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You searched for +publisher:"University of Georgia" +contributor:("Lance Wells"). Showing records 1 – 18 of 18 total matches.

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University of Georgia

1. Teo, Chin-Fen. Detecting O-GlcNAc and understanding its role in insulin action.

Degree: PhD, Biochemistry and Molecular Biology, 2013, University of Georgia

 O-linked β-N-acetylglucosamine (O-GlcNAc) modification is a ubiquitous glycosylation found on the serine and threonine side chains of intracellular proteins. The spatial and temporal distribution of… (more)

Subjects/Keywords: β-O-linked N-acetylglucosamine (O-GlcNAc)

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APA (6th Edition):

Teo, C. (2013). Detecting O-GlcNAc and understanding its role in insulin action. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/teo_chin-fen_201308_phd

Chicago Manual of Style (16th Edition):

Teo, Chin-Fen. “Detecting O-GlcNAc and understanding its role in insulin action.” 2013. Doctoral Dissertation, University of Georgia. Accessed February 24, 2020. http://purl.galileo.usg.edu/uga_etd/teo_chin-fen_201308_phd.

MLA Handbook (7th Edition):

Teo, Chin-Fen. “Detecting O-GlcNAc and understanding its role in insulin action.” 2013. Web. 24 Feb 2020.

Vancouver:

Teo C. Detecting O-GlcNAc and understanding its role in insulin action. [Internet] [Doctoral dissertation]. University of Georgia; 2013. [cited 2020 Feb 24]. Available from: http://purl.galileo.usg.edu/uga_etd/teo_chin-fen_201308_phd.

Council of Science Editors:

Teo C. Detecting O-GlcNAc and understanding its role in insulin action. [Doctoral Dissertation]. University of Georgia; 2013. Available from: http://purl.galileo.usg.edu/uga_etd/teo_chin-fen_201308_phd


University of Georgia

2. Dobson, Christina Marie. Development of a mass spectrometry based blood test for dystroglycanopathies using consecutive reaction monitoring.

Degree: MS, Biochemistry and Molecular Biology, 2013, University of Georgia

 A new mass spectrometry workflow has been developed using the intelligent fragmentation of O-glycans via consecutive reaction monitoring. Using the intensity of selected fragment ions… (more)

Subjects/Keywords: Dystroglycanopathy

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APA (6th Edition):

Dobson, C. M. (2013). Development of a mass spectrometry based blood test for dystroglycanopathies using consecutive reaction monitoring. (Masters Thesis). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/dobson_christina_m_201312_ms

Chicago Manual of Style (16th Edition):

Dobson, Christina Marie. “Development of a mass spectrometry based blood test for dystroglycanopathies using consecutive reaction monitoring.” 2013. Masters Thesis, University of Georgia. Accessed February 24, 2020. http://purl.galileo.usg.edu/uga_etd/dobson_christina_m_201312_ms.

MLA Handbook (7th Edition):

Dobson, Christina Marie. “Development of a mass spectrometry based blood test for dystroglycanopathies using consecutive reaction monitoring.” 2013. Web. 24 Feb 2020.

Vancouver:

Dobson CM. Development of a mass spectrometry based blood test for dystroglycanopathies using consecutive reaction monitoring. [Internet] [Masters thesis]. University of Georgia; 2013. [cited 2020 Feb 24]. Available from: http://purl.galileo.usg.edu/uga_etd/dobson_christina_m_201312_ms.

Council of Science Editors:

Dobson CM. Development of a mass spectrometry based blood test for dystroglycanopathies using consecutive reaction monitoring. [Masters Thesis]. University of Georgia; 2013. Available from: http://purl.galileo.usg.edu/uga_etd/dobson_christina_m_201312_ms


University of Georgia

3. Durning, Sean Patrick. O-GlcNAc is a sensor in the pancreatic beta cell.

Degree: PhD, Biochemistry and Molecular Biology, 2013, University of Georgia

 O-linked β-N-acetylglucosamine (O-GlcNAc) is a ubiquitous post-translational protein modification found on serine and threonine amino acid residues of intracellular proteins. This inducible and dynamic PTM… (more)

Subjects/Keywords: O-GlcNAc

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APA (6th Edition):

Durning, S. P. (2013). O-GlcNAc is a sensor in the pancreatic beta cell. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/durning_sean_p_201312_phd

Chicago Manual of Style (16th Edition):

Durning, Sean Patrick. “O-GlcNAc is a sensor in the pancreatic beta cell.” 2013. Doctoral Dissertation, University of Georgia. Accessed February 24, 2020. http://purl.galileo.usg.edu/uga_etd/durning_sean_p_201312_phd.

MLA Handbook (7th Edition):

Durning, Sean Patrick. “O-GlcNAc is a sensor in the pancreatic beta cell.” 2013. Web. 24 Feb 2020.

Vancouver:

Durning SP. O-GlcNAc is a sensor in the pancreatic beta cell. [Internet] [Doctoral dissertation]. University of Georgia; 2013. [cited 2020 Feb 24]. Available from: http://purl.galileo.usg.edu/uga_etd/durning_sean_p_201312_phd.

Council of Science Editors:

Durning SP. O-GlcNAc is a sensor in the pancreatic beta cell. [Doctoral Dissertation]. University of Georgia; 2013. Available from: http://purl.galileo.usg.edu/uga_etd/durning_sean_p_201312_phd


University of Georgia

4. Koppikar, Anuradha Rajesh. Using chemoenzymatic labeling to probe O-mannose glycosylation.

Degree: MS, Biochemistry and Molecular Biology, 2008, University of Georgia

 O-linked mannose has been implicated in cell-cell and cell-matrix adhesion. Defects in glycosyltransferases that add or extend O-linked mannose on glycoproteins generate neuron migration defects… (more)

Subjects/Keywords: O-mannose

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APA (6th Edition):

Koppikar, A. R. (2008). Using chemoenzymatic labeling to probe O-mannose glycosylation. (Masters Thesis). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/koppikar_anuradha_r_200808_ms

Chicago Manual of Style (16th Edition):

Koppikar, Anuradha Rajesh. “Using chemoenzymatic labeling to probe O-mannose glycosylation.” 2008. Masters Thesis, University of Georgia. Accessed February 24, 2020. http://purl.galileo.usg.edu/uga_etd/koppikar_anuradha_r_200808_ms.

MLA Handbook (7th Edition):

Koppikar, Anuradha Rajesh. “Using chemoenzymatic labeling to probe O-mannose glycosylation.” 2008. Web. 24 Feb 2020.

Vancouver:

Koppikar AR. Using chemoenzymatic labeling to probe O-mannose glycosylation. [Internet] [Masters thesis]. University of Georgia; 2008. [cited 2020 Feb 24]. Available from: http://purl.galileo.usg.edu/uga_etd/koppikar_anuradha_r_200808_ms.

Council of Science Editors:

Koppikar AR. Using chemoenzymatic labeling to probe O-mannose glycosylation. [Masters Thesis]. University of Georgia; 2008. Available from: http://purl.galileo.usg.edu/uga_etd/koppikar_anuradha_r_200808_ms


University of Georgia

5. Fennell, Ashley Monique. Genetic analysis of two mutations that affect neural-specific glycosylation.

Degree: BS, Biology, 2008, University of Georgia

 Complex carbohydrate expression regulates cell-cell interactions that can affect development and normal tissue function. Human genetic disorders that affect glycosylation often result in mental retardation… (more)

Subjects/Keywords: Neural-specific glycosylation

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APA (6th Edition):

Fennell, A. M. (2008). Genetic analysis of two mutations that affect neural-specific glycosylation. (Thesis). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/fennell_ashley_m_200812_bs

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):

Fennell, Ashley Monique. “Genetic analysis of two mutations that affect neural-specific glycosylation.” 2008. Thesis, University of Georgia. Accessed February 24, 2020. http://purl.galileo.usg.edu/uga_etd/fennell_ashley_m_200812_bs.

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

MLA Handbook (7th Edition):

Fennell, Ashley Monique. “Genetic analysis of two mutations that affect neural-specific glycosylation.” 2008. Web. 24 Feb 2020.

Vancouver:

Fennell AM. Genetic analysis of two mutations that affect neural-specific glycosylation. [Internet] [Thesis]. University of Georgia; 2008. [cited 2020 Feb 24]. Available from: http://purl.galileo.usg.edu/uga_etd/fennell_ashley_m_200812_bs.

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

Council of Science Editors:

Fennell AM. Genetic analysis of two mutations that affect neural-specific glycosylation. [Thesis]. University of Georgia; 2008. Available from: http://purl.galileo.usg.edu/uga_etd/fennell_ashley_m_200812_bs

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


University of Georgia

6. Wang, Wei. Cancer biomarker discovery: glycomics study of human serum.

Degree: MS, Chemistry, 2008, University of Georgia

 A biomarker is a detectable characteristic change resulting from a certain stimulus. The stimuli can be tumor growth, virus invasion, drug usage, etc. Biomarker discovery… (more)

Subjects/Keywords: cancer biomarker; serum; enrichment; glycosylation site mapping; Ion Mobility Mass Spectrometry; Multiple Reaction Monitoring

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APA (6th Edition):

Wang, W. (2008). Cancer biomarker discovery: glycomics study of human serum. (Masters Thesis). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/wang_wei_200812_ms

Chicago Manual of Style (16th Edition):

Wang, Wei. “Cancer biomarker discovery: glycomics study of human serum.” 2008. Masters Thesis, University of Georgia. Accessed February 24, 2020. http://purl.galileo.usg.edu/uga_etd/wang_wei_200812_ms.

MLA Handbook (7th Edition):

Wang, Wei. “Cancer biomarker discovery: glycomics study of human serum.” 2008. Web. 24 Feb 2020.

Vancouver:

Wang W. Cancer biomarker discovery: glycomics study of human serum. [Internet] [Masters thesis]. University of Georgia; 2008. [cited 2020 Feb 24]. Available from: http://purl.galileo.usg.edu/uga_etd/wang_wei_200812_ms.

Council of Science Editors:

Wang W. Cancer biomarker discovery: glycomics study of human serum. [Masters Thesis]. University of Georgia; 2008. Available from: http://purl.galileo.usg.edu/uga_etd/wang_wei_200812_ms


University of Georgia

7. Lim, Jae-Min. Secretome and glycome of mammalian adipocytes under insulin resistant conditions.

Degree: PhD, Chemistry, 2009, University of Georgia

 Insulin resistance defines the metabolic syndrome and precedes type 2 diabetes, thus is considered as the hallmark for type 2 diabetes. Prolonged hyperglycemia and hyperinsulinemia… (more)

Subjects/Keywords: O-GlcNAc

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APA (6th Edition):

Lim, J. (2009). Secretome and glycome of mammalian adipocytes under insulin resistant conditions. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/lim_jae-min_n_200905_phd

Chicago Manual of Style (16th Edition):

Lim, Jae-Min. “Secretome and glycome of mammalian adipocytes under insulin resistant conditions.” 2009. Doctoral Dissertation, University of Georgia. Accessed February 24, 2020. http://purl.galileo.usg.edu/uga_etd/lim_jae-min_n_200905_phd.

MLA Handbook (7th Edition):

Lim, Jae-Min. “Secretome and glycome of mammalian adipocytes under insulin resistant conditions.” 2009. Web. 24 Feb 2020.

Vancouver:

Lim J. Secretome and glycome of mammalian adipocytes under insulin resistant conditions. [Internet] [Doctoral dissertation]. University of Georgia; 2009. [cited 2020 Feb 24]. Available from: http://purl.galileo.usg.edu/uga_etd/lim_jae-min_n_200905_phd.

Council of Science Editors:

Lim J. Secretome and glycome of mammalian adipocytes under insulin resistant conditions. [Doctoral Dissertation]. University of Georgia; 2009. Available from: http://purl.galileo.usg.edu/uga_etd/lim_jae-min_n_200905_phd


University of Georgia

8. Marshall, John Benjamin. Microarray analysis of the role of O-GlcNAc in DAF-2 signaling in Caenorhabditis elegans.

Degree: BS, Biochemistry and Molecular Biology, 2009, University of Georgia

 Mutations in genes functioning along the insulin-like signaling pathway in Caenorhabditis elegans extend life span up to three times the wild type phenotype. We sought… (more)

Subjects/Keywords: DAF-2

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APA (6th Edition):

Marshall, J. B. (2009). Microarray analysis of the role of O-GlcNAc in DAF-2 signaling in Caenorhabditis elegans. (Thesis). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/marshall_john_b_200912_bs

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):

Marshall, John Benjamin. “Microarray analysis of the role of O-GlcNAc in DAF-2 signaling in Caenorhabditis elegans.” 2009. Thesis, University of Georgia. Accessed February 24, 2020. http://purl.galileo.usg.edu/uga_etd/marshall_john_b_200912_bs.

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

MLA Handbook (7th Edition):

Marshall, John Benjamin. “Microarray analysis of the role of O-GlcNAc in DAF-2 signaling in Caenorhabditis elegans.” 2009. Web. 24 Feb 2020.

Vancouver:

Marshall JB. Microarray analysis of the role of O-GlcNAc in DAF-2 signaling in Caenorhabditis elegans. [Internet] [Thesis]. University of Georgia; 2009. [cited 2020 Feb 24]. Available from: http://purl.galileo.usg.edu/uga_etd/marshall_john_b_200912_bs.

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

Council of Science Editors:

Marshall JB. Microarray analysis of the role of O-GlcNAc in DAF-2 signaling in Caenorhabditis elegans. [Thesis]. University of Georgia; 2009. Available from: http://purl.galileo.usg.edu/uga_etd/marshall_john_b_200912_bs

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


University of Georgia

9. Hammond, Stephanie Lauren. Inisghts into O-mannosylation revealed by glycoproteomics.

Degree: PhD, Chemistry, 2010, University of Georgia

 O-mannosylation accounts for approximately 30% of the reported O-linked glycan structures detected from mouse brain. However, O-mannosylation has rarely been observed on other mammalian proteins… (more)

Subjects/Keywords: post-translational modifications

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APA (6th Edition):

Hammond, S. L. (2010). Inisghts into O-mannosylation revealed by glycoproteomics. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/hammond_stephanie_l_201008_phd

Chicago Manual of Style (16th Edition):

Hammond, Stephanie Lauren. “Inisghts into O-mannosylation revealed by glycoproteomics.” 2010. Doctoral Dissertation, University of Georgia. Accessed February 24, 2020. http://purl.galileo.usg.edu/uga_etd/hammond_stephanie_l_201008_phd.

MLA Handbook (7th Edition):

Hammond, Stephanie Lauren. “Inisghts into O-mannosylation revealed by glycoproteomics.” 2010. Web. 24 Feb 2020.

Vancouver:

Hammond SL. Inisghts into O-mannosylation revealed by glycoproteomics. [Internet] [Doctoral dissertation]. University of Georgia; 2010. [cited 2020 Feb 24]. Available from: http://purl.galileo.usg.edu/uga_etd/hammond_stephanie_l_201008_phd.

Council of Science Editors:

Hammond SL. Inisghts into O-mannosylation revealed by glycoproteomics. [Doctoral Dissertation]. University of Georgia; 2010. Available from: http://purl.galileo.usg.edu/uga_etd/hammond_stephanie_l_201008_phd


University of Georgia

10. Zhao, Peng. Mass spectrometry-based proteomic analysis of complex biological samples.

Degree: PhD, Chemistry, 2011, University of Georgia

 Proteomics seeks to determine protein structure, modifications, localization, and protein-protein interactions in addition to protein expression levels. Although proteomics is often a large-scale endeavor on… (more)

Subjects/Keywords: mass spectrometry

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APA (6th Edition):

Zhao, P. (2011). Mass spectrometry-based proteomic analysis of complex biological samples. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/zhao_peng_201105_phd

Chicago Manual of Style (16th Edition):

Zhao, Peng. “Mass spectrometry-based proteomic analysis of complex biological samples.” 2011. Doctoral Dissertation, University of Georgia. Accessed February 24, 2020. http://purl.galileo.usg.edu/uga_etd/zhao_peng_201105_phd.

MLA Handbook (7th Edition):

Zhao, Peng. “Mass spectrometry-based proteomic analysis of complex biological samples.” 2011. Web. 24 Feb 2020.

Vancouver:

Zhao P. Mass spectrometry-based proteomic analysis of complex biological samples. [Internet] [Doctoral dissertation]. University of Georgia; 2011. [cited 2020 Feb 24]. Available from: http://purl.galileo.usg.edu/uga_etd/zhao_peng_201105_phd.

Council of Science Editors:

Zhao P. Mass spectrometry-based proteomic analysis of complex biological samples. [Doctoral Dissertation]. University of Georgia; 2011. Available from: http://purl.galileo.usg.edu/uga_etd/zhao_peng_201105_phd


University of Georgia

11. Fang, Meng. Applications of the IDAWG technique to quantitative glycomics of human embryonic stem cells.

Degree: PhD, Chemistry, 2011, University of Georgia

 As the first reported in-vivo stable isotopic labeling strategies for quantitative glycomics, the IDAWG (Isotopic Detection of Aminosugars With Glutamin) takes advantage of the hexosamine… (more)

Subjects/Keywords: IDAWG; stable isotopic labeling; quantitative glycomics; cell culture; glycan analysis; human embryonice stem cells; human definitive endoderms; Pulse-Chase; dynamics; glycan turnover; remodeling

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APA (6th Edition):

Fang, M. (2011). Applications of the IDAWG technique to quantitative glycomics of human embryonic stem cells. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/fang_meng_201112_phd

Chicago Manual of Style (16th Edition):

Fang, Meng. “Applications of the IDAWG technique to quantitative glycomics of human embryonic stem cells.” 2011. Doctoral Dissertation, University of Georgia. Accessed February 24, 2020. http://purl.galileo.usg.edu/uga_etd/fang_meng_201112_phd.

MLA Handbook (7th Edition):

Fang, Meng. “Applications of the IDAWG technique to quantitative glycomics of human embryonic stem cells.” 2011. Web. 24 Feb 2020.

Vancouver:

Fang M. Applications of the IDAWG technique to quantitative glycomics of human embryonic stem cells. [Internet] [Doctoral dissertation]. University of Georgia; 2011. [cited 2020 Feb 24]. Available from: http://purl.galileo.usg.edu/uga_etd/fang_meng_201112_phd.

Council of Science Editors:

Fang M. Applications of the IDAWG technique to quantitative glycomics of human embryonic stem cells. [Doctoral Dissertation]. University of Georgia; 2011. Available from: http://purl.galileo.usg.edu/uga_etd/fang_meng_201112_phd


University of Georgia

12. Vaidyanathan, Krithika. Identification and characterization of a missense mutation in O-GlcNAc transferase that segregates with disease in a family with X-linked intellectual disability.

Degree: PhD, Biochemistry and Molecular Biology, 2014, University of Georgia

 O-GlcNAc transferase (OGT) is responsible for the addition of the β-N-acetylglucosamine post-translational modification to serine/threonine residues of hundreds of nuclear and cytoplasmic proteins. In a… (more)

Subjects/Keywords: O-GlcNAc

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APA (6th Edition):

Vaidyanathan, K. (2014). Identification and characterization of a missense mutation in O-GlcNAc transferase that segregates with disease in a family with X-linked intellectual disability. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/vaidyanathan_krithika_201405_phd

Chicago Manual of Style (16th Edition):

Vaidyanathan, Krithika. “Identification and characterization of a missense mutation in O-GlcNAc transferase that segregates with disease in a family with X-linked intellectual disability.” 2014. Doctoral Dissertation, University of Georgia. Accessed February 24, 2020. http://purl.galileo.usg.edu/uga_etd/vaidyanathan_krithika_201405_phd.

MLA Handbook (7th Edition):

Vaidyanathan, Krithika. “Identification and characterization of a missense mutation in O-GlcNAc transferase that segregates with disease in a family with X-linked intellectual disability.” 2014. Web. 24 Feb 2020.

Vancouver:

Vaidyanathan K. Identification and characterization of a missense mutation in O-GlcNAc transferase that segregates with disease in a family with X-linked intellectual disability. [Internet] [Doctoral dissertation]. University of Georgia; 2014. [cited 2020 Feb 24]. Available from: http://purl.galileo.usg.edu/uga_etd/vaidyanathan_krithika_201405_phd.

Council of Science Editors:

Vaidyanathan K. Identification and characterization of a missense mutation in O-GlcNAc transferase that segregates with disease in a family with X-linked intellectual disability. [Doctoral Dissertation]. University of Georgia; 2014. Available from: http://purl.galileo.usg.edu/uga_etd/vaidyanathan_krithika_201405_phd


University of Georgia

13. Brimble, Sandra Nicole. Investigating the role of O-GlcNAc in the regulation of human Oct4.

Degree: PhD, Biochemistry and Molecular Biology, 2014, University of Georgia

 O-linked β-N-acetylglucosamine (O-GlcNAc) is a single sugar modification found on many different classes of nuclear and cytoplasmic proteins. Addition of this modification, by the enzyme… (more)

Subjects/Keywords: O-GlcNAc

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APA (6th Edition):

Brimble, S. N. (2014). Investigating the role of O-GlcNAc in the regulation of human Oct4. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/brimble_sandra_n_201408_phd

Chicago Manual of Style (16th Edition):

Brimble, Sandra Nicole. “Investigating the role of O-GlcNAc in the regulation of human Oct4.” 2014. Doctoral Dissertation, University of Georgia. Accessed February 24, 2020. http://purl.galileo.usg.edu/uga_etd/brimble_sandra_n_201408_phd.

MLA Handbook (7th Edition):

Brimble, Sandra Nicole. “Investigating the role of O-GlcNAc in the regulation of human Oct4.” 2014. Web. 24 Feb 2020.

Vancouver:

Brimble SN. Investigating the role of O-GlcNAc in the regulation of human Oct4. [Internet] [Doctoral dissertation]. University of Georgia; 2014. [cited 2020 Feb 24]. Available from: http://purl.galileo.usg.edu/uga_etd/brimble_sandra_n_201408_phd.

Council of Science Editors:

Brimble SN. Investigating the role of O-GlcNAc in the regulation of human Oct4. [Doctoral Dissertation]. University of Georgia; 2014. Available from: http://purl.galileo.usg.edu/uga_etd/brimble_sandra_n_201408_phd


University of Georgia

14. Porterfield, Melody Perlman. High throughput glycomics.

Degree: PhD, Chemistry, 2014, University of Georgia

 Over half of all cellular proteins are modified by post translational addition of oligosaccharides. Proper glycosylation plays a critical role in cell-cell communication and changes… (more)

Subjects/Keywords: glycan

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APA (6th Edition):

Porterfield, M. P. (2014). High throughput glycomics. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/porterfield_melody_p_201408_phd

Chicago Manual of Style (16th Edition):

Porterfield, Melody Perlman. “High throughput glycomics.” 2014. Doctoral Dissertation, University of Georgia. Accessed February 24, 2020. http://purl.galileo.usg.edu/uga_etd/porterfield_melody_p_201408_phd.

MLA Handbook (7th Edition):

Porterfield, Melody Perlman. “High throughput glycomics.” 2014. Web. 24 Feb 2020.

Vancouver:

Porterfield MP. High throughput glycomics. [Internet] [Doctoral dissertation]. University of Georgia; 2014. [cited 2020 Feb 24]. Available from: http://purl.galileo.usg.edu/uga_etd/porterfield_melody_p_201408_phd.

Council of Science Editors:

Porterfield MP. High throughput glycomics. [Doctoral Dissertation]. University of Georgia; 2014. Available from: http://purl.galileo.usg.edu/uga_etd/porterfield_melody_p_201408_phd


University of Georgia

15. Praissman, Jeremy Lawrence. The role of [beta]-1,4-glucuronyltransferase 1 in [alpha]-dystroglycan function.

Degree: PhD, Biochemistry and Molecular Biology, 2015, University of Georgia

 Alpha-dystroglycan (α-DG) is a necessary cell-surface receptor in diverse metazoan species and is particularly important in mammalian neural development and muscular structure. However, the complex… (more)

Subjects/Keywords: Congenital muscular dystrophy

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APA (6th Edition):

Praissman, J. L. (2015). The role of [beta]-1,4-glucuronyltransferase 1 in [alpha]-dystroglycan function. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/praissman_jeremy_l_201505_phd

Chicago Manual of Style (16th Edition):

Praissman, Jeremy Lawrence. “The role of [beta]-1,4-glucuronyltransferase 1 in [alpha]-dystroglycan function.” 2015. Doctoral Dissertation, University of Georgia. Accessed February 24, 2020. http://purl.galileo.usg.edu/uga_etd/praissman_jeremy_l_201505_phd.

MLA Handbook (7th Edition):

Praissman, Jeremy Lawrence. “The role of [beta]-1,4-glucuronyltransferase 1 in [alpha]-dystroglycan function.” 2015. Web. 24 Feb 2020.

Vancouver:

Praissman JL. The role of [beta]-1,4-glucuronyltransferase 1 in [alpha]-dystroglycan function. [Internet] [Doctoral dissertation]. University of Georgia; 2015. [cited 2020 Feb 24]. Available from: http://purl.galileo.usg.edu/uga_etd/praissman_jeremy_l_201505_phd.

Council of Science Editors:

Praissman JL. The role of [beta]-1,4-glucuronyltransferase 1 in [alpha]-dystroglycan function. [Doctoral Dissertation]. University of Georgia; 2015. Available from: http://purl.galileo.usg.edu/uga_etd/praissman_jeremy_l_201505_phd

16. Hayden, Edith Elizabeth. Examining the regulation of adipocytokine expression during chronic insulin resistance.

Degree: PhD, Biochemistry and Molecular Biology, 2012, University of Georgia

 Type II diabetes, characterized by hyperglycemia and hyperinsulinemia, results in many costly and debilitating patient complications. A broad range of tissues respond to insulin and… (more)

Subjects/Keywords: O-GlcNAc

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

APA (6th Edition):

Hayden, E. E. (2012). Examining the regulation of adipocytokine expression during chronic insulin resistance. (Doctoral Dissertation). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/hayden_edith_e_201208_phd

Chicago Manual of Style (16th Edition):

Hayden, Edith Elizabeth. “Examining the regulation of adipocytokine expression during chronic insulin resistance.” 2012. Doctoral Dissertation, University of Georgia. Accessed February 24, 2020. http://purl.galileo.usg.edu/uga_etd/hayden_edith_e_201208_phd.

MLA Handbook (7th Edition):

Hayden, Edith Elizabeth. “Examining the regulation of adipocytokine expression during chronic insulin resistance.” 2012. Web. 24 Feb 2020.

Vancouver:

Hayden EE. Examining the regulation of adipocytokine expression during chronic insulin resistance. [Internet] [Doctoral dissertation]. University of Georgia; 2012. [cited 2020 Feb 24]. Available from: http://purl.galileo.usg.edu/uga_etd/hayden_edith_e_201208_phd.

Council of Science Editors:

Hayden EE. Examining the regulation of adipocytokine expression during chronic insulin resistance. [Doctoral Dissertation]. University of Georgia; 2012. Available from: http://purl.galileo.usg.edu/uga_etd/hayden_edith_e_201208_phd

17. Stuart, Ryan Patrick. Establishing genotype-phenotype relationships in POMGnT1 associated with congenital muscular dystrophy.

Degree: MS, Biochemistry and Molecular Biology, 2013, University of Georgia

 Protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase1 (POMGnT1) is an influential glycosyltransferase required for modifying α-dystroglycan. Mutations in POMGnT1, removing GlcNAc modifications, have been associated with muscle-eye-brain (MEB) disease,… (more)

Subjects/Keywords: POMGnT1

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

APA (6th Edition):

Stuart, R. P. (2013). Establishing genotype-phenotype relationships in POMGnT1 associated with congenital muscular dystrophy. (Masters Thesis). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/stuart_ryan_p_201308_ms

Chicago Manual of Style (16th Edition):

Stuart, Ryan Patrick. “Establishing genotype-phenotype relationships in POMGnT1 associated with congenital muscular dystrophy.” 2013. Masters Thesis, University of Georgia. Accessed February 24, 2020. http://purl.galileo.usg.edu/uga_etd/stuart_ryan_p_201308_ms.

MLA Handbook (7th Edition):

Stuart, Ryan Patrick. “Establishing genotype-phenotype relationships in POMGnT1 associated with congenital muscular dystrophy.” 2013. Web. 24 Feb 2020.

Vancouver:

Stuart RP. Establishing genotype-phenotype relationships in POMGnT1 associated with congenital muscular dystrophy. [Internet] [Masters thesis]. University of Georgia; 2013. [cited 2020 Feb 24]. Available from: http://purl.galileo.usg.edu/uga_etd/stuart_ryan_p_201308_ms.

Council of Science Editors:

Stuart RP. Establishing genotype-phenotype relationships in POMGnT1 associated with congenital muscular dystrophy. [Masters Thesis]. University of Georgia; 2013. Available from: http://purl.galileo.usg.edu/uga_etd/stuart_ryan_p_201308_ms


University of Georgia

18. Stuchlik, Olga. Using Caenorhabditis elegans to elucidate the role of O-GlcNAc in insulin signal transduction.

Degree: MS, Biochemistry and Molecular Biology, 2006, University of Georgia

 O-GlcNAc is a regulatory carbohydrate post-translational modification found on serine and threonine residues on cytosolic and nuclear proteins in multicellular organisms. Global elevation of O-GlcNAc… (more)

Subjects/Keywords: O-GlcNAc Insulin Resistance C. elegans lifespan ogt-1 oga-1 O-GlcNAc transferase O-GlcNAcase

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

APA (6th Edition):

Stuchlik, O. (2006). Using Caenorhabditis elegans to elucidate the role of O-GlcNAc in insulin signal transduction. (Masters Thesis). University of Georgia. Retrieved from http://purl.galileo.usg.edu/uga_etd/stuchlik_olga_200612_ms

Chicago Manual of Style (16th Edition):

Stuchlik, Olga. “Using Caenorhabditis elegans to elucidate the role of O-GlcNAc in insulin signal transduction.” 2006. Masters Thesis, University of Georgia. Accessed February 24, 2020. http://purl.galileo.usg.edu/uga_etd/stuchlik_olga_200612_ms.

MLA Handbook (7th Edition):

Stuchlik, Olga. “Using Caenorhabditis elegans to elucidate the role of O-GlcNAc in insulin signal transduction.” 2006. Web. 24 Feb 2020.

Vancouver:

Stuchlik O. Using Caenorhabditis elegans to elucidate the role of O-GlcNAc in insulin signal transduction. [Internet] [Masters thesis]. University of Georgia; 2006. [cited 2020 Feb 24]. Available from: http://purl.galileo.usg.edu/uga_etd/stuchlik_olga_200612_ms.

Council of Science Editors:

Stuchlik O. Using Caenorhabditis elegans to elucidate the role of O-GlcNAc in insulin signal transduction. [Masters Thesis]. University of Georgia; 2006. Available from: http://purl.galileo.usg.edu/uga_etd/stuchlik_olga_200612_ms

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