochemical Characterization of Trypanosoma brucei MRB1590, a kRNA Editing Accessory Protein .” 2015. Web. 16 Jul 2018.

Vancouver:

Shaw P. Structural and Biochemical Characterization of Trypanosoma brucei MRB1590, a kRNA Editing Accessory Protein . [Internet] [Thesis]. Duke University; 2015. [cited 2018 Jul 16]. Available from: http://hdl.handle.net/10161/11343.

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

Council of Science Editors:

Shaw P. Structural and Biochemical Characterization of Trypanosoma brucei MRB1590, a kRNA Editing Accessory Protein . [Thesis]. Duke University; 2015. Available from: http://hdl.handle.net/10161/11343

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


Duke University

7. Krasich, Rachel. Fate of Transcription Elongation Complexes Stalled by DNA Damage and Elongation Inhibitors .

Degree: 2014, Duke University

  Transcription is the process by which cells translate genetic information stored in DNA into RNA. Transcription is a highly regulated and discontinuous process, and… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Krasich, R. (2014). Fate of Transcription Elongation Complexes Stalled by DNA Damage and Elongation Inhibitors . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/8669

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):

Krasich, Rachel. “Fate of Transcription Elongation Complexes Stalled by DNA Damage and Elongation Inhibitors .” 2014. Thesis, Duke University. Accessed July 16, 2018. http://hdl.handle.net/10161/8669.

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

MLA Handbook (7th Edition):

Krasich, Rachel. “Fate of Transcription Elongation Complexes Stalled by DNA Damage and Elongation Inhibitors .” 2014. Web. 16 Jul 2018.

Vancouver:

Krasich R. Fate of Transcription Elongation Complexes Stalled by DNA Damage and Elongation Inhibitors . [Internet] [Thesis]. Duke University; 2014. [cited 2018 Jul 16]. Available from: http://hdl.handle.net/10161/8669.

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

Council of Science Editors:

Krasich R. Fate of Transcription Elongation Complexes Stalled by DNA Damage and Elongation Inhibitors . [Thesis]. Duke University; 2014. Available from: http://hdl.handle.net/10161/8669

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


Duke University

8. Wang, Weina. Structural Mechanisms of Accurate and Mutagenic DNA Replication .

Degree: 2012, Duke University

  High-fidelity DNA polymerases achieve remarkable accuracy by exhibiting exquisite nucleotide substrate selection mechanisms. DNA polymerases not only discriminate highly against base-pair mismatches, but also… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Wang, W. (2012). Structural Mechanisms of Accurate and Mutagenic DNA Replication . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/5607

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):

Wang, Weina. “Structural Mechanisms of Accurate and Mutagenic DNA Replication .” 2012. Thesis, Duke University. Accessed July 16, 2018. http://hdl.handle.net/10161/5607.

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

MLA Handbook (7th Edition):

Wang, Weina. “Structural Mechanisms of Accurate and Mutagenic DNA Replication .” 2012. Web. 16 Jul 2018.

Vancouver:

Wang W. Structural Mechanisms of Accurate and Mutagenic DNA Replication . [Internet] [Thesis]. Duke University; 2012. [cited 2018 Jul 16]. Available from: http://hdl.handle.net/10161/5607.

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

Council of Science Editors:

Wang W. Structural Mechanisms of Accurate and Mutagenic DNA Replication . [Thesis]. Duke University; 2012. Available from: http://hdl.handle.net/10161/5607

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


Duke University

9. Zeng, Daina. Characterization of LpxC inhibitors and resistant mutants .

Degree: 2012, Duke University

  LpxC, the deacetylase that catalyzes the second and committed step of lipid A biosynthesis in E. coli, is an essential enzyme for virtually all… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Zeng, D. (2012). Characterization of LpxC inhibitors and resistant mutants . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/6114

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):

Zeng, Daina. “Characterization of LpxC inhibitors and resistant mutants .” 2012. Thesis, Duke University. Accessed July 16, 2018. http://hdl.handle.net/10161/6114.

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

MLA Handbook (7th Edition):

Zeng, Daina. “Characterization of LpxC inhibitors and resistant mutants .” 2012. Web. 16 Jul 2018.

Vancouver:

Zeng D. Characterization of LpxC inhibitors and resistant mutants . [Internet] [Thesis]. Duke University; 2012. [cited 2018 Jul 16]. Available from: http://hdl.handle.net/10161/6114.

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

Council of Science Editors:

Zeng D. Characterization of LpxC inhibitors and resistant mutants . [Thesis]. Duke University; 2012. Available from: http://hdl.handle.net/10161/6114

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


Duke University

10. Young, Hayley Elizabeth. Biochemical and Genetic Studies of UDP-2,3-Diacylglucosamine Hydrolysis in Lipid A Biosynthesis .

Degree: 2014, Duke University

  The outer-leaflet of the outer membrane of Gram-negative bacteria is composed of lipopolysaccharide (LPS), which is attached to the membrane via a hexa-acylated saccharolipid… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Young, H. E. (2014). Biochemical and Genetic Studies of UDP-2,3-Diacylglucosamine Hydrolysis in Lipid A Biosynthesis . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/8742

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):

Young, Hayley Elizabeth. “Biochemical and Genetic Studies of UDP-2,3-Diacylglucosamine Hydrolysis in Lipid A Biosynthesis .” 2014. Thesis, Duke University. Accessed July 16, 2018. http://hdl.handle.net/10161/8742.

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

MLA Handbook (7th Edition):

Young, Hayley Elizabeth. “Biochemical and Genetic Studies of UDP-2,3-Diacylglucosamine Hydrolysis in Lipid A Biosynthesis .” 2014. Web. 16 Jul 2018.

Vancouver:

Young HE. Biochemical and Genetic Studies of UDP-2,3-Diacylglucosamine Hydrolysis in Lipid A Biosynthesis . [Internet] [Thesis]. Duke University; 2014. [cited 2018 Jul 16]. Available from: http://hdl.handle.net/10161/8742.

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

Council of Science Editors:

Young HE. Biochemical and Genetic Studies of UDP-2,3-Diacylglucosamine Hydrolysis in Lipid A Biosynthesis . [Thesis]. Duke University; 2014. Available from: http://hdl.handle.net/10161/8742

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


Duke University

11. Asllani, Lored. Studies on adenine nucleotide states and their role in human MutSα function .

Degree: 2012, Duke University

  Mismatch repair is a conserved pathway that corrects errors resulting from the misincorporation of bases during DNA synthesis or from the production of damaged… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Asllani, L. (2012). Studies on adenine nucleotide states and their role in human MutSα function . (Thesis). Duke University. Retrieved from http://hdl.handle.net/10161/6140

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):

Asllani, Lored. “Studies on adenine nucleotide states and their role in human MutSα function .” 2012. Thesis, Duke University. Accessed July 16, 2018. http://hdl.handle.net/10161/6140.

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

MLA Handbook (7th Edition):

Asllani, Lored. “Studies on adenine nucleotide states and their role in human MutSα function .” 2012. Web. 16 Jul 2018.

Vancouver:

Asllani L. Studies on adenine nucleotide states and their role in human MutSα function . [Internet] [Thesis]. Duke University; 2012. [cited 2018 Jul 16]. Available from: http://hdl.handle.net/10161/6140.

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

Council of Science Editors:

Asllani L. Studies on adenine nucleotide states and their role in human MutSα function . [Thesis]. Duke University; 2012. Available from: http://hdl.handle.net/10161/6140

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


Temple University

12. Hoffman, Nicholas. Mitochondrial Calcium Influx is Determined by Multiple Protein Components Including SLC25A23 and MICU1.

Degree: PhD, 2014, Temple University

Biochemistry

Ca2+ control mechanisms employed by the cell at the plasma membrane include receptor operated, voltage-sensitive, and store operated channels for Ca2+ import. Upon entry… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Hoffman, N. (2014). Mitochondrial Calcium Influx is Determined by Multiple Protein Components Including SLC25A23 and MICU1. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,287159

Chicago Manual of Style (16th Edition):

Hoffman, Nicholas. “Mitochondrial Calcium Influx is Determined by Multiple Protein Components Including SLC25A23 and MICU1.” 2014. Doctoral Dissertation, Temple University. Accessed July 16, 2018. http://digital.library.temple.edu/u?/p245801coll10,287159.

MLA Handbook (7th Edition):

Hoffman, Nicholas. “Mitochondrial Calcium Influx is Determined by Multiple Protein Components Including SLC25A23 and MICU1.” 2014. Web. 16 Jul 2018.

Vancouver:

Hoffman N. Mitochondrial Calcium Influx is Determined by Multiple Protein Components Including SLC25A23 and MICU1. [Internet] [Doctoral dissertation]. Temple University; 2014. [cited 2018 Jul 16]. Available from: http://digital.library.temple.edu/u?/p245801coll10,287159.

Council of Science Editors:

Hoffman N. Mitochondrial Calcium Influx is Determined by Multiple Protein Components Including SLC25A23 and MICU1. [Doctoral Dissertation]. Temple University; 2014. Available from: http://digital.library.temple.edu/u?/p245801coll10,287159


Temple University

13. Wang, Xizhuo. STIM Protein Coupling Domains and The Activation of Orai Channels.

Degree: PhD, 2015, Temple University

Biochemistry

STIM1 and STIM2 are widely expressed endoplasmic reticulum (ER) Ca2+ sensor proteins able to translocate within the ER membrane to physically couple with and… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Wang, X. (2015). STIM Protein Coupling Domains and The Activation of Orai Channels. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,366037

Chicago Manual of Style (16th Edition):

Wang, Xizhuo. “STIM Protein Coupling Domains and The Activation of Orai Channels.” 2015. Doctoral Dissertation, Temple University. Accessed July 16, 2018. http://digital.library.temple.edu/u?/p245801coll10,366037.

MLA Handbook (7th Edition):

Wang, Xizhuo. “STIM Protein Coupling Domains and The Activation of Orai Channels.” 2015. Web. 16 Jul 2018.

Vancouver:

Wang X. STIM Protein Coupling Domains and The Activation of Orai Channels. [Internet] [Doctoral dissertation]. Temple University; 2015. [cited 2018 Jul 16]. Available from: http://digital.library.temple.edu/u?/p245801coll10,366037.

Council of Science Editors:

Wang X. STIM Protein Coupling Domains and The Activation of Orai Channels. [Doctoral Dissertation]. Temple University; 2015. Available from: http://digital.library.temple.edu/u?/p245801coll10,366037


Cleveland State University

14. Turner, Katherine Ann. Therapeutic Potential of rhTRAIL for Malignant Melanoma.

Degree: PhD, College of Sciences and Health Professions, 2017, Cleveland State University

 The application of recombinant human Tumor Necrosis Factor-Related Apoptosis-Inducing Ligand (rhTRAIL) for the treatment of cancer holds great promise due to its ability to selectively… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Turner, K. A. (2017). Therapeutic Potential of rhTRAIL for Malignant Melanoma. (Doctoral Dissertation). Cleveland State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=csu1493983803123051

Chicago Manual of Style (16th Edition):

Turner, Katherine Ann. “Therapeutic Potential of rhTRAIL for Malignant Melanoma.” 2017. Doctoral Dissertation, Cleveland State University. Accessed July 16, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=csu1493983803123051.

MLA Handbook (7th Edition):

Turner, Katherine Ann. “Therapeutic Potential of rhTRAIL for Malignant Melanoma.” 2017. Web. 16 Jul 2018.

Vancouver:

Turner KA. Therapeutic Potential of rhTRAIL for Malignant Melanoma. [Internet] [Doctoral dissertation]. Cleveland State University; 2017. [cited 2018 Jul 16]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=csu1493983803123051.

Council of Science Editors:

Turner KA. Therapeutic Potential of rhTRAIL for Malignant Melanoma. [Doctoral Dissertation]. Cleveland State University; 2017. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=csu1493983803123051


Arizona State University

15. Bowen, Sara. Insights into the Role of the Metal-Binding Sites of Quercetin 2,3-Dioxygenase from Bacillus subtilis.

Degree: PhD, Biochemistry, 2010, Arizona State University

 The metalloenzyme quercetin 2,3-dioxygenase (QueD) catalyzes the oxidative decomposition of the aromatic compound, quercetin. The most recently characterized example is a product of the bacterium… (more)

Subjects/Keywords: Biochemistry

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

APA (6th Edition):

Bowen, S. (2010). Insights into the Role of the Metal-Binding Sites of Quercetin 2,3-Dioxygenase from Bacillus subtilis. (Doctoral Dissertation). Arizona State University. Retrieved from http://repository.asu.edu/items/8650

Chicago Manual of Style (16th Edition):

Bowen, Sara. “Insights into the Role of the Metal-Binding Sites of Quercetin 2,3-Dioxygenase from Bacillus subtilis.” 2010. Doctoral Dissertation, Arizona State University. Accessed July 16, 2018. http://repository.asu.edu/items/8650.

MLA Handbook (7th Edition):

Bowen, Sara. “Insights into the Role of the Metal-Binding Sites of Quercetin 2,3-Dioxygenase from Bacillus subtilis.” 2010. Web. 16 Jul 2018.

Vancouver:

Bowen S. Insights into the Role of the Metal-Binding Sites of Quercetin 2,3-Dioxygenase from Bacillus subtilis. [Internet] [Doctoral dissertation]. Arizona State University; 2010. [cited 2018 Jul 16]. Available from: http://repository.asu.edu/items/8650.

Council of Science Editors:

Bowen S. Insights into the Role of the Metal-Binding Sites of Quercetin 2,3-Dioxygenase from Bacillus subtilis. [Doctoral Dissertation]. Arizona State University; 2010. Available from: http://repository.asu.edu/items/8650


Purdue University

16. Krisenko, Mariya. Role of Syk in the regulation of cytoskeleton and stress granules in breast cancer.

Degree: PhD, Microbiology, Molecular Biology and Biochemistry, 2015, Purdue University

  The Syk protein-tyrosine kinase, a well-characterized modulator of immune recognition receptor signaling, also plays important, but poorly characterized, roles in tumor progression, acting as… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Krisenko, M. (2015). Role of Syk in the regulation of cytoskeleton and stress granules in breast cancer. (Doctoral Dissertation). Purdue University. Retrieved from http://docs.lib.purdue.edu/open_access_dissertations/492

Chicago Manual of Style (16th Edition):

Krisenko, Mariya. “Role of Syk in the regulation of cytoskeleton and stress granules in breast cancer.” 2015. Doctoral Dissertation, Purdue University. Accessed July 16, 2018. http://docs.lib.purdue.edu/open_access_dissertations/492.

MLA Handbook (7th Edition):

Krisenko, Mariya. “Role of Syk in the regulation of cytoskeleton and stress granules in breast cancer.” 2015. Web. 16 Jul 2018.

Vancouver:

Krisenko M. Role of Syk in the regulation of cytoskeleton and stress granules in breast cancer. [Internet] [Doctoral dissertation]. Purdue University; 2015. [cited 2018 Jul 16]. Available from: http://docs.lib.purdue.edu/open_access_dissertations/492.

Council of Science Editors:

Krisenko M. Role of Syk in the regulation of cytoskeleton and stress granules in breast cancer. [Doctoral Dissertation]. Purdue University; 2015. Available from: http://docs.lib.purdue.edu/open_access_dissertations/492


Purdue University

17. Nasir, Amjad M. Developmentally regulated SUMOylation in the ciliate Tetrahymena thermophila.

Degree: PhD, Biochemistry, 2015, Purdue University

  The Small Ubiquitin-like MOdifier (SUMO) protein regulates numerous nuclear events such as transcription, mitosis and meiosis and DNA repair. These processes are critical to… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Nasir, A. M. (2015). Developmentally regulated SUMOylation in the ciliate Tetrahymena thermophila. (Doctoral Dissertation). Purdue University. Retrieved from http://docs.lib.purdue.edu/open_access_dissertations/524

Chicago Manual of Style (16th Edition):

Nasir, Amjad M. “Developmentally regulated SUMOylation in the ciliate Tetrahymena thermophila.” 2015. Doctoral Dissertation, Purdue University. Accessed July 16, 2018. http://docs.lib.purdue.edu/open_access_dissertations/524.

MLA Handbook (7th Edition):

Nasir, Amjad M. “Developmentally regulated SUMOylation in the ciliate Tetrahymena thermophila.” 2015. Web. 16 Jul 2018.

Vancouver:

Nasir AM. Developmentally regulated SUMOylation in the ciliate Tetrahymena thermophila. [Internet] [Doctoral dissertation]. Purdue University; 2015. [cited 2018 Jul 16]. Available from: http://docs.lib.purdue.edu/open_access_dissertations/524.

Council of Science Editors:

Nasir AM. Developmentally regulated SUMOylation in the ciliate Tetrahymena thermophila. [Doctoral Dissertation]. Purdue University; 2015. Available from: http://docs.lib.purdue.edu/open_access_dissertations/524


Purdue University

18. Yi, Li. Paralogous genes in Arabidopsis thaliana contribute to diversified phenylpropanoid metabolism.

Degree: PhD, Physics, 2015, Purdue University

  Significant evidence supports the idea that gene duplication drives the evolution of new gene function. Besides being silenced, duplicated genes can either neofunctionalize or… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Yi, L. (2015). Paralogous genes in Arabidopsis thaliana contribute to diversified phenylpropanoid metabolism. (Doctoral Dissertation). Purdue University. Retrieved from http://docs.lib.purdue.edu/open_access_dissertations/612

Chicago Manual of Style (16th Edition):

Yi, Li. “Paralogous genes in Arabidopsis thaliana contribute to diversified phenylpropanoid metabolism.” 2015. Doctoral Dissertation, Purdue University. Accessed July 16, 2018. http://docs.lib.purdue.edu/open_access_dissertations/612.

MLA Handbook (7th Edition):

Yi, Li. “Paralogous genes in Arabidopsis thaliana contribute to diversified phenylpropanoid metabolism.” 2015. Web. 16 Jul 2018.

Vancouver:

Yi L. Paralogous genes in Arabidopsis thaliana contribute to diversified phenylpropanoid metabolism. [Internet] [Doctoral dissertation]. Purdue University; 2015. [cited 2018 Jul 16]. Available from: http://docs.lib.purdue.edu/open_access_dissertations/612.

Council of Science Editors:

Yi L. Paralogous genes in Arabidopsis thaliana contribute to diversified phenylpropanoid metabolism. [Doctoral Dissertation]. Purdue University; 2015. Available from: http://docs.lib.purdue.edu/open_access_dissertations/612


Purdue University

19. Chuong, Aurelie. Support Needs of Young Ovarian Cancer Survivors: A Pilot Study.

Degree: MPH, Health and Kinesiology, 2015, Purdue University

  Purpose. Young ovarian cancer survivor (18 years old or older but diagnosed before the age of 34 years old) support needs (i.e., physical and… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Chuong, A. (2015). Support Needs of Young Ovarian Cancer Survivors: A Pilot Study. (Thesis). Purdue University. Retrieved from http://docs.lib.purdue.edu/open_access_theses/541

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):

Chuong, Aurelie. “Support Needs of Young Ovarian Cancer Survivors: A Pilot Study.” 2015. Thesis, Purdue University. Accessed July 16, 2018. http://docs.lib.purdue.edu/open_access_theses/541.

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

MLA Handbook (7th Edition):

Chuong, Aurelie. “Support Needs of Young Ovarian Cancer Survivors: A Pilot Study.” 2015. Web. 16 Jul 2018.

Vancouver:

Chuong A. Support Needs of Young Ovarian Cancer Survivors: A Pilot Study. [Internet] [Thesis]. Purdue University; 2015. [cited 2018 Jul 16]. Available from: http://docs.lib.purdue.edu/open_access_theses/541.

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

Council of Science Editors:

Chuong A. Support Needs of Young Ovarian Cancer Survivors: A Pilot Study. [Thesis]. Purdue University; 2015. Available from: http://docs.lib.purdue.edu/open_access_theses/541

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


Purdue University

20. Bueno, Amy N. An active site loop mutant of a zinc metallo-deubiquitinase suggests the importance of loop dynamics to catalysis.

Degree: MS, Chemistry, 2015, Purdue University

  AMSH is a conserved zinc metalloprotease that functions with endosomal sorting complexes required for transport (ESCRT) machinery in order to down regulate and degrade… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Bueno, A. N. (2015). An active site loop mutant of a zinc metallo-deubiquitinase suggests the importance of loop dynamics to catalysis. (Thesis). Purdue University. Retrieved from http://docs.lib.purdue.edu/open_access_theses/549

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):

Bueno, Amy N. “An active site loop mutant of a zinc metallo-deubiquitinase suggests the importance of loop dynamics to catalysis.” 2015. Thesis, Purdue University. Accessed July 16, 2018. http://docs.lib.purdue.edu/open_access_theses/549.

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

MLA Handbook (7th Edition):

Bueno, Amy N. “An active site loop mutant of a zinc metallo-deubiquitinase suggests the importance of loop dynamics to catalysis.” 2015. Web. 16 Jul 2018.

Vancouver:

Bueno AN. An active site loop mutant of a zinc metallo-deubiquitinase suggests the importance of loop dynamics to catalysis. [Internet] [Thesis]. Purdue University; 2015. [cited 2018 Jul 16]. Available from: http://docs.lib.purdue.edu/open_access_theses/549.

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

Council of Science Editors:

Bueno AN. An active site loop mutant of a zinc metallo-deubiquitinase suggests the importance of loop dynamics to catalysis. [Thesis]. Purdue University; 2015. Available from: http://docs.lib.purdue.edu/open_access_theses/549

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


Arizona State University

21. Seng, Chenda Ouk. Studies on the Three-dimensional Structures of Proteins Using X-ray Crystallography.

Degree: PhD, Biochemistry, 2013, Arizona State University

 X-ray diffraction is the technique of choice to determine the three-dimensional structures of proteins. In this study it has been applied to solve the structure… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Seng, C. O. (2013). Studies on the Three-dimensional Structures of Proteins Using X-ray Crystallography. (Doctoral Dissertation). Arizona State University. Retrieved from http://repository.asu.edu/items/20934

Chicago Manual of Style (16th Edition):

Seng, Chenda Ouk. “Studies on the Three-dimensional Structures of Proteins Using X-ray Crystallography.” 2013. Doctoral Dissertation, Arizona State University. Accessed July 16, 2018. http://repository.asu.edu/items/20934.

MLA Handbook (7th Edition):

Seng, Chenda Ouk. “Studies on the Three-dimensional Structures of Proteins Using X-ray Crystallography.” 2013. Web. 16 Jul 2018.

Vancouver:

Seng CO. Studies on the Three-dimensional Structures of Proteins Using X-ray Crystallography. [Internet] [Doctoral dissertation]. Arizona State University; 2013. [cited 2018 Jul 16]. Available from: http://repository.asu.edu/items/20934.

Council of Science Editors:

Seng CO. Studies on the Three-dimensional Structures of Proteins Using X-ray Crystallography. [Doctoral Dissertation]. Arizona State University; 2013. Available from: http://repository.asu.edu/items/20934


Arizona State University

22. Segerman, Zachary Jay. Study of Site Specific Cleavage of Strongly Bound Hairpin DNAs by Bleomycin.

Degree: MS, Biochemistry, 2011, Arizona State University

 Natural products that target the DNA of cancer cells have been an important source of knowledge and understanding in the development of anticancer chemotherapeutic agents.… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Segerman, Z. J. (2011). Study of Site Specific Cleavage of Strongly Bound Hairpin DNAs by Bleomycin. (Masters Thesis). Arizona State University. Retrieved from http://repository.asu.edu/items/14241

Chicago Manual of Style (16th Edition):

Segerman, Zachary Jay. “Study of Site Specific Cleavage of Strongly Bound Hairpin DNAs by Bleomycin.” 2011. Masters Thesis, Arizona State University. Accessed July 16, 2018. http://repository.asu.edu/items/14241.

MLA Handbook (7th Edition):

Segerman, Zachary Jay. “Study of Site Specific Cleavage of Strongly Bound Hairpin DNAs by Bleomycin.” 2011. Web. 16 Jul 2018.

Vancouver:

Segerman ZJ. Study of Site Specific Cleavage of Strongly Bound Hairpin DNAs by Bleomycin. [Internet] [Masters thesis]. Arizona State University; 2011. [cited 2018 Jul 16]. Available from: http://repository.asu.edu/items/14241.

Council of Science Editors:

Segerman ZJ. Study of Site Specific Cleavage of Strongly Bound Hairpin DNAs by Bleomycin. [Masters Thesis]. Arizona State University; 2011. Available from: http://repository.asu.edu/items/14241


Arizona State University

23. Raghav, Nidhi. Structure Activity Studies of Quinones and Analogues.

Degree: MS, Biochemistry, 2011, Arizona State University

 Many natural and synthetic quinones have shown biological and pharmacological activity. Some of them have also shown anticancer activity. Ubiquinone (CoQ10) which is a natural… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Raghav, N. (2011). Structure Activity Studies of Quinones and Analogues. (Masters Thesis). Arizona State University. Retrieved from http://repository.asu.edu/items/8928

Chicago Manual of Style (16th Edition):

Raghav, Nidhi. “Structure Activity Studies of Quinones and Analogues.” 2011. Masters Thesis, Arizona State University. Accessed July 16, 2018. http://repository.asu.edu/items/8928.

MLA Handbook (7th Edition):

Raghav, Nidhi. “Structure Activity Studies of Quinones and Analogues.” 2011. Web. 16 Jul 2018.

Vancouver:

Raghav N. Structure Activity Studies of Quinones and Analogues. [Internet] [Masters thesis]. Arizona State University; 2011. [cited 2018 Jul 16]. Available from: http://repository.asu.edu/items/8928.

Council of Science Editors:

Raghav N. Structure Activity Studies of Quinones and Analogues. [Masters Thesis]. Arizona State University; 2011. Available from: http://repository.asu.edu/items/8928


University of Kansas

24. Deng, Bin. Structural basis of inter-domain electron transfer in Ncb5or, a redox enzyme implicated in diabetes and lipid metabolism.

Degree: PhD, Physical Therapy & Rehabilitation Sciences, 2011, University of Kansas

 NADH cytochrome b5 oxidoreductase (Ncb5or) is a multi-domain redox enzyme found in all animal tissues and associated with the endoplasmic reticulum (ER). Ncb5or contains (from… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Deng, B. (2011). Structural basis of inter-domain electron transfer in Ncb5or, a redox enzyme implicated in diabetes and lipid metabolism. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/9724

Chicago Manual of Style (16th Edition):

Deng, Bin. “Structural basis of inter-domain electron transfer in Ncb5or, a redox enzyme implicated in diabetes and lipid metabolism.” 2011. Doctoral Dissertation, University of Kansas. Accessed July 16, 2018. http://hdl.handle.net/1808/9724.

MLA Handbook (7th Edition):

Deng, Bin. “Structural basis of inter-domain electron transfer in Ncb5or, a redox enzyme implicated in diabetes and lipid metabolism.” 2011. Web. 16 Jul 2018.

Vancouver:

Deng B. Structural basis of inter-domain electron transfer in Ncb5or, a redox enzyme implicated in diabetes and lipid metabolism. [Internet] [Doctoral dissertation]. University of Kansas; 2011. [cited 2018 Jul 16]. Available from: http://hdl.handle.net/1808/9724.

Council of Science Editors:

Deng B. Structural basis of inter-domain electron transfer in Ncb5or, a redox enzyme implicated in diabetes and lipid metabolism. [Doctoral Dissertation]. University of Kansas; 2011. Available from: http://hdl.handle.net/1808/9724


University of Kansas

25. Petrunak, Elyse Marie. Structural and Functional Evaluation of Steroidogenic Cytochrome P450 Enzymes.

Degree: PhD, Medicinal Chemistry, 2015, University of Kansas

 Cytochromes P450 (CYP450) are heme-containing monooxygenase enzymes that perform a variety of functions in humans, including xenobiotic metabolism and the production of endogenous signaling molecules.… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Petrunak, E. M. (2015). Structural and Functional Evaluation of Steroidogenic Cytochrome P450 Enzymes. (Doctoral Dissertation). University of Kansas. Retrieved from http://hdl.handle.net/1808/23924

Chicago Manual of Style (16th Edition):

Petrunak, Elyse Marie. “Structural and Functional Evaluation of Steroidogenic Cytochrome P450 Enzymes.” 2015. Doctoral Dissertation, University of Kansas. Accessed July 16, 2018. http://hdl.handle.net/1808/23924.

MLA Handbook (7th Edition):

Petrunak, Elyse Marie. “Structural and Functional Evaluation of Steroidogenic Cytochrome P450 Enzymes.” 2015. Web. 16 Jul 2018.

Vancouver:

Petrunak EM. Structural and Functional Evaluation of Steroidogenic Cytochrome P450 Enzymes. [Internet] [Doctoral dissertation]. University of Kansas; 2015. [cited 2018 Jul 16]. Available from: http://hdl.handle.net/1808/23924.

Council of Science Editors:

Petrunak EM. Structural and Functional Evaluation of Steroidogenic Cytochrome P450 Enzymes. [Doctoral Dissertation]. University of Kansas; 2015. Available from: http://hdl.handle.net/1808/23924


The Ohio State University

26. Zhong, Qi. Hyperphosphorylation and Mutation Enhance Tau Aggregation.

Degree: PhD, Neuroscience, 2008, The Ohio State University

  Tauopathies refer to a diverse set of sporadic and familial neurodegenerative disorders including Alzheimer’s disease (AD), and frontotemporal dementia with Parkinsonism linked to chromosome… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Zhong, Q. (2008). Hyperphosphorylation and Mutation Enhance Tau Aggregation. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1228235966

Chicago Manual of Style (16th Edition):

Zhong, Qi. “Hyperphosphorylation and Mutation Enhance Tau Aggregation.” 2008. Doctoral Dissertation, The Ohio State University. Accessed July 16, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=osu1228235966.

MLA Handbook (7th Edition):

Zhong, Qi. “Hyperphosphorylation and Mutation Enhance Tau Aggregation.” 2008. Web. 16 Jul 2018.

Vancouver:

Zhong Q. Hyperphosphorylation and Mutation Enhance Tau Aggregation. [Internet] [Doctoral dissertation]. The Ohio State University; 2008. [cited 2018 Jul 16]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1228235966.

Council of Science Editors:

Zhong Q. Hyperphosphorylation and Mutation Enhance Tau Aggregation. [Doctoral Dissertation]. The Ohio State University; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1228235966


The Ohio State University

27. Glasgow, Shane L., Mr. Determination of the Sequence Specificity of SH2-B1ß and SH2-B3 SH2 Domains by a Combinatorial Library Approach.

Degree: MS, Biochemistry, 2010, The Ohio State University

  Src homology (SH2) domains promote the formation of protein complexes through their interaction with specific phosphotyrosine (pY)-containing motifs in their binding partners, thus playing… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Glasgow, Shane L., M. (2010). Determination of the Sequence Specificity of SH2-B1ß and SH2-B3 SH2 Domains by a Combinatorial Library Approach. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1282240642

Chicago Manual of Style (16th Edition):

Glasgow, Shane L., Mr. “Determination of the Sequence Specificity of SH2-B1ß and SH2-B3 SH2 Domains by a Combinatorial Library Approach.” 2010. Masters Thesis, The Ohio State University. Accessed July 16, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=osu1282240642.

MLA Handbook (7th Edition):

Glasgow, Shane L., Mr. “Determination of the Sequence Specificity of SH2-B1ß and SH2-B3 SH2 Domains by a Combinatorial Library Approach.” 2010. Web. 16 Jul 2018.

Vancouver:

Glasgow, Shane L. M. Determination of the Sequence Specificity of SH2-B1ß and SH2-B3 SH2 Domains by a Combinatorial Library Approach. [Internet] [Masters thesis]. The Ohio State University; 2010. [cited 2018 Jul 16]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1282240642.

Council of Science Editors:

Glasgow, Shane L. M. Determination of the Sequence Specificity of SH2-B1ß and SH2-B3 SH2 Domains by a Combinatorial Library Approach. [Masters Thesis]. The Ohio State University; 2010. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1282240642


The Ohio State University

28. Guo, Yi. Study of the Structure and Function Relationship of Oncoprotein Gankyrin.

Degree: PhD, Ohio State Biochemistry Program, 2009, The Ohio State University

  Gankyrin, a newly defined oncoprotein also known as PSMD10 and P28, functions as a dual-negative regulator of the two most prominent tumor suppressor pathways:… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Guo, Y. (2009). Study of the Structure and Function Relationship of Oncoprotein Gankyrin. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1249579598

Chicago Manual of Style (16th Edition):

Guo, Yi. “Study of the Structure and Function Relationship of Oncoprotein Gankyrin.” 2009. Doctoral Dissertation, The Ohio State University. Accessed July 16, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=osu1249579598.

MLA Handbook (7th Edition):

Guo, Yi. “Study of the Structure and Function Relationship of Oncoprotein Gankyrin.” 2009. Web. 16 Jul 2018.

Vancouver:

Guo Y. Study of the Structure and Function Relationship of Oncoprotein Gankyrin. [Internet] [Doctoral dissertation]. The Ohio State University; 2009. [cited 2018 Jul 16]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1249579598.

Council of Science Editors:

Guo Y. Study of the Structure and Function Relationship of Oncoprotein Gankyrin. [Doctoral Dissertation]. The Ohio State University; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1249579598


The Ohio State University

29. Fowler, Jason David. Investigation of Noncanonical DNA Polymerases and Their Mechanisms.

Degree: PhD, Ohio State Biochemistry Program, 2009, The Ohio State University

  DNA polymerases have evolved complex biological functions to balance the need for faithful DNA replication with the need for subtle genetic flexibility in the… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Fowler, J. D. (2009). Investigation of Noncanonical DNA Polymerases and Their Mechanisms. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1250701062

Chicago Manual of Style (16th Edition):

Fowler, Jason David. “Investigation of Noncanonical DNA Polymerases and Their Mechanisms.” 2009. Doctoral Dissertation, The Ohio State University. Accessed July 16, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=osu1250701062.

MLA Handbook (7th Edition):

Fowler, Jason David. “Investigation of Noncanonical DNA Polymerases and Their Mechanisms.” 2009. Web. 16 Jul 2018.

Vancouver:

Fowler JD. Investigation of Noncanonical DNA Polymerases and Their Mechanisms. [Internet] [Doctoral dissertation]. The Ohio State University; 2009. [cited 2018 Jul 16]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1250701062.

Council of Science Editors:

Fowler JD. Investigation of Noncanonical DNA Polymerases and Their Mechanisms. [Doctoral Dissertation]. The Ohio State University; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1250701062


University of Toledo

30. Zeringo, Nicholas A. Biochemical and Structural Studies of the Circadian Enzymes CLOCK and Casein Kinase 1, and Indolotryptoline Biosynthetic Enzymes.

Degree: PhD, College of Natural Sciences and Mathematics, 2014, University of Toledo

 Circadian rhythms are cyclic changes in physiology and biochemistry with a ~24 hour period. On the cellular level circadian rhythms result in rhythmic gene expression… (more)

Subjects/Keywords: Biochemistry

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APA (6th Edition):

Zeringo, N. A. (2014). Biochemical and Structural Studies of the Circadian Enzymes CLOCK and Casein Kinase 1, and Indolotryptoline Biosynthetic Enzymes. (Doctoral Dissertation). University of Toledo. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=toledo1404132328

Chicago Manual of Style (16th Edition):

Zeringo, Nicholas A. “Biochemical and Structural Studies of the Circadian Enzymes CLOCK and Casein Kinase 1, and Indolotryptoline Biosynthetic Enzymes.” 2014. Doctoral Dissertation, University of Toledo. Accessed July 16, 2018. http://rave.ohiolink.edu/etdc/view?acc_num=toledo1404132328.

MLA Handbook (7th Edition):

Zeringo, Nicholas A. “Biochemical and Structural Studies of the Circadian Enzymes CLOCK and Casein Kinase 1, and Indolotryptoline Biosynthetic Enzymes.” 2014. Web. 16 Jul 2018.

Vancouver:

Zeringo NA. Biochemical and Structural Studies of the Circadian Enzymes CLOCK and Casein Kinase 1, and Indolotryptoline Biosynthetic Enzymes. [Internet] [Doctoral dissertation]. University of Toledo; 2014. [cited 2018 Jul 16]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1404132328.

Council of Science Editors:

Zeringo NA. Biochemical and Structural Studies of the Circadian Enzymes CLOCK and Casein Kinase 1, and Indolotryptoline Biosynthetic Enzymes. [Doctoral Dissertation]. University of Toledo; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=toledo1404132328

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