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Dept: Biochemistry

You searched for subject:( 1 5 ). Showing records 1 – 30 of 58 total matches.

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The Ohio State University

1. Eberley, William Arthur. Hydrogen-bonding residues at the asymmetric dimer site of tRNAHis guanylyltransferase and their contributions to oligomeric state and activity.

Degree: MS, Biochemistry, 2011, The Ohio State University

 tRNAHis guanylyltransferase (Thg1) in eukaryotes plays a critical role in the proper maturation of tRNAHis by catalyzing the 3’-5’ addition of a required non-encoded, guanosine… (more)

Subjects/Keywords: Biochemistry; Thg1; tRNAHis guanylyltransferase; G-1 addition; 3'-5' polymerase

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

APA (6th Edition):

Eberley, W. A. (2011). Hydrogen-bonding residues at the asymmetric dimer site of tRNAHis guanylyltransferase and their contributions to oligomeric state and activity. (Masters Thesis). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1306943230

Chicago Manual of Style (16th Edition):

Eberley, William Arthur. “Hydrogen-bonding residues at the asymmetric dimer site of tRNAHis guanylyltransferase and their contributions to oligomeric state and activity.” 2011. Masters Thesis, The Ohio State University. Accessed October 23, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1306943230.

MLA Handbook (7th Edition):

Eberley, William Arthur. “Hydrogen-bonding residues at the asymmetric dimer site of tRNAHis guanylyltransferase and their contributions to oligomeric state and activity.” 2011. Web. 23 Oct 2019.

Vancouver:

Eberley WA. Hydrogen-bonding residues at the asymmetric dimer site of tRNAHis guanylyltransferase and their contributions to oligomeric state and activity. [Internet] [Masters thesis]. The Ohio State University; 2011. [cited 2019 Oct 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1306943230.

Council of Science Editors:

Eberley WA. Hydrogen-bonding residues at the asymmetric dimer site of tRNAHis guanylyltransferase and their contributions to oligomeric state and activity. [Masters Thesis]. The Ohio State University; 2011. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1306943230


Virginia Tech

2. Liu, Pingyang. Biochemical studies of enzymes in insect cuticle hardening.

Degree: PhD, Biochemistry, 2013, Virginia Tech

 In insects, the cuticle provides protection against physical injury and water loss, rigidness for muscle attachment and mechanical support, and flexibility in inter-segmental and joint… (more)

Subjects/Keywords: aspartate 1-decarboxylase; pyridoxal 5-phosphate; cysteine sulfinic acid; taurine; hypotaurine; beta-alanine; cysteine; glutamat

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APA (6th Edition):

Liu, P. (2013). Biochemical studies of enzymes in insect cuticle hardening. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/50528

Chicago Manual of Style (16th Edition):

Liu, Pingyang. “Biochemical studies of enzymes in insect cuticle hardening.” 2013. Doctoral Dissertation, Virginia Tech. Accessed October 23, 2019. http://hdl.handle.net/10919/50528.

MLA Handbook (7th Edition):

Liu, Pingyang. “Biochemical studies of enzymes in insect cuticle hardening.” 2013. Web. 23 Oct 2019.

Vancouver:

Liu P. Biochemical studies of enzymes in insect cuticle hardening. [Internet] [Doctoral dissertation]. Virginia Tech; 2013. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/10919/50528.

Council of Science Editors:

Liu P. Biochemical studies of enzymes in insect cuticle hardening. [Doctoral Dissertation]. Virginia Tech; 2013. Available from: http://hdl.handle.net/10919/50528


Virginia Tech

3. Miller, Danielle Virginia. Methanocaldococcus jannaschii and the Recycling of S-adenosyl-L-methionine.

Degree: PhD, Biochemistry, 2017, Virginia Tech

 S-Adenosyl-L-methionine (SAM) is an essential metabolite for all domains of life. SAM- dependent reactions result in three major metabolites: S-adenosyl-L-homocysteine (SAH), methylthioadenosine (MTA), and 5'-deoxyadenosine… (more)

Subjects/Keywords: S-adenosyl-L-methionine; SAM; recycling; 6-deoxy-5-ketofructose 1-phosphate; aromatic amino acids; methionine salvage; 5'-deoxyadenosine; S-adenosylhomoysteine; methylthioadenosine

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APA (6th Edition):

Miller, D. V. (2017). Methanocaldococcus jannaschii and the Recycling of S-adenosyl-L-methionine. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/77520

Chicago Manual of Style (16th Edition):

Miller, Danielle Virginia. “Methanocaldococcus jannaschii and the Recycling of S-adenosyl-L-methionine.” 2017. Doctoral Dissertation, Virginia Tech. Accessed October 23, 2019. http://hdl.handle.net/10919/77520.

MLA Handbook (7th Edition):

Miller, Danielle Virginia. “Methanocaldococcus jannaschii and the Recycling of S-adenosyl-L-methionine.” 2017. Web. 23 Oct 2019.

Vancouver:

Miller DV. Methanocaldococcus jannaschii and the Recycling of S-adenosyl-L-methionine. [Internet] [Doctoral dissertation]. Virginia Tech; 2017. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/10919/77520.

Council of Science Editors:

Miller DV. Methanocaldococcus jannaschii and the Recycling of S-adenosyl-L-methionine. [Doctoral Dissertation]. Virginia Tech; 2017. Available from: http://hdl.handle.net/10919/77520


Virginia Tech

4. Burnette, Ryan Nelson. A Physiological, Biochemical and Structural Analysis of Inositol Polyphosphate 5-Phosphatases from Arabidopsis thaliana and Humans.

Degree: PhD, Biochemistry, 2004, Virginia Tech

 The complete role of inositol signaling in plants and humans is still elusive. The plant Arabidopsis thaliana contains fifteen predicted inositol polyphosphate 5- phosphatases (5PTases,… (more)

Subjects/Keywords: 4; inositol (1; 5)-trisphosphate; inositol polyphosphate 5-phosphatase; Arabidopsis thaliana; Lowe syndrome; infrared spectroscopy

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APA (6th Edition):

Burnette, R. N. (2004). A Physiological, Biochemical and Structural Analysis of Inositol Polyphosphate 5-Phosphatases from Arabidopsis thaliana and Humans. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/29874

Chicago Manual of Style (16th Edition):

Burnette, Ryan Nelson. “A Physiological, Biochemical and Structural Analysis of Inositol Polyphosphate 5-Phosphatases from Arabidopsis thaliana and Humans.” 2004. Doctoral Dissertation, Virginia Tech. Accessed October 23, 2019. http://hdl.handle.net/10919/29874.

MLA Handbook (7th Edition):

Burnette, Ryan Nelson. “A Physiological, Biochemical and Structural Analysis of Inositol Polyphosphate 5-Phosphatases from Arabidopsis thaliana and Humans.” 2004. Web. 23 Oct 2019.

Vancouver:

Burnette RN. A Physiological, Biochemical and Structural Analysis of Inositol Polyphosphate 5-Phosphatases from Arabidopsis thaliana and Humans. [Internet] [Doctoral dissertation]. Virginia Tech; 2004. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/10919/29874.

Council of Science Editors:

Burnette RN. A Physiological, Biochemical and Structural Analysis of Inositol Polyphosphate 5-Phosphatases from Arabidopsis thaliana and Humans. [Doctoral Dissertation]. Virginia Tech; 2004. Available from: http://hdl.handle.net/10919/29874


Purdue University

5. Chen, Meng-Chieh. New Strategies To Reveal Protein Candidates In Protein-Protein Interactome Study.

Degree: MS, Biochemistry, 2014, Purdue University

  Comprehensive protein-protein interaction network analysis can help reveal protein functions in a system-wide manner. A reliable knowledgebase of interaction networks is not only important… (more)

Subjects/Keywords: Pure sciences; Biological sciences; Phosphoproteome; Polo-like kinase 1; Protein arginine methyltransferase 5; Protein-protein interaction; Sindbis virus; Virus-host interaction; Analytical Chemistry; Biochemistry; Molecular Biology

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APA (6th Edition):

Chen, M. (2014). New Strategies To Reveal Protein Candidates In Protein-Protein Interactome Study. (Thesis). Purdue University. Retrieved from http://docs.lib.purdue.edu/open_access_theses/310

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):

Chen, Meng-Chieh. “New Strategies To Reveal Protein Candidates In Protein-Protein Interactome Study.” 2014. Thesis, Purdue University. Accessed October 23, 2019. http://docs.lib.purdue.edu/open_access_theses/310.

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

MLA Handbook (7th Edition):

Chen, Meng-Chieh. “New Strategies To Reveal Protein Candidates In Protein-Protein Interactome Study.” 2014. Web. 23 Oct 2019.

Vancouver:

Chen M. New Strategies To Reveal Protein Candidates In Protein-Protein Interactome Study. [Internet] [Thesis]. Purdue University; 2014. [cited 2019 Oct 23]. Available from: http://docs.lib.purdue.edu/open_access_theses/310.

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

Council of Science Editors:

Chen M. New Strategies To Reveal Protein Candidates In Protein-Protein Interactome Study. [Thesis]. Purdue University; 2014. Available from: http://docs.lib.purdue.edu/open_access_theses/310

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


Virginia Tech

6. Ananieva-Stoyanova, Elitsa Antonova. Identification and Functional Role of Myo-Inositol Polyphosphate 5-Phosphatase Protein Complexes.

Degree: PhD, Biochemistry, 2009, Virginia Tech

 To survive, an organism must constantly adjust its internal state to changes in the environment from which it receives signals. The signals set off a… (more)

Subjects/Keywords: myo-inositol polyphosphate 5-phosphatase; 5)P3]; sucrose nonfermenting-1-related kinase; Arabidopsis thaliana; inositol trisphosphate [Ins(1; arabidopsis homolog of p80

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APA (6th Edition):

Ananieva-Stoyanova, E. A. (2009). Identification and Functional Role of Myo-Inositol Polyphosphate 5-Phosphatase Protein Complexes. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/28028

Chicago Manual of Style (16th Edition):

Ananieva-Stoyanova, Elitsa Antonova. “Identification and Functional Role of Myo-Inositol Polyphosphate 5-Phosphatase Protein Complexes.” 2009. Doctoral Dissertation, Virginia Tech. Accessed October 23, 2019. http://hdl.handle.net/10919/28028.

MLA Handbook (7th Edition):

Ananieva-Stoyanova, Elitsa Antonova. “Identification and Functional Role of Myo-Inositol Polyphosphate 5-Phosphatase Protein Complexes.” 2009. Web. 23 Oct 2019.

Vancouver:

Ananieva-Stoyanova EA. Identification and Functional Role of Myo-Inositol Polyphosphate 5-Phosphatase Protein Complexes. [Internet] [Doctoral dissertation]. Virginia Tech; 2009. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/10919/28028.

Council of Science Editors:

Ananieva-Stoyanova EA. Identification and Functional Role of Myo-Inositol Polyphosphate 5-Phosphatase Protein Complexes. [Doctoral Dissertation]. Virginia Tech; 2009. Available from: http://hdl.handle.net/10919/28028


Case Western Reserve University

7. Abbas, Atheir Ibrahim. PSD-95 Regulates Serotonin Receptor Function in vivo.

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

 The 5-hydroxytryptamine 2A (5-HT2A) receptor, a target for hallucinogens and some antipsychotics, is thought to play a prominent role in regulating mood, perception, and cognition.… (more)

Subjects/Keywords: Biochemistry; Pharmacology; 5-HT2A; 5-HT2C; PSD-95; hallucinogen; antipsychotic; clozapine; serotonin receptors

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APA (6th Edition):

Abbas, A. I. (2009). PSD-95 Regulates Serotonin Receptor Function in vivo. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1237990096

Chicago Manual of Style (16th Edition):

Abbas, Atheir Ibrahim. “PSD-95 Regulates Serotonin Receptor Function in vivo.” 2009. Doctoral Dissertation, Case Western Reserve University. Accessed October 23, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1237990096.

MLA Handbook (7th Edition):

Abbas, Atheir Ibrahim. “PSD-95 Regulates Serotonin Receptor Function in vivo.” 2009. Web. 23 Oct 2019.

Vancouver:

Abbas AI. PSD-95 Regulates Serotonin Receptor Function in vivo. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2009. [cited 2019 Oct 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1237990096.

Council of Science Editors:

Abbas AI. PSD-95 Regulates Serotonin Receptor Function in vivo. [Doctoral Dissertation]. Case Western Reserve University; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1237990096


Case Western Reserve University

8. Setola, Vincent. DISCOVERING THE MOLECULAR AND CELLULAR MECHANISMS UNDERLYING FENFLURAMINE-INDUCED CARDIOPULMONARY SIDE EFFECTS.

Degree: PhD, Biochemistry, 2005, Case Western Reserve University

 G protein-coupled receptors (GPCRs) are plasma membrane proteins that act as sensors for extracellular stimuli (e.g., photons, neurohumoral moduluators, odorants and tastants, lipids). The cognate… (more)

Subjects/Keywords: Chemistry, Biochemistry; 5-HT2B; 5-HT2B Receptors; Receptors; SNF; V2.53L; Fenfluramine; 5-HT2C

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APA (6th Edition):

Setola, V. (2005). DISCOVERING THE MOLECULAR AND CELLULAR MECHANISMS UNDERLYING FENFLURAMINE-INDUCED CARDIOPULMONARY SIDE EFFECTS. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1115318623

Chicago Manual of Style (16th Edition):

Setola, Vincent. “DISCOVERING THE MOLECULAR AND CELLULAR MECHANISMS UNDERLYING FENFLURAMINE-INDUCED CARDIOPULMONARY SIDE EFFECTS.” 2005. Doctoral Dissertation, Case Western Reserve University. Accessed October 23, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1115318623.

MLA Handbook (7th Edition):

Setola, Vincent. “DISCOVERING THE MOLECULAR AND CELLULAR MECHANISMS UNDERLYING FENFLURAMINE-INDUCED CARDIOPULMONARY SIDE EFFECTS.” 2005. Web. 23 Oct 2019.

Vancouver:

Setola V. DISCOVERING THE MOLECULAR AND CELLULAR MECHANISMS UNDERLYING FENFLURAMINE-INDUCED CARDIOPULMONARY SIDE EFFECTS. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2005. [cited 2019 Oct 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1115318623.

Council of Science Editors:

Setola V. DISCOVERING THE MOLECULAR AND CELLULAR MECHANISMS UNDERLYING FENFLURAMINE-INDUCED CARDIOPULMONARY SIDE EFFECTS. [Doctoral Dissertation]. Case Western Reserve University; 2005. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1115318623


Virginia Commonwealth University

9. Sukholutsky, Marianna. ADENOVIRUS-5 INFECTION AFFECTS LIPID METABOLISM IN HEPATIC AND ADIPOSE TISSUES.

Degree: MS, Biochemistry, 2010, Virginia Commonwealth University

 Our recent studies have shown a link between Adenovirus-5 (Ad-5) and elevated lipids, which prompted the hypothesis that Ad-5 infection might augment hepatic and/or adipose… (more)

Subjects/Keywords: lipid metabolism; Ad-5; Biochemistry, Biophysics, and Structural Biology; Life Sciences

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APA (6th Edition):

Sukholutsky, M. (2010). ADENOVIRUS-5 INFECTION AFFECTS LIPID METABOLISM IN HEPATIC AND ADIPOSE TISSUES. (Thesis). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/2297

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):

Sukholutsky, Marianna. “ADENOVIRUS-5 INFECTION AFFECTS LIPID METABOLISM IN HEPATIC AND ADIPOSE TISSUES.” 2010. Thesis, Virginia Commonwealth University. Accessed October 23, 2019. https://scholarscompass.vcu.edu/etd/2297.

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

MLA Handbook (7th Edition):

Sukholutsky, Marianna. “ADENOVIRUS-5 INFECTION AFFECTS LIPID METABOLISM IN HEPATIC AND ADIPOSE TISSUES.” 2010. Web. 23 Oct 2019.

Vancouver:

Sukholutsky M. ADENOVIRUS-5 INFECTION AFFECTS LIPID METABOLISM IN HEPATIC AND ADIPOSE TISSUES. [Internet] [Thesis]. Virginia Commonwealth University; 2010. [cited 2019 Oct 23]. Available from: https://scholarscompass.vcu.edu/etd/2297.

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

Council of Science Editors:

Sukholutsky M. ADENOVIRUS-5 INFECTION AFFECTS LIPID METABOLISM IN HEPATIC AND ADIPOSE TISSUES. [Thesis]. Virginia Commonwealth University; 2010. Available from: https://scholarscompass.vcu.edu/etd/2297

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


Virginia Tech

10. Casasanta, Michael Anthony. Laying the Genetic and Molecular Foundation for the Study of Fusobacterium Nucleatum in Relation to Human Health and Disease.

Degree: PhD, Biochemistry, 2019, Virginia Tech

 Fusobacterium nucleatum is a Gram-negative, anaerobic bacterium that is a member of the human oral microbiota. Although it is a normal resident of the mouth,… (more)

Subjects/Keywords: Intracellular pathogen; Fusobacterium nucleatum; colorectal cancer; autotransporter; Type 5 secretion; infection

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APA (6th Edition):

Casasanta, M. A. (2019). Laying the Genetic and Molecular Foundation for the Study of Fusobacterium Nucleatum in Relation to Human Health and Disease. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/88484

Chicago Manual of Style (16th Edition):

Casasanta, Michael Anthony. “Laying the Genetic and Molecular Foundation for the Study of Fusobacterium Nucleatum in Relation to Human Health and Disease.” 2019. Doctoral Dissertation, Virginia Tech. Accessed October 23, 2019. http://hdl.handle.net/10919/88484.

MLA Handbook (7th Edition):

Casasanta, Michael Anthony. “Laying the Genetic and Molecular Foundation for the Study of Fusobacterium Nucleatum in Relation to Human Health and Disease.” 2019. Web. 23 Oct 2019.

Vancouver:

Casasanta MA. Laying the Genetic and Molecular Foundation for the Study of Fusobacterium Nucleatum in Relation to Human Health and Disease. [Internet] [Doctoral dissertation]. Virginia Tech; 2019. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/10919/88484.

Council of Science Editors:

Casasanta MA. Laying the Genetic and Molecular Foundation for the Study of Fusobacterium Nucleatum in Relation to Human Health and Disease. [Doctoral Dissertation]. Virginia Tech; 2019. Available from: http://hdl.handle.net/10919/88484


Queens University

11. Lamparter, Christina L. REGULATION OF THE GABPβ PROMOTER AND THE ROLE OF NRF-1 IN MAMMARY EPITHELIAL MORPHOGENESIS .

Degree: Biochemistry, 2012, Queens University

 Decreased expression of the tumor suppressor gene BRCA1 (breast cancer 1, early onset) is frequently observed in sporadic breast tumors, with the decrease not attributed… (more)

Subjects/Keywords: Breast cancer; GABP; NRF-1

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APA (6th Edition):

Lamparter, C. L. (2012). REGULATION OF THE GABPβ PROMOTER AND THE ROLE OF NRF-1 IN MAMMARY EPITHELIAL MORPHOGENESIS . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/7429

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):

Lamparter, Christina L. “REGULATION OF THE GABPβ PROMOTER AND THE ROLE OF NRF-1 IN MAMMARY EPITHELIAL MORPHOGENESIS .” 2012. Thesis, Queens University. Accessed October 23, 2019. http://hdl.handle.net/1974/7429.

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

MLA Handbook (7th Edition):

Lamparter, Christina L. “REGULATION OF THE GABPβ PROMOTER AND THE ROLE OF NRF-1 IN MAMMARY EPITHELIAL MORPHOGENESIS .” 2012. Web. 23 Oct 2019.

Vancouver:

Lamparter CL. REGULATION OF THE GABPβ PROMOTER AND THE ROLE OF NRF-1 IN MAMMARY EPITHELIAL MORPHOGENESIS . [Internet] [Thesis]. Queens University; 2012. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/1974/7429.

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

Council of Science Editors:

Lamparter CL. REGULATION OF THE GABPβ PROMOTER AND THE ROLE OF NRF-1 IN MAMMARY EPITHELIAL MORPHOGENESIS . [Thesis]. Queens University; 2012. Available from: http://hdl.handle.net/1974/7429

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


University of Pretoria

12. Goolab, Shivani. Optimization of the heterologous expression of folate metabolic enzymes of Plasmodium falciparum.

Degree: Biochemistry, 2011, University of Pretoria

 Malaria is a fatal tropical disease affecting billions of people in impoverished countries world-wide. An alarming fact is that a child in Africa dies of… (more)

Subjects/Keywords: Folate biosynthesis; Recombinant protein expression; Guanosine 5’ triphosphate; Codon harmonization; Malaria; UCTD

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APA (6th Edition):

Goolab, S. (2011). Optimization of the heterologous expression of folate metabolic enzymes of Plasmodium falciparum. (Masters Thesis). University of Pretoria. Retrieved from http://hdl.handle.net/2263/23647

Chicago Manual of Style (16th Edition):

Goolab, Shivani. “Optimization of the heterologous expression of folate metabolic enzymes of Plasmodium falciparum.” 2011. Masters Thesis, University of Pretoria. Accessed October 23, 2019. http://hdl.handle.net/2263/23647.

MLA Handbook (7th Edition):

Goolab, Shivani. “Optimization of the heterologous expression of folate metabolic enzymes of Plasmodium falciparum.” 2011. Web. 23 Oct 2019.

Vancouver:

Goolab S. Optimization of the heterologous expression of folate metabolic enzymes of Plasmodium falciparum. [Internet] [Masters thesis]. University of Pretoria; 2011. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/2263/23647.

Council of Science Editors:

Goolab S. Optimization of the heterologous expression of folate metabolic enzymes of Plasmodium falciparum. [Masters Thesis]. University of Pretoria; 2011. Available from: http://hdl.handle.net/2263/23647


Case Western Reserve University

13. Yu, Yang. REGULATION OF PRE-MRNA SPLICING IN MAMMALIAN CELLS: IDENTIFICATION AND CHARACTERIZATION OF INTRONIC AND EXONIC SILENCERS.

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

  Almost every human pre-mRNA contains introns that must be removed through splicing before translated into proteins. Alternative splicing is a major contributor to proteomic… (more)

Subjects/Keywords: Biology, Molecular; alternative splicing; splicing silencer; functional SELEX; 5' splice site; U1 snRNP

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APA (6th Edition):

Yu, Y. (2007). REGULATION OF PRE-MRNA SPLICING IN MAMMALIAN CELLS: IDENTIFICATION AND CHARACTERIZATION OF INTRONIC AND EXONIC SILENCERS. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1184182785

Chicago Manual of Style (16th Edition):

Yu, Yang. “REGULATION OF PRE-MRNA SPLICING IN MAMMALIAN CELLS: IDENTIFICATION AND CHARACTERIZATION OF INTRONIC AND EXONIC SILENCERS.” 2007. Doctoral Dissertation, Case Western Reserve University. Accessed October 23, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1184182785.

MLA Handbook (7th Edition):

Yu, Yang. “REGULATION OF PRE-MRNA SPLICING IN MAMMALIAN CELLS: IDENTIFICATION AND CHARACTERIZATION OF INTRONIC AND EXONIC SILENCERS.” 2007. Web. 23 Oct 2019.

Vancouver:

Yu Y. REGULATION OF PRE-MRNA SPLICING IN MAMMALIAN CELLS: IDENTIFICATION AND CHARACTERIZATION OF INTRONIC AND EXONIC SILENCERS. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2007. [cited 2019 Oct 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1184182785.

Council of Science Editors:

Yu Y. REGULATION OF PRE-MRNA SPLICING IN MAMMALIAN CELLS: IDENTIFICATION AND CHARACTERIZATION OF INTRONIC AND EXONIC SILENCERS. [Doctoral Dissertation]. Case Western Reserve University; 2007. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1184182785


University of Illinois – Urbana-Champaign

14. Hebbard, Carleigh Fredda Frances. Mechanisms of polyphosphate degradation.

Degree: PhD, Biochemistry, 2016, University of Illinois – Urbana-Champaign

 The goal of my research has been to investigate the mechanisms by which inorganic polyphosphate (polyP) is degraded in vivo. PolyP is a linear chain… (more)

Subjects/Keywords: polyphosphate; polyP; Nudt2; Nudt3; pNP; p-nitrophenol; 4-nitrophenol; Nudix; phosphoanhydride; phosphoester; chromogenic substrate; fluorogenic substrate; phosphatase substrate; spectrophotometry; DAPI; 4-methylumbeliferone; dinucleotide polyphosphate; diadenosine polyphosphate; phosphate; phosphatase; phosphoanhydrase; phosphodiesterase; alkaline phosphatase; acid phosphatase; endopolyphosphatase; exopolyphosphatase; calcium; acidocalcisome; volutin granule; azurophilic granule; chitin; Chs2; ScChs2; cell wall; polysaccharide; oligosaccharide; calcium phosphate sink; ocean phosphate; serum; GlcNAc; UDP-GlcNAc; platelet; clotting; blood; coagulation; coagulation cascade; processive; polymer; TLC; carbohydrate; primer; TCA-insoluble; YO1531; inositol; inositol phosphate; ApnA; Ap3A; Ap4A; Ap6A; NpnA; diadenosine tetraphosphate; diadenosine pentaphosphate; diadenosine hexaphosphate; phytic acid; metaphosphate; phosphate melt; inositol hexaphosphate; 5-phosphoribosyl 1-pyrophosphate; PNPP; p-nitrophenol phosphate; DIPP; diphosphoinositol polyphosphate phosphohydrolase; Ddp1p; YOR163w; Saccharomyces cerevisiae; GlcN; GalNAc; ManNAc; Glc; GlcNAc2; GlcNAc3; N-propanoylglucosamine; GlcNPr; N-butanoylglucosamine; GlcNBu; N-glycolylglucosamine; GlcNGc

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APA (6th Edition):

Hebbard, C. F. F. (2016). Mechanisms of polyphosphate degradation. (Doctoral Dissertation). University of Illinois – Urbana-Champaign. Retrieved from http://hdl.handle.net/2142/91597

Chicago Manual of Style (16th Edition):

Hebbard, Carleigh Fredda Frances. “Mechanisms of polyphosphate degradation.” 2016. Doctoral Dissertation, University of Illinois – Urbana-Champaign. Accessed October 23, 2019. http://hdl.handle.net/2142/91597.

MLA Handbook (7th Edition):

Hebbard, Carleigh Fredda Frances. “Mechanisms of polyphosphate degradation.” 2016. Web. 23 Oct 2019.

Vancouver:

Hebbard CFF. Mechanisms of polyphosphate degradation. [Internet] [Doctoral dissertation]. University of Illinois – Urbana-Champaign; 2016. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/2142/91597.

Council of Science Editors:

Hebbard CFF. Mechanisms of polyphosphate degradation. [Doctoral Dissertation]. University of Illinois – Urbana-Champaign; 2016. Available from: http://hdl.handle.net/2142/91597


Queens University

15. Choi, Heesung. Implementing the Bimolecular Fluorescence Complementation Assay to Study Protein Interactions in the Cell Cycle Checkpoint Response .

Degree: Biochemistry, 2009, Queens University

 The genomic integrity of a cell is constantly being pressured by both intrinsic and extrinsic forces. Cell cycle checkpoints exist to protect the cells by… (more)

Subjects/Keywords: Rad9; Checkpoint; 9-1-1; TopBP1

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APA (6th Edition):

Choi, H. (2009). Implementing the Bimolecular Fluorescence Complementation Assay to Study Protein Interactions in the Cell Cycle Checkpoint Response . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/5361

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):

Choi, Heesung. “Implementing the Bimolecular Fluorescence Complementation Assay to Study Protein Interactions in the Cell Cycle Checkpoint Response .” 2009. Thesis, Queens University. Accessed October 23, 2019. http://hdl.handle.net/1974/5361.

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

MLA Handbook (7th Edition):

Choi, Heesung. “Implementing the Bimolecular Fluorescence Complementation Assay to Study Protein Interactions in the Cell Cycle Checkpoint Response .” 2009. Web. 23 Oct 2019.

Vancouver:

Choi H. Implementing the Bimolecular Fluorescence Complementation Assay to Study Protein Interactions in the Cell Cycle Checkpoint Response . [Internet] [Thesis]. Queens University; 2009. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/1974/5361.

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

Council of Science Editors:

Choi H. Implementing the Bimolecular Fluorescence Complementation Assay to Study Protein Interactions in the Cell Cycle Checkpoint Response . [Thesis]. Queens University; 2009. Available from: http://hdl.handle.net/1974/5361

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


University of Utah

16. Brereton, Melissa Diane Stuchell. The protein network of HIV-1 budding.

Degree: PhD, Biochemistry, 2010, University of Utah

 HIV-1 is an enveloped RNA virus that recruits cellular machinery to facilitate virus budding. HIV-1 Gag, the structural protein that drives the assembly and budding… (more)

Subjects/Keywords: HIV-1; Human ESCRT pathway; Virus budding; Protein network:

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APA (6th Edition):

Brereton, M. D. S. (2010). The protein network of HIV-1 budding. (Doctoral Dissertation). University of Utah. Retrieved from http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/235/rec/2634

Chicago Manual of Style (16th Edition):

Brereton, Melissa Diane Stuchell. “The protein network of HIV-1 budding.” 2010. Doctoral Dissertation, University of Utah. Accessed October 23, 2019. http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/235/rec/2634.

MLA Handbook (7th Edition):

Brereton, Melissa Diane Stuchell. “The protein network of HIV-1 budding.” 2010. Web. 23 Oct 2019.

Vancouver:

Brereton MDS. The protein network of HIV-1 budding. [Internet] [Doctoral dissertation]. University of Utah; 2010. [cited 2019 Oct 23]. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/235/rec/2634.

Council of Science Editors:

Brereton MDS. The protein network of HIV-1 budding. [Doctoral Dissertation]. University of Utah; 2010. Available from: http://content.lib.utah.edu/cdm/singleitem/collection/etd3/id/235/rec/2634


Case Western Reserve University

17. Rodkey, Elizabeth A. INHIBITOR RESISTANCE MECHANISMS AND INHIBITOR DESIGN IN ¿¿-LACTAMASES.

Degree: PhD, Biochemistry, 2013, Case Western Reserve University

 Antibiotic resistance is an ever-present problem and is a natural result of evolution; however, it is anticipated that we may exhaust our antibacterial options if… (more)

Subjects/Keywords: Biochemistry; SHV-1; beta-lactamase; inhibitor-resistant; inhibition mechanism; inhibitor design

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APA (6th Edition):

Rodkey, E. A. (2013). INHIBITOR RESISTANCE MECHANISMS AND INHIBITOR DESIGN IN ¿¿-LACTAMASES. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1354463033

Chicago Manual of Style (16th Edition):

Rodkey, Elizabeth A. “INHIBITOR RESISTANCE MECHANISMS AND INHIBITOR DESIGN IN ¿¿-LACTAMASES.” 2013. Doctoral Dissertation, Case Western Reserve University. Accessed October 23, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1354463033.

MLA Handbook (7th Edition):

Rodkey, Elizabeth A. “INHIBITOR RESISTANCE MECHANISMS AND INHIBITOR DESIGN IN ¿¿-LACTAMASES.” 2013. Web. 23 Oct 2019.

Vancouver:

Rodkey EA. INHIBITOR RESISTANCE MECHANISMS AND INHIBITOR DESIGN IN ¿¿-LACTAMASES. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2013. [cited 2019 Oct 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1354463033.

Council of Science Editors:

Rodkey EA. INHIBITOR RESISTANCE MECHANISMS AND INHIBITOR DESIGN IN ¿¿-LACTAMASES. [Doctoral Dissertation]. Case Western Reserve University; 2013. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1354463033


Case Western Reserve University

18. Wang, Wei-Ming. AP-1-MEDIATED REGULATION OF HPV CHROMATIN TRANSCRIPTION.

Degree: PhD, Biochemistry, 2008, Case Western Reserve University

 AP-1 complexes are a family of transcription factors ubiquitously expressed in different cell types. Transcriptional regulation mediated by AP-1 has been extensively studied; AP-1 mainly… (more)

Subjects/Keywords: AP-1; p300; HPV; chromatin; transcription; Jun; Fos

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APA (6th Edition):

Wang, W. (2008). AP-1-MEDIATED REGULATION OF HPV CHROMATIN TRANSCRIPTION. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1199480473

Chicago Manual of Style (16th Edition):

Wang, Wei-Ming. “AP-1-MEDIATED REGULATION OF HPV CHROMATIN TRANSCRIPTION.” 2008. Doctoral Dissertation, Case Western Reserve University. Accessed October 23, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1199480473.

MLA Handbook (7th Edition):

Wang, Wei-Ming. “AP-1-MEDIATED REGULATION OF HPV CHROMATIN TRANSCRIPTION.” 2008. Web. 23 Oct 2019.

Vancouver:

Wang W. AP-1-MEDIATED REGULATION OF HPV CHROMATIN TRANSCRIPTION. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2008. [cited 2019 Oct 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1199480473.

Council of Science Editors:

Wang W. AP-1-MEDIATED REGULATION OF HPV CHROMATIN TRANSCRIPTION. [Doctoral Dissertation]. Case Western Reserve University; 2008. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1199480473


Boston University

19. Li, Chendi. Myocardin-related transcription factor A regulates conversion of progenitors to beige adipocytes.

Degree: PhD, Biochemistry, 2015, Boston University

 Thermogenic brown adipose tissue generates heat via mitochondrial uncoupling protein-1 (UCP-1), increases whole-body energy expenditure and may protects against obesity and metabolic disorders. White adipocytes… (more)

Subjects/Keywords: Biochemistry; Beige adipocyte; MRTFA; UCP-1; Whole-body metabolism

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APA (6th Edition):

Li, C. (2015). Myocardin-related transcription factor A regulates conversion of progenitors to beige adipocytes. (Doctoral Dissertation). Boston University. Retrieved from http://hdl.handle.net/2144/16110

Chicago Manual of Style (16th Edition):

Li, Chendi. “Myocardin-related transcription factor A regulates conversion of progenitors to beige adipocytes.” 2015. Doctoral Dissertation, Boston University. Accessed October 23, 2019. http://hdl.handle.net/2144/16110.

MLA Handbook (7th Edition):

Li, Chendi. “Myocardin-related transcription factor A regulates conversion of progenitors to beige adipocytes.” 2015. Web. 23 Oct 2019.

Vancouver:

Li C. Myocardin-related transcription factor A regulates conversion of progenitors to beige adipocytes. [Internet] [Doctoral dissertation]. Boston University; 2015. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/2144/16110.

Council of Science Editors:

Li C. Myocardin-related transcription factor A regulates conversion of progenitors to beige adipocytes. [Doctoral Dissertation]. Boston University; 2015. Available from: http://hdl.handle.net/2144/16110


Queens University

20. Price, Phillipe. CRISPR/CAS9-MEDIATED GENE EDITING IN THE ARGINASE-1 DEFICIENT MOUSE GENOME .

Degree: Biochemistry, 2015, Queens University

 Arginase-1 deficiency is a rare, autosomal recessive disorder of the urea cycle that normally converts ammonia to less toxic urea. Symptoms include neurodegeneration, spastic diplegia… (more)

Subjects/Keywords: Arginase-1 Deficiency; Induced Pluripotent Stem Cells; Gene Editing; CRISPR/Cas9

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APA (6th Edition):

Price, P. (2015). CRISPR/CAS9-MEDIATED GENE EDITING IN THE ARGINASE-1 DEFICIENT MOUSE GENOME . (Thesis). Queens University. Retrieved from http://hdl.handle.net/1974/13626

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):

Price, Phillipe. “CRISPR/CAS9-MEDIATED GENE EDITING IN THE ARGINASE-1 DEFICIENT MOUSE GENOME .” 2015. Thesis, Queens University. Accessed October 23, 2019. http://hdl.handle.net/1974/13626.

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

MLA Handbook (7th Edition):

Price, Phillipe. “CRISPR/CAS9-MEDIATED GENE EDITING IN THE ARGINASE-1 DEFICIENT MOUSE GENOME .” 2015. Web. 23 Oct 2019.

Vancouver:

Price P. CRISPR/CAS9-MEDIATED GENE EDITING IN THE ARGINASE-1 DEFICIENT MOUSE GENOME . [Internet] [Thesis]. Queens University; 2015. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/1974/13626.

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

Council of Science Editors:

Price P. CRISPR/CAS9-MEDIATED GENE EDITING IN THE ARGINASE-1 DEFICIENT MOUSE GENOME . [Thesis]. Queens University; 2015. Available from: http://hdl.handle.net/1974/13626

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


The Ohio State University

21. Kasim, Mumtaz. THE ROLE OF THE N(5) INTERACTION AND ASSOCIATED CONFORMATIONAL CHANGES IN THE MODULATION OF THE REDOX PROPERTIES IN FLAVOPROTEINS.

Degree: PhD, Biochemistry, 2002, The Ohio State University

 Many biochemical processes exploit the remarkable versatility of flavoenzymes and their flavin cofactors by modulating the numerous interactions made with the apoflavoprotein. The interaction to… (more)

Subjects/Keywords: Chemistry, Biochemistry; Flavin; Redox Potential; Turn; N(5); Conformational change; P450 reductase

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APA (6th Edition):

Kasim, M. (2002). THE ROLE OF THE N(5) INTERACTION AND ASSOCIATED CONFORMATIONAL CHANGES IN THE MODULATION OF THE REDOX PROPERTIES IN FLAVOPROTEINS. (Doctoral Dissertation). The Ohio State University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=osu1039022224

Chicago Manual of Style (16th Edition):

Kasim, Mumtaz. “THE ROLE OF THE N(5) INTERACTION AND ASSOCIATED CONFORMATIONAL CHANGES IN THE MODULATION OF THE REDOX PROPERTIES IN FLAVOPROTEINS.” 2002. Doctoral Dissertation, The Ohio State University. Accessed October 23, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=osu1039022224.

MLA Handbook (7th Edition):

Kasim, Mumtaz. “THE ROLE OF THE N(5) INTERACTION AND ASSOCIATED CONFORMATIONAL CHANGES IN THE MODULATION OF THE REDOX PROPERTIES IN FLAVOPROTEINS.” 2002. Web. 23 Oct 2019.

Vancouver:

Kasim M. THE ROLE OF THE N(5) INTERACTION AND ASSOCIATED CONFORMATIONAL CHANGES IN THE MODULATION OF THE REDOX PROPERTIES IN FLAVOPROTEINS. [Internet] [Doctoral dissertation]. The Ohio State University; 2002. [cited 2019 Oct 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1039022224.

Council of Science Editors:

Kasim M. THE ROLE OF THE N(5) INTERACTION AND ASSOCIATED CONFORMATIONAL CHANGES IN THE MODULATION OF THE REDOX PROPERTIES IN FLAVOPROTEINS. [Doctoral Dissertation]. The Ohio State University; 2002. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=osu1039022224


Case Western Reserve University

22. Sheffler, Douglas James. The Regulation of G Protein-Coupled Receptor (GPCR) Signal Transduction by p90 Ribosomal S6 Kinase 2 (RSK2).

Degree: PhD, Biochemistry, 2006, Case Western Reserve University

5-hydroxytryptamine 2A (5-HT2A) serotonin receptors are G-protein coupled receptors (GPCRs) that play prominent roles in both the central nervous system and in the periphery and… (more)

Subjects/Keywords: Chemistry, Biochemistry; Serotonin; GPCR; RSK2; 5-HT2A; Coffin-Lowry Syndrome

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APA (6th Edition):

Sheffler, D. J. (2006). The Regulation of G Protein-Coupled Receptor (GPCR) Signal Transduction by p90 Ribosomal S6 Kinase 2 (RSK2). (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1130777469

Chicago Manual of Style (16th Edition):

Sheffler, Douglas James. “The Regulation of G Protein-Coupled Receptor (GPCR) Signal Transduction by p90 Ribosomal S6 Kinase 2 (RSK2).” 2006. Doctoral Dissertation, Case Western Reserve University. Accessed October 23, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1130777469.

MLA Handbook (7th Edition):

Sheffler, Douglas James. “The Regulation of G Protein-Coupled Receptor (GPCR) Signal Transduction by p90 Ribosomal S6 Kinase 2 (RSK2).” 2006. Web. 23 Oct 2019.

Vancouver:

Sheffler DJ. The Regulation of G Protein-Coupled Receptor (GPCR) Signal Transduction by p90 Ribosomal S6 Kinase 2 (RSK2). [Internet] [Doctoral dissertation]. Case Western Reserve University; 2006. [cited 2019 Oct 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1130777469.

Council of Science Editors:

Sheffler DJ. The Regulation of G Protein-Coupled Receptor (GPCR) Signal Transduction by p90 Ribosomal S6 Kinase 2 (RSK2). [Doctoral Dissertation]. Case Western Reserve University; 2006. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1130777469


Virginia Tech

23. Ercetin, Mustafa Edib. Molecular Characterization and Loss-of-Function Analysis of an Arabidopsis thaliana Gene Encoding a Phospholipid-Specific Inositol Polyphosphate 5-Phosphatase.

Degree: PhD, Biochemistry, 2005, Virginia Tech

 The phosphatidylinositol signaling pathway utilizes inositol-containing second messengers to mediate signaling events. The enzymes that metabolize phosphoinositides can in some cases serve to terminate the… (more)

Subjects/Keywords: PIP2; Arabidopsis thaliana; inositol polyphosphate 5-phosphatase; IP3; phosphatidylinositol signaling

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APA (6th Edition):

Ercetin, M. E. (2005). Molecular Characterization and Loss-of-Function Analysis of an Arabidopsis thaliana Gene Encoding a Phospholipid-Specific Inositol Polyphosphate 5-Phosphatase. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/27884

Chicago Manual of Style (16th Edition):

Ercetin, Mustafa Edib. “Molecular Characterization and Loss-of-Function Analysis of an Arabidopsis thaliana Gene Encoding a Phospholipid-Specific Inositol Polyphosphate 5-Phosphatase.” 2005. Doctoral Dissertation, Virginia Tech. Accessed October 23, 2019. http://hdl.handle.net/10919/27884.

MLA Handbook (7th Edition):

Ercetin, Mustafa Edib. “Molecular Characterization and Loss-of-Function Analysis of an Arabidopsis thaliana Gene Encoding a Phospholipid-Specific Inositol Polyphosphate 5-Phosphatase.” 2005. Web. 23 Oct 2019.

Vancouver:

Ercetin ME. Molecular Characterization and Loss-of-Function Analysis of an Arabidopsis thaliana Gene Encoding a Phospholipid-Specific Inositol Polyphosphate 5-Phosphatase. [Internet] [Doctoral dissertation]. Virginia Tech; 2005. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/10919/27884.

Council of Science Editors:

Ercetin ME. Molecular Characterization and Loss-of-Function Analysis of an Arabidopsis thaliana Gene Encoding a Phospholipid-Specific Inositol Polyphosphate 5-Phosphatase. [Doctoral Dissertation]. Virginia Tech; 2005. Available from: http://hdl.handle.net/10919/27884


Virginia Commonwealth University

24. Hobbs, Daniel. PATHOGENIC ROLE OF PHOSPHODIESTERASE TYPE 5 UPREGULATION IN CARDIAC ISCHEMIA/REPERFUSION INJURY.

Degree: MS, Biochemistry, 2010, Virginia Commonwealth University

 Phosphodiesterase Type 5 (PDE5) inhibitors are cardioprotective against ischemia/reperfusion (I/R) injury. However, it remains uncertain if I/R affects PDE5. We hypothesized that generation of reactive… (more)

Subjects/Keywords: Phosphodiesterase 5; Ischemia/Reperfusion Injury; Reactive Oxygen Species; Pharmacological Preconditioning; cGMP-Dependent Protein Kinase; Myocardial Infarction; Biochemistry, Biophysics, and Structural Biology; Life Sciences

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APA (6th Edition):

Hobbs, D. (2010). PATHOGENIC ROLE OF PHOSPHODIESTERASE TYPE 5 UPREGULATION IN CARDIAC ISCHEMIA/REPERFUSION INJURY. (Thesis). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/106

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):

Hobbs, Daniel. “PATHOGENIC ROLE OF PHOSPHODIESTERASE TYPE 5 UPREGULATION IN CARDIAC ISCHEMIA/REPERFUSION INJURY.” 2010. Thesis, Virginia Commonwealth University. Accessed October 23, 2019. https://scholarscompass.vcu.edu/etd/106.

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

MLA Handbook (7th Edition):

Hobbs, Daniel. “PATHOGENIC ROLE OF PHOSPHODIESTERASE TYPE 5 UPREGULATION IN CARDIAC ISCHEMIA/REPERFUSION INJURY.” 2010. Web. 23 Oct 2019.

Vancouver:

Hobbs D. PATHOGENIC ROLE OF PHOSPHODIESTERASE TYPE 5 UPREGULATION IN CARDIAC ISCHEMIA/REPERFUSION INJURY. [Internet] [Thesis]. Virginia Commonwealth University; 2010. [cited 2019 Oct 23]. Available from: https://scholarscompass.vcu.edu/etd/106.

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

Council of Science Editors:

Hobbs D. PATHOGENIC ROLE OF PHOSPHODIESTERASE TYPE 5 UPREGULATION IN CARDIAC ISCHEMIA/REPERFUSION INJURY. [Thesis]. Virginia Commonwealth University; 2010. Available from: https://scholarscompass.vcu.edu/etd/106

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


University of Iowa

25. Zhang, Yanling. The roles and regulation of phosphatidylinositol 3,5-bisphosphates in mammals.

Degree: PhD, Biochemistry, 2008, University of Iowa

  Phosphatidylinositol 3,5-bisphosphate [PI(3,5)P2] is a low-abundance signaling lipid important for the maintenance of the endomembrane system and selected membrane trafficking pathways. In yeast, in… (more)

Subjects/Keywords: Fab1; Vac14; PI(3; 5)P2; CMT; neurodegeneration; Biochemistry; Medical Biochemistry

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APA (6th Edition):

Zhang, Y. (2008). The roles and regulation of phosphatidylinositol 3,5-bisphosphates in mammals. (Doctoral Dissertation). University of Iowa. Retrieved from https://ir.uiowa.edu/etd/1

Chicago Manual of Style (16th Edition):

Zhang, Yanling. “The roles and regulation of phosphatidylinositol 3,5-bisphosphates in mammals.” 2008. Doctoral Dissertation, University of Iowa. Accessed October 23, 2019. https://ir.uiowa.edu/etd/1.

MLA Handbook (7th Edition):

Zhang, Yanling. “The roles and regulation of phosphatidylinositol 3,5-bisphosphates in mammals.” 2008. Web. 23 Oct 2019.

Vancouver:

Zhang Y. The roles and regulation of phosphatidylinositol 3,5-bisphosphates in mammals. [Internet] [Doctoral dissertation]. University of Iowa; 2008. [cited 2019 Oct 23]. Available from: https://ir.uiowa.edu/etd/1.

Council of Science Editors:

Zhang Y. The roles and regulation of phosphatidylinositol 3,5-bisphosphates in mammals. [Doctoral Dissertation]. University of Iowa; 2008. Available from: https://ir.uiowa.edu/etd/1

26. Strachan, Ryan Thomas. P90 Ribosomal S6 Kinase 2 (RSK2) Directly Phosphorylates the 5-HT2A Serotonin Receptor thereby Modulating Signaling.

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

 Given the pivotal role G protein-coupled receptors (GPCRs) play in physiological responses, various mechanisms have evolved to ensure the tight regulation of GPCR signaling. Classically,… (more)

Subjects/Keywords: Biochemistry; Pharmacology; serotonin; 5-HT; 5-HT2A; GPCR; RSK; ERK; phosphorylation; RTK; growth factor; functional selectivity; biased agonism

…133 5-1 Relative agonist potency and efficacy values for 5-HT2A-mediated IP accumulation… …18 1-5 GPCRs activate the ERK/MAPK cascade via integrin-based scaffolds… …kinases modulate GPCR signaling ..27 1-8 Many of the conserved residues in 5-HT… …and secondary 5-HT2A-mediated signal transduction pathways ..39 1-10… …receptor regulation …...43 1-11 5-HT2A receptor interacting proteins and their sites… 

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APA (6th Edition):

Strachan, R. T. (2009). P90 Ribosomal S6 Kinase 2 (RSK2) Directly Phosphorylates the 5-HT2A Serotonin Receptor thereby Modulating Signaling. (Doctoral Dissertation). Case Western Reserve University. Retrieved from http://rave.ohiolink.edu/etdc/view?acc_num=case1247172805

Chicago Manual of Style (16th Edition):

Strachan, Ryan Thomas. “P90 Ribosomal S6 Kinase 2 (RSK2) Directly Phosphorylates the 5-HT2A Serotonin Receptor thereby Modulating Signaling.” 2009. Doctoral Dissertation, Case Western Reserve University. Accessed October 23, 2019. http://rave.ohiolink.edu/etdc/view?acc_num=case1247172805.

MLA Handbook (7th Edition):

Strachan, Ryan Thomas. “P90 Ribosomal S6 Kinase 2 (RSK2) Directly Phosphorylates the 5-HT2A Serotonin Receptor thereby Modulating Signaling.” 2009. Web. 23 Oct 2019.

Vancouver:

Strachan RT. P90 Ribosomal S6 Kinase 2 (RSK2) Directly Phosphorylates the 5-HT2A Serotonin Receptor thereby Modulating Signaling. [Internet] [Doctoral dissertation]. Case Western Reserve University; 2009. [cited 2019 Oct 23]. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1247172805.

Council of Science Editors:

Strachan RT. P90 Ribosomal S6 Kinase 2 (RSK2) Directly Phosphorylates the 5-HT2A Serotonin Receptor thereby Modulating Signaling. [Doctoral Dissertation]. Case Western Reserve University; 2009. Available from: http://rave.ohiolink.edu/etdc/view?acc_num=case1247172805


University of Pretoria

27. Botha, M.E. (Mariette). Two-hybrid analysis and attempted expression of elongation factor 1α from the cattle tick, Rhipicephalus microplus.

Degree: Biochemistry, 2013, University of Pretoria

 Control of Rhipicephalus microplus is predominantly mediated by the application of acaricides, but the rapid acquisition of resistance by this species and environmental pollution resulting… (more)

Subjects/Keywords: Protein-protein interactions; Elongation factor 1-alpha; Anti-tick vaccine; Yeast two-hybrid.; UCTD

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APA (6th Edition):

Botha, M. E. (. (2013). Two-hybrid analysis and attempted expression of elongation factor 1α from the cattle tick, Rhipicephalus microplus. (Masters Thesis). University of Pretoria. Retrieved from http://hdl.handle.net/2263/31568

Chicago Manual of Style (16th Edition):

Botha, M E (Mariette). “Two-hybrid analysis and attempted expression of elongation factor 1α from the cattle tick, Rhipicephalus microplus.” 2013. Masters Thesis, University of Pretoria. Accessed October 23, 2019. http://hdl.handle.net/2263/31568.

MLA Handbook (7th Edition):

Botha, M E (Mariette). “Two-hybrid analysis and attempted expression of elongation factor 1α from the cattle tick, Rhipicephalus microplus.” 2013. Web. 23 Oct 2019.

Vancouver:

Botha ME(. Two-hybrid analysis and attempted expression of elongation factor 1α from the cattle tick, Rhipicephalus microplus. [Internet] [Masters thesis]. University of Pretoria; 2013. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/2263/31568.

Council of Science Editors:

Botha ME(. Two-hybrid analysis and attempted expression of elongation factor 1α from the cattle tick, Rhipicephalus microplus. [Masters Thesis]. University of Pretoria; 2013. Available from: http://hdl.handle.net/2263/31568


Virginia Tech

28. Nourbakhsh, Aida. Molecular Characterization of Inositol Monophosphatase Like Enzymes in Arabidopsis thaliana.

Degree: PhD, Biochemistry, 2012, Virginia Tech

 myo-Inositol synthesis and catabolism are crucial in many multicellular eukaryotes for production of phosphatidylinositol and inositol phosphate signaling molecules. myo-inositol monophosphatase (IMP) is a major… (more)

Subjects/Keywords: inositol; inositol monophosphatase; L-histidine; L-histidinol; L-histidinol 1-phosphate phosphatase; Arabidopsis thaliana

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APA (6th Edition):

Nourbakhsh, A. (2012). Molecular Characterization of Inositol Monophosphatase Like Enzymes in Arabidopsis thaliana. (Doctoral Dissertation). Virginia Tech. Retrieved from http://hdl.handle.net/10919/38695

Chicago Manual of Style (16th Edition):

Nourbakhsh, Aida. “Molecular Characterization of Inositol Monophosphatase Like Enzymes in Arabidopsis thaliana.” 2012. Doctoral Dissertation, Virginia Tech. Accessed October 23, 2019. http://hdl.handle.net/10919/38695.

MLA Handbook (7th Edition):

Nourbakhsh, Aida. “Molecular Characterization of Inositol Monophosphatase Like Enzymes in Arabidopsis thaliana.” 2012. Web. 23 Oct 2019.

Vancouver:

Nourbakhsh A. Molecular Characterization of Inositol Monophosphatase Like Enzymes in Arabidopsis thaliana. [Internet] [Doctoral dissertation]. Virginia Tech; 2012. [cited 2019 Oct 23]. Available from: http://hdl.handle.net/10919/38695.

Council of Science Editors:

Nourbakhsh A. Molecular Characterization of Inositol Monophosphatase Like Enzymes in Arabidopsis thaliana. [Doctoral Dissertation]. Virginia Tech; 2012. Available from: http://hdl.handle.net/10919/38695


Virginia Commonwealth University

29. Anand, Monika. FUNCTION AND REGULATION OF MATRIX METALLOPROTEINASE-1 IN GLIOBLASTOMA MULTIFORME.

Degree: PhD, Biochemistry, 2010, Virginia Commonwealth University

 Glioblastoma Multiforme (GBM) is an aggressive and fatal cancer of the brain. It is characterized with augmented morbidity and elusion to therapies due in part… (more)

Subjects/Keywords: GBM; MMP-1; Invasion; EGFR; MAPK; Biochemistry, Biophysics, and Structural Biology; Life Sciences

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

APA (6th Edition):

Anand, M. (2010). FUNCTION AND REGULATION OF MATRIX METALLOPROTEINASE-1 IN GLIOBLASTOMA MULTIFORME. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/2214

Chicago Manual of Style (16th Edition):

Anand, Monika. “FUNCTION AND REGULATION OF MATRIX METALLOPROTEINASE-1 IN GLIOBLASTOMA MULTIFORME.” 2010. Doctoral Dissertation, Virginia Commonwealth University. Accessed October 23, 2019. https://scholarscompass.vcu.edu/etd/2214.

MLA Handbook (7th Edition):

Anand, Monika. “FUNCTION AND REGULATION OF MATRIX METALLOPROTEINASE-1 IN GLIOBLASTOMA MULTIFORME.” 2010. Web. 23 Oct 2019.

Vancouver:

Anand M. FUNCTION AND REGULATION OF MATRIX METALLOPROTEINASE-1 IN GLIOBLASTOMA MULTIFORME. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2010. [cited 2019 Oct 23]. Available from: https://scholarscompass.vcu.edu/etd/2214.

Council of Science Editors:

Anand M. FUNCTION AND REGULATION OF MATRIX METALLOPROTEINASE-1 IN GLIOBLASTOMA MULTIFORME. [Doctoral Dissertation]. Virginia Commonwealth University; 2010. Available from: https://scholarscompass.vcu.edu/etd/2214


Virginia Commonwealth University

30. Gomez-Arroyo, Jose. Metabolic Remodeling and Mitochondrial Dysfunction in Maladaptive Right Ventricular Hypertrophy Secondary to Pulmonary Arterial Hypertension.

Degree: PhD, Biochemistry, 2013, Virginia Commonwealth University

 Right ventricular dysfunction is the most frequent cause of death in patients with pulmonary arterial hypertension. Although abnormal energy substrate use has been implicated in… (more)

Subjects/Keywords: PGC-1; mitochondria; right ventricle; right ventricular failure; Biochemistry, Biophysics, and Structural Biology; Life Sciences

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

APA (6th Edition):

Gomez-Arroyo, J. (2013). Metabolic Remodeling and Mitochondrial Dysfunction in Maladaptive Right Ventricular Hypertrophy Secondary to Pulmonary Arterial Hypertension. (Doctoral Dissertation). Virginia Commonwealth University. Retrieved from https://scholarscompass.vcu.edu/etd/3257

Chicago Manual of Style (16th Edition):

Gomez-Arroyo, Jose. “Metabolic Remodeling and Mitochondrial Dysfunction in Maladaptive Right Ventricular Hypertrophy Secondary to Pulmonary Arterial Hypertension.” 2013. Doctoral Dissertation, Virginia Commonwealth University. Accessed October 23, 2019. https://scholarscompass.vcu.edu/etd/3257.

MLA Handbook (7th Edition):

Gomez-Arroyo, Jose. “Metabolic Remodeling and Mitochondrial Dysfunction in Maladaptive Right Ventricular Hypertrophy Secondary to Pulmonary Arterial Hypertension.” 2013. Web. 23 Oct 2019.

Vancouver:

Gomez-Arroyo J. Metabolic Remodeling and Mitochondrial Dysfunction in Maladaptive Right Ventricular Hypertrophy Secondary to Pulmonary Arterial Hypertension. [Internet] [Doctoral dissertation]. Virginia Commonwealth University; 2013. [cited 2019 Oct 23]. Available from: https://scholarscompass.vcu.edu/etd/3257.

Council of Science Editors:

Gomez-Arroyo J. Metabolic Remodeling and Mitochondrial Dysfunction in Maladaptive Right Ventricular Hypertrophy Secondary to Pulmonary Arterial Hypertension. [Doctoral Dissertation]. Virginia Commonwealth University; 2013. Available from: https://scholarscompass.vcu.edu/etd/3257

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