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You searched for subject:(S Adenosylmethionine). Showing records 1 – 30 of 32 total matches.

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Case Western Reserve University

1. Peng, Yi. Structural Studies of the S-Adenosylmethionine-Dependent Methyltransferases.

Degree: PhD, Biochemistry, 2009, Case Western Reserve University

S-adenosylmethionine-dependent methyltransferases (AdoMet-dependent MTases) are a main subfamily of MTases, which play critical roles in diverse methylation reactions in many significant biological processes. AdoMet-dependent… (more)

Subjects/Keywords: Biochemistry; S-adenosylmethionine-dependent methyltransferase

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

APA (6th Edition):

Peng, Y. (2009). Structural Studies of the S-Adenosylmethionine-Dependent Methyltransferases. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1228316254

Chicago Manual of Style (16th Edition):

Peng, Yi. “Structural Studies of the S-Adenosylmethionine-Dependent Methyltransferases.” 2009. Doctoral Dissertation, Case Western Reserve University. Accessed September 19, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=case1228316254.

MLA Handbook (7th Edition):

Peng, Yi. “Structural Studies of the S-Adenosylmethionine-Dependent Methyltransferases.” 2009. Web. 19 Sep 2020.

Vancouver:

Peng Y. Structural Studies of the S-Adenosylmethionine-Dependent Methyltransferases. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2009. [cited 2020 Sep 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1228316254.

Council of Science Editors:

Peng Y. Structural Studies of the S-Adenosylmethionine-Dependent Methyltransferases. [Doctoral Dissertation]. Case Western Reserve University; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1228316254


University of Texas Southwestern Medical Center

2. Capota, Emanela. The Role of S-Adenosylmethionine Synthetase in Killing Effects of DFMO in African Trypanosomes.

Degree: 2013, University of Texas Southwestern Medical Center

 T. brucei parasites cause a fatal disease that affects hundreds of thousands of people in sub-Saharan Africa. Since current treatment options show either poor efficacy… (more)

Subjects/Keywords: S-Adenosylmethionine; Trypanosomiasis; Eflornithine

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APA (6th Edition):

Capota, E. (2013). The Role of S-Adenosylmethionine Synthetase in Killing Effects of DFMO in African Trypanosomes. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/1244

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):

Capota, Emanela. “The Role of S-Adenosylmethionine Synthetase in Killing Effects of DFMO in African Trypanosomes.” 2013. Thesis, University of Texas Southwestern Medical Center. Accessed September 19, 2020. http://hdl.handle.net/2152.5/1244.

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

MLA Handbook (7th Edition):

Capota, Emanela. “The Role of S-Adenosylmethionine Synthetase in Killing Effects of DFMO in African Trypanosomes.” 2013. Web. 19 Sep 2020.

Vancouver:

Capota E. The Role of S-Adenosylmethionine Synthetase in Killing Effects of DFMO in African Trypanosomes. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2013. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/2152.5/1244.

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

Council of Science Editors:

Capota E. The Role of S-Adenosylmethionine Synthetase in Killing Effects of DFMO in African Trypanosomes. [Thesis]. University of Texas Southwestern Medical Center; 2013. Available from: http://hdl.handle.net/2152.5/1244

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


Boise State University

3. Stonick, Jason Alan. Examination of Klebsiella pneumoniae 5'-Methylthioadenosine/S-Adenosylhomocysteine Nucleosidase and 5-Methylthioribose Kinase.

Degree: 2016, Boise State University

 Klebsiella pneumoniae is an opportunistic bacterial pathogen that is emerging as a major global threat as an infectious agent. This organism, along with many other… (more)

Subjects/Keywords: klebsiella pneumoniae; s-adenosylmethionine; antibiotic; nucleosidase; Biochemistry

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APA (6th Edition):

Stonick, J. A. (2016). Examination of Klebsiella pneumoniae 5'-Methylthioadenosine/S-Adenosylhomocysteine Nucleosidase and 5-Methylthioribose Kinase. (Thesis). Boise State University. Retrieved from https://scholarworks.boisestate.edu/td/1111

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):

Stonick, Jason Alan. “Examination of Klebsiella pneumoniae 5'-Methylthioadenosine/S-Adenosylhomocysteine Nucleosidase and 5-Methylthioribose Kinase.” 2016. Thesis, Boise State University. Accessed September 19, 2020. https://scholarworks.boisestate.edu/td/1111.

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

MLA Handbook (7th Edition):

Stonick, Jason Alan. “Examination of Klebsiella pneumoniae 5'-Methylthioadenosine/S-Adenosylhomocysteine Nucleosidase and 5-Methylthioribose Kinase.” 2016. Web. 19 Sep 2020.

Vancouver:

Stonick JA. Examination of Klebsiella pneumoniae 5'-Methylthioadenosine/S-Adenosylhomocysteine Nucleosidase and 5-Methylthioribose Kinase. [Internet] [Thesis]. Boise State University; 2016. [cited 2020 Sep 19]. Available from: https://scholarworks.boisestate.edu/td/1111.

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

Council of Science Editors:

Stonick JA. Examination of Klebsiella pneumoniae 5'-Methylthioadenosine/S-Adenosylhomocysteine Nucleosidase and 5-Methylthioribose Kinase. [Thesis]. Boise State University; 2016. Available from: https://scholarworks.boisestate.edu/td/1111

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


University of Louisville

4. Mathews, Stephanie A. Role of HDACs and SAM in interferon-alpha signaling and epigenetic regulation of anti-HCV gene expression.

Degree: PhD, 2011, University of Louisville

 Hepatitis C virus (HCV) infection is a major cause of chronic liver disease in the United States and is a huge burden on the US… (more)

Subjects/Keywords: Interferon-alpha; Hepatitis C; S-adenosylmethionine; Epigenetics

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APA (6th Edition):

Mathews, S. A. (2011). Role of HDACs and SAM in interferon-alpha signaling and epigenetic regulation of anti-HCV gene expression. (Doctoral Dissertation). University of Louisville. Retrieved from 10.18297/etd/919 ; https://ir.library.louisville.edu/etd/919

Chicago Manual of Style (16th Edition):

Mathews, Stephanie A. “Role of HDACs and SAM in interferon-alpha signaling and epigenetic regulation of anti-HCV gene expression.” 2011. Doctoral Dissertation, University of Louisville. Accessed September 19, 2020. 10.18297/etd/919 ; https://ir.library.louisville.edu/etd/919.

MLA Handbook (7th Edition):

Mathews, Stephanie A. “Role of HDACs and SAM in interferon-alpha signaling and epigenetic regulation of anti-HCV gene expression.” 2011. Web. 19 Sep 2020.

Vancouver:

Mathews SA. Role of HDACs and SAM in interferon-alpha signaling and epigenetic regulation of anti-HCV gene expression. [Internet] [Doctoral dissertation]. University of Louisville; 2011. [cited 2020 Sep 19]. Available from: 10.18297/etd/919 ; https://ir.library.louisville.edu/etd/919.

Council of Science Editors:

Mathews SA. Role of HDACs and SAM in interferon-alpha signaling and epigenetic regulation of anti-HCV gene expression. [Doctoral Dissertation]. University of Louisville; 2011. Available from: 10.18297/etd/919 ; https://ir.library.louisville.edu/etd/919


The Ohio State University

5. Allen, George M. Identification of Factors Involved in the Regulation of the <i>Bacillus subtilis metK</i> Gene.

Degree: MS, Microbiology, 2016, The Ohio State University

 Riboswitches are cis-acting regulatory elements that respond to a variety of signals. The S box (SAM-I) riboswitches are <i>S</i>-adenosylmethionine (SAM)-responsive RNA regulatory elements located at… (more)

Subjects/Keywords: Microbiology; Riboswitch; S-adenosylmethionine; regulated mRNA stability; S box riboswitch

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APA (6th Edition):

Allen, G. M. (2016). Identification of Factors Involved in the Regulation of the <i>Bacillus subtilis metK</i> Gene. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1480616278645374

Chicago Manual of Style (16th Edition):

Allen, George M. “Identification of Factors Involved in the Regulation of the <i>Bacillus subtilis metK</i> Gene.” 2016. Masters Thesis, The Ohio State University. Accessed September 19, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1480616278645374.

MLA Handbook (7th Edition):

Allen, George M. “Identification of Factors Involved in the Regulation of the <i>Bacillus subtilis metK</i> Gene.” 2016. Web. 19 Sep 2020.

Vancouver:

Allen GM. Identification of Factors Involved in the Regulation of the <i>Bacillus subtilis metK</i> Gene. [Internet] [Masters thesis]. The Ohio State University; 2016. [cited 2020 Sep 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1480616278645374.

Council of Science Editors:

Allen GM. Identification of Factors Involved in the Regulation of the <i>Bacillus subtilis metK</i> Gene. [Masters Thesis]. The Ohio State University; 2016. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1480616278645374


University of California – Irvine

6. Borrego, Stacey L. Methionine Metabolism and Cell Cycle Control.

Degree: Biomedical Sciences, 2016, University of California – Irvine

 The majority of cancer cells have a unique metabolic addiction to methionine in contrast to normal cells. This “methionine-dependent” phenotype describes the inability of cancer… (more)

Subjects/Keywords: Molecular biology; cancer metabolism; homocysteine; methionine; methionine stress; S-adenosylmethionine; SAM

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APA (6th Edition):

Borrego, S. L. (2016). Methionine Metabolism and Cell Cycle Control. (Thesis). University of California – Irvine. Retrieved from http://www.escholarship.org/uc/item/7f12w8g6

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):

Borrego, Stacey L. “Methionine Metabolism and Cell Cycle Control.” 2016. Thesis, University of California – Irvine. Accessed September 19, 2020. http://www.escholarship.org/uc/item/7f12w8g6.

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

MLA Handbook (7th Edition):

Borrego, Stacey L. “Methionine Metabolism and Cell Cycle Control.” 2016. Web. 19 Sep 2020.

Vancouver:

Borrego SL. Methionine Metabolism and Cell Cycle Control. [Internet] [Thesis]. University of California – Irvine; 2016. [cited 2020 Sep 19]. Available from: http://www.escholarship.org/uc/item/7f12w8g6.

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

Council of Science Editors:

Borrego SL. Methionine Metabolism and Cell Cycle Control. [Thesis]. University of California – Irvine; 2016. Available from: http://www.escholarship.org/uc/item/7f12w8g6

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


Temple University

7. Moncada Benavides, Camilo Andres. EFFECT OF NICOTINE ON LUNG S-ADENOSYLMETHIONINE AND PNEUMOCYSTIS PNEUMONIA DEVELOPMENT.

Degree: PhD, 2012, Temple University

Biochemistry

Infection with "Pneumocystis" causes a ≥ 99% depletion of plasma S-adenosylmethionine (AdoMet) levels in both "Pneumocystis" pneumonia (PcP) animal models and patients. AdoMet is… (more)

Subjects/Keywords: Biochemistry; Laser Capture Microdissection; Lung; Nicotine; Pneumocystis; Polyamines; S-Adenosylmethionine

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APA (6th Edition):

Moncada Benavides, C. A. (2012). EFFECT OF NICOTINE ON LUNG S-ADENOSYLMETHIONINE AND PNEUMOCYSTIS PNEUMONIA DEVELOPMENT. (Doctoral Dissertation). Temple University. Retrieved from http://digital.library.temple.edu/u?/p245801coll10,206623

Chicago Manual of Style (16th Edition):

Moncada Benavides, Camilo Andres. “EFFECT OF NICOTINE ON LUNG S-ADENOSYLMETHIONINE AND PNEUMOCYSTIS PNEUMONIA DEVELOPMENT.” 2012. Doctoral Dissertation, Temple University. Accessed September 19, 2020. http://digital.library.temple.edu/u?/p245801coll10,206623.

MLA Handbook (7th Edition):

Moncada Benavides, Camilo Andres. “EFFECT OF NICOTINE ON LUNG S-ADENOSYLMETHIONINE AND PNEUMOCYSTIS PNEUMONIA DEVELOPMENT.” 2012. Web. 19 Sep 2020.

Vancouver:

Moncada Benavides CA. EFFECT OF NICOTINE ON LUNG S-ADENOSYLMETHIONINE AND PNEUMOCYSTIS PNEUMONIA DEVELOPMENT. [Internet] [Doctoral dissertation]. Temple University; 2012. [cited 2020 Sep 19]. Available from: http://digital.library.temple.edu/u?/p245801coll10,206623.

Council of Science Editors:

Moncada Benavides CA. EFFECT OF NICOTINE ON LUNG S-ADENOSYLMETHIONINE AND PNEUMOCYSTIS PNEUMONIA DEVELOPMENT. [Doctoral Dissertation]. Temple University; 2012. Available from: http://digital.library.temple.edu/u?/p245801coll10,206623


University of Pretoria

8. Smit, Salome. Functional consequences of the inhibition of Malaria S-adenosylmethionine decarboxylase as a key regulator of polyamine and methionine metabolism.

Degree: Biochemistry, 2011, University of Pretoria

 Malaria presents a global health risk that is becoming increasingly difficult to treat due to increased resistance of both the parasite and mosquito to all… (more)

Subjects/Keywords: Methionine metabolism; Malaria; S-adenosylmethionine decarboxylase; Mosquito; Parasite; UCTD

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APA (6th Edition):

Smit, S. (2011). Functional consequences of the inhibition of Malaria S-adenosylmethionine decarboxylase as a key regulator of polyamine and methionine metabolism. (Doctoral Dissertation). University of Pretoria. Retrieved from http://hdl.handle.net/2263/25743

Chicago Manual of Style (16th Edition):

Smit, Salome. “Functional consequences of the inhibition of Malaria S-adenosylmethionine decarboxylase as a key regulator of polyamine and methionine metabolism.” 2011. Doctoral Dissertation, University of Pretoria. Accessed September 19, 2020. http://hdl.handle.net/2263/25743.

MLA Handbook (7th Edition):

Smit, Salome. “Functional consequences of the inhibition of Malaria S-adenosylmethionine decarboxylase as a key regulator of polyamine and methionine metabolism.” 2011. Web. 19 Sep 2020.

Vancouver:

Smit S. Functional consequences of the inhibition of Malaria S-adenosylmethionine decarboxylase as a key regulator of polyamine and methionine metabolism. [Internet] [Doctoral dissertation]. University of Pretoria; 2011. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/2263/25743.

Council of Science Editors:

Smit S. Functional consequences of the inhibition of Malaria S-adenosylmethionine decarboxylase as a key regulator of polyamine and methionine metabolism. [Doctoral Dissertation]. University of Pretoria; 2011. Available from: http://hdl.handle.net/2263/25743


Cornell University

9. Bale, Shridhar. Structural Basis For Putrescine Activation, Substrate Specificity And Inhibitor Design Of Human S-Adenosylmethionine Decarboxylase.

Degree: 2009, Cornell University

 Structure Based Drug Design is an emerging tool employed in industry as well as academia in the design and discovery of therapeutically relevant molecules. The… (more)

Subjects/Keywords: Human S-Adenosylmethionine Decarboxylase

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APA (6th Edition):

Bale, S. (2009). Structural Basis For Putrescine Activation, Substrate Specificity And Inhibitor Design Of Human S-Adenosylmethionine Decarboxylase. (Thesis). Cornell University. Retrieved from http://hdl.handle.net/1813/13514

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):

Bale, Shridhar. “Structural Basis For Putrescine Activation, Substrate Specificity And Inhibitor Design Of Human S-Adenosylmethionine Decarboxylase.” 2009. Thesis, Cornell University. Accessed September 19, 2020. http://hdl.handle.net/1813/13514.

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

MLA Handbook (7th Edition):

Bale, Shridhar. “Structural Basis For Putrescine Activation, Substrate Specificity And Inhibitor Design Of Human S-Adenosylmethionine Decarboxylase.” 2009. Web. 19 Sep 2020.

Vancouver:

Bale S. Structural Basis For Putrescine Activation, Substrate Specificity And Inhibitor Design Of Human S-Adenosylmethionine Decarboxylase. [Internet] [Thesis]. Cornell University; 2009. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/1813/13514.

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

Council of Science Editors:

Bale S. Structural Basis For Putrescine Activation, Substrate Specificity And Inhibitor Design Of Human S-Adenosylmethionine Decarboxylase. [Thesis]. Cornell University; 2009. Available from: http://hdl.handle.net/1813/13514

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


Penn State University

10. Shi, Chenxu. INVESTIGATIONS OF POLYAMINE FUNCTION USING TRANSGENIC MOUSE MODELS WITH SPERMIDINE SYNTHASE AND S-ADENOSYLMETHIONINE DECARBOXYLASE OVEREXPRESSION .

Degree: 2011, Penn State University

 Polyamines, including putrescine, spermidine, and spermine, are ubiquitous polycationic compounds that are essential for cell growth and differentiation. To better understand cellular function of polyamines,… (more)

Subjects/Keywords: Polyamines; S-adenosylmethionine decarboxylase; Spermidine synthase; Transgenic mice; Nonmelanoma skin cancer

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APA (6th Edition):

Shi, C. (2011). INVESTIGATIONS OF POLYAMINE FUNCTION USING TRANSGENIC MOUSE MODELS WITH SPERMIDINE SYNTHASE AND S-ADENOSYLMETHIONINE DECARBOXYLASE OVEREXPRESSION . (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/12128

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):

Shi, Chenxu. “INVESTIGATIONS OF POLYAMINE FUNCTION USING TRANSGENIC MOUSE MODELS WITH SPERMIDINE SYNTHASE AND S-ADENOSYLMETHIONINE DECARBOXYLASE OVEREXPRESSION .” 2011. Thesis, Penn State University. Accessed September 19, 2020. https://submit-etda.libraries.psu.edu/catalog/12128.

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

MLA Handbook (7th Edition):

Shi, Chenxu. “INVESTIGATIONS OF POLYAMINE FUNCTION USING TRANSGENIC MOUSE MODELS WITH SPERMIDINE SYNTHASE AND S-ADENOSYLMETHIONINE DECARBOXYLASE OVEREXPRESSION .” 2011. Web. 19 Sep 2020.

Vancouver:

Shi C. INVESTIGATIONS OF POLYAMINE FUNCTION USING TRANSGENIC MOUSE MODELS WITH SPERMIDINE SYNTHASE AND S-ADENOSYLMETHIONINE DECARBOXYLASE OVEREXPRESSION . [Internet] [Thesis]. Penn State University; 2011. [cited 2020 Sep 19]. Available from: https://submit-etda.libraries.psu.edu/catalog/12128.

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

Council of Science Editors:

Shi C. INVESTIGATIONS OF POLYAMINE FUNCTION USING TRANSGENIC MOUSE MODELS WITH SPERMIDINE SYNTHASE AND S-ADENOSYLMETHIONINE DECARBOXYLASE OVEREXPRESSION . [Thesis]. Penn State University; 2011. Available from: https://submit-etda.libraries.psu.edu/catalog/12128

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


University of Texas Southwestern Medical Center

11. Pendleton, Kathryn Elizabeth. The U6 snRNA m6A Methyltransferase METTL16 Regulates MAT2A Intron Retention Through Co-Transcriptional Splicing.

Degree: 2017, University of Texas Southwestern Medical Center

 Maintenance of proper levels of the methyl donor S-adenosylmethionine (SAM) is critical for a wide variety of biological processes. We demonstrate that the N6-adenosine methyltransferase… (more)

Subjects/Keywords: Introns; Methionine Adenosyltransferase; Methyltransferases; RNA Splicing; S-Adenosylmethionine

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APA (6th Edition):

Pendleton, K. E. (2017). The U6 snRNA m6A Methyltransferase METTL16 Regulates MAT2A Intron Retention Through Co-Transcriptional Splicing. (Thesis). University of Texas Southwestern Medical Center. Retrieved from http://hdl.handle.net/2152.5/7194

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):

Pendleton, Kathryn Elizabeth. “The U6 snRNA m6A Methyltransferase METTL16 Regulates MAT2A Intron Retention Through Co-Transcriptional Splicing.” 2017. Thesis, University of Texas Southwestern Medical Center. Accessed September 19, 2020. http://hdl.handle.net/2152.5/7194.

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

MLA Handbook (7th Edition):

Pendleton, Kathryn Elizabeth. “The U6 snRNA m6A Methyltransferase METTL16 Regulates MAT2A Intron Retention Through Co-Transcriptional Splicing.” 2017. Web. 19 Sep 2020.

Vancouver:

Pendleton KE. The U6 snRNA m6A Methyltransferase METTL16 Regulates MAT2A Intron Retention Through Co-Transcriptional Splicing. [Internet] [Thesis]. University of Texas Southwestern Medical Center; 2017. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/2152.5/7194.

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

Council of Science Editors:

Pendleton KE. The U6 snRNA m6A Methyltransferase METTL16 Regulates MAT2A Intron Retention Through Co-Transcriptional Splicing. [Thesis]. University of Texas Southwestern Medical Center; 2017. Available from: http://hdl.handle.net/2152.5/7194

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


University of Pretoria

12. [No author]. Functional consequences of the inhibition of Malaria S-adenosylmethionine decarboxylase as a key regulator of polyamine and methionine metabolism .

Degree: 2011, University of Pretoria

 Malaria presents a global health risk that is becoming increasingly difficult to treat due to increased resistance of both the parasite and mosquito to all… (more)

Subjects/Keywords: Methionine metabolism; Malaria; S-adenosylmethionine decarboxylase; Mosquito; Parasite; UCTD

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APA (6th Edition):

author], [. (2011). Functional consequences of the inhibition of Malaria S-adenosylmethionine decarboxylase as a key regulator of polyamine and methionine metabolism . (Doctoral Dissertation). University of Pretoria. Retrieved from http://upetd.up.ac.za/thesis/available/etd-06222011-081539/

Chicago Manual of Style (16th Edition):

author], [No. “Functional consequences of the inhibition of Malaria S-adenosylmethionine decarboxylase as a key regulator of polyamine and methionine metabolism .” 2011. Doctoral Dissertation, University of Pretoria. Accessed September 19, 2020. http://upetd.up.ac.za/thesis/available/etd-06222011-081539/.

MLA Handbook (7th Edition):

author], [No. “Functional consequences of the inhibition of Malaria S-adenosylmethionine decarboxylase as a key regulator of polyamine and methionine metabolism .” 2011. Web. 19 Sep 2020.

Vancouver:

author] [. Functional consequences of the inhibition of Malaria S-adenosylmethionine decarboxylase as a key regulator of polyamine and methionine metabolism . [Internet] [Doctoral dissertation]. University of Pretoria; 2011. [cited 2020 Sep 19]. Available from: http://upetd.up.ac.za/thesis/available/etd-06222011-081539/.

Council of Science Editors:

author] [. Functional consequences of the inhibition of Malaria S-adenosylmethionine decarboxylase as a key regulator of polyamine and methionine metabolism . [Doctoral Dissertation]. University of Pretoria; 2011. Available from: http://upetd.up.ac.za/thesis/available/etd-06222011-081539/


University of Pretoria

13. Coertzen, Dina. Structural and functional validation of S-adenosylmethionine decarboxylase as a novel drug target in the malaria parasite, Plasmodium falciparum.

Degree: PhD, Biochemistry, 2014, University of Pretoria

 Malaria is considered the most prevailing human parasitic disease. Despite various chemotherapeutic interventions being available, the parasite responsible for the most lethal form of malaria,… (more)

Subjects/Keywords: UCTD; S-adenosylmethionine decarboxylase; Plasmodium falciparum; Parasite Specific Inserts; Polyamines

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APA (6th Edition):

Coertzen, D. (2014). Structural and functional validation of S-adenosylmethionine decarboxylase as a novel drug target in the malaria parasite, Plasmodium falciparum. (Doctoral Dissertation). University of Pretoria. Retrieved from http://hdl.handle.net/2263/46163

Chicago Manual of Style (16th Edition):

Coertzen, Dina. “Structural and functional validation of S-adenosylmethionine decarboxylase as a novel drug target in the malaria parasite, Plasmodium falciparum.” 2014. Doctoral Dissertation, University of Pretoria. Accessed September 19, 2020. http://hdl.handle.net/2263/46163.

MLA Handbook (7th Edition):

Coertzen, Dina. “Structural and functional validation of S-adenosylmethionine decarboxylase as a novel drug target in the malaria parasite, Plasmodium falciparum.” 2014. Web. 19 Sep 2020.

Vancouver:

Coertzen D. Structural and functional validation of S-adenosylmethionine decarboxylase as a novel drug target in the malaria parasite, Plasmodium falciparum. [Internet] [Doctoral dissertation]. University of Pretoria; 2014. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/2263/46163.

Council of Science Editors:

Coertzen D. Structural and functional validation of S-adenosylmethionine decarboxylase as a novel drug target in the malaria parasite, Plasmodium falciparum. [Doctoral Dissertation]. University of Pretoria; 2014. Available from: http://hdl.handle.net/2263/46163


Penn State University

14. Landgraf, Bradley James. MECHANISTIC STUDIES OF THE METHYLTHIOLATION REACTION CATALYZED BY THE RADICAL SAM ENZYME RIMO.

Degree: 2016, Penn State University

 The S12 protein, a component of the bacterial 30S subunit of the ribosome, contains a universally conserved aspartic acid at position 89 (D89) in Escherichia… (more)

Subjects/Keywords: S-adenosylmethionine; Radical SAM; Methylthiotransferase; Enzymology; 5'-deoxyadenosyl radical; S-adenosylhomocysteine; Post-translational modification

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APA (6th Edition):

Landgraf, B. J. (2016). MECHANISTIC STUDIES OF THE METHYLTHIOLATION REACTION CATALYZED BY THE RADICAL SAM ENZYME RIMO. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/13501bjl230

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):

Landgraf, Bradley James. “MECHANISTIC STUDIES OF THE METHYLTHIOLATION REACTION CATALYZED BY THE RADICAL SAM ENZYME RIMO.” 2016. Thesis, Penn State University. Accessed September 19, 2020. https://submit-etda.libraries.psu.edu/catalog/13501bjl230.

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

MLA Handbook (7th Edition):

Landgraf, Bradley James. “MECHANISTIC STUDIES OF THE METHYLTHIOLATION REACTION CATALYZED BY THE RADICAL SAM ENZYME RIMO.” 2016. Web. 19 Sep 2020.

Vancouver:

Landgraf BJ. MECHANISTIC STUDIES OF THE METHYLTHIOLATION REACTION CATALYZED BY THE RADICAL SAM ENZYME RIMO. [Internet] [Thesis]. Penn State University; 2016. [cited 2020 Sep 19]. Available from: https://submit-etda.libraries.psu.edu/catalog/13501bjl230.

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

Council of Science Editors:

Landgraf BJ. MECHANISTIC STUDIES OF THE METHYLTHIOLATION REACTION CATALYZED BY THE RADICAL SAM ENZYME RIMO. [Thesis]. Penn State University; 2016. Available from: https://submit-etda.libraries.psu.edu/catalog/13501bjl230

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

15. Amaral, Cátia Lira do. Avaliação da metilação do gene TP53 e instabilidade genômica em ratos expostos a metionina e doxorrubicina.

Degree: PhD, Toxicologia, 2010, University of São Paulo

O estado de metilação é suscetível a mudanças quando os organismos são expostos a agentes ambientais tais como componentes dos alimentos e medicamentos. Uma dieta… (more)

Subjects/Keywords: DNA methylation; Gluta; Glutat; Methionine. Doxorubicin; Metilação do DNA; Metionina. Doxorrubicina; S-adenosilhomocisteína; S-adenosilmetionina; S-adenosylhomocysteine; S-adenosylmethionine; TP53; TP53

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APA (6th Edition):

Amaral, C. L. d. (2010). Avaliação da metilação do gene TP53 e instabilidade genômica em ratos expostos a metionina e doxorrubicina. (Doctoral Dissertation). University of São Paulo. Retrieved from http://www.teses.usp.br/teses/disponiveis/60/60134/tde-25042010-134222/ ;

Chicago Manual of Style (16th Edition):

Amaral, Cátia Lira do. “Avaliação da metilação do gene TP53 e instabilidade genômica em ratos expostos a metionina e doxorrubicina.” 2010. Doctoral Dissertation, University of São Paulo. Accessed September 19, 2020. http://www.teses.usp.br/teses/disponiveis/60/60134/tde-25042010-134222/ ;.

MLA Handbook (7th Edition):

Amaral, Cátia Lira do. “Avaliação da metilação do gene TP53 e instabilidade genômica em ratos expostos a metionina e doxorrubicina.” 2010. Web. 19 Sep 2020.

Vancouver:

Amaral CLd. Avaliação da metilação do gene TP53 e instabilidade genômica em ratos expostos a metionina e doxorrubicina. [Internet] [Doctoral dissertation]. University of São Paulo; 2010. [cited 2020 Sep 19]. Available from: http://www.teses.usp.br/teses/disponiveis/60/60134/tde-25042010-134222/ ;.

Council of Science Editors:

Amaral CLd. Avaliação da metilação do gene TP53 e instabilidade genômica em ratos expostos a metionina e doxorrubicina. [Doctoral Dissertation]. University of São Paulo; 2010. Available from: http://www.teses.usp.br/teses/disponiveis/60/60134/tde-25042010-134222/ ;


Penn State University

16. Lanz, Nicholas David. The Role of the Auxiliary Iron-sulfur Cluster of Lipoyl Synthase in the Biosynthesis of the Lipoyl Cofactor.

Degree: 2015, Penn State University

 Lipoic acid is an essential cofactor found in all domains of life. It is a simple cofactor composed of an eight-carbon fatty acid chain with… (more)

Subjects/Keywords: Lipoyl Synthase; Lipoic Acid; Radical SAM; S-Adenosylmethionine; Mössbauer spectroscopy; Iron-sulfur cluster

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APA (6th Edition):

Lanz, N. D. (2015). The Role of the Auxiliary Iron-sulfur Cluster of Lipoyl Synthase in the Biosynthesis of the Lipoyl Cofactor. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/27378

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):

Lanz, Nicholas David. “The Role of the Auxiliary Iron-sulfur Cluster of Lipoyl Synthase in the Biosynthesis of the Lipoyl Cofactor.” 2015. Thesis, Penn State University. Accessed September 19, 2020. https://submit-etda.libraries.psu.edu/catalog/27378.

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

MLA Handbook (7th Edition):

Lanz, Nicholas David. “The Role of the Auxiliary Iron-sulfur Cluster of Lipoyl Synthase in the Biosynthesis of the Lipoyl Cofactor.” 2015. Web. 19 Sep 2020.

Vancouver:

Lanz ND. The Role of the Auxiliary Iron-sulfur Cluster of Lipoyl Synthase in the Biosynthesis of the Lipoyl Cofactor. [Internet] [Thesis]. Penn State University; 2015. [cited 2020 Sep 19]. Available from: https://submit-etda.libraries.psu.edu/catalog/27378.

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

Council of Science Editors:

Lanz ND. The Role of the Auxiliary Iron-sulfur Cluster of Lipoyl Synthase in the Biosynthesis of the Lipoyl Cofactor. [Thesis]. Penn State University; 2015. Available from: https://submit-etda.libraries.psu.edu/catalog/27378

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


University of Illinois – Chicago

17. LaMarre, Jacqueline M. Investigation of the cfr and rlmN genes in linezolid resistance.

Degree: 2012, University of Illinois – Chicago

 Linezolid is an effective antibiotic against pathogens like Staphylococcus aureus. Recently, the Cfr methyltransferase was found to confer resistance to linezolid by methylating C8 of… (more)

Subjects/Keywords: linezolid; antibiotic resistance; Staphylococcus aureus; Staphylococcus epidermidis; cfr; rlmN; Radical SAM; Radical S-adenosylmethionine

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APA (6th Edition):

LaMarre, J. M. (2012). Investigation of the cfr and rlmN genes in linezolid resistance. (Thesis). University of Illinois – Chicago. Retrieved from http://hdl.handle.net/10027/9177

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):

LaMarre, Jacqueline M. “Investigation of the cfr and rlmN genes in linezolid resistance.” 2012. Thesis, University of Illinois – Chicago. Accessed September 19, 2020. http://hdl.handle.net/10027/9177.

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

MLA Handbook (7th Edition):

LaMarre, Jacqueline M. “Investigation of the cfr and rlmN genes in linezolid resistance.” 2012. Web. 19 Sep 2020.

Vancouver:

LaMarre JM. Investigation of the cfr and rlmN genes in linezolid resistance. [Internet] [Thesis]. University of Illinois – Chicago; 2012. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/10027/9177.

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

Council of Science Editors:

LaMarre JM. Investigation of the cfr and rlmN genes in linezolid resistance. [Thesis]. University of Illinois – Chicago; 2012. Available from: http://hdl.handle.net/10027/9177

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


Northeastern University

18. Cleary, Dillon Christian. Synthesis of Se-adenosyl-L-selenohomocysteine selenoxide and potential gram-negative antibacterial analogs.

Degree: MS, Department of Chemistry and Chemical Biology, 2015, Northeastern University

 This paper includes work performed on two separate projects. The first project is the synthesis and characterization of a new analog of S-adenosylmethionine (AdoMet or… (more)

Subjects/Keywords: gram-negative bacteria; oxazolidinone; S-Adenosylmethionine; selenoxide; Chemistry; Pharmaceutical chemistry; Research; Adenosylmethionine; Synthesis; Adenosine; Synthesis; Selenium; Synthesis; Oxazoles; Synthesis; Gram-negative bacteria

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APA (6th Edition):

Cleary, D. C. (2015). Synthesis of Se-adenosyl-L-selenohomocysteine selenoxide and potential gram-negative antibacterial analogs. (Masters Thesis). Northeastern University. Retrieved from http://hdl.handle.net/2047/d20128883

Chicago Manual of Style (16th Edition):

Cleary, Dillon Christian. “Synthesis of Se-adenosyl-L-selenohomocysteine selenoxide and potential gram-negative antibacterial analogs.” 2015. Masters Thesis, Northeastern University. Accessed September 19, 2020. http://hdl.handle.net/2047/d20128883.

MLA Handbook (7th Edition):

Cleary, Dillon Christian. “Synthesis of Se-adenosyl-L-selenohomocysteine selenoxide and potential gram-negative antibacterial analogs.” 2015. Web. 19 Sep 2020.

Vancouver:

Cleary DC. Synthesis of Se-adenosyl-L-selenohomocysteine selenoxide and potential gram-negative antibacterial analogs. [Internet] [Masters thesis]. Northeastern University; 2015. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/2047/d20128883.

Council of Science Editors:

Cleary DC. Synthesis of Se-adenosyl-L-selenohomocysteine selenoxide and potential gram-negative antibacterial analogs. [Masters Thesis]. Northeastern University; 2015. Available from: http://hdl.handle.net/2047/d20128883


Penn State University

19. Arcinas, Arthur. MECHANISTIC STUDIES OF THE RADICAL S-ADENOSYL-L-METHIONINE (SAM) TRNA METHYLTHIOTRANSFERASE MIAB.

Degree: 2017, Penn State University

 Methylthiolation (–SCH3) is a conserved tRNA modification found specifically in adenosines adjacent to the anticodon in tRNAs that decode a leading uridine. The resulting hypermodification… (more)

Subjects/Keywords: MiaB; methylthiolation; methylthiotransferase; Radical SAM; S-adenosylmethionine; iron-sulfur cluster; EPR spectroscopy; Mössbauer spectroscopy; ferrodoxin; electron film voltammetry

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APA (6th Edition):

Arcinas, A. (2017). MECHANISTIC STUDIES OF THE RADICAL S-ADENOSYL-L-METHIONINE (SAM) TRNA METHYLTHIOTRANSFERASE MIAB. (Thesis). Penn State University. Retrieved from https://submit-etda.libraries.psu.edu/catalog/13901aja210

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):

Arcinas, Arthur. “MECHANISTIC STUDIES OF THE RADICAL S-ADENOSYL-L-METHIONINE (SAM) TRNA METHYLTHIOTRANSFERASE MIAB.” 2017. Thesis, Penn State University. Accessed September 19, 2020. https://submit-etda.libraries.psu.edu/catalog/13901aja210.

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

MLA Handbook (7th Edition):

Arcinas, Arthur. “MECHANISTIC STUDIES OF THE RADICAL S-ADENOSYL-L-METHIONINE (SAM) TRNA METHYLTHIOTRANSFERASE MIAB.” 2017. Web. 19 Sep 2020.

Vancouver:

Arcinas A. MECHANISTIC STUDIES OF THE RADICAL S-ADENOSYL-L-METHIONINE (SAM) TRNA METHYLTHIOTRANSFERASE MIAB. [Internet] [Thesis]. Penn State University; 2017. [cited 2020 Sep 19]. Available from: https://submit-etda.libraries.psu.edu/catalog/13901aja210.

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

Council of Science Editors:

Arcinas A. MECHANISTIC STUDIES OF THE RADICAL S-ADENOSYL-L-METHIONINE (SAM) TRNA METHYLTHIOTRANSFERASE MIAB. [Thesis]. Penn State University; 2017. Available from: https://submit-etda.libraries.psu.edu/catalog/13901aja210

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


University of Pretoria

20. Williams, Marni. Biochemical and structural characterization of novel drug targets regulating polyamine biosynthesis in the human malaria parasite, Plasmodium falciparum.

Degree: Biochemistry, 2011, University of Pretoria

 Malaria is prevalent in over 100 countries which is populated by half of the world’s population and culminates in approximately one million deaths per annum,… (more)

Subjects/Keywords: Protein-protein interactions; Polyamines; Plasmodium falciparum; Malaria; X-ray crystallography; Structure-based drug design; S-adenosylmethionine decarboxylase/ornithine de; UCTD

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APA (6th Edition):

Williams, M. (2011). Biochemical and structural characterization of novel drug targets regulating polyamine biosynthesis in the human malaria parasite, Plasmodium falciparum. (Doctoral Dissertation). University of Pretoria. Retrieved from http://hdl.handle.net/2263/26237

Chicago Manual of Style (16th Edition):

Williams, Marni. “Biochemical and structural characterization of novel drug targets regulating polyamine biosynthesis in the human malaria parasite, Plasmodium falciparum.” 2011. Doctoral Dissertation, University of Pretoria. Accessed September 19, 2020. http://hdl.handle.net/2263/26237.

MLA Handbook (7th Edition):

Williams, Marni. “Biochemical and structural characterization of novel drug targets regulating polyamine biosynthesis in the human malaria parasite, Plasmodium falciparum.” 2011. Web. 19 Sep 2020.

Vancouver:

Williams M. Biochemical and structural characterization of novel drug targets regulating polyamine biosynthesis in the human malaria parasite, Plasmodium falciparum. [Internet] [Doctoral dissertation]. University of Pretoria; 2011. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/2263/26237.

Council of Science Editors:

Williams M. Biochemical and structural characterization of novel drug targets regulating polyamine biosynthesis in the human malaria parasite, Plasmodium falciparum. [Doctoral Dissertation]. University of Pretoria; 2011. Available from: http://hdl.handle.net/2263/26237


University of Pretoria

21. [No author]. Biochemical and structural characterization of novel drug targets regulating polyamine biosynthesis in the human malaria parasite, Plasmodium falciparum .

Degree: 2011, University of Pretoria

 Malaria is prevalent in over 100 countries which is populated by half of the world’s population and culminates in approximately one million deaths per annum,… (more)

Subjects/Keywords: Protein-protein interactions; Polyamines; Plasmodium falciparum; Malaria; X-ray crystallography; Structure-based drug design; S-adenosylmethionine decarboxylase/ornithine de; UCTD

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APA (6th Edition):

author], [. (2011). Biochemical and structural characterization of novel drug targets regulating polyamine biosynthesis in the human malaria parasite, Plasmodium falciparum . (Doctoral Dissertation). University of Pretoria. Retrieved from http://upetd.up.ac.za/thesis/available/etd-07122011-104755/

Chicago Manual of Style (16th Edition):

author], [No. “Biochemical and structural characterization of novel drug targets regulating polyamine biosynthesis in the human malaria parasite, Plasmodium falciparum .” 2011. Doctoral Dissertation, University of Pretoria. Accessed September 19, 2020. http://upetd.up.ac.za/thesis/available/etd-07122011-104755/.

MLA Handbook (7th Edition):

author], [No. “Biochemical and structural characterization of novel drug targets regulating polyamine biosynthesis in the human malaria parasite, Plasmodium falciparum .” 2011. Web. 19 Sep 2020.

Vancouver:

author] [. Biochemical and structural characterization of novel drug targets regulating polyamine biosynthesis in the human malaria parasite, Plasmodium falciparum . [Internet] [Doctoral dissertation]. University of Pretoria; 2011. [cited 2020 Sep 19]. Available from: http://upetd.up.ac.za/thesis/available/etd-07122011-104755/.

Council of Science Editors:

author] [. Biochemical and structural characterization of novel drug targets regulating polyamine biosynthesis in the human malaria parasite, Plasmodium falciparum . [Doctoral Dissertation]. University of Pretoria; 2011. Available from: http://upetd.up.ac.za/thesis/available/etd-07122011-104755/


Northeastern University

22. Qu, Wanlu. Identifying unknown substrates of S-adenosyl-methionine-dependent methyltransferases via in situ formation of tight binding bisubstrate adducts.

Degree: PhD, Department of Chemistry and Chemical Biology, 2015, Northeastern University

 Identification of enzyme substrates is an essential step toward understanding the physiological functions of enzymes. However, progress in substrate elucidation is hampered by the transient… (more)

Subjects/Keywords: bisubstrate adduct; native mass spectrometry; S-adenosyl-methionine; S-adenosyl-vinthionine; substrate identification; Enzyme kinetics; Enzymes; Physiology; Methyltransferases; Sulfonium compounds; Adenosylmethionine; Mass spectrometry; Dissertations

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APA (6th Edition):

Qu, W. (2015). Identifying unknown substrates of S-adenosyl-methionine-dependent methyltransferases via in situ formation of tight binding bisubstrate adducts. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/D20194123

Chicago Manual of Style (16th Edition):

Qu, Wanlu. “Identifying unknown substrates of S-adenosyl-methionine-dependent methyltransferases via in situ formation of tight binding bisubstrate adducts.” 2015. Doctoral Dissertation, Northeastern University. Accessed September 19, 2020. http://hdl.handle.net/2047/D20194123.

MLA Handbook (7th Edition):

Qu, Wanlu. “Identifying unknown substrates of S-adenosyl-methionine-dependent methyltransferases via in situ formation of tight binding bisubstrate adducts.” 2015. Web. 19 Sep 2020.

Vancouver:

Qu W. Identifying unknown substrates of S-adenosyl-methionine-dependent methyltransferases via in situ formation of tight binding bisubstrate adducts. [Internet] [Doctoral dissertation]. Northeastern University; 2015. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/2047/D20194123.

Council of Science Editors:

Qu W. Identifying unknown substrates of S-adenosyl-methionine-dependent methyltransferases via in situ formation of tight binding bisubstrate adducts. [Doctoral Dissertation]. Northeastern University; 2015. Available from: http://hdl.handle.net/2047/D20194123


The Ohio State University

23. Pavlovicz, Ryan Elliott. Investigation of Protein/Ligand Interactions Relating Structural Dynamics to Function: Combined Computational and Experimental Approaches.

Degree: PhD, Biophysics, 2014, The Ohio State University

 The use of computers in chemistry has matured significantly since the introduction of the modern personal computer, leading to the development of many tools that… (more)

Subjects/Keywords: Biophysics; computational chemistry; molecular modeling; free energy analysis; biophysics; protein receptors; docking; force field parameterization; SAM; nAChR; RAR; retinoic acid receptor; nicotinic acetylcholine receptor; S-adenosylmethionine

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APA (6th Edition):

Pavlovicz, R. E. (2014). Investigation of Protein/Ligand Interactions Relating Structural Dynamics to Function: Combined Computational and Experimental Approaches. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1397220613

Chicago Manual of Style (16th Edition):

Pavlovicz, Ryan Elliott. “Investigation of Protein/Ligand Interactions Relating Structural Dynamics to Function: Combined Computational and Experimental Approaches.” 2014. Doctoral Dissertation, The Ohio State University. Accessed September 19, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=osu1397220613.

MLA Handbook (7th Edition):

Pavlovicz, Ryan Elliott. “Investigation of Protein/Ligand Interactions Relating Structural Dynamics to Function: Combined Computational and Experimental Approaches.” 2014. Web. 19 Sep 2020.

Vancouver:

Pavlovicz RE. Investigation of Protein/Ligand Interactions Relating Structural Dynamics to Function: Combined Computational and Experimental Approaches. [Internet] [Doctoral dissertation]. The Ohio State University; 2014. [cited 2020 Sep 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1397220613.

Council of Science Editors:

Pavlovicz RE. Investigation of Protein/Ligand Interactions Relating Structural Dynamics to Function: Combined Computational and Experimental Approaches. [Doctoral Dissertation]. The Ohio State University; 2014. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1397220613


University of Cambridge

24. Liu, Ke-di. The Interaction of Obesity and Age and their effect on Adipose Tissue Metabolism in the Mouse.

Degree: PhD, 2019, University of Cambridge

 Numerous studies have investigated how bulk lipid metabolism is influenced in obesity and in particular how the composition of triglycerides found in the cytosol change… (more)

Subjects/Keywords: lipid metabolism; obesity; glycerophospholipid; choline; one-carbon metabolism; S-adenosylmethionine; DNA methylation; lipidomics; transcriptomics; adipose tissue; triglyceride; aging; peroxisome; AMPK signaling; PPAR signaling; metabolic syndrome

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APA (6th Edition):

Liu, K. (2019). The Interaction of Obesity and Age and their effect on Adipose Tissue Metabolism in the Mouse. (Doctoral Dissertation). University of Cambridge. Retrieved from https://www.repository.cam.ac.uk/handle/1810/290384

Chicago Manual of Style (16th Edition):

Liu, Ke-di. “The Interaction of Obesity and Age and their effect on Adipose Tissue Metabolism in the Mouse.” 2019. Doctoral Dissertation, University of Cambridge. Accessed September 19, 2020. https://www.repository.cam.ac.uk/handle/1810/290384.

MLA Handbook (7th Edition):

Liu, Ke-di. “The Interaction of Obesity and Age and their effect on Adipose Tissue Metabolism in the Mouse.” 2019. Web. 19 Sep 2020.

Vancouver:

Liu K. The Interaction of Obesity and Age and their effect on Adipose Tissue Metabolism in the Mouse. [Internet] [Doctoral dissertation]. University of Cambridge; 2019. [cited 2020 Sep 19]. Available from: https://www.repository.cam.ac.uk/handle/1810/290384.

Council of Science Editors:

Liu K. The Interaction of Obesity and Age and their effect on Adipose Tissue Metabolism in the Mouse. [Doctoral Dissertation]. University of Cambridge; 2019. Available from: https://www.repository.cam.ac.uk/handle/1810/290384


Northeastern University

25. Trivedi, Malav Suchin. Redox / methylation signaling: a novel epigenetic-based mechanism of opioid drug action.

Degree: PhD, School of Pharmacy, 2013, Northeastern University

 Drugs of abuse affect the capacity for attention and awareness and produce altered states of consciousness, implying that they act upon the molecular mechanisms, which… (more)

Subjects/Keywords: DNA methylation; glutathione; met enkephalin; mu opioid receptor; oxidative stress; S-adenosyl methionine; DNA; Methylation; Oxidation-reduction reaction; Oxidative stress; Opioids; Receptors; Opioid peptides; Glutathione; Adenosylmethionine

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APA (6th Edition):

Trivedi, M. S. (2013). Redox / methylation signaling: a novel epigenetic-based mechanism of opioid drug action. (Doctoral Dissertation). Northeastern University. Retrieved from http://hdl.handle.net/2047/D20198517

Chicago Manual of Style (16th Edition):

Trivedi, Malav Suchin. “Redox / methylation signaling: a novel epigenetic-based mechanism of opioid drug action.” 2013. Doctoral Dissertation, Northeastern University. Accessed September 19, 2020. http://hdl.handle.net/2047/D20198517.

MLA Handbook (7th Edition):

Trivedi, Malav Suchin. “Redox / methylation signaling: a novel epigenetic-based mechanism of opioid drug action.” 2013. Web. 19 Sep 2020.

Vancouver:

Trivedi MS. Redox / methylation signaling: a novel epigenetic-based mechanism of opioid drug action. [Internet] [Doctoral dissertation]. Northeastern University; 2013. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/2047/D20198517.

Council of Science Editors:

Trivedi MS. Redox / methylation signaling: a novel epigenetic-based mechanism of opioid drug action. [Doctoral Dissertation]. Northeastern University; 2013. Available from: http://hdl.handle.net/2047/D20198517


University of South Florida

26. Schleif, William. Effects of Long-Term Administration of Caffeine in a Mouse Model for Alzheimer’s Disease.

Degree: 2005, University of South Florida

 A recent epidemiological study suggested that higher caffeine intake reduces the risk of Alzheimer's disease (AD). Caffeine, a widely consumed stimulatory drug, is a non-selective… (more)

Subjects/Keywords: Amyloid; S-adenosylmethionine; PS1; Adenosine; Transgenic mice; American Studies; Arts and Humanities

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APA (6th Edition):

Schleif, W. (2005). Effects of Long-Term Administration of Caffeine in a Mouse Model for Alzheimer’s Disease. (Thesis). University of South Florida. Retrieved from https://scholarcommons.usf.edu/etd/854

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):

Schleif, William. “Effects of Long-Term Administration of Caffeine in a Mouse Model for Alzheimer’s Disease.” 2005. Thesis, University of South Florida. Accessed September 19, 2020. https://scholarcommons.usf.edu/etd/854.

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

MLA Handbook (7th Edition):

Schleif, William. “Effects of Long-Term Administration of Caffeine in a Mouse Model for Alzheimer’s Disease.” 2005. Web. 19 Sep 2020.

Vancouver:

Schleif W. Effects of Long-Term Administration of Caffeine in a Mouse Model for Alzheimer’s Disease. [Internet] [Thesis]. University of South Florida; 2005. [cited 2020 Sep 19]. Available from: https://scholarcommons.usf.edu/etd/854.

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

Council of Science Editors:

Schleif W. Effects of Long-Term Administration of Caffeine in a Mouse Model for Alzheimer’s Disease. [Thesis]. University of South Florida; 2005. Available from: https://scholarcommons.usf.edu/etd/854

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


University of Michigan

27. Ghosh, Soumi. Probing the Mechanism of Viral Inhibition by the Radical S-adenosyl-L-methionine (SAM) Dependent Enzyme- Viperin.

Degree: PhD, Chemistry, 2020, University of Michigan

 Viperin (Virus Inhibitory Protein; Endoplasmic Reticulum associated, INterferon inducible) is an endoplasmic reticulum (ER)-associated antiviral responsive protein that is highly up-regulated in eukaryotic cells upon… (more)

Subjects/Keywords: S-adenosylmethionine domain containing protein 2 (RSAD2); anti-viral responsive protein; Radical S-adenosyl-L-methionine enzyme; mammalian cell-based radical SAM enzyme activity; protein-protein interaction in innate immune system; regulation of cellular metabolic and signaling pathways; Chemistry; Science

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

APA (6th Edition):

Ghosh, S. (2020). Probing the Mechanism of Viral Inhibition by the Radical S-adenosyl-L-methionine (SAM) Dependent Enzyme- Viperin. (Doctoral Dissertation). University of Michigan. Retrieved from http://hdl.handle.net/2027.42/155178

Chicago Manual of Style (16th Edition):

Ghosh, Soumi. “Probing the Mechanism of Viral Inhibition by the Radical S-adenosyl-L-methionine (SAM) Dependent Enzyme- Viperin.” 2020. Doctoral Dissertation, University of Michigan. Accessed September 19, 2020. http://hdl.handle.net/2027.42/155178.

MLA Handbook (7th Edition):

Ghosh, Soumi. “Probing the Mechanism of Viral Inhibition by the Radical S-adenosyl-L-methionine (SAM) Dependent Enzyme- Viperin.” 2020. Web. 19 Sep 2020.

Vancouver:

Ghosh S. Probing the Mechanism of Viral Inhibition by the Radical S-adenosyl-L-methionine (SAM) Dependent Enzyme- Viperin. [Internet] [Doctoral dissertation]. University of Michigan; 2020. [cited 2020 Sep 19]. Available from: http://hdl.handle.net/2027.42/155178.

Council of Science Editors:

Ghosh S. Probing the Mechanism of Viral Inhibition by the Radical S-adenosyl-L-methionine (SAM) Dependent Enzyme- Viperin. [Doctoral Dissertation]. University of Michigan; 2020. Available from: http://hdl.handle.net/2027.42/155178

28. 和田, 牧子. マトリックス支援レーザー脱離イオン化飛行時間型質量分析計を用いるポリアミン生合成酵素の構造解析 : マトリックス シエン レーザー ダツリ イオンカ ヒコウ ジカンガタ シツリョウ ブンセキケイ オ モチイル ポリアミン セイゴウセイ コウソ ノ コウゾウ カイセキ.

Degree: 博士(薬学), 2011, Josai University / 城西大学

学位授与機関:城西大学 学位記番号:博乙第56号,学位の種別:博士(薬学), 学位授与年月日:平成23年(2011年) 3月22日, 論文著者名:古屋, 牧子(フルヤ, マキコ). 60p.

Subjects/Keywords: matrix-assisted laser desorption; ionization time of flight mass spectrometry; spermidine synthase; s-adenosylmethionine decarboxylase; primary structure; conformational stabillization

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APA (6th Edition):

和田, . (2011). マトリックス支援レーザー脱離イオン化飛行時間型質量分析計を用いるポリアミン生合成酵素の構造解析 : マトリックス シエン レーザー ダツリ イオンカ ヒコウ ジカンガタ シツリョウ ブンセキケイ オ モチイル ポリアミン セイゴウセイ コウソ ノ コウゾウ カイセキ. (Thesis). Josai University / 城西大学. Retrieved from http://libir.josai.ac.jp/il/meta_pub/G0000284repository_JOS-PhDZ56

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):

和田, 牧子. “マトリックス支援レーザー脱離イオン化飛行時間型質量分析計を用いるポリアミン生合成酵素の構造解析 : マトリックス シエン レーザー ダツリ イオンカ ヒコウ ジカンガタ シツリョウ ブンセキケイ オ モチイル ポリアミン セイゴウセイ コウソ ノ コウゾウ カイセキ.” 2011. Thesis, Josai University / 城西大学. Accessed September 19, 2020. http://libir.josai.ac.jp/il/meta_pub/G0000284repository_JOS-PhDZ56.

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

MLA Handbook (7th Edition):

和田, 牧子. “マトリックス支援レーザー脱離イオン化飛行時間型質量分析計を用いるポリアミン生合成酵素の構造解析 : マトリックス シエン レーザー ダツリ イオンカ ヒコウ ジカンガタ シツリョウ ブンセキケイ オ モチイル ポリアミン セイゴウセイ コウソ ノ コウゾウ カイセキ.” 2011. Web. 19 Sep 2020.

Vancouver:

和田 . マトリックス支援レーザー脱離イオン化飛行時間型質量分析計を用いるポリアミン生合成酵素の構造解析 : マトリックス シエン レーザー ダツリ イオンカ ヒコウ ジカンガタ シツリョウ ブンセキケイ オ モチイル ポリアミン セイゴウセイ コウソ ノ コウゾウ カイセキ. [Internet] [Thesis]. Josai University / 城西大学; 2011. [cited 2020 Sep 19]. Available from: http://libir.josai.ac.jp/il/meta_pub/G0000284repository_JOS-PhDZ56.

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

Council of Science Editors:

和田 . マトリックス支援レーザー脱離イオン化飛行時間型質量分析計を用いるポリアミン生合成酵素の構造解析 : マトリックス シエン レーザー ダツリ イオンカ ヒコウ ジカンガタ シツリョウ ブンセキケイ オ モチイル ポリアミン セイゴウセイ コウソ ノ コウゾウ カイセキ. [Thesis]. Josai University / 城西大学; 2011. Available from: http://libir.josai.ac.jp/il/meta_pub/G0000284repository_JOS-PhDZ56

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

29. Marinelli, Zachary A. Identification of a putative <i>metK</i> selenite resistance gene in <i>Stenotrophomonas maltophilia</i> OR02.

Degree: MSin Biological Sciences, Department of Biological Sciences, 2017, Youngstown State University

 <i>Stenotrophomonas maltophilia</i> OR02 (S02) is a multi-metal resistant strain that was isolated from a metal-contaminated site in Oak Ridge, TN. It grows in the presence… (more)

Subjects/Keywords: Biology; Environmental Science; Genetics; Microbiology; Molecular Biology; Stenotrophomonas maltophilia; metK; S-adenosylmethionine; selenite resistance; selenite detoxification; bioremediation

S-adenosylmethionine involved in selenide methylation. 16 Chapter III: Methods 3.1… …8 Figure 5 – Putative Selenite Detoxification Pathway in S. maltophilia… …10 Figure 6 – Methionine Metabolism in S. maltophilia… …processes were disposed of in four, poorly constructed S-3 ponds near the plant and East Fork… …Stenotrophomonas maltophilia (S. maltophilia) is a gram negative, nonfermentative, aerobic… 

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

APA (6th Edition):

Marinelli, Z. A. (2017). Identification of a putative <i>metK</i> selenite resistance gene in <i>Stenotrophomonas maltophilia</i> OR02. (Masters Thesis). Youngstown State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=ysu1516345597337997

Chicago Manual of Style (16th Edition):

Marinelli, Zachary A. “Identification of a putative <i>metK</i> selenite resistance gene in <i>Stenotrophomonas maltophilia</i> OR02.” 2017. Masters Thesis, Youngstown State University. Accessed September 19, 2020. http://rave.ohiolink.edu/etdc/view?acc_num=ysu1516345597337997.

MLA Handbook (7th Edition):

Marinelli, Zachary A. “Identification of a putative <i>metK</i> selenite resistance gene in <i>Stenotrophomonas maltophilia</i> OR02.” 2017. Web. 19 Sep 2020.

Vancouver:

Marinelli ZA. Identification of a putative <i>metK</i> selenite resistance gene in <i>Stenotrophomonas maltophilia</i> OR02. [Internet] [Masters thesis]. Youngstown State University; 2017. [cited 2020 Sep 19]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1516345597337997.

Council of Science Editors:

Marinelli ZA. Identification of a putative <i>metK</i> selenite resistance gene in <i>Stenotrophomonas maltophilia</i> OR02. [Masters Thesis]. Youngstown State University; 2017. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=ysu1516345597337997

30. Tibrewal, Nidhi. INVESTIGATING KEY POST-PKS ENZYMES FROM GILVOCARCIN BIOSYNTHETIC PATHWAY.

Degree: 2013, University of Kentucky

 Gilvocarcin V (GV) belongs to the angucycline class of antibiotics that possesses remarkable anticancer and antibacterial activities with low toxicity. Gilvocarcin exhibits its light induced… (more)

Subjects/Keywords: Gilvocarcin; S-adenosylmethionine; O-methyltransferase; Baeyer-Villiger monooxygenases; Medicinal and Pharmaceutical Chemistry; Natural Products Chemistry and Pharmacognosy

adenosylmethionine; (B) Cofactor released from GilM; (C) S-adenosylmethionine boiled… …adenosylmethionine; (B) Cofactor released from GilM; (C) S-adenosylmethionine boiled… …35 Figure 0.2 HPLC traces of the released cofactor: (A) standard S… …39 Figure 0.6 HPLC traces of the released cofactor: (A) standard S… …structure activity relationship SAM S-adenosyl methionine TE thioesterase TLC thin layer… 

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

APA (6th Edition):

Tibrewal, N. (2013). INVESTIGATING KEY POST-PKS ENZYMES FROM GILVOCARCIN BIOSYNTHETIC PATHWAY. (Doctoral Dissertation). University of Kentucky. Retrieved from https://uknowledge.uky.edu/pharmacy_etds/14

Chicago Manual of Style (16th Edition):

Tibrewal, Nidhi. “INVESTIGATING KEY POST-PKS ENZYMES FROM GILVOCARCIN BIOSYNTHETIC PATHWAY.” 2013. Doctoral Dissertation, University of Kentucky. Accessed September 19, 2020. https://uknowledge.uky.edu/pharmacy_etds/14.

MLA Handbook (7th Edition):

Tibrewal, Nidhi. “INVESTIGATING KEY POST-PKS ENZYMES FROM GILVOCARCIN BIOSYNTHETIC PATHWAY.” 2013. Web. 19 Sep 2020.

Vancouver:

Tibrewal N. INVESTIGATING KEY POST-PKS ENZYMES FROM GILVOCARCIN BIOSYNTHETIC PATHWAY. [Internet] [Doctoral dissertation]. University of Kentucky; 2013. [cited 2020 Sep 19]. Available from: https://uknowledge.uky.edu/pharmacy_etds/14.

Council of Science Editors:

Tibrewal N. INVESTIGATING KEY POST-PKS ENZYMES FROM GILVOCARCIN BIOSYNTHETIC PATHWAY. [Doctoral Dissertation]. University of Kentucky; 2013. Available from: https://uknowledge.uky.edu/pharmacy_etds/14

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